160 research outputs found

    Effect of Surface Roughness on Elastohydrodynamic Lubrication Performance of Cylindrical Roller Bearing

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    In order to study the effect of surface roughness on the Elastohydrodynamic Lubrication (EHL) performance of cylindrical roller bearing, an EHL model of cylindrical roller bearing with three dimensional surface cosine roughness based on finite length line contact theory is established. The EHL performance of cylindrical roller bearing is calculated by the Finite Difference Method (FDM) program, with which the effects of surface cosine roughness amplitude, wavelength and texture angle on EHL performance of cylindrical roller bearing are analyzed. The numerical results show that the roughness amplitude, wavelength and texture angle have great influence on the EHL performance in the contact area. The increase of roughness amplitude and wavelength in a reasonable range is beneficial to the enhancement of EHL performance of the cylindrical roller bearing, and the transverse roughness is more favorable to enhance the bearing capacity and reduce the friction coefficient

    Dimethyl 3,3′-diphenyl-2,2′-[(S)-thio­phene-2,5-diylbis(carbonyl­aza­nedi­yl)]dipropano­ate tetra­hydro­furan monosolvate

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    The title compound, C26H26N2O6S·C4H8O, a solvated bis-amide derivative, is also a chiral amino acid ester with l-phenyl­alanine methyl ester groups as amine substituents. The thio­phene-2,5-dicarboxamide core approximates C 2 point symmetry. The tetra­hydro­furan solvent mol­ecule is linked to the main mol­ecule through an inter­molecular N—H⋯O hydrogen bond. The central ring makes dihedral angles of 90.0 (2) and 76.5 (2)° with the pendant rings

    Attenuation of kainic acid-induced epilepsy by butyrate is associated with inhibition of glial activation

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    Purpose: To investigate the function and potential therapeutic relevance of butyrate in epilepsy using rat models of kainic acid (KA)-induced epilepsy.Methods: The neurotoxin KA was applied to rats and rat astrocytes to establish models of epilepsy in vivo and in vitro. Multiple parameters, including behavioural seizure scores, were evaluated in rats and rat astrocytes treated with KA alone or in combination with butyrate. Western blot was performed to examine the levels of phosphorylated extracellular signal-related kinase (p-ERK), proinflammatory cytokine (IL-1ß), and glial fibrillary acidic protein (GFAP).Results: Significant increases were observed in the seizure-related proteins p-ERK and GFAP and in the proinflammatory cytokine IL-1ß in KA-treated rats and rat astrocytes (p < 0.05). Butyrate treatment attenuated KA-induced epileptic behaviour in rats and significantly reduced the expression of p-ERK, GFAP, and IL-1ß in a dose-dependent manner (p < 0.05).Conclusion: Butyrate has potential as a treatment for epilepsy by inhibiting the activation of p-ERK, astrogliosis, and inflammation, which were induced by KA in rats and rat astrocytes.Keywords: Kainic acid, Epilepsy, Butyrate, Glial activation, Astrogliosi

    Iterative Nearest Neighborhood Oversampling in Semisupervised Learning from Imbalanced Data

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    Transductive graph-based semi-supervised learning methods usually build an undirected graph utilizing both labeled and unlabeled samples as vertices. Those methods propagate label information of labeled samples to neighbors through their edges in order to get the predicted labels of unlabeled samples. Most popular semi-supervised learning approaches are sensitive to initial label distribution happened in imbalanced labeled datasets. The class boundary will be severely skewed by the majority classes in an imbalanced classification. In this paper, we proposed a simple and effective approach to alleviate the unfavorable influence of imbalance problem by iteratively selecting a few unlabeled samples and adding them into the minority classes to form a balanced labeled dataset for the learning methods afterwards. The experiments on UCI datasets and MNIST handwritten digits dataset showed that the proposed approach outperforms other existing state-of-art methods

    (−)-Dimethyl 3,3′-diphenyl-2,2′-[pyridine-2,6-diylbis(carbonyl­imino)]dipropanoate

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    The title compound, C27H27N3O6, a bis-amide derivative, is also a chiral amino acid ester with l-phenyl­alanine methyl ester groups as amine substituents. The pyridine ring is oriented at dihedral angles of 89.69 (3) and 62.95 (3)° with respect to the phenyl rings, while the dihedral angle between the phenyl rings is 60.76 (3)°. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains. One of the carbonyl O atoms and one of the meth­oxy CH3 groups are disordered over two positions. The O atom was refined with occupancies of 0.69 (13) and 0.31 (13), while C and H atoms were refined with occupancies of 0.69 (8) and 0.31 (8)
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