Hydride Generation Atomic Fluorescence Spectrometry Research Articles

Traces of the past: assessing the impact of potentially toxic elements from an abandoned mine on groundwater and agricultural soil in San Luis Potosí, México.

The study was conducted in Cerritos, San Luis Potosí, México, near the Guaxcama mine, focused on environmental contamination (groundwater and agricultural soil) from antimony (Sb), arsenic (As), lead (Pb), cadmium (Cd), and mercury (Hg). In March 2022, 20 agricultural soil and 16 groundwater samples were collected near the historically cinnabar (HgS)- and arsenopyrite (FeAsS)-rich Guaxcama mine. Hydride generation atomic fluorescence spectrometry (HG-AFS) for As, cold vapor atomic fluorescence spectrometry (CV-AFS) for Hg, and inductively coupled plasma optical emission spectrometry (ICP-OES) for Cd, Pb, and Sb were used for the determinations of potentially toxic elements (PTEs). While concentrations of Cd, Hg, Pb, and Sb in groundwater were below detection limits, As levels exhibited a range from 40.9 ± 1.4 to 576.0 ± 1.0µg/L, exceeding permissible limits for drinking water (10µg/L). In agricultural soil, As was between 7.67 ± 0.16 and 24.1 ± 0.4µg/g, Hg ranged from 0.203 ± 0.018 to 2.33 ± 0.19µg/g, Cd from 2.53 ± 0.90 to 2.78 ± 0.01µg/g, and Pb from 11.7 ± 1.2 to 34.3 ± 4.1µg/g. Only one study area surpassed the Mexican As soil limit of 22µg/g. Sequential extraction (four-step BCR procedure) indicated significant As bioavailability in soil (fractions 1 and 2) ranging from 3.66 to 10.36%, heightening the risk of crop transfer, in contrast to the low bioavailability of Hg, showing that fractions 1, 2, and 3 were below the limit of quantification (LOQ). Crucial physicochemical parameters in soil, including nitrate levels, pH, and organic matter, were pivotal in understanding contamination dynamics. Principal component analysis highlighted the influence of elements like Fe and Ca on phytoavailable As, while Pb and Cd likely originated from a common source. Ecological risk assessments underscored the significant impact of pollution, primarily due to the concentrations of Cd and Hg. Non-cancer and cancer risks to residents through As poisoning via contaminated water ingestion also were found. The hazard index (HI) values varied between 4.0 and 82.2 for adults and children. The total incremental lifetime cancer risk (TILCAR) values for adults ranged from 7.75E - 04 to 1.06E - 02, whereas for children, the values were from 2.47E - 04 to 3.17E - 03.

Selenium speciation analysis of selenium-enriched Shiitake mushrooms (Lentinula edodes) by HPLC-ESI-MS

Selenium (Se) is an essential component of critical enzymes and is intricately linked to human health. Shiitake mushrooms (Lentinula edodes) are considered as good dietary supplements for producing Se-enriched foods due to their high protein content and ability to absorb minerals from growth substrates. In this study, the distribution of soluble Se in Se-enriched L. edodes was analyzed by microwave digestion and hydride generation-atomic fluorescence spectrometry (HG-AFS). In order to evaluate the absorption and conversion effect of Se by L. edodes, the Se-containing compounds in selenized L. edodes were quantitatively and qualitatively analyzed by high-performance liquid chromatography-electrospray ionization tandem mass spectrometry (HPLC-ESI-MS). It can be shown that L. edodes possessed a good biological transformation ability of organic Se enrichment though the quantitative analysis of three seleno-amino acids, selenocystine (Se-Cys2), methylselenocysteine (Se-MeSeCys) and selenomethionine (Se-Met), in selenized L. edodes. The structures of three unknown Se-containing compounds were identified by qualitative analysis, the results indicated that the possible structures were selenomethylmethionine (C6H14NO2Se), N-Acetyl-selenomethionine (C7H13NO3Se) and Se-methyl-5-selenoadenosinese-oxide (C12H18N5O3Se). The discovery of these Se compounds filled the research gap and provided a theoretical basis for molecular structure identification and mechanism study of organic Se in Se-enriched L. edodes.

