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991.
Fang J Shan XQ Wen B Lin JM Lu XC Liu XD Owens G 《Langmuir : the ACS journal of surfaces and colloids》2008,24(19):10929-10935
The sorption and desorption of phenanthrene by three engineered nanoparticles including nanosize zerovalent iron (NZVI), copper (NZVC), and silicon dioxide (NSiO2) were investigated. The sorption of phenanthrene onto NSiO2 was linear and reversible due to the hydrophilic properties of NSiO2. In comparison, sorption of phenanthrene onto NZVI and NZVC was nonlinear and irreversible, which was potentially due to the existence of significantly heterogeneous surface energy distribution patterns detected by a standard molecular probe technique. Naphthalene exerted significant competitive sorption with phenanthrene for NZVI and NZVC, and the isotherm of phenanthrene changed from being significantly nonlinear to nearly linear when naphthalene was simultaneously absorbed. A surface adsorption mechanism was proposed to explain the observed sorption and competition of phenanthrene on both NZVI and NZVC. In contrast, no competition was observed for sorption onto NSiO2. The sorption of phenanthrene on all three nanoparticles significantly decreased with increasing pH. The sorption irreversibility of phenanthrene on NZVI and NZVC were significantly enhanced with decreasing pH. A pH-dependent hydrophobic effect and dipole interactions between the charged surface (electron acceptors) and phenanthrene with electron-rich pi systems (electron donors) were proposed to explain the observed pH-dependent sorption. 相似文献
992.
One- and two-photon circular dichroism spectra of R-(+)-3-methyl-cyclopentanone, a system that has been the subject of recent experimental studies of (2+1) resonance-enhanced multiphoton ionization circular dichroism, have been calculated with an origin-invariant density functional theory approximation in the region of the lowest electronic excited states, both for the gas phase and for a selection of solvents. A polarizable continuum model is used in the calculations performed on the solvated system. Two low-lying conformers are analyzed, and a comparison of the intensities and characteristic features is made with the corresponding two-photon absorption for each species, also for the Boltzmann-averaged spectra. The effect of the choice of geometry, basis set, and exchange-correlation functional is carefully analyzed. It is found that a density functional theory approach using the Coulomb attenuating method variant of Becke's three-parameter exchange and the Lee-Yang-Parr correlation functionals with correlation-consistent basis sets of double-zeta quality can reproduce the experimental electronic circular dichroism spectra very well. The features appearing in experiment are characterized in terms of molecular excitations, and the differences in the response of each state in the one- and two-photon processes are highlighted. 相似文献
993.
Separation of crystal violet dyes and its application to pen ink analysis using CZE and MEKC methods
A crystal violet (CV) standard was irradiated under a Hg-Cd lamp for different exposure times to obtain various N-demethylation products. CZE effectively separated the photodegradation products based on molecular weight differences. In contrast, micellar EKC (MEKC), using SDS as the surfactant, was ineffective because the binding constants of the demethylation products and SDS were too close for separation. Nevertheless, MEKC analysis of ink has applications in forensic science because MEKC separated neutral components in the inks. Thus, MEKC can be used to obtain an ink "fingerprint" since each ink is unique depending on the location and time it was made. In contrast, CZE is useful for dating inks because CV is the primary ink dye and it photodegrades slowly. 相似文献
994.
Certain characteristic fragmentations of tryptamines (indoleethylamine) and phenethylamines are described. Based on the GC-EI/MS, LC-ESI/MS and MALDI/TOFMS, the mass fragmentations of 13 standard compounds, including alpha-methyltryptamine (AMT), N,N-dimethyltryptamine (DMT), 5-methoxy-alpha-methyltryptamine (5-MeO-AMT), N,N-diethyltryptamine (DET), N,N-dipropyltryptamine (DPT), N,N-dibutyltryptamine (DBT), N,N-diisopropyltryptamine (DIPT), 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT), 5-methoxy-N,N-diisopropyltryptamine (5-MeO-DIPT), methamphetamine (MAMP), 3,4-methylenedioxyamphetamine (3,4-MDA), 3,4-methylenedioxymethamphetamine (3,4-MDMA) and 2-methylamino-1-(3,4-methylenedioxyphenyl)butane (MBDB), were compared. As a result, the parent ions of these analytes were hard to be obtained by GC/MS whereas the protonated molecular ions can be observed clearly by means of ESI/MS and MALDI/TOFMS. Furthermore, two major characteristic fragmentations, namely and alpha-cleavage ([M+H](+)-->[3-vinylindole](+)) and beta-cleavage ([M+H](+)-->[CH(2)N(+)R(N1)R(N2)]), are produced when the ESI and MALDI modes are used, respectively. In the case of ESI/MS, the fragment obtained from alpha-cleavage is the major process. In contrast to this, in the case of MALDI/TOFMS, the major fragment is produced via beta-cleavage. The ionization efficiency and fragments formed from either alpha- or beta-cleavages are closely related to the degree of alkylation of the side chain nitrogen in both cases. 相似文献
995.
