US3272689A - Delignification of lignocellulose with an nu-(lower alkyl)-2-pyrrolidone - Google Patents
Delignification of lignocellulose with an nu-(lower alkyl)-2-pyrrolidone Download PDFInfo
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- US3272689A US3272689A US256131A US25613163A US3272689A US 3272689 A US3272689 A US 3272689A US 256131 A US256131 A US 256131A US 25613163 A US25613163 A US 25613163A US 3272689 A US3272689 A US 3272689A
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- United States
- Prior art keywords
- pyrrolidone
- delignification
- water
- lignin
- lower alkyl
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- 238000000034 method Methods 0.000 claims description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 239000003153 chemical reaction reagent Substances 0.000 claims description 11
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 10
- 239000002023 wood Substances 0.000 claims description 9
- 229920005610 lignin Polymers 0.000 description 20
- 238000004537 pulping Methods 0.000 description 13
- 239000001913 cellulose Substances 0.000 description 9
- 229920002678 cellulose Polymers 0.000 description 9
- -1 ethyl- Chemical group 0.000 description 8
- 239000011121 hardwood Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000011122 softwood Substances 0.000 description 7
- 238000001914 filtration Methods 0.000 description 6
- 239000003752 hydrotrope Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 4
- 230000003165 hydrotropic effect Effects 0.000 description 4
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 4
- 235000003339 Nyssa sylvatica Nutrition 0.000 description 3
- 244000018764 Nyssa sylvatica Species 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 235000012054 meals Nutrition 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 241000609240 Ambelania acida Species 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000218691 Cupressaceae Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000010905 bagasse Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- DCALJVULAGICIX-UHFFFAOYSA-N 1-propylpyrrolidin-2-one Chemical compound CCCN1CCCC1=O DCALJVULAGICIX-UHFFFAOYSA-N 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000183024 Populus tremula Species 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- WVHBHPATSLQXGC-UHFFFAOYSA-N benzene;ethanol Chemical compound CCO.C1=CC=CC=C1 WVHBHPATSLQXGC-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 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
- D21C3/00—Pulping cellulose-containing materials
- D21C3/003—Pulping cellulose-containing materials with organic compounds
Definitions
- the present invention relates to a process for the delignification of lignocellulose. More particularly, this invention relates to a process for delignification in which the pulping medium is a mixture of water and an N-(lower alkyl)-2-pyrrolidone.
- lower alkyl is used herein to mean straight or branched chain saturated aliphatic radicals which contain from one to five carbon atoms;
- examples of the N-(lower alkyl)-2-pyrrolidones of this invention are N- methyl-, ethyl-, n-propyl-, isopropyl-, n-butyl-, secbutyl-, iso-butyl-, t-butyl-, 'n-pentyl, iso-pentyl-, and neopentyl, -2-pyrrolidone.
- a hydrotrope is a substance which increases the solubility of another substance in water; the original definition (Neuberg, J. Chem. Soc, 110, II, 555) applied the term only to salts.
- the interaction between solute and hydrotropic agent which effects increased solubility is not thoroughly understood, but it is probable that the solute benefits from the superior solvation of the hydrotrope by bonding to it.
- the resultant bonds are usually readily broken by addition of solvent, which causes precipitation of solute, and it is therefore inferred that solute-hydrotrope interaction does not involve covalent forces, but depends on a combination of van der Waals forces, electrostatic attraction, and coordinate-covalent bonds.
- Hydrotropic pulping usually involves a procedure in which lignocellulose, water and hydrotrope are allowed to react at an elevated temperature for several hours; the resultant pulp is removed by filtration, and water is added to the filtrate to precipitate lignin. Then lignin is separated by mechanical means, and the mother liquor is concentrated by evaporation or distillation of exess water; the resultant liquor is returned to the pulping step. This procedure is readily adapted to a batch or continuous process.
- lignocellulose for example wood chips
- N (lower alkyl) 2 pyrrolidone The weight ratio of these reagents is usually 1:20 to 1:1, respectively.
- the resultant mixture is heated usually at C. to 200 C. for a time of from about one-half to about 24 hours.
- the cellulosic material is removed from the mixture thus obtained by mechanical means, such as by filtration or centrifugation, and the mother liquid is treated with water to precipitate lignin and associated materials. The precipitate is removed, and the remaining liquid is concentrated by distillation; the resultant concentrate may be re-used in the pulping step.
- a particular embodiment of this invention involves treatment of wood chips with a mixture of water and an N-(lower al-kyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at C. to 180 C. for a time of from one to four hours, followed by filtration to remove pulp, addition of water to the filtrate, removal by filtration of the lignin thus precipitated, and concentration of the aqueous N-(lower alkyl)-2-pyrrolidone solution.
