Removal of Cd from solution and in-situ remediation of Cd-contaminated soil by a mercapto-modified cellulose/bentonite intercalated nanocomposite.

A novel intercalated nanocomposite of mercapto-modified cellulose/bentonite (LCS-BE-SH) was synthesized by high-speed shearing method in one step at room temperature, and was applied to remove Cd from solution and remediate Cd-contaminated soil. Results revealed that cellulose long-chain molecules have intercalated into bentonite nanolayers and interlayer spacing was increased to 1.411 nm, and grafting -SH groups improved adsorption selectivity, which enabled LCS-BE-SH to have distinct capability of Cd adsorption (qmax = 147.21 mg/g). Kinetic and thermodynamics showed that Cd adsorption onto LCS-BE-SH was well fitted by pseudo-second-order and Langmuir adsorption isotherm. Characterizations of the adsorbents revealed that synergistic effect of complexation (e.g., CdS, CdO) and precipitation (e.g., Cd(OH)2, CdCO3) mechanism played a major role in Cd removal. In soil remediation, application of LCS-BE-SH was most effective (67.31 %) in Cd immobilization compared to the control (8.85 %), which reduced exchangeable Cd from 37.03 % to 11.44 %. Meanwhile, soil pH, soil organic matter, available phosphorus, and enzyme activities (catalase, urease, and dehydrogenase) were improved LCS-BE-SH treatment. The main immobilization mechanism in soil included complexation (e.g., CdS, CdO) and precipitation (e.g., Cd(OH)2, Cd-Fe-hydroxide). Overall, this work applied a promising approach for Cd removal in aqueous and Cd remediation in soil by using an effective eco-friendly LCS-BE-SH nanocomposites.

Critical assessment of recent advancements in chitosan-functionalized iron and geopolymer-based adsorbents for the selective removal of arsenic from water.

Inorganic arsenic (As), a known carcinogen and major contaminant in drinking water, affects over 140 million people globally, with levels exceeding the World Health Organization's (WHO) guidelines of 10 µg L-1. Developing innovative technologies for effluent handling and decontaminating polluted water is critical. This paper summarizes the fundamental characteristics of chitosan-embedded composites for As adsorption from water. The primary challenge in selectively removing As ions is the presence of phosphate, which is chemically similar to As(V). This study evaluates and summarizes innovative As adsorbents based on chitosan and its composite modifications, focusing on factors influencing their adsorption affinity. The kinetics, isotherms, column models, and thermodynamic aspects of the sorption processes were also explored. Finally, the adsorption process and implications of functionalized chitosan for wastewater treatment were analyzed. There have been minimal developments in water disinfection using metal-biopolymer composites for environmental purposes. This field of study offers numerous research opportunities to expand the use of biopolymer composites as detoxifying materials and to gain deeper insights into the foundations of biopolymer composite adsorbents, which merit further investigation to enhance adsorbent stability.

Removal of chloride ion from drinking water using Ag NPs-Modified bentonite: Characterization and optimization of effective parameters by response surface methodology-central composite design.

The presence of chloride ion as an environmental pollutant is having a devastating and irreversible effect on aquatic and terrestrial ecosystems. To ensure safe and clean drinking water, it is vital to remove this substance using non-toxic and eco-friendly methods. This study presents a novel and highly efficient Ag NPs-modified bentonite adsorbent for removing chloride ion, a common environmental pollutant, from drinking water using a facile approach. The surface chemical properties and morphology of the pristine Na-bentonite and Ag NPs-Modified bentonite were characterized by field emission scanning electron microscopy (FESEM) and X-ray spectroscopy (EDX), X-Ray diffraction (XRD), Fourier transform infrared (FTIR), and zeta potential (ζ). To achieve maximum chloride ion removal, the effects of experimental parameters, including adsorbent dosage (1-9 g/L), chloride ion concentration (100-900 mg/L), and reaction time (5-25 h), were examined using the Response Surface Methodology (RSM). The chloride ion removal of 90% was obtained at optimum conditions (adsorbent dosage: 7 g/L, chloride ion concentration: 500 mg/L, and reaction time: 20 h). The adsorption isotherm and kinetics results indicated that the Langmuir isotherm model and pseudo-second-order kinetics were found suitable to chloride ion removal. Additionally, the regeneration and reusability of the Ag NPs-modified bentonite were further studied. In the regeneration and reusability study, the Ag NPs-modified bentonite has shown consistently ≥90% and ≥87% chloride ion removal even up to 2 repeated cycles, separately. Thus, the findings in this study provided convincing evidence for using Ag-NPs modified bentonite as a high-efficiency and promising adsorbent to remove chloride ion from drinking water.

