Abstract: A Cellulose acylate film, in which X-ray diffraction intensity satisfies following formulae and a half-value width of the peak at 2?2 is greater than 3° and not greater than 7°: 0.40?Ic2/(Iam2+Ic2)?0.75; Iam2I1+{(I3?I1)/(2?3?2?1)×(2?2?2?1)}; and Ic2=I2?Iam2, wherein when it is assumed that ?is the Bragg angle, 2?1 and 2?3 indicate 2? at which the intensity becomes the minimum in the 2? range of 4° to 5° and 14° to 16°, respectively, 2?2 indicates 2? at which the intensity becomes the maximum in the 2? range of 5° to 10°, and I1, I2 and I3 indicate a diffractive intensity at 2?1, 2?2 and 2?3, respectively.

Abstract: A protective film for polarizers which comprises a cellulose ester film and which, even when stored for long, suffers no film deformation failures such as ridging and protrusion failures; a process for producing the protective film; a polarizer; a process for producing the polarizer; and a liquid-crystal display employing the polarizer. The process for producing a protective film for polarizers is characterized by forming a melt comprising a cellulose ester and at least one member selected among compounds respectively represented by the following general formulae (1) to (3) into a continuous cellulose ester film by melt casting and winding the film into a roll. [Chemical formula 1] General formula (1) (In the formula, R1 to R5 each represents a substituent.) [Chemical formula 2] General formula (2) (In the formula, R1 to R6 each represents a substituent.

Abstract: A phase difference plate which comprises one sheet of polymer film containing a compound having a rod-shaped molecular structure and exhibiting a maximum absorption wavelength (?max) of less than 250 nm in an ultraviolet spectrum of its solution and which exhibits a retardation value as measured at a wavelength of 450 nm (Re450) of 60 to 135 nm and a retardation value as measured at a wavelength of 590 nm (Re590) of 100 to 170 nm, where the relationship: Re590?Re450?2 nm is satisfied. The phase difference plate functions as a ?/4 plate.

Abstract: A cellulose ester film that excels in uniformity of retardation as an optical property, especially uniformity of retardation in the direction of film width, and further contrast; a process for producing such a cellulose ester film; and making use of the film, an optical film, polarizing plate and liquid crystal display unit. There is provided a process characterized by subjecting, to melting film formation, a solid cellulose ester having been suspension washed with a poor organic solvent to cellulose ester in the presence of an antioxidant so that the content of free acids in the cellulose ester is 50 ppm or less.

Abstract: A polymer film, wherein when any point in the polymer film is taken as a center, a maximum difference between high and low film thicknesses within a range of 60 mm diameter is not more than 1 ?m, an RMS value of a film thickness is 0 ?m to 0.15 ?m or a difference between maximum and minimum values of slow axis angle in any 60 mm×60 mm square in the polymer film is 0° to 0.40°; and a solution casting film-forming method comprising: casting a dope on a support; peeling the casted film, wherein a dry wind of 3 m/s to 15 m/s is applied to the casted film within 15 seconds from the casting, and wherein before the dry wind is applied to the casted film, an air floating on a surface of the casted film has a wind velocity of less than 3 m/s.

Abstract: Described herein are implantable medical devices comprising a biocompatible polymer comprising a triggerable bioadhesive property that allows the device to adhere to body tissue. The triggerable bioadhesive property of the polymer can be triggered or activated by exposure to a stimulus. Also, the present invention pertains to methods of making an implantable medical device comprising a biocompatible polymer comprising a triggerable bioadhesive property that allows the device to adhere to body tissue.

Abstract: An objective is to provide a cellulose ester film which can reduce a manufacturing burden and a facility burden caused by drying and recovering of a solvent used in the production process, a manufacturing method of the cellulose ester film and an optical film, and to specifically provide a polarizing plate employing the optical film as an excellent polarizing plate protective film exhibiting reduced fluctuation of retardation property in the width direction and a liquid crystal display employing the polarizing plate. Also disclosed is a cellulose ester film containing at least one compound having a phenol structure and a phosphite ester structure in a molecule.

