Chimie douce hydrogen production from Hg contaminated water,with desirable throughput,and simultaneous Hg-removal

Hydrogen's widespread use is fraught with many difficulties. The challenges currently are to do with safety concerns in gas storage and transportation, and low rate of production leading to non-viability of technologies at the point-of-use. Another global concern of immediate relevance involves heavy-metal ion pollution. Viable processes which can simultaneously remove and result in beneficiation of the contaminants are hitherto rarely reported. In this context we report a single-step, in situ co-reduction approach which has the dual advantage of (i) Hg contaminant removal, and (ii) room temperature hydrogen production. Hydrogen is produced via galvanic corrosion of in situ synthesized nanoaluminium amalgam. The production rate (720 mL/min for 0.5 g-Al salt) is far superior to what would be expected from the use of pure hydrides, and/or using bulk amalgams at room temperature. The method is simple, chimie douce (i.e soft chemical), hence potentially affordable, and capable of providing a means of beneficiating Hg contaminated water present in effluents from certain industries (for example, industries which uses chlor-alkali process). The in situ co-reduction approach helps in bypassing the usual rate limiting step which involves formation of an alumina passivation layer on hydrolytic material surface. Given the potential that exists in scale down and up, this approach offers a method to address the long standing challenge of point-of-use hydrogen availability.     

Biopolymeric coatings for delivery of antibiotic and controlled degradation of bioresorbable Mg AZ31 alloys

Magnesium and magnesium alloys are attracting considerable interest as biodegradable materials with high potential for application as temporary implants. The high corrosion rate of Mg-based implants is considered a serious drawback, and it is crucial to design novel surface protection strategies that minimize the detrimental effects of corrosion, while contributing for introducing additional functionalities on the material surface. In this work, a layer-by-layer coating architecture composed of an inner poly(lactic-co-glycolic) acid layer, working as adhesion promoter, and additional polycaprolactone (PCL) layers working as reservoirs for antibiotic (levofloxacin) and for nanohydroxyapatite (nanoHA) particles was applied on the Mg alloy AZ31. The results demonstrate that the composition and number of PCL layers can tailor the biodegradation of the bare magnesium alloy, surface wettability, and the kinetics of release of antibiotic (levofloxacin). The distribution of nanoHA in the coating architecture plays a crucial role on tailoring the desired biocompatible functionalities and corrosion protection of the bare alloy.     

Laminated aluminum thin-films as low-cost opaque moisture ultra-barriers for flexible organic electronic devices

Flexible aluminum moisture barrier films are shown to meet ultra-barrier requirements with water vapor transmission rates as low as 1*10⁻⁴ g/m²/day at 38 °C and 90% R.H. These low transmission rates are achieved by lamination of two films that are independently processed on individual substrates. The integration in organic electronic devices like organic solar cells or OLEDs is particularly easy in a single lamination step, since an existing aluminum electrode can be utilized as one half of the moisture barrier. The resulting laminate maintains flexibility of the device and improves the barrier quality by an order of magnitude compared to conventional stacking of two barriers. Organic solar cells with this type of encapsulation are manufactured and aged in controlled climate. They do not exhibit significant extrinsic degradation.     

谈11G101-1图集的变化

依据相关标准及规范,对11G101-1图集中关于制图规则、钢筋锚固、搭接、节点构造等内容的变化作了分析,以便于设计人员掌握11G101-1图集内容,解决如何执行11G101-1图集的问题。     

Stability of the passive state of Zr–Nb crystalline alloys

Stability of the passive state was assessed for pure Zr and four Zr–Nb alloys (2.5, 5.0, 10.0, 25.0 at.% Nb) after 24 h exposure to naturally aerated 3.5% NaCl solution (pH = 6). Open circuit potential values indicated that all the Zr–Nb alloys studied and the pure Zr undergo spontaneous passivation due to spontaneously formed oxide film passivating the metallic surface. It also indicated that the addition of increasing Nb contents to pure Zr seems to improve the protection characteristics of its spontaneous oxides. Potentiodynamic polarization curves showed an increase of the breakdown potential and the extent of the passive range following an increased niobium amount in the alloy. This leads to the conclusion that a progressive increase of niobium content positively affects the localized corrosion behaviour of the Zr–Nb alloys by enhancing the electrochemical stability of the passive film. Electrochemical impedance spectroscopy (EIS) studies showed high impedance values for all the samples, and its increase on increased niobium content in the alloy indicated an improvement in the corrosion resistance of the spontaneous oxide film. The fit obtained suggests a single passive film present on the metal surface, with resistance improving with the increase of niobium amount in the alloy. All these electrochemical results show the beneficial effect of increasing niobium contents on the passive state stability of the Zr–Nb alloys.     

Environmental fatigue behavior of non‐crimp,E‐glass fiber reinforced polyester composites for marine applications

This study is aimed to find the fatigue behavior of Glass Reinforced Plastics, a material which is a widely preferred material for small marine crafts, as well as several other applications. The type of composite tested is hand‐laid E‐glass non‐crimp reinforcements with an polyester resin matrix. The specimens were produced in two standard thicknesses and with these material directions and were tested both under atmospheric and simulated seawater environments for fatigue. It was seen that the results of fatigue lifetime obtained by testing the material in seawater is much lower than the results obtained from testing similar specimens under atmospheric conditions. However, the stress curves indicate the same slope, suggesting that the fatigue failure mechanism of both testing conditions is the same and the fiber‐related factors dominate. It was found that the thickness and material direction did not have a significant effect on the fatigue behavior of the material.