Degradation of biochanin A in soil

Degradation of biochanin A, 400 μg (1.41 μmol) per gram of dry soil, was studied and the initial degradation products, dihydrobiochanin A, pratensein and genistein were identified and quantified. The maximum concentrations of these compounds were determined as 166 pmol/g dry soil after 2 days of incubation, 175 pmol/g dry soil after 1 day and 1,236 pmol/g dry soil after 1 day, respectively. Biochanin A and the initially formed products degrade too fast to be responsible for clover soil sickness (DT₉₀ <20 days), but could be precursors for the responsible compounds. The immediate degradation products from biochanin A are all biologically active and are the prime candidates for a reduction of weed pressure caused by clover.     

黑曲霉吸附弱酸性艳蓝RAWL机理研究

考察了黑曲霉对染料吸附性能的pH响应模式,红外光谱表征了菌体表面的主要官能团组成,化学修饰定量研究了不同官能团的染料吸附贡献.结果显示,在低pH条件下,菌体表现出最优的染料吸附特性:随着pH值由2.0升至6.0,染料吸附量由39.6mg/g降至9.3mg/g.菌体表面含有氨基、羧基和磷酸根.高pH下,羧基和磷酸根电离导致菌体表面带负电并与染料发生静电斥力,使得染料吸附量下降;低pH下,氨基的质子化使得菌体带正电并通过静电吸引提高染料吸附.甲基化氨基在酸性条件下仍然可以质子化,故氨基甲基化修饰后染料吸附性能不变;乙酰化氨基在酸性体系中失去质子化能力,乙酰化修饰菌体染料吸附性能下降51.6%.氨基质子化引起的菌体正电性和染料负电性之间的静电引力是染料吸附的重要机制.图6参10     

Changes in protein-bound and free amino acids in the muscle of the tiger prawn Penaeus esculentus during starvation

Using the starvation technique, changes in protein and free amino acids were examined in Penaeus esculentus Haswell collected from Moreton Bay, Australia, by trawling in 1985. Prawns of 17.7±0.26 g wet weight were held at 25°C until 2 d after moulting. Groups of seven or eight were then starved fro 5, 10, or 15 d, with appropriate control groups. At the end of each period, ecreted amino acids were collected for 24 h and whole-muscle amino acids and free amino acids (FAA) g^-1 in each prawn were analysed. Concentrations of whole-muscle amino acids showed only minor changes with starvation, but concentrations of many of the FAA changed significantly. Total FAA averaged 1 182±45 mol g^-1 dry weight. Individual FAA, in order of abundance, were glycine, arginine, proline, taurine, threonine, hydroxyproline, alanine, glutamic acid, valine, aspartic acid and lysine; the remaining FAA each contributed <0.2% of the total. Only taurine and alanine did not show significant changes with starvation. Concentrations of glycine, arginine, hydroxyproline, glutamic and aspartic acid increased, while those of proline, threonine, valine and lysine decreased with starvation, that of proline approaching zero after 15 d starvation. Excreted amino acid-nitrogen represented <2% of excreted ammonianitrogen ornithine being the most abundant (35%), followed by leucine (22%) and lysine (17%). The relative abundance of excreted amino acids did not correspond with those of the FAA. It is suggested that, as starvation progresses, the muscle protein is progressively hydrolysed, but with the remaining muscle maintaining its amino acid composition. The liberated amino acids enter the FAA pool and become available for energy production. Proline may have an important role as an energy source, but the ability to synthesise proline may be limited, and thus the artificial food of penaeid prawns may be improved by its addition.     

