US2947657A - Extraction of cellulose from vegetable matter - Google Patents

Extraction of cellulose from vegetable matter Download PDF

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Publication number
US2947657A
US2947657A US640304A US64030457A US2947657A US 2947657 A US2947657 A US 2947657A US 640304 A US640304 A US 640304A US 64030457 A US64030457 A US 64030457A US 2947657 A US2947657 A US 2947657A
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cellulose
hydrosulfite
vegetable matter
alkali
extraction
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US640304A
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Peteri Robert
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Compagnie de Saint Gobain SA
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Compagnie de Saint Gobain SA
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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
    • D21C3/222Use of compounds accelerating the pulping processes

Definitions

  • Another object is to improve the cooking liquors of this type. Another object is to stabilize the improved liquors with novel stabilizers. Yet another object is to improve the homogeneity of the pulps produced by these processes. Another object is to eliminate or minimize the occurrence of black spots in such pulps.
  • the objects of the invention are accomplished by digesting the vegetable matter containing ligno cellulose in a neutral or acid liquor containing at least one of the sulphites ind bisulphites of alkali and alkali earth metals, which are used in the usual concentrations, and a metal hydrosulphite, preferably zinc or sodium hydrosulfite, the liquor preferably being stabilized, especially when the temperature of the cook is to be about 120-l70 C., by the addition of stabilizers of which formaldehyde, complex chelates, and polyphosphates are exemplary.
  • ethylenediaminetetracetic acid is an exceptionally eflicient stabilizer.
  • the cooks thatare carried out under pressure employ temperatures that are relatively high, circa 120 to 170 C., at which the hydrosulfites are relatively unstable, and under such circumstances it is desirable to add a stabilizer for the hydrosulfite to the liquor. Satisfactory stability is obtained with stabilizers of the type of formaldehyde, complex chelates, ethylene diamine tetraacetic acid, polyphosphates.
  • hydrosulfite In carrying out the cook in the presence of hydrosulfite the formation of a part of the colored products is prevented.
  • the hydrosulfites have marked reducing power and prevent the oxidation of the sugars and other organic products released in the disintegration of the vegetable materials, or destroy them after formation, thus producing a clearer and less colored pulp.
  • the hydrosulfites because of their combined sulfur, which occurs in different forms, plays the double role of a delignifying agent and assists in the production of more homogeneous and softer pulps.
  • the products NaI-IS and H 8 are delignifiers of strength and their action is added to that of the cooking liquors of alkali metal, or alkali, sulfite or bisulfite base and produce jointly a disintegration of the vegetable matter that is more thorough and more homogeneous. From this fact, the presence of sodium hydrosulfite in the cooking liquor makes the action of the mineral salt liquors more selective and protects the cellulose better.
  • the invention is applicable to all the liquors employing mineral salts in acid or neutral medium and to all types of vegetable matter from pine wood to straw. This produces clearer pulps which may be used directly without bleaching, particularly if the medium is the neutral sulfite or bisulfite with hydrosulfite.
  • hydrosulfites are the alkali and alkali earth metal hydrosulfites and zinc hydrosulfite.
  • Sodium hydrosulfite is excellent and is generally employed, but it is not exclusively useful.
  • the pulps produced by this method can be bleached by the standard methods. Particularly interesting results are obtained by submitting such pulps to a simple treatment with sodium hydrosulfite under conditions the same as those used for bleaching groundwood pulp. The improvement in whiteness is greater than that obtained with pulps not made in the presence of hydrosulfite.
  • Example 1 The cooking of 2.5 kg. of poplar wood chips, 89% dry, by a mixture of calcium and magnesium sulfite in water at standard concentration, was carried out in a pressure digester (autoclave) of stainless steel.
  • Example 2 2.5 kilos of Austin pine chips, 7075% dry, were cooked in a liquor containing a mixture of bisulfites of calcium and magnesium in an autoclave of stainless steel. The liquor at the start of the operation, mixed with the chips contained:
  • a temperature of 105 C. was reached at 3 hrs. and 45 min. When the pressure reached 5 kg. it was maintained for 5 hrs. When the temperature reached 128, which required 1 hr. min. from 105, a second steady cook of 6 hrs. was used, so that the total cook was 16 hrs.
  • the digester was blown, the product was washed and sent to a disintegrator.
  • the pulp was examined, standard test samples showed reflectance of 45% with a Wratten blue filter and revealed lumps and numerous black spots.
  • Example 3 A pulp was prepared from 2.5 kg. of poplar wood chips, 89% dry, using neutral sodium sulfite liquor buffered with sodium carbonate of which the composition, by weight based on thedry wood, was:
  • Example 2 The same conditions as Example 1 were used except that the steady cook took place at 160 for 7 hrs.
  • the pulp had a reflectance, by like test, of 51%.
  • This pulp could be used directly for making printing paper without bleaching.
  • the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, of a metal from the group Zn and Na, in an amount between about .3 to about 2% by weight of the dry ligno-cellulose matter, and a stabilizer for the hydrosulfite, consisting in its essential operative constituent of ethylene diamine tetraacetic acid, at a temperature of l20l70 C.
  • the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the suliites and bisulfites of alkali and alkali earth metais, a metal hydrosulfite, in an amount between about .3 to about 2% by weight of the dry lignocellulose matter, and as a stabilizer for the hydrosulfite, ethylene diamine tetraacetic acid, at a temperature of -170 C.
  • a cooking liquor of non-alkaline pH composed in its essential delignitying ingredients of at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, and a hydrosulfite stabilizer.

