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GB926034A - Process for producing chemicals from a woody material - Google Patents

Process for producing chemicals from a woody material

Info

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
Application number
GB2336259A
Inventor
Ralph Harper Mckee
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mckee Dev Corp
Original Assignee
Mckee Dev Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mckee Dev Corp filed Critical Mckee Dev Corp
Publication of GB926034A publication Critical patent/GB926034A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05DSYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D23/00Control of temperature
    • G05D23/19Control of temperature characterised by the use of electric means
    • G05D23/20Control of temperature characterised by the use of electric means with sensing elements having variation of electric or magnetic properties with change of temperature
    • G05D23/24Control 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/48Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C53/00Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
    • C07C53/08Acetic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic 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
    • C07D307/38Heterocyclic 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
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/46Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
    • C07D307/48Furfural
    • C07D307/50Preparation from natural products
    • 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
    • D21C3/003Pulping cellulose-containing materials with organic compounds
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24CDOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
    • F24C15/00Details
    • F24C15/10Tops, e.g. hot plates; Rings
    • F24C15/102Tops, e.g. hot plates; Rings electrically heated
    • F24C15/105Constructive 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.
GB2336259A 1959-10-07 1959-07-07 Process for producing chemicals from a woody material Expired GB926034A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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