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51.
52.
Hossein Arayesh Nadereh Golshan Ebrahimi Behnam Khaledi Masood Khabazian Esfahani 《应用聚合物科学杂志》2020,137(41):49243
Chain extension/branching by reactive processing is a well-known method to enhance the rheological properties of polymers. In this study, pyromellitic dianhydride, poly(glycolic acid), triglycidyl isocyanurate, and bisphenol A diglycidyl ether were used as chain extender/branching agents to produce branched Polyethylene terephthalate (PETs) with four different molecular structures. According to the linear rheological characterizations, the storage modulus and complex viscosity of modified PET samples enhanced significantly after branching. The shear viscosities of modified PET show a pronounced shear-thinning behavior and a remarkable increase at low frequencies, which can be an indication of the existence of long-chain branches (LCBs) in the molecular structure of polymer and broadening the molecular weight distribution. Fourier transform infrared (FTIR) and differential scanning calorimetry (DSC) analysis were used to investigate the effect of branching agents on the chemical structure and thermal properties of PET, respectively. DSC results show that higher amounts of LCBs lead to lower melting and crystallization temperatures. 相似文献
53.
Yifei Wang Shouying Huang Xinsheng Teng Hongyu Wang Jian Wang Qiao Zhao Yue Wang Xinbin Ma 《Frontiers of Chemical Science and Engineering》2020,14(5):802
The Fischer–Tropsch synthesis (FTS) continues to be an attractive alternative for producing a broad range of fuels and chemicals through the conversion of syngas (H2 and CO), which can be derived from various sources, such as coal, natural gas, and biomass. Among iron carbides, Fe2C, as an active phase, has barely been studied due to its thermodynamic instability. Here, we fabricated a series of Fe2C embedded in hollow carbon sphere (HCS) catalysts. By varying the crystallization time, the shell thickness of the HCS was manipulated, which significantly influenced the catalytic performance in the FTS. To investigate the relationship between the geometric structure of the HCS and the physic-chemical properties of Fe species, transmission electron microscopy, X-ray diffraction, N2 physical adsorption, X-ray photoelectron spectroscopy, hydrogen temperature-programmed reduction, Raman spectroscopy, and Mössbauer spectroscopy techniques were employed to characterize the catalysts before and after the reaction. Evidently, a suitable thickness of the carbon layer was beneficial for enhancing the catalytic activity in the FTS due to its high porosity, appropriate electronic environment, and relatively high Fe2C content. 相似文献
54.
55.
Marijana Đaković 《Crystallography Reviews》2020,26(2):69-100
Designing crystalline solids with improved properties or performances remains a challenging task, despite great strides that have been made within the field of crystal engineering since its birth several decades ago. Herein, we are bringing examples that illustrate recent successes in taking supramolecular synthetic guidelines from the organic crystal engineering and adjusting those to metal-containing systems, particularly to the lower-dimensional ones. The versatility of calculated molecular electrostatic potential (MEP) as a new crystal engineering tool is demonstrated. 相似文献
56.
Morpholine is a frequently used heterocycle in medicinal chemistry and a privileged structural component of bioactive molecules. This is mainly due to its contribution to a plethora of biological activities as well as to an improved pharmacokinetic profile of such bioactive molecules. The synthesis of morpholines is a subject of much study due to their biological and pharmacological importance, with the last such review being published in 2013. Here, an overview of the main approaches toward morpholine synthesis or functionalization is presented, emphasizing on novel work which has not been reviewed so far. This review is an update on synthetic strategies leading to easily accessible libraries of bioactives which are of interest for drug discovery projects. 相似文献
57.
