scholarly journals The Fabrication of Natural Zeolite Via Co-Precipitation Method as Cu, Pb and Zn Metal Absorbent

2020 ◽  
Vol 57 (3) ◽  
pp. 40-47
Author(s):  
M. Sirait ◽  
K.Sari Dewi Saragih ◽  
S. Gea ◽  

AbstractHeavy metal waste is very dangerous, which can change the condition of water into a solid substance that can be suspended in water and can reduce the cleanliness level of water consumed by living things. To date, heavy metals can be managed through several processes, namely physics, biology or chemistry. One of the ways to overcome heavy metal pollution is to use natural zeolite applying a co-precipitation method, as it is known that zeolite is a powerful natural material to be used for certain purposes. In order to justify the research results, several analyses have been performed, such as X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Surface Area Analyser (SAA), and Atomic Adsorption Spectrophotometric (AAS). From the XRD results, it has been found out that the size of each zeolite with variations in size of 150 mesh, 200 mesh, and 250 mesh is 29.274 nm, 38.665 nm and 43.863 nm, respectively. Moreover, the SEM-EDX has shown that the zeolite under consideration is a type of Na-Zeolite and that the co-precipitation method successfully removes impurity elements, namely, Fe, Ti, and Cl. The results of SAA testing have indicated that the total surface area for each variation of zeolite sizes is 63.23 m2/g, 45.14 m2/g and 59.76 m2/g. The results of the AAS test analysis have demonstrated that the optimal absorption of metal content is observed in a size of 150 mesh zeolite with adsorption power of 99.6 % for Pb metal, 98 % for Cu metal, and 96 % Zn metal.

2018 ◽  
Vol 127 (1A) ◽  
pp. 15
Author(s):  
Ngô Minh Đức

Hydrotalcite was synthesized using the co-precipitation method with  the Mg/Al molar ratio of 3.0 and then  calcined at 450 °C, for 5 h. The obtained solid was characterized by XRD, BET. As seen from results of physical characterization, the synthesized Hydrotalcite material owns large surface area of  309.3 m<sup>2</sup>/g, mean capillary diameter of 11.52 nm. Hydrotalcite application as adsorbent of heavy metal ions. The results of adsorption experiment for Pb<sup>2+</sup> in water showed that the absorption equilibrium was attained after 90 minutes at pH = 5 with maximum adsorption loading capacity of 144.93 mg/g. The synthesized adsorbent could be regenerated with HNO<sub>3</sub> (1M) solution


2013 ◽  
Vol 734-737 ◽  
pp. 2364-2368
Author(s):  
Xiao Guang Ren ◽  
Fu Xia Li ◽  
Peng Li ◽  
Wei Hou

In this study, the hexaaluminate catalyst SrMnMAl10O19-δ(M= Cd、Co、Cu 、Fe、Ni、Zn、Zr、Cr and Y)and SrMnFexAl11-xO19-δ(x=1, 2, 4, 6, 8)have been prepared by co-precipitation method. The catalysts were characterized by powder X-ray diffraction (XRD), surface area (BET), hydrogen temperature programmed reduction (H2-TPR). The reduction catalyst properties of hexaaluminate for deNOx were evaluated by using devices of micro-evaluation. The results showed that the CO could remove NOx very well. The hexaaluminate not only have a good catalytic performance, but also can form a complete crystal calcined at 1200 °C for 4 h.


2006 ◽  
Vol 942 ◽  
Author(s):  
Sang Joon Park ◽  
Tae Wook Eom ◽  
Jae Eun Oh ◽  
Hae Kwang Yang ◽  
Kyung Hwan Kim

ABSTRACTA surfactant-assisted co-precipitation method was employed for obtaining high surface area Ni-SDC with improved structural properties for SOFC applications. In the work, a cationic surfactant, cetyltrimethylammonium bromide(CTAB) was employed with NiCl2, SmCl3 and CeCl3 as precursors and NH4OH as mineralizer. The elimination of surfactants upon calcination gives rise to the formation of high surface area NiO-SDC. When calcined at 600°C, the powders with surface area of 249 m2/g, were obtained and the pore size was 14.45 nm. The powders consist of two phases, the cubic NiO and SDC confirmed with X-ray diffraction identification.


2015 ◽  
Vol 7 (2) ◽  
pp. 1393-1403
Author(s):  
Dr R.P VIJAYALAKSHMI ◽  
N. Manjula ◽  
S. Ramu ◽  
Amaranatha Reddy

Single crystalline nano-sized multiferroic BiFeO3 (BFO) powders were synthesized through simple chemical co-precipitation method using polyethylene glycol (PEG) as capping agent. We obtained pure phase BiFeO3 powder by controlling pHand calcination temperature. From X-ray diffraction studies the nanoparticles were unambiguously identified to have a rhombohedrally distorted perovskite structure belonging to the space group of R3c. No secondary phases were detected. It indicates single phase structure. EDX spectra indicated the appearance of three elements Bi, Fe, O in 1:1:3. From the UV-Vis diffuse reflectance spectrum, the absorption cut-off wavelength of the BFO sample is around 558nm corresponding to the energy band gap of 2.2 eV. The size (60-70 nm) and morphology of the nanoparticles have been analyzed using transmission electron microscopy (TEM).   Linear M−H behaviour and slight hysteresis at lower magnetic field is observed for BiFeO3 nanoparticles from Vibrating sample magnetometer studies. It indicates weak ferromagnetic behaviour at room temperature. From dielectric studies, the conductivity value is calculated from the relation s = L/RbA Sm-1 and it is around 7.2 x 10-9 S/m.


