Fixed bed column adsorption systems to remove 2,4-Dichlorophenoxyacetic acid herbicide from aqueous solutions using magnetic activated carbon.

The widespread use of 2,4-Dichlorophenoxyacetic acid (2,4-D) as a weedkiller has resulted in its persistence in the environment, leading to surface and groundwater pollution. In this study, the fixed bed column experiments were performed to remove 2,4-D from aqueous solutions using magnetic activated carbon derived from Peltophorum pterocarpum tree pods. The evaluation was done on effects of operating parameters such as bed depth (2-4 cm), influent flow rate (4.6-11.4 mL/min), and 2,4-D concentration (25-100 mg/L) on the breakthrough curves. The data fit well with the Yoon-Nelson and Thomas models, exhibiting high R2 values. Results indicated that lower flow rates, lower 2,4-D concentrations, and greater bed depths enhanced adsorption capacity, achieving up to 196.31 mg/g. Reusability studies demonstrated the material's potential for repeated use, while toxicity studies with Vigna radiata seeds confirmed the effectiveness of Fe3O4-CPAC in removing 2,4-D. This investigation highlights the promising application of Fe3O4-CPAC in fixed bed adsorption systems for efficient 2,4-D removal.

Multifunctional hydrophobin-like protein (HFB-NJ1): A versatile solution for wastewater treatment.

As wastewater contains a variety of contaminating bacteria and oily residues, there is an urgent need for environmentally safe bactericidal agents and surfactants which can be applied for wastewater treatment. The present study emphasizes on the potential of hydrophobin-like protein (HFB-NJ1) extracted from sporulating mycelia of Aspergillus sp. NJ1 for wastewater treatment. The purified HFB-NJ1, depicted the presence of one single protein band of molecular size approximately 11-12 kDa on silver-stained SDS-PAGE gel. HFB-NJ1 also presented properties such as surface modification of glass and stable emulsification of sunflower oil. HFB-NJ1 depicted exceptional antibacterial activity against bacterial pathogens such as Bacillus subtilis and Pseudomonas aeruginosa at low MIC of 0.5 µg/mL and 0.75 µg/mL respectively. Additionally, HFB-NJ1 depicted enhanced emulsification of various vegetable and petroleum-based oils (E24 > 80%). HFB-NJ1 effectively reduced gold ions, producing nanospheres with a size of 15.33 nm - a recognized antimicrobial agent. This study underscores the multifunctional attributes of HFB-NJ1, highlighting its efficacy in removing pathogenic bacteria, emulsifying organic compounds from wastewater, and demonstrating a reduction ability for nanoparticle synthesis.

Synthesis of magnetic biochar composite using Vateria indica fruits through in-situ one-pot hydro-carbonization for Fenton-like catalytic dye degradation.

The present study reports the synthesis, characterization, and application of sustainable magnetic biochar composite. The inedible fruits of Vateria indica, a powerful ayurvedic plant were hydrothermally transformed into magnetic biochar (BC-Fe3O4) in a single step and characterized by several sophisticated techniques. FESEM analysis portrayed fibrous irregular mesh-like biochar with surface clustered Fe3O4 nanoparticles, while the incidence of carbon, oxygen, and iron in the elemental analysis by EDS established magnetic biochar formation. Numerous peaks consistent with planes of (220), (311), (400), (422), (511), (440), and (120) also substantiated the occurrence of magnetite nanoparticles and biochar respectively, as analyzed by XRD. XPS analysis showed signals at 285.65 eV, 533.28 eV, 711.08 eV, and 724.68 eV corroborating a strong C-O bond, O1s orbit, Fe2+, and Fe3+ respectively. BC-Fe3O4 was superparamagnetic with saturation magnetization of 4.74 emu/g, as per VSM studies, while its specific surface area, pore volume, and pore diameter were 5.74 m2/g, 0.029 cm3/g, and 20.86 nm respectively. The Fenton-like degradation of methylene blue (5.0-25.0 ppm) was accomplished by synthesized BC-Fe3O4, in the presence of H2O2. Within 180 min, almost complete degradation was achieved, with first-order kinetics having rate constants between 0.0299 and 0.0167 min-1. Stability and recyclability studies performed over 7 cycles exhibited unaltered degradation between 93.98 and 97.59%. This study exhibits the exceptional characteristics and degradation capabilities of BC-Fe3O4 synthesized from a sustainable plant biomass.

