纤维改性硫氧镁基仿木保温材料性能研究

为了提高硫氧镁基仿木保温材料的各项性能, 分别研究了相同长度的聚丙烯纤维(PPF)、聚乙烯醇纤维(PVAF)、玻璃纤维(GF)对其性能的影响. 结果表明: 随着纤维掺量的增加, 硫氧镁基仿木保温材料的流动性有所降低; GF对其抗压抗折强度的提高效果最明显, 其中GF掺量为1.0 kg·m^-3时早期抗压强度最高, PVAF掺量为0.5 kg·m^-3时其早期抗压强度最高; PPF明显提高了硫氧镁基仿木保温材料的耐水性, 其掺量为0.5 kg·m^-3时软化系数最大, 而GF掺量在1.0 kg·m^-3时, 浸水软化系数稍高于未加纤维的对比试件; 掺加PVAF后硫氧镁基保温材料的导热系数出现一定程度的降低, 其中PVAF掺量在1.5 kg·m^-3时其导热系数最低. GF和PPF可以明显地降低硫氧镁基仿木保温材料的收缩值, 其中GF降低自收缩效果较好, 而PPF可以明显地降低其干燥收缩值.     

茂钇-铝双金属配合物催化甲基丙烯酸甲酯立规聚合

立规聚合;茂稀土催化剂;稀土;茂钇-铝双金属配合物催化甲基丙烯酸甲酯立规聚合     

(Triphenylarsine)iodinemonobromine: a charge‐transfer adduct in which arsenic selectively bonds to iodine

The title molecule, (iodobromo)triphenylarsenic(III), [As(BrI)(C₆H₅)₃], has a dart shape, with the phenyl rings arranged in a propeller conformation [I—As—C—C 61.3 (4), 43.8 (4) and 54.1 (4)°]. There is no indication that the halogen atoms have mixed site occupancies. Packing forces displace the I atom away from one phenyl ring [I—As—C 117.3 (2)°] towards the other two [I—As—C 109.8 (2) and 108.3 (2)°] and produce an even more pronounced leaning of the terminal bromine [As—I—Br 174.78 (2)°].     

烯烃聚合高性能FI催化剂的进展

FI催化剂系一近几年发展起来的烯烃聚合高性能催化剂。以它的极高的活性、聚合物分子结构的可控性、多重活性聚合等特性而引人注目。本评述首先进行该催化剂的化学描述,然后分别介绍该催化剂的主要特征、活性中心结构、聚合机理和应用,重点介绍该催化剂的五大特征。     

Statistical theory for hydrogen bonding fluid system of A_aD_d type (I): The geometrical phase transition

The influence of hydrogen bonds on the physical and chemical properties of hydrogen bonding fluid system of AaDd type is investigated from two viewpoints by the principle of statistical mechanics. In detail, we proposed two new ways that can be used to obtain the equilibrium size distribution of the hydrogen bonding clusters, and derived the analytical expression of a relationship between the hydrogen bonding free energy and hydrogen bonding degree. For the nonlinear hydrogen bonding systems, it is shown that the sol-gel phase transition can take place under proper conditions, which is further proven to be a kind of geometrical phase transition rather than a thermodynamic one. Moreover, several problems associated with the geometrical phase transition and liquid-solid phase transition in nonlinear hydrogen bonding systems are discussed.     

Assessing the effects of homosexuals and bisexuals on the intrinsic dynamics of HIV/AIDS in heterosexual settings

A deterministic compartmental sex-structured HIV/AIDS model for assessing the effects of homosexuals and bisexuals on the intrinsic dynamics of the disease in heterosexual settings in which homosexuality and bisexuality issues have remained taboo is presented. The epidemic threshold and equilibria for the model are determined and stabilities are investigated. Comprehensive qualitative analysis of the model including invariance of solutions and permanence are carried out. The epidemic threshold known as the basic reproductive number suggests that heterosexuality, homosexuality, and bisexuality influence the growth of the epidemic in HIV/AIDS affected populations and the partial reproductive number (homosexuality induced or heterosexuality and bisexuality induced) with the larger value influences the overall dynamics of the epidemic in a setting. Numerical simulations of the model show that as long as one of the partial reproductive numbers is greater than unity, the disease will exist in the population. We conclude from the study that homosexuality and bisexuality enlarge the epidemic in a heterosexual setting. The theoretical study highlights the need to carry out substantial research to map homosexuals and bisexuals as it has remained unclear as to what extent this group has contributed to the epidemic in heterosexual settings especially in southern Africa, which has remained the epidemiological locus of the epidemic.     

Crystallographic effects in low energy ion scattering due to local ion-atom neutralisation

New experiments on 1 keV ₄He⁺ ion scattering from Ni {100} and Ni {100} (√2 × √2)R45°?O surfaces show azimuthal anisotropies attributable to variations in ion neutralisation probability for different ion trajectories relative to the position of the surface atoms. These effects are shown to be compatible with a simple localised ion-atom neutralisation mechanism. The results indicate that local neutralization is an important process in substrate shadowing in low energy ion scattering studies of adsorbate structures.