Activated Carbon with Ultrahigh Specific Surface Derived from Bamboo Shoot Shell through K2FeO4 Oxidative Pyrolysis for Adsorption of Methylene Blue.

To effectively remove methylene blue (MB) from dye wastewater, a novel activated carbon (BAC) was manufactured through co-pyrolysis of bamboo shoot shell and K2FeO4. The activation process was optimized to a temperature of 750 °C and an activation time of 90 min based on its excellent adsorption capacity of 560.94 mg/g with a yield of 10.03%. The physicochemical and adsorption properties of BACs were investigated. The BAC had an ultrahigh specific surface area of 2327.7 cm2/g and abundant active functional groups. The adsorption mechanisms included chemisorption and physisorption. The Freundlich model could be used to describe the isothermal adsorption of MB. The kinetics confirmed that the adsorption of MB belonged to the pseudo-second-order model. Intra-particle diffusion was the main rate-limiting step. The thermodynamic study showed that the adsorption process was endothermic and temperature was beneficial for the improvement of adsorption property. Furthermore, the removal rate of MB was 63.5% after three cycles. The BAC will have great potential for commercial development for purifying dye wastewater.

Application of Orange Peel Waste as Adsorbent for Methylene Blue and Cd2+ Simultaneous Remediation.

Pollution by dyes and heavy metals is one of the main concerns at the environmental level due to their toxicity and inefficient elimination by traditional water treatment. Orange peel (OP) without any treatment was applied to effectively eliminate methylene blue (MB) and cadmium ions (Cd2+) in mono- and multicomponent systems. Although the single adsorption processes for MB and Cd2+ have been investigated, the effects and mechanisms of interactions among multicomponent systems are still unclear. Batch experiments showed that in monocomponent systems, the maximum adsorption capacities were 0.7824 mmol g-1 for MB and 0.2884 mmol g-1 for Cd2+, while in multicomponent systems (Cd2+ and MB), both contaminants competed for the adsorption sites on OP. Particularly, a synergic effect was observed since the adsorption capacity of Cd2+ increased compared to the monocomponent system. Results of desorption and adsorbent reuse confirmed that the adsorbent presents good regeneration performance. The low cost of this material and its capacity for the individual or simultaneous removal of Cd2+ and MB in aqueous solutions makes it a potential adsorbent for polluted water treatment processes.

Removal of 142Pr from nuclear purity water using hydroxyapatite.

The adsorption of praseodymium using hydroxyapatite was evaluated. The hydroxyapatite (HAP) was characterized by X-ray diffraction (JCPDS 01-04-3708), scanning electron microscopy, BET specific surface area (54.2 m2/g), and point of zero charge (6.5). Adsorption kinetics and isotherms were evaluated at pH of 3 and 142Pr was determined using a gamma spectrometer. The adsorption of praseodymium was fast (1 min of contact) with an adsorption capacity of 1.68 mg/g and the data were best adjusted to the pseudo-second-order model, whereas the data of adsorption isotherm were best adjusted to the Langmuir model with a maximum adsorption capacity of 39.16 ± 0.20 mg/g. The thermodynamic parameters indicated that a physicochemical mechanism took place in the adsorption of praseodymium by HAP (adsorption enthalpy = 31.65 kJ/mol), the randomness of the system increased (adsorption entropy = 0.16 kJ/mol), and according with Gibbs free energy, the adsorption process was spontaneous at high temperature. The praseodymium in the hydroxyapatite is stable, it could not be desorbed using different solutions (ammonium sulfate, calcium chloride, sodium chloride, hydrochloric acid, and sodium hydroxide).

