US3560331A - Pulping of wood with sulfite base digestion liquor containing acetic acid - Google Patents
Pulping of wood with sulfite base digestion liquor containing acetic acid Download PDFInfo
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- US3560331A US3560331A US709891A US3560331DA US3560331A US 3560331 A US3560331 A US 3560331A US 709891 A US709891 A US 709891A US 3560331D A US3560331D A US 3560331DA US 3560331 A US3560331 A US 3560331A
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- Prior art keywords
- acetic acid
- sulfite
- wood
- pulp
- percent
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 title abstract description 89
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 title abstract description 32
- 239000002023 wood Substances 0.000 title abstract description 18
- 238000004537 pulping Methods 0.000 title description 8
- 238000002419 base digestion Methods 0.000 title description 2
- 230000029087 digestion Effects 0.000 abstract description 29
- 229920001131 Pulp (paper) Polymers 0.000 abstract description 5
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 description 17
- 238000010411 cooking Methods 0.000 description 16
- 229920002678 cellulose Polymers 0.000 description 10
- 239000001913 cellulose Substances 0.000 description 10
- 238000004061 bleaching Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 5
- 229920003043 Cellulose fiber Polymers 0.000 description 4
- 235000005018 Pinus echinata Nutrition 0.000 description 4
- 241001236219 Pinus echinata Species 0.000 description 4
- 235000017339 Pinus palustris Nutrition 0.000 description 4
- 229920005610 lignin Polymers 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 235000007173 Abies balsamea Nutrition 0.000 description 3
- 229920002581 Glucomannan Polymers 0.000 description 3
- 229920002488 Hemicellulose Polymers 0.000 description 3
- 241000218685 Tsuga Species 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- LUEWUZLMQUOBSB-FSKGGBMCSA-N (2s,3s,4s,5s,6r)-2-[(2r,3s,4r,5r,6s)-6-[(2r,3s,4r,5s,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,4r,5s,6r)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](OC3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-FSKGGBMCSA-N 0.000 description 2
- 229920000875 Dissolving pulp Polymers 0.000 description 2
- 229920000057 Mannan Polymers 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 229940046240 glucomannan Drugs 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 240000003021 Tsuga heterophylla Species 0.000 description 1
- 235000008554 Tsuga heterophylla Nutrition 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000002699 waste material Substances 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 well-known and widely used sulfite pulping process for the production of refined cellulose fiber suitable for high-grade paper stock and suitable for dissolving or for chemical pulp uses involves digesting wood (preferably in the form of chips) in an aqueous sulfite digestion liquor at elevated temperatures and pressures to solubilize and remove lignin and other unwanted materials from the cellulose.
- the substantially lignin-free cellulosic fiber that results is then removed from the digestion liquor and subjected to various stages of purification (i.e., bleaching) and washing to remove remaining small amounts of lignin and other impurities and then dried.
- Very white, active pulps of substantially pure cellulose fiber are produced in this manner.
- K No. bleachability of an unbleached pulp is customarily measured by means of the well-known standard TAPPI potassium permanganate number (K No.). Other factors being equal, decreasing K Nos. indicate an increasing ease of bleaching.
- Degradation or depolymerization of the cellulose in the pulp is usually measured by determination of the intrinsic viscosity (I.V.) of its solution in a standardized cuene solution. A decreasing I.V. is indicative of increased degradation or depolymerization of the cellulose and as a rule K No. can only be lowered at the expense of reduction of the I.V.
- I.V. intrinsic viscosity
- Glucomannans are one type of hemicellulose that invariably carries over from the wood to appear at least in trace quantities in most dissolving woodpulps.
- I carried out certain experiments in which various amounts of acetic acid replaced some of the water in the sulfite digestion liquors used.
- the addition of the acetic acid lower the glucomannan content of the resultant pulp, but most unexpectedly, when the acetic acid content of the liquor was within certain limits the K No. of the pulp was significantly decreased without any compensating decrease in the I.V.
