Results 251 to 260 of about 64,556 (304)

Oxidation of Sulfides

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
S. Colonna, N. Gaggero, G. Carrea, P. Pasta   +3 more
openaire   +2 more sources

Transition Metal Catalyzed Synthesis of Aryl Sulfides

Molecules, 2011
The presence of aryl sulfides in biologically active compounds has resulted in the development of new methods to form carbon-sulfur bonds. The synthesis of aryl sulfides via metal catalysis has significantly increased in recent years.
Chad Eichman
exaly   +2 more sources

Adaptations to sulfide in the meiofauna of the sulfide system. I. 35S-sulfide accumulation and the presence of a sulfide detoxification system

Journal of Experimental Marine Biology and Ecology, 1979
Abstract Life in the sulfide system requires the ability to withstand the toxic effects of long-term sulfide stress. The adaptations of sulfide-system interstitial metazoans to sulfide stress have been investigated using 35 S-sulfide. One possible adaptation, the total exclusion of sulfide at the body wall, could not be demonstrated.
Eric N. Powell, Miles A. Crenshaw, Reinhardt M. Rieger   +2 more
openaire   +1 more source

Chemisorption of hydrogen sulfide on lead sulfide

Russian Journal of Electrochemistry, 2006
The hydrogen sulfide chemisorption on lead sulfide at 22–100°C is studied by static testing in a vacuum and by pulsed chromatography. It is established that H2S is sorbed in reversible and irreversible forms and that the process is accompanied by the sample charging.
L. E. Derlyukova, M. V. Vinokurova, T. A. Anufrieva, A. V. Levchenko, A. A. Vinokurov   +4 more
openaire   +1 more source

Fabrication of Ni Sulfides by Thermal Sulfidation

Materials Science Forum, 2006
The microstructure of Ni sulfides prepared by thermal sulfidation of pure Ni and their dependence of fabrication parameters were investigated by means of scanning electron microscopy and X-ray diffractions. Sulfidation was made by isothermally annealing Ni with the sulfur in vacuum sealed glass ampoules at 673 K for 120 – 600s under the sulfur pressure
Tae Hyun Nam, Cheol Am Yu, Dae Won Jung, Kwon Koo Cho   +3 more
openaire   +1 more source

Photooxidation of methyl sulfide, ethyl sulfide, and methanethiol

Environmental Science & Technology, 1984
Products of sunlight-irradiated mixtures of oxides of nitrogen and alkyl sulfides (RSR, R = CH/sub 3/, C/sub 2/H/sub 5/) and methanethiol (CH/sub 3/SH) in air include formaldehyde (R = CH/sub 3/), acetaldehyde and PAN (R = C/sub 2/H/sub 5/), sulfur dioxide, and alkyl nitrates (RONO/sub 2/) as well as particulate alkanesulfonic acids (RSO/sub 2/OH) and ...
openaire   +2 more sources

Sulfides, Arsenides and Complex Sulfides (Sulfosalts)

2020
This mineral class comprises most of the ore minerals. Many of them are opaque, i.e., they are non-transparent, even in thin sections that are not more than 20–30 µm in thickness, and show metallic lustre with different shades of colour.
Martin Okrusch, Hartwig E. Frimmel
openaire   +1 more source

A Sulfide Oxidase Biosensor for Monitoring Sulfide

CORROSION 2008, 2008
Abstract A sulfide oxidase enzyme electrode is proposed for monitoring of biogenic sulfide resulting from the activities of sulfate-reducing bacteria (SRB). The enzyme which is immobilized in a carbon (graphite) paste with 1,1’ dimethylferrocene, catalyses the oxidation of sulfide to sulfur.
Reeta Sooknah, Sankara Papavinasam, R. Winston Revie   +2 more
openaire   +1 more source

Sulfides in organic synthesis. Application of sulfides

Russian Chemical Reviews, 1994
The results of studies on the use of sulfides as synthons in organic synthesis are treated systematically and surveyed. The practical applications of sulfides are examined. The bibliography includes 187 references.
openaire   +1 more source

Reductive Sulfidation. Conversion of Aldehydes into Sulfides

Synthetic Communications, 1976
Abstract Carbonyl compounds have been converted into 1,3-oxathiolanes or 1,3-oxathianes and then reduced with “mixed hydride” to β-hydroxyethyl (or on further reduction ethyl) or γ-hydroxypropyl sulfides, respectively.1 However, this overall conversion of a carbonyl compound to a sulfide (a process for which the name reductive sulfidation is suggested ...
openaire   +1 more source