An Interfacial Layer Based on Polymers of Intrinsic Microporosity to Suppress Dendrite Growth on Li Metal Anodes

The performance and safety of lithium (Li) metal batteries can be compromised owing to the formation of Li dendrites. Here, the use of a polymer of intrinsic microporosity (PIM) is reported as a feasible and robust interfacial layer that inhibits dendrite growth. The PIM demonstrates excellent film-forming ability, electrochemical stability, strong adhesion to a copper metal electrode, and outstanding mechanical flexibility so that it relieves the stress of structural changes produced by reversible lithiation. Importantly, the porous structure of the PIM, which guides Li flux to obtain uniform deposition, and its strong mechanical strength combine to suppress dendrite growth. Hence, the electrochemical performance of the anode is significantly enhanced, promising excellent performance and extended cycle lifetime for Li metal batteries.     

Generalized invexity of nonsmooth functions

In this paper, the concepts of weak invexity and weak quasi invexity are introduced and the relations among several kinds of generalized invexity are studied for nonsmooth functions by means of the properties of limiting subdifferentials. In addition, the relations between generalized invexity of a nonsmooth function and generalized invariant monotonicity of its limiting subdifferential mapping are researched. Our results here are an extension and generalization of those presented by M. Soleimani-damaneh.     

Analyses of gibberellins by capillary electrophoresis-mass spectrometry combined with solid-phase extraction

A new, simple and rapid capillary electrophoresis-mass spectrometry (CE-MS) method, using a cationic polymer-coated capillary to reverse electroosmotic flow, is proposed and validated for the separation and simultaneous quantification of 11 gibberellins (GAs). Under optimum conditions, a baseline separation of 11 GAs, including GA1, GA3, GA4, GA5, GA6, GA7, GA13, GA19, GA20, GA24 and GA53 was accomplished within 25 min using 70 mM ammonium formate/formic acid buffer (pH 3.8) and 2% (v/v) acetonitrile with -25 kV as the separation voltage. Satisfactory results were obtained in terms of linearity (R2 between 0.984 and 0.995), precision (RSD of migration time below 0.8%) and sensitivity (LOD between 0.31 and 1.02 microM). Furthermore, a novel solid-phase extraction (SPE) procedure was developed for the pre-concentration and purification of GAs using Oasis MAX cartridges. The combination of SPE and CE-MS approach was applied to screen for endogenous GAs present in coconut (Cocos nucifera L.) water sample. To illustrate the applicability of the method, GA1 and GA3 were successfully detected and quantified in coconut water. Finally, the GA1 and GA3 identities were further unequivocally confirmed by CE-tandem MS experiments operating in the multiple reaction monitoring mode.     

Natural radioactivity of geothermal water in Beijing,China

In this work, we collected 101 geothermal water samples to investigate comprehensively the radioactivity of geothermal water in Beijing. The concentrations of gross beta, ²²⁶Ra and ²²²Rn were measured and the obtained values were in the range of 0.032–7.060, 0.023–0.363 and 0.470–29.700 Bq/L, respectively. The samples with higher concentration of ²²²Rn were found to be located near large faults. The effective dose of ²²²Rn in the air for three cases were calculated to be greater than radiation dose limit of 1 mSv/a.     

稀土离子(Ho,Er,Yb)与八肋游仆游虫中心蛋白N端半分子作用的光谱研究

在0.01 mol·L-1Hepes,0.15 mol·L-1Na Cl,p H 7.4及室温条件下,采用紫外差光谱和荧光光谱的方法研究了稀土离子Ho(III),Er(III),Yb(III)与八肋游仆虫中心蛋白N端半分子(N-terminal domain of Euplotes octocarinatus centrin,N-Eo Cen)的结合性质。结果表明:稀土离子Ho(III),Er(III),Yb(III)与N-Eo Cen结合导致蛋白质高级结构发生明显变化,疏水区暴露增加。二甲酚橙为竞争配体测得稀土离子Ho(III),Er(III),Yb(III)与N-Eo Cen两个位点的结合能力分别为:lg KI,Ho(III)=5.47±0.37,lg KII,Ho(III)=5.07±0.45;lg KI,Er(III)=5.78±0.42,lg KII,Er(III)=5.36±0.52;lg KI,Yb(III)=5.80±0.65,lg KII,Yb(III)=5.37±0.61。     

控制图法对底排药剂组分结果的探讨

针对烟火剂型底排药剂组分分析结果与生产投料配比存在较大的差异,使用均值-极差(X)-R控制图法对结果数据进行统计分析,判定结果所处状态.结合药剂特性及生产工艺、取样情况、分析方法实际状况,对统计分析结果展开讨论,查找均值失控的原因,采取工艺控制、方法改进等措施,从而利用分析数据实现有效的质量控制,确保产品质量满足要求.     

