Electrochemical and surface-enhanced Raman spectroscopy studies of 4-phenylpyridine adsorption at the gold/solution interface

The adsorption of 4-phenylpyridine (4-PhPy) on the Au electrode was examined using conventional electrochemical techniques: cyclic voltammetry and impedance measurements and also by surface enhanced Raman spectroscopy (SERS) in a wide range of electrode potentials. Electrochemical results indicate the strong adsorption of 4-Phpy molecules, particularly at the positively charged Au electrode. The wide shoulder of capacity close to the pzc suggests that the composition and/or the structure of 4-Phpy monolayer change with the sign of the surface charge on the electrode. Investigation of integrity of adsorbed layer, however, indicates that adsorbed molecules do not form tight, compact monolayer even in the case of adsorption from saturated solution. SERS spectra provided evidence for gradual, potential-induced reorientation of the molecular plane with respect to the surface, from nearly vertical in the negatively charged electrode, to more flat at the positively charged metal surface.     

摩擦材料研究进展

对摩擦材料国内外发展现状进行了综述，简要叙述了摩擦材料的发展历史，以及各种摩擦材料的性能以及应用，阐述了它们的优缺点，说明了纤维在摩擦材料中的重要作用。同时指出陶瓷基复合摩擦材料是今后发展的趋势。     

HYDRODYNAMICS AND MASS TRANSFER IN A NEW TYPE (FG) STACK PACKED EXTRACTION COLUMN

1 INTRODUCTIONOne of the major objectives in the study of extraction column is to minimize column di-mensions to fulfill a certain specific separation process.This has led to the intensiveemployment of structured packings in extraction columns [1].One of the recentdevelopments targeted for greater interfacial areas without excessive dispersion is the useof structure packings contactive claiming advantages,such as lower fluid flow friction     

矿物材料化学加工与合成的研究现状和发展方向

从以矿物原料直接制备矿物材料、矿物材料的化学改性、特殊功能粉体的合成及粉体材料合成中新技术手段的应用等方面,论述了矿物粉体材料的研究进展。聚合物/黏土纳米复合材料,由于其特殊的功能,成为矿物材料改性的新方向;特殊功能粉体赋予材料许多优越的性能,其开发和研究已成为热点,特别是在电池材料、抛光材料、生物材料的研究方面;学科交叉为材料研制带来了又一次兴起,超声波、机械化学、微波和微波等离子体,由于其特殊的功效,解决了粉体制备过程中许多难题。新方法和技术所制得材料具有优越性能和特殊功能。     

高分子材料的微孔发泡方法

介绍了微孔发泡高分子材料的成型方法 ,成型原理和成型工艺及设备。     

以太网在工业应用中的实时能力分析

以工业控制过程为背景，详细分析以太网端到端的通信延迟，给出排队延迟的期望表达式，发送延迟和传输延迟的计算方法；通过仿真，分析网络节点数目、帧的长度和通信速率对以太网实时能力的影响，并提出以太网在工业应用中改善实时能力的方法。     

Improved electrochemical redox performance of 2,5-dimercapto-1,3,4-thiadiazole by poly(3-methoxythiophene)

High electrocatalytic activity of an electropolymerized film of poly(3-methoxythiophene) (PMOT) is reported toward the redox reaction of 2,5-dimercapto-1,3,4-thiadiazole (DMcT) as a promising cathode material for the lithium ion battery. Cyclic voltammetry showed improved electrochemical performance of DMcT on PMOT-coated Pt electrode, indicating accelerated redox kinetics. Moreover, charge-discharge tests exhibited higher discharge capacity and slower capacity fading of the PMOT-doped DMcT composite cathode compared with pure DMcT.     

改性环氧基减摩材料

介绍了一种塑料基减摩材料,它是以改性环氧树脂为主体,加入固体润滑剂及增强材料等组成,具有较为理想的摩擦学特性。还讨论了固体润滑剂、增强材料对制件摩擦学特性的影响,并展望了它们的应用前景。     

Assessment of the relative agronomic effectiveness of phosphate rocks under glasshouse conditions

Six phosphate rocks (PRs) of varying reactivities were compared with monocalcium phosphate (MCP) in a glasshouse experiment growing perennial ryegrass (Lolium perenne cv. Nui) as the test plant on four soils of contrasting P sorption capacity and exchangeable Ca. The cumulative dry matter yield over 10 harvests showed a significant response to P application in all soils. Based on relative yield and P uptake, MCP was the most effective P fertilizer followed by the reactive phosphate rocks, which were superior to the unreactive rocks in all soils. The relative agronomic effectiveness (RAE) and substitution ratio (SR) of individual PR fertilizers, calculated with respect to MCP using the methods of vertical and horizontal comparison, respectively, were similar over a range of fertilizer rate. There was a decline or slight increase in the performance of PRs with time in the low P sorption soils but a consistent increase in the high P sorption soils. Some initial influence of exchangeable Ca content of the soils on the relative performance of PRs was also observed. Generally the PRs performed better in high P sorption soils than low P sorption soils and in low exchangeable Ca soils than high exchangeable Ca soils.     

Development and evaluation of an improved soil test for phosphorus: 1. The influence of phosphorus fertilizer solubility and soil properties on the extractability of soil P

The objective of this work was to develop and evaluate a soil test suitable for estimating the phosphorus status of soils whether they were fertilized with soluble or sparingly soluble P fertilizers or both. Four New Zealand soils of contrasting P sorption capacity and exchangeable Ca content were incubated alone or with monocalcium phosphate (MCP), reactive North Carolina (NC) phosphate rock or unreactive Florida (FRD) rock, at 240 mg P kg^–1 soil, to allow the P sources of different solubilities to react with each soil and provide soil samples containing different amounts of extractable P, Ca and residual phosphate rock. The phosphorus in the incubated soils was fractionated into alkali soluble and acid soluble P fractions using a sequential extraction procedure to assess the extent of phosphate rock dissolution. Eight soil P tests [three moderately alkaline — Olsen (0.5M NaHCO₃) modified Olsen (pretreatment with 1M NaCl) and Colwell; three acid tests — Bray 1, modified Bray 1 and Truog; and two resin tests — bicarbonate anion exchange resin (AER) and combined AER plus sodium cation exchange resin (CER)] were assessed in their ability to extract P from the incubated soils.The 0.5M NaHCO₃ based alkaline tests could not differentiate between the Control and FRD treatments in any soil nor between the Control, NC and FRD treatments in the high P sorption soils. The acid extractants appeared to be affected by the P sorption capacity of the soil probably because of reabsorption of dissolved P in the acid medium. The AER test gave results similar to Olsen. Only the combined AER + CER test extracted P in amounts related to the solubility of the P sources incubated with each soil. Furthermore, when soil samples were spiked with FRD and NC and extracted immediately, the P extracted by the AER + CER test, over and above the control soils, increased with the amount and chemical reactivity of the rocks. There was no extraction of rock P by any of the alkaline extractions.Increases in the amounts of P extracted (P) by each soil test from the fertilized soils, over and above the control soils were compared with the amounts ofP dissolved from the fertilizers during incubation (measured by P fractionation). Soil P sorption capacity had least influence on the amounts of P extracted by the AER + CER and Colwell tests. However, the Colwell test was unable to differentiate between all P sources in all four soils and suffered from the disadvantage of producing coloured extracts. The AER + CER test appeared to have the potential to assess the available P status of soils better than the other tests used because of its ability to extract a representative portion of residual PR (in accordance with the amount and reactivity) and dissolved P, and thus to differentiate between fertilizer treatments in all four soils.