US1268774A - Process of dissociating waste lye from the sulfite-cellulose manufacture. - Google Patents
Process of dissociating waste lye from the sulfite-cellulose manufacture. Download PDFInfo
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- US1268774A US1268774A US22508118A US22508118A US1268774A US 1268774 A US1268774 A US 1268774A US 22508118 A US22508118 A US 22508118A US 22508118 A US22508118 A US 22508118A US 1268774 A US1268774 A US 1268774A
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- Prior art keywords
- sulfite
- liquor
- waste lye
- heating
- cellulose manufacture
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H6/00—Macromolecular compounds derived from lignin, e.g. tannins, humic acids
Definitions
- the waste liquor from the manufacture of Wood pulp and other pulp by the sulfite process may be dissociated by the use of oxidizing agents under high pressure and at a high temperature. It has heretofore been proposed to heat the waste liquor, from which the pulp has been separated, to a temperature of about 100 (1., while introducing an oxidizing gas, such as air, said heating being effected under superatmospheric pressure, in an autoclave, durin which operation the free S0 together w1th that combined with lime as bisulfite becomes oxidized to S0,, and whereby the lignin material is precipitated, but it is found that during such operation sulfate of lime is produced, this being precipitated, and forming a coating on the surfaces of the heating elements.
- an oxidizing gas such as air
- the first part of the heating, for the dissociation of the liquor solids must, for economical reasons be effected by means of exhaust steam, and the coating of the heating elements with calcium sulfate very materially decreases the efficiency of the heating operation.
- the oxidization of the sulfur compound considerable heat is liberated, the amount of which is usually suflicient to raise the temperature of the liquor by about 20 degrees C. This of course further decreases the efiiciency of the heating operation, since in order to get efficient heating by exhaust steam, it is necessary to have a wide temperature difference between this steam and the liquor to be heated.
- the waste liquor is first heated, preferably in an autoclave, by exhaust steam, up to such a temperature (about 80 (3.), that the heat produced by oxidation subsequently, will raise the temperature to about 100 C. and this operation is effected in an atmosphere consisting of non-oxidizing gases, or gases which have only slight oxidizing power. This operation can be carried out at atmospheric, or at a higher pressure.
- the liquor is transferred to another autoclave and is heated therein somewhat, preferably by the introduction of live steam or superheated steam, while compressed oxidizing gases, such as compressed air, or the like, are introduced.
- This air or oxygen oxidizes the sulfur compounds, producing a precipitation of calcium sulfate, simultaneously with the precipitation of the lignin material, but the precipitation of calcium sulfate at this stage of the operation is not objectionable, since there are no heat interchange elements employed in the second autoclave.
- the oxidation in the second autoclave produces heat, and the temperature of the liquor may rise about twenty degrees, from this cause.
- This oxidation treatment is preferably efiected under a considerable super-atmospheric pressure.
- the lignin material produced may be employed, either alone or with other materials, as a fuel, and the presence of precipitated calcium sulfate ther'ein, while of course increasing the ash content materially, is not particularly objectionable.
- a process of precipitating lignin material from the waste liquor separated from pulp made by the sulfite process which comprises firstly, heating up the said liquor while confined in an atmosphere of a non oxidizing gas, to a temperature of not materially below 80 G, and secondly, subjectingthe said liquor to the action of an oxidizing gas under superatrnospheric pressure, while raising the temperature of the liquor to about 100 0., until said lignin material is precipitated.
- the improvement which comprises. introducing compressed air into the liquor during the second heating operation, whereby the oxygen content of said air becomes considerably decreased, and thereafter conveying the remaining gas to the containers in which the first operation is carried out whereby the exit gas of the second operation is used as the 11on o idizing gas for the first operation.
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- Engineering & Computer Science (AREA)
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- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
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Description
Warren srarns arana @FFIQE.
ING-VAR SijRAAS, 0F INDRE .AALVIK, HARDANGER, NORWAY.
PROCESS OF DISSOCIA'IING WASTE LYE FROM THE SULFITE-CELLULOSE MANUFACTURE.
No Drawing.
To all whom it may concern: I
Be it known that I, INGVAR Scams, a
citizen of Norway, residing at Indre Aalvik,
Hardanger, Norway, have invented certain new and useful Improvements in Processes of Dissociating Waste Lye from the Sulfite-Cellu1ose Manufacture, of which the following is a specification.
It is a well known fact that the waste liquor from the manufacture of Wood pulp and other pulp by the sulfite process may be dissociated by the use of oxidizing agents under high pressure and at a high temperature. It has heretofore been proposed to heat the waste liquor, from which the pulp has been separated, to a temperature of about 100 (1., while introducing an oxidizing gas, such as air, said heating being effected under superatmospheric pressure, in an autoclave, durin which operation the free S0 together w1th that combined with lime as bisulfite becomes oxidized to S0,, and whereby the lignin material is precipitated, but it is found that during such operation sulfate of lime is produced, this being precipitated, and forming a coating on the surfaces of the heating elements. The first part of the heating, for the dissociation of the liquor solids must, for economical reasons be effected by means of exhaust steam, and the coating of the heating elements with calcium sulfate very materially decreases the efficiency of the heating operation. During the oxidization of the sulfur compound, considerable heat is liberated, the amount of which is usually suflicient to raise the temperature of the liquor by about 20 degrees C. This of course further decreases the efiiciency of the heating operation, since in order to get efficient heating by exhaust steam, it is necessary to have a wide temperature difference between this steam and the liquor to be heated.
