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Yield of n-propyl radicals as a function of added 1-butene in the mercury-photosensitized decomposition of propane. —C3D8 O—C3Ha .

Yield of naphthalene triplet in the laser photolysis of naphthalene in toluene as a function of naphthalene concentration in moles L . A represents calculated yield as a function of naphthalene concentration, at 1.2 mol dm with various concentrations of nitro-methane. Concentrations in moles L.

Yield of Nb cathode deposits in a pilot-scale cell . Operating current 120 A

Yield of Ni for the feedstocks A and B on Octacat as a hmction of reaction time and temperature .

Yield of nitrotyrosine, relative to metMb, generated by adding one equiv. H202 , 1 mM tyrosine, and different amounts of nitrite at pH 7.0.

Yield of No. 5 still during 72-hour sea water run

Yield of olefins as function of precoke content from i-butanol during MTO

Yield of olefins during dimethyl ether-to-olefins conversion catalyzed by SAPO-34F with various amounts of coke deposited from the reaction of propene before the experiment

Yield of olefins during MTO conversion catalyzed by SAPO-34F with various amounts of coke deposited from the reaction of propene before the experiment

Yield of olefins versus coke content

Yield of olefins versus coke content during

Yield of oligomers

Yield of organic compounds as function of the molar CO2 content of the feed gas

Yield of oxime aa a function of the flow rate in the mercury-photosensitized decomposition of propane, in the presence of NO. —2 mole- NO O—25 mole- NO.

Yield of oxime as a function of the nitric oxide concentration in the mercury-photosensitized decomposition of various propanes. O—C3H3 S—C3Da C —CH CD2CH3 -CDaCH-CIU

Yield of P and R2 obtained using the IRT method and compared with Monte Carlo random flights using a 12 M scavenger concentration. Number of realisations used

Yield of paprika colour

Yield of Pb-212 as function of water flow.

Yield of pentasil zeolites as a function of time. Abbreviations are C, for mono-n-butylair

Yield of pentasil zeolites as a function of time. Abbreviations are C, for mono-n-butylandne, C for mono-n-propylamine, Cy for mono-n-ethylamine, CL for mono-n-methylamine, di-C, for di-n-propylamine, di-Co for di-n-propylamine, di-C2 for di-n-ethylamine, di-n-C. for ai-n-methylamine, TPA Al-free for the alijiminium-free synthesis with the tetrapr pylammonium cation, TPA for tetrapropylammonium cation, TEA Al-free for the aluminium-free synthesis with the tetraethylammonium cation, TEA for tetraethylammonium cation and tri-C for tri-n-propylamine.

Yield of pentasil zeolites as a function on the SiC A O ratio for different crystallization times.

Yield of PHL versus the number of cycles for samples of different compositions, , 1

Yield of Pi for feedstocks A and B on Octacat a fiinction of reaction time and temperature .

Yield of poly

Yield of poly. Methanol, ambient temperature, reaction time



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