US2010818A - Etherification of cellulose - Google Patents
Etherification of cellulose Download PDFInfo
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- US2010818A US2010818A US615036A US61503632A US2010818A US 2010818 A US2010818 A US 2010818A US 615036 A US615036 A US 615036A US 61503632 A US61503632 A US 61503632A US 2010818 A US2010818 A US 2010818A
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- US
- United States
- Prior art keywords
- cellulose
- alkali
- caustic
- parts
- slurry
- 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 - Lifetime
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- 229920002678 cellulose Polymers 0.000 title description 50
- 239000001913 cellulose Substances 0.000 title description 48
- 238000006266 etherification reaction Methods 0.000 title description 5
- 239000003513 alkali Substances 0.000 description 45
- 239000003518 caustics Substances 0.000 description 33
- 238000000034 method Methods 0.000 description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 239000002002 slurry Substances 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920003086 cellulose ether Polymers 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 3
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 3
- 229960003750 ethyl chloride Drugs 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical compound CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 description 1
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 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 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- UNFUYWDGSFDHCW-UHFFFAOYSA-N monochlorocyclohexane Chemical compound ClC1CCCCC1 UNFUYWDGSFDHCW-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000005336 safety glass Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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
Definitions
- Patented Aug. 13, 1935 y SFTATE This invention relates to a process of etherifyingicellulosa'and more particularly, to such a process wherein grindingof the cellulose may be completely avoided.
- object of the present invention is to provide 15 animproved process of the" same general type disclosed in the above mentioned I-Iahn patent, but in which process all grinding of the cellulos'e 'may be aviiided.
- the grinding-of the cellulose is an expensive step' and also has a tendencyto degrade thecellulosepwhich may be slightly objec- -"tionable preparing a very high grade product.
- the above objects'are accomplished according L to the presentinventiomby converting cellulose to alkali cellulose, then mixing thealkali cel "lulose with a slurry of caustic alkali in an inert liq id and then etherifying the alkali cellulose in "The cellulose may be converted toan alkali 'cellulose bytreatmentwith a caustic alkalisolutionand by thus iorm'ing an alkali cellulose and ft nmixing'withacaustic alkali slurry, the mixture is sufliciently homogeneous to obtain uniform 'etheriilcation without the necessityoi grinding ithe cellulose at any stage of the process.
- alkali cellulose is mixed with a slurry of caustic alkali in an inert liquid and then etherified, v
- Example 3 One hundred parts of high alpha cellulose from wood pulp is impregnated with 400 parts of 50% caustic soda solutionand the resulting alkali cellulose is kneaded or shredded iwith fiOO parts of a slurry of 200 parts of caustic sodaand400 parts of toluene, prepared as described in Example 1, until the mixture is uniform. This will require only a. short period of about 15-30 minutes. The mixture is then charged into an autoclave along with 600 parts of benzyl chloride and is agitated and heated for eight hours at 125 C., a high grade of benzyl cellulose being formed at the "end ofthis treatment. r l
- methyl ether, diethyl ether and glycol diethyl ether may be used in place of benzene or toluene; from 1-3 parts by weight of inert liquid to one lulose for best results.
- the slurry of caustic alkali and inert liquid is conveniently produced by grinding solid caustic alkali in the inert liquid in a ball mill, although other grinding apparatus of course may be used.
- the slurry is relatively stable and there is practically no tendency to settle out evenafter standing for several hours. Since it is relatively fluid, it can be advantageously transported through pipe lines by means of pumps.
- the particles of caustic alkali are in an extremely fine state of subdivision compared with any of the commercial powdered caustic alkalies, or compared with caustic alkalies powdered in the absence of the inert liquid.
- the extremely fine particles of caustic alkali in the slurry show no tendency to'clu'mp together,whereas the dry pow- Idered caustic alkali shows a strong tendency to form lumps which possess the same disadvantages as unpowdered caustic in the etherification' proc- 'ess, namely, non-uniform concentration of alkali throughoutthe reaction mass.
- cellulosic material may beused advantageously in the present process besides cotton linters or high alpha cellulose from sulphite pulp.