Perfluoroalkane acids in human milk under the global monitoring plan of the Stockholm Convention on Persistent Organic Pollutants (2008–2019)

● Perfluorooctanesulfonic acid and perfluorooctanoic acid highest in human milk. ● All other perfluoroalkane substances had median values of zero (101 samples). ● Branched PFOS recommended to be analyzed separately from linear isomer. ● PFOS and PFOA showed differentiated regional and income distribution. ● Human health risk assessment values not yet available at global level. Within the global monitoring plan (GMP) established by article 16 of the Stockholm Convention on Persistent Organic Pollutants, perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorohexane sulfonic acid (PFHxS) are recommended for analysis in core matrices to assess occurrence and changes geographically and with time. In 101 samples consisting of 86 national pools and 15 pools from States in Brazil obtained between 2008 and 2019, PFHxS was detected in 17% of the national pools and none in Brazil. PFOA and PFOS had a detection frequency of 100% and 92%, respectively. Other perfluoroalkane substances (PFAS) had either low detection frequencies and median values of zero (carboxylic acids C₄–C₁₁; except PFOA) or could not be quantified in any sample (sulfonic acids, C₄–C₁₀, and long-chain carboxylic acids, C₁₂–C₁₄). Correlation between PFOA and PFOS was moderately (r = 0.58). Whereas median values were almost identical (18.9 pg/g f.w. for PFOS; 18.6 pg/g f.w. for PFOA), PFOS showed larger ranges (< 6.2 pg/g f.w.–212 pg/g f.w.) than PFOA (< 6.2 pg/g f.w.–63.4 pg/g f.w.). It was shown that wealthier countries had higher PFOA concentrations than poorer countries. No difference in concentrations was found for samples collected in countries having or not having ratified the Stockholm Convention amendments to list PFOS or PFOA. The goal to achieve 50% decrease in concentrations within ten years was met by Antigua and Barbuda, Kenya, and Nigeria for PFOS and by Antigua and Barbuda for PFOA. In a few cases, increases were observed; one country for PFOS, four countries for PFOA.     

Photo detoxification of solubilized vat dye effluent using different pH ranges

The removal of solubilized vat dye effluent using photo detoxification method was studied at various pH ranges. Experiments were carried out with synthetic effluent using total dye concentrations of 50, 100, 200, 300, and 350 mg/L. In sunlight photo oxidation, the original soluble vat dye is precipitated and can be filtered and reused by the textile industries. The effect of the different concentrations (1,000, 2,000, 3,000 mg/L) of total dissolved solids on the removal of vat dye was also carried out in the photo detoxification process. The efficiency of the dye removal was found to be 99 %.     

Human hair mercury levels in the Wanshan mercury mining area,Guizhou Province,China

The total mercury (T-Hg) and methyl mercury (Me-Hg) concentrations in the hair were measured to evaluate mercury (Hg) exposure for the residents in Da-shui-xi Village (DSX) and Xia-chang-xi Village (XCX) in the Wanshan Hg mining area, Guizhou Province, Southwestern China. The mean concentrations in the hair of DSX residents were 5.5 ± 2.7 μg/g and 1.9 ± 0.9 μg/g for T-Hg and Me-Hg, respectively. The concentrations in the hair of XCX residents were 3.3 ± 1.4 μg/g and 1.2 ± 0.5 μg/g for T-Hg and Me-Hg, respectively. Hair Me-Hg concentrations were significantly correlated to T-Hg (r = 0.42, P < 0.01) in the two sites; on average, hair Me-Hg concentration accounted for 40 and 44% of T-Hg for DSX and XCX residents, respectively. Age has no obvious correlation with hair Hg and the hair Hg levels showed a significant gender difference, with higher T-Hg and Me-Hg concentrations in the hair from males than females. The rice collected from the two sites showed high levels of T-Hg and Me-Hg concentration. The results indicated a certain Hg exposure for the residents in DSX and XCX in the Wanshan Hg mining area.     

