Butyl rubber

Butyl rubber gloves

Butyl rubber is a synthetic rubber, a copolymer of isobutylene with isoprene. The abbreviation IIR stands for isobutylene isoprene rubber. Polyisobutylene, also known as "PIB" or polyisobutene, (C4H8)n, is the homopolymer of isobutylene, or 2-methyl-1-propene, on which butyl rubber is based. Butyl rubber is produced by polymerization of about 98% of isobutylene with about 2% of isoprene. Structurally, polyisobutylene resembles polypropylene, having two methyl groups substituted on every other carbon atom. Polyisobutylene is a colorless to light yellow viscoelastic material. It is generally odorless and tasteless, though it may exhibit a slight characteristic odor.

Butyl rubber has excellent impermeability, and the long polyisobutylene segments of its polymer chains give it good flex properties.

The formula for PIB is: –(–CH2–C(CH3)2–)n–

The formula for IIR is:

It can be made from the monomer isobutylene or CH2=C(CH3)2 only via cationic addition polymerization.

A synthetic rubber, or elastomer, butyl rubber is impermeable to air and used in many applications requiring an airtight rubber. Polyisobutylene and butyl rubber are used in the manufacture of adhesives, agricultural chemicals, fiber optic compounds, ball bladders, caulks and sealants, cling film, electrical fluids, lubricants (2 cycle engine oil), paper and pulp, personal care products, pigment concentrates, for rubber and polymer modification, for protecting and sealing certain equipment for use in areas where chemical weapons are present, as a gasoline/diesel fuel additive, and even in chewing gum. The first major application of butyl rubber was tire inner tubes. This remains an important segment of its market even today.

History

Isobutylene was discovered by Michael Faraday in 1825. Polyisobutylene (PIB) was first developed by the BASF unit of IG Farben in 1931 using a boron trifluoride catalyst at low temperatures and sold under the trade name Oppanol B. PIB remains a core business for BASF to this day.

It was later developed into butyl rubber in 1937, by researchers William J. Sparks and Robert M. Thomas, at Standard Oil of New Jersey's Linden, N.J., laboratory. Today, the majority of the global supply of butyl rubber is produced by just two companies, ExxonMobil, the successor to Standard Oil, and Polymer Corporation, a Canadian federal crown corporation established in 1942 to produce artificial rubber to substitute for overseas supply cut off by World War II. It was renamed Polysar in 1976 and the rubber component became a subsidiary, Polysar Rubber Corp. The company was privatized in 1988 with its sale to NOVA Corp which, in turn, sold Polysar Rubber in 1990 to Bayer AG of Germany. In 2005 Bayer AG spun off chemical divisions, including most of the Sarnia site, creating LANXESS AG, also of Germany.[1]

PIB homopolymers of high molecular weight (100 000 - 400 000 or more) are polyolefin elastomers: tough extensible rubber-like materials over a wide temperature range; with low density: 0.913-0.920, low permeability and excellent electrical properties.

In the 1950s and 1960s, halogenated butyl rubber (halobutyl) was developed, in its chlorinated (chlorobutyl) and brominated (bromobutyl) variants, providing significantly higher curing rates and allowing covulcanization with other rubbers such as natural rubber and styrene-butadiene rubber. Halobutyl is today the most important material for the inner linings of tubeless tires.

In the spring of 2013 two incidents of PIB contamination in the English Channel, believed to be connected, were described as the worst UK marine pollution 'for decades'. The RSPB estimated over 2,600 seabirds were killed by the chemical and hundreds more were rescued and decontaminated. [2]

Uses

Fuel and lubricant additive

Polyisobutylene can be reacted with maleic anhydride to make polyisobutenylsuccinic anhydride (PIBSA), which can then be converted into polyisobutenylsuccinimides (PIBSI's)by reacting it with various amines. These derivatives have interesting properties when used as an additive in lubricating oils and motor fuels. Polyisobutylene added in small amounts to the lubricating oils used in machining results in a significant reduction in the generation of oil mist and thus reduces the operator's inhalation of oil mist.[3] It is also used to clean up waterborne oil spills as part of the commercial product Elastol. When added to crude oil it increases the oil's viscoelasticity when pulled, causing the oil to resist breakup when it is vacuumed from the surface of the water.