Biodegradable polymers and their nano-composites for the removal of endocrine-disrupting chemicals (EDCs) from wastewater: A review.

Endocrine-disrupting chemicals (EDCs) target the endocrine system by interfering with the natural hormones in the body leading to adverse effects on human and animal health. These chemicals have been identified as major polluting agents in wastewater effluents. Pharmaceuticals, personal care products, industrial compounds, pesticides, dyes, and heavy metals are examples of substances that could be considered endocrine active chemicals. In humans, these chemicals could cause obesity, cancer, Alzheimer's disease, autism, reproductive abnormalities, and thyroid problems. While in wildlife, dysfunctional gene expression could lead to the feminization of some aquatic organisms, metabolic diseases, cardiovascular risk, and problems in the reproductive system as well as its levels of hatchability and vitellogenin. EDCs could be effectively removed from wastewater using advanced technologies such as reverse osmosis, membrane treatment, ozonation, advanced oxidation, filtration, and biodegradation. However, adsorption has been proposed as a more promising and sustainable method for water treatment than any other reported technique. Increased attention has been paid to biodegradable polymers and their nano-composites as promising adsorbents for the removal of EDCs from wastewater. These polymers could be either natural, synthetic, or a combination of both. This review presents a summary of the most relevant cases where natural and synthetic biodegradable polymers have been used for the successful removal of EDCs from wastewater. It demonstrates the effectiveness of these polymers as favorable adsorbents for novel wastewater treatment technologies. Hitherto, very limited work has been published on the use of both natural and synthetic biodegradable polymers to remove EDCs from wastewater, as most of the studies focused on the utilization of only one type, either natural or synthetic. Therefore, this review could pave the way for future exploration of biodegradable polymers as promising and sustainable adsorbents for the removal of various types of pollutants from wastewater.

An Affordable Fabrication of a Zeolite-Based Capacitor for Gas Sensing.

The development of even more compact, inexpensive, and highly sensitive gas sensors is widespread, even though their performances are still limited and technological improvements are in continuous evolution. Zeolite is a class of material which has received particular attention in different applications due to its interesting adsorption/desorption capabilities. The behavior of a zeolite 4A modified capacitor has been investigated for the adsorption of nitrogen (N2), nitric oxide (NO) and 1,1-Difluoroethane (C2H4F2), which are of interest in the field of chemical, biological, radiological, and nuclear threats. Sample measurements were carried out in different environmental conditions, and the variation of the sensor electric capacitance was investigated. The dielectric properties were influenced by the type and concentration of gas species in the environment. Higher changes in capacitance were shown during the adsorption of dry air (+4.2%) and fluorinated gas (+7.3%), while lower dielectric variations were found upon exposure to N2 (-0.4%) and NO (-0.5%). The proposed approach pointed-out that a simple fabrication process may provide a convenient and affordable fabrication of reusable capacitive gas sensor.

Functionalized graphene nanosheets as absorbent for copper (II) removal from water.

Functionalized graphene nanosheets (FGNs) with high surface area and various functional groups were prepared by oxidation method. The characteristics of FGNs were studied by nitrogen adsorption using the Brunauer-Emmett-Teller (BET) method, Fourier transform infrared spectroscopy (FTIR), transmission electron microscope (TEM), scanning electron microscope (SEM), energy dispersion spectrum (EDS), and atomic force microscopy (AFM). The specific surface area of obtained FGNs was measured as 834.06 m2 g-1, which was 20-40% higher than graphene nanosheets (GNs) before oxidation. An abundance of oxygen-containing functional groups, such as carboxyl, hydroxyl and epoxy groups, was grafted on the edge and surface of GNs. Moreover, FGNs demonstrated excellent adsorption and desorption performance when used as absorbent to remove Cu (II) from aqueous solution. The removal percentage could reach 96% within 1 h and remain 72% after 5 adsorption-desorption cycles. Adsorption process and mechanism were elucidated by kinetics models and isotherm models. The results showed FGNs has a great potential to be an adsorbent for removal copper ions from water.

