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51.
Takahiro Gunji Takayoshi Tozune Hironori Kaburaki Kouji Arimitsu Yoshimoto Abe 《Journal of polymer science. Part A, Polymer chemistry》2013,51(22):4732-4741
Polymethyl(alkoxy)siloxane copolymers, poly(MTES‐co‐TEOS), and poly(MTMS‐co‐TMOS), are prepared by acid‐catalyzed controlled hydrolytic co‐polycondensation of methyl(trialkoxy)silane MeSi(OR)3 (R = Et (MTES) and Me (MTMS)) and tetra‐alkoxysilane Si(OR)4 (R = Et (TEOS) and Me (TMOS)), respectively. The products are purified by fractional precipitation to provide polymethyl(alkoxy)siloxane copolymers with molecular weight 1000–10,000 (poly(MTES‐co‐TEOS)) or 1700–100,000 (poly(MTMS‐co‐TMOS)) that are stable to self‐condensation. These polymers are soluble in common organic solvents except for hexane, and form flexible and transparent free‐standing films with a tensile strength of 4.0–10.0 MPa. The structure of the polymethyl(alkoxy)siloxane copolymers is thought to be a random or a block co‐polymer. They are found to provide coating films with an adhesive strength up to 10, a refractive index of 1.36–1.40, and a dielectric constant of 3.5–3.6. The products also show better weathering stability than polyethoxysiloxane due to the hydrolytic polycondensation of TEOS. Field emission‐scanning electron micrography analysis reveals that coating films are composed of a micro‐phase separated structure. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4732–4741 相似文献
52.
Tomohiro Narukawa Takayoshi Kuroiwa Izumi Narushima Koichi Chiba 《Analytical sciences》2008,24(3):355-360
The sensitivity of graphite furnace atomic absorption spectrometry (GFAAS) to arsenobetaine (AB) was 1.3-times higher than to inorganic As. In order to understand the mechanism underlying this observation, the atomization processes for both chemical species were investigated in terms of the enthalpy change (DeltaH) during the atomization process in GFAAS. The enthalpy change of AB was slightly lower than that of inorganic As, which suggested that AB was atomized more efficiently than was inorganic As. Moreover, it was observed that some co-existing organic materials enhanced the analytical sensitivity of inorganic As. The sensitivity difference between inorganic As and AB depended upon the mechanisms of their atomization processes. 相似文献
53.
Takayoshi Kimura Sekai Iwama Satoko Kido Mohammad Abdullah Khan 《The Journal of chemical thermodynamics》2009,41(10):1170-1177
Enthalpies of mixing and the densities of ethanol solution of R- and S-enantiomers of camphor, 10-camphorsulfonamide, 10-camphorsulfonic acid, camphorquinone, and 10-camphorsulfonyl chloride have been measured for a wide range of mole fractions of heterochiral components at 298.15 K. Enthalpies of mixing were exothermic for all concentrations and heterochiral solutions were more stable than each of the homochiral solutions. Enthalpic stabilization of mixing of heterochiral solutions was increased with a decreasing concentration of all the camphor derivatives measured. The sequence of enthalpic stabilization on mixing was 10-camphorsulfonyl chloride, 10-camphorsulfonic acid, 10-camphorsulfonamide, camphor, and camphorquinone. Apparent molar volumes were determined and excess volumes of mixing of heterochiral solutions were small and negative. Enthalpic stabilizations were found to be dependent on dipole–dipole interaction between solutes and solvents. 相似文献
54.
Enthalpies of mixing of ethanol solution of R- and S-enantiomers of limonene in large concentration have been measured at 298.15 K. The enthalpies of mixing were negligibly small
for all concentrations. Enthalpies of mixing showed negative in less than 30 mol%, but positive in more than the high concentration
of limonenes. The heterochiral solutions were more stable than each of the homochiral solutions in dilute solutions. The concentration
dependence on enthalpies of mixing in dilute concentration of less than 10 mol% was much sharper in inclination than the dense
solutions limonene. 相似文献
55.
Hongli Liu Tomoko Yamashita Tadashi Kamiyama Masao Fujisawa Takayoshi Kimura 《Journal of Thermal Analysis and Calorimetry》2010,99(1):95-103
The excess molar enthalpies of 8 binary mixtures for the o-, m-, and p-isomers of fluoroiodobenzene, fluoromethoxybenzene, bromofluorobenzene, chlorofluoro-benzene, difluorobenzene, fluoromethylbenzene,
fluoronitrobenzene, and aminofluoro-benzene were measured at 298.15 K. The changes of the measured enthalpies were very small.
The experimental results revealed that the isomers containing two electron-acceptor groups showed the most positive excess
enthalpy change, while isomers containing both one electron donor and one electron acceptor group, such as aminofluorobenzene,
showed more stable and always the most negative results. 相似文献
56.
