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1.
Zhu R  Sun L 《Chemosphere》2005,59(11):1583-1593
Methane fluxes were measured from three exposed tundra sites and four snowpack sites on the Fildes Peninsula in the maritime Antarctic in the summertime of 2002. The average fluxes at two normal tundra sites were −15.3 μg m−2 h−1 and −14.3 μg m−2 h−1, respectively. The fluxes from tundra site with fresh penguin dropping addition showed positive values with the average of 36.1 μg m−2 h−1, suggesting that the deposition of fresh droppings greatly enhanced CH4 emissions from the poor Antarctic tundra during penguin breeding periods. The summertime variation in CH4 flux was correlated with surface ground temperature and the precipitation. The correlation between the flux and PT0, which is the product of the precipitation and surface ground temperature, was quite strong. The diurnal cycle of CH4 flux from the tundra soils was not obtained due to local fluky weather conditions. The fluxes through four snowpack sites were also obtained by the vertical CH4 concentration gradient and their average fluxes were −46.5 μg m−2 h−1, −28.2 μg m−2 h−1, −46.4 μg m−2 h−1 and −17.9 μg m−2 h−1, respectively, indicating that tundra soils under snowpack also consume atmospheric CH4 in the maritime Antarctic; therefore these fluxes could constitute an important part of the annual CH4 budget for Antarctic tundra ecosystem.  相似文献   

2.
Zhang JB  Song CC  Yang WY 《Chemosphere》2005,59(11):1703-1705
Cold season (winter and thaw) CH4, CO2 and N2O fluxes from freshwater marshes (47°35′N, 133°31′E, Northeast China) were measured, using the static chamber method. The mean CH4 and CO2 fluxes from Carex lasiocarpa (Cl) were 0.5 ± 0.19 and 6.23 ± 1.36 mg C m−2 h−1, respectively, and those from Deyeuxia angustifoli (Da) were 0.18 ± 0.15 and 5.22 ± 2.48 mg C m−2 h−1, respectively in winter. There was no significant difference between Cl and Da (p > 0.05). The contributions of winter CH4 fluxes were about 5.5% and 3% in the Cl and Da, respectively. Marshes are an important potential N2O sink in winter season in northeast China. During thaw, the CH4 and CO2 emissions rapidly increased, 4.5–6 times of winter emissions. Wetland became a source of N2O. Cold season gases flux from northern wetlands play an important role in the seasonal gas exchange.  相似文献   

3.
Fu F  Zeng H  Cai Q  Qiu R  Yu J  Xiong Y 《Chemosphere》2007,69(11):1783-1789
A new dithiocarbamate-type heavy metal precipitant, sodium 1,3,5-hexahydrotriazinedithiocarbamate (HTDC), was prepared and used to remove coordinated copper from wastewater. In the reported dithiocarbamate-type precipitants, HTDC possesses the highest percentage of the effective functional groups. It could effectively precipitate copper to less than 0.5 mg l−1 from both synthetic and actual industrial wastewater containing CuEDTA in the range of pH 3–9. UV–vis spectral investigation and elemental analysis suggested that the precipitate was a kind of coordination supramolecular compound, [Cu3(HTDC)2]n. The toxicity characteristic leaching procedure (TCLP) and semi-dynamic leaching test (SDLT) indicated that the supramolecular precipitate was non-hazardous and stable in weak acid and alkaline conditions. Tests of an anion exchange resin D231 provided a clue to simultaneously remove excess HTDC and residual CuEDTA in practical process of wastewater treatment.  相似文献   

4.
Haggi E  Bertolotti S  García NA 《Chemosphere》2004,55(11):1501-1507
The aerobic visible-light-photosensitised irradiation of methanolic solutions of either of the phenolic-type contaminants model compounds (ArOH) p-phenylphenol (PP), p-nitrophenol (NP) and phenol (Ph), and for two additional phenolic derivatives, namely p-chlorophenol (ClP) and p-methoxyphenol (MeOP), used in some experiments, was carried out. Employing the natural pigment riboflavin (Rf) as a sensitiser, the degradation of both the ArOH and the very sensitiser was observed. A complex mechanism, common for all the ArOH studied, operates. It involves superoxide radical anion (O2√−) and singlet molecular oxygen (O2(1Δg)) reactions. Maintaining Rf in sensitising concentrations levels (≈0.02 mM), the mechanism is highly dependent on the concentration of the ArOH. Kinetic experiments of oxygen and substrate consumption, static fluorescence, laser flash photolysis and time-resolved phosophorescence detection of O2(1Δg) demonstrate that at ArOH concentrations in the order of 10 mM, no chemical transformation occurs due to the complete quenching of Rf singlet excited state. When ArOH is present in concentrations in the order of mM or lower, O2√− is generated from the corresponding Rf radical anion, which is produced by electron transfer reaction from the ArOH to triplet excited Rf. The determined reaction rate constants for this step show a fairly good correlation with the electron-donor capabilities for Ph, PP, NP, ClP and MeOP. In this context, the main oxidative species is O2√−, since O2(1Δg) is quenched in an exclusive physical fashion by the ArOH. The production of O2√− regenerates Rf impeding the total degradation of the sensitiser. This kinetic scheme could partially model the fate of ArOH in aquatic media containing natural photosensitisers, under environmental conditions.  相似文献   

