Efficacy Of Removal Research Articles

Influence of rubber particle inputs on nitrogen removal efficiency of bioretention systems

ABSTRACT Bioretention systems effectively capture rubber particles and other microplastics in stormwater runoff. However, it is uncertain whether long-term particle accumulation affects pollutant removal efficacy. This study investigated the impact of various concentrations of ethylene-propylene-diene-monomer (EPDM) particles (0, 50, 100, and 400 mg/L) on bioretention system nitrogen removal performance. The input of EPDM during short-duration (2 h) rainfall favored the removal of nitrogen, and the total nitrogen effluent concentration of the bioretention system with EPDM was reduced by 0.59–1.52 mg/L compared with that of the system without EPDM. In addition, the input of EPDM reduced the negative effects of drought. During long-duration (24 h) rainfall, higher concentrations of EPDM led to lower nitrate–nitrogen concentrations in the effluent. The bioretention system with EPDM required less time for nitrate–nitrogen removal to reach 50% than that without EPDM input. Microbial community analysis showed that EPDM increased the relative total abundance of denitrifying bacteria (such as Dechloromonas, Zoogloea, Ramlibacter, and Aeromonas) by 7.25–10.26%, which improved the denitrification capacity of the system.

Increase flavour quality of Sichuan pepper(Zanthoxylum bungeanum Maxim.)with optimized cleaning technology: soaking and spraying

The current study presents the development of a specialized cleaning device for Sichuan pepper, which explores the effects of soaking technology, a combined soaking and spraying technology, and uncleaned on the quality of Sichuan pepper and its processed derivatives. The findings reveal that the highest impurity removal ratio achieved through this combined method was 78.385%. Furthermore, after employing the soaking and spraying technology, the concentration of numbing compounds in dried Sichuan pepper increased from 90.86 mg/g to 102.62 mg/g over a storage period of 120 days. Following the application of three distinct methods, the numbing compounds in Sichuan pepper oils ranged 4.88∼4.95 mg/g. Additionally, the volatile oil content in two varieties of cleaned dried Sichuan pepper was recorded at 11.79 mL/100 g and 11.65 mL/100 g, both of which exceeded the levels found in uncleaned pepper. These results suggest that cleaning demonstrated significant efficacy in impurity removal and in mitigating the deterioration of the color of dried Sichuan pepper. Notably, the combined soaking and spraying cleaning method exhibited superior preservation effects on the content of numbing compounds and volatile aromatic components in Sichuan pepper products, thereby effectively prolonging the shelf life of dried Sichuan pepper.

Silicon dioxide incorporated cellulose acetate-mixed matrix membranes for Safranin-O removal from aqueous solutions.

Nanoparticle incorporated-mixed matrix membranes are renowned for their multifaceted advantages, including improved hydrophilicity, elevated solute rejection, enhanced mechanical robustness, and augmented chemical and thermal stability. The inherent hydrophilicity of silicon dioxide (SiO2) nanoparticles, due to silanol groups (Si-OH), along with their high porosity and surface area, renders them an ideal reinforcing filler within polymer matrices, significantly strengthening structural integrity of membranes. In this work, SiO2 nanoparticles were incorporated in a cellulose acetate (CA) matrix to prepare CA/SiO2 adsorptive membranes using phase inversion method. The performance of the membranes was assessed on the removal of Safranin-O (Sf-O) from aqueous solution. The physicochemical characterization of the synthesized membranes was assessed using contact angle, XRD, FE-SEM, EDS, FTIR, TGA, and tensile strength studies. The optimization studies on novel CA/SiO2 membrane revealed that the membrane with 2.5 wt.% of SiO2 in the CA matrix was the best in terms of Sf-O removal (approximately 100% dye removal) when the operating pH, initial dye concentration, and operating pressure were 9, 50 ppm, and 1 bar respectively. It is also found that 2.5 wt.% CA/SiO2 membrane has higher water permeability than other membranes. Incorporating SiO2 nanoparticles into a polymer matrix augments the structural, mechanical, and thermal properties of the resulting membranes while also enhancing water permeability, selectivity, and dye removal efficacy.

