scholarly journals Nano-PAA-CuCl2 Composite as Fenton-Like Reusable Catalyst to Enhanced Degrade Organic Pollutant MB/MO

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 10
Author(s):  
Yang Dang ◽  
Yu Cheng ◽  
Yukun Zhou ◽  
Yifei Huang ◽  
Kaige Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Organic Pollutant ◽  
Energy Dispersive Spectrometer ◽  
Chemical Properties ◽  
Anodic Alumina ◽  
Alumina Substrate ◽  
Reusable Catalyst ◽  
X Ray ◽  
Nanoporous Anodic Alumina

The treatment of organic dye contaminants in wastewaters has now becoming more imperative. Fenton-like degradation of methylene blue (MB) and methyl orange (MO) in aqueous solution was investigated by using a nanostructure that a layer of CuCl2 nanoflake film grown on the top surface of nanoporus anodic alumina substrate (nano-PAA-CuCl2) as catalyst. The new nano-PAA-CuCl2 composite was fabricated with self-assembly approach, that is, a network porous structure film composed of CuCl2 nanoflake grown on the upper surface of nanoporous anodic alumina substrate, and the physical and chemical properties are characterized systematically with the X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and high-resolution transmission electron microscopy (HRTEM), Energy Dispersive Spectrometer (EDS), X-ray photoelectron spectroscopy (XPS). The experimental results showed that the nano-PAA-CuCl2 catalyst presented excellent properties for the degradation of two typical organic pollutants such as MB and MO, which were almost completely degraded with 8 × 10−4mol/L nano-PAA-CuCl2 catalyst after 46 min and 60 min at reaction conditions of H2O2 18 mM and 23 mM, respectively. The effects of different reaction parameters such as initial pH, H2O2 concentration, catalyst morphology and temperature were attentively studied. And more, the stability and reusability of nano-PAA-CuCl2 were examined. Finally, the mechanism of MB and MO degradation by the nano-PAA-CuCl2/H2O2 system was proposed, based on the experimental data of the BCA and the temperature-programmed reduction (H2-TPR) and theoretical analysis, the reaction kinetics belonged to the pseudo-first-order equation. This new nanoporous composite material and preparation technology, as well as its application in Fenton-like reaction, provide an effective alternative method with practical application significance for wastewater treatment.

scholarly journals Improvement of the thermal stability of dendritic silver-coated copper microparticles by surface modification based on molecular self-assembly

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Tae Hyeong Kim ◽  
Hyeji Kim ◽  
Hyo Jun Jang ◽  
Nara Lee ◽  
Kwang Hyun Nam ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Electrically Conductive ◽  
X Ray ◽  
Alkyl Chains ◽  
Conductive Film ◽  
Initial Resistance ◽  
Thermal Stability Of ◽  
Scanning Electron

AbstractIn the study reported herein, silver-coated copper (Ag/Cu) powder was modified with alkanethiols featuring alkyl chains of different lengths, namely butyl, octyl, and dodecyl, to improve its thermal stability. The modification of the Ag/Cu powders with adsorbed alkanethiols was confirmed by scanning electron microscopy with energy dispersive spectroscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis. Each powder was combined with an epoxy resin to prepare an electrically conductive film. The results confirmed that the thermal stability of the films containing alkanethiol-modified Ag/Cu powders is superior to that of the film containing untreated Ag/Cu powder. The longer the alkyl group in the alkanethiol-modified Ag/Cu powder, the higher the initial resistance of the corresponding electrically conductive film and the lower the increase in resistance induced by heat treatment.

scholarly journals Microstructure and Properties of Self-Assembly Graphene Microcapsules: Effect of the pH Value

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 587 ◽  
Author(s):  
Yan-Dong Guo ◽  
Jun-Feng Su ◽  
Ru Mu ◽  
Xin-Yu Wang ◽  
Xiao-Long Zhang ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Chemical Engineering ◽  
Ph Value ◽  
Liquid Paraffin ◽  
Energy Dispersive Spectrometer ◽  
Core Material ◽  
Microstructure And Properties ◽  
Ph Values

