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PubMed2004

Effects of the humic substances of de-inking paper sludge on the antagonism between two compost bacteria and Pythium ultimum.

We investigated the in vitro influence of humic substances (HS) extracted from de-inking paper sludge compost on the inhibition of Pythium ultimum by two compost bacteria, Rhizobium radiobacter (Agrobacterium radiobacter) and Pseudomonas aeruginosa. When low concentrations (5 or 50 mg l(-1)) of HS were added to the culture medium, fungal inhibition by R. radiobacter significantly increased (P<0.01) by 2-3%. In contrast, these low levels of HS had no effect on P. ultimum inhibition by P. aeruginosa. The Fe, chelated by HS, was in part responsible for the decrease of P. ultimum inhibition by the bacteria when increasing amounts of HS were added in the culture medium. The addition of 500 mg l(-1) of humic acids isolated from de-inking paper sludge compost or from fossil origin completely eliminated the inhibition of P. ultimum by R. radiobacter. This Fe effect also stimulated growth of R. radiobacter and reduced its siderophore production in a minimal medium supplemented with HS as sole source of Fe. The results showed that HS influence microbial antagonism when added to a culture medium. However, this effect varies with different factors such as the type of bacteria, concentration of HS, molecular weight and Fe content.

Bacteria↗

PubMed2001

Sorption of pyrene to dissolved humic substances and related model polymers. 1. Structure--property correlation.

Solid-phase microextraction (SPME) was employed to determine sorption coefficients for pyrene on dissolved humic substances (DHS) of various origins and also on model polymers to gain a better understanding of the relationships between sorption potential and sorbent structures. The sorption potential of DHS from very different sources is described by an empirical two-parameter correlation involving the polarity (O/H atomic ratio) and the aromaticity (epsilon 280 nm) as descriptors. On the other hand, sorption experiments with well-defined model polymers, poly(acrylic acid) esters, led to the conclusion that aliphatic chains may be more effective than aromatic moieties in binding PAHs. The molecular weight of the model sorbents was found to have a significant influence on the sorption potential.

Fluorescent Dyes↗

PubMed2004

Effects of humic substances on photodegradation of bensulfuron-methyl on dry soil surfaces.

The photodegradation of the herbicide bensulfuron-methyl on dry soil surfaces in the presence and absence of humic substances was investigated under Xe lamp irradiation. A rapid rate of disappearance occurs in the humus-removed soil. The presence of humic acid (HA) and fulvic acid (FA) reduces degradation rates and has a quenching effect on the photodecomposition of bensulfuron-methyl. The quenching effect increases with increasing HA and FA concentration in soil. HA has a slightly greater ability to quenching the photolysis compared to FA. In addition, co-effects of HA and FA on quenching the photolysis are stronger than single effects of HA or FA.

Benzopyrans↗

PubMed1997

Characterization of humic substances using capillary electrophoresis with photodiode array and laser-induced fluorescence detection.

The effect of organic modifiers (organic solvents and urea) on the electrophoretic buffer was investigated in an attempt to enhance resolution in the finger-printing of two humic substances (HS): an aquatic fulvic acid (FA) and a soil humic acid (HA). Two detection modes, photodiode array and laser-induced fluorescence, were applied. The addition of organic solvents (acetonitrile, acetone, 2-propanol and tetrahydrofuran) in 10 mM Na2B4O7 (pH 9.0) resulted in a clear difference in electrophoretic behavior of the studied HS compared to the absence of organic solvents. There were also marked differences in the electrophoretic profiles using a 2-propanol-borate buffer with urea. The study of the interaction between metals and HS showed that there was a change in the migration pattern in the presence of A1(III), indicating the specific binding sites of aluminum.

1-Propanol↗

PubMed2002

Sorption of pyrene to dissolved humic substances and related model polymers. 2. Solid-phase microextraction (SPME) and fluorescence quenching technique (FHT) as analytical methods.

Sorption coefficients for pyrene on dissolved humic substances and on poly(acrylic acid) esters as well-defined model polymers were determined using solid-phase microextraction (SPME) and the fluorescence quenching technique (FQT). The results of both analytical methods were compared and theoretically evaluated, which led to the conclusion that the sorption coefficients measured by SPME and FQT are inevitably different: SPME measures activity-based and FQT concentration-based sorption coefficients. The environmental relevance of the two types of sorption coefficients is discussed. FQT is inappropriate to measure sorption coefficients for pyrene with the synthetic sorbents. Inspection of the vibrational structure of the fluorescence spectra of those solutions indicates a highly hydrophobic microenvironment of pyrene. This can be explained by an intra- or intermolecular agglomeration of hydrophobic moieties forming a favorable host for hydrophobic solutes.

