Solar photocatalytic degradation of the herbicide isoproturon on a Bi–TiO2/zeolite photocatalyst

The photocatalytic degradation of the herbicide isoproturon under solar light was investigated in aqueous solution containing a Bi–TiO₂/zeolite photocatalyst. The catalysts were characterized using X-ray diffraction, UV-Vis diffuse reflectance spectroscopy, Fourier transform-infrared spectroscopy, scanning electron microscopy, and transmission electron microscopy. The effect of Bi–TiO₂ loading onto the zeolite support and influence of the parameters such as catalyst amount, pH, and initial concentration of isoproturon on the degradation rate were evaluated. The recycling ability of the catalyst was found to be sustainable for elongated periods. The high activity of the Bi–TiO₂/zeolite was attributed to its absorptivity of visible light and its high adsorption capacity for the pollutant molecules.     

Photodegradation of an azo dye by silver-doped nano-particulate titanium dioxide

The synthesis of silver doped nano-particulate titanium dioxide (Ag/TiO₂) using a microemulsion method and an investigation of its photocatalytic activity for the degradation of Acid Red 27 in distilled water under UV-irradiation is reported. The prepared Ag/TiO₂ is characterized using transmission electron microscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy. The size of the Ag nanoparticles is around 5–15?nm, with almost uniform distribution on the TiO₂ particles. The efficiency of the photocatalytic process is evaluated to establish the optimum conditions, found to be at 2?wt% of Ag loading on TiO₂, catalyst dosage of 400?mg?L^?1, and calcination temperature of 300°C. Complete decolorization of the dye solution on Ag/TiO₂ was observed in 20?min of UV irradiation in the optimum conditions.     

Combined sorptional–photocatalytic remediation of dyes by polyaniline Zr(IV) selenotungstophosphate nanocomposite

A polyaniline Zr(IV) selenotungstophosphate nanocomposite was prepared via sol-gel method and characterized by thermogravimetric analysis, scanning electron microscopy, energy dispersive X-ray spectroscopy, and transmission electron microscopy. The combined sorptional–photocatalytic activity of the nanocomposite for degradation of methylene blue and malachite green was investigated and was found to be more efficient than separate adsorption in the dark followed by photocatalysis. The dyes were degraded in 3 h by 96% and 89% by the combined process, as compared to 86% and 72% by the two-step process in 5 h. The nanocomposite material showed antimicrobial activity against Staphylococcus aureus and Escherichia coli.     

Determination of minimum inhibitory concentration and half maximal inhibitory concentration of antibiotics and their degradation products to assess the eco-toxicological potential

Abstract

Numerous studies have been reported on today’s ubiquitous presence of antibiotics in surface waters causing the emergence of multidrug-resistant bacteria. Advanced water treatment procedures aim at the complete prevention and elimination of antibiotics from entering natural water bodies. In this study, photoinduced degradation processes using UVC-irradiation were applied toward selected fluoroquinolone, tetracycline, macrolide, and sulfonamide antibiotics. Photodegradation products were elucidated using high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS). Rate constants and quantum efficiencies were determined for the active substances and their photo-transformation products. As a measure of ecotoxicity, minimum inhibitory and half-maximal inhibitory concentrations were determined against the Gram-negative bacterium Pseudomonas fluorescens and the Gram-positive Bacillus subtilis in a standard assay format. These values were further recorded as a function of UV exposure time. The irradiation time-dependent increase of minimum inhibitory concentration (MIC) values agreed well with the kinetic models. After 10?min of irradiation, the compound solutions ceased to inhibit bacterial cell growth, indicating removal of the pharmaceutical activity. These findings were found in agreement with quantitative structure–activity relationship analysis. The combination of microbiological activity testing, molecular structure analysis, chemical kinetic investigation, and quantitative structure–activity relationship models proved to be able to predict irradiation times and evaluate potential ecotoxicological hazard of the irradiated drugs.     

Iron-doped copper 1,4-benzenedicarboxylate as photo-Fenton catalyst for degradation of methylene blue

Abstract

A metal-organic framework of iron-doped copper 1,4-benzenedicarboxylate was synthesized and, for the first time, utilized as a heterogeneous photo-Fenton catalyst for degradation of methylene blue dye in aqueous solution under visible light irradiation. The synthesized materials were characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction and energy-dispersive X-ray spectroscopy. The influence factors, kinetics, and stability of the synthesized catalysts were investigated in detail. Iron-doped copper 1,4-benzenedicarboxylate showed higher degradation efficiency than pure copper 1,4-benzenedicarboxylate. An almost complete degradation was achieved within 70?min under visible light irradiation at a solution pH of 6, a catalyst loading of 1?g?L^?1, a H₂O₂ dosage of 0.05?mol L^?1 and methylene blue concentration of 50?mg?L^?1. Recycling studies demonstrated that the iron-doped copper 1,4-benzenedicarboxylate is a promising heterogeneous photo-Fenton catalyst for long-term removal of methylene blue dye from industrial wastewater.     

