Low-Cost Carbon Nanoparticles for Removing Hazardous Organic Pollutants from Water: Complete Remediation Study and Multi-Use Investigation

Continuous waste discharge into natural water resources in many countries is a severe global issue, and seeking an effective solution is a researcher’s concern. Herein, toilet paper waste was a low-cost precursor for preparing carbon nanoparticles (TPCNPs). The characterization of TPCNPs revealed a 30 nm to 50 nm particle size, a 264 m2 g−1 surface area, and a cubical graphite lattice XRD pattern. The TPCNPs were tested for removing malachite green (MG), indigo carmine (IC), rhodamine B (RB), and methylene blue (MB) dyes from water. The solution parameters were examined for the sorption process, and a pH of 5.0 suited the MB removal, while a pH of 6.0 was suitable for MG, IC, and RB. The effect of concentration investigation showed an adsorption capacity of 110.9, 64.8, 73.5, and 98 mg g−1 for MG, IC, RB, and MB, respectively. The sorption of the four dyes fitted the Langmuir isotherm model; it was exothermic and spontaneous. The water remediation was tested using groundwater and seawater samples (GW and SW) spiked with pollutants. It is worth mentioning that one treatment sufficed for the remediation of GW and SW contaminated by 5 mg L−1 concentration, while a double treatment was required for 10 mg L−1 pollution in both samples

Insight into the Adsorption Behavior of Carbon Nanoparticles Derived from Coffee Skin Waste for Remediating Water Contaminated with Pharmaceutical Ingredients

Coffee skins, a cheap, agricultural waste, were carbonized in a tubular furnace under a nitrogen stream and then ball milled to fabricate coffee skin-carbon-nanoparticles (CCNPs). SEM showed 35.6–41.6 nm particle size. The 26.64 and 43.16 peaks in the XRD indicated a cubic graphite lattice. The FT-IR broadband revealed a 2500–3500 cm−1 peak, suggesting an acidic O-H group. CCNPs possessed a type-H3-loop in the N2-adsorption-desorption analysis, with a surface of 105.638 m2 g−1. Thereafter, CCNPs were tested for ciprofloxacin (CPXN) adsorption, which reached equilibrium in 90 min. CCNPs captured 142.6 mg g−1 from 100 mg L−1 CPXN, and the 5:12 sorbent mass-to-solution volume ratio was suitable for treating up to 75 mg L−1 contamination. The qt dropped from 142.6 to 114.3 and 79.2 mg g−1 as the temperature rose from 20 °C to 35 °C and 50 °C, respectively, indicating exothermic adsorption. CPXN removal efficiency decreased below pH 5.0 and above pH 8.0. Kinetically, CPXN adsorption fits the second-order model and is controlled by the liquid-film mechanism, indicating its preference for the CCNPs’ surface. The adsorption agreement with the liquid-film and Freundlich models implied the ease of CPXN penetration into the CCNP inner shells and the multilayered accumulation of CPXN on the CCNPs’ surface. The negative ∆H° and ∆G° revealed the exothermic nature and spontaneity of CPXN adsorption onto the CCNP. The CCNPs showed an efficiency of 95.8% during four consecutive regeneration-reuse cycles with a relative standard deviation (RSD) of 3.1%, and the lowest efficiency in the fourth cycle was 92.8%

Fast-simplistic fabrication of MoO3@Al2O3-MgO triple nanocomposites for efficient elimination of pharmaceutical contaminants

