There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality.

Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

I and i

3.2.3. Hydroformylation 2467 3.2.4. Dimerization 2468 3.2.5. Oxidative Cleavage and Ozonolysis 2469 3.2.6. Metathesis 2470 4. Terpenes 2472 4.1. Pinene 2472 4.1.1. Isomerization: R-Pinene 2472 4.1.2. Epoxidation of R-Pinene 2475 4.1.3. Isomerization of R-Pinene Oxide 2477 4.1.4. Hydration of R-Pinene: R-Terpineol 2478 4.1.5. Dehydroisomerization 2479 4.2. Limonene 2480 4.2.1. Isomerization 2480 4.2.2. Epoxidation: Limonene Oxide 2480 4.2.3. Isomerization of Limonene Oxide 2481 4.2.4. Dehydroisomerization of Limonene and Terpenes To Produce Cymene 2481

Chemical Routes for the Transformation of Biomass into Chemicals

Rod Borup is a Team Leader in the fuel cell program at Los Alamos National Lab in Los Alamos, New Mexico. He received his B.S.E. in Chemical Engineering from the University of Iowa in 1988 and his Ph.D. from the University of Washington in 1993. He has worked on fuel cell technology since 1994, working in the areas of hydrogen production and PEM fuel cell stack components. He has been awarded 12 U.S. patents, authored over 40 papers related to fuel cell technology, and presented over 50 oral papers at national meetings. His current main research area is related to water transport in PEM fuel cells and PEM fuel cell durability. Recently, he was awarded the 2005 DOE Hydrogen Program R&D Award for the most significant R&D contribution of the year for his team's work in fuel cell durability and was the Principal Investigator for the 2004 Fuel Cell Seminar (San Antonio, TX, USA) Best Poster Award. Jeremy Meyers is an Assistant Professor of materials science and engineering and mechanical engineering at the University of Texas at Austin, where his research focuses on the development of electrochemical energy systems and materials. Prior to joining the faculty at Texas, Jeremy workedmore » as manager of the advanced transportation technology group at UTC Power, where he was responsible for developing new system designs and components for automotive PEM fuel cell power plants. While at UTC Power, Jeremy led several customer development projects and a DOE-sponsored investigation into novel catalysts and membranes for PEM fuel cells. Jeremy has coauthored several papers on key mechanisms of fuel cell degradation and is a co-inventor of several patents. In 2006, Jeremy and several colleagues received the George Mead Medal, UTC's highest award for engineering achievement, and he served as the co-chair of the Gordon Research Conference on fuel cells. Jeremy received his Ph.D. in Chemical Engineering from the University of California at Berkeley and holds a Bachelor's Degree in Chemical Engineering from Stanford University. Bryan Pivovar received his B.S. in Chemical Engineering from the University of Wisconsin in 1994. He completed his Ph.D. in Chemical Engineering at the University of Minnesota in 2000 under the direction of Profs. Ed Cussler and Bill Smyrl, studying transport properties in fuel cell electrolytes. He continued working in the area of polymer electrolyte fuel cells at Los Alamos National Laboratory as a post-doc (2000-2001), as a technical staff member (2001-2005), and in his current position as a team leader (2005-present). In this time, Bryan's research has expanded to include further aspects of fuel cell operation, including electrodes, subfreezing effects, alternative polymers, hydroxide conductors, fuel cell interfaces, impurities, water transport, and high-temperature membranes. Bryan has served at various levels in national and international conferences and workshops, including organizing a DOE sponsored workshop on freezing effects in fuel cells and an ARO sponsored workshop on alkaline membrane fuel cells, and he was co-chair of the 2007 Gordon Research Conference on Fuel Cells. Minoru Inaba is a Professor at the Department of Molecular Science and Technology, Faculty of Engineering, Doshisha University, Japan. He received his B.Sc. from the Faculty of Engineering, Kyoto University, in 1984 and his M.Sc. in 1986 and his Dr. Eng. in 1995 from the Graduate School of Engineering, Kyoto University. He has worked on electrochemical energy conversion systems including fuel cells and lithium-ion batteries at Kyoto University (1992-2002) and at Doshisha University (2002-present). His primary research interest is the durability of polymer electrolyte fuel cells (PEFCs), in particular, membrane degradation, and he has been involved in NEDO R&D research projects on PEFC durability since 2001. He has authored over 140 technical papers and 30 review articles. Kenichiro Ota is a Professor of the Chemical Energy Laboratory at the Graduate School of Engineering, Yokohama National University, Japan. He received his B.S.E. in Applied Chemistry from the University of Tokyo in 1968 and his Ph.D. from the University of Tokyo in 1973. He has worked on hydrogen energy and fuel cells since 1974, working on materials science for fuel cells and water electrolysis. He has published more than 150 original papers, 70 review papers, and 50 scientific books. He is now the president of the Hydrogen Energy Systems Society of Japan, the chairman of the Fuel Cell Research Group of the Electrochemical Society of Japan, and the chairman of the National Committee for the Standardization of the Stationary Fuel Cells. ABSTRACT TRUNCATED« less

Scientific aspects of polymer electrolyte fuel cell durability and degradation.