Recent advances in boron removal in aqueous media. An approach to the adsorption process and process optimization.

The numerous oxidation states of the element boron bring great challenges in containing its contamination in receptor bodies. This scenario increases significantly due to the widespread use of boron compounds in various industries in recent years. For this reason, the removal of this contaminant is receiving worldwide attention. Although adsorption is a promising method in boron removal, finding suitable adsorbents, that is, those with high efficiency, and feasible remains a constant challenge. Hence, this review presents the boron removal methods in comparison to costs of adsorbents, reaction mechanisms, economic viability, continuous bed application, and regeneration capacity. In addition, the approach of multivariate algorithms in the solution of multiobjective problems can enable the optimized conditions of dosage of adsorbents and coagulants, pH, and initial concentration of boron. Therefore, this review sought to comprehensively and critically demonstrate strategic issues that may guide the choice of method and adsorbent or coagulant material in future research for bench and industrial scale boron removal.

Fabrication of lignosulfonate-derived porous carbon via pH-tunable self-assembly strategy for efficient atrazine removal.

Herein, a straightforward protocol was developed for the one-pot synthesis of N-doped lignosulfonate-derived carbons (NLDCs) with a tunable porous structure using natural amino acids-templated self-assembly strategy. Specifically, histidine was employed as a template reagent, leading to the preparation of 10-NLDC-21 with remarkable characteristics, including the large specific surface area (SBET = 1844.5 m2/g), pore volume (Vmes = 1.22 cm3/g) and efficient adsorption for atrazine (ATZ) removal. The adsorption behavior of ATZ by NLDCs followed the Langmuir and pseudo-second-order models, suggesting a monolayer chemisorption nature of ATZ adsorption with the maximum adsorption capacity reached up to 265.77 mg/g. Furthermore, NLDCs exhibited excellent environmental adaptability and recycling performance. The robust affinity could be attributed to multi-interactions including pore filling, electrostatic attraction, hydrogen bonding and π-π stacking between the adsorbents and ATZ molecules. This approach offers a practical method for exploring innovative bio-carbon materials for sewage treatment.

Investigation into the characteristics of electron beam-aged microplastics and adsorption behavior of dibutyl phthalate.

Microplastics are increasingly prevalent in the environment, and their ability to adsorb various organic additives, posing harm to organisms, has attracted growing attention. Currently, there are no effective methods to age microplastics, and there is limited discussion on the subsequent treatment of aged microplastics. This study focuses on micro polyethylene (PE) and employs electron beam technology for aging treatment, investigating the adsorption and leaching behavior between PE and dibutyl phthalate (DBP) before and after aging. Experimental results indicate that with increasing doses of electron beam irradiation, the surface microstructure of PE worsens, inducing the generation of oxygen-containing functional groups on the surface of polyethylene. Comparative evaluations between electron beam aging and existing methods show that electron beam technology surpasses existing aging methods, achieving a level of aging exceeding 0.7 within an extremely short period of 1 min at doses exceeding 350 kGy. Adsorption experiments demonstrate that the adsorption between PE and DBP conforms to pseudo-second-order kinetics and the Freundlich model both before and after aging. The adsorption capacity of microplastics for DBP increases from 76.8 mg g-1 to 167.0 mg g-1 after treatment, exceeding that of conventional DBP adsorbents. Electron beam irradiation causes aging of microplastics mainly through the generation of ·OH, which lead to the formation of oxygen-containing functional groups on the microplastics' surface, thereby enhancing their adsorption capacity for DBP. This provides a new perspective for the degradation of aged microplastics and composite pollutants.

