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At least 19 recordsLinked to original sources

The chemical fractionation of rabbit and swine thymus.

A chemical fractionation procedure, previously found applicable to bovine thymus and bovine and ovine palatine tonsils, was used to fractionate rabbit and hog thymus. With respect to the chemical fractionation steps, yields of fractions, and optical and electrophoretic properties, extracts from hog and rabbit thymus were indistinguishable from similar extracts prepared from calf thymus. The study provides composition and yield data applicable to the thymus of a small mammal readily available in most laboratories.

Animals↗

Identification of Lilial as a fragrance sensitizer in a perfume by bioassay-guided chemical fractionation and structure-activity relationships.

Fragrance materials are among the most common causes of allergic contact dermatitis. The aim of this study was to identify in a perfume fragrance allergens not included in the fragrance mix, by use of bioassay-guided chemical fractionation and chemical analysis/structure-activity relationships (SARs). The basis for the investigation was a 45-year-old woman allergic to her own perfume. She had a negative patch test to the fragrance mix and agreed to participate in the study. Chemical fractionation of the perfume concentrate was used for repeated patch testing and/or repeated open application test on the pre-sensitized patient. The chemical composition of the fractions giving a positive patch-test response and repeated open application test reactions was obtained by gas chromatography-mass spectrometry. From the compounds identified, those that contained a "structural alert" in their chemical structure, indicating an ability to modify skin proteins and thus behave as a skin sensitizer, were tested on the patient. The patient reacted positively to the synthetic fragrance p-t-butyl-alpha-methylhydrocinnamic aldehyde (Lilial), a widely used fragrance compound not present in the fragrance mix. The combination of bioassay-guided chemical fractionation and chemical analysis/structure-activity relationships seems to be a valuable tool for the investigation of contact allergy to fragrance materials.

Aldehydes↗

Serological reactivity of chemical fractions of Mycoplasma bovis.

Crude chemical fractions, homogenates, and whole cells of Mycoplasma bovis were tested for serological reactivity using agar gel diffusion, ring precipitation, indirect hemagglutination, inhibition of growth inhibition (IGI), and complement-fixation (CF) tests. Only the IGI and the CF tests gave sensitive and reproducible serological information. Preliminary studies indicated lipids to be the serologically reactive components of M. bovis.

Antigens, Bacterial↗

Chemical fractionation of copper, lead and zinc in ombrotrophic peat.

Measurement of operationally defined chemical fractions in ombrotrophic peat samples provides information not obtained by total metal extractions. Examination of such sequential data permits interpretation of process dynamics. Results for copper, lead and zinc chemical fractionation of peat profiles from Ringinglow Bog, near Sheffield, Great Britain, are reported and discussed. Lead and zinc share similar patterns of partitioning. A considerable proportion of these records is in a form predisposed to transformation and mobilisation. In contrast, much of the copper is comparatively immobile, it being associated with the more chemically intractable fractions. The results suggest that peat copper deposition records may be used for reconstruction of pollution history. The use of lead and zinc records for these purposes is problematic.

Journal Article↗

The chemical fractionation of lymphatic organs.

A method for chemically fractionating lymphatic organs has been described. The method has been shown to be applicable to bovine palatine tonsils, sheep palatine tonsils, and bovine thymus. Approximately 50 per cent of the dry weight of tonsils and about 30 per cent of thymus has been found to be soluble in the 0.15 M NaCl extract. Four components have been isolated which together account for 65 per cent by weight of the material in the extracts. Four other components have been identified and partially defined by means of electrophoretic mobility, solubility, or some other chemical or physical property.

Animals↗

Radiocarbon and stable carbon isotope compositions of chemically fractionated soil organic matter in a temperate-zone forest.

To better understand the role of soil organic matter in terrestrial carbon cycle, carbon isotope compositions in soil samples from a temperate-zone forest were measured for bulk, acid-insoluble and base-insoluble organic matter fractions separated by a chemical fractionation method. The measurements also made it possible to estimate indirectly radiocarbon ((14)C) abundances of acid- and base-soluble organic matter fractions, through a mass balance of carbon among the fractions. The depth profiles of (14)C abundances showed that (1) bomb-derived (14)C has penetrated the first 16cm mineral soil at least; (2) Delta(14)C values of acid-soluble organic matter fraction are considerably higher than those of other fractions; and (3) a significant amount of the bomb-derived (14)C has been preserved as the base-soluble organic matter around litter-mineral soil boundary. In contrast, no or little bomb-derived (14)C was observed for the base-insoluble fraction in all sampling depths, indicating that this recalcitrant fraction, accounting for approximately 15% of total carbon in this temperate-zone forest soil, plays a role as a long-term sink in the carbon cycle. These results suggest that bulk soil organic matter cannot provide a representative indicator as a source or a sink of carbon in soil, particularly on annual to decadal timescales.