5.
The influence of intact (FLT) and photomodified (phFLT) fluoranthene (0.05, 0.5 and 5 μmol l−1) and herbicide Basagran (5, 20, 35 and 50 nmol l−1) on the germination, growth of seedlings and photosynthetic processes in pea plants (Pisum sativum L., cv. Garde) was investigated. The germination was significantly inhibited already by the lowest concentration (0.05 μmol l−1) of FLT and phFLT, while Basagran caused inhibition only in higher concentrations (35 and 50 nmol l−1). The growth of roots was significantly inhibited by higher concentration 5 μmol l−1 of both FLT and phFLT and the shoot of seedlings was significantly influenced only by photomodified form. The length of root and shoot was inhibited already by concentration 5 nmol l−1 of Basagran. Organic compounds applied on chloroplasts suspension influenced primary photochemical processes of photosynthesis. In chlorophyll fluorescence parameters, the significant increase of F0 values and the decrease of FV/FM and ΦII values by application of FLT (0.5 and 5 μmol l−1) and phFLT (0.05, 0.5 and 5 μmol l−1) was recorded. The maximum capacity of PSII (FV/FM) was influenced by the highest (50 nmol l−1) and the effective quantum yield of PSII (ΦII) already by the lowest (5 nmol l−1) concentration of Basagran. Hill reaction activity decreased and was significantly inhibited by higher concentration (0.5 and 5 μmol l−1) of FLT and phFLT and already by the lowest concentration (5 nmol l−1) of Basagran.  相似文献   

6.
Yacob S  Hassan MA  Shirai Y  Wakisaka M  Subash S 《Chemosphere》2005,59(11):1575-1581
Anthropogenic release of greenhouse gases, especially CO2 and CH4 has been recognized as one of the main causes of global warming. Several measures under the Kyoto Protocol 1997 have been drawn up to reduce the greenhouse gases emission. One of the measures is Clean Development Mechanisms (CDM) that was created to enable developed countries to cooperate with developing countries in emission reduction activities. In Malaysia, palm oil industry particularly from palm oil mill effluent (POME) anaerobic treatment has been identified as an important source of CH4. However, there is no study to quantify the actual CH4 emission from the commercial scale wastewater treatment facility. Hence, this paper shall address the CH4 emission from the open digesting tanks in Felda Serting Hilir Palm Oil Mill. CH4 emission pattern was recorded for 52 weeks from 3600 m3 open digesting tanks. The findings indicated that the CH4 content was between 13.5% and 49.0% which was lower than the value of 65% reported earlier. The biogas flow rate ranged between 0.8 l min−1 m−2 and 9.8 l min−1 m−2. Total CH4 emission per open digesting tank was 518.9 kg day−1. Relationships between CH4 emission and total carbon removal and POME discharged were also discussed. Fluctuation of biogas production was observed throughout the studies as a result of seasonal oil palm cropping, mill activities, variation of POME quality and quantity discharged from the mill. Thus only through long-term field measurement CH4 emission can be accurately estimated.  相似文献   

7.
Lima IB 《Chemosphere》2005,59(11):1697-1702
Biogeochemical distinction of methane emissions to the atmosphere may essentially rely on the surface area and morphometry of Amazon hydroreservoirs. Tucuruí (deep) and Samuel (shallow) reservoirs released in average 13.82 ± 22.94 and 71.19 ± 107.4 mg CH4 m−2 d−1, respectively. δ13C–CH4 values from the sediments to the atmosphere indicate that the deep reservoir has extended methanotrophic layer, oxidizing large quantities of light isotope methane coming from the sediments, while sediment-generated methane can easily evade the shallow reservoir.  相似文献   

