scholarly journals X-ray-Based Spectroscopic Techniques for Characterization of Polymer Nanocomposite Materials at a Molecular Level

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1053 ◽  
Author(s):  
Dongwan Son ◽  
Sangho Cho ◽  
Jieun Nam ◽  
Hoik Lee ◽  
Myungwoong Kim
Keyword(s):  
Photoelectron Spectroscopy ◽  
Molecular Level ◽  
Polymeric Materials ◽  
Polymer Nanocomposite ◽  
Nanocomposite Materials ◽  
Chemical Compositions ◽  
Spectroscopic Techniques ◽  
Characterization Methods ◽  
X Ray ◽  
Chemical Structures

This review provides detailed fundamental principles of X-ray-based characterization methods, i.e., X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, and near-edge X-ray absorption fine structure, and the development of different techniques based on the principles to gain deeper understandings of chemical structures in polymeric materials. Qualitative and quantitative analyses enable obtaining chemical compositions including the relative and absolute concentrations of specific elements and chemical bonds near the surface of or deep inside the material of interest. More importantly, these techniques help us to access the interface of a polymer and a solid material at a molecular level in a polymer nanocomposite. The collective interpretation of all this information leads us to a better understanding of why specific material properties can be modulated in composite geometry. Finally, we will highlight the impacts of the use of these spectroscopic methods in recent advances in polymer nanocomposite materials for various nano- and bio-applications.

scholarly journals A Comprehensive Review of Characterization Methods for Metallurgical Coke Structures

Materials ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 174
Author(s):  
Heng Zheng ◽  
Runsheng Xu ◽  
Jianliang Zhang ◽  
Oday Daghagheleh ◽  
Johannes Schenk ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Structural Model ◽  
Gas Adsorption ◽  
Diffraction Method ◽  
Metallurgical Coke ◽  
Image Method ◽  
Adsorption Method ◽  
Characterization Methods ◽  
X Ray ◽  
Chemical Structures

The structure of coke affects its reactivity and strength, which directly influences its performance in the blast furnace. This review divides coke structures into chemical structure, physical structure, and optical texture according to their relevant characteristics. The focuses of this review are the current characterization methods and research status of the coke structures. The chemical structures (element composition and functional group) can be characterized by elemental analysis, Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy (Raman), X-ray photoelectron spectroscopy (XPS), and nuclear magnetic resonance imaging technology (13C NMR). The physical structures (pore structure and micro-crystallite structure) can be characterized by image method, X-ray CT imaging technique, mercury intrusion method, nitrogen gas adsorption method, X-ray diffraction method (XRD), and high-resolution transmission electron microscopy (HRTEM). The optical textures are usually divided and counted by a polarizing microscope. In the end, this review provides an idea of the construction of a coke molecular structural model, based on the above characterization. With the coke model, the evolution principles of the coke can be calculated and simulated. Hence, the coke performance can be predicted and optimized.

scholarly journals Structure and Characterization of TiC/GLC Multilayered Films with Various Bilayers Periods

Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 787
Author(s):  
Weiqi Wang ◽  
Xiaoming Ling ◽  
Rui Wang ◽  
Wenhao Nie ◽  
Li Ji ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Chemical Compositions ◽  
Closed Field ◽  
Multilayered Structures ◽  
Multilayered Films ◽  
Sputtering Deposition ◽  
X Ray ◽  
Mechanical And Tribological Properties ◽  
Self Organizing

The spontaneously self-organizing multilayered graphite-like carbon (denoted as GLC) /TiC films with various bilayer periods in the range of 13.3–17.5 nm were deposited on silicon and 1Cr18Mn8Ni5N stainless steel substrates using closed field magnetron sputtering deposition facility. The microstructures and chemical compositions of the prepared multilayered films were characterized by scanning electron microscopy, high resolution transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy respectively. The self-organizing multilayered structures in all of the films consisted of titanium carbide layers and sp2-rich carbon layers periodically alternate arrangement. The TiC contents and bilayer periods of the multilayered films can be controlled by means of adjusting of sputtering current of graphite target. Furthermore, the mechanical and tribological performances of the prepared films were appraised by nano-indentor, scratch measures, and ball-on-plate tribometer respectively. The results indicated that multilayer structure endowed the as-deposited TiC/GLC films outstanding mechanical and tribological properties, especially the multilayer film with 15.9 nm bilayer period deposited at 10 A sputtering current showed the excellent adhesion strength and hardness; Simultaneously it also exhibited the lowest average friction coefficient in the humid environment owing to its high content of sp2 hybrid carbon.

