粘土矿物用于乙烯聚合催化剂的研究 Ⅰ.以凹凸棒石粘土为载体的乙烯聚合催化剂

研究了以凹凸棒石粘土为载体,负载TiCl4制备的乙烯聚合催化剂的结构、性能及制备规律。结果表明,催化剂中Ti的负载量随焙烧温度的提高而逐渐降低,聚合活性随焙烧温度的提高呈上升趋势,但过高的焙烧温度也会导致粘土晶体结构的彻底破坏而不利于活化粘土活性的提高;通过采用烷基铝等有机金属化合物处理粘土同样可以极大地改善粘土性质,提高催化活性。不同助催化剂对以凹凸棒石粘土为载体的催化剂的聚合性能有较大影响。     

Electrochemical Aspects of Electroosmotic Dewatering of Clay Suspensions

An attempt is made to elucidate the electrochemical aspects of the electroosmotic dewatering (EOD) of clays as reported in some recent work, especially that on interrupted DC power electroosmotic dewatering published by Rabie, Mujumdar and Weber (2). These authors showed that the dewatering by EOD stops after the DC power has been on for several minutes or hours; on interruption of their power and on short-circuiting of the electrodes, conditions can be created again for some further dewatering by DC power EOD. This discovery, of Rabie et al. is interpreted as a fuel cell effect and it is shown that it affords clues to several other electrochemical strategies for the possible enhancement of the efficiency of the EOD by DC power.

Further, the open circuit potentials observed by Rabie et al. (2) on the interruption of DC power are given an electrochemical interpretation which leads to quantitative estimates in agreement with the experimental values.     

Ultrasound‐activated Knoevenagel condensation of malononitrile with carbonylic compounds catalysed by alkaline‐doped saponites

α,β‐Unsaturated nitriles have been synthesized by Knoevenagel condensation of a carbonylic compound with malononitrile, assisted by sonochemical irradiation. Two alkaline‐promoted clays (Li⁺‐ and Cs⁺‐exchanged saponites) have been employed as catalysts. The influence of the carbonylic compound (benzaldehyde or cyclohexanone) and the use of a solvent on the catalytic activity have been studied. Remarkable increase in the conversion values has been found when the reaction is activated by ultrasound, as compared with the thermal activation. In this green, solvent‐free procedure, α,β‐unsaturated nitriles have been produced in very high yields (97%) when the Cs⁺‐saponite is used as catalyst. Copyright © 2004 Society of Chemical Industry     

浅谈贵溪冶炼厂岩土工程勘察的几点体会

总结了贵溪冶炼厂岩土工程勘察工作中的一些经验，提出了在勘察中容易出现的若干问题及其处理方法。     

Metal sorption by biomass of melanin‐producing fungi grown in clay‐containing medium

The sorption of toxic metals by fungal mycelia grown in clay‐containing medium is reported in this work. Biomass of melanin‐producing microfungi of the genus Cladosporium (C cladosporioides, C resinae and C herbarum) and Aureobasidium pullulans, clay minerals and fungal mycelia grown in clay‐containing medium were compared for their equilibrium Cu and Cd uptake from pH‐buffered solutions using experimental sorption isotherms. Bentonite (Cherkassy) in the natural form was shown to be the best Cu sorbent compared with the other clays and clay minerals tested. Cu sorption isotherms fitted the Langmuir sorption model for all cases. Comparison of Cu and Cd uptake for biomass and bentonite showed a lower biomass uptake capacity but a considerably higher affinity of the biosorbent for the solute. The presence of kaolinite and palygorskite in the medium generally reduced both Cu and Cd sorption capacity and the metal‐binding ability of the fungal–clay mixtures. In contrast, addition of bentonite into the medium did not appreciably alter the Cd sorption ability but increased the sorption of Cu by A pullulans and C cladosporioides grown in this medium. A common feature for all fungi grown in the presence of bentonite was an increase in the Cu sorption capacity (Q_max) of the biomineral sorbents and a reduction in their affinity (Langmuir parameter b) compared with control biomass. A difference between predicted and experimental data obtained for biomass grown on bentonite medium was also observed. The connection between the sorption capacity of biomass grown in clay‐containing medium, mycelial morphology and the structure of fungal pellets is discussed and a mechanism for the changed sorption capacity of the combined biomineral sorbents is proposed which involves blocking or modification of binding sites on biotic and abiotic components of the ‘biomineral’ association. © 2002 Society of Chemical Industry     

Anhydrous esterification of myristic acid with propylene: Ion exchange resin and acid-treated clay as catalysts

Anhydrous esterification of myristic acid with propylene was carried out in the temperature range of 110–145°C and pressure from 190–195 psig in the presence of Amberlyst-15 (cation exchange resin) and Filtrol-24 (acid-treated clay) as catalysts. The product ester, isopropyl myristate finds use in cosmetic and topical medicinal preparations where good absorption through the skin is desired. Filtrol-24 is the catalyst of choice, and the recommended operating temperature is 130°C with a pressure of 190 psig.     

低电阻率气层测井评价方法

粘土矿物成份是造成气层电阻率低的主要原因。用灰色静态模型计算孔隙度，用BP神经网络计算束缚水饱和度等参数。与岩心分析结果比较，储层参数计算结果精度有所提高。用储层参数建立气层和水层的判别式，判别结果与试油有较好的一致性。综合数字处理结果建立了气层产能评价模型，处理结果与试油结果比较，符合率82％。     

稀土在搪瓷面釉上应用的研究

采用稀土氧化物和无机化合物的复合物（不简称ＲＩ－复合物）作为搪瓷釉浆悬浮剂，使之全部或大部分代替粘土，进行了一系列试验，已获得成功，突破了长期来搪瓷工业离不开粘土的传统工艺，并实现了工业化生产。     

用热失重法确定水合粘土水分含量及存在形式

文章以蒙脱土为例，采用热失重法定性定量确定了水合粘土中结合水类型、界限及其相对含量，并与等温吸附法结果进行了对比。结果表明，用该方法得到的水合蒙脱土中各种水分的相对含量及总含水量与等温吸附实验结果相一致。热失重（25~250 ℃）分析结果表明，水合蒙脱土中水分子主要存在自由水、松散吸附结合水、紧密吸附水（强吸附结合水）3种状态，分别对应于25~75 ℃、75~120 ℃、120~230 ℃区间里的失水。从热失重（25~250 ℃）规律来看，仍存在两个明显的转折点p/ps=0.9、0.98，它们为粘土-水体系的两个特征湿度，前者为粘土表面强结合水与松散结合水（渗透结合水）之间的界限，后者为松散结合水与自由水之间的界限，这验证了等温吸附法确定的两个特征湿度及对粘土表面结合水界限划分的正确性。     

New nanocomposite materials based on polymerization of [oligo(oxyethylene) methacrylates] in the presence of montmorillonite clay

Intercalation of poly[oligo(oxyethylene) methacrylates] onto sodium montmorillonite (MMT) clay has been investigated. A polymer–clay hybrid has been synthesized through intercalation of the monomer followed by its solution free‐radical polymerization. Eight polymer–clay hybrids were prepared using different weight ratios of clay, different oligo(oxyethylene) lengths and different proportions of crosslinker. Evidence of the development of nanostructures is obtained from scanning electron microscopy, and wide‐angle X‐ray diffraction studies support these results which show disappearance of the peak characteristic to d₀₀₁ spacing. In this hybrid MMT is dispersed homogeneously in the polymer matrix. © 2003 Society of Chemical Industry