Styrene-based resins

Unsaturated polyester resin/styrene based filler materials with good adhesive properties. Catalyst tube is inside lid of tins. 

Bio-Rex 70 2.4 0.70 Weakly acidic cation exchanger with car-boxylate groups on a macroreticular acrylic matrix for separation and fractionation of proteins, peptides, enzymes, and amines, particularly high molecular weight solutes. Does not denature proteins as do styrene-based resins. 

This type of adhesive is generally useful in the temperature range where the material is either leathery or mbbery, ie, between the glass-transition temperature and the melt temperature. Hot-melt adhesives are based on thermoplastic polymers that may be compounded or uncompounded ethylene—vinyl acetate copolymers, paraffin waxes, polypropylene, phenoxy resins, styrene—butadiene copolymers, ethylene—ethyl acrylate copolymers, and low, and low density polypropylene are used in the compounded state polyesters, polyamides, and polyurethanes are used in the mosdy uncompounded state. 

The first resins to be produced on a commercial scale were the coumarone—indene or coal-tar resins (1) production in the United States was started before 1920. These resins were dominant until the development of petroleum resins, which were estabHshed as important raw materials by the mid-1940s. Continued development of petroleum-based resins has led to a wide variety of aHphatic, cyclodiene, and aromatic hydrocarbon-based resins. The principal components of petroleum resins are based on piperylenes, dicyclopentadiene (DCPD), styrene, indene, and their respective alkylated derivatives. 

With the improvement of refining and purification techniques, many pure olefinic monomers are available for polymerization. Under Lewis acid polymerization, such as with boron trifluoride, very light colored resins are routinely produced. These resins are based on monomers such as styrene, a-methylstryene, and vinyltoluene (mixed meta- and i ra-methylstyrene). More recently, purified i ra-methylstyrene has become commercially available and is used in resin synthesis. Low molecular weight thermoplastic resins produced from pure styrene have been available since the mid-1940s resins obtained from substituted styrenes are more recent. 

G-5—G-9 Aromatic Modified Aliphatic Petroleum Resins. Compatibihty with base polymers is an essential aspect of hydrocarbon resins in whatever appHcation they are used. As an example, piperylene—2-methyl-2-butene based resins are substantially inadequate in enhancing the tack of 1,3-butadiene—styrene based random and block copolymers in pressure sensitive adhesive appHcations. The copolymerization of a-methylstyrene with piperylenes effectively enhances the tack properties of styrene—butadiene copolymers and styrene—isoprene copolymers in adhesive appHcations (40,41). Introduction of aromaticity into hydrocarbon resins serves to increase the solubiHty parameter of resins, resulting in improved compatibiHty with base polymers. However, the nature of the aromatic monomer also serves as a handle for molecular weight and softening point control. 

The cross-linking reaction mechanism is also influenced by the presence of other monomers. Methyl methacrylate is often used to improve the uv resistance of styrene-based resins. However, the disparate reaction rates of styrene and methacrylate monomer with the fumarate unsaturation not only preclude the use of more than 8% of the methacrylate monomer due to the significant slowing of the cross-linking reaction but also result in undercured products. 

Considerable work has been done on mathematic models of the extmsion process, with particular emphasis on screw design. Good results are claimed for extmsion of styrene-based resins using these mathematical methods (229,232). With the advent of low cost computers, closed-loop control of... 

Beaded acrylamide resins (28) are generally produced by w/o inverse-suspension polymerization. This involves the dispersion of an aqueous solution of the monomer and an initiator (e.g., ammonium peroxodisulfates) with a droplet stabilizer such as carboxymethylcellulose or cellulose acetate butyrate in an immiscible liquid (the oil phase), such as 1,2-dichloroethane, toluene, or a liquid paraffin. A polymerization catalyst, usually tetramethylethylenediamine, may also be added to the monomer mixture. The polymerization of beaded acrylamide resin is carried out at relatively low temperatures (20-50°C), and the polymerization is complete within a relatively short period (1-5 hr). The polymerization of most acrylamides proceeds at a substantially faster rate than that of styrene in o/w suspension polymerization. The problem with droplet coagulation during the synthesis of beaded polyacrylamide by w/o suspension polymerization is usually less critical than that with a styrene-based resin. 

