Growth of organic films on indoor surfaces

We present a model for the growth of organic films on impermeable indoor surfaces. The model couples transport through a gas‐side boundary layer adjacent to the surface with equilibrium partitioning of semivolatile organic compounds (SVOCs) between the gas phase and the surface film. Model predictions indicate that film growth would primarily be influenced by the gas‐phase concentration of SVOCs with octanol‐air partitioning (K_oa) values in the approximate range 10≤log K_oa≤13. Within the relevant range, SVOCs with lower values will equilibrate with the surface film more rapidly. Over time, the film becomes relatively enriched in species with higher log K_oa values, while the proportion of gas‐phase SVOCs not in equilibrium with the film decreases. Given stable airborne SVOC concentrations, films grow at faster rates initially and then subsequently diminish to an almost steady growth rate. Once an SVOC is equilibrated with the film, its mass per unit film volume remains constant, while its mass per unit area increases in proportion to overall film thickness. The predictions of the conceptual model and its mathematical embodiment are generally consistent with results reported in the peer‐reviewed literature.     

A review on carbon nanotube/polymer composites for organic solar cells

Carbon nanotubes (CNTs) have unique properties, such as their electrical conductivity, that enable them to be combined with conducting polymers to form composites for use in organic solar cells (OSCs). It is envisaged that the improved composite has a higher efficiency of green energy and will reduce the cost of these cells. The use of such alternative energy sources also drastically reduces overuse of fossil fuels and consequently limits environmental degradation. This review compares research and performance between conventional silicon solar cells and OSCs. It also discusses OSC photoexcitation and charge carrier generation with the incorporation of CNTs, physicochemical properties of the composites and other factors that affect the efficiencies of OSCs. In addition, properties of CNTs that favour their dispersion in polymer matrices as acceptors and charge carriers to the electrodes are covered. The effects of CNTs containing dopants, such as nitrogen and boron, on charge transfer are discussed. Also, the fabrication techniques of OSCs that include CNT/polymer composite processing and the methods of film deposition on the substrate are described. Finally, the case studies of OSCs containing polymers with single‐walled CNTs, double‐walled CNTs or multi‐walled CNTs are evaluated. Copyright © 2014 John Wiley & Sons, Ltd.     

Analysis on effect of electroless coated SiCp on mechanical properties of polymer matrix composites

ABSTRACT

The versatility of polymer matrix composites in industrial applications has gained reputation and adaptability among advanced materials. Still, treatment of reinforcement for these composites has emerged as a vital domain to be explored. With a continuance to this fact, the present paper aims to analyze the effect of reinforced electroless coated silicon carbide particulates on mechanical properties of composites. The composite is developed using epoxy polymer as matrix and glass fibers as primary reinforcement. The electroless coated and uncoated silicon carbide particulates were used as secondary reinforcement. The phase identification of copper on secondary reinforcement was identified using X-ray powder diffraction technique. Fracture analysis during tensile testing and bonding behavior between matrix and reinforcement is examined using field emission scanning electron microscopy with energy dispersive spectroscopy. The presence of copper particles on secondary reinforcement results in improved interfacial bonding and resistance against fracture during loading.     

[2.2]Paracyclophane as a Target of the Organic Solid State: Emergent Properties via Supramolecular Construction

In this account, we review the synthesis of [2.2]paracyclophanes in the organic solid state. Reactions in crystalline solids provide a means to obtain molecules with high degrees of stereocontrol that can also be unattainable in solution. We show that [2.2]paracyclophanes form in the solid state stereospecifically and in quantitative yield via intermolecular [2+2] double photodimerization reactions. The double cycloaddition that affords a paracyclophane in the solid state does not readily occur in solution. Small molecules in the form of hydrogen-bond-donor templates can provide access to [2.2]paracyclophanes in a solid by design. A [2.2]paracyclophane obtained using a hydrogen-bond template is shown to exhibit attractive optical properties and has been employed as a building block of a metal-organic framework (MOF).     

