CA1251631A - Water-absorbent agents for low ph applications - Google Patents
Water-absorbent agents for low ph applicationsInfo
- Publication number
- CA1251631A CA1251631A CA000478946A CA478946A CA1251631A CA 1251631 A CA1251631 A CA 1251631A CA 000478946 A CA000478946 A CA 000478946A CA 478946 A CA478946 A CA 478946A CA 1251631 A CA1251631 A CA 1251631A
- Authority
- CA
- Canada
- Prior art keywords
- acid salt
- polyelectrolyte
- water
- alkali metal
- sulfonic acid
- 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.)
- Expired
Links
- 239000002250 absorbent Substances 0.000 title claims description 11
- 229920000642 polymer Polymers 0.000 claims abstract description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 24
- -1 alkali metal sulphonic acid salt Chemical class 0.000 claims abstract description 21
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 20
- 239000012736 aqueous medium Substances 0.000 claims abstract description 17
- 229920000867 polyelectrolyte Polymers 0.000 claims abstract description 17
- 239000000178 monomer Substances 0.000 claims description 33
- 238000004132 cross linking Methods 0.000 claims description 9
- 230000002745 absorbent Effects 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical group OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 150000001408 amides Chemical class 0.000 claims description 4
- 150000003460 sulfonic acids Chemical class 0.000 claims description 4
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 150000003839 salts Chemical group 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract description 10
- 230000002378 acidificating effect Effects 0.000 abstract description 7
- 239000000446 fuel Substances 0.000 abstract description 7
- 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 abstract description 6
- 229910052708 sodium Inorganic materials 0.000 abstract description 6
- 239000011734 sodium Substances 0.000 abstract description 6
- 229920006037 cross link polymer Polymers 0.000 abstract 1
- 229940117913 acrylamide Drugs 0.000 description 11
- 239000000243 solution Substances 0.000 description 8
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical class OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 4
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 3
- 125000004964 sulfoalkyl group Chemical class 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 2
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229940047670 sodium acrylate Drugs 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tertâbutyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- BSSNZUFKXJJCBG-OWOJBTEDSA-N (e)-but-2-enediamide Chemical compound NC(=O)\C=C\C(N)=O BSSNZUFKXJJCBG-OWOJBTEDSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- PRAMZQXXPOLCIY-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethanesulfonic acid Chemical compound CC(=C)C(=O)OCCS(O)(=O)=O PRAMZQXXPOLCIY-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- UVDYBBRVDUKNFV-UHFFFAOYSA-N 2-(prop-2-enoylamino)ethanesulfonic acid Chemical class OS(=O)(=O)CCNC(=O)C=C UVDYBBRVDUKNFV-UHFFFAOYSA-N 0.000 description 1
- MVYVKSBVZFBBPL-UHFFFAOYSA-N 2-(prop-2-enoylamino)propane-1-sulfonic acid Chemical class OS(=O)(=O)CC(C)NC(=O)C=C MVYVKSBVZFBBPL-UHFFFAOYSA-N 0.000 description 1
- AIIITCMZOKMJIM-UHFFFAOYSA-N 2-(prop-2-enoylamino)propane-2-sulfonic acid Chemical compound OS(=O)(=O)C(C)(C)NC(=O)C=C AIIITCMZOKMJIM-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- YMUJDPCTVKOZDK-UHFFFAOYSA-N [N].C(C=C)(=O)NCNC(C=C)=O Chemical compound [N].C(C=C)(=O)NCNC(C=C)=O YMUJDPCTVKOZDK-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- JZQAAQZDDMEFGZ-UHFFFAOYSA-N bis(ethenyl) hexanedioate Chemical compound C=COC(=O)CCCCC(=O)OC=C JZQAAQZDDMEFGZ-UHFFFAOYSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000002036 drum drying Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- KUDUQBURMYMBIJ-UHFFFAOYSA-N ethylene glycol diacrylate Substances C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229960000834 vinyl ether Drugs 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
This invention is directed to a process for absorbing water in the form of an aqueous medium having a pH of less than 4. The process comprises contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulphonic acid salt containing polyelectrolyte which is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte.
