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Hockings

The contribution that Hocking wished to make was to refine the sensor system and the instrumentation paekage so as to be able to incorporate the necessary functionality within a lightweight portable battery operated instrument. This implied a lower power level and very low-noise instrumentation. We aimed also for a low cost instrument able to operate for several hours from fully charged batteries and able to operate at a pull speed of 500mm/second. [Pg.321]

You can order the molecular orbitals that arc a solution to etjtia-tion (47) accordin g to th eir en ergy, Klectron s popii late the orbitals, with the lowest energy orbitals first. normal, closed-shell, Restricted Hartree hock (RHK) description has a nia.xirnuin of Lw o electrons in each molecular orbital, one with electron spin up and one w ith electron spin down, as sliowm ... [Pg.220]

I ll c Raffeu etti ill Lcgral form at emph a sizes th e speed of corn piuiri g the Hock matrix. [Pg.264]

The cIcniciiLs of the MNDO Fock niairix bused on thenef/lecL of diuLmnic din ereii liul overlap approximaiion are described below. When and dy are on dilTeren L cen ters the oIT-diagonal elemen Is of 111 e Hock matrix ai e ... [Pg.285]

Because the protonation of ozone removes its dipolar nature, the electrophilic chemistry of HOs, a very efficient oxygenating electrophile, has no relevance to conventional ozone chemistry. The superacid-catalyzed reaction of isobutane with ozone giving acetone and methyl alcohol, the aliphatic equivalent of the industrially significant Hock-reaction of cumene, is illustrative. [Pg.166]

Sales demand for acetophenone is largely satisfied through distikative by-product recovery from residues produced in the Hock process for phenol (qv) manufacture. Acetophenone is produced in the Hock process by decomposition of cumene hydroperoxide. A more selective synthesis of acetophenone, by cleavage of cumene hydroperoxide over a cupric catalyst, has been patented (341). Acetophenone can also be produced by oxidizing the methylphenylcarbinol intermediate which is formed in styrene (qv) production processes using ethylbenzene oxidation, such as the ARCO and Halcon process and older technologies (342,343). [Pg.501]

F. J. Zele2nik and S. Gordon, Ind. Eng. Chem. 60(6), 25 (June 1968) S. Gordon and B. J. McBride, Computer Programfor the Calculation of Complex Chemical Equilibrium Compositions, Pocket Peformance, Incident and Keflected S hocks and Chapman-Jouguet Detonations, NASA SP-273, Lewis Research Center, NTIS N-71-37775, U.S. Department of Commerce, Spriugfield, Va., 1971. [Pg.353]

Ilyoscyamus niger. Leaves, 0-045 to 0-08 roots, 0-16 seeds, 0-06 to 0-1 tops, 0-07 to 0-1. Chiefly hyoscyamine with some atropine and hyoscine cj. Sievers and Lowman, Allan. A historical account of this drug has been published by Hocking. ... [Pg.66]

Exxon Mobil Chemical Hock Loos (Netherlands)... [Pg.28]

Air Products Chemicals Chevron Phillips Chemical Degussa-Huls (Geiinany) Hock Loos (Netherlands) Holox... [Pg.79]

Donghae Gas Industrial Co. (South Korea) Farmland Industries Hock Loos (Netherlands)... [Pg.99]

See other pages where Hockings is mentioned: [Pg.270]    [Pg.319]    [Pg.323]    [Pg.227]    [Pg.265]    [Pg.275]    [Pg.285]    [Pg.481]    [Pg.316]    [Pg.529]    [Pg.423]    [Pg.62]    [Pg.450]    [Pg.529]    [Pg.136]    [Pg.235]    [Pg.83]    [Pg.134]    [Pg.276]    [Pg.285]    [Pg.367]    [Pg.801]    [Pg.48]    [Pg.432]    [Pg.364]    [Pg.364]    [Pg.13]    [Pg.19]    [Pg.28]    [Pg.36]    [Pg.38]    [Pg.76]    [Pg.77]    [Pg.77]    [Pg.91]    [Pg.99]    [Pg.100]   
See also in sourсe #XX -- [ Pg.165 , Pg.173 ]



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Cumene Hock process

Hock cleavage

Hock process

Hock reaction

Hock rearrangement

Hock synthesis

Hocking

Phenol Hock process

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