Surface modification of nanoporous alumina membranes by plasma polymerization

The deposition of plasma polymer coatings onto porous alumina (PA) membranes was investigated with the aim of adjusting the surface chemistry and the pore size of the membranes. PA membranes from commercial sources with a range of pore diameters (20, 100 and 200?nm) were used and modified by plasma polymerization using n-heptylamine (HA) monomer, which resulted in a chemically reactive polymer surface with amino groups. Heptylamine plasma polymer (HAPP) layers with a thickness less than the pore diameter do not span the pores but reduce their diameter. Accordingly, by adjusting the deposition time and thus the thickness of the plasma polymer coating, it is feasible to produce any desired pore diameter. The structural and chemical properties of modified membranes were studied by scanning electron microscopy (SEM), atomic force microscopy (AFM) and x-ray electron spectroscopy (XPS). The resultant PA membranes with specific surface chemistry and controlled pore size are applicable for molecular separation, cell culture, bioreactors, biosensing, drug delivery, and engineering complex composite membranes.     

Novel methods for the characterization of water-soluble polymers

The liquid chromatography of four water-soluble polymers [pullulan, polyacrylamide, poly(ethylene glycol), and poly(ethylene oxide)] have been investigated and used to categorize separation processes which couple enthalpic and entropic mechanisms. Experiments were carried out with a binary mobile phase which combined a thermodynamically good solvent (water or aqueous 0.02M Na₂SO₄) and nonsolvent (methanol). The polymer solute was injected in a good solvent. By varying the solvent–nonsolvent ratio in the eluent, conditions could be obtained where the free energies of exclusion and solvation were balanced. This has been given the nomenclature “liquid chromatography under limiting conditions of solubility” (LC-LCS) since the polymer elutes just in front of the system peak at the “limit” of its solubility. Conditions can also be identified where exclusion is balanced with adsorption (“liquid chromatography under limiting conditions of adsorption,” or LC-LCA). To our knowledge, these are the first experimental reports of LC-LCS for any polymer and the first LC-LCA observation on water-soluble macromolecules. All measurements were carried out over a poly(hydroxymethylacrylate) sorbent. Cloud point curves were found to generally distinguish the regions where LC-LCA or LC-LCS dominate. The data illustrate the need to consider the polymer when analyzing LC-LCA. Conversely, polymer adsorption may play an important role in LC-LCS. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 2549–2557, 1998     

控制气氛下的AgCuTi/TiAl润湿铺展动力学

采用热台原位加热法系统研究了不同保护气体流量对润湿铺展过程、润湿铺展最大半径、润湿铺展动力学以及界面组织结构的影响.保护气体为氩气,保护气体流量分别为5,10,15 mL/s;加热曲线设定最高温度为1273 K,保温时间120 s;采用扫描电镜、能谱分析、光学显微镜等分析了界面组织结构.结果表明,保护气体流量为15 mL/s时,润湿铺展等效半径最大,原始半径0.9 mm的钎料铺展半径达到约1.4 mm.各种保护条件下,AgCuTi/TiAl体系的润湿铺展动力学过程相似,铺展半径与时间之间呈n次幂关系,即rn~kt;润湿铺展中钎料熔敷/TiAl的界面结构为:残余钎料的富银相/AlCuTi三元相层(AlCu₂Ti, AlCuTi, Ti₃Al)/TiAl母材,保护条件对其影响不大.     

