Study on the Reaction Kinetics and Catalytic Stability of Pillared Bentonite in Heterogeneous UV-Fenton Process

2013 ◽  
Vol 690-693 ◽  
pp. 1535-1538
Author(s):  
Xuan Zhang ◽  
Hong Lei Jiang ◽  
Xia Chen
Keyword(s):  
High Stability ◽  
Wave Length ◽  
Interlayer Spacing ◽  
Catalytic Performance ◽  
Fenton Process ◽  
X Ray ◽  
Catalytic Stability ◽  
Doping Technique ◽  
Reaction Constants ◽  
Pillaring Solution

An investigate was carried out to evaluate the catalytic performance of Fe, Al-pillared bentonite in heterogeneous UV-Fenton process. The catalysts were prepared by a cation doping technique. X-ray diffiraction and infraed spectroscopy were used to characterize their properties. Results showed that intercalated process could obtained larger interlayer spacing. Some bands of infrared spectroscopy shifted to lower wave length, indicating that FexAly has intercalated into the layers of the bentonite. The higher ratio of Fe to Al was in the pillaring solution, the higher discolouration rate could be obtained. The discoloration rate reached 79.9% at 20 min and 283K when the ratio of Fe to Al in pillaring solution was 9:1. The reaction constants of the heterogeneous UV-Fenton process increased from 0.074 min-1 at 283K to 0.094min-1 at 323K. Its activation energy was 36.7kJ.mol-1, indicating that temperature had little effect on this process. Little Fe-leaching made it possible for Fe, Al-pillared bentonite to remain a high stability during recycling uses.

scholarly journals Palygorskite Supported AuPd Alloy Nanoparticles as Efficient Nano-Catalysts for the Reduction of Nitroarenes and Dyes at Room Temperature

Nanomaterials ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 1000 ◽  
Author(s):  
Jun Xu ◽  
Shengli Guo ◽  
Lei Jia ◽  
Wensheng Zhang
Keyword(s):  
Room Temperature ◽  
Catalytic Performance ◽  
Atomic Ratio ◽  
Alloy Nanoparticles ◽  
X Ray ◽  
Degradation Of Dyes ◽  
Transmission Electron ◽  
Catalytic Stability ◽  
Nano Catalysts ◽  
Co Reduction

In this work, AuPd alloy palygorskite based Pal-NH2@AuPd nano-catalysts were prepared and used as catalysts for the reduction of nitroarenes and dyes at room temperature. The surface of palygorskite (Pal) was first modified with 3-aminpropyltriethoxysilane, and then covered with AuPd alloy nanoparticles through co-reduction of HAuCl4 and K2PdCl4. The morphology and structures of the Pal-NH2@AuPd nano-catalysts were characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS) and transmission electron microscopy (TEM). The as-synthesized Pal-NH2@AuPd nano-catalysts displayed excellent catalytic performance in reducing 4-nitrophenol (4-NP) and various other nitroaromatic compounds. Moreover, the catalytic activities of the Pal-NH2@AuPd nano-catalysts were adjustable via changing the atomic ratio of AuPd alloy nanoparticles, leading to the Pal-NH2@Au48Pd52 component as having the best atomic ratio. The Pal-NH2@Au48Pd52 continued to display good catalytic stability after being reused for several cycles and there were no obvious changes, either of the morphology or the particle size distribution of the nano-catalysts. Furthermore, these Pal-NH2@Au48Pd52 nano-catalysts also provided a convenient and accessible way for the degradation of dyes in artificial industrial wastewater.

Structural/Texture Evolution During Facile Substitution of Ni into ZSM-5 Nanostructure vs. its Impregnation Dispersion Used in Selective Transformation of Methanol to Ethylene and Propylene

2020 ◽  
Vol 23 ◽  
Author(s):  
Parisa Sadeghpour ◽  
Mohammad Haghighi ◽  
Mehrdad Esmaeili
Keyword(s):  
High Temperature ◽  
Physicochemical Properties ◽  
Active Sites ◽  
Catalytic Performance ◽  
Fixed Bed Reactor ◽  
Light Olefins ◽  
Isomorphous Substitution ◽  
Impregnation Method ◽  
Hydrothermal Temperature ◽  
X Ray

