Abstract: Silated polysaccharides having 0.005 to 2.0 silyl molar substitution per anhydrosaccharide unit form water resistant films when cast from aqueous solution and dried in the presence of atmospheric carbon dioxide. These films are soluble in aqueous caustic. A preferred water soluble polymer is a cellulose ether with 0.005 to 1.0 silyl substitution.

Abstract: A polysaccharide derivative having the structure Sacch--O--Z--Ar--CH.dbd.N--Y or ##STR1## where Sacch--O-- represents a polysaccharide molecule; Z is --(CH.sub.2).sub.n -- or ##STR2## Ar is a divalent aromatic group; Y is (a) a monovalent group derived from a water-soluble substituted or unsubstituted aromatic compound containing only one free primary amine group, or (b) a monovalent group derived from a water-soluble substituted or unsubstituted aliphatic or cycloaliphatic compound containing only one primary amine group, or (c) a multivalent group derived from a water-soluble protein containing more than one primary amine group; n is one or greater; and m is zero or greater, is prepared by first modifying the polysaccharide with a reagent to introduce free aromatic aldehyde groups and then reacting with a suitable amine-containing reagent. The siloxane-containing starch derivaties are useful in glass forming size compositions.

Abstract: Cellulose derivatives are disclosed which have the following formula: ##STR1## wherein Z is selected from the group consisting of alkylene, alkenylene, alkynylene, cycloalkylene or benzylene or xylylene radicals, which may or may not be substituted;X is selected from the group consisting of --H, --NR.sub.2, --N.sup.+ R.sub.3, --CN, --COOH, --SO.sub.3 H, --SO.sub.3 H, --PO(OR).sub.2, CONR.sub.2 or --Si(OR).sub.3 ;R is selected from the group consisting of hydrogen, alkyl and alkenyl groups having from 1 to 25 carbon atoms, and cycloalkyl, tolyl and phenyl groups;Y is selected from the group consisting of alkyl, alkenyl, alkynyl groups having from 1 to 36 carbon atoms, which may or may not be substituted, cycloalkyl, phenyl, tolyl and benzyl groups, ##STR2## (--CH.dbd.CH--COOH), and NHR, where R has the same meaning as in X, andm=0 to 2.5n=0.01 to 2.95,with the provision that, when m=0, n.gtoreq.1.55, if Y is an alkyl radical with 1 to 5 carbon atoms, 3-(CH.sub.2).sub.

Abstract: Carboxymethylhydroxyethyl (CMHEC), starch and guar are preferred polysaccharides providing at least a 1% solution viscosity of 1000 cps at 25 C. An invert emulsion for oil drilling or paper manufacture comprises on a weight percent basis:______________________________________ Diesel, mineral or paraffin oil 40-60 Imidazole surfactant 1-4 Water 0-10 Organophilic clay 0.5-5.

Abstract: A modified cellulose for biocompatible dialysis membranes having a structure represented by the formula ##STR1## wherein cell is cellulose or chitin, in each case without hydroxyl groups, s=3 in the case of cellulose and s=2 in the case of chitin, R' is CH.sub.3 and/or C.sub.2 H.sub.5 and/or C.sub.3 H.sub.7, X denotes specified functional groups, R" is H or R, R"' denotes R, x+t=0.75 to 2.85, t=0 to 2.85, x=0 to 2.85, and r=0 to 1. A process for preparation of the cellulose derivatives is also disclosed.

Abstract: Aqueous dispersion of a multicolored wall coating composition comprising colored minerals in the form of quartz granules having transparent or translucent fibers agglomerated thereto, wherein said minerals are transparent or translucent after drying.

Abstract: Silated polysaccharides having 0.0005 to 2.0 silyl molar substitution per anhydrosaccharide unit form water resistant films when cast from aqueous solution and dried in the presence of atmospheric carbon dioxide. These films are soluble in aqueous caustic. A preferred water soluble polymer is a cellulose ether with 0.005 to 1.0 silyl substitution.

Abstract: Carboxymethylcellulose (CMC) and hydroxyethylcellulose (HEC) are preferred modified polysaccharides providing at least 10% by weight gelatin particles to prevent fluid loss during diaphragm wall construction. A 1% solution of CMC or HEC give a 1000 cps viscosity at 25.degree. C. An oil slurry comprises:______________________________________ Solvent 45 Surfactant 2.5 Water 6 Organophillic clay 1 Modified cellulose 45.