Carbon Isotopes↗

Evaluation of plant availability of soil trace metals by chemical fractionation and multiple regression analysis.

Soil samples with a range of chemical and physical properties were collected from 10 different rural regions of China. Trace metals (Ni, Co, Cu, and Pb) in the soils were partitioned by a sequential extraction procedure into Mg(NO(3))(2) extractable (F1), CH(3)COONa extractable (F2), NH(2)OH.HCl extractable (F3), HNO(3)?H(2)O(2) extractable (F4), and residual (F5) fractions. Chemical fractionation showed that F1 fraction of the metals was less than 1% and residue was the dominant form for Cu and Ni in all samples, and for Co in most of the samples. Significant interrelationships of the fractions varied considerably with the different metals. Winter wheat (Triticum aestivum L.) and alfalfa (Medicago sativa L.) had been grown on the soils in a pot-culture experiment under greenhouse conditions for 40 days. Metal availability to the plants was evaluated by simple and multiple regression analysis. The Mg(NO(3))(2) extractable Co (F1) was significantly correlated with Co concentrations in different parts of wheat and in the whole of alfalfa. For the other metals, the independent variables of the multiple regression models, chosen by stepwise selection, were given as: F1 and F2 + F3 + F4 for Ni; F1, F2 + F3 and F4 for Cu; and F3 + F4 for Pb. The results of this study demonstrate that the sequential extraction procedure, in conjunction with multiple regression models using a combination of correlated fractions as an independent variable, may be useful for the prediction of plant absorption of trace metals in soils.

Journal Article↗

Speciation of phosphorus in phosphorus-enriched agricultural soils using X-ray absorption near-edge structure spectroscopy and chemical fractionation.

Knowledge of phosphorus (P) species in P-rich soils is useful for assessing P mobility and potential transfer to ground water and surface waters. Soil P was studied using synchrotron X-ray absorption near-edge structure (XANES) spectroscopy (a nondestructive chemical-speciation technique) and sequential chemical fractionation. The objective was to determine the chemical speciation of P in long-term-fertilized, P-rich soils differing in pH, clay, and organic matter contents. Samples of three slightly acidic (pH 5.5-6.2) and two slightly alkaline (pH 7.4-7.6) soils were collected from A or B horizons in two distinct agrosystems in the province of Québec, Canada. The soils contained between 800 and 2100 mg total P kg(-1). Distinct XANES features for Ca-phosphate mineral standards and for standards of adsorbed phosphate made it possible to differentiate these forms of P in the soil samples. The XANES results indicated that phosphate adsorbed on Fe- or Al-oxide minerals was present in all soils, with a higher proportion in acidic than in slightly alkaline samples. Calcium phosphate also occurred in all soils, regardless of pH. In agreement with chemical fractionation results, XANES data showed that Ca-phosphates were the dominant P forms in one acidic (pH 5.5) and in the two slightly alkaline (pH 7.4-7.6) soil samples. X-ray absorption near-edge structure spectroscopy directly identified certain forms of soil P, while chemical fractionation provided indirect supporting data and gave insights on additional forms of P such as organic pools that were not accounted for by the XANES analyses.

Adsorption↗

Wastewater COD characterization: biodegradability of physico-chemical fractions.

