Experimental Research on Preparation Technics of High-Purity Quartz Material

2017 ◽  
Vol 748 ◽  
pp. 17-21
Author(s):  
Qi Dong Zhang ◽  
Xiao Li Li ◽  
Yong Sheng Song ◽  
Gui Ying Zhou

In order to make the natural quartz up to the standard of high purity quartz sands, quartz ores are processed to obtain high purity quartz sands by the purifying technologies which include grinding, high-intensity magnetic concentration, flotation and acid leaching, washed by deionized water. The phase, morphology and composition of the prepared quzrtz sands were determined by X-ray diffraction, scanning electron microscope and inductively coupled plasma spectrometers.The results show that impurity minerals adsorb onto the quartz mineral surfaces. Magnetic minerals were removed by magnetic concentration experiment, while other impurities were removed by flotation and acid leaching experiments and they show excellent cleaning effect. Finally a high purity quartz product which contains higher than 99.95% SiO2, less than 0.003% Fe2O3, and less than 0.01% Al2O3 was obtained.

Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 10
Author(s):  
Godfrey Tinashe Bare ◽  
Jean Jacques Kalombo Mbayo ◽  
Sehliselo Ndlovu ◽  
Alan Shemi ◽  
Liberty Chipise

Miners around Zimbabwe used to supply gold concentrates from sulphide flotation to the Kwekwe Roasting Plant (Zimbabwe) for toll treatment. The concentrates were roasted in Edward’s roasters and the calcine product was leached by cyanidation. Due to inefficient roasting, overall gold recoveries of 75–80% left behind a rich calcine leach residue at the Kwekwe Roasting Plant. The characterization performed to establish a potential process route involved several techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), fire assaying and inductively coupled plasma (ICP). Assays conducted on samples from the 350,000 tons tailings dam residue, created over the operational years, gave an average Au grade of 8.58 g/t and 12.54 g/t for Ag. The base metals assayed—0.11% Cu, 0.10% Pb, 0.17% Zn and 26.05% Fe. SiO2 (36.1%), Fe2O3 (36.9%), Mg3Si4O10 (OH)2 (8.9%), NaAlSi3O8 (6.9%), and Fe3O4 (6.4%)—were the major mineral phases in the cyanide leach residue. SEM gold scans on 24 polished sections showed only 2 discrete gold particles of less than 5 µm, with one partially liberated and associated with quartz, while the other was fully liberated. Therefore, the particulate gold in the calcine leach residue was negligible. It was deduced from the analysis after ultrafine milling (P80 < 5 µm) followed by cyanidation that 68.53% of the gold was sub-microscopic. Direct cyanidation using bottle roll resulted in only 2.33% of the total gold being leachable, indicating that the calcine leach residue was highly refractory. Diagnostic leaching by sequential use of acids in order of their strength resulted in HCl leachable phases (CaCO3, CaMg(CO3)2, PbS, Fe1-XS, and Fe2O3) freeing 4.2% of the total Au during subsequent cyanidation leach. H2SO4 leachable phases (Cu–Zn sulphides, labile FeS2) released an additional 26.57% during cyanidation, whereas HNO3 leachable phases (FeS2, FeAsS) released a further 20.98% of Au. After acid treatment and subsequent cyanidation, hot caustic leach of the residue followed by carbon in pulp resulted 4.43% of the total gold being eluted. Therefore, 4.43% of the total gold was surface bound. From the analysis after diagnostic acid leaching, it was deduced that a total of 54.08% of the gold was in the acid-leachable phase. Due to cost and environmental considerations, H2SO4 was selected for the evaluation of acid digestion as a pretreatment stage followed by cyanidation. Increasing the H2SO4 strength for the pretreatment of the calcine leach residue increased gold recoveries during cyanidation.


2020 ◽  
Vol 9 (1) ◽  
pp. 1586-1593
Author(s):  
Tingting Yan ◽  
Shengwen Zhong ◽  
Miaomiao Zhou ◽  
Xiaoming Guo ◽  
Jingwei Hu ◽  
...  

