制造商融资决策:银行、商业信用或区块链供应链金融

基于收益共享契约构建银行信用融资、商业信用融资和区块链供应链金融的对比模型，探讨各模式下供应链的最优决策方案，定量分析各融资模式下供应链绩效随不同参数的变化情况.研究表明，当零售商资金成本低于制造商资金成本时，商业信用融资一定优于银行信用融资;存在两个区块链供应链金融平台费率的阈值，只有当平台费率低于低阈值点时，区块链供应链金融才是同时利于制造商和零售商的最优模式.此外，收益共享比率越高，制造商收益越高，则零售商收益越低.     

基于XPS对硫铁矿去除SeO2-3的机理研究

硒是动植物及人体生长必需的十五种微量元素之一，具有清除体内自由基、抗氧化、增强免疫力等功能，但其安全剂量的范围却很窄。利用扫描电子显微镜（SEM）和X射线衍射仪（XRD）对湿法球磨制备的硫铁矿形貌进行了表征。SEM观测发现加乙醇助磨后的硫铁矿为粒径大小较均匀的球形颗粒团聚体，粒径范围在17～200 nm之间，平均粒径138 nm。XRD衍射图谱中的特征峰与FeS₂衍射图谱中各峰位置基本一致，因此判定硫铁矿中主要化学组分为FeS₂，且图谱中基本没有杂峰，表明制备过程中并未混入杂质，样品纯度较高。实验结果表明，该法制备的硫铁矿具有颗粒粒径小、比表面积大、反应活性高等优点。研究中利用X射线光电子能谱仪（XPS）对硫铁矿去除水体中SeO2-₃的机理进行了研究。研究结果表明, （1）在较为广泛的实验pH范围（pH 2.2～11.5），硫铁矿均能有效去除水体中SeO2-₃，去除效率（除pH值7.8以外）均达到90%以上；（2）硫铁矿与SeO2-₃发生反应后，其主要组成元素的XPS特征峰结合能有所减小，表明硫铁矿表面发生了一定化学变化；（3）酸碱环境下硫铁矿去除SeO2-₃的机理不完全相同，酸性环境下，硫铁矿对SeO2-₃的去除是单纯的氧化还原过程，即硫铁矿中被酸活化的S2-₂将SeO2-₃还原为单质Se(0)，并且酸性越强，SeO2-₃去除效果越好；碱性环境下，SeO2-₃的去除过程中氧化还原与络合反应并存，硫铁矿表面有络合态Fe(OH)SeO₃和单质Se(0)两种存在形态，且碱性越强，络合态Fe(OH)SeO₃含量越高。以上研究结果为硫铁矿去除固定水体和土壤中以SeO2-₃为代表的可变价金属阴离子提供重要理论依据和应用基础。     

考虑多种损坏构成特征的沥青路面预防性养护决策方法

由于沥青路面损坏构成的多样性, 相同的路面状况指数(pavement condition index, PCI)可能代表不同的损坏组合. 当多种损坏并存且损坏程度接近时, 用PCI和主导损坏(最严重、扣分最多的路面损坏)难以得到具有针对性的养护对策. 因此, 通过对PCI的深入分析, 明确了主导损坏代表性不足的路段, 以现行预防性养护决策方法为基础, 补充了一种考虑损坏构成特征、更具针对性的决策方法. 以上海城市道路近5年的检测、养护数据为分析基础, 首先利用有序聚类算法将路段按PCI水平分组, 分析了不同阶段路面损坏构成和差异水平; 然后, 针对多种损坏并存且损坏差异不显著的路段, 根据预防性养护的实施效果筛选了能够反映正确预防性养护经验的有效养护路段; 最后, 基于有效养护路段建立并对比分析了2个基于BP(back propagation)神经网络的养护决策模型. 结果表明: 当PCI水平介于优良(84.4~93.0分)时, 不同损坏程度接近, 主导损坏代表性不足; 考虑多种损坏构成特征的BP神经网络模型表现出更高的决策精度, 测试集决策正确率达86.20%, 优于仅考虑主导损坏的模型(58.50%). BP神经网络与传统决策树法结合能够优化沥青路面决策过程, 提高养护对策选取的针对性.     

