Adsorption Science & Technology

Pristine Macadamia nutshell-based activated carbons were chemically oxidized with different concentrations of H₃PO₄ and HNO₃ to increase their surface adsorption properties and further explore if they could be an attractive alternative low-cost adsorbent for gold recovery from cyanide-leached liquors. The modified activated carbons were labeled MACN₂₀, MACN₄₀ and MACN₅₅ to signify the materials prepared from 20%, 40% and 55% (v/v) HNO₃, respectively. Similar nomenclature was followed for H₃PO₄-modified activated carbons. Brunauer-Emmet-Teller, scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, elemental analysis and X-ray diffraction spectroscopy were used to characterize the prepared activated carbons. The physical properties were attained through determining attrition, ash content, volatile matter and moisture content of all the activated carbons. Various parameters that affect selective adsorption such as the effect of initial concentration, time, agitation speed, interfering species and the dose of the adsorbent were investigated. Optimal parameters for gold ion adsorption were as follows: solution pH, 10; contact time, 6 h; agitation speed, 150 r/min; sorbent amount, 4 g and initial concentration, 5.5 mg/L. The observed selectivity order was not the same for all the adsorbents, but the adsorption of gold was found to be mostly influenced in the presence of nickel and least influenced by copper. MACN₅₅ was found to be the most efficient adsorbent with 74% of gold adsorption from a real-world sample and displayed a similar performance to coconut-based activated carbons.

Expansion/contraction of coal, induced by the sorption of carbon dioxide and methane in isothermal and non-isothermal conditions, was measured. The investigation is of great importance in the context of validating the potential CO₂ sequestration in unmined coal seams. Changes in temperature in underground coal beds can influence the sorption balance, resulting in strains in coal strata, which could lead to the desorption of gas and leaks to the ground surface. The research shows that the strains induced by CO₂ sorption are about twice the size of those resulting from the sorption of CH₄. The linear strains are anisotropic and greater in the direction perpendicular to the bedding plane. The results of the non-isothermal experiments show that a temperature increase gives rise to the sample swelling in the presence of methane, but a different pattern is observed for coal–CO₂ systems, where sample contraction occurs. This behaviour is explained by the different mechanism of CH₄ and CO₂ deposition and by the diversity in the maceral composition of the samples.

In this study, the adsorption capacities of peanut shell activated carbon samples prepared using three types of peanut shell as raw material were compared. The effects of activation state, carbonization temperature, carbonization time, adsorption time during decolorization, and dosage on the performance of the peanut shell activated carbon samples were investigated. The performance of the modified peanut shell (activated carbon) on the decolorization of reactive brilliant blue X-BR and the adsorption kinetics were evaluated systematically. Among the three types of peanut shell activated carbon, the activated carbon that was first activated by phosphoric acid and then carbonized at 450°C for 3 h displayed the best performance, with an optimum dosage of 4 g l⁻¹ and an optimum adsorption time of 2 h. The pseudo-second-order kinetics equation and the intraparticle diffusion equation could well describe the adsorption behavior of the activated carbon prepared by phosphoric acid activation. Intraparticle diffusion was not the only factor affecting the adsorption rate of the activated carbon on reactive brilliant blue X-BR.

In this work, a series of ammonium–lauric salts (ALS) was prepared with lauric acid and amines as small molecular shale swelling inhibitor. The inhibitors were screened by the linear expansion test first, and the result shows that the inhibitor prepared by lauric acid and diethylenetriamine with the mole ratio of 2:1 (ALS-2) displays excellent inhibition effect on the hydration expansion of bentonite. The inhibition of ALS-2 to bentonite was fully evaluated by various methods in the following work, including clay linear swelling test and particle distribution measurement. The results show that ALS-2 has superior performance to inhibit the hydration swelling and dispersion of bentonite, and the swelling rate of bentonite in 0.5% ALS-2 was reduced to 29.7%. In water-based drilling fluid, ALS-2 is compatible with the conventional additives, and it can improve the lubricity of the mud cake obviously after aged under 120°C. Besides, it can control the particle size of bentonite in water. The inhibition mechanism of the ammonium–lauric salts was discussed in detail through physical adsorption, scanning electron microscopy, X-ray diffraction, thermogravimetric analysis, and Fourier transform infrared spectroscopy.

