pH玻璃电极的现状与发展

对pH玻璃电极的结构、原理以及特性进行了综述.与液体充填式玻璃电极比较,固体接触式pH玻璃电极有明显的优点.叙述了固体接触式pH玻璃电极膜的成分及其响应机理,并指出固体接触式pH玻璃电极的发展方向.     

Nanocomposite route to the stabilization of porous ϑ-alumina

Stabilization of -alumina phase by silica was studied in nanocomposite (diphasic) alumina-silica gels by XRD and BET surface areas measurements. Five wt.% of silica (22 nm particles) increased the crystallization temperature of to -alumina by about 100°C from boehmite (10 nm particles) derived alumina. Stabilization of -alumina was caused by the formation of intimate contact (Al-O-Si) between components by diffusion of silica into the defect alumina structure.Also with the Department of Agronomy.     

Monodisperse nanoparticles of poly(ethylene glycol) macromers and N‐isopropyl acrylamide for biomedical applications

Poly(ethylene glycol)‐based nanoparticles have received significant attention in the field of biomedicine. When they are copolymerized with pH‐ or temperature‐sensitive comonomers, their small size allows them to respond very quickly to changes in the environment, including changes in the pH, ionic strength, and temperature. In addition, the high surface‐to‐volume ratio makes them highly functionalized. In this work, nanoparticles composed of temperature‐sensitive poly(N‐isopropylacrylamide), poly(ethylene glycol) 400 dimethacrylate, and poly(ethylene glycol) 1000 methacrylate were prepared by a thermally initiated, free‐radical dispersion polymerization method. The temperature‐responsive behavior of the hydrogel nanoparticles was characterized by the study of their particle size with photon correlation spectroscopy. The size of the nanoparticles varied from 200 to 1100 nm and was a strong function of the temperature of the system, from 5 to 40°C. The thermal, structural, and morphological characteristics were also investigated. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1678–1684, 2003     

Kinetic investigation of the chlorine reduction reaction on electrochemically oxidised ruthenium

The rate and mechanism of the electroreduction of chlorine on electrooxidised ruthenium has been investigated with focus on the effect of solution pH. Current/potential curves for the reduction process in solutions with constant chloride concentration of 1.0 mol dm⁻³ and varying H⁺ concentration have been obtained with the use of the rotating disk electrode technique (RDE). It was found that the chlorine reduction rate is highly inhibited in solutions with high H⁺ concentrations and that it can be satisfactorily described by the Erenburg mechanism, previously suggested for the chlorine evolution on RuO₂ and RTO. The expression of the kinetic current as a function of chlorine and H⁺ concentration was obtained by solving the elementary rate equations of the kinetic mechanism. The kinetic constants obtained from the correlation of the kinetic current expression to the experimental data were used to simulate the dependence of the surface coverages and elementary reaction rates on overpotential.     

过氧化氢处理河流着生刚毛藻的效果研究

以深圳市某河流为研究对象,分析了投加H2O2对刚毛藻生物量的控制效果及其对水体p H、溶解氧、氨氮和总磷的影响。结果表明:H2O2≥1.25 mol/L时能有效抑制刚毛藻生长,使藻类光合活性在10 min内从5.8降低到0,叶绿素浓度在30 min内从5.8 mg/L降低至0.2 mg/L。现场试验投加H2O2处理河流水体中刚毛藻14 d内,藻类生物量、光合活性和叶绿素浓度降幅均高于90%。加药1 h后,河流p H值由原来的9.21~9.74迅速降低至8.23~8.80,14 d内保持在9以下。河流溶解氧、氨氮、总磷和H2O2残留浓度在除藻过程中存在变化,但是1 d后会迅速恢复至加药前水平。投加H2O2是一种有效、无污染的应急去除河流着生刚毛藻的方法。     

Mechanistic investigation of hydrogen-enhanced anodic dissolution of X-70 pipe steel and its implication on near-neutral pH SCC of pipelines

