A novel Ag/ZnO core-shell structure for efficient sterilization synergizing antibiotics and subsequently removing residuals

The massive use of antibiotics has led to the aggravation of bacterial resistance and also brought environmental pollution problems.This poses a great threat to human health.If the dosage of antibiotics is reduced by increasing its bactericidal performance,the emergence of drug resistance is certainly delayed,so that there's not enough time for developing drug resistance during treatment.Therefore,we selected typical representative materials of metal Ag and semiconductor ZnO nano-bactericides to design and synthesize Ag/ZnO hollow core-shell structures(AZ for short).Antibiotics are grafted on the surface of AZ through rational modification to form a composite sterilization system.The research results show that the antibacterial efficiency of the composite system is significantly increased,from the sum(34.7%+22.8%-57.5%)of the antibacterial efficiency of AZ and gentamicin to 80.2%,net synergizes 22.7%,which fully reflects the effect of 1+1>2.Therefore,the dosage of antibiotics can be drastically reduced in this way,which makes both the possibility of bacterial resistance and medical expenses remarkably decrease.Subsequently,residual antibiotics can be degraded under simple illumination using AZ-self as a photocatalyst,which cuts off the path of environmental pollution.In short,such an innovative route has guiding significance for drug resistance.

Green synthesis of three-dimensional magnesium ferrite/titanium dioxide/reduced graphene from Garcinia mangostana extract for crystal violet photodegradation and antibacterial activity

In this study,three-dimensional porous magnesium ferrite/titanium dioxide/reduced graphene oxide(Mg Fe_2O_(4)-GM/TiO_(2)/rGO(MGTG))was successfully synthesized via green and hydrothermal-supported co-precipitation methods using the extract of Garcinia mangostana(G.mangostana)as a reducing agent.The characterization results indicate the successful formation of the nano/micro Mg Fe_(2)O_(4)(MFO)and TiO_(2) on the structure of the reduced graphene oxide(rGO),which can also act as efficient support,alleviating the agglomeration of the nano/micro MFO and TiO_(2).The synergic effects of the adsorption and photodegradation activity of the material were investigated according to the removal of crystal violet(CV)under ultraviolet light.The effects of catalyst dosage,CV concentration,and p H on the CV removal efficiency of the MGTG were also investigated.According to the results,the CV photodegradation of the MGTG-200 corresponded to the pseudo-first-order kinetic model.The reusability of the material after 10 cycles also showed a removal efficiency of 92%.This happened because the materials can easily be recollected using external magnets.In addition,according to the effects of different free radicals·O_(2)^(-),h^(+),and·OH on the photodegradation process,the photocatalysis mechanism of the MGTG was also thoroughly suggested.The antibacterial efficiency of the MGTG was also evaluated according to the inhibition of the Gram-positive bacteria strain Staphylococcus aureus(S.aureus).Concurrently,the antibacterial mechanism of the fabricated material was also proposed.These results confirm that the prepared material can be potentially employed in a wide range of applications,including wastewater treatment and antibacterial activity.

MXene:From synthesis to environment remediation

A new burgeoning family of two-dimensional(2D)transition metal carbides/nitrides,better known as MXenes,have received extensive attention because of their distinct properties,such as metallic conductivity,good hydrophilicity,large surface area,good mechanical stability,and biodegradability.About 40 different MXenes have been synthesized,and dozens more structures and properties have been theoretically predicted.However,the recent progress in MXenes development is not well covered in chronological order based on different applications.This review article focuses on emerging synthesis methods,the properties of MXenes,and mainly the applications of MXenes and MXene-based material family in environmental remediation,a comprehensive review of gaseous and aqueous pollutants treatment.

Oxidation of Partially Hydrolyzed Polyacrylamide from Polymer Flooding Processes Using Fenton Reagents

The degradation of partially hydrolyzed polyacrylamide(HPAM) found in alkaline/surfactant/polymer flooding sewage was investigated using Fenton-type reagents. Different Fenton reagent treatments for HPAM degradation were compared. The effects of pH, hydrogen peroxide(H_(2)O_(2)), ferrous ion(Fe^(2+)), and tartaric ion(C_(4)H_(4)O_(6)^(2-)) concentrations were studied. The degradation reaction occurred within a wide range of pH(3–9). The HPAM degradation performance of photo-Fenton processes using solar light and UV were compared with that of the Fenton process. The degradation rate was found to be strongly dependent on the H_(2)O_(2)/Fe^(2+)/C_(4)H_(4)O_(6)^(2-)molar ratio. The HPAM degradation efficiency was 90%, and the chemical oxygen demand removal efficiency was 85%. HPAM could be degraded into a compound with a lower molecular weight, but it was difficult to achieve complete mineralization to CO_(2). The presence of intermediate products hindered further oxidation in the Fenton process.