Abstract: A modified cellulose for biocompatible dialysis membranes having a structure represented by the formula ##STR1## wherein Cell is cellulose or chitin, in each case without hydroxyl groups, s=3 in the case of cellulose and s=2 in the case of chitin, R' is CH.sub.3 and/or C.sub.2 H.sub.5 and/or C.sub.3 H.sub.7, X denotes specified functional groups, R" is H or R, Z corresponds to the following groups of atoms: SR", SO.sub.3 H and salts thereof, SO-R, SONR".sub.2, SO.sub.2 -R, SO.sub.2 NR".sub.2, SO.sub.2 H and salts thereof, F, Cl, Br, I, NR".sub.2, PR".sub.2, PO.sub.3 H.sub.2 and salts thereof, PO.sub.2 H(OR), PO(OR).sub.2, PO.sub.2 HR" and salts thereof, POR"(OR) and POR".sub.2, x+t=0.75 to 2.85, t=0 to 2.85, x=0 to 2.85, and z=0.01 to 0.45. A process for preparation of the cellulose derivatives is also disclosed.

Abstract: A modified cellulose for biocompatible dialysis membranes having a structure represented by the formula ##STR1## wherein cell is unmodified cellulose or chitin, in each case without hydroxyl groups, s=3 in the case of cellulose and s=2 in the case of chitin, R' is CH.sub.3 and/or C.sub.2 H.sub.5 and/or C.sub.3 H.sub.7, X denotes specified functional groups, m=0.75 to 2.85, and x=0.005 to 2.10. A process for preparation of the cellulose derivatives is also disclosed.

Abstract: Disclosed are a polysaccharide derivative having the structure: ##STR1## and a polysaccharide graft polymer having the structure: Sacch-O-(G).sub.m -(M)-.sub.n, wherein Sacch- is a polysaccharide; m is zero or one; G is the residue of a polymerizable, unsaturated monomer which is bonded to the polysaccharide in an ether or ester linkage; n is greater than one; M is the residue of one or more polymerizable, unsaturated, monomer(s), at least one of which is a siloxane-containing monomer, which have been grafted to the polysaccharide by free radical polymerization; R is an organic group which is bonded to the polysaccharide by an ether or ester linkage and to the silicon by a carbon-silicon linkage; R.sub.1 is a straight or branched C.sub.1 -C.sub.6 alkyl or alkenyl group, or an aryl, aralkyl or alkaryl group; and R.sub.2 and R.sub.3 are, independently, straight or branched C.sub.1 -C.sub.6 alkyl or alkenyl groups, or aryl, aralkyl or alkaryl groups, or alkoxides of straight or branched C.sub.1 -C.sub.

Abstract: A method for preparing cellulose ethers containing tertiary or quaternary nitrogen by reacting alkylene epoxides with cellulose or its derivatives in an alkaline medium in the presence of water. Alkylene epoxides of the formulas ##STR1## or mixtures thereof, in which n=1, 2 or 3, R.sup.1, R.sup.2 and R.sup.3 correspond to the same or different alkyl groups with 1 to 18 carbon atoms or R.sup.1 corresponds to the benzyl group or --C.sub.2 H.sub.4 OH and X is chloride, bromide, sulfate or acetate are used as cationization agents.

Abstract: A release agent comprising a polyfunctional alkoxysiloxane and an organic compound which is solid at room temperature and contains a functional group capable of reacting with said polyfunctional alkoxysiloxane, and a composite material comprising a substrate and a cured film of the release agent are disclosed. The cured film of the release agent exhibits high strength and excellent release properties without causing blocking or contamination on an adherent.

Abstract: A regenerable support matrix useful for immobilization of biologically active materials is prepared by coating a core support with a cellulose ester, removing ester groups by hydrolysis to produce hydroxyl groups and converting the hydroxyl groups to dialkylaminoalkyl ether groups. The support matrix can immobilize biologically active proteinaceous materials with a net negative charge by adsorption. The support matrix is readily regenerated when an immobilized biologically active material becomes inactive by washing the support with a base or salt solution and adsorbing additional biologically active material to the support. Multiple cycles of immobilization and regeneration are possible without significant deleterious affects.

