Decomposition of Hydroxylammonium Nitrate Solution Over Nanoporous CuO Supported on Honeycomb

2021 ◽  
Vol 21 (8) ◽  
pp. 4532-4536
Author(s):  
Munjeong Kim ◽  
Juyoung Kim ◽  
Young Min Jo ◽  
Jong-Ki Jeon

We investigated the influence of a copper loading strategy over a honeycomb structure on the catalytic performance during the decomposition of a hydroxylammonium nitrate (HAN) aqueous solution. Copper was supported on the honeycomb surface by means of a metal coating method (MC), i.e., a method of directly coating a metal, and a metal alumina coating method (MAC), i.e., a method of coating a mixture of metal and alumina. The properties of the catalysts were analyzed by N2 adsorption, X-ray diffraction (XRD), and scanning electron microscopy (SEM). The Cu(16.8)/honeycomb-MC catalyst showed a lower decomposition onset temperature during the decomposition of the HAN aqueous solution compared to that over the Cu(7.0)/honeycomb- MAC catalyst, an outcome ascribed to the higher copper loading and the higher dispersion of copper in the Cu(16.8)/honeycomb-MC catalyst compared to that in the other catalyst. The Cu(16.8)/honeycomb-MC catalyst was confirmed to have both excellent activity and heat resistance during the decomposition of a HAN aqueous solution.

2010 ◽  
Vol 6 (1) ◽  
pp. 891-896
Author(s):  
Manel Halouani ◽  
M. Dammak ◽  
N. Audebrand ◽  
L. Ktari

One nickel 1,4-cyclohexanedicarboxylate coordination polymers, Ni2 [(O10C6H4)(COO)2].2H2O  (I), was hydrothermally synthesized from an aqueous solution of Ni (NO3)2.6H2O, (1,4-CDC) (1,4-CDC = 1,4-cyclohexanedicarboxylic acid) and tetramethylammonium nitrate. Compound (I) crystallizes in the monoclinic system with the C2/m space group. The unit cell parameters are a = 20.1160 (16) Å, b = 9.9387 (10) Å, c = 6.3672 (6) Å, β = 97.007 (3) (°), V= 1263.5 (2) (Å3) and Dx= 1.751g/cm3. The refinement converged into R= 0.036 and RW = 0.092. The structure, determined by single crystal X-ray diffraction, consists of two nickel atoms Ni (1) and Ni (2). Lots of ways of which is surrounded by six oxygen atoms, a carboxyl group and two water molecules.


Author(s):  
Ke Guo ◽  
Shaoyan Wang ◽  
Renfeng Song ◽  
Zhiqiang Zhang

AbstractLeaching titaniferous magnetite concentrate with alkali solution of high concentration under high temperature and high pressure was utilized to improve the grade of iron in iron concentrate and the grade of TiO2 in titanium tailings. The titaniferous magnetite concentrate in use contained 12.67% TiO2 and 54.01% Fe. The thermodynamics of the possible reactions and the kinetics of leaching process were analyzed. It was found that decomposing FeTiO3 with NaOH aqueous solution could be carried out spontaneously and the reaction rate was mainly controlled by internal diffusion. The effects of water usage, alkali concentration, reaction time, and temperature on the leaching procedure were inspected, and the products were characterized by X-ray diffraction, scanning electron microscope, and energy dispersive spectroscopy, respectively. After NaOH leaching and magnetic separation, the concentrate, with Fe purity of 65.98% and Fe recovery of 82.46%, and the tailings, with TiO2 purity of 32.09% and TiO2 recovery of 80.79%, were obtained, respectively.


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.


2013 ◽  
Vol 789 ◽  
pp. 176-179 ◽  
Author(s):  
Eny Kusrini ◽  
Nofrijon Sofyan ◽  
Dwi Marta Nurjaya ◽  
Santoso Santoso ◽  
Dewi Tristantini

Hydroxyapatite/chitosan (HApC) composite has been prepared by precipitation method and used for removal of heavy metals (Cr6+, Zn2+and Cd2+) from aqueous solution. The HAp and 3H7C composite with HAp:chitosan ratio of 3:7 (wt%) were characterized by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy-energy dispersive X-ray spectroscopy. The SEM results showed that HAp is spherical-shaped and crystalline, while chitosan has a flat structure. SEM micrograph of 3H7C composite reveals crystalline of HAp uniformly spread over the surface of chitosan. The crystal structure of HAp is maintained in 3H7C composite. Chitosan affects the adsorption capacity of HAp for heavy metal ions; it binds the metal ions as well as HAp. The kinetic data was best described by the pseudo-second order. Surface adsorption and intraparticle diffusion take place in the mechanism of adsorption process. The binding of HAp powder with chitosan made the capability of composite to removal of Cr6+, Zn2+and Cd2+from aqueous solution effective. The order of removal efficiency (Cr6+> Cd2+> Zn2+) was observed.


2020 ◽  
Vol 8 (2) ◽  
pp. 84-89
Author(s):  
Noor Hindryawati ◽  
Aman Sentosa Panggabean ◽  
Dirgarini Julia Nurlianti Subagyono ◽  
Rinda Anisyah Putri ◽  
Prilianda Kusmiaty ◽  
...  

Degradation of blue dye waste in Sarong Samarinda production using WO3-bleaching earth (BE) has been conducted. Structural and morphological characterization has conducted using X-ray diffraction (XRD), and Scanning electron microscopy-energy dispersive spectroscopy (SEM-EDX). The X-ray diffraction results show the mineral on bleaching earth is rectorite dioctahedral mica layer and dioctahedral smectite with a ratio 2:1. The WO3 pattern is appeared after the calcination. After calcination at 500°C, the WO3 is deposited homogeneously on the BE surface. The catalytic performance of WO3-BE for photodegradation of the blue dye waste under the solar light is 99.85 % within 1 h.