Abstract: Disclosed is an optical film having a hard coat layer on a cellulose ester film, which contains an ester compound composed of a furanose structure or a pyranose structures and a sum of a number of the furanose structures or the pyranose structure is 1 to 12, provided that a part of hydroxy groups of the furanose structure or the pyranose structure has been esterified and a part of hydroxy groups of the furanose structure or the pyranose structure remains.

Abstract: A cellulose ester and film thereof useful for remarkably improving optical properties such as optical isotropy are provided. The cellulose ester is adjusted so that the degree of substitution is from 2.90 to 2.965, the total of degrees of substitution at 2- and 3-positions is not less than 1.97, and the half height width of chemical composition expressed in degree of substitution is not more than 0.09. Such a cellulose ester maybe produced by a method for producing a cellulose ester, which comprises (i) an acylating step for acylating a cellulose with an acylating agent in the presence of a sulfuric acid catalyst, and (ii) a hydrolyzing step for hydrolyzing the acylated product in the presence of a sulfuric acid catalyst, and in which the acylation carried out with from 1.40 to 2.0 molar equivalents of the acylating agent relative to 1 mol of a hydroxyl group in the cellulose in the presence of 6.5 to 9.

Abstract: Disclosed are glucoside alkyl urethanes composed of units of the formula: A(O—CO—NH—R)3 wherein A represents a glucosyl unit of a starch hydrolysate molecule, the starch hydrolysate having a Dextrose Equivalent (D.E.) ranging from 1 to 47, (O—CO—NH—R) represents an N-alkyl aminocarbonyloxy group replacing a hydroxyl group of the glucosyl unit A, and wherein R represents a linear or branched, saturated or unsaturated alkyl group containing from 3 to 22 carbon atoms, and s represents the number of alkyl carbamate groups per glucosyl unit which number is expressed as degree of substitution (DS) with said DS value ranging from about 0.01 to about 2.0 which are useful as surface-active agents. Also disclosed are a method for their manufacture and compositions containing one or more glucoside alkyl urethanes. The glucoside alkyl urethanes have good to excellent tensio-active properties in combination with good biodegrability and they are suitable as surfactants for use in household and industrial applications, e.g.

Abstract: A cellulose acylate film, wherein at least one surface thereof has a contact angle of water of less than 55°, and wherein all or a part of hydroxyl groups of cellulose is substituted for an acyl group having 3 or more carbon atoms. The cellulose acylate film has an excellent bonding property to a polarizer and a small fluctuation in retardation with a variation in humidity.

Abstract: A cellulose acetate solution is filtrated with a filter medium formed of cellulose fiber. Hydroxyl groups on the filter medium are substituted to other functional groups. An acidic material is added to the cellulose acetate solution, and the filtration is preformed. In order to estimate the hydrogen ion concentration of the organic solvent, a sample solvent of thereof is mixed with water so as to transport hydrogen ions from the sample solvent to the water of a predetermined volume. Then the water is separated from the sample solvent, and the pH value of the water is measured with a pH meter. The result of the measurement is regarded as the pH value of the organic solvent.

Abstract: A method of making cellulose ester polymer comprises the steps of: pre-treating a cellulose source; esterifying the pretreated cellulose source to form a cellulose ester; and optionally hydrolyzing the cellulose ester. The pretreatment step further comprises: mixing, in a first stage, the cellulose source with a first solution of a weak acid and water, whereby the cellulose source being suspended in the first solution; de-liquefying the first stage suspension; mixing, in a second stage, the de-liquefied mass with a second solution of weak acid and water, whereby the mass being suspended in the second solution; and de-liquefying the second stage suspension.

Abstract: A nonionic water-soluble cellulose ether is characterized in that when 3 pbw of the nonionic water-soluble cellulose ether is added to a mixture of 90 pbw of cordierite, 10 pbw of ordinary Portland cement, and 33 pbw of water, immediately followed by kneading at 20° C. and 20 rpm, a maximum torque for kneading is reached within 180 seconds from the addition. It is suitable as an admixture for extrudable hydraulic compositions. The hydraulic composition to which the inventive admixture is added can be kneaded within a brief time into a uniform mass which is smoothly extrudable.

