Natural Solar Light Research Articles

Self-Sensitization-Induced Protonation Sites for Weak-Light-Driven Hydrogen Evolution in Coordination Polymers

The exploration on weak-light-driven catalysis is an important approach to reduce the dependence of photocatalysts on strong light and improve the efficiency of solar spectrum utilization. However, the reported photocatalysts typically necessitate high light intensity (e.g., exceeding 100mWcm−2) for catalytic reactions, which cannot be achieved with natural solar light. Herein, a self-sensitization-induced strategy was employed to generate in-situ proton sites, enabling photocatalytic hydrogen evolution reaction (HER) even under low light intensity (10mWcm−2). An indolocarbazole ligand (H2ICDB) was utilized to construct a paddle-wheel dicopper coordination polymer (CuICDB-DMF). By substituting the axially coordinated DMF with methanol or water, CuICDB-MeOH and CuICDB-H2O were obtained. Under weak-light irradiation (10mWcm−2), CuICDB-H2O exhibited the highest photocatalytic HER rate of 838.4 μmol g−1 h−1 when compared to the other two counterparts. Remarkably, the substitution of axially coordinated H2O promotes charge separation and transfer efficiency through optimizing ligand-to-cluster charge transfer (LCCT) process. Moreover, density functional theory (DFT) calculations reveal that coordinated H2O substitution decreases the Gibbs free energy difference of the potential determining step (H2O* → OH* + H*) in CuICDB-H2O.

Insight into efficient photocatalytic degradation of norfloxacin over a simple, economical biochar-based magnetic photocatalyst under solar illumination: a statistical and experimental approach.

The transformation of residual agricultural solid waste into an efficient value-added carbon product has been an ongoing strategy for solid waste management and a sustainable economy. Meanwhile, the upsurgence of antibiotic contamination in water bodies due to their inadvertent use poses a serious threat to human health and leads to antimicrobial resistance. Hence, to neutralize two evils in one stroke simultaneously, a simple, easy, and cost-effective pea shell-based magnetic photocatalyst (PSMC) has been synthesized and characterized by XRD (X-ray diffraction), VSM (vibrating sample magnetometer), XPS (X-ray photoelectron spectroscopy), TGA (thermogravimetric analysis), and FTIR (Fourier-transform infrared) spectroscopy techniques. Batch experimental studies revealed that PSMC efficiently eliminates norfloxacin (91.3%) within 180min from wastewater and mineralizes it into innocuous products at optimum parameters of norfloxacin concentration of 20mg/L, catalyst dosage of 15mg, and pH 3.5. Additionally, statistical parameters for the photodegradation of NX obtained from ANOVA by applying the Box-Behnken design are in close agreement with batch experiment parameters. PSMC has surplus advantages of facile recovery for recycling up to seven consecutive cycles by an external magnet and efficacy in natural solar light, making it cost-effective and economical. Radical scavenging studies revealed that O2•- and OH• were the potent reactive species in the photocatalytic degradation process.

Scaling-up the use of macroscopic photo-CWPO La1-xTixFeO3/SiC alveolar foam catalyst for solar water treatment against micropollutants

Current wastewater treatment plants are not prepared for the removal of micropollutants like phenol, pharmaceuticals and pesticides in water. As their release into the environment has adverse consequences towards the living organisms of ecosystems, the engineering of novel sustainable processes able to ultimately remove the emerging organic contaminants is an objective of paramount importance. Hereby we report for the first time on the successful scale-up of a macroscopic photo-CWPO La1-xTixFeO3/SiC alveolar foam catalyst used at the pilot-plant scale inside a Compound Parabolic Collectors based photoreactor. The removal of a span of organic micropollutants in water matrices of different complexity was efficiently realized under natural solar radiation using H2O2 or persulfates as oxidizing agent. The water matrix composition affected the efficiency of the degradation process. Using H2O2, for a collected energy of ca. 27 KJ/mol, the rate of micropollutant removal ranged from 53 % to 95 % in distilled water depending on the micropollutant in a cocktail configuration. It was lowered to the 17–66 % range in tap water, and to the 8–42 % range in simulated urban wastewater. The results demonstrated the promise of using sodium persulfate as oxidant instead of H2O2, with a better efficiency towards the removal of most of the micropollutants tested. The use of the sodium persulfate oxidant allows for overcoming the drawbacks associated to the treatment of real water matrices observed using H2O2, as better performances were reached when increasing the water matrix complexity. Complete removal of carbamazepine and diclofenac micropollutants was reached in tap water and simulated urban wastewater for ca. 27 KJ/mol of collected energy. The degradation performances combined to the catalyst robustness make this water treatment technology promising for operating in a continuous way under natural solar light.

