Effects of Different TiO2/CNT Coatings of PVDF Membranes on the Filtration of Oil-Contaminated Wastewaters.

Six different TiO2/CNT nanocomposite-coated polyvinylidene-fluoride (PVDF) microfilter membranes (including -OH or/and -COOH functionalized CNTs) were evaluated in terms of their performance in filtering oil-in-water emulsions. In the early stages of filtration, until reaching a volume reduction ratio (VRR) of ~1.5, the membranes coated with functionalized CNT-containing composites provided significantly higher fluxes than the non-functionalized ones, proving the beneficial effect of the surface modifications of the CNTs. Additionally, until the end of the filtration experiments (VRR = 5), notable flux enhancements were achieved with both TiO2 (~50%) and TiO2/CNT-coated membranes (up to ~300%), compared to the uncoated membrane. The irreversible filtration resistances of the membranes indicated that both the hydrophilicity and surface charge (zeta potential) played a crucial role in membrane fouling. However, a sharp and significant flux decrease (~90% flux reduction ratio) was observed for all membranes until reaching a VRR of 1.1-1.8, which could be attributed to the chemical composition of the oil. Gas chromatography measurements revealed a lack of hydrocarbon derivatives with polar molecular fractions (which can act as natural emulsifiers), resulting in significant coalescent ability (and less stable emulsion). Therefore, this led to a more compact cake layer formation on the surface of the membranes (compared to a previous study). It was also demonstrated that all membranes had excellent purification efficiency (97-99.8%) regarding the turbidity, but the effectiveness of the chemical oxygen demand reduction was slightly lower, ranging from 93.7% to 98%.

Photoinhibitive Properties of α-MoO3 on Its Composites with TiO2, ZnO, BiOI, AgBr, and Cu2O.

Orthorhombic molybdenum trioxide (α-MoO3) is well known as a photocatalyst, adsorbent, and inhibitor during methyl orange photocatalytic degradation via TiO2. Therefore, besides the latter, other active photocatalysts, such as AgBr, ZnO, BiOI, and Cu2O, were assessed via the degradation of methyl orange and phenol in the presence of α-MoO3 using UV-A- and visible-light irradiation. Even though α-MoO3 could be used as a visible-light-driven photocatalyst, our results demonstrated that its presence in the reaction medium strongly inhibits the photocatalytic activity of TiO2, BiOI, Cu2O, and ZnO, while only the activity AgBr is not affected. Therefore, α-MoO3 might be an effective and stable inhibitor for photocatalytic processes to evaluate the newly explored photocatalysts. Quenching the photocatalytic reactions can offer information about the reaction mechanism. Moreover, the absence of photocatalytic inhibition suggests that besides photocatalytic processes, parallel reactions take place.

Outstanding Separation Performance of Oil-in-Water Emulsions with TiO2/CNT Nanocomposite-Modified PVDF Membranes.

Membrane filtration is an effective technique for separating micro- and nano-sized oil droplets from harmful oil-contaminated waters produced by numerous industrial activities. However, significant flux reduction discourages the extensive application of this technology; therefore, developing antifouling membranes is necessary. For this purpose, various titanium dioxide/carbon nanotube (TiO2/CNT) nanocomposites (containing 1, 2, and 5 wt.% multi-walled CNTs) were used for the modification of polyvinylidene fluoride (PVDF) ultrafilter (250 kDa) membrane surfaces. The effects of surface modifications were compared in relation to the flux, the filtration resistance, the flux recovery ratio, and the purification efficiency. TiO2/CNT2% composite modification reduced both irreversible and total filtration resistances the most during the filtration of 100 ppm oil emulsions. The fluxes were approximately 4-7 times higher compared to the unmodified PVDF membrane, depending on the used transmembrane pressure (510, 900, and 1340 L/m2h fluxes were measured at 0.1, 0.2, and 0.3 MPa pressures, respectively). Moreover, the flux recovery ratio (up to 68%) and the purification efficiency (95.1-99.8%) were also significantly higher because of the surface modification, and the beneficial effects were more dominant at higher transmembrane pressures. TiO2/CNT2% nanocomposites are promising to be applied to modify membranes used for oil-water separation and achieve outstanding flux, cleanability, and purification efficiency.

Visible-light-driven photocatalytic PVDF-TiO2/CNT/BiVO4 hybrid nanocomposite ultrafiltration membrane for dairy wastewater treatment.

