C08G2310/00

DIHYDROXY LACTAM BASED POLYMERS, COMPOSITIONS AND APPLICATIONS THEREOF

A lactam-functionalized polymer is disclosed. The dihydroxy lactam based polymer includes polyesters, polycarbonates, polyethers, poly (ester ethers), poly (ester amides), poly imides, polyamides, poly acrylates and poly (ester imides), and polyurethanes. The applications of the dihydroxy lactam based polymers are also disclosed.

Sprayable polymer membrane for agriculture

A process for preparing a polymeric membrane for soil materials used in crop production comprising providing an aqueous dispersion of polyurethane and spraying the aqueous dispersion onto soil materials to be used in crop production to form a polymeric membrane.

Polyurethane Moisture Barrier Coatings Containing Thermoplastic Resins

A moisture barrier coating includes the reaction product of (A) at least one polyol and (B) at least one polyisocyanate. The moisture barrier coating further includes at least one amorphous thermoplastic material that forms a homogeneous mixture with the polyol, and is nonreactive with the polyol and with the polyisocyanate. A controlled release fertilizer, a method for the production of a controlled release fertilizer, and a moisture barrier coating composition are also disclosed.

Polyurethanes prepared from oligomeric polyol compositions and polyisocyanates

There is provided an oligomeric polyol composition having (a) an oligomeric network containing residues of at least one polyhydroxylated aromatic compound and residues of at least one polyol having at least three hydroxyl groups; and (b) a plurality of peripheral groups having one or more pendant hydroxyl groups bound to the oligomeric network by a plurality of linking units. The residues of the polyol may optionally contain one or more oxygen ether groups, one or more amino ether groups, or both of one or more oxygen ether groups and one or more amino ether groups. Reaction of the oligomeric polyols with isocyanate monomers affords a new class of polyurethanes having superior heat and water resistance. The new polyurethanes exhibit lower peak exotherms, typically less than 250° F. during in-mold polymerization. Articles prepared from polyurethanes incorporating such oligomeric polyol compositions exhibit flexural strengths and moduli in excess of 10,000 psi and 400,000 psi respectively, and outstanding green strength.

Composition comprising oligomeric polyol compositions and polyisocyanates

There is provided an oligomeric polyol composition having (a) an oligomeric network containing residues of at least one polyhydroxylated aromatic compound and residues of at least one polyol having at least three hydroxyl groups; and (b) a plurality of peripheral groups having one or more pendant hydroxyl groups bound to the oligomeric network by a plurality of linking units. The residues of the polyol may optionally contain one or more oxygen ether groups, one or more amino ether groups, or both of one or more oxygen ether groups and one or more amino ether groups. Reaction of the oligomeric polyols with isocyanate monomers affords a new class of polyurethanes having superior heat and water resistance. The new polyurethanes exhibit lower peak exotherms, typically less than 250° F. during in-mold polymerization. Articles prepared from polyurethanes incorporating such oligomeric polyol compositions exhibit flexural strengths and moduli in excess of 10,000 psi and 400,000 psi respectively, and outstanding green strength.

Method of preparing polyurethanes from oligomeric polyol compositions and polyisocyanates

There is provided an oligomeric polyol composition having (a) an oligomeric network containing residues of at least one polyhydroxylated aromatic compound and residues of at least one polyol having at least three hydroxyl groups; and (b) a plurality of peripheral groups having one or more pendant hydroxyl groups bound to the oligomeric network by a plurality of linking units. The residues of the polyol may optionally contain one or more oxygen ether groups, one or more amino ether groups, or both of one or more oxygen ether groups and one or more amino ether groups. Reaction of the oligomeric polyols with isocyanate monomers affords a new class of polyurethanes having superior heat and water resistance. The new polyurethanes exhibit lower peak exotherms, typically less than 250° F. during in-mold polymerization. Articles prepared from polyurethanes incorporating such oligomeric polyol compositions exhibit flexural strengths and moduli in excess of 10,000 psi and 400,000 psi respectively, and outstanding green strength.