Synthesis of zeolites from fly ash is an ecologically justified process aimed at the transformation of energy sector waste – fly ash into microcrystalline zeolites of broad possible application field. In this study, the synthesis of zeolites from fly ash by using a modified two-step synthesis was presented. The aim of such a planned experiment was to use the waste solutions from previous synthesis, in such a way that minimalization of negative influence of post-synthesis wastes on environment was possible. Received materials were tested for its sulfur dioxide sorption capacity, indicating its future possible application to capture SO2 from exhaust gases.

Adsorption behaviours of humic acid on three natural clays from Ivory Coast were studied. In order to investigate the adsorption mechanism, characterization of clays and the humic acid–clay complex was conducted by using various analytical methods (attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), X-ray diffraction (XRD), specific surface area analysis (BET) and chemical composition). As a result, adsorption process showed that the maximum adsorption capacity of humic acid was achieved at pH = 3 and was found to be to 115 mg/g obtained for the best sample. For all clays, the adsorption was found to be strongly dependent on pH and well fitted by the Langmuir model. In addition, it was shown that the adsorption capacity was linked to the kaolinite content of each sample. The results showed that humic acid adsorption onto clay was made via electrostatic interactions, ligand exchange and hydrophobic interactions. This study showed that clays are valuable adsorbents for the removal of humic acid.

Nanotechnology has been used in different industries for years. In this study, polyurethane filter, modified with nano-sized polypyrrole–ZnO was used for wastewater quality improvement. The effect of coating method and influential parameters on polymer morphology was studied by Fourier transform infrared spectroscopy and scanning electron microscopy. The results revealed that the uniformly synthesized polymers are seed like. The size of synthesized nanoparticles was observed to be about 50–120 nm. The effect of the number of iterative filtration and the height of the filter on improving the quality of the waste water was investigated using central composite design. After filtration, spectroscopy method, gas chromatography method, and some other devices such as biochemical oxygen demand meter and salt meter were used to evaluate the quality of the waste water. The results indicated that the filter efficiency in optimizing parameters such as total dissolved solids, biochemical oxygen demand, chemical oxygen demand, color, salinity, hardness, pH, and organic compounds removal is desirable. After data modeling, the optimal thickness of the filter was 3.8 cm and the most appropriate iteration for filtration was eight times obtained using a graphical method. Results showed that the designed filter had an excellent ability to improve wastewater quality and can be used in water and wastewater refining instruments.

Goethite is a stable and widespread mineral present in soil with many uses, and it affects the transportation and immobilization of heavy metals in solution. Nanogoethite was synthesized by a chemical precipitation method and used to batch adsorb U(VI) in solution. Adsorption experiments were used to understand the role of nanogoethite in controlling the U(VI) adsorption behavior in soil. The morphology and the crystallinity of nanogoethite were characterized by scanning electron microscopy and wide-angle X-ray powder diffractometry, respectively. The results showed that the crystallinity of nanogoethite after the adsorption of uranium did not change, but small particles appeared on the surface of the scales. The surface area was determined from N₂ adsorption–desorption experiments using the Brunauer–Emmett–Teller to be 81.86 m²/g. The effects of factors such as the contact time, pH, adsorbent dosage, and the initial concentration of uranium on the adsorption of U(VI) were investigated. The experimental results showed that nanogoethite removed over 85% of the U(VI) in an aqueous 5.0 mg/L U(VI) solution at pH 4.0 and at 298 K. The pseudo-second-order model was used to simulate the adsorption process. The results show that chemisorption plays a major role in the adsorption process. The results of this study suggest that nanogoethite may play a significant role in controlling the migration and transfer of U(VI) in the soil, thus controlling the presence of U(VI) in soil.