Innovative Use of Spirogyra sp. Biomass for the Sustainable Adsorption of Aflatoxin B1 and Ochratoxin A in Aqueous Solutions

This research investigates the efficacy of Spirogyra sp. biomass as an effective adsorbent for the removal of AFB1 and OTA from aqueous solutions. Several factors, including contact time, adsorbent dosage, pH level, and initial mycotoxin concentration, were analyzed to evaluate their impact on adsorption efficacy. The optimal contact time for equilibrium was determined at 60 min, during which the TPA obtained a 91% reduction in AFB1 and 68% removal of OTA. Although increasing the adsorbent dosage improved effectiveness, excessive quantities led to particle aggregation, hence diminishing adsorption performance. The optimal dosage of 5.0 mg/mL optimized the efficacy and use of resources. Adsorption was more efficacious at acidic to neutral pH levels (5–6), enhancing the accessibility of functional groups on the biomass. Kinetic analysis indicated that adsorption process followed a pseudo second-order model, whereas isotherm studies demonstrated a heterogeneous adsorption mechanism, with the Freundlich model providing the optimal fit. The TPB exhibited enhanced adsorption capacities for both mycotoxins, offering a viable solution for mitigating mycotoxin contamination in food and feed. These findings illustrate the significance of biomass treatment techniques in improving mycotoxin removal efficacy and suggest the potential of algal biomass in food safety applications.

Enhanced nitrogen and phosphorus removal from mariculture water using immobilized bacteria and macroalgae

With the vigorous development of the mariculture industry, the untreated wastewater from mariculture has exerted significant pressure on the water environment. The untreated N and P in the wastewater from mariculture can deteriorate the quality of the mariculture. In this study, a composite in situ treatment system involving macroalgae (Caulerpa lentillifera/Caulerpa sertularoides f. Longipes) and immobilized degrading bacteria was established to handle wastewater from shrimp culture. The changes in nutrients in aquaculture wastewater were studied by chemical analysis, and the microbial community structure was analyzed using molecular biology technology and high-throughput sequencing technology. The removal efficacy of nutrients in aquaculture wastewater and the composition of microorganisms in the wastewater were examined, and the primary causes for the alteration of the microbial community were analyzed. The results demonstrated that when the macroalgae in the system were Caulerpa lentillifera (CL), the removal efficiencies of TN, PO43--P, and COD from shrimp culture were 59.04%, 34.26%, and 68.61% respectively. When the macroalgae was Caulerpa sertularoides f. Longipes (CSF), the removal efficiencies of TN, PO43--P, and COD generated by experimental shrimp culture were 51.50%, 33.69%, and 50.88% respectively. The biomass (wet weight) of both macroalgae species also increased, facilitating the removal of nutrients from the wastewater. Additionally, both Proteobacteria and Bacteroidetes were the dominant bacteria in the three samples, and the addition of the composite in-situ treatment system had no impact on the dominant bacteria in the water. The results of FAPROTAX analysis indicated that compared with the untreated samples, the abundances of methyl-functional bacteria and amino acid-functional bacteria in the samples increased due to organic matter such as COD produced during shrimp culture and the addition of feed, suggesting that shrimp culture can influence the abundances of functional bacteria in the water. In conclusion, the combined in situ treatment system can effectively eliminate nutrients from aquaculture wastewater, and the combined effect of macroalgae and immobilized degrading bacteria plays a vital role in this process.

