Effect of Bimodal Grain Size Distribution on the Strain Hardening Behavior of a Medium-Entropy Alloy

The evolution of strain hardening behavior of the Fe_(50)(CoCrMnNi)_(50) medium-entropy alloy as a function of the fraction of recrystallized microstructure and the grain size was studied using the Hollomon and Ludwigson equations.The specimens under study were partially recrystallized,fully recrystallized with ultrafine-grained microstructure,and fully recrystallized with coarse grains.The yield strength decreases steadily as the fraction of recry stallized micro structure and grain size increases due to the recovery process and the Hall-Petch effect.Interestingly,the bimodal grain distribution was found to have a significant impact on strain hardening during plastic deformation.For instance,the highest ultimate tensile strength was exhibited by a 0.97 μm specimen,which was observed to contain a bimodal grain distribution.Furthermore,using the Ludwigson equation,the effect of the bimodal grain distribution was established from the behavior of K_2 and n1 curves.These curves tend to show very high values in the specimens with a bimodal grain distribution compared to those that show a homogenous grain distribution.Additionally,the bimodal grain distribution contributes to the extensive L(u|")ders strain observed in the 0.97 μm specimen,which induces a significant deviation of the Hollomon equation at lower strains.     

Temporal variation of pharmaceuticals in an urban and agriculturally influenced stream

Pharmaceuticals have become ubiquitous in the aquatic environment. Previous studies consistently demonstrate the prevalence of pharmaceuticals in freshwater but we do not yet know how concentrations vary over time within a given system. Two sites in central Indiana with varying land use in the surrounding watershed (suburban and agricultural) were sampled monthly for pharmaceutical concentrations and stream physiochemical parameters. Sediment samples were also collected at each sampling event for measurement of δ¹⁵N natural abundance and sediment organic content. Across sites and sampling events, twelve pharmaceuticals were detected including acetaminophen, caffeine, carbamazepine, cotinine, N,N-diethyl-meta-toluamide (DEET), gemfibrozil, ibuprofen, sulfadimethoxine, sulfamethazine, sulfamethoxazole, triclosan, and trimethoprim. Sulfathiazole, lincomycin, and tylosin were not detected at either site at any time. The agriculturally-influenced site had comparable pharmaceutical concentrations to the urban-influenced site. In general, pharmaceutical concentrations increased during winter at both sites and decreased during spring and summer. Multiple regression analyses indicated that water column dissolved oxygen, the number of days since precipitation, and solar radiation influenced total pharmaceutical concentration in the urban-influenced site; whereas pH, chlorophyll a concentration, and total amount of rainfall in the previous 10 days influenced total pharmaceutical concentrations in the agriculturally-influenced site. Pharmaceutical concentrations were not correlated with sediment δ¹⁵N across or within sites. However, sediment in the urban-influenced site had higher mean δ¹⁵N signatures relative to sediment in the agriculturally-influenced site. These data indicate pharmaceuticals are persistent in aquatic ecosystems influenced by both agricultural and suburban activity. Pharmaceuticals are designed to have a physiological effect; therefore, it is likely that they may also influence aquatic organisms, potentially threatening freshwater ecosystem health.     

HIPed Tailored Hollandite Waste Forms for the Immobilization of Radioactive Cs and Sr

Hot isostatically pressed tailored hollandite waste forms were used to demonstrate the immobilization of Cs and Sr are separable from spent nuclear fuel, as well as Ba and Rb. Four hollandite formulations were investigated, two samples with ∼12 wt% waste loading (on an oxide basis) and two with ∼18 wt% waste loading. Two of the samples were Al-substituted and the other two contained Mg. The hollandite in the Al-substituted samples contained all the waste cations, as designed, but this was not the case in the Mg-substituted samples. The hollandite in the Mg-substituted samples did not contain all the waste cations, with ∼50% of the Sr forming SrTiO₃ as a secondary phase. This resulted in waste forms that were not as durable, with respect to Cs, as their Al counterparts. The formation of SrTiO₃ had little effect on the Sr release rates and was not detrimental to the Mg-substituted hollandite waste form. For the Al-substituted samples, the MCC-1 normalized release rates were <0.06 g·(m²·day)⁻¹ at 0–28 days for all elements, while the Cs release rates remained at 2.0 g·(m²·day)⁻¹ at 0–28 days for the Mg-substituted samples.     

高k材料／金属栅电极迈向大规模量产

到了45纳米技术节点,高介电常数绝缘材料和金属栅电极将被用于射造逻辑电路器件。而采用高金属功函数和能隙工程电荷陷阱的闪存也能从这些项技术中获益。     

Advances in room temperature curing adhesives and sealants—a review

Room temperature curing adhesives and sealants, defined here as those which cure without a mixing process under the influence of substrates or environmentally available reagents such as daylight, oxygen or moisture, include polyurethane, silicone, anaerobic adhesives, cyanoacrylate and certain acrylic types. Advances in cure chemistry, built-in adhesion promotion, and in formulating techniques have created the scope for significant new properties within all the mentioned systems. In addition, development of resins having two (or more) different functionalities, which respond to substrate and or atmospheric cure agents, has created the potential to achieve new advanced performance levels. Examples of these include compositions which give light curing through acrylic functions while having RTV (room temperature vulcanising) silicone resin chemistry polymerising under the influence of atmospheric moisture. The properties can be tailored by molecular design, formulation and choice of cure accelerators.     

Platinum sulfated zirconia catalysts. Fate of chlorine during activation

The gases evolved during activation of a sulfated zirconia prepared by impregnation with chloroplatinic acid have been followed using mass spectrometry and infrared spectrometry. When the sample is heated in either helium or in air, the halogen is lost from the catalyst as HCl and Cl2. Heating the sample in hydrogen results in the loss of the halogen as HCl, and only traces as Cl2. The loss of halogen occurs over a wide temperature range (200-900°C). The data are consistent with the chloroplatinic acid being converted by loss of halide with the formation of Pt⁰. This revised version was published online in July 2006 with corrections to the Cover Date.     

Self-organizing map network as an interactive clustering tool — An application to group technology

The Self-Organizing Map (SOM) network, a variation of neural computing networks, is a categorization network developed by Kohonen. The theory of the SOM network is motivated by the observation of the operation of the brain. This paper presents the technique of SOM and shows how it may be applied as a clustering tool to group technology. A computer program for implementing the SOM neural networks is developed and the results are compared with other clustering approaches used in group technology. The study demonstrates the potential of using the Self-Organizing Map as the clustering tool for part family formation in group technology.