Grain refinement of DC cast magnesium alloys with intensive melt shearing

A new direct chill (DC) casting process, melt conditioned DC (MC-DC) process, has been developed for the production of high quality billets/slabs of light alloys by application of intensive melt shearing through a rotor-stator high shear device during the DC casting process. The rotor-stator high shear device provides intensive melt shearing to disperse the naturally occurring oxide films, and other inclusions, while creating a microscopic flow pattern to homogenize the temperature and composition fields in the sump. In this paper, we report the grain refining effect of intensive melt shearing in the MC-DC casting processing. Experimental results on DC casting of Mg-alloys with and without intensive melt shearing have demonstrated that the MC-DC casting process can produce magnesium alloy billets with significantly refined microstructure. Such grain refinement in the MC-DC casting process can be attributed to enhanced heterogeneous nucleation by dispersed naturally occurring oxide particles, increased nuclei survival rate in uniform temperature and compositional fields in the sump, and potential contribution from dendrite arm fragmentation

Photoinduced intramolecular charge transfer in self-assembly .1. Aggregation and dual fluorescence of ethyl p-didecylaminobenzoate in dioxane-water binary solvent

Aggregation of ethyl p-didecylaminobenzoate (EDDAB) in dioxane-water binary mixture was shown to occur at water volume fraction of 0.47 and a strong intramolecular charge transfer emission was observed in the aggregate

Weak stability of l_1-minimization methods in sparse data reconstruction

As one of the most plausible convex optimization methods for sparse data reconstruction, l_1-minimization plays a fundamental role in the development of sparse optimization theory. The stability of this method has been addressed in the literature under various assumptions such as the restricted isometry property, null space property, and mutual coherence. In this paper, we propose a unified means to develop the so-called weak stability theory for 1-minimization methods under the condition called the weak range space property of a transposed design matrix, which turns out to be a necessary and sufficient condition for the standard l_1-minimization method to be weakly stable in sparse data reconstruction. The reconstruction error bounds established in this paper are measured by the so-called Robinson’s constant. We also provide a unified weak stability result for standard l_1-minimization under several existing compressed sensing matrix properties. In particular, the weak stability of l_1-minimization under the constant-free range space property of order k of the transposed design matrix is established for the first time in this paper. Different from the existing analysis, we utilize the classic Ho˙man’s lemma concerning the error bound of linear systems as well as Dudley’s theorem concerning the polytope approximation of the unit l_2-ball to show that l_1-minimization is robustly and weakly stable in recovering sparse data from inaccurate measurements

Optimization of fermentation medium for nisin production from Lactococcus lactis subsp. lactis using response surface methodology (RSM) combined with artificial neural network-genetic algorithm (ANN-GA)

Nisin is a bacteriocin approved in more than 50 countries as a safe natural food preservative. Response surface methodology (RSM) combined with artificial neural network-genetic algorithm (ANN-GA) was employed to optimize the fermentation medium for nisin production. Plackett-Burman design (PBD) was used for identifying the significant components in the fermentation medium. After that, the path of steepest ascent method (PSA) was employed to approach their optimal concentrations. Sequentially, Box-Behnken design experiments were implemented for further optimization. RSM combined with ANNGA were used for analysis of data. Specially, a RSM model was used for determining the individual effect and mutual interaction effect of tested variables on nisin titer (NT), an ANN model was used for NT prediction, and GA was employed to search for the optimum solutions based on the ANN model. As the optimal medium obtained by ANN-GA was located at the verge of the test region, a further Box- Behnken design based on the RSM statistical analysis results was implemented. ANN-GA was implemented using the further Box-Behnken design data to locate the optimum solution which was as follow (g/l): Glucose (GLU) 15.92, peptone (PEP) 30.57, yeast extraction powder (YEP) 39.07, NaCl 5.25, KH2PO4 10.00, and MgSO4·7H2O 0.20, with expected NT of 22216 IU/ml. The validation experiments with the optimum solution were implemented in triplicate and the average NT was 21423 IU/ml, which was 2.13 times higher than that without ANN-GA methods and 8.34 times higher than that without optimization.Key words: Response surface methodology, artificial neural network, genetic algorithm, nisin titer

