A Highly Sensitive,Reversible, and Bidirectional Humidity Actuator by Calcium Carbonate Ionic Oligomers Incorporated Poly(Vinylidene Fluoride)

Sensitivity and multi-directional motivation are major two factors for developing optimized humidity-response materials, which are promising for sensing, energy production, etc. Organic functional groups are commonly used as the water sensitive units through hydrogen bond interactions with water molecules in actuators. The multi-coordination ability of inorganic ions implies that the inorganic ionic compounds are potentially superior water sensitive units. However, the particle forms of inorganic ionic compounds produced by classical nucleation limit the number of exposed ions to interact with water. Recent progress on the inorganic ionic oligomers has broken through the limitation of classical nucleation, and realized the molecular-scaled incorporation of inorganic ionic compounds into an organic matrix. Here, the incorporation of hydrophilic calcium carbonate ionic oligomers into hydrophobic poly(vinylidene fluoride) (PVDF) is demonstrated. The ultra-small calcium carbonate oligomers within a PVDF film endow it with an ultra-sensitive, reversible, and bidirectional response. The motivation ability is superior to other bidirectional humidity-actuators at present, which realizes self-motivation on an ice surface, converting the chemical potential energy of the humidity gradient from ice to kinetic energy.     

使能未来工厂的5G能力综述

5G系统将移动通信服务从移动电话、移动宽带和大规模机器通信扩展到新的应用领域，即所谓对通信服务有特殊要求的垂直领域。对使能未来工厂的5G能力进行了全面的分析总结，包括弹性网络架构、灵活频谱、超可靠低时延通信、时间敏感网络、安全和定位，而弹性网络架构又包括对网络切片、非公共网络、5G局域网和边缘计算的支持。希望从广度到深度，对相关的理论及技术应用做透彻、全面的梳理，对其挑战做清晰的总结，从而为相关研究和工程技术人员提供借鉴。     

Characterization of an acrylic polymer under hygrothermal aging as an optically clear adhesive for touch screen panels

Optically clear adhesives (OCAs) are key components of touch screen panels (TSPs). It is important that OCAs do not affect the transparent electrodes in TSPs because OCAs are contacted to the transparent electrodes. Therefore, N-vinyl caprolactam (NVC) was incorporated in the composition of an acrylic pressure sensitive adhesive (PSA) with excluding an acidic component to maintain the cohesion for OCA preparation. With increasing amounts of NVC, the tack and peel strength of UV-cured PSA increased, but high amounts of NVC led to decreased peel strength. The UV-cured PSA films were placed in a high temperature and humidity chamber for 8 weeks to investigate the durability and corrosion property under hygrothermal conditions. In this study, the corrosion test method using copper foil was suggested as a simple and economical method and was used to evaluate the effect of NVC on the corrosion property of PSA. This method helped identify suitable OCAs that do not have corrosive property. PSA films containing more than 20 wt% of NVC promoted the corrosion of copper foil under hygrothermal aging conditions. The caprolactam ring was opened by moisture, and the PSA structure morphed into a polar structure during the aging process. This change caused a glass transition shift, an increase in the storage modulus at the rubbery plateau, and an increase in peel strength. The surface free energy of the PSA films also increased due to the increase in the polar property. However, high amounts of NVC caused a decrease in the peel strength after 8 weeks of aging because of increased molecular interactions.     

拟时移地震气藏剩余潜力研究

时移地震是一种有效的油气藏监测技术，但高投入和高风险造成目前时移地震资料缺乏。由于不同年度采集、处理参数不同，地震资料存在非一致性问题，不能有效开展剩余潜力研究。为此，选择了处于开发后期的南海Y气田，通过对2001年二维和2015年三维地震资料优选和优化，形成拟时移地震资料；再应用拟时移地震资料识别气水关系、划分气藏水侵模式，并利用分频能量属性，结合气田生产数据模拟气藏动态，明确了气藏剩余潜力区。研究结果表明，当前Y气田西北区域隔层为高渗滤型和渗滤型，气藏处于强水侵状态，剩余潜力有限；东南区域隔层为非渗透型，气藏处于水侵初期，剩余潜力大，可作为下一步挖潜目标区。拟时移地震的应用证明了其可作为当前时移地震研究的补充部分发挥重要作用。     

有机硅压敏胶的性能及影响因素

对有机硅压敏胶的几个影响因素进行了考察,在此基础上研制出一种有机硅压敏胶。乙烯基含量为0.3%的MQ硅树脂和相对分子质量为4.0×105的硅橡胶等比例配合,经1.0%的二丁基二月桂酸锡催化缩合,再以1.5%的BPO交联剂200℃下交联10min制得的有机硅压敏胶性能优异,初黏力25#,室温持黏力960min,剥离强度13.45N/25mm。     

