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211.
便携式GC-MS在挥发性有机物应急监测中的应用 总被引:7,自引:0,他引:7
建立了便携式GC-MS测定空气中37种挥发性有机物(VOCs)的方法,采用便携式GC-MS配置的手持探头采集大气样品,然后用便携式GC-MS进行检测.该方法能快速、有效地对空气中的37种挥发性有机物进行定性和定量,具有相关性好(r>0.995)、检出限低(0.070×10-9 ~0.94×10-9 (体积分数))、精密度好(RSD小于7.7%)、准确度高(回收率为92% ~114%)的特点,适用于大气中挥发性有机污染物的应急监测. 相似文献
212.
213.
The effect of a ZnO#ZnS QDs heterojunction (O#SQDs) on the binding affinities of flavonoid glycosides for bovine serum albumin (BSA) was investigated. The fluorescence intensities of BSA decreased remarkably with increasing concentration of O#SQDs. The magnitudes of the binding constants of flavonoid glycosides for BSA in the presence of O#SQDs were in the range of 10(5)-10(7) L mol(-1), and the number of binding sites per BSA (n) was determined as 1.24 ± 0.17. O#SQDs increased the affinities of flavonoid glycosides for BSA by about 2.96% to 114.68% depending on their structures. O#SQDs in blood will enhance the transportation of flavonoid glycosidegs in blood and improve their pharmacology effects. From this point, O#SQDs are a perfect candidate for flavonoid glycosides delivery applications. 相似文献
214.
[reaction: see text] A series of new pyrrolidine derivatives were prepared directly in very good yields, from the substrates containing a basic or nucleophilic N atom via ring-closing enyne metathesis reaction under mild reaction conditions. Moreover, the reaction occurs smoothly without the presence of ethylene gas. 相似文献
215.
Yin P Wang J Xiao Z Wu P Wei Y Liu T 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(30):9174-9178
So emulsional: Two hexavanadate-organic hybrids were synthesized and their amphiphilic properties were confirmed by forming emulsions in mixtures of water and nonpolar organic solvents, and were utilized as "emulsion catalysts" in deep desulfurization reactions (see figure). Their catalytic activities show a pH-dependent behavior, which can be explained by the size-change of emulsions and the appearance of reverse emulsions. 相似文献
216.
This work demonstrates the process of building optoelectrically cooperative surface wetting in smart and precise way. The superhydrophobic photosensitive film is constructed with TiO(2) nanotube arrays. Compared with conventional organic dyes, CdS quantum dots (QDs) as sensitizer layer are modified on TiO(2) nanotubes surface to improve photosensitivity of the composited surface in visible light region, which offer the benefit for designing and fabricating solid state hetero-junction devices. ITO glass is introduced as top electrode to apply electrical and optical stimuli and the patterned wetting is instantly obtained with masking light through ITO. The optoelectrically cooperative wettability conversion occurred on superhydrophobic TiO(2) nanotube surface at critical voltage of 12 V, which was decreased by 18 V comparing with only using electric stimulus. This study provides potential applications for TiO(2) nanotube arrays to the associated research of liquid reprography, location-controlled microfluidic device and lab-on-chip. 相似文献
217.
Pei Y Pal R Liu C Gao Y Zhang Z Zeng XC 《Journal of the American Chemical Society》2012,134(6):3015-3024
Atomic structure of a recently synthesized ligand-covered cluster Au(24)(SR)(20) [J. Phys. Chem. Lett., 2010, 1, 1003] is resolved based on the developed classical force-field based divide-and-protect approach. The computed UV-vis absorption spectrum and powder X-ray diffraction (XRD) curve for the lowest-energy isomer are in good agreement with experimental measurements. Unique catenane-like staple motifs are predicted for the first time in core-stacked thiolate-group (RS-) covered gold nanoparticles (RS-AuNPs), suggesting the onset of structural transformation in RS-AuNPs at relatively low Au/SR ratio. Since the lowest-energy structure of Au(24)(SR)(20) entails interlocked Au(5)(SR)(4) and Au(7)(SR)(6) oligomers, it supports a recently proposed growth model of RS-AuNPs [J. Phys. Chem. Lett., 2011, 2, 990], that is, Au(n)(SR)(n-1) oligomers are formed during the initial growth of RS-AuNPs. By comparing the Au-core structure of Au(24)(SR)(20) with other structurally resolved RS-AuNPs, we conclude that the tetrahedral Au(4) motif is a prevalent structural unit for small-sized RS-AuNPs with relatively low Au/SR ratio. The structural prediction of Au(24)(SR)(20) offers additional insights into the structural evolution of thiolated gold clusters from homoleptic gold(I) thiolate to core-stacked RS-AuNPs. Specifically, with the increase of interfacial bond length of Au(core)-S in RS-AuNPs, increasingly larger "metallic" Au-core is formed, which results in smaller HOMO-LUMO (or optical) gap. Calculations of electronic structures and UV-vis absorption spectra of Au(24)(SR)(20) and larger RS-AuNPs (up to ~2 nm in size) show that the ligand layer can strongly affect optical absorption behavior of RS-AuNPs. 相似文献
218.
219.
Enhanced indirect fluorescence detection with in-column optical-fiber LED-induced fluorescence (LED-IF) detection has been developed for the simultaneous separation and determination of p-nitrophenol, 2,4-dinitrophenol and trinitrophenol. The instrumental set-up is simple, cost-effective and the detection method is stable. Different experimental parameters have been studied. The optimum conditions were determined as: running buffer (pH 9.1) composed of 10 mM borate, 80 mM sodium dodecylsulfate and 0.18 μM fluorescein (as a background reagent); applied voltage of 15 kV; working temperature of 25.0 °C. The limits of detection (S/N = 3) were 11, 18 and 16 μM for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol, respectively. The nitrophenols were completely separated in 13 min and the number of theoretical plates for p-nitrophenol, 2,4-dinitrophenol and trinitrophenol were 8.1 × 10(6), 6.5 × 10(6) and 8.4 × 10(6), respectively. The RSDs (n = 6) for the migration time and the peak area were better than 0.85 and 0.91%, respectively. Our proposed method possesses the advantages of rapidness and good separation efficiency. 相似文献
220.
A series of iron(III) complexes ligated by 2-(benzimidazole)-6-(1-aryliminoethyl)pyridines was synthesized and examined by 1H NMR, ESI-MS, IR spectroscopic, elemental analysis and X-ray photoelectron spectroscopy (XPS). Activated with methylaluminoxane (MAO), all ferric complexes exhibited good activities (up to 5.38 × 106 g mol−1(Fe) h−1) of ethylene oligomerization and polymerization, and resultant oligomers and polyethylene waxes showed high α-olefin feature, meanwhile the distribution of oligomers mostly resembled Schulz-Flory rules. The various reaction parameters were investigated in detail, and the less bulky and electron-withdrawing substituents of ligands could enhance the catalytic activities of their ferric complexes. The observations explain the cause for unstable activities performed by stored iron(II) complexes. 相似文献