Estimated daily intake and health risk assessment of total and organic selenium in crops across areas with different selenium levels

BackgroundThe health risk of Se has gained significant attention. Previous studies mainly focused on the health risk of total Se in high-Se area. Less attention has been paid to the health risk of organic selenium in areas with varying selenium levels. MethodsA total number of 109 crop samples (edible parts) were collected in Langao County, Shannxi Province, China from 2018 to 2020, including 42 corn, 18 rice, 9 sweet potato, 25 potato, 12 radish, and 3 eggplant samples. The hydride generation atomic fluorescence spectrometry (HG-AFS) method was used to determine the total and organic Se contents. Result and conclusion(1) Corn (2.82 mg/kg), rice (0.44 mg/kg), potato (6.56 mg/kg), and eggplant (0.77 mg/kg) in high-Se area, as well as sweet potato (1.07 mg/kg) and radish (4.28 mg/kg) in medium-Se area, exhibited the highest total Se content among all crops in this county, and 5–328 times higher than the values of Se-enriched standard (2) The average daily intake of total/organic Se of residents in high-Se area reached 676/449 μg/day, which was 1–4 times higher than levels observed in medium-Se area (419/257 μg/day) and low-Se area (196/128 μg/day). The organic Se daily intakes from dietary combinations of rice + radish and rice + eggplant in high-Se area lower than 400 μg/day, which could be safely consumed. The organic Se daily intakes from dietary combinations of sweet potato + radish and sweet + eggplant in medium-Se area higher than 400 μg/day, which could not be safely consumed. The total / organic Se daily intakes of all dietary combinations in low-Se area lower than 400 μg/day, which could be safely consumed. (3) The health risk associated with crops might be overestimated due to the higher non-carcinogenic risk attributed to total Se compared to organic Se. The present study demonstrated that daily intake and health risk of total and organic Se in crops across areas with different Se levels varied significantly.

A simple and rapid copper-assisted microprecipitation method for the on-site separation of inorganic arsenic species in water samples followed by hydride generation atomic fluorescence spectrometry determination

A simple and rapid microprecipitation procedure was developed using copper (Cu2+) as precipitating agent for the separation–preconcentration of inorganic arsenic species (As(III) and As(V)) in waters prior to their determination by hydride generation atomic fluorescence spectrometry (HG-AFS). This procedure is based on selective precipitation of anionic species of As(V) with Cu2+, leaving neutral As(III) in the filtrate. The complexation of As(V) with Cu(II) entails the precipitation as copper arsenate, Cu3(AsO4)2 due to its low solubility product. The copper arsenate precipitate was characterized by XRD and EDS measurements. Optimum conditions for efficient microprecipitation process are; pH: 5 to 6, Cu/As mass ratio: 100, equilibration time: 2–3 min and eluent volume: 2 mL of 0.03 mol L−1 HCl. A fast process time of 2 min is enough for the on-site separation of As(III) and As(V) with the detection limits (LOD) 0.012 and 0.034 μg L−1 respectively. The recoveries were found to be in the range of 98–102%. This simple and fast method was successfully utilized for the on-site separation of As(III) and As(V) in wide variety of water samples collected in and around Kiradalli Tanda village, Karnataka state, India, where severe arsenic-contamination exists in various water bodies.

Enzymatic reaction modulated hydride generation of arsenic for parathion-methyl monitoring in traditional Chinese medicine by atomic fluorescence spectrometry

In the production of traditional Chinese medicine (TCM), the frequent use of organophosphorus pesticides (OPs) will lead to a certain residue and affect the quality of TCM. Therefore, the development of simple and rapid methods for OPs residue monitoring is of great significance for the quality control and evaluation of TCM. In this work, a novel method was developed for the indirect determination of parathion-methyl (PM) residue in TCM by hydride generation atomic fluorescence spectrometry (HG-AFS) based on enzyme modulation. The acetylthiocholine (ATCh) can be hydrolyzed by butyrylcholinesterase (BChE) to produce thiocholine (TCh), which contains − SH that can interact with As(III) and inhibits its HG procedure, further reducing its AFS signal. However, OPs like PM can inhibit the activity of BChE to restore the AFS signal. Therefore, the indirect analysis of PM can be achieved by detecting As(III). A low limit of detection (LOD) of 0.043 μg mL−1 and a relative standard deviation (RSD) of 0.5% were obtained, respectively. The proposed method was successfully applied for the analysis of PM residue in 6 kinds of TCMs commonly used in clinical practice. This present strategy offers a unique alternative for OPs assay with high sensitivity, selectivity, and simple operation.

