双相钢板料的单向拉伸断裂失效研究(Ⅱ)——弧长法非线性有限元分析

为了获得docol800DP双相钢板料的等效塑性应变和应力三轴度在单向拉伸断裂失效过程中的变化历程,对其拉伸过程进行了弧长法非线性有限元分析。根据试验得到的材料参数建立了双相钢单向拉伸试件的有限元模型,考虑大变形引起的几何非线性和塑性强化引起的材料非线性,模拟了试件拉伸变形的全过程。计算结果表明:弧长法可较好地模拟试件变形的全程,计算得到的典型变形阶段、集中性失稳带的分布及方向与试验结果吻合很好;发生失稳变形时的应变与理论分析结果一致。最后,给出了起裂点处失效参数的变化历程,为定量化研究双相钢材料的断裂失效模型提供准确的数据支持。     

Study on clarithromycin lactobionate based dual selector systems for the enantioseparation of basic drugs in capillary electrophoresis

In this paper, the use of clarithromycin lactobionate, a kind of antibiotic chiral selector, in combination with four neutral cyclodextrin derivatives (glucose‐β‐cyclodextrin, hydroxyethyl‐β‐cyclodextrin, methyl‐β‐cyclodextrin and hydroxypropyl‐β‐cyclodextrin) was reported for the first time. As a result, these dual systems gave much better resolution of nefopam (the Rs increased to 3.58, 2.72, 1.49 and 1.42, respectively) compared to the single systems. The effects of buffer pH and selector concentration on the separation of nefopam were also investigated. Additionally, some other basic drugs including metoprolol, atenolol, propranolol, bisoprolol, esmolol and ritodrine were tested for the investigation and evaluation of the enantiorecognition capability of the four dual systems. As expected, the synergistic effect was observed in four systems. Different results of these dual systems were also summarized.     

Paper-Based Ratiometric Fluorescence Analytical Devices towards Point-of-Care Testing of Human Serum Albumin

Monitoring of human serum albumin (HSA) in a point-of-care fashion is urgently needed in particular for elderly or chronically ill patients. Herein, a dual-state emissive chalcone probe having the feature of aggregation-induced emission was designed and synthesized. The concentration of HSA can be evaluated by the ratios of emission from probes in aggregated and monomeric state, which gives a visually discernible red-to-green color change. A simple, portable paper-based analytical device have been fabricated by integration of the recognition probe in the detection pad and employed for HSA test using the whole blood samples. This paper-based assay shows the analytical capability comparable to the standard testing methods but is in a point-of-care fashion, providing a promising tool for at-home HSA detection and HSA-related disease diagnosis.     

Real-time HD Exchange Kinetics of Proteins from Buffered Aqueous Solution with Electrothermal Supercharging and Top-Down Tandem Mass Spectrometry

Electrothermal supercharging (ETS) with electrospray ionization produces highly charged protein ions from buffered aqueous solutions in which proteins have native folded structures. ETS increases the charge of ribonuclease A by 34%, whereas only a 6% increase in charge occurs for a reduced-alkylated form of this protein, which is unfolded and its structure is ~66% random coil in this solution. These results indicate that protein denaturation that occurs in the ESI droplets is the primary mechanism for ETS. ETS does not affect the extent of solution-phase hydrogen-deuterium exchange (HDX) that occurs for four proteins that have significantly different structures in solution, consistent with a droplet lifetime that is considerably shorter than observable rates of HDX. Rate constants for HDX of ubiquitin are obtained with a spatial resolution of ~1.3 residues with ETS and electron transfer dissociation of the 10+ charge-state using a single capillary containing a few μL of protein solution in which HDX continuously occurs. HDX protection at individual residues with ETS HDX is similar to that with reagent supercharging HDX and with solution-phase NMR, indicating that the high spray potentials required to induce ETS do not lead to HD scrambling.

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Twisted Diindeno-Fused Dibenzo[a,h]anthracene Derivatives and their Dianions

We report a facile synthesis of diindeno-fused dibenzo[a,h]anthracene derivatives ( DIDBA-2Cl , DIDBA-2Ph , and DIDBA-2H) with different degrees of non-planarity using three substituents (chloro, phenyl, and hydrogen) of various sizes. The planarization of their cores, as evidenced by the decreased end-to-end torsional angles, was confirmed by X-ray crystallography. Their enhanced energy gaps with twisting were investigated by a combination of spectroscopic and electrochemical methods with density functional theory, which showed a transition from singlet open-shell to closed-shell configuration. Moreover, their doubly reduced states, DIDBA-2Ph ²⁻ and DIDBA-2H ²⁻, were achieved by chemical reduction. The structures of dianions were identified by X-ray crystallographic analysis, which elucidated that the electron charging further distorted the backbones. The electronic structure of the dianions was demonstrated by experimental and theoretical approaches, suggesting decreased energy gaps with larger non-planarity, different from the neutral species.     

