To further elucidate interaction of nitroaromatic compounds with mineral surface, the sorption of m-dinitrobenzene （m-DNB） and nitrobenzene to original bentonite in aqueous solution containing different electrolytes...To further elucidate interaction of nitroaromatic compounds with mineral surface, the sorption of m-dinitrobenzene （m-DNB） and nitrobenzene to original bentonite in aqueous solution containing different electrolytes （i.e., KCl, NH4Cl, CaCl2 and Tetramethylammonium bromide （TMAB）） was studied. The sorption of m-DNB was greatly enhanced with the presence of KCl and NH4Cl, while little influence was observed with CaCl2 and TMAB, following the order of KCl 〉 NH4Cl 〉〉 TMAB, CaCl2, or DI water. For nitrobenzene, sorption enhancement only occurred at high nitrobenzene concentrations in the presence of KCl, and the solute equilibrium concentration at inflexion point was lowered with increasing KCl concentration. These sorption enhancements were significantly promoted with the increase of electrolyte concentration. The salting-out effect is insufficient to account for the sorption enhancement by original bentonite with increasing KCI or NH4Cl concentration. X-ray diffraction patterns of bentonite suspensions indicated that the sorption enhancement of m-DNB was attributed to the intercalation of K^＋ or NH4^＋ into bentonite interlayer and then dehydration with m-DNB to form inner-sphere complexes, which caused previously expanded bentonite interlayers to collapse in aqueous suspension, thus further enhanced the interaction of phenyl with siloxane surface. In comparison, the sorption enhancement of NB is attributed to the formation of outer-sphere complexes with K^＋ at high solute-loadings （〉 20（0-400 mg/kg）. The sorption of m-DNB to initially modified TMA^＋-bentonite and K^＋-bentonite was almost the same as respective sorption to original bentonite in solution containing TMA^＋ and K^＋.展开更多
The objective of this work is to determine changes of surface properties of a bentonite after acid activation, using hydrochloric acid solutions (HCl) at room temperature. XRD, FX, FTIR, MEB, and BET analyses of the s...The objective of this work is to determine changes of surface properties of a bentonite after acid activation, using hydrochloric acid solutions (HCl) at room temperature. XRD, FX, FTIR, MEB, and BET analyses of the samples have been carried out to examine the structure of bentonite before and after acid activation. It is found that the raw bentonite is composed of dioctahedral montmorillonite with predominant quantity and certain amounts of quartz, albite and illite, etc. It has an cation exchange capacity (CEC) of 74.32 meq/g which allows it to be characterized as typical sodium bentonite. The changes, at low acid concentrations, are the result from from cation exchange (exchangeable cations with H+ ions). Differences of surface area at high acid concentrations (0.25 - 0.4 M) were caused by structural changes and partial decomposition of the samples. Data of surface area measurements have showed that with increase of concentration of hydrochloric acid, the surface area increased. The maximum value (837.11 m2/g) was reached by the sample activated with 0.4 M HCl. By against, activation with higher concentration (0.6 M) caused a decrease in the surface area.展开更多
In order to study the ability of bentonites to remove heavy metal ions from waste water and its factors affecting it,batch sorption experiments of Cu2+ were conducted on Ca-bentonite and Na-bentonite under various con...In order to study the ability of bentonites to remove heavy metal ions from waste water and its factors affecting it,batch sorption experiments of Cu2+ were conducted on Ca-bentonite and Na-bentonite under various conditions.The results show that the adsorption process of bentonite accorded with the Freundlich isotherm model and that the sorption results of Na-bentonite are better than those of Ca-bentonite.Adsorption behavior of both bentonites was strongly depending on pH,initial concentration and additional amounts of bentonites.There are three kinds of adsorption mechanism at different ranges of pH values:the competition adsorption between Cu2+ and H+(pH<3),ion-exchange adsorption(pH=3～7) and precipitation adsorption of copper hydroxyl compounds(pH>8.3).The removal rate of bentonite decreases with an increase in the initial metal ion concentration.The maximum adsorption capacity of Na-bentonite was 26 mg/g and that of Ca-bentonite 12 mg/g.The removal rate of Cu2+ was practically 100% at the initial concentration of 40 mg/L,when 4 g/L of Na-bentonite and 14 g/L of Ca-bentonite were added to the solution.展开更多
Three organobentonites were synthesized by placing cation surfactants such as octadecyltrimethylammonium bromide (OTMAD ), cetyltrimethylammonium bromide (CTMAB) and dodecyltrimethylammonium bromide(DTMAB) on bentonit...Three organobentonites were synthesized by placing cation surfactants such as octadecyltrimethylammonium bromide (OTMAD ), cetyltrimethylammonium bromide (CTMAB) and dodecyltrimethylammonium bromide(DTMAB) on bentonite. The properties for organobentonites to adsorb phenol, p-nitrophenol, aniline, nitrobenzene and 1-naphthylamine in water were investigated in detail. The mechanism that organic compounds were adsorbed by organobentonites was studied. The removal rates for organobentonites to treat organic compounds from water were associated with the properties of organic compounds, the ammount of cation surfactants exchanged on the bentonite and the length of alkyl chain of the cation surfactant.展开更多