Machine learning and statistical physics modeling of tetracycline adsorption using activated carbon derived from Cynometra ramiflora fruit biomass.

The current investigation reports the usage of adaptive neuro-fuzzy inference system (ANFIS) and artificial neural network (ANN), the two recognized machine learning techniques in modelling tetracycline (TC) adsorption onto Cynometra ramiflora fruit biomass derived activated carbon (AC). Many characterization methods utilized, confirmed the porous structure of synthesized AC. ANN and ANFIS models utilized pH, dose, initial TC concentration, mixing speed, time duration, and temperature as input parameters, whereas TC removal percentage was designated as the output parameter. The optimized configuration for the ANN model was determined as 6-8-1, while the ANFIS model employed trimf input and linear output membership functions. The obtained results showed a strong correlation, indicated by high R2 values (ANNR2: 0.9939 & ANFISR2: 0.9906) and low RMSE values (ANNRMSE: 0.0393 & ANFISRMSE: 0.0503). Apart from traditional isotherms, the dataset was fitted to statistical physics models wherein, the double-layer with a single energy satisfactorily explained the physisorption mechanism of TC adsorption. The sorption energy was 21.06 kJ/mol, and the number of TC moieties bound per site (n) was found to be 0.42, conclusive of parallel binding of TC molecules to the adsorbent surface. The adsorption capacity at saturation (Qsat) was estimated to be 466.86 mg/g - appreciably more than previously reported values. These findings collectively demonstrate that the AC derived from C. ramiflora fruit holds great potential for efficient removal of TC from a given system, and machine learning approaches can effectively model the adsorption processes.

Magnetic activated carbon synthesized using rubber fig tree leaves for adsorptive removal of tetracycline from aqueous solutions.

The current study emphasizes the activated carbon fabrication from rubber fig leaves, the establishment of its composite with iron oxide nanoparticles (RFAC@Fe2O3), and its relevance in the adsorptive elimination of tetracycline. The physical and functional properties of RFAC@Fe2O3 nanocomposite were uncovered by multiple approaches. Elemental analysis portrayed the existence of carbon, oxygen, and iron, while FESEM analysis revealed that Fe2O3 nanoparticle agglomerates were entrenched in the activated carbon matrix rendering it a rough abrasive texture. FT-IR analysis reported the presence of functional groups attributing to CC, -OH, crystalline iron oxide, and Fe-O stretching vibrations, and XRD corroborated graphitic crystalline structure, oxygenated functional groups attached to carbon accompanied by crystalline plane corresponding to Fe2O3 nanoparticles. XPS spectra depicted signature peaks for C, O, and Fe, while VSM studies designated its superparamagnetic nature. The high surface area (662.73 m2/g), pore size (3.12 nm), and mesoporous nature of RFAC@Fe2O3 make it apt for the adsorption of pollutants from contaminated samples. The adsorption of tetracycline (50 ppm) by RFAC@Fe2O3 was maximum at pH 4.0. As the nanocomposite dosage and stirring speed increased to 2.0 g/L and 150 rpm, maximum adsorption was observed due to more active binding sites and improved mixing. Freundlich isotherm along with pseudo-second-order model well described adsorption process divulging that tetracycline was adsorbed onto RFAC@Fe2O3 composite in multi-layers by chemisorption. Thermodynamic analysis signified negative values for ΔG°, while positive values for ΔH° and ΔS were obtained, indicating spontaneous feasible endothermic adsorption.

Green synthesized cobalt oxide nanoparticles with photocatalytic activity towards dye removal.

The present study aimed at the synthesis of cobalt oxide nanoparticles (CONPs) mediated by leaf extract of Muntingia calabura using a rapid and simple method and evaluation of its photocatalytic activity against methylene blue (MB) dye. UV-vis absorption spectrum showed multiple peaks with an optical band gap of 2.05 eV, which was concordant with the literature. FESEM image signified the irregular-shaped, clusters of CONPs, and EDX confirmed the existence of the Co and O elements. The sharp peaks of XRD spectrum corroborated the crystalline nature with a mean crystallite size of 27.59 nm. Raman spectrum substantiated the purity and structural defects. XPS signified the presence of Co in different oxidation states. FTIR image revealed the presence of various phytochemicals present on the surface and the bands at 515 and 630 cm-1 designated the characteristic Co-O bonds. VSM studies confirmed the antiferromagnetic property with negligible hysteresis. The high BET specific surface area (10.31 m2/g) and the mesoporous nature of the pores of CONPs signified the presence of a large number of active sites, thus, indicating their suitability as photocatalysts. The CONPs degraded 88% of 10 mg/L MB dye within 300 min of exposure to sunlight. The degradation of MB dye occurred due to the formation of hydroxyl free radicals on exposure to sunlight, which followed first-order kinetics with rate constant of 0.0065 min-1. Hence, the CONPs synthesized herein could be applied to degrade other xenobiotics and the treatment of industrial wastewater and environmentally polluted samples.

