Optimizing filters of activated carbons obtained from biomass residues for ethylene removal in agro-food industry devices.

A series of adsorbents (activated carbons, ACs) were synthesized by physical and chemical activation of olive stones (OS) and their textural and chemical characteristics determined by complementary techniques such as N2 and CO2 physisorption, pH of the point zero of charge (pHPZC), HRSEM or XPS. Samples with a wide range of physicochemical properties were obtained by fitting the activation procedure. The performance of these adsorbents in filters working under dynamic conditions was studied by determining the corresponding breakthrough curves for the ethylene removal. The physicochemical transformations of OS during activation were related with the adsorptive performance of derivative ACs. Results were compared to those obtained using commercial carbons, in particular ACs, carbon black or carbon fibers, in order to identify the properties of these materials on influencing the adsorptive performance. In general, ACs from OS perform better than the commercial samples, being also easily regenerated and properly used during consecutive adsorption cycles. CO2-activation showed to be the best synthesis option, leading to granular ACs with a suitable microporosity and surface chemistry. These results could favour the integration of this type of inexpensive materials on devices for the preservation of climacteric fruits, in a clear example of circular economy by reusing the agricultural residues.

Magnetite Nanoparticles as Solar Photo-Fenton Catalysts for the Degradation of the 5-Fluorouracil Cytostatic Drug.

Heterogeneous catalysts based on magnetite nanoparticles, Fe3O4, were prepared by the chemical coprecipitation method using iron (III) chloride as a salt precursor. The physicochemical properties of the nanoparticles were determined by different techniques and the efficiency was evaluated for the degradation of the cytostatic drug, 5-fluorouracil (5-FU), in aqueous solution by photo-Fenton process under simulated solar radiation. The most influential parameters, namely pH of the solution, catalyst load, H2O2 dosage, and use of radiation, were studied and optimized in the degradation process. The optimal conditions to achieve a 100% degradation of 5-FU (10 mg L-1) and a high mineralization degree (76%) were established at the acidic pH of 3.0, 100 mg L-1 of catalyst loading, and 58 mM of H2O2 under simulated solar radiation. The contribution of iron leaching to the catalyst deactivation, the role of the dissolved iron ions on homogenous reactions, and the stability of the catalyst were assessed during consecutive reaction cycles.

One-Pot Thermal Synthesis of g-C3N4/ZnO Composites for the Degradation of 5-Fluoruracil Cytostatic Drug under UV-LED Irradiation.

Graphitic carbon nitride (g-C3N4) was used to enhance the photocatalytic activity of ZnO nanoparticles for the degradation of 5-fluorouracil (5-FU) cytostatic drug under UV-LED irradiation. CN/ZnO composites were synthetized by an easy one-pot thermal method, varying the g-C3N4 loading, i.e., from 10 to 67 wt% and a post-thermal exfoliation in air. The physicochemical and optical properties of the materials were analyzed by several techniques. CN/ZnO composites showed a coral-like structure of spherical ZnO wurtzite particles on the g-C3N4 structure. In general, the synergism and heterojunction interface between both phases allowed the enhancement of the mesoporosity, light absorption ability, and the aromaticity of the corresponding composites. Moreover, the photocatalytic activity of the CN/ZnO composites was increased with the addition of g-C3N4 in comparison with pristine ZnO. The highest activity was found for the composite containing 25 wt% of g-C3N4 (i.e., CN25/ZnO), reaching the total degradation of 5-FU and a mineralization of 48% at 180 min, as well as a good photostability during four reuse cycles. Experiments with different pH solutions and scavengers allowed for the assessment of the reactive oxygen species (ROS) involved in the 5-FU degradation pathway, with radicals and non-radical species as the main responsible active species. Furthermore, a tentative photocatalytic mechanism was proposed for CN/ZnO composites.

Photocatalytic Perfomance of ZnO-Graphene Oxide Composites towards the Degradation of Vanillic Acid under Solar Radiation and Visible-LED.

