Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C1835664 (TOC)
 2,763 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Ozonation and O3/H2O2 oxidation of reactive dyestuffs and simulated textile dye-bath were investigated. Effects of reaction pH, initial dye concentration, H2O2 concentration and assisting chemicals on treatment efficiency were examined. We found considerable improvement in COD and colour removal rates at pH = 11, that was almost the actual pH of the prepared textile wastewater, whereas in particular increasing the initial dyestuff concentration had an adverse effect upon oxidation rates. Removal of colour, COD and TOC were found to be fairly sensitive to the introduction of soda that is frequently applied as an auxiliary chemical during the reactive dyeing process. The addition of H2O2 had negligible effect on COD removal efficiency and decolorization rate compared to ozonation alone at different pH values. Accordingly it can be inferred that the theoretically expected effect of OH radical scavengers (e.g. carbonate, chloride) present in the synthetic dye-bath as well as introduced radical formation promoters (e.g. H2O2, OH-) were probably hidden due to the complexity of the synthetic wastewater matrix. Biodegradability of the ozonated dye-bath was accelerated by a factor of three corresponding to a 233% relative enhancement. The inhibition of the oxygen uptake rate decreased from 91% to 75% within only 5 min treatment time.
 ...
PMID:Partial oxidation of reactive dyestuffs and synthetic textile dye-bath by the O3 and O3/H2O2 processes. 1138 Jan 83

The efficiencies of chemical oxidation of organic matter in genuine secondary-treated municipal wastewater by using O3, O3/UV, O3/TiO2, UV/TiO2 and O3/UV/TiO2 methods were compared experimentally. Effects of carbonates on these efficiencies were also investigated. Elimination of carbonates from the water increased TOC reduction efficiency of all the methods. The effect of the carbonates on the O3 method was less significant than that on the other methods. The O3/UV method was the most effective for reducing TOC under both carbonate-present and decarbonated conditions. The catalytic ozone process (O3/TiO2) showed a tendency to increase the ozonation efficiency at the beginning of the reaction under the decarbonated condition, but the addition of the TiO2 catalyst inhibited the ozonation under the carbonate-present condition. The photocatalytic oxidation process (UV/TiO2) did not reduce TOC as much as the other methods, but it could reduce TOC over a long time. And the O3/UV/TiO2 method did not show a synergistic effect of ozonation and photocatalytic oxidation. Furthermore, zonation prior to coagulation increased TOC reduction efficiency of coagulation, but this effect was also affected by the carbonates in water.
 ...
PMID:Chemical oxidation of organic matter in secondary-treated municipal wastewater by using methods involving ozone, ultraviolet radiation and TiO2 catalyst. 1143 94

Carbon-isotopic compositions of total carbonate, inoceramid carbonate, micritic carbonate, secondary cements, total organic carbon, and geoporphyrins have been measured in 76 different beds within a 17-m interval of a core through the Greenhorn Formation, an interbedded limestone and calcareous shale unit of Cretaceous age (Cenomanian-Turonian) from the Western Interior Seaway of North America. Results are considered in terms of variations in the processes of primary production (which led to the biosynthesis of the molecular precursors of the geoporphyrins) and in secondary processes (those mediating the transformation of primary organic material into sedimentary total organic carbon). It is shown that the porphyrin isotopic record reflects primary isotopic variations more closely than the TOC isotopic record, and that, in these sediments, TOC is enriched in 13C relative to its primary precursor by 0.6 to 2.8%. This enrichment is attributed to isotope effects within the consumer foodweb and is associated with respiratory heterotrophy. Variations in this secondary enrichment are correlated with variations in the isotopic composition of marine carbonate. This correlation is attributed to effects of environmental changes on the marine foodweb. These may have included increased atmospheric oxygen associated with the Cenomanian-Turonian oceanic anoxic event. The isotopic fractionation associated with fixation of carbon by primary producers is observed to have varied by 1.5% during the interval of deposition. It is suggested that this change is due to a variation in the makeup of the community of primary producers and/or to a decrease in the atmospheric abundance of CO2 during the oceanic anoxic event.
 ...
PMID:An isotopic study of biogeochemical relationships between carbonates and organic carbon in the Greenhorn Formation. 1153 81

