US20060225852A1 - Process for removing silica from cellulosic material - Google Patents
Process for removing silica from cellulosic material Download PDFInfo
- Publication number
- US20060225852A1 US20060225852A1 US11/103,265 US10326505A US2006225852A1 US 20060225852 A1 US20060225852 A1 US 20060225852A1 US 10326505 A US10326505 A US 10326505A US 2006225852 A1 US2006225852 A1 US 2006225852A1
- Authority
- US
- United States
- Prior art keywords
- silica
- raw material
- black liquor
- liquor
- sodium carbonate
- 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
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 150
- 239000000377 silicon dioxide Substances 0.000 title claims abstract description 74
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000000463 material Substances 0.000 title claims description 11
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 61
- 238000005470 impregnation Methods 0.000 claims abstract description 53
- 239000002994 raw material Substances 0.000 claims abstract description 44
- 229910000029 sodium carbonate Inorganic materials 0.000 claims abstract description 30
- 238000009993 causticizing Methods 0.000 claims abstract description 29
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 18
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 8
- 239000010902 straw Substances 0.000 claims description 27
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- 239000000292 calcium oxide Substances 0.000 claims description 17
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 11
- 239000002023 wood Substances 0.000 claims description 11
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 8
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims description 6
- 235000017491 Bambusa tulda Nutrition 0.000 claims description 6
- 241001330002 Bambuseae Species 0.000 claims description 6
- 235000014676 Phragmites communis Nutrition 0.000 claims description 6
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims description 6
- 239000011425 bamboo Substances 0.000 claims description 6
- 239000000920 calcium hydroxide Substances 0.000 claims description 6
- 241000609240 Ambelania acida Species 0.000 claims description 5
- 239000010905 bagasse Substances 0.000 claims description 5
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 5
- 238000005086 pumping Methods 0.000 abstract 1
- 241000209140 Triticum Species 0.000 description 14
- 235000021307 Triticum Nutrition 0.000 description 14
- 235000012255 calcium oxide Nutrition 0.000 description 14
- 238000000926 separation method Methods 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000000523 sample Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 9
- 235000011941 Tilia x europaea Nutrition 0.000 description 9
- 239000004571 lime Substances 0.000 description 9
- 238000004537 pulping Methods 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 3
- 235000011116 calcium hydroxide Nutrition 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 239000011121 hardwood Substances 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229920002488 Hemicellulose Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241001062472 Stokellia anisodon Species 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 230000008092 positive effect Effects 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- -1 silicate ions Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000003265 pulping liquor Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229910052665 sodalite Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 229920001221 xylan Polymers 0.000 description 1
- 150000004823 xylans Chemical class 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C1/00—Pretreatment of the finely-divided materials before digesting
- D21C1/06—Pretreatment of the finely-divided materials before digesting with alkaline reacting compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C5/00—Other processes for obtaining cellulose, e.g. cooking cotton linters ; Processes characterised by the choice of cellulose-containing starting materials
Definitions
- the present invention relates to a method of removing silica from a cellulosic raw material, such as bamboo, bagasse, reed and straw, prior to the cellulosic raw material being converted into a pulp by a chemical or mechanical delignification processes.
- a cellulosic raw material such as bamboo, bagasse, reed and straw
- Non-wood cellulosic fibers are a percentage of the world's pulp source, representing less than 10% of the total pulp production.
- Non-wood pulp production primarily utilizes straw, bagasse, bamboo and reed.
- Agricultural by-products make up 73% of the world's non-wood pulp capacity while natural plants such as reed and bamboo account for 18% and the remainder consists mainly of industrial crops.
- the macro-chemical composition of non-wood cellulosic raw materials such as wheat straw does not deviate materially from that of hardwood.
- the total holocellulose content of wheat straw is very similar to that of trees. In contrast with wood, straw contains less cellulose.
- the lignin content of wheat straw is typically from 16% to 21% and significantly lower than that of softwoods, which is typically 26% to 34%, and hardwoods, which is typically from 23% to 30%.
- Cereal straws have relatively high silica and potassium content.
- the ash content of straw is invariably much higher than that of most other fibrous materials while Xylans are the principal hemicellulose contained in hardwoods and straws, analytically determined as pentosans.
- silica The greatest impediment to the use of non-wood cellulosic raw materials in commercial pulping is the ash, and more specifically silica, contained therein.
