The adsorption and dispersing mechanisms of sodium lignosulfonate on Al2O3 particles in aqueous solution

Holzforschung ◽  
2013 ◽  
Vol 67 (4) ◽  
pp. 387-394 ◽  
Author(s):  
Rong Li ◽  
Dongjie Yang ◽  
Wenyuan Guo ◽  
Xueqing Qiu
Keyword(s):  
Metal Cation ◽  
Photoelectron Spectroscopy ◽  
Low Ph ◽  
Repulsive Force ◽  
Sodium Lignosulfonate ◽  
Aggregation State ◽  
Potential Measurement ◽  
X Ray ◽  
Ph Values ◽  
Vis Spectroscopy

Abstract The adsorption behavior and dispersion efficiency of sodium lignosulfonate (NaLS) on Al2O3 particles at different pH values were investigated by UV-Vis spectroscopy, zeta potential measurement, X-ray photoelectron spectroscopy, and viscosity measurements. The effects of the additives urea, Na2SO4, and NaCl were tested. At low pH values, NaLS adsorbed on the Al2O3 particles in the form of aggregates and at high pH values as separated single molecules. At pH 3–11, the adsorption was not affected through addition of urea, ruling out hydrogen bond as a controlling factor. By adding Na2SO4 and NaCl, the main driving force was the synergistic effect of the electrostatic interaction and the metal cation-π interaction at pH<pHIEP (IEP, isoelectric point), whereas the metal cation-π interaction was dominant at pH>pHIEP. The dispersing mechanism was mainly attributed to the steric hindrance (at pH<pHIEP) and the electrostatic repulsive force (at pH>pHIEP) owing to the differences in the aggregation state of the adsorbed molecules.

scholarly journals Application of Reverse Micelle Sol–Gel Synthesis for Bulk Doping and Heteroatoms Surface Enrichment in Mo-Doped TiO2 Nanoparticles

Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 937 ◽  
Author(s):  
Roberto Nasi ◽  
Serena Esposito ◽  
Francesca Freyria ◽  
Marco Armandi ◽  
Tanveer Gadhi ◽  
...  
Keyword(s):  
Tio2 Nanoparticles ◽  
Reverse Micelle ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Actual State ◽  
Test Reaction ◽  
Potential Measurement ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Mo Content

TiO2 nanoparticles containing 0.0, 1.0, 5.0, and 10.0 wt.% Mo were prepared by a reverse micelle template assisted sol–gel method allowing the dispersion of Mo atoms in the TiO2 matrix. Their textural and surface properties were characterized by means of X-ray powder diffraction, micro-Raman spectroscopy, N2 adsorption/desorption isotherms at −196 °C, energy dispersive X-ray analysis coupled to field emission scanning electron microscopy, X-ray photoelectron spectroscopy, diffuse reflectance UV–Vis spectroscopy, and ζ-potential measurement. The photocatalytic degradation of Rhodamine B (under visible light and low irradiance) in water was used as a test reaction as well. The ensemble of the obtained experimental results was analyzed in order to discover the actual state of Mo in the final materials, showing the occurrence of both bulk doping and Mo surface species, with progressive segregation of MoOx species occurring only at a higher Mo content.

scholarly journals Colloidal and Deposited Products of the Interaction of Tetrachloroauric Acid with Hydrogen Selenide and Hydrogen Sulfide in Aqueous Solutions

Minerals ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 492 ◽  
Author(s):  
Sergey Vorobyev ◽  
Maxim Likhatski ◽  
Alexander Romanchenko ◽  
Nikolai Maksimov ◽  
Sergey Zharkov ◽  
...  
Keyword(s):  
Zeta Potential ◽  
Photoelectron Spectroscopy ◽  
Ex Situ ◽  
Supersaturated Solution ◽  
Hydrodynamic Diameter ◽  
Elemental Selenium ◽  
Potential Measurement ◽  
Gold Colloids ◽  
X Ray ◽  
Vis Spectroscopy

