دورية أكاديمية

Synchrotron Radiation Based Study of the Catalytic Mechanism of Ag+ to Chalcopyrite Bioleaching by Mesophilic and Thermophilic Cultures

التفاصيل البيبلوغرافية
العنوان: Synchrotron Radiation Based Study of the Catalytic Mechanism of Ag+ to Chalcopyrite Bioleaching by Mesophilic and Thermophilic Cultures
المؤلفون: Zhenyuan Nie, Weiwei Zhang, Hongchang Liu, Jinlan Xia, Wei Zhu, Duorui Zhang, Lei Zheng, Chenyan Ma, Yidong Zhao, Wen Wen
المصدر: Minerals, Vol 8, Iss 9, p 382 (2018)
بيانات النشر: MDPI AG, 2018.
سنة النشر: 2018
المجموعة: LCC:Mineralogy
مصطلحات موضوعية: chalcopyrite, bioleaching, Ag+, mesophilic culture, thermophilic culture, SR-XRD, XANES, Mineralogy, QE351-399.2
الوصف: The catalytic mechanism of Ag+ for chalcopyrite bioleaching by mesophilic culture (at 30 °C) and thermophilic culture (at 48 °C) was investigated using synchrotron radiation-based X-ray diffraction (SR-XRD) and S K-edge and Fe L-edge X-ray absorption near edge structure (XANES) spectroscopy. Bioleaching experiments showed that copper extraction from chalcopyrite bioleaching by both cultures was promoted significantly by Ag+, with more serious corrosion occurring on the minerals surface. SR-XRD and XANES analyses showed that the intermediates S0, jarosite and secondary minerals (bornite, chalcocite and covellite) formed for all bioleaching experiments. For these secondary minerals, the formation of bornite and covellite was promoted significantly in the presence of Ag+ for both cultures, while Ag+ has almost no effect on the formation of chalcocite. These results provided insight into the catalytic mechanisms of Ag+ to chalcopyrite bioleaching by the mesophilic and thermophilic cultures, which are both probably due to the rapid formation of bornite by Ag+ and the conversion of bornite to covellite.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2075-163X
Relation: http://www.mdpi.com/2075-163X/8/9/382; https://doaj.org/toc/2075-163X
DOI: 10.3390/min8090382
URL الوصول: https://doaj.org/article/28926491c0544a549c6c79d32528af87
رقم الأكسشن: edsdoj.28926491c0544a549c6c79d32528af87
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2075163X
DOI:10.3390/min8090382