دورية أكاديمية

Alkaline reactivity of arsenical natrojarosite

التفاصيل البيبلوغرافية
العنوان: Alkaline reactivity of arsenical natrojarosite
المؤلفون: Reyes, Iván A., Patiño, Francisco, Rivera, Isauro, Flores, Mizraím U., Reyes, Martín, Hernández, Juan
المصدر: Journal of the Brazilian Chemical Society. December 2011 22(12)
بيانات النشر: Sociedade Brasileira de Química, 2011.
سنة النشر: 2011
مصطلحات موضوعية: reactivity, arsenical natrojarosite, kinetics, arsenate, decomposition, amorphous
الوصف: Jarosites are compounds that can undergo substitutions with several elements of environmental importance (such as As5+) during precipitation. Arsenic integrated in the structure could influence the solubility of the jarosite, potentially stabilizing the structure under a wide range of conditions that are tolerated by pure jarosite. Alkaline reactivity is characterized by the removal of sulfate and sodium ions from the lattice and by the formation of a gel consisting of iron hydroxides with adsorbed arsenate. The decomposition curves show an induction period, followed by a conversion period. The induction period is independent from the particle size and decreases exponentially as the temperature increases. The conversion period is characterized by the formation of a hydroxide halo around an unreacted arsenical natrojarosite core. The kinetic data are consistent with the chemical control of the process. The expression obtained in NaOH medium for [OH-] concentrations ranging from 3.84 × 10-3 to 1.08 × 10-1 mol L-1 is the following: r0/-v[1 - (1 - x)1/3] = 3.11 × 10(9) exp(-57.110/RT) [OH-]0.7 t. The expression in Ca(OH)2 medium for [OH-] concentrations ranging from 2.21 × 10-2 to 6.98 × 10-2 mol L-1 is the following: r0/-v[1 - (1 - x)1/3] = 9.22 × 10(11) exp(-48.610/RT) [OH-]1.51 t.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 0103-5053
DOI: 10.1590/S0103-50532011001200004
الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001200004Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edssci.S0103.50532011001200004
قاعدة البيانات: SciELO
الوصف
تدمد:01035053
DOI:10.1590/S0103-50532011001200004