Microporous Activated Carbon from Pisum sativum Pods Using Various Activation Methods and Tested for Adsorption of Acid Orange 7 Dye from Water.

This work demonstrates the preparation of high-surface-area activated carbon (AC) from Pisum sativum pods using ZnCl2 and KOH as activating agents. The influence of CO2 and N2 gases during the carbonization process on the porosity of AC were studied. The highest specific surface area of AC was estimated at 1300 to 1500 m2/g, which presented characteristics of microporous materials. SEM micrographs revealed that chemical activation using an impregnation reagent ZnCl2 increases the porosity of the AC, which in turn leads to an increase in the surface area, and the SEM image showed that particle size diameter ranged between 48.88 and 69.95 nm. The performance of prepared AC for adsorption of Acid Orange 7 (AO7) dye was tested. The results showed that the adsorption percentage by AC (2.5 g/L) was equal to 94.76% after just 15 min, and the percentage of removal increased to be ~100% after 60 min. The maximum adsorption capacity was 473.93 mg g-1. A Langmuir model (LM) shows the best-fitted equilibrium isotherm, and the kinetic data fitted better to the pseudo-second-order and Film diffusion models. The removal of AO7 dye using AC from Pisum sativum pods was optimized using a response factor model (RSM), and the results were reported.

Efficiency of Fe3O4 Nanoparticles with Different Pretreatments for Enhancing Biogas Yield of Macroalgae Ulva intestinalis Linnaeus.

In this work, different pretreatment methods for algae proved to be very effective in improving cell wall dissociation for biogas production. In this study, the Ulva intestinalis Linnaeus (U. intestinalis) has been exposed to individual pretreatments of (ultrasonic, ozone, microwave, and green synthesized Fe3O4) and in a combination of the first three mentioned pretreatments methods with magnetite (Fe3O4) NPs, (ultrasonic-Fe3O4, ozone-Fe3O4 and microwave-Fe3O4) in different treatment times. Moreover, the green synthesized Fe3O4 NPs has been confirmed by FTIR, TEM, XRD, SEM, EDEX, PSA and BET. The maximum biogas production of 179 and 206 mL/g VS have been attained when U. intestinalis has been treated with ultrasonic only and when combined microwave with Fe3O4 respectively, where sediment were used as inoculum in all pretreatments. From the obtained results, green Fe3O4 NPs enhanced the microwave (MW) treatment to produce a higher biogas yield (206 mL/g VS) when compared with individual MW (84 mL/g VS). The modified Gompertz model (R2 = 0.996 was appropriate model to match the calculated biogas production and could be used more practically to distinguish the kinetics of the anaerobic digestion (AD) period. The assessment of XRD, SEM and FTIR discovered the influence of different treatment techniques on the cell wall structure of U. intestinalis.

Sources of hydrocarbons and their risk assessment in seawater and sediment samples collected from the Nile Delta coast of the Mediterranean Sea.

The aim of this work is to examine the levels, distribution, bases, and hazards of n-alkanes (n-C9 to n-C20) and PAHs in the seawater and sediments around oil production locations in the whole delta region. The variations in the levels of PAHs and n-alkanes in seawater and sediment of the Nile delta coast of the Mediterranean were investigated using GC-MS/MS. The Σn-alkanes residues ranged between 12.05 and 93.51 mg/L (mean: 50.45 ± 17.49 mg/L) and 4.70 to 84.03 µg/g (mean: 31.02 ± 27.995 µg/g) in seawater and sediments, respectively. Total PAHs concentrations ranged between 4.485 and 16.337 µg/L (average: 9.47 ± 3.69 µg/L) and 1.32 to 28.38 ng/g (average 8.61 ± 7.57 ng/g) in seawater and sediment samples, respectively. The CPI (carbon preference index) values fluctuated between 0.62 and 1.72 (seawater) and from 0.234 to 2.175 (sediment), proposing the variation sources of n-alkane in the studied area. PAHs concentrations were lower than the Effective Range Low (ERL) and Effective Range Median (ERM) levels. The Toxic Equivalent Quotient (TEQ) values oscillated between 0.002 and 6.84 ng/L and from 3.72 to 13.48 ng/g for the seawater and sediment samples, respectively. The Ant/(Ant + Phe) ratio in sediment and seawater samples indicated a pyrolytic source while the BaA/(BaA + Chry) ratio indicates petrogenic sources in most of the studied stations.

