Adsorptive Recovery of Auro-Dicyanide Anions from Aqueous Solutions using Activated Carbon-Magnesium Oxide (C-MgO) Nanocomposite as Adsorbent

MRS Advances ◽  
2018 ◽  
Vol 3 (34-35) ◽  
pp. 1955-1967
Author(s):  
Tatenda C Madzokere ◽  
Gey T Musarurwa ◽  
Godcontrols Jere ◽  
Trymore Chitambwe ◽  
Haledene Chiririwa

ABSTRACTThe reprocessing of tailings or gold mine waste dumps to extract gold has become an attractive proposition for mining houses worldwide because of the availability of gold which was not easily recovered using old technologies. This study seeks to exploit the novel properties of nanostructured materials in enhancing gold extraction from gold mine tailings. The beneficiation of slimes or tailings involved taking samples for mineralogical studies, synthesis of a novel adsorbent medium (nano C-MgO) prepared by using both chemical and mechano-synthesis methods, oxidative pre-treatment of flotation concentrates, cyanidation and final recovery of the precious metal from solution in a Carbon in Column (CIC) system. The nanocomposite adsorbent was studied by powder X-ray Diffraction (XRD) for structural analysis, Field Emission Scanning Electronic Microscopy (FESEM) for surface morphology, Energy-dispersive X-ray spectroscopy (EDX) for elemental analysis and Fourier Transform Infrared (FTIR) spectroscopy for chemical structure analysis. The Brunauer-Emmett-Teller (BET) Surface Area Analysis procedure was employed to determine the total specific surface area of the nano-adsorbent. Representative tailings samples of 100-500 g were obtained for different analytical investigations using a riffle splitter. The tailings grade was analysed using the Atomic Absorption Spectroscopy (AAS) technique and was found to be an average of 0.5 g/tonne. A comparative Pseudo-Equilibrium test showed that the novel C-MgO nano adsorbent had an average of 84% recovery against 70 % for convectional activated carbon. The average crystalline size of 4.5 -11nm for the majority of MgO nanoparticles was obtained using Debye-Scherrer formula. FESEM confirmed that nano MgO was porous in nature and highly agglomerated whilst EDX exhibited the successful synthesis of the nano-composite product. This work also shows that the nano-adsorbent presents a huge potential for application in the conventional processes for gold adsorption.

2021 ◽  
Author(s):  
Ashok Kumar ◽  
Kaman Singh ◽  
Rayees Ahamad Bhat

Adsorption is an important technique that significances the characteristics of porous solid materials and fine powders. The importance of porous solid materials and fine powders has been recognized when porous coal used for various applications such as catalysis, separation, isolation, sensors, chromatography, etc. Herein, the synthesis of mesoporous activated carbon derived from agricultural waste using TiO2. The TiO2-modified carbon was characterized employing scanning electron microscope (SEM), attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, powder X-ray diffraction (pXRD), Brunauer–Emmett–Teller (BET) surface area analyzer and X-ray photoelectron spectroscopy (XPS). The obtained results suggested that the TiO2-modified carbon could be a potential material for various application like dye removal, metal removal and allied areas. This book chapter describes the commonly used classifications of porous bulk materials and also reported here the characterization of porous solid materials and fine powders with special reference to the evaluation of the surface area, pore size distribution and thermodynamic parameters of the different mesoporous material, at various scales of resolution using relevant techniques. These materials comprise several levels of structures that of the mesopores, micropores as well as macropores. The apparent topography analysis of these materials, of various pore diameters, synthesized in our laboratory has been determined at various scales with the help of various characterization techniques.


2018 ◽  
Vol 6 (1) ◽  
pp. 46
Author(s):  
Nkwaju Yanou Rachel ◽  
Baçaoui Abdelaziz ◽  
Ndi Julius Nsami ◽  
Kouotou Daouda ◽  
Yaacoubi Abdelrani ◽  
...  

AgNO3- activated carbon composite based palm kernel shell was prepared by hydrothermal carbonization. The concentration of AgNO3, activation temperature and impregnation time were investigated on five responses (iodine number, methylene blue number, BET surface area, micropore volume and total pore volume). The most influential parameters of the preparation process were optimized using the Doehlert optimal design. From the ANOVA, the following optimal conditions of preparation were retained: 0.068 mol/L, 210°C and 3.7 h for AgNO3 concentration, activation temperature and impregnation time respectively. The activated carbon (AC) and the composite (AC-AgNO3) were characterized using Fourier Transform infrared spectroscopy, X-Ray diffraction, Scanning Electron Microscopy coupled to Energy Dispersive X-ray spectroscopy and measurements of the surface area. The XRD pattern and SEM-EDX clearly confirmed the presence of silver in the composite. The experimental parameters of AC- AgNO3 composite were as followed: 708.44 mg/g; 293.09 mg/g; 713.0 m2/g; 0.49 cm3/g and 0.76 cm3/g, for iodine number, methylene blue number, BET surface area, micropore volume and total pore volume of AC- AgNO3 respectively. The antibacterial test carried on Escherichia Coli showed that AC-AgNO3 composite has a high-improved antibacterial property of 99.99% fixation with a dosage of 1500 ppm for 5 hours of contact time.


