Estimating the extent of surface oxidation by measuring the porosity dependent dielectrics of oxygenated porous silicon

Surface oxidation and porosity variation play significant roles in the dielectric performance of porous silicon (PS) yet discriminating the contribution of these events is a challenge. Here we present an analytical solution that covers contributions from the components of silicon oxide surface, silicon backbone and voids using a serial–parallel capacitance structure. Agreement between modeling predictions and measurement has been realized, which turns out an effective method that enables us to estimate the extent of surface oxidation of a specimen by measuring the porosity dependent dielectric response of the chemically passivated PS, and provides guidelines that could be useful for designing dielectric porous structures with surface oxidation.     

An application of Raman spectroscopy on the measurement of residual stress in porous silicon

The porous silicon film, at micron level, and the bulk silicon substrate is a basic structure in MEMS components. The residual stress, due to the lattice mismatch between the film and the substrate, exists on the interface and may cause cracking and damaging on the component. Micro-Raman spectroscopy is an optical measurement method that was rapidly applied into the fields of chemistry, physics, material science and mechanics. In this paper, the method is introduced and applied to the study of the stress problems in porous silicon as follows. (1) In the electrochemical etching technique for porous silicon preparation, the distribution of the tensile residual stress along the transitional region between etched and un-etched area is experimentally studied and the result reveals the stress is continuous across the region. In the etched region it reaches GPa level, and in the transition region the gradient of the stress is high. (2) In chemical etching preparation of porous silicon, the residual stress rises up seriously in the cracked area, up to 0.92 GPa. With the porosity increasing, the tensile stress on the porous silicon film increases accordingly. The appearance of the porous silicon film surface is also given by metalloscope and atomic force microscope. The structure of the micro-pores is expected to have a close relation with the distribution of the residual stress.     

蓄冷器丝网填料的空隙率的估算方法探讨

首先简要介绍一下目前蓄冷器采用的丝网材料的性能、现状、要求。由于其空隙率对制冷机的性能有很大的影响,以及在进行制冷机设计计算与性能模拟中,丝网材料的空隙率也是一个很重要的参数,文中针对目前存在的多种丝网空隙率的估算方法进行统计分析,并根据较精确的实测结果来对比,得出结论:在蓄冷器进行设计计算以及性能模拟时,可以选择文中的公式(4)对空隙率进行较好的估算。     

The role of Laplace pressure in the formation of the structure of thin layers based on silicon dioxide

Formation of the structure of thin layers deposited from the gas phase occurs not only during film deposition but also during the subsequent annealing. In the present work, porous films were deposited using the catalytic chemical vapor deposition (Cat-CVD) procedure. It was shown that the kinetics of a decrease in the film volume during annealing can be explained taking into account the role of Laplace pressure in the formed pores.     

多孔岩芯渗透率与孔隙度的MRI研究

运用自旋回波序列,得到一系列用盐水饱和的多孔岩芯的磁共振自旋密度象,可以直观、准确地观察岩芯的结构,并对象的信号强度与渗透率和孔隙度之间的相关关系进行了分析,发现它们之间存在良好的定性关系,得到了较好的结果.     

活性炭纤维孔结构控制和表面改性

活性炭纤维（ACF-ActivatedCarbonFiber）是本世纪七十年代发展起来的纤维状吸附剂[1]。其吸附性能与表面积、细孔直径、细孔分布等物理结构密切相关，同时与其表面化学结构密不可分，本文综述介绍ACF的孔结构控制方法和表面化学改性与吸附性能的关系。     

Synthesis,structural and electrical characterization of PbS NCs in titania sol–gel films

Nanocrystals of lead sulfide were grown in TiO₂ (titania) thin films prepared by a sol-gel process. The synthetic procedure as well as the structural, optical, and electrical properties of the films are demonstrated. The structures and morphology of PbS nanocrystals were analyzed using HRTEM, SAED, AFM, HRSEM, XRD and EDAX elemental analysis technique. When the concentration of PbS in the titania matrix is 20 mol%, PbS NCs with a diameter of 2.0 nm are created. At a higher PbS concentration (> 40 mole%) in the titania matrix, PbS NCs and PbS clusters are created not only within the TiO₂ film but also on the external surface of the TiO₂ film. By increasing the PbS concentration up to 50 mol%, PbS nanocrystals of 6–8 nm in diameter are formed within the titania film and PbS clusters with a base size of about 100 nm² and a height up to about 20 nm were self assembled on the external surface of TiO₂ film. Quantum size effect and band gap energies were obtained from shifts of the absorption edge. For electrical measurements, PbS–TiO₂ films were deposited on an ITO/glass substrate, and then covered with gold contact. The electrical properties of ITO/PbS NCs–TiO₂/Au and ITO/PbS NCs–TiO₂/PbS cluster/Au structures were studied. I–V characteristics of the one layer structure are nearly linear and symmetric, while those of the two-layer structure exhibit rectifying behavior.     

