Adsorption Of Acid Research Articles

Adhesion promotion and corrosion resistance of mixed phosphonic acid monolayers on AA 2024

Mixed monolayers were used to prepare surfaces of AA 2024 with precisely controlled corrosion protective and adhesive properties. In this study, the corrosion inhibition and adhesion promotion as a function of the composition of mixed phosphonic acid monolayers on AA 2024 was investigated. Mixed monolayers were formed by competitive adsorption of n-dodecylphosphonic acid (DPA) and 12-aminododecylphosphonic acid (ADPA) from ethanolic solution. Their compositions were determined by X-ray photoelectron spectroscopy. Atomic force microscopy studies and polarization modulation infrared reflection–absorption spectroscopy as well as contact angle studies proved the formation of monolayers with varying surface chemistry. The wet-adhesion strength was tested by 90° peel tests after application of an epoxy-amine adhesive. Linear sweep voltammetry was performed to evaluate the corrosion inhibition of the monolayers, and the corrosion resistance of the metal/adhesive composite was investigated by means of its corrosive delamination behavior. The electrochemical measurements demonstrated that reducing the surface concentration of ADPA improved the corrosion inhibition of the monolayer. However, the corrosive delamination experiments revealed that the improved corrosion inhibition by the self-organized DPA is of minor importance for the corrosion behavior of the metal/adhesive composite, as the adhesive properties dominate.

Programmable Lanthanide Metal-Organic Framework for Ultra-Efficient Nucleic Acids Extraction and Interaction Analysis.

Efficient, mild, and reversible adsorption of nucleic acids onto nanomaterials represents a promising analytical approach for medical diagnosis. However, there is a scarcity of efficient and reversible nucleic acid adsorption nanomaterials. Additionally, the lack of comprehension of the molecular mechanisms governing their interactions poses significant challenges. These issues hinder the rational design and analytical applications of the nanomaterials. Herein, we propose an ultra-efficient nucleic acid affinity nanomaterial based on programmable lanthanide metal-organic frameworks (Ln-MOFs). Through experiments and density functional theory calculations, a rational design guideline for nucleic acid affinity of Ln-MOF was proposed, and a modular and flexible preparation scheme was provided. Then, Er-TPA (terephthalic acid) MOF emerged as the optimal candidate due to its pore size-independent adsorption and desorption capabilities for nucleic acids, enabling ultra-efficient adsorption (about 150% mass ratio) within 1 min. Furthermore, we elucidate the molecular-level mechanisms underlying the Ln-MOF adsorption of single- and double-stranded DNA and G4 structures. The affinity nanomaterial based on Ln-MOF exhibits robust nucleic acid extraction capability (4-fold higher than commercial reagent kits) and enables mild and reversible CRISPR/Cas9 functional regulation. This method holds significant promise for broad application in DNA/RNA liquid biopsy and gene editing, facilitating breakthroughs in analytical chemistry, pharmacy, and medical research.

Phytic Acid-Functional Cellulose Nanocrystals and Their Application in Self-Healing Nanocomposite Hydrogels.

Cellulose nanocrystals (CNCs) have garnered significant attention as a modifiable substrate because of their exceptional performances, including remarkable degradability, high tensile strength, high elastic modulus, and biocompatibility. In this article, the successful adsorption of phytic acid (PA) onto the surface of cellulose nanocrystals @polydopamine (CNC@PDA) was achieved. Taking inspiration from mussels, a dopamine self-polymerization reaction was employed to coat the surface of CNCs with PDA. Utilizing Pickering emulsion, the CNC@PDA-PA nanomaterial was obtained by grafting PA onto CNC@PDA. An environmentally friendly hydrogel was prepared through various reversible interactions using poly(acrylic acid) (PAA) and Fe3+ as raw materials with the assistance of CNC@PDA-PA. By multiple hydrogen bonding and metal-ligand coordination, nanocomposite hydrogels exhibit remarkable mechanical properties (the tensile strength and strain were 1.82 MPa and 442.1%, respectively) in addition to spectacular healing abilities (96.6% after 5 h). The study aimed to develop an innovative approach for fabricating nanocomposite hydrogels with exceptional self-healing capabilities.