Determination of Se and Te by hydride generation-inductively coupled plasma mass spectrometry after mixed-acid digestion of tungsten ores

Se and Te in tungsten ores are important parameters for exploring the metallogenetic process of tungsten ores; however, due to their high refractory, low abundance, extreme volatilization, as well as the complex matrix interference during analysis, it is a challenge to accurately determining their concentrations in tungsten ores. This study presents a method of combining hydride generation device with inductively coupled plasma mass spectrometry (HG-ICP-MS) to determine the contents of Se and Te in tungsten ores. As a pre-processing step, tungsten ores were dissolved in the mixture of HF + HNO3 + HClO4 and microwaved for digestion. The analytical results show that the main matrix components (K, Na, Ca, Mg, Fe, Mn and Pb) in tungsten ores have no interference, and the interference of W, Cu, Zn and Bi can be eliminate by adding an appropriate amount of Fe3+. The method was used to test 6 samples with different tungsten concentrations. Compared with the results of hydride generation atomic fluorescence spectrometry (HG-AFS) method, the mean values of HG-ICP-MS method showed a good consistency and the relative mean deviations of Se and Te contents were in the range of −5.2%­ to 6.2% and − 3.8%­ to 3.4%, respectively. The values of Se, Te and Te/Se ratio determined from various geological samples (30 soil and sediment samples, 30 granite samples, 25 poly-metallic sulfide ore samples and 29 tungsten ore samples) highlight their potential prospecting in the metallogenetic process of tungsten ores.

Novel covalent organic frameworks based electrospun composite nanofiber membranes as pipette-tip strong anion exchange sorbent for determination of inorganic arsenic in rice

Novel covalent organic frameworks (COFs) based PAN@TpBD(NH2)2 electrospun composite nanofiber membranes (ECNMs) were fabricated as strong anion exchange sorbent by implementing electrospinning technology. The finished sorbent was characterized, and key parameters of pipette-tip solid phase extraction (PTSPE) procedures were investigated. Inorganic arsenic (iAs) was successfully separated from rice under the optimal precondition conditions, and quantified by hydride generation-atomic fluorescence spectrometry (HG-AFS). This PTSPE-HG-AFS methodology achieved 0.015 μg L-1 detection limit, 4.67 % relative standard deviation, and 86.48～99.11 % recoveries. In this work, preparation and characterization of this novel COFs-based anion exchange sorbent, PAN@TpBD(NH2)2 ECNMs, is described and its suitability for PTSPE applications is demonstrated.

Comparative pharmacokinetics and urinary excretion of arsenic and mercury after oral administration of realgar, cinnabar and AnGongNiuHuang Pill to rats

Realgar- and cinnabar-containing AnGongNiuHuang Pill (AGNHP) is widely used for treating encephalopathy syndrome. However, it raises great safety concerns due to the adverse effects reported by arsenic or mercury poisoning. Although AGNHP has been generally recognized, little is known about the metabolism of arsenic and mercury and their resulting potential health risk in vivo. Thus, comparative pharmacokinetics and urinary excretion of arsenic and mercury were conducted in rats after oral administration of realgar, cinnabar and AGNHP, respectively. The contents of arsenic and mercury in rat blood and urine were determined by hydride-generation atomic fluorescence spectrometry (HG-AFS) after wet digestion. AGNHP significantly reduced the absorption of arsenic in blood and promoted urinary arsenic excretion. Whereas, it increased the blood mercury absorption and reduced urinary mercury excretion. No significant toxicity was observed in the clinical dose range of AGNHP. However, excessive exposure to arsenic and mercury may still pose risks especially by long-term or excessive medication. The results are helpful for the rational clinical applications of realgar- and cinnabar-containing TCMs.