Abstract: A process for alkali saponification of polymer film is disclosed. The process comprises the steps of applying solution of an alkali onto a polymer film having a temperature of not lower than room temperature, and washing away the alkaline solution from the film.

Abstract: A nonionic water-soluble cellulose ether is characterized in that when 3 pbw of the nonionic water-soluble cellulose ether is added to a mixture of 90 pbw of cordierite, 10 pbw of ordinary Portland cement, and 33 pbw of water, immediately followed by kneading at 20° C. and 20 rpm, a maximum torque for kneading is reached within 180 seconds from the addition. It is suitable as an admixture for extrudable hydraulic compositions. The hydraulic composition to which the inventive admixture is added can be kneaded within a brief time into a uniform mass which is smoothly extrudable.

Abstract: To provide hard coat films having high hardness, and uniform durability against scratching and high flatness even with a small thickness and a large width, and to provide a method producing the same. The hard coat films are provided with an actinic ray curable resin on a cellulose ester film thereof, the cellulose ester film containing a UV absorber and 2 or more plasticizers. One of the plasticizers is a polyalcohol ester type and the other one is a non-phosphate ester type. The cellulose ester film is produced by biaxially stretching of a cellulose ester film with a total acyl substitution degree ranging from 2.6 to 2.9, a number average molecular weight ranging from 80,000 to 200,000, and a ratio of a weight-average molecular weight to a number average molecular weight ranging from 1.4 to 3.0.

Abstract: A resin composition, which comprises a biodegradable polymer and a biodegradable liquid crystalline polymer. The resin composition is useful for producing molded resin articles having good recyclability.

Abstract: The present invention relates to a purification method of hydroxypropylmethyl cellulose phthalate, more particularly to a method of preparing high-purity hydroxypropylmethyl cellulose phthalate through a simple crushing process which comprises: increasing fluidity of reaction product mixture by adding fluidization solvent as a post-treatment process; and spraying it into water through a spray nozzle. As a result, formation of fine granular hydroxypropylmethyl cellulose phthalate particles prevents inter-particle coagulation during the a post-treatment process, and phthalic anhydride reactant, free phthalic acid and remaining acetic acid solvent can be removed effectively.

Abstract: The present inventors have discovered that the solution rheology of cellulose ethers prepared from cellulose pulp is altered by mercerizing and recovering cellulose pulp before preparing the cellulose ethers. For example, the solution viscosity of carboxymethyl cellulose (CMC) produced from mercerized and recovered cellulose pulp is significantly greater than that produced from non-mercerized cellulose pulp. The present invention provides a method of preparing cellulose ethers comprising the steps of (a) obtaining mercerized and recovered cellulose pulp, and (b) converting the mercerized and recovered cellulose pulp into the cellulose ethers. According to one embodiment, the cellulose pulp is southern softwood kraft and the mercerized cellulose pulp has a TAPPI 230 om-89 viscosity of at most 12 cP. This method, however, may be applied to all cellulose pulps, regardless of their viscosities, including those which, when mercerized, have a viscosity greater than 12 cP.

Abstract: The present invention provides compositions comprising at least one GHB moiety bonded to at least one physiologically compatible carrier molecule. The compositions can enhance the uptake of the drug, deliver effective therapeutic doses in a time-delayed fashion, or can target specific organs.

Abstract: A cellulose acylate which is a polymer obtained by substituting cellulose with acyl groups in 2-, 3-, 6-positions. The total degree of acyl substitution in the 2- and 3-positions is regulated to from 1.70 to 1.90. The degree of 6-position acyl substitution is regulated to 0.88 or higher.

Abstract: A cellulose ester film is disclosed which comprises a polyhydric alcohol ester, which is an ester of one or more kinds of monocarboxylic acids with an aliphatic polyhydric alcohol, wherein the cellulose ester film has a water vapor transmission rate of from 20 to 260 g/m2·24 hours measured under conditions of 25° C. and 90% RH.