Supramolecular core-shell nanosilica@liposome nanocapsules for drug delivery

The fabrication of core-shell structural nanosilica@liposome nanocapsules as a drug delivery vehicle is reported. SiO(2) nanoparticles are encapsulated within liposomes by a W/O/W emulsion approach to form supramolecular assemblies with a core of colloidal particles enveloped by a lipid bilayer shell. A nanosilica core provides charge compensation and architectural support for the lipid bilayer, which significantly improves their physical stability. A preliminary application of these core-shell nanocapsules for hemoglobin (Hb) delivery is described. Through the H-bonding interaction between the hydroxyl groups on nanosilicas and the amino nitrogens of Hb, Hb-SiO(2) nanocomplexes in which the saturated adsorption amount of Hb on SiO(2) is 0.47 g g(-1) are coated with lipids to generate core-shell Hb-SiO(2)@liposome nanocapsules with mean diameters of 60-500 nm and Hb encapsulation efficiency of 48.4-87.9%. Hb-SiO(2)@liposome supramolecular nanovehicles create a mode of delivery that stabilizes the encapsulated Hb and achieves long-lasting release, thereby improving the efficacy of the drug. Compared with liposome-encapsulated Hb and Hb-loaded SiO(2) particles, such core-shell nanovehicles show substantially enhanced release performance of Hb in vitro. This finding opens up a new window of liposome-based formulations as drug delivery nanovehicles for widespread pharmaceutical applications.     

A high efficient sorption of U(VI) from aqueous solution using amino-functionalized SBA-15

Uranium is one of the most hazardous heavy metal due to its long half-life radioactivity, high toxicity and mobility as aqueous uranyl ion (UO₂ ²⁺) under ordinary environmental conditions. Herein, amino functionalized SBA-15 (APSS) was developed as a rapid and efficient sorbent for removal of U(VI) from the environment. The APSS sample was synthesized by grafting method and was characterized by SEM, NMR, SAXS, and N₂ sorption/desorption isothermal experiments. The sorption of U(VI) by APSS was investigated under different conditions of pH, contact time, initial U(VI) concentration, ionic strength and solid–liquid ratio. The results show that the sorption of U(VI) by APSS is strongly dependent on pH but independent of ionic strength and solid–liquid ratios (m/V). The sorption is ultrafast with an equilibrium time of less than 30 min, and the sorption capacity is as large as 409 mg/g at pH 5.3 ± 0.1. Besides, the U(VI) sorption by APSS from extremely diluted solution and the desorption of U(VI) from APSS were also studied. It is found that 100 mg of APSS can almost completely remove the U(VI) ions from 4 L aqueous solution with the U(VI) concentration as low as 4.2 ppb and the sorbed U(VI) can be completely desorbed by 0.1 mol/L nitric acid. The results strongly reveal the high performance of the APSS material in the removal and preconcentration of U(VI) from the aqueous solution.     

N-甲酰基哌啶的制备

A modified formylation method of piperidine catalyzed by sulfuric acid is described. The reaction conditions and separation method of the products were presented.     

Studies on the Syntheses of the Side Chains of Brassinolide and Dolicholide

(4R,5S)-2,2-Dimethyl-4-(1',2'-dimethylpropyl)-5-(1'-bromoethyl)--1,3-dioxolane(15) with the side chain of brassinolide and (4R, 5S)--2, 2-dimethyl-4-(l'-methylene-2'-methylpropyl)-5-(1'-bromoethyl) 1,3-dioxolane(14) with the side chain of dolicholide were first synthesized through 11 and 10 stepes from D-mannitol respectively. All of the intermediates 7-13 were first synthesized too.     

Studies on the electrochemical behavior of cytochrome c and its interaction with DNA at a Co/GC ion implantation modified electrode

The electrochemical behavior of cytochrome c (cyt c) and its interaction with DNA at a Co/glassy carbon (GC) ion implantation modified electrode were studied by linear sweep and cyclic voltammetry. In 0.005 mol dm(-3) Tris-0.05 mol dm(-3) NaCl buffer solution (pH = 7.10), a sensitive reduction derivative peak of cyt c was obtained by linear sweep voltammetry. The peak potential was 0.032 V (SCE). The peak current was proportional to the concentration of cyt c. The electrode process was quasi-reversible with adsorption. The electrode reaction rate constant k and the electron transfer coefficient a of cyt c were 4.42 s(-1) and 0.47, respectively. AES and XPS experiments showed that Co was implanted into the surface of the GC electrode (GCE). The implanted Co formed Co-C, which catalyzed the reduction of cyt c. The reaction of DNA with cyt c led to an electrochemically active complex, which resulted in an increase in the reduction current of cyt c. After adding DNA into the solution containing cyt c, the electrode process was still quasi-reversible with adsorption.