Surface water removal of Aluminum(III), Iron(III) and Manganese(II) using sustainable natural serpentinite mining tailings, proof of concept

To remediate surface water as the Doce River and spring waters from Minas Gerais, Brazil, this study examined the possibility of natural serpentinite mining tailings as a sustainable alternative for removing aluminum (III), iron (III), and manganese (II). The study used a Box-Behnken experimental design to examine how initial metal concentration, adsorbate dosage, and adsorption time affect metal removal effectiveness. Results demonstrated impressive performance, with removal rates exceeding 80 % for Al(III) and Fe(III) within the initial 5 min, and 60 % for Mn(II) within 30 min. This study delves deeper into the removal mechanisms, kinetics, adsorption isotherms and characterization identify physisorption and chemisorption pathways in which complex formation with released OH− groups and ion exchange with Mg(II) from serpentinite emerged as key contributors to the removal process. Furthermore, ion metal adsorption and regeneration cycles were assessed, exhibit sustained removal efficacy without notable capacity reduction. Each cycle shows an average metal adsorption capacity of 0.32 mg g−1 and an average Mg(II) release capacity of 0.98 mg g−1. Remarkably, the application of serpentinite successfully lowered the metals content of the Doce River and spring water to drinkable standards. A batch and continuous process is proposed for scaling-up serpentinite's metal adsorption. Overall, this study shows serpentinite's potential as a foundation for sustainable and cost-effective methods to treat surface water contamination with Al(III), Fe(III), and Mn(II).

Numerical Analysis of Optimising Liquid Desiccant Dehumidification for Sustainable Building Cooling: A Data-Driven Method Using Response Surface Methodology

Leveraging data-driven methods such as Response Surface Methodology (RSM) has considerable potential for sustainable building cooling via mitigating energy consumption and environmental impacts. This research focuses on using the RSM to improve liquid desiccant dehumidification for sustainable building cooling performance using a D-optimal design. Specifically, the research intends to investigate the actual influence of the inlet air conditions and desiccant concentration on the performance of liquid desiccant dehumidification systems, i.e., the moisture removal rates and dehumidifier efficiency. To systematically conduct this research, a set of experimental data gathered from the open literature is utilised. This includes a specific set of inlet parameters of air temperature (27–34.5 °C), ratio of air humidity (20.5–25 g/kg), and solution temperature (27.5–38.5 °C) as the independent variables. Also, the feedback variables include the moisture removal rates (MRR) and efficacy (ϵ). The associated results of the analysis of variation indicate that the ratio of air humidity has the greatest influence on the moisture removal rate. However, the solution temperature and the ratio of air humidity have the most influence on efficacy. In the event of response optimisation, the result at MRR and (ϵ) are 0.54 g/s and 0.50, respectively, with a minimum desirability of 0.992 and 1.

Boosting SO2-tolerance of Mn-doped CeO2-ZrO2 for Hg catalytic oxidation via NaOH etching

Manganese-doped CeO2-ZrO2 solid solution (CZM) is a prominent sorbent for extracting Hg0 from flue gas, operating optimally around 150 °C, but impaired by SO2 exposure. In this research, we apply a hydrothermal method, employing a sodium hydroxide (NaOH) solution, to enhance CZM's SO2 resilience. The detrimental effect of SO2 on CZM primarily arises from the reduction of active oxygen species, diminishing Hg0 removal efficacy. After conducting a 10-hour test in the atmosphere comprising N2, 6 %O2, and 500ppmSO2, the mercury removal efficiency of the unmodified CZM significantly decreased from ∼99.5 % to ∼26.0 %. Conversely, the modified sorbents, designated as CZM-1M, demontrasted enhanced stability, with its mercury removal efficiency modestly reducing from ∼97 % to ∼60 %. We then conducted comprehensive characterizations of both sorbents to understand the mechanism behind this improved SO2 tolerance. In CZM-1M, we noted an enhanced conversion rate from Ce4+ to Ce3+, a key factor in boosting the production of active oxygen species, necessary for Hg0 oxidation. Additionally, the formation of SO3 - a result of the interaction between the abundant oxygen species and SO2 - emerged as a novel active site that further promoted Hg0 oxidation. This shift in active site offers a pathway for enhancing SO2 resistance in such material.

