Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Infrared spectroscopy ethylene

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]

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]

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]

The nature of the titanium-containing active site has been investigated with different techniques, including theoretical calculations. The formation of a hydroperoxidic species or of a bidentate side-on titanium peroxo structure was suggested by many authors . Alternatively, some DFT calculations indicated an undissociated molecule of H2O2 weakly interacting with Ti centers or an active Ti-O-O-Si peroxo moiety as a reactive site . Recently, Lin and Frei reported the first direct detection, obtained using in situ FT-infrared spectroscopy, of a Ti-OOH moiety as active species in the oxidation of small olefins like ethylene or propylene . [Pg.1082]

Whatever the precursor, the formation of an intermediate solid phase was always observed. It can be inferred from X-ray diffraction (Fig. 9.2.7) and infrared spectroscopy that this intermediate phase shows a lamellar, incompletely ordered structure (turbostratic structure) built up with parallel and equidistant sheets like those involved in the lamellar structure of the well-crystallized hydroxides Ni(OH)2 or Co(OH)2, these sheets are disoriented with intercalation of polyol molecules and partial substitution of hydroxide ions by alkoxy ions (29). The dissolution of this solid phase, which acts as a reservoir for the M(I1) solvated species, controls the concentration of these species and then plays a significant role in the control of the nucleation of the metal particles and therefore of their final morphological characteristics. For instance, starting from cobalt or nickel hydroxide as precursor in ethylene glycol, the reaction proceeds according to the following scheme (8) ... [Pg.471]

Copper, silver, and gold colloids have been prepared by Chemical Liquid Deposition (CLD) with dimethoxymethane, 2-methoxyethyl ether, and ethylene glycol dimethyl ether. The metals are evaporated to yield atoms which are solvated at low temperatures and during the warm-up process colloidal sols with metal clusters are obtained. Evaporation of the solvent was carried out under vacuum-generating metal films. These films are showing very low carbon/hydrogen content and were characterized by elemental analyses and infrared spectroscopy (Cardenas et al., 1994). [Pg.177]

The spectral properties of ethylene oxides are among the most important, not only for the information derivable from them concerning tbe intimate structure of the three-merabered oxide ring, but also in connexion with the detection and identification of this function in complex molecules of unknown constitution, e.g. natural product. The present review is concerned with the following three types of gpectroBoopy A) infrared spectroscopy, ( ) ultraviolet spectroscopy, and ( 7) nuclear magnetic resonance spectroscopy,... [Pg.10]

Reed 332) has reported that reaction of ethylene oxide with the a,(a-dilithiumpoly-butadiene in predominantly hydrocarbon media (some residual ether from the dilithium initiator preparation was present) produced telechelic polybutadienes with hydroxyl functionalities (determined by infrared spectroscopy) of 2.0 + 0.1 in most cases. A recent report by Morton, et al.146) confirms the efficiency of the ethylene oxide termination reaction for a,ta-dilithiumpolyisoprene functionalities of 1.99, 1.92 and 2.0j were reported (determined by titration using Method B of ASTM method E222-66). It should be noted, however, that term of a, co-dilithium-polymers with ethylene oxide resulted in gel formation which required 1-4 days for completion. In general, epoxides are not polymerized by lithium bases 333,334), presumably because of the unreactivity of the strongly associated lithium alkoxides641 which are formed. With counter ions such as sodium or potassium, reaction of the polymeric anions with ethylene oxide will effect polymerization to form block copolymers (Eq. (80) 334 336>). [Pg.74]

Reaction with ethylene sulfide yields ethylene and, possibly, a silanethione (47). With ethylene oxide, the first step is abstraction of an oxygen atom to yield the silanone (48), which adds to a second ethylene oxide molecule to give the siladioxolane (49). The products were identified mainly by infrared spectroscopy in several cases the reaction kinetics were studied and activation energies determined348. [Pg.2531]


See other pages where Infrared spectroscopy ethylene is mentioned: [Pg.682]    [Pg.341]    [Pg.602]    [Pg.161]    [Pg.358]    [Pg.149]    [Pg.134]    [Pg.185]    [Pg.734]    [Pg.149]    [Pg.125]    [Pg.30]    [Pg.1082]    [Pg.17]    [Pg.140]    [Pg.134]    [Pg.504]   
See also in sourсe #XX -- [ Pg.188 , Pg.189 ]

See also in sourсe #XX -- [ Pg.677 ]




SEARCH



Ethylene spectroscopy

Infrared spectroscopy adsorbed ethylene

Infrared spectroscopy ethylene-propylene copolymer

© 2024 chempedia.info