Migration behaviors of arsenic and sulfur from coal during washing process and their release characteristics during combustion process

Two raw coals and their washery products were collected from two coal-washing plants of Ningwu coal field, Shanxi, China. The migration behaviors of sulfur (S) and arsenic (As) during coal washing process were investigated by the microwave digestion method together with hydride generation-atomic fluorescence spectrometry. Based on the checked mass balance of As, a sequential-chemical-extraction method was used to explore the dependence between speciation transformation and release characteristics of S and As during the combustion process of raw coal, cleaned coal, coal gangue, middling coal, or coal slime. The results show that 20%–28% of S and As in raw coal are migrated to the cleaned coal, and 46%–61% of them to gangue. Pearson correlation coefficient identifies that the inorganic minerals in samples control the migration behavior of S and As. Compared with the elements in raw coal, the proportions of organic S and As in cleaned coal increase to 30%–50%, while the inorganic S and As in coal gangue account for more than 90%, which indicates the dependence between the species of S and As in raw coal and its washery products. The relatively large amount of organic S and As in the cleaned coal obviously release together with water and volatile matters below 500 ℃. While the inorganic bonded As and S in gangue mainly release during the decomposition process of pyrite, sulfate and other inorganic minerals between 500 and 1000 ℃, which shows the consistency of S and As release characteristics during combustion of raw coal or washery product. The release rates of S and As from the cleaned coal are the fastest among all samples and the corresponding maximum release ratios are 80%–95% at 300 s and 60%–75% at 200 s, respectively, whilst their release rates from gangue are the slowest and As reaches the maximum release ratio of 40%–45% at 300 s but S doesn’t get to the maximum release ratio even at 600 s. The release rates of S and As from the middling coal or raw coal are between the cleaned coal and gangue. The different release rates of S and As during the sample combustion are mainly depended on their speciation distributions in nature.

Investigation of selenium nutritional status and dietary pattern among children in Kashin-Beck disease endemic areas in Shaanxi Province, China using duplicate portion sampling method.

Selenium deficiency is a primary risk factor of Kashin-Beck disease (KBD). This study aimed to investigate whether children in endemic areas could maintain sufficient selenium intake after termination of selenium supplement administration, and evaluate their comprehensive nutritional status and dietary structure. Duplicate portion sampling combined with a questionnaire was adopted to collect data on categories and quantity of all food ingested in three consecutive days. Occipital hair was also collected to detect selenium content by hydride generation atomic fluorescence spectrometry (HGAFS). CDGSS3.0 software and factor analysis were integrated to assess the children's comprehensive nutritional status and dietary structure. This study included 240 sex-matched (1:1) children aged 7-12years from KBD endemic (n=120) and non-endemic (n=120) areas. Overall, 720 solid food, 720 liquid, and 240 hair samples were collected for selenium determination. The mean selenium level in hair of children in endemic areas (0.38±0.16mg/kg) was significantly lower than that in children in non-endemic areas (0.56±0.28mg/kg, Z=-5.249, p<0.001). The dietary selenium intake of children in endemic areas was 40.0% lower than that in children in non-endemic areas (Z=-9.374, p<0.001). Children in endemic areas consumed significantly less diverse dietary items leading to significantly less intake of multiple nutrients compared to children in non-endemic areas. The dietary selenium intake of most children in endemic areas was less than the recommended amount. The dietary structure of children was undiversified, which limited the intake of multiple nutrients. Therefore, comprehensive nutrition rather than sole selenium intake should be the primary concern in the future.

Arsenic Trioxide Therapy During Pregnancy: ATO and Its Metabolites in Maternal Blood and Amniotic Fluid of Acute Promyelocytic Leukemia Patients.