The trace metal contents of 71 core samples collected in 1992 from the bottom sediments of the Arabian Gulf are used to determine the regional distribution of concentration and pollution levels of these substances in the region. Chronic contamination was recorded in seven locations: the northwestern area (Fe), the northeastern area (Fe, V and Ni), the north-central area (V and Ni), the central area (Fe, Pb, V and Ni), the south-central area (Cu), the eastern area (Cu) and the southeastern area (Fe, V and Ni). Present-day contamination was identified in three locations only: the north-central area (V), the central area (Pb, V and Ni) and the southeastern area (Fe, V and Ni). Diversified natural and anthropogenic inputs may have provided the sources of this contamination. The V/Ni ratios of recent marine sediments cannot be used in identifying oil spillages or in oil-sediment correlation studies. Positive correlations are found between increasing trace metal concentration and decreasing carbonate content and grain size, verifying that adsorption onto muds is the primary mechanism of trace metal concentration in marine sediments. Correlations with TOC (total organic carbon) contents indicate that organic matter is a significant concentrator only in the case of Pb and Cu. With the exception of the Fe contamination in the northwest area due to river transport, all chronic and present-day trace metal concentrations are within the permissible natural background levels in the western offshore areas, including the two areas thought to be polluted by the Kuwait oil slick, thereby supporting the idea that airborne fallout from oil fires was deposited in a limited coastal area between Kuwait and Bahrain, and verifying that the oil slick had minimal effect on the state of pollution by trace metals in the Arabian Gulf.
 ...
PMID:Bottom sediments of the Arabian Gulf--III. Trace metal contents as indicators of pollution and implications for the effect and fate of the Kuwait oil slick. 1509 27

Acid neutralizing capacity (ANC) is the parameter most commonly used as chemical indicator for fish response to acidification. Empirical relationships between fish status of surface waters and ANC have been documented earlier. ANC is commonly calculated as the difference between base cations ([BC]=[Ca2+]+[Mg2+]+[N+]+[K+]) and strong acid anions ([SAA]=[SO4(2)-]+[NO3-]+[Cl-]). This is a very robust calculation of ANC, because none of the parameters incorporated are affected by the partial pressure of CO2, in contrast to the remaining major ions in waters, pH ([H+]), aluminum ([Aln+]), alkalinity ([HCO3-/CO3(2)-]) and organic anions ([An-]). Here we propose a modified ANC calculation where the permanent anionic charge of the organic acids is assumed as a part of the strong acid anions. In many humic lakes, the weak organic acids are the predominant pH-buffering system. Because a significant amount of the weak organic acids have pK-values<3.0-3.5, these relatively strong acids will permanently be deprotonated in almost all natural waters (i.e. pH>4.5). This means that they will be permanently present as anions, equal to the strong acid inorganic anions, SO4(2)-, NO3- and Cl-. In the literature, natural organic acids are often described as triprotic acids with a low pK1 value. Assuming a triprotic model, we suggest to add 1/3 of the organic acid charge density to the strong acid anions in the ANC calculation. The suggested organic acid adjusted ANC (ANC(OAA)), is then calculated as follows: ANC(OAA)=[BC]-([SAA]+1/3CD*TOC) where TOC is total organic carbon (mg C L(-1)), and CD=10.2 is charge density of the organic matter (microeq/mg C), based on literature data from Swedish lakes. ANC(OAA) gives significant lower values of ANC in order to achieve equal fish status compared with the traditional ANC calculation. Using ANC(OAA) the humic conditions in lakes are better taken into account. This may also help explain observations of higher ANC needed to have reproducing fish populations in lakes with higher TOC concentrations.
 ...
PMID:The influence of total organic carbon (TOC) on the relationship between acid neutralizing capacity (ANC) and fish status in Norwegian lakes. 1514 66

