Formulation and rheological evaluation of liposomes-loaded carbopol hydrogels based on thermal waters.

The aims of this study were to develop topical liposomal hydrogels based on thermal waters (TWs) acquired in the region of Biskra (Northeast Algeria) and also to investigate their rheological properties. Liposomes containing two highly mineralized thermal waters, Baraka (BTW) and Salhine (STW), were prepared by probe sonication using phosphatidylcholine (PC) and cholesterol (Chol), plain or mixed with phosphatidylglycerol (PG). Based on their lipid composition, obtained liposomes presented vesicle sizes of 60 nm, a low polydispersity index, and various negative zeta potentials. It was noted that with increasing counterions charge in TWs the zeta potential of liposomes decreased toward neutral values.Carbopol (1%, w/w) hydrogels prepared with BTW, STW, and also demineralized water (placebo hydrogel) showed a non-Newtonian behavior, pseudoplastic fluid adjusted to Carreau model. The composition of thermal waters influenced highly the rheological properties of Carbopol hydrogels. Liposomal hydrogels were prepared by dispersing liposomes in hydrogels formulated with the same encapsulated thermal water. Regardless of composition or lipid concentration of added liposomes, the viscosity and viscoelastic parameters of Carbopol hydrogels changed negligibly. Indeed, liposome composition and lipid concentration seemed to have no effect on the rheological properties of Carbopol hydrogel in the presence of an important charge of cations. Hence, hydrogels and liposomal hydrogels based on thermal waters had suitable rheological properties for topical application and delivery of minerals in the skin.

Peroxidase enzymes as green catalysts for bioremediation and biotechnological applications: A review.

The fast-growing consumer demand drives industrial process intensification, which subsequently creates a significant amount of waste. These products are discharged into the environment and can affect the quality of air, degrade water streams, and alter soil characteristics. Waste materials may contain polluting agents that are especially harmful to human health and the ecosystem, such as the synthetic dyes, phenolic agents, polycyclic aromatic hydrocarbons, volatile organic compounds, polychlorinated biphenyls, pesticides and drug substances. Peroxidases are a class oxidoreductases capable of performing a wide variety of oxidation reactions, ranging from reactions driven by radical mechanisms, to oxygen insertion into CH bonds, and two-electron substrate oxidation. This versatility in the mode of action presents peroxidases as an interesting alternative in cleaning the environment. Herein, an effort has been made to describe mechanisms governing biochemical process of peroxidase enzymes while referring to H2O2/substrate stoichiometry and metabolite products. Plant peroxidases including horseradish peroxidase (HRP), soybean peroxidase (SBP), turnip and bitter gourd peroxidases have revealed notable biocatalytic potentialities in the degradation of toxic products. On the other hand, an introduction on the role played by ligninolytic enzymes such as manganese peroxidase (MnP) and lignin peroxidase (LiP) in the valorization of lignocellulosic materials is addressed. Moreover, sensitivity and selectivity of peroxidase-based biosensors found use in the quantitation of constituents and the development of diagnostic kits. The general merits of peroxidases and some key prospective applications have been outlined as concluding remarks.

Synthesis, structural, and opto-electrochemical properties of cobalt aluminate type spinel and its use with ZnO for Cr(VI) photoreduction.

The discovery of the occurrence of inorganic pollutants in surface waters is identified in the system assessment quality. The most harmful elements are pesticides, persistent organic pollutants, pharmaceuticals, personal care products, and heavy metals are still dangerous to the environment due to their general uses. Chromate has the largest concentration compared to the other metals in the wastewater industries. This work evaluates the application of the spinel p-CoAl2O4 as a photocatalyst prepared by the nitrate synthesis process to reduce Cr(VI), a hazardous metal for the environment. The photocatalyst was characterized using thermal analysis (TG), X-ray diffraction, UV-diffuse reflectance spectroscopy, scanning electron microscopy, fluorescent X-ray, Fourier transform infrared spectroscopy, electrical conductivity, and photoelectrochemically. The results showed that the efficiency of optimum reduction of Cr(Vl) to Cr(IIl) photoreduction is more effective (77%) for pH = 3.6 than that at high pH values up to 8 (7%). Moreover, the effect of the hetero-system CoAl2O4/ZnO on photocatalytic efficiency was investigated. The photocatalytic activity increases up to 99% with 1 g L-1, a total catalyst dosage over the hetero-system CoAl2O4/ZnO at a ratio of 75%/25%. This data is better relative to CoAl2O4 or ZnO alone. The Cr(VI) photoreduction activity improvement was caused by the best separation and the photogeneration of electron-hole on the CoAl2O4/ZnO surfaces. Finally, the Lagergren pseudo-first-order and the Langmuir-Hinshelwood models fit well the experimental kinetics.