Fabrication of date palm kernel biochar-sulfur (DPKB-S) for super adsorption of methylene blue dye from water.

A novel form of biochar was created by dehydration of Date palm kernel with 85% sulfuric acid. It was examined how the newly produced biochar (DPKB-S) affected the aqueous solution's capacity to extract Methylene Blue (MB) dye. The prepared DPKB-S was categorized by BET, BJH, FT-IR, SEM, EDX, DSC, and TGA analyses. The ideal pH for the MB dye adsorption by DPKB-S is 8. With 0.75 g L-1 of DPKB-S and an initial concentration of 50 ppm MB dye, Date Palm Kernel Biochar-Sulfur (DPKB-S) had the highest removal percentage of 100%. The Langmuir and Freundlich isotherm models were used to investigate the collected data. Freundlich model is the model that best covers MB dye adsorption in DPKB-S at low concentrations (0.75-1.25 g L-1) and the Langmuir model at high concentrations (1.5-1.75 g L-1). The Langmuir model maximum adsorption capacity (Qm) of the DPKB-S was 1512.30 mg g-1. Furthermore, a variety of error function models were applied to investigate the isotherm models derived data, including Marquardt's percent standard deviation (MPSD), the sum of absolute errors (EABS), the sum of the errors squared (ERRSQ), root mean square errors (RMS), Chi-square error (X2), the average relative error (ARE), average percent errors (APE), and hybrid error function (HYBRID). Kinetic data were calculated by intraparticle diffusion (IPD), pseudo-second-order (PSO), pseudo-first-order (PFO), and film diffusion (FD) models. A PSO rate model with a strong correlation (R2 = 1.00) largely regulated the adsorption rate. The removal mechanism of MB dye by DPKB-S is based on the principle that these positively charged dyes are attracted by electrostatic attraction forces due to the growth in the number of negatively charged regions at basic pH value. According to the results, DPKB-S shows promise as an affordable and competent adsorbent for the adsorption of MB dye. It can be used frequently without experiencing a discernible decrease in adsorption efficiency.

Experimental, predictive and RSM studies of H2 production using Ag-La-CaTiO3 for water-splitting under visible light.

Ag-La-CaTiO3 was used in place of sacrificial agents to assess the influence of operational factors on hydrogen generation in a photocatalytic water splitting system. After being synthesized, the physicochemical features of this substance were accurately described. Several characterization techniques including UV-Vis spectroscopy, FTIR, XRD, XPS, EDX, SEM, TGA, DRS and BET were applied to study the prepared Ag-La-CaTiO3 photocatalyst. Ag-La-CaTiO3 shows a band in the visible wavelength between 400 and 800 nm at < 560 nm compared to the main CaTiO3 band at 350 nm. Ag 4d5s electrons transition to the conduction band (CB), which is responsible for the absorption band at ~ 560 nm (> 2.21 eV). The effects of catalyst concentration, light intensity, and beginning solution pH on the H2 generation rate may all be evaluated simultaneously using experimental design procedures. Up to a maximum threshold, where a drop in the rate of gas evolution occurs, it was confirmed that the increase in catalyst dose positively affects system productivity. The initial solution pH plays a crucial role in H2 production, and pH = 4 and 10 are the optimum pH with a higher yield of H2 production. The highest total H2 production rate, 6246.09 µmol, was obtained using a catalyst concentration of 700 mg and solution pH equal to 10 under 1200 W Vis lamp for 3 h. For prediction and optimization, a D-Optimal design was applied and the optimal results were pH 4, the catalyst dose of 645.578 mg and 1200 W with H2 production of 6031.11 µmol.