Abstract: Disclosed are an organic-inorganic hybrid film comprising a cellulose derivative and a polycondensation product of a condensation polymerizable reactive metal compound, wherein the film contains a plasticizer in an amount of 1 to 20% by weight and its manufacturing method.

Abstract: AGE precursors can be removed from blood, plasma or PBS buffer using a modified polymeric shaped body that can be produced by reaction of diaminoguanidine and/or triaminoguannidine with a staring polymeric shaped body carrying R—X residues, where R is an alkylene group that may or may not be substituted with a hydroxyl group and contains from 1 to 3 carbon atom, and X is a group that is substituted during the reaction by carrying residues Y, on to with diaminoguanidine, or with a starting polymeric shaped body during the reaction which diaminoguanidine and/or triaminoguannidine are added during the reaction.

Abstract: The invention relates to low solution viscosity cellulose triacetate and methods of making thereof. The invention also relates to films prepared from the low solution viscosity cellulose triacetate and articles containing the low solution viscosity cellulose triacetate.

Abstract: A method for forming II-type cellulose, which comprises introducing together a slurry having water and a I-type cellulose dispersed therein and water in the state of high temperature and high pressure to a tubular reactor (28) contacting the I-type cellulose with a hot water in a supercritical state or subcritical state for a predetermined time in the tubular reactor (28), to thereby cleave a part of the hydrogen bonds in the I-type cellulose and dissolve the I-type cellulose into the water in a supercritical state or subcritical state, cooling a cellulose solution discharged from the tubular reactor (28) in a cooler (30) to room temperature or lower, followed by allowing to stand, to thereby precipitate crystals of II-type cellulose having a molecular weight lower than that of the I-type cellulose, and separating the resultant II-type cellulose from a solvent. The method allows the preparation of pure II-type cellulose by the use of a simple process.

Abstract: In a cellulose acylate solution, cellulose acylate is dissolved in an essentially non-chlorinated solvent. The essentially non-chlorinated solvent is a mixture of a ketone having a solubility parameter of 19 to 21 and an ester having a solubility parameter of 19 to 21. The solution further contains a releasing agent.

Abstract: An annular fluid or packer fluid, and methods of making the same, that includes a water-miscible solvent, a viscosifying additive, a crosslinking agent, a crosslinking inhibitor having the facility to inhibit crosslinking between the viscosifying additive and the crosslinking agent, and an initiating agent having the facility to overcome an action of the crosslinking inhibitor and to initiate crosslinking between the viscosifying additive and the crosslinking agent, is shown and described. The fluid has a thermal conductivity of no more than about 0.25 btu/(hr·ft·° F.) and a potential to substantially increase its viscosity upon sitting for a selected period of time.

Abstract: The present invention is an enzyme-decomposable polymer compound having recyclable decomposition products. The polymeric compound is a glycopolymer of a saccharide having only glucopyranose rings and a second component. In addition, the glycopolymer may contain molecular chains having at least one type of repeating unit, which chains are crosslinked by a saccharide having only glucopyranose rings.

Abstract: A cellulose acetate film is produced from a solution of a cellulose acylate in a mixed solvent. The mixed solvent comprises a main solvent and an alcohol. The mixed solvent essentially does not contain chlorine atom. The main solvent comprises an ester and a ketone. The ester has a solubility parameter of 16 to 23. The ketone has a solubility parameter of 16 to 23. The alcohol has a solubility parameter of 20 to 30. The mixed solvent comprises the ester in an amount of 58 to 96 wt. %, the ketone in an amount of 2 to 15 wt. %, and the alcohol in an amount of 2 to 40 wt. %.

Abstract: A method of producing a cellueose ether that is predominantly substituted in the C2 position of the anhydroglucose unit of the cellulose is described. The regioselectively substituted saccharide ester produced according to the method of the present invention is selected from the group consisting of oligo-saccharide ester and polysaccharide ester, having a partial average degree of substitution (AS) at the C2 position of its anhydroglucose unit of at least 90% relative to the total AS. Also described is a blood plasma expander comprising the regioselectively substituted ester.