Tomohiro Narukawa Takayoshi Kuroiwa Izumi Narushima Yasujiro Jimbo Toshihiro Suzuki Koichi Chiba 《Analytical and bioanalytical chemistry》2010,397(2):493-499
Arsenate [As(V)] solution reference material, National Metrology Institute of Japan (NMIJ) certified reference material (CRM)
7912-a, for speciation of arsenic species was developed and certified by NMIJ, the National Institute of Advanced Industrial
Science and Technology. High-purity As2O3 reagent powder was dissolved in 0.8 M HNO3 solution and As(III) was oxidized to As(V) with HNO3 to prepare 100 mg kg-1 of As(V) candidate CRM solution. The solution was bottled in 400 bottles (50 mL each). The concentration of As(V) was determined
by four independent analytical techniques—inductively coupled plasma mass spectrometry, inductively coupled plasma optical
emission spectrometry, graphite furnace atomic absorption spectrometry, and liquid chromatography inductively coupled plasma
mass spectrometry—according to As(V) calibration solutions, which were prepared from the arsenic standard of the Japan Calibration
Service system and whose species was guaranteed to be As(V) by NMIJ. The uncertainties of all the measurements and preparation
procedures were evaluated. The certified value of As(V) in the CRM is (99.53 ± 1.67) mg kg-1 (k = 2). 相似文献
57.
Cai HL Zhang W Ge JZ Zhang Y Awaga K Nakamura T Xiong RG 《Physical review letters》2011,107(14):147601
A new organic ferroelectric compound, 4-(cyanomethyl)anilinium perchlorate, proceeds a second-order phase transition from a paraelectric phase (P2(1)/m) to a ferroelectric phase (P2(1)) at 184 K. A perfect ferroelectric hysteresis loop was observed even at 10 KHz. It is the first example of a molecule-based organic ferroelectric whose polarization can be switched at such a high frequency. The temperature dependent second harmonic generation effect shows that the second-order nonlinear coefficient is nearly zero above T(c) and proportional to the spontaneous polarization below T(c), suggesting the occurrence of symmetry breaking, in good agreement with crystal structural determination. The origin of ferroelectricity was ascribed to the displacements of -NH(3)(+) cations and ClO(4)(-) anions from the symmetric positions including a small part of the order-disorder behaviors of the ClO(4)(-) anions. 相似文献
58.
The visible second harmonic of the idler output from a noncollinear optical parametric amplifier was compressed using adaptive dispersion control with a deformable mirror. The amplifier was pumped by and seeded in the signal path by a common 400 nm second-harmonic pulse from a Ti:sapphire regenerative amplifier. Thus, both the idler output and the second harmonic of the idler were passively carrier-envelope phase stabilized. The shortest pulse duration achieved was below 3 fs. 相似文献
59.
Synthesis and healing properties of poly(arylether sulfone)–poly(alkylthioether) multiblock copolymers containing disulfide bonds 下载免费PDF全文
Takayoshi Akiyama Akira Ushio Yoshitaka Itoh Yuya Kawaguchi Kazuya Matsumoto Mitsutoshi Jikei 《Journal of polymer science. Part A, Polymer chemistry》2017,55(21):3545-3553
Thermoplastic elastomers composed of soft and hard segments are important elastic and processable synthetic polymers. The microphase‐separated soft domains show low glass transition temperature and possess sufficient chain mobility at room temperature. In this study, we report the synthesis and healing properties of multiblock copolymers containing disulfide bonds as dynamic covalent bonds. The multiblock copolymers composed of poly(arylether sulfone) and poly(alkylthioether) segments were synthesized by oxidative coupling polymerization of the corresponding thiol‐terminated oligomers. Atomic force microscopy phase images, differential scanning calorimetry, and dynamic mechanical analysis curves indicated the microphase‐separated morphology of the multiblock copolymer. Self‐healing properties of the polymer were evaluated by changes in the elongation at break of the cut/adhered samples. The elongation recovery increased with UV irradiation time, and the multiblock copolymer showed a 93% recovery after UV irradiation for 5 h. The healing efficiency induced by UV irradiation, determined by subtracting the recovery without UV irradiation, was calculated to be 51%. According to the UV spectra and solubility changes after UV irradiation, the main healing factor in this study was the crosslinking reactions caused by thiyl radicals generated from UV irradiation instead of disulfide exchange reactions. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3545–3553 相似文献
60.
To apply the latex agglutination lectin assay (LALA) to carbohydrate ligands, monosaccharide derivatives were incorporated onto latex beads by various methods, and the usefulness of the resulting beads was evaluated. The best outcome, which resulted in aggregation with lectin concentrations of 1 to 4 μg/mL, was obtained when latex beads coated with bovine serum albumin were treated with divinylsulfone, a linker agent, and then with 2-aminoethyl glycosides. Monosaccharides with an amino or anomeric hydroxyl group other than N-acetylglucosamine were applicable in this direct LALA. For example, mannose- and 5-thiomannose-coupled latex beads showed aggregation with minimum concanavalin (ConA) concentrations of 4 and 32 μg/mL, respectively. An inhibition assay was more versatile than the direct LALA, and the standardized inhibition activity (EC0 50) was determined for several compounds. Representative EC0 50 data for mannose, methyl mannoside, and p-nitrophenyl mannoside (1, 0.12, and 0.06 mM, respectively) are consistent with those reported with other methods. We obtained EC0 50 values for some synthetic compounds with slightly different binding abilities to ConA, demonstrating a semiquantitative character of this method. The inhibition LALA can be performed without instrumentation or tedious derivatization and is thus suitable for the rapid evaluation of monovalent ligands prior to assemblage into multivalent ligands. 相似文献