Structural Changes on Photochromism of Organic-Inorganic Hybrid Materials

1999 ◽  
Vol 604 ◽  
Author(s):  
Keiichi Kuboyama ◽  
Kazumi Matsushige
Keyword(s):  
Fourier Transform ◽  
Tungsten Oxide ◽  
Transition Metal Oxides ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Spectroscopic Measurement ◽  
Inorganic Hybrid ◽  
X Ray ◽  
Oxide Hydrate ◽  
Ft Ir

AbstractSome transition metal oxides are known to exhibit the reversible coloration phenomena. Tungsten oxide is one of such materials and exhibits the photochromism and the electrochromism. It is known that the coloration phenomena in the tungsten oxide hydrate are caused by the redox reaction. We found that the photochromic efficiency became extremely higher by addition of some organic materials to the tungsten oxide hydrate and we have studied the mechanism of such a remarkable photochromic enhancement. In some spectroscopic measurement as FT-IR (Fourier transform infrared spectroscopy) and XPS (X-ray photoelectron spectroscopy), we obtained interesting features as follows. The addition of an organic material leads to reducing the tungsten oxide hydrate to smaller pieces, that is, the surface area of the pieces that can react with the additive increases. Moreover, it was found that specific sites in the additive are oxidized when the sample colors. The fact suggests that the additives having such specific sites can enhance the photochromism of the tungsten oxide hydrate

Observation of the Tribo-Film Formation Derived from ZnDTP by Using FT-IR

2015 ◽  
Vol 642 ◽  
pp. 259-263
Author(s):  
Hirotomo Watanabe ◽  
Chiharu Tadokoro ◽  
Shinya Sasaki
Keyword(s):  
Fourier Transform ◽  
Ir Spectra ◽  
Photoelectron Spectroscopy ◽  
Film Formation ◽  
Intensity Change ◽  
Friction Behavior ◽  
Absorption Bands ◽  
X Ray ◽  
Sliding Surfaces ◽  
Ft Ir

To understand the effects of tribo-film formation derived from ZnDTP (zinc dialkyl ditio phosphate) on friction behavior, friction tests were carried out with varying sliding time. The sliding surfaces were analyzed using Fourier transform infrared spectroscopy (FT-IR) and X-ray Photoelectron Spectroscopy (XPS). On the basis of the surface analytical results of the tribo-film, the absorption bands in the region of 1300-1000 cm-1 assigned as polyphosphate appeared in all IR spectra after the sliding. The friction behavior of ZnDTP was related to the intensity change of the IR spectra peak at 1200 cm-1.

scholarly journals Comparative Study of Carbon Nanosphere and Carbon Nanopowder on Viscosity and Thermal Conductivity of Nanofluids

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 608
Author(s):  
Thong Le Ba ◽  
Marcell Bohus ◽  
István Endre Lukács ◽  
Somchai Wongwises ◽  
Gyula Gróf ◽  
...  
Keyword(s):  
Thermal Conductivity ◽  
Thermal Analysis ◽  
Fourier Transform ◽  
Photoelectron Spectroscopy ◽  
Comparative Research ◽  
Base Fluid ◽  
X Ray ◽  
Ft Ir ◽  
High Concentrations ◽  
Scanning Electron

A comparative research on stability, viscosity (µ), and thermal conductivity (k) of carbon nanosphere (CNS) and carbon nanopowder (CNP) nanofluids was performed. CNS was synthesized by the hydrothermal method, while CNP was provided by the manufacturer. Stable nanofluids at high concentrations 0.5, 1.0, and 1.5 vol% were prepared successfully. The properties of CNS and CNP nanoparticles were analyzed with Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), specific surface area (SBET), X-ray powder diffraction (XRD), thermogravimetry/differential thermal analysis (TG/DTA), and energy dispersive X-ray analysis (EDX). The CNP nanofluids have the highest k enhancement of 10.61% for 1.5 vol% concentration compared to the base fluid, while the CNS does not make the thermal conductivity of nanofluids (knf) significantly higher. The studied nanofluids were Newtonian. The relative µ of CNS and CNP nanofluids was 1.04 and 1.07 at 0.5 vol% concentration and 30 °C. These results can be explained by the different sizes and crystallinity of the used nanoparticles.

