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81.
The applicability of pulsed field gradient nuclear magnetic resonance spectroscopy to nanocapsule systems is demonstrated on dispersed poly-n-butylcyanoacrylate nanocapsules as a model system. Spectroscopic data are presented that allow for the structural characterization of the inner cavities, the observation of Brownian motion of the capsules and the detection of rapid molecular exchange through the capsule walls. An analytical formula is proposed that yields equilibrium populations and average residence times of a given tracer molecule, thus leading to crucial information regarding the permeability of the capsule walls. Based on these analytical methods, two varieties of nanocapsules are compared that derive from two different preparation procedures. It is found that thinner capsule walls obtained under acidic conditions of the organic phase during interfacial polymerization lead to correspondingly higher exchange rates of benzene as a tracer molecule. 相似文献
82.
《European Polymer Journal》2002,38(7):1343-1347
In this study, hydrogels of poly(N-isopropylacrylamide-co-acrylamide) having a thermoresponsive character were prepared by a redox polymerization method. NIPAM-co-AAm hydrogels with different thermoresponsive properties were obtained by changing the initial NIPAM/AAm mole ratio and crosslinker concentration.Equilibrium-swelling ratio, dynamic swelling ratio and dynamic deswelling ratio were evaluated for all hydrogel systems. The fast shrinking was observed with all gels. The time required for equilibrium shrinking increased with the increase of acrylamide content in the gel. 相似文献
83.
84.
A kind of inorganic‐organic hybrid 18‐molybdodiphosphate nanoparticles ([(C4H9)4N]6P2Mo18Q62·4H2O) was firstly used as a bulk‐modifier to fabricate a three‐dimensional chemically modified carbon paste electrode (CPE) by direct mixing. The electrochemical behavior of the solid nanoparticles dispersed in the CPE in acidic aqueous solution was characterized by cyclic and square‐wave voltammetry. The hybrid 18‐molybdodiphosphate nanoparticles bulk‐modified CPE (MNP‐CPE) displayed a high electrocatalytic activity towards the reduction of nitrite, bromate and hydrogen peroxide. The remarkable advantages of the MNP‐CPE over the traditional polyoxometalates‐modified electrodes are their excellent reproducibility of surface‐renewal and high stability owing to the insolubility of the hybrid 18‐molybdodiphosphate nanoparticles. 相似文献
85.
Shigeru Matsuo Tomoyoshi Murakami Ryuichi Takasawa 《Journal of polymer science. Part A, Polymer chemistry》1993,31(13):3439-3446
Crystalline poly(arylene ether nitrile) could be prepared by the polycondensation of 2,6-dihalobenzonitrile with resorcinol at 200°C in N-methylpyrrolidone in the presence of sodium carbonate. A reaction temperature of at least 200°C was necessary to attain high molecular weight polymer. Spectral data indicated that the polymer had the structure of a poly(meta-phenylene ether) with pendent nitrile groups on every other phenylene unit. Despite this structure, the crystallinity and the crystallization rate of the polymer were greater than those of the corresponding polymer with a para-linked structure. The glass transition temperature and the melting temperature of the polymer were almost the same as those of poly(etheretherketone) (PEEKTM). A series of other new poly(arylene ether nitriles) were also examined. The polymers derived from 4,4′-biphenol, dihydroxytetra-phenylmethane, dihydroxydiphenylsulfone, and 1,5-isoquinolinediol had high glass transition temperatures. The poly(arylene ether nitriles) exhibited excellent tensile strength compared with the corresponding ketone- or sulfone-containing polymers. Comparing the three different kinds of polymers containing the same bisphenol units, the order of glass transition temperature was found to be sulfone- > nitrile- > ketone-containing polymers, while the order of tensile strength was nitrile- > ketone- > sulfone-containing polymers. The excellent mechanical properties are attributable to dipole-dipole interactions of nitrile groups. © 1993 John Wiley & Sons, Inc. 相似文献
86.
Crespi M. S. Silva A. R. Ribeiro C. A. Oliveira S. C. Santiago-Silva M. R. 《Journal of Thermal Analysis and Calorimetry》2003,72(3):1049-1056
The thermal behavior and non-isothermal kinetics of thermal decomposition of three different kinds of composting of the USR
like: stack with drilled PVC tubes (ST), revolved stack (SR) and stack with material of structure (SM), from the usine of
composing of Araraquara city, Săo Paulo state, Brazil, within a period of 132 days of composting were studied. Results from
TG, DTG and DSC curves obtained on inert atmosphere indicated that the cellulosic fraction present, despite the slow degradation
during the composting process, is thermally less stable than other substances originated from that process. Due to that behavior,
the cellulosic fraction decomposition could be kinetically evaluated through non-isothermal methods of analysis. The values
obtained were: average activation energy, Ea=248, 257 and 259 kJ mol-1 and pre- exponential factor, logA=21.4, 22.5, 22.7 min-1, to the ST, SR and SM, respectively. From Ea and logA values and DSC curves, Málek procedure could be applied, suggesting that the SB (Šesták-Berggren) kinetic model is the appropriated
one to the first thermal decomposition step.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
87.
It is well known that porphyrin derivatives play a key role in the primary process of photo-synthesis[1], in which porphyrins directly absorb the sunlight or indirectly acquire excitation en-ergy from light-harvesting antenna system to reach their excited state, and then donate electrons to quinone acceptors to yield a series of charge-separated species. In general, only first singlet ex-cited state of porphyrins is involved in energy transfer process[2]. However, highly excited state (S2 stat… 相似文献
88.
SynthesesandStudiesofPEG┐b┐PNIPABlockPolymersCAOWei-xiao**andZHANGTao(ColegeofChemistryandMolecularEnginering,PekingUniversit... 相似文献
89.
The influences of Triton X-100 on hemoglobin (Hb) behaviors were studied by the methods of UV-Vis spectrum, fluorescence spectrum, HPLC, conductivity, zeta potential and negative-staining transmission electron microscope in Hb/acyclovir/Triton X-100/H2O system. With the increase of Triton X-100 concentration in the system, the percentage of the free acyclovir increased from 58%--63% to 90%--94%. The static quenching constant and the association number of acyclovir to Hb decreased. The fluorescence spectrum, conductivity, zeta potential, fluorescence polarization and negative-staining morphology of Hb tended to recover to those of the original state of Hb in the same concentration of Hb. The interaction between Triton X-100 and Hb is stronger than that between acyclovir and Hb. Most Triton-X-100 was associated with Hb at low Triton X-100 concentration. But the interaction of Triton X-100 with Hb was apparently dominant in high Triton X-100 concentration. The Hb structure was unfolded and finally denatured. 相似文献
90.
酞侧基聚芳醚酮的热学性能谢红卫,李滨耀(中国科学院长春应用化学研究所长春130022)关键词酞侧基聚芳醚酮,pvT行为,导热系数,定压比热容酞侧基聚芳醚酮(PEK-C)具有较高的玻璃化转变温度,其流变加工性能和力学性能已被广泛研究[1~3],被证明是... 相似文献