High surface area biochar for the removal of naphthenic acids from environmental water and industrial wastewater.

This study reports the production of biochar adsorbents from two major crop residues (i.e., rice and wheat straw) to remove naphthenic acids from water. The alkali treatment approach was used for biochar activation that resulted in a tremendous increase in their surface area, i.e., up to 2252 and 2314 m2/g, respectively, for rice and wheat straw biochars. Benzoic acid was used as a model compound to optimize critical adsorption parameters. Its maximum monolayer adsorption capacity of 459.55 and 357.64mg/g was achieved for activated rice and wheat straw biochars. The adsorption of benzoic acid was exothermic (∆H° = - 7.06 and - 3.89kJ/mol) and identified possibly as physisorption (Gibbs free energy ranges 3.5-4.0kJ/mol). The kinetic study suggested that adsorption follows pseudo-second-order kinetics with qe2 for rice straw and wheat straw-derived adsorbents at 200 and 194mg/g, respectively. As adsorbent, the recyclability of activated biochars was noticed with no significant loss in their efficiency for up to ten successive regeneration cycles. The adsorption results were validated using a commercial naphthenic acid mixture-spiked river water and paper/pulp industrial effluent. The activated rice and wheat straw biochars exhibited excellent adsorption efficiency of 130.3 and 74.6mg/g, respectively. The naphthenic acid adsorption on biochar surface was due to various interactions, i.e., weak van der Waal's, pore filling, π-π stacking, and ionic interactions. This study offers a cost-effective and eco-friendly approach to valorizing agricultural residues for pollutant removal from industrial wastewater, including petroleum refineries.

Adsorption, Orientation, and Speciation of Amino Acids at Air-Aqueous Interfaces for the Direct Air Capture of CO2.

Amino acids make up a promising family of molecules capable of direct air capture (DAC) of CO2 from the atmosphere. Under alkaline conditions, CO2 reacts with the anionic form of an amino acid to produce carbamates and deactivated zwitterionic amino acids. The presence of the various species of amino acids and reactive intermediates can have a significant effect on DAC chemistry, the role of which is poorly understood. In this study, all-atom molecular dynamics (MD) based computational simulations and vibrational sum frequency generation (vSFG) spectroscopy studies were conducted to understand the role of competitive interactions at the air-aqueous interface in the context of DAC. We find that the presence of potassium bicarbonate ions, in combination with the anionic and zwitterionic forms of amino acids, induces concentration and charge gradients at the interface, generating a layered molecular arrangement that changes under pre- and post-DAC conditions. In parallel, an enhancement in the surface activity of both anionic and zwitterionic forms of amino acids is observed, which is attributed to enhanced interfacial stability and favorable intermolecular interactions between the adsorbed amino acids in their anionic and zwitterionic forms. The collective influence of these competitive interactions, along with the resulting interfacial heterogeneity, may in turn affect subsequent capture reactions and associated rates. These effects underscore the need to consider dynamic changes in interfacial chemical makeup to enhance DAC efficiency and to develop successful negative emission and storage technologies.

Differential immobilization of cadmium and changes in soil surface charge in acidic Ultisol by chitosan and citric acid: effect of their functional groups.

Soil organic matter plays an important role in cadmium adsorption and immobilization. Since different organic matter components affect cadmium adsorption processes differently, selecting the right organic substrate and knowing how to apply it could improve cadmium remediation. This study compares the effects of two contrasting organic molecules; chitosan and citric acid, on cadmium adsorption and speciation in acidic Ultisol. The adsorption of chitosan to Ultisol significantly increased the soil positive charge while adsorption of citric acid increased the soil negative charge. At pH 5.0, the maximum amount of cadmium adsorbed in excess chitosan was 341% greater than that in excess citric acid. About 73-89% and 60-62% of adsorbed cadmium were bound to Fe/Mn oxides and organic matter/sulfide at pH 4.0 while this fraction was 77-100% and 57-58% for citric acid and chitosan at pH 5.0, respectively. This decrease in the complexing ability of chitosan was related to the destabilizing effect of high pH on chitosan's structure. Also, the sequence through which chitosan, citric acid, and cadmium were added into the adsorption system influenced the adsorption profile and this was different along a pH gradient. Specifically, adding chitosan and cadmium together increased adsorption compared to when chitosan was pre-adsorbed within pH 3.0-6.5. However, for citric acid, the addition sequence had no significant effect on cadmium adsorption between pH 3.0-4.0 compared to pH 6.5 and 7.5, with excess citric acid generally inhibiting adsorption. Given that the action of citric acid is short-lived in soil, chitosan could be a good soil amendment material for immobilizing cadmium.

