Tailoring the hydrophilic and hydrophobic reaction fields of the electrode interface on single crystal Pt electrodes for hydrogen evolution/oxidation reactions

Interfacial hydrophobic/hydrophilic reaction fields significantly affect various reactions at the electrode surface. The hydrogen evolution reaction (HER) and the hydrogen oxidation reaction (HOR) have been investigated on single crystal Pt electrodes modified with hydrophobic/hydrophilic cations and anion-exchange copolymers in alkaline solutions. In alkali metal hydroxide solutions, Pt (110) exhibits the highest HER/HOR activity in the low-index planes of Pt. On the low-index planes of Pt, the hydrophilicity of the alkali metal cation in the supporting electrolyte activates the HER/HOR depending on its hydration energy. Hydrophilic cations at the interface facilitate the extraction of hydrogen from the hydrated water. The modification of anion-exchange copolymers with a hydrophobic skeleton on Pt (110) further enhanced the HER/HOR activity. The hydrogen bonding network formed around the hydrophobic species facilitated the mobility of water molecules and the OH⁻ as the reactant/product of the HER/HOR. Appropriately forming hydrophilic and hydrophobic reaction fields at the interface improved the HER/HOR activity.     

基于ISIGHT的安全气囊盖板结构优化设计方法研究

选取某款弱化沟槽呈“H”形的聚碳酸酯/丙烯腈?丁二烯?苯乙烯共聚物(PC/ABS)合金材质安全气囊盖板为研究对象，并构建了其有限元仿真模型，对比有限元力学仿真分析结果与理论计算值验证了该有限元仿真模型的可靠性；通过ISIGHT软件集成Catia和ANSYS，选取安全气囊盖板弱化沟槽的横向长度、深度，纵向长度、深度4个参数作为设计变量，选取弱化沟槽横向最大应力与纵向最大应力作为响应变量，分析了设计变量对响应变量的贡献度分布特征并采用NSGA遗传算法对响应变量多目标优化。结果表明,横向长度、纵向深度对横向最大应力为负贡献度，横向深度、纵向长度为正贡献度；横向深度、纵向长度对纵向最大应力为负贡献度，横向长度、纵向深度为正贡献度；在合理范围内，4个参数值的优化设计，实现了横向最大应力提高和纵向最大应力降低的多目标优化，有效减少了安全气囊盖板爆破时产生的碎屑量，提升了产品的安全性能。     

偶联剂对PLA/PBAT/WF复合材料3D打印性能的影响

以聚乳酸（PLA）和聚己二酸/对苯二甲酸丁二酯（PBAT）为基体，杨木粉（WF）为填充增强材料，使用混炼机熔融共混制备PLA/PBAT/WF复合材料，采用熔融沉积成型（FDM）技术制备标准实验试样，通过扫描电子显微镜、红外光谱分析、旋转流变测试以及力学试验等方法，研究不同含量的硅烷偶联剂KH550对PLA/PBAT共混物以及PLA/PBAT/WF的相容性、流变性及力学性能的影响。结果表明，在偶联剂用量为3 %（质量分数，下同）时，拉伸强度提高了136 %；偶联剂KH550与 PLA和PBAT共价键偶联生成接枝聚合物，二者相容性得到提高；同时偶联剂与WF表面羟基发生缩聚反应有效的改善了其与PLA/PBAT的基体相容性，PLA/PBAT/WF复合材料的FDM的制件力学性能得到较大提升；复合材料的黏度随偶联剂含量的增加呈下降的趋势，含量为3 %时线材的综合打印性能及制品质量最佳。     

MAPP/EAA处理对聚丙烯/小麦秸秆粉复合材料性能的影响

研究了马来酸酐接枝聚丙烯（MAPP）、乙烯丙烯酸共聚物（EAA）处理对聚丙烯（PP） /小麦秸秆粉（WSP）复合材料性能的影响。结果表明，随着体系中MAPP质量份数的增加，PP/WSP的拉伸强度和弯曲强度均逐渐增大，但冲击强度却先增加后减小，复合材料达到塑化峰的时间逐渐延长；使用EAA后，无论体系中是否已经使用了MAPP，PP/WSP的拉伸、弯曲和冲击强度均可得以提高，特别对于未使用MAPP的体系，效果更加明显，可分别提高65.04 %、45.42 %和6.75 %，储能模量增加，表面疏水性增强，平衡扭矩从13.9 N·m降至11.8 N·m，吸水尺寸变化率及吸水率下降，吸水平衡时间缩短；使用EAA可改善PP/WSP中WSP与PP间的界面结合，改善PP/WSP力学性能、热稳定性能、表面疏水性能、尺寸稳定性能和加工性能，降低其吸水率。     

Amide-containing segmented copolymers

This review highlights the synthesis, physical properties, and emerging technologies of state-of-the-art segmented copolymers containing amide hydrogen bonding sites. Amide hydrogen bonding plays a crucial role in the physical properties associated with amide-containing segmented copolymers. Amide hard segments are accessible in many different forms from amorphous alkyl amides to crystalline aramids and greatly influence copolymer morphology and mechanical properties. Variations in copolymer structure allow for the fine tuning of physical properties and the ability to predict mechanical performance based upon structural modifications. This review includes various synthetic methods for producing well-defined amide-containing segmented copolymers as well as common applications. Also, the morphological and mechanical properties associated with modifications in copolymer structure are discussed.     

