Modification of a carbon/carbon composite with a thermosetting resin precursor as a matrix by the addition of carbon black

Carbon/carbon composites were made through the pyrolysis of stabilized PAN felt and phenolic resin with the addition of 5 or 10 wt % carbon black to the matrix and then heat treatment at 600–2500°C. The effects of adding carbon black to the matrix precursor on the physical properties, microstructure, and mechanical properties of the resultant composites were investigated. Adding carbon black not only reduced the weight loss but also limited the shrinkage of the resultant composites. Adding carbon black also accelerated the formation of carbon basal planes in the matrix. At 2500°C, the crystalline stacking height in the composite with 10 wt % added carbon black was 200% greater than that with no additive. The flexural strength of the composite also increased from 15 to 42 MPa (almost 300%). © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 333–337, 2006     

Synthesis and properties of fluorinated aromatic poly(amide imide)s based on 4,4′‐bis(4‐amino‐2‐trifluoromethylphenoxy)benzophenone and various bis(trimellitimide)s

A CF₃‐containing diamine, 4,4′‐bis(4‐amino‐2‐trifluoromethylphenoxy)benzophenone ( 2 ), was synthesized from 4,4′‐dihydroxybenzophenone and 2‐chloro‐5‐nitrobenzotrifluoride. Imide‐containing diacids ( 3 and 5B_a – 5B_g ) were prepared by the condensation reaction of aromatic diamines and trimellitic anhydride. Then, two series of novel soluble aromatic poly(amide imide)s (PAIs; 6A_a – 6A_k and 6B_a – 6B_g ) were synthesized from a diamine ( 4A_a – 4A_k or 2 ) with the imide‐containing diacids ( 3 and 5B_a – 5B_g ) via direct polycondensation with triphenyl phosphate and pyridine. The aromatic PAIs had inherent viscosities of 0.74–1.76 dL/g. All of the synthesized polymers showed excellent solubility in amide‐type solvents, such as N‐methyl‐2‐pyrrolidone and N,N‐dimethylacetamide (DMAc), and afforded transparent and tough films by DMAc solvent casting. These polymer films had tensile strengths of 90–113 MPa, elongations at break of 8–15%, and initial moduli of 2.0–2.9 GPa. The glass‐transition temperatures of the aromatic PAIs were in the range 242–279°C. They had 10% weight losses at temperatures above 500°C and showed excellent thermal stabilities. The 6B series exhibited less coloring and showed lower yellowness index values than the corresponding 6A series. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:3641–3653, 2006     

Rattle‐Structured Ag/TiO2 Nanocomposite Capsules with Bactericide and Photocatalysis Activities

A structural design featuring rattle‐type silver/titania (Ag/TiO₂) core/shell, that is, Ag@TiO₂, composite microcapsules is produced. The TiO₂ shell protects the encapsulated, movable Ag nanoparticles from breaking away under moderate loading, minimizing hence adverse environmental and biological exposure due to the metal loss, whereas the mesoporous shell serves as conduits for Ag ions released from the caged Ag nanoparticles to kill Escherichia coli in aqueous solutions under dark condition. The anatase TiO₂ shell imparts an additional, synergistic photocatalysis activity under ultraviolet irradiation. A pronouncedly enhanced photocatalysis activity results when the Ag@TiO₂ composite capsules were thermally annealed under vacuum. This “rattle‐in‐ball” hybrid architecture enables bifunctional bactericide and photocatalysis capability under both light and dark conditions, as well as mitigated environmental and biological impact in practical use.     

Maximizing the Retention of Ganoderic Acids and Water-Soluble Polysaccharides Content of Ganoderma lucidum Using Two-Stage Dehydration Method

Ganoderic acids and water-soluble polysaccharides are the main bioactive ingredients of Ganoderma lucidum and are heat sensitive. Hence, it is crucial to apply a suitable drying method for the drying of G. lucidum to minimize the loss of these bioactive ingredients. In this study, a two-stage drying method was applied to enhance the drying kinetics, as well as the retention of both ganoderic acids and water-soluble polysaccharides in dried G. lucidum fruiting bodies and slices compared to other single-stage-dried products. The results showed that two-stage drying enhanced the overall drying rate, which consequently shortened the total drying time up to 61 and 330% for fruiting bodies and slices, respectively, compared to single-stage drying methods. Furthermore, two-stage drying of Ganoderma fruiting bodies, which involves 18-h vacuum drying followed by 5-h heat pump drying, maximized the retention of ganoderic acids and water-soluble polysaccharides, with the retention of 97.90% of water-soluble polysaccharides and 4.2% more ganoderic acids than freeze-dried products. On the other hand, drying of Ganoderma slices within the shortest total drying time, which is 10-min heat pump drying followed by 50-min oven drying, also retained most of the ganoderic acids and water-soluble polysaccharides in the dried products; that is, about 80% of water-soluble polysaccharides and 11% more ganoderic acids than freeze-dried slices.     

