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SCIENCE OF THE TOTAL ENVIRONMENT · 2020 · IF 6.551

Reducing phenanthrene uptake and translocation, and accumulation in the seeds by overexpressing OsNRT2.3b in rice

Xiaowen Wang,Ajay Jain,Xu Huang,Xiaoxia Lan,Li Xu,Gengmao Zhao,Xin Cong,Zhantian Zhang,Xiaorong Fan,Feng Hu

The uptake and accumulation of polycyclic aromatic hydrocarbons (PAHs) in crops have gained much attention due to their toxicity to humans. Nitrogen (N) is an essential element for plant growth and has also been implicated in the acquisition and acropetal translocation of PAHs. OsNRT2 . 3b encodes a nitrate (NO 3 − ) transporter that is involved in the acquisition and mobilization of N in rice. Here, we investigated whether overexpression of OsNRT2 . 3b would exert any mitigating influence on the uptake and translocation of phenanthrene (Phe, a model PAH) in transgenic rice ( Oryza sativa ). The wild-type seedlings exhibited a reduction in plant height, primary root length, and shoot biomass when grown hydroponically in a medium supplemented with Phe. Acquisition of Phe by the roots and its subsequent translocation to shoots increased concomitantly with an increase in Phe concentration in the medium and duration of the treatment. OsNRT2 . 3b -overexpressing lines (Ox-6 and Ox-8) were generated independently. Compared with the wild-type, the concentration of Phe in Ox-6 and Ox-8 were significantly lower in the roots (47%–54%) and shoots (22%–31%) grown hydroponically with Phe (1 mg/L). Further, the wild-type and Ox lines were grown to maturity in a pot soil under Phe conditions and the concentrations of Phe and total N were assayed in the culms and flag leaves. Compared with the wild-type, in Ox lines the concentration of total N significantly increased in the culms (288%–366%) and flag leaves (12%–25%), while that of Phe significantly reduced in the culms (25%–28%) and flag leaves (18%–21%). The results revealed an antagonistic correlation between the concentration of total N and Phe. The concentration of Phe was also significantly lower (29%–38%) in the seeds of Ox lines than the wild-type. The study highlighted the efficacy of overexpressing OsNRT2 . 3b in mitigating the Phe toxicity by attenuating its acquisition, mobilization, and allocation to the seeds.

CAS / MDL: 85-01-8
研究领域: 植物学 · 环境科学 · 遗传学
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ADSORPTION SCIENCE & TECHNOLOGY · 2018 · IF 0.609

Steel slag as low-cost adsorbent for the removal of phenanthrene and naphthalene

Liyun Yang,Xiaoming Qian,Zhi Wang,Yuan Li,Hao Bai,Hong Li

This study investigates the removal effectiveness and characteristics of phenanthrene and naphthalene using low-cost steel slag with batch experiments. The adsorption characteristics of steel slag were measured and analysed using X-ray fluorescence, X-ray diffraction, and Fourier transform infrared spectroscopy. The batch experiments investigated the effect of the time gradient, pH, and steel slag dosage gradient on the adsorption of the steel slag. The results show that with time and dosage of steel slag increased, the adsorption capacity of phenanthrene and naphthalene increased and gradually became balanced, but pH had no obvious effect on the adsorption of phenanthrene and naphthalene. The Langmuir isotherm model best describes the phenanthrene and naphthalene removal by the steel slag, which shows the adsorption occurring in a monolayer. The maximum adsorption capacity of the steel slag to phenanthrene and naphthalene is 0.043 and 0.041 mg/g, respectively. A pseudo-first-order kinetic model can better represent the adsorption of phenanthrene and naphthalene by steel slag. The research demonstrates that the steel slag has a certain adsorption capacity for phenanthrene and naphthalene.

