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Atmospheric oxidation of pyrite with a novel catalyst and ultra-high elemental sulphur yield

机译:用新型催化剂和超高元素硫产率的大气氧化硫铁矿

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AbstractThe effectiveness of two different carbon based catalysts, Lewatit? AF 5 (AF 5) a new microporous carbonaceous bead, and a granular coconut shell based activated carbon, in aiding atmospheric oxidation of a gold-bearing pyrite concentrate was tested. Oxidation in ferric sulphate media unassisted by a catalyst was incomplete after 96h and resulted in only 60% pyrite oxidation, with an elemental sulphur yield ranging between 16% and 28%. Under the same test conditions, oxidation tests assisted by AF 5 saw approximately 96% pyrite oxidation with elemental sulphur yields ranging between 65% and 74%, while activated carbon assisted oxidation reached 100% pyrite oxidation with elemental sulphur yields between 63% and 64%. Testwork indicated that not only were pyrite oxidation kinetics greatly enhanced by the addition of carbon based catalysts leading to almost if not complete oxidation, but drastic increases in elemental sulphur yields and thus reductions in sulphate yields were also experienced.It is shown that the AF 5 catalyst adsorbs all of the elemental sulphur produced on its surface. The AF 5 beads are large enough (approximately 0.5mm) that after the leach process they can be screened out of the slurry, resulting in negligible elemental sulphur within the residue after solid/liquid separation. AF 5 also showed much stronger mechanical properties than the activated carbon, resulting in only approximately 0.40% AF 5 loss to fines compared to approximately 21.5% activated carbon loss to fines.Graphical abstractDisplay OmittedHighlights?An atmospheric oxidation process of pyrite is investigated.?The effect of two carbon based catalysts on oxidation is presented.?Without a catalyst oxidation of pyrite reached 60% with a maximum 28% S0yield.?With AF 5 addition 96% oxidation was achieved with a maximum 74% S0yield.?Activated carbon addition lead to 100% oxidation with a maximum 64% S0yield.]]>
机译:<![cdata [ 抽象 两种不同碳基催化剂的有效性,Lewatit? AF 5(AF 5)测试了一种新的微孔碳质珠,以及粒状椰子壳的活性炭,用于触及耐金黄铁矿浓缩物的大气氧化。在96h后,催化剂的硫酸铁氧化介质中的氧化在96h后不完全,导致仅60%的硫酸盐氧化,元素硫产率在16%和28%之间。在相同的试验条件下,AF5辅助的氧化试验约为96%的硫铁矿氧化,元素硫产率在65%和74%之间,而活性炭辅助氧化达到100%的硫酸盐氧化,元素硫产率为63%和64%。 。验证表明,不仅通过添加碳基催化剂而导致几乎是不完全氧化的碳基催化剂的大大提高,而且元素硫产率的激烈增加,也经历了硫酸盐产率的急剧增加。 显示AF 5催化剂吸附其表面上产生的所有元素硫。 AF 5珠子足够大(约0.5mm),在浸出过程之后,它们可以被筛分出浆液,在固体/液体分离后残留物内的可忽略的元素硫。 AF 5还比活化碳的机械性能更强大,导致仅大约0.40%的AF 5损失,与约21.5%的活性炭损失进行罚款。 图形抽象 显示省略 突出显示 研究了黄铁矿的大气氧化过程。 呈现了两个碳基催化剂对氧化的影响。 没有催化剂氧化催化剂达到60%,最大28%s 0 产量。 使用AF 5加入96%氧化,最大74%S 0 产量。 活性炭加成导致100%氧化,最大64%S 0 产量。 ]]>

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