铁粉为原料催化改性铁氧化物的储氢性能

以Fe粉为原料, 以金属Mo, Al和Ni可溶性盐作为添加剂, 通过浸渍法制备单金属添加和双金属添加的改性铁氧化物储氢材料Fe-Mo, Fe-Al, Fe-Mo-Ni和Fe-Mo-Al, 并研究了它们的储氢性能. 结果表明样品Fe-Mo改性效果最好: 如放氢温度由改性前的500 ℃降至改性后的290 ℃左右; 300 ℃时放氢速率最高, 由改性前的低于50 μmol•min^－1• Fe-g^－1到改性后的325 μmol•min^－1•Fe-g^－1 (10次平均); 4.53 wt%的平均实验储氢量与理论值4.8 wt%较接近; 储-放氢循环稳定性随着循环次数的增加呈逐渐增加的趋势. SEM微观结构和BET比表面积分析表明添加剂的种类对样品的改性作用更重要.     

四种5-氟尿嘧啶二肽衍生物的合成、晶体结构和抗癌活性

合成了四种新的5-氟尿嘧啶(5-Fu)二肽衍生物, 它们的结构经过元素分析、IR、1H NMR和13C NMR的表征, 比旋光度[a]D的测定结果表明了它们之间的对映异构关系, 用X射线衍射法测定了其中一对对映异构的晶体结构3a (S)和3b (R), 生物活性测试的结果表明这四种化合物都具有一定的抑制活性, 并且R型产物比S型产物抑制率高. 研究了2a和3a与DNA在Au电极上相互作用的伏安行为, 比较了它们跟5-氟尿嘧啶与双链DNA发生相互作用的差别.     

绿色单体二氧化碳参与的新型聚合反应

二氧化碳(CO₂)是一种丰富、廉价、无毒以及可再生的一碳资源,也是一种可用于聚合的绿色单体.基于CO₂的聚合是近年来的研究热点之一.目前广泛报道的是CO₂和环氧单体的聚合反应,经过几十年的发展已经成功实现工业化生产.最近几年,一些CO₂参与的新型聚合反应被陆续报道,这些工作大都通过两种途径实现从CO₂到高分子材料的转变.第一个途径是先将CO₂转化为可以聚合的单体,例如:内酯、环状碳酸酯和2,5-二呋喃甲酸等,再利用开环或者逐步聚合将单体转化为聚合物;另一个途径是直接以CO₂为单体和其他类型单体共聚得到聚合物.这两种途径对于发展CO₂参与的新型聚合反应,拓展CO₂基聚合物种类都具有重要意义.本综述按照CO₂直接还是间接参与聚合反应分类总结了近年来在CO₂制备高分子材料方面的进展,并对未来发展方向进行了简单阐述.     

颗粒毛细效应影响因素的离散元分析

颗粒毛细效应是指将一根细管插入填充有颗粒物质的容器中并对管施加竖直振动时颗粒在管内上升并最终达到一个稳定的高度的现象,该现象为颗粒物料的逆重力输运提供了一种潜在的技术途径.为探究颗粒毛细效应的影响因素,采用离散元方法,模拟再现了颗粒毛细效应过程,展示了不同管径下颗粒竖直方向速度演变特性,考察了不同容器宽度和振动条件下颗粒最终毛细上升高度随管径的演变规律.结果表明,在容器宽度与粒径比为40、管振幅与粒径比为14.33、管振动频率为12 Hz情况下,管径与粒径比D/d=3.33时,管内颗粒堵塞严重,使得颗粒上升缓慢,并造成颗粒柱中断; D/d=8.33时,起初毛细上升高度增加迅速,随后毛细上升高度的增大逐渐减缓,管内颗粒在管径方向几乎不存在速度梯度; D/d=15时,随着颗粒毛细上升高度的增大,管内颗粒柱分离为速度截然不同的两层,上层颗粒在管径方向几乎不存在速度梯度,而下层颗粒存在明显的速度梯度.研究还发现,在毛细效应能够发生的管径范围内,存在一个对应于颗粒最终毛细上升高度最大值的临界管径,当管径小于临界管径时,颗粒最终毛细上升高度随管径的增大而增大,当管径大于临界管径时,颗粒最终毛细上升...     

宽体液腔Janus-Helmholtz换能器

该文使用有限元方法对宽体液腔Janus-Helmholtz(JH)换能器进行了仿真分析,得出了壳体宽度拓展增量对JH换能器工作性能的影响规律。使用三维建模的方式,分析了连接部分对换能器性能的影响及宽体壳体的模态,证明了三维建模的必要性。依据仿真优化结构设计了一款宽体液腔JH换能器并进行了湖上测试。最终测试结果与仿真结果有很好的一致性,相较直筒JH换能器其谐振频率降低300 Hz,发射电压响应最高可达144 dB。     

