表外储油层酸化防膨剂的评价及效果分析

本文论述了采用不同防膨试验方法评价不同类型粘土防膨剂,并以回归曲线和价值工程分析防膨效果。由分子结构理论提出分子保护膜的防膨机理新观点,论述了酸液中添加具有多种功能的非离子型防膨剂QC—1可提高表外储层酸化与排酸效果。     

横波速度各向异性初步探讨：—多波勘探资料的应用

在纵波、SH 型横波资料处理和解释过程中,我们发现四川 HBC 地区地下介质普遍存在方向各向异性。当横波通过方向各向异性介质时,分裂成两个波:一个波的偏振方向与裂缝平行,叫快横波;另一个波的偏振方向与裂缝走向垂直,叫慢横波。采用相应的观测和处理方法,便可获得快横波和慢横波剖面。根据同一界面的快、慢横波的旅行时可以求得各向异性系数。同样,还可以利用 SH 波与转换波的速度比求取各向异性系数。各向异性系数的大小,反映了裂缝的发育程度。如果野外作了 X、Y 分量观测,室内又作了坐标旋转处理,那么,就可以进一步确定裂缝带的方向。如果未作上述工作,也可以根据构造线走向,大致确定裂缝带的发育方向。     

Study on ASTM E399 and ASTM E1921 standards

Costs of ASTM E399 and ASTM E1921 tests, which were developed to determine the fracture toughness (K_Ic) and the ductile–brittle transition temperature of ferritic steels, respectively, are considered high and the procedures are also very complicated. In this study, a method, which is more cost‐effective and easier to carry out, is proposed.     

过渡金属元素催化羟自由基反应机理研究

针对显色剂－过渡金属元素－过氧化氢体系，用分光光度法间接测定羟自由基。通过大量试验，确定了三苯甲烷类酸性酚醌吡喃类为有效显色剂，并确定了溴邻苯三酚红－亚铁离子－过氧化氢体系测定羟自由基的最佳条件，首次推测出其最可能的反应机理为：亚铁离子催化过氧化氢产生羟自由基，羟自由基氧化溴邻苯三酚红上的羰基碳氧双键，破坏其显色的共轭结构，使其褪色，此法可作为筛选羟自由基清除剂的有效方法。     

Visualization and quantification of the mechanical deformation induced by an electrical field in poly(ethylene naphthalene 2,6‐dicarboxylate) (PEN) films

An optical nondestructive strain measurement technique was performed to analyze the mechanical deformation induced by an electrical field within the insulating materials. Poly(ethylene naphthalene 2,6‐dicarboxylate) (PEN) films were then subjected to constant electrical fields right up to their electrical breakdown. The experimental technique made it possible to follow the various stages of the mechanical behavior of PEN in real time. The final breakdown occurred in the observation zone and the related mechanical deformation was captured. A “margarita” structure was observed with a hole at the center. The experimental results indicated that the level of the induced‐mechanical deformations depended on the local environment. We defined two different zones representing the inside and the outside of the damaged area. The induced‐deformations were larger in the damaged zone. It was also observed that deformations increased when the sample had a lower degree of crystallinity. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Influence of third monomer on the crystal phase transition behavior of ethylene-tetrafluoroethylene copolymer

Crystal phase transition between the low- and high-temperature phases has been investigated for ethylene (E)-tetrafluoroethylene (TFE) alternating copolymer (ETFE) containing the third monomeric species by the temperature dependent measurements of wide-angle X-ray diffraction (WAXD) and small-angle X-ray scattering (SAXS) and differential scanning calorimetry. Nonafluoro-1-hexene (NFH) and hexafluoropropylene (HFP) were chosen as the third monomers, where they are different in the side-branch length, -(CF₂)₃CF₃ and -CF₃, respectively. In the case of E/TFE/NFH copolymer (ET-C4F9), the crystal phase transition temperature of the original ETFE two-components copolymer was not very much affected by the existence of NFH in the range of NFH content from 0.7 to 3 mol%. Contrarily, the crystal phase transition temperature of E/TFE/HFP copolymer (ET-CF3) was found to decrease drastically with increasing HFP content. The melting temperature and the higher-order structure were also affected sensitively depending on the HFP content. This difference in phase transition behavior between ET-C4F9 and ET-CF3 copolymers is reasonably interpreted as follows: the short side groups (-CF₃) of HFP monomeric unit are included in the crystal lattice of E/TFE chains and the unit cell is expanded gradually with an increment of the HFP content, resulting in the decrease in phase transition point because of easier thermal motion of the chains. On the other hand, the long side groups [-(CF₂)₃CF₃] of NFH monomeric units are excluded out of the crystal lattice and located on the lamellar surfaces or in the amorphous region and do not affect very much the phase transition temperature even when the NFH content is increased. In association with such a change in crystal structure, the long period of stacked lamellar structure was found to decrease remarkably in the case of NFH, whereas it does not change very much for HFP, consistent with the interpretation of the above-mentioned WAXD data.     

