Recharge Kinetics of the Porous Lead Dioxide Electrode: II . The Effect of Sulfuric Acid Concentration

1985 ◽  
Vol 132 (11) ◽  
pp. 2529-2533 ◽  
Author(s):  
Per Ekdunge ◽  
Daniel Simonsson
2019 ◽  
Vol 116 (2) ◽  
pp. 214
Author(s):  
Hongjun Wang ◽  
Yali Feng ◽  
Haoran Li ◽  
Xiangyi Deng ◽  
Jinxing Kang

The dissolution kinetics of vanadium from spent hydroprocessing catalyst was investigated by leaching with sulfuric acid at atmospheric pressure. The effects of stirring speed (400–800 rpm), initial sulfuric acid concentration (0.60–1.20 mol/l) and reaction temperature (373–423 K) on the vanadium dissolution were studied. The results showed that the vanadium dissolution ratio was practically independent of stirring speed at the investigated range, while increasing with the increases of sulfuric acid concentration and reaction temperature. The experimental data agreed quite well with the shrinking core model, with solid membrane diffusion as the rate controlling step. The apparent activation energy was calculated as 11.44 kJ/mol, and the reaction order with respect to sulfuric acid concentrations was determined to be 1.51. The kinetics equation of the leaching process was established as: 1 − 2x/3 − (1 − x)2/3 = 0.067[H2SO4]1.51exp[ − 11563/RT ]t.


1989 ◽  
Vol 42 (9) ◽  
pp. 1527 ◽  
Author(s):  
TH Randle ◽  
AT Kuhn

Lead dioxide is a strong oxidizer in sulfuric acid, consequently electrochemical oxidation of solution species at a lead dioxide anode may occur by a two-step, C-E process (chemical oxidation of solution species by PbO2 followed by electrochemical regeneration of the reduced lead dioxide surface). The maximum rate of each step has been determined in sulfuric acid for specified lead dioxide surfaces and compared with the rates observed for the electrochemical oxidation of cerium(III) and manganese(II) on the same electrode surfaces. While the rate of electrochemical oxidation of a partially reduced PbO2 surface may be sufficient to support the observed rates of CeIII and MnII oxidation at the lead dioxide anode, the rate of chemical reaction between PbO2 and the reducing species is not. Hence it is concluded that the lead dioxide electrode functions as a simple, 'inert' electron-transfer agent during the electrochemical oxidation of CellI and MnII in sulfuric acid. In general, it will most probably be the rate of the chemical step which determines the feasibility or otherwise of the C-E mechanism.


2021 ◽  
Vol 6 (1) ◽  
pp. 156-164
Author(s):  
Jessica E. Guzmán-Pérez ◽  
◽  
Oscar J. Salinas-Luna ◽  
Ernesto Favela-Torres ◽  
Nohemi López-Ramírez ◽  
...  

Water hyacinth (Eichhornia crassipes) is considered a pernicious herb in many parts of the world due to its rapid growth. However, for its high content of cellulose and hemicellulose, it could be considered as raw material to produce fermentable sugars. In this work, the effect of sulfuric acid concentration by thermochemical pretreatment and enzymatic hydrolysis on the release of sugars from water hyacinth was evaluated. Initially, the effect of the sulfuric acid concentration from 1.5 to 9% at 120 ºC was evaluated. With 1.5%, the release of reducing sugars was 160 milligrams of reducing sugars per gram of dry matter (mg red-sug/g dm). After the thermochemical pretreatment, the enzymatic hydrolysis with the cellulase complex (NS22086) allowed obtaining a reducing sugars concentration up to 317 mg red-sug/g dm. These thermochemical and enzymatic approaches to recover reducing sugars from water hyacinth is promising and should be evaluated for bioprocess using reducing sugars as the main source of carbon, such as bioethanol production.


Minerals ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 565 ◽  
Author(s):  
Norman Toro ◽  
Nelson Herrera ◽  
Jonathan Castillo ◽  
Cynthia Torres ◽  
Rossana Sepúlveda

In this study, the surface optimization methodology was used to assess the effect of three independent variables—time, particle size and sulfuric acid concentration—on Mn extraction from marine nodules during leaching with H2SO4 in the presence of foundry slag. The effect of the MnO2/Fe ratio and particle size (MnO2) was also investigated. The maximum Mn extraction rate was obtained when a MnO2 to Fe molar ratio of 0.5, 1 M of H2SO4, −320 + 400 Tyler mesh (−47 + 38 μm) nodule particle size and a leaching time of 30 min were used.