Abstract: Surface active glycosides are made by reaction of monose or polyose with an alcohol in the presence of an acid catalyst composition containing acid catalyst and reducing agent; the color properties of the glycosodes so made makes them attractive for use in cosmetic, pharmaceutical and household products. Suitable reducing agents include phosphorous, hypophosphorous, sulphurous, hyposulphurous, nitrous and hyponitrous acids. Suitable catalysts include the known etherification catalysts.

Abstract: The invention relates to a process for the preparation of low-viscosity cellulose ethers, in particular of methylcelluloses having viscosities of less than 100 mPa.s, measured in 1.8% aqueous solution. The process is carried out in such a way that an aqueous sodium chlorite solution is added preferably during and/or after alkalization, but before etherification.

Abstract: A process for the preparation of a cellulose ether by reacting in a heterogenous reaction mixture an alkaline solution and an etherifying agent with a fibrous cellulose. The total of the required stoichiometric amount of the alkaline solution and at least a portion of the etherifying agent required in producing the cellulose ether are admixed (e.g. in a mixing nozzle) at sufficiently low temperature to suppress reaction between the alkaline solution and the etherifying agent. The admixture is then contacted with the cellulose fibers, preferably by spraying the admixture thereupon. Additional of the etherifying agent if required is then added to the reaction mixture, and the heterogenous reaction mixture is agitated and reacted at an initial temperature below 40.degree. C. sufficient to produce alkalization of the cellulose. Thereafter the temperature is increased above 40.degree. C., preferably incrementally or gradually up to about 100.degree. C., preferably to 80.degree. C.

Abstract: A chemically modified and activated, hydroxyl-group-containing, natural or synthetic, polymeric solid body surface is disclosed, as well as a process for the activation of such solid body surfaces by means of organo-silanes and, if necessary, homo- or heterobifunctional reagent. The surfaces are used for the stable, simple and economical binding of proteins, nucleic acids, low-molecular ligands, cells, microorganisms and other biological materials, in biology, biotechnology and medicine.

Abstract: High viscosity cellulose ether products are produced by grinding a substantially dry high molecular weight cellulose ether under conditions of mild mechanical impact such as those encountered in a high speed air swept impact mill. It has been found that such a cellulose ether product has several times the intrinsic viscosity of a product of substantially equivalent particle size by ball mill or hammer mill grinding.

Abstract: Polysaccharide aldehydes having the formula ##STR1## or Sacch--O--CH.sub.2 --Ar--CHO (II) such as starch, cellulose, and gum aldehydes, are useful as paper additives for imparting strength and as the granular or gelatinized portion of a corrugating adhesive. Those having formula I are prepared by a nonoxidative method which involves reacting the polysaccharide base, in the presence of alkali, with a derivatizing acetal reagent having the general structure ##STR2## and then hydrolyzing the acetal by adjusting the pH to less than 7, preferably 2-4. In the formula Ar is an aryl group, optionally containing an ether linkage, or an alkaryl group and A and A' are lower alkyls or together form at least a 5-membered cyclic acetal. The polysaccharide aldehydes are crosslinked by the addition of selected polyfunctional crosslinkers such as an aliphatic primary polyamine or polyketone.

Abstract: The process comprises the action of a saturated aliphatic or cycloaliphatic alcohol or an aliphatic or cycloaliphatic alcohol comprising a double ethylenic bound not situated in alpha of the hydroxyl group with an aldose, aldoside or polyaldoside in the solvent and reactant formed by the hydrogen fluoride. Application to the synthesis of surfactants or as additives for rigidifying polyurethane foams.

Abstract: Polysaccharide aldehydes having the general structure ##STR1## such as starch, cellulose and gum aldehydes, are useful for imparting wet, dry, or temporary wet strength to paper. They are prepared by a non-oxidative method which involves reacting the polysaccharide base, in the presence of alkali, with a derivatizing acetal reagent having the general structure ##STR2## and then hydrolyzing the acetal by adjusting the pH to less than 7, preferably 2-4. R is (CH.sub.2).sub.n or a divalent aromatic group and n os 0 or greater; R.sup.1, R.sup.6, and R.sup.7 are hydrogen or an organic group; R.sup.2, R.sup.5, and R.sup.8 are (CH.sub.2).sub.m with m being 1-6; R.sup.3 and R.sup.4 are hydrogen or a lower alkyl; Y is an anion; Z is an organic group capable of reacting with the polysaccharide base to form an ether derivative and selected from the group consisting of an epoxide, ethylenically unsaturated group, halohydrin, and halogen; R.sup.

