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US3773611A - Two-stage sodium sulfite-oxygen pulping - Google Patents

Two-stage sodium sulfite-oxygen pulping Download PDF

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US3773611A
US3773611A US00133395A US3773611DA US3773611A US 3773611 A US3773611 A US 3773611A US 00133395 A US00133395 A US 00133395A US 3773611D A US3773611D A US 3773611DA US 3773611 A US3773611 A US 3773611A
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pulp
digestion
stage
oxygen
sodium sulfite
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H Worster
M Pudek
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MacMillan Bloedel Ltd
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    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21CPRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
    • D21C3/00Pulping cellulose-containing materials
    • D21C3/22Other features of pulping processes
    • D21C3/26Multistage processes
    • D21C3/263Multistage processes at least one stage being in presence of oxygen

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  • alkaline sulfite pulping It has been well established that sodium hydroxide used in both kraft and alkaline sulfite pulping is responsible for the relatively low yields obtained by these two processes.
  • Sodium sulfide used in kraft pulping causes air pollution with volatile sulfur compounds such as hydrogen sulfide and mercaptans.
  • Alkaline sulfite pulping does not give this type of pollution due to the absence of sodium sulfide.
  • These two known alkaline pulping processes give similar yields and strength properties at a given degree of pulping.
  • a serious disadvantage of alkaline sulfite pulping is the very high chemical requirements compared to kraft pulping.
  • the main purpose of the present invention to provide a commerically acceptable alkaline pulping-type process which (a) gives superior yields and quality than kraft, alkaline sulfite or alkaline oxygen pulping (b) does not require a catalyst, and (c) does not create air pollution with volatile sulfur compounds.
  • alkaline sulfite pulps are obtained with extremely high yields and excellent quality when lignocellulosic material, such as wood chips, is subjected to a two-stage pulping process with the second stage being conducted in the presence of oxygen.
  • the lignocellulosic material is first given a mild treatment under heat and pressure with sodium sulfite alone or with sodium sulfite plus sodium bicarbonate, carbonate or hydroxide, or sodium sulfite and sulfur dioxide.
  • the first stage digestion is carried out onlyto a point where it removes only some of the lignin and very little carbohydrate material compared to other pulping methods and is preferably conducted at a temperature in the range of from about 140 to 190C for about to 150 minutes, and a sodium sulfite application of 8 to 18 percent by weight expressed as sodium oxide based on the dry weight of the lignocellulosic material.
  • the optimum temperature of the first stage depends upon the raw material, the available reaction time, the chemical application, and the degree of pulping desired. This is well known in the art.
  • This stage is preferably carried out at a pH value of 6 or higher.
  • the free sulfite spent liquor is separated from the treated material and can be recycled and/or recovered for chemical regeneration.
  • This treated material obtained from the first stage digestion is defiberized, e.g. in a disc refiner, and is then further pulped with an alkali, such as sodium hydroxide, sodium carbonate, sodium bicarbonate or ammonia, and a large excess of oxygen under heat and pressure. It is preferable to use an alkali which is highly water soluble, because it will not lead to operating problems, such as the formation of precipitates and scales.
  • This second stage digestion is preferably conducted at a temperature in the range of from about to 130C for about 15 to 150 minutes, and an alkali application of 2 to 10 percent, e.g. sodium hydroxide expressed as sodium oxide based on the dry weight of the original lignocellulosic material.
  • Oxygen is injected into the digester or any other suitable pressure reactor containing the material to be pulped as soon as the alkali is added at any convenient time during the pulping cycle.
  • a partial oxygen pressure of to 250 psig is desirable.
  • the optimum temperature and oxygen pressure of the second stage depend on the available reaction time, quantity and concentration of alkali chosen, the degree of pulping by the first stage,.and the desired lignin content of the final pulp.
  • the sodium sulfite is necessary in the first stage digestion, while the sodium bicarbonate, sodium carbonate, sodium hydroxide, or sulfur dioxide are used when necessary to control the pH value of this first stage in the customary manner.
  • the spent liquor from the second stage digestion can be recovered either together with the spent liquor from the first stage or separately in order to regenerate sodium hydroxide by well established methods.
  • the alkaline pulping method provided by the present invention does not cause air pollution with volatile sulfur compounds.
  • EXAMPLE 2 The hemlock chips used for Example 1 were also pulped by the alkaline sulfite process under the following conditions:
  • EXAMPLE 3 The hemlock chips used for Example 1 were also pulped by the prior two-stage soda oxygen process under the following conditions:
  • Stage 13 percent sodium hydroxide as Na O based on wood, heating up to 170C in 90 minutes, maintaining at 170C for about 120 minutes.
  • EXAMPLE 6 The hemlock chips used for example 5 were also pulped by the present two-stage alkaline sulfite oxygen process under the time-temperature cycle described in Example 4. The chemical applications and results were as follows:
  • pulps are delignified completely whereas in the present process the pulp is only partially delignified and lignin is modified chemically to make it respond more favorably to subsequent papermaking.
  • Hemlock chips were used in the above tests, but the same tests were made with other wood species; such as Western red cedar and Douglas fir, and similar results were obtained.
  • the lignocellulosic material can be pulped in the first stage of digestion to Kappa numbers 100 to 200, and in the second stage of digestion to Kappa numbers 20 to for bleachable pulps.
  • the linerboard grade pulps can in the second stage of digestion by pulped to Kappa numbers 70 to 130.
  • An alkaline pulping process which comprises subjecting softwood chips to a first mild digestion with sodium sulfite'alone or sodium sulfite in combination with one or more chemical compounds selected from the group consisting of sulfur dioxide, sodium bicarbonate, sodium carbonate, and sodium hydroxide, under conditions of temperature, pressure and time to produce pulp with high residual lignin content while removing little carbohydrate material, the pulp so produced having Kappa number of not less than about 100, defibering the thus treated material, and then subjecting the defibered material to a second digestion with an alkali in the presence of an excess of oxygen under conditions of temperature, pressure and time to produce a high yield and quality pulp of Kappa number 20-50 for bleachable pulp or Kappa number 70-130 for linerboard grade pulp.
  • alkali used in the second digestion is selected from the group consisting of sodium bicarbonate, sodium carbonate. and ammonia.
  • a process according to claim 1 wherein the sodium sulfite or sodium sulfite in combination with the selected chemical compound in the first digestion is from 8 to 18 percent by weight based on the dry weight of the cellulosic material.

