An experimental investigation was performed to compare the boiling heat transfer coefficients and two-phase pressure drops from a square inline and a staggered tube bundle having the same tube pitch-to-diameter ratio (P/D = 1.30) and from two square inline tube bundles having different pitch-to-diameter ratios (P/D = 1.30 and 1.70). Except at the highest heat fluxes the heat transfer coefficients generally were higher in the staggered tube bundle than in the inline tube bundle and higher in the larger P/D tube bundle than in the smaller. As the heat flux increased, the differences decreased. The differences were attributed to the tradeoff between nucleation and convection. The staggered tube bundle had higher pressure drops than the inline bundle except at low mass velocities; the larger pressure drop in the staggered bundle was attributed to the combination of a larger void fraction and a larger friction multiplier, with the frictional component dominating at higher mass velocities. Comparing the inline tube bundle pressure drops, it was concluded that the larger P/D bundle had a larger void fraction than the smaller P/D tube bundle; no conclusions could be drawn regarding the relative magnitude of the two-phase fraction multiplier. 相似文献
In this paper we define a class of two-phase laminate composites for which the constituent elements are either linearly elastic or exhibit viscoelastic effects. We determine the viscoelastic behaviour of the equivalent homogeneous transversely isotropic medium by a single time-independent memory function. 相似文献
We report that the nanostructures of poly(styrene‐block‐4‐vinylpyridine) block copolymer (PS‐b‐P4VP) thin film on a wafer substrate can be re‐assembled by sequential vapor treatment using selected solvents. Metal or other inorganic nanoparticles that were randomly pre‐loaded inside or on the surface of PS‐b‐P4VP thin film could be pulled to the rim of PS and P4VP along with the movements of PS and P4VP blocks during the treatment. As a result, the patterned polymeric or inorganic/polymer composite nanoisland and nanoring arrays were fabricated.
Carbon nanotubes (CNTs) show exceptional properties that render them attractive for incorporation in a new generation of high‐performance engineering composites with tailored properties. While a great deal of work has been done toward using CNTs as a reinforcing agent in polymer composites, the full potential of CNTs has yet to be reached. In this work, two case studies were proposed in order to analyze the effectiveness of CNTs and carbon fibers (CFs) as reinforcing agents. Micromechanics models for the stiffness and strength of hybrid composites, comprising CNTs and CFs are derived by considering the concept of effective fiber. In addition, the 2009 prices of commercially available CNTs are reviewed. The strongest, the stiffest, and the cheapest CFs commercially available are compared with single walled CNTs (SWCNTs) and multiwalled CNTs (MWCNTs). The simulated results from the micromechanics models show that the use of CFs makes the acquisition of composites with maximum tensile strengths of 4.18 GPa possible. Analysis of the cost versus property relation showed that CNTs are the most viable strengthening option for achieving composites with strengths of up to 11.61 GPa. It is also shown that CFs are the most viable stiffening option, making composites with Young's moduli of up to 383 GPa possible at the expense of the material's toughness. Moreover, it is shown that, in order to achieve CNT's true potential, several challenges have to be faced. CNTs have to be produced with higher purity, longer lengths, better integrity, in larger amounts, and at lower cost. Moreover, issues such as orientation of the CNTs, their concentration, interfacial adhesion, distribution, and dispersion have to be overcome.
