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21.
近红外(NIR)光谱技术可用于表征氯仿体系中反胶团增溶水的能力. 对于C12-s-C12•2Br (s=2, 3, 4, 5, 6, 8)系列, 不论体系是否含有NaBr电解质, 由于具有较短联接链的表面活性剂易形成较大的反胶团, 其增溶水的能力随着联接链长度增加而降低. 与未含NaBr电解质的体系相比, 当体系中存在NaBr电解质时所形成的反胶团增溶水能力降低. 相似文献
22.
《Arabian Journal of Chemistry》2020,13(12):8848-8887
Phthalocyanine (Pc) complexes are an important class of dyes with numerous (e.g., biological, photophysical, and analytical) applications. Among the methods used to improve the properties of these complexes, one should mention the introduction of different substituents, variation of the central metal ion, ligand exchange, and conjugation to nanomaterials (e.g., carbon-based nanomaterials and metal nanoparticles (NPs)). This work briefly reviews Pc complex conjugation to Ag and Au NPs, highlights the different NP shapes, and discusses the diversity of conjugation approaches. Moreover, the use of UV–Vis spectroscopy, powder X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, atomic force microscopy, dynamic light scattering and Fourier transform infrared spectroscopy to characterize Pc-NP hybrids is summarized. The effect of conjugation on Pc photo-physicochemical properties (fluorescence, singlet oxygen generation, triplet state formation, and optical limiting behavior) is discussed, and future perspectives for the synthesis and applications of new hybrids are provided. 相似文献
23.
Kristin fischer Stefan Spange Steffen Fischer Cornelia Bellmann Jörg Adams 《Cellulose (London, England)》2002,9(1):31-40
The surface polarity of native celluloses has been investigated by the following solvatochromic dyes: dicyano-bis (1,10)-phenanthroline iron (II) Fe(phen)2 (CN)2 (1), bis(4-N,N-dimethylamino)-benzophenone (2), and cou-marine 153 (3). Linear Solvation Energy (LSE) relationships and the UV/Vis data have been used to characterize the surface polarity of different native cellulose batches in terms of the empirical Kamlet–Taft polarity parameters (hydrogen bond acidity), (hydrogen bond basicity), and * (dipolarity/polarizability). , , *and calculated Reichardt's E T (30) values are reported for various native and regenerated cellulose samples with different degrees of crystallinity. The degree of crystallinity of the cellulose samples has been determined by X-ray. The microcrystalline environment of cellulose can be exactly parameterized in terms of the , and *values. It shows a fairly strong acidity and a low dipolarity/polarizability. For the amorphous sections smaller and larger * values are observed. The correspondence of the empirical polarity parameters determined has been discussed in relation to results from pyrene fluorescence and zetapotential measurements. 相似文献
24.
在氢氧化钡和氢氧化锶水溶液/Triton X-100/环己烷/正己醇四元W/O型反相微乳液中制备了钛酸锶钡纳米棒, 研究了ω0值(水与表面活性剂Triton X-100的物质的量之比)、反应物浓度、陈化时间对产品形貌和尺寸的影响, 用TEM, SAED, SEM, EDS和XRD等技术对产品进行了表征. 结果表明, 所得Ba0.7Sr0.3TiO3纳米棒长约500~1200 nm、直径约为50~120 nm; 具有立方相单晶结构. 产品中钡、锶、钛的物质的量之比约为0.7∶0.3∶1. 相似文献
25.
Antonio Cipiciani Stefania Primieri Antonio Arcelli 《Journal of inclusion phenomena and macrocyclic chemistry》1994,15(3):207-214
The hydrolysis reaction of 2-nitro-4-carboxyphenyl acetate was studied in dichloromethane in the presence of an added electrolyte (NaOH) and cationic surfactants systems with varying quantities of added water at 25°C. The kinetic and conductivity data were correlated. 相似文献
26.
