Mass transfer mechanisms in fixed-bed adsorption of erythromycin

The equilibrium and kinetic characteristics of the adsorption of erythromycin to Sepabeads SP825 were determined. The equilibrium data in a batch system was well described by a Langmuir isotherm. The separation performance was investigated in a fixed-bed system with respect to the adsorption superficial velocity, ionic strength and pH. A mathematical model was used to simulate the mass transfer mechanism, taking film mass transfer, pore diffusion and axial dispersion into account. The model predictions were consistent with the experimental data and were consequently used to determine the mass transfer coefficients.     

Mass transfer mechanisms in fixed-bed adsorption of erythromycin

The equilibrium and kinetic characteristics of the adsorption of erythromycin to Sepabeads SP825 were determined. The equilibrium data in a batch system was well described by a Langmuir isotherm. The separation performance was investigated in a fixed-bed system with respect to the adsorption superficial velocity, ionic strength and pH. A mathematical model was used to simulate the mass transfer mechanism, taking film mass transfer, pore diffusion and axial dispersion into account. The model predictions were consistent with the experimental data and were consequently used to determine the mass transfer coefficients.     

Theoretical and experimental SO2 adsorption onto pistachio-nut-shell activated carbon for a fixed-bed column

The adsorption and desorption behaviours of SO₂ onto activated carbons, which were prepared from pistachio-nut shells, were studied theoretically and experimentally in a fixed-bed column. A mathematical model considering non-equilibrium, non-isothermal and non-adiabatic effects for a single gas adsorbate on a fixed-bed system was derived and the model was solved by a finite-difference method. A linear driving force (LDF) approximation is used for heat and mass transfer rates. The temperature-dependent Langmuir equilibrium isotherm is used to represent gas–solid equilibrium isotherm. The theoretical study was conducted to compare the present model with the isothermal and adiabatic model. The effects of inlet concentration, flow rate and temperature were studied experimentally. These experimental data showed that the breakthrough time decreased with increasing feed concentration, increasing flow rate and increasing temperature and the trends were correctly predicted by the model calculations.     

Single and Multicomponent Sorption of CO2, CH4 and N2 in a Microporous Metal-Organic Framework

Abstract

Single and multicomponent fixed-bed adsorption of CO₂, N₂, and CH₄ on crystals of MOF-508b has been studied in this work. Adsorption equilibrium was measured at temperatures ranging from 303 to 343 K and partial pressures up to 4.5 bar. MOF-508b is very selective for CO₂ and the loadings of CH₄ and N₂ are practically temperature independent. The Langmuir isotherm model provides a good representation of the equilibrium data. A dynamic model based on the LDF approximation for the mass transfer has been used to describe with good accuracy the adsorption kinetics of single, binary and ternary breakthrough curves. It was found that the intra-crystalline diffusivity for CO₂ is one order of magnitude faster than for CH₄ and N₂.     

Effects of non-ideal adsorption equilibria of gas mixtures on column dynamics

A theoretical study has been made for simulating the dynamic behavior of non-ideal gas mixtures in an isothermal fixed-bed adsorber. A mathematical model was developed which takes into account the non-ideality of adsorbable species on the adsorbed phase under equilibrium. The model is based on both the real adsorbed solution theory (RAST), which incorporates the activity coefficients in the multicomponent isotherm equations to account for the deviations from ideality, and the linear driving force (LDF) model for representing diffusion resistance inside the adsorbent particles. To describe the effect of non-ideal adsorption equilibrium of gas mixtures on the breakthrough curves, we considered several model mixtures of binary and ternary components which exhibit non-ideal behavior with azeotropic crossovers in the composition domains at equilibrium. Sample calculations of a fixed-bed adsorption were done with various inlet gas compositions of binary and ternary mixtures, respectively, at a fixed total concentration. From the calculation results, it was shown that the order of breakthrough curves could be changed at a certain value of inlet gas composition ratio. This result implies that the dynamic behaviors of fixed-bed adsorption are greatly influenced by multicomponent equilibrium models. Furthermore, the reversal phenomenon of breakthrough curves could not be simulated by the ideal adsorbed solution theory (IAST).     