8.
Among the many larvicides tested for the control of s.l. larvae, the vector of human onchocerciasis in West Africa, pyraclofos proved to be 100% effective at 100 μg × L−1 for 10 min in river, with a carry of 20 km at 100 m3 × sec−1. Tests were then performed both in laboratory and field conditions to evaluate its toxicity on the non-target aquatic fauna. In experimental short-term gutter tests, the detachment of the total benthic insects was 35% at 100 μg × L−1 for 10 min against 17% for temephos at the same dose and 59% for chlorphoxim at 50μg × L−1 for 10 min. , and were the most affected organisms. The treatment of a river resulted in a considerable detachment of the same taxonomic groups, plus Orthocladiinae. On the other hand, investigations conducted in tanks showed that the 24-hr LC50 for is 150 μg × L−1 and that for 170 μg × L−1, values which are not very different from the operational dose of the larvicide (100 μg × L−1 for 10 min.). Nevertheless, in a river, no fish mortality was recorded. Based on fish LC50 and drift of benthic insects, pyraclofos at 100 μg × L−1 was judged to be less toxic to aquatic fauna in the short term than permethrin and carbosulfan.  相似文献   

9.
The present work focuses on the fate of two cancerostatic platinum compounds (CPC), cisplatin and carboplatin, as well as of two inorganic platinum compounds, [PtCl4]2− and [PtCl6]2− in biological wastewater treatment. Laboratory experiments modelling adsorption of these compounds onto activated sludge showed promising specific adsorption coefficients KD and KOC and Freundlich adsorption isotherms. However, the adsorption properties of the investigated substances were differing significantly. Adsorption decreased following the order cisplatin > [PtCl6]2− > [PtCl4]2− > carboplatin. Log KD-values were ranging from 2.5 to 4.3 , log KOC from 3.0 to 4.7.

A pilot membrane bioreactor system (MBR) was installed in a hospital in Vienna and fed with wastewater from the oncologic in-patient treatment ward to investigate CPC-adsorption in a sewage treatment plant. During three monitoring periods Pt-concentrations were measured in the influent (3–250 μg l−1 Pt) and the effluent (2–150 μg l−1 Pt) of the treatment plant using ICP-MS. The monitoring periods (duration 30 d) revealed elimination efficiencies between 51% and 63% based on averaged weekly input–output budgets. The derived log KD-values and log KOC-values ranged from 2.4 to 4.8 and from 2.8 to 5.3, respectively. Species analysis using HPLC-ICP-MS proofed that mainly carboplatin was present as intact drug in the influent and – due to low log KD – in the effluent of the MBR.  相似文献   


10.
Subbiah D  Kala S  Mishra AK 《Chemosphere》2005,61(11):1580-1586
The fluorescence spectroscopic behavior of bromadiolone (anticoagulant rodenticide), a substituted 4-hydroxycoumarin derivative, was investigated in water and in organized media like micelles and cyclodextrins. A detailed study on various photophysical parameters like fluorescence intensity (IF), quantum yield (), lifetime (τ) and steady state fluorescence anisotropy (r) of bromadiolone in aqueous and in organized media was carried out. Bromadiolone in aqueous solution was observed to be in an aggregated state, thereby showing weak emission due to self-quenching. Marked enhancement of fluorescence intensity was observed in organized media like micelles and β-cyclodextrin. A preliminary investigation has been done to find out whether this enhancement of fluorescence can be used to develop a sensitive analytical method for determination of bromadialone in aqueous media. A linear relationship between the fluorescence intensity and concentration of bromadiolone was observed in the range of 0.15–7.9 μg ml−1 in cetyltrimethylammonium bromide (CTAB) and 0.5–26.4 μg ml−1 in β-cyclodextrin medium. The lower detection limit was found to be 37 ng ml−1 in presence of CTAB and 23 ng ml−1 in β-cyclodextrin. Comparison with 4-hydroxycoumarin, an unsubstituted analogue, was made.  相似文献   