X-Ray Photoelectron Spectroscopy Study on Reduction of Graphene Oxide with Hydrazine Hydrate

2011 ◽  
Vol 287-290 ◽  
pp. 539-543 ◽  
Author(s):  
Wen Shi Ma ◽  
Jun Wen Zhou ◽  
Xiao Dan Lin
Keyword(s):  
Graphene Oxide ◽  
Hydrazine Hydrate ◽  
Photoelectron Spectroscopy ◽  
Reduction Rate ◽  
Reduction Reaction ◽  
Chemical Compositions ◽  
Total Oxygen ◽  
Graphene Oxides ◽  
X Ray ◽  
Oxygen Groups

Graphene oxide was prepared through Hummers' method，then different reduced graphenes were prepared via reduction of graphene oxide with hydrazine hydrate for 1h、12h and 24h. X-ray photoelectron spectroscopy (XPS) was used for the characterization of graphene oxide and the reduced graphenes. The variation of the contents of carbon in carbon and oxygen functional groups and chemical compositions of graphene oxides were investigated through analysis the content of different carbon atoms in different reduced graphenes. The results showed that the reduction reaction was very fast in the first 1 h, the content of total oxygen bonded carbon atoms decreased from 83.6% to 22.1%, and then after the reduction rate became very slow. After 12h, the content of total oxygen bonded carbon atom is 19.56%, only 2.54% lower than that of 1h’s. At the same time, C-N was introduced in the graphene oxides; this increased the stereo-hindrance for hydrazine hydrate attacking the C-Oxygen groups, thus reduced the reduction rate. After reduction for 24h, there still exists 16.4% oxygen bonded carbon atoms and the total conversion ratio of graphene approaches 70%.

Chemical Structures of Native Oxides Formed During Wet Chemical Treatments on NH4F Treated Si(111) Surfaces

1992 ◽  
Vol 259 ◽  
Author(s):  
Takeo Hattori ◽  
Hiroki Ogawa
Keyword(s):  
Photoelectron Spectroscopy ◽  
Attenuated Total Reflection ◽  
Native Oxide ◽  
X Ray ◽  
Chemical Treatments ◽  
Chemical Structures ◽  
Native Oxides ◽  
Ft Ir ◽  
Wet Chemical ◽  
Silicon Interface

ABSTRACTChemical structures of native oxides formed during wet chemical treatments on NH4F treated Si(111) surfaces were investigated using X-ray Photoelectron Spectroscopy (XPS) and Fourier Transformed Infrared Attenuated Total Reflection(FT-IR-ATR). It was found that the amounts of Si-H bonds in native oxides and those at native oxide/silicon interface are negligibly small in the case of native oxides formed in H2SO4-H2O2-H2O solution. Based on this discovery, it was confirmed that native oxides can be characterized by the amount of Si-H bonds in native oxides. Furthermore, it was found that the combination of various wet chemical treatments with the treatment in NH4OH-H2O2-H2O solution results in the drastic decrease in the amount of Si-H bonds in native oxides.

Recyclable Heterogeneous Fe-Mo Nanocatalyst: Application in Solvent Free Synthesis of β-enaminones

2019 ◽  
Vol 6 (3) ◽  
pp. 238-247
Author(s):  
Swapnil R. Bankar
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Significant Loss ◽  
Solvent Free ◽  
Catalyst Loading ◽  
Spectroscopic Techniques ◽  
Impregnation Method ◽  
Molybdenum Catalyst ◽  
X Ray ◽  
Solvent Free Condition

<P>Background: In recent years, green organic transformation has become a challenge for a chemist in areas like social sector, health, and environment. Literature survey revealed that a nano magnetite supported heterogeneous catalysis is an emergent field with huge application in chemical synthesis. </P><P> Objective: In the present article, the aim was to develop a simple and facile method to carry organic reaction under benign media. So, the focus was on the synthesis of nano-magnetite supported molybdenum catalyst and its application in β-enaminones synthesis. </P><P> Methods: Magnetically recyclable heterogeneous ferrite-molybdenum catalyst was prepared by simple impregnation method. The synthesized nanocatalyst Fe-Mo was well analysed by spectroscopic techniques like X-ray diffraction analysis, X-ray photoelectron spectroscopy, transmission electron microscopy, field-emission gun scanning electron microscopy and vibrating-sample magnetometry. The functionalized nanocatalyst Fe-Mo was employed in the synthesis of β-enaminones under solvent free condition. </P><P> Results: The competency of synthesized nanocatalyst-Fe-Mo was observed to be good for the synthesis of β-enaminones derivatives under microwave irradiation and gave excellent yield (86-96%) of the product. The catalyst was recycled for more than five consecutive runs without significant loss in its activity. </P><P> Conclusion: In the present research article, synthesis of highly active, magnetically recyclable Fe- Mo nanocatalyst was obtained from easily available precursor. The MNP was stable under investigated conditions and effective in β-enaminones synthesis. The simple eco-friendly method, low catalyst loading, short transformation time, and reusability of the catalyst thoroughly follow the sustainable protocol.</P>

scholarly journals Synthesis of Phosphorus-Containing Polyanilines by Electrochemical Copolymerization

