Application of Zn-contaminated soil: Feasibility study on the removal of H2S from hot coal-derived gas

In this study, zinc-contaminated soils were chosen as a candidate material for the removal of hydrogen sulfide (H₂S) from hot coal-derived gas. Laboratory experiments showed that H₂S was decreased to less than 10 ppm when the zinc-contaminated soils were reacted with H₂S. The best removal temperature of H₂S was found to be at 550°C in the operating conditions. In addition to zinc species, free iron oxides in contaminated soils also performed an active species to react with H₂S and enhanced the sulfur capacity. Through the XPS analysis, iron sulfide (FeS) and zinc sulfide (ZnS) were the major products after removal experiments. Regeneration experimental results indicated that the zinc-contaminated soils can be regenerated by pass diluted air and thus be reused on the removal of H₂S for many times.     

Study on degradation process of famotidine hydrochloride in aqueous samples

The kinetics of famotidine (FAM) transformation under the influence of various factors, important from the environmental point of view, was investigated in aqueous solutions. The degradation processes using UV, H₂O₂, UV/H₂O₂, H₂O₂/Fe²⁺, and UV/H₂O₂/Fe²⁺ were studied. Direct photolysis and H₂O₂-assisted photolysis showed a pseudo-first-order kinetics, while the Fenton and the photo-Fenton processes fit second-order kinetics. The provided experiments proved a high resistance of FAM to direct photolysis. Its stability depends highly on the pH of the reaction solutions. The rate of FAM direct photolysis in acidic solutions was almost negligible. The reaction rate of FAM photolysis at pH 8–9 was 3.7 × 10^?3 min^?1 with DT₅₀ about 3 h 7 min. It was found that the presence of H₂O₂ in the reaction environment enhances the rate of photolysis of FAM. The observed rates of reaction were 5.1 × 10^?3 min^?1 and 3.7 × 10^?3 min^?1 in acidic and basic solutions, respectively. The used Fenton systems appeared to be the most efficient in FAM removal. The rate of reaction depends on concentration of Fe²⁺ and H₂O₂. It was observed that the presence of UV-light enhances the reaction rate by two to six times in comparison to the classical Fenton system. Additionally, FAM behavior in natural water under solar irradiation was examined. The irradiation experiments were carried out in batch experiments with simulated sunlight.     

Degradation of bisphenol A by photo-fenton processes

The photo-Fenton reactions, which could yield hydroxyl radicals via the catalytic degradation of H₂O₂ by Fe(II), were focused as one of the abiotic degradation processes of bisphenol A (BPA) in surface waters. At pH 6, in the presence of H₂O₂ only, 32% of BPA was degraded after 120?min of irradiation. However, 97% of BPA was degraded in the presence of both H₂O₂ and Fe(II). Without light irradiation, no BPA degradation was observed even in the presence of Fe(II) and H₂O₂. These results show that photo-Fenton processes are effective in the natural attenuation of BPA in surface water. In addition, the presence of humic acids (HAs), which were of more aliphatic nature, resulted in enhancing BPA degradation via the photo-Fenton processes. Therefore, HAs can be one of the important factors in enhancing the degradation of BPA in surface water via the photo-Fenton processes.     

The fluffy sea anemone Metridium senile in periodically oxygen depleted surroundings

In SCUBA-diving monitored field experiments (Flensburg Fjord, 15 m, 1981) and parallel aquarium tests,the behavior of Metridium senile under anoxic conditions and its oxygen-deficiency resistance were studied. When oxygen is lacking the fluffy sea anemone diminishes body surface, and then, successively, shuts off most energy consuming activities. By means of this strategy, 50% of the tested individuals survived 3 weeks of total anoxia.     

Control of hydrogen sulfide emissions using autotrophic denitrification landfill biocovers: engineering applications

Hydrogen sulfide (H₂S) emitted from construction and demolition waste landfills has received increasing attention. Besides its unpleasant odor, longterm exposure to a very low concentration of H₂S can cause a public health issue. In the case of construction and demolition (C&D) waste landfills, where gas collection systems are not normally required, the generated H₂S is typically not controlled and the number of treatment processes to control H₂S emissions in situ is limited. An attractive alternative may be to use chemically or biologically active landfill covers. A few studies using various types of cover materials to attenuate H₂S emissions demonstrated that H₂S emissions can be effectively reduced. In this study, therefore, the costs and benefits of H₂S-control cover systems including compost, soil amended with lime, fine concrete, and autotrophic denitrification were evaluated. Based on a case-study landfill area of 0.04 km², the estimated H₂S emissions of 80900 kg over the 15-year period and costs of active cover system components (ammonium nitrate fertilizer for autotrophic denitrification cover, lime, fine concrete, and compost), ammonium nitrate fertilizer is the most cost effective, followed by hydrated lime, fine concrete, and yard waste compost. Fine concrete and yard waste compost covers are expensive measures to control H₂S emissions because of the large amount of materials needed to create a cover. Controlling H₂S emissions using fine concrete and compost is less expensive at landfills that provide on-site concrete recovery and composting facilities; however, ammonium nitrate fertilizer or hydrated lime would still be more cost effective applications.     