- Silica is distributed throughout the straw stem and is concentrated mostly in small bodies called phytoliths, which cover the outer surface of the stem. Silicon is typically present in living plants in three basic forms: insoluble silica in an amount of 90%, silicate ions in an amount of from 0.5% to 8%, and colloidal silicic acid in the amount of 0 to 3.3%.
- the insoluble silica in plant tissue is generally a clear, colorless and isotropic deposit with an index of refraction of 1.42 to 1.44. This amorphous silica deposit is found in a dumbbell-shaped cell referred to as biological opals.
- U.S. Pat. No. 4,331,507 to Roberts discloses an alkaline-type pulping process for the manufacture of pulp from silica-contaminated raw materials where a quantity of aluminum oxide sufficient to react with silica and sodium hydroxide present in the process is introduced into the pulp liquor to precipitate silica as a sodalite.
- U.S. Pat. No. 4,504,356 to Mülder et al discloses a continuous process for removing silica from spent pulping liquors, which have been obtained by the alkaline digestion of annual plants by pre-concentrating the spent liquor and contacting it with a carbon dioxide-containing gas. Silica precipitates, is removed from the treated liquor and then washed with water and causticized by the addition of lime or milk of lime. The solid and liquid phases are separated from each other and the resulting residue is combusted.
- U.S. Pat. No. 4,941,945 to Pettersson discloses a method of cleaning green liquor of solid particulate impurities by removing solid particles out of unclarified green liquor prior to the subsequent complete causticizing of clarified green liquor by adding caustic lime to the clarified liquor.
- the caustic lime is added to the unclarified green liquor during agitation prior to the removal of the solid particles in an amount of 0.5% to 10% of the caustic lime needed for the subsequent complete causticization.
- Waste liquor obtained during the digestion of wood is evaporated to give concentrated waste liquor, which is then burnt in a soda recovery boiler.
- a smelt is obtained that is led in smelt spouts down into a tank where it is dissolved in green liquor obtained by the washing of lime sludge in the causticizing department to produce green liquor.
- the green liquor is sent to a green liquor clarifier for removing solid particles therefrom by sedimentation.
- Chinese Publication No. 1103450 to Wang et al discloses a process for the removal of silicon from straw pulping black liquor which requires the addition of aluminum oxide and/or aluminum dihydrate from a by-product of an aluminum industry, and optionally a residue from a sodium chloride derived industry, or lime, to a straw pulping black liquor and separating the silica therefrom.
- the present invention is concerned with the removal of silica from a cellulosic raw material, particularly, a non-wood cellulosic material which can be straw, bagasse, reed, bamboo, cornstalks, and combinations thereof.
- a cellulosic raw material particularly, a non-wood cellulosic material which can be straw, bagasse, reed, bamboo, cornstalks, and combinations thereof.
- the cellulosic raw material should be cut into long pieces of approximately 10 to 30 millimeters in length and then screened. This significantly reduces the content of silica in the raw materials up to 50%.
- the raw materials are then moisturized and preheated by steam or hot water to help improve the kinetics of the impregnation of the cellulosic raw material with a silica leaching agent to thereby improve the efficiency of silica removal.
- the pretreated cellulosic raw material is impregnated with a solution comprising sodium carbonate to form silica-containing impregnation black liquor and in at least partially desilicated raw material.
- the sodium carbonate is preferably dissolved in an aqueous medium and, optionally, sodium hydroxide can be contained therein.
- the concentration of sodium carbonate in the impregnating solution is from 2.5 to 100 grams of Na 2 O equivalents per liter of impregnating solution.
- an impregnating solution containing a higher concentration of sodium carbonate may be diluted with any kind of technological water or waste aqueous media containing residual sodium carbonate to achieve the targeted amount of sodium carbonate or sodium carbonate and sodium hydroxide mixture to obtain the desired ratio of impregnating solution to raw material.
- the amount of sodium carbonate contained in the impregnating solution varies depending on the quality of the cellulosic raw material and the desired levels of desilication.
- the charge of sodium carbonate may be up to 25% based on oven dried weight of raw material and preferably is over 5%, most preferably 10%, Na 2 O equivalent.
- the ratio of impregnation liquid to cellulosic raw material can vary significantly depending on the quality of the raw material and normally is maintained in the range of from 1:2.5 up to 1:20. The ratio is maintained as small as possible while maintaining good impregnation operation, including good impregnating solution circulation to achieve even silica removal from the raw cellulosic material.