Aim and Objective: Effect of two different modification methods for introducing Ni into ZSM-5 framework was investigated under high temperature synthesis conditions. The nickel successfully introduced into the MFI structures at different crystallization conditions to enhance the physicochemical properties and catalytic performance. Materials and Methods: A series of impregnated Ni/ZSM-5 and isomorphous substituted NiZSM-5 nanostructure catalysts were prepared hydrothermally at different high temperatures and within short times. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDX), Brunner, Emmett and Teller-Barrett, Joyner and Halenda (BET-BJH), Fourier transform infrared (FTIR) and Temperature-programmed desorption of ammonia (TPDNH3) were applied to investigate the physicochemical properties. Results: Although all the catalysts showed pure silica MFI–type nanosheets and coffin-like morphology, using the isomorphous substitution for Ni incorporation into the ZSM-5 framework led to the formation of materials with lower crystallinity, higher pore volume and stronger acidity compared to using impregnation method. Moreover, it was found that raising the hydrothermal temperature increased the crystallinity and enhanced more uniform incorporation of Ni atoms in the crystalline structure of catalysts. TPD-NH3 analysis demonstrated that high crystallization temperature and short crystallization time of NiZSM-5(350-0.5) resulted in fewer weak acid sites and medium acid strength. The MTO catalytic performance was tested in a fixed bed reactor at 460ºC and GHSV=10500 cm3 /gcat.h. A slightly different reaction pathway was proposed for the production of light olefins over impregnated Ni/ZSM-5 catalysts based on the role of NiO species. The enhanced methanol conversion for isomorphous substituted NiZSM-5 catalysts could be related to the most accessible active sites located inside the pores. Conclusion: The impregnated Ni/ZSM-5 catalyst prepared at low hydrothermal temperature showed the best catalytic performance, while the isomorphous substituted NiZSM-5 prepared at high temperature was found to be the active molecular sieve regarding the stability performance.

scholarly journals Nitration of Jharia basin coals, India: a study of structural modifications by XRD and FTIR techniques

2021 ◽  
Author(s):  
Prabal Boral ◽  
Atul K. Varma ◽  
Sudip Maity
Keyword(s):  
Acetic Acid ◽  
Nitric Acid ◽  
Linear Relationship ◽  
Glacial Acetic Acid ◽  
Vitrinite Reflectance ◽  
Aqueous Media ◽  
Interlayer Spacing ◽  
Acetic Acid Medium ◽  
X Ray ◽  
The Media

AbstractFour coal samples from Jharia basin, India are treated with nitric acid in glacial acetic acid and aqueous media to find out the chemical, petrographic and spatial structure of the organic mass by X-ray diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR) techniques. X-ray parameters of coal like interlayer spacing (d002), crystallite size (Lc), aroamticity (fa), average number of aromatic layers (Nc), and coal rank (I26/I20) have been determined using profile-fitting software. Considerable variation is observed in treated coals in comparison to the demineralized coals. The d002 values of treated coals have increased in both the media showing increase in disordering of organic moieties. A linear relationship has been observed between d002 values with the volatile matter of the coals. Similarly, the d002 values show linear relationship with Cdmf contents for demineralized as well as for the treated coals in both the media. The Lc and Nc values have decreased in treated coals corresponding to demineralized coals. The present study shows that nitration in both the media is capable of removing the aliphatic side chains from the coals and aromaticity (fa) increases with increase in rank and shows a linear relationship with the vitrinite reflectance. The corresponding I26/I20 values are least for treated coals in glacial acetic acid medium followed by raw and then to treated coals in aqueous medium. FTIR studies show that coal arenes of the raw coals are converted into nitro-arenes in structurally modified coals (SMCs) in both the media, the corresponding bands at 1550–1490 and 1355–1315 cm−1 respectively. FTIR study confirms that nitration is the predominant phenomenon, though, oxidation and nitration phenomena takes place simultaneously during treatment with nitric acid to form SMCs. In comparison to raw coals, the SMCs show higher aromaticity and may be easily converted to coal derived products like activated carbon and specialty carbon materials.

scholarly journals A monodispersed CuPt alloy: synthesis and its superior catalytic performance in the hydrogen evolution reaction over a full pH range

RSC Advances ◽  
2021 ◽  
Vol 11 (21) ◽  
pp. 12470-12475
Author(s):  
Xinmei Liu ◽  
Chen Liang ◽  
Wenlong Yang ◽  
Chunyang Yang ◽  
Jiaqi Lin ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
High Stability ◽  
Low Cost ◽  
Catalytic Performance ◽  
Ph Range

An effective approach to achieve the low cost and high stability of electro-catalysts for HER.