Graphene has attracted attention in the material field of functional microcapsules because of its excellent characteristics. The content and state of graphene in shells are critical for the properties of microcapsules, which are greatly affected by the charge adsorption equilibrium. The aim of this work was to investigate the effect of pH value on the microstructure and properties of self-assembly graphene microcapsules in regard to chemical engineering. Microcapsule samples were prepared containing liquid paraffin by a self-assembly polymerization method with graphene/organic hybrid shells. The morphology, average size and shell thickness parameters were investigated for five microcapsule samples fabricated under pH values of 3, 4, 5, 6 and 7. The existence and state of graphene in dry microcapsule samples were analyzed by using methods of scanning electron microscope (SEM), transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS). Fourier Transform Infrared Spectoscopy (FT-IR) and Energy Dispersive Spectrometer (EDS) were applied to analyze the graphene content in shells. These results proved that graphene had existed in shells and the pH values greatly influenced the graphene deposition on shells. It was found that the microcapsule sample fabricated under pH = 5 experienced the largest graphene deposited on shells with the help of macromolecules entanglement and electrostatic adherence. This microcapsules sample had enhanced thermal stability and larger thermal conductivity because of additional graphene in shells. Nanoindentation tests showed this sample had the capability of deforming resistance under pressure coming from the composite structure of graphene/polymer structure. Moreover, more graphene decreased the penetrability of core material out of microcapsule shells.

High Temperature Oxidation Behavior of SUS310S Austenitic Stainless Steel

2014 ◽  
Vol 941-944 ◽  
pp. 212-215
Author(s):  
Tao Zheng ◽  
Jing Tao Han
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidation Behavior ◽  
Layer Structure ◽  
Energy Dispersive Spectrometer ◽  
Austenitic Stainless Steels ◽  
Temperature Oxidation ◽  
X Ray ◽  
High Temperature Oxidation Behavior ◽  
High Oxidation Resistance ◽  
Ray Diffusion

The oxidation behavior of SUS310S austenitic stainless steels was studied in isothermal conditions at different temperatures between 800oC and 1100oC for 96h in air. The oxidation kinetics was analyzed, the surface and cross-section of the oxide scale grown by oxidation were characterized by using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), X-ray diffusion (XRD) and X-ray photoelectron spectroscopy (XPS). The SUS310S steel has high oxidation resistance at 800oC and with the increase of the temperature, the parabolic rate constants is constantly increasing. Examination of the morphology and composition of oxide layers reveals a double-layer structure, The inner layer is mainly chromium oxide (Cr2O3) and is covered by an uneven thinness outer layer of manganese-chromium or iron-chromium spinel oxide.

X-ray Photoelectron Spectroscopy Study of the Deposition of TiO2 Thin Films on Self-assembly Monolayer

1998 ◽  
Vol 14 (01) ◽  
pp. 57-62
Author(s):  
Xiao Zhong-Dang ◽  
◽  
Huang Dan ◽  
Gu Jian-Hua ◽  
Lu Zu-Hong
Keyword(s):  
Thin Films ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Spectroscopy Study ◽  
X Ray

Physical Chemistry of the Interface between Attached Micro-Organisms and Their Support

1990 ◽  
Vol 22 (1-2) ◽  
pp. 1-16 ◽  
Author(s):  
P. G. Rouxhet ◽  
N. Mozes
Keyword(s):  
Photoelectron Spectroscopy ◽  
Bacterial Adhesion ◽  
Surface Composition ◽  
Chemical Properties ◽  
Dlvo Theory ◽  
Support Surface ◽  
X Ray ◽  
Polymer Molecules ◽  
Physico Chemical ◽  
Micro Organisms

The thermodynamic approach of adhesion and DLVO theory are complementary to predict initial bacterial adhesion; the interplay between short- and long-range forces, respectively, may be due to surface roughness. Due to the influence of electrical double layer interactions, adhesion can be promoted by treatments leading to modification of the cell or support surface properties. Adhesion is influenced by cell-cell interactions, by the cpresence of polymer molecules on the surface and by the composition of the medium. X-ray photoelectron spectroscopy can be applied to determine the elemental composition of the surface of microorganisms; some information on the chemical functions can also be obtained. The surface composition is related to physico-chemical properties which play a determining role in adhesion and flocculation, in particular the hydrophobicity and the zeta potential.

scholarly journals Non-Enzymatic Glucose Sensing Based on Incorporation of Carbon Nanotube into Zn-Co-S Ball-in-Ball Hollow Sphere

Sensors ◽  
2020 ◽  
Vol 20 (15) ◽  
pp. 4340
Author(s):  
Han-Wei Chang ◽  
Chia-Wei Su ◽  
Jia-Hao Tian ◽  
Yu-Chen Tsai
Keyword(s):  
Electron Microscopy ◽  
Hollow Sphere ◽  
Photoelectron Spectroscopy ◽  
Chemical Properties ◽  
High Sensitivity ◽  
Glucose Sensing ◽  
Ionic Exchange ◽  
X Ray ◽  
Transmission Electron ◽  
Electro Oxidation

