US20010022282A1 - Process for removing impurities from kaolin clays - Google Patents
Process for removing impurities from kaolin clays Download PDFInfo
- Publication number
- US20010022282A1 US20010022282A1 US09/818,693 US81869301A US2001022282A1 US 20010022282 A1 US20010022282 A1 US 20010022282A1 US 81869301 A US81869301 A US 81869301A US 2001022282 A1 US2001022282 A1 US 2001022282A1
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- US
- United States
- Prior art keywords
- clay
- process according
- dispersion
- substituted
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 97
- 230000008569 process Effects 0.000 title claims abstract description 84
- 239000012535 impurity Substances 0.000 title claims abstract description 73
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 title claims description 20
- 239000005995 Aluminium silicate Substances 0.000 title claims description 18
- 235000012211 aluminium silicate Nutrition 0.000 title claims description 18
- 239000004927 clay Substances 0.000 claims abstract description 189
- 230000003750 conditioning effect Effects 0.000 claims abstract description 104
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 84
- 150000003839 salts Chemical class 0.000 claims abstract description 41
- 239000002270 dispersing agent Substances 0.000 claims abstract description 36
- 239000000654 additive Substances 0.000 claims abstract description 32
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000008394 flocculating agent Substances 0.000 claims abstract description 18
- 239000002253 acid Substances 0.000 claims abstract description 17
- -1 aromatic hydroxamic acids Chemical class 0.000 claims abstract description 14
- 230000003311 flocculating effect Effects 0.000 claims abstract description 8
- 239000006185 dispersion Substances 0.000 claims description 92
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 49
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 35
- 125000003107 substituted aryl group Chemical group 0.000 claims description 27
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 24
- 239000000194 fatty acid Substances 0.000 claims description 24
- 229930195729 fatty acid Natural products 0.000 claims description 24
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 24
- 150000004665 fatty acids Chemical class 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 230000001143 conditioned effect Effects 0.000 claims description 19
- 230000000996 additive effect Effects 0.000 claims description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 17
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical group [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 16
- 239000001110 calcium chloride Substances 0.000 claims description 16
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 15
- 239000004115 Sodium Silicate Substances 0.000 claims description 15
- 150000001768 cations Chemical class 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229920000620 organic polymer Polymers 0.000 claims description 14
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims description 14
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims description 14
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 14
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 14
- 125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 13
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 13
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 12
- 229910052783 alkali metal Inorganic materials 0.000 claims description 12
- 150000001340 alkali metals Chemical class 0.000 claims description 12
- 125000000129 anionic group Chemical group 0.000 claims description 12
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 12
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 12
- 239000003921 oil Substances 0.000 claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 claims description 10
- 229930195733 hydrocarbon Natural products 0.000 claims description 10
- 150000002430 hydrocarbons Chemical class 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 229920002401 polyacrylamide Polymers 0.000 claims description 10
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 7
- 239000005642 Oleic acid Substances 0.000 claims description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 7
- 239000010696 ester oil Substances 0.000 claims description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 6
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- 239000000908 ammonium hydroxide Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 4
- 229920000831 ionic polymer Polymers 0.000 claims 4
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 2
- 238000005189 flocculation Methods 0.000 abstract description 32
- 230000016615 flocculation Effects 0.000 abstract description 22
- 229920000642 polymer Polymers 0.000 abstract description 12
- 125000001931 aliphatic group Chemical group 0.000 abstract description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 27
- 239000007787 solid Substances 0.000 description 17
- 239000002245 particle Substances 0.000 description 15
- 238000000926 separation method Methods 0.000 description 12
- 235000017550 sodium carbonate Nutrition 0.000 description 9
- 238000009291 froth flotation Methods 0.000 description 8
- 238000000746 purification Methods 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- 229920000058 polyacrylate Polymers 0.000 description 7
- 229910052500 inorganic mineral Inorganic materials 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 239000011707 mineral Substances 0.000 description 6
- 235000010755 mineral Nutrition 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 125000002091 cationic group Chemical group 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 150000002431 hydrogen Chemical group 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 238000004061 bleaching Methods 0.000 description 4
- 150000001733 carboxylic acid esters Chemical class 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 4
- 235000013980 iron oxide Nutrition 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 235000019795 sodium metasilicate Nutrition 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 238000005188 flotation Methods 0.000 description 3
- 238000007885 magnetic separation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000005233 alkylalcohol group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical class [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920001560 Cyanamer® Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical class [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229910052788 barium Chemical class 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical class [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013401 experimental design Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000008206 lipophilic material Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Chemical class 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000011591 potassium Chemical group 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- JZWFDVDETGFGFC-UHFFFAOYSA-N salacetamide Chemical group CC(=O)NC(=O)C1=CC=CC=C1O JZWFDVDETGFGFC-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000019794 sodium silicate Nutrition 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical class OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000004876 x-ray fluorescence Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D3/00—Differential sedimentation
- B03D3/06—Flocculation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B1/00—Conditioning for facilitating separation by altering physical properties of the matter to be treated
- B03B1/04—Conditioning for facilitating separation by altering physical properties of the matter to be treated by additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/40—Compounds of aluminium
- C09C1/42—Clays
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/80—Compositional purity
Definitions
- This invention relates to an improved selective flocculation process for the separation of impurities from clay.
- the selective flocculation process of this invention is particularly useful for separating colored impurities from kaolin clays.
- Crude clays often contain well dispersed mineral impurities that must be removed from the clay prior to use.
- naturally occurring kaolin clays are contaminated with highly colored impurities composed of iron oxides and titanium oxides (rutile, anatase) and mixtures thereof.
- Purified kaolin clay is generally white and is suitable for many industrial uses, particularly as a pigment or filler in the paper industry.
- the technique chosen for the purification of crude clays is often determined by the type of clay (e.g. clays having different particle size distributions and/or different mean particle sizes) and the quantity and identity of the impurities that are to be removed from the clay.
- the most commonly used purification techniques include chemical bleaching, magnetic separation, froth flotation and selective flocculation.
- Chemical bleaching is generally used to remove iron impurities, but is not always effective. Chemical bleaching is generally ineffective at removing titanium impurities. Magnetic separation has proven useful for removing titanium impurities from some clays, but it is not useful for purifying clays containing very fine titanium particulates, as found in the ultra-fine kaolin clays mined from the eastern part of Georgia. Froth flotation and selective flocculation processes have proven to be the most useful techniques for the purification of these fine clays. Accordingly, many attempts to improve the efficiency of these processes for producing clays having higher purity have been made.
- U.S. Pat. No. 4,629,556 describes a froth flotation process using alkyl, aryl or alkylaryl hydroxamates as collectors for the removal of colored impurities.
- U.S. Pat. No. 4,871,466 describes a collector composition comprising alkyl or alkaryl hydroxamic acids, or salts thereof, and an aliphatic alcohol for the flotation of colored impurities.
- U.S. Pat. No. 5,522,986 describes a froth flotation process using a combination of a fatty acid and an alkyl hydroxamate compound, as a collector, to remove impurities in the form of a froth from a coarse grained kaolin clay dispersion.
- U.S. Pat. No. 3,138,550 discloses another froth flotation process for metallic minerals comprising adding an anionic polymeric flocculating agent to a mineral pulp already conditioned with a fatty acid, as a collector.
- the success of a froth flotation operation depends on the ability of the collector to effectively bind the impurities and to form a froth. Whereas the froth flotation process is generally effective with coarse grained clays, it has limited effectiveness with very fine clays. For this reason, many non-flotation processes, such as selective flocculation, have been developed as alternatives to flotation.
- U.S. Pat. Nos. 3,701,417 and 3,862,027 describe a selective flocculation process using a soluble source of polyvalent cations, specifically calcium chloride, and an anionic organic polyelectrolyte to selectively flocculate and remove impurities from an aqueous kaolin clay dispersion.
- Other related processes are described in U.S. Pat. Nos. 3,837,482 and 3,371,988.
- the foremost problem associated with the use of polyvalent cationic reagents is that these reagents bind to clay particles as well as to the impurities. These reagent-bound clay particles flocculate together with the impurities, which results in reduced recovery of the purified clay. It is often difficult to quantitate the amount of polyvalent cationic reagent required to purify a given clay sample without reducing clay recovery. Accordingly, balancing clay purity against clay recovery is a constant problem.
- monovalent cation conditioning agents such as ammonium salts
- U.S. Pat. No. 4,604,369 U.S. Pat. No. 3,837,482 describes a reverse flocculation process for purifying clay wherein the clay particles are flocculated, leaving the impurities dispersed in the aqueous suspension.
- the clay particles are flocculated by addition of an anionic polymeric flocculant. While such a process may be effective, its cost would be very disadvantageous.
- U.S. Pat. No. 5,535,890 describes a recent improvement to the selective flocculation process using a conditioning agent composition composed of a water soluble source of polyvalent cations and a fatty acid. Both the polyvalent cation source and the fatty acid are used in quantities insufficient to flocculate the clay particles. Separation of the impurities from clay is accomplished using a highly anionic, high molecular weight copolymer of polyacrylamide and acrylic acid.
- This invention is directed to an improved process for the selective flocculation of impurities from clay, particularly, kaolin clay.
- the process comprises blunging the clay in the presence of dispersing agents, treating the blunged clay with a conditioning agent, or a mixture of conditioning agents, composed of aliphatic or aromatic hydroxamic acids, or salts thereof, flocculating the impurities with a high molecular weight organic polymeric flocculant, and separating the flocculated impurities from the unflocculated clay.
- a conditioning agent or a mixture of conditioning agents, composed of aliphatic or aromatic hydroxamic acids, or salts thereof
- flocculating the impurities with a high molecular weight organic polymeric flocculant and separating the flocculated impurities from the unflocculated clay.
- hydroxamic acid conditioning agents improves the removal of impurities from the clay, thereby providing a clay product having high brightness and low level impurities.
