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71.
WANG Shufang GUO Tianying TAO Jian ZHENG Chenggang ZHANG Banghua SONG Cunjiang 《反应性高分子(英文版)》2005,14(1):1-7
Blends of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHHx) and poly(butylene succinate-adipate) (PBSA), both biodegradable semicrystalline polyesters, were prepared with the ratio of PHBHHx/PBSA ranging from 80/20 to 20/80 by melt mixing method. Differential scanning calorimetry (DSC), thermogravimetry analysis (TGA), dynamic mechanical thermal analysis (DMA), polarizing optical microscopy (POM) and wide angle X-ray diffractometer (WAXD) were used to study the miscibility and crystallization behavior of PHBHHx/PBSA blends. Experimental results indicate that PHBHHx is immiscible with PBSA as shown by the almost unchanged glass transition temperature and the biphasic melt. 相似文献
72.
K3 [Fe(CN)6] and KFe[Fe(CN)6] are classical coordination compounds. However, the mechanism of decomposition reactions has not been well expounded. The gas products of thermal decomposition were examined by gas chroma tography (GC) , and the structure of the solid products by Mossbauer spectroscopy(MS) and X-ray diffraction(XRD). The findings are explained in terms of the theory of coordination chemistry and a decomposition mechanism is proposed in this study. On the basis of various experimental results, the first stage of the decomposition of K3[Fe(CN)6] in He was found to be the evolution of(CN)2 resulting in the reduction of Fe(Ⅲ)12K3 [Fe(CN)6]→9K4[Fe(CN)6] + Fe2 [Fe(CN)6] + 6 ( CN )For KFe [Fe(CN) 6 ], the first stage of decomposition man be represented as6KFe[Fe(CN)6]→3K2Fe[Fe(CN)6] + 2Fe2[Fe(CN)6 + 3(CN)2At higher temperatures, the decomposition of both K3[Fe(CN)6) andKFe[Fe(CN)6] to form KCN and Fe2C was accomplished by the release of(CN)2 and N2. 相似文献
73.
固相热分解反应最可几机制的判断 总被引:1,自引:0,他引:1
固相热分解反应最可几机制的判断高永煜,邹文樵,冯仰婕(华东理工大学化学系上海200237)关键词热分解,动力学方程,反应机制固相热分解反应机制的判断,是热分析动力学中令人感兴趣的领域。常用的方法是从含机制函数的非等温积分动力学方程出发,分别用Sest... 相似文献
74.
Danuta Wrbel Andrzej Boguta 《Journal of photochemistry and photobiology. A, Chemistry》2002,150(1-3):67-76
In this paper we describe conversion of light energy into electric energy in a photoelectrochemical cell containing zinc phthalocyanine (ZnPc) dyes. For all dyes investigated in liquid polyvinyl alcohol with dimethyl sulfoxide solution and located in the photoelectrochemical cell the following measurements have been done: absorption, fluorescence, photoacoustic spectra, photovoltaic spectra, kinetics of photocurrent and current–voltage characteristics. It has been shown that all dyes located in the photoelectrochemical cell are able to convert light into electric energy but with different effectiveness. The influence of substituted different peripheral groups to ZnPc core and the correlation between the molecular structure and effectiveness of solar to electric energy conversion were observed and described. The unique behavior of ZnPc substituted with fluorines was indicated. 相似文献
75.
The thermal behaviour of [Ba(C2H6O2)4][Sn(C2H4O2)3] used as a BaSnO3 precursor, and its phase evolution during thermal decomposition are described. The initially formed transient barium tin oxycarbonate phase disintegrates into BaCO3 and SnO2, reacting subsequently to BaSnO3. The existence of the intermediate oxycarbonate phase is evidenced by Fourier transformed infrared (FT-IR), X-ray powder diffraction (XRD) and electron energy loss spectroscopy (EELS (ELNES)) investigations. 相似文献
76.
J. Borrs R. Carballo A. Castieiras M. C. Gmez‐Conde M. C. Fernndez‐Vidal J. Nicls 《无机化学与普通化学杂志》2005,631(11):2221-2226
Four new dinuclear copper(II) complexes have been synthesized and have the general formula [Cu2(L)(H2O)2], where L = GLYDTO [N,N′‐bis(carboxymethyl)dithiooxamide], ALADTO [N,N′‐bis(carboxyethyl)dithiooxamide], VALDTO [N,N′‐bis(1‐carboxy‐2‐methylpropyl)dithiooxamide] and LEUDTO [N,N′‐bis(1‐carboxy‐3‐methylbutyl)dithiooxamide]. The complexes were characterized by elemental analysis as well as by IR, electronic and EPR spectroscopy. These techniques provided evidence for the presence of the CuNO2S chromophore. Magnetic susceptibility measurements on all the complexes in the range 4–300 K show the existence of a dominant antiferromagnetic interaction with ?J values greater than 300 cm?1. Thermal decomposition behaviour of the complexes was studied by thermogravimetry. 相似文献
77.