The reactions of aqueous gold complexes with H2Se and H2S are important for transportation and deposition of gold in nature and for synthesis of AuSe-based nanomaterials but are scantily understood. Here, we explored species formed at different proportions of HAuCl4, H2Se and H2S at room temperature using in situ UV-vis spectroscopy, dynamic light scattering (DLS), zeta-potential measurement and ex situ Transmission electron microscopy (TEM), electron diffraction, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Metal gold colloids arose at the molar ratios H2Se(H2S)/HAuCl4 less than 2. At higher ratios, pre-nucleation “dense liquid” species having the hydrodynamic diameter of 20–40 nm, zeta potential −40 mV to −50 mV, and the indirect band gap less than 1 eV derived from the UV-vis spectra grow into submicrometer droplets over several hours, followed by fractional nucleation in the interior and coagulation of disordered gold chalcogenide. XPS found only one Au+ site (Au 4f7/2 at 85.4 eV) in deposited AuSe, surface layers of which partially decomposed yielding Au0 nanoparticles capped with elemental selenium. The liquid species became less dense, the gap approached 2 eV, and gold chalcogenide destabilized towards the decomposition with increasing H2S content. Therefore, the reactions proceed via the non-classical mechanism involving “dense droplets” of supersaturated solution and produce AuSe1−xSx/Au nanocomposites.

Silver mirror reaction metallized chromatography paper for supercapacitor application

2021 ◽  
Author(s):  
I-Hsuan Chen ◽  
Jung-Hsien Chang ◽  
Ren-Jie Xie ◽  
Chia-Hui Tseng ◽  
Sheng-Rong Hsieh ◽  
...  
Keyword(s):  
Flexible Electronics ◽  
Photoelectron Spectroscopy ◽  
Cost Effective ◽  
Water Contact ◽  
X Ray ◽  
Supercapacitor Application ◽  
Resource Limited ◽  
Vis Spectroscopy ◽  
Silver Mirror ◽  
Silver Mirror Reaction

Abstract In this study, the easy-to-operate silver mirror reaction (SMR) was used for metallizing chromatography paper. The SMR-metallized paper was characterized by water contact angle measurements, a surface profiler, X-ray photoelectron spectroscopy, UV-vis spectroscopy, X-ray diffraction, and electrical resistance measurement. The characterization results show that Ag was successfully synthesized on cellulose fibers and was electrically conductive after cyclic bending. Moreover, this SMR-metallized paper was used as electrodes for fabricating a supercapacitor. This SMR-metallized paper could be used for realizing cost-effective flexible electronics applied in on-site biochemical sensing in resource-limited settings.

scholarly journals Succinic acid in aqueous solution: connecting microscopic surface composition and macroscopic surface tension

2014 ◽  
Vol 16 (39) ◽  
pp. 21486-21495 ◽  
Author(s):  
Josephina Werner ◽  
Jan Julin ◽  
Maryam Dalirian ◽  
Nønne L. Prisle ◽  
Gunnar Öhrwall ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Surface Tension ◽  
Succinic Acid ◽  
Photoelectron Spectroscopy ◽  
Surface Composition ◽  
Md Simulations ◽  
Vapor Interface ◽  
X Ray ◽  
Ph Values ◽  
Microscopic Surface

The water–vapor interface of aqueous solutions of succinic acid, where pH values and bulk concentrations were varied, has been studied using surface sensitive X-ray photoelectron spectroscopy (XPS) and molecular dynamics (MD) simulations.

scholarly journals Effects of pH and Ca exchange on the structure and redox state of synthetic Na-birnessite

2021 ◽  
Vol 106 (1) ◽  
pp. 15-27
Author(s):  
Chiara Elmi ◽  
Jeffrey E. Post ◽  
Peter J. Heaney ◽  
Eugene S. Ilton
Keyword(s):  
Photoelectron Spectroscopy ◽  
Water Oxidation ◽  
Structure Refinement ◽  
Oxidation Catalysis ◽  
X Ray ◽  
Cell Parameters ◽  
Ph Values ◽  
Water Oxidation Catalysis ◽  
Effects Of Ph ◽  
End Members