CAS / MDL: 91-20-3 85-01-8
研究领域: 环境科学 · 化学工程
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ENVIRONMENTAL RESEARCH · 2021 · IF 6.498

Co-adsorption of As(III) and phenanthrene by schwertmannite and Fenton-like regeneration of spent schwertmannite to realize phenanthrene degradation and As(III) oxidation

Xiaoqing Meng,Xiaomeng Wang,Chunmei Zhang,Su Yan,Guanyu Zheng,Lixiang Zhou

Co-contamination of arsenic and polycyclic aromatic hydrocarbons (PAHs) in groundwater is frequently reported, and it is thus necessary to develop efficient techniques to tackle this problem. Here, we evaluated the feasibility of utilizing schwertmannite to co-adsorb As(III) and phenanthrene from water solution and regenerating spent schwertmannite via a heterogeneous Fenton-like reaction to degrade adsorbed phenanthrene and meanwhile oxidize adsorbed As(III). The results suggested that schwertmannite with a hedgehog-like morphology was superior to that with a smooth surface for the adsorption removal of As(III) or phenanthrene because of the much higher BET surface area and hydroxyl proportion of the former one, and schwertmannite formed at 72 h incubation effectively co-adsorbed As(III) and phenanthrene from water solution. The adsorption of As(III) and phenanthrene on schwertmannite did not interfere with each other, while the acidic initial solution pH delayed the adsorption of As(III) on schwertmannite but enhanced the adsorption capacity for phenanthrene. The adsorption of As(III) on schwertmannite mainly involved its exchange with SO 4 2− (outer-sphere or inner-sphere) and its complexation with iron hydroxyl surface groups, and phenanthrene adsorption mainly occurred through cation-π bonding and OH-π interaction. During the adsorption-regeneration processes, schwertmannite adsorbed As(III) and phenanthrene firstly, and then it can be successfully regenerated via Fenton-like reaction catalyzed by itself to effectively degrade the adsorbed phenanthrene and meanwhile oxidize the adsorbed As(III) to As(V). Therefore, schwertmanite is an outstanding environmental adsorbent to decontaminate As(III) and phenanthrene co-existing in groundwater.

CAS / MDL: 85-01-8
研究领域: 环境科学 · 化学
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JOURNAL OF CHEMICAL THERMODYNAMICS · 2018 · IF 2.631

Ternary phase diagram of phenanthrene and carbazole in different solvents and its application in the separation of them

Suping Ding,Qiuxiang Yin,Wei Du,Xiaowei Sun,Guiping Li,Yafei Mao,Hongxun Hao

The separation of phenanthrene (PHE) and carbazole (CAR) has been a tough job since the formation of solid solutions. Development of new separation strategy for PHE-CAR mixture highly depends on their phase equilibrium behaviour. In this work, ternary phase diagrams of phenanthrene (PHE) and carbazole (CAR) in dimethylformamide (DMF), acetone, acetonitrile (MeCN) and toluene at T  = 308.15 K under normal atmosphere were determined through wet residue method. It was found that PHE-rich solid solution α was formed in the particular composition range of PHE-end. On the contrary, no CAR-rich solid solution was formed in CAR-end. These results were further verified through powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC). Based on the ternary phase diagrams, a difference coefficient of solubility ( Ds ) was put forward to assist screening and evaluation of solvents for solution crystallization. Among the four tested solvents, toluene is the most suitable one for separating PHE-CAR mixture.

研究领域: 化学工程 · 材料科学
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SCIENCE OF THE TOTAL ENVIRONMENT · 2017 · IF 4.9

Removal of phenanthrene from coastal waters by green tide algae Ulva prolifera

Cui Zhang,Jian Lu,Jun Wu,Yongming Luo

Ulva prolifera ( U. prolifera ) has been frequently involved in terrible algal proliferation in coastal areas. Although it is known to be associated with green tide, its contribution to the natural attenuation of the polycyclic aromatic hydrocarbons (PAHs) in seawater has not been evaluated. In this study, the removal of phenanthrene using U. prolifera collected from coastal water with green tide blooming was investigated. The results showed that phenanthrene could be removed efficiently in the presence of both the live and heat-killed U. prolifera . The phenanthrene concentrations of the live algae treatment decreased smoothly from 10.00 to 0.80   μg   L −   1 through the whole process, while those of the heat-killed algae treatment decreased sharply from 10.0 to 2.71   μg   L −   1 in one day and kept constantly after that. The in situ monitoring and visualizing using laser confocal scanning microscopy (LCSM) confirmed the accumulation of phenanthrene in U. prolifera . The increase in nutrient and temperature led to the increase of phenanthrene removal rate, while the salinity had less influence on the removal of phenanthrene. The removal efficiency by U. prolifera had a good linear relationship with phenanthrene initial concentration (r 2   =   0.999) even at 100   μg   L −   1 which was higher than its environmentally relevant concentrations. High removal efficiency (91.3%) was observed when the initial phenanthrene concentration was set at environmental relevant concentration (5   μg   L −   1 ). Results of this study demonstrate a potential new natural attenuation process for typical PAHs in coastal water during the outbreak of green tide. These findings indicate that the outbreak of harmful green tide algae may bring positive environmental benefits in the terms of the removal of harmful organic pollutants from coastal waters.