- a preferred embodiment of this invention involves treatment of hardwood chips with a mixture of water and N-rnethyl-Z-pyrr-olidone in a weight ratio of from 1:4 to 1:2 in a sealed reaction vessel at a temperature of 100 C. to 180 C. for a time of from one to four hours, followed by the separation and concentration steps cited above.
- the process of this invention is applicable to lignocellulose generally including softwoods such as pine and cypresses; hardwoods such as black gum, aspen, oak and fruit woods; and fibers such as those of bagasse and bast. These materials can be used in any convenient form, chips or meal being preferred, and can be previously extracted with organic solvents such as ethanol-benzene to remove fatty acids, sterols and glycerine, without material effect on the pulping procedure of this invention.
- the hardwood pulp thus obtained is suitable for use as a corrugating medium, and softwood pulp prepared by this procedure is useful as liner for corrugated board.
- A In a typical embodiment of this invention a mixture of 30 grams of black gum wood meal, 280 ml. of N-methyl-Z-pyrrolidone and 20 ml. of water was stirred and heated in an autoclave at C. under a nitrogen pressure of 100 p.s.i.g. for three hours. The reaction mixture thus obtained is allowed to cool to room temperature, and then the pulp is removed by filtration; the yield is 69%, based on the weight of wood. The filtrate may be re-used two or three times without further treatment. When the pulp yield drops substantially, the filtrate is diluted with 500 ml. of water, and the precipitated lignin and associated material are removed by filtration;
- a method of delignification which comprises treating wood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating wood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from one to four hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating hardwood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating hardwood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from one to four hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating softwood with a reagent which comprises water and N-methyl-Z-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature of from C. to 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating hardwood with a reagent which comprises water and N-methyl-Z-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature of from C. to C. for a time of from one to four hours and separating a ligninenriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating bagasse with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
- a method of delignification which comprises treating softwood with a reagent which comprises Water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from 1 to 4 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
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- Paper (AREA)
Description
United States Patent "ice 3,272,689 DELTGNTFICATIION 0F LIGNOCELLULOSE WITH AN N-(LOWER ALKYL)-2-PYRROLIDONE Bernard L. lLenz, Stockholm, Sweden, assignor to Owens- Illlinois, Ina, a corporation of Ohio No Drawing. Filed Feb. 4, 1963, Ser. No. 256,131 8 Claims. (Cl. 162-72) The present invention relates to a process for the delignification of lignocellulose. More particularly, this invention relates to a process for delignification in which the pulping medium is a mixture of water and an N-(lower alkyl)-2-pyrrolidone.
The term lower alkyl is used herein to mean straight or branched chain saturated aliphatic radicals which contain from one to five carbon atoms; examples of the N-(lower alkyl)-2-pyrrolidones of this invention are N- methyl-, ethyl-, n-propyl-, isopropyl-, n-butyl-, secbutyl-, iso-butyl-, t-butyl-, 'n-pentyl, iso-pentyl-, and neopentyl, -2-pyrrolidone.
A hydrotrope is a substance which increases the solubility of another substance in water; the original definition (Neuberg, J. Chem. Soc, 110, II, 555) applied the term only to salts. The interaction between solute and hydrotropic agent which effects increased solubility is not thoroughly understood, but it is probable that the solute benefits from the superior solvation of the hydrotrope by bonding to it. The resultant bonds are usually readily broken by addition of solvent, which causes precipitation of solute, and it is therefore inferred that solute-hydrotrope interaction does not involve covalent forces, but depends on a combination of van der Waals forces, electrostatic attraction, and coordinate-covalent bonds.
The ability of certain hydrotropes to increase the water solubility of lignin more than they increase the solubility of cellulose is the basis of hydrotropic pulping. This method of delignification has advantages over procedures which require acidic (sulfite process) or alkaline (kraft and soda processes) reaction media (McKee, Ind. & Eng. Chem. (4), 38, 382 (1946)). An acidic medium usually causes hydrolysis of alpha-cellulose, and consequent decrease in yield of pulp; a further disadvantage is that the lignin is obtained as a highly modified calcium sulfonate. An alkaline medium usually causes extensive destruction of hemicellulose, and converts. the lignin to sodium salts of organic acids which possess mainly fuel value. The ability of hydrotropic processes to operate near neutral pH results in a superior yield of alpha-cellulose, and produces lignin which, because it more closely resembles native lignin, is a more promising material for further applications. Hydrotropic pulping usually involves a procedure in which lignocellulose, water and hydrotrope are allowed to react at an elevated temperature for several hours; the resultant pulp is removed by filtration, and water is added to the filtrate to precipitate lignin. Then lignin is separated by mechanical means, and the mother liquor is concentrated by evaporation or distillation of exess water; the resultant liquor is returned to the pulping step. This procedure is readily adapted to a batch or continuous process.
