# US 5,710,200 A · Natural rubber treated with viscosity stabilizers and production thereof

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- Number: US 5,710,200 A
- Document ID: US5710200A
- Status: Granted
- Kind: A
- Application number: 08/522,221
- Filed: 1995-09-01
- Granted: 1998-01-20
- Earliest claimed: 1993-03-02
- Assignees: Bridgestone Corporation
- Inventors: Hirotoshi Toratani; Eiji Nakamura; Hideki Aoyama; Yasushi Hirata
- Web page: https://patentgrep.com/patent/US5710200A

## CPC

- C08K 5/25: Carboxylic acid hydrazides
- C08K: Use of inorganic or non-macromolecular organic substances as compounding ingredients (paints, inks, varnishes, dyes, polishes, adhesives C09)

## Abstract

Natural rubber containing viscosity stabilizers is treated under drying conditions to result in 10% or less of the difference of gel content and 85% or more of molecular weight retention between before and after drying, and methods for manufacturing natural rubber comprise treating under drying conditions to result in 10% or less of the difference of gel content and 85% or more of molecular weight retention between before and after drying. Natural rubber containing viscosity stabilizers is treated with a strainer, and methods for manufacturing natural rubber comprise treating with a strainer after compounding hydrazide stearate into the natural rubber. Gelation (storage hardening) is suppressed and a decrease in molecular weight is prevented.

## Claims

### Claim 1

A method of treating natural rubber in which gelation of the natural rubber is suppressed, comprising the steps of:
drying the natural rubber;
before the natural rubber gels compounding into the natural rubber based on 100 parts by weight of the natural rubber 0.01 to 0.5 part by weight of a hydrazide compound as a viscosity stabilizer represented by the following general formula:
R--CONHNH.sub.2
wherein R is selected from the group consisting of an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms and an aryl group; and
reacting the hydrazide compound with functional groups of a polyisoprene molecule in the natural rubber to cap the functional groups.

### Claim 2 (depends on 1)

The method of treating natural rubber according to claim 1, wherein the hydrazide compound is present in an amount of 0.03 to 0.25 part by weight based on 100 parts by weight of the natural rubber.

### Claim 3 (depends on 1)

The method of treating natural rubber according to claim 1, wherein R is an alkyl group having 1 to 2 carbon atoms.

### Claim 4 (depends on 1)

The method of treating natural rubber according to claim 1, wherein the drying is conducted under conditions to result in a 10% or less difference of gel content and 85% or more molecular weight retention between before and after the drying.

### Claim 5 (depends on 1)

The method of treating natural rubber according to claim 1, wherein the drying is conducted at a temperature ranging from 80.degree. to 100.degree. C.

### Claim 6 (depends on 1)

The method of treating natural rubber according to claim 1, further comprising the step of:
treating the natural rubber with a strainer.

### Claim 7

A method of treating natural rubber in which gelation of the natural rubber is suppressed, comprising the steps of:
before the natural rubber gels compounding into the natural rubber based on 100 parts by weight of the natural rubber 0.01 to 0.5 part by weight of a hydrazide compound as a viscosity stabilizer represented by the following general formula:
R--CONHNH.sub.2
wherein R is selected from the group consisting of an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms and an aryl group;
drying the natural rubber; and
reacting the hydrazide compound with functional groups of a polyisoprene molecule in the natural rubber to cap the functional groups.

### Claim 8 (depends on 7)

The method of treating natural rubber according to claim 7, wherein the hydrazide compound is present in an amount of 0.03 to 0.25 part by weight based on 100 parts by weight of the natural rubber.

### Claim 9 (depends on 7)

The method of treating natural rubber according to claim 7, wherein R is an alkyl group having 1 to 2 carbon atoms.

### Claim 10

Natural rubber containing 0.01 to 0.5 part by weight of a hydrazide compound based on 100 parts by weight of the natural rubber as a viscosity stabilizer represented by the following general formula:
R--CONHNH.sub.2
wherein R is selected from the group consisting of an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group having 3 to 30 carbon atoms and an aryl group.

### Claim 11 (depends on 10)

The natural rubber according to claim 10, wherein the hydrazide compound is present in an amount of 0.03 to 0.25 part by weight based on 100 parts by weight of the natural rubber.

### Claim 12

Natural rubber containing 0.01 to 0.5 part by weight of a hydrazide compound based on 100 parts by weight of the natural rubber as a viscosity stabilizer represented by the following general formula:
R--CONHNH.sub.2
wherein R is an alkyl group having 1 to 2 carbon atoms.
