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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2018 · IF 2.829

Removal of acenaphthene by biochar and raw biomass with coexisting heavy metal and phenanthrene

Li Lu,Yan Lin,Qiwei Chai,Shanying He,Chunping Yang

Rice bran, bamboo and the biochar derived from them were used as four sorbents for the removal of acenaphthene from aqueous solution. The effects of coexisting metal ions and organic compounds on their sorption performances were investigated. The sorption capacity of acenaphthene by biochar prepared from rice bran and bamboo was significantly higher than the raw biomass. The coexisting Cu 2+ and Cr(VI) both inhibited the sorption of acenaphthene by the biochar, whereas the sorption of acenaphthene by the biomass was less affected by the coexisting ions. The coexisting phenanthrene exhibited obvious competition with acenaphthene on the biochar, but it showed no competition with acenaphthene on the biomass. The partition process was a dominate sorption mechanism for acenaphthene on the biomass, which was not easily affected by the coexisting substances. Both partition and surface adsorption were enabled for acenaphthene on the biochar, and the latter was more affected by coexisting heavy metals and organic compounds.

CAS / MDL: 67-56-1
研究领域: 环境科学 · 生态学
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SYNTHESIS-STUTTGART · 2019 ·Vol. 51 ·期 23 ·4425-4433 · IF 2.867

Nitroacenaphthene as a New Photocatalyst for the Synthesis of Sulfonyl Amidines

Yong Jian,Ming Chen,Chao Yang,Wujiong Xia

A small molecule, namely nitroacenaphthene, is reported for the first time as a recyclable visible-light photocatalyst for the construction of the C=N bond from sulfonyl azides and amines. This scalable, site-selective protocol provides a convenient way to access various sulfonyl amidines under mild conditions. Two reaction pathways are proposed, according to different transformation patterns.

研究领域: 有机化学 · 光催化
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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Photodegradation of acenaphthylene over plasmonic Ag/Ag3PO4 nanopolyhedrons synthesized via in-situ reduction

Yuxuan Dai,Yuting Wang,Gancheng Zuo,Jijie Kong,Yang Guo,Cheng Sun,Qiming Xian

We report a simple strategy to synthesize the Ag 3 PO 4 nanopolyhedrons with regular morphology and uniform size under mild conditions. The photocatalytic properties of the composite were optimized by adjusting the content of Ag nanoparticles. The as-prepared photocatalysts were characterized and the photocatalytic performances were evaluated by the degradation of acenaphthylene (ANY) under visible-light illumination. The surface plasmon resonance (SPR) of appropriate Ag nanoparticles was generated on surface under visible light irradiation, which enhanced the absorption and utilization of visible light. At the same time, the conductivity of Ag promoted the separation and transfer of photogenerated carriers, provided active sites for the reaction, and enhanced the photocatalytic degradation efficiency through the generation of active species. As a result, the optimized composite exhibited enhanced visible-light photocatalytic activity of 0.03512 min −1 and higher removal rate of 97.3% for ANY (4 times and 1.8 times higher than that of pristine Ag 3 PO 4 , respectively), more photogenerated active species (h + and •O 2 – ) and relatively high stability (4 times of cycle experiments). In addition, the possible degradation pathway of ANY was proposed. The work of this paper has a crucial guiding significance for the working principle and design direction of silver semiconductor composite photocatalysts with surface plasmon effect.

CAS / MDL: 1336-21-6
研究领域: 环境科学 · 材料科学
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ANALYTICA CHIMICA ACTA · 2024 · IF 5.7

Core-shell silica@pyridyl conjugated microporous polymer as a stationary phase for high performance liquid chromatography

Min Sun,Jiaqing Feng,Yang Feng,Xubo Xin,Yali Ding,Juanjuan Feng

Background Because of the advantages of good selectivity , high sensitivity, and fast analysis, high performance liquid chromatography (HPLC) has become one of the modern analytical techniques in wide application range, such as biological analysis, environmental detection, pharmaceutical and food inspection, agriculture and other fields. The stationary phase greatly decides the chromatographic separation performance, so the development of novel stationary phase is most important for HPLC. Results Pyridyl conjugated microporous polymers (P-CMP) with one to four layers were modified on the surface of amino silica to obtain a novel core-shell material (SiO2@P-CMP) by the layer-by-layer assembly strategy and Chichibabin reaction . The relationship between the structure of SiO2@P-CMP and chromatographic performance was carefully investigated, and the retention mechanism was revealed. The interactions including π-π stacking, hydrophobic effect and hydrogen bond gradually enhanced with the increase of P-CMP layers on the silica surface. Compared with C18 column, SiO2@P-CMP columns displayed better separation selectivity for polycyclic aromatic hydrocarbons (PAHs). According to the relative retention values ( α ), the separation performance of SiO2@P-CMP columns ( α  = 1.144–1.884) for PAH isomers and other analytes was obviously better than that of C18 column ( α  = 0.998–1.487). Furthermore, the SiO2@P-CMP column with four layers was selected to separate different types of analytes (eight PAHs, four bisphenols , four estrogens and nine phthalates), and the peak order of analytes was different from that on the C18 column due to the influence of hydrogen-bonding and π-π interactions. The relative standard deviations (n = 10) of retention time and peak area on SiO2@P-CMP column were between 0.28 % and 1.98 %. Significance and novelty Pyridyl conjugated microporous polymer was introduced as the stationary phase for the first time in HPLC. The proposed column displayed better separation characteristics compared to Zorbax SB-C 18 column. It provided a new idea for the separation of small molecules and the development of chromatographic packing or extraction material.