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Abstract

Subjecting solftwood chips to a mild digestion with sodium sulfite alone or sodium sulfite and a small amount of sulfur dioxide or mixtures of sodium sulfite with sodium carbonate, bicarbonate or hydroxide to obtain a Kappa number of not less than about 100, defiberizing the thus treated material, and then subjecting the defiberized material to a second digestion with an alkali in the presence of oxygen to obtain a pulp of Kappa number 20-50 for bleachable pulp or Kappa number of 70-130 for linerboard grade pulp.

Description

United States Patent [191 Worster et al.
TWO-STAGE SODIUM SULFITE-OXYGEN PULPING Inventors: Hans E. Worster, Richmond, British Columbia; Marian F. Pudek, Coquitlam, British Columbia, both of Canada US. Cl. 162/25, 162/65 Int. Cl. D2lc 3/00 Field of Search 162/25, 65
[111 3,773,611 1*Nov. 20, 1973 [56] References Cited UNITED STATES PATENTS 3,691,008 9/ l972 Worster et al. 162/25 Primary Examiner-S. Leon Bashore Assistant Examiner--Arthur L. Corbin Att0 meyFetherstonhaugh & Co.
57 ABSTRACT Subjecting solftwood chips to a mild digestion with sodium sulfite alone or sodium sulfite and a small amount of sulfur dioxide or mixtures of sodium sulfite with sodium carbonate, bicarbonate or hydroxide to obtain a Kappa number of not less than about 100, defiberizing the thus treated material, and then subjecting the defiberized material to a second digestion with an alkali in the presence of oxygen to obtain a pulp of Kappa number 20-50 for bleachable pulp or Kappa number of 70-130 for linerboard grade pulp.
9 Claims, No Drawings TWO-STAGE SODIUM SULFITE-OXYGEN PULPING This invention relates to the manufacture of pulp and particularly to a two-stage sulfite oxygen pulping process.
It has been well established that sodium hydroxide used in both kraft and alkaline sulfite pulping is responsible for the relatively low yields obtained by these two processes. Sodium sulfide used in kraft pulping causes air pollution with volatile sulfur compounds such as hydrogen sulfide and mercaptans. Alkaline sulfite pulping does not give this type of pollution due to the absence of sodium sulfide. These two known alkaline pulping processes give similar yields and strength properties at a given degree of pulping. A serious disadvantage of alkaline sulfite pulping is the very high chemical requirements compared to kraft pulping.
It has also been known for some time that lignocellulosic materials can be delignified by sodium hydroxide and an excess of oxygen under pressure. However, this pulping method suffers from penetration problems of wood chips and similar raw materials with oxygen, high alkali requirements, the need for high pressures and low product quality, i.e. similar to the acid sulfite process, and inferior to the kraft process. A more recent development in this area is oxygen bleaching, which applies alkali, oxygen and a catalyst, e.g. magnesium carbonate, for complete delignification of chemical pulps. It is stressed in patents and papers on oxygen bleaching that the catalyst must be used to reduce pulp degradation and retain product quality. Obviously, the use of a catalyst is an additional operating expense.
The main purpose of the present invention to provide a commerically acceptable alkaline pulping-type process which (a) gives superior yields and quality than kraft, alkaline sulfite or alkaline oxygen pulping (b) does not require a catalyst, and (c) does not create air pollution with volatile sulfur compounds.
With the process in accordance with this invention alkaline sulfite pulps are obtained with extremely high yields and excellent quality when lignocellulosic material, such as wood chips, is subjected to a two-stage pulping process with the second stage being conducted in the presence of oxygen. The lignocellulosic material is first given a mild treatment under heat and pressure with sodium sulfite alone or with sodium sulfite plus sodium bicarbonate, carbonate or hydroxide, or sodium sulfite and sulfur dioxide.