For example, a crosslinked polymer containing polymerized acrylamide and sodium 2-acrylamide-2-methylpropane sulfonate can be used to remove acidic water from, for example, fuels, battery casings.
This invention is directed to a process for absorbing water in the form of an aqueous medium having a pH of less than 4. The process comprises contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulphonic acid salt containing polyelectrolyte which is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte.
For example, a crosslinked polymer containing polymerized acrylamide and sodium 2-acrylamide-2-methylpropane sulfonate can be used to remove acidic water from, for example, fuels, battery casings.
Description
,S~3~
A PROCESS FOR ABSORBING WATER HAVING A pH
LESS THAN FOUR
The present invention relates to polymeric agents which are useful as water-absorbents, and in particular, to polymeric agents which are useful in removing water from numerous systems.
Water-swellable polymers have found various uses as absorbents for water. Examples of such polymers are disclosed in U.S. Patent Nos. 3,926,891; 4,190,562 and 4,293,609. Unfortunately, such known water swel~
lable polymers are either non-ionic water-swellable polymers, or polyanionic water-swellable polymers containing anions of weak acids such as carboxylic acids. The weakly acidic groups only function in the ionic form when the pH of the system is above the pK of the acidic group. Thus, the known wa~er-swellable polymers have not been effective in applications in which the p~ is below 4.
In view of the deficiencies of the prior art, it would be highly desirable to provide a means for effectively absorbing an aqueous medium which is acidic in nature.
~k ~2,~l63 The present invention is a process for effectively absorbing water in the form of an aqueous medium having a pH of less than 4 which process comprises contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulfonic acid salt containing polyelectrolyte whic~ is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte, wherein the amount of said sulfonic acid salt moieties in said polyelectrolyte is sufficient to provide water absorbent activity, wherein said sulfonic acid salt containing polyelectrolyte maintains an ionic form over a lower pH range than a swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties having (1) a similar molecular weight and
A PROCESS FOR ABSORBING WATER HAVING A pH
LESS THAN FOUR
The present invention relates to polymeric agents which are useful as water-absorbents, and in particular, to polymeric agents which are useful in removing water from numerous systems.
Water-swellable polymers have found various uses as absorbents for water. Examples of such polymers are disclosed in U.S. Patent Nos. 3,926,891; 4,190,562 and 4,293,609. Unfortunately, such known water swel~
lable polymers are either non-ionic water-swellable polymers, or polyanionic water-swellable polymers containing anions of weak acids such as carboxylic acids. The weakly acidic groups only function in the ionic form when the pH of the system is above the pK of the acidic group. Thus, the known wa~er-swellable polymers have not been effective in applications in which the p~ is below 4.
In view of the deficiencies of the prior art, it would be highly desirable to provide a means for effectively absorbing an aqueous medium which is acidic in nature.
~k ~2,~l63 The present invention is a process for effectively absorbing water in the form of an aqueous medium having a pH of less than 4 which process comprises contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulfonic acid salt containing polyelectrolyte whic~ is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte, wherein the amount of said sulfonic acid salt moieties in said polyelectrolyte is sufficient to provide water absorbent activity, wherein said sulfonic acid salt containing polyelectrolyte maintains an ionic form over a lower pH range than a swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties having (1) a similar molecular weight and
(2) a similar concentration of acid salt moieties to that of said alkali metal sulfonic acid salt poly-electrolyte, and wherein said sulfonic acid salt containing polyelectrolyte provides improved water absorbent capability over a lower pH range than said swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties.
The process of this invention enables one to absorb aqueous solutions or moisture in a wide variety of applications, and is particularly useful in providing disposable absorbent articles where a means for increased absorbency and decreased bulk is desirable. Of particular interest are those situations where it is desirable to remove an acidic aqueous medium from, for example, fuels, hydraulic fluids, or battery applications.