Zn-Co-S ball-in-ball hollow sphere (BHS) was successfully prepared by solvothermal sulfurization method. An efficient strategy to synthesize Zn-Co-S BHS consisted of multilevel structures by controlling the ionic exchange reaction was applied to obtain great performance electrode material. Carbon nanotubes (CNTs) as a conductive agent were uniformly introduced with Zn-Co-S BHS to form Zn-Co-S BHS/CNTs and expedited the considerable electrocatalytic behavior toward glucose electro-oxidation in alkaline medium. In this study, characterization with scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) was used for investigating the morphological and physical/chemical properties and further evaluating the feasibility of Zn-Co-S BHS/CNTs in non-enzymatic glucose sensing. Electrochemical methods (cyclic voltammetry (CV) and chronoamperometry (CA)) were performed to investigate the glucose sensing performance of Zn-Co-S BHS/CNTs. The synergistic effect of Faradaic redox couple species of Zn-Co-S BHS and unique conductive network of CNTs exhibited excellent electrochemical catalytic ability towards the glucose electro-oxidation, which revealed linear range from 5 to 100 μM with high sensitivity of 2734.4 μA mM−1 cm−2, excellent detection limit of 2.98 μM, and great selectivity in the presence of dopamine, uric acid, ascorbic acid, and fructose. Thus, Zn-Co-S BHS/CNTs would be expected to be a promising material for non-enzymatic glucose sensing.

Influence of Thermal Treatments on the Chemistry and Self-Assembly of Ge Nanoparticles on SiO2 Surfaces

2004 ◽  
Vol 830 ◽  
Author(s):  
Scott K. Stanley ◽  
Shawn S. Coffee ◽  
John G. Ekerdt
Keyword(s):  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Chemical Vapor ◽  
Thermal Treatments ◽  
X Ray ◽  
Agglomeration Process ◽  
Oxide Substrate ◽  
Temperature Programmed ◽  
Hot Filament ◽  
Substrate Temperatures

ABSTRACTGeH4 is thermally cracked over a hot filament depositing 0.7–15 ML Ge onto 2–7 nm SiO2/Si(100) at substrate temperatures of 300–970 K. Ge, GeHx, GeO, and GeO2 desorption is monitored through temperature programmed desorption in the temperature range 300–1000 K. Ge bonding changes are analyzed during annealing from 300–1000 K with X-ray photoelectron spectroscopy (XPS). Low temperature desorption features are attributed to GeO and GeH4. No GeO2 desorption is observed, but GeO2 decomposition to Ge through high temperature pathways is seen above 700 K. Germanium oxidization results from Ge etching of the oxide substrate, which is demonstrated through XPS. Ge nanoparticle formation on SiO2 is demonstrated using the agglomeration process. With these results, explanations for the difficulties of conventional chemical vapor deposition to produce Ge nanocrystals on SiO2 surfaces are proposed.

scholarly journals Polyarylene Ether Nitrile and Barium Titanate Nanocomposite Plasticized by Carboxylated Zinc Phthalocyanine Buffer

Polymers ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 418 ◽  
Author(s):  
Shuning Liu ◽  
Chenchen Liu ◽  
Changyu Liu ◽  
Ling Tu ◽  
Yong You ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Barium Titanate ◽  
Photoelectron Spectroscopy ◽  
Energy Dispersive Spectrometer ◽  
Composite Films ◽  
Zinc Phthalocyanine ◽  
Hydroxyl Groups ◽  
X Ray ◽  
Polyarylene Ether Nitrile ◽  
High Dielectric

Barium titanate (BT) and polyarylene ether nitrile (PEN) nanocomposites with enhanced dielectric properties were obtained by using carboxylatedzinc phthalocyanine (ZnPc-COOH) buffer as the plasticizer. Carboxylated zinc phthalocyanine, prepared through hydrolyzing ZnPc in NaOH solution, reacted with the hydroxyl groups on the peripheral of hydrogen peroxide treated BT (BT-OH) yielding core-shell structured BT@ZnPc. Thermogravimetric analysis (TGA), transmission electron microscopy (TEM), TEM energy dispersive spectrometer mapping, scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared (FTIR) demonstrated successful preparation of BT@ZnPc. The fabricated BT@ZnPc was incorporated into the PEN matrix through the solution casting method. Rheological measurements demonstrated that the ZnPc-COOH buffer can improve the compatibility between BT and PEN effectively. With the existence of the ZnPc-COOH buffer, the prepared BT@ZnPc/PEN nanocomposites exhibit a high dielectric constant of 5.94 and low dielectric loss (0.016 at 1000 Hz). BT@ZnPc/PEN dielectric composite films can be easily prepared, presenting great application prospects in the field of organic film capacitors.

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