研究领域: 分析化学 · 材料科学
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SCIENCE OF THE TOTAL ENVIRONMENT · 2024 · IF 8.2

Effect of UV exposure and natural aging on the in vitro PAHs bioaccessibility associated with tire wear particles in soil

Qian Zhang,Xinyan Xu,Chenzhuo Song,Dengke Zhang,Yi Kong,Xinyi Cui

Tire wear particles (TWP), as an emerging type of microplastics, are a significant source of contaminants in roadside soils due to their high concentration of pollutants, including polycyclic aromatic hydrocarbons (PAHs). This study explored the impact of ultraviolet (UV) exposure and natural aging on the in vitro bioaccessibility of PAHs associated with TWP in soil on a China-wide scale. Our findings suggested that UV exposure amplified the negative charge of TWP by 75 % and increased the hydrophobic groups on the particle surface. The bioaccessibility of 3- and 4-ring PAHs in TWP was significantly ( p  < 0.05) heightened by UV exposure. After 20 types of soils containing 2 % UV-exposed TWP underwent natural aging, the bioaccessibility of PAHs saw a significant decrease ( p  < 0.05) to 16–48 %, compared to 28–96 % in the unaged group. Soil pH and electrical conductivity (EC) were the two primary soil properties positively influencing the reduction of in vitro PAHs concentration and PAHs bioaccessibility. According to the prediction results, soils in southern China presented the highest potential region for the release of bioaccessible PAHs from TWP, highlighting the regional specificity of environmental impact. Our study provides valuable insights into the biological impact of PAHs associated with TWP on a regional scale, and offers scientific evidence for targeted soil risk management strategies.

研究领域: 环境科学 · 毒理学
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GREEN CHEMISTRY · 2024 ·Vol. 26 ·期 6 ·3211-3220 · IF 9.3

Development of a high-efficiency and environmentally friendly melamine–formaldehyde resin-based solid phase microextraction fiber for enhanced extraction of polycyclic aromatic hydrocarbons from environmental water

Pengfei Li,Yehong Han,Dandan Han,Hongyuan Yan

An innovative solid-phase microextraction (SPME) fiber coating, melamine–formaldehyde resin (MFR), was synthesized with a green cross-linker (paraformaldehyde), and it exhibited high heat resistance (up to 350 °C). Seven polycyclic aromatic hydrocarbons (PAHs) were chosen as analytes, and the results demonstrated the MFR-based SPME fiber's exceptional enrichment capabilities and efficient extraction, with high enrichment factors and significantly improved efficiency compared to the conventional polydimethylsiloxane (PDMS) fibers. The unique superiority of the MFR was attributed to its strong π–π interactions and amino-associated enhancement, as well as its porous structure and rough surface, which provided abundant adsorption sites and facilitated rapid mass transport of analytes. Furthermore, the preparation conditions of the MFR-coated SPME fiber were compared with those of commercially available and reported fibers, emphasizing the advantages of the MFR-coated fiber, such as its simplicity, cost-effectiveness, reproducibility, and eco-friendliness. The MFR-based SPME fiber exhibited significant advantages, including high enrichment factors (ranging from 1906- to 7153-fold) for PAHs and good fiber-to-fiber reproducibility (8.7–14.6%), outperforming commercially available PDMS fibers by a factor of 4.9–82.8-fold. This study also considered important factors affecting the extraction process, such as ionic strength, temperature, and time, and optimized these parameters for the best extraction efficiency. The greenness of the developed method was assessed using the Analytical Eco-Scale, and the results showed that it was green in terms of reagent dosage, energy consumption, and waste. The developed headspace solid phase microextraction–gas chromatography–tandem mass spectrometry (HS-SPME-GC-MS/MS) method based on the MFR coating exhibited excellent precision, accuracy, and repeatability, making it a reliable method for the determination of trace PAHs in environmental water samples.