- the hydroxamic acid conditioning agents may advantageously be used in combination with other conditioning additives, including alcohols, fatty acids, hydrocarbon oils, and carboxylic acid esters, or with salts containing polyvalent cations. Additionally, the conditioning agents of the present invention are useful with a wide variety of anionic and non-ionic water soluble or water-dispersible polymeric flocculating agents, particularly polymers containing pendant hydroxamate groups.
- a further embodiment of this invention is the use of a hydroxamate-containing polymeric flocculant to selectively flocculate impurities from clay slurries which have been treated with a fatty acid and a polyvalent metal salt as conditioning agents.
- the improved process of this invention utilizes selective flocculation of mineral impurities from an aqueous crude clay dispersion using alkyl or aryl hydroxamic acids, or salts thereof, as conditioning agents.
- This process is particularly useful for selective flocculation of impurities found in ultra-fine kaolin clays, which are not readily purified using conventional techniques, such as froth flotation.
- the clay dispersion is treated with an alkyl, aryl or aralkyl hydroxamate conditioning agent, or a mixture of hydroxamate conditioning agents, that selectively binds to the mineral impurities commonly found in the crude clays.
- Flocculation, and subsequent separation of the conditioned clay impurities is accomplished by addition of high molecular weight organic polymeric flocculating agents.
- strongly anionic polymeric flocculating agents have been commonly used.
- alkyl, aryl or aralkyl hydroxamate conditioning agents advantageously allows for the step of flocculation to be performed using either anionic or non-ionic high molecular weight flocculating agents, and particularly polymeric flocculants containing hydroxamate groups.
- polymers containing hydroxamate groups may be advantageously used when the clay dispersion is treated with fatty acids as conditioning agents.
- flocculation of the impurities occurs rapidly to form a two phase mixture having an upper phase containing the purified milky-white clay suspension, and a lower phase containing the impurity-rich flocculated material. Separation of the two layers may be accomplished by any of the techniques conventionally used in flocculation operations.
- the process of the present invention is flexible and may be used to effectively purify different types of clays containing a variety of different impurities.
- the present process may be advantageously used to separate a wide variety of minerals from one another.
- iron oxides may be readily separated from silica or silicates, or cassiterite (tin oxide) may be separated from gangue in ores, ore concentrates or ore pre-concentrates.
- effective removal of impurities may be obtained using the process of the present invention without the use of polyvalent cationic salts, although these salts may be used in conjunction with alkyl hydroxamic acids and other conditioning aids, such as fatty acids, to enhance the purity of the clay.
- fine kaolin clays generally contain grit, composed of +325 mesh (U.S. Sieve) particles, which generally must be separated from the crude clay prior to the purification process.
- This additional separation step may be eliminated using the selective flocculation process of this invention because the grit may simply be removed with the flocculated impurities.
- the aqueous clay dispersion is prepared by blunging, or mixing, the clay in water to form a finely dispersed mixture having a milk-like consistency.
- This clay dispersion is also called a slip.
- the objective in forming the aqueous clay dispersion is to form a clay composition wherein the crude clay particles are not aggregated with each other, but are uniformly dispersed.
- the concentration of the dry crude clay in the aqueous clay dispersion is generally about 50% to about 70% by weight of the total weight of the dispersion. In the art, this concentration is described as about 50% “solids” to about 70% “solids”.
- a dispersing agent is a material that is used to impart a highly negative overall charge onto the surface of the clay particles, thereby inducing particle-particle repulsion and preventing particle aggregation.
- exemplary dispersing agents that may be useful for preparing a well-dispersed aqueous clay dispersion include sodium silicate, sodium metasilicate, sodium carbonate, sodium or ammonium polyacrylate, hexametaphosphate or the like.
- Preferred dispersing agents include, for example, sodium silicate, soda ash, and sodium polyacrylate.
- the dispersing agent may be added as a solid, or may be pre-dissolved in water and added in an aqueous solution.
- the amount of dispersing agent used to form a finely dispersed clay mixture will vary from sample to sample and for each type of clay, but is generally in the range of about 0.05 to about 10 kilogram (kg) of the dispersing agent per ton of crude clay (on a dry solids basis) depending on the type of dispersing agent and type of clay crude used.
- the concentration of the dispersing agent(s) is selected to provide enhanced dispersion of the clay in the clay dispersion which consequently provides enhanced separation of the colored impurities from the clay. Reduction of the viscosity of the dispersed clay dispersion is frequently used as a guide for obtaining a well dispersed clay slip, but ultimately the preferred dispersion is judged by the separation obtained between colored impurities and clay.
- Combinations of two or more dispersing agents may be used to improve the formation of the aqueous clay dispersion and the efficiency of the overall purification process.
- Effective dispersing agent combinations include, for example, soda ash and low molecular weight sodium polyacrylate (molecular weight in the range of 1000-20,000), or sodium silicate and sodium polyacrylate, or a combination of sodium carbonate, sodium silicate and sodium polyacrylate.
- sodium or ammonium polyacrylate are used as one of the dispersing agents.
- Polyacrylate dispersing agents are commercially available from many suppliers under different trade names, for example, Cyanamer P70® (sodium polyacrylate) sold by Cytec Industries Inc., West Paterson, N.J.
- the agents comprising the combination may be added to the clay dispersion either sequentially or simultaneously.
- the preferred addition method and the individual use rates for each dispersing agent may be established without undue by experimentation by those skilled in the art.
- the use rates for the dispersing agents are in the range of about 1 to about 5 kilograms/ton of clay for sodium silicates, preferably about 2 to about 4 kilograms/ton; in the range of about 0.05 to about 1.0 kilograms/ton for polyacrylates, preferably, about 0.2 to about 0.4 kilograms/ton; and in the range of about 0.25 to about 2.5 kilograms/ton for sodium carbonate, preferably about 0.5 to about 1.5 kilograms/ton.
- the use rates are dictated by the type of crude clay being treated and the overall separation efficiency between colored impurities and the clay.
- Statistical experimental designs such as two- or three-factor, three-level factorial designs, may be useful in determining the use rates, when combinations of dispersing agents are used. See generally, Statistics for Experimenters, by Box, Hunter and Hunter, John Wiley & Sons, Inc., 1978.
- “Conditioning” of the clay dispersion is a conventional process wherein the clay dispersion is mixed with a conditioning agent to develop dissimilar surfaces between the dispersed clay particles and the impurities, to thereby promote the subsequent separation process. Conditioning is accomplished by treatment of the well-dispersed clay slip with a conditioning agent, or a mixture of conditioning agents, comprising compounds that are N-hydroxy derivatives of amides, or hydroxamic acid derivatives. These compounds are referred to herein as “hydroxamate conditioning agents”.
- the hydroxamate conditioning agent, or a mixture of hydroxamate conditioning agents, used herein are represented by the formula:
- R is linear or branched C 2 -C 18 alkyl, linear or branched C 2 -C 18 alkenyl, C 6 -C 20 aryl, substituted aryl, C7-C 26 aralkyl or substituted aralkyl;
- R′′ is H, C 1 -C 12 alkyl or C 7 -C 26 aralkyl;
- M is hydrogen, an alkali metal or ammonium (NH 3 ), wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C 1 -C 6 alkoxy, or C 1 -C 6 alkyl.
- exemplary aralkyl moieties include benzyl, salicyl, and the like.
- aryl is phenyl or naphthyl.
- the hydroxamate conditioning agents are alkyl hydroxamic acids, or salts thereof, wherein R is linear or branched C 8 -C 12 alkyl, linear or branched C 8 -C 12 alkenyl, aryl or substituted aryl; R′′ is hydrogen; and M is selected from hydrogen, sodium, potassium or ammonium.
- the hydroxamate conditioning agent or the mixture of hydroxamate conditioning agents, may be added as a solid, a liquid, or as a solution or a dispersion in water.
- the amount of hydroxamate conditioning agent required for purification of a given clay sample will vary depending on the type of clay and the amount of impurities to be removed, the hydroxamate conditioning agents may generally be used in the process of the present invention in an amount of about 250 grams/ton of clay to about 2,000 grams /ton of clay.
- the hydroxamate conditioning agent, or mixtures thereof may be used alone or may be optionally used in combination with other conditioning additives.
- the conditioning treatment described herein comprises treatment of the aqueous clay dispersion with a hydroxamate conditioning agent and a conditioning additive, either simultaneously or sequentially.
- a conditioning agent composition may be used to condition the clay sample.
- the conditioning agent composition of this invention is comprised of the hydroxamate conditioning agent, or mixtures thereof, in combination with at least one conditioning additive selected from an alkyl or aralkyl alcohol, hydrocarbon oil, carboxylic acid ester, or fatty acid represented by the formula:
- R is a C 10 -C 18 alkyl, C 6 -C 20 aryl, substituted aryl, C 7 -C 26 aralkyl or substituted aralkyl
- M is hydrogen, an alkali metal or ammonium (NH 3 ), wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C 1 -C 6 alkoxy, or C 1 -C 6 alkyl.
- R is C 16 -C 18 alkyl, C 6 -C20 aryl, substituted aryl, C 7 -C 26 aralkyl or substituted aralkyl
- M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C 1 -C 6 alkoxy, or C 1 -C 6 alkyl.
- Conditioning additives are lipophilic materials that have low water solubility in water that enhance the conditioning of the slurry with the conditioning agent and the subsequent separation process.
- Alcohol conditioning additives that may be useful in the process of this invention include long chain branched or linear C 10 to C 22 alkyl alcohols, preferably C 12 to C 16 alkyl alcohols, or C 7 -C 26 aralkyl alcohols.
- decanol or dodecanol may be used as conditioning additives.
- Useful hydrocarbon oil conditioning additives are composed of branched or linear C 12 to C 32 alkanes or alkenes, preferably C 12 to C 20 alkanes or alkenes.
- Useful carboxylic acid ester conditioning additives comprise branched or linear C 9 to C 22 hydrocarbon moieties, comprising alkanes, alkenes, or aryl moieties.
- the hydroxamate conditioning agent may be advantageously pre-dissolved or pre-dispersed in the alkyl alcohol or hydrocarbon oil and added directly to the aqueous clay dispersion.
