天然杜仲胶的改性及应用研究进展

杜仲胶（EUG）主要由反式聚异戊二烯组成,是一种具有良好生物相容性、橡塑二重性和优异力学性能的天然高分子材料。近年来,EUG在新型生物基材料领域备受瞩目。EUG在室温下结晶度高,表现为刚性塑料状态,极大程度限制了其在功能材料领域的应用。因此,将EUG进行物理或化学改性,进而拓宽其应用范围已成为近年来的研究热点。本文详细介绍了EUG分子链结构特点,随后从物理改性和化学改性两个方面系统论述了EUG常见的改性方法及机理,如通过与其它材料共混或环氧化改性、硫化改性等改变EUG的硬度及弹性。对EUG在绿色轮胎与公路建设、形状记忆与自修复材料、减震与吸声材料、医用材料、生物降解复合材料等新型功能材料领域的最新研究进展进行了综述,并在此基础上展望了EUG在生物基高性能材料领域的发展前景。     

Printability,shape-memory,and mechanical properties of PHB/PCL/CNFs composites

Shape-memory polymers have attracted attention as smart implant materials in recent years because they are lightweight, low-cost, easily processable, and because they undergo large deformation. Here, cellulose nanofibers (CNFs) were used as a reinforcement for polyhydroxybutyrate (PHB)/polycaprolactone (PCL) composites to improve mechanical properties. The composites were investigated by rheological tests, differential scanning calorimetry, dynamic mechanical analysis, mechanical property tests, and shape-memory tests. The printability of PHB/PCL/CNFs composites was demonstrated by using them to print interconnected porous structures with a gyroid surface. The results showed that the PHB/PCL (80:20) composites with 1 wt% CNF displayed the best comprehensive mechanical and shape-memory properties. As a functional verification, a model of the self-opening hand was fabricated by 3D printing, and its deformation and recovery capabilities were evaluated.     

石榴石型固态电解质Li7La3Zr2O12的改性研究现状

固态电解质是高安全性、高能量密度的全固态锂电池的核心部件,其典型代表Li₇La₃Zr₂O₁₂(LLZO)具有高离子电导率、高机械强度、高电化学稳定性、低界面阻抗以及对锂金属负极良好的稳定性等优势,是科研人员重点关注的对象之一,但与液态电解质相比,目前LLZO仍存在低离子电导率和与电极固-固界面接触等问题。本文主要简介了LLZO的晶体结构、改性方式等对其离子电导率及界面阻抗的影响,同时对LLZO现存的问题进行了总结,对LLZO的未来发展方向进行了展望,为探索全固态锂电池的实际生产应用提供理论指导。     

Cuprous-based composite ionic liquids for the selective absorption of CO: Experimental study and thermodynamic analysis

Three cuprous-based composite ionic liquids (ILs) [EimH][OAc]–xCuOAc (x = 0.5, 0.6, 0.7) were prepared and employed for efficient absorption of CO. It is shown that the cuprous composite IL [EimH][OAc]–0.6CuOAc exhibited the largest absorption capacity for CO (0.031 g/g at 293.15 K and 1 bar) and had a record CO/N₂ selectivity of 967, which is better than most of common ILs and solvents reported in the literature. The results of Fourier transform infrared (FTIR) spectra, electrospray ionization mass spectrometry (ESI-MS) analysis, and theoretical calculations reveal that such superior CO capacity mainly resulted from two kinds of chemical interaction between CO and the active anionic species [Cu(OAc)₂]⁻ in [EimH][OAc]–0.6CuOAc. Furthermore, a “deactivated IL model” was further proposed to accurately describe the absorption behavior of CO in [EimH][OAc]–0.6CuOAc, in which the thermodynamic parameters including Henry's law constants, reaction equilibrium constants, and absorption enthalpies were estimated by the correlation of the experimental solubilities of CO.     

阳离子型表面活性剂与聚合物复配体系协同减阻作用

为探究阳离子型表面活性剂和聚合物复配体系的协同减阻作用,以阳离子型表面活性剂十六烷基三甲基氯化铵（CTAC）和聚合物聚丙烯酰胺（PAM）为研究对象,设计搭建多功能湍流减阻实验测试装置,实验分析聚合物离子类型对复配体系协同减阻的影响,优选复配体系,进一步研究复配体系协同减阻作用随表面活性剂浓度、聚合物浓度、温度的变化规律。实验结果表明：CPAM-CTAC/NaSal复配体系协同减阻作用>AmPAM-CTAC/NaSal复配体系协同减阻作用>NPAM-CTAC/NaSal复配体系协同减阻作用>APAM-CTAC/NaSal复配体系协同减阻作用。CPAM-CTAC/NaSal复配体系的协同减阻作用在CTAC/NaSal浓度达到聚合物饱和浓度（PSP）0.3g/L时到达顶峰,平均减阻效率高达69.22%;当CTAC/NaSal浓度增加至0.5g/L后,平均减阻率迅速减小至10.08%,复配体系的临界广义雷诺数亦迅速降至7535.20,抗剪切性减弱。随着CPAM浓度由0.05g/L增加到0.2g/L,减阻破坏区减阻率可由9.08%增加至57.49%,临界广义雷诺数由31272.43增加到45033.36,抗剪切性增强;当CPAM浓度超过第二临界缔合浓度（CAC Ⅱ）0.15g/L后,减阻破坏区减阻率增加趋势及抗剪切性增强趋势均变缓。此外,相较于单一减阻剂,复配体系耐温性显著增强,55℃时最大减阻率增至69.05%。     