Development of design charts for fixed-bed adsorption

A mathematical model of the dynamic behaviour of non-isothermal fixed-bed adsorbers has been developed which takes into account the various mass and heat transfer resistances. Comparison of experimental and simulated results confirms that the model can predict the adsorption and desorption breakthrough curves of an adiabatically operated column, using only equilibrium data and tortuosity factors obtained from single pellet experiments. A simplified model with a reduced number of parameters was derived by investigation of the dimensionless transfer parameters under industrial conditions. It becomes evident that the main transfer mechanisms are convective heat and mass transfer in the bulk flow and diffusion within the pores of the particle. Dimensionless effluent concentration is expresses in terms of dimensionless time, a transport parameter, a non-isothermal parameter, the adsorption equilibrium and the inlet and initial concentrations and temperatures in the simplified model. For a chosen system of adsorbate and adsorbent, design charts can be developed by computer simulation, to determine graphically the breakthrough time as a function of significant process parameters, i.e. the dimensionless transfer parameter and the feed concentration.     

Adsorption of CO2 on Hydrotalcite‐like Compounds in a Fixed Bed

Abstract

The reduction of carbon dioxide emission from flue gases can be achieved using post‐combustion technologies, such as adsorption employing efficient solid sorbents. In this work, the adsorption of CO₂ on hydrotalcite‐like Al‐Mg compounds partially carbonated was studied using dynamic and static methods. The breakthrough curves were obtained at different flow gas rates in the range 60 to 100 mL/min and total pressure 1.0 atm. Different mixtures of CO₂ diluted in helium were used (3–20% v/v) at temperatures in the range 29 to 350°C. The experimental equilibrium data were described according to a Langmuir‐like equation. The capacity of adsorption presented a weak dependence on the temperature due to opposite effects of increasing of entropy and increasing of MgO (non‐carbonated) content in the adsorbent at high temperatures. The linear driving force model was suitable to describe the breakthrough curves. The dispersion and mass transfer coefficients were calculated by theoretical correlations and the model described quite very well the adsorption of CO₂ on hydrotalcite‐like compounds in a fixed bed in any temperature.     

AB-8大孔树脂对葡萄籽原花青素的吸附过程

研究葡萄籽原花青素粗提液在AB-8大孔树脂上的吸附过程,建立了AB-8大孔树脂吸附原花青素的相平衡方程和动态吸附模型,计算了不同流速、不同进料浓度下的总传质系数、传质区长度及穿透时间。实验结果表明,原花青素静态吸附符合Langmuir吸附等温方程式;AB-8树脂对原花青素的动态吸附属于外扩散控制过程;穿透时间计算值与实验值一致。建立的数学模型可用于指导实际生产操作,为吸附柱的设计提供参考。     

Adsorption characteristics of benzene on electrospun‐derived porous carbon nanofibers

The adsorption properties of polyacrylonitrile (PAN) carbon nanofibers fabricated by using an electrospinning route were assessed for their applicability as a novel alternative adsorbent. Commercial fiber, A–10, was chosen for comparison. Nitrogen adsorption/desorption isotherms and gravimetric techniques were used to examine the porous structure, adsorption equilibrium, kinetics, and the energetic heterogeneity of the prepared adsorbent. The nitrogen adsorption and desorption isotherms showed that PAN carbon nanofibers are highly microporous with small amounts of mesoporous regions. The equilibrium data of benzene was obtained at three different temperatures (343.15, 383.15, and 423.15) K with pressures up to 4 kPa. The data correlated successfully with the Toth isotherm equation. In addition, by using this isotherm model, the adsorption affinity and isosteric enthalpy of adsorption were determined. The results of the isosteric enthalpy of adsorption and adsorption energy distribution tests/equations revealed that although PAN carbon nanofibers have a heterogeneous surface, they seem to be more homogeneous than commercial carbon fibers. Moreover, the mass transfer and thermal desorption results showed that shallow pores contained within PAN carbon nanofibers may be effective adsorbents for removing toxic compounds. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2454–2462, 2006     

基于改进型吸附等温线模型的空气预纯化TSA双层床模拟

为了掌握空气中CO2和水蒸气在空分装置双层床变温吸附(TSA)纯化器中的动态吸附特性,通过LDF传质假设及非绝热假设,建立了一维二元稀组分系统的双层床TSA过程数学模型。一种改进型的多组分等温线模型用于描述水蒸气的Ⅱ型吸附等温线以及水蒸气和CO2混合物的吸附平衡关系。通过对比模拟结果与TSA纯化器的现场监控数据发现,基于改进型等温线模型的模拟结果与现场数据吻合良好。最后对多种工况下的TSA纯化器中的温度、浓度及吸附量床层分布和穿透曲线进行了数值模拟和分析。     

