摘要:
Oxymethylene copolymers having a high proportion of terminal alkyl ether groups and having terminal hydroxyalkylene groups are described. These polymers are distinguished by high thermal stability and high hot water resistance.Furthermore, a process for the preparation of oxymethylene copolymers is described in which the polymerization of at least one monomer forming —CH2—O— units is effected in the presence of at least one acetal of formaldehyde and of at least one initiator of cationic polymerization and the initiator of cationic polymerization is used in an amount of less than or equal to 10−4 mol %, based on the amount of the monomers present at the beginning of the polymerization and forming —CH2—O— units, in which starting materials of the polymerization are used such that the content of water and formic acid at the beginning of the polymerization is less than or equal to 40 ppm, and in which the initiator and/or the active polymer chains are deactivated by treatment of the prepared polymer with a base-containing protic solvent.
摘要:
Methods of producing macromolecular compositions and using same are provided. The method includes preparing a resin material; forming an acetyl group on the resin material; and oxidizing the acetyl group via a one-step reaction including reacting a sulfoxide and an acid with the acetyl group to form a ketoaldehyde group. The macromolecular compositions are capable of removing an effective amount of one or more constituents from a physiological solution, such as urea during dialysis therapy.
摘要:
The present invention is directed to ion triggerable, water-dispersible cationic polymers. The present invention is also directed to a method of making ion triggerable, water-dispersible cationic polymers and their applicability as binder compositions. The present invention is further directed to fiber-containing fabrics and webs comprising ion triggerable, water-dispersible binder compositions and their applicability in water-dispersible personal care products, such as wet wipes.
摘要:
Copolymers based on ethylenically unsaturated monomers and containing urethane groups, processes for their preparation and their use.Copolymers prepared by free-radical-initiated copolymerization of ethylenically unsaturated copolymerizable monomers, in which the copolymers are preferably synthesized froma) 25 to 85% by weight of ethylenically unsaturated hydrophobic monomers, andb) 1 to 50% by weight of ethylenically unsaturated monomers capable of salt formation, andc) 0.1 to 30% by weight of surface-active urethane derivatives containing ethylenically unsaturated carboxyl or carbamido radicals, andd) 0 to 10% by weight of other ethylenically unsaturated monomers different from a) to c) and containing functional radicals, ande) 0 to 5% by weight of ethylenically unsaturated carbonyl compounds, andf) 0 to 5% by weight of ethylenically polyunsaturated or polyfunctional monomers capable of crosslinking, andg) 0 to 5% by weight of molecular weight regulators, and, if aqueous dispersions or the copolymers isolated therefrom are present, these furthermore containh) 0.1 to 10% by weight, relative to the total amount of all monomer units in the copolymer, of emulsifiers and/or protective colloids, and, if desired, the copolymers are partially or completely neutralized and converted into water-soluble or colloid-water-dispersible copolymer salts and, if desired, are obtained in solid form.Use of the products as viscosity-increasing and rheology-modifying thickener substances in aqueous systems.
摘要:
Suspension polymerization of acrolein type compounds in the presence of appropriate surfactants results in the formation of microspheres in size ranging from 0.03 to 80 microns. Fluorescent and magnetic microspheres are obtained by carrying out the same polymerization in the presence of appropriate fluorochromic or ferrofluidic compounds, respectively. Hybrido-polyacrolein microspheres are obtained by grafting one type of such microspheres on another type. Immunomicrospheres were formed by binding covalently at physiological pH appropriate proteins to the microspheres. The immunomicrospheres can be used for various biological applications, such as specific markers for labeling cell surface receptors, for cell separation, for diagnostic purposes, etc.
摘要:
Homopolymeric polyaldehyde microspheres can be prepared in yields of up to about 90% by preparing an aqueous solution consisting essentially of a suitable concentration of an .alpha.,.beta.-ethylenically unsaturated aldehyde and a suitable concentration of an appropriate surfactant under suitable conditions such that the surfactant has a net electrostatic charge. The solution, which may also contain a ferrofluidic material, fluorescent dye or additional solvent, is then irradiated under an inert atmosphere with a sufficient dose of .gamma.-radiation to effect polymerization and the monodisperse homopolymeric polyaldehyde microspheres so produced are recovered. Copolymeric polyaldehyde microspheres can be prepared by adding to the solution a suitable concentration of a copolymerizable comonomer before initiating polymerization.Monodisperse homopolymeric or copolymeric polyaldehyde microspheres useful for affinity chromatography, cell labeling, cell separation and diagnostic purposes can thus be prepared in significantly higher yield than was previously obtainable.
摘要:
Mixtures of two distinct polyvinyl butyral grades, viz., one high viscosity and one low viscosity grade, both having a narrow molecular weight distribution exhibit good processing characteristics which nearly reach the performance of the high viscosity grades hitherto used.
摘要:
A process for storing a monomer phase which is liquid under the conditions of storage and comprises methacrylic monomers to an extent of ≧95% by weight and has been obtained by condensation out of a gaseous phase or by melting a crystalline phase, in a storage vessel, in which polymer of the monomer present in dissolved form in the liquid monomer phase is removed therefrom on the route from its generation into the storage vessel, and also a process for withdrawing liquid monomer phase from the storage vessel in which polymer of the monomer present in dissolved form in the monomer phase is likewise removed.
