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Ethers

Subclass of:

536 - Organic compounds -- part of the class 532-570 series

536000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

536100110 - Carbohydrates or derivatives

536056000 - Cellulose or derivative

Patent class list (only not empty are listed)

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Class / Patent application numberDescriptionNumber of patent applications / Date published
536084000 Ethers 52
20090326217Process for preparing cellulose ether - The invention relates to a process for preparing a cellulose ether wherein the cellulose ether is prepared in the presence of an ether of the formula R1-O—R2 having a boiling point between 40 and 90° C., or of a solvent mixture comprising an ether and having a boiling point between 40 and 90° C., wherein R1 and R2 maybe the same or different and are independently selected from an alkyl group.12-31-2009
20100168410Hydroxypropyl Methyl Cellulose Hard Capsules and Process of Manufacture - A composition for manufacture of hard hydroxypropyl methyl cellulose capsules comprising a film forming material of hydroxypropyl methyl cellulose having a methoxy content of 27.0-30.0% (w/w), and a hydroxypropoxy content of 4.0-7.5% and as a 2% weight solution, a viscosity of 3.5-6.0 cPs at 20° C., dipping compositions, process for manufacture of hard hydroxypropyl methyl cellulose capsules according to a dip coating process and hard capsule shells.07-01-2010
20120214980METHODS FOR PREPARING ALKALI CELLULOSE AND CELLULOSE ETHER - Provided is a method for efficiently preparing alkali cellulose having a uniform alkali distribution. More specifically, provided are a methods for preparing alkali cellulose comprising a contact filtration step of bringing a pulp into contact with an alkali metal hydroxide solution on a moving filtration plane for vacuum filtration to collect a contact product remaining on the filtration plane, and a draining step of draining the contact product; and a method of preparing cellulose ether by using the alkali cellulose. Also provided is an apparatus for preparing alkali cellulose comprising a continuous horizontal vacuum filter type contactor.08-23-2012
20120214981METHODS FOR PRODUCING ALKALI CELLULOSE AND CELLULOSE ETHER - A degree of polymerization of cellulose ether is accurately controlled, and quality and a manufacturing process of the cellulose ether are stabilized. There is provided a method for producing depolymerized alkali cellulose having a degree of polymerization controlled, comprising at least a step of depolymerizing, in the presence of an oxygen-containing gas flow, alkali cellulose obtained by bringing a pulp into contact with an alkali solution, while measuring feeding and discharging amounts of oxygen in the oxygen-containing gas flow. There is also provided a method for producing cellulose ether, comprising at least a step of adding an etherifying agent to the depolymerized alkali cellulose having a degree of polymerization controlled.08-23-2012
20150299338METHOD FOR PRODUCING CELLULOSE ETHER - Provided is a method for producing a cellulose ether including a drying step capable of continuously and stably drying a highly adhesive wet cellulose ether with high thermal efficiency without causing adhesive growth and solidification of the wet cellulose ether in a dryer. More specifically, the method for producing a cellulose ether includes a step of drying a wet cellulose ether having water content of more than 50% by weight in a rotary type through-flow dryer.10-22-2015
536085000 Subsequent treatment process 13
20080306253MATRIX MADE OF A POLYSACCHARIDE MODIFIED UNDER AN ELECTRON BEAM WITH A FUNCTIONAL ORGANOSILICON COMPOUND - Water-soluble or water-dispersible matrix, made of a polysaccharide modified under an electron beam with an organosilicon compound chosen from organosilanes and/or polyorganosiloxanes having at least one functional group capable of reacting and/or interacting with said polysaccharide.12-11-2008
20090221813Homogeneous synthesis of cellulose ethers in ionic liquids - The invention is directed to a simple and new method for the homogeneous synthesis of cellulose ethers. Ionic liquids are not only used as solvent, but also as reaction media for the homogeneous etherification of cellulose. The dissolved cellulose is treated with the etherification agent in the absence of organic and/or inorganic bases and in the absence and/or in the presence of moderate amounts of water. The obtained cellulose ethers show new distributions of substitution on the polymer chain, resulting in new properties and applications.09-03-2009