2013 ◽  
Vol 699 ◽  
pp. 28-33 ◽  
Author(s):  
Yun Fei Long ◽  
Jing Su ◽  
Xian Jia Ye ◽  
Hai Feng Su ◽  
Yan Xuan Wen

Bagasse, a fibrous residue from sugarcane juice extraction, was used as a reducing agent to roast low-grade pyrolusite in N2. The roasted ore was further leached using sulfuric acid, to convert manganese oxide in the ore to manganese sulfate. The effects of weight ratio of bagasse to manganese ore, roasting temperature, roasting time, leaching temperature, leaching time, stirring speed and sulfuric acid concentration on the leaching recovery of manganese were investigated. Optimal conditions were determined to be a bagasse to manganese ore weight ratio of 0.8:10, roasting temperature of 500°C for 40 min, leaching stirring speed of 100 rpm, sulfuric acid concentration of 3 mol•L-1 and leaching temperature of 50°C for 40 min. The leaching recovery rate of manganese was up to 97.8% at the optimal conditions.


2017 ◽  
Author(s):  
Runlong Cai ◽  
Dongsen Yang ◽  
Yueyun Fu ◽  
Xing Wang ◽  
Xiaoxiao Li ◽  
...  

Abstract. The predominating role of aerosol Fuchs surface area, AFuchs, in determining the occurrence of new particle formation (NPF) events in Beijing was elucidated in this study. Analysis was based on a field campaign from March 12th to April 6th, 2016, in Beijing, during which aerosol size distributions down to ~ 1 nm and sulfuric acid concentration were simultaneously monitored. The 26 days were classified into 11 typical NPF days, 2 undefined days, and 13 non-event days. A dimensionless factor, LΓ, characterizing the relative ratio of the coagulation scavenging rate over the condensational growth rate and predicting whether or not a NPF event would occur (Kuang et al., 2010), was applied. The three parameters determining LΓ are sulfuric acid concentration, the growth enhancement factor characterizing contribution of other gaseous precursors to particle growth, Γ, and AFuchs. Different from other atmospheric environment such as in Boulder and Hyytiälä, the variations of daily maximum sulfuric acid concentration and Γ in Beijing are in a narrow range with geometric standard deviations of 1.40 and 1.31, respectively. Positive correlation was found between estimated new particle formation rate, J1.5, and sulfuric acid concentration with a mean fitted exponent of 2.4. However, sulfuric acid concentration on NPF days is not significantly higher than that on non-event days. Instead, AFuchs varies greatly among days in Beijing with a geometric standard deviation of 2.56, while it is relatively stable at other locations such as Tecamac, Atlanta, and Boulder. Good correlation was found between AFuchs and LΓ in Beijing (R2 = 0.88). It appears that the abundance of gaseous precursors such as sulfuric acid in Beijing is high enough to have nucleation, however, it is AFuchs that determines the occurrence of NPF event in Beijing. 10 in 11 NPF events occurred when AFuchs is smaller than 200 μm2/cm3, and the NPF event was suppressed due to coagulation scavenging when AFuchs is larger than 200 μm2/cm3. Measured AFuchs is in good correlation with PM2.5 mass concentration (R2 = 0.85) since AFuchs in Beijing is mainly determined by particles in the size range of 50–500 nm that also contribute to PM2.5 mass concentration.


Metals ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 1062 ◽  
Author(s):  
Kivanc Korkmaz ◽  
Mahmood Alemrajabi ◽  
Åke Rasmuson ◽  
Kerstin Forsberg

In the present study, the recovery of valuable metals from a Panasonic Prismatic Module 6.5 Ah NiMH 7.2 V plastic casing hybrid electric vehicle (HEV) battery has been investigated, processing the anode and cathode electrodes separately. The study focuses on the recovery of the most valuable compounds, i.e., nickel, cobalt and rare earth elements (REE). Most of the REE (La, Ce, Nd, Pr and Y) were found in the anode active material (33% by mass), whereas only a small amount of Y was found in the cathode material. The electrodes were leached in sulfuric acid and in hydrochloric acid, respectively, under different conditions. The results indicated that the dissolution kinetics of nickel could be slow as a result of slow dissolution kinetics of nickel oxide. At leaching in sulfuric acid, light rare earths were found to reprecipitate increasingly with increasing temperature and sulfuric acid concentration. Following the leaching, the separation of REE from the sulfuric acid leach liquor by precipitation as NaREE (SO4)2·H2O and from the hydrochloric acid leach solution as REE2(C2O4)3·xH2O were investigated. By adding sodium ions, the REE could be precipitated as NaREE (SO4)2·H2O with little loss of Co and Ni. By using a stoichiometric oxalic acid excess of 300%, the REE could be precipitated as oxalates while avoiding nickel and cobalt co-precipitation. By using nanofiltration it was possible to recover hydrochloric acid after leaching the anode material.


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