Autocatalytic oxidation of ferroin by bromate in water-in-oil reverse micelles of AOT has been studied experimentally and theoretically. The simplest models for this process have been constructed. Analytical solutions for these models were found for some limiting cases. It has been shown that the autocatalytic reaction runs much more slowly in reverse micelles than in water. The dependencies of the maximum reaction rate,
max, the exponent of the increase in ferriin concentration, , and induction period, , on micelle concentration have been obtained at =[H2O]/[AOT]=4.6. It was found that there is only one theoretical model which can explain the experimental data. The values of the elementary reaction rate constantsk
i
were estimated on the basis of the theoretical dependencies of
max and on the constantsk
i
. All elementary rate constants turned out to be two or three orders of magnitude smaller than the corresponding constants for the reaction proceeding in water. The decrease in the rate constants is explained by the increase in viscosity and pH in a micellar water core at low .Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1401–1407, August, 1993.This work was supported by the Russian Foundation for Fundamental Investigations through Research Grant 93-03-4090. 相似文献
27.
A relationship is derived to enable the comparison of the dispersion heights of normal and reverse flow injection analysis (FIA). A single channel flow system is employed in the absence of a chemical reaction. The stopped-flow injection method is used to probe the influence of molecular diffusion on the overall dispersion of normal and reverse FIA, which appeared to demonstrate fundamentally different diffusion behaviors. Small discrepancies are observed between the dispersion heights, which are enhanced by the stopped-flow period, especially when unmatched matrix ionic compositions of the indicator and counter solutions were involved. For these conditions, the diffusion flux rate is enhanced considerably, displaying a peak, in addition to the transient, for both methods. The influence of diffusion on the dispersion characteristics of normal and reverse FIA is discussed theoretically. Diffusion in the proposed model is postulated to oppose dispersion by convection. The latter initiates concentration gradients in the injection zone and propagates it with flow time over the dispersion zone profile. The diffusion flux then reacts in order to confine the indicator dispersion for normal FIA and to enhance it for reverse FIA. This model is consistent with the experimental results and accounts for most of the phenomena encountered. Probably owing to the influence of secondary flow phenomena, the use of coiled tubes has suppressed the effects of diffusion on the overall dispersion behavior.Part of the experimental work was performed at IMI Institute for Research and Development, Haifa, Israel. 相似文献
28.
Winghong Chan Suei Yee Lam-Leung Chingfai Ng Junqi Ding Shiping Xi 《Journal of polymer science. Part A, Polymer chemistry》1995,33(15):2525-2531
New diamino monomers IIa – IIg were synthesized in a two-step reaction sequence starting from p-acetamidobenzenesulfonyl chloride. Solution polymerization of these monomers in DMAC with terephthaloyl or isophthaloyl chloride resulted in the formation of a series of 14 poly(amide sulfonamide)s (PASAs) in excellent yield (> 95%). The polymers have in-trinsic viscosities of 0.32–1.11 dL g?1. Except for polymers IIIa ? p and IIId - p , all other PASAs were readily soluble in aprotic polar solvents including DMAC, DMF, and DMSO. Thermogravimetric analyses of the polymers showed moderate thermal stability with 10% weight loss being recorded in the range of 325–408°C. In addition, these polymers exhibit moderate chemical stabilities toward alkali, acidic, and chromic acid solution. © 1995 John Wiley & Sons, Inc. 相似文献
29.
30.
M. M. R. Talukder M. M. Zaman Y. Hayashi J. C. Wu T. Kawanishi 《Applied biochemistry and biotechnology》2007,141(1):77-83
The thermostability of Cromobacterium viscosum lip ase (EC 3.1.1.3) entrapped in AOT (sodium bis-[2-ethylhexyl] sulfosuccinate) reverse micelles was in creased by the addition
of short-chain polyethylene glycol (PEG 400). Two different approaches were considered: (1) the determination of half-life
time and (2) the mechanistic analysis of deactivation kinetics. The half-life of lipase entrapped in AOT/isooctane reverse
micelles with PEG 400 at 60°C was 28h, ninefold higher than that in reverse micelles without PEG 400. The lip ase entrapped
in both reverse micellar systems followed a series-type deactivation mechanism involving two first-order steps. The deactivation
constant for the first step at 60°C in PEG containing reverse micelles was 0.055 h11, 11-fold lower than that in reverse micelles without PEG, whereas it remained almost constant for the second step. The inactivation
energy of the lip ase entrapped in reverse micelles with and without PEG 400 was 88.12 and 21.97 kJ/mol, respectively. 相似文献