- the conditioning additives typically may be used in an amount of about 50% to about 200% by weight, relative to the amount by weight of alkyl hydroxamate conditioning agent.
- Useful fatty acid conditioning additives are comprised of C 12 -C 18 alkyl, C 6 -C 20 aryl, substituted aryl, C 7 -C 26 aralkyl or substituted aralkyl acids or salts thereof.
- oleic acid is used as a fatty acid conditioning agent.
- the aqueous clay dispersion may be conditioned with the hydroxamate conditioning agents and the optional fatty acid conditioning additive, sequentially, in any order, or simultaneously.
- the fatty acid and hydroxamate may be added directly to the aqueous clay dispersion as neat oils, or may be added as a dispersion in water.
- the fatty acid may be advantageously used in an amount of about 500 grams/ton to about 3,000 grams/ton of crude clay, although that amount may vary depending on the type of clay and the amount of impurities to be removed from the clay.
- the process of this invention may also include the use of a salt containing a polyvalent metal cation, particularly the alkaline earth metal salts of calcium, magnesium and barium.
- a polyvalent metal cation particularly the alkaline earth metal salts of calcium, magnesium and barium.
- Incorporation of a polyvalent cationic salt is not required for effective purification of clays using the process of this invention, and may be substantially absent.
- These salts may be optionally added to further improve the overall process.
- Salts that are useful as conditioning additives are well known, and are generally water soluble salts that may be added directly to the aqueous clay dispersion as a solid or in solution.
- a preferred polyvalent metal cation containing salt is calcium chloride.
- the salts may be added simultaneously with, or prior to, the addition of the hydroxamate conditioning agent, or mixtures thereof, in combination with any of the conditioning additives described above.
- the salt may be added in an amount generally in the range of about 0 grams/ton to about 1,000 grams/ton of crude clay, and preferably at about 250 grams/ton of crude clay, depending on the type of clay and the amount of impurities to be removed from the particular clay sample.
- the clay dispersion, conditioned with hydroxamate and other additives, if any, may be transferred from a blunging/conditioning vessel, such as a mixing tank, or a blender pitcher, to another vessel that would permit subsequent removal of the flocculated impurities, e.g., a settling vessel.
- the density or % solids of the clay dispersion may be adjusted by addition of water, as necessary, for enhanced flocculation and separation.
- the clay concentration in the clay dispersion is reduced such that the clay concentration is in the range of about 10% to about 30% solids, prior to addition of the flocculating agent.
- the density of the clay dispersion may be adjusted upon addition of the polymer solution.
- Selective flocculation of the impurities may be accomplished by adding a dilute solution of the polymer, typically, at about 0.01% to about 0.1% by weight, with low shear mixing.
- a pH modifying agent is a material having a basic pH (greater than 7.0) that is capable of maintaining the pH of the aqueous clay dispersion in the range of 7.5-10.5, and preferably in the range of 8.0-9.5.
- Useful pH modifying agents include, without limitation, water soluble agents such as ammonia or ammonium hydroxide, sodium or potassium hydroxide and sodium carbonate.
- the preferred pH modifying agents include, for example, sodium hydroxide or ammonium hydroxide.
- the amount of the pH modifying agent added to the clay dispersion will be that amount necessary to adjust the pH of the aqueous clay dispersion to about 7.5 to about 10.5.
- the pH modifying agent is commonly added during the blunging step, generally as a solid, but it may be pre-dissolved in water and added as a aqueous solution.
- the impurities in the clay dispersion are flocculated (e.g. aggregated and precipitated) from the dispersion by addition of a flocculating agent.
- the flocculating agent may be added to the conditioned clay dispersion as a dilute water solution.
- useful flocculating agents are high molecular weight organic polymers that are anionic or non-ionic water soluble or water-dispersible organic polymers, having a molecular weight in the range of about 0.5 million to about 30 million, and preferably a molecular weight in the range of about 1.0 million to about 20 million.
- organic polymeric flocculants include, but are not limited to hydrolyzed polyacrylamides, co-polymers of acrylamide and acrylic acid, copolymers of acrylamide and acrylamidomethylpropanesulfonic acid, vinyl sulfonic acids, carboxymethyl cellulose, polystyrene sulfonic acids, water soluble polymers containing pendant hydroxamic acid functionality, and salts there of, such as hydroxamated polyacrylamides or polyacrylates, water-soluble or dispersible polyethylene oxide polymers, and other non-ionic water soluble or water-dispersible polymers such as polyacrylamides and polyvinyl alcohols.
- Preferred polymeric flocculants of this invention are hydroxamated polyacrylamides and hydroxamated polyacrylates.
- hydroxamated polyacrylamides and hydroxamated polyacrylates may be used to selectively flocculate impurities from clays that have been treated with conditioning agents comprising fatty acids and alkaline earth metal salts.
- This process comprises the steps of forming an aqueous clay dispersion by blunging the clay with a dispersing agent, or a combination of dispersing agents, in water; treating the aqueous clay dispersion with a conditioning agent represented by the formula:
- R is C 10 -C 18 alkyl, C 6 -C 20 aryl, substituted aryl, C 7 -C 26 aralkyl or substituted aralkyl
- M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C 1 -C 6 alkoxy, or C 1 -C 6 alkyl; flocculating the conditioned clay dispersion by treatment with a water soluble or water dispersible organic polymer containing hydroxamic acid groups or salts thereof, and removing the flocculated impurities to form a purified clay dispersion.
- the amount of polymeric flocculant used to purify a clay sample will vary depending upon the type of clay used and the amount of impurity to be flocculated from the particular clay sample.
- the general use rates of the polymeric flocculant in the process of the present invention are in the range of about 20 grams/ton to about 200 grams/ton of crude clay.
- the aqueous clay dispersion may be also treated with a salt containing a polyvalent metal cation.
- the salt is calcium chloride.
- the clay dispersion is also treated with at least one conditioning additive selected from an aliphatic alcohol, a hydrocarbon oil or a carboxylic acid ester oil.
- the conditioning additive may be decanol or dodecanol.
- Useful dispersing agents include sodium silicate, sodium polyacrylate, or sodium carbonate.
- Rapid flocculation of the colored impurities in the aqueous clay dispersion generally occurs upon addition of the polymeric flocculating agent.
- the flocculated impurities settle to form a highly colored lower layer, leaving a milky-white upper layer of purified clay.
- This upper clay layer may be isolated from the lower impurity-containing layer by any of the conventional processes used in selective flocculation operations which are well known to those skilled in the art.
- the upper layer may be decanted away from the lower layer, or alternatively, the lower layer may be drained off from the bottom.
- Other apparatus such as a drag box or a low shear centrifugal device, may also be used to separate the lower impurity-containing layer from the purified upper clay layer.
- the purified clay produced by the process of this invention possesses high brightness and low levels of impurities.
- the purity of this product may be further improved by using the conventional techniques of magnetic separation or chemical bleaching.
- a 60% solids dispersion of kaolin clay was prepared by blunging (mixing) 386 g. of the crude clay (approximately 330 g. of clay on a dry weight basis) containing 3.0% TiO 2 with 500 grams/ton sodium carbonate, 3000 grams/ton sodium metasilicate, 250 grams/ton of sodium polyacrylate, and 400 grams/ton of sodium hydroxide (to obtain a blunged slurry having a pH of approximately 8.5-9) in water for 5 minutes using a Waring laboratory blender at high speed.
- Aero 6493® a mixture of alkyl hydroxamates, sold by Cytec Industries Inc., West Paterson, N.J.
- a conditioning agent a conditioning agent
- the concentration of the clay in the dispersion was reduced to about 20% by weight by addition of water.
- the clay slurry was mixed gently using a stainless steel plunger with holes, typically used in flocculation tests. The mixture was allowed to stand for 30 min. during which time the physical attributes of the selective flocculation process, such as floc formation, the appearance of flocs, and the rate of settling, were observed. The volumes of settled and suspended phases were noted, and samples from each phase were analyzed for Ti content, using x-ray fluorescence (see Table 1).
- Comparative tests were performed using the procedure described above, but without addition of any conditioning agent(s) prior to flocculant addition.
- the prior art selective flocculation process was conducted using oleic acid as a fatty acid at 2500 grams/ton in combination with calcium chloride at 385 grams/ton.
- the dispersing agents used in this test were 2600 grams/ton of sodium metasilicate and 300 grams/ton of sodium polyacrylate.
- the TiO 2 content in the clay product is reduced from about 3% by weight in the crude clay to about 2.1% by weight, i.e. a reduction of 0.9%.
- Use of alkyl hydroxamic acid as the conditioning agent reduced the TiO 2 content in the clay product by more than 1.3%, relative to the control where no conditioning agent was used, or by about 2.2%, relative to the crude clay.
- the TiO 2 content in the clay product is reduced by about 0.25% relative to the prior art process using fatty acid, CaCl 2 and a highly charged, high molecular weight copolymer of acrylic acid and acrylamide.
- a solids dispersion was prepared according to the procedure set forth in Example 1, except that 1000 grams/ton sodium carbonate, 2000 grams/ton of sodium metasilicate, 175 grams/ton of sodium polyacrylate, and only 600 grams/ton of Aero 6493® were blunged with the kaolin clay.
- the TiO 2 concentration of the clay, after selective flocculation follows: 1.17% for Polymer A (use rate 30 grams/ton), 1.02% for Polymer B (6.5 grams/ton), and 1.00% for Polymer C (18 grams/ton).
- a solids dispersion was prepared according to the procedure set forth in Example 1, except that the conditioning agent was a mixture of C 8 -C 10 alkyl hydroxamic acids.
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- a solids dispersion was prepared according to the procedure set forth in Example 2, except that a conditioning agent combination, consisting of a mixture of C 8 -C 10 alkyl hydroxamic acids (conditioning agent) and a oleic acid (conditioning additive), was used to condition the clay dispersion.
- the conditioning agent combination was added simultaneously with the calcium chloride to the blunged clay dispersion.
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- a solids dispersion was prepared according to the procedure set forth in Example 3, except that the conditioning agent combination consisted of a mixture of C 8 -C 10 alkyl hydroxamic acids (conditioning agent) and a hydrocarbon oil (conditioning additive).