One of the main challenges of the ammonia-based CO₂ capture process is how to further reduce the regeneration energy consumption. An antisolvent crystallization method was proposed to strengthen the crystallization process of carbonized ammonia, and heating the crystal products instead of rich solution can greatly reduce renewable energy consumption. The main component of the crystal product was NH₄HCO₃ analyzed by X-ray diffraction. Therefore, it is very important to study the thermodynamic properties of ammonium bicarbonate in the ternary system of NH₃–H₂O–ethanol. In this paper, the solubility curves under different temperature and solvent compositions were determined by static method and the mathematical model of solubility was established. The effects of the addition of ammonium carbamate which was produced in the initial stage of the CO₂ absorption process and the addition of ammonia on the solubility in ternary system of NH₄HCO₃–H₂O–ethanol were studied. The dissolution heat was also calculated in the end. The research of this article has a guiding significance for the antisolvent method to strengthen the crystallization of carbonized ammonia of ammonia-based carbon capture technology. It is helpful to further strengthen the crystallization process of low carbonized ammonia and improve the crystallization yield.

In this study, a new category of sulfone-modified chitosan derivatives as surface-selective adsorbents for the extraction of toxic Hg(II) metal has been synthesized in good yield. Sulfone-modified chitosan/5–20 based on variable loading of the corresponding phenacyl bromide (5, 10, 15, and 20% with respect to the original weight of the pure chitosan) was synthesized. The β-ketosulfone derivative, namely 1–(4-bromophenyl)-2-(phenylsulfonyl)ethanone, was first prepared by treatment of the corresponding phenacyl bromide with a sufficient amount of sodium benzene sulfinate; its chemical structure was confirmed by spectral analyses, including Fourier transform infrared spectroscopy, ¹H-NMR, ¹³C-NMR, and mass spectrometry. Then, sulfone-modified chitosan/5–20 derivatives were synthesized by the interaction of chitosan with a freshly prepared p-bromo-β-ketosulfone derivative in a mildly acidic aqueous solution using the solution-blending technique. Sulfone-modified chitosan/5–20 derivatives were identified and characterized using common characterization techniques, including Fourier transform infrared spectroscopy, field-emission scanning electron microscope, powder X-ray diffraction, and thermal behaviour. A strong interaction was displayed between chitosan and its corresponding β-ketosulfones in powder X-ray diffraction, which was confirmed by significant 2θ shifts. Sulfone-modified chitosan/5–20 derivatives were detected as catalysts, which efficiently increased the thermal decomposition of pure chitosan. More particularly, the efficiency of sulfone-modified chitosan/5–20 derivatives for Hg(II), Pb(II), Ni(II), Al(III), Sr(II), Cr(III), Fe(III), Zn(II), and Mn(II) detection and adsorption was also investigated using inductively coupled plasma optical emission spectrometry. The sulfone-modified chitosan/5 derivative exhibited the highest adsorption efficiency. The most effective quantitative adsorption onto the sulfone-modified chitosan/5 surface was detected at pH = 2. In addition to that, the adsorption isotherm showed that the adsorption capacity of sulfone-modified chitosan/5 for Hg(II) was 122.47 mg g⁻¹ and that its adsorption isotherm was in agreement with the Langmuir adsorption isotherm.

This study investigates the potential use of activated carbon prepared from coffee waste (CW) as an adsorbent for the removal of congo red dye from aqueous solution. The oxygen-containing groups of activated carbon prepared from CW play an important role in dyes ions adsorption onto activated carbon prepared from CW. The activated carbon is characterized by scanning electron microscopy and Fourier transform infrared (FTIR) spectroscopy. Adsorption experiments were carried out as batch studies at different contact time, pH, and initial dye concentration. The dye adsorption equilibrium was attained after 120 min of contact time. Removal of dye in acidic solutions was better than in basic solutions. The adsorption of dye increased with increasing initial dye concentration. The equilibrium data were revealed that Langmuir model was more suitable to describe the congo red adsorption and demonstrated excellent reusability potential with desorption greater than 90% throughout six consecutive adsorption–desorption cycles. Experimental data founded that kinetics followed a pseudo-second-order equation. Thermodynamic study showed that the adsorption was a spontaneous and exothermic process. According to the FTIR analyses, hydrogen bonding and electrostatic interactions between dyes and oxygen-containing functional groups on activated carbon prepared from CW are dominant mechanisms for dye adsorption.