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排序方式: 共有502条查询结果,搜索用时 31 毫秒
1.
Ying‐Hung So Pamela Foster Jang‐Hi Im Philip Garrou Jack Hetzner Edmund Stark Kayla Baranek 《Journal of polymer science. Part A, Polymer chemistry》2006,44(5):1591-1599
Divinylsiloxane‐bisbenzocyclobutene (DVS‐bisBCB) polymer has very low dielectric constant and dissipation factor, good thermal stability, and high chemical resistance. The fracture toughness of the thermoset polymer is moderate due to its high crosslink density. A thermoplastic elastomer, polystyrene–polybutadiene–polystyrene triblock copolymer, was incorporated into the matrix to enhance its toughness. The cured thermoset matrix showed different morphology when the elastomer was added to the B‐staged prepolymer or when the elastomer was B‐staged with the DVS‐bisBCB monomer. Small and uniformly distributed elastomer domains were detected by transmission electron micrographs (TEM) in the former case, but TEM did not detect a separate domain in the latter case. A high percentage of the polystyrene–polybutadiene–polystyrene triblock copolymer could be incorporated into the DVS‐bisBCB thermoset matrix by B‐staging the triblock copolymer with the BCB monomer. The elastomer increased the fracture toughness of DVS‐bisBCB polymer as indicated by enhanced elongation at break and increased K1c values obtained by the modified edge‐lift‐off test. Elastomer modified DVS‐bisBCB maintained excellent electrical properties, high Tg and good thermal stability, but showed higher coefficient of linear thermal expansion values. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 1591–1599, 2006 相似文献
2.
Bokhee Im 《Results in Mathematics》1995,28(1-2):67-74
For a group G = (G, ·), we define the (internal) quasidirect product f · U = F × U of a certain K-loop (F,+) with F ? G and a suitable subgroup il of G (cf. (3.1)). Let K be a commutative pythagorean field and let L = K(i) be the quadratic extension of K with i2 = ~-1. Then the future cone H:= A ∈ GL(2,L) ¦ A = A*, det A ∈ K+, Tr A ∈ K+ is a K-loop with respect to the binary operation $A?ggsquaredplus B:=sqrt{AB^{2}A},{? where}sqrt{A}=({? Tr}A+2sqrt {{? det}A})^{1?er 2}(sqrt {? det}AE+A)$} (cf. (2.4)), and the (internal) quasidirect product $H^{}</Emphasis>{\mathop \times\limits_{Q}}Q_{1}$ of the K-loop (H},+) and the group Q1:= {X ∈ GL(2,L) ¦ X*X = E) is a subgroup of GL(2,L) (cf. (3.2)). Moreover, S L(2,1) = $H^{1+}{\mathop \times\limits_{Q}}Q^{1}$ , where H1+ = SL(2,L)∩ H ≤} (H},+), Q1 = S L(2, L) ∩ Q1 (cf. (3.4)), and if K is euclidean, then (cf. (3.6)). 相似文献
3.
Lee CS Kim KY Im JB Choi JW Kim HK Park JS Shin EY Kim SR Kim EG 《Experimental & molecular medicine》2004,36(6):582-587
p21-activated kinase (PAK)-interacting exchange factor (PIX) is known to be involved in regulation of Cdc42/Rac GTPases and PAK activity. PIX binds to the proline-rich region of PAK, and regulates biological events through activation of Cdc42/Rac GTPase. To further investigate the role of PIX we produced monoclonal antibodies (Mab) against bPIX. Three clones; N-C6 against N-terminal half and C-A3 and C-B7 against C- terminal half of bPIX were generated and characterized. N-C6 Mab detected bPIX as a major band in most cell lines. C-A3 Mab recognizes GIT-binding domain (GBD), but it does not interfere with GIT binding to bPIX. Using C-A3 Mab possible bPIX interaction with actin in PC12 cells was examined. bPIX Mab (C-A3) specifically precipitated actin of the PC12 cell lysates whereas actin Mab failed to immunoprecipitate bPIX. Co-sedimentation of PC12 cell lysates with the polymerized F-actin resulted in the recovery of most of bPIX in the cell lysates. These results suggest that bPIX may not interact with soluble actin but with polymerized F-actin and revealed that bPIX constitutes a functional complex with actin. These data indicate real usefulness of the bPIX Mab in the study of bPIX role(s) in regulation of actin cyoskeleton. 相似文献
4.
