Separation of Heavy Metal Ions from the Solution Obtained by Leaching Low-Grade Pyrolusite with Pyrite and H2SO4

2013 ◽  
Vol 773 ◽  
pp. 283-288
Author(s):  
Xing Zou ◽  
Xiang Quan Chen ◽  
Hai Chao Xie ◽  
Xiao Dan Qiu

The manganese sulfate solution leached from low-grade pyrolusite with pyrite and H2SO4 contains heavy metal ions of high concentration, influencing the quality of the final products of manganese compounds and causing manganese ions not to be electrolyzed. The present study was focused on the separation of Co, Ni and Zn ions from the leached solution with BaS. By controlling the pH value at 5.0-6.5, temperature at 50-60°C, reaction time at 15 min and mixing velocity at 78 rpm, the heavy metal ions could be separated effectively. Under the above optimized conditions, the ion concentration of Co, Ni, and Zn in the solution was reduced to 0.06 mg.L-1, 0.27mg.L-1 and 0.01mg.L-1, and the separation efficiency was 99.72%, 99.18% and 99.9% respectively. The obtained pure solution meets the demands of manganese electrowinning.

2002 ◽  
Vol 20 (7) ◽  
pp. 607-617 ◽  
Author(s):  
Adil Denizli ◽  
Bora Garipcan ◽  
Sibel Emir ◽  
Süleyman Patir ◽  
Ridvan Say

Details of the adsorption performance of poly(2-hydroxyethylmethacrylate–methacrylamidocysteine) [p(HEMA–MAC)] beads towards the removal of heavy metal ions from aqueous solution were studied. The metal-complexing ligand and/or co-monomer MAC was newly synthesized from methylacrylochloride and cysteine. Spherical beads of average size 150–200 mm were obtained by the radical suspension polymerization of MAC and HEMA conducted in an aqueous dispersion. The p(HEMA–MAC) beads obtained had a specific surface area of 18.9 m2/g. p(HEMA–MAC) beads were characterized by swelling studies, FT-IR spectroscopy and elemental analysis. Such beads with a swelling ratio of 72%, and containing 3.9 mmol MAC/g, were used for heavy metal removal studies. The adsorption capacities of the beads for selected metal ions, i.e. CdII, AsIII, CrIII, HgII and PbII, were investigated in aqueous media containing different amounts of these ions (10–750 mg/l) and at different pH values (3.0–7.0). The adsorption rate was fast in all cases. The maximum adsorption capacities of the p(HEMA–MAC) beads were 1058.2 mg/g for CdII, 123.4 mg/g for AsIII, 199.6 mg/g for CrIII, 639.1 mg/g for PbII and 1018.6 mg/g for HgII. On a molar basis, the following affinity order was observed: CdII > HgII > CrIII > PbII >AsIII. The adsorption capacity of the MAC-incorporated beads was affected significantly by the pH value of the aqueous medium. The adsorption of heavy metal ions from artificial wastewater was also studied. In this case, the adsorption capacities were 52.2 mg/g for CdII, 23.1 mg/g for CrIII, 83.4 mg/g for HgII, 62.6 mg/g for PbII and 11.1 mg/g for AsIII at an initial metal ion concentration of 0.5 mmol/l. The chelating beads could be regenerated easily with a higher effectiveness by 0.1 M HNO3. These features make p(HEMA–MAC) beads potential candidates for heavy metal ion removal at high capacity.


Author(s):  
Shuai Li ◽  
Yulin Zhang ◽  
Ru Feng ◽  
Haoxuan Yu ◽  
Jilong Pan ◽  
...  