Antimicrobial finishing of regular and modified polyethylene terephthalate fabrics

An effective two-stage method has been developed for imparting antimicrobial properties to regular polyethylene terephthalate (R-PET), polyethylene glycol modified polyethylene terephthalate (PEG-M-PET), R-PET/Cotton blend (R-PET/C) and PEG-M-PET/Cotton blend (PEG-M-PET/C) fabrics. The method consists of partial hydrolysis of the fabrics to create carboxylic groups in PET macromolecules followed by subsequent reaction with dimethylalkylbenzyl ammonium chloride (DMABAC) under alkaline conditions. The reaction conditions such as pH, reaction temperature and time, carboxylic content, and DMABAC concentration were studied. Characterization of the finished fabrics was carried out through scanning electron microscopy (SEM) and Fourier transform infrared spectra (FTIR). All the modified PET fabrics showed excellent antibacterial activity towards Gram-positive (Bacillus mycoides), Gram-negative (Escherichia coli), and nonfilamentous fungus (Candida albicans). The achieved antimicrobial functions on the PET fabrics are durable in repeated laundering processes. Even after laundering 10 times the fabrics could still provide more than 85% of its antimicrobial activity against B. mycoides, E. coli, and C. albicans. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Functional copolymer of geraniol and acrylonitrile: Synthesis and characterization

The radical copolymerization of acyclic terpene namely geraniol [GER] with acrylonitrile [AN] in DMF at (70 ± 0.1)°C for 1 h, using benzoylperoxide (BPO) as an initiator has been carried out under inert atmosphere of nitrogen. The kinetic expression for reaction is R_p ∝ [BPO]^0.5 [AN]^1.0 [GER]^1.0. The IR spectrum of the copolymer shows bands at 3432 and at 2244 cm^?1 due to ? OH group of GER and ? CN group of AN, respectively. The ¹³C‐NMR spectrum shows peaks at 73–75 δ ppm and 116–120 δ ppm due to ? OH group of GER and ? CN group of AN, respectively. The thermogravimetric analysis and differential scanning calorimetry study shows that copolymer is thermally stable up to 407°C and has glass transition temperatures (T_g) 56°C. The reactivity ratios r₁ (AN) and r₂ (GER) have been calculated as 0.05 and 0.005, respectively. The Alfrey‐Price Q‐e parameter for GER has been calculated as 0.094 and ?2.0, respectively. The molecular weights of the copolymers have been evaluated by gel‐permeation chromatography. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Time and temperature effect on the linear–nonlinear viscoelastic transition threshold of a polymeric system

In the present study, the transition of a polymeric material from the linear to the nonlinear viscoelastic behavior and the determination of the nonlinearity stress threshold variation with time and temperature are investigated. For this purpose a systematic experimental program consisted of thermal and mechanical characterization of certain polymeric material followed by isothermal creep tests at different stress levels and temperatures was conducted. Through isochronal curves that occurred from creep tests, the nonlinearity threshold dependence on both time and temperature is presented. The reported results provide information that is critical for the design and development of polymer structures and components. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

一种T形高压输电线路故障测距新方法

对T形线路的故障测距，现有方法都是先判断故障支路，再将3端线路等效成2端线路进行测距。但在 T节点附近短路，尤其是经高阻短路时，现有的测距方法由于无法正确判别故障支路而存在一定范围的测距死区。针对上述缺陷，分别假设故障发生在某一支路，由假定正常的2段支路端的电压、电流推算求得 T节点电压和注入假定故障支路的电流，从而分别求得3个故障距离。经证明，求得的3个故障距离有且仅有1个在0和对应支路总长度之间，该距离就是真实的故障距离，故障发生在对应支路上。该方法无需事先判别故障支路即可测距，在 T节点附近经高阻故障时无测距死区。其测距精度理论上不受过渡电阻和故障类型影响，无需故障前数据，且对滤波无高要求。EMTP仿真结果表明该方法正确、有效，测距精度高。