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Description

EXTRACTION OF CELLULOSE FROM VEGETABLE MATTER Robert Peteri, Paris, France, assignor to Compagnie de Saint-Gobain, Paris, France No Drawing. Filed Feb. 15, 1957, Ser. No. 640,304 Claims priority, application France Feb. 18, 1956 7 Claims. (Cl. 162-76) This invention relates to the extraction of cellulose from vegetable matter containing ligno-cellulose by acid or neutral liquors of mineral salt type and constitutes an improvement over known processes.
It is known that during the deligniiication of vegetable matter containing ligno-cellulose by cooking with mineral salts such as neutral sulfite or by bisulphite liquors the fibres become colored of which the intensity and hue depend onthe raw materials employed and the process of digestion adopted. In most cases the fibres must undergo subsequent treatments for clarification or bleachmg.
It is an object of the invention to produce pulp by these processes that is of better color and which requires no after treatment.
Another object is to improve the cooking liquors of this type. Another object is to stabilize the improved liquors with novel stabilizers. Yet another object is to improve the homogeneity of the pulps produced by these processes. Another object is to eliminate or minimize the occurrence of black spots in such pulps.
The objects of the invention, generally speaking, are accomplished by digesting the vegetable matter containing ligno cellulose in a neutral or acid liquor containing at least one of the sulphites ind bisulphites of alkali and alkali earth metals, which are used in the usual concentrations, and a metal hydrosulphite, preferably zinc or sodium hydrosulfite, the liquor preferably being stabilized, especially when the temperature of the cook is to be about 120-l70 C., by the addition of stabilizers of which formaldehyde, complex chelates, and polyphosphates are exemplary. I have also discovered that ethylenediaminetetracetic acid is an exceptionally eflicient stabilizer.
By this invention one produces directly, by digesting cellulosic vegetable matter with mineral salts, pulps which are both less colored and more homogeneous than was previously feasible. The hydrosulfites of sodium and zinc are particularly useful. The amount to use depends on the kind of ligno-cellulosic matter being digested and the conditions, such as temperature, of the cook. In general good results are obtained if one uses a proportion of hydrosulfite on the order of .3% to 2% of the weight of the dry cellulose matter. At the same time one uses of the non-alkaline sulfite or bisulfite the same proportions that are presently recommended.
The cooks thatare carried out under pressure employ temperatures that are relatively high, circa 120 to 170 C., at which the hydrosulfites are relatively unstable, and under such circumstances it is desirable to add a stabilizer for the hydrosulfite to the liquor. Satisfactory stability is obtained with stabilizers of the type of formaldehyde, complex chelates, ethylene diamine tetraacetic acid, polyphosphates.
In carrying out the cook in the presence of hydrosulfite the formation of a part of the colored products is prevented. The hydrosulfites have marked reducing power and prevent the oxidation of the sugars and other organic products released in the disintegration of the vegetable materials, or destroy them after formation, thus producing a clearer and less colored pulp.. In addition, at the relatively high temperatureof such cooks the hydrosulfites, because of their combined sulfur, which occurs in different forms, plays the double role of a delignifying agent and assists in the production of more homogeneous and softer pulps. By decomposition during digestion the hydrosulfite gives, according to the pH of the cooking liquor, the following reactions:
With a neutral liquor, sodium hydrosulfide:
With a sulfurous acid medium, hydrogen sulfide:
The products NaI-IS and H 8 are delignifiers of strength and their action is added to that of the cooking liquors of alkali metal, or alkali, sulfite or bisulfite base and produce jointly a disintegration of the vegetable matter that is more thorough and more homogeneous. From this fact, the presence of sodium hydrosulfite in the cooking liquor makes the action of the mineral salt liquors more selective and protects the cellulose better.
The invention is applicable to all the liquors employing mineral salts in acid or neutral medium and to all types of vegetable matter from pine wood to straw. This produces clearer pulps which may be used directly without bleaching, particularly if the medium is the neutral sulfite or bisulfite with hydrosulfite.
Among the useful hydrosulfites are the alkali and alkali earth metal hydrosulfites and zinc hydrosulfite. Sodium hydrosulfite is excellent and is generally employed, but it is not exclusively useful.
The pulps produced by this method can be bleached by the standard methods. Particularly interesting results are obtained by submitting such pulps to a simple treatment with sodium hydrosulfite under conditions the same as those used for bleaching groundwood pulp. The improvement in whiteness is greater than that obtained with pulps not made in the presence of hydrosulfite.