Polymer resins for recovery of valuable metals

Vinylbenzyl chloride/divinylbenzene gel copolymer beads have been modified using piperidine, hexamethyleneimine, piperazine, 1-(2-aminoethyl)piperazine, and N-cyclohexyl-1,3-propanediamine. These resins were then tested for the sorption of noble metal ions, namely, Re(VII), Pd(II), Pt(IV), and Au(III), from a 0.1 M HCl solution. The effect of these resins on the sorption of other coexisting ions, such as Cu, Ni and Fe, was also studied. Of the resins tested, resin 4 [1-(2-aminoethyl)piperazine groups] showed the highest sorption capacity for Pt(IV) and Re(VII) from single and multicomponent solutions, with the sorption of Pt(IV) from the multicomponent solution (Re, Au, Pd, Pt, Cu, Ni Fe) in 0.1 M HCl reaching 68 mg Pt/g.     

Synthesis of polycaprolactone by microwave irradiation — an interesting route to synthesize this polymer via green chemistry

Poly(ε-caprolactone) has become an important biocompatible and biodegradable polymer. Indeed, due to its multiple biomedical applications, the synthesis of polycaprolactone has received increased attention in the past few decades. Moreover, microwave irradiation is a very clean modern technique widely used for green chemistry. Here, several polymers were synthesized by microwave irradiation, without any solvent, using nontoxic, biologically acceptable lanthanide halides as initiators. Reaction times varied between 2 and 90 min. The molecular weights of the obtained polymer products were between 3,000 and 16,000 g/mol. After polymerization, the polycaprolactone polymers were functionalized by reaction with 2-hydroxyethyl methacrylate. Hydrolytic and enzymatic degradation of the synthesized polymers were compared and discussed.     

Accumulation of cadmium and zinc in <Emphasis Type="Italic">Evodiopanax innovans</Emphasis>

The use of tree species for phytoremediation of contaminated soil offers the advantage of a large biomass in which to store contaminants. We investigated the cadmium (Cd) and zinc (Zn) accumulation ability of Evodiopanax innovans, a common deciduous tree species belonging to the Araliaceae family and widely found in secondary forests in Japan. Sampling was conducted at an old silver mine. Leaf samples were collected from nine tree species, including E. innovans. The seasonal variation of metal concentrations in the leaves and the detailed distribution of metals in the leaves and twigs of E. innovans were measured. We also analyzed the contents of organic acids in the leaves. The highest concentration of Cd in the leaves of E. innovans was 118 μg/g, which exceeds the threshold level for being considered a Cd hyperaccumulator (100 μg/g). For Zn, the highest value was 1040 μg/g in leaves, which is less than required to qualify as a Zn hyperaccumulator. Both Cd and Zn were found to accumulate in the petioles and veins of leaves and the bark of twigs. Since the oxalic acid content of leaves showed a weak correlation with Cd concentration, oxalic acid may play an important role in the accumulation of Cd. Taking both the Cd concentration level and the biomass of this woody plant into consideration, it may be possible to use E. innovans for the phytoremediation of Cd-contaminated soils.     

Exposure profiles of mercury in human hair at a terai belt of North India

Human hair is frequently used as a bioindicator of mercury exposure. Mercury (Hg) has for centuries been a useful metal in a variety of applications. Unfortunately, this usefulness is counterbalanced by its neurotoxicological health impact. The US Environmental Protection Agency recommends keeping the hair Hg level <1.0 µg/g. Therefore, an investigation has been performed in order to ascertain the hair Hg levels among the people living at the terai belt of North India. Hair samples were collected from 111 individuals and were placed in an identified plastic bag, stapled to prevent the shift of the hair strand. Samples were analyzed by combustion, gold amalgamation, atomic absorption spectrometry (C-GA-AAS). The mean Hg level in hair was 0.28 µg/g for the whole group ranging from 0.0012 to 1.9091 µg/g. The mean hair Hg levels were 0.16 µg/g for men and 0.12 µg/g for women, indicating that men had higher hair Hg levels than women. Total hair Hg was found to be significantly associated with age, gender and fish consumption frequency. 98 % of the total sample had hair Hg concentrations less than 1.0 µg/g, i.e, within safe dose, whereas only 2 % had Hg concentrations greater than 1.0 µg/g, thereby exceeding the safe dose.

