Casting properties of ASTM A128 Gr. E1 steel modified with Mn-alloying and titanium ladle treatment

This work aims to produce a high manganese steel with more refined austenite grains and better wear resistance without sacrificing the toughness and tensile properties by Mn alloying and Ti ladle treatment in comparision to ASTM A128 Gr. E1 steel (1.0C-13Mn) that is mostly used in the mining industry. The 1.0C-17Mn-xTi alloys (x=0, 0.05 and 0.1, in wt.%) were prepared. A relationship was established between the microstructures and mechanical properties of the as-cast and solution annealed alloys. Increasing Ti content increases the stable Ti(CN) phase on and beside the grain boundaries and decreases up to 37% the austenite grain size of the as-cast alloy with 0.10wt.% Ti. Correspondingly, after solution annealed, optimized titanium content (0.05wt.%) results in significant improvements in wear resistance, hardness, elongation, yield and tensile strengths by 44%, 31%, 30%, 8% and 12%, respectively, except 9% decrease in impact toughness compared to ASTM A 128 Gr. E1 steel without modification. These results show that 1.0C-17Mn-0.05Ti alloy can be used for parts exposed to high load wear and applied in conditions where relatively high tensile properties with sufficent ductility is needed.

     

Percutaneous absorption of ketoprofen. I. In vitro release and percutaneous absorption of ketoprofen from different ointment bases

Drug-related renal damage is manifold in its origin, clinical picture and prognosis. The disorder can manifest itself as a purely functional phenomenon with tubular elimination of amino acids, enzymes, protein, glucose and electrolytes, or it is due to reversible hemodynamic changes; on the other hand, it may be accompanied by cell necrosis and inflammation. Hemodynamic, toxic, immunologic, or mechanically obstructive mechanisms or a combination of these play a pathogenetic role. It is important to know the renal parameters before and monitor them during treatment with nephrotoxic drugs; to avoid concomitant administration of two or more nephrotoxic drugs; and to make the diagnosis as well as terminate exposure rapidly.     

Bioengineering functional copolymers: synthesis and characterization of poly(<Emphasis Type="Italic">N</Emphasis>-isopropyl acrylamide-<Emphasis Type="Italic">co</Emphasis>-3,4-2H-dihydropyran)s

Novel bioengineering copolymers were synthesized by radical copolymerization of N-isopropylacrylamide (NIPA) and 3,4-2H-dihydropyran (DHP) with 2,2′-azobisisobutyronitrile as an initiator in acetone solution at 70 °C under nitrogen atmosphere. Structure, tacticity and compositons of the copolymers prepared in a wide range of monomer feed were confirmed by FTIR, ¹H{¹³C} NMR-DEPT and elemental analyses. The monomer reactivity ratios (r ₁ and r ₂) were detected using known two methods: r ₁ (NIPA)?=?1.25 and r ₂?=?0.035 (DHP), and r ₁ (NIPA) ?=?0.97 and r ₂?=?0.022 (DHP) by Kelen-Tüdös and Jaacks methods, respectively. It was demonstrated that the studied monomer pair has a tendency to form H-bonding beween amide/ether groups through ?NH...O< complexation which played an important role in the stereoselective chain growth, and significant decrease of allyl degradative chain transfer reactions. This phenomenon is also confirmed by the observed relatively high molecular weights of copolymers (M _v ). The synthesized water-soluble stimuli-responsive poly(NIPA-co-DHP)s exhibit thermal stability, higher glass-transition temperature, polyelectrolyte, pH- and temperature-sensitive behavior and can be attributed to the class of bioengineering functional copolymers useful for various bio- and gene-engineering, and drug delivery applications.     

Understanding the degradation of MEA in PEMFC: Definition of structural markers and comparison between laboratory and on‐site ageing

Different accelerated tests in 12 fuel cells stack were performed in laboratory, namely on/off, back‐up, and base‐load regimes. In parallel, membrane electrode assemblies (MEA) were integrated in two “on‐site” systems for GSM relay application. One of them was dedicated to base‐load power applications while the second fuel cells coupled with photovoltaic panels operated in semibase load mode. To investigate the influence of the power profiles on MEA degradation, over 80 CCB MEAs (5 layers) were studied at different scales using ex situ characterizations such as tensile tests, TGA‐MS, DMTA, and SEM. A series of complementary microstructural ageing markers were thereby identified. The isolated influence of dry‐wet cycling on MEA properties was also established after passive hydro‐thermal (HT) ageing performed continuously for 10 months in the laboratory. The changes of each marker as a function of HT ageing time permitted to define a temporal benchmark. Based on these indicators, the main changes occurred in the MEA properties appear after a 5 months dry‐humid cycling (up to about 1800 cycles). The trends observed were useful to compare and estimate the degree of degradation of each ageing tests. Thus, the accelerated tests performed in laboratory for at least 500 h in stack did not reveal systematic MEA modifications. On the contrary, the 1500 h “on‐site” system operation results in some MEA degradations which origins are discussed. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effective atomic numbers of some composite mixtures including borax

Effective atomic numbers for (PbO and Na₂B₄O₇10H₂O) and (UO₂(NO₃)₂, and Na₂B₄O₇10H₂O) mixtures against changing contents of PbO, Na₂B₄O₇10H₂O, and UO₂(NO₃)₂ were measured in the X-ray energy range from 25.0 to 58.0 keV. The gamma rays emitted by a ²⁴¹Am annular source have been sent on the absorbers which emits their characteristic X-rays to be used in transmission arrangement. The X-rays were counted by a Si(Li) detector with a resolution of 146 eV at 5.90 keV. The changing compositions of the compounds were assigned to be 0, 0.167, 0.333, 0.500, 0.666, 0.833 and total masses of the mixtures were adjusted to be identical. Also, the total effective atomic numbers of each mixture were estimated by using the mixture rule. The measured values were compared with estimated values for the mixtures.