Enhanced photocatalytic performance of colored Ti2O3–Ti3O5–TiO2 heterostructure for the degradation of antibiotic ofloxacin and bactericidal effect

Removing emergent contaminants, such as pharmaceuticals, and inhibiting bacteria by photocatalysis represents an interesting alternative for water remediation. We report the effective preparation of colored powders containing Ti2O3, Ti3O5, and TiO2, by a simple thermal oxidation reaction of a Ti2O3 precursor from 400 °C to 800 °C. The material obtained at 500 °C (P500 sample) exhibited the highest photocatalytic performance under simulated solar light, reaching 54% degradation of antibiotic ofloxacin and a bacteria inactivation of 51% and 62% for Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), respectively. The superoxide anion radical was the main specie contributing to the photodegradation of ofloxacin, while the hydroxyl radical showed negligible effect. A synergy between the physicochemical properties of the phases in the P500 sample contributes to the electrons transfer, visible light absorption capability and generation of reactive oxygen species, resulting in its remarkable photoactivity. The comparison in terms of surface-specific activity revealed that the P500 sample is more efficient than commercially available TiO2 P25. This fact opens the option of using commercially available Ti2O3 and TiO2 P25 to obtain composites for promoting photoinduced reactions using natural solar light.

Enhancement of effluent degradation by zinc oxide, carbon nitride, and carbon xerogel trifecta on brass monoliths.

In recent years, heterogeneous photocatalysis has emerged as a promising alternative for the treatment of organic pollutants. This technique offers several advantages, such as low cost and ease of operation. However, finding a semiconductor material that is both operationally viable and highly active under solar irradiation remains a challenge, often requiring materials of nanometric size. Furthermore, in many processes, photocatalysts are suspended in the solution, requiring additional steps to remove them. This can render the technique economically unviable, especially for nanosized catalysts. This work demonstrated the feasibility of using a structured photocatalyst (ZnO, g-C3N4, and carbon xerogel) optimized for this photodegradation process. The synthesized materials were characterized by nitrogen adsorption and desorption, X-ray diffraction (XRD), and diffuse reflectance spectroscopy (DRS). Adhesion testing demonstrated the efficiency of the deposition technique, with film adhesion exceeding 90%. The photocatalytic evaluation was performed using a mixture of three textile dyes in a recycle photoreactor, varying pH (4.7 and 10), recycle flow rate (2, 4, and 6 L h-1), immobilized mass (1, 2, and 3mgcm-2), monolith height (1.5, 3.0, and 4.5cm), and type of radiation (solar and visible artificials; and natural solar). The structured photocatalyst degraded over 99% of the dye mixture under artificial radiation. The solar energy results are highly promising, achieving a degradation efficiency of approximately 74%. Furthermore, it was possible to regenerate the structured photocatalyst up to seven consecutive times using exclusively natural solar light and maintain a degradation rate of around 70%. These results reinforce the feasibility and potential application of this system in photocatalytic reactions, highlighting its effectiveness and sustainability.

