Resins acrylic

The methyl, ethyl, and butyl esters of acrylic and methacrylic acids are polymerized under the influence of heat, light, and peroxides. The polymerization reaction is exothermic and may be carried out in bulk for castings, or by emulsion, or in solution. The molecular weight decreases as the temperature and catalyst concentration are increased. The polymers are noncrystalline and thus very clear. Such resins are widely used because of their clarity, brilliance, ease of forming, and light weight. They have excellent optical properties and are used for camera, instrument, and spectacle lenses. 

Because of their excellent dielectric strength they are often used for high-voltage line spacers and cable clamps. Emulsions are widely applied as textile finishes and paints. 

Ethylene-acrylate copolymers have been used as modifying agents to improve impact strength and compatibility of other polymers [24, 25]. 

It should be noted that despite their widespread acceptance in the coating industry as a cross-linker of choice for many high performance coatings, aminoplast cross-linkers face many challenges. In the most developed countries, the trend is away from formaidehyde-based polymers due to the highly toxic nature of formaldehyde. 

The terms pure acrylics or 100 % acrylic resin is frequently used to differentiate acrylic resins derived strictly from (meth)acrylate 

---

C4H8O, CH3COCH2CH3. Colourless liquid with a pleasant odour, b.p. 80°C. It occurs with propanone in the products of the destructive distillation of wood. Manufactured by the liquid or vapour phase dehydrogenation of 2-butanol over a catalyst. Used as a solvent, particularly for vinyl and acrylic resins, and for nitrocellulose and cellulose acetate, also for the dewaxing of lubricating oils. U.S. production 1978 300 000 tonnes. 

CHi=CMeCOOH. Colourless prisms m.p. 15-16 C, b.p. 160-5 C. Manufactured by treating propanone cyanohydrin with dilute sulphuric acid. Polymerizes when distilled or when heated with hydrochloric acid under pressure, see acrylic acid polymers. Used in the preparation of synthetic acrylate resins the methyl and ethyl esters form important glass-like polymers. 

CH =C(CH3)C02Me. Colourless liquid b.p. lOO C. Manufactured by healing acetone cyanohydrin with methanol and sulphuric acid. It is usually supplied containing dissolved polymerization inhibitor, on removal of which it is readily polymerized to a glass-like polymer. See acrylate resins. 

Perspex Trade name for cast polymethylmethacrylate sheet - an acrylic resin. 

CHjlCH COOH. Colourless liquid having an odour resembling that of ethanoic acid m.p. 13 C, b.p. I4I°C. Prepared by oxidizing propenal with moist AgO or treating -hy-droxypropionitrile with sulphuric acid. Slowly converted to a resin at ordinary temperatures. Important glass-like resins are now manufactured from methyl acrylate, see acrylic resins. Propenoic acid itself can also be polymerized to important polymers - see acrylic acid polymers. 

As a pharmaceutical, methyl salicylate is used in liniments and ointments for the relief of pain and for rheumatic conditions. As a flavor and fragrance agent, it is used in confectioneries, dentifrices, cosmetics, and perfumes. Other commercial applications for methyl salicylate are as a dye carrier, as a uv-light stabilizer in acrylic resins, and as a chemical intermediate. The May 1996 price was 5.50/kg (18). 

Acrylic Resins. The first synthetic polymer denture material, used throughout much of the 20th century, was based on the discovery of vulcanised mbber in 1839. Other polymers explored for denture and other dental uses have included ceUuloid, phenolformaldehyde resins, and vinyl chloride copolymers. Polystyrene, polycarbonates, polyurethanes, and acryHc resins have also been used for dental polymers. Because of the unique combination of properties, eg, aesthetics and ease of fabrication, acryHc resins based on methyl methacrylate and its polymer and/or copolymers have received the most attention since their introduction in 1937. However, deficiencies include excessive polymerization shrinkage and poor abrasion resistance. Polymers used in dental appHcation should have minimal dimensional changes during and subsequent to polymerization exceUent chemical, physical, and color stabiHty processabiHty and biocompatibiHty and the abiHty to blend with contiguous tissues. 

Thickness of recording dye layer = 10 nm when spincoated from a CHCl solution on an acrylate resin plate. 

Medium 20,000-50,000 4 Acrylic resins, plastics, PVC, ammonium chloride, DMT, copper compounds, lead Ferroalloys, fluorspar, nickel Iron, potash, glass-making mixtures... 

A number of thermosetting acrylic resins for use as surface coatings have appeared during recent years. These are generally complex copolymers and terpolymers such as a styrene-ethyl acrylate-alkoxy methyl acrylamide... 

Carbon, hydrogen and possibly oxygen Resin and derivatives Natural drying oils Cellulose derivatives Alkyd resins Epoxy resins (uncured) Phenol-formaldehyde resins Polystyrene Acrylic resins Natural and synthetic rubbers Carbon monoxide Aldehydes (particularly formaldehyde, acrolein and unsaturated aldehydes) Carboxylic acids Phenols Unsaturated hydrocarbons Monomers, e.g. from polystyrene and acrylic resins... 

Several approaches have been disclosed to make release coatings that can be printed with ink jet or laser jet printers (e.g., to make linerless labels). For example, Khatib and Langan [164] disclose a blend of two different acrylate functional silicones, one with a high level of acrylate functionality to provide the printability and one with a low level of acrylate functionality to provide easy PSA release. Lievre and Mirou [165] describe an aqueous blend of a crosslinkable silicone and poly(vinyl alcohol-vinyl acetate) resins while Shipston and Rice describe a blend of acrylic resin and a surfactant [166]. 