Kim MK Oh S Lee JH Im H Ryu YM Oh E Lee J Lee E Sul D 《Experimental & molecular medicine》2004,36(5):396-410
In this study, we investigated the effects of PAHs and dioxin on mRNA and plasma protein expression using genomic and proteomic analysis for automobile emission inspectors and waste incineration workers. About 54 workers from automobile emission inspection offices, 31 workers from waste incinerating company and 84 unexposed healthy subjects were enrolled in this study. Urine and air samples were collected and analyzed by HPLC and GC/MS. Comet assays were carried out to evaluate any DNA damage in mononuclear and polynuclear cells. A significant difference in Olive tail moments in mononuclear cells was observed between exposed and control subjects (P < 0.0001). To examine the differences of the gene expression profile in automobile emission inspectors and waste incineration workers, radioactive complementary DNA microarrays were used to evaluate changes in the expression of 1,152 total genes. The gene expression profiles showed that 11 genes were up-regulated and 4 genes were down-regulated in waste incinerating workers as compared with controls. Plasma proteins were analyzed by 2-dimentional electrophoresis with pH 3-10 NL IPG Dry strip. The protein expression profiles showed that 8 proteins were up- regulated and 1 protein, haptoglobin, was down- regulated in automobile emission inspectors and waste incineration workers. Serum paraoxonase/ arylesterase was found only in the plasma of waste incineration workers. The expression of genes and proteins involved in oxidative stress were up-regulated in both automobile emission inspectors and waste incineration workers. Several proteins, such as transthyrethin, sarcolectin and haptoglobin, that were highly up- or down-regulated, could serve as biological monitoring markers for future study. 相似文献
5.
We investigate the application of torsion angle molecular dynamics (TAMD) to augment conformational sampling of peptides and proteins. Interesting conformational changes in proteins mainly involve torsional degrees of freedom. Carrying out molecular dynamics in torsion space does not only explicitly sample the most relevant degrees of freedom, but also allows larger integration time steps with elimination of the bond and angle degrees of freedom. However, the covalent geometry needs to be fixed during internal coordinate dynamics, which can introduce severe distortions to the underlying potential surface in the extensively parameterized modern Cartesian-based protein force fields. A "projection" approach (Katritch et al. J Comput Chem 2003, 24, 254-265) is extended to construct an accurate internal coordinate force field (ICFF) from a source Cartesian force field. Torsion crossterm corrections constructed from local molecular fragments, together with softened van der Waals and electrostatic interactions, are used to recover the potential surface and incorporate implicit bond and angle flexibility. MD simulations of dipeptide models demonstrate that full flexibility in both the backbone phi/psi and side chain chi1 angles are virtually restored. The efficacy of TAMD in enhancing conformational sampling is then further examined by folding simulations of small peptides and refinement experiments of protein NMR structures. The results show that an increase of several fold in conformational sampling efficiency can be reliably achieved. The current study also reveals some complicated intrinsic properties of internal coordinate dynamics, beyond energy conservation, that can limit the maximum size of the integration time step and thus the achievable gain in sampling efficiency. 相似文献
6.
In this paper, to improve the slow processing speed of the rule-based visible and NIR (near-infrared) image synthesis method, we present a fast image fusion method using DenseFuse, one of the CNN (convolutional neural network)-based image synthesis methods. The proposed method applies a raster scan algorithm to secure visible and NIR datasets for effective learning and presents a dataset classification method using luminance and variance. Additionally, in this paper, a method for synthesizing a feature map in a fusion layer is presented and compared with the method for synthesizing a feature map in other fusion layers. The proposed method learns the superior image quality of the rule-based image synthesis method and shows a clear synthesized image with better visibility than other existing learning-based image synthesis methods. Compared with the rule-based image synthesis method used as the target image, the proposed method has an advantage in processing speed by reducing the processing time to three times or more. 相似文献
7.
