Synthesis and Characterization of ZnAPSO-34 Membrane on Porous α- Al2O3 Support

2013 ◽  
Vol 291-294 ◽  
pp. 2758-2764 ◽  
Author(s):  
Abbad Brahim ◽  
Azeddine Lounis ◽  
Sylvie Condom ◽  
K. Taibi

Zeolites and other inorganic molecular sieve membranes have shown potential for separation based on molecular size and shape because of their small pore sized, typically less than 1nm, and their narrow pore size distribution. The in situ synthesis of ZnAPSO-34 films supported on alumina substrates is reported in this paper. Organic and water contents, alumina source, and supports have important roles in the syntheses of ZnAPSO-34 film. Traditionally, the role of organic molecules in the synthesis of these materials has been associated to their structure-directing and their protonation abilities. In our work, we were interested in a new family of materials; the alumino-phosphate, which are similar to zeolites. This work concerns the in-situ preparation of films of ZnAPSO-34 on porous α -alumina tubes. These films of ZnAPSO-34 corresponding to the structure Chabazite (CHA) have an effective intracrystal nanopore diameter of 0.38 nm. The hydrothermal synthesis was made in an autoclave under autogenous pressure. The membrane used was characterized by thermo-gravimetric analysis (TGA) and differential thermal analysis, X-ray diffraction and scanning electron microscopy after calcination.

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Luqman Ali Shah ◽  
Rida Javed ◽  
Mohammad Siddiq ◽  
Iram BiBi ◽  
Ishrat Jamil ◽  
...  

AbstractThe in-situ stabilization of Ag nanoparticles is carried out by the use of reducing agent and synthesized three different types of hydrogen (anionic, cationic, and neutral) template. The morphology, constitution and thermal stability of the synthesized pure and Ag-entrapped hybrid hydrogels were efficiently confirmed using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and thermo gravimetric analysis (TGA). The prepared hybrid hydrogels were used in the decolorization of methylene blue (MB) and azo dyes congo red (CR), methyl Orange (MO), and reduction of 4-nitrophenol (4-NP) and nitrobenzene (NB) by an electron donor NaBH4. The kinetics of the reduction reaction was also assessed to determine the activation parameters. The hybrid hydrogen catalysts were recovered by filtration and used continuously up to six times with 98% conversion of pollutants without substantial loss in catalytic activity. It was observed that these types of hydrogel systems can be used for the conversion of pollutants from waste water into useful products.


2011 ◽  
Vol 221 ◽  
pp. 302-307 ◽  
Author(s):  
Hui Huang ◽  
Zhong Cheng Guo ◽  
Wei Zhu ◽  
Fa Chuang Li

Conductive polyaniline/zirconia (PANI/ZrO2) composites have been synthesized by in-situ polymerization of aniline in the presence of ZrO2 nanoparticles. The structure and morph- ology of composites were characterized by Fourier-transform infrared spectra (FTIR), thermo- gravimetric analysis (TGA), X-ray diffraction (XRD) and scanning electron microscope (SEM). The conductivity was also investigated. The results showed that PANI and ZrO2 nanoparticles were not simply blended, and a strong interaction existed at the interface of ZrO2 and PANI. It was probably a composite at molecular level. The composites were more thermal stability than that of the pure PANI. XRD analyses confirmed PANI deposited on the surface of ZrO2 nanoparticles had no effect on crystallization performance of ZrO2 nanoparticles. Electrical conductivity measurements indicated that the conductivity of PANI/ZrO2 composites was much higher than that of PANI and the maximum conductivity obtained was 11.27S/cm at 15 wt% of ZrO2 nanoparticles.


2014 ◽  
Vol 1065-1069 ◽  
pp. 1784-1790 ◽  
Author(s):  
Yan Bing Zong ◽  
Zhao Bo Liu ◽  
Jun Jie Hou ◽  
Hong Xu Li

Slag glass-ceramics were successfully prepared by cold pressing sintering method in different atmospheres from metallurgical solid wastes. The evolution of crystal microstructure and crystalline phase transition of slag glass-ceramics was investigated by thermo-gravimetric analysis (TG-DTA), X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) coupled with Energy Dispersive X-ray spectrometer (EDX). The results indicate that the Na2O composition plays the role of decreasing the crystallization temperature to some extent. Iron oxides make the glass frits have a high driving force to crystallize. This oxidation of ferrum will postpone the process of densification and deteriorate the mechanical properties of product. On the other hand, the slag glass-ceramic products can obtain novel mechanical performance when the samples were sintered under nitrogen atmosphere.


BMC Chemistry ◽  
2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Arefeh Dehghani Tafti ◽  
Bi Bi Fatemeh Mirjalili ◽  
Abdolhamid Bamoniri ◽  
Naeimeh Salehi

AbstractNano-eggshell/Ti(IV) as a novel naturally based catalyst was prepared, characterized and applied for the synthesis of dihydropyrano[2,3-c]pyrazole derivatives. The characterization of nano-eggshell/Ti(IV) was performed using Fourier Transform Infrared spectroscopy, X-ray Diffraction, Field Emission Scanning Electron Microscopy, Energy-Dispersive X-ray Spectroscopy, and Thermo Gravimetric Analysis. Dihydropyrano[2,3-c]pyrazoles were synthesized in the presence of nano-eggshell/Ti(IV) via a four component reaction of aldehydes, ethyl acetoacetate, malononitrile and hydrazine hydrate at room temperature under solvent free conditions. The principal affairs of this procedure are mild condition, short reaction times, easy work-up, high yields, reusability of the catalyst and the absence of toxic organic solvents.