The first stage digestion is carried out onlyto a point where it removes only some of the lignin and very little carbohydrate material compared to other pulping methods and is preferably conducted at a temperature in the range of from about 140 to 190C for about to 150 minutes, and a sodium sulfite application of 8 to 18 percent by weight expressed as sodium oxide based on the dry weight of the lignocellulosic material. The optimum temperature of the first stage depends upon the raw material, the available reaction time, the chemical application, and the degree of pulping desired. This is well known in the art. This stage is preferably carried out at a pH value of 6 or higher. After completion of the first stage digestion, the free sulfite spent liquor is separated from the treated material and can be recycled and/or recovered for chemical regeneration.
This treated material obtained from the first stage digestion is defiberized, e.g. in a disc refiner, and is then further pulped with an alkali, such as sodium hydroxide, sodium carbonate, sodium bicarbonate or ammonia, and a large excess of oxygen under heat and pressure. It is preferable to use an alkali which is highly water soluble, because it will not lead to operating problems, such as the formation of precipitates and scales. This second stage digestion is preferably conducted at a temperature in the range of from about to 130C for about 15 to 150 minutes, and an alkali application of 2 to 10 percent, e.g. sodium hydroxide expressed as sodium oxide based on the dry weight of the original lignocellulosic material. Oxygen is injected into the digester or any other suitable pressure reactor containing the material to be pulped as soon as the alkali is added at any convenient time during the pulping cycle. A partial oxygen pressure of to 250 psig is desirable. The optimum temperature and oxygen pressure of the second stage depend on the available reaction time, quantity and concentration of alkali chosen, the degree of pulping by the first stage,.and the desired lignin content of the final pulp.
The sodium sulfite is necessary in the first stage digestion, while the sodium bicarbonate, sodium carbonate, sodium hydroxide, or sulfur dioxide are used when necessary to control the pH value of this first stage in the customary manner.
The spent liquor from the second stage digestion can be recovered either together with the spent liquor from the first stage or separately in order to regenerate sodium hydroxide by well established methods.
With this process it has been found that excellent pulp yield and quality are obtained without the necessity of any catalyst or cellulose stabilizer in the second stage. It has also been found that both yield and quality are superior to those of the kraft, alkaline sulfite and alkaline oxygen pulping processes.
In addition to the above mentioned advantages, there is the very important advantage that the alkaline pulping method provided by the present invention does not cause air pollution with volatile sulfur compounds.
The present invention is illustrated by the following non-limitative examples:
EXAMPLE 1 the conventional kraft process under the following conditions:
16.3 percent active alkali based on dry wood, 20 percent sulfidity of white liquor, heating to' 170C in minutes by' circulating liquor through a heat exchanger, maintaining the temperature of 170C for minutes. The following results were obtained:
Screened pulp yield, on dry wood 43.9 Screen rejects, on dry wood 0.6 Kappa number 34.5
Unbeaten Pulp Properties: Pulp Brightness 23.8 Freeness, ml GS. 718 Mullen 59 Breaking length, km 4.7
EXAMPLE 2 The hemlock chips used for Example 1 were also pulped by the alkaline sulfite process under the following conditions:
percent sodium sulfite expressed as Na O based on dry wood 14 percent sodium hydroxide expressed as Na O based on dry wood,
heating to 180C in 105 minutes by circulating liquor through a heat exchanger,
maintaining the temperature of 180C for 120 minutes. The following results were obtained:
Screened pulp yield, on dry wood 43.1 Screen rejects, on dry wood 1.5 Kappa number 39 Unbeaten Pulp Properties:
Brightness 29 Freeness, m. C.S. 710
Mullen 58 Breaking Length, km 4.6