Optimization strategy of Co3O4 nanoparticles in biomethane production from seaweeds and its potential role in direct electron transfer and reactive oxygen species formation.

In the present study, three process parameters optimization were assessed as controlling factors for the biogas and biomethane generation from brown algae Cystoceira myrica as the substrate using RSM for the first time. The biomass amount, Co3O4NPs dosage, and digestion time were assessed and optimized by RSM using Box-Behnken design (BBD) to determine their optimum level. BET, FTIR, TGA, XRD, SEM, XPS, and TEM were applied to illustrate the Co3O4NPs. FTIR and XRD analysis established the formation of Co3O4NPs. The kinetic investigation confirmed that the modified model of Gompertz fit the research results satisfactorily, with R2 ranging between 0.989-0.998 and 0.879-0.979 for biogas and biomethane production, respectively. The results recommended that adding Co3O4NPs at doses of 5 mg/L to C. myrica (1.5 g) significantly increases biogas yield (462 mL/g VS) compared to all other treatments. The maximum biomethane generation (96.85 mL/g VS) was obtained with C. myrica at (0 mg/L) of Co3O4NPs. The impacts of Co3O4NPs dosages on biomethane production, direct electron transfer (DIET) and reactive oxygen species (ROS) were also investigated in detail. The techno-economic study results demonstrate the financial benefits of this strategy for the biogas with the greatest net energy content, which was 2.82 kWh with a net profit of 0.60 USD/m3 of the substrate and was produced using Co3O4NPs (5 mg/L).

Hydrothermal fabrication, characterization and RSM optimization of cobalt-doped zinc oxide nanoparticles for antibiotic photodegradation under visible light.

Photodegradation is considered a significant method engaged for the elimination of organic pollutants from water. In this work, hydrothermal cobalt-doped zinc oxide nanoparticles (Hy-Co-ZnO NPs) loaded with 5, 10, and 15% cobalt were prepared in a hydrothermal way and were investigated as a photocatalyst for the Ciprofloxacin (CIPF) degradation under visible irradiation using LED-light. Characterization approaches such as FTIR, XRD, XPS, DRS UV-vis spectroscopy, SEM, TEM, BET, EDX and TGA were used for the investigation of the fabricated Hy-Co-ZnO NPs. The studies indicated that 10% Hy-Co-ZnO NPs was the most efficient catalyst for the CIPF photolysis compared to ZnO NPs and other Hy-Co-ZnO NPs with 5 and 15% cobalt content. Higher photocatalytic activity (> 98%) of 20 mg/L of CIPF solution was attained within 60 min. The reaction kinetics showed that the first-order model is suitable for displaying the rate of reaction and amount of CIPF elimination with R2 = 0.9883. Moreover, Central composite design (CCD) optimization of the 10% Hy-Co-ZnO NPs was also studied.

Central composite design and mechanism of antibiotic ciprofloxacin photodegradation under visible light by green hydrothermal synthesized cobalt-doped zinc oxide nanoparticles.

In this research, different Co2+ doped ZnO nanoparticles (NPs) were hydrothermally synthesized by an environmentally friendly, sustainable technique using the extract of P. capillacea for the first time. Co-ZnO was characterized and confirmed by FTIR, XPS, XRD, BET, EDX, SEM, TEM, DRS UV-Vis spectroscopy, and TGA analyses. Dislocation density, micro strains, lattice parameters and volume of the unit cell were measured using XRD results. XRD suggests that the average size of these NPs was between 44.49 and 65.69 nm with a hexagonal wurtzite structure. Tauc plot displayed that the optical energy bandgap of ZnO NPs (3.18) slowly declines with Co doping (2.96 eV). Near complete removal of the ciprofloxacin (CIPF) antibiotic was attained using Green 5% of Hy-Co-ZnO in the existence of visible LED light which exhibited maximum degradation efficiency (99%) within 120 min for 30 ppm CIPF initial concentration. The photodegradation mechanism of CIPF using Green Hy-Co-ZnO NPs followed the Pseudo-first-order kinetics. The Green Hy-Co-ZnO NPs improved photocatalytic performance toward CIPF for 3 cycles. The experiments were designed using the RSM (CCD) method for selected parameters such as catalyst dosage, antibiotic dosage, shaking speed, and pH. The maximal CIPF degradation efficiency (96.4%) was achieved under optimum conditions of 39.45 ppm CIPF dosage, 60.56 mg catalyst dosage, 177.33 rpm shaking speed and pH 7.57.