Abstract The extraction of Li from the spent LiFePO4 cathode is enhanced by the selective removal using interactions between HCl and NaClO to dissolve the Li+ ion while Fe and P are retained in the structure. Several parameters, including the effects of dosage and drop acceleration of HCl and NaClO, reaction time, reaction temperature, and solid–liquid ratio on lithium leaching, were tested. The Total yields of lithium can achieve 97% after extraction process that lithium is extracted from the precipitated mother liquor, using an appropriate extraction agent that is a mixture of P507 and TBP and NF. The method also significantly reduced the use of acid and alkali, and the economic benefit of recycling is improved. Changes in composition, morphology, and structure of the material in the dissolution process are characterized by inductively coupled plasma optical emission spectrometry, scanning electron microscope, X-ray diffraction, particle size distribution instrument, and moisture analysis.


2006 ◽  
Vol 118 ◽  
pp. 639-644
Author(s):  
Hye Sung Kim ◽  
Su Chak Ryu

Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) powders is synthesized using the mixed powders of CaCO3 refined from oyster shells and phosphoric acid (H3PO4-98%, Daejung) as starting materials. The characteristic evaluation and chemical analysis of the synthesized powders is performed by X-ray diffraction (XRD), Fourier-transformed infra-red spectroscopy (FT-IR), and inductively-coupled plasma atomic emission spectroscopy (ICPAES). XRD analysis of synthetic powder by heat treatment at 1300°C for 2hrs shows only HAp peaks corresponding to stoichiometric HAp. It is confirmed by ICP-AES test that impurities such as Zn, In, Ti, Ba, Cd, Pb, and Mn, is not detected at all, but small amounts of Ti and Be is observed (0.099ppm Ti and 0.002ppm Ba). Variation of bone density is measured by giving medication of HAp powder with drinking water into human body continuously for three month. After the medication, the bone density is higher than the medication before. This means that HAp powder made from this process can be used as improver of bone density.


2012 ◽  
Vol 9 (4) ◽  
pp. 1788-1795 ◽  
Author(s):  
Olushola S. Ayanda ◽  
Olalekan S. Fatoki ◽  
Folahan A. Adekola ◽  
Bhekumusa J. Ximba

In this study, fly ash was obtained from Matla power station and the physicochemical properties investigated. The fly ash was characterized by x-ray fluorescence, x-ray diffraction, scanning electron microscopy, and inductively coupled plasma mass spectrometry. Surface area, particle size, ash and carbon contents, pH, and point of zero charge were also measured. The results showed that the fly ash is alkaline and consists mainly of mullite (Al6Si2O13) and quartz (SiO2). Highly toxic metals As, Sb, Cd, Cr, and Pb as well as metals that are essential to health in trace amounts were also present. The storage and disposal of coal fly ash can thus lead to the release of leached metals into soils, surface and ground waters, find way into the ecological systems and then cause harmful effect to man and its environments.


Author(s):  
Shiying Zhang ◽  
Lei Zhang ◽  
Yueyao Zhong ◽  
Guodong Wang ◽  
Qingjun Xu

High crystal quality GaN nanorod arrays were fabricated by inductively coupled plasma (ICP) etching using self-organized nickel (Ni) nano-islands mask on GaN film and subsequent repaired process including annealing in ammonia and KOH etching. The Ni nano-islands have been formed by rapid thermal annealing, whose density, shape, and dimensions were regulated by annealing temperature and Ni layer thickness. The structural and optical properties of the nanorods obtained from GaN epitaxial layers were comparatively studied by high-resolution X-ray diffraction (HRXRD), Raman spectroscopy and photoluminescence (PL). The results indicate that damage induced by plasma can be successfully healed by annealing in NH3 at 900 °C. The average diameter of the as-etched nanorod was effectively reduced and the plasma etch damage was removed after a wet treatment process in a KOH solution. It was found that the diameter of the GaN nanorod was continuously reduced and the PL intensity first increased, then reduced and finally increased as the KOH etching time sequentially increased.


2013 ◽  
Vol 49 (14) ◽  
pp. 1249-1263 ◽  
Author(s):  
V. K. Karandashev ◽  
K. V. Zhernokleeva ◽  
V. B. Baranovskaya ◽  
Yu. A. Karpov

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