EXAMPLE 3 The hemlock chips used for Example 1 were also pulped by the prior two-stage soda oxygen process under the following conditions:
1st Stage 13 percent sodium hydroxide as Na O based on wood, heating up to 170C in 90 minutes, maintaining at 170C for about 120 minutes.
2nd Stage 4 percent sodium hydroxide as Na O based on wood,
at 160 psig. partial oxygen pressure, heating up to 115C in 90 minutes, maintaining at 115C for about 90 minutes.
The following results were obtained:
Screened pulp yield, on dry wood 44.1
Screen rejects, on dry wood 0.1
Kappa number 35 Unbeaten Pulp Properties:
Brightness 28.7 Freeness, ml C.S. 717 Mullen 58 Breaking Length, km 4.5
EXAMPLE 4 The hemlock chips were pulped according to the process of this invention under the following timetemperature cycle:
to 170 C in 105 minutes at 170 C for 120 minutes The chemical applications are listed in the table below. The alkali oxygen treatment was carried out under the following conditions:
to 115C in 85 minutes at 115C for 90 minutes partial oxygen pressure 160 psig (at C) The alkali applications are listed in the table below.
Experiment No. 1" 2 3 1st Stage (alkaline sulflte) Chemicals, on B1) Wood Na,SO as Na,0 16.0 16.0 12.4
NaHCO, as Na,0 0 0 1.8 Pulp Yield. on BD Wood 72.8 79.7 75.4 Kappa No. 141 147 146 175C maximum temperature 2nd Stage (Oxygen alkali) NaOH as Na,O, on BD Wood 7.9 10.1 9.7 Results Kappa No. 34.5 41 4O Pulp Yield, on BD Wood 50.7 54.3 52.2 Brightness 37.2 36.5 36.5 Frecness, ml C.S. 685 675 679 Mullen 125 113 125 Breaking Length, km 8.8 8.1 8.6
A comparison of these results with the data given in Examples 1, 2 and 3 shows clearly that at a comparable lignin content, the present two stage process gives 6.0 to 10 percent higher yields of bleachable pulps with 8 to 10 points higher brightness and double the mullen and breaking length of conventional kraft, alkaline sulfite and alkaline oxygen pulps without beating. It is surprising that the pulps resulting from this process give these high pulp yields despite the strongly alkaline conditions in the oxygen pulping stage and without the use of a catalyst.
EXAMPLE 5 The hemlock chips were pulped by the conventional kraft process under the following conditions to prepare linerboard pulps:
15 percent active alkali based on dry wood,
20 percent sulfidity of white liquor,
the same time-temperature cycle as described in Example l. The following results were obtained:
Total pulp yield, on BD Wood 50.9
Kappa N0. 87
Brightness 16.4 In the laboratory, 26 lb. duplex linerboard handsheets were also prepared and these had the following properties:
Mullen 85 Ring Crush 58 Breaking Length, km 8.2
Brightness 15.2
EXAMPLE 6 The hemlock chips used for example 5 were also pulped by the present two-stage alkaline sulfite oxygen process under the time-temperature cycle described in Example 4. The chemical applications and results were as follows:
Experiment No. 1 2 3 4 5 1st Stage Chemicals, on DD Wood N21 as Na o 11.0 16.0 11.0 11.0 11.0 NaHCO as Na,0 5.0 143,00, as Na o 5.0 NaOH as Na O 5.0 SO in addition to Na,SO, 2.4 Total as Na O 11.0 16.0 16.0 16.0 16.0 Terminal pH of liquor(20C) 6.9 7.6 8.9 9.1 9.8 Pulp Yield, on BD Wood 80.7 78.9 78.1 71.7 66.8 Kappa No. 142 151 150 155 169 Experiment No. 1 2 3 4 5 2nd Stage Chemicals, on EU Wood NaOl-l as Na,0 5.3 4.9 4.9 4.2 4.0 Results Pulp Yield, on B0 Wood 63.7 63.0 62.8 58.1 53.8 Kappa No. 84 87 89 83 86 Brightness 32.1 31.4 29.3 25.6 25.3 Pulp Yield Increase Over Kraft Process, on Wood at Kappa No. (Extra- 13.2 12.1 11.6 7.8 2.9 polated) Duplex Linerboard Properties Mullen 102 119 115 124 Ring Crush 61.3 66 59 70 58 Breaking Length, km 11.3 11.6 11.8 10.4 9.7 Brightness 28.5 28.6 28.0 25.9 24.0
A comparison of these results with those given in Example 5 show clearly that, at a given lignin content, those two-stage pulps were obtained with up to 13 percent higher yields based on wood and significantly higher strength properties and brightness of duplex linerboards than the comparable conventional kraft pulp.
It is unexpected that despite the significant lignin removal (from 22.5 percent to 12.7 percent lignin in the pulps) in the alkaline oxygen stage, the pulp yields and properties were considerably superior to those of a comparable kraft pulp.