2018 ◽  
Vol 2018 ◽  
pp. 1-14 ◽  
Author(s):  
H. Ait Ahsaine ◽  
Z. Anfar ◽  
M. Zbair ◽  
M. Ezahri ◽  
N. El Alem

Zirconium oxide/activated carbon (Zr3O/AC) composite was synthesized to remove methylene blue (MB) and crystal violet (CV) from the aqueous medium. The Zr3O/AC sample was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analyses (EDS), Raman spectroscopy (RS), BET surface area, and Fourier transform infrared spectroscopy (FTIR). XRD profiles confirmed the successful synthesis of the zirconium oxide/activated carbon composite. SEM images showed multideveloped walls with irregular particle size with channel arrays. The nitrogen physisorption combines I and IV types with a calculated BET surface area of 1095 m2/g. Raman spectrum illustrated a disorder of both crystalline structure and the graphitic structure. The adsorption was better fitted to the pseudo-second-order (PSO) kinetic model. Langmuir model fitted better the experimental results of MB adsorption, whereas the CV was better consistent with the Freundlich model. The obtained results suggested that the MB and CV adsorption might be influenced by the mass transfer that involves multiple diffusion steps. The maximum adsorption capacities are 208.33 and 204.12 mg/g for MB and CV, respectively. The MB and CV removal mechanisms were proposed, and statistical optimization was performed using central composite design combined with the response surface methodology.


2021 ◽  
Vol 14 ◽  
pp. 1-9
Author(s):  
Nur rahimah Said ◽  
Hazirah Syahirah Zakria ◽  
Siti Nor Atika Baharin ◽  
Nurul' Ain Jamion

Azo dyes are recognised as contaminants from the textile and printing industries that lead to human toxicity. Copper(II) activated carbon (CuAC) is an effective removal agent of dyes in these industries. The purpose of this study is to synthesise and characterise CuAC from date seeds. In addition, the efficiency of CuAC as a removal of Congo red (CR) in aqueous solution is also studied. Activated carbon (AC) was prepared from date seeds using phosphoric acid as activating agent, followed by activation process in a furnace at 500 ℃ for 2 hours. Copper(II) nitrate was used in the impregnation of AC to produce CuAC. The AC and CuAC were characterised using Attenuated Total Reflectance Fourier-Transform Infrared Spectroscopy (ATR-FTIR), BET surface area (SBET), Scanning Electron Microscope-Energy Dispersive X-Ray Spectroscopy (SEM-EDX), Atomic Absorption Spectroscopy (AAS) and X-Ray Diffraction (XRD). UV-VIS Spectroscopy was used to determine dye concentrations after treatment with removal agent of CuAC. The characterisation data proved that the CuAC has been successfully synthesised with 0.33% Cu(II) loaded onto AC and its surface area increased from 8.37 m2/g to 384.82 m2/g. The dye removal study was conducted at 10 ppm concentration of dye. Result revealed that 0.2 g of CuAC at pH 2 in 90 min removed 100% of CR dye.


BioResources ◽  
2020 ◽  
Vol 15 (2) ◽  
pp. 2133-2146
Author(s):  
Gervais Kounou Ndongo ◽  
Ndi Julius Nsami ◽  
Ketcha Joseph Mbadcam

Ferromagnetic activated carbon (FAC) was prepared through impregnation of cassava peel with FeCl3 (3.75%) solution and pyrolyzed at 800 °C. Samples were characterized using iodine number, methylene blue number, X-ray fluorescence, Fourier transformation infrared, X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled to energy dispersive X-ray spectroscopy, elemental analysis and N2 adsorption for surface area determination. The proximate analysis of cassava peel showed that the moisture content, fixed carbon, ash content, and the volatile matter were 3.52%, 82.97%, 4.97%, and 8.54%, respectively. The prepared FAC had a BET surface area of 405.9 m2/g, pore size of 2.03 nm and total pore volume of 0.11 cm3/g. The SEM analysis showed the presence of both micro and mesopores on the FAC sample. The XRD pattern of FAC showed the presence of characteristic peaks of magnetite–maghemite, confirming that the prepared material is ferromagnetic. According to the experimental results, the cassava peels are considered as appropriate raw material for FAC preparation.