- sulfite pulping practice involves digesting or cooking wood (usually in the form of chips) in an aqueous sulfite digestion liquor at temperatures ranging from about to C., and pressures of from about 50 to 150 p.s.i.g. for from about 3.5 to 9.0 hours.
- a pulp is produced comprising essentially pure cellulose and a spent liquor containing lignin, soluble carbohydrates, inorganic salts and other soluble or solubilized constituents of the wood.
- the liberated cellulose fiber is then separated from the spent sulfite liquor and purified by various combinations of bleaching, extraction, and washing, and finally dried.
- the result is a reactive, very white, relatively pure cellulose fiber suitable for conversion into high-grade papers and for use in the production of regenerated cellulose and cellulose derivatives such as rayons, cellulose acetates, nitrates, etc.
- the improved process of my invention and the product obtained thereby are based upon my discovery that when about 20 to 75 percent (by volume) of the water in the soluble-base sulfite digestion liquor is replaced by an equal amount of acetic acid, the digestion results in an easy bleaching pulp with an exceptionally high I.V., or conversely a pulp with an exceptionally low K No. for a given I.V.
- the replacement of less than about 20 percent of the water content of the digestion liquor with acetic acid will produce some reduction in the K No./I.V. ratio of the unbleached pulp; however, there is a dramatic and most unexpected reduction in said ratio when the acetic acid is increased above 20 percent.
- some reduction of the K No./I.V. ratio is still obtained at acetic acid replacements in excess of 75 percent by volume, but
- the conditions under which the practice of the invention are most advantageously carried out are essentially the same as those employed in conventional sulfite cooking practices. If a finished bleached product is desired having the same I.V. as a conventional pulp, a compensating increase in the severity of the cooking conditions is required which in turn results in a whiter and purer cellulose end product.
- the length of time, temperature and pressure of a cooking procedure required to obtain a pulp of a specified I.V. and/or K No. are variables that must always be taken into consideration in sulfite cooking operations and the determination of the cooking conditions best adapted to produce a product with desired characteristics in the practice of my invention in a matter well within the skill of workers in this art.
- EXAMPLE 1 Five cooks were made on southern pine chips each using 3.2 kilograms of wood on an oven dry basis in 12 liters of soda base sulfite digestion liquor containing the amounts of acetic acid and under the digestion conditions set out in Table I. The characteristics of the unbleached pulps obtained illustrate the striking increase in bleachability and I.V. afforded by the presence of the indicated percentages of acetic acid (glacial) in the digestion liquors.
- EXAMPLE 4 In a second series of cooks using the process and the same chips as in Example 2, a slight variation in the digestion time at a concentration of 50 percent by volume of acetic acid was made to illustrate how the I.V. ad the K No./I.V. ratio of the unbleached pulp could be varied. From the range of results obtained it is clear that considerable control of the characteristics of the product is easily obtained.
Landscapes
- Paper (AREA)
Abstract
A HIGH-GRADE SULFITE WOOD PULP OF SUBSTANTIALLY INCREASED BLEACHABILITY AND INTRINSIC VISCOSITY IS PRODUCED BY DISGESTING WOOD IN A CONVENTIONAL MANNER WITH A SOLUBLE-BASE SULFITE DIGESTION LIQUOR IN WHICH FROM ABOUT 20 TO 75 PERCENT OF THE WATER, BY VOLUME, HAS BEEN REPLACED WITH ACETIC ACID.
Description
United States Patent 3,560,331 PULPING OF WOOD WITH SULFITE BASE DIGES- TION LIQUOR CONTAINING ACETIC ACID Andrew Beelik, Shelton, Wash., assignor to ITT Rayonier Incorporated No Drawing. Filed Mar. 4, 1968, Ser. No. 709,891 Int. Cl. D21d 3/00 US. Cl. 162-76 3 Claims ABSTRACT OF THE DISCLOSURE A high-grade sulfite wood pulp of substantially increased bleachability and intrinsic viscosity is produced by digesting wood in a conventional manner with a soluble-base sulfite digestion liquor in which from about 20 to 75 percent of the water, by volume, has been replaced with acetic acid.