Synergistic adsorption and singlet oxygenation of humic acid on alkali-activated biochar via peroxymonosulfate activation

Synergistic adsorption and singlet oxygenation of humic acid on alkali-activated biochar via peroxymonosulfate activation

In Ukrainian

An important environmental problem is the removal of contaminants and the purification of domestic and industrial water from pollutants of various nature. There is a separate issue of cleaning the effluents of pharmaceutical enterprises. Various chemical and physical methods are used to solve these problems, such as settling, coagulation, filtration, and sorption techniques. Adsorption with using efficient and reusable adsorbents is the most effective and cheap. In recent years special attention has been paid to the use of sorption materials based on hydrolysis lignin, which has a high sorption activity in relation to ions of some heavy metals, dyes, organic compounds and pharmaceuticals. The use of lignin as an adsorbent simultaneously solves two problems: the disposal of paper production waste and the purification of sewage from various types of pollutants. The aim of this work was to study the sorption properties of hydroylysis lignin in aqueous solution in relation to some medical substances of different chemical nature, existing in solution in cationic, anionic or neutral forms. The point of zero charge of hydrolysis lignin was determined, which is equal to рНPZC = 4.95. The adsorption of rivanol, proflavin, doxorubicin, levofloxacin, furacilin, and salicylic acid by hydrolysis lignin was studied as dependence on the pH of the solutions and the concentration of adsorbates. It was found that adsorption largely depends on the structure of the pharmaceuticals and the pH values of the solutions. It is shown that the studied medical compounds, which exist in the solution in the form of cations, are adsorbed the best (rivanol, proflavin, doxorubicin). Adsorption of these substances occurs mainly due to electrostatic interaction with negatively charged surface groups. Adsorption of anionic form (salicylic acid) is the smallest and is observed only at quite low pH values. Levofloxacin is adsorbed mainly in the form of zwitter ions, and furacilin is in neutral form. The adsorption of these both compounds occupies an intermediate value of adsorption amount. The obtained adsorption isotherms are well lined up in Langmuir coordinates. Quantitative parameters of adsorption values - of maximum adsorption and equilibrium constants were calculated. Quite high values of these parameters indicate that hydrolysis lignin can be used as an adsorbent for the removal of these pharmaceuticals.

Regulation and synthesis of metal–organic frameworks through mixed-ligand strategy: A pathway to enhance adsorption of perfluoroalkyl acids

Metal-organic frameworks (MOFs) have been regarded as extremely promising adsorbent materials, with the repetitive coordination assembly of inorganic metal ions and organic ligands constituting their reticular structure and abundant pores. Herein, a ligand mixing approach to synthesizing and regulating MOFs is provided. By mixing multiple solvents and adding modifiers, imidazole-based linkers can be prepared MOFs with mixed ligand components at room temperature. In this study, we prepared four mixed-ligand MOFs: Zn(aIM + bIM), Zn(mIM + bIM), Zn(aIM + mIM), and Zn(mIM + 2-mbIM). Series of characterizations by SEM, XRD, NMR, etc. confirmed the successful preparation of mixed-ligand MOFs, and they exhibited the different surface areas, pore sizes, and surface properties. And the adsorption capabilities for perfluoroalkyl acids (PFAAs) were compared among the prepared MOFs adsorbents. Among them, Zn(aIM + bIM) consisting of benzimidazole and imidazole-2-formaldehyde linker possessed the optimum adsorption performance, with an equilibrium adsorption capacity qe of 245 mg/g for perfluorobutyric acid, and the calculated maximum adsorption capacity qm of 439 mg/g. And for the other chain lengths of perfluoroalkyl acids, the adsorption results are also acceptable. The potential adsorption mechanism and the reasons for the performance enhancement are discussed based on relevant characterization and simulation. It was proved that the ligand mixing strategy can provide new insights into the development of high-performance MOFs adsorbents for addressing environmental concerns.