Photoinduced intramolecular charge transfer of sodium 4-(N,N-dimethylamino)benzenesulfonate

A new dual fluorescent N,N-dimethylaniline derivative, sodium 4-(N,N-dimethylamino)benzenesulfonate (SDMAS), is reported. In SDMAS, the electron acceptor is linked to the phenyl ring via a sulfur atom at the para-position of the electron donor. It was found that SDMAS emits dual fluorescence only in highly polar solvent water but not in organic solvents such as formamide, methanol and acetonitrile. In organic solvents only a single-band emission at ca.360 nm was observed in the short wavelength region. The dual fluorescence of SDMAS in water was found at 365 and 475 nm, respectively. Introduction of organic solvent such as ethanol, acetonitrile, and 1,4-dioxane into aqueous solution of SDMAS leads to blue-shift and quenching of the long-wavelength emission. Measurements of steady-state and picosecond time-resolved fluorescence indicate that the long wavelength fluorescence is emitted from a charge transfer (CT) state that is populated from the locally excited (LE) state, with the latter giving off the short wavelength fluorescence. The fact that a highly polar solvent is required to bring out the dual fluorescence suggests that the CT process of SDMAS has a high activation energy (E-a). In supporting this assumption the time-resolved fluorescence measurements give an E-a of 15.35 kJ . mol(-1). It was assumed that the participation of the sulfur atom d-orbital in the conjugation of sulfonate group with phenyl ring and the strong twisting and inverting of the dimethylamino plane relative to the phenyl ring could be the reasons for the high activation energy. A molecular configuration change upon charge transfer in water was suggested for SDMAS based on the thermodynamic data. SDMAS reported here represents the example of the dual fluorescent amine substituted aromatic sulfonate

Dual fluorescence from aqueous 1-naphthylamine solutions of high pH - Excited-state acidic dissociation of naphthylamine

Dual fluorescence at ca. 447 nm and 545 nm was observed from the aqueous 1-naphthylamine (NA) solutions at pH higher than 13.6. Similar dual fluorescence was also found with sodium 1-naphthylaminoacetate(NAA), but not with N, N-disubstituted 1-aminonaphthalenes such as sodium 1-naphthylaminodiacetate (NADA) and 1-dimethylaminonaphthalene (DMAN). No change in absorption spectra of NA and NAA was observed in this pH region. It was proposed that the dual fluorescence observed with NA and NAA was due to the excited state dissociation of the primary and secondary amines at high pH. From the dual fluorescence intensity ratio pH titration curve, the pK(a)(.)'s of NA and NAA were estimated to be between 14 and 15 which are much lower than the ground state pK(a). The novel approach is such a simple, convenient and frequent analysis technique that it can be widely used in detecting the substitutional derivatives of aminonaphthalene

Internal conversion with 4-(azetidinyl)benzonitriles in alkane solvents. Influence of fluoro substitution

