Polymer

Patent metadata

Field	Value
Publication number	US-10370467-B2
Application number	US-201515535606-A
Country	US
Kind code	B2
Filing date	Dec 10, 2015
Priority date	Dec 15, 2014
Publication date	Aug 6, 2019
Grant date	Aug 6, 2019

Abstract

A polymer that is capable of affording a heat storage material superior in humidity permeability and shape retention after phase transition and that is superior in molding processability is provided. The polymer includes constitutional units (A) derived from ethylene, constitutional units (B) represented by a specified formula, and optionally includes constitutional units (C) represented by another specified formula. Where the total number of the units (A), the units (B), and the units (C) is 100%, the number of the units (A) accounts for 70% to 99%, the total number of the units (B) and the units (C) accounts for 1% by weight to 30% by weight. Where the total number of the units (B) and the units (C) is 100%, the number of the units (B) accounts for 1% to 100% and the number of the units (C) accounts for 0% to 99%.

First claim

The invention claimed is:

1. A polymer comprising structural units (A) derived from ethylene and constitutional units (B) represented by formula (1) below and optionally comprising at least one type of constitutional units (C) selected from the group consisting of constitutional units represented by formula (2) below and constitutional units represented by formula (3) below,
wherein where the total number of the units (A), the units (B), and the units (C) is 100%, the number of the units (A) accounts for 70% to 99% and the total number of the units (B) and the units (C) accounts for 1% to 30%; and where the total number of the units (B) and the units (C) is 100%, the number of the units (B) accounts for 1% to 100% and the number of the units (C) accounts for 0% to 99%,

in formula (1) R represents a hydrogen atom or methyl group,
L 1 represents —CO—O—, —O—CO—, or —O—,
L 2 represents a single bond, —CH 2 —, —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —, —CH 2 —CH(OH)—CH 2 —, or —CH 2 —CH(CH 2 OH)—,
L 3 represents a single bond, —CO—O—, —O—CO—, —O—, —CO—NH—, —NH—CO—, —CO—NH—CO—, —NH—CO—NH—, —NH—, or —N(CH 3 )—,
L 6 represents an alkyl group having 14 to 30 carbon atoms;

in formula (2),
R represents a hydrogen atom or a methyl group,
L 1 represents —CO—O—, —O—CO—, or —O—,
L 4 represents an alkylene group having 1 to 8 carbon atoms,
L 5 represents a hydrogen atom, an epoxy group, —CH(OH)—CH 2 OH, a carboxyl group, a hydroxyl group, an amino group, or an alkylamino group having 1 to carbon atoms;

in each of the horizontal chemical formulae represented by L 1 , L 2 , or L 3 in formula (1) and formula (2) above, the left side thereof corresponds to the top side of formula (1) or formula (2) and the right side thereof corresponds to the bottom side of formula (1) or formula (2),
wherein a ratio A defined by formula (I) is 0.95 or less, and
wherein A=α 1 /α 0 (I) in formula (I),
wherein α 1 is a value obtained by a method comprising: measuring the absolute molecular weight and the intrinsic viscosity of a polymer by gel permeation chromatography using an apparatus equipped with a light scattering detector and a viscosity detector, plotting the measured data with logarithms of absolute molecular weights as abscissa against logarithms of intrinsic viscosities as ordinate, approximating with formula (I-I) in the least squares sense logarithms of absolute molecular weights and logarithms of intrinsic viscosities within the range of from the logarithm of the weight-average molecular weight of the polymer to the logarithm of the z-average molecular weight of the polymer on the abscissa, and representing the slope of the straight line showing formula (I-I) by α 1 ,
log [η 1 ]=α 1 log M 1 +log K 1   formula (I-I)

in formula (I-I), [η 1 ] represents the intrinsic viscosity (unit: dl/g) of the polymer, M 1 represents the absolute molecular weight of the polymer, and K 1 is a constant; and
wherein in formula (I), α 0 is a value obtained by a method comprising: measuring the absolute molecular weight and the intrinsic viscosity of a polyethylene standard substance 1475a by gel permeation chromatography using an apparatus equipped with a light scattering detector and a viscosity detector, plotting the measured data with logarithms of absolute molecular weights as abscissa against logarithms of intrinsic viscosities as ordinate, approximating with formula (I-II) in the least squares sense logarithms of absolute molecular weights and logarithms of intrinsic viscosities within the range of from the logarithm of the weight-average molecular weight of the polyethylene standard substance 1475a to the logarithm of the z-average molecular weight of the polymer on the abscissa, and representing the slope of the straight line showing formula (I-II) by α 0 ,
log [η 0 ]=α 0 log M 0 +log K 0   formula (I-II)

