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41.
Semens of Astragali Complanati own anti-erectile dysfunction effect; however, the components which contribute to the anti-erectile dysfunction effect remain unclear. This work raised a strategy that integrates liquid chromatography coupled mass spectrometry-based quantitative analysis, anti-erectile dysfunction assessment on impotent rats, and their relationship analysis for pinpointing anti-erectile dysfunction components from semens of Astragali Complanati. For simultaneous quantification of seven major components in raw and salt-processed semens of Astragali Complanati, an accurate and reliable liquid chromatography–mass spectrometry method was developed under multiple reaction monitoring mode. Of note, chloramphenicol was employed as the internal standard. The method showed good linearity and repeatability, where the recovery rates of each component ranged from 98.1 to 104.7%, and the precisions of intra- and interday were all within 3.4%. The method has been used for quantification of the seven major components in 10 batches of raw and salt-processed semens of Astragali Complanati. Then, the anti-erectile dysfunction effects of raw and salt-processed semens of Astragali Complanati were evaluated on impotent rats. Gray relationship analysis and partial least squares regression were combined for elucidating the relationship. As a result, complanatuside, astragalin, complanatoside B, and kaempferol were found to be responsible for anti-erectile dysfunction effect of Astragali Complanati.  相似文献   
42.
Many plants have a high polyphenol content, which causes the matrix effect and makes the analysis of trace pesticide residues highly challenging. A common approach to improving matrix effects is to purify pesticides through the use of sorbents, but this requires a combination of multiple sorbents and extensive use. Zeolitic imidazolate framework-8 is widely used for pesticide analysis due to its high porosity, large specific surface area, and versatility. Here, we established and validated a modified quick, easy, cheap, effective, rugged, and safe method based on a zeolitic imidazolate framework-8 that was used to test the removal ability for polyphenols. To this end, 145 pesticide residues in peppermint, perilla, fennel, and mulberry leaves were analyzed by the modified method coupled with liquid chromatography with tandem mass spectrometry. The mean recoveries of all pesticide residues were in the range of 74.3–103.7%, with mean relative standard deviations ≤9.1% at spiked concentrations of 1, 10, 50, and 100 μg/kg for mulberry leaves. The limits of quantitation of the method ranged from 1 to 50 μg/kg. This study offers a reliable approach for the accurate quantitative analysis of various trace substances in the polyphenol-rich plants.  相似文献   
43.
Adsorptive separation of C2H6 from C2H4 by adsorbents is an energy-efficient and promising method to boost the polymer grades C2H4 production. However, that C2H6 and C2H4 display very similar physical properties, making their separation extremely challenging. In this work, by regulating the pore environment in a family of chitosan-based carbon materials (C-CTS-1, C-CTS-2, C-CTS-4, and C-CTS-6)- we target ultrahigh C2H6 uptake and C2H6/C2H4 separation, which exceeds most benchmark carbon materials. Explicitly, the C2H6 uptake of C-CTS-2 (166 cm3/g at 100 kPa and 298 K) has the second-highest adsorption capacity among all the porous materials. In addition, C-CTS-2 gives C2H6/C2H4 selectivity of 1.75 toward a 1:15 mixture of C2H6/C2H4. Notably, the adsorption enthalpies for C2H6 in C-CTS-2 are low (21.3 kJ/mol), which will facilitate regeneration in mild conditions. Furthermore, C2H6/C2H4 separation performance was confirmed by binary breakthrough experiments. Under different ethane/ethylene ratios, C-CTS-X extracts a low ethane concentration from an ethane/ethylene mixture and produces high-purity C2H4 in one step. Spectroscopic measurement and diffraction analysis provide critical insight into the adsorption/separation mechanism. The nitrogen functional groups on the surface play a vital role in improving C2H6/C2H4 selectivity, and the adsorption capacities depend on the pore size and micropore volume. Moreover, these robust porous materials exhibit outstanding stability (up to 800 °C) and can be easily prepared on a large scale (kg) at a low cost (~$26 per kg), which is very significant for potential industrial applications.  相似文献   
44.
Wu  Hong-Yu  Jiang  Li-Hong 《Nonlinear dynamics》2022,109(3):1993-2002
Nonlinear Dynamics - Vector similar structures for solutions with similar expressions of nonlinear models are paid attention in the previous literature. However, the demand of different localized...  相似文献   
45.
Xiang  Wang-Kai  Xie  Qing  Xu  Shan-Shan  Sun  Chen-Xuan  Yu  Cheng-Tao  Zheng  Ying  Pan  Peng-Ju 《高分子科学》2022,40(6):567-575

Stereocomplex (SC) crystallization has been an effective way to improve the physical performances of stereoregular polymers. However, the competition between homo and SC crystallizations can lead to more complicated crystallization kinetics and polymorphic crystalline structure in stereocomplexable polymers, which influences the physical properties of obtained materials. Herein, we select the medium-molecular-weight (MMW) poly(L-lactic acid)/poly(D-lactic acid) (PLLA/PDLA) asymmetric blends with different PDLA fractions (fD=0.01–0.5) as the model system and investigate the effects of fD and crystallization temperature (Tc) on the crystallization kinetics and polymorphic crystalline structure. We observe the fractionated (i.e., multistep) crystallization kinetics and the formation of peculiar β-form homocrystals (HCs) in the asymmetric blends under quiescent conditions, which are strongly influenced by both fD and Tc. Precisely, crystallization of β-form HCs is favorable in the MMW PLLA/PDLA blends with high fD (≥0.2) at a low Tc (80–100 °C). It is proposed that the formation of metastable β-form HCs is attributed to the conformational matching between β-form HCs and SCs, and the stronger constrain effects of precedingly-formed SCs in the early stage of crystallization. Such effects can also cause the multistep crystallization kinetics of MMW PLLA/PDLA asymmetric blends in the heating process.

