Adsorption Of Components Research Articles

A Surface Charge Approach to Investigating the Influence of Oil Contacting Clay Minerals on Wettability Alteration.

Reservoir rock wettability has been linked to the adsorption of crude fractions on the rock, with much attention often paid to the bulk mineralogy rather than contacting minerals. Crude oil is contacted by different minerals that contribute to rock wettability. The clay mineral effect on wettability alterations is examined using the mineral surface charge. Also, the pH change effect due to well operations was investigated. Clay mineral surface charge was examined using zeta potential computed from the particle electrophoretic mobility. Clay minerals considered in this study include kaolinite, montmorillonite, illite, and chlorite. Results reveal that the clay mineral charge development is controlled by adsorption of ionic species and double layer collapse. Also, clay mineral surface charge considered in this study shows that their surfaces become more conducive for the adsorption of hydrocarbon components due to the presence of salts. The salt effect is greater in the following order: NaHCO3 < Na2SO4 < NaCl < MgCl2 < CaCl2. Furthermore, different well operations induce pH environments that change the clay mineral surface charge. This change results in adsorption prone surfaces and with reservoir rock made up of different minerals, and the effect of contacting minerals is critical as shown in our findings. This is due to the contacting mineral control wettability rather than the bulk mineralogy.

Unexpected effects of mobile phase solvents and additives on retention and resolution of N-acyl-D,L-leucine applying Cinchonane-based chiral ion exchangers

Chiral ion exchangers based on quinine (QN) and quinidine (QD), namely Chiralpak QN-AX and QD-AX as anionic and ZWIX(+) and ZWIX(-) as zwitterionic ion exchanger chiral stationary phases (CSPs) have been investigated with respect to their retention and chiral resolution characteristics. For the evaluation of the effects of the composition of the polar organic bulk solvents of the mobile phase (MP) and those of the organic acid and base additives acting as displacers necessary for a liquid chromatographic ion-exchange process, racemic N-(3,5-dinitrobenzoyl)leucine and other related analytes were applied. The main aim was to evaluate the impact of the MP variations on the observed, and thus the apparent enantioselectivity (αapp), and the retention factor. Significant differences were found using either polar protic methanol (MeOH) or polar non-protic acetonitrile (MeCN) solvents in combination with the acid and base additives as counter- and co-ions. It became clear, that the charged sites of both the chiral selectors of the CSPs and the analytes get specifically solvated, accompanied by the adsorption of all MP components on the CSP, thereby building a stagnant “stationary phase layer” with a composition different from the bulk MP. Via a systematic change of the MP composition, trends of resulting αapp and retention factors have been identified and discussed.In a detailed set of experiments, the effect of the concentration of the acid component in the MP containing MeOH or MeCN was specifically investigated, with the acid considered to be a displacer in anion-exchange type chromatographic systems.Surprisingly, all four chiral columns retained and resolved the tested N-acyl-Leu analytes with αapp values up to 21 within a retention factor window of 0.03 and 10 with pure MeOH as eluent. However, using pure MeCN as eluent, an almost infinite-long retention of the acidic analyte was noticed in all cases. We suggest that the rather different thickness of the solvation shells generated by MeOH or MeCN around the charged/chargeable sites of the chiral selector determines eventually the strength of the electrostatic selector–selectand interactions.As a control experiment we included the non-chiral N-acylglycine derivatives as analyte in all cases to support the interpretations with respect to the contribution of the enantioselective and non-enantioselective retention factor increments as a part of the observed αapp.

An automated multi-component gas adsorption system (MC GAS)

The knowledge gap on adsorption of complex mixtures in the literature relative to single component data represents a persistent obstacle to developing accurate process models for adsorption separations. The collection of mixed gas adsorption data is an imminent need for improved understanding of the behavior of adsorbent systems in these diverse adsorption applications. Current approaches to understanding mixture adsorption using predictive theories based on pure component adsorption experiments often fail to capture the behavior of more complex, non-ideal systems. In this work, we present an automated volumetric instrument for the measurement of mixed gas adsorption isotherms. This instrument was validated by comparison to other in-house instruments and data available in the literature, and the binary adsorption measurements were found to be thermodynamically consistent. The automation of this instrument allows for rapid collection of high-quality mixture adsorption data.