EXAMPLE 7 Hemlock chips were pulped by the present process to Kappa numbers of 94 to 107 under the following c0nditions:
Experiment No. l 2 Stage Na,SO as Na,0, on BD Wood 16.0 16.0 Pulp Yield, on BD Wood 78.9 78.9 Kappa No. l5! l5] 2nd Stage NaOH as Na o, on BD Wood 4.2 2.8
Time-temperature cycles and oxygen pressures were identical with those given in Example 4.
Results Pulp Yield, on BD Wood 65.2 69.4 Kappa No. 94 I07 Linerboard Properties Mullen H7 104 Ring Crush 75 65 Breaking Length, km 11.7 10.7 Brightness 28.3 28.6
A comparison of these data with the results reported in Example 5 show clearly that up to 18.5 percent higher pulp yields based on wood and significantly better linerboard properties were obtained by the twostage alkaline sulfite oxygen process than by kraft pulping to a lower Kappa number (85 vs 94 and 107). These conclusions are entirely unexpected because, normally, pulping to higher Kappa numbers in the range covered has adverse effects on pulp quality, especially mullen, breaking length and brightness. It can probably also be concluded that, in the oxygen pulping stage, the lignosulfonates, which are formed in the alkaline sulfite stage and remain in the pulp, are changed chemically and thus contribute to the improved pulp properties at these very high yield increases. This is an entirely new way of utilizing chemically modified lignin in high yield pulps. Obviously, the benefits of this new principle are two fold: (a) increased pulp yield, and (b) increased pulp quality.
A major difference between the second stage of this novel process and oxygen bleaching is that, in the latter method, pulps are delignified completely whereas in the present process the pulp is only partially delignified and lignin is modified chemically to make it respond more favorably to subsequent papermaking.
Hemlock chips were used in the above tests, but the same tests were made with other wood species; such as Western red cedar and Douglas fir, and similar results were obtained.
With the process of this invention the lignocellulosic material can be pulped in the first stage of digestion to Kappa numbers 100 to 200, and in the second stage of digestion to Kappa numbers 20 to for bleachable pulps. The linerboard grade pulps can in the second stage of digestion by pulped to Kappa numbers 70 to 130.
We claim:
1. An alkaline pulping process which comprises subjecting softwood chips to a first mild digestion with sodium sulfite'alone or sodium sulfite in combination with one or more chemical compounds selected from the group consisting of sulfur dioxide, sodium bicarbonate, sodium carbonate, and sodium hydroxide, under conditions of temperature, pressure and time to produce pulp with high residual lignin content while removing little carbohydrate material, the pulp so produced having Kappa number of not less than about 100, defibering the thus treated material, and then subjecting the defibered material to a second digestion with an alkali in the presence of an excess of oxygen under conditions of temperature, pressure and time to produce a high yield and quality pulp of Kappa number 20-50 for bleachable pulp or Kappa number 70-130 for linerboard grade pulp.
2. A process as claimed in claim 1 wherein the alkali used in the second digestion is selected from the group consisting of sodium bicarbonate, sodium carbonate. and ammonia.
3. A process according to claim 1 wherein the first digestion is conducted at a temperature in the range of 140 to l90C.
4. A process according to claim 1 wherein the Kappa number of softwood pulp from the first digestion is from about 100 to about 200.
5. A process according to claim 1 wherein the pulp from the second digestion is bleachable pulp.
6. A process according to claim 1 wherein the pulp from the second digestion is linerboard grade pulp.
7. A process according to claim 1 wherein the sodium sulfite or sodium sulfite in combination with the selected chemical compound in the first digestion is from 8 to 18 percent by weight based on the dry weight of the cellulosic material.
cellulosic material.