We quantified the concentrations and distributions of metals (Cd, Cr, Cu, Ni, Pb, and Zn) in the sediments of Tuen Mun River, Hong Kong. The potential bioavailability of metals was assessed with a biomimetic extraction method using the sipunculan gut juices. The sediments were characterized by relatively high concentrations of trace metals. Field collected sediments were highly anoxic and the ratio of simultaneously extractable metal (sigmaSEM) to acid volatile sulfide (AVS) was much less than one in these sediments. The majority (>67%) of Cd, Pb, and Zn were bound to AVS, thus their concentrations in the sediment porewater were low. In contrast, Ni was little bound to AVS due to its lower ratios of SEM-Ni to total Ni concentrations. For Cu, relatively high concentrations in the sediment porewater was found, and total organic carbon, AVS and other resistant sulfide phase were the controlling factors for sedimentary Cu partitioning. Net metal adsorption from gut juices to anoxic sediments was observed in metal extraction experiments, suggesting that AVS determined the bioaccumulation and potential bioavailability of most metals in these sediments. Extraction of metals from the oxidized sediments by the gut juices was mainly attributed to metal redistribution from AVS to other geochemical phases. The gut juices were the most effective solvent or extractant than the simple electrolyte solution [I (NaNO(3)) = 0.01 M] and the natural overlying water. Cd was more easily extracted from the oxidized sediments than Zn that tended to have a stronger binding affinity with Fe-Mn oxide, clay and organic matter. The application of partial removal techniques in metal extraction experiments further demonstrated the differential controls of various sediment geochemical phases in affecting metal bioavailability, with the order of TOC > Fe-Mn oxides > carbonate.
 ...
PMID:Metal partitioning in river sediments measured by sequential extraction and biomimetic approaches. 1548 75

Batchwise heterogeneous photocatalytic oxidation of model wastewater (solutions of the azo dye "Acid Orange 7" in tap water) has been performed in a laboratory-scale stirred vessel reactor with non-submerged UV-A lamps using titanium dioxide "P25" as photocatalyst. Comparison to results of solar pilot-scale Plexiglass double-skin sheet reactor (DSSR) experiments indicates that the lab-scale method may predict area demand for technical-scale DSSR design. Characteristic UV-A fluences leading to TOC or COD reduction to e(-1) of the initial concentrations were determined in lab-scale stirred vessel experiments for treated effluents of seven different industrial branches, secondary municipal effluent and biologically treated greywater. Predicted areas for solar photocatalytic oxidation of these effluents in DSSRs yielding mineralization of 95% of organics in 100 m3 of the respective effluents for a TiO2 concentration of 2 g l(-1) and a sky and solar radiation of 3.9kWh m(-2) d(-1) within one day greatly varied from below 6,000 m2 (biologically treated lubricating oil refinery effluent) to more than 100,000 m2 (highly saline biologically treated effluent of chemical industry). Especially municipal and refinery effluents (except oil reclaiming) have been identified as promising candidates for reuse after solar photocatalytic oxidation. Mineralization efficiency was decreasing with increasing alkalinity of effluents. This was interpreted by competition of hydrogen carbonate anions with organics for binding sites on photocatalyst surface and by OH radical scavenging by hydrogen carbonate. Dependence on alkalinity was superimposed by salinity influence as some effluents with high alkalinity also exhibited high salt concentrations (especially chloride).
 ...
PMID:Solar photocatalytic oxidation of pretreated wastewaters: laboratory scale generation of design data for technical-scale double-skin sheet reactors. 1597 68

This research investigates the effect of adding oxidants such as Fe0, Fe2+ and S2O8(2-) in the sonication of 1,4-dioxane (1,4-D). The results indicate that the degradation pattern of 1,4-D kinetically could be divided into three steps (initiation, acceleration, and stabilization), with the first two steps predominating. The initiation step agreed with zero order rate model, while the acceleration step was the pseudo-first order. In the presence of HCO3- as a radical scavenger, the degradations of 1,4-D and TOC were suppressed, indicating that OH radical is an important factor in the sonolysis, especially at the acceleration step. The overall degradation efficiency of 79.0% in the sonolysis of 1,4-D was achieved within 200 min. While Fe0, Fe2+ and S2O8(2-) were individually combined with sonication, the total degradation efficiency of 1,4-D increased 18.6%, 19.1% and 16.5% after 200 min, respectively. The addition of oxidants not only increased the rate constant in the acceleration step, but also changed the kinetic model from zero to pseudo-first order at the initiation step. The addition of oxidants such as Fe2+, Fe0 and S2O8(2-) in the sonication of 1,4-D also improved the mineralization of 1,4-D. However, the degradation efficiencies of 1,4-D and TOC were not statistically different (p = 0.709, ANOVA) with different oxidants such as Fe2+, Fe0 and S2O8(2-).
 ...
PMID:Removal of 1,4-dioxane from water using sonication: effect of adding oxidants on the degradation kinetics. 1642 16