- the time, temperature and pressure for the impregnating step will depend on the variables discussed above, the time of the impregnation may take up to two hours, preferably up to one hour and most preferably 30 minutes.
- the temperature of the impregnation can range from at least 40° centigrade up to 180° centigrade with 100° centigrade being preferable and 70° centigrade being most preferable.
- the impregnation pressure may vary up to 880 kPa of saturated steam but most preferably impregnation is performed at atmospheric pressure.
- the impregnating step at least partially desilicates the cellulosic raw material and will preferably completely desilicates the cellulosic raw material and forms silica-containing impregnation black liquor.
- the silica-containing impregnation black liquor is separated from the at least partially desilicated cellulosic raw material by any known suitable separation technique and is preferably separated by a screw press.
- the time of separation will be dependent upon the retention time needed in the separation device and a preferable temperature is the temperature of the silica-containing impregnation black liquor entering the separation device.
- a preferred pressure of the separation step is atmospheric pressure but any other temperature and time parameters can be varied by one skilled in the arts based on the conditions of the materials to be separated, the desired product quality and the separation device utilized.
- the separated silica-containing impregnation black liquor is causticized to precipitate silica-enriched calcium carbonate.
- Calcium oxide and/or calcium hydroxide is used to causticize the separated silica-containing impregnation black liquor and should be added in an amount at least equal to a 1:1 molar ratio of lime to residual sodium carbonate.
- the conversion efficiency of the causticizing step is dependent on the duration of the causticizing step, the temperature of the causticizing liquor and the quality of the calcium oxide-containing material.
- the causticizing reaction rate curves show two separate zones with an initial period having high values of reaction rate from the initiation of causticization up to 20 minutes at a temperature range of from 70° to 100° centigrade, at which a causticizing efficiency up to 80% is reached.
- the second time period is characterized by a very low reaction rate value and requires a much longer period of causticizing as equilibrium conversion is approached.
- the causticized solution may also contain precipitated calcium carbonate, sodium hydroxide, excess lime that doesn't react with sodium carbonate and other components such as soluble lignin, hemicelluloses and soluble silica, which enter the causticizing reaction and which may or may not be entrapped with the precipitated calcium carbonate.
- precipitated silica-enriched calcium carbonate can be separated from the causticized impregnation liquor by any suitable type of separation process, with sedimentation and filtration techniques being preferred.
- temperature and pressure conditions required for separation of the precipitated silica-enriched calcium carbonate from the causticized impregnation liquor as is generally known, higher temperatures have a positive effect on the settling velocity in a sedimentation process and higher pressures have a positive effect on separation in filtration processes.
- the separated causticized impregnation liquor is considered to be silica-free and can be used as a washing liquor, dilution media or make-up media in different steps in the process.
- the impregnation of the wheat straw sample was conducted in a 6.5 L stationary batch digester (M&K Systems Inc.) equipped with an electrical heat exchanger and a liquor circulation system. The experiment was conducted at the conditions as follows: 160 grams of air dried wheat straw with 6% of moisture content, 38.5 grams of anhydrous Na 2 CO 3 (15% of Na 2 O on o.d. material), liquor to wheat straw ratio—1:20, impregnation temperature—95° C., time of impregnation at the impregnation temperature—30 minutes.
- Control sample A sample of the wheat straw, containing 2.95% of total ash and 1.22% of silica (acid insoluble ash), was treated with the impregnating liquid (12.8 g Na 2 CO 3 /L) under the conditions mentioned above. After the impregnation step, the sample of impregnated wheat straw was washed and stored in wet conditions, and 2160 mL of impregnation black liquor were used for the following analysis and caustisizing experiments.
- the total yield from the wheat straw impregnation was 88.1%.
- the impregnation black liquor contained 23 mg of suspended solids per liter, total solids 19.3 g/L, total ash content (575° C.) 13.6 g/L, silica content 0.582 g/L, and concentration of residual sodium carbonate 8.3 g Na 2 CO 3 /L. Based on the analysis provided, cca 35.2% of sodium carbonate in the impregnation liquor was consumed and 95.8% of silica was removed from the raw material.
- Causticizing step Causticizing of the impregnation black liquor obtained after impregnation of the wheat straw was performed in 50 mL PE ampoules at a temperature of 105° C. and time of 6 hours. The sample of impregnation black liquor was filtered and not diluted. A different amount of quick lime prepared in the laboratory was added directly into the ampoules filled with the impregnation black liquor. After causticizing, the samples were clarified overnight by settling the sediment and then centrifuged at 2300 RPM for 5 minutes. A clear solution (Supernatant I) was separated, stored and used for silica content and residual sodium carbonate analysis. The amount of sediment was determined by drying at 105° C. in an oven.