Enhancing the performance of polymeric membranes by nanomaterials has become of great interest in the field of membrane technology. The present work aimed to fabricate polyvinylidene fluoride (PVDF)-hybrid nanocomposite membranes and modify them with TiO2 and/or BiVO4 nanoparticles and/or carbon nanotubes (CNTs) in various ratios. Their photocatalytic performance under visible light was also investigated. All modified PVDF membranes exhibited higher hydrophilicity (lower contact angle of water droplets) than that of the neat membrane used as a reference. The membranes were characterized by using bovine serum albumin (BSA) as model dairy wastewater. The hybrid membranes had better antifouling properties as they had lower irreversible filtration resistance than that of the neat membrane. Hybrid PVDF membranes containing TiO2/CNT/BiVO4 showed the highest flux and lowest irreversible resistance during the filtration of the BSA solution. PVDF-TiO2/BiVO4 had the highest flux recovery ratio under visible light (70% for the PVDF mixed with 0.5% TiO2 and 0.5% BiVO4). The hydrophilicity of membrane surfaces increased with the incorporation of nanoparticles, preventing BSA to bind to the surface. This resulted in a slight decrease in BSA and chemical oxygen demand rejections, which were still above 97% in all cases.

Co-Crystals of Etravirine by Mechanochemical Activation.

The co-crystals formation of etravirine with three carboxylic acids was investigated. New co-crystals of etravirine with adipic acid, benzoic acid, and 4-hydroxybenzoic acid have been synthesized by wet milling of ingredients for 120 min. The novelty of these solid forms was first evidenced by powder X-ray diffraction. Their different morphology was evidenced by SEM microscopy. Spectroscopic analyses (FT-IR, MAS-NMR, and XPS) highlighted the hydrogen bonds between etravirine and co-formers, as a result of the solid-state reaction of the ingredients by wet milling. Thermal analyses pointed out that the milling process caused in co-crystals a reduction in the fusion enthalpy and the melting temperature, compared to the values obtained for etravirine. These co-crystals are stable up to four months on storage under extreme conditions, excepting the co-crystal with benzoic acid which begins to transform into a polymorph of etravirine after 30 days. The UV absorption spectra of the samples tested in three simulated physiological media with pH values of 6, 6.3, and 7 have evidenced the conformation change of etravirine due to hydrogen bonds between etravirine and carboxylic acids.

Rapid Synthesis Method of Ag3PO4 as Reusable Photocatalytically Active Semiconductor.

The widespread use of Ag3PO4 is not surprising when considering its higher photostability compared to other silver-based materials. The present work deals with the facile precipitation method of silver phosphate. The effects of four different phosphate sources (H3PO4, NaH2PO4, Na2HPO4, Na3PO4·12 H2O) and two different initial concentrations (0.1 M and 0.2 M) were investigated. As the basicity of different phosphate sources influences the purity of Ag3PO4, different products were obtained. Using H3PO4 did not lead to the formation of Ag3PO4, while applying NaH2PO4 resulted in Ag3PO4 and a low amount of pyrophosphate. The morphological and structural properties of the obtained samples were studied by X-ray diffractometry, diffuse reflectance spectroscopy, scanning electron microscopy, infrared spectroscopy, and X-ray photoelectron spectroscopy. The photocatalytic activity of the materials and the corresponding reaction kinetics were evaluated by the degradation of methyl orange (MO) under visible light. Their stability was investigated by reusability tests, photoluminescence measurements, and the recharacterization after degradation. The effect of as-deposited Ag nanoparticles was also highlighted on the photostability and the reusability of Ag3PO4. Although the deposited Ag nanoparticles suppressed the formation of holes and reduced the degradation of methyl orange, they did not reduce the performance of the photocatalyst.

Optimization Method of the Solvothermal Parameters Using Box-Behnken Experimental Design-The Case Study of ZnO Structural and Catalytic Tailoring.

ZnO photocatalysts were synthesized via solvothermal method and a reduced experimental design (Box-Behnken) was applied to investigate the influence of four parameters (temperature, duration, composition of the reaction mixture) upon the photocatalytic activity and the crystal structure of ZnO. The four parameters were correlated with photocatalytic degradation of methyl orange and the ratio of two crystallographic facets ((002) and (100)) using a quadratic model. The quadratic model shows good fit for both responses. The optimization experimental results validated the models. The ratio of the crystal facets shows similar variation as the photocatalytic activity of the samples. The water content of the solvent is the primary factor, which predominantly influence both responses. An explanation was proposed for the effect of the parameters and how the ratio of (002) and (100) crystal facets is influenced and its relation to the photocatalytic activity. The present research laconically describes a case study for an original experimental work, in order to serve as guideline to deal with such complicated subjects as quantifying influence of synthesis parameters upon the catalytic activity of the obtained ZnO.