Green synthesized hydroxyapatite nanoadsorbent for the adsorptive removal of AB113 dye for environmental applications.

The present work reports the synthesis of hydroxyapatite (HAp) via the green chemistry approach by using the leaf extract of copper pod tree and its adsorptive potential to remove Acid blue 113 (AB113) dye. FESEM-EDS characterization of the synthesized HAp confirmed rod-shaped HAp with prominent Ca and P elements. The crystallinity of HAp was ascertained by XRD and thermal stability was analyzed by TGA. The colloidal suspension stability was determined as - 17.7 mV by Zeta potential analyzer. The mesoporous structure was affirmed via BET studies with a high magnitude of specific surface area. TEM studies substantiated the rod-shaped HAp as observed in FESEM. The signals specific to HAp were observed in XPS studies. Adsorption of AB113 on the synthesized HAp was examined by varying the process parameters. Batch experiments resulted in an optimum dye removal of 92.72% at a pH of 8, 1 g/L of CP-HAp nps dosage, 20 ppm AB113 concentration, 120 min contact time, 150 rpm agitation speed and at room temperature. The maximum adsorption capacity reached 120.48 mg/g. Multifarious isotherms characterized the adsorption with Freundlich isotherm (R2 > 0.968) dominating Langmuir indicating multilayer adsorption. The experimental data reasonably matched pseudo-second-order kinetics with R2 exceeding 0.99. Thermodynamic investigations underlined the spontaneity and exothermicity of the processes. Results showed the suitability of the HAp nanoadsorbent to remove AB113 from wastestreams.

Synthesis of hydroxyapatite nanoparticles using Acacia falcata leaf extract and study of their anti-cancerous activity against cancerous mammalian cell lines.

This study deals with the synthesis of hydroxyapatite nanoparticles (HAPnps) mediated by Acacia falcata leaf extract. Aggregates of needle-shaped crystalline nanostructures were confirmed by FE-SEM and TEM analysis. Well-defined rings in the SAED patterns corroborated the polycrystalline nature of the HAPnps. Individual elements present in the HAPnps were attested by the specific signals for Ca, P, and O in the EDS and XPS analyses. The distinct peaks observed in the XRD spectrum matched well with the HAP hexagonal patterns with a mean crystallite size of 55.04 nm. The FTIR study unveiled the coating of the nanoparticles with the biomolecules from Acacia falcata leaves. The suspension HAPnps exhibited polydispersity (0.446) and remarkable stability (zeta potential: - 31.9 mV) as evident from DLS studies. The pore diameter was 25.7 nm as obtained from BET analysis, suggesting their mesoporous nature. The HAPnps showed the cytotoxic effect on A549 lung and MDA-MB231 breast carcinoma cell lines, with an IC50 value of 55 µg/mL. The distortion of the cell membrane and cell morphology, along with the chromatin condensation and cell necrosis on treatment with HAPnps were detected under fluorescence microscopy post acridine orange/ethidium bromide dye staining. This study reports the anti-cancerous potential of non-drug-loaded plant-mediated HAPnps. Therefore, the HAPnps obtained in this investigation could play a vital role in the biomedical field of cancer therapy.

Photocatalytic degradation of methylene blue dye using newly synthesized zirconia nanoparticles.