Fabrication of carbon black nanoparticles from green algae and sugarcane bagasse.

There are several industrial uses for carbon black (CB), an extremely fine powdered form of elemental carbon that is made up of coalesced particle aggregates and almost spherical colloidal particles. Most carbon black is produced from petroleum-derived feedstock, so there is a need to find an alternative method to produce CB, which relies on renewable resources such as algae and agricultural waste. A process involving hydrolysis, carbonization, and pyrolysis of green algae and sugarcane bagasse was developed, as the optimal hydrolysis conditions (16N sulfuric acid, 70 °C, 1 h, 1:30 g/ml GA or SC to sulfuric acid ratio), a hydrolysis ratio of 62% for SC and 85% for GA were achieved. The acidic solution was carbonized using a water bath, and the solid carbon was then further pyrolyzed at 900 °C. The obtained carbon black has a high carbon content of about 90% which is confirmed by EDX, XRD, and XPS analysis. By comparison carbon black from sugar cane bagasse (CBB) and carbon black from green algae Ulva lactuca (CBG) with commercial carbon black (CCB) it showed the same morphology which was confirmed by SEM analysis. The BET data, showed the high specific surface area of prepared CB, which was 605 (m2/g) for CBB and 424 (m2/g) for CBG compared with commercial carbon black (CBB) was 50 (m2/g), also the mean pore diameter of CBB, CBG and CCB indicated that CBB and CBG were rich in micropores, but CCB was rich in mesoporous according to IUPAC classification. This study might have created a technique that can be used to make carbon black from different kinds of biomass.

Green algae Ulva lactuca-derived biochar-sulfur improves the adsorption of methylene blue from water.

The present investigation explores the efficacy of green algae Ulva lactuca biochar-sulfur (GABS) modified with H2SO4 and NaHCO3 in adsorbing methylene blue (MB) dye from aqueous solutions. The impact of solution pH, contact duration, GABS dosage, and initial MB dye concentration on the adsorption process are all methodically investigated in this work. To obtain a thorough understanding of the adsorption dynamics, the study makes use of several kinetic models, including pseudo-first order and pseudo-second order models, in addition to isotherm models like Langmuir, Freundlich, Tempkin, and Dubinin-Radushkevich. The findings of the study reveal that the adsorption capacity at equilibrium (qe) reaches 303.78 mg/g for a GABS dose of 0.5 g/L and an initial MB dye concentration of 200 mg/L. Notably, the Langmuir isotherm model consistently fits the experimental data across different GABS doses, suggesting homogeneous adsorption onto a monolayer surface. The potential of GABS as an efficient adsorbent for the extraction of MB dye from aqueous solutions is highlighted by this discovery. The study's use of kinetic and isotherm models provides a robust framework for understanding the intricacies of MB adsorption onto GABS. By elucidating the impact of various variables on the adsorption process, the research contributes valuable insights that can inform the design of efficient wastewater treatment solutions. The comprehensive analysis presented in this study serves as a solid foundation for further research and development in the field of adsorption-based water treatment technologies.

Formation of self-nitrogen-doping activated carbon from Fish/sawdust/ZnCl2 by hydrothermal and pyrolysis for toxic chromium adsorption from wastewater.