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1029 ◽  
Author(s):  
Beatriz Martínez-Sánchez ◽  
Andrés Felipe Quintero-Jaime ◽  
Francisco Huerta ◽  
Diego Cazorla-Amorós ◽  
Emilia Morallón
Keyword(s):  
Photoelectron Spectroscopy ◽  
Polymeric Materials ◽  
Electroactive Polymers ◽  
Hydrogen Electrode ◽  
X Ray ◽  
Electrochemical Copolymerization ◽  
Phosphorus Containing ◽  
Redox Transitions ◽  
Acid Stable

In this study, the phosphonation of a polyaniline (PANI) backbone was achieved in an acid medium by electrochemical methods using aminophenylphosphonic (APPA) monomers. This was done through the electrochemical copolymerization of aniline with either 2- or 4-aminophenylphosphonic acid. Stable, electroactive polymers were obtained after the oxidation of the monomers up to 1.35 V (reversible hydrogen electrode, RHE). X-ray photoelectron spectroscopy (XPS) results revealed that the position of the phosphonic group in the aromatic ring of the monomer affected the amount of phosphorus incorporated into the copolymer. In addition, the redox transitions of the copolymers were examined by in situ Fourier-transform infrared (FTIR) spectroscopy, and it was concluded that their electroactive structures were analogous to those of PANI. From the APPA monomers it was possible to synthesize, in a controlled manner, polymeric materials with significant amounts of phosphorus in their structure through copolymerization with PANI.

Unexpected Pyramid Texturization of n-Type Ge (100) via Electrochemical Etching: Bridging Surface Chemistry and Morphology

2018 ◽  
Vol 282 ◽  
pp. 94-98
Author(s):  
Graniel Harne A. Abrenica ◽  
Mikhail V. Lebedev ◽  
Hy Le ◽  
Andreas Hajduk ◽  
Mathias Fingerle ◽  
...  
Keyword(s):  
Surface Morphology ◽  
Surface Chemistry ◽  
Photoelectron Spectroscopy ◽  
Chemical Etching ◽  
Electrochemical Etching ◽  
Spectroscopic Techniques ◽  
X Ray ◽  
Etching Behavior ◽  
Effect Of Oxygen

We report on the (electro) chemical etching behavior, surface morphology and composition of n-type Ge (100) in acidic halide solutions using various analytical and spectroscopic techniques. The use of an integrated (electro) chemical etching chamber connected to X-ray photoelectron spectroscopy instrument to exclude the effect of oxygen from atmosphere is highlighted.

scholarly journals X-Ray Photoelectron Spectroscopy Study of Silane Coupling Agents/Basalt Fiber Interface

2011 ◽  
Vol 236-238 ◽  
pp. 1467-1471 ◽  
Author(s):  
Ya Lan Liu ◽  
Shi Jie Shen ◽  
Li Zhang ◽  
Ling Min Shao
Keyword(s):  
Coupling Agent ◽  
Photoelectron Spectroscopy ◽  
Silane Coupling Agent ◽  
Basalt Fiber ◽  
Fiber Surface ◽  
Chemical Compositions ◽  
Hydroxyl Groups ◽  
Silane Coupling Agents ◽  
X Ray ◽  
Silane Coupling

In this paper, two types of fiber surface treatment methods, namely heat treatment and chemical coupling, were used to improve the basalt fiber surface properties. The basalt fiber surface was heated under 250Celsius degree for 30minites, and then was treated by silane coupling agent ethanol solution with different concentrations. X-ray photoelectron spectroscopy (XPS) was utilized to study the surface chemical compositions of basalt fiber after treatments. The XPS analysis indicated that chemical bonds between basalt fiber and KH-550 have occurred, and silanols were adsorbed to the surface of basalt fibers by an ether linkage between the silanols and the hydroxyl groups of the fibers. When the concentration of KH-550 is 0.8wt%, the optimal bonding condition is formed between basalt fiber and silane coupling agent.

X-ray photoelectron spectroscopy investigation of fire retarded polymeric materials

2002 ◽  
Vol 77 (2) ◽  
pp. 203-211 ◽  
Author(s):  
S Duquesne ◽  
M Le Bras ◽  
C Jama ◽  
E.D Weil ◽  
L Gengembre
Keyword(s):  
Photoelectron Spectroscopy ◽  
Polymeric Materials ◽  
X Ray
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