Abstract: Disclosed is a process for producing reactive cellulose for use in the manufacture of cellulose acetate having superior clarity by mercerizing hardwood cellulosic material and reacting it with an hydroxyalkylating agent to a degree of molar substitution ranging from 0.04 to 0.15 per anhydroglucose unit in cellulose.

Abstract: A method for the preparation of a glucose polymer having an ion-exchanging ability comprises the steps of drying a mixed aqueous solution containing a raw glucose polymer and a polyvalent carboxylic acid to thus form a uniform powdery mixture and then subjecting the powdery mixture to a heat treatment. The method of the present invention can ensure the achievement of a high reaction efficiency, is economically advantageous since it never requires the use of any expensive catalyst and does not require the use of any complicated step for the removal of impurities. The glucose polymer prepared by the method of the present invention is biodegradable and can be used in, for instance, various foods and/or builders.

Abstract: The present invention provides a cellulose acetate satisfying at least one requirement selected from the following requirements (A), (B) and (C), provided that the case where (B) alone is satisfied is excluded. Requirement (A): Bright spotty matters in sizes of 20 &mgr;m or more are not more than 20 units/mm3. Requirement (B): Blocking constant (K) is not more than 60. Requirement (C): The ratio (G′/G″) of storage modulus (G′) to loss modulus (G″) at a measuring frequency of 0.016 Hz is not more than 0.2.

Abstract: Cellulose mixed esters are disclosed having low molecular weights and low degrees of polymerization. These new cellulose mixed esters include cellulose acetate propionate and cellulose acetate butyrate. The esters exhibit solubility in a wide range of organic solvents with minimal viscosity increase, are compatible with a wide variety of resins, and are useful in coatings and inks compositions as binder resins and rheology modifiers.

Abstract: Carboxyalkylcellulose esters are disclosed having relatively low degrees of polymerization. These new carboxyalkylcellulose esters include carboxymethylcellulose acetate, carboxymethylcellulose acetate propionate, and carboxymethylcellulose acetate butyrate. The inventive esters exhibit solubility in a range of organic solvents, and are useful in coatings and ink compositions as binder resins and rheology modifiers.

Abstract: A thermoplastic cellulose derivative composition of the present invention contains, as a main component, a cellulose ester having an aliphatic polyester side chain having a repeat unit having 2 to 5 carbon atoms, wherein a rate of heating loss at 200° C. is 5 wt % or less, a melt viscosity at 200° C. and 1000 sec−1 is 50 to 300 Pa·sec, and a melt tension at the time of take-up at 200° C. and 100 m/min is 0.1 to 40 mN. The present invention can provide excellent fiber products by melt spinning of the composition.

Abstract: The present invention provides a cellulose triacetate which exhibits a satisfactory filtration performance Thus, the present invention provides a cellulose triacetate whose occlusion constant (K) determined by the following method is 70 or less. Method: the cellulose triacetate is dissolved in a solvent mixture of methylene chloride/methanol (9/1 w/w) to form a 16% by weight (as a solid concentration) solution, which is then filtered under a constant pressure at the filtration pressure of 3 kg/cm2 and the temperature of 25° C. using a muslin filter to determine a filtered volume with the lapse of time, from which the slope of a linear curve represented by t/V−t (wherein t is a filtration time (sec) and V is a filtered volume (ml)) is calculated to obtain an occlusion constant (K) where K=slope×2×104.

Abstract: An anticancer drug includes a compound represented by Formula (1): where R101 represents an acyl moiety of a saturated higher fatty acid, and R102 represents a hydrogen atom or an acyl moiety of a saturated higher fatty acid, and/or a pharmaceutically acceptable salt thereof.

Abstract: A process for alkali saponification of polymer film is disclosed. The process comprises the steps of applying solution of an alkali onto a polymer film having a temperature of not lower than room temperature, and washing away the alkaline solution from the film.