Abstract Birnessite-like minerals are among the most common Mn oxides in surficial soils and sediments, and they mediate important environmental processes (e.g., biogeochemical cycles, heavy metal confinement) and have novel technological applications (e.g., water oxidation catalysis). Ca is the dominant interlayer cation in both biotic and abiotic birnessites, especially when they form in association with carbonates. The current study investigated the structures of a series of synthetic Ca-birnessite analogs prepared by cation-exchange with synthetic Na-birnessite at pH values from 2 to 7.5. The resulting Ca-exchanged birnessite phases were characterized using powder X-ray diffraction and Rietveld refinement, Fourier transform infrared spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning and transmission electron microscopy. All samples synthesized at pH values greater than 3 exhibited a similar triclinic structure with nearly identical unit-cell parameters. The samples exchanged at pH 2 and 3 yielded hexagonal structures, or mixtures of hexagonal and triclinic phases. Rietveld structure refinement and X-ray photoelectron spectroscopy showed that exchange of Na by Ca triggered reduction of some Mn3+, generating interlayer Mn2+ and vacancies in the octahedral layers. The triclinic and hexagonal Ca-birnessite structures described in this study were distinct from Na- and H-birnessite, respectively. Therefore, modeling X-ray absorption spectra of natural Ca-rich birnessites through mixing of Na- and H-birnessite end-members will not yield an accurate representation of the true structure.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

Thermally Induced Superlow Friction of DLC Films in Ambient Air

2018 ◽  
Vol 37 (8) ◽  
pp. 725-731 ◽  
Author(s):  
Qunfeng Zeng
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ambient Air ◽  
Friction Model ◽  
Repulsive Force ◽  
Hydroxyl Group ◽  
Thermally Induced ◽  
X Ray ◽  
Thermally Activated ◽  
Charged Interface ◽  
Positively Charged

AbstractThermally induced superlow friction (0.008) of diamond-like carbon (DLC) films was achieved in ambient air in the present work. Raman and XPS (X-ray Photoelectron Spectroscopy) measurements and analyses show that superlow friction of the annealed DLC films is involved in the transformation of sp3 to sp2 hybridized carbon during annealing and the tribochemical reactions during sliding. The thermally activated graphitization and oxidation of the annealed DLC films in ambient air is beneficial to form the positively charged interface and achieve the stable superlow friction. A friction model was developed and applied to explain superlow friction, which is attributed to Van de Waals force between graphite layers and the repulsive force between hydroxyl group of graphite oxide and hydrogen terminated DLC films surface.

Inorganic-Framework Molecularly Imprinted CdS/TiO2 for Selectively Photocatalytic Degradation of Di (2-ethylhexyl) phthalate

2019 ◽  
Vol 41 (2) ◽  
pp. 308-308
Author(s):  
Fangyan Chen Fangyan Chen ◽  
Yiming Liu Yiming Liu ◽  
Xi Zhang Xi Zhang ◽  
Lina He and Yubin Tang Lina He and Yubin Tang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Tetrabutyl Titanate ◽  
Template Molecule ◽  
Molecularly Imprinted ◽  
X Ray ◽  
Simulated Solar Light ◽  
Specific Recognition ◽  
Vis Spectroscopy ◽  
Inorganic Framework ◽  
Ethylhexyl Phthalate

In order to improve the photocatalytic efficiency and selectivity of di (2-ethylhexyl) phthalate (DEHP) under solar-driven, the inorganic-framework molecularly imprinted CdS/TiO2, named as MIP-CdS/TiO2, was prepared by using DEHP as template molecule and tetrabutyl titanate as titanium source and functional monomer. The as-prepared MIP-CdS/TiO2 was characterized by scanning electron microscopy (SEM), X-ray energy spectrum (EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-Vis Spectroscopy (UV-vis), X-ray photoelectron spectroscopy (XPS) and photoluminescence spectrum (PL). And the specific recognition and photocatalytic selectivity of MIP-CdS/TiO2 to DEHP were investigated. The results show that inorganic-framework molecular imprinting on the surface of CdS/TiO2 can result in existence of specific recognition sites of DEHP, extend and intensify the absorption visible light of CdS/TiO2, inhibit the recombination of the photo-induced electron-holes pairs. MIP-CdS/TiO2 has a specific recognition to DEHP. The binding selectivity coefficients of DEHP relative to its analogues DBP and DMP are 2.78 and 2.60, respectively. Compared with CdS/TiO2, MIP-CdS/TiO2 exhibits higher photocatalytic activity and selectivity for DEHP. Under simulated solar light irradiation, the degradation efficiency of DEHP photocatalyzed by MIP-CdS/TiO2 is 75.5%, which is 1.63 times as high as that of DEHP photocatalyzed by CdS/TiO2.

