2,808 research outputs found

    Transfer molding of PMR-15 polyimide resin

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    Transfer molding is an economically viable method of producing small shapes of PMR-15 polyimide. It is shown that with regard to flexural, compressive, and tribological properties transfer-molded PMR-15 polyimide is essentially equivalent to PMR-15 polyimide produced by the more common method of compression molding. Minor variations in anisotropy are predictable effects of molding design and secondary finishing operations

    Cash Crop and Foodgrain Productivity in Senegal: Historical View, New Survey Evidence, and Policy Implications

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    Crop Production/Industries, Productivity Analysis, Downloads July 2008 - June 2009: 10,

    Approximate analysis and stability of pressure oscillations in ramjets

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    This paper summarizes work accomplished during the past five years on analysis of stability related to recent experimental results on combustion instabilities in dump combustors. The primary purpose is to provide the information in a form useful to those concerned with design and development of operational systems. Thus most substantial details are omitted; the material is presented in a qualitative fashion

    Analysis of existing mathematics textbooks for use in secondary schools.

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    Thesis (Ed.M.)--Boston University Thesis (M.A.)--Boston Universit

    Calorimetric Analysis Using DNA Thermal Stability to determine protein concentration

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    It was recently reported for two globular proteins and a short DNA hairpin in NaCl buffer that values of the transition heat capacities, Cp,DNA and Cp,PRO for equal concentrations (mg/mL) of DNA and proteins, are essentially equivalent (differ by less than 1%). Additional evidence for this equivalence is presented that reveals this phenomenon does not depend on DNA sequence, buffer salt, or Tm. Sequences of two DNA hairpins were designed to confer a near 20°C difference in their Tm’s. For the molecules, in NaCl and CsCl buffer the evaluated Cp,PRO and Cp,DNA were equivalent. Based on the equivalence of transition heat capacities, a calorimetric method was devised to determine protein concentrations in pure and complex solutions. The scheme uses direct comparisons between the thermodynamic stability of a short DNA hairpin standard of known concentration, and thermodynamic stability of protein solutions of unknown concentrations. In all cases, evaluated protein concentrations determined from the DNA standard curve agreed with the UV-Vis concentration for monomeric proteins. For samples of multimeric proteins, streptavidin (tetramer), Herpes Simplex Virus glycoprotein D (trimer/dimer), and a 16 base pair DNA duplex (dimer), evaluated concentrations were greater than determined by UV-Vis by factors of 3.94, 2.65, and 2.15, respectively
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