Zirconium oxide nanoparticles (ZrO2NPs) were prepared using the leaf extract of Muntingia calabura as a reductant. The absorption peak at 232 nm confirmed the signature peak for ZrO2NPs with band energy at 5.07 eV. The ZrO2NPs were tetragonal and highly crystalline, possessing a mean diameter of 14.83 nm as confirmed by XRD studies. The lattice constants (a = 0.362 nm and c = 0.511 nm) were consistent with the literature. Spherical nanoaggregates (29.25 nm) were seen in FESEM image and the specific signals for Zr and O were noticed in EDS image. The tetragonal phase of the ZrO2NPs were further confirmed from the XPS and Raman studies. PL spectrum had a sharp emission at 493 nm. The FTIR spectrum revealed the presence of various functional groups. ZrO2NPs were thermally stable with 5.76% total weight loss - as revealed from TGA profile. The photocatalytic breakdown of methylene blue (MB) dye under the influence of solar irradiation was performed using ZrO2NPs which exhibited 89.11% degradation within 5 h. Hence, the synthesized ZrO2NPs can be used as an alternate potential photocatalyst for the degradation of various dyes present in waste streams.

Synthesis, characterization and anticancer activity of the green-synthesized hematite nanoparticles.

The conventional synthesis of hematite nanoparticles (HNPs) is expensive and creates secondary contaminants. Therefore, to combat these issues, there is a requirement for a cheap, effective, and eco-friendly technique. Herein, HNPs were prepared using the fruit extract of Spondias pinnata - an abundant source available in Western-coastal India. The polyphenolic compounds aided the synthesis process and the entire procedure was very rapid. The obtained HNPs had needle-like morphology with agglomerations due to the magnetic interactions as seen in FESEM and HRTEM images. Fe and O elements were noticed in EDS results. The crystalline nature and crystal phase were confirmed from XRD and SAED patterns. The lattice parameters of HNPs were in tandem with the literature. Fe-O crystalline vibrations were noticed in FTIR studies. VSM results portrayed the superparamagnetic nature of HNPs with a high magnetic saturation value of 8.949 emu/g and a negligible hysteresis loop. Thermal stability was ascertained using TGA results with 32% overall weight loss. XPS studies revealed the existence of pure HNPs with signature peaks. Raman spectrum showed the bands specific for HNPs, comparable to the commercial one. In addition, the HNPs were mesoporous with a high surface area (72.04 m2/g) - higher than the commercial one. The anticancer potential of the HNPs was successfully demonstrated against two mammalian cancer cell lines. Therefore, the HNPs synthesized in this study could be applied in various biomedical fields, especially for anticancer formulations.

Efficient adsorptive removal of 2,4-dichlorophenoxyacetic acid (2,4-D) using biomass derived magnetic activated carbon nanocomposite in synthetic and simulated agricultural runoff water.

This study focused on evaluating the efficacy of a magnetic activated carbon material (CPAC@Fe3O4) derived from pods of copper pod tree in adsorbing the toxic herbicide, 2,4- (2,4-D) from aqueous solutions. The synthesized CPAC@Fe3O4 adsorbent, underwent various characterization techniques. FESEM images indicated a rough surface, incorporating iron oxide nanoparticles, while EDS analysis confirmed the presence of elements like Fe, O, and C. Notably, the CPAC@Fe3O4 exhibited high surface area (749.10 m2/g) and pore volume (0.5351 cm³/g), confirming its mesoporous nature. XRD investigations identified distinct signals associated with graphitic carbon and magnetite nanoparticles, while VSM analysis verified its magnetic properties with a high magnetic saturation value (2.72 emu/g). The adsorption process was exothermic, with a decrease in adsorption capacity at higher temperatures. Freundlich isotherm provided the best fit for the adsorption, and the pseudo-second-order equation effectively described the kinetics. Remarkably, the maximum adsorption capacity ranged from 246.43 to 261.03 mg/g, surpassing previously reported values. The ΔH° value (-8.67 kJ/mol) suggested a physisorption mechanism, and the negative ΔG° values established the spontaneous nature. Furthermore, the synthesized adsorbent demonstrated exceptional reusability, allowing for up to five cycles of adsorption-desorption operations. When applied to simulated agricultural runoff, CPAC@Fe3O4 showcased a significant adsorption capacity of 160.71 mg/g for 50 mg/L 2,4-D, using a 0.2 g/L dosage at pH 2. This study showcased the transformation of copper pod biomass into a valuable magnetic nanoadsorbent capable of efficiently eliminating the noxious 2,4-D pollutant from aqueous environments.

Machine learning, conventional and statistical physics modeling of 2,4-Dichlorophenoxyacetic acid (2,4-D) herbicide removal using biochar prepared from Vateria indica fruit biomass.