Potentials of African Star Apple (&lt;i&gt;Chrysophyllum albidum)&lt;/i&gt; Fruit Shell Adsorbent in Recovery of Valuable Hydrocarbons for Spent Engine Oil

Inventory of spent engine oil continuously increase and indiscriminately disposed of at auto-mechanics garages. Adsorptive separation established to be indispensable in recovery of these hydrocarbons was carried out using Chrysophyllum albidum (African star apple) fruit shell – a renewable resource. In this study, clay pretreated spent engine oil was recovered in a fixed bed adsorption processes and the recovered adsorbate components determined by GC-MS analysis. The results showed African star apple fruit shell adsorbent effective in recovering n-hexane solubilized spent lubricating oil. The study concluded that using the developed African star apple fruit shell adsorbent, an agricultural waste adsorbent in the recovery of waste lubricating oil will enhance greatly the nation’s economy.

Dynamical coupling of ion adsorption with fluid flow in nanopores

AbstractTo describe the commonly existing coupling between adsorption dynamics and fluid flow, a nonequilibrium molecular model is developed, upon which we systematically investigate the dynamical adsorption of ionic components from confined flows onto the charged surfaces of nanoscale pores, and find that a competition relation exists between the adsorption and flow. Promoting flow speed suppresses the adsorption amount, while enhancing adsorption strength reduces the flow speed. With the increase of flow speed, the contact density of co‐ion is enhanced while that of counterion is suppressed, leading to overall enhanced accumulation charge densities at pore surfaces. Besides, the accumulation charge density increases monotonically with the applied voltage in large pores, while displays a nontrivial relation with the applied voltage in small pores of several ion sizes. This work not only extends the theoretical framework of nonequilibrium molecular theories, but also provides novel insights into the regulation of interfacial dynamic processes.

Potentials of African Star Apple (&lt;i&gt;Chrysophyllum albidum)&lt;/i&gt; Fruit Shell Adsorbent in Recovery of Valuable Hydrocarbons for Spent Engine Oil

Inventory of spent engine oil continuously increase and indiscriminately disposed of at auto-mechanics garages. Adsorptive separation established to be indispensable in recovery of these hydrocarbons was carried out using Chrysophyllum albidum (African star apple) fruit shell – a renewable resource. In this study, clay pretreated spent engine oil was recovered in a fixed bed adsorption processes and the recovered adsorbate components determined by GC-MS analysis. The results showed African star apple fruit shell adsorbent effective in recovering n-hexane solubilized spent lubricating oil. The study concluded that using the developed African star apple fruit shell adsorbent, an agricultural waste adsorbent in the recovery of waste lubricating oil will enhance greatly the nation’s economy.

Storage Material Effects on the Performance of Ru-Based CO2 Capture and Methanation Dual Functioning Materials

In this study, a systematic investigation on Dual Functioning Materials (DFMs) for the capture and methanation of CO2 is carried out. The attention is focused on the nature of the CO2 adsorbent component (storage material, SM) varying between alkaline (Li, Na, K) and alkaline-earth (Mg, Ca, Ba) metal oxides in combination with Ru, both supported on an Al2O3 support. Combining gas phase reactivity analysis and FT-IR characterization, the samples are characterized in terms of CO2 storage capacity. It is found that all the SM-containing samples adsorb significant amounts of CO2 as carbonate species, with the higher amounts being adsorbed when the more thermally stable species are formed, i.e., when Ca, Ba, or K are employed as SMs. In all cases, the hydrogenation of the adsorbed carbonates to CH4 occurs at lower temperature, if compared to their thermal desorption. However, in the case of Ca- and Ba-based DFMs, resilient carbonates are present on the material surface. It was found that the SMs able to form the more thermally stable carbonates upon CO2 adsorption also showed the best performances in capture/methanation cycles at 350 °C, even if some residual carbonates were left on the DFM after the hydrogenation step. In particular, the following order of reactivity has in fact been observed in terms of CH4 production: Ru–K ≥ Ru–Ba > Ru–Ca > Ru–Na ≫ Ru–Mg ≅ Ru–Li ≅ Ru. The presence of steam and O2 during the capture step has a detrimental effect on the CO2 adsorption for all samples and, as a result, on CH4 production due to the competition of CO2 and water for the same adsorption sites. Thus, only SMs able to form strongly bound carbonates species upon CO2 exposure can retain significant CO2 storage capacity also in the presence of water in the adsorption feed.