BACKGROUND OF THE INVENTION The well-known and widely used sulfite pulping process for the production of refined cellulose fiber suitable for high-grade paper stock and suitable for dissolving or for chemical pulp uses involves digesting wood (preferably in the form of chips) in an aqueous sulfite digestion liquor at elevated temperatures and pressures to solubilize and remove lignin and other unwanted materials from the cellulose. The substantially lignin-free cellulosic fiber that results is then removed from the digestion liquor and subjected to various stages of purification (i.e., bleaching) and washing to remove remaining small amounts of lignin and other impurities and then dried. Very white, active pulps of substantially pure cellulose fiber are produced in this manner.
Sulfite digestion and subsequent bleaching of the wood, however, not only remove lignin and impurities, they also attack and degrade or depolymerize the cellulose itself, more or less directly in proportion to their severity. This is, and has to be acceptable to a degree, but on the whole, the art diligently seeks to obtain the highest yield possible of the least degraded (highest I.V.) chemical cellulose having maximum purity and whiteness. Research is constantly going on in an effort to develop improved methods of sulfite pulping that will either yield less degraded (higher I.V.) unbleached pulp of a given easy bleachability or an easier bleaching pulp of a given relatively high I.V. Either object obviously would lead to a final bleached cellulose having a maximum I.V. and whiteness.
As noted above, bleachability of an unbleached pulp is customarily measured by means of the well-known standard TAPPI potassium permanganate number (K No.). Other factors being equal, decreasing K Nos. indicate an increasing ease of bleaching. Degradation or depolymerization of the cellulose in the pulp, on the other hand, is usually measured by determination of the intrinsic viscosity (I.V.) of its solution in a standardized cuene solution. A decreasing I.V. is indicative of increased degradation or depolymerization of the cellulose and as a rule K No. can only be lowered at the expense of reduction of the I.V. Therefore, as one measure of the quality of an unbleached sulfite pulp we have become accustomed to determining the ratio of the K No./I.V. and, other factors remaining equal, the lower the numerical value of the ratio, the better the pulp. Applying this standard to conventional sulfite dissolving pulps we find that they normally exceed a value of 1.0 and in many cases they exceed 1.5. One common use for sulfite dissolving pulps is the production of cellulose acetate. It is well-known that acetylation-grade pulps should have as low a hemicellulose content as possible, the hemicellulose content being an important criterion in evaluation of the quality of said pulps. Glucomannans are one type of hemicellulose that invariably carries over from the wood to appear at least in trace quantities in most dissolving woodpulps. In the course of an investigation, the objective of which was to discover a way to promote the hydrolytic cleavage of glucomannan molecules during the sulfite digestion of wood and thereby facilitate their removal, I carried out certain experiments in which various amounts of acetic acid replaced some of the water in the sulfite digestion liquors used. To my surprise, not only did the addition of the acetic acid lower the glucomannan content of the resultant pulp, but most unexpectedly, when the acetic acid content of the liquor was within certain limits the K No. of the pulp was significantly decreased without any compensating decrease in the I.V. In fact, the I.V. of the pulp was even higher than normal. On further investigation, I found that by cooking the wood with a soluble-base sulfite digestion liquor containing controlled amounts of acetic acid, I could readily obtain pulps having a K No./I.V. ratio significantly below 1.0 and even below 0.5 under the proper conditions, if desired.