Microstructure–mechanical properties relations in SiC–TiB2 composite

Densification and mechanical properties (fracture toughness, flexural strength and hardness) of SiC–TiB₂ composite were studied. Pressureless sintering experiments were carried out on samples containing 0–50 vol% of TiB₂ created by in situ reaction between TiO₂, B₄C and carbon. Al₂O₃ and Y₂O₃ were used as sintering additives to create liquid phase and promote densification at sintering temperature of 1940 °C. The sintered samples were subsequently heat treated at 1970 °C. It was found that the presence of TiB₂ serves as an effective obstacle to SiC grain growth as well as crack propagation thus increasing both strength and fracture toughness of sintered SiC–TiB₂ composite. The subsequent heat treatment of sintered samples promoted the elongation of SiC matrix and further improved mechanical properties of the composite. The best mechanical properties were measured in heat-treated samples containing 12–24 vol% TiB₂. The maximum flexural strength of ∼600 MPa was obtained in samples with 12 vol% TiB₂ whereas the maximum fracture toughness of 6.6 MPa m^1/2 was obtained in samples with 24 vol% TiB₂. Typical microstructures of samples with the mentioned volume fractions of TiB₂ consist of TiB₂ particles (<5 μm) uniformly dispersed in a matrix of elongated SiC plates.     

Nanopore gradients on porous aluminum oxide generated by nonuniform anodization of aluminum

A method for surface engineering of structural gradients with nanopore topography using the self-ordering process based on electrochemical anodization of aluminum is described. A distinct anodization condition with an asymmetrically distributed electric field at the electrolyte/aluminum interface is created by nonparallel arrangement between electrodes (tilted by 45°) in an electrochemical cell. The anodic aluminum oxide (AAO) porous surfaces with ordered nanopore structures with gradual and continuous change of pore diameters from 80 to 300 nm across an area of 0.5-1 cm were fabricated by this anodization using two common electrolytes, oxalic acid (0.3 M) and phosphoric acid (0.3 M). The formation of pore gradients of AAO is explained by asymmetric and gradual distribution of the current density and temperature variation generated on the surface of Al during the anodization process. Optical and wetting gradients of prepared pore structures were confirmed by reflective interferometric spectroscopy and contact angle measurements showing the ability of this method to generate porous surfaces with multifunctional gradients (structural, optical, wetting). The study of influence of pore structures on cell growth using the culture of neuroblastoma cells reveals biological relevance of nanopore gradients and the potential to be applied as the platform for spatially controllable cell growth and cell differentiation.     

Hydro energy potential of cooling water at the thermal power plant

The hydro energy of the gravity water flow from the coal-fired thermal power plant units to the river in an open cooling system of turbine condensers is determined. On the basis of statistical data for a long time period, the water net head duration curve due to the river annual level change, as well as the reduction of the hydro energy potential due to the thermal power plant overhauls periods, are evaluated in the case study of the Thermal Power Plant “Nikola Tesla B” in Serbia. A small hydro power plant is designed for the utilization of this hydro energy, and the economic benefits of the project are calculated. The internal rate of returns and pay back periods are calculated in dependence of the electricity price and total investment costs. The increase of profitability is assessed, bearing in mind that the plant might be realized as the Clean Development Mechanism project according to the Kyoto protocol. The obtained results show that the project is economically attractive, and it can be carried out with standard matured solutions of hydro turbines available at the market. Even for the relatively low electricity price from small hydro power plants in Serbia of 0.08 €/kW h the internal rate of return and the pay back period are 17.5% and 5.5 years.     

Wetting and Spreading Of Liquid Metals Through Open Microgrooves and Surface Alterations

Surface-tension-driven flows (isothermal or non-isothermal) of microlayers of complex liquids over substrates under reactive wetting conditions at elevated temperatures are greatly influenced by interface interactions and topography of surface alterations. For example, understanding of the spreading of molten metals over metal substrates with complex topography may be interpreted as spreading over multiple connected networks of open microchannels. Hence, understanding of the kinetics of wetting and spreading of such reactive systems through microchannels is of a key interest. This article provides an overview of wetting/spreading phenomena related to migration of molten metal microlayer over smooth, rough, and/or well-organized-topography surfaces, such as microchannels. Systems involving a liquid metal medium temperature range (at ～850–873 K, Al-Si over Al), and a low temperature range (～420–520 K, Pb-Sn and Ag-Sn over Cu and Cu-Sn) have been considered. Kinetics data involving triple-line movement and its modeling were supported by real-time in situ visualizations. Targeted applications of these fundamental studies involve the art of brazing of compact aluminum heat exchangers for HVAC&R (heating, ventilation, air conditioning, and refrigeration), thermal management for aerospace, and soldering processes (in particular lead-free) for electronics industries.     