As one of the main industrial solid wastes, there are a large number of free alkaloids, chemically bound alkaloids, fluoride, and heavy metal ions in Bayer process red mud (BRM), which are difficult to remove and easily pollute groundwater as a result of open storage. In order to realize the large-scale industrial application of BRM as a backfilling aggregate for underground mining and simultaneously avoid polluting groundwater, the material characteristics of BRM were analyzed through physical, mechanical, and chemical composition tests. The optimum cement–sand ratio and solid mass concentration of the backfilling were obtained based on several mixture proportion tests. According to the results of bleeding, soaking, and toxic leaching experiments, the fuzzy comprehensive evaluation method was used to evaluate the environmental impact of BRM on groundwater. The results show that chemically bound alkaloids that remained in BRM reacted with Ca2+ in PO 42.5 cement, slowed down the solidification speed, and reduced the early strength of red mud-based cemented backfill (RMCB). The hydration products in RMCB, such as AFT and C-S-H gel, had significant encapsulation, solidification, and precipitation inhibition effects on contaminants, which could reduce the contents of inorganic contaminants in soaking water by 26.8% to 93.8% and the leaching of toxic heavy metal ions by 57.1% to 73.3%. As shown by the results of the fuzzy comprehensive evaluation, the degree of pollution of the RMCB in bleeding water belonged to a medium grade Ⅲ, while that in the soaking water belonged to a low grade II. The bleeding water was diluted by 50–100 times to reach grade I after flowing into the water sump and could be totally recycled for drilling and backfilling, thus causing negligible effects on the groundwater environment.


Materials ◽  
2019 ◽  
Vol 12 (2) ◽  
pp. 241 ◽  
Author(s):  
Jian Guo ◽  
Yaqin Song ◽  
Xiaoyang Ji ◽  
Lili Ji ◽  
Lu Cai ◽  
...  

The aim of this study was to optimize the adsorption performance of activated carbon (AC), derived from the shell of Penaeus vannamei prawns, on heavy metal ions. Inexpensive, non-toxic, and renewable prawn shells were subjected to carbonization and, subsequently, KOH-activation to produce nanoporous K-Ac. Carbonized prawn shells (CPS) and nanoporous KOH-activated carbon (K-Ac) from prawn shells were prepared and characterized by FTIR, XRD, BET, SEM, and TEM. The results showed that as-produced K-Ac samples were a porous material with microporous and mesoporous structures and had a high specific surface area of 3160 m2/g, average pore size of about 10 nm, and large pore volume of 2.38 m3/g. Furthermore, batches of K-Ac samples were employed for testing the adsorption behavior of Cd2+ in solution. The effects of pH value, initial concentration, and adsorption time on Cd2+ were systematically investigated. Kinetics and isotherm model analysis of the adsorption of Cd2+ on K-Ac showed that experimental data were not only consistent with the Langmuir adsorption isotherm, but also well-described by the quasi-first-order model. Finally, the adsorption behaviors of as-prepared K-Ac were also tested in a ternary mixture of heavy metal ions Cu2+, Cr6+, and Cd2+, and the total adsorption amount of 560 mg/g was obtained.


Author(s):  

Water factor plays an important role in formation of healthy environment for human beings. Due to unfavorable anthropogenic impact upon environment certain surface and groundwater water supply sources are contaminated with heavy metal compounds. Clints (siliceous rocks) are considered the most promising materials for the natural and waste waters treatment from such ingredients. The paper presents the results of the siliceous rocks’ physical/chemical and operational properties studying. It has been shown that these siliceous rocks satisfy all requirements to filtering materials. Methods of physical/chemical analysis were applied for studying the adsorption processes nature. It was for the first time stated (with methods of potentiometric titration and infra-red spectroscopy) that siliceous rocks included the fixed functional ion-exchange groups in their composition and were subacid cationits. Beside chemical adsorption heavy metal ions interact with siliceous rocks due to the action of their physical nature forces. Physical adsorption contributes the most in the heavy metal compounds up-taking by filtering materials, this is supported by the fact of low values of the process activation energy: from 3 to 8 kJ/gram-molecule. Parameters of the process of heavy metal ions adsorption with siliceous rocks in static and dynamic conditions have been calculated in accordance with the experimental results. Influence of salt content and the liquid phase pH value on the adsorption process has been stated. Optimal conditions for the worked siliceous rocks regeneration have been determined. New data on heavy metals cations adsorption with nuclear filtering materials confirm principal possibility of their use for natural and waste waters treatment.