In Ukrainian

The paper discusses the results of saponite research from the Tashkiv deposit of Ukraine. X-ray structural analysis proved the necessity of preliminary cleaning of saponites from mineral impurities. The study of the morphology, nanoprofile and topography of the surface of saponite by the methods of SEM-microscopy and Atomic Force Microscopy revealed that the mineral is represented by aggregates of nano- and microparticles of a pyramidal shape. Its characteristic feature is the heterogeneity of isomorphic substitutions of ions in the tetrahedral and octahedral sheets of the structural elementary package. According to X-ray fluorescence analysis, saponite contains a significant amount of Fe3+, which isomorphically replaces magnesium Mg2+ and, accordingly, is located mastly in the octahedral sheet of the structural package with a charge from +0.37 to +0.35. The number and mechanism of isomorphic substitutions determine the presence of a total negative charge of the crystal lattice (from –0.38 to –0.3), the value of which ensures intensive interaction with water molecules of the interpacket space with the formation of surface OH groups. Accordingly, both acidic and alkaline Lewis and Brønsted centers are present on the surface with a predominance of acidic ones, so the acidity function is 5.82, and the point of zero proton charge is pH = 5.5. During dispersion in water, a part of the alkaline centers of the side surface are transformed into Brønsted acid centers as a result of their protonation, which causes an increase in the pH of the dispersion medium to pH = 8–8.6. Accordingly, the isoionic state is reached at pH = 7.5. The difference in pH values characterizing the isoionic state of the surface and the point of zero net proton charge (PZNPC) indicates the presence of weak acid-alkaline centers on the surface. The study of the adsorption of acid-alkaline dyes showed the adsorption of alkaline (pK = 1¸3) and acid (pK = 7¸14) dyes on saponites. The latter is significantly reduced due to the preliminary hydration of the solid surface - mainly the lateral edges of the particles. Acidic dyes are not adsorbed from a dispersion medium with pH < 5.5 (PZNPC), and basic dyes are adsorbed at pH > 5,5( PZNPC).

Highly Efficient Cationic Surfactant Functionalized Alginate Hydrogel for Perfluorooctanoic Acid Adsorption: Optimization through Response Surface Methodology and Performance Evaluation for Aqueous Media

Highly Efficient Cationic Surfactant Functionalized Alginate Hydrogel for Perfluorooctanoic Acid Adsorption: Optimization through Response Surface Methodology and Performance Evaluation for Aqueous Media

Comprehensive batch studies on removal of fluoride from aqueous solution by acid and alkali-activated adsorbents prepared from Dal lake weeds: Mechanism, Kinetics and Thermodynamics

An efficient and economical way of eliminating fluoride from water is being investigated by employing the buoyant aquatic plant (Dal weed). Two post-pyrolysis chemical activation alteration techniques were implemented: acidic activation by employing sulfuric acid (H-activation) and alkaline activation using sodium hydroxide (OH-activation). The batch kinetic studies have been carried out considering varying starting fluoride levels such as 2–10 mg/L. The impact of diverse procedural factors, including dosage of Dal weed, starting fluoride level, pH and contact duration was observed to determine their influence on fluoride adsorption kinetics. Based on analyzed exploratory results, removal efficacy of 63% for the OH-activated carbon and 83% for H-activated carbon was achieved at commencing fluoride level of 10 mg/L, adsorbent dosage of 0.8 g, at 25 °C after 120 min. The maximal fluoride uptake capacity for H-activated carbon was observed to be 78.158 mg/g. Kinetic investigations showed that the Freundlich isotherm model provided a satisfactory match with an R2 value of 0.99. The reaction order nature adhered to kinetics resembling pseudo second order. Thermodynamic investigation revealed endothermic sorption, with negative ΔG indicating spontaneous fluoride uptake. In comparison, the positive number for ΔS suggested random behavior at the contact involving the adsorbent and adsorbate. The investigations into the regeneration capabilities of the adsorbent material revealed that even after undergoing for five consecutive cycles of adsorption and regeneration, the adsorbent exhibited an uptake potential of 45%. The presence of competing ions in the solution negatively impacted defluoridation efficacy, with the influence following the order of HCO3−< NO3−< Cl−< SO42−< PO43−.