     

Equilibrium studies on the adsorption of acid dye into chitin

We report the adsorption isotherm of acid dye on the surface of chitin, a unique solid adsorbent. Adsorption process offers an attractive benefit for a dyeing house treatment. Influences of essential kinetic parameters such as adsorbent particle size, reaction temperature governing the dye adsorption have been investigated. Adsorptions isotherms of dye on chitin were developed and the equilibrium data fitted well to the Langmuir, Freundlich and Redlich Peterson isotherm model. At optimum conditions maximum dye adsorption capacity of chitin estimated with the Langmuir 44.0, 85.0, 104.3 mg/g and 85.0, 114.10, 113.62 mg/g adsorbent. The results showed that chelating polymer of chitin could be considered as potential adsorbents for acid dye removal from dilute solution.     

Amino acid uptake and respiration by marine heterotrophs

The concentration and turnover of dissolved free amino acids were measured in samples from 25 and 100 m on three occasions at a station 6 miles off the California (USA) coast. Individual amino acid concentrations varied from undetectable (<0.05 g/l) to 3 g/l, the total amino acid concentration from 1.8 to 8.5 g/l. The greater concentration of total amino acids was always found at 25 m. The predominant amino acids were serine, lysine, aspartate, glutamate and alanine; reliable analyses could not be made for glycine because of a high blank. For the 10 individual amino acids studied, the rate of heterotrophic turnover ranged from undetectable to 1.2 g/l day^-1; serine, aspartate, alanine and glutamate showed the highest rates. In samples from 25 m, the rates were 15 to 20 times higher than those taken from 100 m. The total calculated flux of the amino acids studied varied from 0.015 to 3.2 g/l day^-1 and amounted to 1–10% of photosynthetic carbon dioxide fixation.     

树脂D001负载纳米Pd/Fe双金属脱溴2,2’,4,4’-四溴联苯醚(BDE-47)的研究

采用大孔树脂D001交换吸附Pd2+、Fe2+并在厌氧条件下以硼氢化钠溶液还原吸附的钯铁离子制备成负载纳米Pd/Fe双金属树脂。利用该树脂对2,2’,4,4’-四溴联苯醚(BDE-47)进行脱溴反应,探讨了该法的可行性和特性。结果表明:当大孔树脂D001、氯化钯、硫酸亚铁用量分别为0.75 g、2μg和0.2 g时所制备的双金属树脂脱溴水-乙醇溶液中的BDE-47效果最佳,反应遵循准一级动力学,速率常数k约为0.161 d-1,半减期为1.21 d。负载Pd/Fe的D001连续3次脱溴反应都有较好的效果,水-乙醇溶液中超过90%以上的BDE-47在反应6 d后被降解。负载Pd/Fe双金属的树脂可以重复活化再生,但再生2次后其脱溴效率变差,反应6 d只有47.3%的BDE-47被降解。用气相色谱-质谱联用仪和离子色谱仪跟踪Pd/Fe双金属树脂脱溴BDE-47反应,可知产物包括溴离子、三溴联苯醚、二溴联苯醚、一溴联苯醚和联苯醚。     

Detecting the effects of coal mining,acid rain,and natural gas extraction in Appalachian basin streams in Pennsylvania (USA) through analysis of barium and sulfate concentrations

