KCl/NaCl/CPI复合盐阳离子聚合物钻井液在南海大斜度井段中的应用

为改善南海东部惠州25-8油田大斜度井因泥岩水化造浆而引起的井壁失稳和钻井液增稠影响携砂的问题,在现有成熟PLUS/KCl钻井液的基础上开展复合盐阳离子聚合物钻井液研究,对钻井液配方进行了优化,评价了优化后钻井液的流变性、抑制性、封堵性和润滑性,并在惠州油田进行了现场应用。结果表明,复合盐阳离子聚合物钻井液配方中,无机盐类抑制剂KCl和NaCl的适宜加量为3%和12%、有机阳离子聚合物抑制剂PF-CPI适宜的加量为2.0%。该钻井液抑制性强,防膨率高达93.32%,钻屑回收率87.56%;受到钻屑侵污后的钻井液流变性能波动小,仍具有较低的黏度和合适的切力,有利于大斜度井携砂;封堵性和润滑性均优于PLUS/KCl钻井液体系。现场应用2口井,钻井液流变性良好,平均起下钻速度提高,钻井过程顺利,无复杂情况发生。复合盐阳离子聚合物钻井液可改善南海大斜度井起下钻阻卡的问题。     

Highly efficient supported AlCl3-based cationic catalysts to produce polyα-olefin oil base stocks

The main aim of this research is to decrease the amount of AlCl₃ content that is very corrosive and hazardous in the catalytic system, required for the α-olefin oligomerization without substantial change of final oil features. This was successfully achieved by supporting AlCl₃ on different carriers. More precisely, a series of supported bimetallic catalysts was synthesized by immobilization of AlCl₃ and TiCl₄ onto Al₂O₃, SiO₂, and mixed supports, that is, Al₂O₃/FeCl₃ and SiO₂/FeCl₃. It was found that silica and alumina-based catalysts had higher catalytic activities compared to support free AlCl₃; however, this enhancement for silica-based supports was more significant. According to gel permeation chromatography (GPC) results, the use of single supports, that is, Al₂O₃ and SiO₂, increased oligomer's molecular weight, while the application of mixed supports resulted in the decrease of molecular weight of the oligomers. Viscosity characteristics of the synthesized oligomers have also been studied at two different temperatures of 40 and 100°C (KV⁴⁰ and KV¹⁰⁰). The viscosity index (VI) values, derived from KV⁴⁰ and KV¹⁰⁰, of the prepared oligomers were in the range of 126–145. The molecular weight and termination mechanisms of the oligomers were studied by ¹H-NMR spectroscopy. The obtained results disclosed that the employed reaction conditions led to the production of oligomer chains with various structures including vinylidene (Vd), and di and three-substituted vinylene (2Vn, 3Vn) structures.     

适用于“一步酸溶法”生产氧化铝工艺中稀释料浆的高分子絮凝剂的合成

为达到"一步酸溶法"生产氧化铝工艺中稀释料浆在高温、高酸度工况下进行固液高效分离的目的,以丙烯酰胺(AM)与阳离子(DMDAAC)为共聚单体,通过水溶液聚合法合成了阳离子聚丙烯酰胺(CPAM)絮凝剂。以转化率和相对分子质量为目标,通过单因素分析法确定了最优的合成工艺条件,即反应温度30℃,单体总质量分数为30%,阳离子度5%,K2S2O8和NaHSO3质量分数均为0.005%,2,2′-偶氮二(2-脒基丙烷盐酸盐)(V50)质量分数为0.0025%,乙二胺四乙酸(EDTA)质量分数为0.05%的条件下,反应时间为6 h,获得相对分子质量为1.2×107溶解性能较好的阳离子型聚丙烯酰胺(CPAM)。     

无硅无氟型食品防油纸的制备及其性能研究

防油纸是食品包装领域常用的一种包装材料。随着人们健康和环保意识的增强,对无硅与无氟型防油纸的需求日益增加。采用阳离子淀粉(CS)、羧甲基纤维素(CMC)和环保防油剂复配,采用一次性涂布,开发了一种环保型防油纸。实验结果表明:CS/CMC复配液与环保防油剂按照质量比1∶1混合后,涂布量为2.5g/m 2的条件下,所制备的食品防油纸接触角达到99.6°,KIT防油等级达到8级。     

Excellent Mechanical and Transparency Properties of Cationic Waterborne Polyurethane Films Modified by Boehmite Sol

The strategies for nanosol from metal alkoxide have enabled production of ultratransparent and mechanically robust polymer nanocomposites at extremely high loading. Herein, a simple approach to fabricate high‐performance polyurethane‐based nanocomposites via unmodified boehmite nanoparticles is reported. Evaluating their physical properties, the uniform dispersion of boehmite in the matrix caused nanocomposites retains ultrahigh transparency. Hydrogen bonding and intermolecular entanglement between boehmite and polyurethane brings about the mechanical properties of the nanocomposites material enhanced, i.e., strength, stiffness, and toughness. Optimized strength, stiffness, and toughness of Boehmite/Cationic waterborne polyurethane at 40 wt% (BNC40) are up to 58.1 MPa, 1096.7 MPa, 249.5 MJ m^?3, respectively. Furthermore, the feasibility and mechanism of polymer strengthening and toughening by inorganic rigid nanoparticles is explored from the aspects of crystallinity and micromorphology.     