2021 ◽  
Vol 12 (2) ◽  
pp. 1884-1898

Natural water gets contaminated with heavy metal ions because of industrial effluents' discharge into the aquatic environment. As these heavy metal ions cause various health hazards, they should be removed from the aqueous solution. Heavy metal ion concentration in the aqueous solution is very less, so conventional metal removal and recovery processes cannot be applied here. The adsorption method is a great alternative to all these processes as it is a cost-effective and easy method. The use of natural, low-cost materials as adsorbents is eco-friendly also. However, metal uptake capacity of low-cost materials is very less. So, modification is required for low-cost materials to increase their efficiency. In the present review, different modification procedures adopted by different researchers have been discussed. Different low-cost materials used are sawdust, fruit and vegetable wastes, soil, minerals, etc. The modifying agents are heat, acids, bases, and other chemicals. Nevertheless, most of the studies are limited to batch tests only. Future research should be carried out on the extension of batch tests to column study for the large-scale treatment of contaminated water, and the cost of modification procedures and their impact on the environment should also be assessed.


2020 ◽  
Vol 20 (12) ◽  
pp. 7231-7254 ◽  
Author(s):  
Yuzhe Zhang ◽  
Bin Wang ◽  
Qian Cheng ◽  
Xinling Li ◽  
Zhongyu Li

How to remove harmful heavy metal ions from waste batteries or lithium cells efficiently has been the focus of scholars. More and more metal oxides had been used to deal with the pollution of heavy metal caused by waste batteries in recent years. Nanostructured metal oxides have great potential because of their large comparative areas. The adsorption for these heavy metal ions can be further improved by using modified metal oxides as adsorbents. At present, iron oxide is widely used in this field. Other metal oxides have also been studied in removing these heavy metal ions. Compared to other metal oxides, the adsorbents made of iron oxide are easy to be separated from the reaction system. pH value in the solution can affect the activity of adsorption sites on metal oxides adsorbents and change the distribution of ions in solution. As a result, pH value can significantly influence the adsorption of metal oxides adsorbents for heavy metal ions from waste batteries or lithium cells.


2011 ◽  
Vol 255-260 ◽  
pp. 2791-2796 ◽  
Author(s):  
Hong Mei Ma ◽  
Zhi Liang Zhu ◽  
Yong Qian Cheng

MnO2-loaded D301 weak basic anion exchange resin was used as adsorbent to simultaneously remove Co2+, Ni2+, Cd2+, Zn2+ andCu2+ from aqueous solution contained high concentration of alkali and alkaline-earth metals ions. The effects of solution pH and coexistent ions on the adsorption were investigated. The results indicated that Co2+, Ni2+, Cd2+, Zn2+ andCu2+ can be simultaneously removed in the wide pH range of 3 to 8. The coexistence of PO43− decreased the heavy metal ions removal rate, but for other high concentrations coexistence cations and anions such as Na+, K+, Cl−, NO3−, SO42− and HCO3−, there is no significant impact on removal rate of heavy metals. The adsorption isotherm can be well described by Langmuir isotherm. The adsorption processes followed the pseudo first-order kinetics model. High adsorption capacity makes it a good promising candidate material for simultaneous removal of Co2+, Ni2+, Cd2+, Zn2+ andCu2+ from aqueous solution with the co-existence of high concentration of alkali and alkaline-earth metals ions.


2014 ◽  
Vol 2014 ◽  
pp. 1-6
Author(s):  
Natsagdorj Narantsogt ◽  
Gunchin Burmaa ◽  
Adiya Perlee-Oidov ◽  
Nyamdorj Shurkhuu ◽  
Namsrai Javkhlantugs

The synthesized poly[N,N′-bis(3-silsesquioxanilpropyl)-thiocarbamide] (PSTM-3T) was used and the surface morphology and microstructure of it were analyzed by scanning electron microscopy with energy dispersive spectrometer (SEM/EDS). The molecular structure change of the PSTM-3T polymer of the PSTM-3T after treatment by acidic solution with different pHs was revealed using FT-IR experiments andab initiocalculations with density functional theory method. The sorption efficiency of the heavy metal ions depends on the molecular structure change of PSTM-3T after treatment of different pH aqueous solutions. After the treatment of acidic solution (pH = 2) of PSTM-3T, the polymer formed the tautomer state to increase the sorption efficiency for chromate ion. For the increment of pH value for acidic solution, the PSTM-3T polymer was dissociated to increase the sorption efficiency for copper ion.


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