- the impregnating liquor with a Total Titratable Alkali of 10.0 g Na 2 O/L was used with a ratio of Na 2 CO 3 :NaOH of 3:1 (in Na 2 O equivalents).
- the impregnating black liquor contained residual sodium carbonate at a concentration of 5.5 g Na 2 O/L and dissolved silica at a concentration of 0.595 g SiO 2 /L.
- Example III shows that the causticizing of the impregnation black liquor with sodium hydroxide contained therein is in principle possible, but with lower dissolved silica reduction efficiency, as well as a lowered causticizing efficiency.
- the present invention allows for the separation of up to 100% of the silica originally contained in the cellulosis raw material and the complete separation of silica from the silica-contained impregnation black liquor in an economical and simple manner to provide a process cellulosis material that can be used at a paper pulping process.
Landscapes
- Paper (AREA)
Abstract
Description
- The present invention relates to a method of removing silica from a cellulosic raw material, such as bamboo, bagasse, reed and straw, prior to the cellulosic raw material being converted into a pulp by a chemical or mechanical delignification processes.
- Non-wood cellulosic fibers are a percentage of the world's pulp source, representing less than 10% of the total pulp production. Non-wood pulp production primarily utilizes straw, bagasse, bamboo and reed. Agricultural by-products make up 73% of the world's non-wood pulp capacity while natural plants such as reed and bamboo account for 18% and the remainder consists mainly of industrial crops.
- Current trends indicate that the global consumption of paper making fibers would increase to approximately 425,000,000 tons by the year 2010. At the present time, it is not known where the estimated millions of tons of fiber needed by the year 2010 will come from. An abundance of agricultural residues are produced in the United States and Canada, which could be used for pulp and paper production with wheat straw and corn stalks representing the most underutilized fiber resources in the United States.
- The macro-chemical composition of non-wood cellulosic raw materials such as wheat straw does not deviate materially from that of hardwood. The total holocellulose content of wheat straw is very similar to that of trees. In contrast with wood, straw contains less cellulose. The lignin content of wheat straw is typically from 16% to 21% and significantly lower than that of softwoods, which is typically 26% to 34%, and hardwoods, which is typically from 23% to 30%. Cereal straws have relatively high silica and potassium content. The ash content of straw is invariably much higher than that of most other fibrous materials while Xylans are the principal hemicellulose contained in hardwoods and straws, analytically determined as pentosans.
- The greatest impediment to the use of non-wood cellulosic raw materials in commercial pulping is the ash, and more specifically silica, contained therein. Silica is distributed throughout the straw stem and is concentrated mostly in small bodies called phytoliths, which cover the outer surface of the stem. Silicon is typically present in living plants in three basic forms: insoluble silica in an amount of 90%, silicate ions in an amount of from 0.5% to 8%, and colloidal silicic acid in the amount of 0 to 3.3%. The insoluble silica in plant tissue is generally a clear, colorless and isotropic deposit with an index of refraction of 1.42 to 1.44. This amorphous silica deposit is found in a dumbbell-shaped cell referred to as biological opals.
- There have been many efforts to accomplish the removal of silica from non-wood cellulosic materials in a simple and economical fashion, including black liquor desilication with carbon dioxide from flue gases, two-stage causticizing desilication, green liquor desilication with lime, evaporation and the use of ammonium- or potassium-based pulping with the by-product liquor being utilized as a fertilizer.
- U.S. Pat. No. 4,331,507 to Roberts discloses an alkaline-type pulping process for the manufacture of pulp from silica-contaminated raw materials where a quantity of aluminum oxide sufficient to react with silica and sodium hydroxide present in the process is introduced into the pulp liquor to precipitate silica as a sodalite.
- U.S. Pat. No. 4,504,356 to Mülder et al discloses a continuous process for removing silica from spent pulping liquors, which have been obtained by the alkaline digestion of annual plants by pre-concentrating the spent liquor and contacting it with a carbon dioxide-containing gas. Silica precipitates, is removed from the treated liquor and then washed with water and causticized by the addition of lime or milk of lime. The solid and liquid phases are separated from each other and the resulting residue is combusted.
