纳米Fe粉的制备研究

总结了纳米Fe粉的制备方法,重点介绍了一种新的制备方法——封闭循环氢还原法。该方法以FeSO·47H2O和NaOH为原料,采用沉淀方法制备粒径为30～70nm的Fe2O3粉末,其反应条件为:反应温度50℃,反应终点pH值大于12,陈化时间1h。用封闭循环氢还原法,在400℃下还原Fe2O3得到了Fe粉。其粒径在20～50nm之间,含量为99.16%。     

UV法测定聚甲基丙烯酸酯纳米粒中胰岛素的包封率

建立一种简便易行的测定聚甲基丙烯酸酯胰岛素纳米粒中游离胰岛素含量方法.用Nanosep OD100C33超滤膜分离纳米粒和游离药物,在276 nm处测定药物的吸光度,建立胰岛素含量测定方法,并对线性、回收率、精密度等指标进行考察,最后测定各种胰岛素和载体比例混合的纳米粒的包封率.结果发现,该超滤膜能较好地分离纳米粒和游离的药物,在0.11～1.10 u/mL范围内,药物在276 nm的吸光度和浓度存在良好的线性关系(r=0.999 8),线性方程为A=0.868 8C-0.001 6,高、中、低3种浓度的回收率和精密度良好.该方法操作简单、结果可靠,可用于胰岛素纳米粒中药物包封率的测定.     

Hydrogen Absorption and Release Behavior in Hydrogen Decrepitation Process of Nd-Fe-B Alloys

The behavior of hydrogen absorption and release in hydrogen decrepitation (HD) process of Nd-Fe-B alloys were investigated. The results reveal that the reactivity and the amount of hydrogen absorption in HD process are related to the surface activity of the alloy so that the fresh and active surface has a higher efficiency. The presence of Nd-rich phase at the grain boundary is an essential factor of the HD activity of the alloy at room temperature. On degassing, hydrogen is released from the HD powder continuously with increasing temperature. And the residual hydrogen is as low as 0.0015% at 1073K, which shows that the hydrogen is almost exhaused. It is feasible to remove the hydrogen from the HD powder by heating treatment at the temperature of 523-723K for 1h prior to the magnetic field forming in order to decrease the harmful effect of hydrogen on the easy axis alignment of HD magnet.     

Conceptual design of a high-efficiency absorption cooling cycle

The search for high-efficiency, gas-fired cooling cycles has led to the development of dual-loop absorption machines with cooling coefficients of performance (COPs) in the 1.2 to 1.7 range. This increased performance may call for high generator temperatures, new working fluids or new materials of construction. In most cases, two different sets of working fluids are required. The conceptual design presented here is aimed at obtaining high efficiencies with relatively low temperatures, employing only one set of fluids. The concept consists of two loops coupled in a configuration aimed at minimizing the loss of thermodynamic availability incurred when transferring refrigerant between the loops. The working fluid pair is a solution of lithium bromide-water. The calculated COPs are of the order of 1.8. The cycle relies on an elaborate evaporator-absorber combination. The paper presents the conceptual design, the critical assumptions, and the performance calculations for the concept.     

InAs／InP_（0．7）Sb_（0．3）热电子晶体管的f_T及f_（max）

用电荷控制及热电子弹道运动模型计算ＩｎＡｓ／ＩｎＰ０．７Ｓｂ０．３热电子晶体管的截止频率ｆＴ及最高振荡频率ｆｍａｘ。结果表明，ｆＴ、ｆｍａｘ分别达到２８０ＧＨｚ及６００ＧＨｚ。并指出，通过生长ＧａＳｂ中间层，ＩｎＡｓ／ＩｎＰ０．７Ｓｂ０．３ＨＥＴ可在ＧａＡｓ衬底上实现单片集成。     

Electrochemical Investigation on the Formation of Dy-Fe Alloy in Molten Chlorides

ＥｌｅｃｔｒｏｃｈｅｍｉｃａｌＩｎｖｅｓｔｉｇａｔｉｏｎｏｎｔｈｅＦｏｒｍａｔｉｏｎｏｆＤｙＦｅＡｌｏｙｉｎＭｏｌｔｅｎＣｈｌｏｒｉｄｅｓＬｉｕＧｕａｎｋｕｎ（刘冠昆），ＴｏｎｇＹｅｘｉａｎｇ（童叶翔），ＨｏｎｇＨｕｉｃｈａｎ（洪惠婵），Ｙａｎｇ...     