In all cases the process produces pulp that is better cooked and more homogeneous than by prior art methods, making bleaching easier. An advantage of technological and commercial nature arises from the fact that the chemicals and steam used in the digesters may be reduced while producing a pulp at least equal to that previously obtainable. No modification of present standard apparatus is necessary.
The following examples are exemplary, not limiting.
Example 1 The cooking of 2.5 kg. of poplar wood chips, 89% dry, by a mixture of calcium and magnesium sulfite in water at standard concentration, was carried out in a pressure digester (autoclave) of stainless steel. The cooking liquor, at the time of admission to the digester, containing its necessary water, had the following composition:
. G./l. S0 total 60 CaO 7.7 MgO 3.3
Example 2 2.5 kilos of Landes pine chips, 7075% dry, were cooked in a liquor containing a mixture of bisulfites of calcium and magnesium in an autoclave of stainless steel. The liquor at the start of the operation, mixed with the chips contained:
S02, total CaO 7.7 h1g0 3.3
A temperature of 105 C. was reached at 3 hrs. and 45 min. When the pressure reached 5 kg. it was maintained for 5 hrs. When the temperature reached 128, which required 1 hr. min. from 105, a second steady cook of 6 hrs. was used, so that the total cook was 16 hrs.
The digester was blown, the product was washed and sent to a disintegrator. The pulp was examined, standard test samples showed reflectance of 45% with a Wratten blue filter and revealed lumps and numerous black spots.
Operating under the same conditions, but with the addition of 2% of sodium hydrosulfite stabilized by .6% formaldehyde there was obtained a pulp free from lumps and with very few black spots. The same test showed a reflectance of.5 1%, an improvement of 6 points.
Example 3 A pulp was prepared from 2.5 kg. of poplar wood chips, 89% dry, using neutral sodium sulfite liquor buffered with sodium carbonate of which the composition, by weight based on thedry wood, was:
Percent Sodium sulfate 14 Sodium carbonate 4.5
The same conditions as Example 1 were used except that the steady cook took place at 160 for 7 hrs. The pulp had a reflectance, by like test, of 51%.
I When the operation was repeated but with the addition of 1% sodium hydrosulfite, stabilized by .3% formaldehyde, the reflectance of a standard sample was 56%, a gain of 5 points.
This pulp could be used directly for making printing paper without bleaching.
Comparable results are obtainable using other hydrosulfites, particularly zinc hydrosulfites.
As many apparently widely different embodiments of the present invention may be made without departing from the spirit and scope thereof, it is to be understood that the invention is not limited .to the specific embodiments.
What is claimed is:
' 1. In the extraction of cellulose from vegetable matter 3 containing ligno-cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, of a metal from the group Zn and Na, in an amount between about .3 to about 2% by weight of the dry ligno-cellulose matter, and a stabilizer for the hydrosulfite, consisting in its essential operative constituent of ethylene diamine tetraacetic acid, at a temperature of l20l70 C.
2. In the extraction of cellulose from vegetable matter containing ligno cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the suliites and bisulfites of alkali and alkali earth metais, a metal hydrosulfite, in an amount between about .3 to about 2% by weight of the dry lignocellulose matter, and as a stabilizer for the hydrosulfite, ethylene diamine tetraacetic acid, at a temperature of -170 C.
3. In the extraction of cellulose from vegetable matter containing ligno cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, in an amount between about .3 to about 2% by weight of the dry ligno cellulose matter, and a stabilizer for the hydrosulfite, at a temperature of 120170 C.
4. In the extraction of cellulose from vegetable matter containing ligno-cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, in an amount between about .3 to 2% by weight of the dry ligno-cellulose matter, and ethylene diamine tetraacetic acid.
5. In the extraction of cellulose from vegetable matter containing ligno-cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the sulfites and bisulfites of 'alkali and alkali earth metals, a metal hydrosulfite, and a stabilizer for the hydrosulfite.
6. In the extraction of cellulosefrom vegetable matter containing ligno-cellulose by mineral salts in neutral and acid media, the improvement which comprises digesting the vegetable matter in a liquor containing at least one of the whites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite from the group consisting of alkali metals and zinc, and ethylene diamine tetraacetic acid.
7. A cooking liquor of non-alkaline pH composed in its essential delignitying ingredients of at least one of the sulfites and bisulfites of alkali and alkali earth metals, a metal hydrosulfite, and a hydrosulfite stabilizer.
References Cited in the file of this patent UNITED STATES PATENTS 1,451,125 Summers Apr. 10, 1923 1,910,613 Kylander May 23,1933 2,070,585 Dreyfus Feb. 16, 1937 2,656,244 Gray et al. Oct. 20, '1953 2,707,145 Sparrow et a1 ,Apr. 26, 1955