厦门小微企业知识产权托管治理的问题及对策

厦门市知识产权托管工作已由政府单向管理向以政府为主引导，企业、服务机构、行业协会、产业园区以及自贸区等载体参与其中的多元治理体系转变，并取得了良好的成效。但存在顶层设计缺失、托管机构服务能力不足、行业协会作用发挥不充分、氛围营造不够等问题。厦门市应通过加强监管力度、提高小微企业参与托管的意识、提升托管机构的服务能力、激励行业协会发挥作用、加强宣传等措施，进一步完善多元共治的治理体系，提升小微企业知识产权托管治理效能。     

Control over Nanostructures and Associated Mesomorphic Properties of Doped Self‐Assembled Triarylamine Liquid Crystals

We have synthesized a series of triarylamine‐cored molecules equipped with an adjacent amide moiety and dendritic peripheral tails in a variety of modes. We show by ¹H NMR and UV/Vis spectroscopy that their supramolecular self‐assembly can be promoted in solution upon light stimulation and radical initiation. In addition, we have probed their molecular arrangements and mesomorphic properties in the bulk by integrated studies on their film state by using differential scanning calorimetry (DSC), variable‐temperature polarizing optical microscopy (VT‐POM), variable‐temperature X‐ray diffraction (VT‐XRD), and atomic force microscopy (AFM). Differences in the number and the disposition of the peripheral tails significantly affect their mesomorphic properties associated with their lamellar‐ or columnar‐packed nanostructures, which are based on segregated stacks of the triphenylamine cores and the lipophilic/lipophobic periphery. Such structural tuning is of interest for implementation of these soft self‐assemblies as electroactive materials from solution to mesophases.     

Self‐Assembly and Gelation of Poly(aryl ether) Dendrons Containing Hydrazide Units: Factors Controlling the Formation of Helical Structures

Self‐assembly of AB₂ and AB₃ type low molecular weight poly(aryl ether) dendrons that contain hydrazide units were used to investigate mechanistic aspects of helical structure formation during self‐assembly. The results suggest that there are three important aspects that control helical structure formation in such systems with acyl hydrazide/hydrazone linkage: i) J‐type aggregation, ii) the hydrogen‐bond donor/acceptor ability of the solvent, and iii) the dielectric constant of the solvent. The monomer units self‐assemble to form dimer structures through hydrogen‐bonding and further assembly of the hydrogen‐bonded dimers leads to macroscopic chirality in the present case. Dimer formation was confirmed by NMR spectroscopy and by mass spectrometry. The self‐assembly in the system was driven by hydrogen‐bonding and π–π stacking interactions. The morphology of the aggregates formed was examined by scanning electron microscopy, and the analysis suggests that aprotic solvent systems facilitate helical fibre formation, whereas introduction of protic solvents results in the formation of flat ribbons. This detailed mechanistic study suggests that the self‐assembly follows a nucleation–elongation model to form helical structures, rather than the isodesmic model.     

Synthesis of self‐healing polyurethane urea‐based supramolecular materials

Supramolecular polyurethane ureas are expected to have superior mechanical properties primarily due to the reversible, noncovalent interactions such as hydrogen bonding interactions. We synthesized polyurethane prepolymers from small molecular weight of poly(tetramethylene ether)glycol and isophorone diisocyanates, which were end capped with propylamine to synthesize polyurethane ureas with high contents of urea and urethane groups for hydrogen‐bonding formations to facilitate self‐healing. The effects of polyurethane urea molecular weight (3000 ≤ M_n ≤ 9000), crosslinking, and cutting direction were studied in terms of thermal, mechanical, and morphological properties with an emphasis on the self‐healing efficiency. It was found that the thermal self‐healability was more pronounced as the molecular weight of polyurethane urea decreased, showing a maximum of more than 96% with 3000 M_n when the sample was cut along the stretch direction. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015 , 53, 468–474     

四-对羟基苯基卟啉的自组装及光电特性

利用X射线光电子能谱(XPS)测试5,10,15,20-四-(对羟基苯基)卟啉单体和5,10,15,20-四-(对羟基苯基)卟啉自组装二聚体,并通过化学模拟得到卟啉自组装二聚体分子的最优构象.结果表明:两种卟啉化合物中氧原子的类型不同;在单体卟啉中未检测到瞬态表面光电压信号,卟啉自组装二聚体表现出较好的瞬态表面光伏特性;卟啉自组装二聚体的光限幅性质优于卟啉1单体.