Mechano-Chemical Modification of Nanodiamond with GW

2008 ◽  
Vol 375-376 ◽  
pp. 87-91
Author(s):  
Yong Wei Zhu ◽  
Xiang Yang Xu ◽  
Bai Chun Wang ◽  
Jian Liang Shen
Keyword(s):  
Fourier Transform ◽  
Chemical Modification ◽  
Photoelectron Spectroscopy ◽  
Silane Coupling Agent ◽  
Xps Spectra ◽  
X Ray ◽  
Silane Coupling ◽  
Before And After ◽  
New Type ◽  
Ft Ir

Mechano-chemical modification (MCM) of nanodiamond was conducted with a stirring mill. A new type of silane coupling agent, GW was chosen as its modifier. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FT-IR) were employed to study the surface properties of nanodiamond before and after treatments. Results showed that the peaks related to GW and the ball (for example, Fe, Si and Cl) appeared obviously after its MCM on their XPS spectra and mostly disappeared after its further purification with acid X or Y. A new peak located at 1382.48cm-1 was very strong after further purification. It was proven by their FT-IR spectra.

scholarly journals Synthesis of Magnetic Ferrocene-Containing Polymer with Photothermal Effects for Rapid Degradation of Methylene Blue

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 558
Author(s):  
Wenhui Zhu ◽  
Caiyun Zhang ◽  
Yali Chen ◽  
Qiliang Deng
Keyword(s):  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Degradation Rate ◽  
Model Compound ◽  
Vibrating Sample Magnetometer ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

Photothermal materials are attracting more and more attention. In this research, we synthesized a ferrocene-containing polymer with magnetism and photothermal properties. The resulting polymer was characterized by Fourier-transform infrared (FT-IR), vibrating sample magnetometer (VSM), scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Its photo-thermocatalytic activity was investigated by choosing methylene blue (MB) as a model compound. The degradation percent of MB under an irradiated 808 nm laser reaches 99.5% within 15 min, and the degradation rate is 0.5517 min−1, which is 145 times more than that of room temperature degradation. Under irradiation with simulated sunlight, the degradation rate is 0.0092 min−1, which is approximately 2.5 times more than that of room temperature degradation. The present study may open up a feasible route to degrade organic pollutants.

scholarly journals Pore Modification and Phosphorus Doping Effect on Phosphoric Acid-Activated Fe-N-C for Alkaline Oxygen Reduction Reaction

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1519
Author(s):  
Jong Gyeong Kim ◽  
Sunghoon Han ◽  
Chanho Pak
Keyword(s):  
Phosphoric Acid ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Electronic States ◽  
Nitrogen Adsorption ◽  
Reduction Reaction ◽  
Phosphorus Doping ◽  
X Ray ◽  
Precious Metal Catalysts ◽  
Adsorption Desorption

The price and scarcity of platinum has driven up the demand for non-precious metal catalysts such as Fe-N-C. In this study, the effects of phosphoric acid (PA) activation and phosphorus doping were investigated using Fe-N-C catalysts prepared using SBA-15 as a sacrificial template. The physical and structural changes caused by the addition of PA were analyzed by nitrogen adsorption/desorption and X-ray diffraction. Analysis of the electronic states of Fe, N, and P were conducted by X-ray photoelectron spectroscopy. The amount and size of micropores varied depending on the PA content, with changes in pore structure observed using 0.066 g of PA. The electronic states of Fe and N did not change significantly after treatment with PA, and P was mainly found in states bonded to oxygen or carbon. When 0.135 g of PA was introduced per 1 g of silica, a catalytic activity which was increased slightly by 10 mV at −3 mA/cm2 was observed. A change in Fe-N-C stability was also observed through the introduction of PA.