Electron beam synergetic removal of microplastics and hexavalent chromium: Synergetic removal process and mechanism.

Microplastics are ubiquitous in the environment and aged microplastics are highly susceptible to absorbing pollutants from the environment. In this study, electron beam was innovatively used to treat PVC composite Cr(VI) pollutants (Composite contaminant formed by polyvinyl chloride microplastics with the heavy metal hexavalent chromium). Experiments showed that electron beam was able to achieve synergistic removal of PVC composite Cr(VI) pollutants compared to degrading the pollutants alone. During the electron beam removal of PVC composite Cr(VI) pollutants, the reduction efficiency of Cr(VI) increased from 57% to 92%, Cl- concentration increased from 3.52 to 12.41 mg L-1, and TOC concentration increased from 16.72 to 26.60 mg L-1. The research confirmed that electron beam can effectively promote the aging degradation of PVC, alter the physicochemical properties of microplastics, and generate oxygen-containing functional groups on the surface of microplastics. Aged microplastics enhanced the adsorption capacity for Cr(VI) through electrostatic and chelation interactions, and the adsorption process followed second-order kinetics and the Freundlich model. Theoretical calculations and experiments demonstrated that PVC consumed oxidizing free radical through dechlorination and decarboxylation processes, generating inorganic ions and small organic molecules. These inorganic ions and small organic molecules further reacted with oxidizing free radical to produce reducing free radicals, facilitating the reduction of Cr(VI). Cr(VI) continuously consumed the educing free radicals to transform into Cr (Ⅲ), enhancing the system oxidative atmosphere and promoting the oxidation degradation of PVC. This study investigated the formation and synergistic removal processes of PVC composite pollutants, offering new insights for controlling microplastics composite pollution.

Enhanced Dye Adsorption on Cold Plasma-Oxidized Multi-Walled Carbon Nanotubes: A Comparative Study.

The oxidation of multi-walled carbon nanotubes (MWCNTs) using cold plasma was investigated for their subsequent use as adsorbents for the removal of dyes from aqueous solutions. The properties of MWCNTs after plasma modification and their adsorption capacities were compared with pristine and chemically oxidized nanotubes. The modification process employed a reactor where plasma was generated through dielectric barrier discharges (DBD) powered by high-voltage nanosecond pulses. Various modification conditions were examined, such as processing time and pulse voltage amplitude. The degree of oxidation and the impact on the chemistry and structure of the nanotubes was investigated through various physicochemical and morphological characterization techniques (XPS, BET, TEM, etc.). Maximum oxidation (O/C = 0.09 from O/C = 0.02 for pristine MWCNTs) was achieved after 60 min of nanopulsed-DBD plasma treatment. Subsequently, the modified nanotubes were used as adsorbents for the removal of the dye methylene blue (MB) from water. The adsorption experiments examined the effects of contact time between the adsorbent and MB, as well as the initial dye concentration in water. The plasma-modified nanotubes exhibited high MB removal efficiency, with adsorption capacity proportional to the degree of oxidation. Notably, their adsorption capacity significantly increased compared to both pristine and chemically oxidized MWCNTs (~54% and ~9%, respectively). Finally, the kinetics and mechanism of the adsorption process were studied, with experimental data fitting well to the pseudo-second-order kinetic model and the Langmuir isotherm model. This study underscores the potential of plasma technology as a low-cost and environmentally friendly approach for material modification and water purification.

Adsorption mechanism of hexavalent chromium on electron beam-irradiated aged microplastics: Novel aging processes and environmental factors.

