Aromatic styrene

The influence of adsorption on the structure of a -chymotrypsin is shown in Fig. 10, where the circular dichroism (CD) spectrum of the protein in solution is compared with that of the protein adsorbed on Teflon and silica. Because of absorbance in the far UV by the aromatic styrene, it is impossible to obtain reliable CD spectra of proteins adsorbed on PS and PS- (EO)8. The CD spectrum of a protein reflects its composition of secondary structural elements (a -helices, / -sheets). The spectrum of dissolved a-chymotrypsin is indicative of a low content of or-helices and a high content of //-sheets. After adsorption at the silica surface, the CD spectrum is shifted, but the shift is much more pronounced when the protein was adsorbed at the Teflon surface. The shifts are in opposite directions for the hydrophobic and hydrophilic surfaces, respectively. The spectrum of the protein on the hydrophilic surface of silica indicates a decrease in ordered secondary structure, i.e., the polypeptide chain in the protein has an increased random structure and, hence, a larger conformational entropy. Adsorption on the hydrophobic Teflon surface induces the formation of ordered structural elements, notably an increase in the content of O -helices (cfi, the discussion in Sect. 3.1.4). 

The species that have been detected at sheet extrusion were mostly aromatics, styrene being the most prominent compound. From the injection molding experiments a wider range of volatiles with significantly higher concentrations was measured in comparison to those for the sheet extrusion experiments. 

Petrochemical Plastics Manufacturing Olefins Polyolefins Aromatics Styrenics Specialty Chemicals... 

Mark Haney, Sr. VP-Specialties, Aromatics Styrenics Tim Taylor, Exec. VP-Olefins Polyolefins Scott Sharp, VP-Environment, Health Safety Dave S. Smith, VP-Polyethylene... 

Metallosilicate mesoporous catalysts prepared by incorporation of transition metals in the MCM-41 molecular sieves and their catalytic activity in selective oxidation of aromatics (styrene and benzene)... 

CIO aromatics. Styrene and vinyl toluene are also aromatic hydrocarbons that act simultaneously as solvents and reactive diluents for chemical crosslinking with unsaturated polyester resins and in UV-cured coatings. 

Chlorosulfonyl styrene-divinylbenzene copolymer is a highly reactive intermediate used in organic synthesis. The aromatic styrene groups of the copolymer are sulfonated with chlorosulfonic acid in dichloroethane, followed by chlorination of the sulfonate groups with phosphorus pentachloride-phosphorus oxychloride mixture. ... 

The composition of a copolymer determines its misdbihty characteristics. PMMA has limited miscibility with polystyrene or polyacrylonitrile individually. However, addition of PMMA to a random copolymer of styrene and acrylonitrile (SAN) can produce a miscible blend at certain compositions. The aromatic styrene group of styrene and polar nitrile group of acrylonitrile of the random copolymer are partially miscible with PMMA. This will be discussed further in Chapter 6. 

Additioneilly, "classes" or types of hydrocarbons were and still are determined based on the capability to isolate them by separation techniques. The four types usually sought eue paraffins, olefins, naphthenes, and aromatics. Paraffinic hydrocarbons include both normal and branched alkanes. Olefins refer to normal and branched alkenes that contain one or more double or triple carbon-carbon bonds. Naphthene (not to be confused with naphthalene ) is a term of the petroleum industry that refers to the saturated cyclic hydrocarbons or cycloalkanes. Finally, aromatics include all hydrocarbons containing one or more rings of the benzenoid structure. These general hydrocarbon classifications are complicated by many combinations of the above types, for example, olefinic aromatics (styrene) or alkylbenzenes (cumene). Table 4 presents a summary of the hydrocarbon types usually found in specific petroleum fractions. 

Benzene, toluene, anthracene, phenanthrene, biphenyl. Aromatic hydrocarbons with unsaturated side-chains. Styrene, stilbene. 

In addition to benzene and naphthalene derivatives, heteroaromatic compounds such as ferrocene[232, furan, thiophene, selenophene[233,234], and cyclobutadiene iron carbonyl complexpSS] react with alkenes to give vinyl heterocydes. The ease of the reaction of styrene with sub.stituted benzenes to give stilbene derivatives 260 increases in the order benzene < naphthalene < ferrocene < furan. The effect of substituents in this reaction is similar to that in the electrophilic aromatic substitution reactions[236]. 

Thallation of aromatic compounds with thallium tris(trifluoroacetate) proceeds more easily than mercuration. Transmetallation of organothallium compounds with Pd(II) is used for synthetic purposes. The reaction of alkenes with arylthallium compounds in the presence of Pd(Il) salt gives styrene derivatives (433). The reaction can be made catalytic by use of CuCl7[393,394], The aryla-tion of methyl vinyl ketone was carried out with the arylthallium compound 434[395]. The /9-alkoxythallium compound 435, obtained by oxythallation of styrene, is converted into acetophenone by the treatment with PdCh[396]. 