CAS / MDL: 85-01-8
研究领域: 环境科学 · 海洋生物学
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SCIENCE OF THE TOTAL ENVIRONMENT · 2023 · IF 9.8

A novel eco-friendly strategy for removing phenanthrene from groundwater: Synergism of nanobubbles and rhamnolipid

Wang Kai Tong,Chaomeng Dai,Jiajun Hu,Jixiang Li,Min-tian Gao,Xueji You,Xin Ru Feng,Zhi Li,Lang Zhou,Yalei Zhang,Xiaoying Lai,Long Kahon,Rongbing Fu

Nanobubbles (NBs), given their unique properties, could theoretically be paired with rhamnolipids (RL) to tackle polycyclic aromatic hydrocarbon contamination in groundwater. This approach may overcome the limitations of traditional surfactants, such as high toxicity and low efficiency. In this study, the remediation efficiency of RL, with or without NBs, was assessed through soil column experiments (soil contaminated with phenanthrene). Through the analysis of the two-site non-equilibrium diffusion model, there was a synergistic effect between NBs and RL. The introduction of NBs led to a reduction of up to 24.3 % in the total removal time of phenanthrene . The direct reason for this was that with NBs, the retardation factor of RL was reduced by 1.9 % to 15.4 %, which accelerated the solute replacement of RL. The reasons for this synergy were multifaceted. Detailed analysis reveals that NBs improve RL's colloidal stability, increase its absolute zeta potential , and reduce its soil adsorption capacity by 13.3 %–19.9 %. Furthermore, NBs and their interaction with RL substantially diminish the surface tension, contact angle, and dynamic viscosity of the leaching solution. These changes in surface thermodynamic and rheological properties significantly enhance the migration efficiency of the eluent. The research outcomes facilitate a thorough comprehension of NBs' attributes and their relevant applications, and propose an eco-friendly method to improve the efficiency of surfactant remediation.

CAS / MDL: 85-01-8 14808-60-7
研究领域: 环境科学 · 生态学
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ENVIRONMENTAL TECHNOLOGY · 2019 · IF 1.918

Enhanced phenanthrene removal in aqueous solution using modified biochar supported nano zero-valent iron

Hongwei Wu,Qiyan Feng,Hong Yang,Ping Lu,Bo Gao,Amir Alansari

The present work investigated the removal behaviour of phenanthrene (PHE) by nano zero-valent iron immobilized on alkali modified biochar (nZVI/MB). Batch studies showed that nZVI/MB enhanced PHE removal by 4.9 times that of the nZVI and 1.2 times that of modified biochar (MB) alone, due to the greater surface area and the inhibited aggregation of nZVI on the surface of MB. Transmission electron microscopy images revealed that the spherical nZVI particulates with an average diameter of 32 nm uniformly dispersed on the surface of MB. The PHE removal fitted well with the pseudo-second-order model (R2>0.98) was an endothermic and spontaneous process. The forces of π–π interaction, hydrophobic interaction and reduction of supported nZVI were contributed to PHE removal process. In addition, the PHE degradation products in solution were determined by gas chromatograph-mass spectrometer after reaction with nZVI/MB.

CAS / MDL: 85-01-8
研究领域: 环境科学 · 材料科学
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JOURNAL OF APPLIED MICROBIOLOGY · 2016 ·Vol. 121 ·期 6 ·1616-1626 · IF 2.156

Biodegradation of phenanthrene by Rhizobium petrolearium SL‐1

Huang X.,Shi J.,Cui C.,Yin H.,Zhang R.,Ma X.,Zhang X.