20100292460WATER-DISPERSIBLE POLYSACCARIDE DERIVATIVES OF REDUCED GLYOXAL CONTENT, AND A PROCESS FOR DECREASING THE GLYOXAL CONTENT IN GLYOXAL-CROSSLINKED POLYSACCHARIDE DERIVATIVES - A description is given of glyoxal-treated polysaccharide derivatives which, to decrease the unbound glyoxal, are treated with an aqueous solution of one or more water-soluble aluminium salts, or one or more water-soluble borates, or a combination of one or more water-soluble aluminium salts and one or more water-soluble borates, and, if appropriate, with suitable buffer substances to set the pH, and then dried.11-18-2010
20130345416METHOD FOR PROCESSING NANOFIBRILLAR CELLULOSE AND PRODUCT OBTAINED BY THE METHOD - The invention relates to a method for processing an aqueous gel of nanofibrillar cellulose by removing water from the aqueous gel by means of an organic solvent miscible with water. In the method: aqueous gel is introduced into a volume of organic solvent miscible with water in a controlled manner so that the aqueous gel is kept as a separate phase and forms discrete physical entities containing the nanofibrillar cellulose within the phase; water is changed with the organic solvent in said discrete physical entities of nanofibrillar cellulose; and the physical entities are separated from the volume of organic solvent.12-26-2013
20150045549METHOD AND APPARATUS FOR PROCESSING FIBRIL CELLULOSE AND FIBRIL CELLULOSE PRODUCT - A method for processing fibril cellulose which is in the form of aqueous fibril cellulose gel includes lowering the pH of the aqueous fibril cellulose gel to provide aqueous fibril cellulose gel of reduced water retention capacity, and dewatering the aqueous fibril cellulose gel of reduced water retention capacity to provide dewatered fibril cellulose. The dewatering is performed by pressure filtration.02-12-2015
20150045550Method For Dehydrating Hydrous Low-Substituted Hydroxypropyl Cellulose and Method for Producing Low-Substituted Hydroxypropyl Cellulose By Using Same - Reduction of the energy burden in a step of drying hydrous low-substituted hydroxypropyl cellulose (L-HPC), reduction of water content of a cake obtained by dehydration, and others are targeted. More specifically, provided is a method for dehydrating hydrous L-HPC with a compression type dehydrator by feeding the hydrous L-HPC to a screw conveyer connected to the inlet of the dehydrator, including steps of: starting the operation of the conveyer to fill the conveyer and the dehydrator with the hydrous L-HPC, starting the operation of the filled dehydrator, and feeding the hydrous L-HPC to the conveyer, while discharging dehydrated L-HPC from an outlet of the dehydrator, wherein a feed rate of feeding the hydrous L-HPC to the conveyer is equal to a discharge rate of discharging the dehydrated L-HPC in terms of net weight of cellulose ether, and a method for producing L-HPC by using the above method.02-12-2015
20160159931HYDROGEL FORMING MATERIAL FROM BYPRODUCT PULP FINES - A process for making a hydrogel forming material from an unbleached cellulose pulp comprised of isolating pulp fines from the cellulose pulp by screening and/or dissolved air filtration, reacting the isolated pulp fines with alkaline hydroxide to form an alkali cellulose composition, preparing a heterogeneous mixture of the alkali cellulose composition and an etherifying agent, and optionally organic cross-linking agent, and reacting the components of the mixture to produce a hydrogel forming material. A polyvalent metal cross-linking agent can optionally be reacted with the hydrogel forming material to enhance its gel strength.06-09-2016
536086000 Comminuting 1
20080207893Process For Grinding Cellulose Ether - The invention relates to a process for grinding cellulose ether comprising the steps of: a) grinding a cellulose ether comprising 20 to 90 wt % of water, based on the total weight of cellulose ether and water, and a cationic surfactant in a mill; and b) optionally drying the mixture while grinding, prior to or following the step of grinding.08-28-2008
536087000 Liquid interaction properties changed (e.g., solubility, absorbability, etc.) 1
