日立835与8800氨基酸分析仪的应用与比较

L 8 8 0 0的Thr -Ser、Gly -Ala、Ile -Leu分离度较 835有很大的提高 ,最低检测浓度为 3pmolAsp ,而 835则为 30pmolAsp ,分析时间也较 835缩短 ,成本大大降低而效率大为提高。比较日立 835 - 5 0型与L - 880 0型氨基酸分析仪在分析中的实际应用情况 ,对这两种机型的应用做个总结 ,使二者得到更合理、充分的利用。     

Ultrasmall Pd‐Cu‐Pt Trimetallic Twin Icosahedrons Boost the Electrocatalytic Performance of Glycerol Oxidation at the Operating Temperature of Fuel Cells

Recently, in order to improve the energy conversion efficiency of direct polyol fuel cells, the engineering of effective Pd‐ and/or Pt‐based electrocatalysts to rupture C? C bonds has received increasing attention. Here, an example is shown to synthesize highly uniform sub‐10 nm Pd‐Cu‐Pt twin icosahedrons by controlling the nucleation phase. Because of the synergies of the electronic effect, synergistic effect, geometric effect, and abundant surface active sites originating from the formation of near surface alloy and special icosahedral shape, the Pd‐Cu‐Pt twin icosahedrons exhibit excellent electrocatalytic performance in glycerol electrocatalysis at the operating temperature of direct alcohol fuel cells (70 °C) in KOH electrolyte. The Pd_50.2Cu_38.4Pt_11.4 icosahedrons show mass activities of 9.7 A mg^?1_Pd+Pt and 13.7 A mg^?1_Pd. Furthermore, the Pd_50.2Cu_38.4Pt_11.4 icosahedrons demonstrate long‐term durability in current–time test for 36 000 s and high in situ anti‐CO poisoning performance. In addition, the introduction of CO can enhance electro‐oxidation endurance on Pd_50.2Cu_38.4Pt_11.4 icosahedrons, and the peak mass activity can reach to 14.4 A mg^?1_Pd+Pt. The in situ Fourier transform infrared spectroscopy spectra indicate that the Pd_50.2Cu_38.4Pt_11.4 icosahedrons possess a high capacity to break C? C bonds and may efficiently convert glycerol into CO₂, thus improving the utilization efficiency of energy‐containing molecule glycerol.     

Adaptive Fuzzy Control for Teleoperation System with Uncertain Kinematics and Dynamics

International Journal of Control, Automation and Systems - In this paper, we address the problem of adaptive tracking control for a teleoperation system with uncertainties in both kinematics and...     

Phase‐Controlled Synthesis of Monolayer W1−xRexS2 Alloy with Improved Photoresponse Performance

Tuning bandgap and phases in the ternary 2D transition metal dichalcogenides (TMDs) alloys has opened up unexpected opportunities to engineer optoelectronic properties and explore potential applications. In this work, a salt‐assisted chemical deposition vapor (CVD) growth strategy is reported for the creation of high‐quality monolayer W_1?xRe_xS₂ alloys to fulfill a readily phase control from 1H to DT by changing the ratio of Re and W precursors. The structures and chemical compositions of doping alloys are confirmed by combining atomic resolution scanning transmission electron microscopy‐annular dark field imaging with energy dispersive X‐ray spectroscopy (EDS) and X‐ray photoelectron spectroscopy, matching well with the calculated results. The field‐effect transistors (FETs) devices fabricated based on 1H‐W_0.9Re_0.1S₂ monolayer exhibit a n‐type semiconducting behavior with the mobility of 0.4 cm² V^?1 s^?1. More importantly, the FETs show high‐performance responsivity with a value of 17 µA W^?1 in air, which is superior to that of monolayer CVD‐grown WS₂. This work paves the way toward synthesizing monolayer ternary alloys with controlled phases for potential optoelectronic applications.     

Mechanical(compressive)form of driving force triggers the phase transformation from βto ω&α"phases in metastable β phase-field Ti-5553 alloy

Most of the structural alloys'applications are under static,dynamic,and cyclic forms of loading.Ti-5553 alloy in the beta phase field is being investigated to confirm the mechanism of deformation and phase transformation upon quasi-static and dynamic compression.The Ti-5553 alloy was heat-treated at 900 C(almost 50℃above beta transus temperature)for one hour of soaking time followed by air quenching to achieve a fully β phase field.After that,Dynamic compression(DC)by Split Hopkinson Pressure Bar(SHPB)and Quasi-static compression(QSC)were performed at a strain rate of～103/s and 10-3/s,respectively.Recovered specimens were thoroughly examined by using different tools,such as an Optical microscope(OM),Scanning electron microscope(SEM),High-resolution transmission electron microscope(HRTEM),and Electron backscatter diffraction(EBSD)to get the reliable data for justification of logical conclusions.It is found that the dominating mode of deformation was dislocation slip along with twinning({332}〈113〉)to some extent in both of QSC and DC,but sliding&spalling of the grain boundary is observed more in the former.Stress-induced phase transformation,i.e.,β to α"and 3 toω,took place in the grains saturated with dislocation slips,where the former transformation occurred simultaneously with{332}〈113〉twinning,while β to ω transformation was completed when a set of two adjacent(110)β planes covered±1/6th of the total separation distance between two(next to each other)(111)β planes,by equal but opposite shear in(111)β direction,and it caused 3％shrinkage of two closed packed(110)β planes after transformation.     

