Catalytic Hydrolysis of Hydrogen Cyanide on Cu-Al Catalyst

2015 ◽  
Vol 1094 ◽  
pp. 15-19
Author(s):  
Lin Xia Yan ◽  
Sen Lin Tian ◽  
Qiu Lin Zhang

Cu-Al catalysts were synthesized by the co-precipitation method to study hydrolysis of hydrogen cyanide. During the synthesis, the impact of Cu/Al molar ratio, pH value and calcination temperature was investigated and the best synthesis condition was found. The results indicate that the remove of hydrogen cyanide first increases and then decreases with increasing Cu/Al molar ratio, pH value and calcination temperature, which reaches the maxima and remains above 95% at 360 min when Cu/Al molar ratio is 2:1, pH value is approximately 8.0 and calcination temperature is 400°C around. The analysis of X-ray diffraction (XRD) shows that Cu content is the main influence factor at Cu/Al molar ratio below 2:1 whereas crystallinity of catalysts is the key factor at Cu/Al molar ratio above 2:1.

2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.


2010 ◽  
Vol 105-106 ◽  
pp. 286-288 ◽  
Author(s):  
Hai Yang Bo ◽  
Guo Qiang Tan ◽  
Hong Yan Miao ◽  
Ao Xia

Bismuth ferrite powders were synthesized by a simple citric acid complexing co-precipitation method at much lower temperature of 600°C. The work studies the calcination temperature and molar ratio of Fe and Bi on the structure and morphology. The as-prepared BiFeO3 powder was characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscope and Fourier transform infrared spectrophotometer. The result shows that the phase pure BiFeO3 powders with cubic morphology were prepared as the calcination temperature was 600°C and molar ratio of Fe and Bi was 1:1. The nanoparticles was uniform with the size of about 200nm.


2018 ◽  
Vol 77 (5) ◽  
pp. 1336-1345 ◽  
Author(s):  
Jicheng Yu ◽  
Jia Lu ◽  
Yong Kang

Abstract Chemical precipitation method was adopted to remove sulfate from wet flue gas desulfurization (FGD) wastewater and mixtures of Ca(OH)2 (CH) and NaAlO2 (SA) were used as precipitants. The mechanisms of sulfate removal were explored according to the experimental and simulated results. These showed that three kinds of precipitations, which were gypsum, ettringite and co-precipitation onto aluminum hydroxides, were formed when sulfate in water reacted with CH and SA. The optimum operation condition for removing sulfate was that the molar ratio of CH/SA was 2, the initial pH value 5, the precipitant dosage 15 g/L, the reaction time 20 min, and the reaction temperature 55 °C. The sulfate was reduced from 4,881 mg/L to 784 mg/L under the optimized condition. In addition, the heavy metals and fluoride were also mostly removed. The post treatments of the supernatant illustrated that removal of sulfate from wet FGD wastewater by co-precipitation with CH and SA was a better choice.


2017 ◽  
Vol 866 ◽  
pp. 73-76
Author(s):  
Thitiyada Taewana ◽  
Rewadee Wongmaneerung

In the present work, hydroxyapatite (HAp) were synthesised from three types eggshells (hen eggshells, duck eggsshells and quail eggsshells) by co-precipitation method. By using recycled eggshells, there were calcined at 700-900 °C for 2 h to form calcium carbonate (CaCO3). Then, CaCO3 and ammonium dihydrogenphosphate (NH4H2PO4) were used as precursor to produce HAp. The molar ratio of Ca to P was 1.67 : 1. In order to determine the most suitable calcination temperature to produce HAp based on purity of CaCO3, HAp were investigated over the temperatures range of 800-1100 °C for 2 h. Phase formation and microstructure evolution of HAp samples were determined by using (XRD), (SEM) and (FTIR) respectively. The results showed that CaCO3 formed at 700 °C for 2 h of all eggshell types. XRD investigations show that HAp powder were stable up to 1100 °C with hexagonal structure. SEMinvestigations demonstrate that the HAp powder obtained with a sphere morphology and FTIR confirmed that the HAp powder calcined at 1100 °C corresponded to the phosphate group in PO43- with significant characteristic peaks at 1026.5 and 563.9 cm-1.


2013 ◽  
Vol 662 ◽  
pp. 520-523
Author(s):  
Ling Ling Niu ◽  
Fang He ◽  
Shang Zhen Zhao

The calcination products of Mg/(Al-Fe) hydrotalcite-like compounds (HMAF) were used as adsorbent to remove perchlorate in affected water. HMAF were synthesized by co-precipitation method at a constant pH value, the best calcined temperature is 500°C and the optimal Mg/Al/Fe molar ratio is 3:0.8:0.2 (CHMAF5%). Factors such as adsorbent dose, initial pH, initial perchlorate concentration affecting perchlorate adsorption were studied. Results showed that the best parameters of adsorbent dose, pH and perchlorate concentration are 0.2g, pH 4-10 and 2000µg/l, respectively. The calcination products of HMAF can be a promising adsorbent for perchlorate removal.