Exemplary nonionic monomers suitably employed in the practice of this invention are those ethylen-ically unsaturated monomers that are sufficiently water-soluble to form at least a 5 weight percent solution when dissolved in water and readily undergo addition homo-poly~erization to form polymers that are water-soluble. Examples of such nonionic monomers include ethylenically unsaturated amides such as acryl-amide, methacrylamide and fumaramide; their water-soluble N-substituted nonionic derivatives such as the N-methylol derivatives of acrylamide and methacrylamide as well as the N-methyl and N,N-dimethyl derivatives of acrylamide and methacrylamide; and hydroxyalkyl esters of unsaturated carboxylic acids such as hydroxyethyl acrylate and hydroxypropyl acrylate. O the foregoing nonionic monomers, the ethylenically unsatura-ted amides are preferred with acrylamide b~iny especially preferred.
Suitable ethylenically unsaturated monomers containing sulfonic acid salt moieties are the water-soluble, ethylenically unsaturated sulfonate monomersincluding, for example, N-sulfoalkyl, ~ ethylenically unsaturated amides such as the alkali metal salts of 2-acrylamido-2-methylpropane sulfonic acid, 2-acrylamido propane sulfonic acid, and 2-acrylamido ethane sulfonic acid such as the sodium and potassium salts thereof, as well as the alkali metal salts of other such monomers listed in U.S. Patent No. 3,692,673; alkali metal salts of sulfoalkyl esters of unsaturated carboxylic acids such as 2-sulfoethyl methacrylate and other such sulfoalkyl esters as listed in U.S. Patent No. 4,075,134;
and alkali metal salts of the sulfoarylalkenes such as vinylbenzyl sulfonic acld and p-styrene sulfonic acid alkali metal salts o sulfoalkenes such as vinyl sulfonic acid. Of the foregoing sulfonate monomers, the alkali metal salts of sulfoalkyl derivatives of acrylamide and methacrylamide are preferred with those of acrylamide being especially preferred, part.icularly 2-acrylamido--2-methylpropane sulfonic acid (AMPS), 2-acrylamido--2-propane sulfonic acid. In th~ most preferred embodiments, the sulfo group is in the form of an alkali metal sulfonate salt such as sulfonate containing sodium or potassium sulfonate. It is also possible to employ said sulfonate containing monomers in preparing polymers in combination with the sulfoni.c acid forms of said monomers.
Also useful herein are the essentially nonionic alkyl acrylates and alkyl methacrylates which are 15 disclosed in U.S. Patent No. 4,293,609. It is also possible to employ other ethylenically unsaturated monomers such as omega hydroxyalkyl acrylates, as well as essentially anionic monomers such as acrylic acid, itaconic acid and maleic anhydride. Examples of omega hydroxyalkyl acrylates and ethylenically unsaturated carboxylic acids are disclosed in U.S. Patent No. 4,293,609.
The polyvinyl crosslinking monomers copolym-erized with the aforementioned ethylenically unsa-turated water-soluble monomers include, for example, divinyl benzene, divinyl esters of polycarboxylic acid, diallyl esters of polycarboxylic acids, diallyl maleate, diallyl fumarate, divinyl adipate, glyceryl.trimethylacrylate, diallyl succinate, divinyl ether, the divinyl esters of ethylene glycol or diethylene glycol diacrylate, and polyethylene ylycol. diacrylates or methacrylates. o~
63~
the aforementioned polyvinyl crosslinking monomers, the most preferred is methylene bisacrylamide.
Pol~mers can also be crosslinked using tech niques and agents disclosed in U.S. Patent No. 4,293,609.
Polymers are prepared by using techniques known in the art for preparing water-soluble polymers.
For example, polymerization is preferably carried out in aqueous medium in the presence of a small but effec-tive amount of a wa-ter soluble oxygen-containing catalyst at a temperature of 80F to 190F. The resulting polymer is recovered from the aqueous medium, as by precipitation or drum drying, and can be subsequently ground to the desired particle size. The particle size should be fine enough to facilitate the dispersion of the polymer in water. Polymers are also prepared using polymerization technigues described in U.S. Patent Nos. 3,284,393; and 4,376,850.
Molecular weights of the polymers of this invention can vary. Molecular weights typically range from 100,000 to 25 million. Most preferably, molecular weights range from l million to 5 million.