Preparation of Polyvinyl Alcohol–Chitosan Nanocellulose–Biochar Nanosilver Composite Hydrogel and Its Antibacterial Property and Dye Removal Capacity

In this research, silver-loaded biochar (C-Ag) was acquired from a waste fish scale, and nanocellulose (CNF) was prepared from the waste wheat stalk. Then C-Ag was loaded into chitosan-polyvinyl alcohol hydrogel (CTS-PVA) with CNC as a reinforcement agent, and a novel nanocomposite material was acquired, which could be efficiently applied for antibacterial and dye removal. By plate diffusion analysis, the inhibition areas of C-Ag-CTS-PVA-CNF (C/CTS/PVA/CNF) hydrogel against E. coli ATCC25922, S. aureus ATCC6538, and P. aeruginosa ATCC9027 could reach 22.5 mm, 22.0 mm, and 24.0 mm, respectively. It was found that the antibacterial rate was 100% in the water antibacterial experiment for 2 h, and the antibacterial activity was more than 90% within 35 days after preparation, and the antibacterial rate was more than 90% after repeated antibacterial tests for five times. Through swelling, water adsorption, water loss rate, and water content tests, the hydrogel manifested good moisturizing properties and could effectually block the loss of water and improve the stability of the C/CTS/PVA/CNF hydrogel. The pseudo-first-order and pseudo-second-order models were built, and the adsorption capacity of hydrogel to dye was analyzed, and the dye removal was more consistent with the pseudo-first-order kinetic model. The best removal effect for Congo red was 96.3 mg/g. The C/CTS/PVA/CNF hydrogel had a remarkable removal efficacy on Malachite green, Methyl orange, Congo red, and Methylene blue. As a result, the C/CTS/PVA/CNF hydrogels had robust antibacterial properties and reusability. In addition, the present research developed a facile strategy for effectual dyes removal from the aqueous medium.

Using syringe filtration after lab-scale adsorption processes potentially overestimates PFAS adsorption removal efficiency from non-conventional irrigation water.

The adsorption process, known for its cost-effectiveness and high efficiency, has been extensively investigated at the laboratory scale for removing per- and polyfluoroalkyl substances (PFAS) from non-conventional irrigation water. However, a syringe filtration step is commonly used when quantifying PFAS removal during this adsorption process, potentially leading to PFAS retention onto the filters and an overestimate of adsorption removal efficiency. Here, we assessed the retention of three prevalent PFAS (i.e., perfluorooctanoic acid [PFOA], perfluorooctane sulfonic acid [PFOS], and perfluorobutanoic acid [PFBA]) on six syringe filters. When filtering distilled deionized water spiked with 1µg/L and 100µg/L of each PFAS, we observed the highest and lowest PFAS recovery percentages by mixed cellulose ester (MCE) (0.20µm, 25mm; 97±11%, 101±4.8%) and polytetrafluoroethylene (0.45µm, 13mm; 61±37%, 80±28%), respectively. Under the initial concentration of 1µg/L and 100µg/L, PFOS had recovery percentages of 55±25% and 68±24%, significantly lower than 96±12% and 99±5% for PFOA and 95±8% and 97±4% for PFBA, highlighting the importance of PFAS functional groups. PFAS recovery percentage increased with filtration volume in the order of 80±28% (1mL)<85±21% (5mL)<90±18% (10mL). Using MCE to filter treated municipal wastewater spiked with 1µg/L and 100µg/L of each PFAS, we found recovery percentages>90% for all three PFAS. Our study underscores the significance of syringe filter selection and potential overestimate of PFAS removal efficacy by the lab-scale adsorption processes.

Post-Space Disinfectants With Sodium Hypochlorite and Methylene Blue Loaded in Silver and Quartz Nanoparticles Activated by Photodynamic Therapy. A SEM Analysis.