Decolorisation of Acid Blue 74 by ultraviolet/H<Subscript>2</Subscript>O<Subscript>2</Subscript>

The photodegradation of Acid blue 74 in aqueous solution employing a H₂O₂/ultraviolet system in a photochemical reactor was investigated. The kinetics of decolorization were studied by application of a kinetic model. The results show that the reaction of decolorization followed pseudo-first order kinetics. We demonstrate that there is an optimum H₂O₂ concentration, at which the rate of the decolorization reaction is maximum. Irradiation at 253.7 nm of the dye solution in the presence of H₂O₂ results in complete discoloration after ten minutes of treatment.     

五氧化二钒类Fenton降解邻苯二甲酸二乙酯的机制研究

发展了基于五氧化二钒(V_2O_5)和过氧化氢(H_2O_2)的新型类Fenton体系,探索了此体系产生羟基(·OH)的机制及降解邻苯二甲酸二乙酯(DEP)的效率;并考察了V_2O_5投加量、H_2O_2浓度,以及草酸对DEP降解的影响。结果表明,当V_2O_5投加量为0.1 g·L-1,H_2O_2浓度为2.0 mmol·L-1,反应24 h后,对DEP(25 mg·L-1)的降解率可达61.1%,增加或降低V_2O_5投加量和H_2O_2浓度均不利于DEP的降解。利用电子顺磁共振技术(Electron Paramagnetic Resonance,EPR)耦合5,5-二甲基-1-吡咯啉氮氧化物(DMPO)为捕获剂对反应体系中的主导自由基进行鉴定,发现·OH是体系降解DEP的主要活性物种,利用苯甲酸作为探针分子实现了·OH的间接定量,并初步推测了V_2O_5活化H_2O_2的过程。     

Simultaneous measurements of arsenic and sulfide using diffusive gradients in thin films technique (DGT)

Diffusive gradients in thin films technique (DGT) is a dynamically passive sampling technique which has been applied increasingly to the environmental monitoring field. In the preliminary period, the DGT with zirconium hydroxide-silver iodide as the binding phase (ZrO-AgI DGT) has been developed for the determination of sulfide (S(II)). On this basis, this paper developed its determination method for inorganic arsenite (As(III)) to further realize the simultaneous and high-resolution measurements of labile inorganic As and S(II) in sediments. ZrO-AgI binding gel had a strong ability in adsorbing and fixing As(III), showing a linear increase in the initial 12.5 min. After saturation of S(II) on ZrO-AgI binding gel, the adsorption rate and adsorption capacity of As(III) reduced by 8 and 14%, respectively. A stable elution rate (89.1 ± 2.2%) was obtained by extraction of As(III) on the binding gel using a mixture solution of 1.0 M NaOH and 1.0 M H₂O₂ (1:1). The DGT capacity of As(III) determined by the ZrO-AgI DGT was 23.6 μg cm^?2. DGT uptakes of As(III) were independent of pH (4.0–9.0) and ionic strength (0.01–100 mM), and they did not interfere with each other during the uptake process. Simultaneous measurements of labile As and S(II) in four sediment cores of Taihu Lake (China) with ZrO-AgI DGT showed that they had similarly vertical distributions in the top 16-mm layer in one core and in the whole profile up to the 35 mm depth in two cores. It likely reflected a simultaneous release of As and S(II) in sediments by synchronous reduction of As-hosted oxidized iron and sulfate, respectively. The simultaneous decreases of labile As and S(II) from their co-precipitation (e.g., As₂S₃) were not obvious in deeper sediment layer through the measurement with ZrO-AgI DGT.     

The effect of preparation conditions of Pt/Al2O3 on its catalytic performance for the H2-SCR in the presence of oxygen

Selective catalytic reduction of NO _x by H₂ in the presence of oxygen has been investigated over Pt/ Al₂O₃ catalysts pre-treated under different conditions. Catalyst preparation conditions exert significant influence on the catalytic performance, and the catalyst pre-treated by H₂ or H₂ then followed by O₂ is much more active than that pre-treated by air. The higher surface area and the presence of metallic Pt over Pt/Al₂O₃ pre-treated by H₂ or pretreated by H₂ then followed by O₂ can contribute to the formation of NO₂, which then promotes the reaction to proceed at low temperatures.     