Oligomeric polyol compositions

There is provided an oligomeric polyol composition having (a) an oligomeric network containing residues of at least one polyhydroxylated aromatic compound and residues of at least one polyol having at least three hydroxyl groups; and (b) a plurality of peripheral groups having one or more pendant hydroxyl groups bound to the oligomeric network by a plurality of linking units. The residues of the polyol may optionally contain one or more oxygen ether groups, one or more amino ether groups, or both of one or more oxygen ether groups and one or more amino ether groups. Reaction of the oligomeric polyols with isocyanate monomers affords a new class of polyurethanes having superior heat and water resistance. The new polyurethanes exhibit lower peak exotherms, typically less than 250° F. during in-mold polymerization. Articles prepared from polyurethanes incorporating such oligomeric polyol compositions exhibit flexural strengths and moduli in excess of 10,000 psi and 400,000 psi respectively, and outstanding green strength.

Method of preparing oligomeric polyol compositions

There is provided an oligomeric polyol composition having (a) an oligomeric network containing residues of at least one polyhydroxylated aromatic compound and residues of at least one polyol having at least three hydroxyl groups; and (b) a plurality of peripheral groups having one or more pendant hydroxyl groups bound to the oligomeric network by a plurality of linking units. The residues of the polyol may optionally contain one or more oxygen ether groups, one or more amino ether groups, or both of one or more oxygen ether groups and one or more amino ether groups. Reaction of the oligomeric polyols with isocyanate monomers affords a new class of polyurethanes having superior heat and water resistance. The new polyurethanes exhibit lower peak exotherms, typically less than 250° F. during in-mold polymerization. Articles prepared from polyurethanes incorporating such oligomeric polyol compositions exhibit flexural strengths and moduli in excess of 10,000 psi and 400,000 psi respectively, and outstanding green strength.

Coated granular fertilizer, method for producing coated granular fertilizer, and fertilizer compostion

Provided is a coated granular fertilizer, which includes a granular fertilizer and a resin coat that coats the granular fertilizer, in which the resin coat contains a urethane resin that is a polyaddition product between a polyisocyanate component and a polyol component, the polyisocyanate component includes an aromatic polyisocyanate, and the polyol component includes a castor oil-modified diol, an alkylene diol having 2 to 8 carbon atoms, and a compound having three or more hydroxyl groups.

FUNCTIONALIZED POLYGLYCINE-POLY(ALKYLENIMINE) COPOLYMERS, THEIR PREPARATION AND USE FOR PREPARING ACTIVE INGREDIENT FORMULATIONS AND SPECIAL-EFFECT SUBSTANCE FORMULATIONS

The invention relates to copolymers that contain structural units of the formula (I), of the formula (II) and optionally of the formula (III) NR.sup.1CHR.sup.3CHR.sup.4 (I), NHCOCHR.sup.7 (II), NHCHR.sup.9CHR.sup.10 (III), or structural units of the formula (IV), of the formula (V) and optionally of the formula (VI) NR.sup.1CHR.sup.3CHR.sup.4CHR.sup.5 (IV), NHCOCHR.sup.7CHR.sup.8 (V), NHCHR.sup.9CHR.sup.10CHR.sup.11 (VI), wherein R.sup.1 is a residue of the formula COR.sup.2, of the formula CONHR.sup.2 or of the formula CH.sub.2CH(OH)R.sup.12, R.sup.3, R.sup.4, R.sup.5, R.sup.7, R.sup.8, R.sup.9, R.sup.10 and R.sup.11 independently of each other represent hydrogen, methyl, ethyl, propyl or butyl, and R.sup.2 and R.sup.12 represent hydrogen or selected organic residues. These copolymers are characterized by good degradability and can be used, for example, for preparing active ingredient formulations.