20110040085PROCESS TO PREPARE CROSSLINKED CELLULOSE ETHERS, CROSSLINKED CELLULOSE ETHERS OBTAINABLE BY SUCH PROCESS AND THE USE THEREOF - The invention relates to a dry or slurry process to prepare phosphate-crosslinked cellulose ethers from a cellulose starting material comprising the steps of adding an alkalizing agent to the cellulose starting material to achieve mercerization, adding an ethehfying agent to the reaction mixture to achieve etherification of the cellulose, and adding a crosslinking agent to the reaction mixture to achieve crosslinking of the cellulose, wherein at least part of the alkalizing agent is added to the cellulose starting material before the etherification and/or crosslinking reactions take place to obtain alkalized cellulose; the crosslinking agent and the etherifying agent are added one after the other in random order or simultaneously; the crosslinking agent is an alkali metal thmetaphosphate; and the crosslinking and etherification steps are performed at an elevated temperature. Additionally, the invention relates to crosslinked cellulose ethers obtainable by the above process having a viscosity and/or water absorption capacity higher than their non-crosslinked equivalents and the use thereof.02-17-2011
536088000 Viscosity, degree of polymerization or heat stability changed (e.g., degrading, cross-linking, etc.) 2
20100063269PROCESS FOR REDUCING THE AVERAGE MOLECULAR WEIGHT OF CELLULOSE ETHERS - A process for reducing the average molecular weight of a cellulose ether comprises the step of contacting a cellulose ether with an acid to partially depolymerize it to a lower molecular weight in a diluent comprising at least 50 weight percent of an organic hydroxylic compound having at least one hydroxy group and at least two carbon atoms.03-11-2010
20150307631PROCESS TO PREPARE CROSSLINKED CELLULOSE ETHERS, CROSSLINKED CELLULOSE ETHERS OBTAINABLE BY SUCH PROCESS AND THE USE THEREOF - The invention relates to a dry or slurry process to prepare phosphate-crosslinked cellulose ethers from a cellulose starting material comprising the steps of adding an alkalizing agent to the cellulose starting material to achieve mercerization, adding an ethehfying agent to the reaction mixture to achieve etherification of the cellulose, and adding a crosslinking agent to the reaction mixture to achieve crosslinking of the cellulose, wherein at least part of the alkalizing agent is added to the cellulose starting material before the etherification and/or crosslinking reactions take place to obtain alkalized cellulose; the crosslinking agent and the etherifying agent are added one after the other in random order or simultaneously; the crosslinking agent is an alkali metal thmetaphosphate; and the crosslinking and etherification steps are performed at an elevated temperature. Additionally, the invention relates to crosslinked cellulose ethers obtainable by the above process having a viscosity and/or water absorption capacity higher than their non-crosslinked equivalents and the use thereof.10-29-2015
536089000 Acid employed in subsequent treatment 2
20090187016METHOD FOR PRODUCING CELLULOSE ACETALS - The present invention describes a process for preparing acetals of polysaccharides, oligosaccharides or disaccharides by dissolving these in at least one ionic liquid and reacting them with a vinyl ether. The acetalated polysaccharides or oligosaccharides obtained in this way can be crosslinked by treatment with acid. The present invention also provides acetals of polysaccharides, oligosaccharides or disaccharides and also crosslinked polysaccharides or oligosaccharides.07-23-2009
20140148591METHOD OF REMOVING ALKYLENE HALOGENOHYDRIN FROM CELLULOSE ETHER - In a method of removing alkylene halogenohydrin from a cellulose ether the cellulose ether is provided, water is added to the cellulose ether and subsequently alkylene halogenohydrin and water is removed from the cellulose ether by evaporation. Alternatively steam or a steam mixture can be sparged across or through the cellulose ether to remove halogenohydrin from the cellulose ether.05-29-2014
536090000 Mixed ethers 9
20080242852Method for Preparation of Hydroxyalkylalkylcellulose Ethers with High Yield - The present invention relates to a method for preparing hydroxyalkylalkylcellulose with high yield, more particularly to a method for preparing hydroxyalkylalkylcellulose with high yield, with at least 60% of alkoxy and hydroxyalkoxy substituted, by treating finely ground pulp with an alkali metal hydroxide at room temperature, reacting it with an alkylene oxide and an alkyl halide, and then adding an alkali metal hydroxide and an alkyl halide thereto. The method of the present invention is highly economical and also environment-friendly because waste of the reactants can be greatly reduced.10-02-2008
20120108805CELLULOSE-BASED RESIN COMPOSITION, MOLDED BODY AND CASE FOR ELECTRIC AND ELECTRONIC DEVICES - A cellulose resin composition for melt molding, containing a cellulose derivative having two or more kinds of aliphatic oxy groups having different carbon numbers (—OR) (wherein R represents an aliphatic group which may be unsubstituted or substituted), wherein a difference in carbon number between the aliphatic oxy group having the largest carbon number and the aliphatic oxy group having the smallest carbon number is 1 to 18. The cellulose resin composition can provide good thermoplasticity and excellent mechanical strength, and can be used to prepare a molded body and a case for electric and electronic devices.05-03-2012