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- a solids dispersion was prepared according to the procedure set forth in Example 3, except that the conditioning agent combination consisted of a mixture of C 8 -C 10 alkyl hydroxamic acids (conditioning agent) and methyl palmitate ester oil (conditioning additive).
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- a solids dispersion was prepared according to the procedure set forth in Example 4, except that the conditioning agent combination, consisting of a mixture of C 8 -C 10 alkyl hydroxamic acids (conditioning agent) and a oleic acid (conditioning additive), was used in combination with calcium chloride to condition the clay dispersion.
- the conditioning agent combination was added simultaneously with the calcium chloride to the blunged clay dispersion.
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- a solids dispersion was prepared according to the procedure set forth in Example 1, except that the flocculant was a polyethylene oxide.
- the reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
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Abstract
An improved process for the selective flocculation of impurities from clays is disclosed. The process comprises blunging the clay in the presence of dispersing agents, conditioning the blunged clay with aliphatic or aromatic hydroxamic acids, or salts thereof, flocculating the impurities with a high molecular weight polymeric flocculant, particularly polymers containing hydroxamate groups, and removing the flocculated impurities from the unflocculated clay. The use of hydroxamic conditioning agents improves the removal of impurities from the clay, thereby providing a clay product having high brightness and low level impurities. The hydroxamic acid conditioning agents may advantageously be used in combination with other conditioning additives and with a wide variety of polymeric flocculating agents.
Description
- 1. Field of the Invention
- This invention relates to an improved selective flocculation process for the separation of impurities from clay. The selective flocculation process of this invention is particularly useful for separating colored impurities from kaolin clays.
- 2. Background of the Invention
- Crude clays often contain well dispersed mineral impurities that must be removed from the clay prior to use. For example, naturally occurring kaolin clays are contaminated with highly colored impurities composed of iron oxides and titanium oxides (rutile, anatase) and mixtures thereof. Purified kaolin clay is generally white and is suitable for many industrial uses, particularly as a pigment or filler in the paper industry. The technique chosen for the purification of crude clays is often determined by the type of clay (e.g. clays having different particle size distributions and/or different mean particle sizes) and the quantity and identity of the impurities that are to be removed from the clay. The most commonly used purification techniques include chemical bleaching, magnetic separation, froth flotation and selective flocculation. Chemical bleaching is generally used to remove iron impurities, but is not always effective. Chemical bleaching is generally ineffective at removing titanium impurities. Magnetic separation has proven useful for removing titanium impurities from some clays, but it is not useful for purifying clays containing very fine titanium particulates, as found in the ultra-fine kaolin clays mined from the eastern part of Georgia. Froth flotation and selective flocculation processes have proven to be the most useful techniques for the purification of these fine clays. Accordingly, many attempts to improve the efficiency of these processes for producing clays having higher purity have been made.
- For example, U.S. Pat. No. 4,629,556 describes a froth flotation process using alkyl, aryl or alkylaryl hydroxamates as collectors for the removal of colored impurities. U.S. Pat. No. 4,871,466 describes a collector composition comprising alkyl or alkaryl hydroxamic acids, or salts thereof, and an aliphatic alcohol for the flotation of colored impurities. U.S. Pat. No. 5,522,986 describes a froth flotation process using a combination of a fatty acid and an alkyl hydroxamate compound, as a collector, to remove impurities in the form of a froth from a coarse grained kaolin clay dispersion. U.S. Pat. No. 3,138,550 discloses another froth flotation process for metallic minerals comprising adding an anionic polymeric flocculating agent to a mineral pulp already conditioned with a fatty acid, as a collector. The success of a froth flotation operation depends on the ability of the collector to effectively bind the impurities and to form a froth. Whereas the froth flotation process is generally effective with coarse grained clays, it has limited effectiveness with very fine clays. For this reason, many non-flotation processes, such as selective flocculation, have been developed as alternatives to flotation.
- For example, U.S. Pat. Nos. 3,701,417 and 3,862,027, describe a selective flocculation process using a soluble source of polyvalent cations, specifically calcium chloride, and an anionic organic polyelectrolyte to selectively flocculate and remove impurities from an aqueous kaolin clay dispersion. Other related processes are described in U.S. Pat. Nos. 3,837,482 and 3,371,988. The foremost problem associated with the use of polyvalent cationic reagents is that these reagents bind to clay particles as well as to the impurities. These reagent-bound clay particles flocculate together with the impurities, which results in reduced recovery of the purified clay. It is often difficult to quantitate the amount of polyvalent cationic reagent required to purify a given clay sample without reducing clay recovery. Accordingly, balancing clay purity against clay recovery is a constant problem.
- To overcome the problems encountered with the use of polyvalent cationic reagents, monovalent cation conditioning agents, such as ammonium salts, are used in the process described in U.S. Pat. No. 4,604,369. U.S. Pat. No. 3,837,482 describes a reverse flocculation process for purifying clay wherein the clay particles are flocculated, leaving the impurities dispersed in the aqueous suspension. The clay particles are flocculated by addition of an anionic polymeric flocculant. While such a process may be effective, its cost would be very disadvantageous. Instead of selectively flocculating the relatively small amount of impurities, typically 2-4% by weight of crude clay, this process selectively flocculates the clay itself, typically 80-95% by weight of crude clay. Ravishanker et al. ( Bull. Mater. Sci., Vol. 10, No. 5, August 1988, pp. 423-433) describe selective flocculation of iron oxide from a 1:1 synthetic mixture of iron oxide and kaolin using hydroxamated polyacrylamide. Clauss et al. (Intl. J. Miner. Process., Vol. 3, 1976, p.27) describe selective flocculation of cassiterite using a modified polyacrylamide flocculant containing hydroxamate functional groups.
- U.S. Pat. No. 5,535,890 describes a recent improvement to the selective flocculation process using a conditioning agent composition composed of a water soluble source of polyvalent cations and a fatty acid. Both the polyvalent cation source and the fatty acid are used in quantities insufficient to flocculate the clay particles. Separation of the impurities from clay is accomplished using a highly anionic, high molecular weight copolymer of polyacrylamide and acrylic acid.
- Despite the many attempts described above to improve the traditional clay purification processes, there remains a need for a highly efficient, high through-put process that can produce purified clays of varying particle size at low cost.
- This invention is directed to an improved process for the selective flocculation of impurities from clay, particularly, kaolin clay. The process comprises blunging the clay in the presence of dispersing agents, treating the blunged clay with a conditioning agent, or a mixture of conditioning agents, composed of aliphatic or aromatic hydroxamic acids, or salts thereof, flocculating the impurities with a high molecular weight organic polymeric flocculant, and separating the flocculated impurities from the unflocculated clay. The use of hydroxamic acid conditioning agents improves the removal of impurities from the clay, thereby providing a clay product having high brightness and low level impurities. The hydroxamic acid conditioning agents may advantageously be used in combination with other conditioning additives, including alcohols, fatty acids, hydrocarbon oils, and carboxylic acid esters, or with salts containing polyvalent cations. Additionally, the conditioning agents of the present invention are useful with a wide variety of anionic and non-ionic water soluble or water-dispersible polymeric flocculating agents, particularly polymers containing pendant hydroxamate groups. A further embodiment of this invention is the use of a hydroxamate-containing polymeric flocculant to selectively flocculate impurities from clay slurries which have been treated with a fatty acid and a polyvalent metal salt as conditioning agents.
- The improved process of this invention utilizes selective flocculation of mineral impurities from an aqueous crude clay dispersion using alkyl or aryl hydroxamic acids, or salts thereof, as conditioning agents. This process is particularly useful for selective flocculation of impurities found in ultra-fine kaolin clays, which are not readily purified using conventional techniques, such as froth flotation. The clay dispersion is treated with an alkyl, aryl or aralkyl hydroxamate conditioning agent, or a mixture of hydroxamate conditioning agents, that selectively binds to the mineral impurities commonly found in the crude clays. Flocculation, and subsequent separation of the conditioned clay impurities, is accomplished by addition of high molecular weight organic polymeric flocculating agents. In the prior art, strongly anionic polymeric flocculating agents have been commonly used. It has been found that the use of alkyl, aryl or aralkyl hydroxamate conditioning agents in the process of this invention, advantageously allows for the step of flocculation to be performed using either anionic or non-ionic high molecular weight flocculating agents, and particularly polymeric flocculants containing hydroxamate groups. Furthermore, it has been found that polymers containing hydroxamate groups may be advantageously used when the clay dispersion is treated with fatty acids as conditioning agents. After addition of the flocculating agent to the conditioned dispersion, flocculation of the impurities occurs rapidly to form a two phase mixture having an upper phase containing the purified milky-white clay suspension, and a lower phase containing the impurity-rich flocculated material. Separation of the two layers may be accomplished by any of the techniques conventionally used in flocculation operations.
- The process of the present invention is flexible and may be used to effectively purify different types of clays containing a variety of different impurities. With appropriate modifications, which are readily accomplished by those skilled in the art, the present process may be advantageously used to separate a wide variety of minerals from one another. For example, iron oxides may be readily separated from silica or silicates, or cassiterite (tin oxide) may be separated from gangue in ores, ore concentrates or ore pre-concentrates. Significantly, effective removal of impurities may be obtained using the process of the present invention without the use of polyvalent cationic salts, although these salts may be used in conjunction with alkyl hydroxamic acids and other conditioning aids, such as fatty acids, to enhance the purity of the clay.
- Use of the selective flocculation process of the present invention provides additional benefits. For example, fine kaolin clays generally contain grit, composed of +325 mesh (U.S. Sieve) particles, which generally must be separated from the crude clay prior to the purification process. This additional separation step may be eliminated using the selective flocculation process of this invention because the grit may simply be removed with the flocculated impurities.