基金supported by the National Natural Science Foundation of China (No. 20577041)the New Century Educational Talents Plan of Chinese Education Ministry (No. NCET-05-0525)+1 种基金the Foundation for the Author of National Excellent Doctoral Dissertation of PR China(No.200765)the Program of Provincial Science and Technology of Zhejiang (No. 2006C33050)
文摘To further elucidate interaction of nitroaromatic compounds with mineral surface, the sorption of m-dinitrobenzene （m-DNB） and nitrobenzene to original bentonite in aqueous solution containing different electrolytes （i.e., KCl, NH4Cl, CaCl2 and Tetramethylammonium bromide （TMAB）） was studied. The sorption of m-DNB was greatly enhanced with the presence of KCl and NH4Cl, while little influence was observed with CaCl2 and TMAB, following the order of KCl 〉 NH4Cl 〉〉 TMAB, CaCl2, or DI water. For nitrobenzene, sorption enhancement only occurred at high nitrobenzene concentrations in the presence of KCl, and the solute equilibrium concentration at inflexion point was lowered with increasing KCl concentration. These sorption enhancements were significantly promoted with the increase of electrolyte concentration. The salting-out effect is insufficient to account for the sorption enhancement by original bentonite with increasing KCI or NH4Cl concentration. X-ray diffraction patterns of bentonite suspensions indicated that the sorption enhancement of m-DNB was attributed to the intercalation of K^＋ or NH4^＋ into bentonite interlayer and then dehydration with m-DNB to form inner-sphere complexes, which caused previously expanded bentonite interlayers to collapse in aqueous suspension, thus further enhanced the interaction of phenyl with siloxane surface. In comparison, the sorption enhancement of NB is attributed to the formation of outer-sphere complexes with K^＋ at high solute-loadings （〉 20（0-400 mg/kg）. The sorption of m-DNB to initially modified TMA^＋-bentonite and K^＋-bentonite was almost the same as respective sorption to original bentonite in solution containing TMA^＋ and K^＋.
文摘The objective of this work is to determine changes of surface properties of a bentonite after acid activation, using hydrochloric acid solutions (HCl) at room temperature. XRD, FX, FTIR, MEB, and BET analyses of the samples have been carried out to examine the structure of bentonite before and after acid activation. It is found that the raw bentonite is composed of dioctahedral montmorillonite with predominant quantity and certain amounts of quartz, albite and illite, etc. It has an cation exchange capacity (CEC) of 74.32 meq/g which allows it to be characterized as typical sodium bentonite. The changes, at low acid concentrations, are the result from from cation exchange (exchangeable cations with H+ ions). Differences of surface area at high acid concentrations (0.25 - 0.4 M) were caused by structural changes and partial decomposition of the samples. Data of surface area measurements have showed that with increase of concentration of hydrochloric acid, the surface area increased. The maximum value (837.11 m2/g) was reached by the sample activated with 0.4 M HCl. By against, activation with higher concentration (0.6 M) caused a decrease in the surface area.
基金Projects D2007000695 and D2009000833 supported by the Natural Science Foundation of Hebei Province, China
文摘In order to study the ability of bentonites to remove heavy metal ions from waste water and its factors affecting it,batch sorption experiments of Cu2+ were conducted on Ca-bentonite and Na-bentonite under various conditions.The results show that the adsorption process of bentonite accorded with the Freundlich isotherm model and that the sorption results of Na-bentonite are better than those of Ca-bentonite.Adsorption behavior of both bentonites was strongly depending on pH,initial concentration and additional amounts of bentonites.There are three kinds of adsorption mechanism at different ranges of pH values:the competition adsorption between Cu2+ and H+(pH<3),ion-exchange adsorption(pH=3～7) and precipitation adsorption of copper hydroxyl compounds(pH>8.3).The removal rate of bentonite decreases with an increase in the initial metal ion concentration.The maximum adsorption capacity of Na-bentonite was 26 mg/g and that of Ca-bentonite 12 mg/g.The removal rate of Cu2+ was practically 100% at the initial concentration of 40 mg/L,when 4 g/L of Na-bentonite and 14 g/L of Ca-bentonite were added to the solution.
文摘Three organobentonites were synthesized by placing cation surfactants such as octadecyltrimethylammonium bromide (OTMAD ), cetyltrimethylammonium bromide (CTMAB) and dodecyltrimethylammonium bromide(DTMAB) on bentonite. The properties for organobentonites to adsorb phenol, p-nitrophenol, aniline, nitrobenzene and 1-naphthylamine in water were investigated in detail. The mechanism that organic compounds were adsorbed by organobentonites was studied. The removal rates for organobentonites to treat organic compounds from water were associated with the properties of organic compounds, the ammount of cation surfactants exchanged on the bentonite and the length of alkyl chain of the cation surfactant.