Accordingly, it is an object of this invention to pro vide a process for the delignification of lignocellulose.
It is a further object to provide a process for delignification in which the pulping agent is readily recovered and recyclized.
It is a still further object to provide a process for delignification in which the pulp and lignin are readily separated in substantially unaltered form.
It is another object to provide a process for delignification in which the pH is near 7.
Other objects and advantages of the present invention will be apparent from the following description.
3,272,689 Patented Sept. 13, 1966 According to the present invention, these and other objects and advantages are met by a process which comprises contacting lignocellulose with a reagent in which the essential ingredients are water and an N-(lower alkyl)- 2-pyrrolid-one to effect delignification. I
In the procedure of the present invention, lignocellulose, for example wood chips, is added to a mixture of water and an N (lower alkyl) 2 pyrrolidone. The weight ratio of these reagents is usually 1:20 to 1:1, respectively. The resultant mixture is heated usually at C. to 200 C. for a time of from about one-half to about 24 hours. The cellulosic material is removed from the mixture thus obtained by mechanical means, such as by filtration or centrifugation, and the mother liquid is treated with water to precipitate lignin and associated materials. The precipitate is removed, and the remaining liquid is concentrated by distillation; the resultant concentrate may be re-used in the pulping step. A particular embodiment of this invention involves treatment of wood chips with a mixture of water and an N-(lower al-kyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at C. to 180 C. for a time of from one to four hours, followed by filtration to remove pulp, addition of water to the filtrate, removal by filtration of the lignin thus precipitated, and concentration of the aqueous N-(lower alkyl)-2-pyrrolidone solution. A preferred embodiment of this invention involves treatment of hardwood chips with a mixture of water and N-rnethyl-Z-pyrr-olidone in a weight ratio of from 1:4 to 1:2 in a sealed reaction vessel at a temperature of 100 C. to 180 C. for a time of from one to four hours, followed by the separation and concentration steps cited above.
The process of this invention is applicable to lignocellulose generally including softwoods such as pine and cypresses; hardwoods such as black gum, aspen, oak and fruit woods; and fibers such as those of bagasse and bast. These materials can be used in any convenient form, chips or meal being preferred, and can be previously extracted with organic solvents such as ethanol-benzene to remove fatty acids, sterols and glycerine, without material effect on the pulping procedure of this invention. The hardwood pulp thus obtained is suitable for use as a corrugating medium, and softwood pulp prepared by this procedure is useful as liner for corrugated board.
In general, less time and/or lower temperatures are required for pulping of hardwood than for pulping of softwood by the procedure of this invention; even with more extensive treatment, softwood pulp thus produced contains a higher precentage of lignin. Hardwood or softwood which has not been extracted will donate fatty acids to the pulping medium; these can precipitate with the lignin or distil during concentration. The presence of fatty acids causes the pH of the solution, originally in the range 9-11, to be reduced. The amount of water required for delignification is low; wood which has not been dried before pulping can contain enough moisture to support the pulping, so that no water need by added with the hydrotrope. Water from this source is included in the cited ratios.
A. In a typical embodiment of this invention a mixture of 30 grams of black gum wood meal, 280 ml. of N-methyl-Z-pyrrolidone and 20 ml. of water was stirred and heated in an autoclave at C. under a nitrogen pressure of 100 p.s.i.g. for three hours. The reaction mixture thus obtained is allowed to cool to room temperature, and then the pulp is removed by filtration; the yield is 69%, based on the weight of wood. The filtrate may be re-used two or three times without further treatment. When the pulp yield drops substantially, the filtrate is diluted with 500 ml. of water, and the precipitated lignin and associated material are removed by filtration;
about 26% of the lignocellulose appears in this fraction. The mother liquor is concentrated by distillation of excess water and the concentrate thus obtained may be reused as a pulping medium.
B. By the procedure of part A, 30 grams of cypress chips are treated with a mixture of 120 m1. of N-propyl- 2-pyrrolidone and 80 ml. of water in a stirred autoclave at 185 C. for ten hours. The resultant pulp and liquor are subjected to the separation procedures described above.