11.
An increasing percentage of agricultural land in Germany is used for oil seed plants. Hence, rape has become an important agricultural plant (in Saxony 1998: 12% of the farmland) in the recent years. During flowering of rape along with intensive radiation and high temperatures, a higher production and emission of biogenic VOC was observed. The emissions of terpenes were determined and more importantly, high concentrations of organic carbonyl compounds were observed during this field experiment. All measurements of interest have been carried out during two selected days with optimal weather conditions. It is found that the origin or the mechanism of formation of different group of compounds had strong influence on the day to day variation of their concentrations. The emission flux of terpenes from flowering rape plants was determined to be 16–32 μg h−1 m−2 (30–60 ng h−1 per g dry plant––540–1080 ng h−1 per plant), in total. Limonene, -thujene and sabinene were the most important compounds (about 60% of total terpenes). For limonene and sabinene reference emission rates (MS) and temperature coefficients were determined: βlimonene=0.108 K−1 and MS=14.57 μg h−1 m−2; βsabinene=0.095 K−1 and MS=5.39 μg h−1 m−2.

The detected carbonyl compound concentrations were unexpectedly high (maximum formaldehyde concentration was 18.1 ppbv and 3.4 ppbv for butyraldehyde) for an open field. Possible reasons for these concentrations are the combination of primary emission from the plants induced by high temperature and high ozone stress, the secondary formation from biogenically and advected anthropogenically emitted VOC at high radiation intensities and furthered by the low wind speeds at this time.  相似文献   


12.
Determination of triazines herbicides (atrazine and simazine) by high performance liquid chromatography (HPLC) in samples of trophic chain were worked out. Determination limits of 0.5 μg g−1 for atrazine, 0.8 μg g−1 for simazine with pesticides recovery of 70–77% in trophic chain samples were obtained. The content of simazine in soils was in range 1.72–57.89 μg g−1, in grass 5–88 μg g−1, in milk 2.32–15.29 μg g−1, in cereals 10.98–387 μg g−1, in eggs 30.14–59.48 μg g−1, for fruits: 2.45–6.19 μg g−1. The content of atrazine in soils was in range 0.69–19.59 μg g−1, in grass 7.85–23.85 μg g−1, in cereals 1.88–43.08 μg g−1. Cadmium, lead and zinc were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES) in the same samples as atrazine and simazine. Determination limits for cadmium 5 × 10−3 μg g−1, for lead 1 × 10−2 μg g−1, and for zinc 0.2 × 10−3 μg g−1, were obtained. The content of cadmium in soil was in range 0.13–5.89 μg g−1, in grass 114–627.72 × 10−3 μg g−1, in milk 8.88–61.88 × 10−3 μg g−1, in cereals 0.20–0.31 μg g−1, in eggs 0.11–0.15 μg g−1, in fruits 0.23–0.59 μg g−1. The content of lead in soils was in range 0.57–151.50 μg g−1, in grass 0.16–136.57 μg g−1, in milk 1.16–3.74 μg g−1, in cereals 1.05–5.47 μg g−1, in eggs 5.79–55.87 μg g−1, in fruits 21.00–87.36 μg g−1. Zinc content in soil was in range 9.15–424.5 μg g−1, in grass 35.20–55.87 μg g−1, in milk 20.00–34.38 μg g−1, in cereals 14.94–28.78 μg g−1, in eggs 15.67–32.01 μg g−1, in fruits 14.94–18.88 μg g−1.

Described below extraction and mineralization methods for particular trophic chains allowed to determine of atrazine, simazine, cadmium, lead and zinc with good repeatability and precision. Emphasis was focused on liquid–liquid extraction and solid-phase extraction of atrazine and simazine from analysed materials, as well as, on monitoring the content of herbicides and metals in soil and along trophic chain. Higher concentration of pesticides in samples from west region of Poland in comparison to that of east region is likely related to common applying them in Western Europe in relation to East Europe. The content of metals strongly depends on samples origin (industry area, vicinity of motorways).  相似文献   


13.
Pang X  Wang DH  Xing XY  Peng A  Zhang FS  Li CJ 《Chemosphere》2002,47(10):1033-1039
In order to improve the plant ability to resist lead stress, effect of 0.05 mg/l La(NO3)3 on the activities of catalase (CAT), superoxide dismutase (SOD), the level of malondialdehyde (MDA) in wheat seedlings under lead stress was studied. The effect of La3+ on plant growth, chlorophyll content in wheat seedlings after adding 0, 50, 100 mg/l Pb(NO3)3 to the nutrient solution for 12 days was observed. The plants were grown in nutrient solution in a strictly controlled climate growth room. Effects of La3+ (with La treatment) compared with check groups was evidently observed. The activities of SOD and CAT in root were enhanced 0.45–1.69 times and 33.20–77.77% respectively and MDA content was reduced 11.05–27.49% in root after treatments from the second day till the end of the experiment. The activities of SOD and CAT was found to be increased slightly (P<0.05) and MDA content decreased in shoot and root of wheat seedlings by La3+ under lead stress within five days after treatments compared with Pb1 and Pb2 groups. It was assumed that antioxidant enzymes was found to be increased by La(NO3)3, the antioxidant potential of the wheat seedlings to resist lead stress enhanced. It is suggested that La3+ could be used to resist lead stress at the beginning under stress while the stress was not so serious.  相似文献   