Acute promyelocytic leukemia (APL) is extremely fatal if treatment is delayed. Management of APL in pregnancy is a challenging situation. Arsenic trioxide (ATO) is successfully applied to treat APL. ATO can be transformed into different arsenic species [arsenite (AsIII), monomethylated arsenic (MMA, consists of MMAIII and MMAV), dimethylated arsenic (DMA, consists of DMAIII and DMAV), and arsenate (AsV)], which produce different toxic effects. Investigating the maternal and fetal exposure to arsenic species is critical in terms of assessing maternal and fetal outcomes, choice of optimal treatment, and making decisions for attempting to preserve the obstetrical and fetal wellbeing. In this study, maternal blood and amniotic fluid (AF) from APL patients treated with ATO in pregnancy and blood samples of non-pregnant patients were collected. Concentrations of inorganic arsenic (iAs, iAs = AsIII+AsV), MMA, and DMA were analyzed by high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry (HPLC–HG–AFS). The difference in arsenic species of plasma between pregnant patients and non-pregnant patients, distribution of arsenic compounds in AF and maternal plasma, and arsenic penetration into AF were explored. The outcomes of pregnant women treated with ATO and their fetus were analyzed. No significant differences in arsenic concentration, percentage, and methylation index [PMI: primary methylation index (MMA/iAs); SMI: secondary methylation index (DMA/MMA)] between pregnant women and non-pregnant women (p > 0.05) were observed. The mean ratios of AF to maternal plasma were as follows: iAs, 2.09; DMA, 1.04; MMA, 0.49; and tAs, 0.98. Abortion rate is higher with the diagnosis at an earlier gestational age, with 0%, 67%, and 100% of pregnancies ending in abortion during the third, second, and first trimester, respectively. The age of the pregnant women, the dose of ATO, and the duration of fetal exposure in utero had no influence on fetal outcomes. All APL women achieved complete remission (CR). Collectively, ATO and its metabolites can easily cross the placenta. Levels and distribution of arsenic species in maternal plasma and AF gave evidence that arsenic species had a different ability to penetrate the placenta into AF (iAs > DMA > MMA) and indicated a relatively high fetal exposure to ATO and its metabolites in utero. Gestational age at diagnosis was more likely to be closely related to fetal outcomes, but had no effects on mother outcomes.

The Status of Selenium and Zinc in the Urine of Children From Endemic Areas of Kashin-Beck Disease Over Three Consecutive Years.

Selenium deficiency is one of the main risk factors for Kashin-Beck disease (KBD). This study aimed to detect the status of selenium and zinc in the urine of children from endemic areas of KBD over three consecutive years and to evaluate whether selenium and zinc levels in children in Shaanxi Province remain normal after stopping selenium supplementation. The samples of urine were collected in consecutive years (2017–2019) to detect selenium content by hydride generation atomic fluorescence spectrometry (HGAFS) and to detect zinc content by atomic absorption spectrophotometry (AAS). Generalized estimation equation (GEE) analysis was integrated to assess the comprehensive nutritional status and dietary structure of children. Data were processed in duplicate and analyzed by SPSS 18.0. This study included 30 X-ray-positive KBD cases and 123 healthy children aged 7–12 years. A total of 424 urine and 137 hair samples were collected over three consecutive years for selenium determination. The mean value of urinary selenium in all subjects was 6.86 μg/l (2017), 8.26 μg/l (2018), and 4.04 μg/l (2019), and the mean value of urinary zinc in all subjects was 0.36 mg/l (2017), 0.39 mg/l (2018), and 0.31 mg/l (2019) for the three consecutive years of 2017–2019. The mean values of urinary selenium were 6.56 and 6.94 μg/l (2017), 8.69 and 8.14 μg/l (2018), and 4.57 and 3.90 μg/l (2019) in the KBD-X and normal groups, respectively; and the mean value of urinary zinc were 0.38 and 0.35 mg/l (2017), 0.41 and 0.39 mg/l (2018), and 0.43 and 0.28 mg/l (2019) in the KBD-X and normal groups, respectively. The mean value of hair selenium in 137 subjects was 275.08 μg/kg and the mean values of hair selenium were 267.48 and 276.61 μg/kg in the KBD-X group and normal group, respectively. The level of selenium/zinc showed a trend of increasing first and then decreasing during the three consecutive years. The level of selenium in all subjects from the endemic areas was lower than normal, which reminds us to monitor the state of KBD constantly and adjust selenium salt supplementation in accordance with the changes in the KBD state.

