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Monika Wawrzkiewicz Zbigniew Hubicki 《Chemical engineering journal (Lausanne, Switzerland : 1996)》2009,150(2-3):509-515
The sorption of Tartrazine, Allura Red, Sunset Yellow and Indigo Carmine from aqueous solutions onto the strongly basic anion-exchanger (Lewatit MonoPlus M-600) of dimethylethanolamine functional groups and styrene–divinylbenzene matrix was investigated. The experimental data obtained at 50, 100, 200, 300 and 500 mg/dm3 initial concentrations at 20 °C were applied to the pseudo-first order, pseudo-second order and Weber–Morris kinetic models. The calculated sorption capacities (q1,cal) and the rate constant of the first-order adsorption (k1) were determined. The pseudo-second order kinetic constants (k2) and capacities (q2,cal) were calculated from the plots of t/qt vs. t, 1/qt vs. 1/t, 1/t vs. 1/qt, qt/t vs. qt and 1/q2 − qt vs. t for type 1, type 2, type 3, type 4 and type 5 of the pseudo-second order expression, respectively. 相似文献
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The precious metals and their alloys are extensively applied in refineries and the chemical and electronic industries as well as in medicine. Their small amounts in nature and extensive exploitation from natural resources are a serious obstacle as far as their application is concerned. High prices of palladium favour its recovery from recyclable materials and industrial wastes. Ion-exchange chromatography is one of the physicochemical methods of noble metal ion recovery. A study was done on the possibility of selective removal of palladium (II) microquantities from the model 0.1-6.0 M HCl, 0.1-0.9 M HCl-0.9 - 0.1 M HNO3, 1.0 M ZnCl2 - 0.1 M HCl and 1.0 M AlCl3-0.1 M HCl systems on weakly, intermediate and strongly basic anion exchangers. The sorption research of Pd (II) on various types of anion exchangers was carried out by means of dynamic and static methods. The working ion-exchange capacities, weight and bed distribution coefficients were calculated from the breakthrough curves of palladium (II) ions. From the static studies the recovery factors of Pd (II) depending on the anion exchanger-solution contact time in the model systems under discussion were determined. 相似文献
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S. Sinha S. S. Behera S. Das A. Basu R. K. Mohapatra B. M. Murmu 《Chemical Engineering Communications》2018,205(4):432-444
Removal of Congo Red (CR) azo dye by adsorption process using Amberlite IRA-400 resin was evaluated in both batch and fixed bed system. From the batch adsorption results, maximum loading efficiency (99.99%) of CR dye was obtained at the conditions pH 4.5, temp. 303?K, contact time 180?min., Amberlite IRA-400 dose 0.5?g. The isotherm study ascertained on favorability of adsorption process as the value of separation factor (KL?=?0.88) and Freundlich constant (1/n?=?0.96?1.0) obtained from Langmuir and Freundlich equations are rational, though, overall adsorption process showed best fit with Langmuir (R2?=?0.99) than Freundlich model (R2?=?0.97). The kinetic data studied at three different CR dye concentration (50, 75, 100?mg) and results were fitted with both pseudo-first-order and second-order model equations. The values of R2 obtained are of 0.95 and 0.99 for former and later one, respectively, ensuring on best fitting of pseudo-second-order kinetics and also suggesting about the chemisorptions type of adsorption. The bed depth service model was applied for competitive analysis of the CR dye adsorption in column variables indicating mass transfer from aqueous solution to Amberlite IRA-400 phase. Fourier transform infrared analysis of CR-loaded resin Amberlite IRA-400 showed a band shifted from 1057 to 1130?cm?1 confirming CR adsorption with Amberlite IRA-400. Scanning electron microscope analysis of resin before and after adsorption was well evident from the phase patterns. Selective separation of CR dye from waste effluent of a textile industry bearing CR dye along with other trace heavy metal was achieved. 相似文献
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The sorption of palladium(II) microquantities from a chloride and chloride-nitrate (V) model 0.1-6.0 M HCl, 0.1-0.9 M HCl-0.9-0.1 M HNO3, 1.0 M ZnCl2-0.1 M HCl and 1.0 M AlCl3-0.1 M HCl systems on strongly basic polyacrylate anion exchangers was studied. The research was carried out by means of dynamic and static methods. The recovery factors of Pd(II) were determined from the static studies. The working ion-exchange capacities as well as weight and bed distribution coefficients of Pd(II) were calculated from the breakthrough curves. The commercial strongly basic anion exchangers of the functional quaternary ammonium groups — Purolite A-850 and Amberlite IRA-958 — can be used in recovery technologies of Pd(II) from anodic slime, wastewaters and spent catalysts due to their high selectivity. 相似文献
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M. Grdeń 《Electrochimica acta》2009,54(3):909-7326
