新疆理化所提出一种基于模拟的使非线性光学晶体材料相匹配区间蓝移的方案

非线性光学晶体是通过频率转换拓宽固态激光器输出波段的关键材料。随着激光微加工,激光通讯和现代科学仪器的持续发展,对紫外/深紫外非线性光学晶体的需求日益增加。但是,很多拥有宽的紫外透过范围和大的倍频效应的晶体因其双折射无法满足深紫外相匹配而无法输出深紫外激光。     

成都中科普瑞净化设备有限公司

正中国科学院高新产业|中国科学院领先技术ISO9001质量管理体系认证ISO14001环境管理体系认证国家高新技术企业(GR200851000218)国家863计划、支撑计划支持企业成都中科普瑞净化设备有限公司是中国科学院全额控股的国家高新技术企业。公司以中国科学院技术力量为依托,自1969年以来,一直专业从事气体纯化技术与设备制造、气体处理工程以及微型反应装置等方面的研究和产     

Biodegradable thermogel as culture matrix of bone marrow mesenchymal stem cells for potential cartilage tissue engineering

Poly（lactide-co-glycolide）-poly（ethylene glycol）-poly（lactide-co-glycolide）（PLGA-PEG-PLGA） triblock copolymer was synthesized through the ring-opening polymerization of LA and GA with PEG as macroinitiator and stannous octoate as catalyst. The amphiphilic copolymer self-assembled into micelles in aqueous solutions, and formed hydrogels as the increase of temperature at relatively high concentrations（〉 15 wt%）. The favorable degradability of the hydrogel was confirmed by in vitro and in vivo degradation experiments. The good cellular and tissular compatibilities of the thermogel were demonstrated. The excellent adhesion and proliferation of bone marrow mesenchymal stem cells endowed PLGA-PEGPLGA thermogelling hydrogel with fascinating prospect for cartilage tissue engineering.     

可拉伸超韧水凝胶的制备和应用

综述了可拉伸超韧水凝胶的设计原理及其在组织工程和柔性电子器件领域的应用. 通过将网络结构层次、 化学结构、 增韧机制与宏观力学性能相结合, 重点讨论了单网络水凝胶、 双网络水凝胶、 纳米复合水凝胶及其它水凝胶等可拉伸超韧水凝胶的研究进展, 并总结和展望了新思路和新方向.     

烷基链工程对两亲有机半导体热力学性能影响的研究

Due to their special polar structure, amphiphilic molecules are simple to process, low in cost and excellent in material properties. Thus, they can be widely applied in the preparation of functional film materials and bionics related to cell membranes. Therefore, amphiphilic organic semiconductor materials are receiving increasing attention in research and industrial fields. The structure of organic amphiphilic semiconductor molecules usually consists of three functional parts: a hydrophilic group, a hydrophobic group, and a linking group between them. The adjustment of their correlation to achieve the target performance is particularly important and needs experimental discussion regarding synthetic methodologies. In this work, we focused on the engineering of a substituent alkyl-chain, and an amphiphilic functional molecule (benzo[b]benzo[4, 5] thieno[2, 3-d]thiophene, named C_nPA-BTBT, n = 3–11) was proposed and synthesized. This molecule links the hydrophobic semiconductor backbone and hydrophilic polar group through alkyl chains of different lengths. Fundamental properties were investigated by nuclear magnetic resonance (NMR) and ultraviolet-visible spectroscopy (UV-Vis) to conform the structure and the band gap properties of the designed organic semiconductor. Thermodynamic features were investigated by thermogravimetric analysis (TGA) and corresponding differential thermal gravity (DTG), which indicate that the functional molecule C_nPA-BTBT (n = 3–11) has a great stability in ambient conditions. Moreover, the results show that the binding ability of the amphiphilic molecule to water molecules was regulated by the odd-even alternating effect of the alkyl chain and the intramolecular coupling with BTBT. Furthermore, differential scanning calorimetry (DSC) and polarized optical microscopy (POM) were used to study the material properties in detail. As the length of the alkyl chain increased, the functional molecule C_nPA-BTBT (n = 3–11) gradually changed from "hard" species with no thermodynamic changes to a transition one with a pair of thermodynamic peaks, and eventually to a "soft" one as a typical liquid crystal with clear observation of Maltese-cross spherulites. The cooling and freezing points were further studied, and the values and trends of their enthalpy and corresponding temperature fluctuated and alternated due to the volume effect, odd-even alternating effect, flexibility, and other functions of the alkyl chain. Three molecular models were proposed according to the thermodynamic study results, namely the brick-like model, transition model, and liquid crystal model. This work presents in-depth discussion on material structure and corresponding thermodynamic properties, and it is an experimental basis for the design, synthesis, optimization, and screening of target performance materials.     

