Organic Semiconducting Luminophores for Near-Infrared Afterglow,Chemiluminescence, and Bioluminescence Imaging

Optical imaging has played a pivotal role in deciphering in vivo bioinformatics but is limited by shallow penetration depth and poor imaging performance owing to interfering tissue autofluorescence induced by concurrent photoexcitation. The emergence of near-infrared (NIR) self-luminescence imaging independent of real-time irradiation has timely addressed these problems. There are two main kinds of self-luminescent agents, namely inorganic and organic luminophores. Inorganic luminophores usually suffer from long-term biotoxicity concerns resulting from potential heavy-metal ions leakage and nonbiodegradability, which hinders their further translational application. In contrast, organic luminophores, especially organic semiconducting luminophores (OSLs) with good biodegradable potential, tunable design, and outstanding optical properties, are preferred in biological applications. This review summarizes the recent progress of OSLs used in NIR afterglow, chemiluminescence, and bioluminescence imaging. Molecular manipulation and nanoengineering approaches of OSLs are discussed, with emphasis on strategies that can extend the emission wavelength from visible to NIR range and amplify luminescence signals. This review concludes with a discussion of current challenges and possible solutions of OSLs in the self-luminescence field.     

H-bond and conformations of donors and acceptors in model polyether based polyurethanes

The molecular mechanics (MM) method with COMPASS force field was used to study the H-bonds in the polyether based polyurethane model molecules. Availability of the calculation was firstly verified in comparison of some H-bonded model molecules, which were studied by using ab initio calculation, and those calculated by MM. Based on a urethane model molecule 1,3-dimethylcarbamate, which can be donor or acceptor and behaves in various conformations, it is reasonable to have a large number of H-bond interactions between various conformational donors and acceptors. For examining all the possible interaction patterns, we studied 57H-bond complexes. This systematic modeling covers well-known four types of interaction patterns, such as NH?OC (Type I), NH?O-CO (Type II), NH?NH (Type III), NH?COC (Type IV) in the system. Obtained H-bond energies were used to analyze the probabilities of the complexes. For the interaction within the hard segments, or Type I, Type II and Type III, a predominant H-bond complex has been found in the present study, which belongs to Type I. For the interaction between the hard segment and the soft segment, two conformations of Type IV were calculated to be existed.     

Influence of ethyl methacrylate content on the volume‐phase transition of temperature‐sensitive poly[(N‐isopropylacrylamide)‐co‐(ethyl methacrylate)] microgels

A novel series of temperature‐sensitive poly[(N‐isopropylacrylamide)‐co‐(ethyl methacrylate)] (p(NIPAM‐co‐EMA)) microgels was prepared by the surfactant‐free radical polymerization of N‐isopropylacrylamide (NIPAM) with ethyl methacrylate (EMA). The shape, size dispersity and volume‐phase transition behavior of the microgels were investigated by transmission electron microscopy (TEM), ultraviolet–visible (UV–Vis) spectroscopy, dynamic light scattering (DLS) and differential scanning calorimetry (DSC). The transmission electron micrographs and DLS results showed that microgels with narrow distributions were prepared. It was shown from UV–Vis, DLS and DSC measurements that the volume‐phase transition temperature (VPTT) of the p(NIPAM‐co‐EMA) microgels decreased with increasing incorporation of EMA, but the temperature‐sensitivity was impaired when more EMA was incorporated, causing the volume‐phase transition of the microgels to become more continuous. It is noteworthy that incorporation of moderate amounts of EMA could not only lower the VPTT but also enhance the temperature‐sensitivity of the microgels. The reason for this phenomenon could be attributed to changes in the complicated interactions between the various molecules. Copyright © 2004 Society of Chemical Industry     

浸胶工艺对Nomex蜂窝性能的影响

本文研究了浸胶工艺对Ｎｏｍｅｘ蜂窝性能的影响，分析探讨了提高Ｎｏｍｅｘ蜂窝性能及外观质量的途径。研究结果表明：采取新的浸胶工艺制作的Ｎｏｍｅｘ蜂窝，各项性能全面达到法国宇航材料标准。     

