水基Fe3O4磁流体的制备工艺研究

用共沉淀法制备Fe3O4磁流体,总结出用十二烷基磺酸钠与聚乙二醇作为表面活性剂制备水基磁流体的合适条件:(1)反应温度为室温或不高于35℃;(2)表面活性剂十二烷基磺酸钠的最佳用量为0.0030～0.0040 g/80 mL;(3)第一次包裹的最佳pH为9～10;(4)聚乙二醇作为第二次包裹的表面活剂时,体系最佳温度为40℃左右;(5)表面活性剂聚乙二醇的最佳用量为0.0050～0.0060 g/80 mL。通过实验制得了能稳定存在180 d的水基磁流体。并用透射电镜、红外光谱、分光光度计、古埃磁天平等进行了初步表征。     

乙烯分离技术分析

从技术先进性、能耗、流程复杂性和运行稳定性等诸多方面对占据乙烯市场的三大分离技术进行了分析。并认为用户在选择分离技术时应综合考虑各方面因素，把握重点，选择出适合的技术。     

乙烯二聚制高纯丁烯－1技术经济评价

本文对生产高纯度丁烯－１的Ａｌｐｈａｂｎｔｏｌ工艺进行了技术经济评价，认为该工艺条件简单、反应条件温和，而且投资少，所以很适合事在发展中国家应用。     

The first measurement of an absolute surface concentration of reaction intermediates in ethylene hydrogenation

The first measurement of a turnover rate with respect to surface intermediate concentration in a high pressure heterogeneous catalytic reaction is reported. By using infrared-visible sum frequency generation to study the hydrogenation of ethylene on Pt(111), it was found that the surface concentration of -bonded ethylene, the key reaction intermediate, represented approximately 4% of a monolayer. Thus the absolute turnover rate per surface adsorbed ethylene molecule is 25 times faster than the rate measured per platinum atom. To explain these results, we propose a model of weakly adsorbed ethylene intermediates reacting on atop sites.     

Thermodynamic studies on the complete phase diagram of aqueous two phase system containing polyethylene glycol dimethyl ether 2000 and di-potassium hydrogen phosphate at different temperatures

The liquid-liquid equilibrium of polyethylene glycol dimethyl ether 2000 (PEGDME₂₀₀₀)+K₂HPO₄+H₂O system has been determined experimentally at T=(298.15,303.15,308.15 and 318.15) K. The liquid-solid and complete phase diagram of this system was also obtained at T=(298.15 and 308.15) K. A nonlinear temperature dependent equation was successfully used for the correlation of the experimental binodal data. Furthermore, a temperature dependent Setschenow-type equation was successfully used for the correlation of the tie-lines of the studied system. Moreover, the effect of temperature on the binodal curves and the tie-lines for the investigated aqueous two-phase system have been studied. Also, the free energies of cloud points for this system and some previously studied systems containing PEGDME₂₀₀₀ were calculated from which it was concluded that the increase of the entropy is the driving force for formation of aqueous two-phase systems. Additionally, the calculated free energies for phase separation of the studied systems were used to investigate the salting-out ability of the salts having different anions. Furthermore, the complete phase diagram of the investigated system was compared with the corresponding phase diagrams of previously studied systems, in which the PEGDME₂₀₀₀ has been used, in order to obtain some information regarding the phase behavior of these PEGDME₂₀₀₀+salt+water systems.     

Preparation of lithium-ion polymer battery using LiNi1/3Co1/3Mn1/3O2 as a cathode material and its electrochemical properties

In this work, LiNi_1/3Mn_1/3Co_1/3O₂ powders were synthesized from co-precipitated spherical metal hydroxide. In the voltage range of 2.8–4.2, 2.8–4.4, and 2.8–4.6 V, the discharge capacities of LiNi_1/3Mn_1/3Co_1/3O₂ electrode were 163, 177, and 193 mAh⋅g⁻¹, respectively. A gel polymer electrolyte (GPE) was also prepared using polyoxyalkylene glycol acrylate (POAGA) as a macromonomer. LiNi_1/3Mn_1/3Co_1/3O₂/GPE/graphite cells were prepared and their electrochemical properties were evaluated at various current densities and temperatures. The ionic conductivity of the GPE was more than 6.2 × 10⁻³ S⋅cm⁻¹ at room temperature. POAGA-based cells were showed good electrochemical performances such as rate capability, low-temperature performance, and cycleability.     

乙二醇在氧化物增强Pd/C催化剂上的电化学氧化

研究了乙二醇在氧化物CeO2、NiO和Co3O4增强Pd/C催化剂上的碱性溶液中电化学氧化活性,结果显示虽然纯Pd/C催化剂对乙二醇的电化学氧化活性非常低以及抗催化剂毒化作用非常弱,其电化学性能远远比不上Pt/C催化剂。但添加氧化物CeO2、NiO和Co3O4后,Pd/C对乙二醇电化学氧化催化活性和抗毒化能力都得到大幅度提高,甚至超过商业催化剂E-TEKPt/C。三种氧化物增强Pd/C催化剂的电化学活性顺序为Pd-Co3O4(质量比为2︰1,以下同)/C>Pd-NiO(4︰1)/C>Pd-CeO2(1.3︰1)/C。     

乙烯裂解炉炉管失效原因分析

利用金相显微镜、X射线衍射仪、光谱分析仪等测试仪器,通过对炉管的材质、外观形貌、金相组织、组分组成等方面进行检测,分析了乙烯裂解炉炉管失效的原因.结果表明,材质为Incoloy 800 H合金的裂解炉管可满足乙烯裂解工况的工艺要求,炉管失效主要是由于高温过热引起的氧化腐蚀破坏所致,另外管内介质对腐蚀也有促进作用.     

Discovery of Five New Ethylene-Forming Enzymes for Clean Production of Ethylene in E. coli

Ethylene is an essential platform chemical with a conjugated double bond, which can produce many secondary chemical products through copolymerisation. At present, ethylene production is mainly from petroleum fractionation and cracking, which are unsustainable in the long term, and harmful to our environment. Therefore, a hot research field is seeking a cleaner method for ethylene production. Based on the model ethylene-forming enzyme (Efe) {"type":"entrez-protein","attrs":{"text":"AAD16440.1","term_id":"4323597","term_text":"AAD16440.1"}}AAD16440.1 (6vp4.1.A) from Pseudomonas syringae pv. phaseolicol, we evaluated five putative Efe protein sequences using the data derived from phylogenetic analyses and the conservation of their catalytic structures. Then, pBAD expression frameworks were constructed, and relevant enzymes were expressed in E. coli BL21. Finally, enzymatic activity in vitro and in vivo was detected to demonstrate their catalytic activity. Our results show that the activity in vitro measured by the conversion of α-ketoglutarate was from 0.21–0.72 μmol ethylene/mg/min, which varied across the temperatures. In cells, the activity of the new Efes was 12.28–147.43 μmol/gDCW/h (DCW, dry cellular weight). Both results prove that all the five putative Efes could produce ethylene.