Ethylbenzene Separation. Ethylbenzene [100-41-4] which is primarily used in the production of styrene, is difficult to separate from mixed Cg aromatics by fractionation. A column of about 350 trays operated at a refluxTeed ratio of 20 is required. No commercial adsorptive unit to accomplish this separation has yet been installed, but the operation has been performed successhiUy in pilot plants (see Table 5). About 99% of the ethylbenzene in the feed was recovered at a purity of 99.7%. This operation, the UOP Ebex process, requires about 40% of the energy that is required by fractional distillation. 

Aqueous mineral acids react with BF to yield the hydrates of BF or the hydroxyfluoroboric acids, fluoroboric acid, or boric acid. Solution in aqueous alkali gives the soluble salts of the hydroxyfluoroboric acids, fluoroboric acids, or boric acid. Boron trifluoride, slightly soluble in many organic solvents including saturated hydrocarbons (qv), halogenated hydrocarbons, and aromatic compounds, easily polymerizes unsaturated compounds such as butylenes (qv), styrene (qv), or vinyl esters, as well as easily cleaved cycHc molecules such as tetrahydrofuran (see Furan derivatives). Other molecules containing electron-donating atoms such as O, S, N, P, etc, eg, alcohols, acids, amines, phosphines, and ethers, may dissolve BF to produce soluble adducts. 

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. 

Coumarone—indene or coal-tar resins, as the name denotes, are by-products of the coal carbonization process (coking). Although named after two particular components of these resins, coumarone (1) and indene (2), these resins are actually produced by the cationic polymerization of predominantly aromatic feedstreams. These feedstreams are typically composed of compounds such as indene, styrene, and their alkylated analogues. In actuaUty, there is very tittle coumarone in this type of feedstock. The fractions used for resin synthesis typically boil in the range of 150—250°C and are characterized by gas chromatography. 

Aromatic. Aromatic feedstreams (C-8, C-9, C-10) derived from the steam cracking of petroleum distillates are composed of styrene, iadene, vinyltoluenes (eg, meta- and i ra-methylstyrene), and their respective alkylated analogues. A typical aromatic feedstream might contain 50% reactive olefins with the remainder being alkylated benzenes and higher aromatics. 

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. 

G-9 Aromatic Petroleum Resins. Feedstocks typically used for aromatic petroleum resin synthesis boil in the approximate range of 100—300°C at atmospheric pressure, with most boiling in the 130—200°C range. The C-9 designation actually includes styrene (C-8) through C-10 hydrocarbons (eg, methylindene). Many of the polymerizable monomers identified in Table 1 for coumarone—indene type cmdes from coal tar are also present in aromatic fractions from cracked petroleum distillates. Therefore, the technology developed for the polymerization of coal-tar cmdes is also appHcable to petroleum-derived aromatic feedstocks. In addition to availabiHty, aromatic petroleum resins offer several advantages over coumarone—indene resins. These include improved color and odor, as weU as uv and thermal stabiHty (46). 

In order to increase the solubiUty parameter of CPD-based resins, vinyl aromatic compounds, as well as other polar monomers, have been copolymerized with CPD. Indene and styrene are two common aromatic streams used to modify cyclodiene-based resins. They may be used as pure monomers or contained in aromatic steam cracked petroleum fractions. Addition of indene at the expense of DCPD in a thermal polymerization has been found to lower the yield and softening point of the resin (55). CompatibiUty of a resin with ethylene—vinyl acetate (EVA) copolymers, which are used in hot melt adhesive appHcations, may be improved by the copolymerization of aromatic monomers with CPD. As with other thermally polymerized CPD-based resins, aromatic modified thermal resins may be hydrogenated. 

Pressure sensitive adhesives typically employ a polymer, a tackifier, and an oil or solvent. Environmental concerns are moving the PSA industry toward aqueous systems. Polymers employed in PSA systems are butyl mbber, natural mbber (NR), random styrene—butadiene mbber (SBR), and block copolymers. Terpene and aUphatic resins are widely used in butyl mbber and NR-based systems, whereas PSAs based on SBR may require aromatic or aromatic modified aUphatic resins. 

Blends ofiPetramethylbisphenolA-PC (TMBPA-PC) with ModfiedPS or Styrene-Ac7ylonitrile(SAN) Copolymer. By installing halogen atoms on the aromatic rings of the PC-backbone, not only the resistance to heat softening can be increased (eg, TMBPA-PC = 203° C) (209), but also the compatibiUty with olefins. 

Sodium naphthalene [25398-08-7J and other aromatic radical anions react with monomers such as styrene by reversible electron transfer to form the corresponding monomer radical anions. Although the equihbtium (eq. 10)... 

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