Photocatalytic Decomposition of Methylene Blue with Lanthanum Doping TiO2 under Visible Light Irradiation

2013 ◽  
Vol 734-737 ◽  
pp. 2163-2167
Author(s):  
Guang Xiu Cao ◽  
Zhong Hou Zhang ◽  
Bin Zhai
Keyword(s):  
Methylene Blue ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Light Irradiation ◽  
Photocatalytic Decomposition ◽  
Lanthanum Doping ◽  
X Ray ◽  
Degradation Rates ◽  
Vis Spectroscopy

Lanthanum doped TiO2 powders were prepared by hydrolysis of titanium tetra-n-butyl oxide and La (NO3)3 in solution. The resulting powders were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis absorption spectroscopy. The photocatalytic activities of doped samples were evaluated by the decomposition of methylene blue under visible light irradiation. The XRD results showed that the doping of lanthanum could not only efficiently inhibit the grain growth but also suppress the phase transition of anatase to rutile. UV-Vis spectroscopy of lanthanum doping TiO2 indicated that the absorption onset red-shifted to the visible light region. XPS results revealed that La2O3 had formed which could enhance the surface area. The degradation rates of methylene blue verified that the visible light photocatalytic activity of TiO2 has been enhanced by the doping of lanthanum.

Growth and Characterizations of Indium-Doped Pentacene Thinfilm Prepared by Thermal Co-Evaporation as a Novel Nanomaterial

2015 ◽  
Vol 1131 ◽  
pp. 35-38
Author(s):  
Navaphun Kayunkid ◽  
Annop Chanhom ◽  
Chaloempol Saributr ◽  
Adirek Rangkasikorn ◽  
Jiti Nukeaw
Keyword(s):  
Thin Films ◽  
Carrier Concentration ◽  
Photoelectron Spectroscopy ◽  
High Vacuum ◽  
Charge Carrier Mobility ◽  
Electrical Measurements ◽  
X Ray ◽  
Force Microscopy ◽  
Vis Spectroscopy ◽  
Hybrid Thin Films

This research is related to growth and characterizations of indium-doped pentacene thin films as a novel hybrid material. Doped films were prepared by thermal co-evaporation under high vacuum. The doping concentration was varied from 0% to 50% by controlling the different deposition rate between these two materials while the total thickness was fixed at 100 nm. The hybrid thin films were characterized by atomic force microscopy (AFM), X-ray diffraction (XRD) and UV-Visible spectroscopy to reveal the physical and optical properties. Moreover, the electrical properties of ITO/indium-doped-pentacene/Al devices i.e. charge mobility and carrier concentration were determined by considering the relationship between current-voltage and capacitance-voltage. AFM results identify that doping of indium into pentacene has an effect on surface properties of doped films i.e. the increase of surface grain size. XRD results indicate that doping of metal into pentacene has an effect on preferential orientation of pentacene’s crystalline domains. UV-Vis spectroscopy results show evolution of absorbance at photon energy higher than 2.7 eV corresponding to absorption from oxide of indium formed in the films. Electrical measurements exhibit higher conductivity in doped films resulting from increment of both charge carrier mobility and carrier concentration. Furthermore, chemical interactions taken place inside the doped films were investigated by x-ray photoelectron spectroscopy (XPS) in order to complete the remaining questions i.e. how do indium atoms interact with the neighbor molecules?, what is the origin of the absorption at E > 2.7 eV? Further results and discussions will be presented in the publication.

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