- U.S. Pat. No. 4,941,945 to Pettersson discloses a method of cleaning green liquor of solid particulate impurities by removing solid particles out of unclarified green liquor prior to the subsequent complete causticizing of clarified green liquor by adding caustic lime to the clarified liquor. The caustic lime is added to the unclarified green liquor during agitation prior to the removal of the solid particles in an amount of 0.5% to 10% of the caustic lime needed for the subsequent complete causticization. Waste liquor obtained during the digestion of wood is evaporated to give concentrated waste liquor, which is then burnt in a soda recovery boiler. A smelt is obtained that is led in smelt spouts down into a tank where it is dissolved in green liquor obtained by the washing of lime sludge in the causticizing department to produce green liquor. The green liquor is sent to a green liquor clarifier for removing solid particles therefrom by sedimentation.
- U.S. Pat. No. 6,074,521 to Engdahl et al discloses that it is known to remove silicon from green liquor by adding lime to the green liquor whereby silicon precipitates with the lime, which may then be removed.
- Chinese Publication No. 1103450 to Wang et al discloses a process for the removal of silicon from straw pulping black liquor which requires the addition of aluminum oxide and/or aluminum dihydrate from a by-product of an aluminum industry, and optionally a residue from a sodium chloride derived industry, or lime, to a straw pulping black liquor and separating the silica therefrom.
- However, none of the prior art references discussed above disclose a simple and economical method of de-silicating a cellulose raw material that is to be used in the pulp manufacture.
- It is an object of the present invention to provide a method for removing silica from a cellulosic raw material, which can be performed in a simple and economical manner.
- It is a further object of the present invention to provide a method from removing silica from a non-wood cellulosic material in a simple and economical manner.
- It is still a further object of the present invention to provide a method for removing silica from a non-wood cellulosic raw material selected from straw, bagasse, bamboo, reed and cornstalks in a simple and economical manner to produce a processed non-wood cellulosic material which can be used subsequently in pulp manufacture.
- DETAILED DESCRIPTION OF THE INVENTION
- The present invention is concerned with the removal of silica from a cellulosic raw material, particularly, a non-wood cellulosic material which can be straw, bagasse, reed, bamboo, cornstalks, and combinations thereof. Initially, the cellulosic raw material should be cut into long pieces of approximately 10 to 30 millimeters in length and then screened. This significantly reduces the content of silica in the raw materials up to 50%. After washing, the raw materials are then moisturized and preheated by steam or hot water to help improve the kinetics of the impregnation of the cellulosic raw material with a silica leaching agent to thereby improve the efficiency of silica removal.
- The pretreated cellulosic raw material is impregnated with a solution comprising sodium carbonate to form silica-containing impregnation black liquor and in at least partially desilicated raw material. The sodium carbonate is preferably dissolved in an aqueous medium and, optionally, sodium hydroxide can be contained therein. The concentration of sodium carbonate in the impregnating solution is from 2.5 to 100 grams of Na2O equivalents per liter of impregnating solution. If desired, an impregnating solution containing a higher concentration of sodium carbonate may be diluted with any kind of technological water or waste aqueous media containing residual sodium carbonate to achieve the targeted amount of sodium carbonate or sodium carbonate and sodium hydroxide mixture to obtain the desired ratio of impregnating solution to raw material. The amount of sodium carbonate contained in the impregnating solution varies depending on the quality of the cellulosic raw material and the desired levels of desilication. The charge of sodium carbonate may be up to 25% based on oven dried weight of raw material and preferably is over 5%, most preferably 10%, Na2O equivalent.
- The ratio of impregnation liquid to cellulosic raw material can vary significantly depending on the quality of the raw material and normally is maintained in the range of from 1:2.5 up to 1:20. The ratio is maintained as small as possible while maintaining good impregnation operation, including good impregnating solution circulation to achieve even silica removal from the raw cellulosic material.
- There are no critical requirements with respect to the time, temperature and pressure for performing the above-described impregnation step. All three of these variables depend on the quality and type of raw material, the extent of desired desilication, the desired quality of the silica-containing impregnation black liquor, the economics of the impregnating step, and subsequent causticization of the silica-containing impregnation black liquor.
- Although the time, temperature and pressure for the impregnating step will depend on the variables discussed above, the time of the impregnation may take up to two hours, preferably up to one hour and most preferably 30 minutes. The temperature of the impregnation can range from at least 40° centigrade up to 180° centigrade with 100° centigrade being preferable and 70° centigrade being most preferable. The impregnation pressure may vary up to 880 kPa of saturated steam but most preferably impregnation is performed at atmospheric pressure.