研究领域: 分析化学 · 环境科学 · 材料科学
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JOURNAL OF MEMBRANE SCIENCE · 2024 · IF 8.4

Excellently conductive fluorinated poly (acenaphthylenyl aryl piperidinium) anion exchange membranes with robust dimensional stability

Jialin Zhao,Jian Gao,Yijia Lei,Jingyi Wu,Na Li,Yan Wang,Junjian Yu,Zhiyan Sui,Jiayao Yang,Zhe Wang

In this work, the polymerization of hydrophobic pentafluorophenylethyl into the high conductivity poly (acenaphthenyl aryl piperidinium) backbone was catalyzed by an efficient and facile one-pot method with super-strong acids to build enhanced phase separation structures while maintaining low swelling. The prepared QPANTP-20-F 15 membrane exhibited the most significant hydrophilic-hydrophobic separation phenomenon, with the conductivity as high as 192.19 mS cm −1 at 80 °C. Due to the incorporation of hydrophobic fluorinated groups, the water uptake of the membrane was limited, and its mechanical (71.0 MPa under hydrated condition) and dimensional stability property (11.32% swelling) showed improved results. In addition, after 1200 h at 80 °C in 3 M/5 M NaOH solution, the structure of the prepared polymer exhibited excellent chemical stability property, with conductivity remaining of 95.04% and 86.38%, respectively. With current density of 706 mA cm −2 at 80 °C, the AEMFCs achieved a peak power density of 321 mW cm −2 .

研究领域: 材料科学 · 能源技术
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GREEN CHEMISTRY · 2025 · IF 9.2

Porous ionic liquids from cyclodextrin carbon for deep extraction of polycyclic aromatic hydrocarbons

Kaihao Mo,Peng Cui,Dongni Liu,Cailan Chen,Hanyu Zhang,Minmeng Tang,Peiwen Wu,Yan Huang,Haiyan Ji,Wenshuai Zhu

In extraction processes, the low mass transfer efficiency of conventional ionic liquids is a refractory problem. Herein, a porous ionic liquid (PIL), β-CD-900-PIL, was innovatively constructed by combining a porous carbon material (β-CD-900) derived from β-cyclodextrin polymer with imidazole bis-trifluoromethylsulfonylimide ionic liquid ([C12mim][NTf2]). The N2 sorption isotherm and CO2 adsorption confirmed the porosity of β-CD-900 and the PIL. With the dispersion amount of β-CD-900 as 20 wt%, the extraction efficiency of naphthalene by β-CD-900-PIL reached 66.6%, which was 24% higher than that of the ionic liquid. After three extractions, the naphthalene content decreased from 500 mg L−1 to 5 mg L−1. The high extraction efficiency was attributed to the high porosity and abundant π–π and C–H⋯π interactions between PILs and naphthalene. The more than 99% extraction performance, low viscosity and low preparation cost make β-CD-900-PIL an ideal extractant for polycyclic aromatic hydrocarbons in the petrochemical industry.

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MARINE POLLUTION BULLETIN · 2025 · IF 4.9

Characterization of the vertical distribution of polycyclic aromatic hydrocarbons in mangrove sediments of Guangxi and ecological risk assessment

Ruicong Gao,Jiaqi Lu,Zhixuan Wei,Hao Xu,Siyuan Jing,Minghuo Wu

PAHs, a group of persistent organic pollutants with significant carcinogenic and mutagenic effects, are widely distributed in the environment and can accumulate in sediments, posing potential threats to mangrove ecosystems and human health. This study is one of the most recent studies that presents an analysis of the vertical contamination characteristics of PAHs in mangrove sediments down to a depth of 80 cm, utilizing a combination of solid-phase extraction and gas chromatography–mass spectrometry. The results showed that the mean value of PAHs was 258.82 ng/g (range from 226.41 to 320.07 ng/g) in the studied mangrove areas (Beihai City, Guangxi). The results indicated a decline in PAH concentrations with increasing sediment depth, with values of 259.3 ng/g in surface sediments (0–10 cm), 240.9 ng/g in intermediate sediments (30–40 cm), and 241.1 ng/g in deeper sediments (60–70 cm). This suggests that PAHs not only remain in the surface layer of the sediment, as in previous studies, but also migrate vertically within the sediment. Based on the results, the potential ecological risks of PAHs were also evaluated by the ERL/ERM model. After environmental risk assessment, it was found that among the six PAHs studied, the contents of all except acenaphthene were lower than the ERL, indicating a low ecological risk. This study elucidates the vertical distribution of PAHs in mangrove sediments, offering crucial data for ecological risk assessment and establishing a foundation for future research on PAH transport mechanisms and their ecological impacts, thereby informing environmental management strategies.