Styrene-based resins, extrusion of, 23 398 Styrene block copolymers, as mixed plastics compatibilizers, 21 454 Styrene-butadiene (SB) block copolymers, 20 324, 23 377, 393 Styrene-butadiene copolymer latex binders, 19 360... 

The introduction of clean air act amendments in 1990, in the USA, may require changes in the formulation of polyester corrosion-resistant resins, which contained styrene, to reduce its emissions. Substitutions, including vinyl toluene which has a much lower vapour pressure, were evaluated. It was established that resin blends containing 15% vinyl toluene had corrosion resistant values comparable to those of styrene-based resins. 

The capacities of styrene-based anion exchangers are not so easily calculated because there may not be an anionic group on every benzene ring. Values of 2.5-4.0 meq/g are typical for strong anion resins. 

Figure 18.1. Formation of styrene-based cationic and anionic resins...

Dowex ion exchange resins include a range of anion and cation resins for multibed demineralization, mixed-bed condensate polishing, as well as nuclear and other specialty applications. Most Dowex resins are based on styrene copolymerized with divinylbenzene (DVB). According to Dow, styrene/DVB structures are the preferred matrices for ion exchange resins because... 

The shape of the dispersed phase droplets was investigated experimentally by Lissant and coworker by scanning electron microscopy (SEM) on cured HIPEs of water in a styrene-based resin [5], At high internal phase volumes, droplets were indeed polyhedral, and appeared to be relatively monodisperse in size. 

Natural supports (agarose, dextran, cellulose, porous glass, silica, the optical fiber itself or alumina) and synthetic resins (acrylamide-based polymers, methacrylic acid-based polymers, maleic anhydride-based polymers, styrene-based polymers or nylon, to name a few) have been applied for covalent attachment of enzymes. These materials must display a high biocatalyst binding capacity (as the linearity and the limit of detection of the sensing layers will be influenced by this value), good mechanical and chemical stability, low cost, and ease of preparation. 

The furan aldehydes were also affected differently by the resins. The fractions from the strong anion exchangers showed decreased concentrations of furan aldehydes, whereas the weak anion exchangers showed increased concentrations of furan aldehydes in the fractions used for fermentation. The lowest concentrations of furan aldehydes were observed in fractions from the strong anion exchangers with styrene-based matrices, Dowex 1x4 and Dowex 2x8, which displayed a decrease in the concentrations of furfural and HMF to approx 60-70%. 

Epoxy vinyl ester resins are a special class of unsaturated resin. This resin is made by capping an epoxy resin with methacrylic acid and then dissolving in styrene monomer to the desired viscosity. This gives mechanical properties similar to epoxy resins, but the processibility (low viscosity allowing for resin infusion processes) of an unsaturated polyester resin. As with unsaturated vinyl esters, the most common fire retardant vinyl ester resin is based on a resin made from a halogenated system, tetrabromobisphenol A. The level of bromine in the resin and the presence of antimony will determine the fire performance of the resin. These resins are normally used for corrosion resistant equipment or when fire performance and high mechanical properties are required. It is very difficult to get a low smoke value with a brominated vinyl ester resin again due to the fact that bromine... 

Ion-exchange polymeric resins are the most important types of exchangers currently in use [113-123], The first, totally organic ion-exchange resin was synthesized in 1935 by Adams and Holmer, when they produced a phenol-formaldehyde cation-exchange resin and an amine-formaldehyde anion-exchange resin, both obtained with the help of condensation polymerization reactions [113], In 1944, D Alelio synthesized styrene-based polymeric resins, which could be modified to obtain both cationic- and anionic-exchange resins. The majority of the resins commercially applied currently are of this type, for example, Amberlite IR-20, Lewatit S-100, Permutit Q, Duolite, C-20, Dowex-50, and Nalcite HCR. 

Most ion-exchange resins based on organic polymers are made by the process of suspension polymerization. The monomers can be neutral as in the case of styrene, divinylbenze, methyl acrylate, and acryonitirle, and the resulting polymer beads are then chemically modihed to introduce the acidic or basic functionality. Styrene-divinylbenzene-based ion exchangers are usually more hydrophobic than their more hydrophilic counterparts. The methacrylate matrix offers a more intermediate polarity and a less hydrophobic surface than styrenic-based materials. 

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