- The impregnating step at least partially desilicates the cellulosic raw material and will preferably completely desilicates the cellulosic raw material and forms silica-containing impregnation black liquor. The silica-containing impregnation black liquor is separated from the at least partially desilicated cellulosic raw material by any known suitable separation technique and is preferably separated by a screw press.
- As with the impregnating step, there are no critical requirements with respect to time, temperature and pressure necessary for performing the separation of the silica-containing impregnation black liquor from the at least partially desilicated raw material. The time of separation will be dependent upon the retention time needed in the separation device and a preferable temperature is the temperature of the silica-containing impregnation black liquor entering the separation device. A preferred pressure of the separation step is atmospheric pressure but any other temperature and time parameters can be varied by one skilled in the arts based on the conditions of the materials to be separated, the desired product quality and the separation device utilized.
- After being separated from the at least partially desilicated cellulosic raw material, the separated silica-containing impregnation black liquor is causticized to precipitate silica-enriched calcium carbonate. Calcium oxide and/or calcium hydroxide is used to causticize the separated silica-containing impregnation black liquor and should be added in an amount at least equal to a 1:1 molar ratio of lime to residual sodium carbonate. The conversion efficiency of the causticizing step is dependent on the duration of the causticizing step, the temperature of the causticizing liquor and the quality of the calcium oxide-containing material.
- In general, the causticizing reaction rate curves show two separate zones with an initial period having high values of reaction rate from the initiation of causticization up to 20 minutes at a temperature range of from 70° to 100° centigrade, at which a causticizing efficiency up to 80% is reached. The second time period is characterized by a very low reaction rate value and requires a much longer period of causticizing as equilibrium conversion is approached.
- For economic reasons, changes in the incoming silica-containing impregnation black liquor are not expected so the time of causticizing will mostly be dependent on the quality and amount charged of calcium oxide. Moreover, an increase in the amount of calcium oxide charge may affect the causticizing step in two ways. It would increase the reaction rate of the causticizing reaction because most of the easily reacting part of the calcium oxide will be presented and it will also negatively affect the kinetics of the causticizing because of the higher particle concentration and higher concentration of residual, non-reactive slaked lime in the final solution which can cause problems with respect to the settling of lime mud, calcium carbonate, in the following step of separating silica-enriched sodium carbonate from the causticized impregnation black liquor.
- The causticized solution may also contain precipitated calcium carbonate, sodium hydroxide, excess lime that doesn't react with sodium carbonate and other components such as soluble lignin, hemicelluloses and soluble silica, which enter the causticizing reaction and which may or may not be entrapped with the precipitated calcium carbonate.
- After the causticization step, precipitated silica-enriched calcium carbonate can be separated from the causticized impregnation liquor by any suitable type of separation process, with sedimentation and filtration techniques being preferred. Although there is no critical time, temperature and pressure conditions required for separation of the precipitated silica-enriched calcium carbonate from the causticized impregnation liquor, as is generally known, higher temperatures have a positive effect on the settling velocity in a sedimentation process and higher pressures have a positive effect on separation in filtration processes. The separated causticized impregnation liquor is considered to be silica-free and can be used as a washing liquor, dilution media or make-up media in different steps in the process.
- The present invention is further shown, but not limited by, the following examples.
- Wheat straw (Triticum aestivum) from Michigan harvest area was chopped into 10 to 30 mm long strips and hand cleaned from sand and dust prior to the experiment. The straw, yellowish in color, was of high quality. The sample was stored at a dry content of about 94%. Whole stems, without leaves and rachis were used.
- The impregnation of the wheat straw sample was conducted in a 6.5 L stationary batch digester (M&K Systems Inc.) equipped with an electrical heat exchanger and a liquor circulation system. The experiment was conducted at the conditions as follows: 160 grams of air dried wheat straw with 6% of moisture content, 38.5 grams of anhydrous Na2CO3 (15% of Na2O on o.d. material), liquor to wheat straw ratio—1:20, impregnation temperature—95° C., time of impregnation at the impregnation temperature—30 minutes.
- Control sample: A sample of the wheat straw, containing 2.95% of total ash and 1.22% of silica (acid insoluble ash), was treated with the impregnating liquid (12.8 g Na2CO3/L) under the conditions mentioned above. After the impregnation step, the sample of impregnated wheat straw was washed and stored in wet conditions, and 2160 mL of impregnation black liquor were used for the following analysis and caustisizing experiments.
