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871.
Jan Bernd Barhorst Roland Kubiak 《Environmental science and pollution research international》2009,16(5):582-589
Background, aim and scope The use of sodium hypochlorite (HYP) in viticulture results in effluents which are contaminated with halogenated substances.
These disinfection by-products (DBPs) can be quantified as group parameter ‘adsorbable organic halogens’ (AOX) and have not
been determined in effluents of viticulture yet. The substances that are detected as AOX are unknown. The AOX can be composed
of harmless substances, but even toxic contaminants. Thus, it is impossible to assess ecological impacts. The aim of this
study is to determine the quantification of AOX and DBPs after the use of HYP. This will be helpful to reduce environmental
pollution by AOX.
Materials and methods The potential of HYP to generate AOX was determined in laboratory-scale experiments. Different model solutions were treated
with HYP according to disinfection processes in viticulture and conditions of AOX formation in effluents were simulated. AOX
were quantified using the flask-shaking method and identified DBPs were investigated by gas chromatography–mass spectrometry.
Results Treatment with HYP resulted in the formation of AOX. The percentage conversion of HYP to AOX was up to 11%. Most important
identified DBPs in viticulture are chloroform, dichloroacetic acid and trichloroacetaldehyde. In addition, the formation of
carbon tetrachloride (CT), 1,1,1-trichloropropanone, 2,4-dichlorobenzoic acid and 2-chloro-/2,4-dichlorophenylacetic acid
was investigated. It was demonstrated that reaction temperature, concentration of HYP and type of organic matter have important
influence on the formation of chlorinated DBPs.
Discussion The percentage conversion of HYP to AOX was similar to other published studies. Although a correlation of single compounds
and AOX is difficult, chloroform was the predominant AOX. Generation of the volatile chloroform should be avoided due to possible
adverse effects. The generation of dichloroacetic acid is of minor importance on account of biodegradation. Trichloroacetaldehyde
and 1,1,1-trichloropropanone are weak mutagens and their formation should be avoided.
Conclusions The generation of AOX and chlorinated DBPs can be minimised by reducing the concentrations of the organic materials in the
effluents. The removal of organic matter before disinfection results in a decreased formation of AOX. HYP is an effective
disinfectant; therefore, it should be used at low temperatures and concentrations to reduce the amount of AOX. If possible,
disinfection should be accomplished by the use of no chlorine-containing agents. By this means, negative influences of HYP
on the quality of wine can also be avoided.
Recommendations and perspectives Our results indicate that HYP has a high potential to form AOX in effluents of viticulture. The predominant by-products are
chloroform, dichloroacetic acid and trichloroacetaldehyde. In further research, wastewaters from a winery and the in- and
outflows of two sewage treatment plants were sampled during vintage and analysed. These results will be discussed in a following
paper. 相似文献
872.
Vinicius F. Farjalla André M. Amado Albert L. Suhett Frederico Meirelles-Pereira 《Environmental science and pollution research international》2009,16(5):531-538
Background, aim, and scope Dissolved humic substances (HS) usually comprise 50–80% of the dissolved organic carbon (DOC) in aquatic ecosystems. From
a trophic and biogeochemical perspective, HS has been considered to be highly refractory and is supposed to accumulate in
the water. The upsurge of the microbial loop paradigm and the studies on HS photo-degradation into labile DOC gave rise to
the belief that microbial processing of DOC should sustain aquatic food webs in humic waters. However, this has not been extensively
supported by the literature, since most HS and their photo-products are often oxidized by microbes through respiration in
most nutrient-poor humic waters. Here, we review basic concepts, classical studies, and recent data on bacterial and photo-degradation
of DOC, comparing the rates of these processes in highly humic ecosystems and other aquatic ecosystems.
Materials and methods We based our review on classical and recent findings from the fields of biogeochemistry and microbial ecology, highlighting
some odd results from highly humic Brazilian tropical lagoons, which can reach up to 160 mg C L−1.