The introduction of a fluoro-substituent in the phenyl ring of 4-(1-azetidinyl)benzonitrile (P4C) leads to smaller fluorescence quantum yields Phi (f) and shorter decay times tau in alkane solvents (cyclopentane, n-hexadecane, n-hexane and 2-methylpentane). In cyclopentane at 25 degreesC, Phi (f) and tau equal 0.02 and 0.14 ns for 2-fluoro-4-(1-azetidinyl)benzonitrile (P4CF2) and 0.11 and 0.85 ns for 3-fluoro-4-(1-azetidinyl)benzonitrile (P4CF3), as compared with 0.27 and 4.55 ns for P4C. The fluorescence originates from a locally excited (LE) state and dual fluorescence due to intramolecular charge transfer is not observed for the three aminobenzonitriles at any temperature in the alkane solvents. By measuring the yields of intersystem crossing Phi (ISC), it follows that this enhancement of the radiationless deactivation of the first excited singlet state S-1 is due to thermally activated internal conversion (IC). The IC yield Phi (IC) in cyclopentane at 25 degreesC, as an example, is considerably larger for P4CF2 (0.93) than for P4CF3 (0.35) and of minor importance for P4C (0.03). The IC activation energies E-IC of P4CF2 (12.6 kJ mol(-1)), P4CF3 (19.3 kJ mol(-1)) and P4C (38.1 kJ mol(-1)) in cyclopentane were determined by fitting tau measured as a function of temperature, together with data for Phi (f) and Phi (ISC). Similar E-IC values were obtained in n-hexane and n-hexadecane. These data show that the increase in IC efficiency from P4C via P4CF3 to P4CF2 is caused by a decrease in E-IC. The radiative rate constants k(f) in cyclopentane of P4CF2 and P4CF3 are about twice that of P4C, probably due to the mixing of the S-2(L-1(a),CT) and S-1(L-1(b)) states of P4C caused by the molecular asymmetry introduced by the F-substituents. It is assumed that the lowering of the IC barriers in P4CF2 and P4CF3 is governed by an F-substituent-dependent difference in the energies of the molecular configuration of the azetidinylbenzonitriles that can be reached in S-1 as compared with those in S-0

3D visualization and information interaction in biomedical applications

2001-2002 > Academic research: refereed > Publication in refereed journalVersion of RecordPublishe

A Review: Cytochrome P450 in Alcoholic and Non-Alcoholic Fatty Liver Disease

Yu-Jie Jiang,1,2 Ye-Ming Cao,1 Yong-Bing Cao,1 Tian-Hua Yan,2 Cheng-Lin Jia,1 Ping He1 1Institute of Vascular Anomalies, Shanghai Academy of Traditional Chinese Medicine, Shanghai, 200082, People’s Republic of China; 2Department of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, 211100, People’s Republic of ChinaCorrespondence: Cheng-Lin Jia; Ping He, Institute of Vascular Anomalies, Shanghai Academy of Traditional Chinese Medicine, Shanghai, 200082, People’s Republic of China, Tel/Fax +1 522 136 9352 ; +1 301 693 1191, Email [email protected]; [email protected]: Alcoholic fatty liver disease (FALD) and non-alcoholic fatty liver disease (NAFLD) have similar pathological spectra, both of which are associated with a series of symptoms, including steatosis, inflammation, and fibrosis. These clinical manifestations are caused by hepatic lipid synthesis and metabolism dysregulation and affect human health. Despite having been studied extensively, targeted therapies remain elusive. The Cytochrome P450 (CYP450) family is the most important drug-metabolising enzyme in the body, primarily in the liver. It is responsible for the metabolism of endogenous and exogenous compounds, completing biological transformation. This process is relevant to the occurrence and development of AFLD and NAFLD. In this review, the correlation between CYP450 and liver lipid metabolic diseases is summarised, providing new insights for the treatment of AFLD and NAFLD.Keywords: CYP450, liver metabolism, lipid accumulation, monooxygenases, alcoholic fatty liver disease, non-alcoholic fatty liver diseas

Imaging Oxygen Defects and their Motion at a Manganite Surface

Manganites are technologically important materials, used widely as solid oxide fuel cell cathodes: they have also been shown to exhibit electroresistance. Oxygen bulk diffusion and surface exchange processes are critical for catalytic action, and numerous studies of manganites have linked electroresistance to electrochemical oxygen migration. Direct imaging of individual oxygen defects is needed to underpin understanding of these important processes. It is not currently possible to collect the required images in the bulk, but scanning tunnelling microscopy could provide such data for surfaces. Here we show the first atomic resolution images of oxygen defects at a manganite surface. Our experiments also reveal defect dynamics, including oxygen adatom migration, vacancy-adatom recombination and adatom bistability. Beyond providing an experimental basis for testing models describing the microscopics of oxygen migration at transition metal oxide interfaces, our work resolves the long-standing puzzle of why scanning tunnelling microscopy is more challenging for layered manganites than for cuprates.Comment: 7 figure