C08G2261/418

NORBORNENE CROSS-LINKED POLYMER AND METHOD FOR PRODUCING SAME
20180319912 · 2018-11-08 · ·

The present invention relates to a norbornene-based crosslinked polymer containing at least one member selected from the group consisting of dicyclopentadiene-based monomer units, tetracyclododecene-based monomer units, and tricyclopentadiene-based monomer units in an amount of 50% by mass or more, wherein the norbornene-based crosslinked polymer has a glass transition temperature of 240 C. or higher. Further, the present invention relates to a method for producing a norbornene-based crosslinked polymer as defined above, including step (1): heating a blend containing at least one member of the above monomer components, and a metathesis polymerization catalyst to a temperature lower than a deactivation temperature of the metathesis polymerization catalyst to carry out a primary curing; and step (2): heating a cured product obtained in the step (1) to a temperature equal to or higher than the deactivation temperature of the above metathesis polymerization catalyst to carry out a secondary curing.

AQUEOUS COMPOSITIONS BASED ON POLYALKENAMERS

The invention relates to aqueous compositions comprising a) at least one polymer PALK in the form of dispersed polymer particles, wherein the polymer PALK is obtainable by ring-opening metathesis polymerization of at least one cyclic olefin monomer, and b) at least one polymer P2 in the form of dispersed polymer particles, wherein the polymer P2 comprises no olefinically unsaturated CC-bond and has repeating units bearing at least one polar group.

The aqueous compositions are suitable in particular for producing sheetings and barrier coatings having a very good barrier action toward gases, such as air, oxygen, nitrogen, argon, carbon dioxide, and in particular toward oxygen and oxygenous gases, such as air. The sheetings and coatings also have very good mechanical properties, in particular a high elongation at break coupled with good tear strength.

Hydrocarbon-based polymers bearing dithiocyclocarbonate end groups

1) Hydrocarbon-based polymer of formula (I): ##STR00001## in which F.sup.1 and F.sup.2 have the respective formulae (IIa) and (IIb) or (IIa) and (IIb): ##STR00002## a process for its preparation, and use as an adhesive.

Associative polymers to control formation of particulate matter from ignitable compositions and related compositions, methods and systems

Described herein are associative polymers capable of controlling formation of particulate matter from a non-polar ignitable composition upon ignition of the non-polar ignitable composition, alone or in combination with control of a physical and/or chemical property of the non-polar compositions and related compositions, methods and systems. Associative polymers herein described have a non-polar backbone and functional groups presented at ends of the non-polar backbone, with a number of the functional groups presented at the ends of the non-polar backbone formed by associative functional groups capable of undergoing an associative interaction with another associative functional group with an association constant (k) such that the strength of each associative interaction is less than the strength of a covalent bond between atoms and in particular less than the strength of a covalent bond between backbone atoms.

Molecular sieves mediated unsaturated hydrocarbon separation and related compositions, materials, methods and systems

Described herein are compositions having an eight-membered monocyclic unsaturated hydrocarbon, methods and system to separate the eight-membered monocyclic unsaturated hydrocarbon from a hydrocarbon mixture including additional nonlinear unsaturated C.sub.8H.sub.2m hydrocarbons with 4?m?8, by contacting the hydrocarbon mixture with a 10-ring pore molecular sieve having a sieving channel with a 10-ring sieving aperture with a minimum crystallographic free diameter greater than 3 ? and a ratio of the maximum crystallographic free diameter to the minimum crystallographic free diameter between 1 and 2, the molecular sieve having a T1/T2 ratio?20:1 wherein T1 is an element independently selected from Si and Ge, and T2 is an element independently selected from Al, B and Ga, the 10-ring pore molecular sieve further having a counterion selected from NH.sub.4.sup.+, Li.sup.+, Na.sup.+, K.sup.+ and Ca.sup.++.

Polymer proppant material and method for producing same

A polymer material for proppant in the form of a metathesis-radically cross-linked mixture of oligocyclopentadienes and methylcarboxy norbornene esters is obtained by mixing dicyclopentadiene with methacrylic esters and polymer stabilizers, heating the mixture to a temperature of 150-220 C., holding at said temperature for 15-360 minutes, and then cooling down to 20-50 C. A radical initiator and a catalyst are added successively to the resultant mixture of oligocyclopentadienes and methylcarboxy norbornene esters. The polymer matrix is heated to a temperature of 50-340 C., is held at this temperature for 1-360 minutes and then is cooled to room temperature. A technical result achieved by implementation of the present invention is an increase in thermal strength of the proppant material, providing a compressive strength of at least 150 MPa at a temperature of not less than 100 C.

BUOYANCY COMPONENT INCLUDING DICYCLOPENTADIENE RESIN

A method of forming a buoyancy providing component, the method comprising locating a plurality of macrospheres in a mould, providing a composition including DCPD (dicyclo pentadiene) resin, a ruthenium or osmium catalyst, and a plurality of microspheres, dispensing the composition in liquid form into the mould to encapsulate the macrospheres, and allowing the mixture to set in the mould.

Hydrocarbon polymers having two azlactone end groups

1) Hydrocarbon polymer having two azlactone end groups ##STR00001##
F.sup.1 is formula (IIa) and F.sup.2 is formula (IIb): ##STR00002## g and d are 0, 1, 2 or 3; R.sup.14 and R.sup.15 are C.sub.1-C.sub.4 or a cyclohexyl radical; R.sup.1 to R.sup.12 represents hydrogen or alkyl with 1 to 22 carbon atoms; x and y are integers, x+y is 0 to 2; R.sup.13 is oxygen or sulphur or divalent CH.sub.2 n1, n2, m, p1 and p2 are an integer or equal to 0 and such that the molecular weight Mn of the polymer of formula (I) is between 400 and 100 000 g/mol; a process for preparation of the polymer; and use as adhesive in mixture with an amino compound with at least two amine groups.

AZIDE-MODIFIED OLEFIN AS POLYMERIC COUPLING AGENT
20180298120 · 2018-10-18 ·

This invention relates to a process for forming a long-chain branched polymer and a long-chain branched polymer resulting from the process. The process comprises reacting (a) a polyolefin base polymer with (b) a coupling agent comprising a polymeric coupling agent, optionally blended with a molecular coupling agent, the polymeric coupling agent being a modified polyolefin having a reactive coupling group at one or more terminal ends of the modified polyolefin chain, to couple the polyolefin base polymer (a) with the coupling agent (b) to form a long-chain branched polymer having a long-chain branching and/or higher surface energy relative to the polyolefin base polymer.

AZIDE-MODIFIED POLYNORBORNENE AS POLYMERIC COUPLING AGENT
20180298141 · 2018-10-18 ·

This invention relates to a process for forming a long-chain branched polymer and a long-chain branched polymer resulting from the process. The process comprises reacting (a) a polyolefin base polymer with (b) a coupling agent comprising a polymeric coupling agent, optionally blended with a molecular coupling agent, the polymeric coupling agent being a modified polyolefin having a reactive coupling group at one or more terminal ends of the modified polyolefin chain, to couple the polyolefin base polymer (a) with the coupling agent (b) to form a long-chain branched polymer having a long-chain branching and/or higher surface energy relative to the polyolefin base polymer.