Adsorption↗

PubMed2000

The influence of humic substances on the speciation and bioavailability of dissolved mercury and methylmercury, measured as uptake by Chaoborus larvae and loss by volatilization.

The influence of dissolved humic substances (HS) on the bioavailability of dissolved inorganic and methyl mercury (Hg) was quantified by measuring the direct uptake of 203Hg in Chaoborus larvae using laboratory microcosms containing artificial freshwater. The animals were exposed individually in triplicate aquaria at 10 different concentrations of HS covering the whole range found in natural freshwaters (0-110 mg C l(-1)). Mercury-203 concentrations were monitored repeatedly in the same individuals and in their ambient water during up to 10 days. Near-steady state Hg concentrations in Chaoborus were usually reached within 5 days. The bioconcentration factor (BCF, direct uptake only) for the larvae in the absence of HS was 0.55+/-0.09 (S.E.) ml individual(-1) for inorganic Hg and 5.3+/-0.7 ml individual(-1) for methyl Hg, thus showing a 10-fold difference. Normalizing to the organic carbon content of the larvae yields a BCF(OC) in the absence of HS of 2.8+/-0.4 x 10(3) ml (gC)(-1) for inorganic Hg and 2.7+/-0.3 x 10(4) ml (gC)(-1) for methyl Hg. The uptake of both inorganic and methyl Hg decreased markedly with increasing concentration of HS. For inorganic Hg, the decrease in uptake was most pronounced at HS concentrations below 0.2 mg C l(-1). For methyl Hg, the relationship between uptake and log([HS]) was sigmoid, showing a reduction by > 90% when increasing HS concentrations from 1 to 50 mg C l(-1). Similar patterns were observed for losses of Hg from the water phase, mainly through volatilization. These results have implications for both the biouptake and the abiotic cycling of Hg in natural ecosystems and suggest that most dissolved inorganic Hg is bound to dissolved organic matter in most natural freshwaters, whereas dissolved methyl Hg is bound only in humic waters. Assuming that only free aqueous Hg is taken up by the organisms, the rather simple methodology employed here can be used for estimating distribution coefficients (K(OC)) for Hg between HS and water. In this study, the K(OC) values were 2.5+/-0.7 (S.E.) x 10(7) ml (gC)(-1) for inorganic Hg and 1.5+/-0.6 x 10(5) ml (gC)(-1) for methyl Hg. Values of similar magnitude were derived from observed losses of Hg from the water phase, supporting the assumption of an immobilization of both inorganic and methyl Hg by HS. The strong negative influence of dissolved HS on the bioavailability of both inorganic and methyl Hg in freshwater suggests that the high Hg levels often found in fish from humic lakes in the boreal forest zone cannot be explained alone by direct uptake of methyl Hg from the water phase into biota at low trophic levels.

Animals↗

PubMed2001

Increased retention of polycyclic aromatic hydrocarbons in soils induced by soil treatment with humic substances.

The analytical recovery of a mixture of polycyclic aromatic hydrocarbons (PAHs) was determined from a soil before and after oxidation with hydrogen peroxide, and subsequently treated with increasing amounts of an exogenous humic acid and subjected to different incubation periods. The release of PAHs from soil depended on the specific structure and physico-chemical properties of each PAH, and increased with additions of exogenous humic materials for both the oxidized and non-oxidized soil as well as with time of PAH permanence in soil. PAH recoveries were lower in the non-oxidized soil, thereby revealing the importance of native organic matter in increasing PAH retention in soils. This study shows that mobility of PAHs in soils can be controlled by soil conditioning with humic substances.

Environmental Pollution↗

PubMed2005

Removal of arsenic and humic substances (HSs) by electro-ultrafiltration (EUF).