Self-dispersion of photocatalysts at oil-water interface accelerates H2O2 production and separation

Enhancing the efficiency of photocatalytic charge transfer for H2O2 production and in situ separation of H2O2 from aqueous suspension are crucial, especially when sacrificial agents are involved, for the advancement of this environmental-friendly process. In this study, we propose that the production and separation of H2O2 can be significantly enhanced at a self-assembled tri-phase system (water/photocatalyst/benzyl alcohol) compared to the suspension system. To prove this, we have employed titania nanotube (TNT) as a representative photocatalyst with efficient oxygen adsorption and modified it with organic ligand (octadecyl phosphate, OPA) and nickel species to modulate its hydrophobicity and dispersity at the interface, resulting in improved H2O2 yield. The modified TNT photocatalyst demonstrates efficient H2O2 production reaching a concentration of 5.1 mM after 75 mins under optimized conditions and an initial rate of 7500 μmol/g/h within first 6 h that even exceeding reported noble metals modified TiO2 photocatalysts. This enhanced activity is attributed to multiple effects including homogeneous dispersion of photocatalyst at the oil-water interface, efficient O2 adsorption and transfer, separated redox reactions at different phases, timely diffusion of H2O2 into bulk aqueous solution, and potential solvent-induced polarization effect on charge transfer, which result from the special oil-water interface that stabilizing photocatalysts and inducing photocatalytic O2 reduction. As proof-of-concept demonstrations show successful photosynthesis of H2O2 using natural solar light followed by utilizing the generated pure H2O2 solution for bacteria inactivation, indicating that interfacial photocatalytic systems offer promising potential for green H2O2 synthesis and application.

Rational design and synthesis of TFPACu nanowires for natural solar light driven photocatalysis

In this study, a novel photocatalyst, 4-OMe-2,3,5,6-tetrafluorophenyl acetylide copper (TFPACu), was synthesized by introducing more electron-withdrawing groups (−F) onto the benzene ring of PhC2Cu. The physicochemical properties of TFPACu were investigated using a variety of characterization techniques. The result of Mott-Schottky test suggested that TFPACu is an n-type semiconductor. The active species involved in thephotocatalyticdegradation process were investigated by electron spin resonance (ESR). The results indicate that OH and h+ was the main active species in the photodegradation process. Under natural solar light irradiation, the degradation rate of TC reached 96 % within 30 min. This work will offer a viable idea for the rational design and development of efficient and cost-effective photocatalysts.

Photoinduced oxidation of chromium picolinate to hexavalent chromium in the presence of ferric ions

The occurrence of chromium picolinate (Cr(pic)3) in environment has attracted raising concerns on its fate and the associated risks. Herein, the photoinduced oxidation of Cr(pic)3 in the presence of ferric ions (Fe(III)) under simulated sunlight and natural solar light irradiation were investigated. Cr(pic)3 was stable under dark or without Fe(III). 87.9 % of Cr(pic)3 (C0 = 1.0 μM) was degraded in the presence of 50 μM Fe(III) after 90 min simulated sunlight irradiation at initial pH of 4.0. •OH was the main cause for Cr(pic)3 oxidation, it attacked the chromium center to generate hexavalent chromium (Cr(VI)) and picolinic acid (k = 5.9 ×108 M−1·s−1). Picolinic acid could be further oxidized to NH4+ and small organics. Relative higher Fe(III) content (25 – 75 μM) and Cr(pic)3 concentration (0.5 – 2.0 μM) promoted both of Cr(pic)3 degradation and Cr(VI) accumulation. While, the degradation of Cr(pic)3 decreased with pH at the range of 3.0 – 8.0, more Cr(VI) was accumulated at pH 5.0 and 6.0. The co-existence of inorganic ions and dissolved organic matter (DOM) in river water inhibited Cr(pic)3 oxidation by scavenging the •OH formed and shielding the light. 8.0 – 16.7 μg/L of Cr(VI) was accumulated after 9.0 h simulated sunlight irradiation of Cr(pic)3 in river water matrix ([Fe(III)]0 = 50 – 100 μM). The generation of Cr(VI) under solar light was slower than that under simulated sunlight due to the weaker light intensity (43.2 – 85.0 mW/cm2 vs. 750 – 1300 mW/cm2). These results consistently suggest photoinduced oxidation of Cr(pic)3 in environment generates the toxic Cr(VI), which deserves significant attention.