Adsorption of Carbon Dioxide, Water Vapor, Nitrogen, and Sulfur Dioxide on Activated Carbon for Capture from Flue Gases: Competitive Adsorption and Selectivity Aspects

There is extensive interest in postcombustion flue gas treatment for mitigating CO2 emissions and removal of acid gases. In this study we investigate the adsorption of the main flue gas components (CO2, N2, SO2, and water vapor) on Filtrasorb 400 activated carbon to understand adsorption characteristics of the main components and competitive adsorption effects. The adsorption isotherms of the pure components of flue gas, CO2 (273.15–318.15 K and 0–50 bar), N2 (298.15–313.15 K and 0–150 bar), SO2 (273.15–303.15 K and 0–3.6 bar), and water vapor (293.15–303.15 K and 0–41 mbar), were investigated. The isosteric enthalpies of adsorption were determined to be a function of surface excess. The enthalpies at zero surface coverage have the order SO2 > H2O > CO2 > N2. However, the SO2 isosteric enthalpy decreases with increasing surface excess and is lower than that of water vapor at high surface excess uptake values. The temperature range for CO2 adsorption covers the subcritical to supercritical gas transition. There was no evidence for isosteric enthalpy differences over this temperature range. The adsorption kinetics for SO2 (290.65–303.15 K) and H2O (293.15–303.15 K) adsorption were measured for each isotherm pressure increment. In both cases the adsorption kinetics followed the linear driving force model. The adsorption mechanisms for both SO2 and H2O kinetic trends are discussed in terms of the adsorption mechanisms. The water vapor adsorption kinetics showed a minimum in the region where water molecules form clusters around functional groups, which merge in the pores. The SO2 adsorption kinetics also show a minimum with increasing surface coverage, and this is attributed to dipole–dipole interactions. The activation energies for diffusion of both SO2 and H2O into F400 were very low. Both the N2 and CO2 adsorption kinetics were too fast to be measured accurately by the gravimetric method used in this study. Ideal adsorbed solution theory (IAST) was used to calculate competitive adsorption of SO2/CO2 and CO2/N2 from the isotherms of the pure components. The competitive adsorption of CO2/N2 was investigated by using the integral mass balance (IMB) experimental method, and this was used for validation of the IAST. The results provide an insight into the role of competitive adsorption in the capture of CO2 and SO2 from flue gases by adsorption from both thermodynamic and kinetic perspectives.

Neutralization of solvent vapors of brand 646 by the adsorption-catalytic method

The aim of the paper is investigation of neutralization of solvent vapors of the brand 646 by an adsorption-catalytic method. The adsorption-catalytic method includes the following stages: adsorption of the solvent components by adsorbent, thermal desorption and periodic flameless catalytic oxidation of organic substances to carbon dioxide and water. Synthetic zeolite of the NaX brand was used as a sorbent, catalyst was porous Al2O3/SiO2 ceramic foam material with an active catalytic phase. Solvent contains aceton, toluene, butylacetate, ethanol, ethyl cellosolve, n-butanol. It is shown that the value of the sorption volume of zeolite for each class of compounds depends on the certain factors: the length and structure of the carbon skeleton, the position of the hydroxyl group (for alcohols and esters), number of methyl groups in the molecules (for benzene derivatives). The conversion of the mixed solvent components was 65.4–90.1 %.

Adsorption of Crude Oil Components onto Carbonate and Sandstone Outcrop Rocks and Its Effect on Wettability

The processes of establishing and altering reservoir wettability are still subjects of discussion due to the complexity of the underlying crude oil–brine–rock interactions. This study was aimed at ...

Photothermal Fabrics for Efficient Oil-Spill Remediation via Solar-Driven Evaporation Combined with Adsorption.