Aqueous oxytetracycline degradation and the toxicity change of degradation compounds in photoirradiation process

The extensive use of antibiotics has been a worldwide environmental issue.In this study the fate of oxytetracycline (OTC),under photoirradiation,was investigated.The results showed that OTC photolysis followed first order model kinetics.Direct photolysis rate was found to be dependent on the initial OTC concentration,with k value ranging from 0.0075 to 0.0141 min^(-1),in the OTC concentration from 40 to 10 mg/L.OTC photolysis was highly pH-dependent and strongly enhanced at a high pH value,with a k value of...

Effect of copper on the degradation of pesticides cypermethrin and cyhalothrin

The influence of coexisting copper （Cu） ion on the degradation of pesticides pyrethroid cypermethrin and cyhalothrin in soil and photodegradation in water system were studied. Serial concentrations of the pesticides with the addition of copper ion were spiked in the soil and incubated for a regular period of time, the analysis of the extracts from the soil was carded out using gas chromatography （GC）. The photodegradation of pyrethroids in water system was conducted under UV irradiation. The effect of Cu^2＋ on the pesticides degradation was measured with half life 00.5） of degradation. It was found that a negative correlation between the degradation of the pyrethroid pesticides in soil and Cu addition was observed. But Cu^2＋ could accelerate photodegradation of the pyrethroids in water. The t0.5 for cyhalothrin extended from 6.7 to 6.8 d while for cypermethrin extended from 8.1 to 10.9 d with the presence of copper ion in soil. As for photodegradation, t0.5 for cyhalothrin reduced from 173.3 to 115.5 min and for cypermethrin from 115.5 to 99.0 min. The results suggested that copper influenced the degradation of the pesticides in soil by affecting the activity of microorganisms. However, it had catalyst tendency for photodegradation in water system. The difference for the degradation efficiency of pyrethroid isomers in soil was also observed. Copper could obviously accelerate the degradation of some special isomers.

氧化铈纳米粒子光催化降解亚甲基蓝的动力学和机理(英文)

CeO2 nanocrystals were synthesized by a simple precipitation method and calcination at 600℃.(NH4)2Ce(NO3)6 and ammonia were used as precursors.The CeO2 nanoparticles were characterized by X-ray diffraction,Fourier transform infrared spectroscopy,transmission electron microscopy,and N2 adsorption.The photodegradation of methylene blue catalyzed by CeO2 nanoparticles was studied under UV and sunlight irradiation.The highest degradation was obtained with 1.0 g/L CeO2 at pH 11 within 125 min.The pseudo first order rate constants of dye bleaching were calculated as 16.2×10-3 and 15.7×10-3 min-1 under UV and sunlight irradiation,respectively.The effect of iso-PrOH,iodide ion,and H2O2 was studied to predict the pathway of dye degradation.The obtained results indicate the effect of photogenerated holes in the degradation mechanism of the dye.Also,the photocatalytic activity of the prepared photocatalyst was studied in the presence of several negative ions.

Photochemical behavior of benzo[a]pyrene on soil surfaces under UV light irradiation

The rates of photodegradation and photocatalysis of benzo [a]pyrene （BaP） on soil surfaces under UV light have been studied. Different parameters such as temperature, soil particle sizes, and soil depth responsible for photodegradation, catalyst loads and wavelength of UV irradiation blamed for photocatalysis have been monitored. The results obtained indicated that BaP photodegradation follows pseudo-first-order kinetics. BaP photodegradation was the fastest at 30℃ . The rates of BaP photodegradation at different soil particle size followed the order： less than 1 mm〉less than 0.45 mm〉less than 0.25 mm. When the soil depth increased from 1 mm to 4 ram, the half-life increased from 13.23 d to 17.73 d. The additions of TiO2 or Fe2O3 accelerated the photodegradation of BaP, and the photocatalysis of BaP follows pseudo-first-order kinetics. Changes in catalyst loads of TiO2 （0.5%, 1%, 2%, and 3% （wt）） or Fe203 （2%, 5%, 7%, and 10% （wt）） did not significantly affect the degradation rates. Both BaP photocatalysis in the presence of TiO2 and Fe2O3 were the fastest at 254 nm UV irradiation.