- The total yield from the wheat straw impregnation was 88.1%. The impregnation black liquor contained 23 mg of suspended solids per liter, total solids 19.3 g/L, total ash content (575° C.) 13.6 g/L, silica content 0.582 g/L, and concentration of residual sodium carbonate 8.3 g Na2CO3/L. Based on the analysis provided, cca 35.2% of sodium carbonate in the impregnation liquor was consumed and 95.8% of silica was removed from the raw material.
- Causticizing step: Causticizing of the impregnation black liquor obtained after impregnation of the wheat straw was performed in 50 mL PE ampoules at a temperature of 105° C. and time of 6 hours. The sample of impregnation black liquor was filtered and not diluted. A different amount of quick lime prepared in the laboratory was added directly into the ampoules filled with the impregnation black liquor. After causticizing, the samples were clarified overnight by settling the sediment and then centrifuged at 2300 RPM for 5 minutes. A clear solution (Supernatant I) was separated, stored and used for silica content and residual sodium carbonate analysis. The amount of sediment was determined by drying at 105° C. in an oven.
- In a step of causticizing impregnation black liquor containing predominantly residual sodium carbonate and dissolved silica, 25 mL of filtered impregnation black liquor was treated in a 50 mL PE ampoule under the conditions described above. 0.0778 g of powdered calcium oxide (quick lime) was added into the sample, which contained dissolved silica at a concentration of 0.582 g/L. The amount of quick lime added was 71.2% stoichiometrically equivalent to the amount of sodium carbonate present in the sample. After the causticizing reaction, an analysis of centrifuged and clarified spent liquor was provided. 42.4% of causticizing efficiency was determined, and the concentration of dissolved silica in the liquor dropped to a level of 0.542 g/L. Thus, the amount of dissolved silica was reduced by 9.3%.
- The following experiment was provided under the same conditions, except the calcium oxide (quick lime) was added at the amount of 120% stoichiometrically equivalent to the amount of sodium carbonate present in the sample. After the causticizing reaction, an analysis of centrifuged and clarified liquor was provided. 100% causticizing efficiency was determined and the concentration of dissolved silica in the liquor dropped to a level of 0.014 g/L. The treatment was effective in that the dissolved silica was reduced to 2.4% of the silica dissolved in the original impregnation black liquor. The concentration of residual dissolved silica (0.014 g/L) most probably comes from quick lime used for the causticizing steps, which contained 0.13% silica by weight. Taking that into consideration, the residual silica content may come from sources other than the raw material (wheat straw), so the desilication efficiency in this example may be considered to be 100%.
- For the impregnation/desilication of wheat straw, under the same conditions as mentioned above, the impregnating liquor with a Total Titratable Alkali of 10.0 g Na2O/L was used with a ratio of Na2CO3:NaOH of 3:1 (in Na2O equivalents). The impregnating black liquor contained residual sodium carbonate at a concentration of 5.5 g Na2O/L and dissolved silica at a concentration of 0.595 g SiO2/L. Into the sample containing dissolved silica at the concentration of 0.595 g/L, calcium oxide (quick lime) was added at the amount of 120% stoichiometrically equivalent to the amount of sodium carbonate present in the sample of impregnation black liquor (the same as in Example II). After the causticizing reaction, an analysis of centrifuged and clarified liquor was provided. 56.8% of causticizing efficiency was determined and the concentration of dissolved silica in the liquor dropped to a level of 0.249 g/L. The treatment had been effective in that the dissolved silica had been reduced to 41.8% of the silica dissolved in the original impregnation black liquor. Thus, 58.2% reduction of dissolved silica was achieved. Example III shows that the causticizing of the impregnation black liquor with sodium hydroxide contained therein is in principle possible, but with lower dissolved silica reduction efficiency, as well as a lowered causticizing efficiency.
- The present invention allows for the separation of up to 100% of the silica originally contained in the cellulosis raw material and the complete separation of silica from the silica-contained impregnation black liquor in an economical and simple manner to provide a process cellulosis material that can be used at a paper pulping process.
