Analytical breakthrough curves for inert core adsorbent with sorption kinetics

AIChE Journal ◽  
2003 ◽  
Vol 49 (11) ◽  
pp. 2974-2979 ◽  
Author(s):  
Ping Li ◽  
Guohua Xiu ◽  
Alirio E. Rodrigues
2007 ◽  
Vol 20-21 ◽  
pp. 635-638 ◽  
Author(s):  
Karol Campos ◽  
Eric Guibal ◽  
Francisco Peirano ◽  
M. Ly ◽  
Holger Maldonado

Mercury sorption on chitosan was investigated in batch and continuous systems. Chitosan sorption properties were determined through sorption isotherms. Langmuir and Freundlich equations were used for the modeling of isotherms at pH 5. In batch systems, maximum sorption capacities reached 550 mg Hg/g. Sorption kinetics have been studied as a function of sorbent particle size and stirring rate. Dynamic removal of mercury was tested in a fixed bed reactor investigating the following parameters: particle size, column size, flow velocity and metal ion concentration. Clark and Adams-Bohart models were evaluated for the simulation of breakthrough curves. This study shows that chitosan is an effective sorbent for the treatment and recovery of mercury from dilute effluents at near neutral pH.


2003 ◽  
Vol 58 (15) ◽  
pp. 3361-3371 ◽  
Author(s):  
Ping Li ◽  
Guohua Xiu ◽  
Alirio E. Rodrigues

1992 ◽  
Vol 23 (2) ◽  
pp. 89-104 ◽  
Author(s):  
Ole H. Jacobsen ◽  
Feike J. Leij ◽  
Martinus Th. van Genuchten

Breakthrough curves of Cl and 3H2O were obtained during steady unsaturated flow in five lysimeters containing an undisturbed coarse sand (Orthic Haplohumod). The experimental data were analyzed in terms of the classical two-parameter convection-dispersion equation and a four-parameter two-region type physical nonequilibrium solute transport model. Model parameters were obtained by both curve fitting and time moment analysis. The four-parameter model provided a much better fit to the data for three soil columns, but performed only slightly better for the two remaining columns. The retardation factor for Cl was about 10 % less than for 3H2O, indicating some anion exclusion. For the four-parameter model the average immobile water fraction was 0.14 and the Peclet numbers of the mobile region varied between 50 and 200. Time moments analysis proved to be a useful tool for quantifying the break through curve (BTC) although the moments were found to be sensitive to experimental scattering in the measured data at larger times. Also, fitted parameters described the experimental data better than moment generated parameter values.


1996 ◽  
Vol 34 (1-2) ◽  
pp. 153-160 ◽  
Author(s):  
S. H. Lee ◽  
S. Vigneswaran ◽  
K. Bajracharya

Excessive phosphorus (P as orthophosphate) is one of the major pollutants in natural water that are responsible for algal blooms and eutrophication. P removal by slag is an attractive solution if the P sorption capacity of slag is significant. To design an efficient land treatment facility, basic information on the behaviour of P in the media-water environment is required. In this study, detailed column experiments were conducted to study the P transport under dynamic condition, and mathematical models were developed to describe this process. The column experiments conducted with dust and cake waste products (slag) from a steel industry as adsorbing indicated that they had higher sorption capacity of P than that of a sandy loam soil from North Sydney, Australia. P transport in the dust and cake columns exhibited characteristic S-shaped or curvilinear breakthrough curves. The simulated results from a dynamic physical nonequilibrium sorption model (DPNSM) and Freundlich isotherm constants satisfactorily matched the corresponding experimental breakthrough data. The mobility of P is restricted by the adsorbents and it is proportional to the sorption capacity of them.


1991 ◽  
Vol 24 (2) ◽  
pp. 309-314 ◽  
Author(s):  
G. Teutsch ◽  
K. Herbold-Paschke ◽  
D. Tougianidou ◽  
T. Hahn ◽  
K. Botzenhart

In this paper the major processes governing the persistence and underground transport of viruses and bacteria are reviewed in respect to their importance under naturally occurring conditions. In general, the simulation of the governing processes is based on the macroscopic mass-conservation equation with the addition of some filter and/or retardation factor and a decay coefficient, representing the natural “die-off” of the microorganisms. More advanced concepts try to incorporate growth and decay coefficients together with deposition and declogging factors. At present, none of the reported concepts has been seriously validated. Due to the complexity of natural systems and the pathogenic properties of some of the microorganisms, experiments under controlled laboratory conditions are required. A laboratory setup is presented in which a great variety of natural conditions can be simulated. This comprises a set of 1 metre columns and an 8 metre stainless-steel flume with 24 sampling ports. The columns are easily filled and conditioned and therefore used to study the effects of different soil-microorganism combinations under various environmental conditions. In the artificial flume natural underground conditions are simulated using sand and gravel aquifer material from the river Neckar alluvium. A first set of results from the laboratory experiments is presented together with preliminary model simulations. The large variety of observed breakthrough curves and recovery for the bacteria and viruses under investigation demonstrates the great uncertainty encountered in microbiological risk assessment.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Shazia Perveen ◽  
Raziya Nadeem ◽  
Shaukat Ali ◽  
Yasir Jamil

