β-2CaO＇SiO2 was obtained with analytical grade reagents. Polyethylene glycol （PEG）, sodium polyacrylate （PAAS） and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate so...β-2CaO＇SiO2 was obtained with analytical grade reagents. Polyethylene glycol （PEG）, sodium polyacrylate （PAAS） and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate solution. The potential of solid-liquid interface and the adsorption mechanism were studied by the methods of Zeta potential measurement and XPS. The results indicate that PEG and PAAS have synergistic effect on the inhibition of secondary reaction. The inhibitory effect is the best when the volume ratio of PAAS to PEG is 1：1 and the total concentration is 12.5 mg/L. PAAS adsorbs on the surface of β-2CaO-SiO2 by the formation of --COOCa coordinate bond, and the negative charge enters into Stem layer, which results in the decrease of particle potential and the obvious change of binding energy of Ca 2p, Si 2p and O Is. PEG only physically adsorbs on the surface ofβ-2CaO·SiO2, and had little effect on particle potential and binding energy of Ca 2p, Si 2p and O Is.展开更多
Four modified starches with selected charge characteristics including cationic starch(CAS),carboxymethyl starch(CMS),amphoteric starch(AMS) and soluble starch(SS) were investigated as depressants for diaspore in rever...Four modified starches with selected charge characteristics including cationic starch(CAS),carboxymethyl starch(CMS),amphoteric starch(AMS) and soluble starch(SS) were investigated as depressants for diaspore in reverse flotation test using cationic collector(dodecylamine).Adsorption examination,Zeta potential measurement and Fourier transform infrared(FTIR) spectroscopy were used to clarify the role of the surface charge characteristics of starches in determining the adsorption behavior and depression performance as well as the mineral-starch interaction.Results show that the positively charged starches(CAS and AMS) display higher adsorption amounts and also better depression performance compared with the non-ionic(SS) and anionic starch(CMS),benefiting from the favorable electrostatic attraction with diaspore and also electrostatic repulsion with collector.FTIR spectroscopy proves the presence of hydrogen bonds and chemical complexation between mineral and starches in an integrated manner.展开更多
CCl4 （carbon tetrachloride） and n-C6H14 （n-hexane） sorption studies have been carried out on natural and dealuminated clinoptilolite-type zeolites. External surface area of the materials has been assessed using t...CCl4 （carbon tetrachloride） and n-C6H14 （n-hexane） sorption studies have been carried out on natural and dealuminated clinoptilolite-type zeolites. External surface area of the materials has been assessed using the αs-plots method. The high resolution αs-plots show that the isotherms are divided into four parts corresponding to adsorption in ultramicropores, intersections, supermicropores and external surface area, respectively. The mineralogies of natural zeolites are determined by X-ray analysis. N： low-pressure hysteresis loops, displayed by some substrata, are related to the micropore structure and to the ion-exchange treatment at which the natural precursors were subjected. The adsorption behavior of these substrata was examined in the range of relative pressures between 10^-5-1. Natural samples were used as reference materials to carry out the sorption analyses of the dealuminated samples. The effect of narrow micropore constrictions on the adsorption behavior of clinoptilolites was explored. The occurrence of a low-pressure hysteresis loop on the sorption isotherm of a modified sample is associated to the strong adsorption of the adsorbate molecules at the entrance of the necked-shape micropores, which interfere with the diffusion of the adsorbate molecules inside the porous structure.展开更多
The arrangement of oligothiophenes is essential for understanding the relationship between structure and properties particularly in the organic electronic field. The self-assembly behaviors of helical(TMS)2-[7]helicen...The arrangement of oligothiophenes is essential for understanding the relationship between structure and properties particularly in the organic electronic field. The self-assembly behaviors of helical(TMS)2-[7]helicene(T1), naphthalene-cored double(TMS)2-[7]helicene(T2), and saddle-shaped cyclooctatetrathiophene(T3), its derivative α,α,α,α-tetraphenyl-cyclooctatetrathiophene(T4) on solid surface are firstly investigated by using a combination of scanning tunneling microscopy(STM) and density functional theory(DFT) calculation. 1,3,5-Tris(10-carboxydecyloxy)-benzene(TCDB) is selected to build flexible host networks to immobilize these oligothiophenes in order to capture their molecular adsorption images successfully. The observed monodisperse or polydisperse filling and long-range alignment of oligothiophenes are described based on the non-covalent interactions and commensurate structure between olihothiophene and cavity. We speculate that those molecularly defined alignments could lead to significantly understanding the application of such ordered monolayer in organic electronic devices.展开更多
文摘β-2CaO＇SiO2 was obtained with analytical grade reagents. Polyethylene glycol （PEG）, sodium polyacrylate （PAAS） and their mixture were used to inhibit the decomposition of β-2CaO·SiO2 in sodium aluminate solution. The potential of solid-liquid interface and the adsorption mechanism were studied by the methods of Zeta potential measurement and XPS. The results indicate that PEG and PAAS have synergistic effect on the inhibition of secondary reaction. The inhibitory effect is the best when the volume ratio of PAAS to PEG is 1：1 and the total concentration is 12.5 mg/L. PAAS adsorbs on the surface of β-2CaO-SiO2 by the formation of --COOCa coordinate bond, and the negative charge enters into Stem layer, which results in the decrease of particle potential and the obvious change of binding energy of Ca 2p, Si 2p and O Is. PEG only physically adsorbs on the surface ofβ-2CaO·SiO2, and had little effect on particle potential and binding energy of Ca 2p, Si 2p and O Is.