Claims (12)
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| US11/103,265 US20060225852A1 (en) | 2005-04-11 | 2005-04-11 | Process for removing silica from cellulosic material |
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| US11/103,265 US20060225852A1 (en) | 2005-04-11 | 2005-04-11 | Process for removing silica from cellulosic material |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080142176A1 (en) * | 2006-12-18 | 2008-06-19 | Van Heiningen Adriaan Reinhard | Process of treating a lignocellulosic material |
| US20080196847A1 (en) * | 2006-12-18 | 2008-08-21 | Pieter Van Heiningen Adriaan R | Pre-extraction and solvent pulping of lignocellulosic material |
| US20110094692A1 (en) * | 2008-03-18 | 2011-04-28 | The Research Foundation Of State University Of New York | Methods of pretreating comminuted cellulosic material with carbonate-containing solutions |
| CN102877361A (en) * | 2012-09-28 | 2013-01-16 | 湖南文理学院 | Silicon retention agent for pulping by grass materials and cooking method |
| CN103334329A (en) * | 2013-06-28 | 2013-10-02 | 陕西科技大学 | Bamboo pulp green liquor silica pre-removing method through utilizing sodium bentonite and application of method |
| CN109266693A (en) * | 2017-07-18 | 2019-01-25 | 湖南湘易康制药有限公司 | A kind of method of straw biological alcohol prepared by fermenting |
| CN115652676A (en) * | 2022-11-17 | 2023-01-31 | 陕西科技大学 | Green liquor desilicication process preposed in desilicication process |
| WO2025043331A1 (en) * | 2023-08-25 | 2025-03-06 | Red Leaf Sustainable Ip Corp. | Apparatus and methods for extracting lignin from non-wood black liquor |
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| US4331507A (en) * | 1979-12-10 | 1982-05-25 | Dorr-Oliver Incorporated | Desilication in alkaline pulp processes |
| US4504356A (en) * | 1982-03-06 | 1985-03-12 | Metallgesellschaft Aktiengesellschaft | Continuous process of removing silica from spent pulping liquors |
| US4941945A (en) * | 1987-02-12 | 1990-07-17 | Hedemora Ab | Method for clarifying green liquor |
| US6074531A (en) * | 1997-03-11 | 2000-06-13 | Valmet-Karlstad Ab | Device in a measuring station |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080142176A1 (en) * | 2006-12-18 | 2008-06-19 | Van Heiningen Adriaan Reinhard | Process of treating a lignocellulosic material |
| US20080196847A1 (en) * | 2006-12-18 | 2008-08-21 | Pieter Van Heiningen Adriaan R | Pre-extraction and solvent pulping of lignocellulosic material |
| US7824521B2 (en) * | 2006-12-18 | 2010-11-02 | University Of Maine System Board Of Trustees | Process of treating a lignocellulosic material with hemicellulose pre-extraction and hemicellulose adsorption |
| US7842161B2 (en) * | 2006-12-18 | 2010-11-30 | The University Of Maine System Board Of Trustees | Pre-extraction and solvent pulping of lignocellulosic material |
| US8475627B2 (en) | 2006-12-18 | 2013-07-02 | University Of Maine System Board Of Trustees | Process of treating a lignocellulosic material |
| US20110214826A1 (en) * | 2006-12-18 | 2011-09-08 | University Of Maine System Board Of Trustees | Process of treating a lignocellulosic material |
| US8303767B2 (en) | 2008-03-18 | 2012-11-06 | The Research Foundation Of State University Of New York | Methods of pretreating comminuted cellulosic material with carbonate-containing solutions |
| US20110094692A1 (en) * | 2008-03-18 | 2011-04-28 | The Research Foundation Of State University Of New York | Methods of pretreating comminuted cellulosic material with carbonate-containing solutions |
| CN102877361A (en) * | 2012-09-28 | 2013-01-16 | 湖南文理学院 | Silicon retention agent for pulping by grass materials and cooking method |
| CN103334329A (en) * | 2013-06-28 | 2013-10-02 | 陕西科技大学 | Bamboo pulp green liquor silica pre-removing method through utilizing sodium bentonite and application of method |
| CN109266693A (en) * | 2017-07-18 | 2019-01-25 | 湖南湘易康制药有限公司 | A kind of method of straw biological alcohol prepared by fermenting |
| CN115652676A (en) * | 2022-11-17 | 2023-01-31 | 陕西科技大学 | Green liquor desilicication process preposed in desilicication process |
| WO2025043331A1 (en) * | 2023-08-25 | 2025-03-06 | Red Leaf Sustainable Ip Corp. | Apparatus and methods for extracting lignin from non-wood black liquor |
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