- any cellulose-of good 'quality produced from wood, bagasse, or other .cellulosic materials may be used.
- etherifying agents may be used, among which may be mentioned not only ethyl chloride and benzyl chloride, but etherifying .agents such as methyl chloride, ethylene chlorohydrin, ethylene chloridacrotyl chloride, cyclohexyl chloride, amyl chloride, lauryl. chloride, propyl chloride, and the like.
- the present invention is applicable to any alkali cellulose regardless of how produced.
- the alkali cellulose prior to the addition of solid caustic alkali should contain 0.45 to 36.0 mols of water and 0.04-10.0 mols of caustic alkali for each mol of cellulose, although it is preferred to use 4.5 to 36.0 mols of water and 2.0-10.0 mols of caustic alkali per mol of'cel- It is advantageous to use high concentrations of caustic.
- the total causticalkali should amount to not more than one mol per mol of water in the reaction mixture where there is a high ratio of water to cellulose, for example, 4 parts by weight of water to one part by weight of cellulose.
- a caustic: water ratio of two mols to one may be used.
- a higher caustic water ratio may be used, 1. e., 4 mols of caustic per mol of water.
- the cellulose ethers produced according to the present invention may be used for any of the purposes for which cellulose ethers or esters are now used, such as for plastics, molding compositions, lacquers and other coating compositions, interlayers for safety glass, artificial fibers,
- An advantage of the present invention resides in the elimination of the necessity for grinding cellulose or alkali cellulose at any stage in the process.
- an ether satisfactory from the standpoint of viscosity, uniformity of etherification, film properties, plastic properties, et cetera could not be obtained without grinding cellulose alone, or alkali, cellulose with solid caustic, at some stage in the process;
- prior art processes involving intimate admixture of cellulose and caustic by means of grinding the optimum properties of the cellulose ether were not obtained.
- the present process improves on all prior art processes by obtaining practically the optimum properties in the product.
- Process of etherifying cellulose comprising the steps of converting the cellulose to an alkali cellulose containing 4.5 to 36.0 mols of water and 2.0 to 10.0 mols of caustic alkali per mol of cellulose, mixing the alkali cellulose with a slurry of caustic alkali in an inert liquid, and then cellulose.
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- 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)
Description
Patented Aug. 13, 1935 y SFTATE This invention relates to a process of etherifyingicellulosa'and more particularly, to such a process wherein grindingof the cellulose may be completely avoided.
In Hahn'U. SQ Patent 1,81-9,600,granted August 18, 1931, the process of etherifying'cellulose as disclosed and"claimed, wherein the cellulose'is ground and then added without further grinding a to a slurry of caustic alkali in an inertliquidinti- I mately mixed therewith, and tIienetherified. That process was afmaterial-improvement over the prior art processes because it avoided grinding thebellulose with caustic alkali.
object of the present invention is to provide 15 animproved process of the" same general type disclosed in the above mentioned I-Iahn patent, but in which process all grinding of the cellulos'e 'may be aviiided. The grinding-of the cellulose is an expensive step' and also has a tendencyto degrade thecellulosepwhich may be slightly objec- -"tionable preparing a very high grade product.
'Other objects of the invention willbe'apparent from the description given hereinafter.