Acid mine drainage (AMD), which contains high concentrations of sulphate and dissolved metals, is a serious environmental problem. It can be treated in situ by sulphate reducing bacteria (SRB), but effectiveness of the treatment process depends on the organic substrate chosen to supply the bacteria's carbon source. Six natural organic materials were characterized in order to investigate how well these promote sulphate reduction and metal precipitation by SRB. Maple wood chips, sphagnum peat moss, leaf compost, conifer compost, poultry manure and conifer sawdust were investigated in terms of their carbon (TOC, TIC, DOC) and nitrogen (TKN) content, as well as their easily available substances content (EAS). Single substrates, ethanol, a mixture of leaf compost (30% w/w), poultry manure (18% w/w), and maple wood chips (2% w/w), and the same mixture spiked with formaldehyde were then tested in a 70-day batch experiment to evaluate their performance in sulphate reduction and metal removal from synthetic AMD. Metal removal efficiency in batch reactors was as high as 100% for Fe, 99% for Mn, 99% for Cd, 99% for Ni, and 94% for Zn depending on reactive mixtures. Early metal removal (0-12d) was attributed to the precipitation of (oxy)hydroxides and carbonate minerals. The lowest metal and sulphate removal efficiency was found in the reactor containing poultry manure as the single carbon source despite its high DOC and EAS content. The mixture of organic materials was most effective in promoting sulphate reduction, followed by ethanol and maple wood chips, and single natural organic substrates generally showed low reactivity. Formaldehyde (0.015% (w/v)) provided only temporary bacterial inhibition. Although characterization of substrates on an individual basis provided insight on their chemical make-up, it did not give a clear indication of their ability to promote sulphate reduction and metal removal.
 ...
PMID:Characterization and reactivity assessment of organic substrates for sulphate-reducing bacteria in acid mine drainage treatment. 1648 66

A greenhouse experiment was performed to investigate the influence of pH TOC, and fractionation of Pb on phytoavailability of Pb in the rhizosphere of lettuce. And the Low molecular-weight organic acids (LMWOAs) were used to evaluate the phytoavailability of soil Pb to lettuce. The results show that the pH is lower in the rhizosphere compared to the bulk soil, and the rhizosphere becomes more acidic with increasing Pb (NO3)2 applied. In contrast, the TOC content is higher in the rhizospherer compared to the bulk soil, and more TOC accumulates in the rhizosphere with increasing Pb (NO3)2 applied. The concentrations of different fractions in rhizosphere soils follow the order of exchangeable > carbonate bound > Fe-Mn oxide bound > organic bound > residual, and for bulk soil the order is carbonate bound > Fe-Mn oxide bound > exchangeable > organic bound > residual. Compared with bulk soils, exchangeable Pb increases significantly in rhizosphere. With increasing Pb (NO3)2 applied, the transformation of residual Pb to carbonate bound and exchangeable Pb may have happened and results in the accumulation of carbonate bound and exchangeable Pb. The air-drying increases the concentration of exchangeable, carbonate bound and Fe-Mn oxide bound Pb and decreases organic bound and residual Pb. Rhizosphere and bulk soils were extracted by low molecular-weight organic acids(LMWOAs) to fractionate Pb fraction of soil pools, which is considered as the phytoavailable Pb. The results show that phytoavailable Pb in rhizosphere is much higher compared to bulk soil, and phytoavailable Pb increases with increasing Pb (NO3)2 applied due to acidification processes and accumulated TOC in the rhizosphere. Air-drying process also increases the phytoavailable Pb. The root-induced changes of Pb availability in the rhizosphere might also be related to the Pb species, especially carbonate bound and exchangeable Pb. Correlation analysis indicates that application of wet fresh rhizosphere soils and LMWOAs should be recommended in the future study on the phytoavailability of soil Pb to lettuce.
 ...
PMID:[Phytoavailable lead in rhizosphere of lettuce]. 1711 30


1 2 3 4 Next >>