Anionic Redox Chemistry as a Clue for Understanding the Structural Behavior in Layered Cathode Materials

The anionic redox chemistries of layered cathode materials have been in focus recently due to an intriguing phenomenon that cannot be described by the number of electrons of transition metal ions. However, even though several studies have investigated the anionic redox chemistry of layered materials in terms of the charge compensation, the relationship between the origin of the structural behavior and anionic redox chemistry in layered materials remains poorly understood. In addition, a simultaneous redox process of transition metal ions could occur through the d bands interaction. Here, it is demonstrated that the anionic redox chemistry is associated with the anisotropic structural behavior of the layered cathode materials albeit without providing additional capacities exceeding the theoretical values. These findings will provide a foundation of a new chapter in the understanding of the properties of materials.     

油水界面上阴/阳离子型复配表面活性剂体系的分子动力学模拟

采油过程中阴/阳离子型表面活性剂复配使用可显著增强驱油效果，对其微观机理的深入研究有助于驱油用表面活性剂的结构优化设计及使用。采用分子动力学方法研究了不同摩尔比的阴离子表面活性剂聚醚羧酸钠(PECNa)和阳离子表面活性剂十八烷基三甲基氯化铵(OTAC)复配体系在油水界面上的分子行为和物理性质。结果表明，复配体系比单种表面活性剂体系更有利于降低油水界面张力。不同复配比体系中，两种表面活性剂头基相反电荷间的吸引作用使表面活性剂之间对各自反离子的静电吸引作用减弱，且等摩尔比体系尤为明显。阴离子表面活性剂的亲水头基对阳离子表面活性剂亲水头基形成的水化层内水分子的结构取向无显著影响，反之亦然。通过调节两种离子型表面活性剂的复配比例，可调整油水界面吸附层微观结构，有望降低油水界面张力，提高采收率。     

A Multiscale-Porous Anion Exchange Membrane for Convenient and Scalable Electrokinetic Concentration of Cationic Species

A device able to electrokinetically concentrate cationic samples has many potential medical and industrial applications, but until now has remained undeveloped due to the lack of a commercial anion-permselective material leading to a prohibitively complex fabrication procedure. Herein, a novel multiscale-porous anion exchange membrane (MP-AEM) that enables the convenient and scalable electrokinetic concentration of cationic species is proposed. A mechanically enhanced multiscale-porous structure with a solid framework is realized by adopting polyester resin as an additive to overcome the intrinsic limitations of the AEM material. The scalable MP-AEM-embedded electrokinetic concentrator is devised based on the peculiar properties of the MP-AEM that for allow both ion and fluid transport. With the MP-AEM, the concentrator is fabricated in a highly streamlined manner consisting only of a simple insertion and assembly. The concentration performance of the MP-AEM-embedded electrokinetic concentrator is demonstrated with a positively charged fluorescent dye and a fluorescein-labeled protein, and the results show enrichment factors of 250 and 500, respectively. The MP-AEM makes cationic electrokinetic concentration more accessible and scalable, thereby enabling further progress in a wide range of fields.     

Novel microscopy-based approaches to study the film formation mechanism and associated mechanical response in polymer lattices

In this paper, we present the results from novel microscopy-based approaches aimed at providing further insight into the mechanism of film formation and associated mechanical response in polymer lattices. Firstly, a ‘simple’ methodology, combining the use of variable pressure scanning electron microscopy and a recently introduced enhanced coolstage (–50 to +50°C), was successfully developed and not only used to study dynamic processes, e.g. different stages of latex film formation, but also for high-resolution imaging of ‘freeze-dried’ structures. By using the enhanced freeze-drying capability of the system, it was also possible to preserve the structure and features of the studied system with minimum shrinkage and distortion and in the case of polymer lattices at a desired stage of film formation. Moreover, specimens can then be readily imaged, without the need of conductive coatings and at much lower chamber gas pressures, thus minimizing the beam skirting effects and allowing higher resolutions to be achieved. The second and final part of our study consider the mechanical response of the studied latex dried under different conditions, with the particular emphasis on the effects of drying rate [% relative humidity (RH)]. Atomic force microscopy force distance curve measurements revealed that while the %RH did not have an effect on the structures formed, it did have an effect on the adhesive properties of the studied system. It is strongly believed that the methodologies developed and used here can be applied to other material systems, including biologicals and pharmaceuticals.