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9010-85-9

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9010-85-9 Usage

Description

A synthetic copolymer containing from 0.5 to 2.0 molar percent of isoprene, the remainder, respectively, consisting of isobutylene. It is prepared by copolymerization of isobutylene and isoprene in methyl chloride solution, using aluminum chloride as the catalyst. After completion of polymerization, the rubber particles aretreated with hot water containing a suitable food-grade deagglomerating agent, such as stearic acid. Finally, the coagulum is dried to remove residual volatiles.

Chemical Properties

Different sources of media describe the Chemical Properties of 9010-85-9 differently. You can refer to the following data:
1. Viscosity controlling agent.
2. Butyl rubber has the chemical resistance characteristic of saturated hydrocarbons. Oxidative degradation is slow, and the rubber may be further protected by incorporating antioxidants. Isobutylene is the major component of bulk rubber. It provides good aging resistance and low gas permeability. Isoprene, a minor component, enhances vulcanizability.

Uses

Butyl rubber is formed from the polymerization of isobutene (isobutylene) with small amounts of chloroprene, isoprene, or butadiene and may be halogenated. The reaction is carried out in a closed system with an aluminum chloride catalyst. Butyl rubber is highly impervious to gases, which makes it the rubber best suited for inner tubes and tires, air chambers, adhesives, and dielectrics. Isobutene is an anesthetic and asphyxiant gas and can be hazardous in concentrations high enough to produce asphyxia. At these concentrations, explosion is an additional hazard.

Preparation

Commercial butyl rubbers generally contain 1-3 mole % isoprene. In a typical process, a solution of the monomers in methyl chloride is pre-cooled to -lOO°C and then fed continuously into the base of a reactor together with a solution of aluminium chloride (initiator) in the same diluent. The reaction is highly exothermic and in order to maintain the temperature at -100°C the reactor is fitted with a powerful stirrer and cooling coils containing liquid ethylene. The polymer forms as a granular slurry which is displaced continuously from the top of the reactor. The slurry passes into a flash tank where it is vigorously agitated with hot water. This treatment deactivates the initiator and extracts water-soluble products. At the same time the diluent and unreacted monomers are flashed off and are purified and re-used. Also at this point a lubricant and an antioxidant are introduced into the polymer. The lubricant, usually zinc stearate, prevents agglomeration of wet crumb and the antioxidant, usually phenyl-p-naphthylamine, reduces degradation during drying operations. The slurry then passes to a screen where wet polymer crumb is isolated. The crumb is dried at about 95-170°C, fed through an extruder and then hot milled. The object of these last operations is to compact the polymer and remove all traces of residual water. In butyl rubber the isoprene is present as random l,4-units and the copolymer thus has the following form:

Production Methods

The bulk of butyl rubber is made by a slurry process using aluminum chloride at 98–99°C and methyl chloride as a diluent. The extremely rapid reaction is unique, and proceeds via cationic polymerization to completion at 100°C in less than a second. Butyl rubber may be vulcanized by three basic methods: accelerated sulfur vulcanization, cross-linking with dioxime and related dinitroso compounds, and polymethylol– phenol resin cure. Halogenated butyl rubber allows broadened vulcanization latitude and rate, and enhanced covulcanization to general-purpose elastomers while it maintains the unique attributes of the basic butyl molecule.

Industrial uses

Butyl rubbers have outstanding impermeabilityto gases and excellent oxidation andozone resistance. The chemical inertness is furtherreflected in lack of molecular-weightbreakdown during processing, thus permittingthe use of hot-mixing techniques for betterpolymer/filler interaction.

Check Digit Verification of cas no

The CAS Registry Mumber 9010-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,1 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 9010-85:
(6*9)+(5*0)+(4*1)+(3*0)+(2*8)+(1*5)=79
79 % 10 = 9
So 9010-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H8.C4H8/c1-4-5(2)3;1-4(2)3/h4H,1-2H2,3H3;1H2,2-3H3

9010-85-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Butadiene, 2-methyl-, polymer with 2-methyl-1-propene

1.2 Other means of identification

Product number -
Other names 1-Propene, 2-methyl-, polymer with 2-methyl-1,3-butadiene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:9010-85-9 SDS

9010-85-9Upstream product

9010-85-9Downstream Products

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