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Ethylene spectroscopy

Studies to determine the nature of intermediate species have been made on a variety of transition metals, and especially on Pt, with emphasis on the Pt(lll) surface. Techniques such as TPD (temperature-programmed desorption), SIMS, NEXAFS (see Table VIII-1) and RAIRS (reflection absorption infrared spectroscopy) have been used, as well as all kinds of isotopic labeling (see Refs. 286 and 289). On Pt(III) the surface is covered with C2H3, ethylidyne, tightly bound to a three-fold hollow site, see Fig. XVIII-25, and Ref. 290. A current mechanism is that of the figure, in which ethylidyne acts as a kind of surface catalyst, allowing surface H atoms to add to a second, perhaps physically adsorbed layer of ethylene this is, in effect, a kind of Eley-Rideal mechanism. [Pg.733]

Figure B2.1.6 Femtosecond spectrometer for transient hole-burning spectroscopy with a continuum probe. Symbols used bs, 10% reflecting beamsplitter p, polarizer. The continuum generator consists of a focusing lens, a cell containing flowing water or ethylene glycol or, alternatively, a sapphire crystal and a recollimating lens. Figure B2.1.6 Femtosecond spectrometer for transient hole-burning spectroscopy with a continuum probe. Symbols used bs, 10% reflecting beamsplitter p, polarizer. The continuum generator consists of a focusing lens, a cell containing flowing water or ethylene glycol or, alternatively, a sapphire crystal and a recollimating lens.
Commercial Hquid sodium alumiaates are normally analyzed for total alumiaa and for sodium oxide by titration with ethylene diaminetetraacetic acid [60-00-4] (EDTA) or hydrochloric acid. Further analysis iacludes the determiaation of soluble alumiaa, soluble siHca, total iasoluble material, sodium oxide content, and carbon dioxide. Aluminum and sodium can also be determiaed by emission spectroscopy. The total iasoluble material is determiaed by weighing the ignited residue after extraction of the soluble material with sodium hydroxide. The sodium oxide content is determiaed ia a flame photometer by comparison to proper standards. Carbon dioxide is usually determiaed by the amount evolved, as ia the Underwood method. [Pg.140]

The cadmium chalcogenide semiconductors (qv) have found numerous appHcations ranging from rectifiers to photoconductive detectors in smoke alarms. Many Cd compounds, eg, sulfide, tungstate, selenide, teUuride, and oxide, are used as phosphors in luminescent screens and scintiUation counters. Glass colored with cadmium sulfoselenides is used as a color filter in spectroscopy and has recently attracted attention as a third-order, nonlinear optical switching material (see Nonlinear optical materials). DiaLkylcadmium compounds are polymerization catalysts for production of poly(vinyl chloride) (PVC), poly(vinyl acetate) (PVA), and poly(methyl methacrylate) (PMMA). Mixed with TiCl, they catalyze the polymerization of ethylene and propylene. [Pg.392]

The stmctural parameters of ethylene oxide have been determined by microwave spectroscopy (34). Bond distances iu nm determined are as follows C—C, 0.1466 C—H, 0.1085 and C—O, 0.1431. The HCH bond angle is 116.6°, and the COC angle 61.64°. Recent ah initio studies usiug SCF, MP2, and CISD have predicted bond lengths that are very close to the experimental values (35,36). [Pg.452]

Ethylene, /3-(dimethylamino)-nitro-in pyrrole synthesis, 4, 334 Ethylene, dithienyl-in photochromic processes, 1, 387 Ethylene, furyl-2-nitro-dipole moments, 4, 555 Ethylene, l-(3-indolyl)-2-(pyridyl)-photocyclization, 4, 285 Ethylene, l-(2-methyl-3-indolyl)-l,2-diphenyl-synthesis, 4, 232 Ethylene, (phenylthio)-photocyclization thiophenes from, 4, 880 Ethylene carbonate C NMR, 6, 754 microwave spectroscopy, 6, 751 photochemical chlorination, 6, 769 synthesis, 6, 780 Ethylene oxide as pharmaceutical, 1, 157 thiophene synthesis from, 4, 899 Ethylene sulfate — see 2,2-dioxide under 1,3,2-Dioxathiolane... [Pg.623]

Low-temperature spectroscopy is indispensable for the studies of processes on the ice surface, illustrated by ozone adsorption and ethylene ozonolysis. Such results are important to clarify the mechanism of atmospheric pollutant elimination and air purification in the nature. [Pg.431]

