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1.
In laboratory experiments the adsorption of eleven different organic substances in water is individually tested in the range of concentration of 0.2… 5.0 mg/l on EP 60 and EP 61 (styrene-divinylbenzene, non-polar) and EP 62 and Y 59 (acrylic-acid-ester-divinylbenzene, polar). In batch experiments the elimination at 1… 2 g/l adsorber quantity was 35… 80%, strongly dissociated anionic substances as benzoic acid being adsorbed only to a low degree and weakly cationic and undissociated substances being adsorbed well. Within a homologous series adsorption increases with the molar mass until the pore diameter will become too small for the taking up of substances. Under dynamic conditions (filtration technology) an elimination of 90… 100% can be expected. As a whole, the adsorption on activated carbon was better in all cases than the adsorption on the polymers. The desorption for the regeneration of the polymers is the more difficult the better the substance contained is adsorbed. By repeated loading and regeneration only a slight influence on the adsorption and desorption of a substance was found. 相似文献
2.
The water supply of Prague is based upon three different water resources: artesian groundwater and infiltrate of the Jizera river, water of the Vltava and Zelivka rivers. The processing techniques are different; consequently for the purpose of increasing capacity one has to search for the suitable raw water quality as well as for the optimum treatment process. An essential parameter for this is the contents of organic substances whose molar mass distribution is investigated by gel chromatography with the aid of Sephadex G-10, G-25 and G-50. With respect to the total load of organic matter the Jizera shows the lowest values, in the Vltava the C.O.D. values are the highest, in the Zelivka the organic carbon shows the highest values. 80% of the organic substances in water have molar masses below 700. By flocculation 60… 70% of the C.O.D.-Cr can be eliminated, the optimum removal of the high-molecular substances occurring at pH = 6 and with 50… 60 g/m3 aluminium sulphate. 相似文献
3.
Results of studying Fe(III) hydrolysis and sorption of heavy metal compounds by organic matter of bottom sediments are discussed. The rate of Fe(III) hydrolysis is found to be largely determined by the concentration of dissolved organic substances. Values of kinetic parameters are obtained for heavy metal compounds sorption under static and dynamic conditions. Calculating the solubility of Fe, Cu, Cd, Zn, and Pb sulfides allowed the assessment of the amount of metals lost by bottom sediments due to the formation of metal complexes with dissolved organic substances contained in natural waters. 相似文献
4.
In batch experiments with the metals labelled with their radionuclides the cumulation of zinc, cadmium and mercury on Scenedesmus obliquus in dependence on the pH-value is measured, because the original pH-value of the solution is changed by the algae due to their absorption of hydrogen-ions. For the uptake of zinc and cadmium the logarithm of the cumulation factor in the range of 2 … 5 is a linear function of the pH-value in the range of 5 … 9, cumulation increasing with rising pH-value. In contrast, the mercury cumulation is pH-independent. If the changed pH-value is taken into account, the cumulation factors are independent of the metal concentration in the range = 10?4 mol/l. The degree of cumulation is not changed by the presence of other metals. The cumulation factor is reduced by substances forming negatively charged complexes with the metals. 相似文献
5.
Dewatering Behaviour of Sludge in the Presence of Polyelectrolytes Interactions of sludge particles with well defined synthetic polyelectrolytes of different charge, molecular mass, and molecular geometry were investigated by means of zeta- and streaming potential measurements and polyelectrolyte titrations. Different mechanisms of flocculation were discussed with regard to the dewatering behaviour of the sludge. In dependence on the flocculation procedure (cationic monoflocculation, anionic-cationic, and cationicanionic dual flocculation) as well as on the chain length and branching of the polyelectrolytes used, different mechanisms of sludge dewatering were discussed: Polyanions are not adsorbed on the sludge particles and lead to a decline of the dewatering results. Linear short chain polycations result in a flocculation after surface charge neutralization of the particles according to a patch mechanism. Long chain linear polycations cause a bridging of the particles leading to a flocculation without charge neutralization of the aggregates formed. With branched polycations, a flocculation according to a patch mechanism is observed. These polycations form sludge particle aggregates which are surface charge neutralized at the flocculation point. In anionic-cationic dual flocculations using long chain polycations, an inclusion flocculation due to polyanion-polycation complex formation is the predominating mechanism. The cationic-anionic dual flocculation with complete covering of the particles with polycations in the first step can be discussed by a patch mechanism quite similar to an anionic monoflocculation of cationic particles. By knowing the mechanism of interaction for a given flocculation agent, an optimal sludge dewatering procedure can be predicted. 相似文献
6.