Claims (8)

  1. 2. A process as claimed in claim 1 wherein the alkali used in the second digestion is selected from the group consisting of sodium bicarbonate, sodium carbonate and ammonia.
  2. 3. A process according to claim 1 wherein the first digestion is conducted at a temperature in the range of 140* to 190*C.
  3. 4. A process according to claim 1 wherein the Kappa number of softwood pulp from the first digestion is from about 100 to about 200.
  4. 5. A process according to claim 1 wherein the pulp from the second digestion is bleachable pulp.
  5. 6. A process according to claim 1 wherein the pulp from the second digestion is linerboard grade pulp.
  6. 7. A process according to claim 1 wherein the sodium sulfite or sodium sulfite in combination with the selected chemical compound in the first digestion is from 8 to 18 percent by weight based on the dry weight of the cellulosic material.
  7. 8. A process according to claim 1 wherein the second digestion is carried on at a temperature of from about 95* to 130*C for from about 15 to 150 minutes at a pressure from about 100 to 250 p.s.i.g.
  8. 9. A process according to claim 1 wherein the alkali in the second digestion is from about 2 to 10 percent by weight based on the dry weight of the original lignocellulosic material.
US00133395A 1971-04-12 1971-04-12 Two-stage sodium sulfite-oxygen pulping Expired - Lifetime US3773611A (en)

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CA110383A CA936310A (en) 1971-04-12 1971-04-15 Two stage process for the production of chemical pulps

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4552616A (en) * 1982-10-20 1985-11-12 New Fibers International Inc. Pulping process pretreatment using a lower alkanolamine in the presence of ammonium hydroxide
US5464563A (en) * 1993-08-25 1995-11-07 Burlington Chemical Co., Inc. Bleaching composition
CN101736427B (en) * 2009-12-22 2011-08-03 唐山三友集团东光浆粕有限责任公司 Bamboo alpha-pulp for viscose and production method thereof
US20130081769A1 (en) * 2010-06-10 2013-04-04 Packaging Corporation Of America Method of manufacturing pulp for corrugated medium
CN104407098A (en) * 2014-09-23 2015-03-11 王朝辉 Rapid method for evaluation of birch caustic soda anthraquinone pulping process

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4552616A (en) * 1982-10-20 1985-11-12 New Fibers International Inc. Pulping process pretreatment using a lower alkanolamine in the presence of ammonium hydroxide
US5464563A (en) * 1993-08-25 1995-11-07 Burlington Chemical Co., Inc. Bleaching composition
CN101736427B (en) * 2009-12-22 2011-08-03 唐山三友集团东光浆粕有限责任公司 Bamboo alpha-pulp for viscose and production method thereof
US20130081769A1 (en) * 2010-06-10 2013-04-04 Packaging Corporation Of America Method of manufacturing pulp for corrugated medium
US8961740B2 (en) * 2010-06-10 2015-02-24 Packaging Corporation Of America Method of manufacturing pulp for corrugated medium
US9399835B2 (en) 2010-06-10 2016-07-26 Packaging Corporation Of America Method of manufacturing pulp for corrugated medium
CN104407098A (en) * 2014-09-23 2015-03-11 王朝辉 Rapid method for evaluation of birch caustic soda anthraquinone pulping process
CN104407098B (en) * 2014-09-23 2016-04-20 黄伟洪 A kind of method of Fast Evaluation birch soda anthraquinone process technique

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