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Ethylene Os

A few illustrative examples are the following. Photohydrogenation of acetylene and ethylene occurs on irradiation of Ti02 exposed to the gases, but only if TiOH surface groups are present as a source of hydrogen [319]. The pho-toinduced conversion of CO2 to CH4 in the presence of Ru and Os colloids has been reported [320]. Platinized Ti02 powder shows, in the presence of water, photochemical oxidation of hydrocarbons [321,322]. Some of the postulated reactions are ... [Pg.738]

FIGURE 9.24 Analysis of ultrahigh poly(ethylene oxide), MW about 37 million. Eluent O.OS M NaNOj. Flow rate 0.3 ml/min. Columns PSS Suprema 20 /tim, 30000, 8 x 300 mm. Oven temp 30°C. Detector Rl. Standards PSS PEO standards. [Pg.297]

The polymerization filling was effected by the ion-coordination mechanism [17-19]. The monomers were ethylene, propylene, allene, os-butylene, butadiene. The fillers were mineral materials such as ash, graphite, silica gel, glass fibers. The ultimate aim of filler conditioning prior to polymerization is to secure, on its surface, metal complex or organometallic catalysts by either physical or chemical methods [17-19],... [Pg.42]

Polyethylene Formation Investigated in Micro Reactors Organic synthesis 62 [OS 62] Radical polymerization of ethylene... [Pg.506]

OS 62] ]R 1] ]P 45] Improved pressure control was exerted for catalyst plug-induced ethylene polymerization by using advanced pressure control electronics [1]. In the regions of large temperature increase, the pressure fluctuated slightly this effect diminished downstream. [Pg.507]

OS 62] ]R 1] ]P 45] Catalyst plug-induced micro-channel ethylene polymerization allows to process about 10 runs per hour [1]. This is considerably more than achievable with conventional equipment (Parr reactors) processing only 4 to 6 runs per day. [Pg.508]

In 1961, Vaska and Diluzio6 showed that hydride-carbonylphosphine complexes of the formula MHX(CO)(PPh3)3 (M = Ru, Os X = Cl, Br) can be directly obtained from the metal halides and triphenylphosphine, using 2-methoxyethanol or ethylene glycol at 120-190°C. In agreement with this, in 1971, Moers7 reported the... [Pg.2]

The role of Os" in the oxidation of various reactants, including hydrocarbons, has been briefly investigated but no definitive data has been obtained. In most of the studies the ESR spectra have been observed following addition of a reactant to a surface which has the superoxide ion. The ESR spectrum of the superoxide ion remains essentially unperturbed upon addition of hydrogen, methane, carbon monoxide or ethylene how-... [Pg.313]

We have previously seen examples of the carbon-like formulas of mononuclear and dinuclear osmium compounds, namely the methane-like tetrahydride (4.50c), ethylene-like H20s=CH2 (4.51c) and H2Os = OsH2 (Table 4.15), acetylenelike HOs = CH (4.54c) and HOs = OsH (Table 4.15), allene-like H2C = Os = CH2 (4.55a), and so forth. While the coordination numbers and Lewis-like formulas are formally analogous, the actual structures of Os and C species may be quite similar (e.g., the Td structures of OsfL and CH4) or dissimilar (e.g the strongly bent Cs structure of H20s = CH2 [Fig. 4.13(c)] versus the planar D2h structure of H2C = CH2). [Pg.419]

First, o - Os(CO)3Cl2 2 (0.188 g 0.272 mmol) is dissolved in ethylene glycol (40 mL) in a three-necked flask containing a magnetic stirring bar and equipped... [Pg.223]

These reactiona exhibit a great difference between the behaviour of ethylenic ether and that of ethylic ether. This difference arises from the fact that in ethylic ether the ethyl atoms are held together by the oxygen only, whereas in ethylenic ether the link-ing of the atoms of CH, does not depend on the oxygen atom alone, os will be seen from the Mowing formula —... [Pg.278]


See other pages where Ethylene Os is mentioned: [Pg.689]    [Pg.514]    [Pg.535]    [Pg.535]    [Pg.542]    [Pg.689]    [Pg.514]    [Pg.535]    [Pg.535]    [Pg.542]    [Pg.439]    [Pg.357]    [Pg.507]    [Pg.508]    [Pg.328]    [Pg.6]    [Pg.109]    [Pg.294]    [Pg.202]    [Pg.284]    [Pg.261]    [Pg.281]    [Pg.282]    [Pg.282]    [Pg.339]    [Pg.113]    [Pg.58]    [Pg.647]    [Pg.647]    [Pg.660]    [Pg.662]    [Pg.663]    [Pg.678]    [Pg.664]    [Pg.183]    [Pg.460]    [Pg.218]    [Pg.223]    [Pg.224]    [Pg.407]    [Pg.19]   
See also in sourсe #XX -- [ Pg.2 , Pg.4 , Pg.138 ]




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