Anodic oxidation of Pd in basic solutions (0.1 M KOHaq and 0.1 M NaOHaq) has been examined via cyclic voltammetry (CV) and an electrochemical quartz crystal microbalance (EQCM). Admittance tests show that Pd(II) layer behaves as a rigid one. The anodic vertex potential influences mass response during formation of the Pd(II) layer. For low anodic vertex potentials, obtained absolute mass per mole values suggest Pd(OH)2 or PdO·H2O to be oxidation products. At this stage of the oxidation process, contribution from adsorbed H2O/OH− in Pd(II) layer formation could explain the lower-than-expected mass gain, although the extent of H2O/OH− adsorption is unclear. The mass gain decreases with further increase in the anodic vertex potential, eventually reaching the value of ca. 8 g mol−1 at about 700 mV vs. SCE. Comparing the influence of vertex potential in CV experiments on the mass and reduction potential of the Pd(II) species points to the formation of PdO at higher oxidation potentials. At this stage of the process, a fraction of the PdO species is generated during transformation of previously formed Pd(OH)2/PdO·H2O. A shift of the main Pd(II) reduction potential peak depends on both the anodic vertex potential and on the composition of the Pd(II) film. The order of the Pd(II) reduction process is the opposite of that observed for the oxidation process. The Pd(IV) species formed at E ≥ 500 mV vs. SCE and those reduced between 50 and 350 mV are hydrated or contain hydroxyl groups. 相似文献
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介绍了聚合物驱油原理,概括了聚合物驱所采用的聚合物品类,介绍了疏水缔合聚合物、两性聚合物及梳形聚合物的特点和发展概况,分析了提高采收率的系列方法。在新型驱油剂的研制过程中,要满足其苛刻的使用条件,开发出耐井下高温,不易在电解质溶液中被剪切破坏的高分子量聚合物驱油剂。 相似文献
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The electrodeposition of palladium–silver alloys was investigated in a basic 1-ethyl-3-methylimidazolium chloride/tetrafluoroborate ionic liquid containing Pd(II) and Ag(I). Cyclic voltammetry experiments showed that the reduction of Ag(I) occurs prior to the reduction Pd(II). Both electrodeposition processes require nucleation overpotential. Energy-dispersive spectroscopy data indicated that the composition of the Pd–Ag alloys could be varied by deposition potential and concentrations of Pd(II) and Ag(I) in the solution. The Pd content in the deposited Pd–Ag alloy increased with decreasing deposition potential and the Pd mole fraction in the plating bath. At potentials where the deposition of both Pd and Ag was mass-transport limited, the Pd/Ag ratio in the electrodeposited alloys was slightly less than the Pd(II)/Ag(I) ratio in the ionic liquid due to the smaller diffusion coefficient of Pd(II). Scanning electron micrographs of the electrodeposits showed that in general, the Pd–Ag alloys were nodular and become more compact upon increasing the temperature up to 120 °C. 相似文献
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溶剂萃取在有机化合物提取和分离方面的应用(上) 总被引:4,自引:0,他引:4
回顾了溶剂萃取技术发展的历史。对于该技术在有机化合物提取和分离方面的研究和应用现状进行了综述。展望了未来的发展趋势。 相似文献
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Giuliana GorrasiMariarosaria Tortora Vittoria Vittoria Dirk KaempferRolf Mülhaupt 《Polymer》2003,44(13):3679-3685
Syndiotactic polypropylene (sPP) nanocomposites were obtained by melt blending synthetic fluorohectorite modified octadecyl ammmonium ions (OLS), and maleic-anhydride-grafted isotactic polypropylene (iPP-g-MA) as compatibilizer. The composition of the inorganic material was varied between 5 and 20 w/w%. Films of the composites were obtained by hot press molding the pellets. Melt-direct polymer intercalation of sPP into the OLS gave rise to nanocomposites in which the silicate layers were delaminated at low clay contents, and ordered to intercalated structures at the highest clay content. The elastic modulus was higher than for the pure polymer in a wide temperature range and increased with the inorganic content. The transport properties were measured for dichloromethane and n-pentane. The sorption was reduced compared to pure sPP. There were not significative differences between the samples having different inorganic contents. The diffusion coefficient decreased with increasing clay content. Permeability (P) showed a strong decreasing dependence on the clay content. The improvement of the barrier properties was largely caused by the reduced diffusion. 相似文献
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Preeti Chandra 《Polymer》2009,50(1):236-12050
This paper reports the sorption and diffusion characteristics of methanol vapor in polyethylene terephthalate (PET). Amorphous PET, semicrystalline, biaxially oriented annealed and non-annealed samples have been studied for equilibrium sorption and kinetics of methanol. At activities of methanol less than 0.30, uptake shows Fickian kinetics and isotherm follows the Dual Mode model. Diffusion coefficients increase with penetrant concentration and are of the order of 10−10 cm2/s. Hysteresis during desorption and increase in solubility during resorption suggest methanol induced conditioning effects which may have detrimental effects on the barrier efficacy of PET. At activities greater than 0.30, swelling and relaxation effects occur and the isotherms show Flory-Huggins behavior for all three samples. Uptake follows two-stage kinetics fit by the Berens-Hopfenberg model. Greater polymer chain stability due to annealing reduces the extent of relaxation and improves the barrier efficacy over amorphous and non-annealed, oriented PET. For amorphous PET, at 80% activity and above, an induction time is observed which is absent in the semicrystalline films, suggesting strong relaxation effects in the amorphous phase of PET. 相似文献
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