微织构超声振动铣削系统的研究

为了在金属切削过程中在7075铝合金表面形成稳定的微织构以提高其服役性能,提出一种微织构超声铣削加工工艺。为此,该文首先基于运动合成原理获得了刀尖的运动轨迹特征和工件表面的织构形貌特征。然后,基于等效电路原理和传输矩阵法建立了超声铣削系统的频率方程,并应用牛顿迭代法获得了准确的数值解,通过有限元软件对建立的超声振动系统分别进行模态分析和谐响应分析,获得了具有微织构特征的纵扭复合超声铣削系统。最后,对加工制造出的微织构纵扭复合超声铣削系统进行振动测试、切削力测试和加工测试,结果表明:工件表面形成的"鱼鳞网纹"微观织构能够改变其润湿性能。     

Molybdenum Cofactor Deficiency in Humans

Molybdenum cofactor (Moco) deficiency (MoCD) is characterized by neonatal-onset myoclonic epileptic encephalopathy and dystonia with cerebral MRI changes similar to hypoxic–ischemic lesions. The molecular cause of the disease is the loss of sulfite oxidase (SOX) activity, one of four Moco-dependent enzymes in men. Accumulating toxic sulfite causes a secondary increase of metabolites such as S-sulfocysteine and thiosulfate as well as a decrease in cysteine and its oxidized form, cystine. Moco is synthesized by a three-step biosynthetic pathway that involves the gene products of MOCS1, MOCS2, MOCS3, and GPHN. Depending on which synthetic step is impaired, MoCD is classified as type A, B, or C. This distinction is relevant for patient management because the metabolic block in MoCD type A can be circumvented by administering cyclic pyranopterin monophosphate (cPMP). Substitution therapy with cPMP is highly effective in reducing sulfite toxicity and restoring biochemical homeostasis, while the clinical outcome critically depends on the degree of brain injury prior to the start of treatment. In the absence of a specific treatment for MoCD type B/C and SOX deficiency, we summarize recent progress in our understanding of the underlying metabolic changes in cysteine homeostasis and propose novel therapeutic interventions to circumvent those pathological changes.     

Optical Anisotropy of Porphyrin Nanocrystals Modified by the Electrochemical Dissolution

Reflectance anisotropy spectroscopy (RAS) coupled to an electrochemical cell represents a powerful tool to correlate changes in the surface optical anisotropy to changes in the electrochemical currents related to electrochemical reactions. The high sensitivity of RAS in the range of the absorption bands of organic systems, such as porphyrins, allows us to directly correlate the variations of the optical anisotropy signal to modifications in the solid-state aggregation of the porphyrin molecules. By combining in situ RAS to electrochemical techniques, we studied the case of vacuum-deposited porphyrin nanocrystals, which have been recently observed dissolving through electrochemical oxidation in diluted sulfuric acid. Specifically, we could identify the first stages of the morphological modifications of the nanocrystals, which we could attribute to the single-electron transfers involved in the oxidation reaction; in this sense, the simultaneous variation of the optical anisotropy with the electron transfer acts as a precursor of the dissolution process of porphyrin nanocrystals.     

α-Diimine Cisplatin Derivatives: Synthesis,Structure, Cyclic Voltammetry and Cytotoxicity

Three new Pt(II) complexes [(dpp-DAD)PtCl₂] (I), [(Mes-DAD(Me)₂)PtCl₂] (II) and [(dpp-DAD(Me)₂)PtCl₂] (III) were synthesized by the direct reaction of [(CH₃CN)₂PtCl₂] and corresponding redox-active 1,4-diaza-1,3-butadienes (DAD). The compounds were isolated in a single crystal form and their molecular structures were determined by X-ray diffraction. The purity of the complexes and their stability in solution was confirmed by NMR analysis. The Pt(II) ions in all compounds are in a square planar environment. The electrochemical reduction of complexes I–III proceeds in two successive cathodic stages. The first quasi-reversible reduction leads to the relatively stable monoanionic complexes; the second cathodic stage is irreversible. The coordination of 1,4-diaza-1,3-butadienes ligands with PtCl₂ increases the reduction potential and the electron acceptor ability of the DAD ligands. The synthesized compounds were tested in relation to an adenocarcinoma of the ovary (SKOV3).     

连体构架避雷针风振计算的简化方法

为简化构架避雷针风振时域计算从而有效降低计算耗时,以单跨和三跨构架避雷针结构为例,根据构架体系的结构特性和风振特点,提出一种简化计算方法,即对每个塔架单独建模并考虑结构刚度和质量系统的一致性和横梁荷载的等效加载,从而对每个塔架单独进行动力计算,并对这种简化方法的合理性进行了验证。研究发现,构架避雷针的频率较小,风振效应较为显著,但在各方向均以一阶振型为绝对主力;构架避雷针的塔架在平面外的荷载耦联效应极小,平面内也仅表现有位移均值的耦联效应:这两个结构特性也为风振简化计算提供了便利。对每个塔架的简化模型,通过在塔架与原横梁连接处设置弹簧和附加质量来实现对原结构一阶振型的等效,并通过影响线法将横梁分布风荷载等效为塔架的集中荷载。由此简化方法所得的结构风振静动力响应结果均与原始结构有良好一致性,并且计算效率得以显著提升。