基金Projects(50804055,50974134) supported by the National Natural Science Foundation of ChinaProject(09JJ3100) supported by Hunan Provincial Natural Science Foundation,China
文摘Four modified starches with selected charge characteristics including cationic starch(CAS),carboxymethyl starch(CMS),amphoteric starch(AMS) and soluble starch(SS) were investigated as depressants for diaspore in reverse flotation test using cationic collector(dodecylamine).Adsorption examination,Zeta potential measurement and Fourier transform infrared(FTIR) spectroscopy were used to clarify the role of the surface charge characteristics of starches in determining the adsorption behavior and depression performance as well as the mineral-starch interaction.Results show that the positively charged starches(CAS and AMS) display higher adsorption amounts and also better depression performance compared with the non-ionic(SS) and anionic starch(CMS),benefiting from the favorable electrostatic attraction with diaspore and also electrostatic repulsion with collector.FTIR spectroscopy proves the presence of hydrogen bonds and chemical complexation between mineral and starches in an integrated manner.
文摘CCl4 （carbon tetrachloride） and n-C6H14 （n-hexane） sorption studies have been carried out on natural and dealuminated clinoptilolite-type zeolites. External surface area of the materials has been assessed using the αs-plots method. The high resolution αs-plots show that the isotherms are divided into four parts corresponding to adsorption in ultramicropores, intersections, supermicropores and external surface area, respectively. The mineralogies of natural zeolites are determined by X-ray analysis. N： low-pressure hysteresis loops, displayed by some substrata, are related to the micropore structure and to the ion-exchange treatment at which the natural precursors were subjected. The adsorption behavior of these substrata was examined in the range of relative pressures between 10^-5-1. Natural samples were used as reference materials to carry out the sorption analyses of the dealuminated samples. The effect of narrow micropore constrictions on the adsorption behavior of clinoptilolites was explored. The occurrence of a low-pressure hysteresis loop on the sorption isotherm of a modified sample is associated to the strong adsorption of the adsorbate molecules at the entrance of the necked-shape micropores, which interfere with the diffusion of the adsorbate molecules inside the porous structure.
基金supported by the National Basic Research Program of China(2016YFA0200700)the National Natural Science Foundation of China(21472029,21773041,21672054)
文摘The arrangement of oligothiophenes is essential for understanding the relationship between structure and properties particularly in the organic electronic field. The self-assembly behaviors of helical(TMS)2-[7]helicene(T1), naphthalene-cored double(TMS)2-[7]helicene(T2), and saddle-shaped cyclooctatetrathiophene(T3), its derivative α,α,α,α-tetraphenyl-cyclooctatetrathiophene(T4) on solid surface are firstly investigated by using a combination of scanning tunneling microscopy(STM) and density functional theory(DFT) calculation. 1,3,5-Tris(10-carboxydecyloxy)-benzene(TCDB) is selected to build flexible host networks to immobilize these oligothiophenes in order to capture their molecular adsorption images successfully. The observed monodisperse or polydisperse filling and long-range alignment of oligothiophenes are described based on the non-covalent interactions and commensurate structure between olihothiophene and cavity. We speculate that those molecularly defined alignments could lead to significantly understanding the application of such ordered monolayer in organic electronic devices.