The adsorption properties of 2,4-Dichlorophenoxyacetic acid (2,4-D) onto biochar, obtained through HCl-assisted hydrothermal carbonization process of Vateria indica fruits (VI-BC), were extensively studied using traditional and statistical physics approaches. The traditional adsorption investigations encompassed kinetics, equilibrium, and thermodynamics studies. Subsequently, the Hill statistical physics model was employed to interpret the mechanism. Also, artificial neural network (ANN) and adaptive neuro-fuzzy inference system (ANFIS) machine learning tools were successfully employed to model the adsorption data wherein both models had high prediction potential (R2 > 0.99). The outcomes demonstrated that the produced VI-BC exhibited remarkable adsorptive traits, having a considerable specific surface area (111.54 m2/g), pore size (5.89 nm), a variety of functional groups, and appropriate attributes for efficiently adsorbing 2,4-D. For 10 mg/L 2,4-D, at pH 2.0 and with 0.3 g/L dose, an impressive 91.67% adsorption efficiency was achieved within a 120-min. Pseudo-second-order model aptly depicted the kinetic behavior of 2,4-D adsorption, while the Freundlich model provided a more accurate representation of the isotherms. 2,4-D maximum adsorption capacity stood at 131.39 mg/g at 303 K. The Hill statistical physics model elucidated that the adsorption primarily occurred via physisorption mechanisms, involving electrostatic attractions, π-π conjugation, and pore filling. This conclusion was further substantiated by post-adsorption characterization of the VI-BC. Thermodynamic analysis indicated that the interactions between VI-BC and 2,4-D were favorable, spontaneous, and exothermic. The calculated low energy of adsorption (1.255 kJ/mol) and ΔH° value (-20.49 kJ/mol) further supported physisorption as the dominant mechanism. In summary, this study underscores the significant potential of the newly developed biochar as a promising alternative material for efficiently removing the 2,4-D herbicide from polluted environments.

Biodegradation of benzo(a)pyrene by Pseudomonas strains, isolated from petroleum refinery effluent: Degradation, inhibition kinetics and metabolic pathway.

Benzo(a)pyrene, a five-ring polyaromatic hydrocarbon, originating from coal tar, crude oil, tobacco, grilled foods, car exhaust etc, is highly persistent in the environment. It has been classified as a Group I carcinogen, as on its ingestion in human body, diol epoxide metabolites are generated, which bind to DNA causing mutations and eventual cancer. Among various removal methods, bioremediation is most preferred as it is a sustainable approach resulting in complete mineralization of benzo(a)pyrene. Therefore, in this study, biodegradation of benzo(a)pyrene was performed by two strains of Pseudomonas, i. e WDE11 and WD23, isolated from refinery effluent. Maximum benzo(a)pyrene tolerance was 250 mg/L and 225 mg/L against Pseudomonas sp. WD23 and Pseudomonas sp. WDE11 correspondingly. Degradation rate constants varied between 0.0468 and 0.0513/day at 50 mg/L with half-life values between 13.5 and 14.3 days as per first order kinetics, while for 100 mg/L, the respective values varied between 0.006 and 0.007 L/mg. day and 15.28-16.67 days, as per second order kinetics. The maximum specific growth rate of strains WDE11 and WD23 was 0.3512/day and 0.38/day accordingly, while concentrations over 75 mg/L had an inhibitory effect on growth. Major degradation metabolites were identified as dihydroxy-pyrene, naphthalene-1,2-dicarboxylic acid, salicylic acid, and oxalic acid, indicating benzo(a)pyrene was degraded via pyrene intermediates by salicylate pathway through catechol meta-cleavage. The substantial activity of the catechol 2,3 dioxygenase enzyme was noted during the benzo(a)pyrene metabolism by both strains with minimal catechol 1,2 dioxygenase activity. This study demonstrates the exceptional potential of indigenous Pseudomonas strains in complete metabolism of benzo(a)pyrene.

Enhanced adsorption of 2,4-dichlorophenoxyacetic acid using low-temperature carbonized Peltophorum pterocarpum pods and its statistical physics modeling.