Adsorption of o-Cresol and Benzoic Acid in an Adsorber Packed with an lon-Exchange Resin: A Comparative Study of Diffusional Models

Abstract

Both solid- and pore-diffusion models were employed to simulate the adsorption of o-cresol and benzoic acid in a fixed-bed adsorber packed with an anion-exchange resin. The equilibrium adsorption data were modeled by a Langmuir isotherm. When the shape of the adsorption isotherm was approximately linear (as in the case of o-cresol), both models agreed well with the experimental breakthrough data, and they could be effectively applied to predict the breakthrough curve of longer columns. For a favorable adsorption isotherm (say, benzoic acid), however, better results were obtained by using the solid-diffusion model. In addition to the shape of the adsorption isotherm, several factors, such as the type of adsorbent, modeling of equilibrium data, compution efficiency, and concentration dependence of the intraprticle diffusivity, should also be taken into account for selecting a suitable diffusion model.     

Adsorption separation of N2, O2, CO2 and CH4 gases by β-zeolite

In the present study, adsorption equilibrium and kinetic separation potential of β-zeolite is investigated for N₂, O₂, CO₂ and CH₄ gases by using concentration pulse chromatography. Adsorption equilibrium and kinetic parameters have been studied. Henry’s Law constants, heat of adsorption values, micro-pore diffusion coefficients and adsorption activation energies are determined experimentally. The three different mass transfer mechanisms, that have to take place for adsorption to occur, are discussed. From the equilibrium and kinetic data, the equilibrium and kinetic selectivities are determined for the separation of the gases studied.With β-zeolite, carbon dioxide has the highest adsorption Henry’s Law constant at all the temperatures studied, followed by methane, nitrogen and oxygen. Carbon dioxide separation from oxygen, nitrogen and methane has good equilibrium separation factors. This factor is not very high for methane/nitrogen and methane/oxygen systems and is the lowest for nitrogen/oxygen system. Micro-pore diffusion is the dominant mass transfer mechanism for all the systems studied, except CH₄, with β-zeolite. The kinetic separation factors are very small at high temperatures for all the systems studied. Nitrogen/carbon dioxide and oxygen/carbon dioxide can be separated in kinetic processes with reasonable separation factors at low temperatures. Both equilibrium and kinetic separation factors decrease as column temperature increases. Considering all the observations from this study, it was concluded that β-zeolite is a good candidate for applications in flue gas separations, as well as natural gas and landfill gas purifications.     

基于DA模型的煤表面甲烷吸附线预测

采用高低温甲烷吸附解吸测试系统,在243.15, 263.15, 283.15, 303.15和323.15 K下用不同变质程度的煤(气肥煤、焦煤、贫煤和无烟煤等)对甲烷进行等温吸附,基于微孔填充Dubinbin?Astakhov(DA)模型对其它环境温度下煤的CH4吸附等温线进行预测. 结果表明,不同变质程度的煤对甲烷的吸附量均随温度降低而增大,且饱和吸附量和特征吸附能与温度具有良好的线性关系. 模型预测的等温吸附曲线与实验结果吻合较好,相对误差不超过5%.     

EQUILIBRIUM,KINETICS, AND BREAKTHROUGH STUDIES FOR ADSORPTION OF Cr(VI) ON CHITOSAN

Wastewater containing low levels of pollutants can be effectively treated by the adsorption technique. In the present work, an adsorption study was carried out using chitosan as adsorbent in a fixed-bed column for the removal of Cr(VI) from wastewater solutions. The column performance of Cr(VI) adsorption onto chitosan was studied at different bed heights (3–9 cm), flow rates (50–200 mL/min), initial metal concentrations (2–10 mg/L), pH values (2–7), and temperatures (30°–60°C). The equilibrium data for the batch adsorption of Cr(VI) on chitosan were tested using the Langmuir, Freundlich, and BET isotherm models. The Langmuir model was found to be the most suitable, with a maximum adsorption capacity of 35.7 mg/g and a correlation coefficient (R ²) = 0.952. The experimental data were found to fit well with the pseudo-second-order kinetic model, with R ² = 0.999. The dynamics of the adsorption process was modeled using the Adams-Bohart, Thomas, and mass transfer models. The models were used to predict the breakthrough curves of adsorption systems and to determine the characteristic design parameters of the column. The adsorption data were observed to fit well with all three models. The model parameters were derived using MATLAB software. In order to compare quantitatively the applicability of adsorption dynamic models in fitting to experimental data, the percentage relative deviation (P) was calculated and found to be less than 5, confirming that the fit is good for all three models.     