This study gives a description of the formation of self-nitrogen doped activated carbon (NDAC) by a novel way of employing fish meal (mixture of Atherina hepseetus and Sardina pilchardus of 60% protein) as nitrogen dopant, ZnCl2 as impregnate agent, sawdust as carbon source and water with a mass ratio (2:1:1:12), which subjected to the hydrothermal process. The hydrothermal mixture was oven dried and carbonized under a flow of nitrogen for one h at 600, 700, and 800 °C. The characterization of NDAC was performed by using various analytical techniques analyses. The synthesized NDAC exhibited unique features such as microporous structure (1.84 ~ 2.01 nm), high surface area (437.51 ~ 680.86 m2/g), the volume of total pores (0.22 ~ 0.32 cm3/g) and nitrogen content (12.82 ~ 13.73%). Batch removal tests were achieved to investigate the impact of chromium ions starting concentration (100-400 mg/L), NDAC dose (0.5-2.5 g/L), pH and contact time (5-120 min). Such helpful characteristics of NDAC, particularly for NDAC600, were suitable to use as an excellent adsorbent for Cr6+ ions with a maximum adsorption capacity (Qm) (769.23 mg/g), and the highest chromium ions adsorption uptake (81.18%) was obtained at pH value 1.5 at room temperature. Both Halsey and Temkin models fitted the adsorption data quite reasonably. The uptake of toxic chromium ions is best represented with pseudo-second-order rate kinetics data.

Fabrication of N-doping activated carbons from fish waste and sawdust for Acid Yellow 36 dye removal from an aquatic environment.

Acid Yellow 36 (AY36) dye is a synthetic azo dye that is excessively used in various industries, causing hazardous environmental effects. The main target of this study is the preparation of self-N-doped porous activated carbon (NDAC) and the investigation in eliminating the AY36 dye from the water solution. The NDAC was prepared by mixing fish waste (60% protein content) which was considered a self-nitrogen dopant. A combination of Fish waste, sawdust, zinc chloride and urea with a mass ratio (5:5:5:1) was submitted to hydrothermal process at 180 °C for 5 h followed by pyrolysis for 1 h under N2 stream at 600, 700, and 800 °C. Fabricated NDAC was qualified as an adsorbent for recovering AY36 dye from water using batch trials. The fabricated NDAC samples were characterized by FTIR, TGA, DTA, BET, BJH, MP, t-plot, SEM, EDX, and XRD methods. The results showed the successful formation of NDAC with nitrogen mass percentage content (4.21, 8.13 and 9.85%). The NDAC prepared at 800 °C had the largest nitrogen content (9.85%) and was labeled as NDAC800. This later had 727.34 m2/g, 167.11 cm3/g, and 1.97 nm for specific surface area, the monolayer volume and the mean pores diameter respectively. By being the more efficient adsorbent, NDAC800 was chosen to test AY36 dye removal. Therefore, it is selected to investigate the removal of AY36 dye from aqueous solution by varying important parameters such as solution pH, initial dye concentration, adsorbent dosage and contact time. The removal of AY36 dye by NDAC800 was pH-dependent, with the optimum pH value 1.5 giving 85.86% removal efficiency and 232.56 mg/g maximum adsorption capacity (Qm). The kinetic data exhibited the best fit model with the pseudo-second-order (PSOM), while the equilibrium data fit well with the Langmuir (LIM) and Temkin (TIM). The mechanism of AY36 dye adsorption may be ascribed to the electrostatic contact between the dye and the available charged sites on NDAC800 surface. The prepared NDAC800 may be considered as an efficient, available, and eco-friendly adsorbent for AY36 dye adsorption from simulated water.

n-Alkanes and PAHs baseline distributions and sources in the sediments of the Nile Delta coast of the southeastern Mediterranean.