The usage of various herbicides in the agricultural field leads to water pollution which is a big threat to the environment. Herein, the pods of the Peltophorum pterocarpum tree were used as a cheap resource to synthesize activated carbon (AC) by low-temperature carbonization to remove 2,4-dichlorophenoxyacetic acid (2,4-D) - an abundantly used herbicide. The exceptional surface area (1078.34 m2/g), mesoporous structure, and the various functional groups of the prepared AC adsorbed 2,4-D effectively. The maximum adsorption capacity was 255.12 mg/g, significantly higher than the existing AC adsorbents. The adsorption data satisfactorily modelled using Langmuir and pseudo-second-order models. Also, the adsorption mechanism was studied using a statistical physics model which substantiated the multi-molecular interaction of 2,4-D with the AC. The adsorption energy (<20 kJ/mol) and thermodynamic studies (ΔH°: -19.50 kJ/mol) revealed the physisorption and exothermicity. The practical application of the AC was successfully tested in various waterbodies by spiking experiments. Hence, this work confirms that the AC prepared from the pods of P. pterocarpum can be applied as a potential adsorbent to remove herbicides from polluted waterbodies.

A critical review on the environmental applications of carbon dots.

The discovery of zero-dimensional carbonaceous nanostructures called carbon dots (CDs) and their unique properties associated with fluorescence, quantum confinement and size effects have intrigued researchers. There has been a substantial increase in the amount of research conducted on the lines of synthesis, characterization, modification, and enhancement of properties by doping or design of composite materials, and a diversification of their applications in sensing, catalysis, optoelectronics, photovoltaics, and imaging, among many others. CDs fulfill the need for inexpensive, simple, and continuous environmental monitoring, detection, and remediation of various contaminants such as metals, dyes, pesticides, antibiotics, and other chemicals. The principles of green chemistry have also prompted researchers to rethink novel modes of nanoparticle synthesis by incorporating naturally available carbon precursors or developing micro reactor-based techniques. Photocatalysis using CDs has introduced the possibility of utilizing light to accelerate redox chemical transformations. This comprehensive review aims to provide the reader with a broader perspective of carbon dots by encapsulating the concepts of synthesis, characterization, applications in contaminant detection and photocatalysis, demerits and research gaps, and potential areas of improvement.

Microplastics occurrence, detection and removal with emphasis on insect larvae gut microbiota.

Microplastics have been identified in all living forms including human beings, the present need is to restrain its spread and devise measures to remediate microplastics from polluted ecosystems. In this regard, the present review emphasizes on the occurrence, sources detection and toxic effects of microplastics in various ecosystems. The removal of microplastics is prevalent by various physico-chemical and biological methods, although the removal efficiency by biological methods is low. It has been noted that the degradation of plastics by insect gut larvae is a well-known aspect, however, the underlying mechanism has not been completely identified. Studies conducted have shown the magnificent contribution of gut microbiota, which have been isolated and exploited for microplastic remediation. This review also focuses on this avenue, as it highlights the contribution of insect gut microbiota in microplastic degradation along with challenges faced and future prospects in this area.

Adsorptive removal of tetracycline from aqueous solutions using magnetic Fe2O3 / activated carbon prepared from Cynometra ramiflora fruit waste.

Herein, the sustainable fabrication of magnetic iron oxide nanoadsorbent prepared with activated carbon of inedible Cynometra ramiflora fruit has been investigated. Activated carbon was obtained from phosphoric acid-treated C. ramiflora fruit, which was then utilized for the synthesis of magnetic nanocomposite (CRAC@Fe2O3). The formed nanocomposite was a porous irregular dense matrix of amorphous evenly sized spherical nanoparticles, as visualized by FESEM, and also contained carbon, oxygen, iron, and phosphorous in its elemental composition. FT-IR spectrum depicted characteristic bands attributing to Fe-O, C-OH, C-N, CC, and -OH bonds. VSM and XRD results proved that CRAC@Fe2O3 was superparamagnetic with a moderate degree of crystallinity and high saturation magnetization value (1.66 emu/g). Superior surface area, pore size, and pore volume of 766.75 m2/g, 2.11 nm, and 0.4050 cm3/g respectively were measured on BET analysis of CRAC@Fe2O3 nanocomposite, indicating their suitability for use as an adsorbent. On application of this nanocomposite for adsorption of tetracycline, maximum removal of 95.78% of 50 ppm TC at pH 4, CRAC@Fe2O3 0.4 g/L in 240 min. The adsorption of TC by CRAC@Fe2O3 was confirmed as monolayer sorption by ionic interaction (R2 = 0.9999) as it followed pseudo-second-order kinetics and Langmuir isotherm (R2 = 0.9801). CRAC@Fe2O3 showed a maximum adsorption capacity of 312.5 mg/g towards TC antibiotics indicating its potential for the treatment of antibiotic-contaminated samples. Since negative ΔGo and positive ΔHo and ΔSo values were obtained at all tested temperatures during the thermodynamic studies, the adsorption was confirmed to be endothermic, spontaneous, and feasible with an enhanced degree of randomness.