Abstract: An improved reactor (and process using the same) comprising multistage stirrer elements and baffles, which has particular dimensional ratios between the reactor diameter, the width and spacing of the stirrer elements, and the baffles. The reactor is particularly adapted for the production of polysaccharide ethers, especially cellulose ethers.

Abstract: Polysaccharide aldehydes having the formula Sacch--O--CH.sub.2 --CH.dbd.CH--CHO, ##STR1## such as starch, cellulose, and gum aldehydes, are useful for imparting wet, dry, or temporary wet strength to paper. They are prepared by a non-oxidative method which involves reacting the polysaccharide base, in the presence of alkali, with a derivatizing acetal reagent having the general structure ##STR2## and then hydrolyzing the acetal by adjusting the pH to less than 7, preferably 2-4. In the formulas, n is 1-3; R.sup.11 and R.sup.12 are independently an alkyl, aryl, aralkyl, or alkaryl group when n is 1, R.sup.11 or R.sup.12 is one of the groups when n is 2, or R.sup.11 and R.sup.12 are not present when n is 3; R.sup.13 is an alkyl group, optionally containing an ether linkage, or an aralkyl group; R.sup.14 and R.sup.15 are individually a hydrogen or a methyl group; R.sup.16, R.sup.17, and R.sup.

Abstract: Polysaccharide aldehydes having the general structure ##STR1## such as starch, cellulose and gum aldehydes, are useful for imparting wet, dry, or temporary wet strength to paper. They are prepared by a non-oxidative method which involves reacting the polysaccharide base, in the presence of alkali, with a derivatizing acetal reagent having the general structure ##STR2## and then hydrolyzing the acetal by adjusting the pH to less than 7, preferably 2-4. R is (CH.sub.2).sub.n or a divalent aromatic group and n is 0 or greater; R.sup.1, R.sup.6, and R.sup.7 are hydrogen or an organic group; R.sup.2, R.sup.5, and R.sup.8 are (CH.sub.2).sub.m with m being 1-6; R.sup.3 and R.sup.4 are hydrogen or a lower alkyl; Y is an anion; Z is an organic group capable of reacting with the polysaccharide base to form an ether derivative and selected from the group consisting of an epoxide, ethylenically unsaturated group, halohydrin, and halogen; R.sup.

Abstract: The process for preparing water-soluble mixed cellulose ethers proceeds in the following steps:(a) alkalization of the cellulose,(b) etherification of the alkali cellulose in the presence of a base, using at least one etherifying agent which requires, for the reaction with cellulose, a catalytic and sub-stoichiometric quantity of a base, and(c) after increasing the quantity of base, further etherification of the cellulose ether so prepared, using at least one etherifying agent which requires, for the reaction with cellulose, an at least stoichiometric quantity of a base or a catalytic and sub-stoichiometric quantity of a base, increased over the quantity used in (a),with at least one inert organic solvent being used as a dispersing auxiliary in at least one of the steps and water being present in all steps. The organic solvent used is dimethyl ether, which either is used alone or in a mixture with dimethoxyethane, an alkanol, an alkanediol and/or an alkoxyalkanol.

Abstract: A manufacturing method for cellulose ether having a high degree of substitution characterized in that an etherifying agent represented by a general formula RCH.sub.2 X (where R is aromatic group, heterocyclic group, vinyl group or ethynyl group or the same group substituted and X is chlorine or bromine) is reacted with a uniform solution of cellulose acetate having a degree of substitution of 2.0 and over in an organic solvent in the presence of a base to manufacture a highly substituted cellulose ether having a degree of substitution of 2.0 and over per anhydrous glucose unit by a one stage reaction at a good yield.As a general method for manufacturing cellulose ether, a method for reacting an etherifying agent with alkali cellulose is now in use. For the general method, several improved methods have been proposed. However, it is difficult to manufacture cellulose ether having a degree of substitution of 2.5 and over by a one stage reaction using the general method.

