JOURNAL OF FOOD PROCESSING AND PRESERVATION
·
2022
·Vol. 46
·期 5
·e16550
·
IF 2.609
Zhen Liu,Da-Cheng Kang,Xin-Rui Li,Ling-Xiao Liu,Yun-Guo Liu
In this study, garlic bulbs after harvesting blanched garlic leaves at four different growth periods were used as the main experimental objects, and black garlic was prepared by solid-state fermentation at variable temperatures. The volatile organic compounds and flavor fingerprints of black garlic were analyzed by headspace-gas chromatography-ion mobility spectrometry (HS-GC-IMS), and the differences of volatile organic compounds in black garlic were compared by principal component analysis (PCA). The physical and chemical indexes of black garlic changed slightly. As the Maillard reaction went on more thoroughly, the content of 5- HMF in black garlic increased. GC-IMS provided information on the characteristics and intensity of 55 volatile organic compounds (monomers and dimers). The results showed that the relative content of organosulfur compounds in black garlic decreased gradually with the extension of the garlic bulb growth period, which was due to the inherent instability of the organosulfur compounds and more complex compounds being formed as precursors in further reactions. The results by PCA showed that BG0 samples can be well distinguished from BG20 samples. Novelty impact statement In this study, garlic bulbs after harvesting blanched garlic leaves at four different growth periods were used as the main experimental objects, and black garlic was prepared by solid-state fermentation at variable temperatures. The volatile organic compounds and flavor fingerprints of black garlic were analyzed by headspace-gas chromatography-ion mobility spectrometry (HS-GC-IMS), and the differences of volatile organic compounds in black garlic were compared by principal component analysis (PCA).
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Food Analytical Methods
·
2025
·
IF 3
Yuan Haiyue,Wang Jiafu,Fu Jiqiang,Wang Jishi,Zhang Yanwei,Geng Yue,Li Bei,He Zeying
A multiresidue method for simultaneously detecting 523 pesticides and metabolites in vegetables using ultra-high-performance liquid chromatography and gas chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS and GC–MS/MS) was developed and rigorously validated for accuracy, precision, linearity, quantification limits, and matrix effects. The validated method was applied to analyze 300 vegetable samples from Shandong province, China, collected in 2023. Results showed the detection of 94 pesticides overall, with a detection rate of 31.67% and a 4.00% exceedance rate of maximum residue limits. Leafy vegetables exhibited the highest detection rate, and insecticides were commonly used in vegetable production. Thiamethoxam was the most frequently detected pesticide. Some banned and restricted pesticides were found at low levels. Celery, Chinese cabbage, tomato, cucumber, eggplant, sweet pepper, and spinach showed the highest frequency of multiple residues. In several rare cases, potential risks to adults and children were identified, highlighting the need for continuous monitoring of pesticide residues to ensure consumer safety.
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WATER AIR AND SOIL POLLUTION
·
2018
·Vol. 229
·期 8
·1-11
·
IF 1.769
Zhang Xiaojun,Ma Xiaoguo,Li Xin,Li Chunying,Wang Rui,Chen Meiqin
Atrazine is one of the most widely used herbicides and has caused much concern about its toxic effects on human and ecosystem. In the present work, a new and efficient method for ultra-trace determination of atrazine in water was developed, using magnetic graphene oxide-based solid-phase extraction combined with dispersive liquid-liquid microextraction, followed by gas chromatography-mass spectrometric determination. The effects of sample pH, contact time, type and volume of elution solvent and extraction solvent, desorption time, and salt addition on the extraction efficiency of atrazine were examined and optimized. Under the optimum conditions, an enrichment factor of 1033 and a detection limit of 0.6 ng L −1 for atrazine were achieved. The developed method was applied to the detection of atrazine in river water, lake water, pond water, and groundwater samples, with spiked recovery of 96–102% and RSD of 2.9–10.5%. Therefore, the proposed method allows proper monitoring of trace atrazine in various environmental waters.