Assessment of the Raceway Pond Reactor for Degradation of Methylene Blue Dye in Different Types of Water: A Systematic Kinetics Study under Natural Solar Light

Assessment of the Raceway Pond Reactor for Degradation of Methylene Blue Dye in Different Types of Water: A Systematic Kinetics Study under Natural Solar Light

Fabrication of hierarchical BiOBr with oxygen vacancies for photocatalytic degradation assisted by SDS additive

Photodegradation is a significant approach to protecting the environment. The BiOBr has attracted great interest due to its unique layered structure and narrow energy band. Herein, the hierarchical BiOBr with oxygen vacancy is fabricated via a facial solvothermal method using the Sodium dodecyl sulfate (SDS) additive. The concentration of oxygen vacancies improves with the increase of SDS content, which could enhance the band gap and the redox ability of BiOBr. The hierarchical BiOBr modified by SDS presents excellent photodegradation activity for RhB and MO under visible light due to the synergistic effect of the oxygen vacancies, the redox ability, porous structure, the separation of photoinduced electron-hole pairs, and light absorption capacity. Furthermore, the BiOBr0.70 presented outstanding photodegradation ability under natural solar light, suggesting the photocatalysts could meet certain practical applications.

Gd and Ni co-doped BiFeO3 ferrite/r-GO nanocomposite for photocatalytic environmental remediation applications

Synergistic effects of the co-doping of rare earth and transition metals on the structural, electrical and optical, in multi-ferroic BiFeO3 nanoferrites (NFs) combined with reduced graphene oxide (r-GO) nanosheets, photocatalytic degradation properties can be boosted. In this current study gadolinium and nickel-co-doped Bi1-xGdxFe1-yNiyO3 were synthesised via the tartaric acid-assisted sol-gel method and their composite Bi1-xGdxFe1-yNiyO3/r-GO with 10 % reduced graphene oxide (r-GO) via the ultra-sonication route. Phase and structural investigation were carried out using x-ray diffraction (P-XRD), Raman scattering, and Fourier transform infrared (FTIR) analysis, which confirms the successful fabrication of co-doping in the rhombohedral geometry of the perovskite-type Bi1-xGdxFe1-yNiyO3. Electrical conductivity of the fabricated composite material was observed to increase because of the co-doping and the addition of r-GO. Photoluminescence (PL) spectra of co-doped and r-GO composite material exhibited a decline in PL intensity because optical bandgap energies exhibited narrowing of 1.99 eV and 1.91 eV respectively, which indicates the excellent separation and stabilization of photo-excited charge pairs. Special conduction properties of r-GO nanosheets improved electrical and optical properties, a well-porous nature, large surface area, lower bandgap, and increased dye degradation in the Bi1-xGdxFe1-yNiyO3/r-GO photocatalyst showing excellent photo-degradation of cationic malachite green (M.G.) dye, achieving a degradation efficiency of 96.4 % under natural solar light. Hence, the photocatalyst shows excellent stability where quenching of radicals using selective scavengers shows that OH* radicals and e−/h+ pairs are primarily involved in the mechanism of photo-degradation in a basic pH medium, making the as-fabricated material a potential material for photo-catalytic environmental remediation.

Ultrafast photosensitized degradation of xanthates by using methylene blue as photosensitizer under simulated and natural solar light irradiation: Operational parameters, mechanism and toxicity evolution

Xanthates have attracted considerable attention due to their broad applications in mineral flotation process and unique natures including environmental persistence and toxicity. This study proposed an innovative approach for the efficient xanthates treatment from mineral processing wastewater. Methylene blue (MB) with good water solubility and strong light absorption in visible range was used as the photosensitizer to degrade potassium ethyl xanthate (PEX) under homogeneous conditions. MB, even at a very low concentration (0.5 mg/L), was found to rapidly remove PEX in only 10 min whether under simulated or natural solar light irradiation. Besides, the influences of various operational parameters, including photosensitizer dosage, PEX concentration, pH, light intensity, common ions, and water source on the photosensitized oxidation process was evaluated and analyzed. The possible degradation path of PEX was investigated depending on the intermediates detected by Liquid chromatography-mass spectrometry (LC-MS), and the photosensitized degradation mechanism was further speculated and validated by the radicals quenching experiments and electron paramagnetic resonance (EPR) spectroscopy. Furthermore, the toxicity of PEX was assessed against Bullfrog tadpole and Lemna minor, and it was found to be greatly reduced after treating with MB photosensitization. Overall, it is the first time that MB is proved to be an outstanding candidate for actual flotation wastewater treatment, providing a more efficient, economical and greener alternative to conventional methods.