High-Stability Flexible X-ray Detectors Based on Lead-Free Halide Perovskite Cs2TeI6 Films

2021 ◽  
Author(s):  
Jun Guo ◽  
Yadong Xu ◽  
Wenhui Yang ◽  
Bao Xiao ◽  
Qihao Sun ◽  
...  
Keyword(s):  
High Stability ◽  
Lead Free ◽  
X Ray ◽  
Halide Perovskite

scholarly journals The Effect of Mg and Zn Dopants on Pt/Al2O3 for the Dehydrogenation of Perhydrodibenzyltoluene

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 490
Author(s):  
Rudaviro Garidzirai ◽  
Phillimon Modisha ◽  
Innocent Shuro ◽  
Jacobus Visagie ◽  
Pieter van Helden ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
Flow Reactor ◽  
Plug Flow ◽  
Optical Emission ◽  
Catalytic Performance ◽  
Emission Spectrometry ◽  
Hydrogen Yield ◽  
X Ray ◽  
Temperature Programmed

The effects of Mg and Zn dopants on the catalytic performance of Pt/Al2O3 catalyst were investigated for dehydrogenation of perhydrodibenzyltoluene (H18-DBT) as a liquid organic hydrogen carrier. Al2O3 supports were modified with Mg and Zn to produce Mg-Al2O3 and Zn-Al2O3 with a target loading of 3.8 wt.% for dopants. The modified supports were impregnated with chloroplatinic acid solution to produce the catalysts Pt/Al2O3, Pt/Mg-Al2O3 and Pt/Zn-Al2O3 of 0.5 wt.% Pt loading. Thereafter, the catalysts were characterised using inductively coupled plasma- optical emission spectrometry, scanning electron microscopy-energy dispersive X-ray spectroscopy, hydrogen temperature-programmed reduction, carbon-monoxide pulse chemisorption, ammonia temperature-programmed desorption, X-ray diffraction and transmission electron microscopy. The dehydrogenation experiments were performed using a horizontal plug flow reactor system and the catalyst time-on-stream was 22 h. Pt/Mg-Al2O3 showed the highest average hydrogen flowrate of 29 nL/h, while an average of 27 nL/h was obtained for both Pt/Al2O3 and Pt/Zn-Al2O3. This has resulted in a hydrogen yield of 80% for Pt/Mg-Al2O3, 71% for Pt/Zn-Al2O3 and 73% for Pt/Al2O3. In addition, the conversion of H18-DBT ranges from 99% to 92%, Pt 97–90% and 96–90% for Pt/Mg-Al2O3, Pt/Zn-Al2O3 and Pt/Al2O3, respectively. Following the latter catalyst order, the selectivity to dibenzyltoluene (H0-DBT) ranges from 78% to 57%, 75–51% and 71–45%. Therefore, Pt/Mg-Al2O3 showed improved catalytic performance towards dehydrogenation of H18-DBT.

scholarly journals Control of zeolite microenvironment for propene synthesis from methanol

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Longfei Lin ◽  
Mengtian Fan ◽  
Alena M. Sheveleva ◽  
Xue Han ◽  
Zhimou Tang ◽  
...  
Keyword(s):  
Active Sites ◽  
Inelastic Neutron Scattering ◽  
Sustainable Manufacturing ◽  
Methanol Conversion ◽  
Acid Sites ◽  
Light Olefins ◽  
Carbon Bond ◽  
X Ray ◽  
Carbon Carbon Bond ◽  
Catalytic Stability