One method which has been proposed, for the overcoming of these difficulties, is to first treat the Waste liquor with sodium bisulfate, for the precipitation of the calcium as sulfate and the removal of this before the heating with air under pressure is effected. This of course requires the use of a large supply of bisulfate, which in many cases considerably increases the cost of the final product. 7
In accordance with the present invention,
Specification of Letters Patent.
Patented June 4, 1918.
a different procedure is followed, as follows:
The waste liquor is first heated, preferably in an autoclave, by exhaust steam, up to such a temperature (about 80 (3.), that the heat produced by oxidation subsequently, will raise the temperature to about 100 C. and this operation is effected in an atmosphere consisting of non-oxidizing gases, or gases which have only slight oxidizing power. This operation can be carried out at atmospheric, or at a higher pressure. Thereafter, as the second step of the process, the liquor is transferred to another autoclave and is heated therein somewhat, preferably by the introduction of live steam or superheated steam, while compressed oxidizing gases, such as compressed air, or the like, are introduced. This air or oxygen oxidizes the sulfur compounds, producing a precipitation of calcium sulfate, simultaneously with the precipitation of the lignin material, but the precipitation of calcium sulfate at this stage of the operation is not objectionable, since there are no heat interchange elements employed in the second autoclave. The oxidation in the second autoclave produces heat, and the temperature of the liquor may rise about twenty degrees, from this cause. This oxidation treatment is preferably efiected under a considerable super-atmospheric pressure.
As the gases for the first step of the process, I find it preferable to employ the waste gases from the second step of the process, the oxidation of the sulfur compounds in said second step removing the major portion of the free oxygen therefrom. I find that it is not necessary to employ, during the first step of the process, such a high pressure as is required in the second step.
The lignin material produced may be employed, either alone or with other materials, as a fuel, and the presence of precipitated calcium sulfate ther'ein, while of course increasing the ash content materially, is not particularly objectionable.
I claim: 1 y
1. A process of precipitating lignin material from the waste liquor separated from pulp made by the sulfite process, which comprises firstly, heating up the said liquor while confined in an atmosphere of a non oxidizing gas, to a temperature of not materially below 80 G, and secondly, subjectingthe said liquor to the action of an oxidizing gas under superatrnospheric pressure, while raising the temperature of the liquor to about 100 0., until said lignin material is precipitated.
2. In the process as set forth in claim 1, the improvement which comprises. introducing compressed air into the liquor during the second heating operation, whereby the oxygen content of said air becomes considerably decreased, and thereafter conveying the remaining gas to the containers in which the first operation is carried out whereby the exit gas of the second operation is used as the 11on o idizing gas for the first operation.
In testimony whereof Ihave affixed my signature in presence of two witnesses.
INGVAR SORAAS.
Vitnesses AXEL LAKIR, HAROLD NALlvL Copies of this patent may be obtained for five cents each, by addressing the Commissioner of Patents,
Washington, 1). c.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22508118A US1268774A (en) | 1918-03-27 | 1918-03-27 | Process of dissociating waste lye from the sulfite-cellulose manufacture. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22508118A US1268774A (en) | 1918-03-27 | 1918-03-27 | Process of dissociating waste lye from the sulfite-cellulose manufacture. |
Publications (1)
Publication Number | Publication Date |
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US1268774A true US1268774A (en) | 1918-06-04 |
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US22508118A Expired - Lifetime US1268774A (en) | 1918-03-27 | 1918-03-27 | Process of dissociating waste lye from the sulfite-cellulose manufacture. |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2491832A (en) * | 1946-09-23 | 1949-12-20 | Marathon Corp | Lignin dispersing agents and method of making same |
US2680113A (en) * | 1949-12-22 | 1954-06-01 | Svenska Cellulosaforeningens C | Method of producing water-soluble products from black liquor lignin |
US2690425A (en) * | 1950-03-23 | 1954-09-28 | Du Pont | Waste disposal process |
US2773026A (en) * | 1953-07-02 | 1956-12-04 | Stora Kopparbergs Bergslags Ab | Removal of dissolved or dispersed organic material from aqueous solutions and suspensions |
US2824058A (en) * | 1953-12-14 | 1958-02-18 | Sterling Drug Inc | Method for the continuous self-sustaining flameless oxidation of combustible materials |
US2903425A (en) * | 1955-01-24 | 1959-09-08 | Frederick J Zimmermann | Oxidation regulation |
US2935473A (en) * | 1959-05-25 | 1960-05-03 | Puget Sound Pulp And Timber Co | Drilling fluid composition and process |
-
1918
- 1918-03-27 US US22508118A patent/US1268774A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2491832A (en) * | 1946-09-23 | 1949-12-20 | Marathon Corp | Lignin dispersing agents and method of making same |
US2680113A (en) * | 1949-12-22 | 1954-06-01 | Svenska Cellulosaforeningens C | Method of producing water-soluble products from black liquor lignin |
US2690425A (en) * | 1950-03-23 | 1954-09-28 | Du Pont | Waste disposal process |
US2773026A (en) * | 1953-07-02 | 1956-12-04 | Stora Kopparbergs Bergslags Ab | Removal of dissolved or dispersed organic material from aqueous solutions and suspensions |
US2824058A (en) * | 1953-12-14 | 1958-02-18 | Sterling Drug Inc | Method for the continuous self-sustaining flameless oxidation of combustible materials |
US2903425A (en) * | 1955-01-24 | 1959-09-08 | Frederick J Zimmermann | Oxidation regulation |
US2935473A (en) * | 1959-05-25 | 1960-05-03 | Puget Sound Pulp And Timber Co | Drilling fluid composition and process |
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