ABSTRACT
Three widths of manufacturing S-ribs carbon-fiber filaments acting as turbulence promoters were implemented into the flow channel of direct contact membrane distillation (DCMD) modules to augment the permeate flux improvement in the present study. Attempts to reduce the disadvantageous temperature polarization effect were made by inserting S-ribs turbulence promoters in improving pure water productivity, in which both heat- and mass-transfer boundary layers were diminished due to creating vortices in the flow pattern and increasing turbulence intensity. The temperature polarization coefficient ttemp was studied and found to enhance device performance (less thermal resistance) under inserting various S-ribs carbon-fiber thicknesses and operating both cocurrent- and countercurrent-flow patterns. The permeate fluxes in the DCMD modules with inserted S-ribs carbon-fiber turbulence promoters were investigated theoretically by developing the mathematical modeling equations and were conducted experimentally with various design and operating parameters. The theoretical predictions and experimental results exhibited a great potential to considerably achieve permeate flux enhancement in the new design of the DCMD system. The DCMD module with inserted S-ribs carbon-fiber turbulence promoters in the flow channel could provide a relative permeate flux enhancement up to 37.77% under countercurrent-flow operations in comparisons with the module of using the empty channel. An economic consideration on both permeate flux enhancement and power consumption increment for the module with inserted S-ribs carbon-fiber filaments was also delineated.
ABSTRACT
This research theoretically and experimentally develops a hollow-fiber dialysis module coupled with ultrafiltration operations by introducing a trans-membrane pressure during the membrane dialysis process, which can be applied to the waste metabolic end products in the human body for improving the dialysis efficiency. The solutes were transported by both diffusion and convection from the concentration driving-force gradient between retentate and dialysate phases across the membrane, compared to the traditional dialysis processes by diffusion only. A two-dimensional modeling of such a dialysis-and-ultrafiltration system in the hollow-fiber dialysis module was formulated and solved using the stream function coupled with the perturbation method to obtain the velocity distributions of retentate and dialysate phases, respectively. The purpose of the present work is to investigate the effect of ultrafiltration on the dialysis rate in the hollow-fiber dialyzer with ultrafiltration operations. A highest level of dialysis rate improvement up to about seven times (say 674.65% under Va=20 mL/min) was found in the module with ultrafiltration rate Vw=10 mL/min and membrane sieving coefficient θ=1, compared to that in the system without operating ultrafiltration. Considerable dialysis rate improvements on mass transfer were obtained by implementing a hollow-fiber dialysis-and-ultrafiltration system, instead of using the hollow-fiber dialyzer without ultrafiltration operation. The experimental runs were carried out under the same operating conditions for the hollow-fiber dialyzers of the two experimental runs with and without ultrafiltration operations for comparisons. A very reasonable prediction by the proposed mathematical model was observed.
ABSTRACT
The absorption efficiencies of CO2 in ceramic hollow-fiber membrane contactors using monoethanolamine (MEA) absorbent under both cocurrent- and countercurrent-flow operations were investigated theoretically and experimentally; various MEA absorbent flow rates, CO2 feed flow rates, and inlet CO2 concentrations were used as parameters. Theoretical predictions of the CO2 absorption flux were analyzed by developing the mathematical formulations based on Happel's free surface model in terms of mass transfer resistances in series. The experiments of the CO2 absorption were conducted by using alumina (Al2O3) hollow-fiber membranes to confirm the accuracy of the theoretical predictions. The simplified expression of the Sherwood number was formulated to calculate the mass transfer coefficient of the CO2 absorption incorporating experimental data. The data were obtained numerically using the fourth-order Runge-Kutta method to predict the concentration distribution and absorption rate enhancement under various fiber packing configurations accomplished by the CO2/N2 stream passing through the fiber cells. The operations of the hollow-fiber membrane contactor encapsulating N = 7 fiber cells and N = 19 fiber cells of different packing densities were fabricated in this work to examine the device performance. The accuracy derivation between experimental results and theoretical predictions for cocurrent- and countercurrent-flow operations were 1.31×10-2≤E≤4.35×10-2 and 3.90×10-3≤E≤2.43×10-2, respectively. A maximum of 965.5% CO2 absorption rate enhancement was found in the module with embedding multiple fiber cells compared with that in the device with inserting single-fiber cell. Implementing more fiber cells offers an inexpensive method of improving the absorption efficiency, and thus the operations of the ceramic hollow-fiber membrane contactor with implementing more fiber cells propose a low-priced design to improve the absorption rate enhancement. The higher overall CO2 absorption rate was achieved in countercurrent-flow operations than that in cocurrent-flow operations.
