Evaluation of methemoglobin and polymerized methemoglobin for detoxification of cyanide, azide, and sulfide in in vitro binding models. [PDF]
Beyer GJ, Khan MA, Salvi T, Palmer AF.
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Determining biocide efficacy for treating established sulfate-reducing biofilms using flow cell systems. [PDF]
Okpala GN +4 more
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Gamma Irradiation Effects on Oxidation, Microbial Growth, and Volatile Compounds in Beef Aged at High Temperatures. [PDF]
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Electro-Chemo-Mechanical Coupling in Composite Cathodes of Sulfide-Based All-Solid-State Batteries: Pathways, Degradation, and Design Rules. [PDF]
Song G, Lee S, Lee M, Park J, Lee KT.
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An Exploratory Pilot Study to Investigate the Potential Relationship Between Porcine Reproductive and Respiratory Syndrome (PRRS) Virus Viremia Changes and Barn Manure Pit Management Procedures. [PDF]
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The Aryl Sulfide Synthesis via Sulfide Transfer
Chemistry – A European Journal, 2022AbstractAryl sulfides are in great demands in drugs and materials sciences. To avoid using nucleophilic and noxious thiols, many efforts have been focused on exploring novel sulfide resources. Herein, a reductive Pd‐catalyzed, Ni‐mediated method to synthesize aryl sulfides via a sulfide transfer reaction is developed.
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ChemInform Abstract: Roasting of Zinc Sulfide, Lead Sulfide, Copper Sulfide, and Iron Sulfide
ChemInform, 1991AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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The mineralogy, mineral chemistry and geological occurrence of metal sulfides, the major sources of world supplies of many metals, are reviewed. Emphasis is placed on the major sulfide minerals pyrite, pyrrhotite, mackinawite, galena, sphalerite and chalcopyrite, and the sulfarsenide mineral arsenopyrite.
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Reductive Sulfidation. Conversion of Aldehydes into Sulfides
Synthetic Communications, 1976Abstract 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 ...
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