US3773611A - Two-stage sodium sulfite-oxygen pulping - Google Patents
Two-stage sodium sulfite-oxygen pulping Download PDFInfo
- Publication number
- 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
- Authority
- US
- United States
- Prior art keywords
- pulp
- digestion
- stage
- oxygen
- sodium sulfite
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004537 pulping Methods 0.000 title description 25
- XODPQKCXGFBFHX-UHFFFAOYSA-M sodium;hydrogen sulfite;hydrate Chemical compound O.[Na+].OS([O-])=O XODPQKCXGFBFHX-UHFFFAOYSA-M 0.000 title description 3
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims abstract description 36
- 230000029087 digestion Effects 0.000 claims abstract description 29
- 239000003513 alkali Substances 0.000 claims abstract description 18
- 235000010265 sodium sulphite Nutrition 0.000 claims abstract description 18
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 16
- 239000000463 material Substances 0.000 claims abstract description 14
- 229910000029 sodium carbonate Inorganic materials 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 44
- 239000012978 lignocellulosic material Substances 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000011122 softwood Substances 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 45
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 26
- 229910052760 oxygen Inorganic materials 0.000 abstract description 26
- 239000001301 oxygen Substances 0.000 abstract description 26
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000002023 wood Substances 0.000 description 31
- 239000002655 kraft paper Substances 0.000 description 13
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 11
- 229920005610 lignin Polymers 0.000 description 9
- 239000011734 sodium Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 235000007173 Abies balsamea Nutrition 0.000 description 7
- 241000218685 Tsuga Species 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000003915 air pollution Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 150000003464 sulfur compounds Chemical class 0.000 description 3
- GRNVJAJGRSXFFZ-UHFFFAOYSA-N sulfurous acid;hydrate Chemical compound O.OS(O)=O GRNVJAJGRSXFFZ-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 2
- 229910001948 sodium oxide Inorganic materials 0.000 description 2
- 229910052979 sodium sulfide Inorganic materials 0.000 description 2
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 235000014466 Douglas bleu Nutrition 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241000218683 Pseudotsuga Species 0.000 description 1
- 235000005386 Pseudotsuga menziesii var menziesii Nutrition 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 241000218638 Thuja plicata Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- D21C3/22—Other features of pulping processes
- D21C3/26—Multistage processes
- D21C3/263—Multistage processes at least one stage being in presence of oxygen
Definitions
- 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.
Landscapes
- Paper (AREA)
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)
- 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 190*C.
- 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.
- 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.
- 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.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13339571A | 1971-04-12 | 1971-04-12 | |
| CA110383A CA936310A (en) | 1971-04-12 | 1971-04-15 | Two stage process for the production of chemical pulps |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3773611A true US3773611A (en) | 1973-11-20 |
Family
ID=25666772
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00133395A Expired - Lifetime US3773611A (en) | 1971-04-12 | 1971-04-12 | Two-stage sodium sulfite-oxygen pulping |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3773611A (en) |
| CA (1) | CA936310A (en) |
Cited By (5)
| 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 |
-
1971
- 1971-04-12 US US00133395A patent/US3773611A/en not_active Expired - Lifetime
- 1971-04-15 CA CA110383A patent/CA936310A/en not_active Expired
Cited By (8)
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA936310A (en) | 1973-11-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4486267A (en) | Chemithermomechanical pulping process employing separate alkali and sulfite treatments | |
| US4012280A (en) | Delignification of lignocellulosic material with an alkaline liquor in the presence of a cyclic keto compound | |
| US4294653A (en) | Process for manufacturing chemimechanical cellulose pulp in a high yield within the range from 65 to 95% | |
| US8475627B2 (en) | Process of treating a lignocellulosic material | |
| US4248662A (en) | Oxygen pulping with recycled liquor | |
| US3888727A (en) | Treatment of lignocellulosic material in an alkaline pulping liquor containing anthraquinone sulphonic acid followed by oxygen delignification | |
| US4869783A (en) | High-yield chemical pulping | |
| US3691008A (en) | Two-stage soda-oxygen pulping | |
| US4552616A (en) | Pulping process pretreatment using a lower alkanolamine in the presence of ammonium hydroxide | |
| US5529663A (en) | Delignification of lignocellulosic materials with peroxymonophosphoric acid | |
| US4091749A (en) | Alkaline pulping of lignocellulosic material with amine pretreatment | |
| US3919041A (en) | Multi-stage chlorine dioxide delignification of wood pulp | |
| US3707437A (en) | Pulping and bleaching of wood chips in a single stage with tertiary butyl hydroperoxide | |
| US5183535A (en) | Process for preparing kraft pulp using black liquor pretreatment reaction | |
| US3811995A (en) | Method of high yield semichemical pulp production | |
| US3773611A (en) | Two-stage sodium sulfite-oxygen pulping | |
| US3532597A (en) | Preparation of dissolving pulps from wood by hydrolysis and alkaline sulfite digestion | |
| US2783146A (en) | Semi-hydrotropic chemical lignocellulose pulping process | |
| CA2049322C (en) | Process for preparing kraft pulp | |
| US3981765A (en) | Treatment of wood chips with an alkali metal borohydride solution followed by mechanical defibration | |
| US3520773A (en) | Alkaline pulping processes with chemical pretreatment | |
| US4329200A (en) | Method and system for selective alkaline defiberization and delignification | |
| US3617432A (en) | Delignifying lignocellulose with an incomplete soda cook followed by gaseous bleaching | |
| US3262839A (en) | Neutral to weakly alkaline sulfite process for the extraction of cellulose from cellulosic material | |
| US3795574A (en) | Impregnation of wood with a formaldehyde free alkaline solution of sodium hydroxide at a ph between 12.4 and 13 |