高分子铁盐絮凝剂制备及其应用研究

研究了以废铁屑和工业硫酸亚铁为原料,在常压和加热条件下,用氯酸钾作为氧化剂制取聚合硫酸铁(PFS)的工艺条件,并在PFS制备的基础上,合成了聚磷硫酸铁(PPFS)和聚氯硫酸铁(PFCS)。将所制备的聚铁用于污水处理实验,结果表明:用该方法制备的聚铁絮凝剂对实际水样具有较好的混凝处理效果,且制备工艺简单、速度快,从根本上消除了用NaNO_2催化氧化法制备聚铁对环境造成的二次污染。     

提高科技创新实力实现我国炼油工业的持续发展

分析了21世纪我国炼油工业要持续发展，国际竞争能力要大力提高，涉及到的原油资源战略、现代化企业管理、行业体制和机制、企业机构调整、人才机制及科技创新等多方面问题，并就产品质量、深度加工、油化一体化、信息技术和运输燃料替代技术，以及如何提高科技创新能力、加强科技开发等技术发展战略，提出了一些对策和建议。     

m-LLDPE／纳米SiO2的力学性能和光学性能研究

采用熔融共混法制备了m-LLDPE／纳米SiO2复合材料，并对该体系的力学性能和光学性能进行了系统研究。结果表明，纳米SiO2对m-LLDPE具有一定的增强、增韧作用。复合材料的红外吸收能力较m-LLDPE明显提高，此外，m-LLDPE／纳米SiO2复合材料的可见光透光度有所降低，雾度却有明显的上升。通过SEM电镜得出，表面处理方法对纳米SiO2在基体中的分散性能有显著影响。     

Investigation of CH4 Reforming with CO2 on Meso-Porous Al2O3-Supported Ni Catalyst

Meso-porous Al₂O₃-supported Ni catalysts exhibited the highest activity, stability and excellent coke-resistance ability for CH₄ reforming with CO₂ among several oxide-supported Ni catalysts (meso-porous Al₂O₃ (Yas1-2, Yas3-8), -Al₂O₃, -Al₂O₃, SiO₂, MgO, La₂O₃, CeO₂ and ZrO₂). The properties of deposited carbons depended on the properties of the supports, and on the meso-porous Al₂O₃-supported Ni catalyst, only the intermediate carbon of the reforming reaction formed. XRD and H₂-TPR analysis found that mainly spinel NiAl₂O₄ formed in meso-porous Al₂O₃ and -Al₂O₃-supported catalysts, while only NiO was detected in -Al₂O₃, SiO₂, CeO₂, La₂O₃ and ZrO₂ supports. The strong interaction between Ni and meso-porous Al₂O₃ improved the dispersion of Ni, retarded its sintering and improved the activated adsorption of CO₂. The coking reaction via CH₄ temperature-programed decomposition indicated that meso-porous Al₂O₃-supported Ni catalysts were less active for carbon formation by CH₄ decomposition than Ni/-Al₂O₃ and Ni/-Al₂O₃.     

多孔羟基磷灰石生物陶瓷的进展

多孔羟基磷灰石生物陶瓷是一种性能优异的人体硬组织修复材料，在植入界面后它具生物降解性，置入体内能逐步参与代谢以至最终与人体骨结合成一体。本文在综合大量国内外文献的基础上，阐述了多孔羟基磷灰石生物陶瓷的性质、研究和发展。     

Seasonal evolution of the interannual variability of chlorophyll-a concentration and its forcing factors in the northwestern Pacific from 1998 to 2010

The northwestern Pacific Ocean is a complex region with significant biological spatial variations on a seasonal timescale. To investigate the joint variation patterns on both seasonal and interannual timescales, a season-reliant empirical orthogonal function (S-EOF) analysis was applied to seasonal mean chlorophyll-a concentration (chl-a) anomalies in the northwestern Pacific Ocean during the period 1998–2010. The first two dominant modes accounted for nearly 31% of the total interannual variance, with the second S-EOF mode (S-EOF2) lagging behind the first S-EOF mode (S-EOF1) by one year. S-EOF1 featured a strong variation pattern to the north of 30° N, with maximum chl-a in winter and minimum chl-a in summer. However, S-EOF2 indicated an opposite seasonally evolving pattern compared with S-EOF1, with chl-a increasing along the Kuroshio and extension current from boreal winter to autumn. Both these modes revealed significant relationships with climate-related indices. The two modes corresponded to the central Pacific (CP) La Niña developing episodes and the turnaround from eastern Pacific (EP) La Niña to CP El Niño, respectively. Both modes were associated with the cold phase of the Pacific Decadal Oscillation, which played an important role in prolonging the impact of the El Niño/Southern Oscillation on chl-a seasonal evolution from 1998 to 2010. In addition, we discuss the possible factors dominating chl-a seasonal variation, in terms of the subregions of the northwestern Pacific Ocean. In the subtropical northwestern Pacific Ocean (15° N – 30° N), the chl-a growth was primarily nutrient-limited, whereas in the mid-latitude northwestern Pacific Ocean (35° N – 50° N), the chl-a growth was mainly light-limited.     

基体韧性对PS改性PVC体系性能的影响

研究了PS对未增韧PVC体系及用CPE预增韧PVC体系韧性的影响,发现在用CPE预增韧PVC基体后,PS的增韧效果更为显著,但增韧机理井无改变,仍可用"空穴增韧"的机理来解释。     

ZrO2增韧Al2O3／SiCnano复合陶瓷的力学性能及微结构

本文对Al_2O_3/SiC nano ZrO_2(3Y)复相陶瓷的力学性能和微结构进行了研究,探讨了ZrO_2(t)应力诱导相交增韧机制和纳米粒子增韧机制相互迭加的可能性。结果表明:适量的第二相纳米粒子ZrO_2(3Y)加入对材料的微结构有很大影响,同时对材料的力学性能的提高作出贡献。     

聚合型受阻酚抗氧剂的合成及应用

研究了以对甲酚为主要原料合成聚合型受阻酚抗氧剂的工艺。结果表明，树脂缩合反应条件是对甲酚与双环戊二烯为3：1～1．25，ZnCl2催化剂为对甲酚质量分数的2．0％，反应温度为75～80℃，双环戊二烯滴加时间为2h。烷基化反应温度为70～75℃，H2S04催化剂为缩合树脂质量分数的2．0％。制得的聚合型受阻酚抗氧剂产品对聚氨酯泡沫用聚醚2802具有较好的抗氧化性，起燃温度达224℃。     

Optimization of membrane gas separation systems using genetic algorithm

Genetic algorithm is applied for the optimization of the membrane gas separation systems. Air separation for enriched oxygen production is the selected system for investigation. Optimizations for single and triple objective functions are studied. The optimization problem involves the selection of the optimal system configurations from three alternatives, including continuous membrane column (CMC), single stripper permeator (SSP), and two stripper in series permeator (TSSP), as well as the optimal operating conditions. Models of the three configurations and the genetic algorithm procedure are computerized. The objective functions discussed are the Rony separation index, power consumption per unit equivalent pure oxygen, and the membrane area. Both high-pressure and low-pressure (vacuum) operation modes are optimized and the effects of different oxygen product purity and feed rate are analyzed. For single objective function optimization, the solutions obtained using genetic algorithm are slightly inferior in one case but superior in other cases compared to those by pure mathematical optimization methods. For triple objective function optimization, the Pareto plots presenting multiple trade-off solutions are generated. In general, compared to high-pressure operation mode, the product recovery and power consumption for low-pressure operation mode are lower. For almost all the cases studied, CMC configuration with its high flexibility appears in the optimal solutions.