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1.
研究了UV/H2O2/草酸高铁铵体系下孔雀绿(Malachite green,MG)光降解过程中的影响因素,包括MG的初始浓度、初始pH值、投加H2O2浓度和草酸高铁铵浓度等。结果表明:MG初始浓度越低光降解越快,碱性条件有利于MG的降解,其最佳降解pH为11.0;随H2O2浓度的增加,MG降解率先增加后减少,在100mmol/L时,降解率最高;MG降解率随草酸高铁铵浓度增加而增加,于10.0mmol/L时MG降解率最高;UV/H2O2/草酸高铁铵体系的降解效果较强,交叉实验结果表明H2O2:草酸高铁铵浓度比在1~20:1时降解率均高于。因此该体系具有快速、简单、经济并高效率等特点,可应用于染料废水的降解和脱色工艺中。 相似文献
2.
Mouheb Sboui Mohamed Faouzi Nsi Ali Rayes Meenakshisundaram Swaminathan Ammar Houas 《环境科学学报(英文版)》2017,29(10):3-13
A novel photocatalyst based on TiO_2–PANI composite supported on small pieces of cork has been reported. It was prepared by simple impregnation method of the polyaniline(PANI)–modified TiO_2 on cork. The TiO_2–PANI/Cork catalyst shows the unique feature of floating on the water surface. The as-synthesized catalyst was characterized by X-ray diffraction(XRD),scanning electron micrograph(SEM), transmission electron microscopy(TEM), thermogravimetric analysis(TGA), Fourier transform infrared spectroscopy(FT-IR), UV–vis diffuse reflectance spectra(UV–vis DRS) and the Brunauer–Emmett–Teller(BET) surface area analysis. Characterization suggested the formation of anatase highly dispersed on the cork surface. The prepared floating photocatalyst showed high efficiency for the degradation of methyl orange dye and other organic pollutants under solar irradiation and constrained conditions, i.e., no-stirring and no-oxygenation. The TiO_2–PANI/Cork floating photocatalyst can be reused for at least four consecutive times without significant decrease of the degradation efficiency. 相似文献
3.
Quantum chemical investigation on photodegradation mechanisms of sulfamethoxypyridazine with dissolved inorganic matter and hydroxyl radical 总被引:1,自引:0,他引:1
Sulfamethoxypyridazine(SMP) is one of the commonly used sulfonamide antibiotics(SAs).SAs are mainly studied to undergo triplet-sensitized photodegradation in water under natural sunlight with other coexisting aquatic environmental organic pollutants.In this work,SMP was selected as a representative of SAs.We studied the mechanisms of triplet-sensitized photodegradation of SMP and the influence of selected dissolved inorganic matter,i.e.,anions(Br~-,Cl~-,and NO~-_3) and cations ions(Ca~(2+),Mg~(2+),and Zn~(2+)) on SMP photodegradation mechanism by quantum chemical methods.In addition,the degradation mechanisms of SMP by hydroxyl radical(OH·) were also investigated.The creation of SO_2 extrusion product was accessed with two different energy pathways(pathway-1 and pathway-2) by following two steps(step-I and step-II) in the tripletsensitized photodegradation of SMP.Due to low activation energy,the pathway-1 was considered as the main pathway to obtain SO_2 extrusion product.Step-II of pathway-1 was measured to be the rate-limiting step(RLS) of SMP photodegradation mechanism and the effect of the selected anions and cations was estimated for this step.All selected anions and cations promoted photodegradation of SMP by dropping the activation energy of pathway-1.The estimated low activation energies of different degradation pathways of SMP with OH·radical indicate that OH·radical is a very powerful oxidizing agent for SMP degradation via attack through benzene derivative and pyridazine derivative ring. 相似文献
4.