The variations in the levels of n-alkanes and Polycyclic Aromatic Hydrocarbons (PAHs) in the sediment of the Nile Delta coast and extended to Bardaweel Lagoon along the Mediterranean were investigated during September 2021. The total n-alkane concentrations in the sediment samples ranged from 18.85 to 164.37 µg/g with an average value of 51.98 ± 17.49 µg/g. Similarly, the ΣPAHs concentrations ranged between 4.55 and 207.48 ng/g with an average of 27.89 ± 49.82 ng/g. The carbon preference index (CPI) values were in the 0.21 to 1.39 range, indicating variations in the sources of n-alkane at the analyzed locations. The mean carbon number (MCN) values ranged from 7.41 to 15.47, with an average of 13.34 ± 1.69. The levels of both low and high molecular weight PAHs were lower than the median and low effective range values (ERM and ERL). The computed total TEQ value varied from 0.102 to 4.129 ng/g in the sediment samples under investigation.

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in water-sediment system of southern Mediterranean: Concentration, source and ecological risk assessment.

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were studied in the Nile Delta area of Egypt's southern Mediterranean for their environmental impacts, probable sources, and ecological risk assessment. Using the Gas Chromatography Triple Quadrupole technique, the residues of 16 OCPs and 18 PCBs were determined. The total OCPs content in the seawater and sediment samples ranged from 0.108 to 10.97 µg/L and 0.301 to 5.268 ng/g, respectively, while the PCBs residues had values between 0.808 and 1069.75 µg/L in seawater and between not detected and 575.50 ng/g in sediment samples. The findings of the risk evaluation showed that, except for endosulfan-I, OCPs caused little harm in seawater. However, PCB180, PCB153, PCB156, PCB126 and PCB138 posed a comparatively significant risk. The concentration of DDTs was higher than the effect range low and threshold effect level but remained below the effect range median and probable effect level, posing a minimal ecological concern.

Soft Pneumatic Muscles: Revolutionizing Human Assistive Devices with Geometric Design and Intelligent Control.

Soft robotics, a recent advancement in robotics systems, distinguishes itself by utilizing soft and flexible materials like silicon rubber, prioritizing safety during human interaction, and excelling in handling complex or delicate objects. Soft pneumatic actuators, a prevalent type of soft robot, are the focus of this paper. A new geometrical parameter for soft artificial pneumatic muscles is introduced, enabling the prediction of actuation behavior using analytical models based on specific design parameters. The study investigated the impact of the chamber pitch parameter and actuation conditions on the deformation direction and internal stress of three tested soft pneumatic muscle (SPM) models. Simulation involved the modeling of hyperelastic materials using finite element analysis. Additionally, an artificial neural network (ANN) was employed to predict pressure values in three chambers at desired Cartesian positions. The trained ANN model demonstrated exceptional performance. It achieved high accuracy with training, validation, and testing residuals of 99.58%, 99.89%, and 99.79%, respectively. During the validation simulations and neural network results, the maximum errors in the x, y, and z coordinates were found to be 9.3%, 7.83%, and 8.8%, respectively. These results highlight the successful performance and efficacy of the trained ANN model in accurately predicting pressure values for the desired positions in the soft pneumatic muscles.

Improved methylene blue adsorption from an aqueous medium by ozone-triethylenetetramine modification of sawdust-based biochar.

In this study, sawdust biochar-O3-TETA (SDBT), a novel biochar, was prepared via treatment with 80% sulfuric acid, followed by oxidation by ozone and subsequent treatment with boiling Triethylenetetramine (TETA). Characterization studies of the prepared SDBT adsorbent were performed with SEM-EDX, BET, XRD, BJH, FT-IR, DTA and TGA analyses. The adsorption efficiency of MB dye by SDBT biochar from water was investigated. Methylene Blue (MB) dye absorption was most effective when the solution pH was 12. The maximum removal % of MB dye was 99.75% using 20 mg/L as starting MB dye concentration and 2.0 g/L SDBT dose. The Qm of the SDBT was 568.16 mg/g. Actual results were fitted to Temkin (TIM), Freundlich (FIM), and Langmuir (LIM) isotherm models. The experimental results for SDBT fitted well with all three models. Error function equations were used to test the results obtained from these isotherm models, which showed that the experimental results fit better with TIM and FIM. Kinetic data were investigated, and the pseudo-second-order (PSOM) had R2 > 0.99 and was mainly responsible for guiding the absorption rate. The removal mechanism of the MB dye ions in a base medium (pH 12) may be achieved via physical interaction due to electrostatic interaction between the SDBT surface and the positive charge of the MB dye. The results show that SDBT effectively removes the MB dye from the aqueous environment and can be used continually without losing its absorption efficiency.