2020 ◽  
Vol 32 (3) ◽  
pp. 519-527
Author(s):  
S.R. Kande ◽  
B.H. Zaware ◽  
G.G. Muley ◽  
A.B. Gambhire

A series of SnO2/activated carbon (AC) nanomaterials were prepared by co-doping V(III), Cr(III), Mn(II), Fe(III), Co(III), Ni(II), Cu(II), Zn(II) with nitrogen and sulphur, separately by co-precipitation method, combined with surfactant incorporation method. The as-prepared sample were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), Brunauer-Teller method (BET), diffuse reflectance spectroscopy (DRS), photoluminescence (PL) and Raman spectroscopy. The results showed that the phase composition, crystallite size, BET surface area and optical absorption of samples varied significantly with the nature dopants. The photocatalytic activities of these co-doped SnO2/AC catalysts were investigated by degradation rhodamine B in aqueous solution under solar-light illumination. The results showed an appreciable enhancement in the photoactivity of Fe/N/SnO2/AC as compared to other co-doped SnO2/AC because of smaller particle size, higher specific surface area, photogenerated carrier′s separation and solar light absorption. The degradation rate of rhodamine B dye reached 98 % in 30 min, which is about 10 times higher than that of pure SnO2.


Processes ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 1238
Author(s):  
Garven M. Huntley ◽  
Rudy L. Luck ◽  
Michael E. Mullins ◽  
Nick K. Newberry

Four naturally occurring zeolites were examined to verify their assignments as chabazites AZLB-Ca and AZLB-Na (Bowie, Arizona) and clinoptilolites NM-Ca (Winston, New Mexico) and NV-Na (Ash Meadows, Nevada). Based on powder X-ray diffraction, NM-Ca was discovered to be mostly quartz with some clinoptilolite residues. Treatment with concentrated HCl (12.1 M) acid resulted in AZLB-Ca and AZLB-Na, the chabazite-like species, becoming amorphous, as confirmed by powder X-ray diffraction. In contrast, NM-Ca and NV-Na, which are clinoptilolite-like species, withstood boiling in concentrated HCl acid. This treatment removes calcium, magnesium, sodium, potassium, aluminum, and iron atoms or ions from the framework while leaving the silicon framework intact as confirmed via X-ray fluorescence and diffraction. SEM images on calcined and HCl treated NV-Na were obtained. BET surface area analysis confirmed an increase in surface area for the two zeolites after treatment, NM-Ca 20.0(1) to 111(4) m2/g and NV-Na 19.0(4) to 158(7) m2/g. 29Si and 27Al MAS NMR were performed on the natural and treated NV-Na zeolite, and the data for the natural NV-Na zeolite suggested a Si:Al ratio of 4.33 similar to that determined by X-Ray fluorescence of 4.55. Removal of lead ions from solution decreased from the native NM-Ca, 0.27(14), NV-Na, 1.50(17) meq/g compared to the modified zeolites, 30 min HCl treated NM-Ca 0.06(9) and NV-Na, 0.41(23) meq/g, and also decreased upon K+ ion pretreatment in the HCl modified zeolites.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer–Emmett–Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of –COOH and –NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.


2013 ◽  
Vol 594-595 ◽  
pp. 73-77 ◽  
Author(s):  
Sze Mei Chin ◽  
Suriati Sufian ◽  
Jeefferie Abd Razak

This paper highlights on the hydrogen production through photocatalytic activity by using hematite nanoparticles synthesized from self-combustion method based on different stirring period. The morphologies and microstructures of the nanostructures were determined using Field-Emission Scanning Electron Microscope (FESEM), X-Ray Diffractometer (XRD) and Particle Size Analyser (PSA). Besides that, surface area analyser was used to determine the BET surface area of the hematite samples. The hematite nanocatalyst as-synthesized are proven to be rhombohedral crystalline hematite (α-Fe2O3) with particle diameters ranging from 60-140 nm. The BET specific surface area of hematite samples increased from 5.437 to 7.6425 m2/g with increasing stirring period from 1 to 4 weeks. This caused the amount of hydrogen gas produced from photocatalytic water splitting to increase as well.


2021 ◽  
Author(s):  
Emmanuel Ayodele ◽  
Victoria Ezeagwula ◽  
Precious Igbokwubiri

Abstract Bamboo trees are one of the fastest growing trees in tropical rainforests around the world, they have various uses ranging from construction to fly ash generation used in oil and gas cementing, to development of activated carbon which is one of the latest uses of bamboo trees. This paper focuses on development of activated carbon from bamboo trees for carbon capture and sequestration. The need for improved air quality becomes imperative as the SDG Goal 12 and SDG Goal13 implies. One of the major greenhouse gases is CO2 which accounts for over 80% of greenhouse gases in the environment. Eliminating the greenhouse gases without adding another pollutant to the environment is highly sought after in the 21st century. Bamboo trees are mostly seen as agricultural waste with the advent of scaffolding and other support systems being in the construction industry. Instead of burning bamboo trees or using them for cooking in the local communities which in turn generates CO2 and fly ash, an alternative was considered in this research work, which is the usage of bamboo trees to generate activated, moderately porous and high surface area carbon for extracting CO2 from various CO2 discharge sources atmosphere and for water purification. This paper focuses on the quality testing of activated carbon that can effectively absorb CO2. The porosity, pore volume, bulk volume, and BET surface area were measured. The porosity of the activated carbon is 27%, BET surface area as 1260m²/g. Fixed carbon was 11.7%, Volatility 73%, ash content 1.7%.


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