《Continental Shelf Research》1995,15(7):843-869
The temporal variations of the superficial (0–1 cm) sedimentary organic matter were studied at a depth of 26 m on the continental shelf of the Gulf of Lions (northwestern Mediterranean). The samples were analyzed for total organic carbon, coarse organic carbon (>40 μm), hydrolyzable organic carbon, nitrogen, total amino acids, total and individual sugars (HPLC), lignin-derived compounds (HPLC) and kerogens (acid-soluble, humic substances and humin). Seasonal variations of the organic compounds are related to the sedimentological, hydrodynamical and physico-chemical environmental conditions.The mean annual values of the different organic compounds analyzed show the low quantities and their evolved character at the sediment-water interface: 0.5% total org C (TOC) (d.w.), 0.049% N (d.w.), : 11.2, coarse org C (COQ: 62% of TOC, hydrolyzable org C: 45% TOC. The labile compounds represent a low percentage of the total organic matter (TOM), amino-acids: 12% of TOM and sugars: 5% of TOM. The relative proportions of soluble (humic) and insoluble kerogens (humin), respectively 6% and 94% of TOC are typical of a highly evolved organic matter. The large contribution of plant remains confirmed by the high proportion of COC, corresponds to a low proportion of humic substances and a high degree of condensation (). The infrared spectroscopy determination of the functional groups of the humic substances permits us to confirm both autochtonous (marine) and allochtonous (terrestrial) sources of organic matter in the Têt prodeltaïc accumulation area. Numerous functional groups identified reveal the fresh quality of the organic inputs at the sediment-water interface. Aliphaticity is well marked and nitrogenous compounds (1 and 2 amines) correspond to autochtonous production (in spring: phyto- and zoo-planktonic blooms in the euphotic zone; in summer: primary production under the thermocline and phytobenthic blooms). Sugars are well represented, but from two origins: phytoplanktonic, and issue from terrestrial high plants (ligno-cellulosic complexes). The aromatic functional groups are well identified (aromatic ether, phenol) as are the markers of a large contribution of terrestrial organic matter.The active hydrodynamical (resuspension) and biological, (consumption, bioturbation) events participate in the frequent reworking of the superficial deposits (muddy-silts) and, consequently, the active degradation (oxidization) of the organic matter. The more labile organic matter is rapidly consumed by the intense biological benthic activity. The organic C content is low (0.5% d.w.) except during the autumnal input (2.5% d.w.). This input (8 cm thick) disappears one month later, because of the resuspension induced by littoral currents. This same phenomenon induces during all the year the reworking of the first centimeter of the deposit. In terms of budget of the carbon cycle in the coastal area, this active hydrodynamical environment shows the supremacy of the carbon degradation over its burial. 相似文献
7.
A novel and efficient protocol optimising deep‐bed filtration of surface water was developed. The innovation lies in ballasted‐flocculation filtration and an intermediate downwash. The approach is based on the assumption that kaolin particles with a partial positive charge may adsorb onto the surface of C. parvum oocysts and neutralize their negative charge. Application of this technology enhanced removal of inorganic particles and Cryptosporidium parvum oocysts by approximately 30 % and shortened the ripening stage of the filtration process from 1 h to about 10 min. 相似文献
8.
J. Vymazal 《洁净——土壤、空气、水》1989,17(3):309-313
The heavy metal content of river water samples with 12 and 15 mg/l dry matter of seston is increased to 400 … 3900μg/l by the addition of inorganic heavy metal salts, and after three days the distribution of the heavy metals is determined by fractional filtration (8, 3, 1.2, 0.8, 0.65, 0.45 and 0.22 μm pore size). More than 80% of Ni, Co and Mn are found in the fraction <0.22 μm, 60% of Pb and Cu in >8 μm as well as 40 and 25%, resp., in <0.22 μm, Cd, Cr and Zn are found in all fractions, 60 … 80% being in the fraction <0.22 μm, 90% of Fe occurring in the fraction >8 μm. The influence of specific parameters of water quality as pH-value and seston concentration on the distribution requires further investigations. 相似文献
9.