ABSTRACT
The absorption efficiencies of CO2 in hollow-fiber membrane contactors using an ethanolamine (MEA) solvent under both concurrent- and countercurrent-flow operations were investigated theoretically and experimentally. Two-dimensional mathematical modeling was developed by Happel's free surface model, and the resultant partial differential equations were solved analytically using the separated variables method with the use of an orthogonal expansion technique. A simplified expression of Sherwood number variations was reported by employing the relevant operations conditions and expressed in terms of the computed eigenvalues for predicting concentration distribution and absorption efficiency. It is emphasized that, in comparing various fiber packing configurations, both theoretical predictions and experimental results should be compared to find the absorption flux increment accomplished by the CO2/N2 stream passing through the fiber cells under the same mass flow rate. The value of the present mathematical treatment is evident to propose a simplified expression of the averaged Sherwood number variations, and provides the predictions of the absorption flux, absorption efficiency, average Sherwood number with the absorbent Graetz number, inlet CO2 concentration, and absorbent flow rates as parameters. The availability of such concise expressions, as developed directly from the analytical formulations, is the value of the present study. The experiments of the CO2 absorption using MEA with alumina (Al2O3) hollow fiber membranes are also set up to confirm the accuracy of the theoretical predictions. The accuracy derivations between the experimental results and theoretical predictions for concurrent- and countercurrent-flow operations are 4.10×10-2≤E≤1.50×10-2 and 1.40×10-2≤E≤9.0×10-1, respectively. The operations of the hollow-fiber membrane contactor implementing N = 7 fiber cells and N = 19 fiber cells offer an inexpensive method of improving absorption efficiency by increasing fiber numbers with consideration of device performance.
ABSTRACT
CO2/H2 separation using membrane technology is an important research area in order to obtain high purity hydrogen as one source of clean energy. Finding a suitable inorganic membrane is one of the critical issues, which needs to be explored for CO2/H2 separation. In the present study, Ba-SAPO-34 zeolite membrane was synthesized and followed by a modification process. CO2/H2 separation of the membrane was investigated by varying the independent process variables (CO2 % in the feed, pressure difference across the membrane and temperature). Modeling and optimization for the responses (CO2/H2 separation selectivity and CO2 permeance) was performed by applying response surface methodology and central composite design, which is available in Design Expert software. The accuracy of the models in predicting the response was tested by comparing with the experimental value of response and the two values were in good agreement. The optimization of the models gave CO2 permeance of 19.23 × 10-7 mol/m2 s Pa and CO2/H2 separation selectivity of 11.6 at 5% CO2 in the feed, a pressure difference of 100 kPa, and temperature of 30 °C for Ba-SAPO-34 zeolite membrane.
ABSTRACT
Effect of external-recycle operations on the heat-transfer efficiency, specifically for the power-law fluid flowing in double-pass concentric circular heat exchanger under sinusoidal wall fluxes, is investigated theoretically in the developed countries. Given that the fluid is heated twice on both sides of the impermeable sheet, four flow patterns proposed in recycling double-pass operations are expected to make substantial improvements in the performance of heat exchanger device in this study. Theoretical predictions point out that the heat-transfer efficiency increases with the ratio of channel thickness of double-pass concentric circular heat exchanger for all new designs under the same working dimension and the operational condition. The fluid velocity within the double-pass heat exchanger is increased by the fluids flowing through divided subchannels, which contributed to the higher convective heat-transfer efficiency. A simplified mathematical formulation was derived for double-pass concentric circular heat exchangers and would be a significant contribution to analyze heat transfer problems with sinusoidal wall fluxes at boundaries. The results deliver the optimal performance for the proposed four configurations with the use of external recycle compared to those conducted in single-pass, where an impermeable sheet is not inserted. The influences of power-law index and impermeable-sheet position on average Nusselt numbers under various flow patterns are also delineated. The distribution of dimensionless wall temperature was lower at the level of relative smaller thickness of annular channel, and the average Nusselt numbers for four external-recycle configurations and single-pass device were more suitable for operating under same condition. The ratio of the power consumption increment to heat-transfer efficiency enhancement demonstrates the economic feasibility among various configurations of double-pass concentric circular heat exchanger. The results also show that the external-recycle configuration (say Type B in the present study) serves as an important economic advantage in designing concentric circular heat exchangers for heating power-law fluids due to the smaller volumetric flow rate in annular channel with exiting outlet temperature.