in formula (I-II), [η 0 ] represents the intrinsic viscosity (unit: dl/g) of the polyethylene standard substance 1475a, M 0 represents the absolute molecular weight of the polyethylene standard substance 1475a, and K 0 is a constant; and
wherein in the measurement of the absolute molecular weight and the intrinsic viscosity of the polymer and the polyethylene standard substance 1475a by gel permeation chromatography, the mobile phase is orthodichlorobenzene and the measurement temperature is 155° C.

2. The polymer according to claim 1 , the fusion enthalpy (ΔH) of which observed within a temperature range of not lower than 10° C. and lower than 60° C. by differential scanning calorimetry is 50 J/g or more.

3. The polymer according to claim 1 , having been crosslinked.

4. The polymer according to claim 1 , having a gel fraction of 20% or more.

5. The polymer according to claim 1 , wherein where the total number of all the constitutional units contained in the polymer is 100%, the total number of the units (A), the units (B), and the units (C) accounts for 90% or more.

6. A molded article comprising the polymer according to claim 1 .

7. A foamed article comprising the polymer according to claim 1 .

8. A resin composition comprising a polymer (1) that is the polymer according to claim 1 , and a polymer (2) that is a polymer whose melting peak temperature or glass transition temperature observed by differential scanning calorimetry is 50° C. to 180° C. except for the exceptive polymers defined below, wherein where the total amount of the polymer (1) and the polymer (2) is 100% by weight, the content of the polymer (1) is 30% by weight to 99% by weight and the content of the polymer (2) is 1% by weight to 70% by weight;
wherein exceptive polymer is any polymer comprising constitutional units (A) derived from ethylene and constitutional unit (B) represented by formula (1) below and optionally comprising at least one type of constitutional units (C) selected from the group consisting of constitutional units represented by formula (2) below and constitutional units represented by formula (3) below, where the total number of the units (A), the units (B), and the units (C) is 100%, the number of the units (A) accounts for 70% to 99% and the total number of the units (B) and the units (C) accounts for 1% to 30%; where the total number of the units (B) and the units (C) is 100%, the number of the units (B) accounts for 1% to 100% and the number of the units (C) accounts for 0% to 99%,

in formula (1),
R represents a hydrogen atom or a methyl group,
L 1 represents —CO—O—, —O—CO—, or —O—,
L 2 represents a single bond, —CH 2 —, —CH 2 —CH 2 —, —CH 2 —CH 2 —CH 2 —, —CH 2 —CH(OH)—CH 2 —, or —CH 2 —CH(CH 2 OH)—,
L 3 represents a single bond, —CO—O—, —O—CO—, —O—, —CO—NH—, —NH—CO—, —CO—NH—CO—, —NH—CO—NH—, —NH—, or —N(CH 3 )—,
L 6 represents an alkyl group having 14 to 30 carbon atoms;

in formula (2),
R represents a hydrogen atom or a methyl group,
L 1 represents —CO—O—, —O—CO—, or —O—,
L 4 represents an alkylene group having 1 to 8 carbon atoms,
L 5 represents a hydrogen atom, an epoxy group, —CH(OH)—CH 2 OH, a carboxyl group, a hydroxyl group, an amino group, or an alkylamino

Assignees

• Sumitomo Chemical Co

Inventors

• Miura Yu
• Kawashima Yasutoyo
• Ueda Kohei
• Nozue Yoshinobu

Classifications

• C08J2201/026

  Crosslinking before of after foaming · CPC title

• C08K5/14

  Peroxides · CPC title

• C08F8/00

  Chemical modification by after-treatment (graft polymers, block polymers, crosslinking with unsaturated monomers or with polymers C08F251/00 - C08F299/00; of conjugated diene rubbers C08C) · CPC title

• C08F8/14

  Esterification · CPC title

• C08J2323/26

  modified by chemical after-treatment · CPC title