离子液体反应型萃取燃油脱硫研究进展

随着社会不断发展,汽、柴油的消耗量逐年增大,开发温和条件下对芳香族硫化物具有优异脱除性能的非加氢脱硫方法对我国汽、柴油标准升级具有重要意义。萃取脱硫法能够在室温常压条件下脱除油品中的芳香族硫化物,且能够通过萃取剂结构设计实现选择性脱硫。综述了近年来离子液体反应型萃取脱硫方法的研究进展,主要探讨了离子液体反应型萃取脱硫方法的原理和萃取作用机制,重点论述了离子液体反应型萃取脱硫方法中离子液体设计、氧化剂类型、外场强化作用、离子液体的分离回收等研究现状,分析了制约反应型萃取脱硫广泛工业化应用的瓶颈,并提出合适的解决策略,以期推动基于离子液体反应型萃取脱硫方法和技术的进一步工业化应用。     

离子液体型超级电容器软包高温老化性能评测研究

构筑了介孔炭,离子液体（EMIMBF₄）与泡沫铝极片结构的超级电容器软包（容量为40 F）,评测了其在2.7 V,65℃,1500 h老化实验中的性能。利用恒流充放电、恒流-恒压充放电模式评测,该电容器经过连续1500 h的高温处理后电容值衰减约10%,内阻增加比例低于40%。与传统的乙腈基电解液软包对比,虽然乙腈基软包起始内阻低,但产气多,且高温循环条件下容量衰减比例和内阻增加比例均劣于离子液体基电解液。上述对比说明,离子液体基电解液在泡沫铝三维导电导热结构的配合下,具有了良好的长周期循环性能。同时,由于其无毒性,可以用于封闭的楼宇空间或其他场所,提供本质安全性。     

Enhanced gravimetric CO2 capacity and viscosity for ionic liquids with cyanopyrrolide anion

Ionic Liquids (ILs) are considered as alternative solvents for the separation of CO₂ from flue gas due mainly to their CO₂ affinity and thermal stability. The cation architecture in a matrix of ammonium and mostly phosphonium‐based ILs with 2‐cyanopyrrolide as the anion to evaluate its impact on gravimetric CO₂ absorption capacity, viscosity, and thermal stability and the three fundamental properties vital for application realization are systematically investigated. Among the investigated ILs, [P2,2,2,8][2‐CNpyr] demonstrated the lowest viscosity, 95 cP at 40°C, and highest CO₂ uptake, 114 mg CO₂ per g IL at 40°C. Combined effects of asymmetry and the optimized chain lengths also resulted in improved thermal stability for [P2,2,2,8][2‐CNpyr], with a mass loss rate of 1.35 × 10^?6 g h^?1 (0.0067 mass % h^?1) at 80°C. © 2015 American Institute of Chemical Engineers AIChE J, 61: 2280–2285, 2015     

Mass‐transfer rate enhancement for CO2 separation by ionic liquids: Theoretical study on the mechanism

To promote the development of ionic liquid (IL) immobilized sorbents and supported IL membranes (SILMs) for CO₂ separation, the kinetics of CO₂ absorption/desorption in IL immobilized sorbents was studied using a novel method based on nonequilibrium thermodynamics. It shows that the apparent chemical‐potential‐based mass‐transfer coefficients of CO₂ were in three regions with three‐order difference in magnitude for the IL‐film thicknesses in microscale, 100 nm‐scale, and 10 nm‐scale. Using a diffusion‐reaction theory, it is found that by tailoring the IL‐film thickness from microscale to nanoscale, the process was altered from diffusion‐control to reaction‐control, revealing the inherent mechanism for the dramatic rate enhancement. The extension to SILMs shows that the significant improvement of CO₂ flux can be obtained theoretically for the membranes with nanoscale IL‐films, which makes it feasible to implement CO₂ separation by ILs with low investment cost. © 2015 American Institute of Chemical Engineers AIChE J, 61: 4437–4444, 2015     

Use of ionic liquids based on phosphonium salts for preparing biocomposites by in situ polymerization

A sodium montmorillonite, Dellite HPS, was modified with ionic liquids based on phosphonium salts, such as octadecyltriphenylphosphonium tetrafluoroborate and octadecyltriphenylphosphonium bromide. Thanks to their high thermal stability, these salts can be used during in situ polymerization, a method that favors the achievement of a good dispersion of the clay. Poly(1,4‐dimethylcyclohexane adipate) (PCHA), was chosen as an example of aliphatic polyester which can be a suitable matrix for new biocomposites with organo‐clays. The organo modified clays prepared were characterized by X‐ray diffraction (XRD), ATR‐FTIR spectroscopy, and thermal gravimetric analysis (TGA) while biocomposites were analyzed in terms of molecular structure, thermal and thermomechanical properties. The degree of dispersion of the clays in the polymer matrix was studied by XRD. The results show that the clays are well dispersed in the biocomposites, despite an intercalated structure highlighted by XRD analysis. Moreover, the clays confer a certain improvement in mechanical properties to the final materials. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42467.