Results and discussion Highly humic tropical lagoons showed proportionally lower bacterial production rates and higher bacterial respiration rates
(i.e., lower bacterial growth efficiency) than other lakes. Zooplankton showed similar δ13C to microalgae but not to humic DOC in these highly humic lagoons. Thus, the data reviewed here do not support the microbial
loop as an efficient matter transfer pathway in highly humic ecosystems, where it is supposed to play its major role.
In addition, we found that some tropical humic ecosystems presented the highest potential DOC photo-chemical mineralization
(PM) rates reported in the literature, exceeding up to threefold the rates reported for temperate humic ecosystems. We propose
that these atypically high PM rates are the result of a joint effect of the seasonal dynamics of allochthonous humic DOC input
to these ecosystems and the high sunlight incidence throughout the year. The sunlight action on DOC is positive to microbial
consumption in these highly humic lagoons, but little support is given to the enhancement of bacterial growth efficiency,
since the labile photo-chemical products are mostly respired by microbes in the nutrient-poor humic waters.
Conclusions HS may be an important source of energy for aquatic bacteria in humic waters, but it is probably not as important as a substrate
to bacterial growth and to aquatic food webs, since HS consumption is mostly channeled through microbial respiration. This
especially seems to be the case of humic-rich, nutrient-poor ecosystems, where the microbial loop was supposed to play its
major role. Highly humic ecosystems also present the highest PM rates reported in the literature. Finally, light and bacteria
can cooperate in order to enhance total carbon degradation in highly humic aquatic ecosystems but with limited effects on
aquatic food webs.
Recommendations and perspectives More detailed studies using C- and N-stable isotope techniques and modeling approaches are needed to better understand the
actual importance of HS to carbon cycling in highly humic waters. 相似文献
873.
Siedlecka EM Stepnowski P 《Environmental science and pollution research international》2009,16(4):453-458
Background, aim, and scope Ionic liquids are regarded as essentially “green” chemicals because of their insignificant vapor pressure and, hence, are
a good alternative to the emissions of toxic conventional volatile solvents. Not only because of their attractive industrial
applications, but also due to their very high stability, ionic liquids could soon become persistent contaminants of technological
wastewaters and, moreover, break through into natural waters following classical treatment systems. The removal of harmful
organic pollutants has forced the development of new methodologies known as advanced oxidation processes (AOPs). Among them,
the Fenton and Fenton-like reactions are usually modified by the use of a higher hydrogen peroxide concentration and through
different catalysts. The aim of this study was to assess the effect of hydrogen peroxide concentration on degradation rates
in a Fenton-like system of alkylimidazolium ionic liquids with alkyl chains of varying length and 3-methyl-N-butylpyridinium chloride.
Materials and methods The ionic liquids were oxidized in dilute aqueous solution in the presence of two different concentrations of hydrogen peroxide.
All reactions were performed in the dark to prevent photoreduction of Fe(III). The concentrations of ionic liquids during
the process were monitored with high-performance liquid chromatography. Preliminary degradation pathways were studied with
the aid of 1H NMR.
Results Degradation of ionic liquids in this system was quite effective. Increasing the H2O2 concentration from 100 to 400 mM improved ionic liquid degradation from 57–84% to 87–100% after 60 min reaction time. Resistance
to degradation was weaker, the shorter the alkyl chain.
Discussion The compound omimCl was more resistant to oxidation then other compounds, which suggests that the oxidation rates of imidazolium
ionic liquids by OH· are structure-dependent and are correlated with the n-alkyl chain length substituted at the N-1-position. The level of degradation was dependent on the type of head group. Replacing
the imidazolium head group with pyridinium increased resistance to degradation. Nonetheless, lengthening the alkyl chain from
four to eight carbons lowered the rate of ionic liquid degradation to a greater extent than changing the head group from imidazolium
to pyridinium. 1H-NMR spectra show, in the first stage of degradation, that it is likely that radical attack is nonspecific,
with any one of the carbon atoms in the ring and the n-alkyl chain being susceptible to attack.