介绍了Kirk—Othmer Encyclopedia of Chemical Technology（化工技术百科全书）（第五版）电子图书网络版数据库，并对该数据库使用方法和检索途径作出了说明，且结合实例简单地介绍了该数据库的检索方法。

Kirk-Othmer Encyclopedia of Chemical Technology数据库介绍及实例

The science and technology of ultracapacitors are reviewed for a number of electrode materials, including carbon, mixed metal oxides, and conducting polymers. More work has been done using microporous carbons than with the other materials and most of the commercially available devices use carbon electrodes and an organic electrolytes. The energy density of these devices is 3¯5 Wh/kg with a power density of 300¯500 W/kg for high efficiency (90¯95%) charge/discharges. Projections of future developments using carbon indicate that energy densities of 10 Wh/kg or higher are likely with power densities of 1¯2 kW/kg. A key problem in the fabrication of these advanced devices is the bonding of the thin electrodes to a current collector such the contact resistance is less than 0.1 cm2. Special attention is given in the paper to comparing the power density characteristics of ultracapacitors and batteries. The comparisons should be made at the same charge/discharge efficiency.

Ultracapacitors: Why, How, and Where is the Technology

Optimization of Parameters Affecting Adsorption of Nickel (II), Zinc (II) and Lead (II) on Dowex 50 W Resin Using a Response Surface Methodology Approach

This paper describes a fabrication of poly (2-hydroxylethyl methacrylate) poly(HEMA) grafted on polyurethane (PU) film prepared by radiation-induced grafting (RIG) copolymerization method using electron beam irradiation for the first time. This method was well known to be fast technique, clean method without involve any chemical initiator, chemically bond the materials, and at the same time is a sterile technique suitable for further potential of biomedical application. This poly(HEMA) grafted on PU film or called as PU-g-poly(HEMA) films was analysed using Fourier-transform infrared (FTIR), scanning electron microscope (SEM), water contact angle analyser (WCA), platelet adhesion and clotting time measurement. As the results, poly(HEMA) was confirmed successful grafted on PU based on the shifting of the functional group, no significant changes in surface morphology, lowering the water contact angle from 78.28° to 70.02°, nearly no platelet adhesion and no excessive disturbance of the clotting time was observed. This means that PU-g-poly(HEMA) was improved its hydrophilicity, thus significantly reduced the platelet adhesion and maintain the normal range of time taken for blood to clot. Therefore, the present PU-g-poly(HEMA) films not only improved hydrophilicity, however, was also compatible with blood. Thus, it may be potential candidates in the biomedical devices or new biomaterial useful for future tissue engineering fields.

https://iopscience.iop.org/article/10.1088/1757-899X/808/1/012035/pdf

Fabrication and Characterization of PU-g-poly(HEMA) Film for Clotting Time and Platelet Adhesion

Breakthrough curves for the removal of Ni(II), Zn(II), and Pb(II) from aqueous solutions using cation exchange resin (Dowex 50W) were determined at dynamic conditions in a fixed-bed column under ambient temperature. The experiments and data obtained were designed and analyzed using response surface methodology, respectively. Three operating parameters: flow rate (15–25 mL min−1), pH (3–9), and bed height (3–5 cm) were investigated. Fixed-bed adsorption models namely Thomas model and Bohart–Adam model were adopted to describe the dynamics of metal adsorption in the column. The obtained experimental data were fitted to these models based on the kinetic constant kBA (mg min cm−3), kTH (cm3 mg−1 min), the maximum amount of metal exchange N0 (mg cm−3), and the maximum adsorption capacities qtm (mg), accordingly. The Thomas model was found to best fit all the experimental conditions studied with correlation coefficients of 0.91, 0.97, and 0.92 for Ni(II), Zn(II), and Pb(II), respectively.

Removal of Ni(II), Zn(II) and Pb(II) from aqueous solutions using cation-exchange resin in fixed-bed column

Enhanced hydrogen storage properties of NaAlH4 with the addition of CoTiO3 synthesised via a solid-state method

Electrospinning is a very simple and robust method for producing nano and microfibers from a wide variety of polymers. Viscosity of polymeric solutions is one of the most important parameters affecting morphological properties of electrospun nanofibers. In this study, the effect of nylon-6,6 solution’s viscosity and concentration on the diameter and morphology of electrospun nanofibers was studied. Nine different concentrations (5-25% wt/v) of nylon 6,6 in formic acid (90%) were prepared to provide various viscosities. A programmable viscometer was used to measure solutions’ viscosity. Electrospinning was carried out using the following conditions: voltage: 20 kV, flow rate: 0.4 ml/h, tip-to-collector distance: 10 cm, drum rotation speed: 200 rpm. Scanning Electron Microscopy (SEM) was used to characterize electrospun nanofibers morphology and measure fibers’ diameter. It was found that there is a threshold viscosity required for the formation of a stable polymeric jet during electrospinning. With increasing viscosity, fiber diameter increased and more uniform fibers were formed. This study shows that modifying solution’s viscosity provides a straightforward method for changing morphological properties of electrospun nanofibers for specific applications.

Mohamed Mahmoud Nasef

Papers

Optimization of Parameters Affecting Adsorption of Nickel (II), Zinc (II) and Lead (II) on Dowex 50 W Resin Using a Response Surface Methodology Approach

Fabrication and Characterization of PU-g-poly(HEMA) Film for Clotting Time and Platelet Adhesion

Removal of Ni(II), Zn(II) and Pb(II) from aqueous solutions using cation-exchange resin in fixed-bed column

Enhanced hydrogen storage properties of NaAlH4 with the addition of CoTiO3 synthesised via a solid-state method

The Effect of Solution Viscosity and Concentration on Morphological Properties of Electrospun Nylon-6,6 Nanofibers