Few‐Layer GeAs Field‐Effect Transistors and Infrared Photodetectors

The family of 2D semiconductors (2DSCs) has grown rapidly since the first isolation of graphene. The emergence of each 2DSC material brings considerable excitement for its unique electrical, optical, and mechanical properties, which are often highly distinct from their 3D counterparts. To date, studies of 2DSC are majorly focused on group IV (e.g., graphene, silicene), group V (e.g., phosphorene), or group VIB compounds (transition metal dichalcogenides, TMD), and have inspired considerable effort in searching for novel 2DSCs. Here, the first electrical characterization of group IV–V compounds is presented by investigating few‐layer GeAs field‐effect transistors. With back‐gate device geometry, p‐type behaviors are observed at room temperature. Importantly, the hole carrier mobility is found to approach 100 cm² V^?1 s^?1 with ON–OFF ratio over 10⁵, comparable well with state‐of‐the‐art TMD devices. With the unique crystal structure the few‐layer GeAs show highly anisotropic optical and electronic properties (anisotropic mobility ratio of 4.8). Furthermore, GeAs based transistor shows prominent and rapid photoresponse to 1.6 µm radiation with a photoresponsivity of 6 A W^?1 and a rise and fall time of ≈3 ms. This study of group IV–V 2DSC materials greatly expands the 2D family, and can enable new opportunities in functional electronics and optoelectronics based on 2DSCs.     

A Versatile Nonviral Delivery System for Multiplex Gene-Editing in the Liver

Recent advances in CRISPR present attractive genome-editing toolsets for therapeutic strategies at the genetic level. Here, a liposome-coated mesoporous silica nanoparticle (lipoMSN) is reported as an effective CRISPR delivery system for multiplex gene-editing in the liver. The MSN provides efficient loading of Cas9 plasmid as well as Cas9 protein/guide RNA ribonucleoprotein complex (RNP), while liposome-coating offers improved serum stability and enhanced cell uptake. Hypothesizing that loss-of-function mutation in the lipid-metabolism-related genes pcsk9, apoc3, and angptl3 would improve cardiovascular health by lowering blood cholesterol and triglycerides, the lipoMSN is used to deliver a combination of RNPs targeting these genes. When targeting a single gene, the lipoMSN achieved a 54% gene-editing efficiency, besting the state-of-art Lipofectamine CRISPRMax. For multiplexing, lipoMSN maintained significant gene-editing at each gene target despite reduced dosage of target-specific RNP. By delivering combinations of targeting RNPs in the same nanoparticle, synergistic effects on lipid metabolism are observed in vitro and vivo. These effects, such as a 50% decrease in serum cholesterol after 4 weeks of post-treatment with lipoMSN carrying both pcsk9 and angptl3-targeted RNPs, could not be reached with a single gene-editing approach. Taken together, this lipoMSN represents a versatile platform for the development of efficient, combinatorial gene-editing therapeutics.     

泡沫镍负载石墨烯/钯复合电极催化H2O2电还原研究

采用简单的一步浸渍法制备了还原氧化石墨烯-贵金属Pd复合改性的泡沫镍电极,采用X射线衍射和扫描电镜对复合电极的微观结构和表面形貌进行分析,通过循环伏安法、线性伏安法、计时电流法对H₂O₂还原反应的催化活性及稳定性进行了测试。结果表明,石墨烯包覆在泡沫镍骨架表面,在石墨烯内均匀分散着贵金属Pd纳米颗粒,直径约为100nm。该复合电极对H₂O₂电还原表现出较好的催化性能。在1mol/L NaOH+0.5mol/L H₂O₂混合溶液中,电位为-0.5V时,电流密度可达164mA/cm²,同时表现出较好的稳定性。     

高温多向异步轧制对LZ91镁锂合金组织和力学性能的影响EI北大核心CSCD

采用异步轧制、多向异步轧制、高温异步轧制、高温多向异步轧制四种不同的方式轧制双相镁锂合金板材。通过光学显微镜、MTS E43拉伸试验机和X射线衍射仪观察不同工艺轧制后合金的显微组织、力学性能以及织构特征,综合分析温度和轧制方向条件耦合对镁锂合金组织和力学性能的影响。结果表明:四种轧制工艺可以使α-Mg相沿轧制方向伸长,同时沿着轧制方向法向细化。高温多向异步轧制后α相厚度最低为2.6μm。多向异步轧制后材料的屈服强度、抗拉强度、伸长率分别为149,167 MPa,14.5%,其综合力学性能最优。多向轧制使双峰织构沿ND方向45°偏转,高温轧制使双峰织构由基极向RD方向偏转的角度降低。轧制后样品R-cube织构组分最强,高温多向异步轧制使β-Li相轧制织构转变成为{001}〈100〉织构,有利于{011}〈111〉滑移系发生多滑移。