- The aqueous clay dispersion is prepared by blunging, or mixing, the clay in water to form a finely dispersed mixture having a milk-like consistency. This clay dispersion is also called a slip. The objective in forming the aqueous clay dispersion is to form a clay composition wherein the crude clay particles are not aggregated with each other, but are uniformly dispersed. The concentration of the dry crude clay in the aqueous clay dispersion is generally about 50% to about 70% by weight of the total weight of the dispersion. In the art, this concentration is described as about 50% “solids” to about 70% “solids”.
- Advantageously, in the method of this invention, at least one dispersing agent is added during the blunging step, to increase the dispersibility of the clay in water. As used herein, a dispersing agent is a material that is used to impart a highly negative overall charge onto the surface of the clay particles, thereby inducing particle-particle repulsion and preventing particle aggregation. Exemplary dispersing agents that may be useful for preparing a well-dispersed aqueous clay dispersion include sodium silicate, sodium metasilicate, sodium carbonate, sodium or ammonium polyacrylate, hexametaphosphate or the like. Preferred dispersing agents include, for example, sodium silicate, soda ash, and sodium polyacrylate.
- The dispersing agent may be added as a solid, or may be pre-dissolved in water and added in an aqueous solution. The amount of dispersing agent used to form a finely dispersed clay mixture will vary from sample to sample and for each type of clay, but is generally in the range of about 0.05 to about 10 kilogram (kg) of the dispersing agent per ton of crude clay (on a dry solids basis) depending on the type of dispersing agent and type of clay crude used. The concentration of the dispersing agent(s) is selected to provide enhanced dispersion of the clay in the clay dispersion which consequently provides enhanced separation of the colored impurities from the clay. Reduction of the viscosity of the dispersed clay dispersion is frequently used as a guide for obtaining a well dispersed clay slip, but ultimately the preferred dispersion is judged by the separation obtained between colored impurities and clay.
- Combinations of two or more dispersing agents may be used to improve the formation of the aqueous clay dispersion and the efficiency of the overall purification process. Effective dispersing agent combinations include, for example, soda ash and low molecular weight sodium polyacrylate (molecular weight in the range of 1000-20,000), or sodium silicate and sodium polyacrylate, or a combination of sodium carbonate, sodium silicate and sodium polyacrylate. Preferably, sodium or ammonium polyacrylate are used as one of the dispersing agents. Polyacrylate dispersing agents are commercially available from many suppliers under different trade names, for example, Cyanamer P70® (sodium polyacrylate) sold by Cytec Industries Inc., West Paterson, N.J. When a combination of dispersing agents is used, the agents comprising the combination may be added to the clay dispersion either sequentially or simultaneously. The preferred addition method and the individual use rates for each dispersing agent may be established without undue by experimentation by those skilled in the art. Generally, the use rates for the dispersing agents are in the range of about 1 to about 5 kilograms/ton of clay for sodium silicates, preferably about 2 to about 4 kilograms/ton; in the range of about 0.05 to about 1.0 kilograms/ton for polyacrylates, preferably, about 0.2 to about 0.4 kilograms/ton; and in the range of about 0.25 to about 2.5 kilograms/ton for sodium carbonate, preferably about 0.5 to about 1.5 kilograms/ton. The use rates are dictated by the type of crude clay being treated and the overall separation efficiency between colored impurities and the clay. Statistical experimental designs, such as two- or three-factor, three-level factorial designs, may be useful in determining the use rates, when combinations of dispersing agents are used. See generally, Statistics for Experimenters, by Box, Hunter and Hunter, John Wiley & Sons, Inc., 1978.
- “Conditioning” of the clay dispersion is a conventional process wherein the clay dispersion is mixed with a conditioning agent to develop dissimilar surfaces between the dispersed clay particles and the impurities, to thereby promote the subsequent separation process. Conditioning is accomplished by treatment of the well-dispersed clay slip with a conditioning agent, or a mixture of conditioning agents, comprising compounds that are N-hydroxy derivatives of amides, or hydroxamic acid derivatives. These compounds are referred to herein as “hydroxamate conditioning agents”. The hydroxamate conditioning agent, or a mixture of hydroxamate conditioning agents, used herein are represented by the formula:
- R−C(=O)N(R″)−OM
- wherein R is linear or branched C 2-C18 alkyl, linear or branched C2-C18 alkenyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl; R″ is H, C1-C12 alkyl or C7-C26 aralkyl; and M is hydrogen, an alkali metal or ammonium (NH3), wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl. As used herein, aralkyl represents a moiety comprising an alkyl moiety bonded at either R, R″, or both, of R−C(=O)N(R″)−OM, wherein the alkyl moiety possesses an aryl, or a substituted aryl substituent. Exemplary aralkyl moieties include benzyl, salicyl, and the like. Preferably, aryl is phenyl or naphthyl. More preferably, the hydroxamate conditioning agents are alkyl hydroxamic acids, or salts thereof, wherein R is linear or branched C8-C12 alkyl, linear or branched C8-C12 alkenyl, aryl or substituted aryl; R″ is hydrogen; and M is selected from hydrogen, sodium, potassium or ammonium.
- The hydroxamate conditioning agent, or the mixture of hydroxamate conditioning agents, may be added as a solid, a liquid, or as a solution or a dispersion in water. Although the amount of hydroxamate conditioning agent required for purification of a given clay sample will vary depending on the type of clay and the amount of impurities to be removed, the hydroxamate conditioning agents may generally be used in the process of the present invention in an amount of about 250 grams/ton of clay to about 2,000 grams /ton of clay. The hydroxamate conditioning agent, or mixtures thereof, may be used alone or may be optionally used in combination with other conditioning additives. The conditioning treatment described herein comprises treatment of the aqueous clay dispersion with a hydroxamate conditioning agent and a conditioning additive, either simultaneously or sequentially.
- Optionally, a conditioning agent composition may be used to condition the clay sample. The conditioning agent composition of this invention is comprised of the hydroxamate conditioning agent, or mixtures thereof, in combination with at least one conditioning additive selected from an alkyl or aralkyl alcohol, hydrocarbon oil, carboxylic acid ester, or fatty acid represented by the formula:
- R−C(=O)OM
- wherein R is a C 10-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium (NH3), wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl. Preferably, R is C16-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl. Conditioning additives are lipophilic materials that have low water solubility in water that enhance the conditioning of the slurry with the conditioning agent and the subsequent separation process.
- Alcohol conditioning additives that may be useful in the process of this invention include long chain branched or linear C 10 to C22 alkyl alcohols, preferably C12 to C16 alkyl alcohols, or C7-C26 aralkyl alcohols. Preferably, decanol or dodecanol may be used as conditioning additives. Useful hydrocarbon oil conditioning additives are composed of branched or linear C12 to C32 alkanes or alkenes, preferably C12 to C20 alkanes or alkenes. Useful carboxylic acid ester conditioning additives comprise branched or linear C9 to C22 hydrocarbon moieties, comprising alkanes, alkenes, or aryl moieties. The hydroxamate conditioning agent, or mixtures thereof, may be advantageously pre-dissolved or pre-dispersed in the alkyl alcohol or hydrocarbon oil and added directly to the aqueous clay dispersion. The conditioning additives typically may be used in an amount of about 50% to about 200% by weight, relative to the amount by weight of alkyl hydroxamate conditioning agent.
- Useful fatty acid conditioning additives are comprised of C 12-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl acids or salts thereof. Preferably, oleic acid is used as a fatty acid conditioning agent. The aqueous clay dispersion may be conditioned with the hydroxamate conditioning agents and the optional fatty acid conditioning additive, sequentially, in any order, or simultaneously. The fatty acid and hydroxamate may be added directly to the aqueous clay dispersion as neat oils, or may be added as a dispersion in water. The fatty acid may be advantageously used in an amount of about 500 grams/ton to about 3,000 grams/ton of crude clay, although that amount may vary depending on the type of clay and the amount of impurities to be removed from the clay.
- Optionally, the process of this invention may also include the use of a salt containing a polyvalent metal cation, particularly the alkaline earth metal salts of calcium, magnesium and barium. Incorporation of a polyvalent cationic salt, a critical component in many of the prior art process, is not required for effective purification of clays using the process of this invention, and may be substantially absent. These salts, however, may be optionally added to further improve the overall process. Salts that are useful as conditioning additives are well known, and are generally water soluble salts that may be added directly to the aqueous clay dispersion as a solid or in solution. A preferred polyvalent metal cation containing salt is calcium chloride. The salts may be added simultaneously with, or prior to, the addition of the hydroxamate conditioning agent, or mixtures thereof, in combination with any of the conditioning additives described above. The salt may be added in an amount generally in the range of about 0 grams/ton to about 1,000 grams/ton of crude clay, and preferably at about 250 grams/ton of crude clay, depending on the type of clay and the amount of impurities to be removed from the particular clay sample.
- During processing, the clay dispersion, conditioned with hydroxamate and other additives, if any, may be transferred from a blunging/conditioning vessel, such as a mixing tank, or a blender pitcher, to another vessel that would permit subsequent removal of the flocculated impurities, e.g., a settling vessel. The density or % solids of the clay dispersion may be adjusted by addition of water, as necessary, for enhanced flocculation and separation. Typically, the clay concentration in the clay dispersion is reduced such that the clay concentration is in the range of about 10% to about 30% solids, prior to addition of the flocculating agent. Alternatively, the density of the clay dispersion may be adjusted upon addition of the polymer solution. Selective flocculation of the impurities may be accomplished by adding a dilute solution of the polymer, typically, at about 0.01% to about 0.1% by weight, with low shear mixing.
- Optionally, the stability of the dispersion and the effectiveness of subsequent impurity separation may be enhanced by the addition of a pH modifying agent. A pH modifying agent is a material having a basic pH (greater than 7.0) that is capable of maintaining the pH of the aqueous clay dispersion in the range of 7.5-10.5, and preferably in the range of 8.0-9.5. Useful pH modifying agents include, without limitation, water soluble agents such as ammonia or ammonium hydroxide, sodium or potassium hydroxide and sodium carbonate. The preferred pH modifying agents include, for example, sodium hydroxide or ammonium hydroxide. Optionally, the amount of the pH modifying agent added to the clay dispersion will be that amount necessary to adjust the pH of the aqueous clay dispersion to about 7.5 to about 10.5. The pH modifying agent is commonly added during the blunging step, generally as a solid, but it may be pre-dissolved in water and added as a aqueous solution.