Abstract: Water-soluble polysaccharides, including cellulose ethers, containing pendent vicinal dihydroxy structure capable of cis geometry, which upon crosslinking with a polyvalent metal, have shear-thermal stability characteristics of at least about 30 at 250.degree. F., are useful in oilfield applications.

Abstract: Improved reaction efficiencies are obtained when water is removed during a reaction of alkali cellulose and an etherifying agent to produce cellulose ethers. The removal of water during the etherification reaction reduces the amount of by-products formed during the reaction.

Abstract: Absorbent, coherent, flexible structures in the form of fibrous webs and porous sponges comprising water-insoluble, ring oxidized cellulosic bases consisting of water-insoluble cellulose ethers, cellulose mixed ethers ring oxidized forms of these cellulose, cellulose ether mixed esters and mixtures of the bases. The cellulose bases have a DS of between about 0.05 and about 0.35. Upon application of the structures to the body and wet with aqueous body liquids, sharp edges and protruding fibers and fibrils or hairs become highly swollen or may dissolve thereby eliminating irritation. The ring oxidized forms of the cellulose bases contain between about 2% and about 52% added carboxyl groups. The structures may have hemostatic properties and the structure may include uniformly dispersed therein chitin and/or starch derivatives or contain starch or gelatin compounds to enhance the hemostatic efficacy.

Abstract: In modern processes for the preparation of cellulose ethers containing one or more types of substituents (such as MC, CMC, HEC, HPC, MHEC or EHEC), cellulose is reacted with etherifying agents in the presence of water, base and a mixture of preferably inert organic solvents (as a dispersing auxiliary). Dimethoxyethane (ethylene glycol dimethyl ether) and at least one organic solvent selected from the group including alkanols, alkane diols and alkoxy alkanols (for example, methanol and/or isopropanol) are employed in the mixture of organic solvents used for these syntheses, particularly in quantities of 1 to 30 parts by weight per 1 part by weight of cellulose.

Abstract: An endotoxin binding material affixed to a support is disclosed. One embodiment is a matrix material capable of binding endotoxins and comprising a polar, water-insoluble, high molecular weight polymer support to which is attached groups which adsorb endotoxin molecules. The groups comprise bifunctional aliphatic molecules, one end of which is bound to the support, the other end of which is bound to an aryl molecule. The invention has utility in the removal of endotoxins from biological fluids and other solutions and for concentrating endotoxins so that they may be subsequently detected and quantified.

Abstract: A process is disclosed for the preparation of water-soluble cellulose ethers, comprising the steps of activating cellulose with ammonia, alkalizing the activated cellulose, and etherifying the alkali cellulose. In the process, the activated cellulose is alkalized in the presence of ammonia and, optionally, in the presence of an organic solvent, and the ammonia is removed from the alkali cellulose in the presence of the alkalizing agent and, optionally, the organic solvent. Etherification proceeds in a medium which contains at least portions of said organic solvent. The organic solvent comprises, in particular, an alkanol which has from 1 to 6 carbon atoms. For the etherification step, carboxymethylation or hydroxyethylation is preferred.

Abstract: In modern processes for preparing cellulose ethers containing one or more types of substituents, such as MC, CMC, HEC, HPC, MHEC or EHEC, cellulose is reacted with an etherifying agent in the presence of water, base and at least one inert organic solvent (as a dispersing auxiliary). Dimethoxyethane (ethylene glycol dimethyl ether) is employed as a new organic solvent for these syntheses, particularly in quantities of 1 to 30 parts by weight per part by weight of cellulose.

Abstract: This invention provides a method for controlling the reaction between cellulose and an etherifying agent which comprises the steps of (a) combining cellulose with an alkylene oxide and alkyl halide in a reactor wherein an etherification reaction is initiated which includes a vapor phase, (b) periodically measuring the quantity of at least one of the reactants or products in the vapor phase of the reactor and therewith determining the rate of the etherification reaction taking place, and (c) regulating the reaction temperature continuously while the reaction is taking place by using the rate of reaction determined in step (b) to determine the amount of heating or cooling needed for the reactor.

