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101.
Keiji Nakayama 《Lubrication Science》1993,5(2):113-127
Radical scavenger, radical anion scavenger, and peroxide decomposer were added to aromatic hydrocarbons and phosphates in aromatic rings with and without side chain, and the effect of these inhibitors on tribopolymerisation and the lubrication characteristics of the aromatic compounds were investigated, in various atmospheres, in order to clarify the reaction mechanism. The aromatics of both hydrocarbons and phosphates with a methyl group in aromatic rings react readily at the rubbing surfaces to form polymer or polymer-like products, improving the lubricating characteristics. The tribochemical reactions of alkylaromatic compounds is shown to differ from those of trialkyl or triarylphosphates. It was concluded that the reaction proceeds through the radical or radicalanion and via peroxide to cause polymerisation. 相似文献
102.
Takehiro Matsunaga Yoshio Nakayama Mitsuaki Iida Senzo Oinuma Noboru Ishikawa Katsumi Tanaka 《Propellants, Explosives, Pyrotechnics》1992,17(2):63-69
Molecular properties of benzene nitro derivatives were investigated by using semi-empirical MO calculations. As the results, the molecular structures and the rotational barrier of the nitro group calculated by AM1 showed a good agreement with the experimental values. The heats of formation in gaseous and condensed phases were obtained by considering isodesmic reactions. By this procedure, the heat of formation of hexanitrobenzene in solid phase was calculated to be +22.7 kcal/mol. The detonation parameters were also calculated by using four equations of state. The predicted detonation velocities showed a good agreement with the experimental values. 相似文献
103.
Previous studies on polyamide 4, excellent properties, functionalities, and biodegradation in natural condition have been shown. In this study, three-branched (star-shaped) copolyamides constituted of polyamide 4 and polyamide 6 constitutional unit were synthesized by anionic ring-opening copolymerization of 2-pyrrolidone with ε-caprolactam. The thermal and mechanical properties and the biodegradability of the obtained copolyamides have been systematically investigated. The weight-average molecular weight of the copolyamides was as high as tens of thousands (Mw 10–80 × 103 g/mol). The composition of the copolyamides was approximately in accord with the monomer feed ratio, thereby being controllable. The thermal and mechanical properties changed readily as the composition was varied (Tm 146–266°C, ΔHm 10–70 J/g, Td 278–369°C, tensile strength 28–64 MPa, elongation at break 80–750%). The copolyamide having 2-pyrrolidone unit of 96–51 mol% exhibited biodegradability by an activated sludge. The biodegradation of the copolyamide proceeded uniformly without disproportion in constitutional unit. 相似文献
104.
Electron beam sterilization of cyclo olefin polymer leads to polymer degradation and production of alkyl radicals
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Hideaki Kiminami Yasufumi Imae Eiji Takahashi Hong Wei Satoshi Oomura Yoshihiko Abe 《应用聚合物科学杂志》2016,133(23)
We investigated the effects of electron‐beam (EB) sterilization on syringe barrels manufactured from cyclo olefin polymer (COP). The chemical structure of the polymer was determined by interpreting the 13C NMR and DEPT‐135 spectra of the COP resin. The antioxidants in the resin were identified by analyzing the liquid chromatography‐photo diode array‐mass spectrometry (LC‐PDA‐MS) data for the methanol extract of the resin and the gas chromatography‐mass spectrometry (GC‐MS) data for the supercritical methanol degradation products of the extract. NMR and LC‐PDA‐MS analyses revealed that EB sterilization produces degradation products in the COP main chain and reduces the quantity of the antioxidants in the COP resin. ESR spectra of the EB‐sterilized syringe barrels indicated the presence and location of alkyl radicals, which were generated in the COP main chain by EB sterilization. ESR analyses also indicated that the quantity of alkyl radicals decreased over time. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43498. 相似文献
105.
Crack-Healing Behavior of Si3 N4 /SiC Ceramics under Cyclic Stress and Resultant Fatigue Strength at the Healing Temperature 总被引:1,自引:0,他引:1
Kotoji Ando Koji Takahashi Shin Nakayama Shinji Saito 《Journal of the American Ceramic Society》2002,85(9):2268-2272
Si3 N4 /SiC composite ceramics were sintered and subjected to three-point bending. A semi-elliptical surface crack of 100 μm surface length was made on each specimen. The crack-healing behavior under cyclic stress of 5 Hz, and resultant cyclic fatigue strengths at healing temperatures of 1100° and 1200°C, were systematically investigated. The main conclusions are as follows: (1) Si3 N4 /SiC composite ceramics have an excellent ability to heal a crack at 1100° and 1200°C. (2) This sample could heal a crack even under cyclic stress at a frequency of 5 Hz. (3) The crack-healed sample exhibited quite high cyclic fatigue strength at each crack-healing temperature, 1100° and 1200°C. 相似文献
106.