Hydrothermal Crystallization of Bismuth Oxychlorides (BiOCl) Using Different Shape Control Reagents.

Bismuth oxychloride photocatalysts were obtained using solvothermal synthesis and different additives (CTAB-cetyltrimethylammonium bromide, CTAC-cetyltrimethylammonium chloride, PVP-polyvinylpyrrolidone, SDS-sodium dodecylsulphate, U-urea and TU-thiourea). The effect of the previously mentioned compounds was analyzed applying structural (primary crystallite size, crystal phase composition, etc.), morphological (particle geometry), optical (band gap energy) parameters, surface related properties (surface atoms' oxidation states), and the resulted photocatalytic activity. A strong dependency was found between the surface tension of the synthesis solutions and the overall morpho-structural parameters. The main finding was that the characteristics of the semiconductors can be tuned by modifying the surface tension of the synthesis mixture. It was observed after the photocatalytic degradation, that the white semiconductor turned to grey. Furthermore, we attempted to explain the gray color of BiOCl catalysts after the photocatalytic decompositions by Raman and XPS studies.

The Effect of the Reducing Sugars in the Synthesis of Visible-Light-Active Copper(I) Oxide Photocatalyst.

In the present work, shape tailored Cu2O microparticles were synthesized by changing the nature of the reducing agent and studied subsequently. d-(+)-glucose, d-(+)-fructose, d-(+)xylose, d-(+)-galactose, and d-(+)-arabinose were chosen as reducing agents due to their different reducing abilities. The morpho-structural characteristics were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and diffuse reflectance spectroscopy (DRS), while their photocatalytic activity was evaluated by methyl orange degradation under visible light (120 min). The results show that the number of carbon atoms in the sugars affect the morphology and particle size (from 250 nm to 1.2 µm), and differences in their degree of crystallinity and photocatalytic activity were also found. The highest activity was observed when glucose was used as the reducing agent.

Shape-Tailored TiO2 Photocatalysts Obtained in the Presence of Different Types of Carbon Materials.

Titania and carbon materials are intensively studied in composite materials including photocatalytic applications. Both positive and negative effects were described in the literature, including charge separation, adsorption enhancement and short-circuiting of the photoelectrons as well. In the present study a more sparsely investigated properties of carbon materials will be highlighted, namely their role as crystallization promoters for titania, during hydrothermal synthesis of the composites. Therefore, carbon nanotubes, carbon coils, activated carbon, graphite and carbon aerogel was used to identify the importance of carbon during the time dependent crystallization of titanium dioxide. The crystal phase composition, morphology, optical properties and photocatalytic activity was followed, and it was found that the anatase and rutile crystallization depended on the used carbon material. The morphology of the particles varied from single anatase sheet-like crystals to hierarchical microball-like structures, while in some cases no specific morphology was observed. Furthermore, it was found that despite the low carbon content (2 wt.%) and microcrystalline structure of TiO2 the composites were proven to be efficient in the degradation of Rhodamine B under UV light irradiation.

Mechanistic insight of structural and optical properties of BiOCl in the presence of CNTs and investigating photodegradation of phenol by BiOCl/CNT composites.

In this work, we have synthesized composites of BiOCl with carbon nanotubes (CNTs) via a hydrothermal method. Different compositions of CNTs were used to study their influence on the physicochemical properties of BiOCl. Based on the interesting results obtained, various significant correlations were made. This study explored how use of CNTs and different hydrothermal crystallization conditions can influence the photocatalytic activity of composites. The CNTs have an impact on the primary crystallite size and morphology of BiOCl. Also, a higher degree of crystallization was obtained in the case of samples containing CNTs. However, in some cases, the synthesis parameters such as high temperature and longer duration also promoted crystallinity in BiOCl/CNT samples. Further, the samples were investigated for their photocatalytic activity to study the photodegradation of RhB and phenol, as model pollutants, under visible and UV light, respectively. The maximum degradation efficiency of 83% for RhB under visible light and almost 40% for phenol under UV light was obtained using BiOCl/CNT composites. Surprisingly, pure BiOCl showed higher performance for the removal of both the pollutants. This is why some comparisons and correlations between the structural and optical properties of BiOCl and CNTs were made. Finally, this study illustrates how a nanostructure like conductive multiwalled carbon nanotubes can sometimes have detrimental effects on the overall photocatalytic properties of a photocatalyst like BiOCl under certain conditions. Therefore, understanding the synergy between physico-chemical properties of BiOCl and nanostructured-modifiers like CNTs could help in designing a photocatalyst system which could benefit wastewater treatment.