SUMMARY OF THE INVENTION I have devised an improved process for producing easybleaching sulfite woodpulp having a significantly increased I.V. value. In the process of my invention, wood (preferably in the form of conventional chips) is digested in the usual manner with an aqueous soluble-base sulfite digestion liquor containing from about 20 to percent by volume (preferably about 50 percent) of acetic acid in place of an equivalent amount of the water normally present in the digestion liquor. This modification of the digestion process will produce an unbleached pulp suitable for use in the production of high-grade paper or as an improved dissolving or chemical-grade cellulose which has a significantly higher than normal I.V. and a controllable K No./I.V. ratio of 1.0 or below. The mannan content of the pulp is also reduced.
DETAILED DESCRIPTION Commercial sulfite pulping practice involves digesting or cooking wood (usually in the form of chips) in an aqueous sulfite digestion liquor at temperatures ranging from about to C., and pressures of from about 50 to 150 p.s.i.g. for from about 3.5 to 9.0 hours. A pulp is produced comprising essentially pure cellulose and a spent liquor containing lignin, soluble carbohydrates, inorganic salts and other soluble or solubilized constituents of the wood. The liberated cellulose fiber is then separated from the spent sulfite liquor and purified by various combinations of bleaching, extraction, and washing, and finally dried. The result is a reactive, very white, relatively pure cellulose fiber suitable for conversion into high-grade papers and for use in the production of regenerated cellulose and cellulose derivatives such as rayons, cellulose acetates, nitrates, etc.
The improved process of my invention and the product obtained thereby are based upon my discovery that when about 20 to 75 percent (by volume) of the water in the soluble-base sulfite digestion liquor is replaced by an equal amount of acetic acid, the digestion results in an easy bleaching pulp with an exceptionally high I.V., or conversely a pulp with an exceptionally low K No. for a given I.V. The replacement of less than about 20 percent of the water content of the digestion liquor with acetic acid will produce some reduction in the K No./I.V. ratio of the unbleached pulp; however, there is a dramatic and most unexpected reduction in said ratio when the acetic acid is increased above 20 percent. Similarly, some reduction of the K No./I.V. ratio is still obtained at acetic acid replacements in excess of 75 percent by volume, but
3 additions of acetic acid much in excess of this amount are accompanied by adverse effects on products produced therefrom such as the haze and color of cellulose acetate films and also the beneficial eifects are reduced drastically,
The conditions under which the practice of the invention are most advantageously carried out are essentially the same as those employed in conventional sulfite cooking practices. If a finished bleached product is desired having the same I.V. as a conventional pulp, a compensating increase in the severity of the cooking conditions is required which in turn results in a whiter and purer cellulose end product. The length of time, temperature and pressure of a cooking procedure required to obtain a pulp of a specified I.V. and/or K No. are variables that must always be taken into consideration in sulfite cooking operations and the determination of the cooking conditions best adapted to produce a product with desired characteristics in the practice of my invention in a matter well within the skill of workers in this art.
The following examples are illustrative, but not limitative of the practice of my invention.
EXAMPLE 1 Five cooks were made on southern pine chips each using 3.2 kilograms of wood on an oven dry basis in 12 liters of soda base sulfite digestion liquor containing the amounts of acetic acid and under the digestion conditions set out in Table I. The characteristics of the unbleached pulps obtained illustrate the striking increase in bleachability and I.V. afforded by the presence of the indicated percentages of acetic acid (glacial) in the digestion liquors.
TABLE I Cook No.
Digestion liquor:
Acetic acid, percent by volume- 25 50 97 Total S02, g./O ml 6. 6. 13 6.13 6. 10 6.10
Free S02, g./100 ml 5. 43 5. 41 5. 41 5. 38 5. 38 Cooking schedule:
Maximum temp, C. 134 134 139 142 144 Maximum pressure, p.s. 105 110 112 109 120 Total time, hrs.: mins 6:45 7:12 6:47 7:00 9:03 Pulp (unbleached):
Screened yield percent 46. 3 44. 2 44. 9 43. 9 54.3
Tappi K No 18.