Conclusions The proposed method has proven to be an efficient and reliable method for the degradation of imidazolium ionic liquids by
a Fenton-like reagent deteriorated with lengthening n-alkyl substituents and by replacing the imidazolium head group with pyridinium. The enhanced resistance of 1-butyl-3-methylpyridinium
chloride when the resistance of imidazolium ionic liquids decreases with increasing H2O2 concentration is probably indicative of a change in the degradation mechanism in a vigorous Fenton-like system. H-NMR spectra
showed, in the first stage of degradation, that radical attack is nonspecific, with any one of the carbon atoms in the ring
and the n-alkyl chain being susceptible to attack.
Recommendations and perspectives Since ionic liquids are now one of the most promising alternative chemicals of the future, the degradation and waste management
studies should be integrated into a general development research of these chemicals. In the case of imidazolium and pyridinium
ionic liquids that are known to be resistant to bio- or thermal degradation, studies in the field of AOPs should assist the
future structural design as well as tailor the technological process of these chemicals 相似文献
874.
The present study deals with the application of self-organizing maps (SOM) in order to model, classify and interpret seasonal and spatial variability of 210Po, 238U and 239+240Pu levels in the Vistula river basin. The data set represents concentration values for 3 alpha emitters (210Po, 238U and 239+240Pu) measured in surface water samples collected at 19 different sampling locations (8 in major Vistula stream while 11 in right or left Vistula tributaries) during four seasons (winter, spring, summer and autumn) in the framework of a one-year quality monitoring study. The advantages of an SOM algorithm, its classification and visualization ability for environmental data sets, are stressed. The neural-network based classification made it possible to reveal specific patterns related to both seasonal and spatial variability. In the middle and upper part of Vistula catchment as well as in the right-shore tributaries, concentrations of 210Po and 238U during summer and winter are the lowest. Concentrations of 210Po and 238U increase significantly during spring and autumn in the Vistula river catchment, especially in the delta of Vistula river. High concentration of anthropogenic originated 239+240Pu indicates “site-specific” character of pollution in two large left-shore tributaries located in the middle part of the Vistula drainage area. Efficient classification of sampling locations could lead to an optimization of river radiochemical sampling networks and to a better tracing of natural and anthropogenic changes along Vistula river stream. 相似文献
875.
David W. Ostendorf Baoshan Xing Niki Kallergis 《Journal of contaminant hydrology》2009,106(3-4):118-130
At a former wood preservation plant severely contaminated with coal tar oil, in situ bulk attenuation and biodegradation rate constants for several monoaromatic (BTEX) and polyaromatic hydrocarbons (PAH) were determined using (1) classical first order decay models, (2) Michaelis–Menten degradation kinetics (MM), and (3) stable carbon isotopes, for o-xylene and naphthalene. The first order bulk attenuation rate constant for o-xylene was calculated to be 0.0025 d− 1 and a novel stable isotope-based first order model, which also accounted for the respective redox conditions, resulted in a slightly smaller biodegradation rate constant of 0.0019 d− 1. Based on MM-kinetics, the o-xylene concentration decreased with a maximum rate of kmax = 0.1 µg/L/d. The bulk attenuation rate constant of naphthalene retrieved from the classical first order decay model was 0.0038 d− 1. The stable isotope-based biodegradation rate constant of 0.0027 d− 1 was smaller in the reduced zone, while residual naphthalene in the oxic part of the plume further downgradient was degraded at a higher rate of 0.0038 d− 1. With MM-kinetics a maximum degradation rate of kmax = 12 µg/L/d was determined. Although best fits were obtained by MM-kinetics, we consider the carbon stable isotope-based approach more appropriate as it is specific for biodegradation (not overall attenuation) and at the same time accounts for the dominant electron-accepting process. For o-xylene a field based isotope enrichment factor εfield of − 1.4 could be determined using the Rayleigh model, which closely matched values from laboratory studies of o-xylene degradation under sulfate-reducing conditions. 相似文献
876.