MoO_3-TiO_2纳米晶体复合材料光降解糖蜜(英文)

A MoO3-TiO2 nanocrystalline composite material was prepared by a simple solgel method.The synthesized material was charac-terized by X-ray diffraction,scanning electron microscopy with an electron dispersion spectroscopy,transmission electron microscopy,and Fourier transform infrared spectroscopy.Melanoidin is a dark brown pigment found in wastewater from the sugar industry and it pollutes water.This polluted water is generally referred to as molasses and it undergoes fermentation and is solely responsible for water,soil,and air pollution.The synthesized catalytic material was found to be effective in degrading molasses under UV-visible radiation.Analysis of treated and untreated molasses was carried out by measuring its color,chemical oxygen demand,biological oxygen demand,pH,and total dissolved solid.Results from these analyses indicate the effective photodegradation of the molasses.This methodology has several advantages such as high photocatalytic activity,non-toxicity,cleanliness,and reusability of the catalytic material.

Mechanism study on UV-induced photodegradation of nonylphenol ethoxylates by intermediate products analysis

Photodegradation of nonylphenol ethoxylates （NPloEO） was investigated in laboratory scale under UV irradiation. The intermediate photodegradation products were analyzed by LC-ESI-MS. Three kinds of intermediate products including aldehydic compounds, carboxylic compounds and cyclohexanyl compounds were identified. Five main degradation routes involving the oxidation of the alkyl chain and ethoxylate unit, shortening of the alkyl chain and ethoxylate unit, hydrogenation of the benzene ring were proposed.

Photoreductive degradation of sulfur hexafluoride in the presence of styrene

Sulfur hexafluoride （SF6） is known as one of the most powerful greenhouse gases in the atmosphere. Reductive photodegradation of SF6 by styrene has been studied with the purpose of developing a novel remediation for sulfur hexafluoride pollution. Effects of reaction conditions on the destruction and removal efficiency （DRE） of SF6 are examined in this study. Both initial styrene-to-SF6 ratio and initial oxygen concentration exert a significant influence on DRE. SF6 removal efficiency reaches a maximum value at the initial styrene-to-SF6 ratio of 0.2. It is found that DRE increases with oxygen concentration over the range of 0 to 0.09 mol/m^3 and then decreases with increasing oxygen concentration. When water vapor is fed into the gas mixture, DRE is slightly enhanced over the whole studied time scale. The X-ray Photoelectron Spectroscopy （XPS） analysis, together with gas chromatography-mass spectrometry （GC-MS） and Fourier Transform Infrared spectroscopy （FT-IR） analysis, prove that nearly all the initial fluorine residing in the gas phase is in the form of SiF4, whereas, the initial sulfur is deposited in the form of elemental sulfur, after photodegradation. Free from toxic byproducts, photodegradation in the presence of styrene may serve as a promising technique for SF6 abatement.

Photodegradation of acetochlor in water and UV photoproducts identified by mass spectrometry

The sunlight photodegradation half-lives of 20 mg/L acetochlor were 151, 154 and 169 days in de-ionized water, river water and paddy water, respectively. When exposed to ultraviolet (UV) light, acetochlor in aqueous solution was rapidly degraded. The half-lives were 7.1, 10.1, and 11.5 min in de-ionized water, river water and paddy water, respectively. Photoproducts of acetochlor were identified by gas chromatography/mass spectrometry(GC/MS) and found at least twelve photoproducts resulted from dechlorination with subsequent hydroxylation and cyclization processes. The chemical structures of ten photoproducts were presumed on the basis of mass spectrum interpretation and literature data. Photoproducts are identified as 2-ethyl-6-methylaniline; N,N-diethylaniline; 4,8-dimethyl-2-oxo-1,2,3,4- tetrahydroquino-line; 2-oxo-N-(2-ethyl-6-methylphenyl)-N-(ethoxymethyl)acetamide; N-(ethoxymethyl)-2′-ethyl-6′-methylformanilide;1-hydroxyacetyl-2-ethoxyl-7-ethylind ole; 8-ethyl-1-ethoxymethyl-2-oxo-1,2,3,4-tetrahydroquinoline; 4,8-dimethyl-1-ethoxymethyl-2-oxo-1,2,3,4-tetrahydroquinoline; 2-hydroxy-2′-ethyl-6′-methyl-N-(ethoxymethyl)acetanilide and a compound related to acetochlor. The other two photoproducts were detected by GC/MS although their chemical structure was unknown.