Microplastics are widely present in the natural environment and exhibit a strong affinity for heavy metals in water, resulting in the formation of microplastics composite heavy metal pollutants. This study investigated the adsorption of heavy metals by electron beam-aged microplastics. For the first time, electron beam irradiation was employed to degrade polypropylene, demonstrating its ability to rapidly age microplastics and generate a substantial number of oxygen-containing functional groups on aged microplastics surface. Adsorption experiments revealed that the maximum adsorption equilibrium capacity of hexavalent chromium by aged microplastics reached 9.3 mg g-1. The adsorption process followed second-order kinetic model and Freundlich model, indicating that the main processes of heavy metal adsorption by aged microplastics are chemical adsorption and multilayer adsorption. The adsorption of heavy metals on aged microplastics primarily relies on the electrostatic and chelation effects of oxygen-containing functional groups. The study results demonstrate that environmental factors, such as pH, salinity, coexisting metal ions, humic acid, and water matrix, exert inhibitory effects on the adsorption of heavy metals by microplastics. Theoretical calculations confirm that the aging process of microplastics primarily relies on hydroxyl radicals breaking carbon chains and forming oxygen-containing functional groups on the surface. The results indicate that electron beam irradiation can simultaneously oxidize and degrade microplastics while reducing hexavalent chromium levels by approximately 90%, proposing a novel method for treating microplastics composite pollutants. Gas chromatography-mass spectrometry analysis reveals that electron beam irradiation can oxidatively degrade microplastics into esters, alcohols, and other small molecules. This study proposes an innovative and efficient approach to treat both microplastics composite heavy metal pollutants while elucidating the impact of environmental factors on the adsorption of heavy metals by electron beam-aged microplastics. The aim is to provide a theoretical basis and guidance for controlling microplastics composite pollution.

Activated Carbon Prepared from Waste Coffee Grounds: Characterization and Adsorption Properties of Dyes.

Spent coffee grounds (SCGs) have great potential as a useful, value-added biological material. In this context, activated carbon (AC) was prepared from SCGs by an activation process using H3PO4 at 600 °C in the air and used as an adsorbent for the azo dye AO7, a model molecule for dye colorants found in textile industry effluents. X-ray diffraction, SEM and BET revealed that the AC was predominantly amorphous, consisting of a powder of 20-100 µm particles with mesopores averaging 5.5 nm in pore size. Adsorption kinetics followed a pseudo-second-order law, while the Langmuir model best fitted the experimental isotherm data (maximum capacity of 119.5 mg AO7 per AC g). The thermodynamic parameters revealed that adsorption was endothermic and spontaneous. All the characterizations indicated that adsorption occurred by physisorption via mainly π-π interactions. The best experimental removal efficiency optimized by means of a Box-Behnken design and response surface methodology was 98% for an initial AO7 concentration of 20 mg·L-1 at pH 7.5 with a dose of 0.285 g·L-1 of AC and a contact time of 40 min. These results clearly show that activated carbon prepared from SCGs can be a useful material for efficiently removing organic matter from aqueous solutions.

Tecoma stans floral extract-mediated synthesis of MgFe2O4/ZnO nanoparticles for adsorption and photocatalytic degradation of coomassie brilliant blue dye.

Toxic organic dyes-containing wastewater treatment by adsorption and photocatalytic techniques is widely applied, but adsorbents and photocatalysts are often synthesized through chemical methods, leading to secondary pollution by released chemicals. Here, we report a benign method using Tecoma stans floral extract to produce MgFe2O4/ZnO (MGFOZ) nanoparticles for adsorption and photocatalytic degradation of coomassie brilliant blue (CBB) dye. Green MGFOZ owned a surface area of 9.65 m2/g and an average grain size of 54 nm. This bio-based nanomaterial showed higher removal percentage and better recyclability (up to five cycles) than green MgFe2O4 and ZnO nanoparticles. CBB adsorption by MGFOZ was examined by kinetic and isotherm models with better fittings of Bangham and Langmuir or Temkin. RSM-based optimization was conducted to reach an actual adsorption capacity of 147.68 mg/g. Moreover, MGFOZ/visible light system showed a degradation efficiency of 89% CBB dye after 120 min. CBB adsorption can be controlled by both physisorption and chemisorption while •O2- and •OH radicals are responsible for photo-degradation of CBB dye. This study suggested that MGFOZ can be a promising adsorbent and catalyst for removal of organic dyes in water.