Application of Bi12ZnO20 Sillenite as an Efficient Photocatalyst for Wastewater Treatment: Removal of Both Organic and Inorganic Compounds.

This work aims to synthesize and characterize a material that can be used as an effective catalyst for photocatalytic application to remove both organic and inorganic compounds from wastewater. In this context, sillenite Bi12ZnO20 (BZO) in a pure phase was synthesized using the sol-gel method. Before calcination, differential scanning calorimetry (DSC) analysis was done to determine the temperature of the formation of the sillenite phase, which was found to be 800 °C. After calcination, the phase was identified by X-ray diffraction (XRD) and then refined using the Rietveld refinement technique. The results prove that BZO crystals have a cubic symmetry with the space group I23 (N°197); the lattice parameters of the structure were also determined. From the crystalline size, the surface area was estimated using the Brunauer-Emmett-Teller (BET) method, which was found to be 11.22 m2/g. The formation of sillenite was also checked using the Raman technique. The morphology of the crystals was visualized using electron scanning microscope (SEM) analysis. After that, the optical properties of BZO were investigated by diffuse reflectance spectroscopy (DRS) and photoluminescence (PL); an optical gap of 2.9 eV was found. In the final step, the photocatalytic activity of the BZO crystals was evaluated for the removal of inorganic and organic pollutants, namely hexavalent chromium Cr(VI) and Cefixime (CFX). An efficient removal rate was achieved for both contaminants within only 3 h, with a 94.34% degradation rate for CFX and a 77.19% reduction rate for Cr(VI). Additionally, a kinetic study was carried out using a first-order model, and the results showed that the kinetic properties are compatible with this model. According to these findings, we can conclude that the sillenite BZO can be used as an efficient photocatalyst for wastewater treatment by eliminating both organic and inorganic compounds.

Bio-based and cost effective method for phenolic compounds removal using cross-linked enzyme aggregates.

This work aimed at presenting a green method using a new source of peroxidase isolated from Raphanus sativus var. niger (RSVNP) in immobilized form, for the treatment of wastewater. To ensure stability and enzymatic activity in the biodegradation process, RSVNP was immobilized as a cross-linked enzyme aggregate (CLEAs). With more than 29% of recovered activity and 85% aggregation yield, acetone was selected as the best precipitating agent. The formed protein aggregates required 2% (v/v) of glutaraldehyde (GA) concentration and a ratio of 9:1 (v/v) enzyme (E) amount to cross-linker (E/GA). Compared to the free enzyme, RSVNP-CLEAs were found more chemically and thermally stable and exhibited good storage stability for more than 8 weeks. In addition, RSVNP-CLEAs were evaluated for their ability to remove phenol and p-cresol from aqueous solution by varying several operating conditions. A maximal yield (98%) of p-cresol conversion was recorded after 40 min; while 92% of phenol was degraded after 1 h duration time. The reusability of RSVNP-CLEAs was tested, displaying 71% degradation of phenol in the third batch carried out and more than 54% was achieved for p-cresol after four successive reuses in the presence of hydrogen peroxide at 2 mM concentration.

Artificial neural network modeling of cefixime photodegradation by synthesized CoBi2O4 nanoparticles.

