Abstract:
Partially and fully fluorinated alkyl substituted thienothiophene monomers (and polymers thereof) wherein the monomers are represented by the formula: wherein R is a partially or fully fluorinated primary, secondary or tertiary alkyl having from 1 to 8 carbon atoms; and X and X′ are independently selected from the group consisting of H, F, Cl, Br, I, MgCl, —COR″, —C≡CH, and a polymerizable cyclic pi-conjugated carbon-ring structure optionally comprising S, N or O heteroatoms; wherein R′ is a primary, secondary or tertiary alkyl having from 1 to 6 carbon atoms, and R″ is H or a primary, or tertiary alkyl having from 1 to 6 carbon atoms.
Abstract:
This invention presents polymers and copolymers comprising repeating units of thieno[3,4-b]thiophene. Water-borne dispersions of such polymers and copolymers can be cast by conventional methods to provide uniform, thin films which possess utility in numerous electroactive applications including electrochromic displays, optically transparent electrodes and antistatic coatings. The compositions of this invention can be doped with conventional p-dopants or n-dopants. The invention also presents an aqueous process for preparing such compositions of matter.
Abstract:
The present invention is directed to an improvement in the wet tensile of a nonwoven web, whether the web is for a pre-moistened nonwoven wet wipe that is both safe to use and also flushes, disperses and finally biodegrades in appropriate environments or for a nonwoven web which requires high tensile strength when in contact with liquids. An improvement in the wet tensile of the nonwoven webs is achieved by incorporating a finite amount of poly(acrylic acid) into a polymeric binder system that is applied to the web.
Abstract:
Polyurethane prepolymer which can be converted into a final product by reaction with a curative or chain extending agent is made by reacting polyisocyanate with polyol in the presence of an amount of an aliphatic hydrocarbon which is a solvent for the polyisocyanate but a non-solvent for the prepolymer. In order to minimize the formation of unwanted oligomers the polyisocyanate is present in stoichiometric excess with respect to the polyol and the amount of hydrocarbon solvent present in the reaction mixture is limited so that a single liquid phase is present in the mixture during most of the synthesis. Solvent containing dissolved isocyanate is then removed from the prepolymer by liquid phase separation. A portion of the solvent can be distilled from this isocyanate solution for use in liquid--liquid extraction of residual isocyanate from the prepolymer, and the remaining solution of isocyanate in hydrocarbon solvent can be used in prepolymer synthesis. A preferred method of liquid--liquid extraction of unreacted polyisocyanate from prepolymer is by counter-current flow of the prepolymer and hydrocarbon solvent through a vertically elongated contact column. This technique can be used independently or in combination with the use of hydrocarbon solvent in the prepolymer synthesis.
Abstract:
The present invention is directed to novel poly(arylene ethers), their synthesis and use in electronics applications as low dielectric insulating layers such as spin-on materials in integrated circuits. The polymers have repeating units of the structure: ##STR1## wherein m=0.2 to 1.0; and n=1.0-m; and Ar.sub.1, Ar.sub.2 and Ar.sub.3 are individually divalent arylene radicals selected from the group consisting of; ##STR2##
Abstract:
Olefin/CO linear alternating copolymers which are useful in hot melt adhesive applications are disclosed. The linear alternating copolymers have melting points ranging from 50 to 165° C. and exhibit a combination of properties which are desired for hot melt adhesives. Single olefins or combinations of olefins ranging from ethylene to C12 olefins can be used to form the linear alternating copolymer.
Abstract:
Acetylenic alcohols and diols have been found which are soluble in liquid/supercritical CO.sub.2 and exhibit surface active properties. These alcohols and diols act as surfactants by lowering the surface tension between CO.sub.2 and mobile CO.sub.2 -phobic substances which are contacted with the CO.sub.2.
Abstract:
Water dispersible polymeric powders are prepared in liquid/supercritical CO.sub.2 by the sequential polymerization of a water soluble polymer after the polymerization of a non-water soluble polymer using core-shell polymerization technology.
Abstract:
Partially and fully fluorinated alkyl substituted thienothiophene monomers (and polymers thereof) wherein the monomers are represented by the formula: wherein R is a partially or fully fluorinated primary, secondary or tertiary alkyl having from 1 to 8 carbon atoms; and X and X′ are independently selected from the group consisting of H, F, Cl, Br, I, MgCl, MgBr, Mgl, Sn(R′)3, CH═CHR″, —OR″, —COOR″, —S—COR″, —B(OR″)2, —COR″, —C≡CH, and a polymerizable cyclic pi-conjugated carbon-ring structure optionally comprising S, N or O heteroatoms; wherein R′ is a primary, secondary or tertiary alkyl having from 1 to 6 carbon atoms, and R″ is H or a primary, secondary or tertiary alkyl having from 1 to 6 carbon atoms.
Abstract:
Hybrid polymeric compositions of epoxy resin and vinyl acetate polymer are combined in an aqueous emulsion also containing an emulsifying agent and isophoronediamine as a hardener for the epoxy resin. The emulsion is stable for long periods of time but can be cast and cured at room temperature, providing a one-pot system for the preparation of protective coatings, laminating adhesives, and the like. The vinyl acetate polymer must be emulsion polymerized independently of the epoxy resin and is preferably a copolymer of vinyl acetate with ethylene or n-butyl acrylate. The pot life of these hybrid polymer emulsions containing the epoxy hardening agent is at least one month and frequently as long as a year.