Description of Carbon Dioxide Adsorption and Desorption onto Malaysian Coals under Subcritical Condition

AbstractCoal bed seams have been considered as promising sequestration reservoirs for CO2 disposal to mitigate the green house gas emissions. The CO2 adsorption and desorption attributes of CO2 on dry Malaysian coals (Sarawak, volatile bituminous) were performed using a sorptomat apparatus (ASAP 2010, Micromeritics, USA) and BELSORP-mini II machine (BEL Japan, Inc.) at 273K, 298K and pressure up to 1bar. The CO2 adsorption was favourable at low temperature and dry coal conditions. However, S3 and S4 coals have the highest adsorption capacity by 0.71 and 0.73 mmol/g respectively. According to IUPAC classification of adsorption isotherms, CO2 adsorption isotherm of all coal samples follow type I which most probably describe the adsorption limited to a few molecular layers (micropores). The results of adsorption and desorption isotherm demonstrate a positive hysteresis in all coal samples. The S1 coal and S2 coal have the highest hysteresis between adsorption and desorption isotherm compared to S3 coal and S4 coal. According to hysteresis classifications, the hysteresis during CO2 adsorption and desorption process for all coal samples follows type H3 which describes micropores and mesopores. The evaluation of the equilibrium adsorption data where fitted using by Langmuir, Freundlich, Redlich-Peterson, Koble-Corrigan, Toth and Sips models. Toth model provided the best fit for all adsorption experimental data that predicting all coals having heterogeneous surface properties

Kinetic Assessment of Tetramethyl Ammonium Hydroxide (Ionic Liquid) for Carbon Dioxide, Methane and Binary Mix Gas Hydrates

This present work highlights the impact of ammonium-based ionic liquid tetramethylammonium hydroxide (TMAOH) on the formation kinetics of carbon dioxide (CO2), methane (CH4), and their binary mixed gas (50–50 mole%) hydrates. The TMAOH (IL) is applied in varying concentrations (0.5, 1, and 2 wt%) at different experimental temperatures, i.e., 1 and 4°C. The kinetic experiments are conducted in a high-pressure reactor equipped with two-bladed impeller, to provide sufficient agitation. The experimental pressures of CO2, CH4, and mixed 50% CO2 + 50% CH4 were 3.50, 8.0, and 6.50 MPa, respectively. Induction time, the initial apparent rate of formation and the total gas consumed are the kinetic parameters used to evaluate the performance of TMAOH as KHI. The results are further compared with commercial KHI (PVP), at higher subcooling condition of 1°C and 1 wt% of all the studied gaseous systems. Furthermore, the KHI performance of TMAOH is also evaluated via the relative inhibition performance (RIP) compared with other ILs for CO2 and CH4 hydrates. Results revealed that TMAOH delays the induction time for all the considered systems. The presence of TMAOH also reduced the total gas consumed and the initial rate of hydrate formation in most of the studied systems

Quantitative and qualitative analyses of grafted okra for corrosion inhibition of mild steel in acidic medium

Introduction: Natural plant polymers demonstrate effective corrosion inhibition abilities, because of their numerous binding sites and excellent adsorption abilities.Methodology: In this study, the Box-Behnken method, gravimetric and electrochemical analyses were used to design and investigate the corrosion inhibition potential of a modified graft polymer of okra for mild steel in a 1M HCl medium. The influence of inhibitor concentration, temperature, and time were also investigated. Qualitatively, the Fourier Transform Infrared (FTIR) spectroscopy, Thermogravimetric Analysis (TGA), and Field emission scanning electron microscopy (FESEM) were used to characterize the extracts and evaluate the metal’s surface morphology.Results and discussion: The quantitative analyses showed that the modified natural polymer’s inhibition efficiency (IE) increased with concentration and reached 73.5% at 800 ppm, with a mixed-type mode of inhibition. From the response surface methodology, it was revealed that temperature influences the IE more than concentration and immersion time. The optimized IE using the desirability function showed the possibility of attaining 88.2% inhibition with inhibitor concentration at 142.3 ppm, temperature at 60.4°C, and an immersion time of 22.4 h. The new functional groups in the hybrid polymer revealed by FTIR analysis shows that grafting improved the inhibitor’s adsorption abilities. TGA analysis confirmed the extract’s high thermal stability, which highlights the inhibitor’s strong adsorption and efficiency for high temperatures. FESEM analysis indicated evidence of inhibitor adsorption onto the metal surface.Conclusion: These findings suggest that the grafting of okra with acrylamide enhances its inhibition properties and contributes to its functionality as a cost-effective plant-based alternative inhibitor against corrosion for mild steel facilities