To understand how extraction of different energy sources impacts water resources requires assessment of how water chemistry has changed in comparison with the background values of pristine streams. With such understanding, we can develop better water quality standards and ecological interpretations. However, determination of pristine background chemistry is difficult in areas with heavy human impact. To learn to do this, we compiled a master dataset of sulfate and barium concentrations ([SO₄], [Ba]) in Pennsylvania (PA, USA) streams from publically available sources. These elements were chosen because they can represent contamination related to oil/gas and coal, respectively. We applied changepoint analysis (i.e., likelihood ratio test) to identify pristine streams, which we defined as streams with a low variability in concentrations as measured over years. From these pristine streams, we estimated the baseline concentrations for major bedrock types in PA. Overall, we found that 48,471 data values are available for [SO₄] from 1904 to 2014 and 3243 data for [Ba] from 1963 to 2014. Statewide [SO₄] baseline was estimated to be 15.8 ± 9.6 mg/L, but values range from 12.4 to 26.7 mg/L for different bedrock types. The statewide [Ba] baseline is 27.7 ± 10.6 µg/L and values range from 25.8 to 38.7 µg/L. Results show that most increases in [SO₄] from the baseline occurred in areas with intensive coal mining activities, confirming previous studies. Sulfate inputs from acid rain were also documented. Slight increases in [Ba] since 2007 and higher [Ba] in areas with higher densities of gas wells when compared to other areas could document impacts from shale gas development, the prevalence of basin brines, or decreases in acid rain and its coupled effects on [Ba] related to barite solubility. The largest impacts on PA stream [Ba] and [SO₄] are related to releases from coal mining or burning rather than oil and gas development.

     

Radionuclide concentrations in raw and purified phosphoric acids from Brazil and their processing wastes: implications for radiation exposures

Radionuclides from the U and Th natural series are present in alkaline rocks, which are used as feedstock in Brazil for the production of raw phosphoric acid, which can be considered as a NORM (naturally occurring radioactive material). As a result of the purification of raw phosphoric acid to food-grade phosphoric acid, two by-products are generated, i.e., solid and liquid wastes. Taking this into account, the main aim of this study was to evaluate the fluxes of natural radionuclide in the production of food-grade phosphoric acids in Brazil, to determine the radiological impact caused by ingestion of food-grade phosphoric acid, and to evaluate the solid waste environmental hazards caused by its application in crop soils. Radiological characterization of raw phosphoric acid, food-grade phosphoric acid, solid waste, and liquid waste was performed by alpha and gamma spectrometry. The ²³⁸U, ²³⁴U, ²²⁶Ra, and ²³²Th activity concentrations varied depending on the source of raw phosphoric acid. Decreasing radionuclides activity concentrations in raw phosphoric acids used by the producer of the purified phosphoric acid were observed as follows: Tapira (raw phosphoric acid D) > Catal?o (raw phosphoric acids B and C) > Cajati (raw phosphoric acid A). The industrial purification process produces a reduction in radionuclide activity concentrations in food-grade phosphoric acid in relation to raw phosphoric acid produced in plant D and single raw phosphoric acid used in recent years. The most common use of food-grade phosphoric acid is in cola soft drinks, with an average consumption in Brazil of 72 l per person per year. Each liter of cola soft drink contains 0.5 ml of food-grade phosphoric acid, which gives an annual average intake of 36 ml of food-grade phosphoric acid per person. Under these conditions, radionuclide intake through consumption of food-grade phosphoric acid per year per person via cola soft drinks is not hazardous to human health in Brazil. Considering these annual additions of ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K, and since these radionuclide should be homogeneously distributed in the upper 10 cm of soils with an assumed apparent density of 1.5 g/cm³, a maximum increase of 0.19 ± 0.03 Bq kg⁻¹ of soil is expected for ²³⁸U and ²³⁴U. Thus, the addition of solid waste as phosphate fertilizers to Brazilian agricultural soils does not represent a hazard to the ecosystem or to human health.     