碳纳米管影响无机砷(As(III)和As(V))对大型蚤毒性的研究：特定砷形态的作用

作为一种新兴的纳米材料,羟基多壁碳纳米管(OH-MWCNTs)可能与其他污染物在水环境中共存,并进一步影响它们的毒性、输移和归趋。因此,评价碳纳米管存在下砷的毒性变化需要得到更多的关注。该试验探索了在不同pH值条件下,OH-MWCNTs诱导砷(As(III)和As(V))对水生生物大型蚤的毒性变化的潜在机制。发现了H₂AsO₃^-和H₂AsO₄^-是对大型蚤毒性最大的As(III)和As(V)。比较As(III)和As(V)的结果,发现pH值是影响砷毒性最重要的因素。此外,OH-MWCNTs影响砷对大型蚤毒性的结果表明,OH-MWCNTs的存在可以提高砷的毒性。通过吸附实验进一步研究了砷与OH-MWCNTs的相互作用。OH-MWCNTs 对As(V)吸附容量高于As(III)。总而言之, OH-MWCNTs对某些形态砷的吸附是解释砷毒性增强的可靠证据。
精选自Xinghao Wang, Ruijuan Qu, Ahmed A. Allam, Jamaan Ajarem, Zhongbo Wei, Zuoyao Wang. Impact of carbon nanotubes on the toxicity of inorganic arsenic [As(III) and As(V)] to Daphnia magna: the role of the certain arsenic species. Environmental Toxicology and Chemistry: Volume 35, Issue 7, pages 1852–1859, July 2016. DOI: 10.1002/etc.3340
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.3340/full
     

Toxic effect assessment of aminotetrazoles and high-energetic azotetrazole salts on soil microbial respiration

The influence of energetic heterocyclic high-nitrogen salts on microbial activity in soil enrichment was investigated. 5-Aminotetrazole, a sodium salt of 5-aminotetrazole, ammonium azotetrazolate, sodium azotetrazolate, guanidinium azotetrazolate, triaminoguanidine azotetrazolate and triaminoguanidine hydrochloride were examined. Respiration tests determined the amount and rate of production of CO₂, H₂ and H₂S from microbial activity. Aminotetrazoles, triaminoguanidine azotetrazolate and triaminoguanidine hydrochloride substantially reduced the amount and rate of microbial CO₂ production. The total amount of CO₂ produced in the soil enrichments was affected by the cation from the azotetrazole salt, whereas the azotetrazolate anion did not seem to inhibit microbial CO₂ production. In contrast, all applied compounds stopped the production of H₂S completely and modified the rate of H₂ production in the cultures compared with the control. The influence of ammonium azotetrazolate and sodium azotetrazolate on the activity of isolated sulfate-reducing bacteria was also determined. The compounds did not have bactericidal activity towards sulfate-reducing bacteria, but the compounds decreased the amount of H₂S produced or slowed the growth of these bacteria in comparison with the control.     

Degradation of trace nitrobenzene in water by microwave-enhanced H2O2-based process

To evaluate possible use of microwave-enhanced H₂O₂-based (MW/H₂O₂) process to degrade trace nitrobenzene (NB) in water, a series of batch experiments were conducted. The results showed that 2450MHz microwave irradiation significantly enhanced oxidative decomposition of nitrobenzene (NB) in a H₂O₂ system. About 90% NB was degraded by the MW/ H₂O₂ process in 30 min. Moreover, the MW/ H₂O₂ process could enhanced the oxidative degradation of NB even at relatively low temperature (50°C). When the initial concentration of NB was 300??g/L, the optimum ratio of H₂O₂ to NB and MW power were 70 and 300W respectively. The presence of humic acid significantly increased H₂O₂ dosage. The ultraviolet absorbance at 254 nm (UV₂₅₄) indicated degradation of NB was stepwise and some intermediates were produced. The gas chromatography-mass spectrometric (GC-MS) analysis showed that main intermediates were nitrophenolic and carbonyl compounds.     