The diffusion coefficient (D) values of tert‐butyloxycarbonyl‐glycine, tert‐butyloxycarbonyl‐L ‐tryptophan, tert‐butyloxycarbonyl‐L ‐phenylalanine (Boc‐Phe), and 9‐fluorenylmethoxycarbonyl‐L ‐phenylalanine in Merrifield polystyrene (MPS) gels, poly(ethylene glycol)‐grafted polystyrene (PEG–PS) gels, and crosslinked ethoxylate acrylate (CLEAR) gels, as used in solid‐phase peptide synthesis, were determined by the pulsed‐field‐gradient spin‐echo 1H‐NMR method. From these experimental results, it was found that the amino acids in MPS gels, PEG–PS gels, and CLEAR gels with N,N‐dimethylformamide‐d7 (DMF‐d7) as a solvent had multidiffusion components within a measurement timescale of 10 ms. The D value of Boc‐Phe in polystyrene gels (1% divinylbenzene crosslinked) with tetrahydrofuran‐d8 was much larger than that in the same gels with DMF‐d7. Furthermore, the required time in which an amino acid transferred from a reactive site to a reactive site was estimated, within which the solvents and amino acids in the polymer supports diffused in the swollen beads.© 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 413–421, 2003 相似文献
107.
Masahiko Nakase Tohru Kobayashi Hideaki Shiwaku Shinichi Suzuki Travis S. Grimes Bruce J. Mincher 《溶剂提取与离子交换》2013,31(7):633-646
ABSTRACTTo effectively separate lanthanides (Ln(III)) from actinides (An(III)), symmetrical 2,2′-bipyridyl (Bpy), 1,10-phenanthroline (Phen), and unsymmetrical N-methyl-N-tolyl-1,10-phenanthroline-2-carboxamide (MeTol-PTA) were investigated. According to the crystal structures and EXAFS experiments, the decreasing ionic radius from light to heavy Ln led to decreases in the Ln–N (Bpy) and Ln–N (Phen) distances, while log β simply increased due to the electrostatic interaction and the order of Ln–O (MeTol-PTA) < Ln–N (Bpy, Phen) < Ln–N (MeTol-PTA) was obtained. This indicated that the bulky phenanthroline moiety of MeTol-PTA may not allow N (MeTol-PTA) to come close to Ln. Consequently, the log β of MeTol-PTA exhibited a local maximum (around Nd). 相似文献
108.
Tetsuya Nanba Asima Sultana Shouichi Masukawa Masaaki Haneda Junko Uchisawa Akira Obuchi Hideaki Hamada 《Topics in Catalysis》2009,52(13-20):1766-1770
Selective catalytic reduction of NO x by NH3 over Cu–FER and Cu–ZSM-5 in the presence of n-decane and SO2 was investigated. NO x conversion over Cu–ZSM-5 decreased in the presence of n-decane, owing to inhibition of the active sites by coke formation. In contrast, coke formation was negligible over Cu–FER, which maintained its NO x conversion activity even in the presence of decane. Coke formation was negligible over H–ZSM-5 and H–FER supports, which suggests that Cu species were involved in coke formation. Temperature-programmed reduction by H2 and electron spin resonance spectroscopy indicated that [Cu–O–Cu]2+ was probably the Cu species involved in coke formation over Cu–ZSM-5. 相似文献
109.
Masaaki Haneda Ohki Houshito Hiromitsu Takagi Kiyoshi Shinoda Yuunosuke Nakahara Kazumi Hiroe Tadahiro Fujitani Hideaki Hamada 《Topics in Catalysis》2009,52(13-20):1868-1872
The activity of Rh/CeO2 for NO reduction by C3H6 was gradually deceased by mixing with ZrO2 until 68 mol%. Rh supported on CeO2–ZrO2 with higher OSC was found to show lower catalytic activity. High OSC of CeO2–ZrO2 would probably stabilize the surface of Rh in oxidized state, resulting in low activity and low efficiency of C3H6 utilization for NO reduction. In situ FT-IR spectroscopy suggested that mononitrosyl species such as Rh(NO)δ? and Rh(NO)δ+ are reaction intermediates in the NO–C3H6–O2 reaction over Rh/CeO2–ZrO2 catalysts. 相似文献
110.
A Multiple‐Labeling Strategy for Nonribosomal Peptide Synthetases Using Active‐Site‐Directed Proteomic Probes for Adenylation Domains
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Dr. Fumihiro Ishikawa Dr. Takehiro Suzuki Dr. Naoshi Dohmae Prof. Hideaki Kakeya 《Chembiochem : a European journal of chemical biology》2015,16(18):2590-2594
Genetic approaches have greatly contributed to our understanding of nonribosomal peptide biosynthetic machinery; however, proteomic investigations are limited. Here, we developed a highly sensitive detection strategy for multidomain nonribosomal peptide synthetases (NRPSs) by using a multiple‐labeling technique with active‐site‐directed probes for adenylation domains. When applied to gramicidin S‐producing and ‐nonproducing strains of Aneurinibacillus migulanus (DSM 5759 and DSM 2895, respectively), the multiple technique sensitively detected an active multidomain NRPS (GrsB) in lysates obtained from the organisms. This functional proteomics method revealed an unknown inactive precursor (or other inactive form) of GrsB in the nonproducing strain. This method provides a new option for the direct detection, functional analysis, and high‐resolution identification of low‐abundance active NRPS enzymes in native proteomic environments. 相似文献