C. By the procedure of part A, 30 grams of black gum wood meal is treated with a mixture of 140 ml. of N-(Z-butyl)-2-pyrrolidone and 60 ml. of water in a stirred autoclave at 100 C. for 1 /2 hours. The resultant pulp and liquor are subjected to the separation procedure described above.
I claim:
1. A method of delignification which comprises treating wood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
2. A method of delignification which comprises treating wood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from one to four hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
3. A method of delignification which comprises treating hardwood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
4. A method of delignification which comprises treating hardwood with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from one to four hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
5. A method of delignification which comprises treating softwood with a reagent which comprises water and N-methyl-Z-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature of from C. to 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
6. A method of delignification which comprises treating hardwood with a reagent which comprises water and N-methyl-Z-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature of from C. to C. for a time of from one to four hours and separating a ligninenriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
7. A method of delignification which comprises treating bagasse with a reagent which comprises water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:20 to 1:1 at a temperature between 80 C. and 200 C. for a time of about /2 hour to 24 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
8. A method of delignification which comprises treating softwood with a reagent which comprises Water and an N-(lower alkyl)-2-pyrrolidone in a weight ratio of from 1:4 to 1:2 at a temperature between 100 C. and 180 C. for a time of from 1 to 4 hours and separating a lignin-enriched phase containing said pyrrolidone from a cellulose-enriched pulp phase.
References Cited by the Examiner UNITED STATES PATENTS 2,945,863 7/1960 Buc 162-72 3,036,950 5/1962 Martin 162-168 3,081,219 3/1963 Drennen 162-72 DONALL H. SYLVESTER, Primary Examiner.
HOWARD R. CAINE, Assistant Examiner.
Claims (1)
1. A METHOD OF DELIGNIFICATIN WHICH COMPRISES TREATING WOOD WITH A REAGENT WHICH COMPRISES WATER AND AN N-(LOWER ALKYL)-2-PYRROLIDONE IN A WEIGHT RATIO OF FROM 1:20 TO 1:1 AT A TEMPERATURE BETWEEN 80*C. AND 200*C. FOR A TIME OF ABOUT 1/2 HOUR TO 24 HOURS AND SEPARATING A LIGNIN-ENRICHED PHASE CONTAINING SAID PYRROLIDONE FROM A CELLULOSE-ENRICHED PULP PHASE.
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US256131A US3272689A (en) | 1963-02-04 | 1963-02-04 | Delignification of lignocellulose with an nu-(lower alkyl)-2-pyrrolidone |
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US256131A US3272689A (en) | 1963-02-04 | 1963-02-04 | Delignification of lignocellulose with an nu-(lower alkyl)-2-pyrrolidone |
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US256131A Expired - Lifetime US3272689A (en) | 1963-02-04 | 1963-02-04 | Delignification of lignocellulose with an nu-(lower alkyl)-2-pyrrolidone |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4462865A (en) * | 1981-09-30 | 1984-07-31 | The Dow Chemical Company | Delignification of lignocellulosic materials with 2-imidazolidinones and 2-oxazolidinones |
US6051143A (en) * | 1997-11-14 | 2000-04-18 | The Trustees Of Columbia University In The City Of New York | Solid-liquid separation using phase transitional N-substituted pyrrolidones |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2945863A (en) * | 1958-06-24 | 1960-07-19 | Gen Aniline & Film Corp | Amides of aminoalkyl pyrrolidones |
US3036950A (en) * | 1959-06-22 | 1962-05-29 | Burgess Cellulose Company | Process for incorporating resins into paper |
US3081219A (en) * | 1960-02-10 | 1963-03-12 | Rohm & Haas | Prevention of deposition of pitch in papermaking |
-
1963
- 1963-02-04 US US256131A patent/US3272689A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2945863A (en) * | 1958-06-24 | 1960-07-19 | Gen Aniline & Film Corp | Amides of aminoalkyl pyrrolidones |
US3036950A (en) * | 1959-06-22 | 1962-05-29 | Burgess Cellulose Company | Process for incorporating resins into paper |
US3081219A (en) * | 1960-02-10 | 1963-03-12 | Rohm & Haas | Prevention of deposition of pitch in papermaking |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4462865A (en) * | 1981-09-30 | 1984-07-31 | The Dow Chemical Company | Delignification of lignocellulosic materials with 2-imidazolidinones and 2-oxazolidinones |
US6051143A (en) * | 1997-11-14 | 2000-04-18 | The Trustees Of Columbia University In The City Of New York | Solid-liquid separation using phase transitional N-substituted pyrrolidones |
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