Sn/n3O4-x heterostructure rich in oxygen vacancies with enhanced visible light photocatalytic oxidation performance

Sn3O4, a common two-dimensional semiconductor photocatalyst, can absorb visible light.However, owing to its rapid recombination of photogenerated electron-hole pairs, its absorption is not sufficient for practical application.In this work, a Sn nanoparticle/Sn3O4-x nanosheet heterostructure was prepared by in situ reduction of Sn3O4 under a H2 atmosphere.The Schottky junctions formed between Sn and Sn3O4-x can enhance the photogenerated carrier separation ability.During the hydrogenation process, a portion of the oxygen in the semiconductor can be extracted by hydrogen to form water, resulting in an increase in oxygen vacancies in the semiconductor.The heterostructure showed the ability to remove Rhodamine B.Cell cytocompatibility experiments proved that Sn/Sn3O4-x can significantly enhance cell compatibility and reduce harm to organisms.This work provides a new method for the fabrication of a Schottky junction composite photocatalyst rich in oxygen vacancies with enhanced photocatalytic performance.

Calculation method of quantum efficiency to TiO_2 nanocrystal photocatalysis reaction

The quantum yield is an important factor to evaluate the efficiency of photoreactor. This article gives an overall calculation method of the quantum efficiency( Φ ) and the apparent quantum efficiency( Φ a) to the TiO 2/UV photocatalysis system. Furthermore, for the immobility system (IS), the formulation of the faction of light absorbed by the TiO 2 thin film is proposed so as to calculate the quantum efficiency by using the measured value and theoretic calculated value of transmissivity (T). For the suspension system(SS), due to the difficulty to obtain the absorption coefficient ( α ) of TiO 2 particulates, the quantum efficiency is calculated by means of the relative photonic efficiency ( ζ r) and the standard quantum yield ( Φ standard ).

New Application of Stainless Steel

Several rigid substrates such as stainless steel, titanium alloy, aluminum alloy, nickel foil, silicon, and sodium lime glass have been employed for manufacturing high quality TiO2 films by metal organic chemical vapor deposition （MOCVD）. The as-deposited TiO2 films have been characterized with SEM/EDX and XRD. The photocatalytic properties were investigated by decomposition of aqueous orange Ⅱ. UV VIS photospectrometer was employed to check the absorption characteristics and photocatalytic degradation activity. The results show that films synthesized on metal substrates display higher photoactivities than that on absolute substrates such as silicon and glass. It is found that solar light is an alternative to UV-light used for illumination during photodegradation of orange Ⅱ. TiO2 film on stainless steel substrate was regarded as the best one for photocatalysis.

Degradation of phenol in industrial wastewater over the F–Fe/TiO_2 photocatalysts under visible light illumination

F–Fe/TiO_2 composite photocatalyst was synthesized by a facile one-step hydrothermal method and then characterized by XRD, XPS and UV–Vis DRS. The catalyst of F–Fe/TiO_2 exhibited the highest photodegradation rate for phenol as compared with pure TiO_2, F/TiO_2, Fe/TiO_2, F0.38–Fe0.13–TiO_2 and Fe(III)/F-TiO_2 under visible light irradiation. The simulated conditions of industrial phenolic wastewater including initial phenol concentration,visible light intensity, p H and different anions were investigated in the presence of F–Fe/TiO_2 photocatalyst. In addition, as expected, the F–Fe/TiO_2 photocatalyst displayed excellent stability, showing a potential industrial application for the treatment of phenolic wastewater.

Effects of ultraviolet(UV) radiation and litter layer thickness on litter decomposition of two tree species in a semi-arid site of Northeast China

Forests and grasslands in arid and semi-arid regions receive high-intensity ultraviolet（UV） radiation year-round. However, how the UV radiation affects the litter decomposition on the forest floor remains unclear. Here, we conducted a field-based experiment in 2011 in the southeastern Horqin Sandy Land, Northeast China, to investigate the effects of UV radiation, litter layer thickness, and their interaction on the mass loss and chemical properties of decomposing litter from Xiaozhuan poplar（Populus × xiaozhuanica） and Mongolian pine（Pinus sylvestris var. mongolica） plantation trees. We found that UV radiation accelerated the decomposition rates of both the Xiaozhuan poplar litter and Mongolian pine litter. For both species, the thick-layered litter had a lower mass loss than the thin-layered litter. The interaction between UV radiation and litter layer thickness significantly affected the litter mass loss of both tree species. However, the effects of UV radiation on the chemical properties of decomposing litter differed between the two species, which may be attributed to the contrasting initial leaf litter chemical properties and morphology. UV radiation mostly had positive effects on the lignin concentration and lignin/N ratio of Xiaozhuan poplar litter, while it had negative effects on the N concentration of Mongolian pine litter. Moreover, litter layer thickness and its interaction with UV radiation showed mostly positive effects on the N concentration and lignin/N ratio of Xiaozhuan poplar litter and the ratios of C/N and lignin/N of Mongolian pine litter, and mostly negative effects on the C/N ratio of Xiaozhuan poplar litter and the N concentration of Mongolian pine litter. Together, these results reveal the important roles played by UV radiation and litter layer thickness in the process of litter decomposition in this semi-arid region, and highlight how changes in the litter layer thickness can exert strong influences on the photodegradation of litter in tree plantations.