Physico-chemical and biological characterization methods were applied to wastewater samples originating from 7 French WWTPs. The settleable fraction (S), unsettleable-coagulable fraction (US-C) and unsettleable-uncoagulable fraction (US-UC) were separated. Special emphasis was put on the determination of hydrolysis kinetics associated with coagulable- and settleable-fractions in order to model their behaviour in activated sludge processes, as both these fractions are influenced by the SRT. The "soluble" fraction (i.e. US-UC) was composed of readily biodegradable COD (2 to 27%), readily hydrolysable COD (37 to 90%) and inerts (2 to 47%). The "colloidal" fraction (i.e. US-C) was composed of heterotrophic biomass (9 to 24%) and readily hydrolysable COD (6 to 82%), with the rest being inerts or very slowly biodegradable COD (0 to 70%). The "particulate" fraction (i.e. settleable) was composed of biomass (14 +/- 6%), readily hydrolysable COD (21 +/- 14%), slowly hydrolysable COD (about 45-50%) and 15 to 20% which can be considered as inert matter (X(I)). "Readily hydrolysable COD" was correctly modeled by a global first-order reaction. First-order constants (KH) were 9 +/- 2 d(-1) for raw-wastewater, 12 +/- 3 d(-1) for primary settled-wastewater and 16 +/- 5 d(-1) for coagulated-wastewater. "Slowly hydrolysable COD" was correctly modeled by a limited surface reaction. Concerning this fraction, the specific hydrolysis rate (kH) ranged from 0.25 to 1.05 d(-1), and the affinity constant (K(X)) ranged from 0.33 to 0.95 gCOD/gCOD based on settleable solids analysis.

Biodegradation, Environmental↗

Investigations of chemical fraction of Co and Ni in industrial fly ash and mobility of metals in environmental conditions.

The quantitative evaluation of chemical fraction of Co and Ni in the industrial fly ash by methods of five step sequential extraction was carried out in order to characterize metal mobility in environmental conditions. The research involved (i) water-soluble (pH=7), (ii) acid-soluble (pH=5), (iii) oxide, (iv) sulfide and (v) residue metal fractions. It was discovered, that the total extraction of the studied metals from fly ash to solutions take place in the following quantities Co - 35.5 and Ni - 153.0mgkg(-1). The investigations of chemical fractions proved that the subject metals occur mainly in fly ash as: oxide (Co - 7.0, Ni - 28.5mgkg(-1)) and residue (Co - 11.5, Ni - 42.5mgkg(-1)) as well as sulfide (Co - 8.5, Ni - 46.5mgkg(-1)). Low concentrations of metals for water-soluble fraction (Co - 0.7, Ni - 1.2mgkg(-1)) and acid-soluble fraction (Co - 4.5, Ni - 23.5mgkg(-1)) were observed. The fractions of Co and Ni leachable from the ash in environmental conditions contain: 24.0% (Co) and 23.3% (Ni) of metal total amount in the industrial fly ash. The obtained mobility parameter of Co and Ni can be applied to estimate the concentration increase of mobile and hardly mobile forms of these metals in soil polluted with the ash.

Carbon↗

Accumulation and chemical fractionation of heavy metals in andisols after a different, 6-year fertilization management.

GOAL, SCOPE AND BACKGROUND: Andisols are widespread in Japan and have some special properties such as high anion exchange capacity, low bulk density, and high organic matter content, which might influence the accumulation or chemical fractionation of heavy metals. However, few such data exist in Japanese andisols. The primary objective of this study was to investigate the distribution and chemical fractions of Cu, Zn, Ni, and Cr in the soil profiles and subsequently to assess their potential environmental hazard. MATERIALS AND METHODS: Soil samples were taken from a field experiment conducted on Japanese andisols, which had received either swine compost or chemical fertilizers for 6 years. Concentrations of Cu, Zn, Ni, and Cr were determined for all of the obtained extract solutions by ICP-AES. RESULTS AND DISCUSSION: Considerably higher total concentrations of Cu and Zn were observed in the top 20 cm layer of the compost-amended soil, relative to the unfertilized soil, while chemical fertilizers had little effect. Application of the swine compost increased the concentrations of Cu and Zn, but not Ni and Cr, in all fractions in the top 20 cm layer. The greatest increase in the organically bound fraction (OM) Cu and dilute acid-exchangeable fraction (DAEXCH) Zn was observed. This suggests that Cu and Zn are potentially bioavailable and mobile in the andisol profiles after 6-year consecutive applications of the swine compost. On the other hand, distribution of Cu, Zn, Ni and Cr among various soil fractions was generally unaffected by chemical fertilizers. CONCLUSIONS: We observed that 6-year consecutive applications of the swine compost led to an increase in total metals of Cu and Zn, as well as their all-chemical fractions, in the top 20 cm soil layers. Potential hazard of heavy metals, especially of Cu and Zn, as a result of the use of swine compost on andisols, must be taken into account. RECOMMENDATIONS AND OUTLOOK: The long-term effect of the accumulation of heavy metals, particularly Cu and Zn, in various plant tissues and soils, as well as their potential risk to surface water via runoff and groundwater via leaching, needs to be carefully considered. Further investigations in the long-term experiments are therefore necessary.