Selection of poly(R)-3-hydroxybutyric acid utilising bacteria by enrichment,optimisation and compatibility testing for consortia development

Bacterial strains with poly-3-hydroxybutyrate (PHB) degradation potential were isolated from waste yard soil samples of selected industrial sites in Uttarakhand, India, and two microbial consortia were developed, i.e. Consortium I comprises Pseudomonas sp. strain Rb10, Pseudomonas sp. strain Rb11 and Bacillus sp. strain Rb18, and Consortium II is composed of Lysinibacillus sp. strain Rb1, Pseudomonas sp. strain Rb13 and Pseudomonas sp. strain Rb19. The current study involved enrichment selection via liquid and semi-solid media, followed by isolation and screening of bacterial strains using PHB pellets and films. Furthermore, the identification and characterisation was done by triphasic approach. The utilisation of PHB by the characterised strains was confirmed by Fourier transform infrared spectroscopy and scanning electron microscopy. Moreover, the minimum inhibitory concentration of solubilised PHB was found to be 2.5?mg/mL, which was detected through ‘clear zone assay’. Further, the selection and biocompatibility testing of potential isolates were performed for the formation of bacterial consortia. Thus, the present work would provide direct and standardised protocol for screening and selection of potential microbiomes for biodegradation of polymers by overcoming the negative effect of organic solvents. Moreover, indigenously developed consortia would be evaluated for their in situ biodegradation potential against various bioplastic films.     

Removal of toluene from air streams by cobalt-copper bimetallic catalysts supported on sepiolite

Abstract

Oxidative removal of toluene using copper and cobalt bimetallic catalysts with varying molar ratios supported on sepiolite was investigated. The catalysts prepared by a deposition precipitation method and were characterized using X-ray diffraction, nitrogen adsorption-desorption, field emission scanning electron microscopy, H₂-temperature-programmed reduction, transmission electron microscope, and inductive coupled plasma atomic emission spectroscopy. The species supported on sepiolite are Co₃O₄, CuO, and CuCo₂O₄. The activities of the tested catalysts increased in the order 0Co-4Cu/Sep <1Co-3Cu/Sep <4Co-0Cu/Sep <1Co-1Cu/Sep <3Co-1Cu/Sep. The latter exhibiting 90% toluene oxidative degradation at 288?°C within 15?h, having high selectivity towards CO₂, and being stable at 300?°C up to 15?h. In conclusion, this study showed that sepiolite has excellent properties as a support.     

Fine structure of endonucleobiotic bacteria in the gill epithelium of Ruditapes decussatus

The ultrastructural organization of an endonucleobiotic bacteria found in the branchial epithelium of the clam Ruditapes decussatus from an estuarine region of Faro (South of Portugal) collected during 1987, was studied by transmission electron microscopy (TEM). This endonucleobiosis is constituted by a variable number of gram-negative bacteria irregularly distributed among the chromatin dots. The nuclear membranes and pores of the host cells, as well as the different cytoplasmic organelles, seemed well preserved. No signs of the infection process were observed.     

Supramolecular complex formation,a possible antigenotoxic mechanism of glucomannan against aflatoxin B1

Abstract

Glucomannan is a highly branched polysaccharide with glycosidic linkages, constituted of mannoses and glucoses. In recent years, its usefulness due to its immunological, antioxidant and antimutagenic activity has been recognized. The aim of the study was to determine the antigenotoxic ability of glucomannan extracted from Candida utilis orally administered (100–700?mg/kg) to mice, which subsequently received 1?mg/kg aflatoxin B₁. Hepatocytes obtained from these animals 4–16?h post administration were examined by means of the comet assay. The antigenotoxic effect was found to be higher than that observed in previous studies with α-mannan and β-D-glucan isolated from Saccharomyces cerevisiae., In order to explore the possibility of formation of a supramolecular complex between glucomannan and aflatoxin B₁, both compounds were co-crystallized, their melting points determined, and the complex analyzed through ultraviolet spectroscopy. The spectroscopy data suggest that the protective effect of glucomannan is related to the formation of a supramolecular complex between the two compounds.     