Treatment of quinoline with ethylene oxide gave oxazolo[3,2-u]quinoline 597 whereas 2-methylquinoline did not react with ethylene oxide (79JOC285). The oxazolidine 597 is labile as monitored by H NMR spectroscopy its colorless solution in CDCI3 became dark red within several hours (Scheme 100). [Pg.148]

Tosi, C. and Ciampelli, F. Applications of Infrared Spectroscopy to Ethylene-Propylene Copolymers. Vol. 12, pp. 87-130. [Pg.186]

Infrared spectroscopy. Due to experimental difficulties, infrared spectroscopy is used infrequently in these kinetic studies. However, continuous measurements have been carried out by Schumann28 in the study of the poly(ethylene terepthalate) synthesis. [Pg.57]

As previously discussed, solvents that dissolve cellulose by derivatization may be employed for further functionahzation, e.g., esterification. Thus, cellulose has been dissolved in paraformaldehyde/DMSO and esterified, e.g., by acetic, butyric, and phthalic anhydride, as well as by unsaturated methacrylic and maleic anhydride, in the presence of pyridine, or an acetate catalyst. DS values from 0.2 to 2.0 were obtained, being higher, 2.5 for cellulose acetate. H and NMR spectroscopy have indicated that the hydroxyl group of the methy-lol chains are preferably esterified with the anhydrides. Treatment of celliflose with this solvent system, at 90 °C, with methylene diacetate or ethylene diacetate, in the presence of potassium acetate, led to cellulose acetate with a DS of 1.5. Interestingly, the reaction with acetyl chloride or activated acid is less convenient DMAc or DMF can be substituted for DMSO [215-219]. In another set of experiments, polymer with high o -celliflose content was esterified with trimethylacetic anhydride, 1,2,4-benzenetricarboylic anhydride, trimellitic anhydride, phthalic anhydride, and a pyridine catalyst. The esters were isolated after 8h of reaction at 80-100°C, or Ih at room temperature (trimellitic anhydride). These are versatile compounds with interesting elastomeric and thermoplastic properties, and can be cast as films and membranes [220]. [Pg.138]

Protonation of the TMM complexes with [PhNMe2H][B(C6Fs)4] in chlorobenzene at —10 °C provided cationic methallyl complexes which are thermally robust in solution at elevated temperatures as determined by NMR spectroscopy. In contrast, addition of BfCgFsls to the neutral TMM precursors provided zwitterionic allyl complexes (Scheme 98). Surprisingly, it was found that neither the cationic nor the zwitterionic complexes are active initiators for the Ziegler-Natta polymerization of ethylene and a-olefins. °°... [Pg.257]

A preparation of the third nitrogenase from A. vinelandii, isolated from a molybdenum-tolerant strain but lacking the structural genes for the molybdenum and vanadium nitrogenases, was discovered to contain FeMoco 194). The 8 subunit encoded by anfG was identified in this preparation, which contained 24 Fe atoms and 1 Mo atom per mol. EPR spectroscopy and extraction of the cofactor identified it as FeMoco. The hybrid enzyme could reduce N2 to ammonia and reduced acetylene to ethylene and ethane. The rate of formation of ethane was nonlinear and the ethane ethylene ratio was strongly dependent on the ratio of nitrogenase components. [Pg.209]

This is a nonpolar rubber with very little unsamration. Nanoclays as well as nanotubes have been used to prepare nanocomposites of ethylene-propylene-diene monomer (EPDM) rubber. The work mostly covers the preparation and characterization of these nanocomposites. Different processing conditions, morphology, and mechanical properties have been smdied [61-64]. Acharya et al. [61] have prepared and characterized the EPDM-based organo-nanoclay composites by X-ray diffracto-gram (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy... [Pg.35]


See other pages where Ethylene spectroscopy is mentioned: [Pg.529]    [Pg.529]    [Pg.784]    [Pg.231]    [Pg.208]    [Pg.148]    [Pg.315]    [Pg.315]    [Pg.633]    [Pg.635]    [Pg.790]    [Pg.921]    [Pg.295]    [Pg.483]    [Pg.682]    [Pg.733]    [Pg.341]    [Pg.602]    [Pg.161]    [Pg.358]    [Pg.289]    [Pg.290]    [Pg.140]    [Pg.247]    [Pg.121]    [Pg.7]    [Pg.79]    [Pg.326]    [Pg.876]    [Pg.893]    [Pg.109]    [Pg.36]    [Pg.207]   
See also in sourсe #XX -- [ Pg.4 , Pg.155 ]

See also in sourсe #XX -- [ Pg.4 , Pg.155 ]




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