固液界面的力?电?化学耦合及在电催化体系中的应用

目前许多新型高效金属催化剂在设计制备中都考虑到表面力学因素, 例如层状结构、核壳结构等, 其表面高活性原子受到不同程度的应变作用. 应变可直接改变金属的能带带隙, 对催化剂表面的电化学反应产生显著影响, 是一种有效提升材料催化活性的新思路和制备高性能催化剂的新途径, 因此受到了科研工作者的广泛关注. 传统的材料应变工程手段存在着活性物质层的应变值难以精确定量, 并缺少实时调控以及制备工艺繁琐等难题, 导致应变与电催化活性相关性规律识别方面的理论和实验研究进展缓慢. 相比于传统的材料手段, 交变载荷产生的应变具有幅值和频率的可变性以及连续的调控性, 在实验中可以完全排除噪声、缺陷、空位、基底效应等其他外部或材料本征的影响因素. 该综述从经典固液界面热力学表述出发, 简要介绍了电催化体系中的力?电?化学耦合效应, 归纳总结目前电催化体系中应变施加的实验手段和分析方法, 并基于目前相关研究着重讨论在交变载荷作用下应变对金属表面电催化反应的作用机理, 最后从力学角度展望了表面力学在电催化体系中的研究重点及发展趋势.      

聚乳酸组织工程支架结构的精密调控

采用糖球模板法结合热致相分离技术,制备了孔径尺寸、内连通度及孔隙率高度可控的左旋聚乳酸(PLLA)支架材料,并通过扫描电镜(SEM)、红外光谱(FTIR)以及示差扫描量热法(DSC)对其空间结构及性能进行了系统研究.支架材料孔径从50μm到800μm及内连通孔径从10μm到200μm连续可调,微观孔壁结构根据不同溶剂可形成各异的微纳米结构.支架的制备对PLLA化学结构无显著影响,但相分离过程会不同程度地降低PLLA的结晶度.     

苏州大学光学工程

苏州大学光学工程学科,依托苏州大学现代光学技术研究所和苏州大学信息光学工程研究所,是苏州大学的重点优势学科。经过多年的建设,目前拥有江苏省光学工程重点学科、微纳光学优势学科、教育部/江苏省现代光学技术     

2HN缓凝高效减水剂

<正>中科翔-2HN缓凝高效减水剂具有高效减水、缓凝、保坍和增强等功能。适合于各种混凝土结构施工。产品对水泥适应性强,掺量少,使用方便,特别适合于具有缓凝、保坍和高增强要求的商品混凝土工程。主要性能指标减水率20%～25%。对水泥适应性强,引     

决策者具有(严格)凸性偏好结构下的一类交互式多目标决策方法

为了更好地解决决策者具有(严格)凸性偏好结构下的多目标决策问题,一般目标空间为有界凸域的情形常常可以转化为目标空间为有界闭凸区域的情形,首先分析了切割平面及该平面上偏好最优点与被切割平面分割成的为有界闭凸区域的目标空间或目标空间的子集的两个部分之间的关系;然后分析并指出了对于包含全局偏好最优目标方案点的为有界闭凸域的目标空间及其子集(准最优目标集),在确定了切割平面上的偏好最优点后,通过适当地选取供决策者与切割平面的偏好最优点进行比较判断的目标方案点,经过一次比较就可以确定一个新的范围更小的包含全局偏好最优目标方案点的目标空间的有界闭凸子区域(准最优目标集).为获取切割平面上的偏好最优点,提出了改进的坐标轮换法.在这些结论和方法的基础上,提出了决策者具有(严格)凸性偏好结构下的一类交互式多目标决策方法,要求决策者提供较易的偏好性息,决策效能较好.