Visible light sensitive activated carbon-metal oxide (TiO2, WO3, NiO,and SnO) nano-catalysts for photo-degradation of methylene blue: a comparative study

Four composites of metal oxide doped with activated carbon with a metal oxide weight of 20% were prepared using mechano-mixing method. The nano-catalysts were characterized by N₂-adsorption–desorption, X-ray diffraction analysis, transmission electron microscopy, Fourier-transform infrared spectroscopy, UV-diffuse reflectance, and photoluminescence spectroscopy. Photo-catalytic degradation of methylene blue dye under UV 254 nm and visible light was examined. In general, prepared catalysts are more active for degradation of dye under visible light than UV, reaching 96% within 180?min irradiation using the SnO catalyst. Photo-degradation of methylene blue followed pseudo first order reaction mechanism with a rate constant of 14.8?×?10^?3?min^?1, and the time required for removal of 50% of dye was 47?min.     

Ag–TiO2 doped photo catalytic degradation of Procion blue H-B dye in textile washwater

The photocatalytic degradation of Procion blue H-B dye in biodegraded textile washwater has been investigated for the complete removal of color and maximum reduction of chemical oxygen demand (COD). Pseudomonas putida was utilized for obtaining biodegraded textile washwater. In this process, silver-doped TiO₂ photocatalyst was prepared and experiments were carried out to study the effects of UV and mercury lamp irradiations on COD reduction and removal of color. The thus prepared silver-doped TiO₂ catalyst was characterized by thermogravimetric and differential thermal analysis, UV-visible spectrometer, X-ray diffraction, scanning electron microscope, energy dispersive X-ray microanalysis, and BET surface area techniques. Adsorption studies were also carried out to evaluate the fitness of isotherm models. The results show that the silver-doped TiO₂ has enhanced the photodegradation of Procion blue H-B dye under UV and mercury lamp irradiations. The enhanced activity of silver-doped TiO₂ is due to the enrichment of electron–hole separation by electron trapping of silver particles.     

A morphological and structural study of the larval shell from the abalone <Emphasis Type="Italic">Haliotis tuberculata</Emphasis>

The larval shell of the marine gastropod Haliotis tuberculata was investigated by polarised light microscopy, scanning electron microscopy, Raman microspectroscopy and infra-red spectroscopy. Trochophore and veliger larval sections were used for histological examination of the growing shell and each larval stage was related to the shell development and the appearance of calcified formations. We determined the stage of initial calcification by specific staining combined with polarised light examination. The shell of 30-h-old pre-veliger larvae was found to be mineralized, confirming that calcification occurred before larval torsion. Using both infra-red and Raman spectroscopy, we showed that CaCO₃ deposition occurred at the pre-veliger stage and that the mineral phase initially deposited was essentially composed of aragonite.     

Synthesis and antibacterial activity of a Fe3O4–AgCl nanocomposite against Escherichia coli

In this investigation, Fe₃O₄ magnetic nanoparticles (MNPs) were prepared by the alkalinization of an aqueous medium containing ferrous sulfate and ferric chloride. In the next step, a Fe₃O₄–AgCl magnetic nanocomposite was fabricated by the drop-by-drop addition of silver nitrate solution into a NaCl solution containing Fe₃O₄ MNPs. All prepared nanoparticles were characterized by transition electron microscopy (TEM), X-ray diffraction (XRD), and energy-dispersive X-ray spectroscopy (EDS). Both particle types varied in size from 2.5 to 20?nm, with an average size of 7.5?nm for Fe₃O₄ MNPs and 12.5?nm for Fe₃O₄–AgCl nanocomposites. The antibacterial effect of the Fe₃O₄ MNPs and fabricated Fe₃O₄–AgCl nanocomposites against Escherichia coli (ATCC 35218) were investigated by conventional serial agar dilution method using the Müller–Hinton Agar medium. The minimum inhibitory concentration was 4?mg?mL^?1 for Fe₃O₄ MNPs and 2?mg?mL^?1 for the Fe₃O₄–AgCl magnetic nanocomposites. Time-kill course assays showed that the Fe₃O₄–AgCl magnetic nanocomposites successfully killed all inoculated bacterial cells during an exposure time of 60?min. The antibacterial activity of recycled Fe₃O₄–AgCl magnetic nanocomposites over four 60?min cycles of antibacterial treatment was further tested against E. coli by the colony-forming unit (CFU) method. The antibacterial efficiency of the nanocomposites was constant over two cycles of antibacterial testing.     

