GB926034A - Process for producing chemicals from a woody material - Google Patents
Process for producing chemicals from a woody materialInfo
- Publication number
- GB926034A GB926034A GB2336259A GB2336259A GB926034A GB 926034 A GB926034 A GB 926034A GB 2336259 A GB2336259 A GB 2336259A GB 2336259 A GB2336259 A GB 2336259A GB 926034 A GB926034 A GB 926034A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- lignin
- autoclave
- furfural
- acetic acid
- 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
Links
Classifications
-
- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
- G05D23/00—Control of temperature
- G05D23/19—Control of temperature characterised by the use of electric means
- G05D23/20—Control of temperature characterised by the use of electric means with sensing elements having variation of electric or magnetic properties with change of temperature
- G05D23/24—Control of temperature characterised by the use of electric means with sensing elements having variation of electric or magnetic properties with change of temperature the sensing element having a resistance varying with temperature, e.g. a thermistor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/08—Acetic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/46—Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
- C07D307/48—Furfural
- C07D307/50—Preparation from natural products
-
- 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
- D21C3/003—Pulping cellulose-containing materials with organic compounds
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24C—DOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
- F24C15/00—Details
- F24C15/10—Tops, e.g. hot plates; Rings
- F24C15/102—Tops, e.g. hot plates; Rings electrically heated
- F24C15/105—Constructive details concerning the regulation of the temperature
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Automation & Control Theory (AREA)
- Furan Compounds (AREA)
Abstract
Woody materials are converted into chemicals by reaction in an autoclave at 120 DEG to 180 DEG C. and at a pressure of 20 to 80 p.s.i. for a plurality of hours with an aqueous catalytic reaction solution of an alkali metal salt of cymenesulphonic acid, xylene-sulphonic acid, toluenesulphonic acid, benzoic acid or salicylic acid, lignin and insoluble cellulose are removed from the lower part of the autoclave and a vapour mixture including furfural, acetic acid, carbon dioxide and water is removed from the top of the autoclave and condensed, acetic acid being thereafter extracted from the condensed mixture by means of furfural. The resulting extract may be subjected to a multiple distillation process whereby the furfural is recovered for use as a solvent in the extraction of the acetic acid. The concentration of the alkali metal salt is preferably in the range of 25-40% by weight, the lignin being then formed as a solution in the catalyst, or in the range of 1-4% by weight, the lignin and cellulose being then formed as an integral solid mixture. In Example 3, where Loblolly pine is used as the woody material, turpentine is amongst the products. Specification 841,229 is referred to.ALSO:Woody materials are converted into chemicals by reaction in an autoclave at 120 DEG to 180 DEG C. and at a pressure of 20 to 80 p.s.i. for a plurality of hours with an aqueous catalytic reaction solution of an alkali metal salt of cymenesulphonic acid, xylenesulphonic acid, toluenesulphonic acid, benzoic acid or salicylic acid, lignin and insoluble cellulose are removed from the lower part of the autoclave and a vapour mixture including furfural, acetic acid, carbon dioxide and water is removed from the top of the autoclave and condensed, acetic acid being thereafter extracted from the condensed mixture by means of furfural. The resulting extract may be subjected to a multiple distillation process whereby the furfural is recovered for use as a solvent in the extraction of the acetic acid. The concentration of the alkali metal salt is preferably in the range of 25-40% by weight, the lignin being then formed as a solution in the catalyst, or in the range of 1-4% by weight, the lignin and cellulose being then formed as an integral solid mixture. Specification 841,229 is referred to.ALSO:Woody materials are converted into chemicals by reaction in an autoclave at 120 to 180 DEG C. and at a pressure of 20 to 80 p.s.i. for a plurality of hours with an aqueous catalytic reaction solution of an alkali metal salt of cymenesulphonic acid, xylenesulphonic acid, toluenesulphonic acid, benzoic acid or salicylic acid, lignin and insoluble cellulose are removed from the lower part of the autoclave, and a vapour mixture including furfural, acetic acid, carbon dioxide and water is removed from the top of the autoclave and condensed, the acetic acid being thereafter extracted from the condensed mixture by means of furfural. The resulting extract may be subjected to a multiple distillation process whereby the furfural is recovered for use as a solvent in the extraction of the acetic acid. The concentration of the alkali metal salt is preferably in the range of 25-40% by weight, the lignin being then formed as a solution in the catalyst, or in the range of 1-4% by weight, the lignin and cellulose being then formed as an integral solid mixture. When the lignin is obtained as a solution, said solution is preferably diluted with water after filtering off the cellulose, the temperature of the diluted solution being from 60-70 DEG C., the precipitated lignin filtered off and the filtrate concentrated for re-use in the autoclave. Lignin prepared in this way may be used as an extender for plastics, a soil conditioner, a rubber additive or as a tanning material. Specification 841,229 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH7911959A CH391731A (en) | 1959-10-07 | 1959-10-07 | Process for the production of chemical substances, such as furfural, acetic acid, carbonic acid, lignin and cellulose, from wood-containing materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB926034A true GB926034A (en) | 1963-05-15 |
Family
ID=4536997
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2336259A Expired GB926034A (en) | 1959-10-07 | 1959-07-07 | Process for producing chemicals from a woody material |
Country Status (3)
Country | Link |
---|---|
CH (1) | CH391731A (en) |
GB (1) | GB926034A (en) |
NL (1) | NL243319A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479336A (en) * | 1966-05-13 | 1969-11-18 | Columbia Cellulose Co Ltd | Production of cellulose esters from particulate lignocellulosic material |
CN114351493A (en) * | 2021-12-08 | 2022-04-15 | 华南理工大学 | Method for removing intercellular layer lignin |
-
0
- NL NL243319D patent/NL243319A/xx unknown
-
1959
- 1959-07-07 GB GB2336259A patent/GB926034A/en not_active Expired
- 1959-10-07 CH CH7911959A patent/CH391731A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479336A (en) * | 1966-05-13 | 1969-11-18 | Columbia Cellulose Co Ltd | Production of cellulose esters from particulate lignocellulosic material |
CN114351493A (en) * | 2021-12-08 | 2022-04-15 | 华南理工大学 | Method for removing intercellular layer lignin |
Also Published As
Publication number | Publication date |
---|---|
NL243319A (en) | |
CH391731A (en) | 1965-05-15 |
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