  相似文献   
46.
Guo  Jiayun  Ma  Dongge  Sun  Fulin  Zhuang  Guilin  Wang  Qi  Al-Enizi  Abdullah M.  Nafady  Ayman  Ma  Shengqian 《中国科学:化学(英文版)》2022,65(9):1704-1709
Science China Chemistry - The heterojunction constructed of covalent organic frameworks (COFs) with adjustable structure and other photocatalysts has great potential in the field of photocatalysis....  相似文献   
47.
Zhang  X. L.  Hu  Y.  Gao  R. X.  Ge  S. X.  Zhang  D. X. 《Fluid Dynamics》2022,56(1):S34-S52

The microfluidic chip for nucleic acid detection in vitro is an essential application of microfluidic technology to the process of in vitro diagnosis. The 90° bend microchannels in chip designed for facilitating assay reagent delivery may cause reagent residues and cast mutual contamination between detection reagents, which significantly affects the detection accuracy. In this paper, a two-dimensional gas–liquid two-phase flow model is constructed to simulate the liquid residue phenomenon. Using the results of simulation, the residual liquid generation can be observed and the area of residual liquid can be obtained. The accuracy of the numerical simulation is verified by comparison with the experimental results. The effects of the fillet radius R, the diameter ratio d1/d2 of the vertical to horizontal sections, the flow velocity v, and the surface roughness Ra on the residual amount are studied. We find that the fillet radius is inversely proportional to the residual amount within the range v = 20–100 mm/s and there is almost no liquid residue in the channel when the radius increases to R = 1 mm. When the channel diameter ratio d1/d2 increases, the liquid residual amount also increases by approximately 98%. The increased surface roughness Ra significantly increases the residual amount. The results of this study provide a reference for the optimal design of microchannels on chips.

  相似文献   
48.
This paper presents a nonlinear thickness-shear vibration model for onedimensional infinite piezoelectric plate with flexoelectricity and geometric nonlinearity. The constitutive equations with flexoelectricity and governing equations are derived from the Gibbs energy density function and variational principle. The displacement adopted here is assumed to be antisymmetric through the thickness due to the thickness-shear vibration mode. Only the shear strain gradient through the thickness is considered in the present model. With geometric nonlinearity, the governing equations are converted into differential equations as the function of time by the Galerkin method. The method of multiple scales is employed to obtain the solution to the nonlinear governing equation with first order approximation. Numerical results show that the nonlinear thickness-shear vibration of piezoelectric plate is size dependent, and the flexoelectric effect has significant influence on the nonlinear thickness-shear vibration frequencies of micro-size thin plates. The geometric nonlinearity also affects the thickness-shear vibration frequencies greatly. The results show that flexoelectricity and geometric nonlinearity cannot be ignored in design of accurate high-frequency piezoelectric devices.  相似文献   
49.
Zinc-ion batteries(ZIBs), in particular quasi-solid-state ZIBs, occupy a crucial position in the field of energy storage devices owing to the superiorities of abundant zinc reserve, low cost, high safety and high theoretical capacity of zinc anode. However, as divalent Zn2+ions experience strong electrostatic interactions when intercalating into the cathode materials, which poses challenges to the structural stability and higher demand in Zn2+ions diffusion kinetics of the ...  相似文献   
50.
《中国化学快报》2022,33(8):3931-3935
Iron fluoride (FeF3) is considered as a promising cathode material for Li-ion batteries (LIBs) due to its high theoretical capacity (712 mAh/g) with a 3e? transfer. Herein, we have designed a strategy of hierarchical and mesoporous FeF3/rGO hybrids for LIBs, where the hollow FeF3 nanospheres are the main contributor to the specific capacity and the 2D rGO nanosheets are the matrix elevating the electronic conductivity and buffering the volume expansion. The unique FeF3/rGO hybrid can be rationally synthesized by a non-aqueous in-situ precipitation method, offering the merits of large specific surface area with rich active sites, fast transport channels for lithium ions, effective alleviation of volume expansion during cycles, and accelerating the electrochemical reaction kinetics. The FeF3/rGO hybrid electrode possesses a high initial discharge capacity of 553.9 mAh/g at a rate of 0.5 C with 378 mAh/g after 100 cycles, acceptable rate capability with 168 mAh/g at 2 C, and feasible high-temperature operation (320 mAh/g at 70 °C). The superior electrochemical behaviors presented here demonstrates that the FeF3/rGO hybrid is a potential electrode for LIBs, which may open up a new vision to design high-efficiency energy-storage devices such as LIBs based on transition metal fluorides.  相似文献   
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