Claims (1)

  1. 5. IN THE EXTRACTION OF CELLULOSE FROM VEGETABLE MATTER CONTAINING LIGNO-CELLULOSE BY MINERAL SALTS IN NEUTRAL AND ACID MEDIA, THE IMPROVEMENT WHICH COMPRISES DIGESTING THE VEGETABLE MATTER IN A LIQUOR CONTAINING AT LEAST ONE OF THE SULFITES AND BISULFITES OF ALKALI AND ALKALI EARTH METALS, A METAL HYDROSULFITE, AND A STABILIZER FOR THE HYDROSULFITE.
US640304A 1956-02-18 1957-02-15 Extraction of cellulose from vegetable matter Expired - Lifetime US2947657A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3088861A (en) * 1960-08-03 1963-05-07 Weyerhaeuser Co Method of manufacturing chemical pulp from lignocellulose material
US3363970A (en) * 1963-11-29 1968-01-16 Geigy Ag J R Alkali metal salts of oxygen acids tetravalent sulfur and metal complexing agents inan acidic dyebath and polyamide dyeing therewith
US3448003A (en) * 1966-01-03 1969-06-03 Dow Chemical Co On-stream cleaning of wood chip digesters using chelating agents
US4135967A (en) * 1969-09-26 1979-01-23 Societe Generale De Brevets Industriels Et Ohimiques Process for producing cellulose pulp by solid phase digestion
US4767500A (en) * 1985-05-18 1988-08-30 Kraftanlagen Aktiengesellschaft Sulfite cooking method for the production of cellulose from materials containing lignocellulose with recovery of the cooking chemicals

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1451125A (en) * 1922-04-21 1923-04-10 Bertrand S Summers Process for the production of paper pulp and the like
US1910613A (en) * 1927-03-17 1933-05-23 Kylander Karl Yrjo Preliminary boiling or cooking process for cellulose
US2070585A (en) * 1933-03-07 1937-02-16 Dreyfus Henry Manufacture of cellulose from ligno-cellulosic products
US2656244A (en) * 1950-07-15 1953-10-20 Rayonier Inc Process of recovering chemicals from smelts obtained in pulping operation
US2707145A (en) * 1952-09-11 1955-04-26 Scott Paper Co Method of bleaching mechanically disintegrated wood pulp

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE742617C (en) * 1941-03-28 1943-12-14 Chem Fab Joh A Benckiser G M B Process for preventing resin precipitations in paper manufacture
AT175782B (en) * 1951-02-28 1953-08-10 Waldhof Zellstoff Fab Process for the production of semi-pulp
DE912169C (en) * 1952-02-22 1954-05-24 Georg Jayme Dr Ing Process for the alkaline digestion of plant substances
DE942553C (en) * 1954-03-11 1956-05-03 Basf Ag Process for the production of cellulose from plant material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1451125A (en) * 1922-04-21 1923-04-10 Bertrand S Summers Process for the production of paper pulp and the like
US1910613A (en) * 1927-03-17 1933-05-23 Kylander Karl Yrjo Preliminary boiling or cooking process for cellulose
US2070585A (en) * 1933-03-07 1937-02-16 Dreyfus Henry Manufacture of cellulose from ligno-cellulosic products
US2656244A (en) * 1950-07-15 1953-10-20 Rayonier Inc Process of recovering chemicals from smelts obtained in pulping operation
US2707145A (en) * 1952-09-11 1955-04-26 Scott Paper Co Method of bleaching mechanically disintegrated wood pulp

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3088861A (en) * 1960-08-03 1963-05-07 Weyerhaeuser Co Method of manufacturing chemical pulp from lignocellulose material
US3363970A (en) * 1963-11-29 1968-01-16 Geigy Ag J R Alkali metal salts of oxygen acids tetravalent sulfur and metal complexing agents inan acidic dyebath and polyamide dyeing therewith
US3448003A (en) * 1966-01-03 1969-06-03 Dow Chemical Co On-stream cleaning of wood chip digesters using chelating agents
US4135967A (en) * 1969-09-26 1979-01-23 Societe Generale De Brevets Industriels Et Ohimiques Process for producing cellulose pulp by solid phase digestion
US4767500A (en) * 1985-05-18 1988-08-30 Kraftanlagen Aktiengesellschaft Sulfite cooking method for the production of cellulose from materials containing lignocellulose with recovery of the cooking chemicals

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DE1063893B (en) 1959-08-20

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