Graphene oxide (GO) is used to enhance the photocatalytic activity of ZnO nanoparticles for the degradation of vanillic acid (VA) under simulated solar light and visible-LED (λ > 430 nm). ZnO-GO composites are prepared by a mixing and sonication process with different GO loadings (i.e., from 1.8 to 6.5 wt.%). The materials are extensively characterized by thermogravimetric analysis (TGA), physisorption of N2, X-ray diffraction (XRD), infrared spectroscopy (FTIR), scanning electron microscopy (SEM), point of zero charge (pHPZC), and UV-Vis diffuse reflectance spectroscopy (DRUV). The presence of GO increases the photocatalytic activity of all the prepared composites in comparison with the pristine ZnO. The highest photocatalytic activity is found for the composite containing 5.5 wt.% of GO (i.e., ZnO-GO5.5), reaching a VA degradation of 99% and 35% under solar light and visible-LED, respectively. Higher TOC removal/VA degradation ratios are obtained from the experiments carried out under visible-LED, indicating a more effective process for the mineralization of VA than those observed under simulated solar light. The influence of hole, radical, and non-radical scavengers is studied in order to assess the occurrence of the reactive oxygen species (ROS) involved in the photocatalytic mechanism. The study of the photo-stability during three reuse experiments indicates that the presence of GO in the composites reduces the photocorrosion in comparison with pristine ZnO.

Supported Biofilms on Carbon-Oxide Composites for Nitrate Reduction in Agricultural Waste Water.

Escherichia coli colonies were grown on different supports for the removal of nitrates from water. A carbon material and different commercial metal oxides, such as SiO2, TiO2 and Al2O3, and their corresponding carbon-metal oxide composites were studied. The physicochemical properties were analyzed by different techniques and the results were correlated with their performance in the denitrification process. Developed biofilms effectively adhere to the supports and always reach the complete reduction of nitrates to gaseous products. Nevertheless, faster processes occur when the biofilm is supported on mesoporous and non-acid materials (carbon and silica).

Functionalized Graphene Derivatives and TiO2 for High Visible Light Photodegradation of Azo Dyes.

Functionalized graphene derivatives including graphene oxide (GO), reduced graphene oxide (rGO), and heteroatom (nitrogen/sulphur (N/S) or boron (B))-doped graphene were used to synthesize composites with TiO2 (T). The photocatalytic performance of composites was assessed for the degradation of Orange G dye (OG) under simulated solar light. All the prepared graphene derivatives-TiO2 composites showed better photocatalytic performance than bare TiO2. A higher photocatalytic activity was found for the composites containing GO and N/S co-doped rGO (kapp = 109.2 × 10-3 and 48.4 × 10-3 min-1, for GO-T and rGONS-T, respectively). The influence of both initial solution pH and the reactive species involved in the OG degradation pathway were studied. The photocatalytic activity of the samples decreased with the increase of the initial pH (from 3.0 to 10.0) due to the occurrence of electrostatic repulsive forces between the photocatalysts surface and the molecules of OG, both negatively charged. The use of selective scavengers showed that although the photogenerated holes dominate the degradation mechanism, radicals and singlet oxygen also participate in the OG degradation pathway. In addition, reutilization experiments indicated that the samples were stable under the reaction conditions used.

Antiparasitic, anti-inflammatory and cytotoxic activities of 2D coordination polymers based on 1H-indazole-5-carboxylic acid.

We report on the formation of two novel multifunctional isomorphous (4,4) square-grid 2D coordination polymers based on 1H-indazole-5-carboxylic acid. To the best of our knowledge, these complexes are the first examples of 2D-coordination polymers constructed with this novel ligand. We have analysed in detail the structural, magnetic and anti-parasitic properties of the resulting materials. In addition, the capability of inhibiting nitric oxide production from macrophage cells has been measured and was used as an indirect measure of the anti-inflammatory response. Finally, the photocatalytic activity was measured with a model pollutant, i.e. vanillic acid (phenolic compound), with the aim of further increasing the functionalities and applicability of the compounds.

Hummers' and Brodie's graphene oxides as photocatalysts for phenol degradation.