CoS_2-碳(C_(60),石墨,碳纳米管)/TiO_2复合光敏剂光降解有机染料(英文)

CoS2,CoS 2-C60 /TiO2,CoS2-CNT/TiO2,and CoS2-Graphene/TiO2 were prepared.The TiO2 products had the anatase phase structure and interesting surface compositions.X-ray diffraction patterns of the CoS2-carbon/TiO2 composites showed a single and clear anatase phase and the CoS2 structure.Scanning electron microscopy characterization of the texture on the CoS 2-carbon/TiO2 composites showed a homogenous composition.Energy-dispersive X-ray spectra for elemental identification showed the presence of C and Ti with strong Co and S peaks from the CoS2-carbon/TiO2 composites.The composites obtained were also characterized by transmission electron microscopy and UV-Vis spectroscopy.CoS2-carbon/TiO2 composites showed excellent photocatalytic activity for the degradation of methylene blue under visible light irradiation.This was attributed to both photocatalysis on the TiO2 support and charge transfer by the carbon nanomaterial,and the introduction of CoS2 to enhance transfer of photogenerated electrons.

Visible Light Induced Photodegradation and Phototoxicity of Phloxine B and Uranine

Ohjective To determine the visible light-induced photodegradation kinetics of two xanthene photosensitizers, phloxine B and uranine, in solution and on the surface of silica TLC plates, and to examine the phototoxicity of residues of degradation, which could provide valuable safety data on the two photosensitizers and other xanthene chemicals when applied in the environment. Methods UV-Vis absorption during photodegradation was monitored with a Unico 2102 spectrophotometer. Organic content of samples was measured with a Shimadzu TOC 4100. Phototoxicity tests were carried out using Saccharomyces cerevisiae with the methods modified from Daniels. Results When phloxine B and uraniue degraded in solution, their apparent rate constant k was 0.0019 and 0.0027 min^-1, respectively. The total organic carbon （TOC） content decreased by approximately 50% during the 8 h irradiation period, which led to a gradual decrease in phototoxicity of the residues. The photodegradation of photosensitizers on the surface of silica TLC plates was much faster than that in the solution. The apparent rate constant k and the half life of phloxine B were 0.0073 min^-1 and 95 min, respectively. Conclusion Visible light can rapidly induce photodegradation of phloxine B and uranine. The phototoxicity of residues is also decreased. The environmental risk of applications of phloxine B and uranine is minimal.

Enhanced photodegradation of phenolic compounds by adding TiO_2 to soil in a rotary reactor

Photodegradation ofpentachlorophenol （PCP） and p-nitrophenol （PNP） in soil was carried out in a designed rotary reactor, which can provide the soil particles with continually uniform irradiation, and on a series of thin soil layers. TiO2, as a kind of environmental friendly photocatalyst, was introduced to the soil to enhance the processes. Compared with that on the soil layers, photodegradation of PCP at initial concentration of 60 mg/kg was improved dramatically in the rotary reactor no matter whether TiO2 was added, with an increase of 3.0 times in the apparent first-order rate constants. The addition of 1 wt% TiO2 furthered the improvement by 1.4 times. Without addition of TiO2, PNP （initial concentration of 60 mg/kg） photodegradation rate in the rotary reactor was similar to that on the soil layers. When 1 wt% additional TiO2 was added, PNP photodegradation was enhanced obviously, and the enhancement in the rotary reactor was 2 times of that on the soil layers, which may be attributed to the higher frequency of the contact between PNP on soil particles and the photocatalyst. The effect of soil pH and initial concentrations of the target compounds on the photodegradation in the rotary reactor was investigated. The order of the degradation rate at different soil pH was relative to the aggregation of soil particles during mixing in the rotary reactor. Photodegradation of PCP and PNP at different initial concentrations showed that addition of TiO2 to enhance the photodegradation was more suitable for contaminated soil with higher concentration of PCP, while was effective for contaminated soil at each PNP concentration tested in our study.