Shape tailoring of AgBr microstructures: effect of the cations of different bromide sources and applied surfactants.

Investigations regarding AgBr-based photocatalysts came to the center of attention due to their high photosensitivity. The present research focuses on the systematic investigation regarding the effect of different alkali metal cation radii and surfactants/capping agents applied during the synthesis of silver-halides. Their morpho-structural and optical properties were determined via X-ray diffractometry, diffuse reflectance spectroscopy, scanning electron microscopy, infrared spectroscopy, and contact angle measurements. The semiconductors' photocatalytic activities were investigated using methyl orange as the model contaminant under visible light irradiation. The correlation between the photocatalytic activity and the obtained optical and morpho-structural properties was analyzed using generalized linear models. Moreover, since the (photo)stability of Ag-based photoactive materials is a crucial issue, the stability of catalysts was also investigated after the degradation process. It was concluded that (i) the photoactivity of the samples could be fine-tuned using different precursors and surfactants, (ii) the as-obtained AgBr microcrystals were transformed into other Ag-containing composites during/after the degradation, and (iii) elemental bromide did not form during the degradation process. Thus, the proposed mechanisms in the literature (for the degradation of MO using AgBr) must be reconsidered.

Innovative and Cost-Efficient BiOI Immobilization Technique on Ceramic Paper-Total Coverage and High Photocatalytic Activity.

In the present work, visible light active bismuth oxyiodide (BiOI) was immobilized on a commercial, non-conductive support (an Al2O3 based ceramic paper) using a novel two-step spray coating technique and investigated with different characterization methods (e.g., SEM, Raman, XPS). Our main goal was to eliminate the separation costs after the photocatalytic measurement and investigate the chemical relevance and opportunity to use this technique in the industry. Our as-prepared uniform BiOI layer had similar properties to the well-known reference BiOI powder. The Raman and XPS measurements confirmed that the enriched amount of the surface iodine defined the color and as well the band gap of the BiOI layer. The durable BiOI layers have prominent photocatalytic activity under UV and visible light irradiation as well. The scale-up procedure proved that the designed BiOI coated paper was reusable and potentially applicable in the industry by straightforward scale-up, which is due to the elaborated non-conventional BiOI coverage estimation method. This immobilization technique could open several opportunities for immobilizing many other visible light active photocatalysts with simple materials and low cost.

New Insights into The Photoactivity of Shape-Tailored BiVO4 Semiconductors via Photocatalytic Degradation Reactions and Classical Reduction Processes.

In the present study, additive-free, pH-driven, hydrothermal crystallization was used to obtain shape-tailored monoclinic BiVO4 photocatalysts. The as-prepared BiVO4 products were systematically characterized, uncovering their crystallographic, morphologic and optical properties, while their applicability was verified in the visible light-driven photodegradation of oxalic acid and rhodamine B. Monoclinic clinobisvanite was obtained in most cases, with their band gap values located between 2.1 and 2.4 eV. The morphology varied from large, aggregated crystals, individual microcrystals to hierarchical microstructures. It was found that the degradation efficiency values obtained in the case of oxalic acid were directly related to the presence of (040) crystallographic plane, while the degradation of rhodamine B was partially independent by the presence of this structural feature. The importance of (040) crystallographic plane was also demonstrated via the reduction of Cu2+ to Cu, by analyzing the Raman spectra of the Cu containing samples, the mean primary crystallite size of Cu and Cu content. Furthermore, the presence of (040) crystallographic plane was directly proportional with the hydrodynamic properties of the powders as well.

Controlled Synthesis of Visible Light Active CuxS Photocatalyst: The Effect of Heat Treatment on Their Adsorption Capacity and Photoactivity.

The effects of different precursor salts, stabilizing agents, and heat treatment parameters are already known to have an influence on the synthesis of nano-sized semiconductors in heterogenous photocatalysis. In the present work, CuxS materials were prepared by using different precursors (copper (II) chloride dihydrate or copper (II) acetate monohydrate) and shape tailoring/stabilizing agents, such as ethylenediaminetetraacetic acid/polyvinylpyrrolidone, and thiourea as the sulfur source. The polyvinylpyrrolidone (PVP) kinetically controlled the growth rate of the nanoplates, while ethylenediaminetetraacetic acid (EDTA) adjusted the nucleation process through the complexation of copper. A one-step hydrothermal method was used for the synthesis, and the materials were characterized by means of morphological and structural complementary investigation methods. Furthermore, the adsorption capacity and photocatalytic activity were also measured for these materials. It was found that the vacancy sites formed by changing the precursor salt, as confirmed by Raman measurements, affect the photocatalytic activity. The rise of the specific surface area was achieved by heat treatment, and concomitantly, the adsorption capacity of the treated samples was found to increase likewise.