Post-space disinfectants methylene blue loaded with silver (Ag) and Quartz nanoparticles (NPs) and MB alone activated by photodynamic therapy (PDT) on the survival of Enterococcus faecalis, smear layer (SL) removal efficacy, and extrusion bond strength (EBS) of fiber posts to canal dentin. Hundred mandibular premolars underwent root canal treatment using the rotary ProTaper system. The canals were obturated and post-space was prepared up to a length of 8 mm, maintaining a 5 mm seal. To assess antibacterial efficacy E. faecalis were inoculated in the canal (n = 20). The samples were then randomly allocated into four groups according to the canal disinfectant used to sterilize the canals. Group 1: 2.5% NaOCl+17% EDTA, Group 2: MB-PDT, Group 3: MB@QP-PDT, and Group 4: MB@AgNP-PDT (n = 25). SEM analysis was conducted on five samples from each disinfectant group to assess the removal of the SL. Survival rates were calculated (n = 5 from each group). Glass fiber post (GFP) was cemented to the root dentin of the remaining samples followed by artificial aging. Sectioning of the specimens was performed in all three-thirds of the canals. PBS was assessed followed by failure evaluation. ANOVA and Tukey post hoc test were used to compare the E. faecalis survival rate and PBS of fiber post among different investigated groups. Group 4 (MB@AgNP-PDT) treated canals exhibited the minimum survival rate (0.30 ± 0.04 CFU/mL) of E. faecalis and maximum PBS. However, the highest survival rate and minimum bond strength of GFP were observed in Group 1 (NaOCl+17% EDTA) and Group 2 (MB-PDT) treated teeth respectively. The highest SL removal was recorded in the coronal section of the samples of Group-4 disinfected with MB@AgNP-PDT. The lowest removal of SL was recorded in Group 2 samples sterilized with MB-PDT at apical one-third. Silver nanoparticles when utilized as nano-carriers to enhance the efficiency of MB activated by PDT, have been shown to exhibit the highest antimicrobial potency, improved capacity for SL removal and improved PBS.

Immobilization of Cadmium Via Ureolytic Bacteria Isolated from Greywater Waste and Horse Faeces

With the constant growth of technology and pollution caused by urban expansion, heavy metal contamination has become an alarming concern. The performance of Microbial induced carbonate precipitation technology in immobilizing heavy metal has been demonstrated by several researchers. While various studies have successfully isolated ureolytic bacteria from a variety of sources, there are very limited studies that have focused on isolating them from local waste sources, specifically Greywater and Horse Faeces for MICP application, which benefits in terms of economical, sustainability, and efficiency for engineering purposes. The study aims to investigate the effect of urease-producing bacteria derived from Greywater and horse faeces on heavy metal immobilization. The methods include collecting waste samples, isolating and subculturing of ureolytic bacteria, testing the physiological characteristics of ureolytic bacteria, examining the tolerance test and evaluating heavy metal removal efficacy through Atomic Absorption Spectrophotometry (AAS) analysis, and last but not least, Scanning Electron Microscopy (SEM) and Energy-Dispersive X-ray (EDX) analyses of morphological and mineralogical properties of biominerals formed after heavy metal immobilization treatment. The study found that bacteria from Greywater were more effective at heavy metal immobilization than those from Horse Faeces. Additionally, AAS analysis indicates the greywater-derived bacteria from the residential area sample's exceptional competence in Cd2+ removal, with a significant 80.19% removal rate exceeding the horse faeces bacteria sample's removal rate of 65.26%. The morphological analysis confirmed the presence of heavy metal carbonate in treated heavy metal samples, as well as presenting insight into the effectiveness and application of local ureolytic bacteria's potential for heavy metal toxicity degradation.