14.
Khwaja HA  Narang A 《Chemosphere》2008,71(11):2030-2043
Measurements of carbonyls and C2–C6 non-methane hydrocarbons (NMHCs) were made in ambient air at a rural site at the summit of Whiteface Mountain (WFM) in New York State. Alkanes dominated in the samples, with ethane and propane making up about 55% of the total on a carbon-atom basis. Ethane, the longest-lived of the NMHCs, showed a mixing ratio in the range of 0.86–2.1 ppbv. Photochemical ageing analysis indicated an anthropogenic influence on the NMHC levels. The photochemical reactivity of the hydrocarbons, calculated in terms of propylene-equivalent concentration, was dominated by alkenes (propene and ethene), which accounted for 74% of the total NMHC sum. Air mass back-trajectories have been used to investigate the origin of the observed NMHCs and carbonyls. Higher concentrations were found when air masses arrived from the midwestern US corridor. Acetone was the most abundant species, comprising from 31% to 53% of the total detected carbonyls, followed by MEK (15–53%), HCHO (7–39%), and CH3CHO (7–19%). Average concentrations were determined to be 1.61 ppbv for CH3C(O)CH3, 1.40 ppbv for MEK, 1.16 ppbv for HCHO, and 0.49 ppbv for CH3CHO. The variations in carbonyl concentrations were observed to follow patterns similar to variations in O3 concentrations, typical of secondary products. Correlations and statistical analysis of the carbonyls and NMHCs were performed, and showed that most of the compounds derived from mixing and photochemical transformation of long-range transported pollutants from the major source areas. Ranking of the carbonyls with respect to removal of the OH radical showed HCHO to be the most important species, followed by CH3CHO, MEK, and CH3C(O)CH3.  相似文献   

15.
Neamtu M  Siminiceanu I  Kettrup A 《Chemosphere》2000,40(12):1407-1410
The photodegradation of five representative nitromusk compounds in water has been performed in a stirred batch photoreactor with a UV low-pressure immersed mercury lamp, at constant temperature and different doses of hydrogen peroxide. The rate constants have been calculated on the basis of experimental data and a postulated first-order kinetic model. The rate constants, at 298 K and a dose of 1.1746 μmol l−1 H2O2 ranges from 0.3567 × 10−3 s−1 for musk tibetene, to 1.785 × 10−3 s−1 for musk ambrette.  相似文献   

16.
Orlando US  Baes AU  Nishijima W  Okada M 《Chemosphere》2002,48(10):1041-1046
Anion exchangers were prepared from different agricultural residues (AR) after reaction with epichlorohydrin and dimethylamine in the presence of pyridine and N,N-dimethylformamide (EDM method). Agricultural residues anion exchangers (AR-AE) produced by the EDM method were inexpensive and showed almost the same NO3 removal capacities as Amberlite IRA-900. AR-AE produced from AR with higher hemicelluloses, lignin, ash and extractive contents resulted in the lower yields. Sugarcane bagasse with the highest -cellulose contents of 51.2% had the highest yield (225%) and lowest preparation cost. The highest maximum adsorption capacity (Qmax) for nitrate was obtained from rice hull (1.21 mmol g−1) and pine bark natural exchangers (1.06 mmol g−1). No correlation was found between Qmax and -cellulose content in the original AR. AR-AE produced from different AR demonstrated comparable Qmax due to the removal of non-active compounds such as extractives, lignin and hemicelluloses from AR during the preparation process. Similar preparation from pure cellulose and pure alkaline lignin demonstrated that the EDM method could not produce anion exchangers from pure lignin due to its solubilization after the reaction with epichlorohydrin.  相似文献   