Removal of Methylene Blue from Aqueous Solutions by Surface Modified Talc.

In this study, raw talc powder surface modification was conducted, and the powder was modified in two different methods using acid washing and ball milling. Modified talc was characterized by X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). In order to investigate the adsorption capacity of modified talc on dyes, adsorption experiments were carried out with methylene blue (MB) in aqueous solutions as the target contaminant. The findings of the characterization revealed that both modifications increased the adsorption capacity of talc, which was attributed to changes in specific surface area and active groups. The influence of process parameters such as contact time, pH, dye concentration, and adsorbent dosage on the adsorption performance was systematically investigated. Modified talc was able to adsorb MB rapidly, reaching equilibrium within 60 min. Additionally, the adsorption performance was improved as the pH of the dye solution increased. The isotherms for MB adsorption by modified talc fitted well with the Langmuir model. The pseudo-second-order model in the adsorption kinetic model properly described the adsorption behavior. The results show that the modified talc can be used as an inexpensive and abundant candidate material for the adsorption of dyes in industrial wastewater.

Effects of activated earth, activated alumina, and chitosan adsorption processes on thermal and rheological and chemical characteristics of menhaden oil.

The objective of this study was the effectiveness of using activated earth, activated alumina, and/or chitosan, either separately or in combination, as adsorbents to remove free fatty acids (FFA) and peroxides from unpurified menhaden oil (MO). Thermal and rheological properties of MO were also evaluated. Five different combinations of absorbents were used to purify MO: Processes 1-3 involved purifications of MO by 5% chitosan (wt/wt of oil), 5% activated earth, and 5% activated alumina, respectively, process 4 involved MO purification with a combination of 6.5% chitosan, 3.5% activated earth, and 5% activated alumina, and process 5 involved MO purification process with a combination of adsorbents of 9% chitosan, 1% activated earth, and 5% activated alumina. All the adsorption processes were conducted at 25°C. Purified MO and MO were evaluated for their fatty acid profile, FFA, peroxide value (PV), moisture content (MC), minerals, and color. Triplicate experiments were conducted, and data were statistically analyzed using α = 0.05. Processes 4 and 5 were effective in reducing PV, FFA, and MC in MO. Thermal properties indicated processes 4 and 5 produced purer MO than processes 1-3. All the oil samples became less viscous, and the flow behavior index of MO was close to 1 after the adsorption processes. This study demonstrated that adsorption processes that include chitosan, activated earth, and activated alumina could effectively improve MO quality.

Occurrence and removal of benzotriazole and benzothiazole in drinking water treatment plants.

The occurrence and removal of four benzotriazoles (BTRs) and five benzothiazoles (BTHs) in drinking water treatment plants (DWTPs) and bottled water were investigated. The mean total BTR and BTH concentrations were 390 and 117 ng/L in raw water, 51.2 and 66.5 ng/L in treated water, and 0.758 and 48.4 ng/L in bottled water, respectively. Different distribution patterns were observed according to the water type, with the dominant BTR being 1H-BTR (mean: 57.8%) in raw water and a predominance of BTH in bottled water (mean: 84.6%). In the DWTPs, the mean removal of BTRs (90.9%) was better than that of BTHs (29.3%). The BTRs were efficiently removed in DWTPs, and in particular during adsorption processes. 5Cl-BTR had a high removal efficiency (75.7%) in the adsorption processes, followed by 5M-BTR (70.0%), 5,6-di-MeBTR (58.4%), and 1H-BTR (50.1%). By contrast, BTHs were not efficiently removed in DWTPs, although relatively high removal efficiencies were achieved with an ozonation process (43.1%) compared to other treatment processes. In treated drinking and bottled water, the hazard quotients (HQs) of the representative BTRs and BTHs were acceptable (defined as HQ < 1), with a safety margin of 2-5 orders of magnitude.