分别对Al2O3和SiO2担载的不同含量铱(Ir)催化剂进行了H2程序升温还原、CO微量吸附量热和红外研究.结果表明,还原后,Ir/Al2O3上存在金属态Ir0和氧化态Irδ 两种物种,CO在催化剂表面主要以线式和孪生吸附态存在,测量的CO吸附热为两种吸附形式的平均吸附热.提高还原温度和Ir担载量,Ir/Al2O3表面CO线式吸附物种的比例增加,从而导致CO吸附热值的升高.而在Ir/SiO2上Ir物种主要为金属态Ir0,CO吸附都以线式吸附为主,在所考察的条件下CO吸附热随Ir担载量和还原温度的变化不明显。 相似文献
996.
多溴联苯醚代谢物的色谱保留和质谱特征 总被引:1,自引:0,他引:1
研究了多溴联苯醚(PBDEs)代谢物中常见的18种羟基PBDEs(HO-BDEs)、15种甲氧基PBDEs(MeO-BDEs)的气相色谱、反相液相色谱分离和质谱碎片特征。MeO-BDEs在反相液相色谱(RPLC)的保留行为受疏水作用支配,而HO-BDEs则还受到除疏水作用以外的特殊作用影响。LC/MS中大气压化学电离(APCI)源适用于HO-BDEs检测,而APCI源以及电喷雾离子源(ESI)对MeO-BDEs都没有响应。质谱碎片具有显著取代位效应:在LC/APCI-MS中,邻位取代HO-BDEs的碎片离子基峰均为脱一个溴的结构[M-H]--HBr,而对位取代的基峰则为准分子离子[M-H]-;在电子电离(EI)源质谱仪下,邻位取代MeO-BDEs有脱溴甲烷碎片离子(M. -BrCH3),对位取代有特征的脱甲基自由基结构(M. -.CH3),间位取代则无上述两种碎片离子。 相似文献
997.
The importance of anharmonic effect in dissociation of molecular systems especially clusters has been noted. In this paper, we shall study the effect of coupled anharmonic oscillator of the standard bilinear form (SBF) Morse oscillator (MO) potential on unimolecular reaction. We shall use the systematic theoretical approach, YL method, proposed by Yao and Lin (YAO L, et. al. J Phys Chem A, 2007, 111(29): 6722-6729), which can evaluate anharmonic effects on the rate constants based on the transition state theory. In treating the anharmonic effect with the Morse oscillator potential on unimolecular reactions under collision-free conditions by using the RRKM (Rice-Ramsperger-Kassel-Marcus) theory, the in-verse Laplace transformation of the partition functions was used to obtain the total amount of state and density of state by using the first-order and the second-order approximations of the saddle-point method. To demonstrate the anharmonic effect of the SBF Morse model, we choose some model systems and a real reaction as examples. 相似文献
998.
Yong Hong Wang Ting Fang Tian Xing Qin Liu Guang Yao Meng 《Journal of membrane science》2006,280(1-2):261-269
The high-quality tubular titania MF membranes are successfully prepared by dip-coating techniques and systematically investigated with regard to their corrosive resistances. The experiments show that dispersants PAA and anatase powder were preferably employed to prepare desired suspensions with solid loading 10–15 wt.% and that suspensions properties significantly affect the final membranes quality. The titania MF membranes with pure water permeability 742.42 l m−2 h−1 bar−1 and 0.1 μm pore diameter have been obtained using the prepared suspensions. The corrosion resistance of titania membranes exhibits that the anatase layers are more stable than the alumina supports in boiling corrosive medium and that the poor quality titania MF membranes become more deteriorated due to its top layer pore blockages and fouling layer formation, which provides a wide range of practical application fields in very hash environments with reliable data supports. 相似文献
999.
The effect of pH on the dilution enthalpies of D-p-hydroxyphenylglycine in phosphate buffer solutions has been investigated by isothermal titration microcalorimetry at 298.15 K. The corresponding homogeneous enthalpic interaction coefficients have been calculated according to the excess enthalpy concept. The results show that the enthalpies of dilution of D-p-hydroxyphenylglycine in phosphate buffer solutions at different pH are all positive. The overall trend is that enthalpies of dilution become more positive with an increase of pH, but there is a minimum of the enthalpy of dilution at pH = 7.0. The enthalpic pair interaction coefficients, h
2, all have negative values. The results are interpreted from the point of view of solute-solute and solute-solvent interactions involved in the solvent effects. 相似文献
1000.
Matrix-enhanced surface-assisted laser desorption ionization mass spectrometry imaging (ME-SALDI MSI) has been previously
demonstrated as a viable approach to improving MS imaging sensitivity. We describe here the employment of ionic matrices to
replace conventional MALDI matrices as the coating layer with the aims of reducing analyte redistribution during sample preparation
and improving matrix vacuum stability during imaging. In this study, CHCA/ANI (α-cyano-4-hydroxycinnamic acid/aniline) was
deposited atop tissue samples through sublimation to eliminate redistribution of analytes of interest on the tissue surface.
The resulting film was visually homogeneous under an optical microscope. Excellent vacuum stability of the ionic matrix was
quantitatively compared with the conventional matrix. The subsequently improved ionization efficiency of the analytes over
traditional MALDI was demonstrated. The benefits of using the ionic matrix in MS imaging were apparent in the analysis of
garlic tissue sections in the ME-SALDI MSI mode. 相似文献