Equilibrium and Kinetic Studies on Adsorption of Neutral and Ionic Species of Organic Adsorbates from Aqueous Solutions on Activated Carbon.

This work presents comprehensive studies of the adsorption of neutral and ionic forms of organic adsorbates from aqueous solutions on activated carbon. The influence of pH on the equilibrium and kinetics of the adsorption of methylene blue (MB) and organic acids, benzoic (BA), 2-nitrobenzoic (2-NBA), 3-nitrobenzoic (3-NBA), and 4-nitrobenzoic (4-NBA) acid, was investigated. Experimental adsorption isotherms were analyzed using the generalized Langmuir isotherm equation (R2 = 0.932-0.995). Adsorption rate data were studied using multiple adsorption kinetics equations, of which the multi-exponential equation gave the best fit quality (R2 - 1 = (6.3 × 10-6)-(2.1 × 10-3)). The half-time was also used to represent the effect of pH on adsorption kinetics. Strong dependences of the adsorption efficiency on the solution pH were demonstrated. In the case of organic acid adsorption, the amount and rate of this process increased with a decrease in pH. Moreover, larger adsorbed amounts of methylene blue were recorded in an alkaline environment in a relatively short time. The maximum absorbed amounts were 11.59 mmol/g, 6.57 mmol/g, 9.38 mmol/g, 2.70 mmol/g, and 0.24 mmol/g for BA, 2NBA, 3-NBA, 4-NBA, and MB. The pure activated carbon and the selected samples after adsorption were investigated using thermal analysis and X-ray photoelectron spectroscopy.

Studies of the Dependency between Salt Content and the Adsorption of Glycolic Acid on Carriers in Aqueous Solutions

Studies of the Dependency between Salt Content and the Adsorption of Glycolic Acid on Carriers in Aqueous Solutions

A phosphorylated guanidine chitosan and UiO-66-NH2 modified magnetic nanoparticle platform for enrichment and detection of multiple bacteria

Wastewater-based epidemiology (WBE) is a powerful tool for early warning of infectious disease outbreaks. Hence, a rapid and portable pathogen monitoring system is urgent needed for on-site detection. In this work, we first reported synthesis of an artificial modulated wide-spectrum bacteria capture nanoparticle (Arg-CSP@UiO@Fe3O4). Arginine-modified phosphorylated chitosan (Arg-CSP) coating could provide strongly positive charged guanidinium group for pathogen interaction by electrostatic attraction, and UiO-66-NH2 layer could help Arg-CSP graft onto Fe3O4 magnetic particles. The capture efficiency of Arg-CSP@UiO@Fe3O4 reached 92.2 % and 97.3 % for Escherichia coli (E.coli) and Staphylococcus epidermidis (S.epidermidis)within 40 min, in 10 mL sample. To prevent pathogen degradation in sewage, a portable nucleic acid extraction-free method was also developed. UiO-66-NH2 could disintegrate in buffer with high concentration of PO43− for bacterium desorption, and then nucleic acid of the bacteria was released by heating. The DNA template concentration obtained by this method was 779.28 times higher than that of the direct thermal lysis product and 8.63 times higher than that of the commercial kit. Afterwards, multiple detection of bacteria was realized by loop-mediated isothermal amplification (LAMP). Artificial regulated pathogen desorption could prevent non-specific adsorption of nucleic acid by nanoparticles. The detection limit of Arg-CSP@UiO@Fe3O4-LAMP method was 80 cfu/mL for E.coli and 300 cfu/mL for S.epidermidis. The accuracy and reliability of the method was validated by spiked sewage samples. In conclusion, this bio-monitoring system was able to detect multiple bacteria in environment conveniently and have good potential to become an alternative solution for rapid on-site pathogen detection.