20120165518CERAMIC EXTRUSION MOLDING COMPOSITION AND BINDER - A non-crosslinked, nonionic, water-soluble cellulose ether having a syneresis value of at least 25% by weight in which the hydrogen atom of a hydroxyl group is substituted by a C06-28-2012
536091000 Hydroxyalkyl containing 6
20110077391HYDROXYALKYL METHYLCELLULOSE HAVING SOLUBILITY AND THERMOREVERSIBLE GELATION PROPERTIES IMPROVED - Provided is hydroxyalkyl methylcellulose which can be dissolved at room temperature of 20 to 30° C. and has high thermoreversible gel strength during thermoreversible gelation. More specifically, provided is water-soluble hydroxyalkyl methylcellulose having a molar substitution of hydroxyalkoxyl groups of 0.05 to 0.1 and a substitution degree of methoxyl groups of 1.6 to 1.9, wherein the hydroxyalkoxyl groups are classified into substituted hydroxyalkoxyl groups having hydroxyl groups of hydroxyalkoxyl groups substituted further with methoxyl groups and unsubstituted hydroxyalkoxyl groups having hydroxyl groups of hydroxyalkoxyl groups not further substituted; and a ratio (A/B) of a molar fraction (A) of the substituted hydroxyalkoxyl groups to a molar fraction (B) of unsubstituted hydroxyalkoxyl groups is 0.4 or greater.03-31-2011
20110144322Hydroxypropylmethylcellulose Having High Thermal Gel Strength, Method For Producing The Same And Food Comprising The Hydroxypropylmethylcellulose - Provided is hydroxypropylmethylcellulose having a high thermal gelation temperature and a high thermal gel strength and a method for producing the same and a food comprising the hydroxypropylmethylcellulose. More specifically, provided is hydroxypropylmethylcellulose having an average substitution degree of a methoxy group of 1.0 to 2.0 per glucose unit, an average substitution degree of a hydroxypropoxy group of 0.05 to 0.4 per glucose unit, and a A/B value of 0.305 or greater wherein A represents a substitution degree of a methoxy group directly substituted for a hydroxy group on carbon at position 6 in a glucose unit free from a hydroxypropoxy group-substituted hydroxy group, B represents a substitution degree of a methoxy group per glucose unit, and the A/B represents a value of A divided by B.06-16-2011
20110282050METHOD OF PREPARING ALKALI CELLULOSE OR A CELLULOSE DERIVATIVE - The throughput of a reactor for producing alkali cellulose and/or a cellulose derivative can be increased by using a granulated cellulose-based material for the preparation of alkali cellulose and/or a cellulose derivative. Cellulose derivatives of essentially the same quality can be produced as in known processes wherein powdered cellulose-based material is used for alkalization and derivatization.11-17-2011
20120214982METHOD FOR PRODUCING ALKALI CELLULOSE COMPRISING REMOVAL OF CELLULOSE PARTICLES - There is provided a method for producing alkali cellulose comprising efficiently removing cellulose particles which are introduced by a pulp and have accumulated in a circulating alkali metal hydroxide solution. More specifically, there is provided a method for producing alkali cellulose, comprising at least the steps of bringing a pulp into contact with an alkali metal hydroxide solution to obtain a contact product, draining the contact product by a drainer, reusing an alkali metal hydroxide solution recovered in the step of draining for contact with a pulp, and adjusting an amount of cellulose particles in the recovered alkali metal hydroxide solution to 0.5% by weight or less prior to reusing for contact with the pulp.08-23-2012
20130245249Hydroxypropylmethylcellulose Having High Thermal Gel Strength, Method For Producing The Same And Food Comprising The Hydroxypropylmethylcellulose - Provided is hydroxypropylmethylcellulose having a high thermal gelation temperature and a high thermal gel strength and a method for producing the same and a food comprising the hydroxypropylmethylcellulose. More specifically, provided is hydroxypropylmethylcellulose having an average substitution degree of a methoxy group of 1.0 to 2.0 per glucose unit, an average substitution degree of a hydroxypropoxy group of 0.05 to 0.4 per glucose unit, and a A/B value of 0.305 or greater wherein A represents a substitution degree of a methoxy group directly substituted for a hydroxy group on carbon at position 6 in a glucose unit free from a hydroxypropoxy group-substituted hydroxy group, B represents a substitution degree of a methoxy group per glucose unit, and the A/B represents a value of A divided by B.09-19-2013