AimsWe aimed to investigate the phenanthrene degradation characteristics and possible phenanthrene degradation pathways of Rhizobium petrolearium SL‐1.Methods and ResultsUsing high‐performance liquid chromatography (HPLC), UV‐visible and gas chromatography‐mass spectrometry (GC‐MS) analysis, the phenanthrene‐degrading properties and metabolites of Rh. petrolearium SL‐1 were analysed, and then combined with genome‐based analysis to elucidate the possible biodegradation pathway of phenanthrene in Rh. petrolearium SL‐1. The results of the analyses showed that phenanthrene (100 mg l−1) was completely degraded by strain SL‐1 at 35°C, 0·02% salinity and pH 9·0 within 3 days. A wide range of polycyclic aromatic hydrocarbons, including naphthalene, fluorene, anthracene and pyrene, could also be degraded by this strain.ConclusionsBased on the identified metabolites, the utilization of probable intermediates and the presence of putative phenanthrene catabolic genes, we concluded that phenanthrene was degraded via two different routes, namely the ‘naphthalene’ and the ‘phthalic acid’ routes.Significance and Impact of the StudyFor the first time, this study shows the degradation pathway of phenanthrene by a Rhizobium strain. Because of its excellent stress resistance, metabolic versatility, high degradation efficiency and potential application in phytoremediation, Rh. petrolearium SL‐1 is a potential candidate for the bioremediation of polycyclic aromatic hydrocarbons‐contaminated areas.

研究领域: 环境微生物学 · 分子生物学 · 生态学
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CHEMOSPHERE · 2024 · IF 8.1

Design and construction of an artificial labor-division consortium for phenanthrene degradation with three-functional modules

Yiyang Liu,Ruolin Qin,Xiaoqiang Jia

Polycyclic Aromatic Hydrocarbons (PAHs) are highly toxic organic pollutants. Phenanthrene often serves as a model compound for studying PAHs biodegradation. In this work, we firstly engineered Escherichia coli M01 containing seven phenanthrene degradation genes and combined it with existing engineered strains E. coli M2 and M3 to form an artificial three-bacteria consortium, named M0123, which exhibited a degradation ratio of 64.66% for 100 mg/L of phenanthrene over 8 days. Subsequently, we constructed engineered Pseudomonas putida KTRL02 which could produce 928.49 mg/L rhamnolipids and integrated it with M0123, forming a four-bacteria consortium with an impressive 81.62% phenanthrene degradation ratio. Assessment of extracellular adenosine levels during the degradation process indicated high cellular energy demand in the four-bacteria consortium. Then, we introduced Bacillus subtilis RH33, a riboflavin-producing strain, as an energy-supplying bacterium, to create a five-bacteria consortium, which exhibited an 88.19% degradation ratio for phenanthrene. The NADH/NAD + ratio in the five-bacteria consortium during the degradation process was monitored, which was consistently higher than that of the four-bacteria consortium over the eight-day period, indicating a higher overall intracellular reduction capacity. Furthermore, the five-bacteria consortium displayed good tolerance to phenanthrene, even achieving a degradation ratio of 79.38% for 500 mg/L of phenanthrene. This study demonstrates that designing and constructing artificial consortia from the functional perspective and various angles can effectively enhance the degradation of phenanthrene after the addition of the energy-supplying bacterium. This study demonstrates that designing and constructing artificial labor-division consortia from the functional perspective and various angles can effectively enhance the degradation of phenanthrene.