Synthesis of CdTe Quantum Dots with Tunable Photoluminescence Using Tellurium Dioxide as Tellurium Source

A simple and convenient method has been developed for synthesis of water‐soluble CdTe quantum dots (QDs) under ambient atmospheric conditions. In contrast to the traditional aqueous synthesis, green to red emitting CdTe QDs were prepared by using TeO₂ to replace Te or Al₂Te₃ as tellurium source in this method. The influences of experimental variables, including pH value, 3‐mercaptopropionic acid (MPA)/Cd and Te/Cd molar ratios, on the emission peak and photoluminescence (PL) quantum yield (QY) of the obtained CdTe QDs have been systematically investigated. Experimental results indicate that green to red emitting CdTe QDs with a maximum photoluminescence quantum yield of 35.4% can be prepared at pH 11.3 and n_(Cd):n_(Te):n_(MPA)=1:0.1:1.7.     

Enantioseparation of Three β-Agonists Using Di-n-butyl d-Tartrate-Boric Acid Complex as Chiral Selector by Means of MEEKC

In this study, a self-prepared complex chiral selector, di-n-butyl d-tartrate-boric acid complex, by the reaction of di-n-butyl d-tartrate with boric acid in a running buffer was used as a chiral selector for the enantioseparation of three β-agonists including clenbuterol, cycloclenbuterol and tulobuterol by means of microemulsion electrokinetic chromatography (MEEKC). Three β-agonists were successfully enantioseparated using the chiral system, indicating that the di-n-butyl d-tartrate-boric acid complex was a useful chiral selector. The effects of di-n-butyl d-tartrate and sodium tetraborate concentration, surfactant concentration, cosurfactant, phosphate, buffer pH and composition, as well as applied voltage were extensively investigated to achieve a good enantioseparation. The di-n-butyl d-tartrate and sodium tetraborate concentration in the running buffer had great influence on the chiral resolution (R _s). Three β-agonists which could not be separated with only di-n-butyl d-tartrate, obtained good chiral separation using the complex chiral selector; among them, two pairs including clenbuterol and cycloclenbuterol could be baseline resolved in 7 min under optimized experimental conditions of 0.8% (w/v) di-n-butyl d-tartrate, 40 mM sodium tetraborate, 3.0% (w/v) Tween-20 and 60 mM sodium dihydrogen phosphate with 25 kV as running voltage. The results indicated that the method could be used for the enantioseparation of three β-agonists.

     

Preparation and in vitro evaluation of an ultrasound-triggered drug delivery system: 10-hydroxycamptothecin loaded PLA microbubbles

10-Hydroxycamptothecin (HCPT) loaded PLA microbubbles, used as an ultrasound-triggered drug delivery system, were fabricated by a double emulsion-solvent evaporation method. The obtained microbubbles were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and confocal laser scanning microscope (CLSM). In addition, the effect of diagnostic ultrasound exposure on BEL-7402 cells combined with HCPT-loaded PLA microbubbles was evaluated using cytotoxicity assay, CLSM and flow cytometry (FCM). It was found that the HCPT-loaded PLA microbubbles showed smooth surface and spherical shape, and the drug was amorphously dispersed within the shell and the drug loading content reached up to 1.69%. Nearly 20% of HCPT was released upon exposure to diagnostic ultrasound at frequency of 3.5 MHz for 10 min. Moreover, HCPT fluorescence in the cells treated only with the HCPT-loaded PLA microbubbles was discernible, but less intense, while those treated with the microbubbles in conjunction with ultrasound exposure was evident and intense, indicating an increased cellular uptake of HCPT by ultrasound exposure. Cytotoxicity test on BEL-7402 cells indicated that the HCPT-loaded PLA microbubbles combined with ultrasound exposure were more cytotoxic than the microbubbles alone. The results suggest that the combination of drug loaded PLA microbubbles and diagnostic ultrasound exposure exhibit an effective intracellular drug uptake by tumor cells, indicating their great potential for antitumor therapy.