A laboratory scale electro-ultrafiltration (EUF) system was developed and used to explore the removal of arsenic and humic substances (HSs) from water. As a negatively charged species, arsenate(V) was readily removed after applying voltage to the EUF cell. Arsenite(III) was removed via EUF after the pH of the water had been adjusted. Meanwhile, the rejection of HSs increased due to the presence of an electric field. This study also showed that the removal of arsenite(III) from water relies primarily on electrostatic and non-electrostatic mechanisms. In the presence of HSs, arsenate(V) complexed with the HSs and was then able to be removed by EUF. This study demonstrates that EUF is a highly promising means of removing arsenic from water.

Adsorption↗

PubMed2005

Characterization of high molecular weight disinfection byproducts from chlorination of humic substances with/without coagulation pretreatment using UF-SEC-ESI-MS/MS.

Chlorinated disinfection byproducts (DBPs) generated from the reaction of the disinfectant chlorine with naturally occurring humic substances in raw water have been intensively studied over the past three decades, yet only a fraction of the total organic halogen (TOX) formed during chlorination has been chemically identified or even well characterized. The majority of the unknown portion of the TOX is likely attributable to high molecular weight (MW) DBPs (above 500), which may have potential adverse health effects. In this work, typically dosed chlorinated Suwannee River fulvic acid (SRFA) samples with and without coagulation pretreatment were separated and fractionated by using ultrafiltration (UF) and size exclusion chromatography (SEC) techniques. The SEC fractions corresponding to the high MW region were concentrated with nitrogen sparging and characterized by negative ion electrospray ionization mass spectrometry (ESI-MS) and ESI-MS/MS. The results demonstrate that the ESI-MS/MS precursor ion scan is an effective tool for the selective detection of the electrospray ionizable chlorine-containing compounds in a complex mixture. Many high MW chlorine-containing DBPs were tentatively found in the UF-SEC fractions of the chlorinated SRFA samples with/without coagulation pretreatment. The SEC-UV chromatograms and SEC-ESI-MS spectra show that coagulation could significantly reduce the formation of high MW chlorinated DBPs.

Benzopyrans↗

PubMed2005

Carbon isotope fractionation of organic contaminants due to retardation on humic substances: implications for natural attenuation studies in aquifers.

Experimental approaches were developed which permit the measurement of carbon isotope effects during partitioning of organic compounds between water and humic substances. Fractionation factors alpha(sorption) = K(OC)12C/K(OC)13C for carbon isotopomers of benzene (1.00044 +/- 0.00015) and toluene (1.00060 +/- 0.00010) were determined from a 10-step batch experiment. Similar fractionation factors were estimated for benzene (1.00017), 2,4-dimethylphenol (1.00035), and o-xylene (< or = 1.00092) from chromatographic experiments. The latter method is based on chromatographic amplification of the fractionation effect (deltadelta13C) in an HPLC column with humic acid (HA) as the stationary phase. Possible implications of the sorption-based isotope fractionation for assessment of natural attenuation processes in contaminated aquifers are discussed. Depending on the aquifer properties (organic carbon content, heterogeneity) together with the plume source, length, and status (stationary or expanding), scenarios may be constructed where sorption-based isotope fractionation competes significantly with that caused by chemical or microbial degradation processes.

Carbon Isotopes↗

PubMedDate not supplied

Structural and elemental investigations of isolated aquatic humic substances using X-ray photoelectron spectroscopy.

Structural and elemental investigations of aquatic humic substances (HS) by means of X-ray photoelectron spectroscopy (XPS) are described. For that purpose small amounts (10-50 microg) of dissolved reference HS, which were characterized within the German research program DFG-ROSIG, were dried as thin films on small pieces of a high-purity silicon wafer. The photoelectrons from such HS layers exhibited characteristic signals of carbon C1s, nitrogen N1s, oxygen O1s and sulfur S2s, which could be fitted by Gaussian curves and used for the quantification of various moieties of HS: carbon (C-C, C-O, C=O, O=C-O), oxygen (C-O, C=O), nitrogen (C-N, C-N+) and sulfur. Moreover, by adding up the element signals of the HS samples their elemental composition of C, O, N and S was assessed. A comparison of the data based on solution state NMR and conventional elementary analysis revealed a satisfactory accuracy with those obtained by XPS.

Journal Article↗

PubMed1996

[The effect of a low molecular weight synthetic humic substance on selected reproductive parameters of male rats].