Polyampholyte acrylic latexes for tablet coating applications

Polyampholyte latexes can exist within a certain pH range as low‐viscosity aqueous dispersions, while upon a pH shift to the vicinity of the isoelectric point they undergo ionic coacervation. Three classes of coacervation latexes were synthesized and evaluated for their suitability for use in tablet coating applications. Pharmaceutical tablet coatings are commonly based on hydroxypropyl methyl cellulose, poly(vinyl alcohol), and acrylic polymers. Because of the high viscosity of their aqueous solutions, and to the consequent required low concentrations of the tablet coating polymers in the coating solutions to enable sufficiently low viscosity for effective spray application, the current commercial pharmaceutical tablet coating technology requires the removal of large amounts of water during the manufacturing process. In this work, films prepared from high‐solids, low‐viscosity coacervated acrylic latexes showed good hardness, very low tackiness, an excellent combination of optical properties, and very low water vapor permeability. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40049.     

Effect of phenol end functional switching segments on the shape memory properties of epoxy‐cyanate ester system

The effect of phenol end functional shape memory oligomers on the shape memory properties of an epoxy‐cyanate ester resin system was examined. The basic resin system consisted of diglycidyl ether of bisphenol A (DGEBA) cured with bisphenol A dicyanate (BADC). For conferring the shape memory properties, the switching segment (SS) components selected are α, ω‐phenol‐terminated poly(tetramethyleneoxide) (PPTMO), poly(ε‐caprolactone) (PPCL), and poly(propylene glycol) (PPPG). Epoxy‐cyanate ester blend of defined composition was analyzed for thermal, mechanical, thermo‐mechanical, and shape memory properties at two concentrations of the three SSs. The transition temperature of heavily SS loaded matrix increased in the order: PPTMO < PPCL < PPPG commensurate with crystallizability of SS segments at ambient. For same reason flexural property showed an increasing trend. This is in league with the increased crystallizability of the shape memory polymer components. The shape fixity, recovery extent, and recovery time followed a reverse order: PPPG < PPCL < PPTMO. In contrast to the alcohol terminated shape memory components, phenol terminal groups were helpful in integrating the shape memory segments into the matrix by way of reaction with both epoxy and cyanate groups. The coreaction was conducive for achieving better shape memory properties and decreasing the transition temperature. A direct relation existed between the modulus ratio and the shape recovery property. Higher concentration of the SSs caused a diminution in transition temperature but enhanced the shape memory properties, though the mechanical properties were adversely affected. The shape recovery increased with increase in temperature. All polymers possessed good mechanical properties and thermal stability. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41196.     

Effect of diisocyanate on pyridine containing shape memory polyurethanes based on N,N‐bis(2‐hydroxylethyl)isonicotinamide

This article demonstrates a comparative investigation about the effect of diisocyanate on pyridine containing shape memory polyurethanes (Py‐SMPUs), which are synthesized with N,N‐bis(2‐hydroxylethyl)isonicotinamide (BINA) and four different diisocyanates: 1,6‐hexanediisocyante (HDI), isophorone diisocyanate (IPDI), methylene diphenyl diisocyanate (MDI), and tolylene diisocyanate (TDI). Results show that all BINA–SMPU systems have amorphous reversible phase. Comparatively, the MDI–BINA and TDI–BINA systems show higher T_g; and the HDI–BINA and IPDI–BINA systems show better thermal stability. In addition, the HDI–BINA and the IPDI–BINA systems exhibit good thermal‐induced shape memory effect and good moisture‐sensitive shape memory effect due to their better moisture absorption properties. Particularly, the HDI–BINA system has better response speed and better shape recovery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40721.     

Ethanol‐responsive characteristics of polyethersulfone composite membranes blended with poly(N‐isopropylacrylamide) nanogels

Ethanol‐responsive smart membranes with different microstructures are prepared from blends of polyethersulfone (PES) and poly(N‐isopropylacrylamide) (PNIPAM) nanogels by immersion precipitation phase inversion method in a convenient and controllable manner. The introduction of PNIPAM nanogels forms the microporous structures on the surface of the top skin layer and on the pore walls of the finger‐like porous sublayer of membranes. The ethanol‐responsive characteristics of the proposed PES composite membranes are systematically investigated. With increasing ethanol concentration in the range from 0 to 15 wt %, the trans‐membrane flux of ethanol solution increases. The microstructures and the resultant ethanol‐responsive characteristics of the composite membranes can be regulated by the content of PNIPAM nanogels blended in the membranes. The more the content of PNIPAM nanogels blended in the membranes, the more the number of the submicron pores is, and thus the better the ethanol‐responsive characteristics of the composite membranes. The proposed ethanol‐responsive smart membranes are expected to be combined with the traditional pervaporation membranes as a smart vavle to achieve continuous and highly efficient ethanol production during the biological fermentation. The preparation technique and results in this study provide valuable guidance for further design and the industrial‐scale fabrication of novel composite membranes for application in ethanol separation systems. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41032.