Heavy Metal Removal from Water Using Graphene Oxide in Magnetic-Assisted Adsorption Systems: Characterization, Adsorption Properties, and Modelling

This study investigated the adsorption properties of graphene oxide in a magnetic-assisted adsorber for the depollution of water containing heavy metals. Two samples of graphene oxide with different surface chemistry were synthetized and assessed using the magnetic-assisted adsorption systems. One graphene oxide sample exhibited a dual magnetic behavior presenting both diamagnetic and ferromagnetic phases, while the other graphene oxide was diamagnetic. The adsorption properties of these graphene oxide samples for removing Pb2+ and Cu2+ were tested and compared with and without a magnetic field exposure. The results showed that the Pb2+ removal increased using both graphene oxide samples in the magnetic-assisted configuration, while Cu2+ adsorption was less sensitive to the application of the magnetic field. A monolayer model was used to simulate all the heavy metal adsorption isotherms quantified experimentally. It was concluded that the adsorption mechanism designed to remove Pb2+ and Cu2+ using tested graphene oxide samples was mainly multi-ionic where two metallic cations could interact with one active site (i.e., oxygenated functional groups) from the adsorbent surface. The oxygenated surface functionalities of graphene oxide samples played a relevant role in determining the impact of magnetic field exposure on the heavy metal removal efficacy. Magnetic-assisted adsorption using graphene oxide is an interesting alternative to reduce the concentration of Pb2+ in polluted effluents, and it can also be applied to improve the performance of adsorbents with a limited concentration of oxygenated functional groups, which usually show poor removal of challenging water pollutants such as toxic heavy metals.

Adsorption performance and mechanism of single-component and multi-component VOCs by Beta zeolites with different Si/Al ratios

The physical and chemical properties of VOCs and zeolite materials generally affect adsorption efficacy for VOCs removal. Here, toluene and methanol were chosen as typical VOCs with different polarities and molecular diameters to investigate the performance and mechanism of their adsorption on Beta zeolites with various Si/Al ratios. It was found that high-silica Beta exhibited superior toluene adsorption capacity, while low-silica Beta showed higher methanol adsorption capacity. Compared with single-component adsorption, in the case of co-adsorption of toluene and methanol, the saturation adsorption capacities for toluene and methanol only changed slightly even with the existence of competitive adsorption and weakened adsorption strength. Importantly, there was almost no decrease in absorption capacity after 10 repeated adsorption-regeneration cycles, showing the excellent reusability of Beta zeolites for toluene and methanol removal. Whether on low-silica or high-silica Beta, physical adsorption of toluene and methanol was dominant, along with a small proportion of chemical adsorption on low-silica Beta based on acid sites. Similar size between the diameters of toluene and the pore channels of Beta zeolites was responsible for strong adsorption force, increase of adsorption capacity, and minor effect on absorption performance in the process of competitive adsorption. Strong interaction between acid sites and polar methanol through H-bond or non-polar toluene by electrostatic attraction promoted chemical adsorption. Furthermore, toluene and methanol both tended to absorb in the twelve-membered-ring of Beta zeolites on Si-OH-Al, Al-OH, and Si-OH sites. This study provides insight into the factors influencing the adsorption performance and mechanism of toluene and methanol on zeolites, which gives potential guidance for the selection of adsorbents for high-efficiency VOCs removal.

Unravelling the efficiency of CoAl-LDH / g-C3N4 nanosheets: Type-II heterojunction for photocatalytic hydrogen production and dye degradation under solar light irradiation

The generation of hydrogen fuel, and wastewater treatment according to solar-driven catalysis possesses considerable prospective for establishing a carbon-neutral and ecologically sound power infrastructure. Driven by this problem, we suggest in this study, adopting a simple impregnation method, a customized association of CoAl-LDH and graphitic carbon nitride (CN), a visible light active narrow and wide band gap semiconductors. Several characterization approaches were implemented to understand the CoAl-LDH@g-C3N4 (CACN) composites' physiochemical and optical features. The CACN hetero structural forms exhibited significantly improved solar light-induced photocatalytic H2 generation and dye pollutants decomposition in contrast with pristine materials. The most effective catalyst 5 wt% CoAl-LDH@g-C3N4 (5-CACN) generated the highest hydrogen (∼430.7 μmolg−1h−1), which is 11.9-fold H2 production efficiency compared with CN and depicted significant Brilliant black dye removal efficacy via photocatalytic degradation (up to ∼79%). This was primarily ascribed to the development of the Type-II CACN heterojunctions, which promoted the separation of charges and expanded the abundance of surface-active sites while absorbing the visible spectrum of solar light.