The polymers of this invention comprise suf-ficient monomer containing sulfonic acid salt moieties (i.e. sulfonate moieties) in order that the process for absorbing water can be achieved. For example, a polymer containing a sodium salt of 2-acrylamido-2-methylpropane sulfonic acid provides particularly ~S~63~
~6--good water absorbing character to the polymer at low pH. The polymers also comprise sufficient essentially nonionic mon~mer, which is preferably acrylamide, or an alkyl acrylate or alkyl methacrylate, in order that the polymer will provide sufficient gelling ability. That is, such monomer typically provides high molecular weight and go~d gelling ability to the polymer. The amount of polyvinyl crosslinking monomer which is employed will depend upon the type of crosslinker which is employed and the molecular weight of the polymer.
The crosslinking monomer is employed to provide increased molecular weight and, hence, swelling character or increased viscosity to the polymer.
The polymers of -this invention typically comprise 0 to 95, preferably 20 to 70, most preferably 30 to 50, mole percent essentially nonionic ethylenically unsaturated monomer or combination of monomers, which are preferably acrylamide; from 5 to 100, preferably from 30 to 80, most preferably from 50 to 70, mole percent ethylenically unsaturated monomer containing a sulfonate moie-ty, which is preferably a sodium salt of 2-acrylamido-2-methyl pr~pane sulfonic acid; and when crosslinking is provided by polyvinyl crosslinking agents, Erom 100 to 2, 500 ppm, pre~erably :rom 300 to 1,000 ppm, most preferably from 400 to 700 ppm polyvinyl crosslinking monomer, which is preferably methylene bisacrylamide. It is understood that the amount of ethylenically unsaturated monomer containiny sulfonic acid salt moieties within the polymer can vary depending on the desired behavior of the polymer. It is also understood that the essen-tially nonionic monomer within the poiymer can undergo an amount of hydrolysis. That is, a portion of the essentially nonionic monomers can undergo hydrolysis. These polymers are particularly well suited for absorbing water from acidic formula-tions and are preerred.
.
Water absorbent polymers absorb several times their weight of an aqueous medium, preferably more than 15 times their weigh~ water. The amount of water which a particular polymer will absorb (i.e. water absorbent capability) is dependen~ upon the pH of the aqueous medium which is being absorbed, the molecular weight of the polymer, the amount of sulfonate moieties present in the polymer, and the amount of crosslinking.
The previously defined polymers can be employed in preparing articles such as laminates as are described in U.S. Patent Nos. 3,980,663; 4,117,184; 4,293,609 and 4,424,247.
The water-swellable polymers which are used in the process of this invention can be employed in those applications in which water-absorbency is desir-able. Most preferred are those applications wherein the pH of the aqueous medium is less than 4, preferably less than 3, most preferably from 0.2 to 2. Of particular interest are those applications wherein the removal of an aqueous medium having a low pH is desirable. For example, the process of this invention can be employed in providing covers and casings for batteries, or in fuel filter applications. That is, fuels or hydraulic fluids having high sulfur contents can introduce problems to internal machine parts upon the formation of sulfuric ~ ~5~i3~
acid. The process of this invention can be employed, for example, in fuel filter applications in order to ~remove the acidic aqueous medium from such fuels or fluids. For example, the polymers of the invention can be mixed with clays, etc. to yield a water-absorbent material having good gel strength, and can be used as a fuel filter. Particularly desirable is that the polymers employed in the process of this invention are capable of swelling rapidly in order to absor~ water at a rapid rate. In this regard, water is removed from a system quickly and efficiently.
The following examples are given for the purposes of illustrating the present invention and shQuld not be construed as limiting its scope. Unless otherwise indicated, all parts and percentages are by weight.
Examples 1 Throuqh 6 and Comparative Runs A and B
The following general procedure is used to prepare the polymers used in the process of this inven-tion and those used for comparison purposes.
