Masterbatch with semi-crystalline polyolefin carrier resin

Patent metadata

Field	Value
Publication number	US-11952470-B2
Application number	US-201816961455-A
Country	US
Kind code	B2
Filing date	Feb 1, 2018
Priority date	Feb 1, 2018
Publication date	Apr 9, 2024
Grant date	Apr 9, 2024

Abstract

A coagent masterbatch comprising a semi-crystalline polyolefin carrier resin and an alkenyl-functional coagent. A peroxide curable formulation comprising the coagent masterbatch and a polyolefin compound. A method of making the masterbatch and formulation; a peroxide-cured polyolefin product prepared therefrom; a manufactured article comprising or made from the masterbatch, formulation, or product; and a method of using the manufactured article.

First claim

The invention claimed is:

1. A coagent masterbatch comprising (A) a semi-crystalline polyolefin carrier resin and (B) an alkylene-functional coagent disposed in the (A) semi-crystalline polyolefin carrier resin, and (C) an organic peroxide disposed on and/or in the (A) semi-crystalline polyolefin carrier resin; wherein the (A) semi-crystalline polyolefin carrier resin has a crystallinity of from 55.0 to less than 100 weight percent (wt %) as measured by Crystallinity Test Method using differential scanning calorimetry (DSC); wherein the (A) semi-crystalline polyolefin carrier resin is a semi-crystalline polyethylene or a semi-crystalline poly(ethylene-co-alpha-olefin) copolymer; wherein (A) has a density of greater than 0.935 gram per cubic centimeter (g/cm 3 ); wherein (A) is 70.0 to 99.9 weight percent (wt %) and (B) is from 30.0 to 0.1 wt % of the combined weight of constituents (A) and (B); and wherein (C) is from 0.01 to 4.5 wt % of the total weight of the coagent masterbatch.

2. The coagent masterbatch of claim 1 characterized by any one of limitations (i) to (x): (i) the coagent masterbatch is free of (D) an peroxide-curable polyolefin compound (host polymer) other than constituent (A); (ii) the coagent masterbatch further comprises at least one additive independently selected from optional additives (E) to (M): (E) an antioxidant, (F) a processing aid, (G) a colorant, (H) a metal deactivator, (I) an (unsaturated carbon-carbon bond)-free hydrolyzable silane, (J) a corrosion inhibitor, (K) a hindered amine light stabilizer, (L) an ethylene-based copolymer that is different than constituents (A) and (D) and is an ethylene/(C 4 -C 20 )alpha-olefin copolymer, an ethylene/unsaturated carboxylic ester copolymer, or a propylene/ethylene-based copolymer, and (M) a flame retardant; (iii) the coagent masterbatch does not contain an alkenyl-functional coagent-containing porous resin; (iv) the coagent masterbatch does not contain any porous resin; (v) the coagent masterbatch consists of constituents (A), (B) and (C); (vi) both (i) and (ii); (vii) both (i) and (iii); (viii) both (i) and (iv); (ix) the coagent masterbatch can be maintained for at least 20 days at a temperature of 23° C. without sweat out of the alkenyl-functional coagent as measured by Sweat Out Test Method (Quantitative); and (x) both (ix) and any one of (i) to (viii).

3. The coagent masterbatch of claim 1 wherein the (A) semi-crystalline polyolefin carrier resin has a melt index (I 2 , 190° C./2.16 kg load) of 0.1 to 20 grams per 10 minutes (g/10 min.) measured according to the Melt Index Test Method.

4. The coagent masterbatch of claim 1 wherein the (B) alkenyl-functional coagent is as described by any one of limitations (i) to (viii): (i) (B) is 2-allylphenyl allyl ether; 4-isopropenyl-2,6-dimethylphenyl allyl ether; 2,6-dimethyl-4-allylphenyl allyl ether; 2-methoxy-4-allylphenyl allyl ether; 2,2′-diallyl bisphenol A; O,O′-diallyl bisphenol A; or tetramethyl diallylbisphenol A; (ii) (B) is 2,4-diphenyl-4-methyl-1-pentene or 1,3-diisopropenylbenzene; (iii) (B) is triallyl isocyanurate; triallyl cyanurate; triallyl trimellitate; N,N,N′,N′,N″,N″-hexaallyl-1,3,5-triazine-2,4,6-triamine; triallyl orthoformate; pentaerythritol triallyl ether; triallyl citrate; or triallyl aconitate; (iv) (B) is trimethylolpropane triacrylate, trimethylolpropane trimethylacrylate, ethoxylated bisphenol A dimethacrylate, 1,6-hexanediol diacrylate, pentaerythritol tetraacrylate, dipentaerythritol pentaacrylate, tris(2-hydroxyethyl) isocyanurate triacrylate, or propoxylated glyceryl triacrylate; (v) (B) is a polybutadiene having at least 50 wt % 1,2-vinyl content or trivinyl cyclohexane; (vi) (B) is an alkenyl-functional organosiloxane of formula (I): [R 1 ,R 2 SiO 2/2 ] n (I), wherein subscript n is an integer greater than or equal to 3; each R 1 is independently a (C 2 -C 4 )alkenyl or a H 2 C═C(R 1a )—C(═O)—O—(CH 2 ) m — wherein R 1a is H or methyl and subscript m is an integer from 1 to 4; and each R 2 is independently H, (C 1 -C 4 )alkyl, phenyl, or R 1 ; (vii) (B) is an alkenyl-functional monocyclic organosiloxane of formula (II): (R 1 ) x Si(OR 2 ) (4-x) (II), wherein subscript x is an integer from 0 to 4; each R 1 is independently a (C 2 -C 4 )alkenyl or a H 2 C═C(R 1a )—C(═O)—O—(CH 2 ) m — wherein R 1a is H or methyl and subscript m is an integer from 1 to 4; and each R 2 is independently H, (C 1 -C 4 )alkyl, phenyl, or R 1 ; with the proviso that the alkenyl-functional monocyclic organosiloxane of formula (II) contains from 2 to 4 R 1 groups; (viii) a combination or any two or more of (i) to (vii).