Jason A. Dittman James B. Shanley George R. Aiken Janet E. Towse 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1953-1956
Stream water samples were collected over a range of hydrologic and seasonal conditions at three forested watersheds in the northeastern USA. Samples were analyzed for dissolved total mercury (THgd), DOC concentration and DOC composition, and UV254 absorbance across the three sites over different seasons and flow conditions. Pooling data from all sites, we found a strong positive correlation of THgd to DOC (r2 = 0.87), but progressively stronger correlations of THgd with the hydrophobic acid fraction (HPOA) of DOC (r2 = 0.91) and with UV254 absorbance (r2 = 0.92). The strength of the UV254 absorbance-THgd relationship suggests that optical properties associated with dissolved organic matter may be excellent proxies for THgd concentration in these streams. Ease of sample collection and analysis, the potential application of in-situ optical sensors, and the possibility for intensive monitoring over the hydrograph make this an effective, inexpensive approach to estimate THgd flux in drainage waters. 相似文献
877.
Li Lu 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1794-1799
Reducing the transfer of contaminants from soils to plants is a promising approach to produce safe agricultural products grown on contaminated soils. In this study, 0-400 mg/kg cetyltrimethylammonium bromide (CTMAB) and dodecylpyridinium bromide (DDPB) were separately utilized to enhance the sorption of PAHs onto soils, thereby reducing the transfer of PAHs from soil to soil solution and subsequently to plants. Concentrations of phenanthrene and pyrene in vegetables grown in contaminated soils treated with the cationic surfactants were lower than those grown in the surfactant-free control. The maximum reductions of phenanthrene and pyrene were 66% and 51% for chrysanthemum (Chrysanthemum coronarium L.), 62% and 71% for cabbage (Brassica campestris L.), and 34% and 53% for lettuce (Lactuca sativa L.), respectively. Considering the impacts of cationic surfactants on plant growth and soil microbial activity, CTMAB was more appropriate to employ, and the most effective dose was 100-200 mg/kg. 相似文献
878.
通过恒温振荡平衡法研究了Pb~(2+)在针铁矿上的等温吸附和吸附动力学特征,探讨了吸附的影响因素.结果表明:(1)随Pb~(2+)平衡浓度和pH的增大,针铁矿对Pb~(2+)的吸附量逐渐增大.(2)针铁矿对Pb~(2+)的等温吸附可用Freundlich和Langmuir方程较好地拟合.(3)在相同温度和pH下,随离子强度的提高,针铁矿对Pb~(2+)的吸附量增大.(4)在相同离子强度和pH下,针铁矿对Pb~(2+)的吸附量总体随温度升高而增大.针铁矿对Pb~(2+)的吸附是自发进行的吸热反应.(5)针铁矿吸附Pb~(2+)的过程可分为初始的快吸附和随后的慢吸附2个阶段.pH影响吸附反应快慢,随pH增大吸附速率增大;随着pH的增大,达到平衡吸附的时间缩短.吸附动力学方程用Elovich方程拟合最佳. 相似文献
879.
生活垃圾加载介质层填埋法对初期渗滤液污染抑制效果研究 总被引:1,自引:0,他引:1
以传统卫生填埋柱R2为对照,通过往生物反应器填埋柱R1内加载可渗透反应介质层1和2进行模拟试验,主要探讨了填埋柱R1垃圾渗滤液COD、总氮、氨氮及总磷的变化趋势,探索一种新型的加载介质层垃圾填埋处理方法。试验结果表明,填埋20周后, R1柱COD浓度基本维持在40 000~45 000 mg/L间,约为R2柱的20%~30%;第24周,R1柱总氮和氨氮分别为206.5 mg/L和167.3 mg/L,在16~24周内,R1总氮和氨氮分别约为R2的14.5%~17.5%和36.2%~43.6%;18周时,R1柱总磷达最大值1.704 mg/L,至第24周降为0.673 mg/L, 整个实验过程R1柱总磷约为R2的0.15%~0.56%。 相似文献
880.