Into a liter reaction kettle equipped with astirrer, thermocouple, nitrogen inlet tube, gas vent and a heating mantle are charged the following with stirring:
(1) 60 g of a 50 percent solution of sodium 2-acrylamido-2-methylpropane sulfonate in water (pH = 9-9.5) (2) 140 g of a 50 percent solu-tion of acrylamide in water (p~I = 5.5)
The process of this invention enables one to absorb aqueous solutions or moisture in a wide variety of applications, and is particularly useful in providing disposable absorbent articles where a means for increased absorbency and decreased bulk is desirable. Of particular interest are those situations where it is desirable to remove an acidic aqueous medium from, for example, fuels, hydraulic fluids, or battery applications.
Exemplary nonionic monomers suitably employed in the practice of this invention are those ethylen-ically unsaturated monomers that are sufficiently water-soluble to form at least a 5 weight percent solution when dissolved in water and readily undergo addition homo-poly~erization to form polymers that are water-soluble. Examples of such nonionic monomers include ethylenically unsaturated amides such as acryl-amide, methacrylamide and fumaramide; their water-soluble N-substituted nonionic derivatives such as the N-methylol derivatives of acrylamide and methacrylamide as well as the N-methyl and N,N-dimethyl derivatives of acrylamide and methacrylamide; and hydroxyalkyl esters of unsaturated carboxylic acids such as hydroxyethyl acrylate and hydroxypropyl acrylate. O the foregoing nonionic monomers, the ethylenically unsatura-ted amides are preferred with acrylamide b~iny especially preferred.
Suitable ethylenically unsaturated monomers containing sulfonic acid salt moieties are the water-soluble, ethylenically unsaturated sulfonate monomersincluding, for example, N-sulfoalkyl, ~ ethylenically unsaturated amides such as the alkali metal salts of 2-acrylamido-2-methylpropane sulfonic acid, 2-acrylamido propane sulfonic acid, and 2-acrylamido ethane sulfonic acid such as the sodium and potassium salts thereof, as well as the alkali metal salts of other such monomers listed in U.S. Patent No. 3,692,673; alkali metal salts of sulfoalkyl esters of unsaturated carboxylic acids such as 2-sulfoethyl methacrylate and other such sulfoalkyl esters as listed in U.S. Patent No. 4,075,134;
and alkali metal salts of the sulfoarylalkenes such as vinylbenzyl sulfonic acld and p-styrene sulfonic acid alkali metal salts o sulfoalkenes such as vinyl sulfonic acid. Of the foregoing sulfonate monomers, the alkali metal salts of sulfoalkyl derivatives of acrylamide and methacrylamide are preferred with those of acrylamide being especially preferred, part.icularly 2-acrylamido--2-methylpropane sulfonic acid (AMPS), 2-acrylamido--2-propane sulfonic acid. In th~ most preferred embodiments, the sulfo group is in the form of an alkali metal sulfonate salt such as sulfonate containing sodium or potassium sulfonate. It is also possible to employ said sulfonate containing monomers in preparing polymers in combination with the sulfoni.c acid forms of said monomers.
Also useful herein are the essentially nonionic alkyl acrylates and alkyl methacrylates which are 15 disclosed in U.S. Patent No. 4,293,609. It is also possible to employ other ethylenically unsaturated monomers such as omega hydroxyalkyl acrylates, as well as essentially anionic monomers such as acrylic acid, itaconic acid and maleic anhydride. Examples of omega hydroxyalkyl acrylates and ethylenically unsaturated carboxylic acids are disclosed in U.S. Patent No. 4,293,609.
The polyvinyl crosslinking monomers copolym-erized with the aforementioned ethylenically unsa-turated water-soluble monomers include, for example, divinyl benzene, divinyl esters of polycarboxylic acid, diallyl esters of polycarboxylic acids, diallyl maleate, diallyl fumarate, divinyl adipate, glyceryl.trimethylacrylate, diallyl succinate, divinyl ether, the divinyl esters of ethylene glycol or diethylene glycol diacrylate, and polyethylene ylycol. diacrylates or methacrylates. o~
63~
the aforementioned polyvinyl crosslinking monomers, the most preferred is methylene bisacrylamide.
Pol~mers can also be crosslinked using tech niques and agents disclosed in U.S. Patent No. 4,293,609.
Polymers are prepared by using techniques known in the art for preparing water-soluble polymers.
