CaO—SiO2-FeO—Cl体系中Zn、Pb挥发物的热力学研究

应用FaetSage热力学软件对不同温度下的FeO—CaO—SiO2-Cl体系中Zn、Ph挥发行为进行分析,采用气流携带法对FeO—CaO-SiO2-Cl体系中Zn、Pb挥发物的饱和蒸气压进行测定,并通过试验分析了温度对其体系中Zn、Pb挥发率的影响。结果表明,温度为970～1030K条件下FeO-CaO-SiO2-Cl体系中Zn、Pb主要以氯化物形式存在,氯化物的饱和蒸气压均随着温度的升高而增加,且InP～1／T呈较好的线性关系,其体系中Zn、Pb挥发率亦随着温度的升高而增加。     

FeO-CaO-SiO2-Al2O3-ZnO—PbO-Cl体系中Zn、Pb氯化物饱和蒸气压的测定

采用气流携带法对FeO-CaO-SiO2-Al2O3-ZnO-PbO-Cl体系中Zn、Pb氯化物的饱和蒸气压进行测定,并对温度、渣成分、Cl含量等影响因素进行了分析。结果表明,温度为970～1030K条件下FeO-CaO-SiO2-Al2O3-ZnO-PbO-Cl体系中Zn、Pb氯化物饱和蒸气压均随着温度的升高而增加,且P1）氯化物蒸气压值的对数与温度的倒数之间呈较好的线性关系。碱度、FeO含量均对Zn、Pb氯化物的饱和蒸气压影响很大,低碱度可提高Zn、Pb氯化物的饱和蒸气压,高FeO含量虽可增加ZnCl2饱和蒸气压,却降低了Pb氯化物的饱和蒸气压。Cl含量越高,该体系中Zn、Pb氯化物的饱和蒸气压越大。     

蒸发过程中饱和土壤水稳定同位素运移规律浅析

基于Fick定律和质量守恒定律推导了饱和土壤水在蒸发过程中的稳定同位素微分方程模型,分析了饱和土壤水的边界条件,给出了解析解,为数值模拟蒸发、蒸发过程中土壤水的稳定同位素组成变化提供了确定性的数学基础,对土壤水分运动以及土壤水稳定同位素的研究具有一定的理论意义.     

冻结方式影响试样内部结构变化的CT研究

利用CT技术可以在不破坏土体结构的情况下,连续不间断的观测到土体试样内各局部区域参数的变化.研究了两种粉质黏土试样分别以不同冻结方式进行冻结,并对试样进行了无损CT扫描,比较了冻结前后的CT数变化,由此定量得到试样内部各区域含水量和干密度的变化程度.结果表明:对于初始均匀的试样而言,不同冻结方式,对试样冻结后其内部含水量和干密度的变化的影响程度及趋势是不同的,比较而言,轴向冻结方式对冻土试样内部含水量的变化影响要小于径向冻结方式.     

膨胀石墨的饱和吸附量与微观结构的关系

采用不同的方法测定膨胀石墨对不同油质的饱和吸附量,来探讨膨胀石墨的结构与饱和吸附量的关系.由扫描电镜可知,膨胀石墨具有较大的比表面积,其孔结构是以中、大孔为主;蠕虫石墨的表面结构与其内部结构不同,其内部为典型的片层结构.通过观察石墨内部孔结构特征变化,可以分析膨胀石墨对油的去除效率以及影响因素.     

Enhancement of radiation‐resistant effect in ethylene–vinyl acetate copolymers by the formation of ethylene–vinyl acetate copolymers/clay nanocomposites

Ethylene–vinyl acetate (EVA) copolymers/clay nanocomposites, prepared by using nonreactive organophilic clay and reactive organophilic clay, were characterized by X‐ray diffraction and by high‐resolution transmission electron microscopy. The influence of gamma irradiation on the structure and properties of the pure EVA and EVA/clay nanocomposites was systematically investigated. In the presence of gamma radiation, the clay can effectively restrain the increase of the storage modulus of EVA/clay nanocomposites, which was supported by dynamical mechanical analysis. Gamma irradiation had almost no effect on the thermal properties of EVA/clay nanocomposites by using nonreactive organophilic clay, but it obviously improved the thermal stability of EVA/clay nanocomposites by using reactive organophilic clay. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2532–2538, 2005     

Preparation and characterization of carboxymethyl konjac glucomannan/sodium montmorillonite hybrid films

