282 research outputs found

    Determination method of the structure size interval of dynamic similar models for predicting vibration characteristics of the isotropic sandwich plates

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    A method is studied for determining the structure size interval of dynamic similar models of the isotropic sandwich plates. Firstly, a comparison between the two theories of plates, the Resineer theory and the Hoff theory, is conducted, including their governing equations and the ANSYS analytic solutions of frequency. The Resineer theory is chosen as the basic theory of this paper finally. Secondly, the scaling laws between the model and prototype of isotropic sandwich plate are established by combining the dimensional analysis and governing analysis. Both complete and incomplete geometric similarity conditions are discussed. Thirdly, the determination method of the structure size interval of the models is proposed. The nature vibration mode keeps the same and the nature frequency and harmonic response keep in proportion with the prototype of the sandwich plate. At last, the flow step of the intervals determination method is given

    Influence of uron resins on the performance of uf resins as adhesives for plywood

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    Uron resin, a kind of urea-formaldehyde (UF) resin containing much more uron structure, were prepared. Several modifi ed UF resins were obtained from mixing uron resins with normal UF resins as well as synthesizing UF resin with uron resin as raw material. This work demonstrated that the introducing of the uron structure reduced free formaldehyde content of UF resin and formaldehyde emission levels in bonded plywood panels signifi cantly, the former were reduced by 76% and 84% in the latter. The synthesis time of uron resin can be shortened to 8 hours. The test result of free formaldehyde content, formaldehyde emission levels and bond strength indicated that specimen of 20 parts uron resin synthesized in 8 hours mixed with 100 parts UF resins (F/U molar ratio of 1.3) had a potential advantage to industrial application. The benefi cial effect of uron resin on the performance of UF resin can be attributed to the opening of uron cycle structure and the following reaction with free formaldehyde and its oligomeric glycol forms

    High strength mullite-bond SiC porous ceramics fabricated by digital light processing

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    Fabricating SiC ceramics via the digital light processing (DLP) technology is of great challenge due to strong light absorption and high refractive index of deep-colored SiC powders, which highly differ from those of resin, and thus significantly affect the curing performance of the photosensitive SiC slurry. In this paper, a thin silicon oxide (SiO2) layer was in-situ formed on the surface of SiC powders by pre-oxidation treatment. This method was proven to effectively improve the curing ability of SiC slurry. The SiC photosensitive slurry was fabricated with solid content of 55 vol% and viscosity of 7.77 Pa s (shear rate of 30 s-1). The curing thickness was 50 μm with exposure time of only 5 s. Then, a well-designed sintering additive was added to completely convert low-strength SiO2 into mullite reinforcement during sintering. Complexshaped mullite-bond SiC ceramics were successfully fabricated. The flexural strength of SiC ceramics sintered at 1550 °C in air reached 97.6 MPa with porosity of 39.2 vol%, as high as those prepared by spark plasma sintering (SPS) techniques.</p

    (E)-1-(4-Meth­oxy­phen­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one

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    In the title compound, C19H20O5, the dihedral angle between the two aromatic rings is 18.23 (4)°. The crystal structure exhibits only weak C—H⋯π and C—H⋯O contacts between the mol­ecules

    1-(4-Amino­phen­yl)-3-[2-(trifluoro­meth­yl)phen­yl]prop-2-en-1-one

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    The title compound, C16H12F3NO, a derivative of biologically active chalcones, comprises two benzene rings and a central –CH=CH—C(=O)– unit. The dihedral angle between the two rings is 10.9 (1)° and the mol­ecule adopts an E configuration about the central olefinic bond. The crystal structure is stabilized by inter­molecular N—H⋯O and N—H⋯N hydrogen bonds
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