Oil spill rapidly destroys aquatic system and threatens humans, requiring fast and efficient remedy for removal of oil. The conventional remedy employs water-floating oil adsorbents whose volume should be large enough to accommodate all oil ingredients. Here, we suggest a new concept for efficient oil-spill remediation, which combines solar-driven evaporation of light oil components and simultaneous adsorption of heavy oil components, namely, solar-driven evaporation of oil combined with adsorption (SEOA). To design photothermal oil absorbents for the efficient SEOA, we designed carbonaceous fabrics with high photothermal heating performance and oil-adsorption capacity by carbonizing nonwoven cotton fabrics. For three model organic solvents of octane, decane, and dodecane floating on water, the fabrics, respectively, accelerated the evaporation in factors of 2.0, 4.4, and 2.3 through photothermal heating under simulated sunlight condition. For the 1.18 mm thick crude oil floating on water, 70 and 77 wt % of crude oil were evaporated within 2 and 16 h, respectively, with the photothermal fabrics, whereas only 22 and 34 wt % was evaporated in the absence of the fabrics, indicating the dramatic enhancement of oil removal by solar-driven evaporation. The remaining heavy oil components were accommodated in the pores of the fabrics, removal of which showed an additional 18 wt % reduction; that is, a total 95 wt % of the crude oil was removed. The oil-treatment capacity is as high as 110 g g-1, which has never been achieved with conventional oil adsorbents to the best of our knowledge. We believe that our combinatorial SEOA approach potentially contributes to minimizing the environmental disaster through a fast and efficient oil-spill remediation.

Boosting molecular recognition of acetylene in UiO-66 framework through pore environment functionalization

The potential of metal–organic frameworks (MOFs) for application in gas separation processes has been widely recognized. Nonetheless, due to their structural instability and high cost, few MOFs have been utilized in the industry. Among them, UiO-66 is one of the most promising materials which displays good structural stability and its preparation is considered economical. Notably, it also provides a valuable platform for the construction of other robust MOFs for various applications. Herein, trifluoromethyl ligands were introduced into the UiO-66 framework to optimize pore environment also to improve its C2H2 recognition ability. Single component adsorption and the corresponding IAST calculation confirmed that compared to UiO-66, UiO-66-(CF3)2 exhibited 2 ~ 3 times higher selectivity for C2H2/C2H4 and C2H2/CO2 separation. Enhanced selectivity resulted in a significantly improved C2H4 separation productivity (56 compared to 36 cm3/cm3) and a reduction in the co-adsorption time. Importantly, the modified UiO-66 framework could be prepared using a simple method and inherited a highly stable structure and good cycling performance of the original material.

Some Theoretical Aspects of Tertiary Treatment of Water/Oil Emulsions by Adsorption and Coalescence Mechanisms: A Review

The massive increase in the volumes of oily contaminated produced waters associated with various industrial sectors has initiated considerable technological and scientific efforts related to the development of new cleaning strategies. The petrochemical industry (oil and gas production and processing) contributes to those volumes by approximately 340 billion barrels per year. The removal of emulsified oily components is a matter of particular interest because the high emulsion stability necessitates sophisticated technological approaches as well as a deep theoretical understanding of key mechanisms of oil/water separation. This review deals with the theoretical aspects of the treatment of emulsified oil/water mixtures and is particularly focused on tertiary treatment, which means the reduction of the oil content from 70–100 ppm to below 10 ppm, depending on national regulations for water discharge. The review concerns the mechanisms of oil/water separation and it covers the (i) adsorption isotherms, (ii) kinetics of adsorption, (iii) interfacial interactions between oil/water mixtures and solid surfaces, and (iv) oil/water separation techniques based on the wettability of solid/oil/water interfaces. The advantages and drawbacks of commonly used as well as newly proposed kinetic and adsorption models are reviewed, and their applicability for the characterization of oil/water separation is discussed. The lack of suitable adsorption isotherms that can be correctly applied for a description of oil adsorption at external and internal solid surfaces of both nonporous and porous structures is pointed out. The direct using of common isotherms, which were originally developed for gas adsorption, often leads to the incorrect data description because the adsorption of oily components at solid surfaces does not fit the assumptions from which these models were originally derived. Particularly, it results in problematic calculations of the thermodynamic parameters of sorption. The importance of nonlinear analysis of data is discussed, since recent studies have indicated that the error structure of experimental data is usually changed if the original nonlinear adsorption isotherms are transformed into their linearized forms. The comparison between the pseudo-first-order and pseudo-second-order kinetic models was performed. It was shown that the correlation between data and models strongly depends on the selection of data, particularly on the frequency of collected data in time scale. The wettability of solid surfaces by oil in air and under water is discussed, regarding the surface morphology of surfaces. We demonstrate that the combination of surface chemistry and topology strongly influences the separation of oil/water emulsions.