ZnBiYO4 was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiYO4 were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance. ZnBiYO4 crystallized with a tetragonal spinel structure with space group I41/A. The lattice parameters for ZnBiYO4 were a = b = 11.176479 Å and c= 10.014323 Å. The band gap of ZnBiYO4 was estimated to be 1.58 eV. The photocatalytic activity of ZnBiYO4 was assessed by photodegradation of methyl orange under visible light irradiation. The results showed that ZnBiYO4 had higher catalytic activity compared with N-doped TiO2 under the same experimental conditions using visible light irradiation. The photocatalytic degradation of methyl orange with ZnBiYO4 or N-doped TiO2 as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01575 and 0.00416 min-1 for ZnBiYO4 and N-doped TiO2, respectively. After visible light irradiation for 220 min with ZnBiYO4 as catalyst, complete removal and mineralization of methyl orange were observed. The reduction of total organic carbon, formation of inorganic products, SO42- and NO3-, and evolution of CO2 revealed the continuous mineralization of methyl orange during the photocatalytic process. The intermediate products were identified using liquid chromatography- mass spectrometry. The ZnBiYO4/(visible light) photocatalysis system was found to be suitable for textile industry wastewater treatment and could be used to solve other environmental chemical pollution problems. 相似文献
5.
Sudha Rani Batchu Venkata R. Panditi Piero R. Gardinali 《Journal of environmental science and health. Part. B》2013,48(3):200-211
The photochemical fate of seven sulfonamides was investigated in matrices representative of natural water bodies under various light sources. Fundamental photolysis parameters such as molar absorption coefficient, quantum yield (QY) and first-order rate constants were determined. The photolysis decay rate was dependent on the protonation state of the molecule, pH of the water sample and dissolved organic matter. Natural organic matter was the most significant factor in the indirect photolysis of sulfonamides. Half-lives were in the range of minutes at 254 nm to days under natural sunlight. Under natural sunlight, all sulfonamides showed higher removal rates in natural waters implying that indirect photolysis is the predominant mechanism. 相似文献
6.
Tao Tang Kun QianTianyu Shi Fang WangPingliang Li Jianqiang LiYongsong Cao 《Chemosphere》2012,89(11):1419-1425
Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through sewage discharge and waste disposal produced by human excretions. In this study, the photodegradation kinetics of quinestrol in various conditions was investigated by UV and solar irradiation. The affecting factors were studied including concentration of hydrogen peroxide, different water types, and the initial concentrations of quinestrol. Concurrently, the transformation products and presumed pathways of quinestrol in distilled water by UV irradiation were identified and proposed. The results showed that the degradation of quinestrol in both irradiation conditions followed the pseudo-first-order kinetics. More rapid degradation was observed by UV irradiation (k = 0.018 min−1) than solar irradiation (k = 0.004 h−1), and the photodegradation rate of quinestrol depended on the concentration of hydrogen peroxide, the initial concentration of quinestrol and water types. The transformation products of quinestrol in distilled water were identified by gas chromatography/mass spectrometry. When exposed to UV irradiation, quinestrol in aqueous solution was rapidly degraded, giving at least ten photodegradation products. The chemical structures of ten degradation products were identified on the basis of mass spectrum interpretation and literature data. 相似文献
7.