CoBi2O4 (CBO) nanoparticles were synthesized by sol-gel method using polyvinylpyrrolidone (PVP) as a complexing reagent. For a single phase with the spinel structure, the formed gel was dried and calcined at four temperatures stages. Various methods were used to identify and characterize the obtained spinel, such as X-ray diffraction (XRD), scanning electron micrograph (SEM-EDX), transmission electron microscope (TEM), Fourier transform infrared (FT-IR), X-ray fluorescence (XRF), Raman, and UV-Vis spectroscopies. The photocatalytic activity of CBO was examined for the degradation of a pharmaceutical product cefixime (CFX). Furthermore, for the prediction of the CFX degradation rate, an artificial neural network model was used. The network was trained using the experimental data obtained at different pH with different CBO doses and initial CFX concentrations. To optimize the network, various algorithms and transfer functions for the hidden layer were tested. By calculating the mean square error (MSE), 13 neurons were found to be the optimal number of neurons and produced the highest coefficient of correlation R2 of 99.6%. The relative significance of the input variables was calculated, and the most impacting input was proved to be the initial CFX concentration. The effects of some scavenging agents were also studied. The results confirmed the dominant role of hydroxyl radical OH• in the degradation process. With the novel CoBi2O4/ZnO hetero-system, the photocatalytic performance has been enhanced, giving an 80% degradation yield of CFX (10 mg/L) at neutral pH in only 3 h.

A comparative study of ceramic nanoparticles synthesized for antibiotic removal: catalysis characterization and photocatalytic performance modeling.

The heterogeneous photocatalysis process has been known to provide significant levels of degradation and mineralization of emerging contaminants including antibiotics. For that, nanoparticle CuCr2O4 (CCO) ceramics were successfully prepared via sol-gel (SG) and co-precipitation (CP) methods to obtain spinel with desired structural features and properties and also to improve the photocatalytic performances. The CCO crystallite phase was produced at 750 °C all ceramics, disregarding the synthesis route. CCO physical and chemical properties were checked by X-ray diffraction (XRD) with Rietveld refinement, Brunauer-Emmett-Teller (BET), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM), and diffuse reflectance solid (DRS). The XRD patterns demonstrated that the synthesized catalysts displayed a small crystallite size between 17.45 and 26.24 nm for SG and 20.97 and 36.86 nm for the CCOCP samples. The observation by SEM and TEM of the nanopowders showed a typical morphology with comparable particle sizes for both synthesized routes (20-30 nm). SG agglomeration rates were higher, and particles stick together more efficiently considering the CP method, while the CCOCP method led to a more significant porosity. Their photocatalytic and adsorption performances were examined for cefaclor (CFC) removal chosen as a target pharmaceutical contaminant in water. The results obtained by the methods differed since nanoparticles prepared by SG led to high photocatalytic activity. In contrast, a high CFC adsorption was observed for those prepared via the CP method, and that agreed with the findings of the characterization analysis. The kinetics of the adsorption process was found to follow the pseudo-second-order rate law. In contrast, the data of the photodegradation process were further found to comply with the Lagergren kinetic law. Nevertheless, the global reaction rate is probably controlled by the intra-particular diffusion of CFC, regardless of the elimination process.

Photocatalytic treatment of petroleum industry wastewater using recirculating annular reactor: comparison of experimental and modeling.

In this study, the treatment of petroleum wastewater has been investigated by applying heterogeneous photocatalytic process using a recirculating annual reactor. An attempt has been made to study the effect of operating parameters such as TiO2 load, initial concentration of the pollutant, emitted photonic flux, and pH of the solution. The degradation efficiency of toluene and benzene, as target molecules, was studied. In fact, result showed that the toluene is better degraded alone than when it is in a mixture. The rate of elimination of toluene separately was 89.5%, while it was 76.19 and 79.55% in the binary (toluene/benzene) and the ternary mixtures (toluene/benzene/xylene), respectively. Moreover, the mineralization of the solution decreased more rapidly when toluene was pure with a rate of 83.13% compared to binary and ternary mixtures. A mathematical model is proposed taking into account the parameters influencing the process performances. The mass transfer step, the degradation, and the mineralization kinetics of the pollutants were defined as model parameters. To build the model, mass balances are written in bulk region and catalyst phase (solid phase). The degradation mechanism on solid phase is divided in two stages. Firstly, the removal of toluene gives an equivalent intermediate (EI). Secondly, EI is oxidized into carbon dioxide (CO2). This approach gives a good agreement between modeling and empirical data in terms of degradation and mineralization. It also allows for the simulation of toluene kinetics without knowing the plausible chemical pathway. A satisfactory fit with experimental data was obtained for the degradation and mineralization of toluene.