Commercial poly(p-phenylene sulfide) (PPS) was thermally cured, which resulted in an increase of molecular weight due to cross-linking. Non-isothermal crystallization studies of samples cured for up to 7 days at 250?C...Commercial poly(p-phenylene sulfide) (PPS) was thermally cured, which resulted in an increase of molecular weight due to cross-linking. Non-isothermal crystallization studies of samples cured for up to 7 days at 250?C showed a monotonous increase of crystallization temperature compared to pure PPS. However, a further increase of curing time decreased the crystallization temperature. The change in the half-crystallization time (t1/2) was similar to the crystallization temperature. Thus, the cross-linking of PPS affected crystallization behaviors significantly. To a certain extent, crosslinks acted as nucleation agents, but excessive cross-linking hindered the crystallization. Morphologies observed by polarized optical microscopy suggested that thermal curing for as little as 1 day contributed to the spherulitic structure having a smaller size, that was not observed with pure PPS.展开更多
Hierarchical tin（Ⅲ） oxide, Sn3O4, nanospheres were synthesized via hydrothermal reaction under strongly acidic ambient conditions. The morphology of Sn3O4 varied with decreasing pH. The prickly SnaO4 nanospheres ch...Hierarchical tin（Ⅲ） oxide, Sn3O4, nanospheres were synthesized via hydrothermal reaction under strongly acidic ambient conditions. The morphology of Sn3O4 varied with decreasing pH. The prickly SnaO4 nanospheres changed into SnaO4 nanospheres covered with single-crystalline nanoplates having a high BET surface area of ca. 55.05 m^2·g^-1 and a band gap of ca. 2.25 eV. Small amounts （0.05 g） of the hierarchical Sn3O4 nanostructures completely decomposed a 30% methyl orange （MO） solution in 100 mL deionized water within 15 min under one sun condition （UV ＋ visible light）. The Sn3O4 photocatalyst exhibited a fast decomposition rate of 1.73 ×10^-1 min^-1, which is a 90.86% enhancement relative to that of the commercially available P25 photocatalyst. The high photocatalytic activity of the hierarchical Sn3O4 nanostructures is attributed to its ability to absorb visible light and its high surface-to-volume ratio.展开更多
文摘Commercial poly(p-phenylene sulfide) (PPS) was thermally cured, which resulted in an increase of molecular weight due to cross-linking. Non-isothermal crystallization studies of samples cured for up to 7 days at 250?C showed a monotonous increase of crystallization temperature compared to pure PPS. However, a further increase of curing time decreased the crystallization temperature. The change in the half-crystallization time (t1/2) was similar to the crystallization temperature. Thus, the cross-linking of PPS affected crystallization behaviors significantly. To a certain extent, crosslinks acted as nucleation agents, but excessive cross-linking hindered the crystallization. Morphologies observed by polarized optical microscopy suggested that thermal curing for as little as 1 day contributed to the spherulitic structure having a smaller size, that was not observed with pure PPS.
文摘Hierarchical tin（Ⅲ） oxide, Sn3O4, nanospheres were synthesized via hydrothermal reaction under strongly acidic ambient conditions. The morphology of Sn3O4 varied with decreasing pH. The prickly SnaO4 nanospheres changed into SnaO4 nanospheres covered with single-crystalline nanoplates having a high BET surface area of ca. 55.05 m^2·g^-1 and a band gap of ca. 2.25 eV. Small amounts （0.05 g） of the hierarchical Sn3O4 nanostructures completely decomposed a 30% methyl orange （MO） solution in 100 mL deionized water within 15 min under one sun condition （UV ＋ visible light）. The Sn3O4 photocatalyst exhibited a fast decomposition rate of 1.73 ×10^-1 min^-1, which is a 90.86% enhancement relative to that of the commercially available P25 photocatalyst. The high photocatalytic activity of the hierarchical Sn3O4 nanostructures is attributed to its ability to absorb visible light and its high surface-to-volume ratio.