Quantitative Estimation of Biocapped Surface Chemistry Driven Interparticle Interactions and Growth Kinetics of Gold Nanoparticles

In phytosynthesis of gold nanoparticles (AuNPs), biomolecules play a vital role in biocapping the surface of particles and generating the electrostatic repulsive forces to inhibit their growth kinetics. However, estimation of bioactive compounds influencing their surface characteristics through formation of electric repulsive forces (Velec\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$V_{elec}$$\end{document}), Van der Waals attraction forces (Vvdw\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$V_{vdw}$$\end{document}) and ultimately hindering their growth is still in the phase of obscurity. Current study, based on surface chemistry approach has been performed for identification of bioactive compounds in Elaeis guineensis leaves (EGL/OPL), acting as biocapping agents and directing the growth of AuNPs over a period of time. The quantitative estimation of interparticle interactions and modification in Ostwald ripening (MOR) model were also done to correlate the growth kinetic of AuNPs. The X-ray photoelectron spectroscopy (XPS) showed the major contribution of oxygen, carbon and nitrogen elements, corresponding to polyphenolic, carboxylic and amides, in biocapping the surface of AuNPs and directing their interparticle interactions associated with growth kinetics. The Velec\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$V_{elec}$$\end{document} forces were reduced with an enhancement in the Vvdw\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$V_{vdw}$$\end{document} forces, depicting their major role in impeding growth of AuNPs. The MOR model exhibited an excellent agreement of predicted growth with experimental size enlargements of AuNPs, having 4.8% average absolute relative percentage error

Effect of gold and iron nanoparticles on photocatalytic behaviour of titanium dioxide towards 1-butyl-3-methylimidazolium chloride ionic liquid

© 2019 Elsevier B.V. The high water solubility, chemical stability and low volatility of ionic liquids (ILs) have made them potentially persistent than conventional pollutants and toxic to the aquatic organisms. Therefore, extensive research efforts are being directed with an aim to develop cheap and efficient protocols to reduce the uncontrolled release of ILs in the environment. In the same line of action, titanium dioxide (TiO2) loaded with gold and iron nanoparticles were trialled for the photocatalytic degradation of highly concentrated 1-butyl-3-methylimidazolium chloride [BmimCl] ionic liquid. Furthermore, results pertaining to the degradation of the [BmimCl] using TiO2 loaded with gold nanoparticles (AuNPs) were compared with results obtained by using TiO2 loaded with Fe (NO3)3.9H2O and pristine TiO2 under same set of conditions. It was found that TiO2 decorated AuNPs demonstrated 7 times higher photocatalytic degradation for highly concentrated [BmimCl] in 60 min of reaction time in comparison to the pristine TiO2. Congruently, investigations also revealed that TiO2 loaded AuNPs expressed 3.3 times higher photocatalytic degradation of [BmimCl] in comparison to conventional photocatalyst TiO2@Fe under same reaction conditions. The higher photocatalytic performance associated with TiO2 loaded AuNPs was due to the enhanced Schottky barrier, which could have minimized the photocharge carrier resistance separation and migration. The mechanism for photocatalytic degradation of [BmimCl] using TiO2 loaded AuNPs has been also been described

Photocatalytic Degradation of DIPA Using Bimetallic Cu-Ni/TiO 2

Bimetallic Cu-Ni/TiO2 photocatalysts were synthesized using wet impregnation (WI) method with TiO2 (Degussa-P25) as support and calcined at different temperatures (180, 200, and 300°C) for the photodegradation of DIPA under visible light. The photocatalysts were characterized using TGA, FESEM, UV-Vis diffuse reflectance spectroscopy, fourier transform infrared spectroscopy (FTIR) and temperature programmed reduction (TPR). The results from the photodegradation experiments revealed that the Cu-Ni/TiO2 photocatalysts exhibited much higher photocatalytic activities compared to bare TiO2. It was found that photocatalyst calcined at 200°C had the highest photocatalyst activities with highest chemical oxygen demand (COD) removal (86.82%). According to the structural and surface analysis, the enhanced photocatalytic activity could be attributed to its strong absorption into the visible region and high metal dispersion

Controllable phytosynthesis of gold nanoparticles and investigation of their size and morphology-dependent photocatalytic activity under visible light