Physiological adaptations of the invasive cordgrass<Emphasis Type="Italic"> Spartina anglica</Emphasis> to reducing sediments: rhizome metabolic gas fluxes and enhanced O<Subscript>2</Subscript> and H<Subscript>2</Subscript>S transport

Cordgrasses of the genus Spartina form dense monospecific stands worldwide, profoundly influencing the ecology of estuaries. One species, Spartina anglica, originated by allopolyploidy in the 1800s and has been particularly prolific as an invasive species worldwide. S. anglica tolerates low-lying estuarine mudflats that its progenitor species and other coastal halophytes cannot. However, very little is known of the physiology of S. anglica. In the present study, an automated flow-through respirometry system was used to quantify metabolic gas fluxes (O₂, H₂S, CO₂, and NH₃) of S. anglica rhizomes. Enhanced physiological mechanisms to transport O₂ and H₂S in both directions between the rhizosphere and the atmosphere were exhibited by S. anglica, but not by the native North American species S. alterniflora. These results suggest that tolerance of anoxia and H₂S may assist S. anglica in colonizing extensively flooded environments. Enhanced sediment oxygenation by S. anglica may be potentially useful for phytoremediation of contaminated sediments, since microbial degradation of organic pollutants is often limited by O₂ availability.     

A comprehensive model to estimate the simultaneous release of acidic and basic gaseous pollutants from swine slurry under different scenarios

Swine slurry is a source of atmospheric pollutants. Emissions of basic and acidic compounds from slurry are largely dependent on the surface pH. In a storage system, the pH at the surface layers changes over time due to the volatilisation of ammonia (NH₃), carbon dioxide (CO₂) and acetic acid (HAc). In this article, a comprehensive gas emission–pH (GE–pH) coupled model is proposed to describe the simultaneous release of acidic and basic gaseous pollutants from swine slurry. The model was applied to describe the release of NH₃, CO₂, HAc and hydrogen sulphide (H₂S) from standard slurries stored in animal houses, outside storage tanks and lagoons. The modelled results agreed well with values reported in the literature and could be reasonably interpreted. The key parameters affecting the release of gases were: initial pH, initial concentration of total ammonium nitrogen and inorganic carbon, slurry temperature and air velocity. This study suggests that future modelling studies on gas emissions from animal slurry should consider the concentration of inorganic carbon and the frequency in which the slurry surface is mixed or altered, because they affect the surface pH and the release of gaseous pollutants from slurry.     

Plasmatic resistance and rate of respiration and photosynthesis of Zostera marina at different salinities and temperatures

Zostera marina L. was studied at the Izembek Lagoon, Alaska Peninsula. Two morphologically different forms, tidepool and subtidal, can be distinguished. Both show a high tolerance to different salinities and temperatures. The plasmatic resistance was found in a range of distilled H₂O up to 3.0 seawater (24 h) and between-6° and 34°C (12 h). Within these resistance limits, the photosynthesis, which has its maximum in normal (1.0) seawater, decreases nearly to zero not only in distilled H₂O but even in 2.0 seawater, and increases with the temperature in the tidepool form up to 35°C, but in the subtidal form up to 30°C only. At higher temperatures photosynthesis declines sharply in both forms. Respiration has its minimum in distilled H₂O and at 0°C and increases with increasing salinity and temperature.Dedicated to Prof. Dr. Dr. h. c. mult. K. Mothes, Halle, Germany (DDR) on the occasion of his 70th birthday.     

Marine food-web analysis: An experimental study of demersal zooplankton using isotopically labelled prey species

Short-term incubations in seawater containing H¹⁴CO₃ ^- or ³H₂O in place of the naturally predominant isotopes can yield highly radioactive preparations of living phytoplankton or zooplankton. Subsequent in situ incubation of these labelled organisms with the community from which they were taken results in the rapid transfer of radioisotope to those species which prey upon them. This technique has been employed to map a portion of a marine food web involving demersal zooplankton; experiments were conducted in summer and autumn on a coral reef and in a subtropical estuary. Similar results were obtained from these initial experiments at each study site during both seasons. Prey supplied as zooplankton (124 to 410 m nominal diameter), which consisted mainly of Oithona oculata, was fed upon by zooplankton size classes ranging from 410 to 850 m and containing amphipods, ostracods, cumaceans and polychaetes. In experiments employing labelled phytoplankton as prey a wide size spectrum was used (10 to 106 m) in order to include representative samples of most of the available planktonic autotrophs as estimated by primary production measurements. In two separate experiments, only 7 out of 63 samples evidenced grazing of phytoplankton by demersal zooplankters. In contrast, labelled diatom auxospores, employed in one experiment as they constituted the most numerically abundant species in the water column, were found to be grazed upon in nearly half the samples examined.     

