一种制备细胞色素C的方法

为了保证细胞色素Ｃ药用的安全性，需要高纯度的细胞色素Ｃ。对新鲜猪心采取提取、吸附、洗脱、去杂、沉淀、树脂纯化等一系列方法，从而制得了纯度较高的细胞色素Ｃ。     

Tetrahydroindoles as Multipurpose Screening Compounds and Novel Sirtuin Inhibitors

Indoles are privileged structures in medicinal and bioorganic chemistry that are particularly well suited to serve as platforms for diversity. Among many other therapeutic areas, the indole scaffold has been used to design aromatic compounds useful to interfere with enzymes engaged in the regulation of substrate acylation status, such as sirtuins. However, the planarity of the indole ring is not necessarily optimal for all target enzymes, especially when functionalization with aromatic side chains is required. Replacement of flat scaffolds by nonplanar molecular cores dominated by sp³ hybridization is a common strategy to avoid the disadvantages associated with poor solubility and high promiscuity, while covering less-well-explored areas of chemical space. Thus, we synthesized fragment-like tetrahydroindoles suitable for fragment-based drug discovery as well as a well-characterized small library intended as multipurpose screening compounds. For proof of principle, these compounds were screened against sirtuins 1–3, enzymes known to be addressable by indoles. We found that 2,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-1H-indole-3-carboxamides are potent and selective SIRT2 inhibitors. Compound 16 t displayed an IC₅₀ value of 0.98 μm and could serve as exquisite starting point for hit-to-lead profiling.     

Fe/beta分子筛催化N2O分解

通过液相离子交换法对H-beta分子筛进行改性得到Fe/beta分子筛,并应用于催化N2O直接分解反应,考察加入HNO3后的体系pH值对Fe/beta催化性能的影响。采用N2物理吸附-脱附、XRD、IR、DR UV-Vis、NH3-TPD和ICP-OES等对Fe/beta分子筛进行分析表征。结果表明,溶液pH值降低过程中催化剂的结晶度、比表面积、孔容及Fe3+含量呈现先增加后减少。溶液pH为2.0时所制备的Fe/beta分子筛催化N2O完全分解温度明显低于pH为2.6和1.0时制备的Fe/beta催化剂,显示了较好的催化活性。     

Nanogrooved carbon microtubes for wet three‐dimensional printing of conductive composite structures

Recent advances in three‐dimensional (3D) printing have enabled the fabrication of interesting structures which are not achievable using traditional fabrication approaches. The 3D printing of carbon microtube composite inks allows fabrication of conductive structures for practical applications in soft robotics and tissue engineering. However, it is challenging to achieve 3D printed structures from solution‐based composite inks, which requires an additional process to solidify the ink. Here, we introduce a wet 3D printing technique which uses a coagulation bath to fabricate carbon microtube composite structures. We show that through a facile nanogrooving approach which introduces cavitation and channels on carbon microtubes, enhanced interfacial interactions with a chitosan polymer matrix are achieved. Consequently, the mechanical properties of the 3D printed composites improve when nanogrooved carbon microtubes are used, compared to untreated microtubes. We show that by carefully controlling the coagulation bath, extrusion pressure, printing distance and printed line distance, we can 3D print composite lattices which are composed of well‐defined and separated printed lines. The conductive composite 3D structures with highly customised design presented in this work provide a suitable platform for applications ranging from soft robotics to smart tissue engineering scaffolds. © 2019 Society of Chemical Industry     

SPTES-b-PI质子交换膜的制备及表征

质子交换膜作为质子交换膜燃料电池的核心部件具有提供离子通道传递质子和隔绝两极气体的双重作用,其性能的好坏直接影响着电池性能的优劣。主链引入亲水和疏水段的嵌段芳香族共聚物,由于各嵌段之间具有热力学不相容性会产生微相分离结构,进而形成高效的质子传导通道。本文以磺化双（4-氟苯基）砜（SDFDPS）和4,4'-硫代双苯硫酚（TBBT）为单体,以间羟基苯胺为封端剂合成了带有氨端基的磺化聚芳硫醚砜（SPTES-NH₂）。嵌段聚合物SPTES-b-PI通过亲水段SPTES-NH₂与以1,4,5,8-萘四羧酸二酐（NDA）和4,4'-双（3-氨基苯氧基）二苯基砜（m-BAPS）为单体缩聚而成的疏水段聚酰亚胺（PI）的酰亚胺化偶联反应来合成,制备出了PI分子量不同的SPTES-b-PIx（x=5~20kg/mol）。SPTES-b-PIx膜显示出优异的热力学稳定性,SPTES-b-PIx膜的脱磺化反应开始于290℃高于260℃的SPTES膜,与SPTES-70相比吸水率降低。随着聚酰亚胺分子量的增大,热稳定性增加,质子传导率增加。SPTES-b-PIx的质子传导率25℃下达到0.045~0.124S/cm。     