In vitro degradation of porous poly(dl-lactide-co-glycolide) (PLGA)/bioactive glass composite foams with a polar structure

In vitro degradation of porous 50/50, 70/30 and 90/10 PLGA (poly(dl-lactide-co-glycolide)) foams and PLGA/bioactive glass (20 wt%) composite foams was studied up to 16 weeks in TRIS (pH 7.4; 37 °C). Polar PLGA/bioactive glass composite films were prepared by applying the bioactive glass (S53P4) on one side of the composite. Porous foams were made by solvent casting and pressure quenching with CO₂. The fabricated foams had an initial pore size of 50-500 μm and thickness of 2-2.5 mm. In vitro degradation of the prepared foams was evaluated after 1, 2, 4, 6, 8, 12 and 16 weeks. Weight loss, water uptake, molecular mass and the amount of dissolved bioactive glass were measured after each time period. Changes in pore morphology were analysed with SEM. The present in vitro results will be evaluated and compared with the results from ongoing animal studies where comparable implants are used for bone defect treatment under non-load-bearing conditions.     

Effect of preparative conditions on the surface characteristics of mixed zirconium and titanium oxides

The surface characteristics of mixed zirconium and titanium oxides prepared from different starting materials are investigated. One mode of preparation entailed the use of zirconium sulfate and titanium oxysulfate as starting materials and ammonium hydroxide as precipitating agent. The produced oxides were washed to different extents to obtain samples with different sulfate content. A second preparative mode used zirconium oxychloride and titanous chloride as starting materials also with ammonium hydroxide as precipitating agent. The oxidation of the titanous to the titanic form for these oxides was carried out by means of oxygen gas. Resulting samples were heat treated at 400 °C and 600 °C, and textural characteristics determined from the adsorption of N₂ at 77 K, complemented by infrared and thermal studies. The samples precipitated from the oxychloride and chloride salts of zirconium and titanium, as well as those precipitated from the sulfate and oxysulfate salts and washed free of the sulfate ions displayed quite similar textural characteristics. The unheated samples and those heat-treated at 400 °C were mesoporous, with some microporosity, and relatively large surface areas in the order of 200–300 m²/g. Heat treatment to 600 °C led to a relative decrease in surface area, in the order of 100 m²/g, and to the disappearance of microporosity. The mixed zirconium and titanium oxides with a sulfate content of ≈17% displayed significantly lower surface areas, smaller than 10 m²/g, with a prevalence of micro and mesoporosity. Infrared and thermal studies indicated the presence of differently bounded sulfato groups, which seem to have a blocking effect on the pores, resulting in the observed smaller surface areas.     

Lithium adsorption properties of porous LiAl-layered double hydroxides synthesized using surfactants

Porous LiAl-layered double hydroxides (LiAl-LDHs) of [Li₂Al₄(OH)₁₂](CO₃)·4H₂O were hydrothermally synthesized in one-pot by mixing LiCl, AlCl₃, urea, and one surfactant each (sodium dodecyl sulfate (SDS), octadecyl amine (OA), and sodium lauryl sulfonate (SLS)) as soft templates. The LiAl-LDHs were granulated by crosslinked sodium alginate. The LiAl-LDHs were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and porosity. Special attention was focused on the rise of Li⁺ adsorption capacity based on the porous morphology in synthetic and real salt lake brine. The adsorption capacity of granulated LiAl-LDHs-SLS reaches 8.48 mg/g in a solution containing 300 mg/L of Li⁺ at pH = 7 and 11.8 mg/g from Da Qaidam brine with 1.0 g/L of Li⁺. Lithium adsorption followed the Langmuir isotherm and pseudo-second-order kinetics. Temperature, solution pH, and other electrolytes had a minor effect on the adsorption performance of porous LiAl-LDHs. The structure of surfactants had a significant influence on the porosity of synthesized LiAl-LDHs, and thus on the adsorption capacity.