An apparatus, designed to simulate bubbling of sieve tray operatedin froth regime, was employed. Bubble contact angles in and above theincipient weeping regime for an air-water-plexiglas system wereinvestigated. The i...An apparatus, designed to simulate bubbling of sieve tray operatedin froth regime, was employed. Bubble contact angles in and above theincipient weeping regime for an air-water-plexiglas system wereinvestigated. The influence of both liquid cross-flow and gas up-flowupon bubble contact angles was examined. A model consider- Ing theinfluence of liquid cross-flow was developed to predict bubble sizefrom a sieve hole in froth operation regime. The comparison showsthat the bubble sizes predicted by the present model are consistentwith our experimental Values and the available published experimentaldata.展开更多
Five humic fractions were obtained from a uniformly 15N-labelled soil by extraction with 0.1 mol L-1 Na4P207, 0.1 mol L-1 NaOH, and HF/HCI-0.1 mol L-1 NaOH, consecutively, and analyzed by 13C and 15N CPMAS NMR (cross ...Five humic fractions were obtained from a uniformly 15N-labelled soil by extraction with 0.1 mol L-1 Na4P207, 0.1 mol L-1 NaOH, and HF/HCI-0.1 mol L-1 NaOH, consecutively, and analyzed by 13C and 15N CPMAS NMR (cross polarization and magic angle spinning nuclear magnetic resonance). Compared with those of native soils humic fractions studied as a whole contained more alkyls, methoxyls and O-alkyls, being 27%-36%, 17%-21% and 36%-40%, respectively, but fewer aromatics and carboxyls (being 14%-20% and 13%-90%, respectively). Among those humic fractions, the humic acid (HA) and fulvic acid (FA) extracted by 0.1 mol L-1 Na4P207 contained slightly more carboxyls than corresponding humic fractions extracted by 0.1 mol L-1 NaOH, and the HA extracted by 0.1 mol L-1 NaOH after treatment with HF/HCI contained the least aromatics and carboxyls. The distribution of nitrogen functional groups of soil humic fractions studied was quite similar to each other and also quite similar to that of humic fraction from native soils. More than 75% of total N in each fraction was in amide form, with 9%-13% present as aromatic and/or aliphatic amines and the remainder as hoterocyclic N.展开更多
文摘An apparatus, designed to simulate bubbling of sieve tray operatedin froth regime, was employed. Bubble contact angles in and above theincipient weeping regime for an air-water-plexiglas system wereinvestigated. The influence of both liquid cross-flow and gas up-flowupon bubble contact angles was examined. A model consider- Ing theinfluence of liquid cross-flow was developed to predict bubble sizefrom a sieve hole in froth operation regime. The comparison showsthat the bubble sizes predicted by the present model are consistentwith our experimental Values and the available published experimentaldata.
基金Project (No. 39790100) supported by the National Natural Science Foundation of China.
文摘Five humic fractions were obtained from a uniformly 15N-labelled soil by extraction with 0.1 mol L-1 Na4P207, 0.1 mol L-1 NaOH, and HF/HCI-0.1 mol L-1 NaOH, consecutively, and analyzed by 13C and 15N CPMAS NMR (cross polarization and magic angle spinning nuclear magnetic resonance). Compared with those of native soils humic fractions studied as a whole contained more alkyls, methoxyls and O-alkyls, being 27%-36%, 17%-21% and 36%-40%, respectively, but fewer aromatics and carboxyls (being 14%-20% and 13%-90%, respectively). Among those humic fractions, the humic acid (HA) and fulvic acid (FA) extracted by 0.1 mol L-1 Na4P207 contained slightly more carboxyls than corresponding humic fractions extracted by 0.1 mol L-1 NaOH, and the HA extracted by 0.1 mol L-1 NaOH after treatment with HF/HCI contained the least aromatics and carboxyls. The distribution of nitrogen functional groups of soil humic fractions studied was quite similar to each other and also quite similar to that of humic fraction from native soils. More than 75% of total N in each fraction was in amide form, with 9%-13% present as aromatic and/or aliphatic amines and the remainder as hoterocyclic N.