Kinetics of microwave roasting of zinc slag oxidation dust with concentrated sulfuric acid and water leaching

Author(s):  
Jun Chang ◽  
Li-bo Zhang ◽  
Chang-jiang Yang ◽  
Qianxu Ye ◽  
Jing Chen ◽  
...  
1992 ◽  
Vol 25 (24) ◽  
pp. 6495-6499 ◽  
Author(s):  
Nobuhiro Shibuya ◽  
Roger S. Porter

Life ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 400
Author(s):  
William Bains ◽  
Janusz Jurand Petkowski ◽  
Zhuchang Zhan ◽  
Sara Seager

The chemistry of life requires a solvent, which for life on Earth is water. Several alternative solvents have been suggested, but there is little quantitative analysis of their suitability as solvents for life. To support a novel (non-terrestrial) biochemistry, a solvent must be able to form a stable solution of a diverse set of small molecules and polymers, but must not dissolve all molecules. Here, we analyze the potential of concentrated sulfuric acid (CSA) as a solvent for biochemistry. As CSA is a highly effective solvent but a reactive substance, we focused our analysis on the stability of chemicals in sulfuric acid, using a model built from a database of kinetics of reaction of molecules with CSA. We consider the sulfuric acid clouds of Venus as a test case for this approach. The large majority of terrestrial biochemicals have half-lives of less than a second at any altitude in Venus’s clouds, but three sets of human-synthesized chemicals are more stable, with average half-lives of days to weeks at the conditions around 60 km altitude on Venus. We show that sufficient chemical structural and functional diversity may be available among those stable chemicals for life that uses concentrated sulfuric acid as a solvent to be plausible. However, analysis of meteoritic chemicals and possible abiotic synthetic paths suggests that postulated paths to the origin of life on Earth are unlikely to operate in CSA. We conclude that, contrary to expectation, sulfuric acid is an interesting candidate solvent for life, but further work is needed to identify a plausible route for life to originate in it.


Rare Metals ◽  
2010 ◽  
Vol 29 (2) ◽  
pp. 121-125 ◽  
Author(s):  
Xiuyan Wang ◽  
Jiemin Liu ◽  
Mei Li ◽  
Huili Fan ◽  
Qishan Yang

2000 ◽  
Vol 65 (9) ◽  
pp. 619-630
Author(s):  
Lucijana Arman-Zubic ◽  
Nada Perisic-Janjic ◽  
Marija Lazarevic

The acid-base behaviour of 4-phenyl-5-(4-R-benzyl)-1,2,4-triazoline-3-thione (1(R = OH); 2(R = OC2H5)) was studied in aqueous sulfuric acid and sodium hydroxide solutions. Three ionisation equilibria of compound 1 (pKBH3+ = -4.64, pKBH2 = 7.50, pKBH- = 10.06) and two ionisation equilibria of compound 2 (pKBH2+ = -4.82, pKBH = 7.45) were found. The first equilibrium belongs to the protonation of 1,2,4-triazoline-3-thione, while the second belongs to the dissociation of the same part of the molecule. The third equilibrium represents the dissociation process of the phenolic OH group of compound 1. The kinetics of hydrolysis of compounds 1 and 2 were studied in high concentrated sulfuric acid solutions. The hydrolysis follows an irreversible first-order consecutive reaction path.


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