ABSTRACT
The challenges in developing high CO2 gas fields are governed by several factors such as reservoir condition, feed gas composition, operational pressure and temperature, and selection of appropriate technologies for bulk CO2 separation. Thus, in this work, we report an optimization study on the separation of CO2 from CH4 at high CO2 feed concentration over a functionalized mixed matrix membrane using a statistical tool, response surface methodology (RSM) statistical coupled with central composite design (CCD). The functionalized mixed matrix membrane containing NH2-MIL-125 (Ti) and 6FDA-durene, fabricated in our previous study, was used to perform the separation performance under three operational parameters, namely, feed pressure, temperature, and CO2 feed concentration, ranging from 3.5-12.5 bar, 30.0-50.0 °C and 15-70 mol%, respectively. The CO2 permeability and CO2/CH4 separation factor obtained from the experimental work were varied from 293.2-794.4 Barrer and 5.3-13.0, respectively. In addition, the optimum operational parameters were found at a feed pressure of 12.5 bar, a temperature of 34.7 °C, and a CO2 feed concentration of 70 mol%, which yielded the highest CO2 permeability of 609.3 Barrer and a CO2/CH4 separation factor of 11.6. The average errors between the experimental data and data predicted by the model for CO2 permeability and CO2/CH4 separation factor were 5.1% and 3.3%, respectively, confirming the validity of the proposed model. Overall, the findings of this work provide insights into the future utilization of NH2-MIL-125 (Ti)/6FDA-based mixed matrix membranes in real natural gas purification applications.
ABSTRACT
An analytical formulation, referred to as conjugated Graetz problems, is developed to predict the temperature distribution and Nusselt numbers for the power-law fluid flowing in a double-pass concentric circular heat exchanger under sinusoidal wall fluxes. A new design of inserting an impermeable sheet into a concentric tube, in parallel, to conduct recycling double-pass operations has been studied theoretically in the fully developed region, resulting in substantial improvements in the performance of heat exchanger device. The analytical solution was derived using the complex functions by transforming the boundary value problem into ordinary differential equations with the aid of the Frobenius method. The influences of power-law index and impermeable-sheet position on average Nusselt numbers with various designs and operating parameters are also delineated. The theoretical predictions show that the heat transfer efficiency is considerably improved through operating the double-pass device compared to via a single-pass circular heat exchanger (where an impermeable sheet is not inserted). The economic feasibility of operating double-pass concentric circular heat exchanger for power-law fluids is exemplified by the ratio of the heat-transfer efficiency enhancement and the increment in power consumption. The double-pass effect from increasing the convective heat-transfer coefficient can compensate for the rise in power consumption, which serves as important economic advantage of this design.
ABSTRACT
In recent years, mixed matrix membranes (MMMs) have received worldwide attention for their potential to offer superior gas permeation and separation performance involving CO2 and CH4. However, fabricating defect-free MMMs still remains as a challenge where the incorporation of fillers into MMMs has usually led to some issues including formation of undesirable interfacial voids, which may jeopardize the gas separation performance of the MMMs. This current work investigated the incorporation of zeolite RHO and silane-modified zeolite RHO (NH2-RHO) into polysulfone (PSf) based MMMs with the primary aim of enhancing the membrane's gas permeation and separation performance. The synthesized zeolite RHO, NH2-RHO, and fabricated membranes were characterized by X-ray diffraction (XRD) analysis, Fourier transform infrared-attenuated total reflection (FTIR-ATR), thermogravimetric analysis (TGA) and field emission scanning election microscopy (FESEM). The effects of zeolite loading in the MMMs on the CO2/CH4 separation performance were investigated. By incorporating 1 wt% of zeolite RHO into the MMMs, the CO2 permeability and ideal CO2/CH4 selectivity slightly increased by 4.2% and 2.7%, respectively, compared to that of a pristine PSf membrane. On the other hand, a significant enhancement of 45% in ideal CO2/CH4 selectivity was attained by MMMs incorporated with 2 wt% of zeolite NH2-RHO compared to a pristine PSf membrane. Besides, all MMMs incorporated with zeolite NH2-RHO displayed higher ideal CO2/CH4 selectivity than that of the MMMs incorporated with zeolite RHO. By incorporating 1-3 wt% zeolite NH2-RHO into PSf matrix, MMMs without interfacial voids were successfully fabricated. Consequently, significant enhancement in ideal CO2/CH4 selectivity was enabled by the incorporation of zeolite NH2-RHO into MMMs.