The presence of antibiotics in water is considered one of the most significant global tragedies. The study successfully devised a practical and straightforward operational approach for synthesizing environmentally safe nanocomposites for removing antibiotics from water. Mainly, Al2O3MgO (0-MoO3), 5 %MoO3@Al2O3MgO (5-MoO3), and 10 %MoO3@Al2O3MgO (10-MoO3) nanocomposites were fabricated as environmentally friendly sorbents. The morphology inspections of 0-MoO3, 5-MoO3, and 10-MoO3 showed mean size ranges of 42.8 – 54.9, 33.6 – 44.5, and 39.3 – 44.9 nm, respectively, while their surface areas were 56.8, 112.8, and 75.6 m2/g, respectively. The X-ray diffraction indicated the purity of the nanocomposites and showed MoO3 phases in the triple nanocomposites pattern. The adsorption of chloro-tetracycline (CTTC) on 0-MoO3, 5-MoO3, and 10-MoO3 resulted in qt values of 96.3, 150.1, and 125.9 mg g−1, respectively. The CTTC sorption onto the three sorbents took approximately 90 min; the best removal was noticed at a pH = 6.0 at 25℃, and the solution: sorbent ratio of 5:12 is proper for treating up to 100 mg L-1 CTTC contamination. The Langmuir model was the best isotherm describing CTTC sorption onto 5-MoO3, with an R2 of 0.96, and the Dubinin- Radushkevich (DM) revealed a physisorption process. The thermodynamic evaluation of CTTC sorption on 5-MoO3 indicated exothermicity and spontaneity of the physisorption. The 5-MoO3 nanocomposite has shown outstanding performance in treating natural water samples and in experiments on its regenerative and reusing ability. These findings indicate that the 5-MoO3 nanocomposite has the potential for effective decontamination of polluted water

Removal of ciprofloxacin and indigo carmine from water by carbon nanotubes fabricated from a low-cost precursor: Solution parameters and recyclability

Water contamination is one of humanity's threatening problems. This study synthesized pristine carbon nanotubes (PCNTs) from commercial gasoline (CG) as a relatively low-cost precursor. 200 mL of CG yielded an average CNTs mass of 26.23 ± 0.97 g. The functionalized carbon nanotubes (FCNTs) were produced by acid-treatment of PCNTs, and the yield was 93.3%. The surface area of PCNTs and FCNTs was 29.69 and 66.16 m2 g−1. The FTIR and EDX indicated an introduction of oxygenated groups on the FCNTs. The FCNTs removed ciprofloxacin (CIP) and indigo carmine (IC) from water with an adsorption capacity of 95.5 and 93.0 mg g−1, respectively, while the PCNTs showed 78.9 and 63.7 mg g−1, respectively. The pH 4.0 and 6.0 suited the adsorption of CIP and IC on both sorbents. The adsorption processes for all sorbent-sorbate systems were spontaneous and exothermic. The FCNTs and PCNTs recyclability showed an average efficiency of 90.0%

Efficient Disposal of Basic Fuchsin Dye from Aqueous Media Using ZrO₂/MgMn₂O₄/Mg(Mg_0.333Mn_1.333)O₄ as a Novel and Facilely Synthesized Nanocomposite

In this work, amorphous and crystalline novel products based on Zr, Mg, and Mn were facilely fabricated through the Pechini sol–gel procedure using inexpensive chemicals and an uncomplicated apparatus. Also, these products showed high efficiency as novel adsorbents in getting rid of basic fuchsin dye from aqueous solutions. The adsorbent, which was fabricated before calcination, was abbreviated as KE. In addition, the adsorbents, which were created at 500 and 700 °C, were designated as KE500 and KE700, respectively. The created adsorbents were characterized using high-level transmission electron microscopy (HR-TEM), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), N2 adsorption/desorption analyzer, and field emission scanning electron microscope (FE-SEM). The XRD showed that the KE adsorbent is amorphous, whereas the KE500 and KE700 adsorbents are mixtures of ZrO2, MgMn2O4, and Mg(Mg0.333Mn1.333)O4 nanostructures. The HR-TEM exhibited that the KE adsorbent consists of very fine irregular shapes, whereas the KE500 adsorbent contains quasi-spherical particles with a mean diameter of 45.16 nm. Furthermore, the HR-TEM exhibited that the KE700 adsorbent consists of polyhedral shapes with a mean diameter of 76.28 nm. Furthermore, the BET surface area of the KE, KE500, and KE700 adsorbents is 67.85, 20.15, and 13.60 m2/g, respectively. Additionally, the elimination of basic fuchsin dye by the KE, KE500, and KE700 adsorbents is exothermic, physical in nature, and follows the pseudo-first-order as well as Langmuir equations. Further, the maximum uptake capabilities of the KE, KE500, and KE700 adsorbents toward basic fuchsin dye are 239.81, 174.83, and 93.19 mg/g, respectively