Utilization of Carbon Nanospheres in Photocatalyst Production: From Composites to Highly Active Hollow Structures.

Titanium dioxide-carbon sphere (TiO2-CS) composites were constructed via using prefabricated carbon spheres as templates. By the removal of template from the TiO2-CS, TiO2 hollow structures (HS) were synthesized. The CS templates were prepared by the hydrothermal treatment of ordinary table sugar (sucrose). TiO2-HSs were obtained by removing CSs with calcination. Our own sensitized TiO2 was used for coating the CSs. The structure of the CSs, TiO2-CS composites, and TiO2-HSs were characterized by scanning electron microscopy (SEM), infrared spectroscopy (IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and diffuse reflectance spectroscopy (DRS). The effect of various synthesis parameters (purification method of CSs, precursor quantity, and applied furnace) on the morphology was investigated. The photocatalytic activity was investigated by phenol model pollutant degradation under visible light irradiation (λ > 400 nm). It was established that the composite samples possess lower crystallinity and photocatalytic activity compared to TiO2 hollow structures. Based on XPS measurements, the carbon content on the surface of the TiO2-HS exerts an adverse effect on the photocatalytic performance. The synthesis parameters were optimized and the TiO2-HS specimen having the best absolute and surface normalized photocatalytic efficiency was identified. The superior properties were explained in terms of its unique morphology and surface properties. The stability of this TiO2-HS was investigated via XRD and SEM measurements after three consecutive phenol degradation tests, and it was found to be highly stable as it entirely retained its crystal phase composition, morphology and photocatalytic activity.

Decoration of Vertically Aligned Carbon Nanotubes with Semiconductor Nanoparticles Using Atomic Layer Deposition.

Vertically aligned carbon nanotubes (VACNTs or "CNT forest") were decorated with semiconductor particles (TiO2 and ZnO) by atomic layer deposition (ALD). Both the structure and morphology of the components were systematically studied using scanning (SEM) and high resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and X-ray diffraction (XRD) methods. Characterization results revealed that the decoration was successful in the whole bulk of VACNTs. The effect of a follow-up heat treatment was also investigated and its effect on the structure was proved. It was attested that atomic layer deposition is a suitable technique for the fabrication of semiconductor/vertically aligned carbon nanotubes composites. Regarding their technological importance, we hope that semiconductor/CNT forest nanocomposites find potential application in the near future.

The Comparison of the Photocatalytic Performance Shown by TiO2 and TiO2/WO3 Composites- A Parametric and Kinetic Study.

Kinetic and mechanistic related approaches for mostly titania were intensively studied in the literature. However, combined modelling and kinetic studies are few. Therefore, the present work focuses on modelling the dependence of the degradation kinetics of two model compounds (salicylic acid-SA and methyl orange-MO) on Evonik Aeroxide P25, hydrothermally prepared hierarchical TiO2 and P25/WO3 nanostars, obtained also by hydrothermal crystallization. The obtained individual semiconductors and the composites were characterized using XRD, DRS, SEM, while the photocatalytic degradation of the model pollutants were carried out varying the catalyst load, the initial pollutant concentration and incident light intensity. It was found that the degradation kinetics were independent from the hierarchical nature of the material, while significant dependencies of the degradation efficiency was found from the previously mentioned investigation parameters. All these parametric interdependences were successfully studied and a kinetic model was proposed for both bare TiO2 and TiO2/WO3 composite systems.

Detailed Investigation of Phenol Degradation on Au/TiO2 Composite Materials.

Photocatalytic applicability of different TiO2-based nanomaterials is a current hot topic. Therefore, our interest for the present research was to elucidate the formation of primary and secondary intermediates during the phenol degradation by photocatalysis, in the presence of Au/TiO2 nanocomposites. The composites consisted of differently shaped gold nanoparticles and commercial titania (Evonik Aeroxide P25). The obtained composites and the noble metal nanoparticles' morphology was investigated by Transmission Electron Microscopy (TEM), their optical properties were explored using Diffuse Reflectance Spectroscopy (DRS), while the crystal structure was characterized by X-ray diffraction (XRD). The photocatalytic activity was investigated by photodegradation of phenol and methyl orange. In case of phenol it was shown that, the formation of degradation intermediates, was dependent on the Au nanoparticles' shape, leading to high amounts of different intermediates as follows: hydroquinone for composites with spherical Au nanoparticles, 1,2,4-trihydroxy-benzene for triangle shaped nanoparticles, and pyrocatechol for TiO2.