Interfacial properties of binary mixtures of Lennard-Jones chains in planar interfaces by molecular dynamics simulation.

Binary mixtures of fully flexible linear tangent chains composed of bonded Lennard-Jones interaction sites (monomers) were studied using the molecular dynamics simulation in the NVT ensemble. Their interfacial properties were investigated in planar interfaces by direct simulation of an explicit liquid film in equilibrium with its vapor. A method for the calculation of long-range interactions in inhomogeneous fluids was implemented to take into account the potential truncation effects. Surface tension and the pressure tensor were calculated via the classical Irving-Kirkwood method; vapor pressure, orthobaric densities, density profiles, and Gibbs relative adsorption of the volatile component with respect to the heavy component were also obtained. The properties were studied as a function of the temperature, molar concentration of the heavy component, and the asymmetry of the mixture. According to the results of this work, the temperature loses influence on the surface tension, vapor pressure, and Gibbs relative adsorption curves as the molecular length of the heavy component increases. This suggests that the universal behavior observed in pure fluids of Lennard-Jones chains also holds for binary mixtures. The contribution of the long-range interactions turned out to account for about 60%, 20%, and 10% of the surface tension, vapor pressure, and orthobaric density final values, respectively. This contribution was even larger at high temperatures and for large molecules. Strong enrichment of the volatile component at the interface was observed in the asymmetric mixtures. One of these mixtures even showed a barotropic effect at elevated pressures and a class III phase behavior.

Oat extract as a natural alkaline scale inhibitor for carbon steel in seawater: electrochemical (AC and DC) studies

Abstract The controlling of alkaline scale deposition on carbon steel surface in seawater by Oat extract was probed by means of current/time transients, electrochemical impedance spectroscopy (EIS) tests and scanning electron microscopy (SEM), high-performance liquid chromatography (HPLC), Fourier-transform infrared (FT-IR), X-ray diffraction (XRD) examinations. Nucleation, scale formation and coverage of carbon steel with alkaline scales were detected by current/time curves. The results demonstrate that the retardation in alkaline scale formation is controlled by Oat extract, with 86% efficiency at the highest concentration. The scale growth inhibition is due to the adsorption of Oat extract components on the active growth sites of crystal surfaces.

Modified bamboo-based activated carbon as the catalyst carrier for the gas phase synthesis of vinyl acetate from acetylene and acetic acid

Abstract As a significant component of catalyst system, catalyst carrier can impact on coating amount of active component, and in turn catalytic activity. In this work, study of bamboo-based activated carbon as the catalyst carrier for gas phase synthesis of vinyl acetate from acetylene and acetic acid was carried out. Characterization and experimental results showed that bamboo-based activated carbon possessed the conditions and potential of being a catalyst carrier and characterized a greater advantage in structure and properties after modification. After ultrasonic treatment, it was found that the mesoporous distribution of activated carbon increased, which promoted the adsorption to zinc acetate and resulted in 23% increase in productivity of catalyst. Simultaneously, it had a different effect on surface area and pore-size distribution of activated carbon by thermal treatment at high temperatures in N2 and CO2 atmosphere. The productivity of catalyst with bamboo-based activated carbon as catalyst carrier after thermal treatment in N2 and CO2 can be increased by 14 and 20%, respectively. Furthermore, based on the influence of pore size on adsorption and reaction of active components, the necessity of expanding pores of carbon was explained in this paper, which pointed out the direction of activated carbon modification.