Sweep-Out of Tigecycline, Chlortetracycline, Oxytetracycline, and Doxycycline from Water by Carbon Nanoparticles Derived from Tissue Waste

Pharmaceutical pollution has pervaded many water resources all over the globe. The propagation of this health threat drew the researchers’ concern in seeking an efficient solution. This study introduced toilet paper waste as a precursor for carbon nanoparticles (CRNPs). The TEM results showed a particle size range of 30.2 nm to 48.1 nm, the BET surface area was 283 m2 g−1, and the XRD pattern indicated cubical-graphite crystals. The synthesized CRNPs were tested for removing tigecycline (TGCN), chlortetracycline (CTCN), oxytetracycline (OTCN), and doxycycline (DXCN) via the batch process. The adsorption equilibrium time for TGCN, DXCN, CTCN, and OTCN was 60 min, and the concentration influence revealed an adsorption capacity of 172.5, 200.1, 202.4, and 200.0 mg g−1, respectively. The sorption of the four drugs followed the PSFO, and the LFDM models indicated their high sorption affinity to the CRNPs. The adsorption of the four drugs fitted the multilayer FIM that supported the high-affinity claim. The removals of the four drugs were exothermic and spontaneous physisorption. The fabricated CRNPs possessed an excellent remediation efficiency for contaminated SW and GW; therefore, CRNPs are suggested for water remediation as low-cost sorbent

Optimization, Nature, and Mechanism Investigations for the Adsorption of Ciprofloxacin and Malachite Green onto Carbon Nanoparticles Derived from Low-Cost Precursor via a Green Route

The spread of organic pollutants in water spoils the environment, and among the best-known sorbents for removing organic compounds are carbonaceous materials. Sunflower seed waste (SFSW) was employed as a green and low-cost precursor to prepare carbon nanoparticles (CNPs) via pyrolysis, followed by a ball-milling process. The CNPs were treated with a nitric–sulfuric acid mixture (1:1) at 100 °C. The scanning electron microscopy (SEM) showed a particle size range of 38 to 45 nm, and the Brunauer–Emmett–Teller (BET) surface area was 162.9 m2 g−1. The elemental analysis was performed using energy-dispersive X-ray spectroscopy, and the functional groups on the CNPs were examined with Fourier transform infrared spectroscopy. Additionally, an X-ray diffractometer was employed to test the phase crystallinity of the prepared CNPs. The fabricated CNPs were used to adsorb ciprofloxacin (CFXN) and malachite green (MLG) from water. The experimentally obtained adsorption capacities for CFXN and MLG were 103.6 and 182.4 mg g−1, respectively. The kinetic investigation implied that the adsorption of both pollutants fitted the pseudo-first-order model, and the intraparticle diffusion step controlled the process. The equilibrium findings for CFXN and MLG sorption on the CNPs followed the Langmuir and the Fredulich isotherm models, respectively. It was concluded that both pollutants spontaneously adsorbed on the CNPs, with physisorption being the likely mechanism. Additionally, the FTIR analysis of the adsorbed CFXN showed the disappearance of some functional groups, suggesting a chemisorption contribution. The CNPs showed an excellent performance in removing CFXN and MLG from groundwater and seawater samples and possessed consistent efficiency during the recycle–reuse study. The application of CNPs to treat synthetically contaminated natural water samples indicated the complete remediation of polluted water using the ball-mill-fabricated CNPs