scholarly journals Synthesis of Novel Arginine-Based Flame Retardant and Its Application in Lyocell Fabric

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3588
Author(s):  
Jiayi Chen ◽  
Yansong Liu ◽  
Jiayue Zhang ◽  
Yuanlin Ren ◽  
Xiaohui Liu
Keyword(s):  
Fourier Transform ◽  
Heat Release ◽  
Flame Retardant ◽  
Photoelectron Spectroscopy ◽  
Fourier Transform Infrared ◽  
Ftir Analysis ◽  
Excellent Thermal Stability ◽  
X Ray ◽  
Cone Calorimeter Test ◽  
Before And After

Lyocell fabrics are widely applied in textiles, however, its high flammability increases the risk of fire. Therefore, to resolve the issue, a novel biomass-based flame retardant with phosphorus and nitrogen elements was designed and synthesized by the reaction of arginine with phosphoric acid and urea. It was then grafted onto the lyocell fabric by a dip-dry-cure technique to prepare durable flame-retardant lyocell fabric (FR-lyocell). X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FTIR) analysis demonstrated that the flame retardant was successfully introduced into the lyocell sample. Thermogravimetric (TG) and Raman analyses confirmed that the modified lyocell fabric featured excellent thermal stability and significantly increased char residue. Vertical combustion results indicated that FR-lyocell before and after washing formed a complete and dense char layer. Thermogravimetric Fourier-transform infrared (TG-FTIR) analysis suggested that incombustible substances (such as H2O and CO2) were produced and played a significant fire retarding role in the gas phase. The cone calorimeter test corroborated that the peak of heat release rate (PHRR) and total heat release (THR) declined by 89.4% and 56.4%, respectively. These results indicated that the flame retardancy of the lyocell fabric was observably ameliorated.

Effects of in-Office and at-Home Bleaching on Human Enamel and Dentin: An in vitro Application of Fourier Transform Infrared Study

2008 ◽  
Vol 62 (11) ◽  
pp. 1274-1279 ◽  
Author(s):  
Feride Severcan ◽  
Kurtulus Gokduman ◽  
Ayca Dogan ◽  
Sukran Bolay ◽  
Saadet Gokalp
Keyword(s):  
Fourier Transform ◽  
Structural Changes ◽  
Protein Denaturation ◽  
Random Coil ◽  
Protein Ratio ◽  
Band Frequency ◽  
Human Enamel ◽  
Ft Ir ◽  
At Home

In-office and at-home bleaching techniques are widely used methods for the whitening of teeth. However, the safety of these techniques has not been clarified yet. The aim of the current study is to investigate the in-office- and at-home-bleaching-induced structural and quantitative changes in human enamel and dentin at the molecular level, under in vitro conditions. The Fourier transform mid-infrared (mid-FT-IR) spectroscopic technique was used to monitor bleaching-induced structural changes. Band frequency and intensity values of major absorptions such as amide A, amide I, phosphate (PO4), and carbonate (CO3−2) bands, for treatment groups and control, were measured and compared. The results revealed that both procedures have negligible effects on dentin constituents. In office-bleached enamel, in addition to demineralization, a decrease in protein and polysaccharide concentrations, mineral-to-protein ratio, and the strength of hydrogen bonds around NH groups, as well as a change in protein secondary structure were observed. The protein structure changed from β-sheet to random coil, which is an indication of protein denaturation. However, no significant variations were observed for at-home bleached enamel. The control, at-home, and in-office bleached enamel samples were differentiated with a high accuracy using cluster analysis based on FT-IR data. This study revealed that office bleaching caused deleterious alterations in the composition and structure of enamel that significantly affected the crystallinity and mineralization of the tissue. Therefore, at-home bleaching seems to be much safer than in-office bleaching in terms of molecular variations.

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