For example, polymerization is preferably carried out in aqueous medium in the presence of a small but effec-tive amount of a wa-ter soluble oxygen-containing catalyst at a temperature of 80F to 190F. The resulting polymer is recovered from the aqueous medium, as by precipitation or drum drying, and can be subsequently ground to the desired particle size. The particle size should be fine enough to facilitate the dispersion of the polymer in water. Polymers are also prepared using polymerization technigues described in U.S. Patent Nos. 3,284,393; and 4,376,850.
Molecular weights of the polymers of this invention can vary. Molecular weights typically range from 100,000 to 25 million. Most preferably, molecular weights range from l million to 5 million.
The polymers of this invention comprise suf-ficient monomer containing sulfonic acid salt moieties (i.e. sulfonate moieties) in order that the process for absorbing water can be achieved. For example, a polymer containing a sodium salt of 2-acrylamido-2-methylpropane sulfonic acid provides particularly ~S~63~
~6--good water absorbing character to the polymer at low pH. The polymers also comprise sufficient essentially nonionic mon~mer, which is preferably acrylamide, or an alkyl acrylate or alkyl methacrylate, in order that the polymer will provide sufficient gelling ability. That is, such monomer typically provides high molecular weight and go~d gelling ability to the polymer. The amount of polyvinyl crosslinking monomer which is employed will depend upon the type of crosslinker which is employed and the molecular weight of the polymer.
The crosslinking monomer is employed to provide increased molecular weight and, hence, swelling character or increased viscosity to the polymer.
The polymers of -this invention typically comprise 0 to 95, preferably 20 to 70, most preferably 30 to 50, mole percent essentially nonionic ethylenically unsaturated monomer or combination of monomers, which are preferably acrylamide; from 5 to 100, preferably from 30 to 80, most preferably from 50 to 70, mole percent ethylenically unsaturated monomer containing a sulfonate moie-ty, which is preferably a sodium salt of 2-acrylamido-2-methyl pr~pane sulfonic acid; and when crosslinking is provided by polyvinyl crosslinking agents, Erom 100 to 2, 500 ppm, pre~erably :rom 300 to 1,000 ppm, most preferably from 400 to 700 ppm polyvinyl crosslinking monomer, which is preferably methylene bisacrylamide. It is understood that the amount of ethylenically unsaturated monomer containiny sulfonic acid salt moieties within the polymer can vary depending on the desired behavior of the polymer. It is also understood that the essen-tially nonionic monomer within the poiymer can undergo an amount of hydrolysis. That is, a portion of the essentially nonionic monomers can undergo hydrolysis. These polymers are particularly well suited for absorbing water from acidic formula-tions and are preerred.
.
Water absorbent polymers absorb several times their weight of an aqueous medium, preferably more than 15 times their weigh~ water. The amount of water which a particular polymer will absorb (i.e. water absorbent capability) is dependen~ upon the pH of the aqueous medium which is being absorbed, the molecular weight of the polymer, the amount of sulfonate moieties present in the polymer, and the amount of crosslinking.
The previously defined polymers can be employed in preparing articles such as laminates as are described in U.S. Patent Nos. 3,980,663; 4,117,184; 4,293,609 and 4,424,247.
The water-swellable polymers which are used in the process of this invention can be employed in those applications in which water-absorbency is desir-able. Most preferred are those applications wherein the pH of the aqueous medium is less than 4, preferably less than 3, most preferably from 0.2 to 2. Of particular interest are those applications wherein the removal of an aqueous medium having a low pH is desirable. For example, the process of this invention can be employed in providing covers and casings for batteries, or in fuel filter applications. That is, fuels or hydraulic fluids having high sulfur contents can introduce problems to internal machine parts upon the formation of sulfuric ~ ~5~i3~
acid. The process of this invention can be employed, for example, in fuel filter applications in order to ~remove the acidic aqueous medium from such fuels or fluids. For example, the polymers of the invention can be mixed with clays, etc. to yield a water-absorbent material having good gel strength, and can be used as a fuel filter. Particularly desirable is that the polymers employed in the process of this invention are capable of swelling rapidly in order to absor~ water at a rapid rate. In this regard, water is removed from a system quickly and efficiently.