Inhibitory effect of the iron chelator desferrioxamine (Desferal) on the generation of activated oxygen species by Chattonella marina

Recent studies demonstrated that the toxic red tide phytoplankton Chattonella spp. produce activated oxygen species such as superoxide anion (O ₂ ^- ), hydrogen peroxide (H₂O₂), and hydroxyl radicals (·OH), which may be responsible for the toxicity of this flagellate. However, the mechanism behind the production of these oxygen radicals and H₂O₂ by Chattonella spp. is largely unknown, and the physiological significance of activated oxygen species for Chattonella spp. is also unclear. In the present study, we investigated the involvement of iron in the generation of O ₂ ^- and H₂O₂ by C. marina. The generation of O ₂ ^- by C. marina was related to the growth phase; the highest rate of O ₂ ^- production was observed during the exponential growth phase. However, no such increase during the exponential growth phase was observed in C. marina growing in an iron-deficient medium, even though the growth of C. marina was not significantly affected by iron-deficiency during the first 4 d. In addition, the iron chelator desferrioxamine (Desferal) strongly inhibited the generation of both O ₂ ^- and H₂O₂ by C. marina in a concentration-dependent manner. The growth of C. marina was also inhibited by Desferal. Furthermore, in the presence of 500 M Desferal, C. marina-induced growth inhibition of the marine bacteria Vibrio alginolyticus was almost completely abolished. These results suggest that iron is required for the generation of activated oxygen species by C. marina, as well as for its own growth.     

Rate evaluation of marble damage by SO2-acidity in the vicinity of stacks

A laboratory modelling for the assessment of damage to marble by the SO₂-acidity in the vicinity of stacks has been devised. The modelling is based on the role of metal oxide particulates (also emitted by smoke-stacks) which catalytically convert SO₂ to SO₃ forming H₂SO₄ (in presence of water), which has an excessively high selectivity, compared with HNO₃, for corroding marble. The requisites of the modelling are: (1) determination of composition of the marble, (2) immersion of samples of marble blocks (after measurement of surface areas) in H₂SO₄ solutions of known concentrations, maintaining pH and temperature at their initial values, (3) determination of concentrations of Ca and Mg (major components of marble) in the leachate, and thereby evaluating the mass loss of the marble, in terms of mg marble cm^–2 day^–1, for each level of H₂S0₄ concentration, (4) application of derived data for evaluation of duration (in years) for the decay of 1 cm thickness of marble block by the process of surface corrosion. From the modelling, it was found that the duration for the damage of 1 cm thickness of the marble sample used here by SO₂ acidities of 1, 5, 10, 50 and 100 ppm are 83.01, 69.02, 31.24, 8.19 and 4.31 years respectively.     

Removal of organophosphorus pesticides from water by electrogenerated Fenton's reagent

Aqueous solutions of organophosphorus pesticides were completely mineralized via in-situ generated hydroxyl radicals (HO^·) by the Electro-Fenton process. Formation of Fenton's reagent (H₂O₂, Fe²⁺) was carried out by simultaneous reduction of O₂ and Fe³⁺ on carbon cathode in acidic medium. The electrochemistry combined with Fenton's reagent provides an excellent way to continuously produce the hydroxyl radical, a powerful oxidant. We demonstrate the efficiency of the Electro-Fenton process to degrade three organophosphorus insecticides: malathion, parathion ethyl and tetra-ethyl-pyrophosphate (TEPP). Degradation kinetics and removals of chemical oxygen demand (COD) have been investigated. Here we show that the mineralization efficiency was over 80% for three organophosphorus pesticides.     

Use of the “Acetylene blockage” technique for assaying denitrification in a salt marsh

The acetylene blockage technique was evaluated for measurement of denitrification in salt-marsh sediments (near Halifax, Nova Scotia, Canada). N₂O in the gas phase of closed Spartina alterniflora marsh-sediment systems was analyzed with use of a thermal conductivity gas chromatograph sensitive to approximately 0.1 nmoles ml^-1 gas. No N₂O was detected for unfertilized sediment samples taken through the growing season and incubated in sealed buckets with 10% C₂H₂. For sediment samples amended with nitrate and for enrichments, initial rates of N₂O evolution were higher in the presence of 10% C₂H₂ than in the absence of C₂H₂, but after longterm incubation N₂O was consumed in some samples containing C₂H₂ as well as in samples without C₂H₂. In addition, total gaseous nitrogen (N₂ and N₂O) production in the absence of C₂H₂ was higher than in the presence of C₂H₂. Acetylene appears to be an inconsistent inhibitor of N₂O reduction in salt-marsh sediments. The usefulness of the acetylene-denitrification technique in this habitat is, therefore, questionable.