Bappaditya Kanrar Anjan Bhattacharyya 《Journal of environmental science and health. Part. B》2013,48(8):788-797
The photolysis of a rice herbicide Bispyribac sodium (Sodium 2, 6-bis [(4, 6-dimethoxypyrimidin-2-yl) oxy] benzoate) has been studied in different aqueous medium (distilled water, pond water and Irrigation water) under the influence of UV (λ max ≥ 250 nm) and sunlight in presence or absence of sensitizers (TiO2 and KNO3). The study was conducted under laboratory simulated condition which made it possible to evaluate the contribution of different factors viz. source of irradiation, solvent and sensitizers towards the photolysis of bispyribac sodium. The photodegradation proceeds via first order reaction Kinetics in all the cases. Five photo metabolites (M1-M5) were isolated in pure form by column chromatographic method from the irradiation system under UV influenced and TiO2 as sensitizer. From the different spectral data (IR, NMR, UV-VIS, Mass) the structure of these five metabolites were assigned as M1 (Phenol), M2 [2, 6-Dihydroxy benzoic acid], M3 [2, 6-bis [(4, 6 dimethoxypyrimidin-2yl) oxy] benzoic acid], M4 [2-(3-Hydroxy-phenoxy)-pyrimidine-4, 6-diol] and M5 as [2,4-Dihydroxy-3, 5-dimethoxy-6-(4-methoxy pyrimidine-2-yloxy)-benzoic acid]. Moreover, another six photometabolites (M6-M11) were identified from the different irradiation system on the basis of Micromass analysis. On the basis of MS/MS data analysis, the structure of these six photometabolites were assigned as M6 [2-(4, 6-Dimethoxy-pyrimidin-2-yloxy)-6-hydroxy-benzoic acid], M7 [2-Hydroxy-6-(4-hydroxy-6-methoxy-pyrimidin-2-yloxy)-benzoic acid], M8 [4, 6-Dimethoxy-pyrimidin-2-ol], M9 [6-Methoxy-pyrimidine-2, 4-diol], M10 [2-Hydroxy-6-(pyrimidin-2-yloxy)-benzoic acid] and M11 [2, 4, 6-Trimethoxy-pyrimidine]. The plausible Photodegradation pathways of bispyribac sodium in the present investigation were portrayed which proceeds via hydrolysis, hydrolytic cleavage, O-dealkylation, decarboxylation, dehydroxylation, O-alkylation and hydroxylation. 相似文献
8.
Chenchen Li Lijie Yan Yiming Li Dan Zhang Mutai Bao Limei Dong 《Frontiers of Environmental Science & Engineering》2021,15(4):72
9.
The photooxidation of dye solutions containing Fe(III)-citrate complexes was studied. The photodegradation under near-UV light of the five dyes, C. I. reactive red 2, C. I. reactive blue 4, C. I. reactive black 8, C. I. basic red 13 and C. I. basic yellow 2, in aqueous solutions at pH2.0 containing Fe(III)-citrate complexes was found to follow pseudo-first order kinetics. The photodegradation rates of the dye, C. I. reactive red 2, decreased with increasing the initial dye concentration in range of 20 – 60 mg/L . A comparatively higher photodegradation efficiency of the dye was gained under the condition of pH2.0 and the Fe(III) to citrate ratio 1:2. 相似文献
10.
Takashi Yamamoto Atsushi Ohara Yukio Noma Katsushi Nishizawa Akio Yasuhara Shin-ichi Sakai 《Journal of Material Cycles and Waste Management》2007,9(2):188-193
The photodegradation of tetraphenyltin (TePT) contained in polychlorinated biphenyl (PCB)-based transformer oil simulants
by ultraviolet (UV) irradiation in alkaline 2-propanol solutions was examined. In the absence of PCBs, the TePT level fell
to below 1% of the initial concentration within 30 min. In the absence of both PCBs and an alkali, the concentrations of tri-,
di-, and monophenyltins initially increased to a few milligrams per liter, and then reduced to below the detection limits
within 90 min. The addition of an alkali to the reaction solution slightly accelerated the photodecomposition of TePT. The
decomposition of other phenyltins (PTs) was also accelerated. When PCBs with concentrations of approximately 80 times the
initial TePT concentration were added, only a small fraction of the TePT decomposed within 100 min. Moreover, the levels of
PTs did not change during irradiation. TePT and other PTs did decompose when the level of PCBs was reduced to the same concentration
as that of TePT; however, the decomposition rates were slower than those in the absence of PCBs. In the actual treatment process,
TePT and other PTs in PCB-based transformer oil are decomposed by catalytic reduction, which is used after UV irradiation.
Therefore, in the actual treatment of PCB-based transformer oil wastes, pollution due to PTs can be prevented. 相似文献