- The impurities in the clay dispersion are flocculated (e.g. aggregated and precipitated) from the dispersion by addition of a flocculating agent. The flocculating agent may be added to the conditioned clay dispersion as a dilute water solution. In the process of this invention, useful flocculating agents are high molecular weight organic polymers that are anionic or non-ionic water soluble or water-dispersible organic polymers, having a molecular weight in the range of about 0.5 million to about 30 million, and preferably a molecular weight in the range of about 1.0 million to about 20 million. Examples of useful organic polymeric flocculants include, but are not limited to hydrolyzed polyacrylamides, co-polymers of acrylamide and acrylic acid, copolymers of acrylamide and acrylamidomethylpropanesulfonic acid, vinyl sulfonic acids, carboxymethyl cellulose, polystyrene sulfonic acids, water soluble polymers containing pendant hydroxamic acid functionality, and salts there of, such as hydroxamated polyacrylamides or polyacrylates, water-soluble or dispersible polyethylene oxide polymers, and other non-ionic water soluble or water-dispersible polymers such as polyacrylamides and polyvinyl alcohols. Preferred polymeric flocculants of this invention are hydroxamated polyacrylamides and hydroxamated polyacrylates.
- An additional feature of this invention is that hydroxamated polyacrylamides and hydroxamated polyacrylates may be used to selectively flocculate impurities from clays that have been treated with conditioning agents comprising fatty acids and alkaline earth metal salts. This process comprises the steps of forming an aqueous clay dispersion by blunging the clay with a dispersing agent, or a combination of dispersing agents, in water; treating the aqueous clay dispersion with a conditioning agent represented by the formula:
- R−C(=O)OM
- wherein R is C 10-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl; flocculating the conditioned clay dispersion by treatment with a water soluble or water dispersible organic polymer containing hydroxamic acid groups or salts thereof, and removing the flocculated impurities to form a purified clay dispersion. The amount of polymeric flocculant used to purify a clay sample will vary depending upon the type of clay used and the amount of impurity to be flocculated from the particular clay sample. However, the general use rates of the polymeric flocculant in the process of the present invention are in the range of about 20 grams/ton to about 200 grams/ton of crude clay. Advantageously, the aqueous clay dispersion may be also treated with a salt containing a polyvalent metal cation. Preferably, the salt is calcium chloride. Optionally, the clay dispersion is also treated with at least one conditioning additive selected from an aliphatic alcohol, a hydrocarbon oil or a carboxylic acid ester oil. Preferably, the conditioning additive may be decanol or dodecanol. Useful dispersing agents include sodium silicate, sodium polyacrylate, or sodium carbonate.
- Rapid flocculation of the colored impurities in the aqueous clay dispersion generally occurs upon addition of the polymeric flocculating agent. The flocculated impurities settle to form a highly colored lower layer, leaving a milky-white upper layer of purified clay.
- This upper clay layer may be isolated from the lower impurity-containing layer by any of the conventional processes used in selective flocculation operations which are well known to those skilled in the art. The upper layer may be decanted away from the lower layer, or alternatively, the lower layer may be drained off from the bottom. Other apparatus, such as a drag box or a low shear centrifugal device, may also be used to separate the lower impurity-containing layer from the purified upper clay layer.
- The purified clay produced by the process of this invention possesses high brightness and low levels of impurities. The purity of this product may be further improved by using the conventional techniques of magnetic separation or chemical bleaching.
- The Examples which follow are intended as an illustration of certain preferred embodiments of the invention, and no limitation of the invention is implied. All quantities are reported on a dry weight basis unless otherwise indicated. The crude kaolin clay used in these Examples was obtained from a mine in the eastern part of Georgia, USA, having a titanium oxide concentration of about 3.0% by weight. The crude clay possessed a particle size distribution of 80-90% finer than 2 microns.
- A 60% solids dispersion of kaolin clay was prepared by blunging (mixing) 386 g. of the crude clay (approximately 330 g. of clay on a dry weight basis) containing 3.0% TiO 2 with 500 grams/ton sodium carbonate, 3000 grams/ton sodium metasilicate, 250 grams/ton of sodium polyacrylate, and 400 grams/ton of sodium hydroxide (to obtain a blunged slurry having a pH of approximately 8.5-9) in water for 5 minutes using a Waring laboratory blender at high speed. At the end of blunging, 1200 grams/ton of Aero 6493® (a mixture of alkyl hydroxamates, sold by Cytec Industries Inc., West Paterson, N.J.), a conditioning agent, was added to the clay slurry, and the resulting mixture was mixed, or conditioned, in the blender at high speed, for 5 minutes. The conditioned slurry was then divided into three equal portions, each of which was transferred to a 500 ml graduated cylinder. A different selective flocculation polymer was added to each cylinder, at a use rate of 30 grams/ton, to induce flocculation. After addition of a dilute solution (0.01 or 0.03% by weight) of the flocculation polymer, the concentration of the clay in the dispersion was reduced to about 20% by weight by addition of water. The clay slurry was mixed gently using a stainless steel plunger with holes, typically used in flocculation tests. The mixture was allowed to stand for 30 min. during which time the physical attributes of the selective flocculation process, such as floc formation, the appearance of flocs, and the rate of settling, were observed. The volumes of settled and suspended phases were noted, and samples from each phase were analyzed for Ti content, using x-ray fluorescence (see Table 1).
- Comparative tests were performed using the procedure described above, but without addition of any conditioning agent(s) prior to flocculant addition. The prior art selective flocculation process was conducted using oleic acid as a fatty acid at 2500 grams/ton in combination with calcium chloride at 385 grams/ton. The dispersing agents used in this test were 2600 grams/ton of sodium metasilicate and 300 grams/ton of sodium polyacrylate.
TABLE 1 % TiO2 in Clay Conditioning Test Flocculation Agents Agents Agent A* Agent B* Agent C* None (Control) 2.01 2.11 2.13 Fatty Acid + CaCl2 1.00 — — (Prior art) Aero 6493 ® 0.73 0.76 0.75 Fatty Acid + CaCl2 — — 1.06 # molecular weight >10 million. # molecular weight >10 million. - In the control test with no conditioning agent the TiO 2 content in the clay product is reduced from about 3% by weight in the crude clay to about 2.1% by weight, i.e. a reduction of 0.9%. Use of alkyl hydroxamic acid as the conditioning agent, reduced the TiO2 content in the clay product by more than 1.3%, relative to the control where no conditioning agent was used, or by about 2.2%, relative to the crude clay. The TiO2 content in the clay product is reduced by about 0.25% relative to the prior art process using fatty acid, CaCl2 and a highly charged, high molecular weight copolymer of acrylic acid and acrylamide.
- A solids dispersion was prepared according to the procedure set forth in Example 1, except that 1000 grams/ton sodium carbonate, 2000 grams/ton of sodium metasilicate, 175 grams/ton of sodium polyacrylate, and only 600 grams/ton of Aero 6493® were blunged with the kaolin clay. The TiO 2 concentration of the clay, after selective flocculation follows: 1.17% for Polymer A (use rate 30 grams/ton), 1.02% for Polymer B (6.5 grams/ton), and 1.00% for Polymer C (18 grams/ton).
- A solids dispersion was prepared according to the procedure set forth in Example 1, except that the conditioning agent was a mixture of C 8-C10 alkyl hydroxamic acids. The reduction in TiO2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- A solids dispersion was prepared according to the procedure set forth in Example 2, except that a conditioning agent combination, consisting of a mixture of C 8-C10 alkyl hydroxamic acids (conditioning agent) and a oleic acid (conditioning additive), was used to condition the clay dispersion. The conditioning agent combination was added simultaneously with the calcium chloride to the blunged clay dispersion. The reduction in TiO2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- A solids dispersion was prepared according to the procedure set forth in Example 3, except that the conditioning agent combination consisted of a mixture of C 8-C10 alkyl hydroxamic acids (conditioning agent) and a hydrocarbon oil (conditioning additive). The reduction in TiO2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- A solids dispersion was prepared according to the procedure set forth in Example 3, except that the conditioning agent combination consisted of a mixture of C 8-C10 alkyl hydroxamic acids (conditioning agent) and methyl palmitate ester oil (conditioning additive). The reduction in TiO2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- A solids dispersion was prepared according to the procedure set forth in Example 4, except that the conditioning agent combination, consisting of a mixture of C 8-C10 alkyl hydroxamic acids (conditioning agent) and a oleic acid (conditioning additive), was used in combination with calcium chloride to condition the clay dispersion. The conditioning agent combination was added simultaneously with the calcium chloride to the blunged clay dispersion. The reduction in TiO2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- A solids dispersion was prepared according to the procedure set forth in Example 1, except that the flocculant was a polyethylene oxide. The reduction in TiO 2 concentration in the clay product was substantially similar to that observed for Aero 6493®, as reported in Table 1.
- Other variations or modifications, which will be obvious to those skilled in the art, are within the scope and teachings of this invention. This invention is not to be limited except as set forth in the following claims.
Claims (48)
1. A process for removing colored impurities from clay comprising the steps of:
a) blunging the clay with a dispersing agent, or a combination of dispersing agents, in water to form an aqueous clay dispersion;
b) forming a conditioned dispersion by treating the aqueous clay dispersion with a conditioning agent, or a mixture of conditioning agents, represented by the formula:
R−C(=O)N(R″)−OM
wherein R is linear or branched C2-C18 alkyl, linear or branched C2-C18 alkenyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl; R″ is H, C1-C12 alkyl or aralkyl; and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl, to form a conditioned dispersion;
c) treating the conditioned dispersion with a flocculating agent comprising a water soluble or water dispersible organic polymer to flocculate the impurities; and
d) removing the flocculated impurities to form a purified clay dispersion.