Substrate preference of Tetrasphaera in dual PAOs synergistic EBPR system and its phosphorus removal performance

In this study, an alternated anaerobic/aerobic sequencing batch reactor (SBR) was employed to investigate the effect of the substrate conversion from casein hydrolysate (Cas aa) to a mixture of amino acids (glutamate, aspartate, glycine and proline) on the efficacy of nitrogen and phosphorus removal in an enhanced biological phosphorus removal (EBPR) system characterized by dual polyphosphate-accumulating organisms (PAOs), mainly focusing on the substrate preference of fermentative PAOs. The results indicated that a stable removal efficiency was found to be above 90 % as the substrate was converted to the mixture of amino acids. Meanwhile, the removal efficiency of ammonium eventually increased to over 95 % in stage III, despite an increase of ammonia nitrogen by hydrolysis with the rising proportion of mixed amino acids in influent. Moreover, shortening the anaerobic duration did not significantly affect the phosphorus removal performance, even enhancing anaerobic phosphorus release capacity. Nevertheless, the ammonia nitrogen removal was influenced. 16 s rRNA high-throughput sequencing results demonstrated that the detected fermentative PAO like Tetrasphaera in the EBPR system exhibited a clear preference for utilizing mixed amino acids and could cooperate with traditional PAO like Accumulibacter for phosphorus removal. In addition, the fermentation of amino acids mixture by Tetrasphaera was more pronounced and its abundance increased under the condition of a shorter anaerobic duration, leading to a relatively stable and high abundance of Accumulibacter in the presence of sufficient substrates from Tetrasphaera. However, considering the nitrogen removal performance and steady operation of the EBPR system, a longer anaerobic duration was more reasonable.

Copper removal with chemically reinforced Leptolyngbya sp. GUEco 1015

Leptolyngbya sp. GUEco 1015, an autochthonous cyanobacterial strains isolated from copper rich hydrocarbon contaminated waterbodies of Assam (India), was subjected to different grades of two acids and one salt to retrieve their copper (Cu2+) removal efficacy. Pretreated Leptolyngbya biomass when considered as an alternative adsorbent showed better removal rate of toxic Cu2+in vitro. The experimental data confirmed that the strain could remove up to 96.77 %, 92.1 % and 88.14 % of Cu2+ with 0.3 mM HCl, 0.1 mM CaCl2, and 0.1 mM CH3COOH in pretreated in-vitro condition respectively from 0.1 ppm of initial Cu2+ concentration. A number of negatively charged functional groups (FG) like O-H, -NH, CO, diketones, C-O stretching and phenols are known to be involved in the adsorption events during the process. The study thus revealed that pretreated biomass of Leptolyngbya sp. GUEco 1015 with 0.3 mM HCl is obviously a feasible alternative as compared to CaCl2 and CH3COOH for Cu2+ removal.

Waste biomass-based graphene oxide decorated with ternary metal oxide (MnO-NiO-ZnO) composite for adsorption of methylene blue dye

In this study, a novel approach for the removal of methylene blue (MB) dye is effectively illustrated by using biomass based composite adsorbent. The investigation employed areca nut husk (AH) to produce graphene oxide (GO) by a single step calcination method. Thereafter, AH-GO was incorporated by using ternary metal oxide (TMO) via hydrothermal treatment. The developed AH-GO@MnO-NiO-ZnO composite was characterized by various analytical techniques, including FT-IR, XRD, FESEM, HRTEM, BET surface area and Raman spectroscopy which exhibited promising properties for dye adsorption. To study the adsorption efficiency of prepared composite, optimization experiments were performed for adsorbent dose, initial dye concentration and contact time. The optimized parameters during adsorption phenomenon were found to be 0.5g/L of dose, 20mg/L of initial concentration and 180min of time exhibiting removal efficacy of 93.05 ± 0.93%. Moreover, adsorption isotherm and kinetic models were analysed to explore the adsorption behaviour of AH-GO@MnO-NiO-ZnO towards MB dye. The adsorption isotherm and kinetic studies followed Langmuir isotherm model and pseudo-second-order (PSO) model respectively. AH-GO@MnO-NiO-ZnO has demonstrated a maximum adsorption capability of 127.06mg/g. These findings collectively underscore the potential of AH-based adsorbent as a viable, inexpensive, and environment friendly for the treatment of wastewater contaminated with MB dye.