Agriculture↗

Assessment of the bioavailability of rare earth elements in soils by chemical fractionation and multiple regression analysis.

The bioavailability of rare earth elements (REEs) in soils was evaluated, based on the combination of chemical fractionation and multiple regression analysis. REEs in soils were partitioned by a sequential extraction procedure into water soluble (F(ws)), exchangeable (F(ec)), bound to carbonates (F(cb)), bound to organic matter (F(om)), bound to Fe-Mn oxides (F(fm)) and residual (F(rd)) fractions. Alfalfa (Medicago Staiva Linn.) had been grown on the soils in a pot-culture experiment under greenhouse conditions for 35 days. The concentrations of REEs in fractions and plant were determined by inductively coupled plasma-mass spectrometry (ICP-MS). Chemical fractionation showed that (F(ws)) fraction of REEs was less than 0.1% and residual (F(rd)) was the dominant form, more than 60% in soils. Bioaccumulation of REEs was observed in Alfalfa. REE availability to the plant was evaluated by multiple regression analysis. F(ws), F(ec), F(cb) and F(om) fractions were significantly correlated with REE uptake by alfalfa. But the exchangeable Pr(F(ec)) was significantly correlated with Pr concentration in alfalfa. F(ec), F(cb) and F(om) greatly contributed to La and Nd bioavailability; F(ec) and F(om) to Ce, Gd and Dy; F(ec) and F(cb) to Yb; and F(ws), F(ec) and F(om) to total REEs. This meant that the bioavailability of different species of REEs varied with individual REE. The results of this study indicated that the sequential extraction procedure, in conjunction with multiple regression analysis, may be useful for the prediction of plant uptake of REEs from soils.

Biological Availability↗

Chemical fractionation of elements in airborne particulate matter: primary results on PM10 and PM2.5 samples in the Lazio region (central Italy).

This paper describes how a two-step chemical fractionation method that allows the determination of 17 elements in airborne particulate matter, has been applied to a monitoring campaign of PM10 and PM2.5 in the Lazio region (Italy). This method involved an extraction in a pH buffered aqueous solution followed by a microwave-assisted acid digestion of the residue. With respect to the determination of the total elemental contents, the evaluation of a soluble fraction provides more reliable information on the presence and of the destiny of heavy metals in the environment. Furthermore, the pH buffered extraction conditions chosen, rendered the results independent of the intrinsic acidity of the collected samples and, although the chemical fractionation has a purely operational function, it facilitates the study of the relationship between the distribution of solubility and the different emission sources. Results are discussed in relation to the different concentration and the different degrees of solubility of the elements observed in two sampling sites; one in an urban and one in a rural environment. Since in-parallel sampling of PM2.5 and PM10 were performed in both sites, the influence of particle size is also discussed. Behaviour of some tracers deriving from both vehicular traffic, with particular attention to re-suspended road dusts, and naturally generated particulate matter, such as marine aerosol and Saharian dust, are discussed.

Air Pollutants↗

Use of chemical fractionation and proton nuclear magnetic resonance to probe the physical structure of the primary plant cell wall.

Proton magnetic resonance has been used to monitor the microscopic physical properties of etiolated hypocotyl cell walls from Phaseolus vulgaris L. at all stages in a series of chemical fractionations with ammonium oxalate and potassium hydroxide. Solid echo measurements indicate that 75% of the polymers in the intact cell wall, including the cellulose and most of the hemicelluloses, are arranged such that there is almost complete restraint of molecular motion. The chemical fractionations generally altered the physical structures of the remaining cell wall components. Digestion with 0.25% ammonium oxalate/oxalic acid solubilized the pectin and increased the mobility of the hemicellulose I component. Extraction with 4% potassium hydroxide removed the hemicellulose I component and loosened the hemicellulose II. Further extraction with 24% potassium hydroxide removed the hemicellulose II and loosened some of the cellulose. The cellulose crystallinity, as monitored by Jeener echo measurements decreased from 83% to 63% during these fractionations. We conclude that, while hemicellulose I is firmly attached to hemicellulose II, it is not in a closely packed structure. Hemicellulose II is strongly bound to cellulose and has a much more closely packed structure.