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Chemosensors · 2024 ·Vol. 12 ·期 10 ·220 · IF 3.7

Fast Determination and Source Apportionment of Eight Polycyclic Aromatic Hydrocarbons in PM10 Using the Chemometric-Assisted HPLC-DAD Method

Ting Hu,Yitao Xia,You Wang,Li Lin,Rong An,Ling Xu,Xiangdong Qing

Polycyclic aromatic hydrocarbons (PAHs) are a group of organic compounds that are both toxic and hazardous to human health and ecological systems. In recent work, a novel analytical strategy based on the chemometric-assisted HPLC-DAD method was proposed for the quantification and source apportionment of eight PAHs in PM10 samples. Compared to traditional chromatographic methods, this approach does not require the purification of complex PM10 samples. Instead, it utilizes a mathematical separation method to extract analytes’ profiles from overlapping chromatographic peaks, enabling precise quantification of PAHs in PM10. Firstly, 40 PM10 samples collected in Loudi city during two sampling periods were used for analysis. Subsequently, the second-order calibration method based on alternating trilinear decomposition (ATLD) was employed to handle the three-way HPLC-DAD data. Finally, the pollution sources of PAHs were analyzed by the feature component analysis method according to the obtained relative concentration matrix. For the validation model, the average recoveries of eight PAHs were between (88.8 ± 7.6)% and (105.6 ± 7.5)%, and the root-mean-square errors of prediction ranged from 0.03 μg mL−1to 0.47 μg mL−1. The obtained limits of quantification for eight PAHs were in the range of 0.0050 μg mL−1to 0.079 μg mL−1. For actual PM10 samples, results of the feature component analysis indicated that the main source of PAHs in PM10 may be traffic emissions and coal combustion. In summary, the proposed method provided a new and rapid analysis method for the accurate determination and source apportionment of PAHs in atmospheric aerosols.

研究领域: 环境科学 · 分析化学 · 公共卫生
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JOURNAL OF HAZARDOUS MATERIALS · 2024 · IF 12.2

Nanoscale-controlled organicinorganic hybrid spheres for comprehensive enrichment of ultratrace chlorobenzenes in marine and fresh water

Yixin Kuang,Suxin Zhou,Yuefan Liu,Xiaoying Feng,Luyi Chen,Juan Zheng,Gangfeng Ouyang

The size of the adsorbent has the potential to influence extraction performance, but the size effect at the nanoscale is still poorly understood. In this study, organic-inorganic hybrid nanospheres (OIHNs) with controllable nanoscale sizes of 30, 50, and 100 nm were successfully prepared. These materials were further fabricated as solid phase microextraction (SPME) coatings with similar thicknesses, and coupled with gas chromatography-mass spectrometry (GC-MS) to investigate their extraction performance. The results showed that the extraction capacities of OIHNs for chlorobenzenes (CBs) and polycyclic aromatic hydrocarbons (PAHs) were much better than those of their corresponding derived carbon materials, despite the smaller specific surface areas and lower porosities of them. In addition, the enrichment performance increased significantly with decreasing particle size, and the OIHN-30 coating demonstrated the best performance, with enrichment factors ranging from 1098 to 6853 for CBs. Finally, a highly sensitive and practical analytical method was established with a wide linear range of 0.5–5000 ng·L −1 , and the limits of quantification (LOQs) were 0.43–1.7 ng·L −1 . The determinations of ultratrace CBs in five marine water samples and five fresh water samples were realized successfully. This study is expected to contribute to a deep understanding of the environmental effects of nanoparticles and the design of high-performance adsorbents.

研究领域: 环境科学 · 分析化学
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ANALYTICA CHIMICA ACTA · 2015 · IF 4.513

Monodisperse microporous carbon nanospheres: An efficient and stable solid phase microextraction coating material

Juan Zheng,Kun Wang,Erlun Luo,Dingcai Wu,Fang Zhu,Ruifen Jiang,Chengyong Su,Chaohai Wei,Gangfeng Ouyang

The monodisperse microporous carbon nanospheres (MMCNSs) were applied in solid phase microextraction for the first time. The MMCNSs-fiber was prepared by sol–gel technique and good repeatability and reproducibility were obtained, due to the excellent monodispersity of the MMCNSs . The sol–gel-MMCNSs fiber exhibited superior extraction ability for polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs), compared with the commercial polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber and the fiber prepared with its precursor, the monodisperse microporous polystyrene nanospheres (MMPNSs). Moreover, the fiber has good thermostability and strong acid/base durability. The sol–gel-MMCNSs fiber was then employed to detect PAHs and OCPs in aqueous samples by combining with gas chromatography–mass spectrometer (GC–MS). Under the optimized conditions, the detection limits of the proposed method ranged from 0.10 to 5.5   ng   L −1 . Furthermore, the method was successfully utilized for the analysis of PAHs and OCPs in real samples, with satisfactory recoveries in the range of 81.0–120% for the Pearl River water samples and 72.8–118% for the coking wastewater samples.

研究领域: 分析化学 · 环境科学
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