Patent classifications
C08G18/5021
AMPHIPHILIC BLOCK COPOLYMER
The invention relates to block copolymer comprising i) A first block wherein at least 65 mol-% of the repeating units of the first block are repeating units of the formula (I)—[CH.sub.2—CH.sub.2—O]—, ii) A second block wherein at least 90 mol-% of the repeating units of the second block are repeating units of at least one of formulae (II) or (III), wherein the groups R.sup.1, R.sup.2, and R.sup.3 independent of each occurrence are selected from hydrocarbyl groups having 1 to 40 carbon atoms, which are optionally substituted by ether or hydroxyl groups, and wherein the groups R.sup.1 and R.sup.2 are optionally linked to each other such that a nitrogen heterocyclic structure is present, iii) A third block which is different from the first block and the second block and which is more hydrophobic than the first block.
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Hollow particles and manufacturing method thereof, pore forming material, particles for cosmetics, and weight reducing material
According to an embodiment of the present invention, provided are hollow particles which have a wall portion containing polyurethane or polyurea, have an internal porous structure, and have a plurality of opening spaces blocked by the wall portion in an outermost portion of the porous structure, and a manufacturing method thereof, and a pore forming material, particles for cosmetics, and a weight reducing material.
Processes for producing aromatic diamine-initiated polyether polyols
Processes are described for producing an aromatic diamine-initiated polyether polyol having a measured OH number of 300 to 500 mg KOH/g and a viscosity at 25° C. of 5000 to 50,000 mPas. The processes include a first alkoxylation step in which an alkylene oxide consisting essentially of propylene oxide is reacted with a starter consisting essentially of aromatic diamine at a molar ratio of propylene oxide to aromatic diamine of 1.4:1 to 2.0:1 to form an alkoxylated product; and a second alkoxylation step in which an alkylene oxide consisting essentially of propylene oxide is reacted with the alkoxylated product, in the presence of an added catalyst, until the ratio of moles of propylene oxide added in the process to the moles of aromatic diamine added in the process is 4:1 to 9:1.
Filled polyurethane or polyisocyanurate foam and method of making same
Polyurethane or polyisocyanurate foam stock and methods of manufacturing are described herein. The foam stock can include (a) a polyurethane or polyisocyanurate formed by the reaction of (i) one or more isocyanates selected from the group consisting of diisocyanates, polyisocyanates, and mixtures thereof, and (ii) one or more polyols; and (b) a filler present in an amount from greater than 50% to 90% by weight, based on the total weight of the foam stock. The density of the foam stock can be from 10 lb/ft.sup.3 to 35 lb/ft.sup.3. The flexural strength of the foam stock can be at least 100 psi. The resulting foam stock can be used to produce polyurethane or polyisocyanurate foam to be used in composite panels.
HFO-CONTAINING COMPOSITIONS AND METHODS OF PRODUCING FOAMS
Polyurethane foam-forming compositions, methods of producing polyurethane foams, polyurethane foams produced from such compositions made by such methods, as well as isocyanate-reactive compositions. The polyurethane foam-forming compositions include a polyisocyanate; a polyol blend, and a physical blowing agent composition. The polyol blend includes an aromatic amine-initiated polyether polyol having an OH number of at least 200 mg KOH/g and a functionality of at least 3, wherein (i) the aromatic amine-initiated polyether polyol having an OH number of at least 200 mg KOH/g is present in amount of at least 20% by weight, based on the total weight of polyol, and (ii) the polyol blend has a content of —C.sub.2H.sub.4O— units of 2 to 7% by weight, based on total weight of the polyurethane foam-forming composition. The physical blowing agent composition includes cis-1,1,1,4,4,4-hexafluoro-2-butene and trans-1,1,1,4,4,4-hexafluoro-2-butene.
FORMULATED POLYOL COMPOSITONS
Embodiments of the present disclosure are directed towards formulated polyol compositions that include a sucrose propoxylated, a propoxylated homopolymer triol, and an amine-initiated polyether alcohol.
Two-Part Urethane Adhesive Composition
There is provided a two-part urethane adhesive composition including: a main agent containing a polyisocyanate component (A); and a curing agent containing water and an active hydrogen-containing compound (B). The (B) contains a compound represented by Formula (4); the (A) contains a urethane prepolymer (A-3); an average active hydrogen concentration of the (B) is 0.50 to 3.50 mol/kg; an average active hydrogen concentration of the (B) and the water is 2.00 to 8.00 mol/kg. The main agent and the curing agent are mixed in such amounts as to satisfy conditions that: a ratio of the number of isocyanate groups of the (A) to the number of active hydrogens of the (B) is 1 to 5; and a ratio of the number of isocyanate groups of the (A) to the total number of active hydrogens of the (B) and the water is 0.5 to 2.5.
COMPOSITIONS AND USES OF CIS-1,1,1,4,4,4-HEXAFLUORO-2-BUTENE AND CYCLOPENTANE
Disclosed is a thermoset, thermal insulating foams having desirable and unexpectedly low thermal conductivity, and to compositions, method and systems which use and/or are used to make such foams comprising: (a) providing thermosetting foam forming component and a blowing agent for forming predominantly closed cells in the foam, wherein the blowing agent comprises: (i) cis-1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzzm(Z)) and cyclopentane, with the HFO-1336mzzm(Z) and cyclopentane in the blowing agent together comprising at least about 50% by weight of the total of all components in the blowing agent and (ii) the weight ratio of HFO-1336mzzm(Z) to cyclopentane in the blowing agent is from about 45:55 to less than 68:32 and (b) forming foam from said provided foamable composition.
Two component polyurethane composition
The invention relates to a polyurethane composition comprising one first component and one second component, said first component comprising an alkoxylated aromatic diol, a low molecular aliphatic or cycloaliphatic diol, a specific polybutadiene polyol and a specific polyetherpolyol, in specific ratios. The hardened composition is characterized by having good adhesion characteristics, a resistance which is only slightly dependent on the temperature, in the temperature range of −35 to +85° C. and also very high resistances. It is particularly suitable as a structural adhesive for bonding two substrates.
Waterborne azido-alkyne click compositions
A waterborne alternative polyurethane composition is provided which comprises a reaction product of: an azidated polyol; and a waterborne poly(alkynyl carbamate) prepolymer comprising a reaction product of a polyisocyanate and from 1 wt. % to 20 wt. % of an alkynol-polyether having a formula (I),
R.sub.1—R.sub.2—O—R.sub.3—OH (I),
wherein, R.sub.1=a monovalent group selected from either HC≡C— or HC≡C—CO—, R.sub.2=a divalent alkylene group from 1 to 8 carbon atoms, and may be straight chain or branched and may contain cyclic moieties, and R.sub.3=a polyethylene glycol with number average molecular weight from 300-1,200 g/mol, wherein the wt. % is based on the weight of the prepolymer, wherein reaction of the azidated polyol and the waterborne poly(alkynyl carbamate) occurs at a temperature of from 20° C. to 200° C. and optionally in the presence of a catalyst. The inclusion of an alkynol-polyether does not materially alter the performance properties and reactivity of the waterborne polyurethane composition relative to a solventborne polyurethane control composition. Inclusion of the alkynol-polyether reduces the need for organic solvents by allowing for the use of water as a carrier. The inventive waterborne alternative polyurethane compositions may find use in or as coatings, adhesives, sealants, films, elastomers, castings, foams, and composites.