scholarly journals Direct Acid Leaching of Sphalerite: An Approach Comparative and Kinetics Analysis

Minerals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 359
Author(s):  
Nallely G. Picazo-Rodríguez ◽  
Ma. de Jesus Soria-Aguilar ◽  
Antonia Martínez-Luévanos ◽  
Isaias Almaguer-Guzmán ◽  
Josue Chaidez-Félix ◽  
...  
Keyword(s):  
Acid Leaching ◽  
Dissolution Kinetics ◽  
Pilot Scale ◽  
Influential Factors ◽  
Acid Media ◽  
Rate Limiting Step ◽  
Leaching Solution ◽  
Direct Leaching ◽  
Media Lab ◽  
Rate Limiting

The present work reports the direct leaching of zinc from a sphalerite concentrate in acid media. Lab-scale and pilot-scale experiments were conducted in atmospheric-pressure and low-pressure reactors, respectively. Leaching of zinc and precipitation of iron was achieved in the same stage using different reagents like Fe3+, O2, O3, and Fe2+ (which is continuously oxidized in the leaching solution by H2O2 and O2). The highest percentage of zinc extraction (96%) was obtained in pilot-scale experiments using H2SO4, Fe2+, and O2. Experimental results were compared with those of other researchers to provide a better understanding of the factors influencing the dissolution of zinc. In the first instance, it was determined from analysis of variance that leaching time and the use of an oxidant agent (O2 or O3) were the most influential factors during the direct leaching of zinc from the sphalerite concentrate. Kinetic models were also evaluated to determine the rate-limiting step of the sphalerite leaching; it was concluded that the type of the sulfur layer formed in the residue (porous or non-porous) depends on the type of the oxidant used in the leaching media, which determines the dissolution kinetics of zinc.

Adsorptive removal of As(III) from aqueous solution by waste litchi pericarps

2016 ◽  
Vol 74 (9) ◽  
pp. 2135-2144 ◽  
Author(s):  
Xiaochen Li ◽  
Jinqiu Qi ◽  
Ruixue Jiang ◽  
Jie Li
Keyword(s):  
Contact Time ◽  
Influential Factors ◽  
Isotherm Models ◽  
Solution Ph ◽  
Rate Limiting Step ◽  
Pseudo Second Order ◽  
Solid Liquid Interface ◽  
Solid Liquid ◽  
Rate Limiting ◽  
Adsorbent Dose

The present study investigated the removal of arsenite anions (AsO33−, referred to as As(III)) from aqueous solutions by waste litchi pericarps (LPs). Influential factors such as the adsorbent dose, contact time, solution pH, and initial As(III) concentration were investigated. The optimum conditions for As(III) adsorption by the LPs occurred at a contact time of 60 min, adsorbent dose of 10.0 g/L, solution pH of 5.0, and initial As(III) concentration of 1 mg/L. A Box–Behnken design with three variables (adsorbent dose, contact time, and solution pH) at three different levels was studied to identify the correlations between the influential factors and the As(III) adsorption; the results showed a significant interaction between the adsorbent dosage and pH. Additionally, adsorption isotherms, kinetics, and thermodynamics were investigated to explore the As(III) adsorption mechanism. Adsorption by the LPs conformed to the Langmuir, Redlich–Peterson, and Koble–Corrigan isotherm models, suggesting that the process proceeds via monolayer, homogeneous adsorption. In addition, the As(III) adsorption could be characterized by a pseudo-second-order mechanism, revealing that the rate-limiting step might be chemisorption. The thermodynamic studies showed that As(III) adsorption by the LPs was spontaneous and endothermic, and disorder at the solid–liquid interface increased in the adsorption process.