Performance of a Solar-Driven Photocatalytic Membrane Reactor for Municipal Wastewater Treatment

The increasing demand for efficient wastewater treatment technologies, driven by global population growth and industrialisation, highlights the necessity for advanced, reliable solutions. This study investigated the efficacy of a slurry photocatalytic membrane reactor (PMR) for the advanced removal of organic pollutants, quantified via chemical oxygen demand (COD), under natural and simulated solar light irradiation. Employing two variants of iron-doped titania as photocatalysts and a polysulfone-based polymeric membrane for the separation process, the investigation showcased COD removal efficiencies ranging from 66–85% under simulated solar light to 52–81% under natural sunlight over a 7 h irradiation period. The overall PMR system demonstrated COD removal efficiencies of 84–95%. The results confirmed the enhanced photocatalytic activity afforded by iron doping and establish solar-powered slurry PMRs as an effective, low-energy, and environmentally friendly alternative for the advanced treatment of municipal wastewater, with the research providing valuable insights into sustainable water management practices.

An Innovative Sunlight‐Driven Device for Photocatalytic Drugs Degradation: from laboratory‐ to real‐Scale Application. A First Step Toward Vulnerable Communities

AbstractFreshwater represents one of the most precious resources on the planet, so it is fundamental to preserve it. In this work, an innovative sunlight‐driven device composed of bismuth oxybromide (BiOBr) grown on a material derived from natural sources, i.e., Lightweight Expanded Clay Aggregates (LECA), is developed to clean surface waters under natural solar light irradiation. For this purpose, the photodegradation of two non‐steroidal anti‐inflammatory drugs, ibuprofen, and diclofenac, is investigated under varying operative conditions. Laboratory‐ and real‐scale experiments reveal that the fabricated floating BiOBr/LECA photocatalyst fully degrades diclofenac, whereas limited abatement of ibuprofen is observed. Based on the identification of specific transformation products (TPs) during the degradation, this behavior seems to be strongly related to the different structures of the two drugs. In fact, the main TP produced during diclofenac degradation derives from dechlorination and ring condensation: this type of photocatalytic degradation pathway is generally favored over the C─C bonds's cleavage, which is a unique possibility for IBU abatement. Moreover, the potential partial adsorption of these species on the photocatalyst's active sites can cause their deactivation. Finally, reusability tests demonstrate the high stability of the floating composite.

Evaluation of photocatalytic activity of Cu3(PO4)2/MgO nanocomposite for the efficient removal of amaranth dye under solar light irradiation

The amaranth dye was removed using photocatalysis on a Cu3(PO4)2/MgO nanocomposite synthesized by co-precipitation method. The crystalline component and the nanostructure of the samples were analyzed by XRD, FTIR, UV–vis-DRS, SEM, EDS, HR-TEM and EIS confirming the successful formation of the nanocomposite. In powder XRD, the average crystallite size is found to be ∼ 26–37 nm. Electrochemical impedance spectroscopy, Nyquist plots represents the charge-transfer resistance at contact interface and the arc diameter of Cu3(PO4)2/MgO is much smaller than that of pure MgO and Thermo gravimetric analysis (TGA), from TGA curve the weight-loss of Cu3(PO4)2 and Cu3(PO4)2/MgO nanocomposite was calculated as 14.18 % and 18.16 % which gives the more contribution to the large enhancement of photocatalytic activity. The photocatalytic degradation efficiency of Cu3(PO4)2/MgO nanocomposite (0.1 g/L, 10 μM and 150 min) was investigated under natural direct solar light irradiation against the dyes. The rate of degradation of amaranth with Cu3(PO4)2/MgO followed pseudo–first order kinetics in the dye concentration. Degradation efficiency (99 %) and degradation rates of amaranth were increases with increasing Cu3(PO4)2/MgO concentration. Generally, this research work advances the possible utilization of Cu3(PO4)2/MgO as an efficient catalyst for taking away of dye from aqueous solution and improvement the catalyst to be used for a numerous cycles. The Cu3(PO4)2/MgO nanocomposites showed good activity against bacteria of Staphylococcus aureus, Staphylococcus pyogenes and Klebsilla pneumoniae.