Polymerized ionic liquids with guanidinium cations as host for gel polymer electrolytes in lithium metal batteries

Polymerized ionic liquids (PILs) having guanidinium cations with different counter‐anions, such as PF₆^? and N(CF₃SO₂)₂^? (TFSI^?), were synthesized by copolymerization of a guanidinium ionic liquid monomer with methyl acrylate followed by an anion exchange reaction. Furthermore, incorporating a guanidinium ionic liquid, LiTFSI salt and nano‐size SiO₂, a quaternary gel polymer electrolyte based on one of the PILs as the polymer host was prepared. The quaternary gel polymer electrolyte was chemically stable even at a higher temperature of 80 °C in contact with the lithium anode. In particular, the electrolyte exhibited high lithium ion conductivity, wide electrochemical stability window and good lithium stripping/plating performance. Li/LiFePO₄ batteries with the quaternary gel polymer electrolyte at 80 °C had capacities of 140 and 130 mA h g^?1 respectively at 0.1 and 0.2 C current rates. Copyright © 2011 Society of Chemical Industry     

Corrosion protection of mild steel with nanofibrous polyaniline-based coatings

Polyaniline (PANI) nanofibers were successfully synthesized by a modified rapid mixing method, that is, by the rapid mixing of solutions of aniline and ammonium peroxydisulfate in either hydrochloric acid or filtrates of oxidative polymerization of aniline. Scanning electron microscopy examination showed that nanofibrous PANI products were achieved in all cases; this indicated that the initially presented excessive anions and cations had no evident effect on the formation of nanosized PANI. The nanofibrous PANI exhibited excellent dispersability in both water and organic solvents, and an ultraviolet–visible spectrum was successfully recorded by dispersion in cyclohexanone. Composite coatings were fabricated with the dispersions of nanofibrous PANI and solutions of epoxy. Greatly enhanced corrosion protection performances were demonstrated by the coatings loaded with a small quantity of nanofibrous PANI. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

High-Valent Iron-Oxo and -Nitrido Complexes: Bonding and Reactivity

Multiple-bonded iron-oxo and -nitrido species have been identified or proposed as key intermediates in a range of important chemical transformations. The reported model complexes feature various coordination geometries and distinct electronic structures, and therefore exhibit diverse reactivity. The present contribution highlights the synergy from both experimental and theoretical standpoints to elucidate their different bonding situations and delineate their common mechanistic features in hydrogen-atom abstraction processes. Our analysis reveals that a radical centered on the abstracting atom E (E=O, N), which is generated via homolysis of covalent Fe−E bonds upon approaching the transition state, is an intrinsic C−H cleaving agent. The iron-oxo species is predicted to be more reactive than its nitride congener, in general, because the O−H bond formed in the H-atom transfer process is often stronger than the corresponding N−H bond.     

Comparison of the performance of masterbatch and liquid color concentrates for mass coloration of polypropylene

The properties of polypropylene (PP) mixed with masterbatch (MB) and liquid color concentrates (LCC), respectively, were compared by preparing samples of PP with MB and PP with LCC and neat PP as a reference material using 1–4 extrusion cycles. Two colors were examined, i.e., a white color consisting of pigment white 6, and a green color consisting of pigment white 6, pigment blue 15:3, and pigment green 7. The color difference between PP prepared with MB and LCC was determined and the mechanical, rheological, and crystalline properties of PP prepared with MB and LCC were found to be generic. The color of PP obtained from MB and LCC were comparable. Further, it was found that the tensile strength, the viscosity, and the crystal structure obtained were similar when using LCC instead of MB. The viscosity of the treated PP generally decreased with increasing extruder retention time due to thermal degradation. The tensile strength and the crystal structure were independent of increased extruder retention time. © 2015 Wiley Periodicals, Inc. Col Res Appl, 41, 484–492, 2016     

硼颗粒的包覆机理及工艺研究进展

阐述了不同包覆材料对硼颗粒的包覆机理,从5个方面总结了硼颗粒包覆材料的选取原则,包括:去除硼颗粒表面氧化膜、提高燃烧温度、降低硼的点火温度、提高表面相容性、催化硼颗粒的氧化反应。总结了沉淀法、表面反应包覆法、高分子吸附聚合法、气相包覆法和机械球磨法等多种硼颗粒包覆工艺的研究状况,分析并比较了不同工艺的作用机理和实际应用效果。介绍了现代硼颗粒表面包覆效果测试技术的特点和应用范围。评述了目前硼颗粒包覆技术的研究现状和不足,并对未来的研究方向进行了展望。     

Soft Matter Technology at KIT: Chemical Perspective from Nanoarchitectures to Microstructures

Bioinspiration has emerged as an important design principle in the rapidly growing field of materials science and especially its subarea, soft matter science. For example, biological cells form hierarchically organized tissues that not only are optimized and designed for durability, but also have to adapt to their external environment, undergo self‐repair, and perform many highly complex functions. Being able to create artificial soft materials that mimic those highly complex functions will enable future materials applications. Herein, soft matter technologies that are used to realize bioinspired material structures are described, and potential pathways to integrate these into a comprehensive soft matter research environment are addressed. Solutions become available because soft matter technologies are benefitting from the synergies between organic synthesis, polymer chemistry, and materials science.