Integrated High-Throughput Centrifugal Microfluidic Chip Device for Pathogen Detection On-Site.

An integrated and high-throughput device for pathogen detection is crucial in point-of-care testing (POCT), especially for early diagnosis of infectious diseases and preventing the spread of infection. We developed an on-site testing platform that utilizes a centrifugal microfluidic chip and automated device to achieve high-throughput detection. The low-power (<32 W), portable (220 mm × 220 mm × 170 mm, 4 kg) device can complete bacterial lysis, nucleic acid extraction and purification, loop-mediated isothermal amplification (LAMP) reaction, and real-time fluorescence detection. Magnetic beads for nucleic acid adsorption can be mixed by applying electromagnetic fields and centrifugal forces, and the efficiency of nucleic acid extraction is improved by 60% compared to the no-mixing group. The automated nucleic acid extraction process achieves equivalent nucleic acid extraction efficiency in only 40% of the time consumed using the kit protocol. By designing the valve system and disc layout, the maximum speed required for the centrifugal microfluidic chip is reduced to 1500 rpm, greatly reducing the equipment power consumption and size. In detecting E. coli, our platform achieves a limit of detection (LOD) of 102 CFU/mL in 60 min. In summary, our active centrifugal microfluidic platform provides a solution for the integration of complex biological assays on turntables, with great potential in the application of point-of-care diagnosis.

Adsorption of Humic Acid from Water Using Metal-Organic Frameworks (MOFs): An Effective Removal Strategy

The escalating presence of humic acid (HA) in aquatic systems poses significant ecological and potable water treatment challenges, altering the color, taste, and odor of water and fueling algal blooms that deplete oxygen levels to the detriment of aquatic life. Traditional techniques like coagulation-flocculation, membrane filtration, oxidation fall short in efficiency due to its small fraction of HA, Humic acids (HAs) can interact with various organic and inorganic substances, affecting their characteristics and behavior in water. These interactions can influence the efficiency of water treatment processes like adsorption and coagulation. Specifically, HAs may compete with other contaminants for treatment sites or alter the chemical conditions of the treatment processes, impacting their effectiveness. This thesis confronts the pervasive issue of HA contamination by leveraging the advanced properties of metal-organic frameworks (MOFs). In this work, four representative MOFs are synthesized and well characterized. Then, their capability to enhance coagulation processes in water for HA and HA-kaolin treatment are detailed evaluated. The findings from this research extend beyond academic curiosity, offering actionable insights for water treatment facilities and environmental management agencies. The synthesis of MOFs which are UiO-66(Zr), MIL-100(Fe), ZIF-8, and Al-fum. Each MOFs have been applied to remove HA by adsorption under different condition, effect of contact time, effect of initial pH, effect of adsorbent dosage. After adsorption experiment, MOF samples prepared to dry and went through characterization. Removal of HA by MOF adsorption showed UiO-66(Zr) and MIL-100(Fe) examined shortest reaching equilibrium state with 10-15 min, however, ZIF-8 and Al-fum gradually reached equilibrium state after 60 min. Among various pH conditions, UiO-66(Zr) and MIL-100(Fe) showed the highest adsorption capacity under acidic conditions, while ZIF-8 excelled at neutral pH, and Al-fum exhibited the highest adsorption capacity under both acidic and basic conditions. ZIF-8 has the highest adsorption capacity among the MOFs with capacity of 754 mg/g. MOF after adsorption samples went through characterizations and their remained characteristics indicating the adsorption not affected the structure of the MOFs.