Nitrogen rejection from low quality natural gas by pressure swing adsorption experiments and simulation using dynamic adsorption isotherms

In order to remove N₂ from low quality natural gas, a mathematical model has been established by Aspen adsorption, using the CH₄-selective sorbent silicalite-1 pellets. The dynamic adsorption isotherm was first simulated by breakthrough simulation of a CH₄/N₂ mixture at different adsorption pressures and feed flow rates based on breakthrough experiments. The resulting simulated CH₄ dynamic adsorption amounts were very close to the experimental data at three different adsorption pressures (100, 200, and 300 kPa). Moreover, a single-bed, three-step pressure swing adsorption (PSA) experiment was performed, and the results were in good agreement with the simulated data, further corroborating the accuracy of the gas dynamic adsorption isotherm obtained by the simulation method. Finally, based on the simulated dynamic adsorption isotherm of CH₄ and N₂, a four-bed, eight-step PSA process has been designed, which enriched 75% (vol) CH₄ and 80% (vol) CH₄ to 95% (vol) and 99% (vol), and provided 99% (vol) recovery.     

Copper removal from effluents using a sulphonated lignite Bath and fixed-bed studies

Copper(ll) retention by a sulphonated lignite has been studied under equilibrium (adsorption isotherms) and dynamic (fixed-bed) conditions. Adsorption isotherms were fitted to the Langmuir equation from which saturation capacity and distribution coefficient for the sulpholignite were calculated. Breakthrough curves were determined and the overall mass transfer coefficients and exchange zone height were calculated from them. A model for the exchange mechanism is proposed.     

ADSORPTION AND DESORPTION KINETICS FOR NONLINEAR ADSORPTION ISOTHERMS

The theoretical calculations of the mass transfer rate are based on a model which considers a nonlinear adsorption isotherms and simultaneous resistance to mass transfer in The pore adsorbent and the convective mass transfer. Numerical solutions to the diffusive-convective-controlled adsorption and desorption processes are calculated for the Langmuir and rectangular adsorption isotherms. It is shown that for the rectangular adsorption isotherm the adsorption kinetics is governed by the diffusive-convective mass transfer over a wide range of times and the desorption kinetics is irreversible process. The equations are derived to calculate from the experimental kinetics data: (a) the coefficient diffusion in the pore adsorbent, (b) the relaxation times characterizing the adsorption and desorption processes, and (c) the times needed to reach the quasiequilibrium state for the adsorption and desorption processes.     

Isotherm parameters and intraparticle mass transfer kinetics on molecularly imprinted polymers in acetonitrile/buffer mobile phases

The equilibrium isotherm and the intraparticle mass transfer kinetics of the enantiomers of the template were investigated on an Fmoc-L-tryptophan (Fmoc-L-Trp) imprinted polymer at different pHs and water concentrations in acetonitrile/aqueous buffer mobile phases. The equilibrium isotherm data were measured using frontal analysis at . The adsorption energy distribution was found to be trimodal, with narrow modes. Consistent with this distribution, the adsorption data were modeled using a tri-Langmuir isotherm equation and the best estimates of the isotherm parameters were determined. The intraparticle mass transfer parameters were derived by comparing the profiles of experimental overloaded bands and the profiles calculated using the isotherm model and the lumped pore diffusion (POR) model of chromatography. These results showed that different adsorption and mass transfer mechanisms exist in mobile phases made of acetonitrile/aqueous buffer and of acetonitrile/acetic acid solutions.     

A Modified Peng-Robinson Equation State for Prediction of Gas Adsorption Isotherm

This research proposes a modified two-dimensional Peng-Robinson equation model to predict adsorp-tion isotherm in adsorbate-adsorbent systems. The parameters of the proposed model are calculated by using the op-timization of experimental data for the different single gas adsorption systems at various temperatures. The experi-mental adsorption equilibrium data of adsorbate-adsorbent systems was compared with the calculated results in our proposed model and the two-dimensional Hill-deBoer equation model. The proposed model as indicated in the re-sults shows a better prediction of the experimental results compared with two others.