scholarly journals Surface Complexation Reactions in a Mixed α-Fe2O3,γ-Al2O3 and SiO2 Suspension

2011 ◽  
Vol 27 (01) ◽  
pp. 186-192 ◽  
Author(s):  
LIU Jia ◽  
◽  
ZHANG Wei-Min ◽  
HUANG Pei-Pei ◽  
FAN Jia-Ni ◽  
...  
2012 ◽  
Vol 384 (1) ◽  
pp. 99-104 ◽  
Author(s):  
Kazuya Morimoto ◽  
Sohtaro Anraku ◽  
Jun Hoshino ◽  
Tetsuro Yoneda ◽  
Tsutomu Sato

2016 ◽  
Vol 74 (10) ◽  
pp. 2446-2453 ◽  
Author(s):  
Yanpeng Mao ◽  
Wenlong Wang ◽  
Chunyuan Ma

As one of the major soluble organic compounds in membrane bioreactors, soluble microbial product (SMP) can combine the surface sites on hydrous ferric oxides (HFO), which can compete with HFO for the uptake of phosphate. In this study, SMP was extracted from an MBR plant with long-term stable operation, and the effects of SMP on phosphate adsorption onto fresh HFO (FHFO) were investigated at pH values of 6.0 and 7.8 in a two-phase system composed of FHFO (solid phase) and SMP/phosphate (liquid phase). The phosphate adsorption capacity of FHFO was found to decrease significantly with increase in the pH value and SMP concentration. A diffuse layer model (DLM) and a charge distribution multisite complexation (CD-MUSIC) model, which take these factors into account, were developed to describe the speciation of SMP and phosphate on FHFO surface. Both of the models provided good description of phosphate adsorption behavior in the presence of SMP at different pH. The equilibrium constants of surface complexation reactions between SMP and HFO were obtained by inversion calculation as log10K = 15.1 ± 0.11 in DLM model and log10K = 12.1 ± 0.5 in CD-MUSIC model, which can improve the equilibrium constants database of surface complexation models.


2021 ◽  
Author(s):  
Nadine Kabengi ◽  
Anastasia Ilgen ◽  
James Kubicki ◽  
Michael Machesky

2021 ◽  
Author(s):  
Ilyas Khurshid ◽  
Emad W. Al-Shalabi ◽  
Imran Afgan

Abstract Several laboratory experiments demonstrated that the use of sodium hydroxide could increase the solution pH and reduce the adsorption of anionic surfactants. However, a better understanding of rock-oil-brine interactions and their effect on surfactant adsorption during alkaline-surfactant-polymer (ASP) flooding is needed for realistic and representative estimations of surfactant adsorption levels. Therefore, this study presents a novel approach to capture these interactions and better predict their effect on surfactant adsorption as well as effluent concentrations of surfactant and various aqueous species. Currently, surface complexation models (SCM) consider rock-brine, oil-brine, and surfactant-brine reactions. In this work, four new surface complexation reactions with intrinsic stability constants that honor oil-surfactant interactions have been proposed for the first time and then validated against experimental data reported in the literature. In addition, we analyzed the effect of various parameters on surface adsorption under harsh conditions of high-temperature and high-salinity using the proposed surface complexation model (SCM). The results showed that the developed surfactant-based SCM is robust and accurate for estimating surfactant adsorption and its concentration in the effluent during chemical floods. The model was validated against two sets of ASP corefloods from the literature including single-phase and two-phase dynamic surfactant adsorption studies. The findings highlighted that oil-surfactant surface complexation reactions are important and should be captured for more representative and accurate estimation of surfactant adsorption during chemical flooding. Moreover, the detail and comprehensive analysis showed that surfactant adsorption increases and its concentration in the effluent decreases with the increase in temperature of the chemical flood, which could be due to the increase in kinetic energy of the species. It was also showed that a decrease in water total salinity decreases the surfactant adsorption on the rock surface, which is related to the increase in the repulsive forces between the adsorbed species. Additionally, with the increase in surfactant concentration in the chemical flood, the effluent surfactant concertation increases, with a slight increase in surfactant adsorption. This slight increase in adsorption can be neglected compared to the injected and produced masses of the surfactant that are proportional. Moreover, the effect of sulfate spiking is significant where the increase in sulfate concentration reduces the surfactant adsorption. Furthermore, it is worth highlighting that the lowest surfactant adsorption levels were achieved through injected water dilution; less than 0.1 mg/g of rock. This is the first study to test a novel formulation of surface complexation modeling considering oil-surfactant effect on surfactant adsorption properties. The proposed framework to estimate surfactant adsorption is conducted for high-temperature and high-salinity reservoir condition. Thus, it could be used in numerical reservoir simulators to estimate oil recovery due to wettability alteration by chemical flooding in carbonates, which will be investigated in our future work. The surfactant adsorption mechanisms during chemical flooding is very case-dependent and hence, the findings of this study cannot be generalized.


2021 ◽  
Author(s):  
Ricardo A. Lara Orozco ◽  
Ryosuke Okuno ◽  
Larry W. Lake

Abstract The potential of tuned-composition waterflooding to enhance oil recovery from carbonate reservoirs has been widely investigated in the literature. The consensus is that wettability alteration occurs because of the electrostatic interactions between the carbonate rock surface and the potential determining ions, Ca2+, Mg2+, CO32−, and SO42−. Recently, glycine, the simplest amino acid, has also been investigated as a wettability modifier for carbonates that acts similarly as the sulfate ions in brine. The impact of wettability modifiers like glycine and calcite's potential determining ions has been described by surface complexation models (SCM) and the wetting-state of the rock has been related to change of the surface potential. However, determining the relevance of the geochemical reactions is obstructed by the complexity of the SCM. Moreover, the surface potential as a surrogate of the wetting-state of the rock does not correlate with the experimental results with glycine reported in the literature. The present research analyzed the results of single-phase displacement using a SCM for calcite to determine the important surface complexation reactions. Then, wettability alteration is modeled as a set of anion exchange reactions between wettability modifiers, like SO42− and Gly−, and adsorbed carboxylic acids. Finally, analytical solutions are presented for the coupled two-phase and multicomponent reactive-transport model with anion exchange reactions.


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