Kinetics of Disproportionation of Elemental Sulfur in Aqueous Solutions
|更新时间:2025-12-16
|
Kinetics of Disproportionation of Elemental Sulfur in Aqueous Solutions
CIESC JournalIssue 4, (1984)
作者机构:
中国科学院化工冶金研究所,中国科学院化工冶金研究所,中国科学院化工冶金研究所
作者简介:
基金信息:
DOI:
CLC:
Online First:25 December 1984,
Published:25 December 1984
稿件说明:
移动端阅览
Deng Tong, Ke Jiajun and Chen JiayongInstitute of Chemical Metallurgy, Academia Sinica. Kinetics of Disproportionation of Elemental Sulfur in Aqueous Solutions[J]. CIESC Journal, 1984, (4).
DOI:
Deng Tong, Ke Jiajun and Chen JiayongInstitute of Chemical Metallurgy, Academia Sinica. Kinetics of Disproportionation of Elemental Sulfur in Aqueous Solutions[J]. CIESC Journal, 1984, (4).DOI:
Kinetics of Disproportionation of Elemental Sulfur in Aqueous Solutions
involves the disproportionation of elemental sulfur in aqueous solution. The kinetics of this disproportionation reaction was carried out. The effect of cupric ions in aqueous solution on this reaction was also investigated. The reaction was carried out in an autoclave. It was shown that elemental sulfur disproportionated in aqueous solutions of pH 6-10 according to the following equation: Experimental results can be correlated by a model of diffusion of elemental sulfur from sulfur droplets to the aqueous solution followed by a pseudo-first-order disproportionation reaction in the aqueous phase. The rate expression has the following form: -ln(1-α)=kt·t where kt = aCs
a is the interfacial area of 1 g of liquid sulfur in water
k1 is the pseudo-first-order reaction rate constant
Cs and D1 are solubility and diffusion coefficient respectively of sulfur in the aqueous phase
α is the fraction of conversion of elemental sulfur
and t is the time of reaction. The effect of pH on reaction rate was studied at 130℃. It was shown that the pseudo-first-order rate constant k1 is directly proportional to the concentration of OH- in the pH range of 6-7.5. The temperature dependence of k
was also studied at pH 6.3 and the apparent activation energy derived was 24.0 kcal/mol.