医院门诊就诊流程优化研究

以业务流程再造、程序分析等相关理论方法为基础,以J市R医院消化内科为例,对医院门诊就诊流程进行优化研究。通过实地走访与问卷调查发现消化内科现行门诊服务流程中存在的问题,基于业务流程再造理论优化门诊服务流程,使用程序分析方法和Flexsim仿真对门诊就诊流程进行对比分析,验证了优化方案的有效性。     

相对压强对白炭黑氮吸附表面积测试稳定性的影响

研究相对压强对白炭黑氮吸附表面积测试稳定性的影响。结果表明:在相同液氮纯度、脱气温度、脱气时间、氮吸附点数量条件下,与相对压强范围为0.05~0.1时相比,相对压强范围为0.05~0.2时白炭黑的氮吸附表面积测量值偏低,且差值随氮吸附表面积的增大呈增大趋势;相对压强范围较小时,氮吸附表面积测试结果的线性相关因数较大,再现性较好,测试结果较稳定。     

Dissipative Particle Dynamics Simulation: A Review on Investigating Mesoscale Properties of Polymer Systems

Polymer systems have typical multiscale characteristics, both in space and time. The mesoscopic properties of polymers are difficult to describe through traditional experimental approaches. Dissipative particle dynamics (DPD) is a simulation method used for solving mesoscale problems of complex fluids and soft matter. The mesoscopic properties of polymer systems, such as conformation, dynamics, and transport properties, have been studied extensively using DPD. This paper briefly summarizes the application of DPD to research involving microchannel flow, electrospinning, free-radical polymerization, polymer self-assembly processes, polymer electrolyte fuel cells, and biomedical materials. The main features and possible development avenues of DPD are described as well.     

锦屏一级水电站左岸1601m廊道岩体质量指标研究

岩石质量指标(RQD)是评价岩体质量的一个重要参数,被广泛应用于岩石质量评价,但通过钻孔取芯方式获取RQD存在明显不足,给岩体质量评价带来了一定的误差。以锦屏一级水电站左岸廊道岩体为实例,结合结构面三维网络模拟技术,采用测线法研究了广义RQD_t随测线布置长度与角度的变化情况。在此基础上分析了岩体的尺寸效应和各向异性。研究结果表明:RQD_t存在显著的尺寸效应,随着测线长度增大至10 m,RQD_t收敛于一个稳定的值;随着测线倾向和倾角的变化,RQD_t沿空间不同方向呈现出不同的分布。研究发现锦屏一级水电站左岸1 601 m廊道岩体具有显著的尺寸效应和各向异性,基于广义RQD_t的岩石质量指标能克服传统RQD在这方面的不足。     

Raman spectroscopic study of conformational changes in the amorphous phase of poly(lactic acid) during deformation

The conformational distribution change of amorphous poly(lactic acid) (PLA) induced by deformation has been studied using Raman spectroscopy. Spectroscopic features associated with the rotational isomeric states (ttt, ttg′, tg′t, tg′g′) have been established experimentally and supported by normal coordinate analysis. Deformation induced a significant increase in the most favorable tg′t conformation. Based on the relative intensities of Raman-active skeletal modes, a quantitative method has been developed that can be used to elucidate structural changes in a variety of deformed polymer samples. For biaxially oriented PLA films, the overall tg′t conformation increased from the 76% in undeformed sample to a value as high as 92%. The change in conformational distribution in the amorphous phase follows a different trend (76-88%) as compared to the increase in sample crystallinity (0-43%). A large change in amorphous chain conformation occurred at relatively low draw ratios. In contrast, the large change in the degree of crystallinity occurred at higher draw ratios.     

陶瓷坯体增强剂聚丙烯酸钠在艺术瓷成形过程的应用

本文合成了一系列不同相对分子质量的聚丙烯酸钠,应用于艺术瓷的坯体中,研究了聚丙烯酸钠对艺术瓷坯体强度、变形率的影响,并对聚丙烯酸钠增强机理进行了探讨。结果表明:聚丙烯酸钠可有效地提高艺术瓷坯体的成形强度,减少了坯体的变形率,当增强剂c加入的质量分数为0.6%时,坯体的干燥强度增加率达167.5%,坯体的变形率从50%降低到10%。