GB478255A - Improvements in or relating to the production of alkali cellulose or other cellulosederivatives, for example, cellulose ethers - Google Patents
Improvements in or relating to the production of alkali cellulose or other cellulosederivatives, for example, cellulose ethersInfo
- Publication number
- GB478255A GB478255A GB1958936A GB1958936A GB478255A GB 478255 A GB478255 A GB 478255A GB 1958936 A GB1958936 A GB 1958936A GB 1958936 A GB1958936 A GB 1958936A GB 478255 A GB478255 A GB 478255A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- alkali
- emulsion
- added
- water
- 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 19
- 239000001913 cellulose Substances 0.000 title abstract 19
- 239000003513 alkali Substances 0.000 title abstract 14
- 238000004519 manufacturing process Methods 0.000 title abstract 5
- 229920003086 cellulose ether Polymers 0.000 title abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 15
- 239000000839 emulsion Substances 0.000 abstract 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 8
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- -1 glycol ethyl Chemical class 0.000 abstract 4
- 239000000725 suspension Substances 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 239000003518 caustics Substances 0.000 abstract 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 abstract 2
- 230000001804 emulsifying effect Effects 0.000 abstract 2
- 229960003750 ethyl chloride Drugs 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 239000000080 wetting agent Substances 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical group CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 abstract 1
- 239000001856 Ethyl cellulose Substances 0.000 abstract 1
- 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 abstract 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 229920001131 Pulp (paper) Polymers 0.000 abstract 1
- 229920000297 Rayon Polymers 0.000 abstract 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical group C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000004945 emulsification Methods 0.000 abstract 1
- 238000006266 etherification reaction Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229920001249 ethyl cellulose Polymers 0.000 abstract 1
- 235000019325 ethyl cellulose Nutrition 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000010408 film Substances 0.000 abstract 1
- 239000003502 gasoline Substances 0.000 abstract 1
- 239000011810 insulating material Substances 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000004033 plastic Substances 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 abstract 1
- 239000002964 rayon Substances 0.000 abstract 1
- 239000005336 safety glass Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- TWEGKFXBDXYJIU-UHFFFAOYSA-M sodium;2-methylpropanoate Chemical compound [Na+].CC(C)C([O-])=O TWEGKFXBDXYJIU-UHFFFAOYSA-M 0.000 abstract 1
- 239000008096 xylene 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
- C08B1/00—Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
- C08B1/08—Alkali cellulose
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
Alkali cellulose is obtained by mixing cellulose material with an emulsion of caustic soda solution in an inert liquid. The process avoids any contact of the cellulose with solid caustic soda. The process may be carried out by dissolving the alkali in water and then emulsifying the solution by agitating with benzene. Cellulose is then mixed with the emulsion so that fine globules of caustic solution are transferred to the cellulose, and there results a suspension of alkali cellulose in the inert liquid. The alkali cellulose may be used in the production of cellulose derivatives such as cellulose ethers. An etherifying agent may be added to the suspension and the mixture may be heated to effect etherification. In general, the cellulose is added to an emulsion containing the desired amount of alkali and water, but in some cases, part only of the alkali is used in the emulsion, and the remainder is added to the suspension of alkali cellulose in the inert liquid. The process may be carried out in the absence of air. Instead of benzene, there may be used toluene, ether, gasoline, xylene, dibutyl-, dibenzyl-, or dipropyl-ether, or dioxane. Emulsifying assistants such as ethyl, benzyl, butyl, methyl, or glycol cellulose, or cellulose glycollic acid may be used. The cellulose ethers obtained may be used in the production of plastics, safety glass, films, rayon, lacquers, coatings, and electric insulating material. In an example, caustic soda, water, benzene, and a small proportion of ethyl cellulose are mixed and heated until the soda has dissolved in the water and the solution has been emulsified. Granulated high grade wood pulp board is added to the emulsion. The mixture is agitated at raised temperature till the benzene is clear. Ethyl chloride is added and the mixture is heated for several hours. Water is added to the reaction mixture to dissolve salt crystals and form an emulsion, if desired with the aid of turkey red oil or similar assistant. The emulsion is steam distilled and the product is filtered and washed. In other examples, ether is used as the organic diluent and solid caustic soda is added to the suspension of alkali cellulose. In another example, alkali cellulose of low caustic soda content is prepared by the emulsion process, ethylated to a low degree, and then treated with additional solid caustic soda and ethyl chloride. In other examples, benzyl cellulose, and mixed ethers such as glycol ethyl, methyl ethyl, benzyl ethyl, and ethyl butyl cellulose ethers are prepared. In other examples, granulated pulp board is mixed with a wetting agent, "alkanol-M," and then with an emulsion in benzene of a highly concentrated caustic soda solution. Sodium isobutyrate may be used instead of "alkanol." Wetting agents may be added to the reagents or reaction mixtures at any stage of the production of the alkali cellulose. The ratio of caustic alkali to water in the production of alkali cellulose may be 125--200 parts of alkali per 100 parts of water, and there may be 40--300 parts of water per 100 parts of cellulose.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1958936A GB478255A (en) | 1936-07-14 | 1936-07-14 | Improvements in or relating to the production of alkali cellulose or other cellulosederivatives, for example, cellulose ethers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1958936A GB478255A (en) | 1936-07-14 | 1936-07-14 | Improvements in or relating to the production of alkali cellulose or other cellulosederivatives, for example, cellulose ethers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB478255A true GB478255A (en) | 1938-01-14 |
Family
ID=10131897
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1958936A Expired GB478255A (en) | 1936-07-14 | 1936-07-14 | Improvements in or relating to the production of alkali cellulose or other cellulosederivatives, for example, cellulose ethers |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB478255A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2767170A (en) * | 1951-08-29 | 1956-10-16 | Hercules Powder Co Ltd | Preparation of alkali cellulose |
| WO2009070168A1 (en) * | 2007-01-24 | 2009-06-04 | Dow Global Technologies Inc. | Method of preparing alkali cellulose or a cellulose derivative |
-
1936
- 1936-07-14 GB GB1958936A patent/GB478255A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2767170A (en) * | 1951-08-29 | 1956-10-16 | Hercules Powder Co Ltd | Preparation of alkali cellulose |
| WO2009070168A1 (en) * | 2007-01-24 | 2009-06-04 | Dow Global Technologies Inc. | Method of preparing alkali cellulose or a cellulose derivative |
| CN101663325B (en) * | 2007-01-24 | 2012-05-30 | 陶氏环球技术有限责任公司 | Method of preparing alkali cellulose or a cellulose derivative |
| JP2013241620A (en) * | 2007-01-24 | 2013-12-05 | Dow Global Technologies Llc | Method of preparing alkali cellulose or cellulose derivative |
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