2. The process according to , wherein the clay is a kaolin clay.
claim 1
3. The process according to , wherein the dispersing agent is selected from the group consisting of sodium silicate, sodium polyacrylate, and sodium carbonate.
claim 1
4. The process according to , comprising blunging the clay with a dispersing agent, or combination of dispersing agents, and a pH modifying agent, in water.
claim 1
5. The process according to , wherein the pH modifying agent is sodium hydroxide or ammonium hydroxide.
claim 1
6. The process according to , wherein the conditioning agent is a hydroxamic acid, or salt thereof, or a mixture of hydroxamic acids, or salts thereof, represented by the formula:
claim 1
R−C(=O)N(R″)−OM
wherein R is an aralkyl moiety selected from the group consisting of (R′-phenyl), (R′-hydroxy-phenyl), (R′-naphthyl), or (R′-hydroxy-naphthyl), wherein R′ is linear or branched C1-C12 alkyl, or linear or branched C2-C12 alkenyl.
7. The process according to , wherein the conditioning agent is a hydroxamic acid, or salt thereof, or a mixture of hydroxamic acids, or salts thereof, represented by the formula:
claim 1
R−C(=O)NH−OM
wherein R is linear or branched C8-C12 alkyl or linear, branched C8-C12 alkenyl, C6-C20 aryl, or substituted aryl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl is substituted with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl.
8. The process according to , wherein the water soluble or water dispersible organic polymer is an anionic or a non-ionic polymer having a molecular weight in the range of about 0.5 million to about 30 million.
claim 1
9. The process according to , wherein the water soluble or water dispersible organic polymer is an anionic or a non-ionic polymer having a molecular weight in the range of about 1 million to about 20 million.
claim 1
10. The process according to , wherein the water soluble or water dispersible organic polymer contains at lease one hydroxamic acid moiety, or salts thereof.
claim 1
11. The process according to , comprising forming a conditioned dispersion by treating the aqueous clay dispersion with a conditioning agent, or a mixture of conditioning agents, and at least one conditioning additive, wherein said conditioning additive is selected from the group consisting of an aliphatic alcohol, a hydrocarbon oil, a carboxylic acid ester oil, and a fatty acid having the formula:
claim 1
R−C(=O)OM
wherein R is a C10-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl.
12. The process according to , wherein the aliphatic alcohol is decanol or dodecanol.
claim 11
13. The process according to , further comprising the step of treating the aqueous clay dispersion with a salt containing a polyvalent metal cation.
claim 1
14. The process according to , wherein the salt is calcium chloride.
claim 13
15. A process for removing colored impurities from clay comprising the steps of:
a) blunging the clay with a dispersing agent, or a combination of dispersing agents, in water to form an aqueous clay dispersion;
b) treating the aqueous clay dispersion with a conditioning composition comprising at least one conditioning agent and at least one conditioning additive, wherein
(i) the at least one conditioning agent is represented by the formula:
R−C(=O)N(R″)−OM
wherein R is linear or branched C2-C18 alkyl, linear or branched C2-C18 alkenyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl; R″ is H, C1-C12 alkyl or aralkyl; and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl, to form a conditioned dispersion; and
(ii) the at least one conditioning additive is a fatty acid represented by the formula:
R−C(=O)OM
wherein R is a C10-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl, to form a conditioned clay dispersion;
c) flocculating the conditioned clay dispersion by treatment with a flocculating agent comprising a water dispersible organic polymer, to form flocculated impurities; and
d) removing the flocculated impurities to form a purified clay dispersion.
16. The process according to , wherein the clay is a kaolin clay.
claim 15
17. The process according to , wherein the dispersing agent is selected from the group consisting of sodium silicate, sodium polyacrylate, and sodium carbonate.
claim 15
18. The process according to , comprising blunging the clay with a dispersing agent, or combination of dispersing agents, and a pH modifying agent, in water.
claim 15
19. The process according to , wherein the pH modifying agent is sodium hydroxide or ammonium hydroxide.
claim 15
20. The process according to , wherein the conditioning agent is a hydroxamic acid, or salt thereof, or a mixture of hydroxamic acids, or salts thereof, represented by the formula:
claim 15
R−C(=O)N(R″)−OM
wherein R is an aralkyl moiety selected from the group consisting of (R′-phenyl), (R′-hydroxy-phenyl), (R′-naphthyl), or (R′-hydroxy-naphthyl), wherein R′ is linear or branched C1-C12 alkyl, or linear or branched C2-C12 alkenyl.
21. The process according to , wherein the conditioning agent is a hydroxamic acid, or salt thereof, or a mixture of hydroxamic acids, or salts thereof, represented by the formula:
claim 15
R−C(=O)NH−OM
wherein R is linear or branched C8-C12 alkyl or linear, branched C8-C12 alkenyl, C6-C20 aryl, or substituted aryl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl is substituted with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl.
22. The process according to , wherein the fatty acid is a compound represented by the formula:
claim 15
R−C(=O)OM
wherein R is a C16-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl.
23. The process according to , wherein the fatty acid is oleic acid.
claim 15
24. The process according to , comprising treating the aqueous clay dispersion with at least two conditioning additives, wherein the second conditioning additive is selected from the group consisting of an aliphatic alcohol, a hydrocarbon oil and a carboxylic acid ester oil.
claim 15
25. The process according to , wherein the aliphatic alcohol is decanol or dodecanol.
claim 24
26. The process according to , further comprising the step of treating the aqueous clay dispersion with a salt containing a polyvalent metal cation.
claim 15
27. The process according to , wherein the salt is calcium chloride.
claim 26
28. The process according to , wherein the water soluble or water dispersible organic polymer is an anionic or a non-ionic polymer having a molecular weight in the range of about 0.5 million to about 30 million.
claim 15
29. The process according to , wherein the water soluble or water dispersible organic polymer is an anionic or a non-ionic polymer having a molecular weight in the range of about 1 million to about 20 million.
claim 15
30. The process according to , wherein the water soluble or water dispersible organic polymer contains at lease one hydroxamic acid moiety, or salts thereof.
claim 15
31. A process for removing colored impurities from clay comprising the steps of:
a) blunging the clay with a dispersing agent, or a combination of dispersing agents, in water to form an aqueous clay dispersion;
b) treating the aqueous clay dispersion with a conditioning agent represented by the formula:
R−C(=O)OM
wherein R is C10-C18 alkyl, C6-C20 aryl, substituted aryl, C7-C26 aralkyl or substituted aralkyl, and M is hydrogen, an alkali metal or ammonium, wherein the substituted aryl or substituted aralkyl are substituted on aryl with hydroxy, C1-C6 alkoxy, or C1-C6 alkyl;
c) flocculating the conditioned clay dispersion by treatment with a flocculating agent comprising a water soluble or water dispersible organic polymer containing hydroxamic acid groups or salts thereof, to form flocculated impurities; and
d) removing the flocculated impurities to form a purified clay dispersion.
32. The process according to , wherein the clay is a kaolin clay.
claim 31
33. The process according to , wherein the dispersing agent is selected from sodium silicate, sodium polyacrylate, and sodium carbonate.
claim 31
34. The process according to , wherein the water soluble or water dispersible flocculant is an organic polymer containing hydroxamic acid groups or salts thereof having a molecular weight in the range of about 0.5 million to about 30 million.
claim 31
35. The process according to , wherein the water soluble or water dispersible flocculant is an organic polymer containing hydroxamic acid groups or salts thereof having a molecular weight in the range of about 1 million to about 20 million.
claim 31
36. The process according to , further comprising treating the clay dispersion with at least one conditioning additive selected from the group consisting of an aliphatic alcohol, a hydrocarbon oil and a carboxylic acid ester oil.
claim 31
37. The process according to , wherein the additive is decanol or dodecanol.
claim 31
38. The process according to , further comprising the step of treating the aqueous clay dispersion with a salt containing a polyvalent metal cation.
claim 31
39. The process according to , wherein the salt containing a polyvalent metal cation is calcium chloride.
claim 31
40. A process for removing colored impurities from clay comprising the following steps:
a) blunging the clay with sodium silicate and sodium polyacrylate in water to form an aqueous clay dispersion;
b) treating the aqueous clay dispersion with a oleic acid fatty acid and calcium chloride,
c) flocculating the conditioned clay dispersion by treatment with hydroxamated polyacrylamide of molecular weight of about 10-20 million, to form flocculated impurities; and
d) removing the flocculated impurities to form a purified clay dispersion.
41. The process according to , wherein the conditioning agent further comprises an additive selected from aliphatic alcohol, hydrocarbon oil or a carboxylic acid ester oil.
claim 40
42. The process according to , wherein the additive is decanol or dodecanol.
claim 41
43. The process according to , further comprising the step of treating the aqueous clay dispersion with a salt containing a polyvalent metal cation.
claim 40
44. The process according to , wherein the salt containing a polyvalent metal cation is calcium chloride.
claim 43
45. A process for removing colored impurities from kaolin clay comprising the following steps:
a) blunging the clay with sodium silicate and sodium polyacrylate in water to form an aqueous clay dispersion;
b) treating the aqueous clay dispersion with a mixture of C8-C10 hydroxamic acid and C12 alcohol;
c) flocculating the conditioned clay dispersion by treatment with hydroxamated polyacrylamide of molecular weight of about 10-20 million, to form flocculated impurities; and
d) removing the flocculated impurities to form a purified clay dispersion.
