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    Abstract:
    Reactions of alkaline metal carbonates with sulfur are investigated in detail. The evolution of CO and a trace of were observed in the course of reaction with major component of polysulfides. Some evidences that the reaction proceeds with breaking of terminal sulfur-sulfur bond in the sulfur polymer, and forming CO, and polysulfide are presented. Polysulfides have the role of keeping free sulfur and allow it to react with other chemicals to rather high temperatures.plexes, whereas the binuclear and mononuclear complexes of Mn and Co$^{2+}$
    Keywords:
    Polysulfide
    ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTOrigin and Decomposition of Carbon Disulfide in Gas Making III—Some Chemical and Thermodynamic Effects in Formation of Organic Sulfur Compounds1,2Wilbert J. Huff and John C. HoltzCite this: Ind. Eng. Chem. 1930, 22, 6, 639–645Publication Date (Print):June 1, 1930Publication History Published online1 May 2002Published inissue 1 June 1930https://pubs.acs.org/doi/10.1021/ie50246a025https://doi.org/10.1021/ie50246a025research-articleACS PublicationsRequest reuse permissionsArticle Views27Altmetric-Citations4LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access options Get e-Alerts
    Carbon disulfide
    Carbon fibers
    Citations (5)
    Oxidation of sulfide to sulfate is known to consist of several steps. Key intermediates in this process are the so-called small oxoacids of sulfur (SOS)-sulfenic HSOH (hydrogen thioperoxide, oxadisulfane, or sulfur hydride hydroxide) and sulfoxylic S(OH)2 acids. Sulfur monoxide can be considered as a dehydrated form of sulfoxylic acid. Although all of these species play an important role in atmospheric chemistry and in organic synthesis, and are also invoked in biochemical processes, they are quite unstable compounds so much so that their physical and chemical properties are still subject to intense studies. It is well-established that sulfoxylic acid has very strong reducing properties, while sulfenic acid is capable of both oxidizing and reducing various substrates. Here, in this review, the mechanisms of sulfide oxidation as well as data on the structure and reactivity of small sulfur-containing oxoacids, sulfur monoxide, and its precursors are discussed.
    Oxidizing agent
    Reactivity
    Sulfenic acid
    Citations (21)
    The influence of mixed sulfur–nitrogen oxides on the redox chemistry of iron-(III) and -(II) species in aqueous solution was studied kinetically as a function of various concentrations. Two oxides, viz. HONH(SO3)– and HON(SO3)22–, were found to reduce FeIII to FeII, whereby these oxides undergo an iron(III)-induced hydrolysis reaction. The hydrolysis products were analysed by ion chromatography. These redox reactions can in principle account for the inhibiting effect of sulfur–nitrogen oxides on the metal-catalysed autoxidation of sulfur(IV) oxides. Possible reaction mechanisms are suggested.
    Autoxidation
    Half-reaction
    Citations (15)