Abstract: Disclosed is a cellulose ether having at least one phosphorus-containing substituent or a mixed ether of said cellulose ether having in addition at least one phosphorus-free substituent comprising alkyl, hydroxyalkyl, carboxyalkyl, sulfonoalkyl, aminoalkyl, or diaminoalkyl, wherein the phosphorus-containing substituent(s) comprise(s) groups of the formula ##STR1## wherein R.sup.1 and R.sup.2 are OX; or R.sup.1 is OX and R.sup.2 is OY; or R.sup.1 is OX and R.sup.2 is (CH.sub.2).sub.n --CH.sub.3 ; or R.sup.1 and R.sup.2 are (CH.sub.2).sub.n --CH.sub.3 ; or R.sup.1 is (CH.sub.2).sub.n --CH.sub.3 and R.sup.2 is (CH.sub.2).sub.p --CH.sub.3, whereinX,Y are identical or different and comprise a hydrogen atom or a monovalent cation;m is an integer from 1 to 4; andn,p are identical or different and are 0 or 1; with the proviso that when m is 1 or 2, R.sup.1 and R.sup.2 may not be OX and R.sup.1 and R.sup.2 may not be OX and OY, respectively. Also disclosed is a process for producing these cellulose ether products.

Abstract: Cellulose derivatives having a controlled molecular weight are prepared by adjusting oxygen concentration as measured by analyzing the quantity of oxygen in the head space of the reaction vessel to a level such that the cellulose derivative prepared therein has a desired solution viscosity. The cellulose derivative is then prepared in the reaction vessel without substantially increasing the quantity of oxygen in said reaction vessel.

Abstract: The application discloses a gel-forming composition based on (a) water, (b) a water-soluble cellulose mixed ether having at least one nonionic substituent from the group comprising hydroxyalkyl and alkyl and at least one anionic phosphorus-containing substituent, and (c) a salt containing a cation which is at least divalent. The phosphorus-containing substituent is a phosphonoalkyl group or a p-alkylphosphinoalkyl group. The application also relates to a process for the preparation of a gel from this composition, to the reversible reversing of the gel by the addition of an agent which complexes the cation, e.g. in the case of Al.sup.3+ ions, Fe.sup.3+ ions, Zr.sup.4+ ions or ZrO.sup.2+ ions, by means of an amount of fluoride ions, and to the use of this gel-forming compostion in the secondary production of petroleum.

Abstract: This invention provides a method for the preparation of trimethylsilyl cellulose ethers. The method comprises reacting cellulose with hexamethyldisilazane in the presence of a small amount of catalyst, wherein the catalyst is acetamide, acetamide and an ammonium halide, N,N-dimethylformamide and an ammonium halide, N,N-dimethylformamide and trimethylsilyl chloride, 2-oxazolidinone and an ammonium halide, or a mixture thereof.

Abstract: Improved basic polysaccharides are prepared by contacting a polysaccharide with a tetravalent onium salt such as tetramethylammonium chloride prior to contacting it with a strong base such as sodium hydroxide. Polysaccharide derivatives having a greater degree and uniformity of substitution are prepared from such improved basic polysaccharides.

Abstract: A method for producing fire-retarded blend fibers having a fire resistance LOl-value of at least 21% O.sub.2, made from cellulose and chlorine containing polymer. Chlorine containing polymer having a chlorine content of 30-75% by weight, is blended, either as such or dissolved in a solvent, with a DMSO/formaldehyde solution of cellulose so that the obtained blend has 10-70% by weight of chlorine containing polymers, based on the total amount of cellulose and said polymers. Fibers are produced of the obtained mixture by bringing it into contact with an aqueous or alcoholic solution.

Abstract: Disclosed is a process for preparing water-soluble phosphonomethyl ethers of cellulose from cellulose and halogenomethane phosphonic acid or one of its salts or acid derivatives, in an aqueous, alkaline medium. The process is carried out in such a way that, for each mole of the cellulose, from about 2.1 to 15 moles of hydroxide ions and from about 0.4 to 3.0 moles of halogenomethane phosphonate ions as etherifying agent are caused to react in from about 3 to 50 parts by weight, per part by weight of the cellulose, of a mixture which is composed of an inert, preferably water-miscible organic solvent and water and in which the proportion of water ranges from about 2 to 60 percent by weight, the reaction is continued until the phosphonomethyl cellulose has a DS of at least about 0.13.