A confocal laser scanning microscopic analysis of efficacy of different activated irrigants in the removal of calcium hydroxide medicament and subsequent penetrability of Bio-C sealer – An in vitro study

Abstract Aim: The aim of the study was to investigate the efficacy of different irrigants activated by pro-agitator tip system (PATS) Vario on the removal of calcium hydroxide medicament and subsequent penetration depth of Bio-C sealer. Materials and Methods: Fifty single-rooted mandibular premolars were selected. Access cavities were prepared; biomechanical preparation was done. Metapex that had been combined with rhodamine B dye was used to fill each sample. All the samples were divided into five groups (n = 10) – Group I: chitosan–citrate, Group II: intracanal heated sodium hypochlorite (NaOCl), Group III: phytic acid, Group IV: SmearClear, and Group V: saline. All samples were obturated using gutta-percha and Bio-C sealer (combined with fluorescein dye). Later, all samples were sectioned at 3, 6, and 9 mm from the apex and observed under a confocal microscope for residual Ca(OH)2 and sealer penetration into dentinal tubules. Results: The saline group exhibited the least amount of sealer penetration and high residual Ca(OH)2, both of which were statistically significant (P ≤ 0.05). Conclusion: The use of PATS Vario for irrigant activation enhanced the calcium hydroxide removal efficacy and penetration of Bio-C sealer into dentinal tubules. The elimination of calcium hydroxide and sealer penetration, from the apical region of the tooth, can be accelerated by intracanal heating of NaOCl.

Nutrient removal efficacy and microbial dynamics in constructed wetlands using Fe(III)-mineral substrates for low carbon-nitrogen ratio sewage treatment.

This study evaluated the roles of two common sources of Fe(III)-minerals-volcanic rock (VR) and synthetic banded iron formations from waste iron tailings (BIF-W)-in vertical flow-constructed wetlands (VFCWs). The evaluation was conducted in the absence of critical environmental factors, including Fe(II), Fe(III), and soil organic matter (SOM), using metagenomic analysis and integrated correlation networks to predict nitrogen removal pathways. Our findings revealed that Fe(III)-minerals enhanced metabolic activities and cellular processes related to carbohydrate decomposition, thereby increasing the average COD removal rates by 10.7% for VR and 5.90% for BIF-W. Notably, VR improved nitrogen removal by 1.70% and 5.40% compared to BIF-W and the control, respectively. Fe(III)-mineral amendment in bioreactors also improved the retention of denitrification and nitrification bacteria (phylum Proteobacteria) and anammox bacteria (phylum Planctomycetes), with increases of 3.60% and 3.20% using VR compared to BIF-W. Metagenomic functional predictionindicated that the nitrogen removal mechanisms in VFCWs with low C/N ratios involve simultaneous partial nitrification, ANAMMOX, and denitrification (SNAD). Network-based analyses and correlation pathways further suggest that the advantages of Fe(III)-minerals are manifested in the enhancement of denitrification microorganisms. Microbial communities may be activated by the functional dissolution of Fe(III)-minerals, which improves the stability of SOM or the conversion of Fe(III)/Fe(II). This study provides new insights into the functional roles of Fe(III)-minerals in VFCWs at the microbial community level, and provides a foundation for developing Fe-based SNAD enhancement technologies.