摘要:
A cross-linking polymer for an organic anti-reflective coating that is able to improve the uniformity of an ultra-fine photoresist pattern formed using a photolithography process and an ArF light source with 194 nm wavelength. Organic anti-reflective coatings including the same and a method for forming a photoresist pattern using the same are also disclosed. The disclosed cross-linking polymer is capable of preventing scattered reflection from a bottom film layer, eliminating standing wave effect due to alteration of thickness of the photoresist film, and increasing uniformity of the thickness of photoresist pattern. At the same time, the disclosed cross-linking pattern increases the etching velocity of the organic anti-reflective coating so that it can be easily removed.
摘要:
Novel polyacrylic acid resins are prepared by polymerizing a monomer selected from the group consisting of H.sub.2 C.dbd.CHCO.sub.2 X, H.sub.2 C.dbd.CR.sup.1 CO.sub.2 X, HR.sup.2 C.dbd.CHCO.sub.2 X, HR.sup.2 C.dbd.CR.sup.1 CO.sub.2 X, HR.sup.2 C.dbd.CHCOX, H.sub.2 C.dbd.CHCOX, H.sub.2 C.dbd.CR.sup.1 COX, HR.sup.2 C.dbd.CR.sup.1 COX, H.sub.2 C.dbd.CHCSO.sub.v X, HR.sup.2 C.dbd.CHCSO.sub.v X, HR.sup.2 C.dbd.CR.sup.1 CSO.sub.v X, H.sub.2 C.dbd.CR.sup.1 CSO.sub.v X, H.sub.2 C.dbd.CHCON(R.sup.3).sub.2, HR.sup.2 C.dbd.CHCON(R.sup.3).sub.2, H.sub.2 C.dbd.CR.sup.1 CON(R.sup.3).sub.2, OR HR.sup.2 C.dbd.CR.sup.1 CON(R.sup.3).sub.2, or a combination thereof, in the presence of at least 10% by weight of reaction components of an aromatic sulfonic acid or its salt, wherein:R.sup.1 and R.sup.2 are independently a substituted or unsubstituted alkyl, alkenyl, aromatic, aralkyl or alkaryl moiety of C.sub.1 to C.sub.20 ;R.sup.3 is independently hydrogen or a substituted or unsubstituted alkyl, alkenyl, aromatic, aralkyl or alkaryl moiety of C.sub.1 to C.sub.20 ; andX is hydrogen, substituted or unsubstituted alkyl, alkenyl, aromatic, aralkyl, or alkaryl moiety of C.sub.1 to C.sub.20 ; --CH.sub.2 CH.sub.2 (CF.sub.2 CF.sub.2).sub.n CF.sub.2 CF.sub.3, wherein n is 1-7; polyoxyalkylene; --C(R.sup.2).sub.2 R.sup.3 Y, wherein R.sup.3 is alkylene or polyoxyalkylene (or a combination thereof), and Y is --OSO.sub.3 H, --SO.sub.3 H, --CO.sub.2 H, --PO.sub.3 H, --OPO.sub.3 H, or a salt thereof; CF.sub.3 (CF.sub.2).sub.q -, wherein q is 1-11, hexafluorobutyl, tetrafluoropropyl, sodium, potassium, lithium, ammonium, or quaternary amine; and v is 0, 1, or 2.
摘要翻译:通过聚合选自H 2 C = CHCO 2 X,H 2 C = CR 1 CO 2 X,HR 2 C = CHCO 2 X,HR 2 C = CR 1 CO 2 X,HR 2 C = CHCOX,H 2 C = CHCOX,H 2 C = CR 1 COX,HR 2 C = CR 1 COX,H 2 C = CHCSOvX,HR2C = CHCSOvX,HR2C = CR1CSOvX,H2C = CR1CSOvX,H2C = CHCON(R3)2,HR2C = CHCON(R3)2,H2C = CR1CON(R3)2,或HR2C = CR1CON(R3) 在至少10重量%的芳族磺酸或其盐的反应组分的存在下,其中:R 1和R 2独立地是C 1 -C 20的取代或未取代的烷基,烯基,芳基,芳烷基或烷芳基部分; R 3独立地为氢或C1至C20的取代或未取代的烷基,烯基,芳族,芳烷基或烷芳基部分; 且X为氢,C1至C20的取代或未取代的烷基,烯基,芳族,芳烷基或烷芳基部分; -CH 2 CH 2(CF 2 CF 2)n CF 2 CF 3,其中n为1-7; 聚氧化烯 -C(R 2)2 R 3 Y,其中R 3是亚烷基或聚氧化烯(或其组合),Y是-OSO 3 H,-SO 3 H,-CO 2 H,-PO 3 H,-OPO 3 H或其盐; CF 3(CF 2)q - ,其中q为1-11,六氟丁基,四氟丙基,钠,钾,锂,铵或季胺; v为0,1或2。