GB200834A - Improvements in and relating to a process of preparing cellulose derivatives - Google Patents
Improvements in and relating to a process of preparing cellulose derivativesInfo
- Publication number
- GB200834A GB200834A GB18187/23A GB1818723A GB200834A GB 200834 A GB200834 A GB 200834A GB 18187/23 A GB18187/23 A GB 18187/23A GB 1818723 A GB1818723 A GB 1818723A GB 200834 A GB200834 A GB 200834A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- etherification
- alkali
- soluble
- methyl
- 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
- 229920002678 cellulose Polymers 0.000 title abstract 6
- 239000001913 cellulose Substances 0.000 title abstract 6
- 238000000034 method Methods 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 17
- 239000003513 alkali Substances 0.000 abstract 13
- 238000006266 etherification reaction Methods 0.000 abstract 10
- 239000000047 product Substances 0.000 abstract 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- 239000003795 chemical substances by application Substances 0.000 abstract 4
- 229960000583 acetic acid Drugs 0.000 abstract 3
- 150000002170 ethers Chemical class 0.000 abstract 3
- 229960003750 ethyl chloride Drugs 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000002168 alkylating agent Substances 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 2
- 239000012362 glacial acetic acid Substances 0.000 abstract 2
- 239000000543 intermediate Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- QZJVWTNHFOMVHX-UHFFFAOYSA-N methanol;methyl acetate Chemical compound OC.COC(C)=O QZJVWTNHFOMVHX-UHFFFAOYSA-N 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 229920000297 Rayon Polymers 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 239000012435 aralkylating agent Substances 0.000 abstract 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 abstract 1
- 229940073608 benzyl chloride Drugs 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003518 caustics Substances 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 abstract 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 abstract 1
- 239000012084 conversion product Substances 0.000 abstract 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 abstract 1
- ORXJMBXYSGGCHG-UHFFFAOYSA-N dimethyl 2-methoxypropanedioate Chemical compound COC(=O)C(OC)C(=O)OC ORXJMBXYSGGCHG-UHFFFAOYSA-N 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 238000007689 inspection Methods 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 abstract 1
- 239000002966 varnish Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Cellulose ethers of a high degree of etherification are obtained by a multistage process with small amounts of alkalies and alkylating agents by the further alkylation or aralkylation of alkyl or aralkyl derivatives of cellulose prepared by treating cellulose or a conversion product or derivative thereof with alkylating or aralkylating agent in the presence of less than 2 mols (preferably less than 1.5 mols) of caustic alkali to 1 mol of C6H10O5, the water content being less than 0.5 part to 1 part of air-dried raw material, or the material being substantially free from water. When the quantity of water is not too small the product is at least partly soluble in aqueous alkalies, while if the water content is very small they are at least partly soluble in cold water and may be soluble in glacial or strong acetic acid, and also in hydrochloric acid. The product of the first stage of etherification is treated as it is for the next stage, or may be first isolated from the reaction mixture. By suitably choosing the conditions of the further etherification, products may be obtained which are soluble in or swell in very cold water which are advantageous when the product (say threads) is required to absorb water-soluble substance such as dyes. For this purpose the conditions are large quantity of water, small quantity of alkali and low reaction temperature. Or hard brittle ethers suitable for instance for lacquers and varnishes, may be obtained by using small quantities of water, large quantities of alkali and higher temperatures. Examples describe the production of the alkali cellulose containing the requisite proportions of alkali and water for the initial material the cellulose being mixed in a disintegrator edge runner machine &c. with the alkali solution or with solid and dissolved alkali or with solid alkali with or without water and excess being removed by for instance hydraulic presses, or the excess water may be removed to the necessary degree by drying. The alkyl or aralkyl esters of inorganic acids are preferably used for the etherification, such as ethyl or methyl chloride, ethyl bromide, dialkyl sulphates, benzyl chloride and ethyl iodide those agents with low boiling points requiring autoclaves while the others may be used in open vessels with or without reflux condensers. Examples describe the use of ethyl chloride. If it is desired to separate the product of the first etherification, the reaction mixture may be washed with hot water and dried, the ether being almost insoluble in hot water. Those of the intermediates (first products of etherification) which dissolve in alkalies may be converted into films or threads by treatment of the solution with acids or other precipitants known in the viscose art. The intermediates may be treated for further etherification in one or more stages so as to produce ethers of different degrees of etherification by using different quantities of alkalies and etherifying agents; products which dissolve or swell in cold water are obtained by using smaller quantities of these agents and products insoluble in and unaffected by water by using larger quantities. The ethers produced when ethyl chloride is used for the final etherification, are soluble in volatile solvents such as alcohol, benzol, alcohol-benzol mixtures, glacial acetic acid, chloroform, chloroform-alcohol mixture, and methyl-acetate-methyl-alcohol mixture and yield flexible films. The ether produced, in an example in which the final etherification is effected with di-ethyl sulphate is soluble in volatile solvents such as glacial acetic acid, benzol-alcohol mixture, chloroform-methyl-alcohol mixture, methyl-acetate-methyl-alcohol mixture. Specifications 177,089, 177,810, 200,816, 203,346, and 203,347 are referred to. The Specification, as open to inspection under Sect. 91 (3) (a) includes also the preparation of the intermediate products by treating a cellulose having a low water content or substantially free from water and a low alkali content with an etherifying-agent. This subject-mater does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT200834X | 1922-07-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB200834A true GB200834A (en) | 1925-01-13 |
Family
ID=3669097
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18187/23A Expired GB200834A (en) | 1922-07-13 | 1923-07-13 | Improvements in and relating to a process of preparing cellulose derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB200834A (en) |
-
1923
- 1923-07-13 GB GB18187/23A patent/GB200834A/en not_active Expired
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