IP Library Granted Patent US 6,939,903
Granted Patent B2
US 6,939,903 · App. 10/417,031 · Granted Sep 6, 2005

Natural fiber-filled polyolefin composites

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Quick Facts
Patent No.
US 6,939,903
App. No.
10/417,031
Granted
Sep 6, 2005
Kind
B2
Abstract

A process for preparing a composite material is disclosed wherein the process comprises: A) sizing a natural fiber with a reactive organosilane; B) mixing the sized natural fiber with a polyolefin resin; and C) adding a functionalized polyolefin coupling agent to the mixture of the sized natural fiber and the polyolefin resin to provide said composite material.

Claims (26)

1. A process for preparing a composite material consisting essentially of the steps of:

A) sizing a natural fiber with a reactive organosilane;

B) mixing the sized natural fiber with a high density polyethylene resin; and

C) adding a functionalized polyolefin coupling agent to the mixture of the sized natural fiber and the high density polyethylene resin to provide said composite material;

wherein the functionalized polyolefin coupling agent is selected from the group consisting of maleic anhydride modified polypropylenes having a weight average molecular weight in the range of from about 20,000 to about 300,000 and comprising from about 0.6 to 310 moles of maleic anhydride per mole of polymer and maleic anhydride modified high density polyethylenes having a weight average molecular weight in the range of from about 20,000 to about 300,000 and comprising from about 0.6 to 310 moles of maleic anhydride per mole of polymer.

2. The process of claim 1 wherein the natural fiber is selected from the group consisting of wood flour, wood fiber, and agricultural fiber.

3. The process of claim 2 wherein the natural fiber is selected from the group consisting of wood flour, wood fiber, hemp, flax, and kenaf.

4. The process of claim 1 wherein the natural fiber is employed at a level in the range of from about 20 to about 85 weight % based on the weight of the total formulation.

5. The process of claim 1 wherein the reactive organosilane is selected from the group consisting of aminosilanes, epoxysilanes, alkoxysilanes, methacrylic silanes, mercaptosilanes, chlorosilanes, and oligomers, mixtures, and blends thereof.

6. The process of claim 1 wherein the reactive organosilane is γ-aminopropyltriethoxysilane.

7. The process of claim 1 wherein the reactive organosilane is selected from the group consisting of γ-aminopropyltriethoxysilane, γ-methacryloxypropyl trimethoxysilane, propyl triethoxy silane, vinyltriethoxysilane, vinyltri(2-methoxy-ethoxy)silane, β-(3,4-epoxycyclohexyl)-ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, n-β-(aminoethyl)-γ-aminopropyltrimethoxysilane, n-β-(aminoethoxyl)-γ-aminopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane, and silylating agents having the general formula

or an oligomer thereof, wherein R 1 , R 2 , and R 3 are independently selected from the group consisting of alkoxy, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, and organo-functional moieties.

8. The process of claim 1 wherein the natural fiber is employed at a level in the range of from about 40 to about 70 weight % based on the weight of the total formulation.

9. A composite material prepared by a process consisting essentially of the steps of:

A) sizing a natural fiber with a reactive organosilane;

B) mixing the sized natural fiber with a high density polyethylene resin; and

C) adding a functionalized polyolefin coupling agent to the mixture of the sized natural fiber and the high density polyethylene resin to provide said composite material;

wherein the functionalized polyolefin coupling agent is selected from the group consisting of maleic anhydride modified polypropylenes having a weight average molecular weight in the range of from about 20,000 to about 300,000 and comprising from about 0.6 to 310 moles of maleic anhydride per mole of polymer and maleic anhydride modified high density polyethylenes having a weight average molecular weight in the range of from about 20,000 to about 300,000 and comprising from about 0.6 to 310 moles of maleic anhydride per mole of polymer.

10. The composite material of claim 9 wherein the natural fiber is selected from the group consisting of wood flour, wood fiber, and agricultural fiber.

11. The composite material of claim 10 wherein the natural fiber is selected from the group consisting of wood flour, wood fiber, hemp, flax, and kenaf.

12. The composite material of claim 9 wherein the natural fiber is employed at a level in the range of from about 20 to about 85 weight % based on the weight of the total formulation.

13. The composite material of claim 9 wherein the reactive organosilane is selected from the group consisting of aminosilanes, epoxysilanes, alkoxysilanes, methacrylic silanes, mercaptosilanes, chlorosilanes, and oligomers, mixtures, and blends thereof.

14. The composite material of claim 9 wherein the reactive organosilane is selected from the group consisting of γ-aminopropyltriethoxysilane, γ-methacryloxypropyl trimethoxysilane, propyl triethoxy silane, vinyltriethoxysilane, vinyltri(2-methoxy-ethoxy)silane, β-(3,4-epoxycyclohexyl)-ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-mercaptopropyltrimethoxysilane, n-β-(aminoethyl)-γ-aminopropyltrimethoxysilane, n-β-(aminoethoxyl)-y-aminopropyltrimethoxysilane, γ-chloropropyltrimethoxysilane, and silylating agents having the general formula

or an oligomer thereof, wherein R 1 , R 2 , and R 3 are independently selected from the group consisting of alkoxy, alkyl, alkenyl, cycloalkyl, aryl, aralkyl, and organo-functional moieties.

15. The composite material of claim 9 wherein the reactive organosilane is γ-aminopropyltriethoxysilane.

16. The composite material of claim 9 wherein the natural fiber is employed at a level in the range of from about 40 to about 70 weight % based on the weight of the total formulation.

Assignments (9)
RELEASE OF SECURITY INTEREST RECORDED AT REEL 030872 FRAME 0810 Recorded Oct 16, 2018
From: WELLS FARGO BANK
To: ADDIVANT USA, LLC
Reel/Frame 047240/0580 →
RELEASE OF FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042447/0508 →
RELEASE OF SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042449/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 1, 2014
From: CHEMTURA CORPORATION
To: ADDIVANT USA LLC
Reel/Frame 031895/0895 →
SECURITY INTEREST Recorded Jul 19, 2013
From: ADDIVANT USA, LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION
Reel/Frame 030872/0810 →
CHANGE OF NAME Recorded Jan 14, 2013
From: CROMPTON CORPORATION
To: CHEMTURA CORPORATION
Reel/Frame 029699/0278 →
FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT. Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 026028/0622 →
INTELLECTUAL PROPERTY SECURITY RELEASE AGREEMENT Recorded Mar 21, 2011
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; ASCK, INC; BIOLAB COMPANY STORE, LLC; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIOLAB TEXTILES ADDITIVES, LLC; BIOLAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GT SEED TREATMENT, INC.; ISCI, INC; GREAT LAKES CHEMICAL GLOBAL, INC.; HOMECARE LABS, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; NAUGATUCK TREATMENT COMPANY; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); MONOCHEM, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC; WRL OF INDIANA, INC.; BIOLAB FRANCHISE COMPANY, LLC
Reel/Frame 026039/0142 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 22, 2010
From: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; AQUA CLEAR INDUSTRIES, LLC; ASCK, INC.; ASEPSIS, INC.; BIOLAB COMPANY STORE, LLC; BIOLAB FRANCHISE COMPANY, LLC; BIOLAB TEXTILE ADDITIVES, LLC; BIO-LAB, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; CROMPTON MONOCHEM, INC.; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; ISCI, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; MONOCHEM, INC.; NAUGATUCK TREATMENT COMPANY; RECREATIONAL WATER PRODUCTS, INC.; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); WEBER CITY ROAD LLC; WRL OF INDIANA, INC.
To: CITIBANK, N.A.
Reel/Frame 023998/0001 →