Styrene//-propyl acrylate copolymer

Clear transparent foils, which are used as covers for documents, are in wide use as are polystyrene windows in letter envelopes. These may be directly scanned with the AFM and rescanned after irradiation. The changes are initially on the nanometer scale—and nanostructures can be formed and found quite easily. This has been done with a commercial styrene//-propyl-acrylate copolymer which was purchased in 1975 and which had abrasive... 

Figure 34. Atomic force microscopy surfaces of a styrene/i -propyl-acrylate copolymer transparent foil (a) before irradiation (b) after 2 h irradiation under vacuum. 

Polyarylate resin Polyarylether ketone resin Polyester carbonate resin Polyetherimide resin Polyethylene, chlorinated Polyethylene glycol Polyethylene, medium density Poly (p-methylstyrene) Poly (p-methylstyrene), rubber-modified Poly (oxy-1,2-ethanediyloxycarbonyl-2,6-naphthalenediylcarbonyl) resin Poly (oxy-p-phenylenesulfonyl-p-phenyleneoxy-p-phenyleneisopropylidene-p-phenylene) resin Poly (phenyleneterephthalamide) resin Polysulfone resin Poly (tetramethylene terephthalate) Polyvinylidene chloride Potassium sorbate Potato (Solanum tuberosum) starch Silica, colloidal Silicone Sodium N-alkylbenzenesulfonate Sodium bicarbonate Sodium tetraborate pentahydrate Starch, pregelatinized Styrene/acrylates copolymer Styrene/butadiene polymer Styrene/DVB copolymer , 1,1 -Sulfonylbis (4-chlorobenzene) polymer with 4,4 -(1-methylethylidene) bis (phenol) and 4,4 -sulfonylbis (phenol) Synthetic wax Tapioca starch Tetrafluoroethylene/perfluoro (propyl vinyl ether) copolymer Tocopherol Triglycidyl isocyanurate VA/crotonates copolymer Vinyl chloride/ethylene copolymer Wheat (Triticum vulgare) starch... 

A significant number of works are concerned with the development of new membranes for the separation of mixtures of aromatic/alicyclic hydrocarbons [10,11,77-109]. For example, the following works can be mentioned. A mixture of cellulose ester and polyphosphonate ester (50 wt%) was used for benzene/cyclohexane separation [113]. High values of the separation factor and flux were achieved (up to 2 kg/m h). In order to achieve better fluxes and separation factors the attention was shifted to the modification of polymers by grafting technique. Grafted membranes were made of polyvinylidene fluoride with 4-vinyl pyridine or acrylic acid by irradiation [83]. 2-Hydroxy-3-(diethyl-amino) propyl methacrylate-styrene copolymer membranes with cyanuric chloride were prepared, which exhibited a superior separation factor /3p= 190 for a feed aromatic component concentration of 20 wt%. Graft copolymer membranes based on 2-hydroxyethyl methylacrylate-methylacrylate with thickness 10 pm were prepared [85]. The membranes yielded a flux of 0.7 kg/m h (for feed with 50 wt% of benzene) and excellent selectivity. Benzene concentration in permeate was about 100 wt%. A membrane based on polyvinyl alcohol and polyallyl amine was prepared [87]. For a feed containing 10 wt% of benzene the blend membrane yielded a flux of 1-3 kg/m h and a separation factor of 62. 

Kim et al. [46,47] reported the synthesis of fluorosilicone block copolymers of poly(perfluoroalkylethyl acrylate)-fc-poly(3-[m s(trimethylsilyloxy)-silyl] propyl methacrylates) (PFA-i>-PSiMAs) by a three-step synthetic approach. In the first step, a PFA macromonomer (PFAM) was made by free radical polymerization. Thereafter, a condensation reaction was applied to prepare the PFAM initiator (PFAMI). Finally, the PFAMI and SiMA were reacted to prepare the PFA-i>-PSiMAs block copolymers. In early studies, synthesis of fluorosilicone block copolymers was reported by Boutevin et al. [48-50]. However, two-step hydrosilylation was carried out to prepare the photo-cross-linkahle fluorinated PDMS as reported by Boutevin et al. [48]. In another study, Luo et al. [51] prepared poly(dimethylsiloxane)- -poly(2,2,3,3, 4,4,4-heptafluorobutyl methacrylate- -poly(styrene)... 

The effects of varying composition in random copolymers can also be seen in isochronal or pseudoisochronal studies such as those in Fig. 12-3. Thus, Jenckel and Herwig found in copolymers of styrene and methyl acrylate that the maximum in tan 5 (measured in torsion at a frequency of 0.14 sec ) on the temperature scale shifted from about 20 to 110° with increasing proportions of styrene the sharpness of the maximum was not much affected. Similar progressive changes with composition have been described for random copolymers of styrene and a-methyl styrene and of methyl methacrylate and tri- -propyl tin methacry-... 

Dispersions of copolymers of butadiene with acrylic acid or methacrylic acid in aqueous potassium hydroxide have been mentioned in the patent literature" as a dip for adhering rayon tire cord to rubber. The effect is most evident when carboxyl groups are present in the adhesive, the tie cement, and the cover stocks. The adhesive may be applied as latex, aqueous dispersion, or cement. A patent issued to the Dunlop Company Ltd." describes the use of a styrene-butadiene-itaconic acid copolymer with Gen-Tac Latex (GenCorp) in formulating an RFL (resorcinol formaldehyde latex) type adhesive for bonding a natural rubber compound to Nylon 66 and rayon tire cords. Brodnyan" also claims carboxylic adhesives for rayon, nylon, and Dacron cords. In this case, the tire cords were treated with a mixed polymer latex containing resorcinol-formaldehyde condensate, a butadiene-vinyl pyridine copolymer, an SBR copolymer, and a multifunctional copolymer from methyl acrylate, 2-hydroxy propyl methacrylate, and acrylic acid. A different approach was reported by Badenkov" whereby rayon or nylon tire cords were coated with... 

Pressure sensitive and contact adhesives are made from a variety of polymers including acrylic acid esters, polyisobutylene, polyesters, polychloroprene, polyiuethane, silicone, styrene-butadiene copolymer and natural rubber. With the exception of acrylic acid ester adhesives which can be processed as solutions, emulsions, UV curable, 100% solids, and silicones (which may contain only traces of solvents), all remaining rubbers are primarily formulated with substantial amounts of solvents such as hydrocarbon solvents (mainly heptane, hexane, naphtha), ketones (mainly acetone and methyl ethyl ketone), esters (propyl acetate), and aromatic solvents (mainly toluene and xylene). 

---