Table 3 lists the selected properties [16] that we have measured for several commercially available acrylate resins manufactured by the Sartomer Company and the Rohm and Haas Company. The resins were cured in an AECL Gammacell Model 240. The temperature rise was measured for an 8-g sample using Acsion s (formerly AECL Radiation Applications Branch) Gamma Calorimetry method [17]. All of this information is being used to evaluate the applicability of EB-cured acrylate adhesives for repairing composite structures. Combinations of these adhesives can be used to create electron-curable adhesives suitable for composite repair. 

Electron-cured panel Hercules AS4, 5HS, 6K fiber, FW3 epoxy acrylate resin. 

Acrylharz, n. acrylic resin, activieren, v.t. activate, acyclisch, acyklisch, a. acyclic, acylieren, v.t. acyUte. 

Organic peroxide-aromatic tertiary amine system is a well-known organic redox system 1]. The typical examples are benzoyl peroxide(BPO)-N,N-dimethylani-line(DMA) and BPO-DMT(N,N-dimethyl-p-toluidine) systems. The binary initiation system has been used in vinyl polymerization in dental acrylic resins and composite resins [2] and in bone cement [3]. Many papers have reported the initiation reaction of these systems for several decades, but the initiation mechanism is still not unified and in controversy [4,5]. Another kind of organic redox system consists of organic hydroperoxide and an aromatic tertiary amine system such as cumene hydroperoxide(CHP)-DMT is used in anaerobic adhesives [6]. Much less attention has been paid to this redox system and its initiation mechanism. A water-soluble peroxide such as persulfate and amine systems have been used in industrial aqueous solution and emulsion polymerization [7-10], yet the initiation mechanism has not been proposed in detail until recently [5]. In order to clarify the structural effect of peroxides and amines including functional monomers containing an amino group, a polymerizable amine, on the redox-initiated polymerization of vinyl monomers and its initiation mechanism, a series of studies have been carried out in our laboratory. 

Acrylic acid and its esters are used to produce acrylic resins. Depending on the polymerization method, the resins could he used in the adhesive, paint, or plastic industry. 

Self-leveling epoxy, polyester or reactive acrylic resin systems 9/105... 

Resin solution penetrating sealers are now available which, for very large warehouse floors, are comparable in applied costs with the concrete surface hardeners and are now being increasingly specified. Experience indicates that certain acrylic resin solutions are proving more durable and offer better protection to chemical and oil spillage than concrete surface hardeners. Acrylic resin solution sealers can markedly improve the abrasion resistance of concrete floors and have rescued a number of poor-quality floors. 

Polyester resin systems and, more recently, acrylic resins are also used. Polyester resin-based systems have a tendency to shrinkage during and after application and application is very critical. 

Acrylic resin systems developed in Germany are similar to polyester resins but, by careful formulation, the problems due to shrinkage have been largely overcome. The acrylic resin-based systems are currently based on highly flammable materials (flash point 10°C), which can present hazards during laying. However, there are systems available that can take foot traffic 2-3 hours after application and full service conditions within 24 hours, even at very low temperatures. 

Emulsion-based primer plus alkyd finish These are based on acrylic resin dispersions and have the advantage of a rapid rate of drying. They generally have excellent adhesion and flexibility but lack the sealing properties of aluminum primers. 

Atmospheres polluted by oxidising agents, e.g. ozone, chlorine, peroxide, etc. whose great destructive power is in direct proportion to the temperature, are also encountered. Sulphuric acid, formed by sulphur dioxide pollution, will accelerate the breakdown of paint, particularly oil-based films. Paint media resistant both to acids, depending on concentration and temperature, and oxidation include those containing bitumen, acrylic resins, chlorinated or cyclised rubber, epoxy and polyurethane/coal tar combinations, phenolic resins and p.v.c. 

Oil-base (including oil-modified alkyd resin) paint films should not be used in alkaline environments as the paint will deteriorate owing to saponification alkali-resistant coatings are provided by some cellulose ethers, e.g. ethyl cellulose, certain polyurethane, chlorinated rubber, epoxy, p.v.c./ p.v.a. copolymer, or acrylic-resin-based paints. In particular, aluminium and its alloys should be protected by alkali-resistant coatings owing to the detrimental effects of alkali on these metals. 

With these lacquers, nitrocellulose-based primer-surfacers are used. As well as liquid plasticisers, a wide range of materials are used as plasticising resins short oil alkyds, maleinised oils, ester gum, rosin and bodied castor oils. Pigmentation is usually inert. Thermoplastic acrylics are often preferred under acrylic lacquers these are based on acrylic resins and cellulose acetate butyrate. 

These requirements are usually met with two-pack paints based on hydroxyl-rich polyester or acrylic resins in the pigmented pack and aliphatic polyisocyanates in the activator pack. Cure with this type of finish is relatively fast and complete even at low ambient temperatures. An alternative finish is an acrylic lacquer, similar to the lacquer used for refinishing motor cars. These finishes are applied to the assembled aircraft by operators protected by air-fed hoods and using airless or conventional spray guns. High durability pigments are included. 

---