Antimicrobial TMSAH-Added Wood-Inorganic Composites Prepared by the Sol-Gel Process

Holzforschung ◽  
1998 ◽  
Vol 52 (4) ◽  
pp. 365-370 ◽  
Author(s):  
Fumie Tanno ◽  
Shiro Saka ◽  
Akira Yamamoto ◽  
Keiji Takabe
Keyword(s):  
Sol Gel ◽  
Inorganic Composites ◽  
Sol Gel Process

scholarly journals Long-Term Creep Behavior Prediction of Sol-Gel Derived SiO2- and TiO2-Wood Composites Using the Stepped Isostress Method

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1215 ◽  
Author(s):  
Ke-Chang Hung ◽  
Tung-Lin Wu ◽  
Jyh-Horng Wu
Keyword(s):  
Creep Behavior ◽  
Creep Resistance ◽  
Flexural Modulus ◽  
Sol Gel ◽  
Untreated Wood ◽  
Behavior Prediction ◽  
Inorganic Composites ◽  
Sol Gel Process ◽  
Term Creep

In this study, methyltrimethoxysilane (MTMOS), methyltriethoxysilane (MTEOS), tetraethoxysilane (TEOS), and titanium(IV) isopropoxide (TTIP) were used as precursor sols to prepare wood-inorganic composites (WICs) by a sol-gel process, and subsequently, the long-term creep behavior of these composites was estimated by application of the stepped isostress method (SSM). The results revealed that the flexural modulus of wood and WICs were in the range of 9.8–10.5 GPa, and there were no significant differences among them. However, the flexural strength of the WICs (93–103 MPa) was stronger than that of wood (86 MPa). Additionally, based on the SSM processes, smooth master curves were obtained from different SSM testing parameters, and they fit well with the experimental data. These results demonstrated that the SSM was a useful approach to evaluate the long-term creep behavior of wood and WICs. According to the Eyring equation, the activation volume of the WICs prepared from MTMOS (0.825 nm3) and TEOS (0.657 nm3) was less than that of the untreated wood (0.832 nm3). Furthermore, the WICs exhibited better performance on the creep resistance than that of wood, except for the WICMTEOS. The reduction of time-dependent modulus for the WIC prepared from MTMOS was 26% at 50 years, which is the least among all WICs tested. These findings clearly indicate that treatment with suitable metal alkoxides could improve the creep resistance of wood.

Photostable wood–inorganic composites prepared by the sol-gel process with UV absorbent

2004 ◽  
Vol 50 (2) ◽  
pp. 130-135 ◽  
Author(s):  
Hisashi Miyafuji ◽  
Hideki Kokaji ◽  
Shiro Saka
Keyword(s):  
Sol Gel ◽  
Inorganic Composites ◽  
Sol Gel Process

Comparison of physical and thermal properties of various wood-inorganic composites (WICs) derived by the sol-gel process

Holzforschung ◽  
2018 ◽  
Vol 72 (5) ◽  
pp. 379-386 ◽  
Author(s):  
Ke-Chang Hung ◽  
Jyh-Horng Wu
Keyword(s):  
Thermal Decomposition ◽  
Reaction Order ◽  
Sol Gel ◽  
Inorganic Composites ◽  
Conversion Rates ◽  
Sol Gel Process ◽  
Apparent Activation Energies ◽  
Kinetics Of ◽  
Thermal Stability Of ◽  
Better Than

AbstractThe physical properties and thermal decomposition kinetics of wood-inorganic composites (WICs) were in focus, which were prepared from methyltriethoxysilane (MTEOS), tetraethoxysilane (TEOS) and titanium (IV) isopropoxide (TTIP) by the sol-gel process. The hydrophobicity and dimensional stability of the composites were better than those of unmodified wood (Wcontr), but the performance of SiO2-based WICs (WICSiO2) was the best. The SEM-EDX micrographs show that silica is only distributed within the cell wall of the WICSiO2. By contrast, titania was deposited principally in the cell lumens of the WICTiO2. The thermal decomposition kinetic experiments show that the average apparent activation energies with conversion rates between 10% and 70% were 156–168 (Wcontr), 178–180 (WICMTEOS), 198–214 (WICTEOS) and 199–204 (WICTTIP) kJ mol−1at the impregnation level of 20% weight gain. The reaction order values calculated based on the Avrami theory were 0.51–0.57, 0.39–0.51, 0.36–0.47 and 0.28–0.51 in the same order of species indicated above. Accordingly, the dimensional and thermal stability of the wood could be enhanced effectively by the sol-gel process with silicon- and titanium-based alkoxides.

The crystallization of thin-film ceramics

1992 ◽  
Vol 50 (1) ◽  
pp. 338-339
Author(s):  
J.M. Schwartz ◽  
L.F. Francis ◽  
L.D. Schmidt ◽  
P.S. Schabes-Retchkiman
Keyword(s):  
Thin Films ◽  
Grain Size ◽  
Sol Gel ◽  
Processing Route ◽  
Small Areas ◽  
Ceramic Thin Films ◽  
Complex Shapes ◽  
Sol Gel Process ◽  
Ceramic Precursors ◽  
Crystalline Ceramic

Ceramic thin films and coatings are of interest for electrical, optical, magnetic and thermal barrier applications. Critical for improved properties in thin films is the development of specific microstructures during processing. To this end, the sol-gel method is advantageous as a versatile processing route. The sol-gel process involves depositing a solution containing metalorganic or colloidal ceramic precursors onto a substrate and heating the deposited layer to form a crystalline or non-crystalline ceramic coating. This route has several advantages, including the ability to create tailored microstructures and properties, to coat large or small areas, simple or complex shapes, and to more easily prepare multicomponent ceramics. Sol-gel derived coatings are amorphous in the as-deposited state and develop their crystalline structure and microstructure during heat-treatment. We are particularly interested in studying the amorphous to crystalline transformation, because many key features of the microstructure such as grain size and grain size distribution may be linked to this transformation.

Epitaxial Growth of Sr0.3Ba0.7Nb2O6 Thin Films Prepared by Sol-Gel Process

1999 ◽  
Vol 606 ◽  
Author(s):  
Keishi Nishio ◽  
Jirawat Thongrueng ◽  
Yuichi Watanabe ◽  
Toshio Tsuchiya
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Epitaxial Growth ◽  
Raw Materials ◽  
Substrate Surface ◽  
Sol Gel ◽  
Tungsten Bronze ◽  
Monomethyl Ether ◽  
Tetragonal Tungsten Bronze ◽  
Sol Gel Process

AbstructWe succeeded in the preparation of strontium-barium niobate (Sr0.3Ba0.7Nb2O6 : SBN30)that have a tetragonal tungsten bronze type structure thin films on SrTiO3 (100), STO, or La doped SrTiO3 (100), LSTO, single crystal substrates by a spin coating process. LSTO substrate can be used for electrode. A homogeneous coating solution was prepared with Sr and Ba acetates and Nb(OEt)5 as raw materials, and acetic acid and diethylene glycol monomethyl ether as solvents. The coating thin films were sintered at temperature from 700 to 1000°C for 10 min in air. It was confirmed that the thin films on STO substrate sintered above 700°C were in the epitaxial growth because the 16 diffraction spots were observed on the pole figure using (121) reflection. The <130> and <310> direction of the thin film on STO were oriented with the c-axis in parallel to the substrate surface. However, the diffraction spots of thin film on LSTO substrate sintered at 700°C were corresponds to the expected pattern for (110).

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