GB778732A - Ethyl cellulose and manufacture thereof - Google Patents
Ethyl cellulose and manufacture thereofInfo
- Publication number
- GB778732A GB778732A GB35446/54A GB3544654A GB778732A GB 778732 A GB778732 A GB 778732A GB 35446/54 A GB35446/54 A GB 35446/54A GB 3544654 A GB3544654 A GB 3544654A GB 778732 A GB778732 A GB 778732A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- per cent
- alkali metal
- ethyl
- ethyl cellulose
- 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
- 239000001856 Ethyl cellulose Substances 0.000 title abstract 11
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 title abstract 11
- 229920001249 ethyl cellulose Polymers 0.000 title abstract 11
- 235000019325 ethyl cellulose Nutrition 0.000 title abstract 11
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 11
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 8
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 7
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 6
- 229960003750 ethyl chloride Drugs 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- 229920002678 cellulose Polymers 0.000 abstract 4
- 239000001913 cellulose Substances 0.000 abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000011541 reaction mixture Substances 0.000 abstract 3
- 239000002002 slurry Substances 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 2
- 238000013019 agitation Methods 0.000 abstract 2
- 239000007864 aqueous solution Substances 0.000 abstract 2
- 235000019441 ethanol Nutrition 0.000 abstract 2
- -1 ethoxyl groups Chemical group 0.000 abstract 2
- 239000008103 glucose Substances 0.000 abstract 2
- 229920000742 Cotton Polymers 0.000 abstract 1
- 229960000583 acetic acid Drugs 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 239000012670 alkaline solution Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 238000006266 etherification reaction Methods 0.000 abstract 1
- 239000012362 glacial acetic acid Substances 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 238000005406 washing Methods 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
As a preliminary step in the manufacture of ethyl cellulose, there are mixed together in a closed vessel cellulose, hot aqueous alkali metal hydroxide of 50-80 per cent concentration and ethyl chloride, at 75-90 DEG C. and under a pressure sufficiently high to maintain the ethyl chloride in the liquid phase and in such proportions that the mixture contains, per part of cellulose, 0.5-0.8 part of sodium hydroxide (or a chemically equivalent proportion of another alkali metal hydroxide), 0.2-0.5 part of water and at least 6 parts of ethyl chloride, a slurry of alkali cellulose in ethyl chloride being formed. The slurry may then be maintained at 100-140 DEG C. until ethyl cellulose containing 0.8-1.3 ethoxyl groups per glucose anhydride unit is formed and the alkali metal hydroxide concentration (based on the combined weight of alkali metal hydroxide and water) is reduced to about 5 to 30 per cent. The ethyl cellulose thus formed may be further etherified in stages until an organosoluble ethyl cellulose containing at least 2.2 ethoxyl groups per glucose anhydride unit is formed. At each stage additional alkali metal hydroxide is added to the reaction mixture sufficient to increase the alkali metal hydroxide concentration to at least 55 per cent, preferably 55-65 per cent, based on the combined weight of alkali metal hydroxide and water, and the etherification is continued at 100-140 DEG C. until the alkali metal concentration has been reduced to not more than 50 per cent, but not substantially below 40 per cent, the total alkali metal hydroxide being 2-4 parts per part of cellulose. In an example, to one part by weight of air-dry purified cotton linters and 6 parts by weight of ethyl chloride agitated in an autoclave at 75 DEG C. in absence of air there are added 0.5 part caustic soda and 0.2 part water in the form of an aqueous solution at 75 DEG C., and the mixture is agitated for 2 hours at 75 DEG C. Agitation is then continued for 3 hours at 100 DEG C., the sodium hydroxide concentration being thereby reduced to 9.7 per cent, based on the sodium hydroxide and water present, and the fibrous ethyl cellulose is recovered by adding hot water to the reaction mixture and then removing the aqueous liquor from the resultant slurry by centrifuging, followed by washing of the ethyl cellulose with hot water and drying. The ethyl cellulose has a D.S. of 1.1 and is completely soluble at 2 per cent concentration in cold water, in 2 per cent aqueous sodium hydroxide solution at room temperature and at 5 per cent concentration in a 9 : 1 by weight water/ethyl alcohol mixture, and is insoluble in glacial acetic acid. When the aqueous and alkaline solutions are heated above 80 DEG C., the ethyl cellulose coagulates as a highly swollen gel. In a second example, after the reaction mixture has been agitated for 3 hours at 100 DEG C. in the autoclave, 1 part of sodium hydroxide and 0.4 part of water are added to the autoclave and its contents are agitated for 1.5 hours at 120 DEG C., a further 2 parts of sodium hydroxide and 0.8 parts water are then added and agitation is continued for 1.5 hours at 120 DEG C. The ethyl cellulose recovered from the mixture has a D.S. of 2.45 and is soluble in an 8 : 2 parts by weight toluene/ethyl alcohol mixture. The process increases the conversion efficiency of the ethyl chloride into ethyl cellulose.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US778732XA | 1954-04-19 | 1954-04-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB778732A true GB778732A (en) | 1957-07-10 |
Family
ID=22140546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB35446/54A Expired GB778732A (en) | 1954-04-19 | 1954-12-07 | Ethyl cellulose and manufacture thereof |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB778732A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2635403A1 (en) * | 1976-08-06 | 1978-02-09 | Fritz Loedige | METHOD OF PREPARING CELLULOSE ETHERS |
| US4311833A (en) | 1979-03-06 | 1982-01-19 | Daicel Chemical Industries Ltd. | Process for preparing ethylcarboxymethylcellulose |
| CN102643356A (en) * | 2012-03-20 | 2012-08-22 | 邸勇 | Two-step production process of ethyl cellulose with high degree of substitution |
-
1954
- 1954-12-07 GB GB35446/54A patent/GB778732A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2635403A1 (en) * | 1976-08-06 | 1978-02-09 | Fritz Loedige | METHOD OF PREPARING CELLULOSE ETHERS |
| US4117223A (en) * | 1976-08-06 | 1978-09-26 | Loedige Wilhelm | Process for the preparation of cellulose alkyl ethers |
| US4311833A (en) | 1979-03-06 | 1982-01-19 | Daicel Chemical Industries Ltd. | Process for preparing ethylcarboxymethylcellulose |
| CN102643356A (en) * | 2012-03-20 | 2012-08-22 | 邸勇 | Two-step production process of ethyl cellulose with high degree of substitution |
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