Cuene I.V. ratio. K N0./I.V. ratio. Mannan percent EXAMPLE 2 Five portions of a batch of western hemlock wood chips each weighing 2.5 kilograms (oven dry basis) were cooked in 12 liter portions of soda base sulfite digestion liquor containing varying amounts of acetic acid under the conditions and with the results set out in Table 11 below:
TABLE II Cook No.
Digestion liquor:
Acetic acid, percent by volume. 0 5 25 50 ca.97 Total S02, g./l00 m1. 6. 7 6. 77 6. 69 6. 75 6. 75 Free S02, g./100 ml 6.10 6. 02 6. 07 6.07 Cooking Schedule:
Maximum temp., C 139 139 143 145 150 Maximum pressure p.s.i.g 110 110 110 111 105 Total time, hrs. mins 5:33 5:32 6:27 6:30 11:50 Pulp (unbleached):
Screened yield percent 50. 5 49. 5 45. 4 49.0 49.0 Tappi l6. 1 13. 6 6. 2 s. 5 13. 4 10. 66 15. 37 0. 80 0. 87 4. 8 9. 1
' 4 EXAMPLE 3 Samples of unbleached pulps produced in Examples 1 and 2 from southern pine and western hemlock wood chips were bleached by a conventional bleaching process and then acetylated to triacetates by a conventional method. Comparative color and haze density determinations were then run on the acetate solutions thus formed by methods developed at Tennessee Eastman Corporation, with the results listed in Table III.
TABLE III Acetic acid in cooking liquor by volume percent Southern pine pulp:
Haze, p.p.m 150 45 150+ Color, p.p.m 570 580 650 Hemlock pulp:
Haze, p.p.m 55 Color, p.p.m 480 350 650 The use of acetic acid in the cooking liquor at the 50 percent level in the modified sulfite pulping process of the invention substantially lowers the triacetate haze levels. The color level improvement obtained in the triacetate solution prepared from hemlock pulp of the invention, however, did not appear in the southern pine pulp equivalent. It is evident, however, that the use of high concentrations of acetic acid such as 97 percent when cooking the wood by the process of the invention is detrimental to both the color and haze densities of triacetates prepared therefrom.
EXAMPLE 4 In a second series of cooks using the process and the same chips as in Example 2, a slight variation in the digestion time at a concentration of 50 percent by volume of acetic acid was made to illustrate how the I.V. ad the K No./I.V. ratio of the unbleached pulp could be varied. From the range of results obtained it is clear that considerable control of the characteristics of the product is easily obtained.
The improvements in bleachability and I.V. resulting from the presence of acetic acid in the cooking liquor are substantial when using soluble-base sulfite liquors. These improvements, however, do not carry over, or at least are substantially less when cooking with a calciumbase sulfite liquor. This example illustrates this phenomena, the exact reason for which is not known.
A large uniform sample of hemlock wood chips was prepared and six experimental cooks made thereon using 2.5 kilogram portions on a dry weight basis and the process of Example 2. The acetic acid contents of the liquors, the digestion conditions and the results obtained are set out in Table V. It will be noted that substantial improvement in results was obtained only for the solublebase sodium and ammonium-base sulfite liquors.
TABLE V Cook No.
Digestion liquor:
Base Na Na NH3 NH; Ca Ca Acetic acid, percent by volume. 50 0 50 0 50 Cooking schedule:
Maximuln temp. C 138 145 140 145 140 145 Maximum pressure p.s.l.g 110 110 110 110 110 110 Total time, hrs.: mins :16 7:40 5:12 6:30 6:08 7:00 Pulp (unbleached):
Screened yield percent 47. 7 46. 4 44. 8 43. 7 45. 1 44. 3
Tappi K No 16. 2 4. 9 ll. 9 8. 7 12.3 10.8
Cuene I.V l1. 6 12. 2 10.8 11.6 10. 5 10.2
K N0./I.V. ratio 1. 40 0. 40 1. l0 0. 75 l. 17 1.06
From the data presented in the foregoing examples, it is apparent that the substitution of from about 20 to 75, and preferably about 50, percent by volume of acetic acid for the equivalent volume of water normally present in sulfite digestion liquors lowers the permanganate number of the unbleached pulp or in other words increases it bleachability. At the same time, unbleached I.V. values increase despite increases in cooking time and temperature. As a result, remarkably low K No./I.V. values are obtained. Moreover, it is also apparent that the mannan content of the pulp is lowered substantially by the use of up to about 50 percent acetic acid in the digestion liquor.
