US1971564A - Process of manufacturing sulphite pulp - Google Patents
Process of manufacturing sulphite pulp Download PDFInfo
- Publication number
- US1971564A US1971564A US674222A US67422233A US1971564A US 1971564 A US1971564 A US 1971564A US 674222 A US674222 A US 674222A US 67422233 A US67422233 A US 67422233A US 1971564 A US1971564 A US 1971564A
- Authority
- US
- United States
- Prior art keywords
- stage
- fibre
- liquor
- cooking
- temperature
- 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
- 238000000034 method Methods 0.000 title description 16
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 title description 12
- 238000004519 manufacturing process Methods 0.000 title description 8
- 238000010411 cooking Methods 0.000 description 16
- 239000000835 fiber Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
- 229920005610 lignin Polymers 0.000 description 4
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- -1 bisulphite ions Chemical class 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 101100348341 Caenorhabditis elegans gas-1 gene Proteins 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 101100447658 Mus musculus Gas1 gene Proteins 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- LPHFLPKXBKBHRW-UHFFFAOYSA-L magnesium;hydrogen sulfite Chemical compound [Mg+2].OS([O-])=O.OS([O-])=O LPHFLPKXBKBHRW-UHFFFAOYSA-L 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 description 1
- 239000000243 solution 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
- D21C3/04—Pulping cellulose-containing materials with acids, acid salts or acid anhydrides
- D21C3/06—Pulping cellulose-containing materials with acids, acid salts or acid anhydrides sulfur dioxide; sulfurous acid; bisulfites sulfites
Definitions
- This invention relates to the manufacture of sulphite pulp and particularly to a two-stage cooking process resulting in substantial economies of operation and in the production of a 15? high quality pulp.
- a two-stage cooking process is employed.
- the cellulose material is cooked with a liquor capable of supplying the bisulphite ions required to effect 'Isulphonation of the lignin.
- This liquor may be an aqueous solution of calcium and/or magnesium bisulphite, containing an excess of free sulphurous acid, alkali sulphite or bisulphite with or without free sulphurous acid, or a mixture of 25. these constituents.
- liberation of the fibre is substantially avoided and reaction products, harmful in later stages of the process, are removed.
- the liquor is removed without substantially 3llj'jlowering'the temperature and pressure in the digester, preferably by the introduction of direct steam into the top portion of the digester;
- the second stage requires the cooking of the charge with water, preheated to the temperature of the charge in the digester.
- the temperature and pressure in the digester are then raised above the limits employed in the usual one-stage sulphite process and these conditions are maintained until fibre liberation is complete and the remaining encrusting materials about the cellulose fibre are dissolved.
- the hydrolysis of the sulphonated lignin is Bo -(effected without damage to the cellulose fibre and without the use of added expensive reagents. This is probably due to the release of hydrogen ions from reaction products, such as organic acids, formed during the cooking operation.
- Chips of coniferous wood or the like are treated in a digester with a liquor consisting of an aqueous solution of calcium and magnesium tially constant, and preheated water is added.
- the temperature is then raised to 160 to 170 C. with a pressure of to 100 pounds and maintained for 3 to 9 hours,'until fibre liberation, is complete.
- the contents of the digester are then dumped in the usual way.
- the chips may be cooked with a first-stage liquor consisting of a solution of substantially pure sodium bisulphite, having a combined S02 content in the proportion of substantially 50% of the total S02 and containing, for example, 6 to 80.
- a process for manufacturing sulphite pulp which comprises cooking cellulosic material with 1101.
- a two-stage process of manufacturing sulphite pulp which comprises cooking cellulose ma terial with sulphite liquor until a temperature of 120 to 150 C. is reached, removing the liquor without substantially lowering the temperature or pressure, introducing preheated water and cooking the material to completely liberate the fibre.
- a two-stage process of manufacturing sulphite pulp which comprises cooking wood chips with a sulphite liquor in which substantially 50% of the S02 is in the combined form, removing the liquor without substantially lowering the temperature or pressure, and cooking the chips with water at a temperature of 160 to 170 C. to liberate the fibre and hydrolyze the sulphonated lignin.
Landscapes
- Paper (AREA)
Description
Patented Aug. 28, 1934 No SULPHITE Ernstf Hocl1berger Hawks-shu s, criteria, (a... ada'yassignorto'Canadian International Paper i Gompany,-"Montreal,'QuebecQCanada 7N6 Drawing. App ication June 3', i933, gas-1 No. 674,222. In Canada June .z d lggg 8 Claims. (Cl, 92L 11 :l'
This invention relates to the manufacture of sulphite pulp and particularly to a two-stage cooking process resulting in substantial economies of operation and in the production of a 15? high quality pulp.
In co-pending applications Serial No. 674,223 and Serial No. 674,224, processes of this character are disclosed. The present invention relates to a further improvement in these processes.
10? Economy in operation in the manufacture of pulp is an important consideration but in addition it is an object of this invention to provide a process whereby full advantage may be taken of the hydrogen ion concentration developed during the ifinal stage of the cooking operation.