Removal of rhodamine B from aqueous solution by BiPO4 hierarchical architecture

Hexahedron-like BiPO₄ microcrystals were sucessfully synthesized via a template-free hydrothermal method. The resulting samples were characterized by Xray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and UV-vis spectroscopy. The BiPO₄ samples were of pure monoclinic phase, and the initial amount of PO_3–4 during synthesis did not show obvious effect on the phase properties of the materials. The hexahedron-like BiPO₄ microcrystal had explicitly cut edges, and its thickness was about 1 μm. The photocatalytic performance of the BiPO₄ catalysts was evaluated by photodegradation of RhB under UV light irradiation with commerial Degussa P25 TiO₂ as reference. Compared with P25, the BiPO₄ catalysts displayed higher photocatalytic activity, with 98.7% of RhB degraded during 60-min experiment. Cost evaluation analysis was adopted to describe the energy consumption of the degradation process, and the results suggested the potential application of this material in the field of dye-contaminated wastewater treatment or environmental matrices remediation.     

Branchial and intestinal osmoregulatory acclimation in the four-eyed sleeper, <Emphasis Type="Italic">Bostrychus sinensis</Emphasis> (Lacepède), exposed to seawater

Bostrychus sinensis is a facultative air breather that inhabits waters of a wide range of salinities. This study aimed to elucidate whether branchial and intestinal osmoregulatory acclimation occurred in B. sinensis transferred from 5‰ water through a progressive increase in salinities to seawater. Our results indicate that B. sinensis acted as a hyperosmotic regulator in 5‰ water, but exhibited hypoosmotic hypoionic regulation in seawater. During short- (1 day) and medium- (10 days) term acclimation to seawater, there were only minor perturbations in plasma osmolality and [Na⁺], which returned to control levels after 45 days of exposure to seawater. Branchial Na⁺/K⁺-ATPase activity was unaffected by 1, 10 or 45 days of exposure to seawater. However, prolonged (45 days) acclimation to seawater led to a significant increase in Na⁺/K⁺-ATPase α-subunit protein abundance. Taken together, these results indicate that there could be changes in the expression of Na⁺/K⁺-ATPase isoforms and/or post-translational modification of Na⁺/K⁺-ATPase in the gills of fish exposed to seawater. Immunofluorescence microscopy revealed that acclimation to seawater for 10 days only resulted in no change in branchial Na⁺/K⁺-ATPase protein expression, but there were increases in protein expression of cystic fibrosis transmembrane regulator (CFTR)-like chloride channel and Na⁺:K⁺:2Cl⁻ cotransporter (NKCC; probably NKCC1). Indeed, NKCC was undetectable in gills of fish kept in 5‰ water by Western blotting, but it became weakly detectable in fish exposed to seawater for 10 days and prominently expressed in fish exposed to seawater for 45 days. Therefore, our results indicate that branchial CFTR-like chloride channel and NKCC1 were the determining factors in the transition between hyperosmotic regulation and hypoosmotic hypoionic regulation in B. sinensis. Furthermore, the intestine of B. sinensis also served as an important osmoregulatory organ, since there were significant increases in both the activity and protein abundance of intestinal Na⁺/K⁺-ATPase in fish acclimated to seawater for 45 days. The effectiveness of branchial and intestinal osmoregulatory acclimation in B. sinensis during seawater acclimation led to only a minor increase in plasma osmolality, and thus resulted in relatively unchanged free amino acid contents in muscle and liver.     

Bio-mediated silver nanoparticle synthesis: mechanism and microbial inactivation

Even though plenty of literature is available on the biosynthesis of metal nanoparticles, there are serious lacunae on the mechanisms of their formation. In the present study, the mechanism of formation of mono-crystalline silver nanoparticles using a fruit extract of the ornamental tree Thevetia peruviana is emphasized, i.e. how the pH of the reaction mixture affected reaction kinetics and size of the nanoparticles. The facilitation of formation of Ag₂O at higher pH resulted in a faster rate of particle formation. The diameter of the bare particles at neutral pH determined by field emission scanning electron microscopy and the hydrodynamic diameter determined by dynamic light scattering were 53 and 104 nm, respectively. The silver nanoparticles exhibited good inactivation of Escherichia coli due to participation of free radicals as evidenced by electron spin resonance spectroscopy.     

