Propylene preparation

It should also be noted that the probability of secondary insertion becomes higher when occurring on a metal-secondary carbon bond(7,10). The interested reader is referred to th quoted papers for a detailed discussion. In the spectrum of isotactic poly-3- 30-propylene prepared with the catalyst, 8TiCl3-Al(CH3 (sample 3 Figure 1.4) only enriched isobutyl end groups are detected. Therefore in this case the insertion of the monomer is always primary. 

Figure 5 shows this region of the spectrum for copolymers of 10-13 and 36 -39 % propylene prepared by both a soluble and a heterogeneous catalyst. The low propylene materials both show crystallinity, with the vanadium catalyzed product being less crystalline at a given propylene content. In the 36-39% propylene region, the vanadium catalyzed product shows no crystallinity (amorphous) however, substantial polyethylene crystallinity is present in the titanium catalyzed copolymer. 

NMR analysis of similar copolymers (40-45% propylene) prepared with VOCl3-Al(C2H5)2Q and with TiCl3Al(C2H5)2Cl showed the latter to have much more order than the former and to show clearly recognizable spectra due to isotactic, heterotactic, and possibly syndio-tactic propylene triads (21). 

An elastomeric copolymer based on ethylene and propylene prepared in Ziegler-Natta polymerization. When small amount of a diene monomer is added, the resulting polymer becomes ethylene-propylene terpolymer, EPDM. 

Cheng, H. N. Ewen, J. A. Carbon-13 nuclear magnetic resonance characterization of poly(propylene) prepared with homogeneous catalysts. Makromol. Chem. 1989,190, 1931-1943. 

Fig. 4. 220 MHz spectra of atactic poly propylenes prepared from (a) trans- and (b) cis-1,2,3,3,3-45-propylene (refs. 6—8)...

CH3 CH0H CH20H, a colourless, almost odourless liquid. It has a sweet taste, but is more acrid than ethylene glycol b.p. 187. Manufactured by heating propylene chlorohydrin with a solution of NaHCO under pressure. It closely resembles dihydroxyethane in its properties, but is less toxic. Forms mono-and di-esters and ethers. Used as an anti-freeze and in the preparation of perfumes and flavouring extracts, as a solvent and in... 

This form of limited-conversion hydrocracking is a process that selectively prepares high quality residues for the special manufacture of base oils of high viscosity index or treating residues having low BMCl for the conversion of heavy fractions to ethylene, propylene, butadiene and aromatics. 

Ethylene (as well as propylene) produced from carbon dioxide subsequently allows ready preparation of the whole array of hydrocarbons, as well as their derivatives and products that have become essential to our everyday life. Whereas the nineteenth century relied mostly on coal for energy as well as derived chemical products, the twentieth century greatly supplemented this with petroleum and nat-... 

PROPENE The major use of propene is in the produc tion of polypropylene Two other propene derived organic chemicals acrylonitrile and propylene oxide are also starting materials for polymer synthesis Acrylonitrile is used to make acrylic fibers (see Table 6 5) and propylene oxide is one component in the preparation of polyurethane polymers Cumene itself has no direct uses but rather serves as the starting material in a process that yields two valuable indus trial chemicals acetone and phenol... 

Poly (methyl Acrylate). The monomer used for preparing poly(methyl acrylate) is produced by the oxidation of propylene. The resin is made by free-radical polymerization initiated by peroxide or azo catalysts and has the following formula ... 

An interesting material with both electro- and therm ochromism behavior, Li VO2 was evaluated for a "smart window" appHcation (25). Films of Li V02 were prepared by reactive sputtering and annealing an electrolyte of LiClO and propylene carbonate. 

Today the most efficient catalysts are complex mixed metal oxides that consist of Bi, Mo, Fe, Ni, and/or Co, K, and either P, B, W, or Sb. Many additional combinations of metals have been patented, along with specific catalyst preparation methods. Most catalysts used commercially today are extmded neat metal oxides as opposed to supported impregnated metal oxides. Propylene conversions are generally better than 93%. Acrolein selectivities of 80 to 90% are typical. 

Early catalysts for acrolein synthesis were based on cuprous oxide and other heavy metal oxides deposited on inert siHca or alumina supports (39). Later, catalysts more selective for the oxidation of propylene to acrolein and acrolein to acryHc acid were prepared from bismuth, cobalt, kon, nickel, tin salts, and molybdic, molybdic phosphoric, and molybdic siHcic acids. Preferred second-stage catalysts generally are complex oxides containing molybdenum and vanadium. Other components, such as tungsten, copper, tellurium, and arsenic oxides, have been incorporated to increase low temperature activity and productivity (39,45,46). 

Hydroxyethyi and 2-hydroxypropyl acrylates are prepared by the addition of ethylene oxide or propylene oxide to acryhc acid (104,105). 

Diester/Ether Diol of Tetrabromophthalic Anhydride. This material [77098-07-8] is prepared from TBPA in a two-step reaction. First TBPA reacts with diethylene glycol to produce an acid ester. The acid ester and propylene oxide then react to give a diester. The final product, a triol having two primary and one secondary hydroxyl group, is used exclusively as a flame retardant for rigid polyurethane foam (53,54). 

Uses. Besides polymerizing TFE to various types of high PTEE homopolymer, TEE is copolymerized with hexafluoropropylene (29), ethylene (30), perfluorinated ether (31), isobutylene (32), propylene (33), and in some cases it is used as a termonomer (34). It is used to prepare low molecular weight polyfluorocarbons (35) and carbonyl fluoride (36), as well as to form PTEE m situ on metal surfaces (37). Hexafluoropropylene [116-15-4] (38,39), perfluorinated ethers, and other oligomers are prepared from TEE. 

Propylene Glycol Esters. These emulsifiers are formed by an alcoholysis reaction of propylene glycol and fatty acids, and are predominantly used in cakes, prepared mixes, whipped toppings, and breads (36). 

Polymer-type antioxidants have been prepared by Eriedel-Crafts reaction of -cresol andp- and/or y -chloromethylstyrene in the presence of boron trifluoride-etherate (198). The oligomeric product resulting from the alkylation of phenyl-a-naphthylamine using C12—15 propylene oligomer in the presence of AlCl or activated white clays is used as an antioxidant additive for lubricating oils (199). 

Other possible chemical synthesis routes for lactic acid include base-cataly2ed degradation of sugars oxidation of propylene glycol reaction of acetaldehyde, carbon monoxide, and water at elevated temperatures and pressures hydrolysis of chloropropionic acid (prepared by chlorination of propionic acid) nitric acid oxidation of propylene etc. None of these routes has led to a technically and economically viable process (6). 

Poly(alI lene glycol)s. While these can be made from polymeri2ation of any alkylene oxide, they are usually prepared either from propylene oxide as the water-insoluble type, or as water-soluble copolymers of propylene oxide and up to 50% ethylene oxide (35,36) (see Polyethers, propylene OXIDE polymers). Current worldwide production is estimated to be about 45,000 t. 

Uses. About 35% of the isophthahc acid is used to prepare unsaturated polyester resins. These are condensation products of isophthahc acid, an unsaturated dibasic acid, most likely maleic anhydride, and a glycol such as propylene glycol. The polymer is dissolved in an inhibited vinyl monomer, usually styrene with a quinone inhibitor. When this viscous hquid is treated with a catalyst, heat or free-radical initiation causes cross-linking and sohdification. A range of properties is possible depending on the reactants used and their ratios (97). 

---