Metal complexation studies of amylopectin‐graft‐poly[(N,N‐dimethylacrylamide)‐co‐(acrylic acid)]: a biodegradable synthetic graft copolymer

Synthesis of amylopectin‐graft‐poly[(N,N‐dimethylacrylamide)‐co‐(acrylic acid)] was carried out using solution polymerization technique with potassium persulfate as the initiator. The graft copolymer was characterized by measuring molecular weight using size exclusion chromatography, thermal analysis and Fourier transform infrared (FTIR) spectroscopy. The synthetic graft copolymer was used for the removal of some potentially toxic metal ions, Cu(II), Zn(II) and Ni(II), from their aqueous solutions. Various operating parameters like the amount of adsorbent, solution pH, contact time and temperature were studied. The adsorption data were well described by the pseudo‐second‐order and Langmuir isotherm models. Metal complexation studies were carried out experimentally using cyclic voltammetry and UV‐visible and FTIR spectroscopies. The metal complex structure was also studied theoretically using density functional theory with the Gaussian 09 program and the geometry of the complex structure was optimized. The metal complexation ability of the graft polymer was in the order Cu(II) > Ni(II) > Zn(II). Calculation of the various thermodynamic parameters was also done. The negative value of free energy change indicates the spontaneous nature of the adsorption. © 2015 Society of Chemical Industry     

Polydimethylsiloxane macromonomer bearing N‐vinylcaprolactam as end group: thermosensitive graft copolymers via free radical polymerization

A polydimethylsiloxane macromonomer was synthesized via anionic ring‐opening polymerization of hexamethylcyclotrisiloxane using N‐vinylcaprolactam anion as initiator and trimethylsilyl chloride as terminating agent. The polydimethylsiloxane macromonomer was copolymerized with N‐vinylcaprolactam in different molar ratios via a free radical mechanism. The new class of graft copolymers thus obtained shows cloud points in water because of an excess of N‐vinylcaprolactam units in the polymer chain. These cloud points can be shifted using randomly methylated β‐cyclodextrin as complexing agent. © 2015 Society of Chemical Industry     

The improvement of electro‐optical properties of polymer‐dispersed liquid crystals with graft copolymer matrix synthesized by reversible addition–fragmentation chain transfer and atom transfer radical polymerization

Aiming to decrease the memory effect of polymer‐dispersed liquid crystals (PDLCs), a type of graft macroinitiator, synthesized by reversible addition–fragmentation chain transfer and atom transfer radical polymerization, was employed to prepare PDLCs with graft copolymer matrix in our previous work. Compared with linear copolymer matrix PDLCs prepared using a linear macroinitiator, it was found that, although low‐memory‐effect PDLCs were obtained, the driving voltage and transmittance of the PDLCs were unfortunately sacrificed to some extent. Thus, it is necessary to improve the electro‐optical properties of PDLCs on the basis of the original research performed by us. In the work reported in this article, a kind of linear macroinitiator with high refractive index and another graft macroinitiator with flexible branched chains were employed to prepare PDLCs. The results showed that by using mixed macroinitiators, the electro‐optical properties of PDLCs could be improved, and a possible mechanism is proposed.     

Synthesis and characterization of copolymers with the same proportions of polystyrene and poly(ethylene oxide) compositions but different connection sequence by the efficient Williamson reaction

The AB type diblock PS‐b‐PEO and ABA type triblock PS‐b‐PEO‐b‐PS copolymers containing the same proportions of polystyrene (PS) and poly(ethylene oxide) (PEO) but different connection sequence were synthesized and investigated. Using the sequential living anionic polymerization and ring‐opening polymerization mechanisms, diblock PS‐b‐PEO copolymers with one hydroxyl group at the PEO end were obtained. Then, using the classic and efficient Williamson reaction (realized in a ‘click’ style), triblock PS‐b‐PEO‐b‐PS copolymers were achieved by a coupling reaction between hydroxyl groups at the PEO end of PS‐b‐PEO. The PS‐b‐PEO and PS‐b‐PEO‐b‐PS copolymers were well characterized by ¹H NMR spectra and SEC measurements. The critical micelle concentration (CMC) and thermal behaviors were also investigated by steady‐state fluorescence spectra and DSC, respectively. The results showed that, because the PEO segment in triblock PS‐b‐PEO‐b‐PS was more restricted than that in diblock PS‐b‐PEO copolymer, the former PS‐b‐PEO‐b‐PS copolymer always gave higher CMC values and lower crystallization temperature (T_c), melting temperature (T_m) and degree of crystallinity (X_c) parameters. © 2015 Society of Chemical Industry     

One-pot synthesis of soluble wholly aromatic liquid crystalline copoly(ester amide)s with high thermal and dimensional stability

Abstract

Thermotropic liquid crystalline polymers (LCPs) have been of great interest for electronic packaging. Herein, we introduce a series of wholly aromatic, thermotropic LCPs from copoly(ester amide)s of 6-hydroxy-2-naphthalic acid, isophthalic acid, terephthalic acid, and 4-aminophenol, prepared by a convenient one-pot melt polycondensation. Almost synthesized copoly(ester amide)s exhibited good solubility in common organic solvents at room temperature. Furthermore, they possessed high thermal stability with 2% degradation temperatures (T_id) of 359–368?°C and the char yields (at 600?°C) of 50.3–55.6%. The synthesized copoly(ester amide)s had relatively low coefficient of thermal expansion (CTE) values, which were 35.85–41.21?ppm °C^?1 in the temperature range of 50–200?°C. Furthermore, an annealing process could be employed to improve the thermomechanical properties of synthesized polymers. For instance, the CTE of sample LCP3 in range temperature of 275–315?°C was reduced by more than 90% after annealing at 320?°C for 1?h, implying the feasibility for electronic packaging.