A comparative study on arsenic and humic substances in alluvial aquifers of Bengal delta plain (NW Bangladesh), Chianan plain (SW Taiwan) and Lanyang plain (NE Taiwan): implication of arsenic mobilization mechanisms

Humic substances in groundwater and aquifer sediments from the arsenicosis and Blackfoot disease (BFD) affected areas in Bangladesh (Bengal delta plain) and Taiwan (Lanyang plain and Chianan plain) were characterized using fluorescence spectrophotometry and Fourier transform infrared (FT-IR) spectroscopy. The results demonstrate that the mean concentration of As and relative intensity of fluorescent humic substances are higher in the Chianan plain groundwater than those in the Lanyang plain and Bengal delta plain groundwater. The mean As concentrations in Bengal delta plain, Chianan plain, and Lanyang plain are 50.65 μg/l (2.8–170.8 μg/l, n = 20), 393 μg/l (9–704 μg/l, n = 5), and 104.5 μg/l (2.51–543 μg/l, n = 6), respectively. Average concentrations and relative fluorescent intensity of humic substances in groundwater are 25.381 QSU (quinine standard unit) and 17.78 in the Bengal delta plain, 184.032 QSU and 128.41 in the Chianan plain, and 77.56 QSU and 53.43 in the Lanyang plain. Moreover, FT-IR analysis shows that the humic substances extracted from the Chianan plain groundwater contain phenolic, alkanes, aromatic ring and amine groups, which tend to form metal carbon bonds with As and other trace elements. By contrast, the spectra show that humic substances are largely absent from sediments and groundwater in the Bengal delta plain and Lanyang plain. The data suggest that the reductive dissolution of As-adsorbed Mn oxyhydroxides is the most probable mechanism for mobilization of As in the Bengal delta plain. However, in the Chianan plain and Lanyang plain, microbially mediated reductive dissolution of As-adsorbed amorphous/crystalline Fe oxyhydroxides in organic-rich sediments is the primary mechanism for releasing As to groundwater. High levels of As and humic substances possibly play a critical role in causing the unique BFD in the Chianan plain of SW Taiwan.     

Fatty acids in fish scales

This study represents the first determination of lipids and fatty acids in fish scales. Scales collected from groups of Atlantic salmon reared on fish farms and in experimental tanks were analyzed by chromatography. The complete suite of fatty acids normally found in marine organisms was detected in the scales, with the following fatty acids dominating: 16:0, 18:0, 18:1n9, 20:5n3, 22:6n3 and 24:1n9. Scales contained relatively high levels of furan fatty acids, and the level of cholesterol (2.5–5 mg/g tissue) was much higher than the levels found in the edible parts of marine fishes (0.2–1 mg/g tissue). The fatty acid profile of scales was distinct between groups of salmon originating from different commercial strains reared on the same farm, between salmon groups originating from the same strains but reared at different farms, and between groups of fed and unfed salmon in experimental tanks. Together, these data indicate that the fatty acid composition of fish scales is dependent upon both environmental and genetic factors. The fatty acid composition of fish scales may be used in stock/population identification, for example identification of escaped Atlantic salmon to farm of origin.     

Metabolic enzymes in coelomic cells (eleocytes) of the polychaete Nereis virens: sex specific changes during sexual maturation