8.
The study focuses on finding the pulse sequences depicting a rat’s tumor when the size of the field of view was reduced, using coils specifically designed for rats, and obtaining an optimized image of a rat by transforming the parameters, according to each pulse sequence. The manufactured coil is 8-channel phased array coils, and the type is a receive-only coil. The diameter of the coil is 80 mm, and the length is 150 mm. The overlapped distance among each channel was 8 mm, and the lab rats used in the experiment were the commonly used Sprague–Dawley rats. The study used three types of pulse sequences, which are the diffusion weight imaging (DWI), three-dimensional dual echo steady state (3-D DESS), and three-dimensional volumetric interpolated breath-hold (3-D VIBE). Along with the DWI results, pulse sequences of 3-D DESS and 3-D VIBE enabled to distinguish the tumors from that of normal tissues in the brain by optimizing a mediator variable and to illustrate the whole body imaging of a rat. 相似文献
9.
Sylvain Cousinet Ali Ghadban Imène Allaoua Frédéric Lortie Daniel Portinha Eric Drockenmuller Jean‐Pierre Pascault 《Journal of polymer science. Part A, Polymer chemistry》2014,52(23):3356-3364
Vinyl levulinate (VL) is used as a biobased reactive diluent in styrene (St)‐free unsaturated polyester resins (UPR). The reactivity ratios for the radical copolymerization of VL with diethyl fumarate (DEF) are determined by the Jaacks method (rVL = 0.01 and rDEF = 0.81 at 60 °C in DMSO‐d6). The properties of UPRs having a stoichiometric ratio between unsaturated groups from the UPR and either St or VL are compared. Defect‐free, slightly yellow, transparent, and rigid thermosets are obtained after a mild curing cycle. Due to unfavorable reactivity ratios about 5.5 wt % of unpolymerized VL remains inside the network and acts as plasticizer. Consequently, compared with St‐based ones, VL‐based UPRs exhibit lower α relaxation (Tα = 180 and 100 °C, respectively), lower elastic moduli at the rubbery plateau (G′ = 108 and 107 Pa) and lower mechanical properties as measured by three points bending tests. Strain at break (εf = 1.8 ± 0.2%) and Charpy impact strength (~2.7 ± 0.3 kJ m?2) are comparable independently of the RD chemical nature. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 3356–3364 相似文献
10.
Detailed gas-phase chemical kinetic models are widely used in combustion research, and many new mechanisms for different fuels and reacting conditions are developed each year. Recent works have highlighted the need for error checking when preparing such models, but a useful community tool to perform such analysis is missing. In this work, we present a simple online tool to screen chemical kinetic mechanisms for bimolecular reactions exceeding collision limits. The tool is implemented on a user-friendly website, cloudflame.kaust.edu.sa, and checks three different classes of bimolecular reactions; (ie, pressure independent, pressure-dependent falloff, and pressure-dependent PLOG). In addition, two other online modules are provided to check thermodynamic properties and transport parameters to help kinetic model developers determine the sources of errors for reactions that are not collision limit compliant. Furthermore, issues related to unphysically fast timescales can remain an issue even if all bimolecular reactions are within collision limits. Therefore, we also present a procedure to screen ultrafast reaction timescales using computational singular perturbation. For demonstration purposes only, three versions of the rigorously developed AramcoMech are screened for collision limit compliance and ultrafast timescales, and recommendations are made for improving the models. Larger models for biodiesel surrogates, tetrahydropyran, and gasoline surrogates are also analyzed for exemplary purposes. Numerical simulations with updated kinetic parameters are presented to show improvements in wall-clock time when resolving ultrafast timescales. 相似文献