2021 ◽  
Vol 13 (1) ◽  
pp. 21-30
Author(s):  
O.K. Sharutina ◽  

By mixing solutions of tris(2-methoxy-5-bromophenyl)antimony and silver nitrate in a methanol : acetonitrile mixture (1:1 vol.), nitrato-O,O'-(acetonitrile)[tris(2-methoxy-5-bromophenyl)antimony]silver complex with the general formula [(C6H3ОMe-2-Br-5)3SbAg(μ2-NO3)(Ме3CN)]2•2[(C6H3ОMe-2-Br-5)3SbAgNO3(Ме3CN)] (1) has been obtained. An addition of silver nitrate solution in the methanol : acetonitrile mixture to the tris(2-methoxy-5-bromophenyl)antimony dioxane solution has led to the formation of a small amount of dark crystals of the ionic complex [(2-MeО-5-Br-C6H3)3SbAg(H2O)Sb(C6H3Br-5-OMe-2)3]+[(2-MeО-5-Br-C6H3)3SbAg(m-NO3)3 AgSb(C6H3Br-5-OMe-2)3]-×3C4H8O2 (2). Complexes 1 and 2 have been characterized by IR spectroscopy, and their structures have been determined by X-ray diffraction analysis. The IR spectra of complexes 1 and 2 contain the bands characterizing the Sb-O, Sb-C, С≡N-, and NO3-group band vibrations. X-ray diffraction analysis of the complexes has been carried out on an automatic four-circle D8 Quest Bruker diffractometer (МоКα radiation, λ = 0.71073 Å, graphite monochromator) at 293 K. Crystallographic characteristics of 1: triclinic, P-1 space group, a = 9.32(3), b = 17.50(7), c = 17.97(5) Å, a = 97.56(14), β = 92.90(19), g = 99.45(19) grad., V = 2859(16) Å3, Z = 2, rcalc = 2.069 g/cm3, 2: monoclinic, С2/с space group, a = 17.417(14), b = 21.041(15), c = 32.01(2) Å, a = 90, β = 97.79(3), g = 90 grad., V = 11624(15) Å3, Z = 4, rcalc = 2.006 g/cm3. In the monomeric and dimeric molecules of crystal 1, nitrate ligands are chelating and bridging, respectively. In the cation of complex 2, the silver atom is bonded to two antimony ligands, the third coordination site is occupied by a water molecule. In the dimeric anion there are one antimony ligand and three bridging nitrate groups surrounding each silver atom.


1998 ◽  
Vol 23 (0) ◽  
pp. 09-16
Author(s):  
Marco Aurélio da Silva CARVALHO FILHO ◽  
Massao IONASHIRO

Compounds of cinnamic acid with manganese, zinc and lead have been prepared in aqueous solution. Thermogravimetry, derivative thermogravimetry (TG, DTG), differential scanning calorimetry (DSC), X-ray diffraction and complexometry have been used in the characterization as well as in the study of the thermal stability and interpretation concerning the thermal decomposition.


2021 ◽  
Vol 11 (3) ◽  
pp. 215
Author(s):  
Achraf El Hallaoui ◽  
Tourya Ghailane ◽  
Soukaina Chehab ◽  
Youssef Merroun ◽  
Rachida Ghailane ◽  
...  

<p>This work aims to prepare a new bimetallic phosphate catalyst using a new simple and effective method. This new catalyst was ready for the first time by a modification of Triple Super Phosphate (TSP) fertilizer with silver sulfate (AgSO<sub>4</sub>), followed by the impregnation of the aluminum atoms using aluminum nitrate (Al(NO<sub>3</sub>)<sub>3</sub>). The use of Al/Ag<sub>3</sub>PO<sub>4</sub>, for the first time as a heterogeneous catalyst in organic chemistry, offers a new, efficient, and green pathway for synthesizing 1,2-dihydro-l-phenyl-3H-naphth[1,2-e]-[1,3]oxazin-3-one derivatives by one-pot three-component cyclocondensation of b-naphthol, aryl aldehyde, and urea. The structure and the morphology of the prepared catalyst were characterized by spectroscopic methods such as X-Ray Diffraction (XRD), Fourier Transform Infrared spectroscopy (FT-IR), and dispersive X-ray spectrometry coupled with a scanning electron microscope (EDX-SEM). In addition, the optimization of the reaction parameters was carried out considering the effect of catalyst amount, the temperature, and the solvent. The procedure described herein allowed a comfortable preparation of oxazine derivatives with excellent yields, short reaction times, and in the absence of organic solvent.</p>


Catalysts ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1238
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Damian C. Onwudiwe

In this paper, spherical-shaped pure phase djurleite (Cu31S16) and roxbyite (Cu7S4) nanoparticles were prepared by a solvothermal decomposition of copper(II) dithiocarbamate complex in dodecanthiol (DDT). The reaction temperature was used to control the phases of the samples, which were represented as Cu31S16 (120 °C), Cu31S16 (150 °C), Cu7S4 (220 °C), and Cu7S4 (250 °C) and were characterized by using X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM and TEM), and absorption spectroscopy. The samples were used as photocatalysts for the degradation of tetracycline (TC) under visible light irradiation. The results of the study showed that Cu7S4 (250 °C) exhibited the best activity in the reaction system with the TC degradation rate of up to 99% within 120 min of light exposure, while the Cu31S16 (120 °C) system was only 46.5% at the same reaction condition. In general, roxbyite Cu7S4 (250 °C) could be considered as a potential catalyst for the degradation of TC in solution.


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