Enhanced performance of dual-functional ZIF-8/red phosphorus photocatalysts for concurrent degradation of organic dyes and hydrogen generation under natural solar light irradiation.

Herein, zeolitic imidazole framework (ZIF)-8/red phosphorus photocatalysts were prepared via a solvothermal method for simultaneous organic dye degradation and hydrogen (H2) generation. The 5 wt% ZIF-8/RP photocatalyst achieved the highest H2 generation rate of 822.5 μmol h-1 g-1 and 92% rhodamine dye degradation under natural sunlight irradiation. This approach offers an effective strategy to replace costly and toxic traditional electron donors with organic dye pollutants for H2 generation.

Surface plasmon resonance effect of silver decorated on BiOCl and its enhanced sunlight-active photodegradation of rhodamine B (RhB) dye and ofloxacin (OFL) antibiotic

Fast electron-hole recombination rate is the major problem concerning low photocatalytic performance of the UV-active BiOCl photocatalyst. To overcome this drawback, decoration of noble metals on the surface of semiconducting photocatalysts can be regarded as one of the promising strategies to improve the photoactivity due to a synergy of heterojunction formation and surface plasmon resonance effect. However, the huge dosage (larger than 10 wt%) of the noble metal incorporated on photocatalyst surface causes high cost in production of the final product. In this work, solvothermally grown BiOCl photocatalyst was decorated with low silver metal loading of 2.5–10 wt%. The tetragonal 2.5 wt%Ag/BiOCl photocatalyst exhibited complete photodegradation of Rhodamin B (RhB) dye and ofloxacin (OFL) antibiotic under natural solar light. The enhancement of the resultant photocatalytic efficiency is possibly due to increasing of charge carrier separation efficiency at the interface together with the formation of the Schottky barrier at the Ag/BiOCl interface so that an improvement in quantum efficiency and an increase in the photocatalytic activity are expected. In addition, well dispersion of silver on BiOCl also leads to red shift in the absorption of light toward visible regime. This is due to the local surface plasmon resonance (LSPR) effect of Ag on BiOCl surface. The synthesized Ag/BiOCl photocatalyst displays enhanced photocatalytic activity with great structural stability after five times of use indicating its excellent cycling ability. The present finding offers a new pathway to create a silver decorated BiOCl for complete removal of harmful dye and antibiotic in aqueous solution. The treatment of toxic organic pollutants in the natural water can be done very easily by utilization of the green technology based on photocatalytic method with the beneficial of abundant solar energy.

A solar evaporator fabricated from corncob waste for the desalination of seawater and removal of oil/herbicides from contaminated water

Corncob (CC) based solar evaporators were employed to desalinize seawater brought from the Vallarta coast in Mexico. The pure CC produced an evaporation-rate and evaporation-efficiency of 0.63 kg m−2 h−1 and 38.4%, respectively, under natural solar light. Later, the CC was coated with carbonized CC (CCCE evaporator) or was coated with graphene (CCGE evaporator). Those evaporators were used for the desalination of seawater and obtained higher evaporation rates of 1.59–1.67 kg m−2 h−1, and higher evaporation efficiencies of 92–94% (under natural solar light). The desalination experiments were repeated under artificial solar light and the evaporation-rates/evaporation-efficiencies slightly decreased to 1.43–1.52 kg m−2 h−1/88–92%. The surface analysis of the evaporators by FTIR, XPS and Raman revealed that the CCGE evaporator had on its surface a lower content of defects and a higher amount of OH groups than the CCCE evaporator. Therefore, the CCGE evaporator had higher evaporation-rates/evaporation-efficiencies in comparison with the CCCE evaporator. Furthermore, we purified water contaminated with three different herbicides (fomesafen, 2–6 dichlorobenzamide and 4-chlorophenol at 30 ppm) by evaporation and using natural solar light. Interestingly, the CCCE and CCGE evaporators also removed the herbicides by physical adsorption with efficiencies of 12–22.5%. Moreover, the CCGE evaporator removed vegetable oil from contaminated water by adsorption and its maximum adsorption capacity was 1.72 g/g. Overall, our results demonstrated that the corncob-based evaporators studied here are a low-cost alternative to obtain clean water under natural solar light and this one was more effective for the desalination of seawater than the artificial sunlight (Xe lamp).