Journal Article↗

Effects of Nidus Vespae extract and chemical fractions on the growth and acidogenicity of oral microorganisms.

Nidus Vespae is the honeycomb of Polistes Olivaceous (De Geer), P. Japonicus Saussure, and Parapolybiavaria Fabricius. It is known to have a number of pharmacological effects, including antimicrobial, anti-inflammatory, anti-virus, anti-tumor and anesthetic properties. The present study evaluated the antimicrobial activity and acid inhibition properties of extracts and chemical fractions of Nidus Vespae. The raw material was first extracted using 95% ethanol/water. Subsequent fractions were prepared from this extract using cyclohexane/ethyl acetate, petroleum ether/ethyl acetate, and chloroform/methanol. For the antimicrobial activity assays, minimum inhibitory concentrations (MIC) and minimum bactericidal concentrations (MBC) were determined using the microdilution method. The chloroform/methanol (Chl/MeOH) fraction showed the highest antibacterial activities with a MIC of 8-16mg/ml and an MBC of 16-32mg/ml. In addition, the extract and chemical fractions of Nidus Vespae showed a remarkable capacity for inhibiting the acid production of common oral bacteria at sub-MIC concentrations. Sub-MIC levels of the petroleum ether/ethyl acetate fraction significantly inhibited acid production by Streptococcus mutans ATCC 25175. The significant antiacidogenic activity demonstrated by Nidus Vespae shows it to be a promising source of novel anticariogenic agents.

Acids↗

Assessment of heavy metal removal technologies for biowaste by physico-chemical fractionation.

In the Netherlands, the heavy metal content of biowaste-compost frequently exceeds the legal standards for heavy metals. In order to assess heavy metal removal technologies a physico-chemical fractionation scheme was developed to gain insight into the distribution of heavy metals (Cd, Cu, Pb and Zn) over the physical entities of biowaste and to determine the binding strength of heavy metals to these physical entities. The scheme was based on a particle fractionation on size and density followed by sequential chemical extraction of the fractions. The organic fraction >1 mm contributed to 40% of the mass of biowaste and this fraction met the legal standards for compost after composting. About 28% of biowaste was composed of sand, which can be reused in road and building construction as the heavy metal content is very low. The heavy metals were concentrated in the organic particles from 0.05-1 mm and the organo-mineral fraction <0.05 mm. The heavy metal content has to be reduced to reach the legal standards for compost. The extractability from the inorganic organic and organo-mineral fractions showed the order Cd>>Zn>Pb>Cu. The order of extractability for Pb and that for Zn were sometimes reversed most probably because the extraction is not only determined by the adsorption strength but also by the accessibility of adsorbed metals. The results of sequential chemical extraction showed that the amount of heavy medals available for extraction was sufficient. Citric acid turned out to be the best option for the removal of heavy metals from solid organic waste streams.

Agriculture↗

Mercury in chemical fractions of recent pelagic sediments of the sea of Japan.

The distribution of mercury (Hg) in chemical fractions (H2O, 0.05 M Na2-EDTA pH 3, 1 M HCl, humic and fulvic acids, and non-hydrolysing residue) of recent pelagic sediment cores of the Sea of Japan (East Sea) was studied. Total Hg content in the sediments was rather low: 83 +/- 30 (21-173) etag g(-1), indicating the absence of substantial specific sources of the element in the deep part of the sea. Hg content within the sediment core varied by a factor of 1.3-1.8, showing peaks that coincide with the near-surface and buried sediment slices of light brown and brown "oxidized" colours and evidencing Hg redox-sensitive diagenetic redistribution. Hg exerted its maximum mobility in the near-surface sediment strata as a component of water-soluble organic matter. Despite the predominance of fulvic acids in extracted humus fractions, humic acids were a much more efficient concentrator for Hg (0-79 vs. 188-233 microg Hg g(-1) C(org), respectively). Nevertheless, the most refractory non-hydrolyzing residue (humin) fraction contained the principal Hg pool in the sediments. Hg content in all the extracted fractions decreased with core depth, thus indicating Hg immobilization as a principal tendency in Hg fate during post-depositional diagenesis.

Benzopyrans↗