20140018531PROCESS FOR REDUCING THE AMOUNT OF WATER-INSOLUBLE FIBERS IN A WATER-SOLUBLE CELLULOSE DERIVATIVE - The amount of water-insoluble fibers in a water-soluble cellulose derivative is reduced in a process comprising the steps of a) providing a water-soluble cellulose derivative having a residual amount of at least 20 ppm by weight of water-insoluble fibers in a 2 weight percent aqueous solution of the water-soluble cellulose derivative; b) mixing the water-soluble cellulose derivative of step a) with a liquid in a compounder to provide a moist water-soluble cellulose derivative having a temperature of at least 50 C and a moisture content of from 35 to 90 percent, based on the total weight of the moist cellulose derivative; and c) drying-grinding the mixture of step b) in a gas-swept impact mill to obtain a dried and ground cellulose derivative.01-16-2014
536092000 Sulfur containing 3
20100317844METAL SALT OF CROSSLINKED CELLULOSE DERIVATIVE - The invention provides a metal salt of a crosslinked cellulose derivative represented by the following formula (I), wherein the degree of substitution of the hydroxyl group of glucose unit of the crosslinked cellulose derivative by a functional group a is 1 or more.12-16-2010
20100324280SODIUM ABSORPTION INHIBITOR, POTASSIUM ABSORPTION INHIBITOR, PHOSPHORUS ABSORPTION INHIBITOR AND PREVENTIVE AGENT, THERAPEUTIC AGENT AND FOOD CONTAINING THE SAME - The present invention provides a sodium absorption inhibitor, a potassium absorption inhibitor, and a phosphorus absorption inhibitor, and a preventive agent, a therapeutic agent and a food for diseases caused by overconsumption of common salt, potassium and phosphorus or diseases which require restriction of ingestion of common salt, potassium and phosphorus to actively and safely excrete overconsumed common salt, potassium and phosphorus excreted outside the body.12-23-2010
20140371443Multifunctional Materials And Composites - Forming multifunctional materials and composites thereof includes contacting a first material having a plurality of oxygen-containing functional groups with a chalcogenide compound, and initiating a chemical reaction between the first material and the chalcogenide compound, thereby replacing oxygen in some of the oxygen-containing functional groups with chalcogen from the chalcogen-containing compound to yield a second material having chalcogen-containing functional groups and oxygen-containing functional groups. The first material is a carbonaceous material or a macromolecular material. A product including the second material is collected and may be processed further to yield a modified product or a composite.12-18-2014
536093000 Unsaturated 1
20140142292(METH)ALLYLSILANE COMPOUND, SILANE COUPLING AGENT THEREFOR, AND FUNCTIONAL MATERIAL USING SAME - A (meth)allylsilane compound chemically bonded to various alcohol derivatives including polyol derivatives such as saccharides, is raw material used to cause a substrate to express functionalities such as a defogging property and separation characteristics for column chromatography, can be easily prepared, is easily purified, and is stable and easy to handle, and a functional material in which those functionalities are expressed, while silyl group-containing groups are conveniently carried at a high density on the surface of the substrate, by using the (meth)allylsilane compound as a silane coupling agent for silane-coupling to the substrate. The (meth)allylsilane compound includes a (meth)allylsilyl group-containing alkyl group or a (meth)allylsilylalkyl group-containing aralkyl group that is bonded to an alcohol derivative. In the functional material, the silane coupling agent is ether-bonded to surface hydroxyl groups exposed on a substrate through the surface hydroxyl groups by silane coupling to have an ether bond on the functional material.05-22-2014
536095000 Hydroxyalkyl containing 12
20080262216HYDROXYALKYL METHYLCELLULOSE HAVING SOLUBILITY AND THERMOREVERSIBLE GELATION PROPERTIES IMPROVED - Provided is hydroxyalkyl methylcellulose which can be dissolved at room temperature of 20 to 30° C. and has high thermoreversible gel strength during thermoreversible gelation. More specifically, provided is water-soluble hydroxyalkyl methylcellulose having a molar substitution of hydroxyalkoxyl groups of 0.05 to 0.1 and a substitution degree of methoxyl groups of 1.6 to 1.9, wherein the hydroxyalkoxyl groups are classified into substituted hydroxyalkoxyl groups having hydroxyl groups of hydroxyalkoxyl groups substituted further with methoxyl groups and unsubstituted hydroxyalkoxyl groups having hydroxyl groups of hydroxyalkoxyl groups not further substituted; and a ratio (A/B) of a molar fraction (A) of the substituted hydroxyalkoxyl groups to a molar fraction (B) of unsubstituted hydroxyalkoxyl groups is 0.4 or greater.10-23-2008