The following examples are given for the purposes of illustrating the present invention and shQuld not be construed as limiting its scope. Unless otherwise indicated, all parts and percentages are by weight.
Examples 1 Throuqh 6 and Comparative Runs A and B
The following general procedure is used to prepare the polymers used in the process of this inven-tion and those used for comparison purposes.
Into a liter reaction kettle equipped with astirrer, thermocouple, nitrogen inlet tube, gas vent and a heating mantle are charged the following with stirring:
(1) 60 g of a 50 percent solution of sodium 2-acrylamido-2-methylpropane sulfonate in water (pH = 9-9.5) (2) 140 g of a 50 percent solu-tion of acrylamide in water (p~I = 5.5)
(3) 400 g of water t4) 9 g of sodium carbonate.
(5) 0.5 g of methylene bisacrylamide Nitrogen is bubbled through the stirred solution for 1 hour. To this stirred solution are then added the f411Owing solutions:
(1) 2 ml of an aqueous solution of 10 percent pentasodium salt of (carboxymethylimino)bis-(ethylenenitrilo)tetraacetic acid.
(2) 0.5 ml of an aqueous solution of 7 percent t-butyl hydroperoxide.
(3) 1 ml of an aqueous solution of 0.06 percent sodium borohydrid~ (NaBH4).
The temperature of the stirred solution rises from 25C
to about 40C and is maintained at such temperature for 1 hour. The mixture is heated to 60C for another 90 minutes. The resulting aqueous solution of AAM/AMPS
copolymer is removed and placed on a steam bath for 1 to 3 hours and drum dried to a white solid. The polymer contains 63 percent acrylamide, 7 percent sodium acrylate and 30 percent sodium 2-acrylamido-2 methylpropane sulfonate acid.
Polymers containing varying degrees of anionic character are prepared as described above. Each polymer is individually dissolved in water to provide a 0.25 g of polymer in 500 ml of water. The solution is allowed 3~
to stand for a period of 20 minutes. The resulting polymer gel is filtered -through a 150 mesh nylon screen and is allowed to drip dry for 20 minutes. The gel is then weighed.
TABLE I
Examples And Capacity3 Comparative Description1 (gm H 0/
_Runs (weight Eercent monomers) ~ gm poly~er) AAm NaAAmNaAMPS
1 Z5 -- 75 1 63.6 2 50 -- 50 1 56.0 3 63 7 30 1 49.6
(5) 0.5 g of methylene bisacrylamide Nitrogen is bubbled through the stirred solution for 1 hour. To this stirred solution are then added the f411Owing solutions:
(1) 2 ml of an aqueous solution of 10 percent pentasodium salt of (carboxymethylimino)bis-(ethylenenitrilo)tetraacetic acid.
(2) 0.5 ml of an aqueous solution of 7 percent t-butyl hydroperoxide.
(3) 1 ml of an aqueous solution of 0.06 percent sodium borohydrid~ (NaBH4).
The temperature of the stirred solution rises from 25C
to about 40C and is maintained at such temperature for 1 hour. The mixture is heated to 60C for another 90 minutes. The resulting aqueous solution of AAM/AMPS
copolymer is removed and placed on a steam bath for 1 to 3 hours and drum dried to a white solid. The polymer contains 63 percent acrylamide, 7 percent sodium acrylate and 30 percent sodium 2-acrylamido-2 methylpropane sulfonate acid.
Polymers containing varying degrees of anionic character are prepared as described above. Each polymer is individually dissolved in water to provide a 0.25 g of polymer in 500 ml of water. The solution is allowed 3~
to stand for a period of 20 minutes. The resulting polymer gel is filtered -through a 150 mesh nylon screen and is allowed to drip dry for 20 minutes. The gel is then weighed.
TABLE I
Examples And Capacity3 Comparative Description1 (gm H 0/
_Runs (weight Eercent monomers) ~ gm poly~er) AAm NaAAmNaAMPS
1 Z5 -- 75 1 63.6 2 50 -- 50 1 56.0 3 63 7 30 1 49.6
4 63 7 30 3 98.8 15 5 75 10 15 1 2g.6 6 75 10 15 3 49.2 A 70 30 -~ 1 20 B 70 30 -- 3 22.4 1AAm is acrylamide NaAAm is sodium acrylate NaAMPS is sodium 2-acrylamide-2-methylpropane sulfonate All polymer samples are crosslinked with 500 ppm methylene bisacrylamide.