I claim:
1. In the process of pulping wood in aqueous solublebase sulfite digestion liquor at elevated temperature and pressure, the improvement which comprises replacing from 20 to 75 percent by volume of the water in the digestion liquor with an equal volume of acetic acid, thereby producing a substantially less degraded unbleached pulp of increased average degree of polymerization as measured by its intrinsic viscosity and increased ease of bleaching as measured by its potassium permanganate number.
2. The process according to claim 1 in which the sulfite digestion liquor contains about 50 percent by volume acetic acid based on the volume of Water normally present in said liquor.
3. The process according to claim 1 in which the unbleached pulp obtained by digesting the wood chips with said acetic acid-containing digestion liquor has a 20 K No./I.V. ratio no greater than one.
References Cited UNITED STATES PATENTS 27 2,214,125 9/1940 Dreyfus 16276X 0 2,442,332 1/1948 Haney et al. 16276X OTHER REFERENCES Haaglund: The Chemistry of the Sulphite Pulping 30 Process and the Evaporation of Its Waste Liquor, TAPPI Manual, vol. 33, No. 10, pp. 520-527, October 1950.
Paper Technology Highlights, vol. 47, No. 6, June 1965, D69, column 2, paragraph 2.
S. LEON BASHORE, Primary Examiner A. L. CORBIN, Assistant Examiner US. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70989168A | 1968-03-04 | 1968-03-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3560331A true US3560331A (en) | 1971-02-02 |
Family
ID=24851706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US709891A Expired - Lifetime US3560331A (en) | 1968-03-04 | 1968-03-04 | Pulping of wood with sulfite base digestion liquor containing acetic acid |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3560331A (en) |
| DE (1) | DE1815667A1 (en) |
| NO (1) | NO120397B (en) |
| SE (1) | SE338498B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4094735A (en) * | 1974-09-06 | 1978-06-13 | Kopparfors Ab | Method of pulping with sulfite liquor containing formic acid esters |
| USRE32408E (en) * | 1982-09-29 | 1987-04-28 | Masonite Corporation | Lignosulfonate-phenol-formaldehyde resin binder |
| US20150051385A1 (en) * | 2012-04-26 | 2015-02-19 | Archer Daniels Midland Company | Liquid / Liquid Separation of Lignocellulosic Biomass to Produce Sugar Syrups and Lignin Fractions |
-
1968
- 1968-03-04 US US709891A patent/US3560331A/en not_active Expired - Lifetime
- 1968-10-01 SE SE13262/68A patent/SE338498B/xx unknown
- 1968-10-12 NO NO4062/68A patent/NO120397B/no unknown
- 1968-12-19 DE DE19681815667 patent/DE1815667A1/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4094735A (en) * | 1974-09-06 | 1978-06-13 | Kopparfors Ab | Method of pulping with sulfite liquor containing formic acid esters |
| USRE32408E (en) * | 1982-09-29 | 1987-04-28 | Masonite Corporation | Lignosulfonate-phenol-formaldehyde resin binder |
| US20150051385A1 (en) * | 2012-04-26 | 2015-02-19 | Archer Daniels Midland Company | Liquid / Liquid Separation of Lignocellulosic Biomass to Produce Sugar Syrups and Lignin Fractions |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1815667A1 (en) | 1969-10-16 |
| NO120397B (en) | 1970-10-12 |
| SE338498B (en) | 1971-09-06 |
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