In carrying out the invention a two-stage cooking process is employed. In the first stage the cellulose material is cooked with a liquor capable of supplying the bisulphite ions required to effect 'Isulphonation of the lignin. This liquor may be an aqueous solution of calcium and/or magnesium bisulphite, containing an excess of free sulphurous acid, alkali sulphite or bisulphite with or without free sulphurous acid, or a mixture of 25. these constituents. In this cooking operation liberation of the fibre is substantially avoided and reaction products, harmful in later stages of the process, are removed. At the conclusion of this step the liquor is removed without substantially 3llj'jlowering'the temperature and pressure in the digester, preferably by the introduction of direct steam into the top portion of the digester; In some cases, it is preferable to wash the charge with hot water, a preheated sulphurous acid soflo'zilution or with a portion of preheated liquor, such s is used in the cooking operation. This insures complete removal of undesired products and leaves the charge in best condition for the final fibre-liberating cook.
The second stage requires the cooking of the charge with water, preheated to the temperature of the charge in the digester. The temperature and pressure in the digester are then raised above the limits employed in the usual one-stage sulphite process and these conditions are maintained until fibre liberation is complete and the remaining encrusting materials about the cellulose fibre are dissolved. Under these conditions it is found that the hydrolysis of the sulphonated lignin is Bo -(effected without damage to the cellulose fibre and without the use of added expensive reagents. This is probably due to the release of hydrogen ions from reaction products, such as organic acids, formed during the cooking operation.
555; To further illustrate the method of carrying out theinvention the following specific examples may be given.
(1) Chips of coniferous wood or the like are treated in a digester with a liquor consisting of an aqueous solution of calcium and magnesium tially constant, and preheated water is added.
The temperature is then raised to 160 to 170 C. with a pressure of to 100 pounds and maintained for 3 to 9 hours,'until fibre liberation, is complete. The contents of the digester are then dumped in the usual way.
(2) The chips may be cooked with a first-stage liquor consisting of a solution of substantially pure sodium bisulphite, having a combined S02 content in the proportion of substantially 50% of the total S02 and containing, for example, 6 to 80.
8% total S02 and 3 to 4% combined S02. Cooking is continued for 3 to 11 hours until a temperature of 100 to 150 C. is reached. The duration of the cook after this temperature is reached may vary from 1 to 8 hours. This liquor is then re- 85 moved as before and the second-stage treatment is effected with preheated water. The temperature is raised to 160 to 170 C. with a pressure of 85 to 100 pounds. Fibre liberation is completed within 10 to 14 hours from the start and the digester contents are dumped and washed as required.
It will be apparent that the invention provides for substantial economy in the use of chemical reagents employed, these reagents being used only in the first stage cooking operation for removal of fibre-encrusting materials and the fibre being liberated in the next stage by the use of water only. As indicated, it appears that hydrogen ions liberated during this stage assist in freeing the cellulose fibre but in any event the relatively mild treatment avoids loss of and damage to to the fibre.
I claim:
1. A process for manufacturing sulphite pulp which comprises cooking cellulosic material with 1101.
sulphite liquor to sulphonate the lignin, discontinuing the cook before liberating the fibre, removing the liquor and further cooking the material with water to liberate the fibre.
3. In a two-stage process of manufacturing sulphite pulp, the steps which comprise discontinuing the first-stage cook before liberation of the fibre of the cellulose material and cooking with water to liberate the fibre.
4. A two-stage process of manufacturing sulphite pulp which comprises cooking cellulose ma terial with sulphite liquor until a temperature of 120 to 150 C. is reached, removing the liquor without substantially lowering the temperature or pressure, introducing preheated water and cooking the material to completely liberate the fibre.
5. A process as defined in claim 4, wherein said second-stage cook is effected at a temperature of 160 to 170 C. and a pressure of 85 to 100 pounds.
6. A process as defined in claim 4, wherein said first-stage liquor contains an excess of free sulphurous acid and wherein the second-stage cook is effected at a temperature of 160 to 170 C.
'7, A two-stage process of manufacturing sulphite pulp which comprises cooking wood chips with a sulphite liquor in which substantially 50% of the S02 is in the combined form, removing the liquor without substantially lowering the temperature or pressure, and cooking the chips with water at a temperature of 160 to 170 C. to liberate the fibre and hydrolyze the sulphonated lignin.
8. A process as defined in claim 7, wherein after the removal of the first stage liquor the material is washed with a preheated fluid to remove impurities.
' ERNST HOCHBERGER.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA1971564X | 1932-06-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1971564A true US1971564A (en) | 1934-08-28 |
Family
ID=4174597
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US674222A Expired - Lifetime US1971564A (en) | 1932-06-24 | 1933-06-03 | Process of manufacturing sulphite pulp |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1971564A (en) |
-
1933
- 1933-06-03 US US674222A patent/US1971564A/en not_active Expired - Lifetime
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