Preparation of core–shell type nanoparticles of diblock copolymers of poly(L‐lactide)/poly(ethylene glycol) and their characterization in vitro

Core–shell type nanoparticles of poly(L ‐lactide)/poly(ethylene glycol) (LE) diblock copolymer were prepared by a dialysis technique. Their size was confirmed as 40–70 nm using photon correlation spectroscopy. The ¹H‐NMR analysis confirmed the formation of core–shell type nanoparticles and drug loading. The particle size, drug loading, and drug release rate of the LE nanoparticles were slightly changed by the initial solvents that were used. The drug release behavior of LE core–shell type nanoparticles showed an initial burst during the first 12 h and then a sustained release until 100 h. The degradation behavior of LE block copolymer nanoparticles was divided into three phases: the initial rapid degradation phase, the stationary phase, and the rapid degradation phase until complete degradation. It was suggested that lidocaine release kinetics were predominantly governed by the diffusion mechanism in the initial burst phase and after that by both of the diffusion and degradation mechanisms. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 2625–2634, 2002     

Benefits to 0+ fishes of connecting man‐made waterbodies to the lower River Trent,England

Floodplain waterbodies are reputed to enhance recruitment of riverine fish populations via provision of spawning and nursery habitat, refuge from floods, and increased availability of planktonic food resources compared with main river channels. Notwithstanding, there have been few parallel studies of fishes and their food resources at both main river and floodplain sites. Thus, this study investigated the 0+ fishes, zooplankton and phytoplankton (chlorophyll a) at four main river and four (man‐made) floodplain sites on the lower River Trent, England, between May 1999 and October 2004 inclusive. All sites shared the same key fish species, and there were no consistent differences in the densities, growth or condition of 0+ fishes from main river and floodplain sites. Similarly, all sites shared the same key zooplankton taxa. However, zooplankton densities, notably of large‐bodied cladocerans, and chlorophyll a concentrations, were significantly higher at floodplain sites than at main river sites. Thus, connection of man‐made waterbodies has the potential to enhance recruitment of riverine fish populations via provision of important spawning and nursery habitat, and superior feeding opportunities for 0+ fishes compared with main river channels. Copyright © 2007 John Wiley & Sons, Ltd.     

Hydrothermal synthesis and in situ surface modification of boehmite nanoparticles in supercritical water

In situ surface modification of boehmite (AlOOH) nanoparticles during hydrothermal synthesis in supercritical water was examined by adding CH₃(CH₂)₄CHO and CH₃(CH₂)₅NH₂ as modifier reagents to the reactants. Changes in surface properties of the nanoparticles by surface modification was observed by FTIR, dispersion in solvents and TEM analyses, which demonstrated that reagents chemically binded onto the surface of the AlOOH nanoparticles. The results of SEM and TEM pictures show that the surface modification affects crystal growth and reduces the particle size and changes the morphology of the particles.     

Synthesis and activation of Pt nanoparticles with controlled size for fuel cell electrocatalysts

Well-dispersed Pt nanoparticles with controlled size and narrow size distribution were prepared by polyalcohol reduction of platinum acetylacetonate, using oleylamine as a capping agent. The particle size was varied from 3.5 nm to 11.5 nm by decreasing the amount of oleylamine added in the synthesis. Size selection of the as-prepared particles by solvent fractionation yielded nearly monodispersed Pt particles. The as-prepared particles were loaded on a carbon support by physical deposition, but showed no electrocatalytic activity due to the oleylamine bound to the particle surface. The particles were activated for electrocatalysis after heating the particles in air at 185 °C for 5 h, conditions that gave no particle-sintering and no oxidation. Cyclic voltammetry showed that the particles after the heat treatment in air were electrocatalytically active for methanol oxidation. The smaller 3.5 nm and 4.0 nm Pt particles had a higher intrinsic activity for methanol oxidation, but a lower tolerance to CO poisoning, compared with 6.0 nm, 9.5 nm and 11.5 nm particles. CO-stripping results suggest that CO is more easily oxidized on larger Pt particles.