20110230656Low-Substituted Hydroxypropylcellulose and Solid Preparation Comprising the Same - Provided is nonionic and excellently stable low-substituted hydroxypropylcellulose having improved compressibility and flowability, and further having improved disintegration and texture in oral cavity. More specifically provided is low-substituted hydroxypropylcellulose having a crystallinity of 60% or less, a degree of hydroxypropoxyl substitution of 5 to 9% by weight, and an aspect ratio of less than 2.5, wherein the crystallinity is calculated based on a diffraction intensity by wide-angle X-ray diffraction measurement according to the following formula (1):09-22-2011
20120041187Process for Improved Production of Alkali Cellulose and Cellulose Derivatives - The present invention relates to a process for the production of alkali cellulose for the production of alkali cellulose and, optionally, cellulose ethers from cellulose in the presence of alkali and, if applicable, with alkylating and/or hydroxyalkylating agent(s) comprising the reaction of a cellulose with an alkali metal hydroxide, wherein the alkali metal hydroxide is mixed with cellulose in a mixing apparatus, the mixing apparatus (02-16-2012
20120065390Method for Producing Low-Substituted Hydroxypropylcellulose - Provided is a method for producing low-substituted hydroxypropylcellulose in which depolymerization capable of achieving a target viscosity in a short time is carried out safely after an etherification reaction step. More specifically, provided is a method for producing low-substituted hydroxypropylcellulose having a degree of hydroxypropoxy substitution of from 9.5 to 16.0% by weight, comprising at least a step of reacting alkali cellulose with an etherifying agent and a step of carrying out depolymerization after the reaction.03-15-2012
20120157674COATING AGENT COMPRISING HYDROXYALKYL CELLULOSE - There are provided a coating agent containing a hydroxyalkyl cellulose in which a content of hydroxyalkyl groups within the hydroxyalkyl cellulose is within a range of 40 to 50% by mass, preferably a coating agent containing a hydroxyalkyl cellulose in which the content of hydroxyalkyl groups is within a range of 40 to 50% by mass and also a viscosity of 2% aqueous solution at 20° C. is within a range of 3.0 to 5.9 mPa·s; and a solid preparation coated with the coating agent.06-21-2012
20120214983METHOD FOR PRODUCING CELLULOSE ETHER - Provided is a method for producing cellulose ether whose aqueous solution is transparent and contains a smaller amount of water-insoluble portion. The method comprises at least the steps of providing at least two alkali cellulose materials having different compositions, each of the materials having been prepared by bringing a pulp into contact with a solution of alkali metal hydroxide and draining; and mixing the at least two alkali cellulose materials having different compositions, wherein each weight ratio of the alkali metal hydroxide in each of the alkali cellulose materials having different compositions to a solid component in the pulp (alkali metal hydroxide/solid component in pulp) is equal to 0.4 to 2.5 times of a weight ratio of alkali metal hydroxide in the alkali cellulose obtained in the step of mixing to solid components in a sum of pulps used for preparation of the alkali cellulose materials.08-23-2012
20120214984METHODS FOR PRODUCING ALKALI CELLULOSE AND CELLULOSE ETHER - When a combination of pulps having different alkali metal hydroxide solution absorption rates is as a raw material, contact conditions such as a contact temperature and a contact time have to be changed frequently, depending on the absorption rate of pulps currently processed, thereby causing a problem of reduced productivity. For solving the problem, provided is a method for producing alkali cellulose, comprising at least the steps of: bringing two or more types of pulps having different alkali metal hydroxide solution absorption rates into contact with an alkali metal hydroxide solution to obtain a contact product; and draining the contact product, wherein the highest absorption rate is not more than 4.0 times as fast as the lowest absorption rate.08-23-2012