Crystals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 832
Author(s):  
Edna X. Figueroa-Rosales ◽  
Javier Martínez-Juárez ◽  
Esmeralda García-Díaz ◽  
Daniel Hernández-Cruz ◽  
Sergio A. Sabinas-Hernández ◽  
...  

Hydroxyapatite (HAp) and hydroxyapatite/multi-walled carbon nanotube (MWCNT) composites were obtained by the co-precipitation method, followed by ultrasound-assisted and microwave radiation and thermal treatment at 250 °C. X-ray diffraction (XRD) confirmed the presence of a hexagonal phase in all the samples, while Fourier-transform infrared (FTIR) spectroscopy elucidated the interaction between HAp and MWCNTs. The photoluminescent technique revealed that HAp and the composite with non-functionalized MWCNTs present a blue luminescence, while the composite with functionalized MWCNTs, under UV-vis radiation shows an intense white emission. These findings allowed presentation of a proposal for the use of HAp and HAp with functionalized MWCNTs as potential materials for optoelectronic and medical applications.


2015 ◽  
Vol 827 ◽  
pp. 19-24 ◽  
Author(s):  
Nur Afifah ◽  
Nadia Febiana Djaja ◽  
Rosari Saleh

In this study, the photocatalytic activity of pure Fe- doped ZnO and Fe- doped ZnO/Montmorillonite nanocomposite has been investigated for the degradation of malachite green under UV light irradiation. Both photocatalysts were synthesized using co-precipitation method and characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, Fourier-transform infrared absorption, and electron spin resonance. The results showed that the photocatalytic efficiency is better in the presence of montmorillonite compared to pure Fe- doped ZnO. To detect the possible reactive species involved in degradation of organic dyes control experiments with introducing scavengers into the solution of organic dyes were carried out. It is found that electron plays an important role in the degradation of malachite green.


MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.


2011 ◽  
Vol 311-313 ◽  
pp. 1713-1716 ◽  
Author(s):  
Yan Rong Sun ◽  
Tao Fan ◽  
Chang An Wang ◽  
Li Guo Ma ◽  
Feng Liu

Nano-hydroxyapatite with different morphology was synthesized by the co-precipitation method coupled with biomineralization using Ca(NO3)2•4H2O and (NH4)2HPO4 as reagents, adding chondroitin sulfate, agarose and aspartic acid as template. The structure and morphology of the prepared powders were characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM).


2015 ◽  
Vol 645-646 ◽  
pp. 1339-1344 ◽  
Author(s):  
Yan Ting Yin ◽  
Qing Hua Chen ◽  
Ting Ting Yan ◽  
Qing Hua Chen

The objective of this study was to develop a novel silica modified large-sized hydroxyapatite whiskers with improved properties for use in bone repair applications. Large-sized whiskers with a mean length of 250μm were obtained by a hydrothermal co-precipitation method at 150°C, 7.5Mpa in high-pressure reactor. Silica modified hydroxyapatite whiskers were prepared by dissolving TEOS in ethanol solution, then sintering with hydroxyapatite. The compositional and morphological properties of prepared whiskers were studied by means of x-ray diffraction (XRD), Fouier transform infrared (FT-IR), scanning electron microscopy (SEM). The results indicated the evidence of nanosilicon dioxide particles on the surface of HAP whiskers. The size of nanosilicon dioxide particles depends on dropping and stirring rate. Hence, this new type of silica modified large-sized hydroxyapatite whiskers is a valuable candidate for biomedical applications.Key words: hydroxyapatite, hydrothermal co-precipitation, surface modified, whiskers


2020 ◽  
Vol 1 (4) ◽  
pp. 187-193
Author(s):  
Elaheh Gharibshahian

KTiOPO4 nanoparticles are known as the best candidate to utilize for second-harmonic generation in multiphoton microscopes and bio labels. Size and shape are important and effective parameters to control the properties of nanoparticles. In this paper, we will investigate the role of capping agent concentration on the size and shape control of KTP nanoparticles. We synthesized KTP nanoparticles by the co-precipitation method. Polyvinyl alcohol with different mole ratios to titanium ion (1:3, 1:2, 1:1) was used as a capping agent. Products were examined by X-ray diffraction patterns and scanning electron microscopy analyses. X-ray diffraction patterns confirmed the formation of the KTP structure. The biggest (56.36nm) and smallest (39.42nm) grain size were obtained by 1:3 and 1:1 mole ratios of capping agent, respectively. Dumbly, spherical and polyhedral forms of KTP nanoparticles were observed by the change in capping agent mole ratio. The narrowest size distribution of KTiOPO4 nanoparticles was obtained at 1:1 mole ratio of capping agent. Doi: 10.28991/HIJ-2020-01-04-06 Full Text: PDF


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