Photovoltaic and spectral properties of tetraphenyloporphyrin and metallotetraphenyloporphyrin dyes 总被引:1,自引:0,他引:1
Spectroscopical properties and photocurrent (or photovoltage) of tetraphenyloporphyrins and metallotetraphenyloporphyrins in nematic liquid crystal have been studied. Photoelectric response has been measured in an electrochemical cell made of the semitransparent semiconducting and golden electrodes with porphyrin dyes embedded in liquid crystal. Fluorescence, time-resolved luminescence in microsecond time scale and photoacoustic spectra have also been measured. The competition between radiative, non-radiative processes and charge transfer is discussed. It has been shown that effectivity of porphyrins for photocurrent generation depends on the presence/absence of central metal in the macrocycle of porphyrin skeleton and the kind of metal. The schematic model of the contributions of the dye molecule and semiconducting electrode in the electron transfer process is shown. 相似文献
78.
Yong Zhong DU Fu Qiang HU Hong YUAN Shinzo OMI 《中国化学快报》2006,17(4):553-556
Stable poly(styrene-co-sodium styrene sulfonate) (P(St-NaSS) nanoparticles with broader size distribution were synthesized by thermal emulsion polymerization without any conventional initiators and emulsifiers. The obtained polymer nanoparticles have higher ξ potential, and the particle sizes have broad distribution. The stability of polymer particles originated from the addition of small amounts of ionic comonomer, NaSS, which can act as an emulsifier in somewhat. The monomer conversion could reach up to about 28 wt% in 48 h, and did not increase by further polymerization when higher polymerization temperature (120 ℃) was employed. This polymerization system may be give some further understand for mechanism of emulsion polymerization. 相似文献
79.
Enzo Giannetti 《Journal of fluorine chemistry》2005,126(4):623-630
Intrinsic bond dissociation energies (BDEs) of selected fluorinated polymers are critically evaluated. Two distinctive approaches were followed. In the first one, according to Wu and Rodgers [E.-C. Wu, A.S. Rodgers, J. Am. Chem. Soc. 98 (1976) 6112-6115], starting from the gas-phase enthalpy of polymerization we obtained the polymer backbone BDE through appropriate thermodynamic cycles. Revised experimental results indicate that the CC BDEs of all the polymers taken into account fall within a limited energy interval, comparable to the average experimental uncertainty. Central to the second methodology adopted, is a model compound approach. Thanks to the large number of reliable thermodynamic data available in the scientific literature and to simple end-capping rules, C2 molecules were chosen as suitable models for infinite linear polymers and alternating copolymers between ethylene and fluorinated olefins. For partially fluorinated polymers, like polyvinylidene fluoride (PVDF), alternating ethylene-tertrafluoroethylene (ETFE) and alternating ethylene-chlorotrifluoroethylene (ECTFE), the weight loss due to HF and HCl evolution during heating experiments was successfully related to the threshold energy Eo(HX) for 1,2-elimination from chemically activated hydrofluoro and hydrofluorochlorocarbons according to the modified Rice-Rampsberger-Kassel (RRKM) unimolecular theory. 相似文献
80.
Matthias Weil 《Journal of solid state chemistry》2003,172(1):35-44
Mercury(I) selenite(IV) is polymorphic and crystallizes at least in three modifications, named α-, β-and γ-Hg2SeO3. Polycrystalline β-Hg2SeO3 was prepared by precipitation of a concentrated mercurous nitrate solution with selenous acid. Hydrothermal treatment of the colorless β-Hg2SeO3 powder in demineralized water at 250°C (10 days) yields light-yellow single crystals of α-Hg2SeO3 which show the highest density of the three modifications. Colorless needle-shaped single crystals of β-Hg2SeO3 and very few single crystals of γ-Hg2SeO3 co-crystallize from strongly diluted Hg2(NO3)2 and H2SeO3 solutions and were grown by a diffusion technique. All crystal structures were solved and refined from single crystal diffractometer data sets and are based on Hg22+ dumbbells and trigonal pyramidal SeO32− anions as the main building units. A common structural feature of all modifications is the formation of open channels extending parallel to the shortest crystallographic axis. The non-bonding orbitals of the SeIV atoms are stereochemically active and protrude into the channels. Upon heating in an open system under N2 atmosphere, both α- and β-Hg2SeO3 decompose in a well-separated three-step mechanism. The first step (T > 250°C) involves disproportionation into elementary mercury and α-HgSeO3 which at ca. 400°C subsequently transforms into β-HgSeO3. The second step between T = 400 and 500°C is accompanied by a loss of Hg and SeO2 and the formation of the basic salt Hg3SeO6. In the third step, at temperatures between T = 500° and 600°C, this material decomposes completely. Upon heating in a closed system (sealed silica capillaries), β-Hg2SeO3 transforms between 320-340°C into the more dense α-Hg2SeO3 which on further heating likewise converts into elementary mercury and β-HgSeO3. 相似文献