Abstract: Molecular coordination complexes are formed between a cellulose polymer and a non-polar solid aliphatic alcohol containing 8 to 18 carbon atoms optionally substituted with an aliphatic group containing 8 to 18 carbon atoms by solvating the polymer with a volatile polar solvent and reacting the solvated cellulose polymer directly with the aliphatic alcohol, preferably as a melt. The resulting composition may be dried. This constitutes the complex. The composition has utility as a matrix in controlled release formulations since it has a uniform porosity which may be varied.

Abstract: The present invention relates to new polymer solutions which make it possible to produce shaped articles, such as yarns and fibres, films, sheets and the like.These solutions consist of cellulose having a degree of polymerisation of at least 200, polyamide-imide, dimethyl sulphoxide and formaldehyde, with a weight ratio cellulose/polyamide-imide of 0.05 to 1, preferably 0.1 to 1, a ratio formaldehyde/cellulose of 0.2 to 2 and a total concentration of 6 to 25%, preferably 15 to 20%.These solutions are particularly suitable for the production of filaments which consist of fibrils substantially orientated along the axis of the fibre and closely intersecting, the cellulose macromolecules being partially involved in a crystal lattice characteristic of cellulose II. The filaments possess valuable properties for use in textiles.

Abstract: This invention is directed to a method for the continuous production of alkyl cellulose by reacting alkali cellulose with alkylating agents in the presence of inert liquids, wherein:(a) powdered cellulose is reacted with aqueous-alcoholic alkali metal hydroxide solution at temperatures of from about 20.degree. to 80.degree. C. to form alkali cellulose;(b) oxygen is completely removed from the alkali cellulose reaction mixture of step (a) and the water content is reduced to about 2.5 to 6.0 moles per anhydroglucose unit; and(c) the reaction mixture from step (b) is reacted with at least a stoichiometric amount, but not more than with a molar excess of up to about 50%, based on the alkali metal hydroxide, of an alkylating agent in an inert liquid boiling at a temperature of from about 80.degree. to 160.degree. C., the reaction being carried out continuously in stirred tanks-in-series with 2 to 10 units.

Abstract: This invention relates to an improved process for preparing cellulose derivatives by alkalizing cellulose to form alkali cellulose, alkylating the alkali cellulose to form alkylated alkali cellulose, and recovering the alkylated alkali cellulose. According to the process of the invention, finely-divided, preferably powdered, cellulose is reacted with an aqueous-alcoholic alkali metal hydroxide solution at a temperature of from about 20.degree. to 120.degree. C., to form alkali cellulose, oxygen is removed, and the water content is reduced to from about 2.5 to 6.0 moles per anhydroglucose unit, prior to alkylization.

Abstract: Non-thrombogenic material comprising a base polymer treated with heparin, the improvement in which the heparin is covalently bonded with the base polymer through only one acetal bond or hemiacetal bond at each bonding site between the heparin and the base polymer.

Abstract: A contact lens solution is provided for wetting, soaking and lubricating of hard contact lenses, particularly those carrying an ionic charge. The solution contains an ionic polymer of cationic or anionic charge that interacts with an oppositely charged surface of a contact lens forming an interfacial polyelectrolyte complex. This polyelectrolyte complex provides increased, long lasting lens wettability leading to a cushioning and lubricating effect with the eyelid and the cornea.

Abstract: Solubilized cellulosic material is modified through a condensation reaction with organotin halides. The modified products exhibit lower heats of combustion in air than unmodified cellulose, are hydrophobic and resistant to hydrolysis, and inhibit the growth of a variety of common fungi. The modified products are useful as insulation materials, mildew and mold resistant fabrics, and as material for topical bandages.

Abstract: A continuous process for manufacturing water-soluble hydroxyalkyl cellulose, and water-soluble mixed ethers based on hydroxyalkyl cellulose, comprising producing a slurry comprising (by weight) 1 part cellulose, 0.02 to 0.6 parts alkali metal hydroxide, 5 to 10 parts inert organic solvent, and 0.4 to 2.5 parts water; continuously feeding the slurry to a first elevated pressure reactor and mixing the slurry therein with at least one normally gaseous etherifying agent which has been liquified under pressure; maintaining the slurry at a temperature up to 40.degree. C., and a gauge pressure up to 3 bars, for 15 to 90 minutes, to give a degree of substitution from 0.2 to 1.