© 2020 Elsevier B.V. Plants mediated synthesis of gold nanoparticles (AuNPs) containing desired characteristics for their suitable potential applications has been a challenging task, which is causing a major hindrance towards its commercialization. Therefore, herein phytosynthesis of AuNPs with required size and morphology has been achieved through manipulating the reaction conditions including reaction temperature and volume of Elaeis guineensis leaves (EGL) extract. Furthermore, photocatalytic potential of EGL mediated AuNPs having different size and shape has also been explored for the removal of methylene blue (MB) under visible light irradiation. The reaction temperature and volume of EGL strongly influenced the size and morphology of AuNPs, which are directly associated with the photocatalytic activities. The experimental results revealed that predominantly spherical and ultra-smaller size AuNPs with particle size of 16.26 ± 5.84 nm, formed at 70 °C showed the highest removal efficiency up to 92.55 % in 60 min. This highest photocatalytic activity of AuNPs could be attributed to the availability of higher number of low-coordinated gold (Au) atoms in the MB aqueous solution, which might have boosted the adsorption of the MB on the surface of particles and accelerated the degradation phenomenon. The proposed photocatalytic degradation mechanism of AuNPs for MB was also explained. The highly photoactive EGL mediated AuNPs with controllable morphology and size could be an advance step in future in chemical and biomedical applications

Effect of Membrane Materials and Operational Parameters on Performance and Energy Consumption of Oil/Water Emulsion Filtration

Membrane technology is one of reliable options for treatment of oil/water emulsion. It is highly attractive because of its effectiveness in separating fine oil droplets of 3000 ppm to a point of no flux

Performance evaluation of phosphonium based deep eutectic solvents coated cerium oxide nanoparticles for CO2 capture

The critical challenge being faced by our current modern society on a global scale is to reduce the surging effects of climate change and global warming, being caused by anthropogenic emissions of CO2 in the environment. Present study reports the surface driven adsorption potential of deep eutectic solvents (DESs) surface functionalized cerium oxide nanoparticles (CeNPs) for low pressure CO2 separation. The phosphonium based DESs were prepared using tetra butyl phosphoniumbromide as hydrogen bond acceptor (HBA) and 6 acids as hydrogen bond donors (HBDs). The as-developed DESs were characterized and employed for the surface functionalization of CeNPs with their subsequent utilization in adsorption-based CO2 adsorption. The synthesis of as-prepared DESs was confirmed through FTIR measurements and absence of precipitates, revealed through visual observations. It was found that DES6 surface functionalized CeNPs demonstrated 27% higher adsorption performance for CO2 capturing. On the contrary, DES3 coated CeNPs exhibited the least adsorption progress for CO2 separation. The higher adsorption performance associated with DES6 coated CeNPs was due to enhanced surface affinity with CO2 molecules that must have facilitated the mass transport characteristics and resulted an enhancement in CO2 adsorption performance. Carboxylic groups could have generated an electric field inside the pores to attract more polarizable adsorbates including CO2, are responsible for the relatively high values of CO2 adsorption. The quadruple movement of the CO2 molecules with the electron-deficient and pluralizable nature led to the enhancement of the interactive forces between the CO2 molecules and the CeNPs decorated with the carboxylic group hydrogen bond donor rich DES. The current findings may disclose the new research horizons and theoretical guidance for reduction in the environmental effects associated with uncontrolled CO2 emission via employing DES surface coated potential CeNPs

Screening of gallate-based metal-organic frameworks for single-component CO

Adsorption using porous adsorbents is widely applied in carbon dioxide (CO2) capture due to its potential energy saving with low operating cost. Metal-organic frameworks (MOFs) are preferable over conventional adsorbents as MOFs have tunable structure properties. Organic linkers from phytochemical-based give a new idea in forming MOFs. Gallic acid is classified under phytochemicals can act as an alternative organic linker in a new family of hybrid framework materials due to low cost, low toxicity, easy availability and naturally abundant. Due to unique property of MOFs that can be tailored, screening using systematic tool is very important. Molecular modeling is proven to play a crucial role in providing an estimation on adsorption capacity, selectivity and adsorbent selection. Grand Canonical Monte Carlo (GCMC) method via Sorption module in Material Studio was performed to compute loading curves of CO2 and methane (CH4) in MOFs. Based on the simulation results, it shows that gallate-based MOFs can be a new promising adsorbent in CO2 capture as the predicted CO2 loading is significantly higher than CH4. The highest predicted CO2 adsorption capacity is achieved by Mg-gallate and the lowest is by Ag-gallate with 7.79 mmol/g and 6.35 mmol/g respectively. The applicability of gallic acid to act as an alternative linker is relevant for practical applications