As a fuel additive, polyisobutylene has detergent properties. When added to diesel fuel, it resists fouling of fuel injectors, leading to reduced hydrocarbon and particulate emissions.[4] It is blended with other detergents and additives to make a "detergent package" that is added to gasoline and diesel fuel to resist buildup of deposits and engine knock.[5]

Polyisobutylene is used in some formulations as a thickening agent.

Explosives

Polyisobutylene is often used by the explosives industry as a binding agent in plastic explosives such as C-4.[6] Polyisobutylene binder is used because it makes the explosive more insensitive to premature detonation as well as making it easier to handle and mold.

Sporting equipment

Butyl rubber is used for the bladders in sporting balls (e.g. Rugby balls, footballs, basketballs, netballs) to provide a tough, airtight inner compartment.

Damp proofing and roof repair

Butyl rubber sealant is used for damp proofing, rubber roof repair and for maintenance of roof membranes (especially around the edges). It is important to have the roof membrane fixed, as a lot of fixtures (i.e., air conditioner vents, plumbing and other pipes, etc.) can considerably loosen it.

Rubber roofing typically refers to a specific type of roofing materials that are made of ethylene propylene diene monomers (EPDM rubber). It is crucial to the integrity of such roofs to avoid using harsh abrasive materials and petroleum-based solvents for their maintenance.

Polyester fabric laminated to butyl rubber binder provides a single-sided waterproof tape that can be used on metal, PVC, and cement joints. It is used for repairing and waterproofing metal roofs.

Gas masks and chemical agent protection

Butyl rubber is one of the most robust elastomers when subjected to chemical warfare agents and decontamination materials. It is a harder and less porous material than other elastomers, such as natural rubber or silicone, but still has enough elasticity to form an airtight seal. While butyl rubber will break down when exposed to agents such as NH3 (ammonia) or certain solvents, it breaks down more slowly than comparable elastomers. It is therefore used to create seals in gas masks and other protective clothing.

Medical Stoppers

Butyl and Bromobutyl rubber are commonly used for manufacturing rubber stoppers used for sealing medicine vials and bottles.[7]

Chewing gum

Most modern chewing gum uses food-grade butyl rubber as the central gum base, which contributes not only the gum's elasticity but an obstinate, sticky quality which has led some municipalities to propose taxation to cover costs of its removal.[8]

Tires

Butyl rubber and halogenated rubber are used for the innerliner that holds the air in the tire.

Notes

  1. ↑ "Butyl Rubber: A Techno-commercial Profile". Chemical Weekly 55 (12): 207–211. November 3, 2009.
  2. ↑ "biggest UK pollution incident for decades". London Guardian.
  3. ↑ "Case Studies: Minimizing Worker Exposure to Mist in the Auto Industry". Green Engineering. Environment Protection Agency.
  4. ↑ Hammerle R, Schuetzle D, Adams W (October 1994). "A perspective on the potential development of environmentally acceptable light-duty diesel vehicles". Environ. Health Perspect. 102 (Suppl 4): 25–30. doi:10.1289/ehp.94102s425. PMC 1566943. PMID 7529704.
  5. ↑ "04-87 BASF Corp. v. United States" (PDF). Slip Opinions. United States Court of International Trade. 2004-07-15.
  6. ↑ "Explosives - Compounds". Global Security.
  7. ↑ "Halobutyl rubber for pharmaceutical stoppers and seals". ExxonMobil Chemical.
  8. ↑ "Making "Greener" Chewing Gum". American Chemical Society.

External links

This article is issued from Wikipedia - version of the Wednesday, December 23, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.