Undoped metal-free graphene oxide (GO) materials prepared by either a modified Hummers' (GO-H) or a Brodie's (GO-B) method were tested as photocatalysts in aqueous solution for the oxidative conversion of phenol. In the dark, the adsorptive capacity of GO-B towards phenol (~35%) was higher than that of GO-H (~15%). Upon near-UV/Vis irradiation, GO-H was able to remove 21% of phenol after 180 min, mostly through adsorption. On the other hand, by using less energetic visible irradiation, GO-B removed as much as 95% in just 90 min. By thorough characterization of the prepared materials (SEM, HRTEM, TGA, TPD, Raman, XRD, XPS and photoluminescence) the observed performances could be explained in terms of their different surface chemistries. The GO-B presents the lower concentration of oxygen functional groups (in particular carbonyl groups as revealed by XPS) and it has a considerably higher photocatalytic activity compared to GO-H. Photoluminescence (PL) of liquid dispersions and XRD analysis of powders showed lower PL intensity and smaller interlayer distance for GO-B relative to GO-H, respectively: this suggests lower electron-hole recombination and enhanced electron transfer in GO-B, in support of its boosted photocatalytic activity. Reusability tests showed no efficiency loss after a second usage cycle and over three runs under visible irradiation, which was in line with the similarity of the XPS spectra of the fresh and used GO-B materials. Moreover, scavenging studies revealed that holes and hydroxyl radicals were the main reactive species in play during the photocatalytic process. The obtained results, establish for the first time, that GO prepared by Brodie's method is an active and stable undoped metal-free photocatalyst for phenol degradation in aqueous solutions, opening new paths for the application of more sustainable and metal-free materials for water treatment solutions.

Syngas production by bi-reforming methane on an Ni-K-promoted catalyst using hydrotalcites and filamentous carbon as a support material.

Steam reforming of methane (SRM) and dry reforming of methane (DRM) are frequently used in the production of syngas; however, the bi-reforming of methane (BRM) is an interesting and alternative process. In this study, BRM was studied over MgO, a layered double hydroxide (LDH) phase that was destroyed between 600 °C and 900 °C during the reaction. It showed good sorption capacity for CO2 at relatively low temperatures (<500 °C), with CO2 adsorption being a pre-requisite for its catalytic conversion. Among the tested materials, the potassium-promoted LDH showed the highest activity, achieving a maximum CO2 conversion of 75%. The results suggest that at high temperature, the electronic structure of the used materials influences the destabilization of the feed in the order of methane, water and carbon dioxide. K promotes the catalytic activity, compensates the presence of large Ni particle sizes originating from the high metal loading, and favors the formation of Mg-Al-spinel. K is known to be an electronic promoter that releases electrons, which flow to the active metal. This electron flow induces instability on the molecule to be converted, and most probably, also induces size variations on the respective active nickel metal. The influence of the operating conditions in the range of 300 °C to 900 °C on the conversion of the reactants and product distribution was studied. Accordingly, it was concluded that it is only possible to obtain molar ratios of hydrogen-to-carbon monoxide close to two at high temperatures, a pre-requisite for the synthesis of methanol.

Correction: Syngas production by bi-reforming methane on an Ni-K-promoted catalyst using hydrotalcites and filamentous carbon as a support material.

[This corrects the article DOI: 10.1039/D0RA03264F.].

From Polyethylene to Highly Graphitic and Magnetic Carbon Spheres Nanocomposites: Carbonization under Pressure.

Carbon nanocomposites microspheres were synthesized from Low-Density Polyethylene (LDPE) by a facile one-step strategy under solvent-free conditions. The synthesis of these materials was carried out in a closed Hastelloy® reactor at 700 °C. The treatment, during which autogenic pressure was generated, leads to highly graphitic materials with stunning properties, particularly concerning the oxidation resistance (compared to the graphite stability). The metallic doping triggers the growth of nanostructures with diverse morphologies around the spheres, obtaining samples with magnetic properties.

TiO2-based (Fe3O4, SiO2, reduced graphene oxide) magnetically recoverable photocatalysts for imazalil degradation in a synthetic wastewater.