ABSTRACT
The CO2 absorption rate by using a Monoethanolamide (MEA) solution through the spiral wired channel in concentric circular membrane contactors under both concurrent-flow and countercurrent-flow operations was investigated experimentally and theoretically. The one-dimensional mathematical modeling equation developed for predicting the absorption rate and concentration distributions was solved numerically using the fourth Runge-Kutta method under various absorbent flow rate, CO2 feed flow rate and inlet CO2 concentration in the gas feed. An economical viewpoint of the spiral wired module was examined by assessing both absorption flux improvement and power consumption increment. Meanwhile, the correlated average Sherwood number to predict the mass-transfer coefficient of the CO2 absorption mechanisms in a concentric circular membrane contactor with the spiral wired annulus channel is also obtained in a generalized and simplified expression. The theoretical predictions of absorption flux improvement were validated by experimental results in good agreements. The amine solution flowing through the annulus of a concentric circular tube, which was inserted in a tight-fitting spiral wire in a small annular spacing, could enhance the CO2 absorption flux improvement due to reduction of the concentration polarization effect. A larger concentration polarization coefficient (CPC) was achieved in the countercurrent-flow operations than that in concurrent-flow operations for various operations conditions and spiral-wire pitches. The absorption flux improvement for inserting spiral wire in the concentric circular module could provide the maximum relative increment up to 46.45%.
ABSTRACT
The development of mixed matrix membranes (MMMs) for effective gas separation has been gaining popularity in recent years. The current study aimed at the fabrication of MMMs incorporated with various loadings (0-4 wt%) of functionalized KIT-6 (NH2KIT-6) [KIT: Korea Advanced Institute of Science and Technology] for enhanced gas permeation and separation performance. NH2KIT-6 was characterized by field emission scanning electron microscope (FESEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), and N2 adsorption-desorption analysis. The fabricated membranes were subjected to FESEM and FTIR analyses. The effect of NH2KIT-6 loading on the CO2 permeability and ideal CO2/CH4 selectivity of the fabricated membranes were investigated in gas permeation and separation studies. The successfulness of (3-Aminopropyl) triethoxysilane (APTES) functionalization on KIT-6 was confirmed by FTIR analysis. As observed from FESEM images, MMMs with no voids in the matrix were successfully fabricated at a low NH2KIT-6 loading of 0 to 2 wt%. The CO2 permeability and ideal CO2/CH4 selectivity increased when NH2KIT-6 loading was increased from 0 to 2 wt%. However, a further increase in NH2KIT-6 loading beyond 2 wt% led to a drop in ideal CO2/CH4 selectivity. In the current study, a significant increase of about 47% in ideal CO2/CH4 selectivity was achieved by incorporating optimum 2 wt% NH2KIT-6 into the MMMs.
ABSTRACT
In recent years, there are increasing interest on applying ultrasonic irradiation for the synthesis of zeolite due to its advantages including remarkable shortened synthesis duration. In this project, the potential of ultrasonic irradiation treatment on the synthesis of zeolite RHO was investigated. Ultrasonic irradiation treatment time was varied from 30 to 120 minutes for the synthesis of zeolite RHO. The zeolite RHO solid samples were characterized with X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA) and nitrogen adsorption-desorption analysis. The application of ultrasonic irradiation treatment in this study has accelerated the synthesis of zeolite RHO where the synthesis duration has been significantly shortened to 2 days compared to 8 days required by conventional hydrothermal heating without ultrasonic irradiation treatment. Highly crystalline zeolite RHO crystals in truncated octahedron morphology were successfully formed.