Sorption of Pb(II), Cd(II), and Ni(II) From Single- and Multimetal Solutions by Recycled Waste Porous Glass

Selective sorption of lead, cadmium, and nickel ions on recycled waste porous glass beads was investigated. Single-metal equilibrations were carried out in demineralized water and ternary metal equilibrations were carried out in demi- and tap water. Freundlich isotherm gave a good correlation of the experimental data. Maximum metal retention (q_max) in single-ion solutions were 18.66 mg/g_RPWG (0.090 mmol/g_RPWG), 4.83 mg/g_RPWG (0.043 mmol/g_RPWG), 4.00 mg/g_RPWG (0.068 mmol/g_RPWG), respectively, for Pb⁺², Cd⁺², and Ni⁺², and lower figures were in the case of ternary systems: 13.50 mg/g_RPWG(0.065 mmol/g_RPWG), 2.23 (0.020 mmol/g_RPWG), 2.05 mg/g_RPWG(0.034 mmol/g_RPWG), respectively, for Pb⁺², Cd⁺², and Ni⁺², with further drastic reduction in tap water. Metal exhausted beads were used as thermal insulators in cement mortars, minimizing their potential impact in the environment.     

阳离子交换树脂改性研究进展

强酸性阳离子交换树脂含有大量的强酸性基团,具有选择、交换、吸收和催化等功能,但其存在耐高温性能差、酸强度低等问题,故需要对其进行改性。改性的阳离子交换树脂广泛应用于水处理、有机合成、分离处理、环境保护及生物制药等领域。本文简要介绍了近年来强酸性阳离子交换树脂的改性方法,主要包含:金属离子改性(Al³⁺、Sn⁴⁺、Zn²⁺、Ti⁴⁺、Fe³⁺和Fe²⁺、Ce⁴⁺和Ga³⁺、Ni²⁺、Zr⁴⁺、Pd²⁺等)、磺化改性、巯基改性、胺化改性及其他类改性等方法;指出了其存在的问题,分析了改性阳离子交换树脂的未来发展方向,开发和研制具有耐高热和化学稳定性的树脂载体材料成为其研究的关键。除此之外,对树脂进行各种改性处理也是改善树脂综合性能、扩大其应用范围的重要方法。     

P-950哌啶树脂吸附钯的动力学研究

研究了P－950哌啶树脂吸附钯的动力学．结果表明，该树脂从氯化物溶液中吸附钯的动力学符合Boyd液膜扩散方程，吸附速率随盐酸浓度的增加而下降；当温度升高时吸附钯的分配比降低．测得的液膜扩散系数K＝1．34×10-2／s，吸附表现热焓△H＝-13.77kJ／mol，表明该树脂吸咐钯是放热反应.     

Changes of copper location in CuY zeolites induced by preparation methods

The location of transition ions in copper- and copper-zinc-loaded Y type zeolites prepared by different procedures has been studied by temperature-programmed reduction, infrared spectroscopy of CO adsorbed on pretreated samples and X-ray photoelectron spectroscopy. Samples outgassed at 673 K showed Cu⁺ species due likely to reduction of Cu²⁺ ions under vacuum. Over exchanged CuY zeolites copper species in exchange sites were detected, while an impregnated sample exhibited bands of CO adsorbed on both Cu²⁺ and Cu⁺ ions developed at the surface of CuO crystals, and small proportions of Cu⁺ ions located in accessible exchange sites S_II and Sn_II. Similar findings were observed in Zn- and Cu-exchanged zeolites although the relative proportion of Cu in S_I positions was decreased due to competition between Cu²⁺ and Zn²⁺ ions. Samples reduced in hydrogen at 523 K showed the appearance of Cu⁰ species in impregnated samples, whereas Cu⁺ dominated in the exchanged counterparts. Reduction at 598 K led to substantial changes in Cu-exchanged samples in water. The proportion of Cu⁺ species decreased by reduction to Cu⁰ and simultaneously migration to Cu⁺ to S_II sites occurred. While Cu²⁺ or Cu⁺ were found on outgassed samples, only Cu⁰ and intrazeolite Cu⁺ were observed after H₂-reduction at 623 K. Changes in copper exposure as a function of sample pretreatments were also revealed by X-ray photoelectron spectroscopy.