Analysis of Fin-Tube Joints in a Compact Heat Exchanger

This article deals with an analysis of fin-tube joints as functions of topological alterations of the joint fillet size. Based on numerical predictions of a joint topology formed by the surface tension driven reactive flow of molten metal, and subsequently verified by empirical evidence gathered through both laboratory and industrial testing, the topology alterations were identified for thermal integrity studies. Subsequently, thermal characteristics of corresponding fin-tube joints were determined in terms of two models of the thermal contact resistance. Model predictions of the fin efficiency with an altered topology of the joint zone were compared with the simulation results from a computational fluid dynamics study, and the results fit well. Numerical predictions of joint topology were devised using an in-house-developed finite-element code, and verified by the Surface Evolver code. Such prediction provided quantitative joint topology information that was needed in assessments of the joint thermal performance. Experimental data were obtained using a computer-controlled transparent hot zone with an ultra-high-purity nitrogen background atmosphere under tightly controlled conditions, and also by an analysis of the state-of-the-art manufacturing process data obtained from an industrial setting. It is demonstrated that a value of fin efficiency, assumed as recommended by traditional sizing design procedures, may drastically differ from actual values.     

Chemical functionalization of diatom silica microparticles for adsorption of gold (III) ions

Diatom silica microparticles from natural diatomaceous earth (DE) silica have been functionalized with 3-mercaptopropyltrimethoxysilane (MPTMS) and their application for adsorption of gold (III) ions from aqueous solutions is demonstrated. Fourier transform infrared spectroscopy (FTIR) and X-ray Photoelectron spectroscopy (XPS) analyses of the MPTMS modified diatom microparticles revealed that the silane layer with functional group (-SH) was successfully introduced to the diatom surface. The adsorption study of Au(III) ions using MPTMS-DE indicated that the process depends on initial gold (III) concentration and pH showing maximum adsorption capacity at pH = 3. The Au(III) adsorption kinetics results showed that the adsorption was very fast and followed a pseudo-second-order reaction model. The Langmuir model was used to provide a sound mechanistic basis for the theoretical of the adsorption equilibrium data. Gold recovery from MPTMS-DE structures was also investigated by using acidified thiourea solution and found to be high (> 95%). These results show that chemically modified DE microparticles can be used as a new, cost effective and environmentally benign adsorbent suitable for adsorption of gold metal ions from aqueous solutions.     

A nanoporous interferometric micro-sensor for biomedical detection of volatile sulphur compounds

ABSTRACT: This work presents the use of nanoporous anodic aluminium oxide [AAO] for reflective interferometric sensing of volatile sulphur compounds and hydrogen sulphide [H2S] gas. Detection is based on changes of the interference signal from AAO porous layer as a result of specific adsorption of gas molecules with sulphur functional groups on a gold-coated surface. A nanoporous AAO sensing platform with optimised pore diameters (30 nm) and length (4 μm) was fabricated using a two-step anodization process in 0.3 M oxalic, followed by coating with a thin gold film (8 nm). The AAO is assembled in a specially designed microfluidic chip supported with a miniature fibre optic system that is able to measure changes of reflective interference signal (Fabry-Perrot fringes). When the sensor is exposed to a small concentration of H2S gas, the interference signal showed a concentration-dependent wavelength shifting of the Fabry-Perot interference fringe spectrum, as a result of the adsorption of H2S molecules on the Au surface and changes in the refractive index of the AAO. A practical biomedical application of reflectometric interference spectroscopy [RIfS] Au-AAO sensor for malodour measurement was successfully shown. The RIfS method based on a nanoporous AAO platform is simple, easy to miniaturise, inexpensive and has great potential for development of gas sensing devices for a range of medical and environmental applications.