Coatings ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 348 ◽  
Author(s):  
Baolei Liu ◽  
Mingqian Wang ◽  
Ying Liang ◽  
Zhicheng Zhang ◽  
Guohong Ren ◽  
...  

This work launches the first-ever report on the fabrication of waterborne epoxy-graphene oxide (GO) coatings (WEGC) using a block polymer as a dispersant of GO, wherein the block polymer was synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization of acrylic acid and oligo(ethylene glycol) methyl ether methacrylate A number of analytical techniques, such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), thermo gravimetric analysis (TGA), and salt spray tests, were utilized to explore the morphology and performance of the WEGC. It was confirmed that POEGMA950-b-PAA attached to the GO nanosheets, increasing the integral space of the sheets. Modified GO (MGO) layers were well-dispersed in the epoxy matrix through the formation of a GO-dispersant-epoxy ternary molecular structure. Furthermore, the presence of MGO substantially influenced the thermal properties, mechanical properties, and anticorrosion performance of the WEGC. TGA, salt spray tests, and pull-off testsshowed that 0.5 wt.% MGO content achieved the greatest improvement in the evaluated properties.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.


2017 ◽  
Vol 50 ◽  
pp. 18-31 ◽  
Author(s):  
Rudzani Sigwadi ◽  
Simon Dhlamini ◽  
Touhami Mokrani ◽  
Patrick Nonjola

The paper presents the synthesis and investigation of zirconium oxide (ZrO2) nanoparticles that were synthesised by precipitation method with the effects of the temperatures of reaction on the particles size, morphology, crystallite sizes and stability at high temperature. The reaction temperature effect on the particle size, morphology, crystallite sizes and stabilized a higher temperature (tetragonal and cubic) phases was studied. Thermal decomposition, band structure and functional groups were analyzed by Brunauer-Emmett-Teller (BET), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA) and Fourier transform infrared (FT-IR). The crystal structure was determined using X-ray diffraction. The morphology and the particle size were studied using (SEM) and (TEM). The shaped particles were confirmed through the SEM analysis. The transmission electron microscopic analysis confirmed the formation of the nanoparticles with the particle size. The FT-IR spectra showed the strong presence of ZrO2 nanoparticles.


2016 ◽  
Vol 30 (32n33) ◽  
pp. 1650347
Author(s):  
Amarjeet ◽  
Vinod Kumar

[Formula: see text] ([Formula: see text] = 0.1, 0.3 and 0.5) nanoparticles were prepared by chemical co-precipitation method. The developed nanoparticles were characterized for structural properties by powder X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) techniques. Peak position in the X-ray diffraction pattern confirmed the single spinel phase of the developed particles. Infrared (IR) spectroscopy in mid-IR range showed the presence of characteristic absorption bands corresponding to octahedral and tetrahedral bonds in the spinel structure of prepared samples. Thermo-gravimetric analysis (TGA) measurements showed a considerable weight loss in the developed samples above 700[Formula: see text]C. Frequency dependence of the electrical properties of the developed material pellets was studied in the frequency range of 1 kHz–5 MHz. Temperature dependence of the dielectric constant of [Formula: see text] was studied at different temperatures, i.e. at 425, 450 and 475 K, in the frequency range of 1 kHz–5 MHz. It was found that the electrical conductivity decreases with increasing Cu[Formula: see text] ion content while it increases with the increase in temperature.


Author(s):  
Nitu Bhatnagar ◽  
Avani Pareek

The present study is aimed to observe the difference in the Physico-Chemical characteristics of the marketed and formulated bhasma samples through X-Ray Diffraction analysis (XRD), Dynamic Light Scattering (DLS), Zeta potential, Thermo-Gravimetric analysis (TGA), Scanning Electron Microscopy (SEM) and Energy Dispersive X-Ray analysis (EDAX), apart from organoleptic methods. Inductively Coupled Plasma Mass Spectroscopy (ICPMS) analysis was also done to observe the presence of trace and heavy metals so that the safety of all these samples could be ensured. XRD shows variation in oxide nature of zinc as well crystallite size in all bhasma samples. DLS and SEM results show difference in particle size of marketed bhasma samples as compared to formulated Yashada bhasma. EDAX and ICPMS also confirm the alteration in elemental composition of all these bhasma samples. Thus, it can be concluded that these ayurvedic medicines should be prepared strictly using the formulation methods as mentioned in the Ayurvedic texts. This will help the prepared products to adopt the inherent quality of the ancient system of medicine, which shall be useful and devoid of any side effects for human consumption.


2001 ◽  
Vol 73 (4) ◽  
pp. 525-532 ◽  
Author(s):  
MELLATIE R. FINISIE ◽  
ATCHE JOSUÉ ◽  
VALFREDO T. FÁVERE ◽  
MAURO C. M. LARANJEIRA

Bioceramic composites were obtained from chitosan and hydroxyapatite pastes synthesized at physiological temperature according to two different syntheses approaches. Usual analytical techniques (X-ray diffraction analysis, Fourier transformed infrared spectroscopy, Thermo gravimetric analysis, Scanning electron microscopy, X-ray dispersive energy analysis and Porosimetry) were employed to characterize the resulting material. The aim of this investigation was to study the bioceramic properties of the pastes with non-decaying behavior from chitosan-hydroxyapatite composites. Chitosan, which also forms a water-insoluble gel in the presence of calcium ions, and has been reported to have pharmacologically beneficial effects on osteoconductivity, was added to the solid phase of the hydroxyapatite powder. The properties exhibited by the chitosan-hydroxyapatite composites were characteristic of bioceramics applied as bone substitutes. Hydroxyapatite contents ranging from 85 to 98% (w/w) resulted in suitable bioceramic composites for bone regeneration, since they showed a non-decaying behavior, good mechanical properties and suitable pore sizes.


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