Excellent Adsorption of Dyes via MgTiO₃@g-C₃N₄ Nanohybrid: Construction, Description and Adsorption Mechanism

This report investigates the elimination of hazardous Rhodamine B dye (RhB) from an aqueous medium utilizing MgTiO3@g-C3N4 nanohybrids manufactured using a facile method. The nanohybrid MgTiO3@g-C3N4 was generated using an ultrasonic approach in the alcoholic solvent. Various techniques, including HRTEM, EDX, XRD, BET, and FTIR, were employed to describe the fabricated MgTiO3@g-C3N4 nanohybrids. RhB elimination was investigated utilizing batch mode studies, and the maximum removal was attained at pH 7.0. The RhB adsorption process is more consistent with the Langmuir isotherm model. The highest adsorption capacity of MgTiO3@g-C3N4 nanohybrids for RhB was determined to be 232 mg/g. The dye adsorption followed a pseudo-second-order model, and the parameters calculated indicated that the kinetic adsorption process was spontaneous. Using ethanol and water, the reusability of the nanomaterial was investigated, and based on the results; it can be concluded that the MgTiO3@g-C3N4 nanohybrids are easily regenerated for dye removal. The removal mechanism for the removal of RhB dye into MgTiO3@g-C3N4 nanohybrids was also investigated

Excellent Adsorption of Dyes via MgTiO3@g-C3N4 Nanohybrid: Construction, Description and Adsorption Mechanism

This report investigates the elimination of hazardous Rhodamine B dye (RhB) from an aqueous medium utilizing MgTiO3@g-C3N4 nanohybrids manufactured using a facile method. The nanohybrid MgTiO3@g-C3N4 was generated using an ultrasonic approach in the alcoholic solvent. Various techniques, including HRTEM, EDX, XRD, BET, and FTIR, were employed to describe the fabricated MgTiO3@g-C3N4 nanohybrids. RhB elimination was investigated utilizing batch mode studies, and the maximum removal was attained at pH 7.0. The RhB adsorption process is more consistent with the Langmuir isotherm model. The highest adsorption capacity of MgTiO3@g-C3N4 nanohybrids for RhB was determined to be 232 mg/g. The dye adsorption followed a pseudo-second-order model, and the parameters calculated indicated that the kinetic adsorption process was spontaneous. Using ethanol and water, the reusability of the nanomaterial was investigated, and based on the results; it can be concluded that the MgTiO3@g-C3N4 nanohybrids are easily regenerated for dye removal. The removal mechanism for the removal of RhB dye into MgTiO3@g-C3N4 nanohybrids was also investigated

Spontaneous Adsorption and Efficient Photodegradation of Indigo Carmine under Visible Light by Bismuth Oxyiodide Nanoparticles Fabricated Entirely at Room Temperature

Bismuth oxyiodide (BiOI) is a targeted material for its relative safety and photocatalytic activity under visible light. In this study, a successful simple and energy-saving route was applied to prepare BiOI through a sonochemical process at room temperature. The characterization of the prepared BiOI was conducted by physical means. The transmission electron microscope (TEM) image showed that the BiOI comprises nanoparticles of about 20 nm. Also, the surface area of the BiOI was found to be 34.03 m2 g−1 with an energy gap of 1.835 eV. The adsorption and photocatalytic capacities of the BiOI were examined for the indigo carmine dye (IC) as a model water-pollutant via the batch experiment methodology. The solution parameters were optimized, including pH, contact time, IC concentration, and temperature. Worth mentioning that an adsorption capacity of 185 mg·g−1 was obtained from 100 mg L−1 IC solution at 25 °C within 60 min as an equilibrium time. In addition, the BiOI showed a high degradation efficiency towards IC under tungsten lamb (80 W), where 93% was removed within 180 min, and the complete degradation was accomplished in 240 min. The fabricated BiOI nanoparticles completely mineralized the IC under artificial visible light, as indicated by the total organic carbon analysis