Abstract: A method of making cellulose polymer solution comprises dissolving a cellulose polymer raw material in a chlorine-free organic solvent system under a high temperature and a high pressure condition belonging to the nearcritical or the supercritical region of the system. By removing the solvent from the thus obtained cellulose polymer solution, cellulose polymer powders are also produced.

Abstract: The present invention provides a controlled release pharmaceutical composition comprising a polydextrose, a drug that is complexed with the polydextrose, and a polymer matrix having the drug complexed with the polydextrose, wherein the polymer matrix and the polydextrose provide for a time release of the drug. A method of therapeutically treating a patient for an illness employing the controlled release pharmaceutical composition is also provided.

Abstract: Improved anti-reflective coating compositions for use in integrated circuit manufacturing processes and methods of forming these compositions are provided. Broadly, the compositions are formed by heating a solution comprising a compound including specific compounds (e.g., alkoxy alkyl melamines, alkoxy alkyl benzoguanamines) under acidic conditions so as to polymerize the compounds and form polymers having an average molecular weight of at least about 1,000 Daltons. The monomers of the resulting polymers are joined to one another via linkage groups (e.g., —CH2—, —CH2—O—CH2—) which are bonded to nitrogen atoms on the respective monomers. The polymerized compound is mixed with a solvent and applied to a substrate surface after which it is baked to form an anti-reflective layer. The resulting layer has high k values and can be formulated for both conformal and planar applications.

Abstract: An anticancer drug includes a compound represented by Formula (1): where R101 represents an acyl moiety of a saturated higher fatty acid, and R102 represents a hydrogen atom or an acyl moiety of a saturated higher fatty acid, and/or a pharmaceutically acceptable salt thereof.

Abstract: Cellulosic fibrids can be made by mixing together under turbulent conditions viscose and a coagulating and regenerating liquor containing preformed fibrids to form a suspension of fibrids in a spent liquor, and collecting the fibrids from the spent liquor.

Abstract: A method for forming II-type cellulose, which comprises introducing together a slurry having water and a I-type cellulose dispersed therein and water in the state of high temperature and high pressure to a tubular reactor (28) contacting the I-type cellulose with a hot water in a supercritical state or subcritical state for a predetermined time in the tubular reactor (28), to thereby cleave a part of the hydrogen bonds in the I-type cellulose and dissolve the I-type cellulose into the water in a supercritical state or subcritical state, cooling a cellulose solution discharged from the tubular reactor (28) in a cooler (30) to room temperature or lower, followed by allowing to stand, to thereby precipitate crystals of II-type cellulose having a molecular weight lower than that of the I-type cellulose, and separating the resultant II-type cellulose from a solvent. The method allows the preparation of pure II-type cellulose by the use of a simple process.

Abstract: The present invention is directed to particulate drug carriers, such as vesicles, formed from polysaccharide derivatives. A polysaccharide bearing at least one non-ionic hydrophilic group attached to an individual monosaccharide unit is hydrophobised to form a derivative bearing at least one long chain alkyl residue. Particle formation is then induced in the presence of cholesterol. The particles are suited for entrapment or conjugation of pharmaceutically active ingredients.

Abstract: A regioselectively substituted member selected from the group consisting of oligo-saccharide ester and polysaccharide ester is disclosed. The ester has a partial average degree of substitution AS at the C2 position of its anhydroglucose unit of at least 90% relative to the total AS. Also disclosed is a method of producing the regioselectively substituted ester. The method entails reacting in the presence of a catalyst a dissolved or a highly swollen oligo-saccharide or polysaccharide with an esterification reagent.

Abstract: Cationized hydroxyalkylcelluloses, which are highly compatible with surfactants, are represented by the following formula (I): wherein R1, R2 and R3 represent a hydrogen atom or a group represented by the formula CH2CH2OCH2CH (OH) CH2N+(CH3)Cl−, etc.; and “n” is a number of from 50 to 2,000; which have a mobility distribution (&Dgr;U) determined by electrophoresis ranging from 0.1×105 10−5 to 2.0×105 10−5 cm2sec·V.