芳烃与烯烃的反应在有机合成中应用广泛。随着环保要求的提高,用于芳烃烷基化反应的传统催化剂逐渐被新型绿色催化剂所替代。近年来研究发现离子液体和分子筛对该反应具有高效催化作用且环境友好。本文探讨了离子液体和分子筛的酸性,总结了相应的的催化机理,对有关实验和理论研究工作进行了分析。同时揭示了离子液体和分子筛的结构对其催化性能的影响,为烷基化反应进一步研究奠定了基础。分析表明离子液体既能作为B酸,也能作为L酸起催化作用;分子筛主要作为B酸起催化作用,同时其催化性能与孔道结构、孔径大小及反应物尺寸密切相关。离子液体的稳定性较差、成本较高,而分子筛失活较快,未来需围绕提高离子液体稳定性、改进其制备方法以降低成本及改善分子筛结构以延长使用周期等方面展开研究。 相似文献
58.
以纯度大于99.9%(质量分数)的高纯ZrO2和SiO2为原料,少量TiO2为添加剂,采用高温固相法合成高纯锆英石(ZrSiO4)粉料。研究温度和反应时间对高纯锆英石合成效率的影响,发现粒度小于50 μm的原料粉末经1 500 ℃反应48 h后,ZrSiO4相的含量可以达到95.77%(质量分数)。将合成的高纯锆英石粉料球磨并冷等静压成型后,在1 550 ℃高温烧结成高纯致密锆英石砖。高纯致密锆英石中杂质Fe的含量仅为29 μg/g,Cu的含量小于1 μg/g,是普通商用致密锆英石的1/10;对磷酸盐玻璃静态光吸收损耗的影响仅为普通致密锆英石材料的1/3。将这种高纯致密锆英石材料用于激光玻璃窑炉,有助于降低玻璃对1 053 nm激光的损耗,提升激光玻璃的激光性能。 相似文献
59.
Dr. Guangze Yang Dr. Yun Liu Song Jin Prof. Chun-Xia Zhao 《Chembiochem : a European journal of chemical biology》2020,21(20):2871-2879
Among various drug-delivery systems, core-shell nanoparticles have many advantages. Inspired by nature, biomimetic synthesis has emerged as a new strategy for making core-shell nanoparticles in recent years. Biomimetic mineralization is the process by which living organisms produce minerals based on biomolecule templating that leads to the formation of hierarchically structured organic–inorganic materials. In this minireview, we mainly focus on the synthesis of core-shell nanoparticle drug-delivery systems by biomimetic mineralization. We review various biomimetic mineralization methods for fabricating core-shell nanoparticles including silica-based, calcium-based and other nanoparticles, and their applications in drug delivery. We also summarize strategies for drug loading in the biomolecule-mineralized core-shell NPs. Current challenges and future directions are also discussed. 相似文献
60.
Tomoyo Okumura Kenya Sonobe Asami Ohashi Harumi Watanabe Katsushi Watanabe Hiroshi Oyamada Masaaki Aramaki Toshiaki Ougizawa 《Polymer Engineering and Science》2020,60(7):1699-1711
Simultaneous one-pot syntheses of PA66 and HAp were carried out by extracting H2O and CO2 from PA66 monomers and HAp raw materials, respectively, resulting in the formation of a polyamide (PA) 66-hydroxyapatite (HAp) nanocomposite. During the process, a spherical nano-sized HAp particle was precipitated following dissolution of micro-sized CaHPO4・2H2O. The PA66 monomers were subsequently adsorbed onto the generated HAp product. Some of the adsorbed PA66 monomers formed a bound polymer on HAp, and an increase in the adhesiveness of the PA66-HAp interface was observed as the polymerization progressed. During this process, the synthesis of a nanocomposite from a micro-sized raw material and creation of an autonomous strong interface between the matrix and filler was achieved. In addition, the shape of the resultant HAp was controllable and could be modified to needle shape by the addition of F− and Mg2+ ions to the raw material. HAp could also be changed to plate shape via octa-calcium phosphate (OCP). Notably, during the synthesis, the filler shape of the nanocomposite could be controlled to 0D (particle), 1D (needle), and 2D (plate). 相似文献