20120214985PRODUCTION METHOD FOR CATIONIC HYDROXYPROPYL CELLULOSE - The present invention relates to a process for producing a cationic hydroxypropyl cellulose including the step of reacting a low-crystalline powdery cellulose with a cationizing agent represented by the following general formula (1) and/or a cationizing agent represented by the following general formula (2), and propylene oxide in the presence of water in an amount of from 10 to 60% by mass on the basis of the low-crystalline powdery cellulose, and a catalyst:08-23-2012
20140142293Method for Producing Purified Low-Substituted Hydroxypropyl Cellulose - Provided is a method for producing low-substituted hydroxypropyl cellulose with less yellowing. More specifically, the method for producing purified low-substituted hydroxypropyl cellulose includes the steps of: reacting alkali cellulose and an etherifying agent to obtain a reaction mixture; dispersing the reaction mixture in water containing a portion of acetic acid necessary for neutralizing the total amount of the reaction mixture to neutralize a portion of the reaction mixture, and then completely neutralizing with the remaining acetic acid to cause precipitation, to obtain a slurry containing crude low-substituted hydroxypropyl cellulose; disintegrating a solid component in the slurry through a cutter pump, the solid component containing the crude low-substituted hydroxypropyl cellulose, and discharging the slurry containing the disintegrated solid component; washing the discharged slurry with water to obtain a cake of purified low-substituted hydroxypropyl cellulose; and drying the cake.05-22-2014
20160083483METHOD FOR CONTINUOUSLY PRODUCING CELLULOSE ETHER - Provided is a method for efficiently and continuously producing a cellulose ether containing a reduced amount of indissoluble component. Specifically, the method includes a contact step of bringing pulp into contact with an alkali metal hydroxide solution in the presence of a heat removal solvent to obtain alkali cellulose; a reaction step of subjecting the alkali cellulose to a reaction with an etherifying agent; a partial condensation step, after completion of the reaction, of partially condensing a gas present in a reaction vessel used for the reaction to separate the gas into gas and liquid components for returning some or all of the gas component to the contact step for reuse as some or all of the heat removal solvent; and a step of incinerating the liquid component and, when all of the gas component is not returned to the contact step, the remainder of the gas component.03-24-2016
20160374945PHARMACEUTICAL COMPOSITIONS OF DISPERSIONS OF DRUG AND NEUTRAL POLYMERS - In one aspect, pharmaceutical compositions comprising dispersions of an acid-sensitive drug and a neutral dispersion polymer are disclosed. The acid-sensitive drug has improved chemical stability relative to dispersions of the drug and acidic polymers. In another aspect, pharmaceutical compositions of low-solubility drugs and amphiphilic, hydroxy-functional vinyl copolymers are disclosed.12-29-2016
536096000 Hydroxyethyl 1
20140073777METHOD FOR PRODUCING ALKALI CELLULOSE - The present invention relates to a method for producing an alkali cellulose with suppressed decrease in the degree of polymerization as well as with small use amount of a basic compound, and to a method for producing a cellulose ether by using the alkali cellulose thus obtained. Provided by the present invention are: (A) a method for producing an alkali cellulose, comprising Step 1 wherein a cellulose-containing raw material (I) is treated by a pulverizing machine thereby obtaining a cellulose-containing raw material (II) which contains a cellulose having crystallinity in the range of 10 to 55% and Step 2 wherein the cellulose-containing raw material (II) obtained in Step 1 is added by a basic compound with the amount thereof being in the range of 0.6 to 1.5 mol relative to 1 mol of an anhydroglucose unit that constitutes the said cellulose as well as by water with the amount thereof being in the range of 20 to 100% by mass relative to the said cellulose thereby obtaining the alkali cellulose; and (B) a method for producing a cellulose ether by reacting the alkali cellulose produced by the foregoing production method with an etherification agent.03-13-2014
536097000 Carboxyalkyl or salts thereof 5
536098000 Carboxymethyl or salts thereof 5
20120130065Guar process monitoring methods - Disclosed are methods relating to monitoring the processing of polysaccharides and, in particular, monitoring the processing of guar in order to improve guar yield and/or lower impurity concentration in the wash effluent fluid.05-24-2012