Influences of the low molecular humic substance HS 1500 on parameters of organs (testis weight, epididymis weight), FSH-, and LH-levels in plasma as well as on the spermatogenesis of male rats were studied. After a daily oral application of 1000 mg/kg b.w. and 2000 mg/kg b.w., respectively over a period of 60 days (40th to 100th day of life) only 2 animals of the high dose group were observed with bilateral testicular atrophy. Despite of the two animals with testicular atrophy no significant differences between treated and control rats were observed with respect to testis morphology and spermatogenesis. There is no evidence whether the differences between the hormone levels and the testicular atrophy revealed is regarded to a HS 1500-effect or not. But otherwise a direct influence of HS 1500 can be ruled out with high certainty. Possibly because of the thin covering layer on the gastrointestinal mucous membrane formed by HS 1500, the absorption of nutritive substances is inhibited. Therefore the growth of sensitive organs like testis and epididymis, in the development period, can be decreased. Nevertheless, even after long time application the spermatogenesis is not influenced.

Administration, Oral↗

PubMed2002

Effect of solution parameters on the removal efficiency of humic substances by a reuse material.

This paper provides an overview of the ability of polypropylene (PPL), a synthetic polymeric adsorbent made from reused plastic material. The removal of humic substances (HS) in a solution pretreated with dedoxyltrimethylammoniumbromide (DDTMAB), a cationic quaternary ammonium compound (QAC), was studied under various conditions. The removal of HS was achieved in its solute complexed form but also as suspended solids. The conditions of the HS solution, which fluctuation was suspected to have an impact on the performance of the adsorbent, were tested. The parameters investigated included the pH, the initial concentration of the surfactant, and the presence of suspended solids in solution. The results of the laboratory scale experiments showed that PPL removal efficiency of HS is strongly pH dependant with higher removal achieved at pH greater than 7. However, the shift for pH above 7 induced an increase in the optimum doses of DDTMAB as more and more deprotonated HS become available to react with DDTMAB. Ionic strength did have the opposite effect: the increase of ionic strength by addition of NaCl decreased PPL removal of HS.

Adsorption↗

PubMed2001

Effect of detector wavelength on the determination of the molecular weight of humic substances by high-pressure size exclusion chromatography.

High-pressure size exclusion chromatography (HPSEC) has proven to be an effective method for determining the molecular weights (MW) of humic substances (HS) from a variety of aquatic and terrestrial environments. HPSEC systems often use a variable wavelength UV-vis detector, which detects the analytes based upon their chromophoric composition. HS contain a range of moieties with chromophores having unique molar absorptivities (for a given wavelength), and the calculated MW may be dependent upon the wavelength chosen for the analysis. As a consequence, the choice of wavelength becomes an important parameter for the reliable determination of MW by HPSEC. The effect of UV-vis detector wavelength on the determination of the MW distribution of selected humic and fulvic acids by HPSEC is examined in this paper. For the HS examined, both the number (Mn) and weight average (Mw) MW increased with increasing wavelength. The relative increase in MW was most pronounced for Lake Fryxell fulvic acid, with a 63 and 21% increase in Mn and Mw, respectively, between 220 and 380 nm. The increases observed for Suwannee River humic and fulvic acids were less pronounced. Mn was more sensitive to changes in detector wavelength than Mw, and as a result the target HS appeared to be less polydisperse at higher wavelengths. Within the range of wavelengths commonly used for the determination of MW of HS by HPSEC (i.e., 220-280 nm), the magnitude of the increases in MW was not significant compared to variability in MW that results from changes to other operational parameters in HPSEC.

Benzopyrans↗

PubMed2003

Effects of humic substances on the pattern of oxidation products of pentachlorophenol induced by a biomimetic catalytic system using tetra(p-sulfophenyl)porphineiron(III) and KHSO5.

In the presence of humic substances (HSs), the oxidative conversion of pentachlorophenol (PCP) was found to be efficiently catalyzed by tetra(p-sulfophenyl)porphineiron(III) (Fe(III)-TPPS) using KHSO5 as an oxygen donor. Ortho-tetrachloroquinone (o-TeCQ), 2-hydroxyl-nonachlorodiphenyl ether (2H-NCDE), 4-hydroxyl-nonachlorodiphenyl ether (4H-NCDE), and octachlorodibenzo-p-dioxin (OCDD) were identified as the major byproducts of the reaction. Decreased amounts of these byproducts were produced in the presence of HS. In particular, the addition of HSs with a lower degree of humification resulted in a large decrease in the formation of dimers, such as 2H-NCDE, 4H-NCDE, and OCDD. More than 60% of the chlorine, which was released from PCP, was found in the HS fractions after the reaction. This suggests that chlorinated intermediates from PCP were incorporated into the HS. Pyrolysis-GC/MS and 13C NMR studies confirmed that the binding of the chlorinated intermediates was covalent in nature and that the intermediates were copolymerized with HS via oxidative coupling reactions. A Microtox test demonstrated that the toxicity of the HS fraction containing PCP-derived intermediates was much lower than that of the mixture of PCP and HS in the absence of a catalytic reaction.