ABSTRACT
Mixed matrix membranes (MMMs) separation is a promising technology for gas permeation and separation involving carbon dioxide (CO2). However, finding a suitable type of filler for the formation of defect-free MMMs with enhancement in gas permeability remains a challenge. Current study focuses on synthesis of KIT-6 silica and followed by the incorporation of KIT-6 silica as filler into polysulfone (PSF) polymer matrix to fabricate MMMs, with filler loadings of 0-8 wt %. The effect of KIT-6 incorporation on the properties of the fabricated MMMs was evaluated via different characterization techniques. The MMMs were investigated for gas permeability and selectivity with pressure difference of 5 bar at 25 °C. KIT-6 with typical rock-like morphology was synthesized. Incorporation of 2 wt % of KIT-6 into PSF matrix produced MMMs with no void. When KIT-6 loadings in the MMMs were increased from 0 to 2 wt %, the CO2 permeability increased by ~48%, whereas the ideal CO2/CH4 selectivity remained almost constant. However, when the KIT-6 loading in PSF polymer matrix was more than 2 wt %, the formation of voids in the MMMs increased the CO2 permeability but sacrificed the ideal CO2/CH4 selectivity. In current study, KIT-6 was found to be potential filler for PSF matrix under controlled KIT-6 loading for gas permeation.
ABSTRACT
Separation of carbon dioxide (CO(2)) from gaseous mixture is an important issue for the removal of CO(2) in natural gas processing and power plants. The ordered mesoporous silicas (OMS) with uniform pore structure and high density of silanol groups, have attracted the interest of researchers for separation of carbon dioxide (CO(2)) using adsorption process. These mesoporous silicas after functionalization with amino groups have been studied for the removal of CO(2). The potential of functionalized ordered mesoporous silica membrane for separation of CO(2) is also recognized. The present paper reviews the synthesis of mesoporous silicas and important issues related to the development of mesoporous silicas. Recent studies on the CO(2) separation using ordered mesoporous silicas (OMS) as adsorbent and membrane are highlighted. The future prospectives of mesoporous silica membrane for CO(2) adsorption and separation are also presented and discussed.
Subject(s)
Carbon Dioxide/isolation & purification , Membranes, Artificial , Silicon Dioxide/chemistry , Adsorption , Carbon Dioxide/chemistry , Porosity , Silicon Dioxide/chemical synthesis , Surface PropertiesABSTRACT
Catalytic cracking of crude palm oil (CPO) and used palm oil (UPO) were studied in a transport riser reactor for the production of biofuels at a reaction temperature of 450 degrees C, with residence time of 20s and catalyst-to-oil ratio (CTO) of 5 gg(-1). The effect of HZSM-5 (different Si/Al ratios), beta zeolite, SBA-15 and AlSBA-15 were studied as physically mixed additives with cracking catalyst Rare earth-Y (REY). REY catalyst alone gave 75.8 wt% conversion with 34.5 wt% of gasoline fraction yield using CPO, whereas with UPO, the conversion was 70.9 wt% with gasoline fraction yield of 33.0 wt%. HZSM-5, beta zeolite, SBA-15 and AlSBA-15 as additives with REY increased the conversion and the yield of organic liquid product. The transport riser reactor can be used for the continuous production of biofuels from cracking of CPO and UPO over REY catalyst.
Subject(s)
Bioelectric Energy Sources , Bioreactors , Plant Oils/chemistry , Catalysis , Gasoline , Palm Oil , Surface Properties , Zeolites/chemistryABSTRACT
In Malaysia, there has been interest in the utilization of palm oil and oil palm biomass for the production of environmental friendly biofuels. A biorefinery based on palm oil and oil palm biomass for the production of biofuels has been proposed. The catalytic technology plays major role in the different processing stages in a biorefinery for the production of liquid as well as gaseous biofuels. There are number of challenges to find suitable catalytic technology to be used in a typical biorefinery. These challenges include (1) economic barriers, (2) catalysts that facilitate highly selective conversion of substrate to desired products and (3) the issues related to design, operation and control of catalytic reactor. Therefore, the catalytic technology is one of the critical factors that control the successful operation of biorefinery. There are number of catalytic processes in a biorefinery which convert the renewable feedstocks into the desired biofuels. These include biodiesel production from palm oil, catalytic cracking of palm oil for the production of biofuels, the production of hydrogen as well as syngas from biomass gasification, Fischer-Tropsch synthesis (FTS) for the conversion of syngas into liquid fuels and upgrading of liquid/gas fuels obtained from liquefaction/pyrolysis of biomass. The selection of catalysts for these processes is essential in determining the product distribution (olefins, paraffins and oxygenated products). The integration of catalytic technology with compatible separation processes is a key challenge for biorefinery operation from the economic point of view. This paper focuses on different types of catalysts and their role in the catalytic processes for the production of biofuels in a typical palm oil and oil palm biomass-based biorefinery.