20130012696NEW HIGH VISCOSITY CARBOXYMETHYL CELLULOSE AND METHOD OF PREPARATION - The invention is directed to a process of preparing carboxymethyl cellulose comprising the steps of (a) reacting non-regenerated cellulose with an alkalization agent in the presence of water and isopropyl alcohol and (b) reacting the alkalized cellulose with monohaloacetic acid or a salt thereof, wherein 1.0 to 1.6 mol of the alkalization agent and 15 to 30 mol of water are used in step (a) and 0.5 to 0.8 mol of monohaloacetic acid or a salt thereof are used in step (b), each based on 1 mol of anhydroglucose unit of the cellulose. The invention also relates to carboxymethyl cellulose prepared by that process.01-10-2013
20130324711PROCESS FOR OBTAINING CARBOXYMETHYL CELLULOSE FROM AGRO-INDUSTRIAL RESIDUES AND CARBOXYMETHYL CELLULOSE AND USE THEREOF - An advantageous and effective process for obtaining carboxymethyl cellulose (CMC) from agro-industrial residues, comprising the steps of a) Preparing the raw material, wherein the raw material is washed, dried, grounded and washed again; b) a pumping step, wherein the product obtained from the step a) is reacted with sodium hydroxide; c) a synthesis step, wherein consists in grounding the pulp; adding a solution of isopropanol and distilled water under stirring at room temperature; adding NaOH aqueous solution up to the alkalization of the mixture; adding monochloroacetic acid in isopropanol; filtrating; suspending in methanol solution and neutralizing with acetic acid. The CMC obtained from the process can be employed in a several industrial processes.12-05-2013
20150094464METHOD FOR THE PREPARATION OF CELLULOSE ETHERS WITH A HIGH SOLIDS PROCESS, PRODUCT OBTAINED AND USES OF THE PRODUCT - The present invention provides a method for production of cellulose ethers in a high solids process substantially without use of organic solvents as reaction and/or washing medium. In the method of the invention the first alkalization step is carried out by using high solids content cellulose pulp and solid sodium hydroxide. This is followed by an etherification step where the solids content is preferably further increased and the use of solid etherification reactant is preferred. As no organic solvents are used as reaction media the invented method enables production of cellulose ethers directly from never dried pulp with significant savings in energy and investment costs. The method is especially suitable for the production of carboxymethyl cellulose sodium salt (CMC) with low degree of substitution (DS<0.3). The use of the resulting none or low water soluble carboxymethylated cellulosic fibres is suitable for example for producing microfibrillated cellulose.04-02-2015
20160102153PROCESS FOR MANUFACTURING LITHIUM CARBOXYMETHYL CELLULOSE - Prepare lithium carboxymethyl cellulose by treating sodium carboxymethyl cellulose with a weak acid to form an acid from of carboxymethyl cellulose and then treating the acid form of the carboxymethyl cellulose with lithium chloride.04-14-2016
536099000 Alkyl or cycloalkyl 4
20100274001METHOD FOR PRODUCING CELLULOSE ETHER DERIVATIVE - The present invention relates to a process for producing a cellulose ether derivative in an industrially convenient and efficient manner by reacting a low-crystalline powdery cellulose with an epoxy compound in the presence of a catalyst.10-28-2010
20100298555METHOD FOR PRODUCING METHYL CELLULOSE - The present invention relates to a process for efficiently producing methyl cellulose in an industrially convenient manner. The production process of the present invention includes the step of reacting cellulose with methanol in a subcritical state.11-25-2010
20140194618Method For Preparing Cellulose Ether Having Low Degree Of Polymerization And Cellulose Ether Prepared Thereby - Provided is a method for preparing a cellulose ether having a low degree of polymerization and undergoing less yellowing and a cellulose ether prepared thereby. Specifically, provided is a method for preparing a cellulose ether having a low degree of polymerization, the method including a step of bringing pulp and an alkali metal hydroxide solution into contact with each other or mixing them to obtain a corresponding alkali cellulose, a first depolymerization step of reacting the alkali cellulose with oxygen to adjust a viscosity reduction percentage of the alkali cellulose to from 10 to 95%, a step of reacting the depolymerized alkali cellulose with an etherifying agent, a step of washing and drying the reaction product to obtain a cellulose ether, and a second depolymerization step of bringing the cellulose ether into contact with hydrochloric acid to adjust a viscosity reduction percentage of the cellulose ether from 40 to 99.9%.07-10-2014
20160168271METHOD FOR PRODUCING ALKYL CELLULOSE06-16-2016

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