The above objects'are" accomplished according L to the presentinventiomby converting cellulose to alkali cellulose, then mixing thealkali cel "lulose with a slurry of caustic alkali in an inert liq id and then etherifying the alkali cellulose in "The cellulose may be converted toan alkali 'cellulose bytreatmentwith a caustic alkalisolutionand by thus iorm'ing an alkali cellulose and ft nmixing'withacaustic alkali slurry, the mixture is sufliciently homogeneous to obtain uniform 'etheriilcation without the necessityoi grinding ithe cellulose at any stage of the process. Where cellulose is mixed directly with the caustic alkali slurry Without being first converted into, an alkali jcellulose; it has been found necessary to grind cellulose inorder to get uniform e'therifica Aslls well known inflthe, artait is necessary to alkali tocelliilose'during the "etherification "step ordertohobtain economical operation and a maintain," certain;.,jratios ,of. water and caustic V :4 2,010,818 4 ETHERIFICATI ONEOF oELLULosE Frederick C. Hahn, Wilmington, Dell, assignor to E. I. du P ontde Nemours & Company, Wilmington,,Del., a corporation of Delaware No Drawing. Application June 2, 1932 l Serial No.v615,036
i Claim. (01. zed-152) caustic alkali slurry. In either case, alkali cellulose is mixed with a slurry of caustic alkali in an inert liquid and then etherified, v
The followinglexamples are given to illustrate the present invention, parts being given by weight:
Example .1.-One hundred parts of cotton lint'ers' (in board form) are steeped in an excess of caustic soda solution and pressed to. a weight of 475 parts. The resulting alkali cellulosenis shreddedand then added, either directly or after ageing, to an autoclave. Six hundred parts of a slurry of 200 parts of caustic soda in 400v parts of benzene, preparedby grinding these materials together in a ball mill, 500 parts ethyl chloride and 400',parts benzene are added to the alkali cellulose, and the mixture agitated and heated for parts of caustic soda and 600 parts of benzene, prepared as described in Example L'are added and the mixture is kneaded orshredded until it is uniform. The resulting. alkali cellulose is charged into an autoclave together with'500 parts "of "ethyl chloride and-200 parts of benzene, and
the mixture agitated and heated for five hours at 150 C. A high grade of ethyl cellulose is prepared in this manner. Example 3.-One hundred parts of high alpha cellulose from wood pulp is impregnated with 400 parts of 50% caustic soda solutionand the resulting alkali cellulose is kneaded or shredded iwith fiOO parts of a slurry of 200 parts of caustic sodaand400 parts of toluene, prepared as described in Example 1, until the mixture is uniform. This will require only a. short period of about 15-30 minutes. The mixture is then charged into an autoclave along with 600 parts of benzyl chloride and is agitated and heated for eight hours at 125 C., a high grade of benzyl cellulose being formed at the "end ofthis treatment. r l
The above examples have been given merely to illustrate the present invention; which is of broad application. Caustic potash and other caustic alkalies may be used in place of caustic soda and any other inert liquid such as xylene, chlorobena.
zene, chlorotoluene, Hi-f lashnaphtha, unsaturated hydrocarbons of thetype of amylene, di-
methyl ether, diethyl ether and glycol diethyl ether, may be used in place of benzene or toluene; from 1-3 parts by weight of inert liquid to one lulose for best results.
centration of the etherifying agent to some extent.
The slurry of caustic alkali and inert liquid is conveniently produced by grinding solid caustic alkali in the inert liquid in a ball mill, although other grinding apparatus of course may be used.
, The slurry is relatively stable and there is practically no tendency to settle out evenafter standing for several hours. Since it is relatively fluid, it can be advantageously transported through pipe lines by means of pumps. The particles of caustic alkali are in an extremely fine state of subdivision compared with any of the commercial powdered caustic alkalies, or compared with caustic alkalies powdered in the absence of the inert liquid. Furthermore, the extremely fine particles of caustic alkali in the slurry show no tendency to'clu'mp together,whereas the dry pow- Idered caustic alkali shows a strong tendency to form lumps which possess the same disadvantages as unpowdered caustic in the etherification' proc- 'ess, namely, non-uniform concentration of alkali throughoutthe reaction mass.
Various types of cellulosic material may beused advantageously in the present process besides cotton linters or high alpha cellulose from sulphite pulp. In fact, practically any cellulose-of good 'quality produced from wood, bagasse, or other .cellulosic materials, may be used.
As will be obvious to those skilled in the art, a Wide variety of etherifying agents may be used, among which may be mentioned not only ethyl chloride and benzyl chloride, but etherifying .agents such as methyl chloride, ethylene chlorohydrin, ethylene chloridacrotyl chloride, cyclohexyl chloride, amyl chloride, lauryl. chloride, propyl chloride, and the like.