Nicole Kowalski Olaf Dellwig Melanie Beck Maik Grunwald Sibylle Fischer Maike Piepho Thomas Riedel Holger Freund Hans-Jürgen Brumsack Michael E. Böttcher 《Ocean Dynamics》2009,59(2):333-350
Tidal and seasonal behaviour of the redox-sensitive trace metals Mn, Fe, Mo, U, and V have been investigated in the open-water
column and shallow pore waters of the backbarrier tidal flats of the island of Spiekeroog (Southern North Sea) in 2002 and
2007. The purpose was to study the response of trace metal cycles on algae blooms, which are assumed to cause significant
changes in the redox state of the entire ecosystem. Trace metal data were complemented by measurements of nutrients and enumeration
of algae cells in 2007. Generally, Mn and V show a tidal cyclicity in the water column with maximum values during low tide
which is most pronounced in summer due to elevated microbial activity in the sediments. Mo and U behave almost conservatively
throughout the year with slightly increasing levels towards high tide. Exceptions are observed for both metals after summer
algae blooms. Thus, the seasonal behaviour of the trace metals appear to be significantly influenced by productivity in the
water column as the occurrence of algae blooms is associated with an intense release of organic matter (e.g. transparent exopolymer
particles, TEP) thereby forming larger organic-rich aggregates. Along with elevated temperatures in summer, the deposition
of such aggregates favours microbial activity within the surface sediments and release of DOC, nutrients and trace metals
(Mn, Mo and V) during the degradation of the aggregates. Additionally, pronounced reducing conditions lead to the reduction
of Mn(IV)-oxides and Fe(III)-(oxihydr)oxides, thereby releasing formerly scavenged compounds as V and phosphate. Therefore,
pore-water profiles show significant enrichments in trace metals especially from July to September. Finally, the trace metals
are released to the open water column via draining pore waters (esp. Mo, Mn, and V) and/or fixed in the sediment as sulphides
(Fe, Mo) and bound to organic matter (U). Non-conservative behaviour of Mo in oxygenated seawater, first observed in the investigation
area by Dellwig et al. (Geochim Cosmochim Acta 71:2745–2761, 2007a), was shown to be a recurrent phenomenon which is closely coupled to bacterial activity after the breakdown of algae blooms.
In addition to the postulated fixation of Mo in oxygen-depleted micro-zones of the aggregates or by freshly formed organic
matter, a direct removal of Mo from the water column by reduced sediment surfaces may also play an important role. 相似文献
10.
In this paper, size‐exclusion chromatography (SEC) was used to determine the metal concentration in different size fractions of a bog lake water. Two methods were applied: (a) preparative SEC with off‐line metal concentration analysis and (b) direct coupling of an analytical SEC system on‐line with an inductively‐coupled plasma mass spectrometer (ICP‐MS). In the preparative SEC measurements, maximum concentrations were found for different metal ions in different size fractions of the natural organic matter (NOM). Normalization of metal concentrations to dissolved organic carbon concentration (DOC) yielded two maxima in the high and in the very low molecular‐weight fractions. Whereas good recoveries were found for Al, Fe, and Ni, only 40% were obtained for Pb. This indicates that Pb formed labile complexes with NOM, and hence could strongly interact with the column material. In the experiments with the analytical SEC‐ICP‐MS system, the same trends were observed, but with even lower recoveries than in the preparative system. Sample preconcentration and storage were also investigated with respect to decrease in metal concentration. During the ultrafiltration preconcentration step Al and Fe were removed only to a small extent, whereas about half of the initial Pb was lost. This indicates that Al and Fe were mainly bound to high molecular‐weight fractions of NOM. In contrast to that, Al and in particular Fe were removed from solution more than proportionally with respect to DOC because of aggregation of the NOM during storage, whereas Pb and Ni were concentrated relative to the DOC. 相似文献
11.
The effectiveness of coagulation (at pH values of 6, 7.5, and 9), flocculation (at pH 9), and coagulation plus flocculation (at pH 9) on turbidity removal from natural stone (travertine) processing wastewaters (NSPW) were examined by applying classical sedimentation tests. FeCl3·6 H2O, AlCl3, and Al2(SO4)3·16 H2O were used as coagulants and a polyacrylamide based anionic polymer was used as the flocculant. In this way, it was found that the coagulation method alone was not sufficient to purify NSPW, whereas flocculation and coagulation plus flocculation methods provided superior purification. Among the coagulants used, AlCl3 gave the best result in terms of turbidity removal by coagulation from NSPW at pH 6 and 9, whereas the turbidity removal performances of the three coagulants were almost identical at pH 7.5. In addition, relatively low pH (i. e., pH 6) improved the purification performance of all coagulants. During coagulation of NSPW at pH 6, a charge neutralization mechanism played a decisive role in turbidity removal. However, in neutral (pH 7.5) and slightly basic (pH 9) media, a sweep coagulation mechanism was predominant. For flocculation of NSPW, the basic mechanism comprised of polymer bridging. 相似文献
12.