Discussion on Determination of Trace Germanium in Copper-lead-zinc Ore by Hydride Generation-atomic Fluorescence Spectrometry

Discussion on Determination of Trace Germanium in Copper-lead-zinc Ore by Hydride Generation-atomic Fluorescence Spectrometry

Fast automated method for the direct determination of total antimony in grape juice samples by hydride generation and atomic fluorescence spectrometric detection without external pretreatment

Matrix complexity of fruit juices and their low antimony level requires sensitive, cost-effective instruments, time-consuming and error-prone sample pretreatment methods. Therefore, a flow-batch procedure (HG-FBA-AFS) was developed for the fast and sensitive determination of total inorganic Sb in grape juice samples by hydride generation atomic fluorescence spectrometry. The sample pretreatment, pre-reduction and stibine formation steps run through the mixing chamber. The HCl and NaBH4 concentrations, and carrier gas flowrate were optimized through a Box-Behnken design. The detection limit (LOD) was 20 ng L−1, intra and inter-day precision ranged in 3.0 – 3.5 %, and low errors within (- 2.4 to 6.6 %) for samples containing 1.23 – 4.58 µg L−1 total Sb. Both HG-FBA-AFS and reference method agreed at 95% confidence level. An 87 h−1 sample throughput, and a 1.15 mL total waste per determination attest that HG-FBA-AFS is a fast, and ecofriendly tool for determining Sb in grape juices.

Arsenic-Related Health Risk Assessment of Realgar-Containing NiuHuangJieDu Tablets in Healthy Volunteers Po Administration

Realgar, an arsenic-containing traditional Chinese medicine of As2S2, has significant therapeutic effects for hundreds of years. NiuHuangJieDu tablets (NHJDT) is one of the most commonly prescribed realgar-containing preparations for the treatment of sore throat, swelling, and aching of gums. However, realgar-containing TCMs raise great safety concerns due to the adverse effects reported by arsenic poisoning. In this study, the arsenic-related health risk assessment of NHJDT was conducted in healthy volunteers after single and multiple doses oral administration. Blood, plasma, and urine samples were collected after dosing at predetermined time points or periods. Simple, rapid, and sensitive methods were established for the quantification of total arsenic and arsenic speciation in biological samples. The total arsenic and arsenic speciation were determined by hydride generation-atomic fluorescence spectrometry (HG-AFS) and high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry (HPLC-HG-AFS), respectively. No significant fluctuation of total arsenic was observed in human blood, and no traces of arsenic speciation were found in human plasma. Dimethylarsenic acid was detected as the predominated arsenic species in human urine after dosing. Therapeutic dose administration of NHJDT was relatively safe in single dose for the limited blood arsenic exposure, but long-term medication may still pose health risks due to the accumulation of arsenics in blood and its extremely slow excretion rate. Therefore, arsenic exposure should be carefully monitored during realgar-containing TCM medication, especially for long-term regimen. The results obtained in this study will provide scientific references for the clinical application of realgar and its-containing TCMs.

Multi-Commutated Flow System for Inorganic Selenium Speciation in Infusion Tea Samples by Hydride Generation Atomic Fluorescence Spectrometry

Multi-Commutated Flow System for Inorganic Selenium Speciation in Infusion Tea Samples by Hydride Generation Atomic Fluorescence Spectrometry

Effect of dietary selenium intake on gut microbiota in older population in Enshi region

BackgroundThe microbial ecosystem in the human gut varies between individuals with differences in diet. Selenium is one of most common trace elements in everyday diet, and selenium intake affects the human gut microbiota. We studied the effect of selenium intake on the gut microbiota in regions of Enshi with different distributions of selenium.MethodsOne hundred elderly subjects (>65 years) were recruited from high-selenium and low-selenium areas in Enshi and blood, nail, and fecal specimens were obtained. The selenium contents in these samples were determined in triplicate by hydride generation atomic fluorescence spectrometry. DNA was extracted from fecal specimens and the microbial diversity was analyzed by 16 S RNA.ResultsThe selenium contents in the blood and nails were significantly different between the high- and low-selenium areas, and the composition of the intestinal microbiota, including abundance and extent of intestinal flora, was altered. The function and metabolic pathways of the gut microbiota showed clear differences.ConclusionsAs a trace element in human diet, selenium intake is an important factor that affects the intestinal microbiota and is likely involved in many human diseases. This study provides new clues and ideas for studying the correlation between selenium and human health.