Magnetite (Fe3O4), a core-shell material (SiO2@Fe3O4), and reduced graphene oxide-Fe3O4 (referred as rGO-MN) were used as supports of a specific highly active TiO2 photocatalyst. Thermal treatments at 200 or 450 °C, different atmospheres (air or N2), and TiO2:support weight ratios (1.0, 1.5, or 2.0) were investigated. X-ray diffractograms revealed that magnetite is not oxidized to hematite when the core-shell SiO2@Fe3O4 material-or a N2 atmosphere (instead of air) in the thermal treatment-was employed to prepare the TiO2-based catalysts (the magnetic properties being preserved). The materials treated with N2 were first tested for degradation of imazalil (a well-known fungicide) in deionized water. The best compromise between the photocatalytic activity, magnetic separation, and Fe leached (1.61 mg L-1, i.e., below the threshold for water reuse in irrigation) was found for the magnetic catalyst prepared with SiO2@Fe3O4, an intermediate TiO2:support ratio (1.5), and treated at 200 °C under N2 atmosphere (i.e., SiO2@Fe3O4-EST-1.5-200-N2). This material was then tested for the treatment of imazalil in a synthetic wastewater, SW (with a chemical composition simulating an effluent resulting from fruit postharvest activity). This SW has a pH of 4.2 and the experiments were carried out at this natural pH0 and at neutral conditions (keeping pH at 7 along the reaction). The magnetic catalyst was more active than bare TiO2 for the treatment of imazalil in SW at natural pH. Since Fe leaching was observed (3.53 mg L-1), added H2O2 enhanced both imazalil degradation and mineralization. Conveniently, these catalysts can be readily recovered by using a conventional magnetic field, as demonstrated over three consecutive recycling runs. Graphical abstract % Imazalil conversion using different magnetic catalysts and comparison with bare TiO2.

Solar treatment (H2O2, TiO2-P25 and GO-TiO2 photocatalysis, photo-Fenton) of organic micropollutants, human pathogen indicators, antibiotic resistant bacteria and related genes in urban wastewater.

Solar-driven advanced oxidation processes were studied in a pilot-scale photoreactor, as tertiary treatments of effluents from an urban wastewater treatment plant. Solar-H2O2, heterogeneous photocatalysis (with and/or without the addition of H2O2 and employing three different photocatalysts) and the photo-Fenton process were investigated. Chemical (sulfamethoxazole, carbamazepine, and diclofenac) and biological contaminants (faecal contamination indicators, their antibiotic resistant counterparts, 16S rRNA and antibiotic resistance genes), as well as the whole bacterial community, were characterized. Heterogeneous photocatalysis using TiO2-P25 and assisted with H2O2 (P25/H2O2) was the most efficient process on the degradation of the chemical organic micropollutants, attaining levels below the limits of quantification in less than 4 h of treatment (corresponding to QUV < 40 kJ L-1). This performance was followed by the same process without H2O2, using TiO2-P25 or a composite material based on graphene oxide and TiO2. Regarding the biological indicators, total faecal coliforms and enterococci and their antibiotic resistant (tetracycline and ciprofloxacin) counterparts were reduced to values close, or beneath, the detection limit (1 CFU 100 mL-1) for all treatments employing H2O2, even upon storage of the treated wastewater for 3-days. Moreover, P25/H2O2 and solar-H2O2 were the most efficient processes in the reduction of the abundance (gene copy number per volume of wastewater) of the analysed genes. However, this reduction was transient for 16S rRNA, intI1 and sul1 genes, since after 3-days storage of the treated wastewater their abundance increased to values close to pre-treatment levels. Similar behaviour was observed for the genes qnrS (using TiO2-P25), blaCTX-M and blaTEM (using TiO2-P25 and TiO2-P25/H2O2). Interestingly, higher proportions of sequence reads affiliated to the phylum Proteobacteria (Beta- and Gammaproteobacteria) were found after 3-days storage of treated wastewater than before its treatment. Members of the genera Pseudomonas, Rheinheimera and Methylotenera were among those with overgrowth.

Graphene oxide based ultrafiltration membranes for photocatalytic degradation of organic pollutants in salty water.

Flat sheet ultrafiltration (UF) membranes with photocatalytic properties were prepared with lab-made TiO2 and graphene oxide-TiO2 (GOT), and also with a reference TiO2 photocatalyst from Evonik (P25). These membranes were tested in continuous operation mode for the degradation and mineralization of a pharmaceutical compound, diphenhydramine (DP), and an organic dye, methyl orange (MO), under both near-UV/Vis and visible light irradiation. The effect of NaCl was investigated considering simulated brackish water (NaCl 0.5 g L(-1)) and simulated seawater (NaCl 35 g L(-1)). The results indicated that the membranes prepared with the GOT composite (M-GOT) exhibited the highest photocatalytic activity, outperforming those prepared with bare TiO2 (M-TiO2) and P25 (M-P25), both inactive under visible light illumination. The best performance of M-GOT may be due to the lower band-gap energy (2.9 eV) of GOT. In general, the permeate flux was also higher for M-GOT probably due to a combined effect of its highest photocatalytic activity, highest hydrophilicity (contact angles of 11°, 17° and 18° for M-GOT, M-TiO2 and M-P25, respectively) and higher porosity (71%). The presence of NaCl had a detrimental effect on the efficiency of the membranes, since chloride anions can act as hole and hydroxyl radical scavengers, but it did not affect the catalytic stability of these membranes. A hierarchically ordered membrane was also prepared by intercalating a freestanding GO membrane in the structure of the M-GOT membrane (M-GO/GOT). The results showed considerably higher pollutant removal in darkness and good photocatalytic activity under near-UV/Vis and visible light irradiation in continuous mode experiments.