5. The coagent masterbatch of claim 1 wherein the (C) organic peroxide is a monoperoxide of formula R O —O—O—R O or a diperoxide of formula R O —O—O—R—O—O—R O , wherein R is a divalent hydrocarbon group and each R O independently is a (C 1 -C 20 )alkyl group or (C 6 -C 20 )aryl group.

6. A method of storing a coagent masterbatch, the method comprising maintaining for at least 20 days the coagent masterbatch of claim 1 at a temperature from 20° to 25° C. to give a stored coagent masterbatch without sweat out of the alkenyl-functional coagent as measured by Sweat Out Test Method (Quantitative).

7. A peroxide-curable formulation comprising the coagent masterbatch of claim 1 , and (D) a peroxide curable (PC) polyolefin compound.

8. The peroxide-curable formulation of claim 7 characterized by any one of limitations (i) to (xiii): (i) the (D) PC polyolefin compound is a low density polyethylene (LDPE) having a density from 0.910 to 0.925 g/cm 3 ; (ii) the (D) PC polyolefin compound is a linear low density polyethylene (LLDPE) having a density from 0.910 to 0.925 g/cm 3 ; (iii) the (D) PC polyolefin compound is a medium density polyethylene (MDPE) having a density from 0.926 to 0.940 g/cm 3 ; (iv) the (D) PC polyolefin compound is a high density polyethylene (HDPE) having a density from 0.941 to 0.990 g/cm 3 ; (v) the (D) PC polyolefin compound is a polyethylene elastomer selected from an ethylene-propylene rubber (EPR), ethylene-1-butene rubber (EBR), and ethylene-1-octene rubber (EOR); (vi) the (D) PC polyolefin compound is an ethylene/(C 3 -C 20 )alpha-olefin) copolymer; (vii) the (D) PC polyolefin compound is an ethylene-propylene copolymer (EPP); (viii) the (D) PC polyolefin compound is an ethylene-propylene-diene monomer (EPDM) copolymer; (ix) the (D) PC polyolefin compound is a combination of any two or more of (i) to (viii); (x) the peroxide-curable formulation further comprises at least one additive that is not a constituent of the coagent masterbatch and is independently selected from optional additives (E) to (M): (E) an antioxidant, (F) a processing aid, (G) a colorant, (H) a metal deactivator, (I) an (unsaturated carbon-carbon bond)-free hydrolyzable silane, (J) a corrosion inhibitor, (K) a hindered amine light stabilizer, (L) an ethylene-based copolymer additive that is different than constituents (A) and (D) and is an ethylene/(C 4 -C 20 )alpha-olefin copolymer, an ethylene/unsaturated carboxylic ester copolymer, or a propylene/ethylene-based copolymer, and (M) a flame retardant; (xi) limitation (x) and any one of limitations (i) to (viii); (xii) (B) is from 0.1 to 20 wt % of the combined weight of constituents (A), (B) and (D); and (xiii) limitation (xii) and any one of limitations (i) to (xi).

9. A method of making a peroxide-curable formulation, the method comprising mixing together a divided solid form of the coagent masterbatch of claim 1 , and a (D) PC polyolefin compound in divided solid or melt form so as to give a mixture; and melt mixing or extruding the mixture so as to make the peroxide-curable (PC) formulation.

10. A method of peroxide curing a formulation in need thereof

Assignees

• Dow Global Technologies Llc

Inventors

• Li Dachao
• Sun Yabin
• Yang Yongyong
• Person Timothy J
• Cogen Jeffrey M
• Patel Rajen M

Classifications

• C08J3/226 Primary

  using a polymer as a carrier · CPC title

• C08K5/06

  Ethers; Acetals; Ketals; Ortho-esters · CPC title

• C08L23/06

  Polyethylene · CPC title

• C08L23/0815

  with aliphatic 1-olefins containing one carbon-to-carbon double bond · CPC title

• C08L23/12

  Polypropene · CPC title