Removal of high-concentration of arsenic in acidic wastewater through zero-valent aluminium powder and characterisation of products

Untreated arsenic in acidic wastewater causes serious environmental pollution. Zero-valent aluminium (ZVAl), without pretreatment, was used in this study to remove arsenic from acidic wastewater. We demonstrated that ZVAl could remove arsenic from acidic wastewater in 30 min with over 99% efficiency. Inductively coupled plasma mass spectrometry (ICP-MS) and hydride-generation atomic fluorescence spectrometry (HG-AFS) were employed to determine the change in ion concentration in acidic wastewater before and after the experiment. The success of using ZVAl for removing arsenic from acidic wastewater was investigated using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy-energy dispersive spectrometer (SEM-EDS), fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TG). Characterisation of the precipitate after the reaction revealed that arsenic removal took place through a complex process which included reduction, surface corrosion, adsorption, co-precipitation, and chemical reactions to form precipitates. These results indicated that ZVAl is a promising material to efficiently remove arsenic from acidic wastewater in an environment friendly manner. The findings of this study will help to develop ZVAl as a method for treating arsenic-contaminated acidic wastewater.

Arsenic contamination caused by roxarsone transformation with spatiotemporal variation of microbial community structure in a column experiment

Arsenic contamination from roxarsone in livestock manure is common, and livestock manure continuously accumulates in the open environment. Evaluations of the environmental processes of As mobilization and transformation are critical for predicting the fate of As compounds after roxarsone degradation. In this study, spatiotemporal variations in As species and microbial community structure were characterized using laboratory column experiments with background soil collected from Yanggu County (northern Shandong Plain, China), a region of intense poultry production. Organic and inorganic arsenic were detected by high-performance liquid chromatography (HPLC) and HPLC with hydride generation atomic fluorescence spectrometry (HPLC-HG-AFS), respectively. High-throughput sequencing technology was used to describe microbial diversity. Results showed that roxarsone was transformed completely within 7 days, and As(Ⅲ) and As(Ⅴ) were the major degradation products. The concentration of As(Ⅲ) was much lower than that of As(Ⅴ). The As(Ⅲ) concentration increased significantly after Day 14, whereas the As(Ⅴ) concentration increased significantly after Day 84, indicating that As(Ⅲ) was initially produced. The microbial community structure changed significantly as roxarsone transformed into various As compounds. A critical and dominant bacterial strain, norank_f__Family_XVⅢ, was found to be related to the degradation of roxarsone into As(Ⅲ). This study improves our understanding of the fate of As species released from poultry litter to soil and groundwater, which is a threat to human health and environment.

Interaction between humic substances and arsenic species simulating environmental conditions

The importance of evaluating how natural organic matter influences the mobility of arsenic species in an ecosystem is an environmental concern. This work aimed to evaluate the interaction between humic substances (HS) and four arsenic species of high toxicity [As(III), As(V), MMA(V), and DMA(V)] (HS-As) under the influence of HS concentration and pH. Next, the complexing capacity (CC) of HS by As(III) was determined in function of pH, ionic strength and co-existing ions. The free arsenic (Asfree) was determined after a tangential flow ultrafiltration procedure by hydride generation atomic fluorescence spectrometry. The better HS-As interactions for As(III) and As(V) at pH 10.5 reached 52% and 61%, respectively. The increase in pH and ionic strength, as well as co-existing ions increased the CC, which reached 1.57 mg of As(III) g−1 HS. We proposed a HS-As interaction model based on the inner and outer binding sites of HS from these results. The inner sites were occupied through hydrogen bonds, Pearson acid-base, hydrophobic, and van der Waals interactions for trivalent arsenic species, while the interactions through the outer sites for pentavalent arsenic species were mostly by hydrogen bonds and electrostatic forces. According to ecotoxicological studies against Artemia salina, the presence of HS decreased the toxicity of As(III) and As(V) as the lethal concentration increased from 5.81 to 8.82 mg L−1 and from 8.82 to 13.37 mg L−1, respectively. From the results through the proposed model, it was possible to successfully understand the interaction dynamic between soil HS and As(III), As(V), MMA(V) and DMA(V) under simulated environmental conditions.