2021 ◽  
Vol 55 (5) ◽  
Author(s):  
Jing Zhang

Antimony tin oxide (ATO) nanoparticles were prepared using co-precipitation with tin chloride and antimony chloride as the main raw materials. X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and ultraviolet-visible spectrophotometry were used to characterize the crystal structure, morphology and laser reflectivity. The effects of the pH value, co-precipitation reaction temperature, calcination temperature and calcination time on the laser reflectivity of ATO nanoparticles were studied. The results show that, compared with the undoped SnO2 powder, the reflectivity of a Sb-doped ATO powder at a laser wavelength of 1.06 µm is significantly reduced, and with an increase in the Sb doping, the reflectivity of the ATO powder at 1.06 µm first decreases and then increases. When the Sb/Sn molar ratio is 2/10, the reflectivity decreases to the lowest point, which is caused by the high concentration of Sb5+. ATO powders (Sb/Sn = 2/10) prepared at a titration-end-point pH of 2, co-precipitation temperature of 70 °C, calcination temperature of 800 °C and calcination time of 6 h have the lowest laser reflectivity at the laser wavelength of 1.06 µm, which is less than 0.02 %.


Author(s):  
Buyan-Ulzii Battulga ◽  
Tungalagtamir Bold ◽  
Enkhsaruul Byambajav

AbstractNi based catalysts supported on γ-Al2O3 that was unpromoted (Ni/γAl2O3) or promoted (Ni–Fe/γAl2O3, Ni–Co/γAl2O3, and Ni–Fe–Co/γAl2O3) were prepared using by the impregnation – co-precipitation method. Their catalytic performances for CO methanation were studied at 3 atm with a weight hourly space velocity (WHSV) of 3000 ml/g/h of syngas with a molar ratio of H2/CO = 3 and in the temperature range between 130 and 350 °C. All promoters could improve nickel distribution, and decreased its particle sizes. It was found that the Ni–Co/γAl2O3 catalyst showed the highest catalytic performance for CO methanation in a low temperature range (<250 °C). The temperatures for the 20% CO conversion over Ni–Co/γAl2O3, Ni–Fe/γAl2O3, Ni–Fe–Co/γAl2O3 and Ni/γAl2O3 catalysts were 205, 253, 263 and 270 °C, respectively. The improved catalyst distribution by the addition of cobalt promoter caused the formation of β type nickel species which had an appropriate interacting strength with alumina support in the Ni–Co/γAl2O3. Though an addition of iron promoter improved catalyst distribution, the methane selectivity was lowered due to acceleration of both CO methanation and WGS reaction with the Ni–Fe/γAl2O3. Moreover, it was found that there was no synergetic effect from the binary Fe–Co promotors in the Ni–Fe–Co/γAl2O3 on catalytic activity for CO methanation.


Author(s):  
Ghazanfar Abbas ◽  
Rizwan Raza ◽  
Muhammad Ashraf Chaudhry ◽  
Bin Zhu

The entire world’s challenge is to find out the renewable energy sources due to rapid depletion of fossil fuels because of their high consumption. Solid Oxide Fuel Cells (SOFCs) are believed to be the best alternative source which converts chemical energy into electricity without combustion. Nanostructured study is required to develop highly ionic conductive electrolyte for SOFCs. In this work, the calcium doped ceria (Ce0.8Ca0.2O1.9) coated with 20% molar ratio of two alkali carbonates (CDC-M: MCO3, where M = Na and K) electrolyte was prepared by co-precipitation method in this study. Ni based electrode was used to fabricate the cell by dry pressing technique. The crystal structure and surface morphology was characterized by X-Ray Diffractometer (XRD), Scanning Electron Microscopy (SEM) and High Resolution Transmission Electron Microscopy (HRTEM). The particle size was calculated in the range of 10–20nm by Scherrer’s formula and compared with SEM and TEM results. The ionic conductivity was measured by using AC Electrochemical Impedance Spectroscopy (EIS) method. The activation energy was also evaluated. The performance of the cell was measured 0.567W/cm2 at temperature 550°C with hydrogen as a fuel.


2013 ◽  
Vol 785-786 ◽  
pp. 449-454
Author(s):  
Yan Zhao ◽  
Chun Yan Wu ◽  
Dan Qin ◽  
Xin Lai ◽  
Si Wu ◽  
...  

SrWO4 octahedrons, flowers, bundles, ellipsoids and dendrites had been successfully synthesized via surfactant-assisted method. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), photo-luminescent spectra techniques (PL) and fourier transrform infrared spectrometer (FTIR). By through various comparison experiments, it can be found that some related experimental parameters including the reagent concentration, [Sr2+]/[WO42-] molar ratio (R), aging temperature and the pH value had great influences on morphology of the products.


2013 ◽  
Vol 781-784 ◽  
pp. 239-242
Author(s):  
Lei Wang ◽  
Peng Xiao

In this paper, SiMgAl hydotalcite synthesis conditions were investigated using co-precipitation method, within a relatively stable pH environment of 8~9. Our research, analysis and discussion focused on the effects of major factors, such as material molar ratio ,silicon content and aged condition, on the structures of synthetic products. To achieve stable and accurate data, synthetic products were characterized by XRD and IR under the identical conditions. As shown in the results, it is suggested that the best Crystallization temperature is 70°C, molar ratio of Mg to Al is 3:1, and the best content of Silicon is 0.015mol/mol.


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