CAS / MDL: 85-01-8 129-00-0
研究领域: 环境生物学 · 微生物工程 · 生物化学
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JOURNAL OF CHEMICAL AND ENGINEERING DATA · 2015 · IF 2.037

Formation of Solid Solution and Ternary Phase Diagrams of Anthracene and Phenanthrene in Different Organic Solvents

Suping Ding,Qiuxiang Yin,Wei Du,Xiaowei Sun,Baohong Hou,Meijing Zhang,Zhao Wang

Crash cooling crystallization of different anthracene (ANT) and phenanthrene (PHE) mixtures in toluene, xylene, and N,N-dimethylformamide (DMF) was investigated. The crystals obtained were identified by powder X-ray diffraction, differential scanning calorimetry, and high-performance liquid chromatography. To verify the formation of different solid solutions, ternary phase diagrams of ANT and PHE in toluene, xylene, and DMF at 308.15 K and 0.1 MPa were determined through experiments. Two solid solutions, α and β, respectively, formed at PHE-rich and ANT-rich ends but coexisted in the middle section of the composition. The effect of solvent and separation process optimization of ANT and PHE were further investigated based on the ternary phase diagrams.

研究领域: 化学 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2022 ·Vol. 29 ·期 41 ·62272-62280 · IF 5.19

The association between phenanthrene and nutrients uptake in lotus cultivar 'Zhongguo Hong Beijing'

Wang Xiaowen,Wang Yanjie,Zhao Xiaoyan,Chen Bingqiong,Kong Nannan,Shangguan Lingfei,Zhang Xiaobin,Xu Yingchun,Hu Feng

It has been well documented that polycyclic aromatic hydrocarbon (PAHs) can be taken up from the environment by the plants and translocated into the shoots. However, the mechanisms underlying this process are poorly understood. Nelumbo nucifera L. (lotus) is a highly ornamental aquatic plant known to possess strong phytoremediation capability. In the present study, the association between phenanthrene (Phe) and nutrients, including nitrogen (N) and phosphorus (P), in lotus was investigated. Over 2 years, all eight lotus cultivars tested accumulated Phe to various degrees when grown in PAH-polluted sediment (0.46 mg/kg Phe). Cluster analysis showed N. nucifera 'Zhongguo Hong Beijing (ZHB)' was the one with the highest Phe levels in the leaves and petals in 2 years. The Phe concentrations in the tissues of 'ZHB' were 3.14 mg/kg and 1.63 mg/kg on average in the first and second year, respectively. Interestingly, 'ZHB' was also the cultivar with the lowest N and P levels considering 2 years and tissues. Hydroponic studies further revealed a negative association between the concentrations of Phe and those of N and P in the aerial tissues under 0.5 and 1.0 mg/L Phe treatments in 'ZHB'. Furthermore, the significant reductions of the roots number (72.6%), longest root length (75.8%), and petiolar height (34.6%) in 'ZHB' seedlings exposed to 1.0 mg/L Phe were observed, indicating that Phe retarded the growth of lotus. These results provide a new understanding of the accumulation of Phe in plants and the association with nutrients and enrich the basis of phytoremediation to the contaminated environment.

研究领域: 环境科学 · 植物学
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KOREAN JOURNAL OF CHEMICAL ENGINEERING · 2015 ·Vol. 32 ·期 6 ·1129-1136 · IF 1.166

Adsorption behavior of phenanthrene onto coal-based activated carbon prepared by microwave activation

Xiao Xuemin,Tian Fei,Yan Yujun,Wu Zhilin,Wu Zhansheng,Cravotto Giancarlo

Coal-based activated carbon (CAC) was prepared from coal produced in Xinjiang of China by microwave activation. CAC was characterized and used as an adsorbent for phenanthrene adsorption. The effects of temperature, adsorption time, CAC amount, initial concentration and pH value of solution on phenanthrene adsorption were studied. The adsorption rate of phenanthrene onto CAC was obtained nearly 100% with initial concentration of 100 mg/L and CAC dosage of 0.3 g at 25 °C. Phenanthrene adsorption was well described with the Langmuir isotherm. The pseudo-second-order model was found to more effectively explain the adsorption kinetics of phenanthrene. The lower temperature was favorable to the adsorption rate and equilibrium adsorption capacity of phenanthrene onto CAC. The thermodynamic parameters ΔH θ , ΔS θ and ΔG θ computed for phenanthrene adsorption onto CAC demonstrate the process was spontaneous, radiative, and entropically driven. Thus, CAC prepared by microwave activation could be effective for removing phenanthrene.

CAS / MDL: 85-01-8
研究领域: 环境科学 · 材料科学
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