In this paper a new method for predicting the hydrodynamic performance of the flap rudder behind a propeller was presented. The hydrodynamics of the rudder was calculated by the panel method and the performance of the...In this paper a new method for predicting the hydrodynamic performance of the flap rudder behind a propeller was presented. The hydrodynamics of the rudder was calculated by the panel method and the performance of the propeller was predicted by the simplified propeller theory. The interaction between the rudder and propeller was determined by iterative procedure. The pressure distribution on rudder surface and the hydrodynamic performance of the flap rudder were discussed in the paper.展开更多
A synthetic strategy toward the cyclic addition of 2,2'-dihydroxybiphenyl to terminal alkynes has been developed using Lewis acid TICl4 as catalyst. The reactions generated dibenzo[d,f][1,3]dioxepines derivatives in ...A synthetic strategy toward the cyclic addition of 2,2'-dihydroxybiphenyl to terminal alkynes has been developed using Lewis acid TICl4 as catalyst. The reactions generated dibenzo[d,f][1,3]dioxepines derivatives in good yields with excellent regio-selectivity in the presence of catalytic amount of TICl4 under mild reaction conditions.展开更多
文摘In this paper a new method for predicting the hydrodynamic performance of the flap rudder behind a propeller was presented. The hydrodynamics of the rudder was calculated by the panel method and the performance of the propeller was predicted by the simplified propeller theory. The interaction between the rudder and propeller was determined by iterative procedure. The pressure distribution on rudder surface and the hydrodynamic performance of the flap rudder were discussed in the paper.
基金Project supported by the National Natural Science Foundation of China (No. 20972057).
文摘A synthetic strategy toward the cyclic addition of 2,2'-dihydroxybiphenyl to terminal alkynes has been developed using Lewis acid TICl4 as catalyst. The reactions generated dibenzo[d,f][1,3]dioxepines derivatives in good yields with excellent regio-selectivity in the presence of catalytic amount of TICl4 under mild reaction conditions.