17.
An experiment was carried out to decompose chlorinated dioxins (PCDDs, PCDFs) Chlorobenzenes, NOx and odourous compounds (H2S, CH4S, C2H6S2, C8H8, C2H6S, C2H4O, NH3) simultaneously using a catalyst in the MSW incineration plant. The experiments were conducted at temperatures from 200°C to 400°C and from 3000h−1 to 6000h−1 at space velocity. A catalyst containing V2O5 and WO3 on the basis of TiO2 is used, an oxidizing catalyst of the honeycomb type. The average decomposition efficiencis were 95%, 98%, 92% for PCDDs(48CDDs), PCDFs(48CDFs) and Chlorobenzenes(36CLBs) at a reaction temperature of 350°C and a space velocity of 3000h−1, more than 90% for NOx at a reactiont temperature of 300°C and more than 80% for odourous compounds at the reaction temperature of 300°C and a space velocity of 6000h−1. All those compounds were decomposed successfully with increasing contact time and surface. The rate-determing step was the chemical reaction of catalyst surface.  相似文献   

18.
Verge C  Moreno A  Bravo J  Berna JL 《Chemosphere》2001,44(8):1749-1757
In the present work, the influence of Ca2+ concentration on the toxicity of single cut linear alkylbenzene sulfonate (LAS) homologues was studied. Precipitation boundary diagrams for each homologue were obtained, indicating turbid and clear zones depending on the LAS and Ca2+ concentrations. The separation between transparent and turbid zones is given by the so-called precipitation line. LAS toxicity to Daphnia magna was determined at concentrations close to this precipitation line. It was observed that when Ca(LAS)2 precipitation progresses, LAS bioavailability decreases for test animals, and the toxicity diminishes even at high nominal LAS concentrations. According to the “free ion activity model” (FIAM), the toxicity of a given chemical compound is mainly due to the ionic species (Ca2+–LAS) and not due to the precipitated molecule, Ca(LAS)2. The significance of the present study is in connection with the assessment of LAS sorption/precipitation studies in soils and sediments, where in situ toxicity is strongly influenced by Ca2+/Mg2+ ions, according to the results presented in this work.  相似文献   

19.
The Ti02-mediated photomineralization of 8–1000 ppm of methanoic acid, of 6–100 ppm of ethanoic acid, of 6–180 ppm of propanoic acid, and of 6–90 ppm of n-decanoic acid in aqueous solutions was studied at 296± 2 K or 308 ± 2 K, with low and high pressure mercury arc lamps (radiant power in the absorption range 8 and 145 W respectively), using PHOTOPERM® CPP/313 membranes containing immobilized 30±3 wt.% Ti02, and, in parallel runs, 7 wt.% of a synergic mixture of tri(t-butyl)- and tri-(i-propyl) vanadate(V) as photocatalytic promoter. Stoichiometric H202 was used or, in some of the runs, 03, at saturation, as oxygen suppliers. Disappearance of total organic carbon (TOC) was followed as a function of time. To fit kinetic curves up to complete photomineralization, a kinetic model was employed, already used successfully in previous studies, which considers appearance and disappearance of all intermediates, as if they were represented by a hypothetical single molecule, mediating all of them. The photocatalytic activity of trialkyl vanadates was evaluated from quantum yields at “infinite” concentration, with respect to the maximum allowable efficiencies. When using O3, a dark catalysis effect clearly appeared towards intermediate species produced during the photocatalysed degradation.  相似文献   

20.
The electrochemical performance of pure Ti–Pt/β-PbO2 electrodes, or doped with Fe and F (together or separately), in the oxidation of simulated wastewaters containing the Blue Reactive 19 dye (BR-19), using a filter-press reactor, was investigated and then compared with that of a boron-doped diamond electrode supported on a niobium substrate (Nb/BDD). The electrooxidation of the dye simulated wastewater (volume of 0.1 l, with a BR-19 initial concentration of 25 mg l−1) was carried out under the following conditions: current density of 50 mA cm−2, volume flow rate of 2.4 l h−1, temperature of 25 °C and electrode area of 5 cm2. The performances of the electrodes in the dye decolorization were quite similar, achieving 100% decolorization, and in some cases 90% decolorization was achieved by applying only ca. 0.3 A h l−1 (8 min of electrolysis). The reduction of the simulated wastewater organic load, monitored by its total organic carbon content (TOC), was greater for the Ti–Pt/β-PbO2–Fe,F electrode obtained from an electrodeposition bath containing 1 mM Fe3+ and 30 mM F. In this case, after 2 h of electrolysis the obtained TOC reduction was 95%, while for the pure β-PbO2 and the Nb/BDD electrodes the reductions were 84% and 82%, respectively.  相似文献   

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