Green synthesis and characterization of metal ions-mixed titania for application in dye-sensitized solar cells

Abstract

The objective of the present study is to synthesize various metal ions mixed TiO₂ nanoparticles using a continuous hydrothermal synthesis pilot reactor for dye-sensitized solar cells (DSCs). In the pilot plant, aqueous solutions of the metal salts are mixed with a flow of supercritical water (450?°C and 24.1?MPa) in a confined jet mixer for continuous synthesis of metal ions-mixed nano-titania. Characterization of the particles was made using Brunauer–Emmett–Teller technique for specific surface area, powder X-ray diffraction analysis and transmission electron microscopy for identification and crystallite size, X-ray photoelectron spectroscopy for surface analysis and infrared spectroscopy for distinct group identification. Following the already existing procedures and using the titanates synthesized, dye-sensitized cells of 1?cm² area were assembled and their photovoltaic parameters were evaluated under standard test conditions. The power conversion efficiencies (η %) for 40?mol % Zn²⁺, 5?mol % Zr⁴⁺ and 10?mol % Zn⁴⁺ titania were obtained to be 4.8, 4.95 and 4.9, respectively. The promising efficiency results from a greener and large-scale production of nano-titania is a step forward towards commercializing DSC technology.     

Mitochondrial toxicity and in vitro biological effects of ambient PM2.5 from an urban site in China

Abstract

The roles of PM_2.5-induced mitochondrial damage and oxidative stress on mast cell degranulation were examined in vitro. Mast cells were treated with suspensions of PM_2.5 in Dulbecco’s modified Eagle’s medium at concentrations from 25 to 200?mg/L in the absence or presence of 10?mmol/L N-acetyl-L-cysteine. Biological effects and mitochondrial function were assessed by determining cell viability, β-hexosaminidase release, interleukin-4 secretion, reactive oxygen species generation, adenosine triphosphate production, potential alteration of mitochondrial membrane, and activities of mitochondrial electron transport chain complexes I and III. Exposure of mast cells to PM_2.5 induced reduction of adenosine triphosphate production, collapse of mitochondrial membrane potential, and inhibition of the activity of complex III. Co-treatment of mast cells exposed to PM_2.5 with N-acetyl-L-cysteine attenuated cytotoxicity and the production of reactive oxygen species, and decreased the release of β-hexosaminidase and interleukin-4. Evidently, PM_2.5-induced oxidative stress plays an essential role in mitochondrial toxicity and mast cell activation.     

Nano-titanium dioxide (TiO2)-induced changes affecting Cu2+-mediated alterations in bacterium Bacillus subtilis and α-amylase

Titanium dioxide (TiO₂) nanoparticles possess the potential to coexist with Copper (Cu²⁺) in soil. The individual and combined toxicity of these two chemicals was evaluated using the bacterium Bacillus subtilis, a known soil model bacterium. Cu²⁺ (6.25–50?µg?mL^?1) alone produced toxicity to bacteria as evidenced by the decreased cell viability and deceased α-amylase production. The addition of TiO₂ (50?mg?mL^?1) enhanced the Cu²⁺-induced decrease in cell viability but elevated amylase activity. TiO₂ did not markedly affect the growth rate and lag period. A primary cause of TiO₂ increasing Cu²⁺ toxicity is presumed to be associated with hydroxyl radical formation, while increased amylase activity is considered to arise from Cu²⁺ facilitating TiO₂ degradation ability.     

山西工矿区土壤二氧化硫与多环芳烃复合污染对小麦种子萌发和幼苗生长的影响

以小麦为供试植物,山西工矿区生黄土为供试土壤,进行了土壤中二氧化硫(SO2)与多环芳烃(PAHs)单一及复合污染对小麦种子萌发率及小麦幼苗株高、根伸长和地下生物量影响的研究,以期考察复合污染的生态毒性效应。结果表明,小麦种子萌发对SO2与PAHs单一及复合污染均不敏感;SO2和PAHs单一污染时,小麦幼苗的株高与根伸长均受到一定程度的影响,低浓度SO2或PAHs处理对小麦生长起促进作用,高浓度则为抑制作用;小麦幼苗株高与SO2浓度呈显著负相关(r=-0.954,P<0.05),但与PAHs浓度的相关性不显著;SO2与PAHs复合污染条件下,对小麦幼苗株高或根伸长的联合作用多体现为协同作用,在低浓度情况下(SO2<500mg·kg-1)表现为协同促进;当SO2达到500～1000mg·kg-1时,对小麦幼苗株高或根伸长的联合作用均体现为协同抑制。SO2和PAHs单一污染时,小麦幼苗地下生物量与SO2、PAHs浓度均为显著负相关(rPAHs=-0.953,rSO2=-0.916,P<0.05);复合污染条件下,在SO2浓度为10mg·kg-1时,对地下生物量的联合作用多体现协同促进作用;而在SO2浓度为1000mg·kg-1,PAHs为50～100mg·kg-1时,对地下生物量的联合作用均体现为协同抑制作用。多元逐步回归分析进一步表明,SO2与PAHs复合污染条件下,小麦幼苗株高、根伸长都受到了SO2及PAHs的共同影响,而SO2是影响小麦幼苗地下生物量的主要因素。