Isotherm and kinetic investigations of sawdust-based biochar modified by ammonia to remove methylene blue from water.

Chemical industry effluent may pose significant environmental risks to both human health and the economy if it is not properly managed. As a result, scientists and decision-makers are paying increasing attention to developing a sustainable, low-cost wastewater treatment technique. This work aims to investigate the adsorption of Methylene Blue (MB) dye present in water using biochar derived from sawdust modified by boiling in an ammonia solution (SDBA). The properties of SDBA were characterized by BET, SEM, XRD, BJH, FT-IR, DTA, EDX and TGA analyses. The presence of -OH and -NH groups in SDBA was confirmed by FTIR, which proved that the NH4OH treatment of biochar successfully added nitrogen groups on its surface. The influence of pH (2 to 12), MB dye initial concentration (20 to 120 mg/L), adsorbent dosage (0.5 to 4.0 g/L) and contact time (0 to 180 min) on the adsorption process has been investigated. The adsorption of MB dye is more favorable at basic pH, with optimum adsorption at pH 8. Using a starting concentration of 20 mg/L of MB dye and a 4.0 g/L SDBA dose, the maximum percent clearance of MB dye was 99.94%. Experimental results were fitted to the Freundlich (FIM), Tempkin (TIM) and Langmuir (LIM) isotherm models (IMs). The FIM fitted the equilibrium data well, with a 643.74 mg/g Qm. Various error function models were used to test the data obtained from IMs. According to Error Function results, experimental data showed that it fits better for LIM and FIM. Kinetic studies indicated that the MB dye adsorption procedure followed pseudo-second-order (PSOM) kinetics based on film diffusion (FDM), pseudo-first-order (PFOM) and intra-particle diffusion models (IPDM). MB dye sorption on the SDBA involved electrostatic interaction, surface participation, hydrogen bond and π-π interactions. The adsorption mechanism of MB dye by SDBA was proposed as physical adsorption via the electrostatic attraction process. SDBA is an effective adsorbent in removing MB dye from water. Six adsorption-desorption cycles of the MB dye were run through the regeneration of SDBA with only a minimal amount of adsorption capacity loss, demonstrating the reusability of manufactured SDBA.

Chlorinated pesticides and PCB residues in the Egyptian Western Desert oases sediments.

This preliminary investigation aimed to detect concentrations of chlorinated pesticides and PCBs in 40 sediment samples from three desert oases located in Kharga, Dakhla and Farafra in western Egypt. The residues of 18 PCBs and 16 chlorinated pesticides were measured by GC-MS/MS (SRM) method. The results showed that PCBs and pesticides were present in all studied samples. The concentrations of individual PCBs ranged from undetected to 3.99 ng/g dw in all these sediment samples. The total residue of pesticides (ng/g, dry weight) in sediment samples also varied from 5.18 to 25.92, 5.41 to 29.49, and 5.93 to 24.19 ng/g dw for the Kharga, Dakhla and Farafra Oases, respectively. The concentrations of PCBs and chlorinated pesticides detected in these oasis sediments were lower than that reported for other worldwide locations. According to the recorded concentrations in this baseline study of PCBs and total DDTs, the results revealed the minimal risks to organisms and people in the studied area according to the Effects Range-Low (ERL) and Effects Range-Median (ERM) guideline values.