Abstract Biochar caged zirconium ferrite (BC-ZrFe2O5) nanocomposites were fabricated and their adsorption capacity for Reactive Blue 19 (RB19) dye was evaluated in a fixed-bed column and batch sorption mode. The adsorption of dye onto BC-ZrFe2O5 NCs followed pseudo-second-order kinetics (R 2 = 0.998) and among isotherms, the experimental data was best fitted to Sips model as compared to Freundlich and Langmuir isotherms models. The influence of flow-rate (3–5 mL min−1), inlet RB19 dye concentration (20–100 mg L−1) and quantity of BC-ZrFe2O5 NCs (0.5–1.5 g) on fixed-bed sorption was elucidated by Box-Behnken experimental design. The saturation times (C t /C o  = 0.95) and breakthrough (C t /C o  = 0.05) were higher at lower flow-rates and higher dose of BC-ZrFe2O5 NCs. The saturation times decreased, but breakthrough was increased with the initial RB19 dye concentration. The treated volume was higher at low sorbent dose and influent concentration. Fractional bed utilization (FBU) increased with RB19 dye concentration and flow rates at low dose of BC-ZrFe2O5 NCs. Yan model was fitted best to breakthrough curves data as compared to Bohart-Adams and Thomas models. Results revealed that BC-ZrFe2O5 nanocomposite has promising adsorption efficiency and could be used for the adsorption of dyes from textile effluents.


Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 510
Author(s):  
Majeda Khraisheh ◽  
Fares. Almomani ◽  
Gavin Walker

The separation of C3H4/C3H6 is one of the most energy intensive and challenging operations, requiring up to 100 theoretical stages, in traditional cryogenic distillation. In this investigation, the potential application of two MOFs (SIFSIX-3-Ni and NbOFFIVE-1-Ni) was tested by studying the adsorption–desorption behaviors at a range of operational temperatures (300–360 K) and pressures (1–100 kPa). Dynamic adsorption breakthrough tests were conducted and the stability and regeneration ability of the MOFs were established after eight consecutive cycles. In order to establish the engineering key parameters, the experimental data were fitted to four isotherm models (Langmuir, Freundlich, Sips and Toth) in addition to the estimation of the thermodynamic properties such as the isosteric heats of adsorption. The selectivity of the separation was tested by applying ideal adsorbed solution theory (IAST). The results revealed that SIFSIX-3-Ni is an effective adsorbent for the separation of 10/90 v/v C3H4/C3H6 under the range of experimental conditions used in this study. The maximum adsorption reported for the same combination was 3.2 mmolg−1. Breakthrough curves confirmed the suitability of this material for the separation with a 10-min gab before the lighter C3H4 is eluted from the column. The separated C3H6 was obtained with a 99.98% purity.


2021 ◽  
Vol 5 (1) ◽  
pp. 9
Author(s):  
Muhammad Yusuf Prajitno ◽  
Mohamad Taufiqurrakhman ◽  
David Harbottle ◽  
Timothy N. Hunter

Natural clinoptilolite was studied to assess its performance in removing caesium and strontium ions, using both static columns and an agitated tube reactor (ATR) for process intensification. Kinetic breakthrough curves were fitted using the Thomas and Modified Dose Response (MDR) models. In the static columns, the clinoptilolite adsorption capacity (qe) for 200 ppm ion concentrations was found to be ~171 and 16 mg/g for caesium and strontium, respectively, highlighting the poor material ability to exchange strontium. Reducing the concentration of strontium to 100 ppm, however, led to a higher strontium qe of ~48 mg/g (close to the maximum adsorption capacity). Conversely, halving the column residence time to 15 min decreased the qe for 100 ppm strontium solutions to 13–14 mg/g. All the kinetic breakthrough data correlated well with the maximum adsorption capacities found in previous batch studies, where, in particular, the influence of concentration on the slow uptake kinetics of strontium was evidenced. For the ATR studies, two column lengths were investigated (of 25 and 34 cm) with the clinoptilolite embedded directly into the agitator bar. The 34 cm-length system significantly outperformed the static vertical columns, where the adsorption capacity and breakthrough time were enhanced by ~30%, which was assumed to be due to the heightened kinetics from shear mixing. Critically, the increase in performance was achieved with a relative process flow rate over twice that of the static columns.


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