Carboxymethyl konjac glucomannan (CKGM)/ sodium montmorillonite (MMT) hybrid films of various compositions were prepared by casting from a polymer/silicate water suspension. The structure and properties of the hybrid films were investigated by wide angle X‐ray diffraction (WAXD), transmission electron microscopy (TEM), attenuated total reflection infrared spectroscopy (ATR‐IR), differential scanning calorimetry (DSC), and tensile tests. The results from WXRD and TEM indicated that an intercalated CKGM/MMT nanocomposite film was obtained by polymer solution intercalation. WXRD and DSC showed that the high‐T_m crystal phase was induced by the presence of lower MMT loading, but the T_m of the hybrid films became weak with the increase of MMT content due to the polymer confinement. The hybrid films showed higher thermal stability and mechanical properties than that of the neat polysaccharide due to the strong interaction between hydroxyl and carbonyl group of CKGM and the silicate layer of MMT. Furthermore, the degree of swelling of the hybrid films was investigated in acidic buffer solutions. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2954–2961, 2007     

Morphology and mechanical properties of polypropylene/organoclay nanocomposites

Polypropylene (PP) nanocomposites were prepared by melt intercalation in an intermeshing corotating twin‐screw extruder. The effect of molecular weight of PP‐MA (maleic anhydride‐ modified polypropylene) on clay dispersion and mechanical properties of nanocomposites was investigated. After injection molding, the tensile properties and impact strength were measured. The best overall mechanical properties were found for composites containing PP‐MA having the highest molecular weight. The basal spacing of clay in the composites was measured by X‐ray diffraction (XRD). Nanoscale morphology of the samples was observed by transmission electron microscopy (TEM). The crystallization kinetics was measured by differential scanning calorimetry (DSC) and optical microscopy at a fixed crystallization temperature. Increasing the clay content in PP‐ MA330k/clay, a well‐dispersed two‐component system, caused the impact strength to decrease while the crystallization kinetics and the spherulite size remained almost the same. On the other hand, PP/PP‐MA330k/clay, an intercalated three‐component system containing some dispersed clay as well as the clay tactoids, showed a much smaller size of spherulites and a slight increase in impact strength with increasing the clay content. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1562–1570, 2002     

Preparation and properties of styrene–butadiene rubber based nanocomposites: The influence of the structural and processing parameters

Rubber‐based nanocomposites were prepared with octadecyl amine modified sodium montmorillonite clay and styrene–butadiene rubber with different styrene contents (15, 23, and 40%). The solvent used to prepare the nanocomposites, the cure conditions, and the cure system were also varied to determine their effect on the properties of the nanocomposites. All the composites were characterized with X‐ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, and transmission electron microscopy (TEM). The XRD studies revealed exfoliation for the modified clay–rubber composites. The TEM photomicrographs showed a uniform distribution of the modified clay in the rubber matrix. The thickness of the particles in the exfoliated composites was around 10–15 nm. Although the FTIR study of the unmodified and modified clays showed extra peaks due to the intercalation of the amine chains into the gallery, the spectra for the rubber–clay nanocomposites were almost the same because of the presence of a very small amount of clay in the rubber matrix. All the modified clay–rubber nanocomposites displayed improved mechanical strength. The styrene content of the rubber had a pronounced effect on the properties of the nanocomposites. With increasing styrene content, the improvement in the properties was greater. Dicumyl peroxide and sulfur cure systems displayed similar strength, but higher elongation and slightly lower modulus values were obtained with the sulfur cure system. The curing of the samples at four different durations at 160°C showed that the cure time affected the properties. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 698–709, 2004     

Effect of montmorillonite on the swelling behavior and drug‐release behavior of nanocomposite hydrogels

A series of nanocomposite hydrogels were prepared from various ratios of N‐isopropylacrylamide (NIPAAm) and organic montmorillonite (MMT). The influence of the extent of MMT in the NIPAAm/MMT nanocomposite hydrogels on the physical properties and drug‐release behavior was the main purpose of this study. The microstructure and morphology were identified by X‐ray diffraction (XRD) and scanning electronic microscopy (SEM). The results showed that the swelling ratios for these nanocomposite hydrogels decreased with increase in the content of MMT. The gel strength and Young's modulus of the gels also increased with increase in the content of MMT. XRD results indicated that the exfoliation of MMT was achieved in the swollen state. Finally, the drug‐release behavior for the gels was also assessed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3652–3660, 2003