Adsorption kinetics and thermodynamic properties of a binary mixture of hard-core particles on a square lattice.

The adsorption kinetics and thermodynamic properties of a binary mixture on a square lattice are studied using the random sequential adsorption with surface diffusion (RSAD). We compare the adsorption of binary species with different equilibrium rate constants and effective rates of adsorption to a surface and find that the temporal evolution of surface coverages of both species can be obtained through the use of the blocking function of a system with irreversible adsorption of highly diffusive particles. Binary mixtures, when one of the components follows the random sequential adsorption (RSA) without surface diffusion and the other follows the RSAD model, display competitive adsorption in addition to cooperative phenomena. Specifically, (i) species replacement occurs over a long period of time, while the total coverage remains unchanged after a short time, (ii) the presence of the RSAD component shifts the jamming coverage to the higher values, and (iii) the maximum jamming coverage is obtained when the effective adsorption of the RSA type components is lower than the other adsorbing particles.

Environmentally Induced Changes of Commercial Carbon Nanotubes in Aqueous Suspensions. Adaptive Behavior of Bacteria in Biofilms

The effects of environmental factors such as sunlight irradiation and the presence of humic acid (HA) on the physicochemical properties of commercial multiwall carbon nanotubes (MWCNT) suspended in a simulated inorganic matrix (SIM) and their impacts on bacteria growing in biofilms were evaluated. Both solar irradiation and the presence of HA lead to the dissolution of adsorbed metals on the MWCNT, which are residues of synthesis catalysts. Also, preferential adsorption of certain HA components on the MWCNT induces important modifications in the aliphatic/aromatic relationship of HA components in solution and the generation and release of new moieties. Results demonstrated that the variation of such physicochemical parameters strongly affects the interactions of MWCNT with Pseudomonas aeruginosa sessile bacteria. Thus, the number of attached bacteria increased, and stress responses such as decrease in bacterial size were found in the presence of sunlight-irradiated MWCNT with a particular distribution of extracellular polymeric substances (EPS) strands. A shielding effect was observed when HA was added. It was concluded that physicochemical alterations caused by environmental conditions (with/without irradiation, presence/absence of HA) on MWCNT-containing SIM trigger distinctive adaptive behavior of bacteria in biofilms. This information must be taken into account in the development of biologically assisted treatments for organic metal co-contamination of MWCNT-containing media since MWCNT discharge alters the physicochemical properties and composition of the aqueous environment and the response of the biofilms that interact with it.

Impact of Iron Minerals in Promoting Wettability Alterations in Reservoir Formations.

Asphaltene adsorption and deposition onto rock surfaces are predominantly the cause of wettability and permeability alterations which result in well productivity losses. These alterations can be induced by rock–fluid interactions which are affected by well operations such as acidizing, stimulation, gas injections, and so forth. Iron minerals are found abundantly in sandstone reservoir formations and pose a problem by precipitation and adsorption of polar crude components. This is due to rock–fluid interactions, which are dependent on reservoir pH; thus, this research work studied the surface charge development of pyrite, magnetite, and hematite. To ascertain conditions that will result in iron mineral precipitation and adsorption of asphaltene on iron mineral surfaces, zeta potential measurement was carried out. This is to determine the charge and colloidal stability of the iron mineral samples across wide pH values. Experimental results show that the charge development of iron minerals is controlled by mineral dissolution, the formation of complexes, adsorption of ions on the mineral surface, and the collapse of the double layer. The findings provide insights into the implications of iron mineral contacting crude oil in reservoir formations and how they contribute to wettability alterations due to different well operations.

Isosteric heat of adsorption from thermodynamic Langmuir isotherm

The recently developed thermodynamic Langmuir isotherm model is used to estimate the isosteric heat of adsorption for pure component adsorption. Specifically, pure component adsorption isotherms at different temperatures are first correlated with the thermodynamic Langmuir isotherm model. Then the pure component isosteric heat of adsorption is calculated with the Clausius–Clapeyron equation. We show the thermodynamic Langmuir isotherm model correctly estimates the isosteric heat of adsorption as a function of surface loading for pure component adsorption.