The effects of hydrogen-charging on anodic dissolution of pipe steel under near-neutral pH condition were studied by electrochemical techniques. Hydrogen-charging enhances the anodic dissolution rate of the steel. The hydrogen-enhanced dissolution increases with increasing charging current density. The hydrogen effect is attributed to the alteration of chemical potential and exchange current density of steel. Hydrogen-charging affects the corrosion process of the steel. In particular, at a high charging current density, a layer of corrosion product forms on the electrode surface to change corrosion potential and interfacial double-charge layer capacitance as well as charge-transfer resistance. The hydrogen effect factor for enhanced anodic dissolution of steel at an anodic potential of −0.4 V (SCE) is 1.53 only. Hydrogen-enhanced anodic dissolution of steel by itself may not be the major factor contributing to the high rate of crack growth in pipe steel in near-neutral pH electrolyte. A further investigation of the synergistic effect of hydrogen and stress on dissolution at the crack-tip is essential to determine the mechanism of near-neutral pH stress corrosion cracking of pipelines.     

Shape memory polymers based on uniform aliphatic urethane networks

Aliphatic urethane polymers have been synthesized and characterized, using monomers with high molecular symmetry, to form amorphous networks with very uniform supermolecular structures, which can be used as photo‐thermally actuable shape memory polymers (SMPs). The monomers used include hexamethylene diisocyanate (HDI), trimethylhexamethylenediamine (TMHDI), N,N,N′,N′‐tetrakis(hydroxypropyl)ethylenediamine (HPED), triethanolamine (TEA), and 1,3‐butanediol (BD). The new polymers were characterized by solvent extraction, NMR, XPS, UV/VIS, DSC, DMTA, and tensile testing. The resulting polymers were found to be single phase amorphous networks with very high gel fraction, excellent optical clarity, and extremely sharp single glass transitions in the range of 34–153°C. Thermomechanical testing of these materials confirms their excellent shape memory behavior, high recovery force, and low mechanical hysteresis (especially on multiple cycles), effectively behaving as ideal elastomers above T_g. We believe these materials represent a new and potentially important class of SMPs, and should be especially useful in applications such as biomedical microdevices. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

乙炔清净废水再利用研究

本文主要是关注乙炔清净废水循环利用的问题,考察了废次钠液温度、新次钠液有效氯含量,以及pH值等因素对新、废次钠液混合的影响。发现废次钠液温度、新次钠液有效氯含量影响甚微,pH值有较大影响。控制pH值在5.5以上,循环利用废次钠液是可行的。     

Effect of pH on a gossypol complex with phospholipids: Gossypol-PE

PE, one of the major phospholipids in oilseed soapstock, may react with gossypol to form Schiff bases. PE amounts to 20–30% of the phosphorus compounds in soap-stock. In this report, the dependence on pH of the Schiff base products between PE and gossypol was investigated using a spectrophotometer, an HPLC equipped with an ELSD, and an LC-MS system. We observed that at pH 7 the Schiff reaction product and reactants were clearly detected by ELSD, absorption, and LC-MS spectra. The absorption spectra displayed the characteristic peak for the Schiff bases around 430–440 nm. The absorption spectra also indicated that the reaction was pH dependent. The reaction temperatures were 60 and 90°C. The LC-MS spectra supported the formation of Schiff bases as well as methyl ether derivatives of gossypol in alcohol at the elevated temperatures. The implications of these experimental findings are presented in this paper.     

Enhanced strain hardening in elongational viscosity for HDPE/crosslinked HDPE blend. I. Characteristics of crosslinked HDPE

Blending a crosslinked high‐density polyethylene (xHDPE) enhances melt strength and strain hardening behavior in elongational viscosity of high‐density polyethylene (HDPE) to a great degree. Gel fraction of xHDPE has a stronger effect on the strain hardening than sol fraction, although sol fraction also enhances the strain hardening to some degree. Further, the xHDPE crosslinked by peroxide in a compression mold exhibits more pronounced effect than xHDPE by radiation, which is attributed to the difference in the amount of the gel fraction. The xHDPE, which enhances the strain hardening, has sparse crosslink points in the network. Moreover, it was found from linear viscoelastic measurements, such as oscillatory modulus and relaxation modulus, that the xHDPE is characterized as a critical gel, which was also supported by the result of tensile testing. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 73–78, 2002