Effects of organophilic clay on the solvent‐maintaining capability,dimensional stability,and electrochemical properties of gel poly(vinylidene fluoride) nanocomposite electrolytes

Four quaternary alkyl ammonium salts were used in an organophilic procedure, performed on montmorillonite clay, and resulted in intercalation in dimethylformamide (DMF) or ethylene carbonate (EC)/propylene carbonate (PC) as a cosolvent between poly(vinylidene fluoride) (PVdF) and the organophilic clay. An examination using X‐ray diffraction revealed that PVdF entered galleries of montmorillonite clay, and it exhibited exfoliation and intercalation phenomena when it was analyzed with transmission electron microscopy. Gel PVdF nanocomposite electrolyte materials were successfully prepared by the addition of the appropriate percentages of DMF or PC/EC as a cosolvent, organophilic clay, and lithium perchlorate to PVdF. The maximum ionic conductivity was 1.03 × 10^?2 S/cm, and the materials exhibited better film formation, solvent‐maintaining capability, and dimensional stability than electrolyte films without added organophilic clays. The results of cyclic voltammetry testing showed that the addition of the organophilic clays significantly enhanced the electrochemical stability of the polymer electrolyte system. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3873–3882, 2002     

Organic clays. Synthesis and structure of Na5[calix[4] arene sulfonate] · 12 H2O,K5[calix[4]arene sulfonate]·8 H2O,Rb5[calix[4]arene sulfonate]·5 H2O,and Cs5[calix[4] arene sulfonate] ·4 H2O

The title calixarenes all exist in the solid state as bilayers of anionic calixarenes in the cone configuration. These layers alternate with inorganic regions which contain the cations and the water molecules. The overall structures bear a close resemblance to those found for clay minerals. The sodium salt crystallizes in the triclinic space groupP witha = 10.998(6),b = 13.582(5),c = 14.472(5) Å, = 74.01(3), = 89.09(4), = 86.50(4)°, andZ = 2 forD _calc = 1.72 g cm^–3. Refinement based on 4727 observed reflections led to a conventionalR = 0.050. The potassium salt crystallizes in the triclinic space groupP witha = 11.815(9),b = 13.636(6),c = 14.040(9) Å, = 100.24(5), = 111.86(9), = 95,14(9)°, andZ = 2 forD _calc = 1.77 g cm^–3. Refinement based on 2977 observed reflections led toR = 0.15. The rubidium and cesium salts are isostructural and crystallize in the monoclinic space groupP2₁/n with parameters for Rb[Cs]a = 11.603(5) [11.704(3)],b = 28.607(8) [29.747(9)],c = 12.512(5) [12.604(4)] Å, = 91.70(4) [91.63(2)°], andZ = 4 forD _calc = 2.01 [2.24] g cm^–3. Refinement based on 1750 [4257] observed reflections led toR = 0.108 [0.075]. Disorder of the cations was observed for the rubidium and cesium salts. Supplementary Data relating to this article are deposited with the British Library as Supplementary Publication No. SUP 82074 (95 pages).     

Synthesis and characterization of hybrids derived from vermiculite chloropropyl and aliphatic diamines

Silylation of vermiculite surface with organosilane (H₃CO)₃SiR, being R is the corresponding organic moieties –CH₂CH₂CH₂Cl, were carried out to yield organofunctionalized nanomaterial, named as VCl. The product reacted subsequently with three aliphatic diamines H₂N (CH₂)_nNH₂ (n=2, 4 and 6). The new hybrids were characterized by elemental analysis, infrared spectroscopy, X-ray diffraction and thermogravimetry. The grafting chloro derivates onto surface amounted to 2.1 mmol g^–1. The incorporation of alkyl amines was more effective for butyl>ethylene>hexyldiamines. The sequence is in agreement with thermogravimetry and elemental analysis data.     

Adsorption of nitrobenzene andn-pentanol from aqueous solution on hydrophilic and hydrophobic clay minerals

The sorption of nitrobenzene andn-pentanol from dilute aqueous solution on swelling clay minerals and their organophilized derivatives (organo clays) was studied. Adsorption excess isotherms were obtained by the immersion method. The basal spacings of the clay minerals were determined by X-ray diffraction measurements. By combining these two independent methods, composition and structure of the interlamellar space could be calculated. On the hydrophilic surface of montmorillonite negative adsorption of the organic component was observed at low molar fractions of nitrobenzene or pentanol, i.e., water was preferentially adsorbed. On organophilized montmorillonite and vermiculite adsorption of nitrobenzene and pentanol was positive over the whole range of liquid composition. The amount of interlamellar alkyl chains which is determined by the surface charge of clay mineral inversely affected the adsorption of both solutes.     

