The pioneering work on polyurethane polymers was conducted by Otto Bayer and his coworkers in 1937 at the laboratories of I.G. Farben in Leverkusen, Germany.1 They recognized that using the polyaddition principle to produce polyurethanes from liquid diisocyanates and liquid polyether or polyester diols seemed to point to special opportunities, especially when compared to already existing plastics that were made by polymerizing olefins, or by polycondensation. The new monomer combination also circumvented existing patents obtained by Wallace Carothers on polyesters.2 Initially, work focused on the production of fibres and flexible foams. With development constrained by World War II (when PUs were applied on a limited scale as aircraft coating2), it was not until 1952 that polyisocyanates became commercially available. Commercial production of flexible polyurethane foam began in 1954, based on toluene diisocyanate (TDI) and polyester polyols. The invention of these foams (initially called imitation swiss cheese by the inventors2) was thanks to water accidentally introduced in the reaction mix. These materials were also used to produce rigid foams, gum rubber, and elastomers. Linear fibres were produced from hexamethylene diisocyanate (HDI) and 1,4-butanediol (BDO).
The first commercially available polyether polyol, poly(tetramethylene ether) glycol, was introduced by DuPont in 1956 by polymerizing tetrahydrofuran. Less expensive polyalkylene glycols were introduced by BASF and Dow Chemical the following year, 1957. These polyether polyols offered technical and commercial advantages such as low cost, ease of handling, and better hydrolytic stability; and quickly supplanted polyester polyols in the manufacture of polyurethane goods. Another early pioneer in PUs was the Mobay corporation.2 In 1960 more than 45,000 tons of flexible polyurethane foams were produced. As the decade progressed, the availability of chlorofluoroalkane blowing agents, inexpensive polyether polyols, and methylene diphenyl diisocyanate (MDI) heralded the development and use of polyurethane rigid foams as high performance insulation materials. Rigid foams based on polymeric MDI (PMDI) offered better thermal stability and combustion characteristics than those based on TDI. In 1967, urethane modified polyisocyanurate rigid foams were introduced, offering even better thermal stability and flammability resistance to low density insulation products. Also during the 1960s, automotive interior safety components such as instrument and door panels were produced by back-filling thermoplastic skins with semi-rigid foam.
In 1969, Bayer AG exhibited an all plastic car in Dusseldorf, Germany. Parts of this car were manufactured using a new process called RIM, Reaction Injection Molding. RIM technology uses high-pressure impingement of liquid components followed by the rapid flow of the reaction mixture into a mold cavity. Large parts, such as automotive fascia and body panels, can be molded in this manner. Polyurethane RIM evolved into a number of different products and processes. Using diamine chain extenders and trimerization technology gave poly(urethane urea), poly(urethane isocyanurate), and polyurea RIM. The addition of fillers, such as milled glass, mica, and processed mineral fibres gave arise to RRIM, reinforced RIM, which provided improvements in flexural modulus (stiffness) and thermal stability. This technology allowed production of the first plastic-body automobile in the United Sates, the Pontiac Fiero, in 1983. Further improvements in flexural modulus were obtained by incorporating preplaced glass mats into the RIM mold cavity, also known as SRIM, or structural RIM.
Starting in the early 1980s, water-blown microcellular flexible foam was used to mold gaskets for panel and radial seal air filters in the automotive industry. Since then, increasing energy prices and the desire to eliminate PVC plastisol from automotive applications have greatly increased market share. Costlier raw materials are offset by a significant decrease in part weight and in some cases, the elimination of metal end caps and filter housings. Highly filled polyurethane elastomers, and more recently unfilled polyurethane foams are now used in high-temperature oil filter applications.
Polyurethane foam (including foam rubber) is often made by adding small amounts of volatile materials, so-called blowing agents, to the reaction mixture. These simple volatile chemicals yield important performance characteristics, primarily thermal insulation. In the early 1990s, because of their impact on ozone depletion, the Montreal Protocol led to the greatly reduced use of many chlorine-containing blowing agents, such as trichlorofluoromethane (CFC-11). Other haloalkanes, such as the hydrochlorofluorocarbon 1,1-dichloro-1-fluoroethane (HCFC-141b), were used as interim replacements until their phase out under the IPPC directive on greenhouse gases in 1994 and by the Volatile Organic Compounds (VOC) directive of the EU in 1997 (See: Haloalkanes). By the late 1990s, the use of blowing agents such as carbon dioxide, pentane, 1,1,1,2-tetrafluoroethane (HFC-134a) and 1,1,1,3,3-pentafluoropropane (HFC-245fa) became more widespread in North America and the EU, although chlorinated blowing agents remained in use in many developing countries.3
Building on existing polyurethane spray coating technology and polyetheramine chemistry, extensive development of two-component polyurea spray elastomers took place in the 1990s. Their fast reactivity and relative insensitivity to moisture make them useful coatings for large surface area projects, such as secondary containment, manhole and tunnel coatings, and tank liners. Excellent adhesion to concrete and steel is obtained with the proper primer and surface treatment. During the same period, new two-component polyurethane and hybrid polyurethane-polyurea elastomer technology was used to enter the marketplace of spray-in-place load bed liners. This technique for coating pickup truck beds and other cargo bays creates a durable, abrasion resistant composite with the metal substrate, and eliminates corrosion and brittleness associated with drop-in thermoplastic bed liners.
The use of polyols derived from vegetable oils to make polyurethane products began garnering attention beginning around 2004, partly due to the rising costs of petrochemical feedstocks and partially due to an enhanced public desire for environmentally friendly green products.4 One of the most vocal supporters of these polyurethanes made using natural oil polyols is the Ford Motor Company.5
Pawling designs and manufactures rubber and plastic seals, actuators, clamps and structural bumpers and barriers for global industrial (1,2,3, 4), scientific (5) and architectural applications (6,7,8). The company?? Engineered Products Division has been IS0 9001 certified since 1994.
General industrial; building and construction; medical/lab/scientific; material handling; transportation; aerospace; energy; semiconductor processing; nuclear power. History
In 1945, a small rubber extrusion business with fifteen employees opened in Pawling, NY, to make gaskets for military ammunition cases. After WW II, the company diversified into plastics processing and launched several consumer products. In the mid-50s, Pawling Rubber Corporation entered into two strategic alliances. It acquired Presray Corporation, which had developed a successful inflatable gripper to handle fragile unfired grinding wheels, and formed an extrusion licensing agreement with the French firm FLT.
In the 1960s, the combined companies established a line of standard wall and corner guards for the architectural market; introduced fabric-reinforced rubber seals and expanded their inflatable seal, actuator and gripper business. Midway through the decade, Pawling diversified into mill mixing and extruding of high-purity silicone, then a leading-edge elastomer for electrical wire and cable insulation. By the end of the decade, the company had branched out into molding of silicone and plastics.
For the next thirty years, all three business areas grew steadily. Reflecting the diversification, the company shortened its name to Pawling Corporation in 1987.he next thirty years, all three business areas grew steadily. Reflecting the diversification, the company shortened its name to Pawling Corporation in 1987.
More recently, the company has focused on high-value branded product lines for demanding growth markets such as healthcare, medical and scientific, nuclear power, solar energy and semiconductor processing. Continuing that focus, in 2006 the company created the strategic business unit Pawling Scientific Products, which provides high-purity elastomeric products (5) to the environmental testing, analytical, and pharmaceutical lab markets.
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