Process for making crosslinked cable insulation using high melt strength ethylene-based polymer made in a tubular reactor and optionally modified with a branching agent
US-11912852-B2 · Feb 27, 2024 · US
US9340498B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9340498-B2 |
| Application number | US-201013145993-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2010 |
| Priority date | Jan 23, 2009 |
| Publication date | May 17, 2016 |
| Grant date | May 17, 2016 |
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A method of preparing polymer, the method comprising polymerizing one or more ethylenically unsaturated monomers of formula (I) where U is selected from H, C 1 -C 4 alkyl or halogen; V is halogen or of the form O-G where G is selected from —C(O)R 1 and —R 1 , or V is of the form NGG a where G is as defined above and G a is selected from H and R 1 , G and G a form together with N a heterocyclic ring, or V is of the form CH 2 G b where G b is selected from H, R 1 , OH, OR 1 , NR 1 2 , PR 1 2 , P(O)R 1 2 , P(OR 1 ) 2 , SR 1 , SOR 1 , and SO 2 R 1 ; and where the or each R 1 is independently selected from optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted alkylaryl, optionally substituted alkylheteroaryl, and an optionally substituted polymer chain, under the control of a RAFT agent of formula (II) or (III), where Y is a Lewis base moiety and Y* is an n-valent Lewis base moiety; X is O or NR 1 , R 1 is as defined above or forms together with Y or Y* and N a heterocyclic ring; m is an integer ≧1; n is an integer ≧2; and where R* is a m-valent radical leaving group that affords R*. which initiates free radical polymerization of the one or more ethylenically unsaturated monomers of formula (I), and R is a free radical leaving group that affords R. which initiates free radical polymerization of the one or more ethylenically unsaturated monomers of formula (I).
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The invention claimed is: 1. A RAFT agent of formula (XI), where X is NR 1 , R 1 is independently selected from optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted arylalkyl, optionally substituted heteroarylalkyl, optionally substituted alkylaryl, optionally substituted alkylheteroaryl, and an optionally substituted polymer chain; R* is a m-valent radical leaving group that affords R*. which initiates free radical polymerisation of one or more ethylenically unsaturated monomers; m is an integer ≧1; R* is selected from the group consisting of primary, secondary and tertiary cyanoalkyls, primary, secondary and tertiary alkoxycarbonylalkyls, and primary, secondary and tertiary carboxyalkyls; and where Y a is a Lewis base moiety selected from optionally substituted heteroaryl. 2. The RAFT agent of claim 1 , wherein R* is selected from cyanomethyl, 1-cyanoethyl, 2-cyanopropan-2-yl, ethoxycarbonylmethyl, 1-ethoxycarbonylethyl, 2-cyanobutan-2-yl, 1-cyanocyclohexyl, 2-cyano-4-methylpentan-2-yl, 2-cyano-4-methoxy-4-methylpentan-2-yl, 2-cyano-4-carboxybutan-2-yl, 2-cyano-5-hydroxypentan-2-yl, cyano(phenyl)methyl, 2-alkoxycarbonylpropan-2-yl, 1-(butylamino)-2-methyl-1-oxopropan-2-yl, phenyl(ethoxycarbonyl)methyl, 1-(cyclohexylamino)-2-methyl-1-oxopropan-2-yl, 1-(2-hydroxyethylamino)-2-methyl-1-oxopropan-2-yl, and 1-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-ylamino)-2-methyl-1-oxopropan-2-yl, 2-(4,5-dihydro-1H-imidazol-2-yl)propan-2-yl, and 2-(1-(2-hydroxyethyl)-4,5-dihydro-1H-imidazol-2-yl)propan-2-yl. 3. The RAFT agent of claim 1 selected from: where R x is selected from an optionally substituted alky group or R y ; and R y is an optionally substituted pyridyl group (all isomers). 4. The RAFT agent of claim 3 , wherein R* is selected from primary, secondary or tertiary cyanoalkyl.
having nitrogen atoms of dithiocarbamate groups bound to carbon atoms of six-membered aromatic rings · CPC title
Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals · CPC title
Use of a di- or tri-thiocarbonylthio compound, e.g. di- or tri-thioester, di- or tri-thiocarbamate, or a xanthate as chain transfer agent, e.g . Reversible Addition Fragmentation chain Transfer [RAFT] or Macromolecular Design via Interchange of Xanthates [MADIX] · CPC title
with substituted hydrocarbon radicals attached to ring carbon atoms · CPC title
Polymerisation using regulators, e.g. chain terminating agents {, e.g. telomerisation} · CPC title
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