聚合物基粘土纳米复合材料的流变行为研究

聚合物基粘土纳米复合材料具有与常规颗粒填充体系类似的流变特性 :在整个频率范围内 ,储能模量和损耗模量均随粘土含量的增加而变高 ,其频率依赖性会表现出非未端行为 :且当粘土含量超过临界值以后 ,储能模量会在低频区表现出似固体的平台发展。但与之不同的是前者在低粘土含量的条件下 (<10 % (wt) )就会表现出似固体行为或非末端行为。这些流变特性还会受到粘土的径厚比、化学特性、聚合物基体的分子结构参数和粘土与基体间的相互作用强度等因素的影响。聚合物基粘土纳米复合材料的流变行为是与其微观结构的形成和演化以及聚合物分子链在特定环境下的粘弹松弛过程紧密联系在一起的。本文综述了插层型、剥离型和聚合物分子链一端受限剥离型聚合物基粘土纳米复合材料在力场作用下的流变特性和粘弹松弛机理方面的研究进展。     

(R)-(+)-[VCD(+)945]-4-Ethyl-4-methyloctane, the simplest chiral saturated hydrocarbon with a quaternary stereogenic center

Enantiopure (R)-(+)-[VCD(+)945]-4-ethyl-4-methyloctane, the simplest chiral saturated hydrocarbon with a quaternary stereogenic center, was synthesized by the use of MαNP acid method, and its absolute configuration was first unambiguously determined by the ¹H NMR anisotropy, X-ray crystallography, and VCD methods.     

Properties of rubber filled with montmorillonite with various surface modifications

Layered silicate/natural rubber composites were prepared by direct polymer melt intercalation. Na‐montmorillonite Kunipia‐F and its organic derivates (organo‐clays) prepared by ion exchange were used as clay fillers. Silica (SiO₂) Ultrasil VN3, a filler commonly used in the rubber industry, was used in combination with clay fillers. The effect of clay or organo‐clay loading from 1 up to 10 phr without (0 phr) or with silica (15 phr) showed significant improvement of the tensile properties (stress at break, strain at break and modulus M100). Modification of montmorillonite by three alkylammonium cations with the same length of alkylammonium chain (18 carbons) and different structure resulted in altered reinforcing and plasticizing effects of the filler in composites with rubber matrix. Copyright © 2011 John Wiley & Sons, Ltd.     

Impact of spectral saturation on leaf area index and aboveground biomass estimation of winter wheat

ABSTRACT

The saturation problem associated with the use of normalized difference vegetation index for crop variable estimation is well known. However, its physical mechanism is not systemically explored. The wavebands computing the vegetation indices also suffered saturation when the leaf area index and aboveground biomass reached to 2.5 and 1 kg m^?2, respectively. We thought that the saturation might be not only referred to normalized difference vegetation index, but also to certain wavebands. Furthermore, the performances of seven different vegetation indices were assessed on overcoming the saturation. The findings will improve our understanding of the spectral saturation.     

NATURAL-CONVECTION AND DROP MORPHOLOGY IN LIQUID-LIQUID DIRECT CONTACT

An optical Fourier transform system is applied to visualize natural-convectire flow patterns inside an evaporating liquid drop floating on an immiscible liquid. Strong cellular convective patterns prevail inside the drop at room temperature, which play an important role in the evaporation of the drop. A grating-shearing interferometry with a 4t system is developed for a real-time determination of a change in the drop morphology during the process of evaporation. Various types of drop geometry, which are derived from the moire fringes, are identified. An unstable, interfacial evaporation mode is disclosed and the mechanism for the augmentation of drop evaporation is determined. The study has potential applications in the process industry and in environmental control.     

饱和砂岩的滞弹性弛豫衰减特征及微观机理的探索

应用Metravib热机械分析仪,以饱和岩石进行正弦波加载的方式, 分别对三种不同孔隙度的泵油饱和彭山砂岩、泵油和甘油饱和自贡长石砂岩进行了衰减实验研究,得到衰减的热弛豫规律.据此规律求得它们的激活能和原子振动频率, 其激活能和原子的振动频率比间隙原子的激活能和振动的频率低, 此现象用饱和砂岩中产生的缺陷原子簇的整体振动比单个或孤立的原子的振动频率低做出了解释. 在饱和岩石的晶粒间界缺陷处参与扩散的是固体原子、液体及气体原子. 并得出随孔隙度和黏滞系数增大,衰减强度和激活能增大,原子的振动频率增高,弛豫时间减小的结论. 在正弦波应力作用下,由多种矿物晶体胶结而成的饱和砂岩是一种多晶、多相的固体, 由于内部结构复杂、缺陷广布,产生弛豫衰减是普遍现象.砂岩中存在点缺陷、位错、 晶界及孪晶界面等许多缺陷及缺陷间的相互作用都可以产生弛豫型衰减峰. 用饱和砂岩中特有的饱和液体及砂岩内部结构的复杂性解释了饱和砂岩的衰减机理, 很自然地将其宏观衰减特征与微观结构紧密连在一起.饱和砂岩中的各种缺陷、 相界等会导致多重弛豫,使它们的弛豫衰减峰变宽,分布参数增大.这项研究既具有理论意义,也具有实用价值.