Modification of the surface chemistry of single- and multi-walled carbon nanotubes by HNO3 and H2SO4 hydrothermal oxidation for application in direct contact membrane distillation.

A specific methodology based on nitric acid hydrothermal oxidation was used to control the surface chemistry of multi-walled (MWCNTs) and single-walled (SWCNTs) carbon nanotubes (CNTs) with different lengths, and this methodology was adapted to the use of sulphuric acid containing ammonium persulfate as an oxidizing agent. The amount of oxygen-containing surface groups depends on the number and length of the graphene layers of the CNTs, thicker and shorter CNTs having more reactive sites for surface functionalization. In particular, the oxidation of MWCNTs was more pronounced than that of short SWCNTs and less surface groups were introduced into long SWCNTs, regardless of the acid used at any fixed concentration. It was also possible to tailor the surface chemistry of both SWCNTs and MWCNTs by using the adopted methodologies, and the amount of both oxygen- and sulphur-containing functional groups was correlated with the concentration of each oxidizing agent used. Mathematical functions that allow precise control of the amount and type of the surface groups introduced into carbon nanotubes were obtained. Buckypapers were also prepared over a polytetrafluoroethylene commercial membrane. These membranes were tested in direct contact membrane distillation and, under salinity conditions, the membrane prepared using oxidized MWCNTs (instead of SWCNTs) was the most efficient, the permeate flux of the commercial membrane significantly increasing in the presence of these CNTs, while completely rejecting chloride ions. In addition, the permeate flux was precisely correlated with the amount of oxygenated functional surface groups (as well as with the pH of point of zero charge) of the oxidized MWCNTs.

Nanodiamond-TiO2 Composites for Heterogeneous Photocatalysis.

Invited for this month's cover are collaborators from the University of Porto in Portugal and KU Leuven in Belgium. The image shows that nanodiamond-TiO2 composites can effectively degrade organic water pollutants by photocatalysis under ambient conditions. This process will reduce human impact on freshwater systems, thereby contributing to meet worldwide targets on water footprint reduction. Read the full text of the article at 10.1002/cplu.201300094.

Nanodiamond-TiO2 Composites for Heterogeneous Photocatalysis.

This is a pioneering study on the synthesis and application of composites based on micro- and nanodiamonds for the photocatalytic degradation of environmental water pollutants. Micro- and nanodiamond powders (with particle sizes of 1-3 µm and 2-10 nm, respectively) were combined with TiO2 , by varying the carbon-phase content, and tested as composite photocatalysts for the degradation of diphenhydramine, which is a pharmaceutical water pollutant, under near-UV/Vis irradiation. These composites exhibited higher photocatalytic activity than the respective bare materials. In addition, composites prepared with pristine nanodiamonds were always more active than those prepared with microdiamonds of the same carbon content. A significant enhancement in the photocatalytic performance was observed on preparation of the composite with 15 wt % of nanodiamonds oxidised in air at 703 K; these oxidised nanodiamonds contained mainly carboxylic anhydrides, lactones, phenols and, to a lesser extent, carbonyl/quinone groups on their surface.

Design of graphene-based TiO2 photocatalysts--a review.

There is a recent increase in the interest of designing high-performance photocatalysts using graphene-based materials. This review gathers some important aspects of graphene-TiO(2), graphene oxide-TiO(2), and reduced graphene oxide-TiO(2) composites, which are of especial relevance as next generation photocatalysts. The methods used for the preparation of these materials, the associated mechanistic fundamentals, and the application of graphene-based composites on the photocatalytic degradation of pollutants are reviewed. Some structural, textural, and chemical properties of these materials and other photo-assisted applications, such as hydrogen production from water splitting and dye-sensitized solar cells, are also briefly included.