The activities of some enzymes of the intermediary metabolism and the content of soluble protein and carbohydrate (glycogen plus free glucose) were measured in one type of coelomic cells (eleocytes) of the polychaete Nereis virens. Specimens used in this study were collected between 1989 and 1991 in Oosterscheldt Bay, The Netherlands, and divided into six different stages of sexual maturation as determined by the mean oocyte volume. In both sexes, the soluble protein content in eleocytes of immature individuals (11 mg ml^–1 cell vol) increased three-fold. In prespawning N. virens the soluble protein content decreased to less than 2 mg protein ml^–1 cell vol in females but not in males. In both sexes, the carbohydrate content decreased continuously from immature [300 mol glucose equivalent (equiv) ml^–1 cell vol] to prespawning individuals (< 40 mol glucose equiv ml^–1 cell vol). During the time course of maturation, the specific activities (expressed as units mg^–1 protein) of pyruvate kinase, phosphoenolpyruvate carboxykinase, malate dehydrogenase, alanine aminotransferase and glutamate dehydrogenase decreased in both sexes. A transient increase in the specific activities was found for glycogen phosphorylase and aspartate aminotransferase. No major changes were found for hexokinase, lactase dehydrogenase, glucose-6-phosphate dehydrogenase and malic enzyme. Sex specific differences were found for the activities of citrate synthase and isocitrate dehydrogenase, which were higher in males. the specific activities of the latter enzyme increased more than ten-fold in males, but only four-fold in female eleocytes during maturation. In eleocytes of prespawning females, the activities of most enzymes showed extremely high variations not found in prespawning males. For two enzymes of fatty acid catabolism, -hydroxyacyl-CoA dehydrogenase and -hydroxybutyrate dehydrogenase, only traces of activities were detected, suggesting the absence of significant fatty acid catabolism in the eleocytes. Compared to the eleocytes, the body wall tissue showed ten-fold higher activities of phosphofructokinase, whereas the eleocytes displayed higher activities of the amino acid interconverting enzymes glutamate dehydrogenase and alanine aminotransferase and the glyconeogenic enzyme phosphoenolpyruvate carboxykinase. Citrate synthase activities were similar for both tissues. In the coelomic fluid of N. virens, glucose (< 0.1 to 3.5 mM) and d-lactate (0.1 to 4 mM) were present and represent exogenous substrates for the eleocyte metabolism.     

The influence of iron stores on cadmium body burden in a Thai population

Cadmium is a toxin of increasing public health concern due to its presence in most human foodstuffs and in cigarette smoke. Exposure to cadmium leads to tissue bioaccumulation and, in particular, has nephrotoxic effects. The aim of the present study was to investigate the association between cadmium body burden and iron stores in a Thai population. A total of 182 healthy adult Thai subjects of both genders (89 males, 93 females) aged between 18 and 57 years and weighing 40–95 kg were included in this study. The total amounts of cadmium excreted in urine over 2 h (μg/g creatinine) were used as an index of long-term cadmium exposure. Quantitation of cadmium was performed using electrothermal (graphite furnace) atomic absorption spectrometry. The urinary cadmium excreted displayed a normal frequency distribution. The average urinary cadmium level did not exceed the WHO maximum tolerable internal dose for the non-exposed population (2 μg/g creatinine). Body iron stores reflected by serum ferritin levels did not show any correlation with cadmium burden in both males and females, although a relatively stronger influence of body iron store status on cadmium burden was shown in females. When the levels of serum ferritin were stratified into five levels (<20, 20–100, 101–200, 201–300, and >300 μg/l), a significant difference in total cadmium body burden was observed between females and males only in the group with a low level of serum ferritin of <20 μg/l. The cadmium body burden in females was about twice that in males in this group.     

树脂D001负载纳米Pd/Fe双金属脱溴2,2＇,4,4＇-四溴联苯醚（BDE-47）的研究

采用大孔树脂D001交换吸附Pd2＋、Fe2＋并在厌氧条件下以硼氢化钠溶液还原吸附的钯铁离子制备成负载纳米Pd/Fe双金属树脂。利用该树脂对2,2＇,4,4＇-四溴联苯醚（BDE-47）进行脱溴反应,探讨了该法的可行性和特性。结果表明：当大孔树脂D001、氯化钯、硫酸亚铁用量分别为0.75 g、2μg和0.2 g时所制备的双金属树脂脱溴水-乙醇溶液中的BDE-47效果最佳,反应遵循准一级动力学,速率常数k约为0.161 d-1,半减期为1.21 d。负载Pd/Fe的D001连续3次脱溴反应都有较好的效果,水-乙醇溶液中超过90%以上的BDE-47在反应6 d后被降解。负载Pd/Fe双金属的树脂可以重复活化再生,但再生2次后其脱溴效率变差,反应6 d只有47.3%的BDE-47被降解。用气相色谱-质谱联用仪和离子色谱仪跟踪Pd/Fe双金属树脂脱溴BDE-47反应,可知产物包括溴离子、三溴联苯醚、二溴联苯醚、一溴联苯醚和联苯醚。