Rebar corrosion in chloride environment

Chloride induced reinforcement corrosion in concrete is a serious durability problem. Different sources of chloride, i.e. chloride introduced at the fresh stage of concrete (i.e. internal chloride) and chloride entered during the hardened state (i.e. external chloride) may affect the performance of concrete in different ways. For the performance evaluation of reinforced concrete in chloride environment (i.e. both internal and external chloride), there is a need for performing different electrochemical tests to obtain various corrosion parameters that will specify the possibility and the magnitude of corrosion in concrete. In the present study, the results of an experimental investigation that includes different corrosion tests namely potential measurement, corrosion rate measurement and potentiodynamic polarization test have been presented and analyzed to evaluate the performance of concrete both in internal chloride and external chloride exposure conditions. In addition an attempt is made to correlate the corrosion parameters obtained from internal and external chloride exposure conditions. From the results it was observed that, dropped half-cell potential value obtained from external chloride exposure mostly lie in the active zone obtained from internal chloride exposure. In addition it was observed that there was significant difference in corrosion current values obtained from both internal and external chloride exposure conditions. Further on the basis of overall ranking obtained from the results of critical parameters from different exposure conditions, the performance of different cement–steel combinations against chloride induced rebar corrosion has been evaluated.     

Recent advances in indium metallurgy: A review

The by-products of zinc refineries are used as the primary mineral resources for the commercial production of indium. The discarded LCDs containing adequate amount of indium is rather worth as its secondary resources compared to the by-products of zinc refineries. Mining and recycling rates of indium, respectively from minerals and waste LCDs are in progress to meet its huge demand. Recycling of the LCDs has been dominating over mining, as presently 480t of indium are produced annually from mining, however, that of 650t annually from recycling. Different aspects of the extractive metallurgy of indium are summarized in this review paper.     

Radial Sub-band Allocation with Downlink Interference Mitigation in Macro–Femto Environment

Wireless Personal Communications - Femtocell deployment is an important strategy when it comes to improvement of QoS metrics in areas of poor cell coverage like indoors in an LTE environment. This,...     

Transplantation for end stage liver disease related to alpha 1 antitrypsin

Alpha 1 antitrypsin deficiency (AT) is an autosomal recessive disease associated with chronic liver disease in adults and children and emphysema in adults. The disease is one of the most common inherited disorders of the Caucasian population of North Europe and North America and is the most common genetic reason for pediatric orthotopic liver transplantation (OLTx), although it is a rare indication in adults. The natural history of the disease is unpredictable and the pathogenesis of the liver injury unclear. Thirty-five patients with histologically apparent alpha 1 AT accumulation in the liver (22 adults, 13 children) have been transplanted in this center. Clinical features were correlated with the pretransplant phenotype, serum alpha 1 antitrypsin levels and potential precipitating factors. All children were PiZZ homozygotes, most of whom had presented with neonatal hepatitis. The majority of adult patients were heterozygotes presenting with portal hypertension and liver cirrhosis. Current one-year posttransplant survival figures are 73% for adults and 87.5% for children. Replacement of the cirrhotic liver results in acquisition of the donor phenotype, a rise in serum levels of alpha 1 antitrypsin, and apparent prevention of associated disease.     

Actinoplanic acids A and B as novel inhibitors of farnesyl-protein transferase

Actinoplanic acids A and B are macrocyclic polycarboxylic acids that are potent reversible inhibitors of farnesyl-protein transferase. Actinoplanic acids A and B were isolated from Actinoplanes sp. MA 7066 while actinoplanic acid B was isolated from both MA 7066 and Streptomyces sp. MA 7099. Actinoplanic acids A and B are competitive with respect to farnesyl diphosphate and are selective inhibitors of farnesyl-protein transferase because they do not inhibit geranylgeranyl-protein transferase type 1 or squalene synthase. MA 7066 is believed to be a novel species of actinomycetes while MA 7099 is believed to be a novel strain of Streptomyces violaceusniger on the basis of morphological, biochemical and chemotaxonomic characteristics as well as its production of actinoplanic acids.