In carrying out the process, it is advantageous to treat the cellulose with a caustic alkali solution having a concentration of from 18-50%, but it is to be understood that the present invention is applicable to any alkali cellulose regardless of how produced. The alkali cellulose prior to the addition of solid caustic alkali should contain 0.45 to 36.0 mols of water and 0.04-10.0 mols of caustic alkali for each mol of cellulose, although it is preferred to use 4.5 to 36.0 mols of water and 2.0-10.0 mols of caustic alkali per mol of'cel- It is advantageous to use high concentrations of caustic. alkali solution in treating the cellulose, since higher concentrations minimize the formation of heat when the solid caustic alkali is added to the alkali cellulose. As will be obvious to those skilled in the art, the quantities of solid caustic alkali; inert liquid, and etherifying agent, as well as the conditions of time and temperature during the etherification, may be varied depending on the characteristics desired in the resulting cellulose ether. In the mol proportions given throughout the specification and claims, a mol of cellulose is taken as 162 for the monoglucose unit as is customary.
The total causticalkali; including that originally added as caustic solution and that added in slurry form, should amount to not more than one mol per mol of water in the reaction mixture where there is a high ratio of water to cellulose, for example, 4 parts by weight of water to one part by weight of cellulose. At lower ratios, for example, 2 parts by weight of water toone part by weight of cellulose, a caustic: water ratio of two mols to one; may be used. At still lower ratios of water to cellulose, for example, one-half part by weight of water to one part by weight of cellulose, a higher caustic water ratio may be used, 1. e., 4 mols of caustic per mol of water. In general, it may be stated that the higher the ratio of water to cellulose, the lower high a proportion as 20 mols of .etherifying agent per grams of cellulose accelerates the reaction and theexcess etherifying'agent may be recovered. Suitable ratios of etherifying agent to cellulose are known in the prior art,
The cellulose ethers produced according to the present invention may be used for any of the purposes for which cellulose ethers or esters are now used, such as for plastics, molding compositions, lacquers and other coating compositions, interlayers for safety glass, artificial fibers,
film for photographic or other purposes, and the like.
An advantage of the present invention resides in the elimination of the necessity for grinding cellulose or alkali cellulose at any stage in the process. In processes heretofore known, an ether satisfactory from the standpoint of viscosity, uniformity of etherification, film properties, plastic properties, et cetera, could not be obtained without grinding cellulose alone, or alkali, cellulose with solid caustic, at some stage in the process; In prior art processes involving intimate admixture of cellulose and caustic by means of grinding, the optimum properties of the cellulose ether were not obtained. The present process improves on all prior art processes by obtaining practically the optimum properties in the product. The elimination of this grinding of cellulose or alkali cellulose efiects a Very material economy in the process and,.furthermore, avoids any danger of obtaining an inferior cellulose ether due to. degradation of the cellulose by grinding.
As many apparently widely difierent embodiments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that the invention is not limited to the specific embodiments thereof except as defined in the appended claim, Process of etherifying cellulose comprising the steps of converting the cellulose to an alkali cellulose containing 4.5 to 36.0 mols of water and 2.0 to 10.0 mols of caustic alkali per mol of cellulose, mixing the alkali cellulose with a slurry of caustic alkali in an inert liquid, and then cellulose.
etherifying the alkali FREDERICK c.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US615036A US2010818A (en) | 1932-06-02 | 1932-06-02 | Etherification of cellulose |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US615036A US2010818A (en) | 1932-06-02 | 1932-06-02 | Etherification of cellulose |
Publications (1)
Publication Number | Publication Date |
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US2010818A true US2010818A (en) | 1935-08-13 |
Family
ID=24463746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US615036A Expired - Lifetime US2010818A (en) | 1932-06-02 | 1932-06-02 | Etherification of cellulose |
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US (1) | US2010818A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4228277A (en) * | 1979-02-12 | 1980-10-14 | Hercules Incorporated | Modified nonionic cellulose ethers |
US4243802A (en) * | 1979-06-06 | 1981-01-06 | Hercules Incorporated | Surfactant-soluble cellulose derivatives |
-
1932
- 1932-06-02 US US615036A patent/US2010818A/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4228277A (en) * | 1979-02-12 | 1980-10-14 | Hercules Incorporated | Modified nonionic cellulose ethers |
US4243802A (en) * | 1979-06-06 | 1981-01-06 | Hercules Incorporated | Surfactant-soluble cellulose derivatives |
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