Catalysis↗

PubMed2003

Sorption of humic substances on aquifer material at artificial recharge of groundwater.

Experiments in batch equilibrium system were carried out to evaluate the importance of physical and chemical factors determining the sorption efficiency of humic substances (HS) on aquifer material, which has been used for artificial recharge of groundwater (ARG) in drinking water production. Results showed that an increase of the amount of clay in the aquifer material and a decrease of pH in water increased the sorption efficiency. The sorption of higher molecular weight, more hydrophobic and aromatic HS (Aldrich and forest soil humic acids) were greater than the sorption of acidic HS (river fulvic acids), either on the aquifer material or to its representative sorbing phases, clay and organic matter. The sorption on the aquifer material was largely due to physical sorption (hydrophobic attractions). This study showed the importance of HS composition on their removal during ARG and contributed to an understanding of the HS sorption mechanisms in this process.

Adsorption↗

PubMedDate not supplied

Increased conformational rigidity of humic substances by oxidative biomimetic catalysis.

A synthetic water-soluble meso-tetra(2,6-dichloro-3-sulfonatophenyl)porphyrinate of iron(III) chloride, Fe(TDCPPS)Cl, was employed as a biomimetic catalyst in the oxidative coupling of terrestrial humic materials. High-performance size-exclusion chromatography (HPSEC), solid-state nuclear magnetic resonance (CPMAS-(13)C NMR), electron paramagnetic resonance (EPR), and diffuse reflectance infrared spectroscopy (DRIFT) were used to follow conformational and structural changes brought about in different humic materials by the oxidative coupling. Increase in apparent weight-average molecular weight (Mw(a)) occurred invariably for all humic substances with the oxidative polymerization catalyzed by Fe(TDCPPS)Cl. HPSEC further showed that the polymerization reaction turned the loosely bound humic supramolecular structures into more stable conformations which could no longer be disrupted by the disaggregating effect of acetic acid. DRIFT spectroscopy suggested the formation of new alkyl and aromatic ethers following the oxidative coupling with the biomimetic catalyst. CPMAS-(13)C NMR and EPR spectra suggested a reduced molecular mobility of humic components and enhanced stabilization of free radicals in larger oxidized fragments. All findings concur in indicating that the biomimetic catalysis by Fe(TDCPPS)Cl increased the molecular mass and chemical rigidity of humic materials by formation of intermolecular covalent bonds via a free-radical mechanism. The development of a technology based on oxidative polymerization by biomimetic catalysis may be of importance in controlling the properties and reactivity of humic matter for industrial and environmental applications.

Biomimetics↗

PubMed2001

Concentrations of monosaccharides in humic substances in the early stages of humification.

Deteriorated liquid packaging board (LPB) and biowaste compost are matrices, mainly consisting of cellulose, in the early stages of humification. Degradative studies on these matrices allow an examination of the role of carbohydrates in the synthesis of humic substances. Samples of different age were collected and divided by extraction into hot water extract (HWE), bitumen, humic acid (HA), fulvic acid (FA) and humin or residual fibre fractions. The following monosaccharides were identified in these fractions: L-arabinose, D-ribose, D-xylose, L-fucose, D-mannose, D-fructose, D-galactose, D-glucose, L-rhamnose and xylitol. The main component in all fractions was glucose. The concentrations of monosaccharides in humic acids (HAs) of LPB ranged from 67 to 503 mg/g of organic matter, and the concentrations in HAs of compost from 52 to 101 mg/g. As a general trend, the concentrations of monosaccharides decreased during LPB degradation and composting in all fractions. At the same time the relative amounts of D-xylose, D-mannose and D-galactose increased in HAs of compost samples.

Cellulose↗