Ornithine Decarboxylase Activity in Cultured Endothelial Cells Stimulated by Serum, Thrombin and Serotonin

1978 ◽  
Vol 39 (02) ◽  
pp. 496-503 ◽  
Author(s):  
P A D’Amore ◽  
H B Hechtman ◽  
D Shepro
Keyword(s):  
Endothelial Cells ◽  
Ornithine Decarboxylase ◽  
Decarboxylase Activity ◽  
Aortic Endothelial Cells ◽  
Ornithine Decarboxylase Activity ◽  
Rate Limiting Step ◽  
Bovine Aortic Endothelial Cells ◽  
Limiting Step ◽  
Rate Limiting ◽  
Serum Serotonin

SummaryOrnithine decarboxylase (ODC) activity, the rate-limiting step in the synthesis of polyamines, can be demonstrated in cultured, bovine, aortic endothelial cells (EC). Serum, serotonin and thrombin produce a rise in ODC activity. The serotonin-induced ODC activity is significantly blocked by imipramine (10-5 M) or Lilly 11 0140 (10-6M). Preincubation of EC with these blockers together almost completely depresses the 5-HT-stimulated ODC activity. These observations suggest a manner by which platelets may maintain EC structural and metabolic soundness.

Dynamics of hepatic and peripheral insulin effects suggest common rate-limiting step in vivo

Diabetes ◽  
1993 ◽  
Vol 42 (2) ◽  
pp. 296-306 ◽  
Author(s):  
D. C. Bradley ◽  
R. A. Poulin ◽  
R. N. Bergman
Keyword(s):  
Rate Limiting Step ◽  
Limiting Step ◽  
Rate Limiting

Cobalt/Lewis Acid Catalysis for Hydrocarbofunctionalization of Alkynes via Cooperative C–H Activation

2020 ◽  
Author(s):  
Chang-Sheng Wang ◽  
Sabrina Monaco ◽  
Anh Ngoc Thai ◽  
Md. Shafiqur Rahman ◽  
Chen Wang ◽  
...  
Keyword(s):  
Catalytic System ◽  
Lewis Acid ◽  
Hydrogen Transfer ◽  
Acid Catalysis ◽  
Rate Limiting Step ◽  
Site Selectivity ◽  
Set Up ◽  
Site Selective ◽  
First Time ◽  
Rate Limiting

A catalytic system comprised of a cobalt-diphosphine complex and a Lewis acid (LA) such as AlMe3 has been found to promote hydrocarbofunctionalization reactions of alkynes with Lewis basic and electron-deficient substrates such as formamides, pyridones, pyridines, and azole derivatives through site-selective C-H activation. Compared with known Ni/LA catalytic system for analogous transformations, the present catalytic system not only feature convenient set up using inexpensive and bench-stable precatalyst and ligand such as Co(acac)3 and 1,3-bis(diphenylphosphino)propane (dppp), but also display distinct site-selectivity toward C-H activation of pyridone and pyridine derivatives. In particular, a completely C4-selective alkenylation of pyridine has been achieved for the first time. Mechanistic stidies including DFT calculations on the Co/Al-catalyzed addition of formamide to alkyne have suggested that the reaction involves cleavage of the carbamoyl C-H bond as the rate-limiting step, which proceeds through a ligand-to-ligand hydrogen transfer (LLHT) mechanism leading to an alkyl(carbamoyl)cobalt intermediate.

Kinetics of cyclization of S-ethoxycarbonylmethylisothiouronium chloride to 2-imino-4-thiazolidone

1979 ◽  
Vol 44 (3) ◽  
pp. 912-917 ◽  
Author(s):  
Vladimír Macháček ◽  
Said A. El-bahai ◽  
Vojeslav Štěrba
Keyword(s):  
Hydrochloric Acid ◽  
Dilute Hydrochloric Acid ◽  
Base Catalysis ◽  
General Base ◽  
Rate Limiting Step ◽  
Limiting Step ◽  
Kinetics Of Formation ◽  
Acid Catalyzed ◽  
Rate Limiting ◽  
Kinetics Of

Kinetics of formation of 2-imino-4-thiazolidone from S-ethoxycarbonylmethylisothiouronium chloride has been studied in aqueous buffers and dilute hydrochloric acid. The reaction is subject to general base catalysis, the β value being 0.65. Its rate limiting step consists in acid-catalyzed splitting off of ethoxide ion from dipolar tetrahedral intermediate. At pH < 2 formation of this intermediate becomes rate-limiting; rate constant of its formation is 2 . 104 s-1.

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