46. The process according to , further comprising blunging the clay with sodium hydroxide or ammonium hydroxide.
claim 45
47. The process according to , further comprising treating the aqueous clay dispersion with oleic acid.
claim 45
48. The process according to , further comprising treating the aqueous clay dispersion with calcium chloride.
claim 45
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/818,693 US20010022282A1 (en) | 1998-03-27 | 2001-03-27 | Process for removing impurities from kaolin clays |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4976198A | 1998-03-27 | 1998-03-27 | |
| US09/618,463 US6390301B1 (en) | 1998-03-27 | 2000-07-18 | Process for removing impurities from kaolin clays |
| US09/818,693 US20010022282A1 (en) | 1998-03-27 | 2001-03-27 | Process for removing impurities from kaolin clays |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/618,463 Continuation US6390301B1 (en) | 1998-03-27 | 2000-07-18 | Process for removing impurities from kaolin clays |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20010022282A1 true US20010022282A1 (en) | 2001-09-20 |
Family
ID=21961577
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/618,463 Expired - Lifetime US6390301B1 (en) | 1998-03-27 | 2000-07-18 | Process for removing impurities from kaolin clays |
| US09/818,693 Abandoned US20010022282A1 (en) | 1998-03-27 | 2001-03-27 | Process for removing impurities from kaolin clays |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/618,463 Expired - Lifetime US6390301B1 (en) | 1998-03-27 | 2000-07-18 | Process for removing impurities from kaolin clays |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US6390301B1 (en) |
| EP (1) | EP1068162B1 (en) |
| AU (1) | AU750165B2 (en) |
| BR (1) | BR9909117A (en) |
| ES (1) | ES2203083T3 (en) |
| PT (1) | PT1068162E (en) |
| WO (1) | WO1999050202A1 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030028059A1 (en) * | 2000-02-02 | 2003-02-06 | Simon Hamper | Integrated process for producing an alkenyl-substituted aromatic compound |
| WO2004026973A1 (en) * | 2002-09-17 | 2004-04-01 | Imerys Minerals Limited | Grinding method |
| US20050119115A1 (en) * | 2000-03-14 | 2005-06-02 | Camlio Machado | Catalyst for thermal cracking of vegetable and mineral oils, plastics, rubbers and dehydration of castor oil |
| US8967383B1 (en) * | 2012-10-19 | 2015-03-03 | KaMin, LLC | Processes for producing high-brightness kaolin in high yields, and kaolin materials produced therefrom |
| US9914137B1 (en) * | 2015-11-13 | 2018-03-13 | Arr-Maz Products, L.P. | Selective flocculation of impurities from silicates and clays |
| US10233330B2 (en) | 2014-12-03 | 2019-03-19 | Coatex | Dispersion and/or grinding aid agents of kaolin in aqueous suspension, aqueous suspensions obtained and uses thereof |
| US20210155512A1 (en) * | 2018-06-08 | 2021-05-27 | Coatex | Recycling of water in a mining by-product |
| CN113600333A (en) * | 2021-08-04 | 2021-11-05 | 中南大学 | Selective flocculation column flotation and fine selection process for micro-fine-particle rutile ore |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU763786B2 (en) | 1999-05-07 | 2003-07-31 | Imerys Pigments, Inc. | A method of treating an aqueous suspension of kaolin |
| US6378703B1 (en) * | 2000-11-30 | 2002-04-30 | Engelhard Corporation | Flotation method for removing colored impurities from kaolin clay |
| ES2241494B2 (en) * | 2004-04-13 | 2006-07-01 | Industrias Quimicas Del Ebro, S.A. | PROCEDURE FOR MANUFACTURING CRYSTALLIZED DISODIO TRIOXOSILICATES WITH OCLUSIONS IN ITS CRYSTAL STRUCTURE OF ORGANIC POLYMER TYPES AND / OR POLYPHOSPHATES AND ITS APPLICATION IN CLAY DEFLOCULATION. |
| US7393462B2 (en) | 2004-05-13 | 2008-07-01 | Cytec Technology Corp. | Process and reagent for separating finely divided titaniferrous impurities from Kaolin |
| BRPI0922547B1 (en) * | 2008-12-18 | 2019-05-21 | Basf Corporation | METHOD FOR STABILIZING A HYDRATED KAULIN FLUTE FOLDER |
| AU2013260133B2 (en) * | 2012-05-10 | 2017-02-02 | Imerys Pigments, Inc. | Rare earth element compositions obtained from particulate material comprising kaolinite and methods for obtaining rare earth element compositions from particulate material comprising kaolinite |
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| US3138550A (en) | 1960-11-28 | 1964-06-23 | Union Carbide Corp | Froth flotation process employing polymeric flocculants |
| GB1103585A (en) | 1964-03-02 | 1968-02-14 | English Clays Lovering Pochin | Improvements in or relating to the processing of clay |
| US3371998A (en) | 1965-05-06 | 1968-03-05 | Dow Chemical Co | Process for the removal of bromine, air and co2 from saline water |
| US3701417A (en) | 1970-09-28 | 1972-10-31 | Engelhard Min & Chem | Purification of clay by selective flocculation |
| US3862027A (en) | 1972-06-13 | 1975-01-21 | Engelhard Min & Chem | Purification of clay by selective flocculation |
| US3837482A (en) | 1973-05-03 | 1974-09-24 | Engelhard Min & Chem | Process for purifying clay by selective flocculation |
| US4492628A (en) | 1982-08-25 | 1985-01-08 | Freeport Kaolin Company | Method of treating clay to improve its whiteness |
| US4604369A (en) * | 1984-08-27 | 1986-08-05 | Thiele Kaolin Company | Method of beneficiating kaolin clay utilizing ammonium salts |
| US4629556A (en) | 1984-11-29 | 1986-12-16 | Thiele Kaolin Company | Purification of kaolin clay by froth flotation using hydroxamate collectors |
| US4871466A (en) | 1987-10-15 | 1989-10-03 | American Cyanamid Company | Novel collectors and processes for making and using same |
| GB8726857D0 (en) | 1987-11-17 | 1987-12-23 | Fospur Ltd | Froth floatation of mineral fines |
| US4931190A (en) | 1988-12-27 | 1990-06-05 | Envirotech Corporation | Flocculating agent combinations for mineral slime filtration systems |
| US5180511A (en) | 1989-09-14 | 1993-01-19 | J.M. Huber Corporation | Flotation aid and process for removal of impurities from silicate minerals |
| US5223463A (en) | 1991-08-01 | 1993-06-29 | Ecc International Inc. | Process for producing a kaolin clay product |
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| US5535890A (en) * | 1994-12-07 | 1996-07-16 | Engelhard Corporation | Method for separating mixture of finely divided minerals |
| US5522986A (en) | 1995-03-03 | 1996-06-04 | Thiele Kaolin Company | Process for removing impurities from kaolin clays |
| US5584394A (en) | 1995-03-15 | 1996-12-17 | Engelhard Corporation | Colored titaniferous coating pigment obtained as a flocculated by-product in a kaolin purification process |
| US5685899A (en) * | 1995-07-28 | 1997-11-11 | Thiele Kaolin Company | Process for conditioning kaolin clays prior to removing impurities |
| US5951955A (en) | 1995-11-07 | 1999-09-14 | Cytec Technology Corp. | Concentration of solids in the Bayer process |
| US5938833A (en) | 1996-09-18 | 1999-08-17 | Engelhard Corporation | Chemical process for fractionating mineral particles based on particle size |
| US5922207A (en) | 1997-05-16 | 1999-07-13 | Engelhard Corporation | Filter aid for clay processing |
| US6041939A (en) | 1998-03-20 | 2000-03-28 | Thiele Kaolin Company | Beneficiation with selective flocculation using hydroxamates |
-
1999
- 1999-03-02 BR BR9909117-8A patent/BR9909117A/en active Search and Examination
- 1999-03-02 WO PCT/US1999/004481 patent/WO1999050202A1/en not_active Ceased
- 1999-03-02 PT PT99909717T patent/PT1068162E/en unknown
- 1999-03-02 EP EP99909717A patent/EP1068162B1/en not_active Expired - Lifetime
- 1999-03-02 ES ES99909717T patent/ES2203083T3/en not_active Expired - Lifetime
- 1999-03-02 AU AU28860/99A patent/AU750165B2/en not_active Ceased
-
2000
- 2000-07-18 US US09/618,463 patent/US6390301B1/en not_active Expired - Lifetime
-
2001
- 2001-03-27 US US09/818,693 patent/US20010022282A1/en not_active Abandoned
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030028059A1 (en) * | 2000-02-02 | 2003-02-06 | Simon Hamper | Integrated process for producing an alkenyl-substituted aromatic compound |
| US20050119115A1 (en) * | 2000-03-14 | 2005-06-02 | Camlio Machado | Catalyst for thermal cracking of vegetable and mineral oils, plastics, rubbers and dehydration of castor oil |
| WO2004026973A1 (en) * | 2002-09-17 | 2004-04-01 | Imerys Minerals Limited | Grinding method |
| US20060106118A1 (en) * | 2002-09-17 | 2006-05-18 | Imerys Minerals Limited | Grinding method |
| US20100219269A1 (en) * | 2002-09-17 | 2010-09-02 | Imerys Minerals Limited | Grinding method for inorganic particulate material |
| US7938346B2 (en) | 2002-09-17 | 2011-05-10 | Imerys Minerals Limited | Grinding method for inorganic particulate material |
| US8967383B1 (en) * | 2012-10-19 | 2015-03-03 | KaMin, LLC | Processes for producing high-brightness kaolin in high yields, and kaolin materials produced therefrom |
| US10233330B2 (en) | 2014-12-03 | 2019-03-19 | Coatex | Dispersion and/or grinding aid agents of kaolin in aqueous suspension, aqueous suspensions obtained and uses thereof |
| US9914137B1 (en) * | 2015-11-13 | 2018-03-13 | Arr-Maz Products, L.P. | Selective flocculation of impurities from silicates and clays |
| US20210155512A1 (en) * | 2018-06-08 | 2021-05-27 | Coatex | Recycling of water in a mining by-product |
| CN113600333A (en) * | 2021-08-04 | 2021-11-05 | 中南大学 | Selective flocculation column flotation and fine selection process for micro-fine-particle rutile ore |
Also Published As
| Publication number | Publication date |
|---|---|
| US6390301B1 (en) | 2002-05-21 |
| ES2203083T3 (en) | 2004-04-01 |
| AU2886099A (en) | 1999-10-18 |
| EP1068162B1 (en) | 2003-07-23 |
| WO1999050202A1 (en) | 1999-10-07 |
| AU750165B2 (en) | 2002-07-11 |
| BR9909117A (en) | 2000-12-19 |
| PT1068162E (en) | 2003-11-28 |
| EP1068162A1 (en) | 2001-01-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: EXPRESSLY ABANDONED -- DURING EXAMINATION |