A novel method was developed and validated for determination of benzene, toluene, p-xylene, m-xylene, o-xylene (BTEX) in a solid–liquid mixing matrix. It makes use of solid phase extraction and thermal desorption (SPE-TD), followed by gas chromatographic flame ionization detector analysis (GC-FID). The trapped BTEX can be measured directly after thermal desorption onto the stainless-steel packed chromatographic column. The effect of tailing area of solvent was removed with the use of SPE-TD technique, and the result shows good reproducibility with very little matrix dependency. The study also supports that the lifetime of the Tenax adsorption tube could be extended over 150 desorption operation at 200 °C, which enables performing excellent stability and reproducibility of BTEX analysis.
The counter-intuitive behaviors of pin-ended beams under the projectile impact are investigated with ANSYS/LS-DYNA in this paper. It studies in detail their displacement-time history curves, final deformed shapes, energy relationships and projectile impact velocity ranges related to their counter-intuitive behaviors. The influences of the impact positions on their counterintuitive behaviors are also discussed. The results show that no matter where the impact position on the beam is, the counter-intuitive behaviors of pinned beams will occur as long as the impacting velocity lies within a proper range. Corresponding to the occurring of the counter-intuitive behaviors, the rebounding number in the displacement history curves of the beams decreases from a few times to zero with an increase of the impact velocity. The final deformation modes of the beam corresponding to the counter-intuitive behaviors will appear in symmetrical and unsym-metrical forms no matter where the impact position is; the impact velocity of the first-occurring of the counter-intuitive behaviors of the beam increases slowly with the deviation of the impact position away from the mid-span. 相似文献
Time‐resolved pump–probe gas‐phase X‐ray scattering signals, extrapolated to zero momentum transfer, provide a measure of the number of electrons in a system, an effect that arises from the coherent addition of elastic scattering from the electrons. This allows to identify reactive transients and determine the chemical reaction kinetics without the need for extensive scattering simulations or complicated inversion of scattering data. We examine the photodissociation reaction of trimethylamine and identify two reaction paths upon excitation to the 3p state at 200 nm: a fast dissociation path out of the 3p state to the dimethyl amine radical (16.6±1.2 %) and a slower dissociation via internal conversion to the 3s state (83.4±1.2 %). The time constants for the two reactions are 640±130 fs and 74±6 ps, respectively. Additionally, it is found that the transient dimethyl amine radical has a N?C bond length of 1.45±0.02 Å and a C?N?C bond angle of 118°±4°. 相似文献
Nanostructured materials are attractive to researchers because of their unique optical, magnetic, thermodynamic, electrical, mechanical, and chemical properties. Controlling the morphology of nanomaterials could provide structural systems for a wide range of technologies. As a result, the development of nanofabrication techniques that are convenient and offer design flexibility is the subject of many studies. In order to progress beyond the conventional morphologies, we have turned to hydrogels, which can serve as organic templates for nanoscale objects with continuous microstructures. Transmission electron microscopy showed that the obtained nanonetwork had a continuous microstructure, which was several microns in length and width, with a cross-sectional diameter of 5–10 nm synthesized from a 35-g hexamethylenetetramine solution and a 1.5 g Zn(NO3)2 solution, and the cross-sectional diameter can be adjusted from 5 to 200 nm by controlling the concentration of the Zn(NO3)2 solution. Our results also showed that the nanostructures based on a superabsorbent polymer template could be controlled easily in terms of size and morphology by changing the concentration of the reaction solution. This protocol could be easily extended to synthesize a variety of nanostructured materials with novel morphologies. 相似文献
Recently, microfluidic techniques have been widely applied for biomaterial droplet manipulations due to their precision and efficiency. Many biosamples such as deoxyribonucleic acid and blood samples are non-Newtonian fluids with complex rheology, which brings challenges in control over them. The electric field is characterized by fast response and excellent adaptation to control microscale fluid flow. Here, we systematically investigate the alternating current electric field–assisted formation of non-Newtonian droplet in a flow-focusing microchannel with different sizes of channel orifice. The dependencies of flow conditions, microchannel geometries and electric parameters on the dynamics of non-Newtonian droplet formation are thus elucidated. An effective capacitance electric model is developed to reveal and predict the interaction between the fluid flow and the electric field. Furthermore, the flow field of non-Newtonian droplet formation is captured via the high-speed microparticle image velocimetry system. The characteristics of the regimes of droplet formation and the influences of the channel orifice are revealed quantitatively. Our work offers elaborate references to the control of non-Newtonian droplet formation, which benefits a wide range of applications in biology and chemistry. 相似文献
In this study, we designed a methacrylate molecule with an alkyl-substituted trichloro salicylic acid pendant as a transformable bulky monomer to enable the synthesis of an alternating copolymer of methyl methacrylate (MMA) and n-butyl acrylate (nBA). The adamantyl-substituted methacrylate monomer ( 1-Ad ) showed very low homopolymerization propensity in radical polymerizations, but afforded the alternating copolymer with nBA via copolymerization. The 1-Ad units in the resultant copolymer were quantitatively and selectively transformed into MMA via transesterification with methanol to yield the alternating copolymer of MMA and nBA. Its alternating sequence was clearly demonstrated by a structural analysis via 13C NMR spectroscopy as well as the low reactivity ratios for the 1-Ad and nBA pair. Finally, we verified the superior self-healing ability of the alternating copolymer compared to that of the corresponding 1 : 1 statistical copolymer. 相似文献