AbstractOptimising the balance between propene selectivity, propene/ethene ratio and catalytic stability and unravelling the explicit mechanism on formation of the first carbon–carbon bond are challenging goals of great importance in state-of-the-art methanol-to-olefin (MTO) research. We report a strategy to finely control the nature of active sites within the pores of commercial MFI-zeolites by incorporating tantalum(V) and aluminium(III) centres into the framework. The resultant TaAlS-1 zeolite exhibits simultaneously remarkable propene selectivity (51%), propene/ethene ratio (8.3) and catalytic stability (>50 h) at full methanol conversion. In situ synchrotron X-ray powder diffraction, X-ray absorption spectroscopy and inelastic neutron scattering coupled with DFT calculations reveal that the first carbon–carbon bond is formed between an activated methanol molecule and a trimethyloxonium intermediate. The unprecedented cooperativity between tantalum(V) and Brønsted acid sites creates an optimal microenvironment for efficient conversion of methanol and thus greatly promotes the application of zeolites in the sustainable manufacturing of light olefins.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

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.

Degradation of Odontologic X-Ray Film Developing Wastewaters by Photo-Fenton Process

2007 ◽  
Vol 5 (1) ◽  
Author(s):  
Luciana Igarashi-Mafra ◽  
Edmilson César Bortoletto ◽  
Maria Angelica Simões Dornella Barros ◽  
Amanda Cristina Alfredo Contrucci Sorbo ◽  
Naiara Aguiar Galliani ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Total Phenol ◽  
Process Conditions ◽  
Phenol Removal ◽  
Total Phenols ◽  
Fenton Process ◽  
X Ray ◽  
Control Factors ◽  
Fenton Oxidation Process ◽  
Wastewater Samples

Effluents from radiographic X-ray film developing processes feature a high contaminant load (COD about 70000 mg/L and total phenols concentration about 16956 mg/L). Photo-Fenton's are potentially useful oxidation processes for destroying toxic organic compounds in water. In these reactions, hydrogen peroxide is combined with ferrous or ferric iron in the presence of light to generate hydroxyl radicals (·OH). The photo-Fenton process was explored as a photochemical treatment to degrade wastewater from radiographic X-ray film developing processes coming from odontologic clinics. A response surface methodology was applied to optimize the photo-Fenton oxidation process conditions using total phenol removal as the target parameter to be optimized, and the reagent concentrations, as related to the initial concentration of organic matter in the effluent, and time and pH as the control factors to be optimized. The best results in terms of maximal total phenol removal and economic process were achieved when wastewater samples were treated at pH 5 in the presence of hydrogen peroxide and iron in the ratios [total phenols]:[H2O2] 1:3 w/w and [Fe2+]:[H2O2] 1:18 w/w and time 1 h.

Preparation of Novel Ag–Si–TiO2 Composite and Research on Its Photocatalytic Degradation of Formaldehyde

2021 ◽  
Vol 13 (3) ◽  
pp. 371-380
Author(s):  
Yongjun Wu ◽  
Nina Xie ◽  
Lu Yu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Removal Rate ◽  
Sol Gel ◽  
Catalytic Performance ◽  
Formaldehyde Concentration ◽  
Order Kinetic ◽  
Solution Ph ◽  
Visible Absorption ◽  
X Ray ◽  
Co Doped

A novel Ag–Si–TiO2 composite was prepared via sol–gel method for removing residual formaldehyde in shiitake mushroom. The structure of Ag–Si–TiO2 composite was characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses. Ultraviolet-visible absorption spectroscopy (UV-Vis) and N2 adsorption-desorption tests showed that Ag and Si co-doped decreased the band gap, the Brunauer-Emmett-Teller (BET) specific surface area of the samples increased and the recombination probability of electron-hole pairs (e--h+) reduced. Effect on removal rate of formaldehyde with different Ag-Si co-doped content, formaldehyde concentration and solution pH were investigated, and the results showed that 6.0 wt%Ag-3.0 wt%Si-TiO2 samples had an optimum catalytic performance, and the degradation efficiency reached 96.6% after 40 W 365 nm UV lamp irradiation for 360 min. The kinetics of formaldehyde degradation by Ag–Si–TiO2 composite photocatalyst could be described by Langmuir-Hinshelwood first-order kinetic model.

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