Highly adsorptive removal of ciprofloxacin and E. coli inactivation using amino acid tryptophan modified nano-gibbsite

Adsorption of essential amino acid, Tryptophan (Tryp) on synthesized gibbsite nanoparticles and their applications in eliminating of antibiotic ciprofloxacin (CFX) and bacteria Escherichia coli (E. coli) in aqueous solution. Nano-gibbsite which was successfully fabricated, was characterized by XRD, TEM-SAED, FT-IR, SEM-EDX and zeta potential measurements. The selected parameters for Tryp adsorption on nano-gibbsite to form biomaterial, Tryp/gibbsite were pH 11, gibbsite dosage 20 mg/mL and 1400 mg/L Tryp. The optimum conditions for CFX removal using Tryp/gibbsite were adsorption time 60 min, pH 5, and 20 mg/mL Tryp/gibbsite dosage. The CFX removal significantly raised from 63 to 90% when using Tryp/gibbsite. The Freundlich and pseudo-second-order models achieved the best fits for CFX adsorption isotherm and kinetic on Tryp/gibbsite, respectively. The amount of CFX increased with increasing ionic strength, suggesting that both electrostatic and non-electrostatic interactions were important. After four reused time, CFX removal was greater than 66%, demonstrating that Tryp/gibbsite is reusable with high performance in removing CFX. The application in bacterial activity in term of E. coli reached greater than 98% that was the best material for bacteria inactivation. The present study reveals that Tryp/gibbsite is an excellent bio-material for removing CFX and E. coli.

Preparation, characterization, and adsorption capacity of pyrophosphoric acid sustainable activated carbon from baijiu spent grains for risk factor mitigation

The increasing societal concern regarding the safety of alcoholic beverages necessitates the implementation of effective and safe intervention measures to enhance their safety. This study aims to repurpose the substantial spent grains generated during Baijiu production, which have a significant environmental impact, into sustainable activated carbon (as an adsorbent) by pyrophosphoric acid to alleviate these concerns directly. Precise optimization strategies were employed for simulated and authentic Baijiu samples to determine ideal conditions for carbon synthesis suitable for different alcoholic beverages (with fewer flavor compounds and rich in flavor compounds). Characterization via FT-IR and SEM confirmed the porous structure of the activated carbon. The adsorption experiments indicate that calcination temperature significantly influences adsorption efficiency, favoring selective adsorption of higher alcohols, acetaldehyde, and methanol, while simultaneously reducing acid adsorption. Compared to commercial activated carbon, spent grain carbon exhibited superior acid retention effects. Through sensory evaluation to determine application parameters, activated carbon can reduce acetaldehyde and higher alcohols in Baijiu by 9.67 % and 14.94 %, respectively, without compromising aroma. Thus, this research not only provides a novel recycling strategy for the significant waste generated in Baijiu production but also offers a green and sustainable assurance measure for the quality and safety of alcoholic beverages.

Comparison of perfluoroalkyl substance adsorption performance by inorganic and organic silicon modified activated carbon

Owing to the persistence and increasingly stringent regulations of perfluoroalkyl substances (PFAS), it is necessary to improve their adsorption capacities using activated carbon (AC). However, their adsorption capacities are suppressed by dissolved organic matter (DOM). In this study, two ACs modified with organic silicon (C-OS) and inorganic silicon (C-IS) were synthesized and used for the adsorption of PFAS in raw water (RW). The results showed that the PFAS adsorption capacity of C-IS was much less influenced by DOM than that of the original AC (C-virgin). In RW, perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) adsorption capacities on C-IS were 15.08 and 3.65 times higher than those on C-virgin, respectively. DOM had less influence on the PFOA and PFOS adsorption kinetics of C-IS than C-OS and C-virgin. Under multi-PFAS condition, C-IS also exhibited slower desorption of short-chain PFAS and breakthrough in batch and column tests, respectively. Characterization of the ACs before and after adsorption and independent gradient modelling indicated that hydrogen bond interactions between the O-Si of C-IS and the –COOH or –CSO3H groups of PFAS contributed to PFAS adsorption. Density functional theory calculations demonstrated that the adsorption energy of C-IS was much lower than that of C-OS and C-virgin. The arrangement of PFAS molecules on C-OS was chaotic owing to the hydrophobic siloxane chain, whereas the arrangement of PFAS on C-IS was orderly in multi-layer or semi-micelle status and more favorable to PFAS adsorption. This study provides a new strategy for avoiding adverse effects of DOM on PFAS adsorption.