2,4-Dichlorophenoxyacetic acid (2,4-D) adsorptive removal by algal magnetic activated carbon nanocomposite.

In the present study, ferric oxide nanoparticles impregnated with activated carbon from Ulva prolifera biomass (UPAC-Fe2O3) were prepared and employed to remove 2,4-Dichlorophenoxyacetic acid (2,4-D) by adsorption. The UPAC-Fe2O3 nanocomposite was characterized for its structural and functional properties by a variety of techniques. The nanocomposite had a jagged, irregular surface with pores due to uneven scattering of Fe2O3 nanoparticles, whereas elemental analysis portrayed the incidence of carbon, oxygen, and iron. XRD analysis established the crystalline and amorphous planes corresponding to the iron oxide and carbon phase respectively. FT-IR analyzed the functional groups that confirmed the integration of Fe2O3 nanoparticles onto nanocomposite surfaces. VSM and XPS studies uncovered the superparamagnetic nature and presence of carbon and Fe2O3, respectively, in the UPAC-Fe2O3 nanocomposite. While the surface area was 292.51 m2/g, the size and volume of the pores were at 2.61 nm and 0.1906 cm3/g, respectively, indicating the mesoporous nature and suitability of the nanocomposites that could be used as adsorbents. Adsorptive removal of 2,4-D by nanocomposite for variations in process parameters like pH, dosage, agitation speed, adsorption time, and 2,4-D concentration was studied. The adsorption of 2,4-D by UPAC-Fe2O3 nanocomposite was monolayer chemisorption owing to Langmuir isotherm behavior along with a pseudo-second-order kinetic model. The maximum adsorption capacity and second order rate constant values were 60.61 mg/g and 0.0405 g/mg min respectively. Thermodynamic analysis revealed the spontaneous and feasible endothermic adsorption process. These findings confirm the suitability of the synthesized UPAC-Fe2O3 nanocomposite to be used as an adsorbent for toxic herbicide waste streams.

Advances in the utilisation of carbon-neutral technologies for a sustainable tomorrow: A critical review and the path forward.

Global industrialisation and overexploitation of fossil fuels significantly impact greenhouse gas emissions, resulting in global warming and other environmental problems. Hence, investigations on capturing, storing, and utilising atmospheric CO2 create novel technologies. Few microorganisms, microalgae, and macroalgae utilise atmospheric CO2 for their growth and reduce atmospheric CO2 levels. Activated carbon and biochar from biomasses also capture CO2. Nanomaterials such as metallic oxides, metal-organic frameworks, and MXenes illustrate outstanding adsorption characteristics, and convert CO2 to carbon-neutral fuels, creating a balance between CO2 production and elimination, thus zeroing the carbon footprint. The need for a paradigm shift from fossil fuels and promising technologies on renewable energies, carbon capture mechanisms, and carbon sequestration techniques that help reduce CO2 emissions for a better tomorrow are reviewed to achieve the world's sustainable development goals. The challenges and possible solutions with future perspectives are also discussed.

Plant-mediated gold and silver nanoparticles as detectors of heavy metal contamination.

Heavy metals are dumped into the environment as a result of human activities, posing a serious threat to ecology and human health. Surface water, potable drinking water, potable groundwater, and majority of wastewater include their traces, due to which, their detection by nanoparticles has received a lot of attention in recent years. Although microorganisms are utilized for green nanoparticle production, plant materials have recently been explored because they are more environmentally friendly, easier to scale up, and require fewer specific growth conditions. The production and attributes of nanoparticles synthesized by plant mediation could be enhanced through design of experiments approach, extending their feasibility in the detection of heavy metals in polluted environmental samples. A concise review on green synthesis of silver and gold nanoparticles utilizing plant phytochemicals, its mechanism of synthesis along with significance of design of experiments for enhancement, and their use as heavy metal contamination detectors is presented in the current study.