Wasted scrub pad functionalized with graphene and porous BiFeO3 microparticles for the desalination/decontamination of water by solar evaporation

Solar water evaporators were fabricated with wasted scrub pad (SP) and their performance for the desalination/decontamination of water was evaluated. Firstly, bare SP was utilized for the desalination of seawater obtained from Puerto Vallarta beach, Mexico. SP produced an evaporation rate (ER)/efficiency of 2.18 kg m−2 h−1/72.6 %, respectively, under natural solar light. Subsequently, the SP evaporator was coated with graphene (G) + porous BiFeO3 (BFO) microparticles. This SPG + BFO evaporator produced an outstanding evaporation rate/efficiency of 2.93 kg m−2 h−1/94.6 %. Thus, the evaporation rate and evaporation efficiency increased by 33 % and by 22 % after adding the graphene + BFO coating. Absorbance and Raman analysis on the evaporators’ surface revealed that the evaporators made with graphene + BFO had higher absorbance of NIR light and higher content of defects. This favored the transformation of light to heat and steam generation. Additionally, the SPG + BFO evaporator was employed for the decontamination of water. Laundry wastewater (LWW) and domestic-wastewater contaminated with coke-soda (WCS) or coffee-drink (WCD) were also decontaminated using the SPG + BFO evaporator. The LWW contained mainly suspended solids, while the WCS and the WCD contained caffeine. The clean water obtained from the evaporation of LWW, WCS and WCD was completely free of suspended solids or caffeine as demonstrated by the FTIR and absorbance measurements. Overall, the results of this investigation demonstrate that low-cost evaporators can be fabricated from wasted scrub pads and those ones are very efficient for the evaporation/decontamination of water. Giving a second use to the wasted scrub pads benefits the environment because this delays its contamination by plastics.

Visible light-mediated activation of periodate for bisphenol A degradation in the presence of Fe3+ and gallic acid at neutral pH

The current study demonstrates, for the first time, the effectiveness of an innovative visible light (VL) photo-Fenton like system using periodate (PI) mediated by Fe3+ and gallic acid (GA) for bisphenol A (BPA) elimination at neutral pH. The promotion of VL irradiation and GA on the Fe2+/Fe3+ cycle in the system allowed the VL/GA/Fe3+/PI system to exhibit excellent performance for BPA removal. Complete degradation of BPA was carried out in the VL/GA/Fe3+/PI process after 30 min reaction under the optimum conditions (0.10 mM Fe3+, 0.10 mM GA, 1 mM PI, and initial pH 7.0). Electron paramagnetic resonance analysis and quenching tests confirmed that the singlet oxygen, iodate radical, and hydroxyl radical were primarily involved in the elimination of BPA with minor contribution from superoxide anion radical and high-valent iron species (Fe4+ and Fe5+). BPA abatement was slightly inhibited by the addition of Cl−, NO3−, and SO42−, whereas the addition of HCO3− obviously hindered this process. Notably, Huimic acid dramatically expedited BPA decomposition. Besides, the VL/GA/Fe3+/PI process demonstrated remarkable removal efficiency over a broad range of initial pH values (3.01–8.97). Meanwhile, based on the eight identified intermediates, the possible degradation pathways of BPA were predicted. The phytotoxicity test concluded that a decrease in toxicity of the degraded intermediates to the growth of radish seed compared to BPA. In addition, the VL/GA/Fe3+/PI system demonstrated favorable potential for application in different actual water matrices. Moreover, efficient and simultaneous abatement of various organic contaminants by the GA/Fe3+/PI process was success accomplished under natural solar light or VL. Consequently, all results implied that the VL/GA/Fe3+/PI process might be a perspective technique for the treatment of organic contaminants.