2The pH is that of the water sample to which each polymer is added.
3Capacity is the amount of water absorbed in grams per gram of polymer.
The data in Table I indicates that examples of the process of this invention exhibit superior water holding capacity than Comparative Runs A and B which do not contain sodium sulfona-te moieties in a very low pH
ra~ge.
2The pH is that of the water sample to which each polymer is added.
3Capacity is the amount of water absorbed in grams per gram of polymer.
The data in Table I indicates that examples of the process of this invention exhibit superior water holding capacity than Comparative Runs A and B which do not contain sodium sulfona-te moieties in a very low pH
ra~ge.
Claims (7)
1. A process for effectively absorbing water in the form of an aqueous medium having a pH of less than 4 which process comprises:
contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulfonic acid salt containing polyelectrolyte which is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte, wherein the amount of said sulfonic acid salt moieties in said polyelectrolyte is sufficient to provide water absorbent activity, wherein said sulfonic acid salt containing polyelec-trolyte maintains an ionic form over a lower pH range than a swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties having (1) a similar molecular weight and (2) a similar concentration of acid salt moieties to that of said alkali metal sulfonic acid salt polyelectrolyte, and wherein said sulfonic acid salt containing polyelectro-lyte provides improved water absorbent capability over a lower pH range than said swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties.
contacting said aqueous medium with a water-swellable polymer comprising an alkali metal sulfonic acid salt containing polyelectrolyte which is crosslinked in an amount sufficient to provide swellability to said polyelectrolyte, wherein the amount of said sulfonic acid salt moieties in said polyelectrolyte is sufficient to provide water absorbent activity, wherein said sulfonic acid salt containing polyelec-trolyte maintains an ionic form over a lower pH range than a swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties having (1) a similar molecular weight and (2) a similar concentration of acid salt moieties to that of said alkali metal sulfonic acid salt polyelectrolyte, and wherein said sulfonic acid salt containing polyelectro-lyte provides improved water absorbent capability over a lower pH range than said swellable polyelectrolyte containing alkali metal carboxylic acid salt moieties.
2. A process of Claim 1 wherein said aqueous medium has a pH of less than 3.
3. A process of Claim 1 wherein said aqueous medium has a pH of from 0.2 to 2.
4. A process of Claim 1 wherein said alkali metal sulfonic acid salt containing polyelectrolyte is a copolymer of an essentially nonionic ethylenically unsaturated monomer and an alkali metal salt of an N-sulfoalkyl, .alpha.,.beta.-ethylenically unsaturated amide.
5. A process of Claim 1 wherein said alkali metal sulfonic acid salt containing polyelectrolyte is a copolymer of a nonionic ethylenically unsaturated monomer, an alkali metal 2-acrylamide-2-methylpropane sulfonate and a polyvinyl crosslinking monomer.
6. A process of Claim 1 wherein said water-swellable polymer comprises from 0 to 95 mole percent essentially nonionic ethylenically unsaturated monomer, from 5 to 100 mole percent ethylenically unsaturated monomer containing a sulfonic acid salt moiety, and from 100 to 2,500 ppm polyvinyl crosslinking monomer.
7. A process of Claim 6 wherein a portion of said essentially nonionic monomer units within the polymer have undergone hydrolysis.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000478946A CA1251631A (en) | 1985-04-12 | 1985-04-12 | Water-absorbent agents for low ph applications |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000478946A CA1251631A (en) | 1985-04-12 | 1985-04-12 | Water-absorbent agents for low ph applications |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1251631A true CA1251631A (en) | 1989-03-28 |
Family
ID=4130251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000478946A Expired CA1251631A (en) | 1985-04-12 | 1985-04-12 | Water-absorbent agents for low ph applications |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1251631A (en) |
-
1985
- 1985-04-12 CA CA000478946A patent/CA1251631A/en not_active Expired
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