The role of the benthic ciliofauna of the Tsibulnik bay of the Kremenchug reservoir in the comsumption of the primary production of phytomicrobenthos and the destruction of organic Substances is shown. In July all over the buy ciliates had consumed 41 % of the benthic primary production. During the process, consumption rates had reached 1.34 kJ/m2 d on seperate sections of the bottom. Sufficiently high is the role of these protists in the destruction of organic substances. They had destroyed 1.4… 1.5% of the whole mineralised organic substances in summer and 10… 11% in autumn. The authors made a conclusion on the importance of the benthic ciliofauna in the transformation of organic substances in an eutrophic bay. 相似文献
13.
Metals in the sea may form complexes with organic compounds, a process known as chelation, and this may modify their properties very greatly. Here the effect of chelation on the toxicity of copper to algae has been studied in the laboratory using the powerful chelating agent EDTA. Similar phenomena in the sea have implications both for anti-fouling paints, which usually contain copper, and for metal pollution in waters with a high organic content. 相似文献
14.
15.
D. R. Lovley J. L. Fraga E. L. Blunt-Harris L. A. Hayes E. J. P. Phillips J. D. Coates 《洁净——土壤、空气、水》1998,26(3):152-157
The potential for humic substances to serve as a terminal electron acceptor in microbial respiration and to function as an electron shuttle between Fe(III)-reducing microorganisms and insoluble Fe(III) oxides was investigated. The Fe(III)-reducing microorganism Geobacter metallireducens conserved energy to support growth from electron transport to humics as evidenced by continued oxidation of acetate to carbon dioxide after as many as nine transfers in a medium with acetate as the electron donor and soil humic acids as the electron acceptor. Growth of G. metallireducens with poorly crystalline Fe(III) oxide as the electron acceptor was greatly stimulated by the addition of as little as 100 μM of the humics analog, anthraquinone-2,6-disulfonate. Other quinones investigated, including lawsone, menadione, and anthraquinone-2-sulfonate, also stimulated Fe(III) oxide reduction. A wide phylogenetic diversity of microorganisms capable of Fe(III) reduction were also able to transfer electrons to humics. Microorganisms which can not reduce Fe(III) could not reduce humics. Humics stimulated the reduction of structural Fe(III) in clay and the crystalline Fe(III) forms, goethite and hematite. These results demonstrate that electron shuttling between Fe(III)-reducing microorganisms and Fe(III) via humics not only accelerates the microbial reduction of poorly crystalline Fe(III) oxide, but also can facilitate the reduction of Fe(III) forms that are not typically reduced by microorganisms in the absence of humics. Addition of humic substances to enhance electron shuttling between Fe(III)-reducing microorganisms and Fe(III) oxides may be a useful strategy to stimulate the remediation of soils and sediments contaminated with organic or metal pollutants. 相似文献
16.
G. Proft 《洁净——土壤、空气、水》1983,11(6):631-636
The method after Strickland and Parsons is modified for fresh water as follows: filtration on glass-fibre paper, oxidation with K2Cr2O7 in cone. H2SO4 for 2 h at 130 °C, dilution to 2.5 times the volume by aqua dest., centrifuging-off of the turbidity and extinction measurement at 445 nm against the blank value, the sample solution being balanced to the transmission of 100% (extinction = 0). Here, the following calibration line holds for the concentration C and the quantity of oxidation solution Ox: C = E1cmc · 0.162 · Ox, C in mg filter. The oxidation solution contains 4.8 g K2Cr2O7 as dissolved in 20 ml aqua dest. and made up with conc. H2SO4 to 11. With 5 ml of this solution one is able to determine 0.05 … 1 mg C/filter. Calibration is performed with 125 mg/l glucose solution. Comparative investigations have shown a good agreement with elementary-analytically obtained measured values. The occurring errors have been determined mainly by sampling. In the range of very small values we have to take into account a blank value of the filter due to the adsorption of dissolved organic substances on the filter. 相似文献
17.