Catalytic Asymmetric Conjugate Addition of Mercaptans to β‐Substituted‐β‐Trifluoromethyl Oxazolidinone Enoates: Access to Chiral Trifluoromethylated Tertiary Thioethers and Thiols

The first asymmetric conjugate addition of mercaptans to β‐substituted‐β‐trifluoromethyl oxazolidinone enoates has been developed. The opposite enantiomers of adducts, containing a trifluoromethylated hetero‐quaternary stereogenic centers, could be obtained by utilizing two pseudo‐enantiomeric Cinchona alkaloid‐derived tertiary amine/squaramides as catalysts. Potassium dihydrogen phosphate was found to accelerate the reaction rate without compromising the enantioselective excess. A variety of chiral trifluoromethylated tertiary thioethers and thiols were readily prepared with excellent enantioselectivity.

     

Physical study of room‐temperature‐cured epoxy/thermally reduced graphene oxides with various contents of oxygen‐containing groups

In this study, the effects of different oxygen‐containing group contents in thermally reduced graphene oxides (TRGs) for enhancing the physical properties of epoxy nancomposites was examined. The epoxy/TRG nanocomposites (ETNs) were prepared by a room temperature curing method in the presence of TRGs containing different oxygen‐containing groups and were then characterized by Fourier transform infrared spectroscopy. TRG contents with higher oxygen‐containing group contents (ca 33%) were found to show better dispersion capability in the epoxy matrix than TRGs with lower oxygen‐containing group contents (ca 11%) based on morphological observations by transmission electron microscopy. The better dispersion capability of TRGs with higher oxygen‐containing group contents in ETN membranes was found to lead to significantly enhanced mechanical strength, thermal stability and thermal conductivity based on measurements of dynamic mechanical analysis, tensile tests, thermogravimetric analysis and by the transient plane source technique. © 2014 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry     

Fabrication of Embedded Microstructures Via Lamination of Thick Gel‐Casted Ceramic Layers

This article describes a new approach to fabricate various embedded ceramic microstructures. Design geometries of the microstructures are replicated onto a soft reusable polydimethylsiloxane (PDMS) mold. Rapid consolidation of ceramic suspension on the molds using gel‐casting technique produces structured ceramic layers. 85% aqueous glycerol solution has been identified as suitable adhesive agent to laminate the ceramic layers. Capability of the approach in fabricating embedded microstructures of 3‐dimensional and aspect ratio as high as 20 and 50 has been demonstrated. Ceramic microthruster and Y‐shaped microfluidic reactor are fabricated using this new approach to show its potential to construct various ceramic microdevices.     

Structural study of titanium oxide films synthesized by ion beam-assisted deposition

The application of titanium dioxide (TiO(2)) films as surgical implant coatings for antibiotic attachment depends crucially on their available surface area and thus their surface morphology and crystallinity. Here, we report our fabrication of high Wenzel ratio TiO(2) films targeted to increase the film surface area using the ion beam-assisted deposition (IBAD) technique at high-deposition temperatures (approximately 610 degrees C). The modulation of the films' surface morphology was accomplished by varying the chemical identity of the concurrent ion beams bombarded on the films during the e-beam evaporation process. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) were employed to investigate the surface morphology of the as-deposited films. X-ray diffractometry (XRD) revealed that these nanocrystalline films primarily consist of anatase phase TiO(2). Wenzel ratio, the ratio of the actual surface area to the projected area, of IBAD films prepared with argon, oxygen, and nitrogen ion beams was measured to be 1.52, 1.31 and 1.49, respectively. The effect of the differences in chemical reactivity and ion size of these three type ion beams are discussed to explain the present results.     

Conversion of allylic hydroxy oleate to conjugated linoleic acid and methoxy oleate by acid-catalyzed methylation procedures

Conjugated linoleic acid (CLA), a term describing a group of conjugated octadecadienoic acids that are both naturally occurring and formed during food processing, is the subject of considerable current research because of the recently reported antioxidant and anticarcinogenic properties of these compounds. Allylic hydroxy oleates (AHOs), secondary products of lipid autoxidation, have also been found in foods. By means of high-performance liquid chromatography with ultraviolet detection, gas chromatography/mass spectrometry and gas chromatography/matrix isolation/Fourier transform infrared spectroscopy, we determined that currently used acid-catalyzed methylation procedures convert AHOs to CLA and other products that potentially yield high values in determination of CLA in foods. A mixture of AHOs, containing mainly (8- and 11-)hydroxy-9-octadecadecenoates, was synthesized and tested by methylation procedures with the following catalysts: BF₃, HCl, NaOMe and tetramethylguanidine. Both the BF₃ and the HCl procedures converted AHOs to CLA. The base-catalyzed procedures did not convert AHOs to CLA.     

Strengths and weaknesses of finite element modeling deep hole drilling as compared with beam and column equations

Deep hole drilling has been studied mainly experimentally in the past. Recently, some theories using beam or column equations have been proposed, which involved complicated mathematical efforts. This work analyzed deep hole drilling by a finite element model (FEM). Results of modal analysis on the established FEM were compared with results from Euler beam equations. Further analysis showed that the FEM could also predict straightness deviation as did the column equation. In addition, FEM could analyze the effects of variable support distance which neither beam nor column equation could. Other analysis results are also presented. The results in this study showed the strength and weakness of the FEM.