Isotherm and kinetic studies of acid yellow 11 dye adsorption from wastewater using Pisum Sativum peels microporous activated carbon.

In this study, Pea Peels-Activated Carbon (PPAC), a novel biochar, was created from leftover pea peels (Pisum sativum) by wet impregnation with ZnCl2 and subsequent heating to 600, 700, and 800 °C in a CO2 atmosphere. Investigated how the newly acquired biochar affected the capacity to extract the AY11 dye from the aqueous solution. Through the use of FTIR, XRD, SEM, BJH, BET, DSC, EDX, and TGA studies, the prepared PPAC was identified. It was found that a pH of 2 is optimum for the AY11 dye elimination. The highest removal percentage of AY11 dye was 99.10% using a beginning AY11 dye concentration of 100 mg/L and a 1.0 g/L dose of PPAC. The highest adsorption capacity (Qm) of the PPAC was 515.46 mg/g. Freundlich (FIM), Halsey (HIM), Langmuir (LIM), Tempkin (TIM), and Gineralize (GIM) isotherm models were useful in examining the adsorption results. A variety of error functions, including the average percent errors (APE), root mean square errors (RMS), Marquardt's percent standard deviation (MPSD), hybrid error function (HYBRID), Chi-square error (X2) and a sum of absolute errors (EABS) equations, were also applied to test the isotherm models data. The PPAC experimental data were best suited by the HIM and FIM isotherm models. Elovich (EM), Pseudo-first-order (PFOM), Intraparticle diffusion (IPDM), Pseudo-second-order (PSOM), and Film diffusion (FDM) models were applied to study the kinetic adsorption results. The PSOM had a strong correlation coefficient (R2 > 0.99), and it was principally responsible for controlling the adsorption rate. Anions are typically absorbed during the adsorption mechanism of AY11 dye by PPAC owing to attractive electrostatic forces created with an increase in positively charged areas at acidic pH levels. The regenerated PPAC was used in six successive adsorption/desorption cycles. This study's outcomes show that PPAC successfully removes the AY11 dye from the aqueous solution; as a result, PPAC can be used repeatedly without experiencing considerable loss in effectiveness.

Cube-shaped Cobalt-doped zinc oxide nanoparticles with increased visible-light-driven photocatalytic activity achieved by green co-precipitation synthesis.

From the perspective of environmental protection, the highly efficient degradation of antibiotics and organic dyes in wastewater needs to be tackled as soon as possible. In this study, an ecofriendly and green cube-shaped cobalt-doped zinc oxide nanoparticles (Co-ZnO NPs) photocatalyst using Pterocladia Capillacea (P. Capillacea) water extract loaded with 5, 10, and 15% cobalt ions were formed via co-precipitation process to degrade antibiotics. The prepared Co-ZnO NPs were tested as a photocatalyst for the photodegradation of ciprofloxacin (CIPF) in the presence of a visible LED-light source. Co-ZnO NPs have been obtained through the co-precipitation method in the presence of P. Capillacea extract as a green capping agent and reducing agent, for the first time. Several characterization techniques including FTIR, XRD, BET, XPS, TEM, EDX, SEM, TGA and DRS UV-Vis spectroscopy were applied to study the prepared Co-ZnO NPs. XRD results suggested that the average size of these NPs ranged between 42.82 and 46.02 nm with a hexagonal wurtzite structure. Tauc plot shows that the optical energy bandgap of ZnO NPs (3.19 eV) gradually decreases to 2.92 eV by Co doping. Examinations showed that 5% Co-ZnO NPs was the highest efficient catalyst for the CIPF photodegradation when compared with ZnO NPs and other 10 and 15% Co-ZnO NPs. A 10 mg/L solution of CIPF was photo-degraded (100%) within the first 15 min irradiation. The kinetics showed that the first-order model is suitable for displaying the rate of reaction and amount of CIPF elimination with R2 = 0.952. Moreover, central composite design optimization of the 5% Co-doped ZnO NPs was also investigated.