Patent classifications
C08G2650/24
Product-to-product process for preparation of low viscosity polyoxyalkylene polyether polyols
This invention relates to a semi-batch process for preparing low viscosity polyoxyalkylene polyether polyols (P) that have a narrow molecular weight distribution. This process comprises reacting a H-functional starter substance (S.sub.i), a H-functional starter substance (S.sub.x) and a H-functional starter substance (S.sub.c) with one or more alkylene oxides in the presence of a double metal cyanide (DMC) catalyst. The resultant polyoxyalkylene polyols (P) have a functionality of 2 to 8 and a hydroxyl number of 5 to 35 mg KOH/g polyol. In addition, the polyoxyalkylation can be completed with a low continuous addition of starter (CAOS) cap.
PROCESS FOR PREPARING POLYOXYALKYLENE POLYOLS BY THE CONTINUOUS ADDITION OF STARTER
This invention relates to an improved process for the preparation of a high molecular weight polyoxyalkylene polyether polyol by the continuous addition of starter (CAOS) process. This process enables a shorter cycle time while maintaining a low viscosity in high molecular weight polyoxyalkylene polyether polyols.
PRODUCT-TO-PRODUCT PROCESS FOR PREPARATION OF LOW VISCOSITY POLYOXYALKYLENE POLYOLS
This invention relates to a process for preparing low viscosity polyoxyalkylene polyols (P) that have a narrow molecular weight distribution. This process comprises reacting a H-functional starter substance (S.sub.i), a H-functional starter substance (S.sub.x) and a H-functional starter substance (S.sub.c) with one or more alkylene oxides in the presence of a double metal cyanide catalyst. The resultant polyoxyalkylene polyols (P) have a functionality of 2 to 8 and a hydroxyl number of 5 to 35 mg KOH/g polyol.
PRODUCT-TO-PRODUCT PROCESS FOR PREPARATION OF LOW VISCOSITY POLYOXYALKYLENE POLYOLS
This invention relates to process for preparing low viscosity polyoxyalkylene polyols (P) that have a narrow molecular weight distribution. This process comprises reacting a H-functional starter substance (S.sub.i), a H-functional starter substance (S.sub.x) and a H-functional starter substance (S.sub.c) with one or more alkylene oxides in the presence of a double metal cyanide catalyst. The resultant polyoxyalkylene polyols (P) have a functionality of 2 to 8 and a hydroxyl number of greater than 35 to 115 mg KOH/g polyol.
POLYMER COMPOSITIONS BASED ON PXE
New polymer compositions based on poly(2,6-dimethyl-1,4-phenylene oxide) and other high-softening-temperature polymers are disclosed. These materials have a microphase domain structure that has an ionically-conductive phase and a phase with good mechanical strength and a high softening temperature. In some arrangements, the structural block has a softening temperature of about 210 C. These materials can be made with either homopolymers or with block copolymers. When these polymers are combined with electrolyte salts, they can be used as electrolytes that have both high ionic conductivity and good mechanical properties.
Heavy oil demulsifier
This invention provides a composite type heavy oil demulsifier and its preparation methods. The demulsifier includes two effective constituents. The constituent I is an amino nonionic dendritic polyether and the constituent II is a dendritic ester acid. The structural formula is presented as Formula I and II, respectively. The demulsifier has good abilities in interfacing between oil and water and reducing viscosity. It has good demulsification performance in breaking crude oil emulsion and is useful in heavy crude oil production and petroleum refining.
AQUEOUS POLYGLYCIDOL SYNTHESIS WITH ULTRA-LOW BRANCHING
Disclosed herein are glycidol-based polymers, nanoparticles, and methods related thereto useful for a variety of applications, including, but not limited to, drug delivery. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
POROUS MEMBRANES INCLUDING PENTABLOCK COPOLYMERS AND METHOD OF MAKING THE SAME
The present disclosure provides a porous membrane made of pentablock copolymer. The porous membrane includes an ABCBA block copolymer and has a number of pores. The A block is immiscible with each of the B block and the C block, the B block has a glass transition temperature (T.sub.g) of 90 degrees Celsius or greater, and the C block has a T.sub.g of 25 degrees Celsius or less. The A block comprises a poly(alkylene oxide), a substituted epoxide, a polylactam, or a substituted carbonate; B block comprises a vinyl aromatic monomer or a polyalkylmethacrylate and C block comprises a polyacrylate, a polysiloxane or a polyisoprene. A method of making a porous membrane is also provided. The method includes forming a film or a hollow fiber from a solution including a solvent and solids containing an ABCBA block copolymer. The method further includes removing at least a portion of the solvent from the film or the hollow fiber and contacting the film or the hollow fiber with a nonsolvent.
White photosensitive resin composition, white spacer, light conversion layer, and light-emitting device
A white photosensitive resin composition, a white spacer, a light conversion layer, and a light-emitting device are provided. The white photosensitive resin composition includes a polymerizable compound (A), an alkali-soluble resin (B), a photopolymerization initiator (C), a solvent (D), and a white pigment (E). The polymerizable compound (A) includes an ethylenically-unsaturated monomer (A-1) represented by formula (I-1) and a thiol compound (A-2) having two or more thiol groups in one molecule, wherein based on 100 mass % of the polymerizable compound (A), a total content of the ethylenically-unsaturated monomer (A-1) and the thiol compound (A-2) is 10 mass % to 98 mass %. ##STR00001##
COMPOUND, COMPOSITION, BIOTISSUE EMBRITTLEMENT AGENT, BIOTISSUE SURFACE DETACHMENT METHOD, AND BIOTISSUE DETACHMENT KIT
Provided is a compound (Z) represented by the formula (1) or (2) below. In the formulas (1) and (2), Xs in each of the formulas (1) and (2) are each independently a carboxy group, a carboxylate group, or a monovalent group represented by the formula (3); at least one of Xs in each of the formulas (1) and (2) is a carboxy group or a carboxylate group; and at least one of Xs in each of the formulas (1) and (2) is a monovalent group represented by the formula (3) C(O)Y-(AO).sub.nR (3). In the formula (3), Y is O, NH, or S; A is a C2-C4 alkylene group; R is a hydrogen atom or a C1-C15 monovalent hydrocarbon group in which a hydrogen atom is optionally substituted with a C1-C10 alkoxy group; n is an integer of 4 to 1000; at least one of n As is an ethylene group; and when the formulas (1) and (2) each have multiple monovalent groups represented by the formula (3), each of Y, A, R, and n is the same or different among the monovalent groups.
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