Organism relics or kerogens in oils are first obsenred by a confocal laser scanning microscope (CLSM) and a transmission electron
microscope (TEM). The complexes of kerogens in oils are characterized by the presence of a great variety of microfossils or
macerals. These kerogens in oils are mainly the residues of the original organic substances from which oil formed, and minor
kerogens from enclosing rocks enter the oils, therefore, the components and types of the kerogens in crude oils can serve
as an indirect indicator of oil-source rock correlation. This method was applied to Jurassic oils in the Junggar Basin and
the Turpan-Hami Basin, and there are two types of the kerogens in oils: one containing a lot of macerals from terrestrial
plants may derive from coals, and the other, characterized by a high content of microscopic algae, fungus spores and Acritarch,
may originate from Permian organic matter. In addition, the reflectance of the vitrodetrinites in oils can be used as an indicator
of oil-source rock correlation. 相似文献
18.
Arsenic in glacial aquifers: sources and geochemical controls 总被引：1，自引：0，他引：1
A total of 176 wells in sand-and-gravel glacial aquifers in central Illinois were sampled for arsenic (As) and other chemical parameters. The results were combined with archived and published data from several hundred well samples to determine potential sources of As and the potential geochemical controls on its solubility and mobility. There was considerable spatial variability in the As concentrations. High concentrations were confined to areas smaller than 1 km in diameter. Arsenic and well depth were uncorrelated. Arsenic solubility appeared to be controlled by oxidation-reduction (redox) conditions, especially the presence of organic matter. Geochemical conditions in the aquifers are typically reducing, but only in the most reducing water does As accumulate in solution. In wells in which total organic carbon (TOC) was below 2 mg/L and sulfate (SO4(2-)) was present, As concentrations were low or below the detection limit (0.5 microg/L). Arsenic concentrations >10 microg/L were almost always found in wells where TOC was >2 mg/L and SO4(2-) was absent or at low concentrations, indicating post-SO4 (2-)reducing conditions. Iron (Fe) is common in the aquifer sediments, and Fe oxide reduction appears to be occurring throughout the aquifers. Arsenic is likely released from the solid phase as Fe oxide is reduced. 相似文献
19.
Yurkovskis A 《Marine pollution bulletin》2004,49(3):249-263
Suspended particulate matter (SPM) was collected in the freshwater-seawater mixing zone in the lower reaches of the Daugava River (Latvia) and adjacent marine area, during five cruises in 1998-2001. The study focused on biogeochemical phase exchange processes. SPM in the freshwater was found to be mainly allochthonous with a high content of organic matter, Mn and sorbed phosphate. Property-salinity plots suggested flocculation of humic-Fe complexes across the salinity gradient. The variability of sorbed phosphate was related to particulate Fe, although no dependence on pH and ionic strength was observed. The Mn contents of SPM mainly follow conservative mixing, but there are also indications of interface exchange of Mn in the mixing zone. The geochemical behaviour of particulate Al appears to differ from that of Fe. In early spring, trace element contents in SPM (Cr, Ni, Cu, Zn, Cd, Pb) correlate tightly with particulate organic matter, whose distribution is linked to phytoplankton distributions. 相似文献
20.
Degradations of reactive brilliant red X‐3B solution by both conventional UV irradiation and microwave electrodeless UV irradiation were investigated. Degradation processes were studied by UV–VIS spectrophotometry, total organic carbon (TOC), high performance capillary electrophoresis (HPCE), conductivity, pH value, and ion chromatography. The results of color removal (%) and TOC removal (%) showed that the degradation by microwave electrodeless UV irradiation was more effective than by conventional UV irradiation. The results of UV–VIS absorption spectra and HPCE analyses indicated that the degradation of reactive brilliant red X‐3B was occurred at the conjugation system first, the benzene ring and the naphthalene ring later. The reactive brilliant red X‐3B was cleaved into some new small compounds and eventually most of the organic substances were mineralized to CO2 and H2O. The results of the conductivity analysis suggested that the degradation has mainly occurred in the first 40 min of reaction. The pH value of reactive brilliant red X‐3B solution was decreased first and then was increased. The results of inorganic anions analysis hinted that many of the N, Cl, and S elements from reactive brilliant red X‐3B were still attached in organic molecules. 相似文献