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
·
2019
·
IF 3.571
Xuejin Mao,Aiping Yan,Yiqun Wan,Dongmei Luo,Hongshun Yang
A QuEChERS-type method without matrix interference was designed and developed to determine organophosphorus pesticide residues in edible vegetable oils, based on dispersive solid-phase extraction with cleanup using UiO-66 as sorbent. Microporous UiO-66 directly and selectively adsorbed organophosphorus pesticides and excluded interfering compounds. Clean analytes were obtained by elution and analyzed using gas chromatography–tandem mass spectrometry. The dispersive solid-phase extraction conditions (amount of adsorbent, extraction time, desorption solvent volume, and elution time) were optimized. The limits of detection of the pesticides in vegetable oils were 0.16–1.56 ng/g. Under optimized conditions, the average pesticide recoveries were 81.1–113.5%. The intraday and interday relative standard deviations for analyte recovery were <8.2 and <13.9%, respectively. Thus, the method is reliable and could detect organophosphorus pesticide residues in edible vegetable oils. Furthermore, UiO-66 can be easily recycled and reused at least 10 times, reducing the cost of analysis.
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JOURNAL OF CHROMATOGRAPHY A
·
2024
·
IF 3.8
Manman Wu,Qin Ma,Mei Li,Zhen Zhou,Jingwei Xu,Geoffrey I.N. Waterhouse,Ninghui Song,Wei-Wei Zhao,Guangxu Chen
The monitoring of organic compounds in aquatic matrices poses challenges due to its complexity and time-intensive nature. To address these challenges, we introduce a novel approach utilizing a dual-channel mono ( 1 D) and comprehensive two-dimensional ( 2 D) gas chromatography coupled with time-of-flight mass spectrometry (GC × GC–TOFMS) system, integrated with a robotic pretreatment platform, for online monitoring of both volatile organic compounds (VOCs) and semivolatile organic compounds (SVOCs) in water matrices. Employing the robotic platform, we establish a suite of online liquid–liquid extraction (LLE) pretreatment processes for water samples, marking the first instance of such procedures. Leveraging the automatic headspace (HS) module, dual robotic preparations of HS and LLE are sequentially executed to extract VOCs and SVOCs from water matrices. The GC × GC–TOFMS system is distinguished by its dual-channel analytical column configuration, facilitating sequential analysis of VOCs in GC–TOFMS mode and SVOCs in GC × GC–TOFMS mode. Quantitative detection of 55 target VOCs and 104 SVOCs is achieved in a water sample using the instrument system. Our method demonstrates excellent correlation coefficients ranging from 0.990 to 1.000, method detection limits ranging from 0.08 to 4.78 μg L –1 , relative standard deviations below 19.3 %, and recovery rates ranging from 50.0 % to 124.0 %. To validate the online monitoring capabilities of our system, we assess target SVOCs at three different concentration levels over a 3-day period. Most compounds exhibit recovery rates ranging from 70.0 % to 130.0 %. Furthermore, we apply our method to analyze a real water sample, successfully identifying over 100 target and nontarget VOCs/SVOCs, including alcohols, aldehydes, ketones, acids, esters, and phenols. These results highlight the efficacy of the proposed analysis system, capable of conducting two distinct analyses in automatic sequence, thereby enhancing the efficiency and accuracy of organic compound analysis in water matrices.
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PubMed
高影响因子
DALTON TRANSACTIONS
·
2022
·Vol. 52
·期 2
·376-383
·
IF 4.569
Enming Ping,Lingyun Kong,Mengyao Liu,Yunshan Zhou,Lijuan Zhang,Nan Chen
The reaction of porous γ-Al2O3 particles acting as both a sacrificial template and an aluminum source with 1,4-naphthalene diacid (H2NDC) resulted in the formation of γ-AlOOH@Al(OH)(1,4-NDC) composites, in which ZIF-67 was then loaded by the in situ crystallization method, leading to the formation of γ-AlOOH@Al(OH)(1,4-NDC)@ZIF-67 composites. The deliberately designed composite was used to separate H2/D2 at 77 K in a 1 m chromatographic column. The results demonstrated that the optimized composite can achieve the effective separation of H2/D2 in gas chromatography due to the additive effects of kinetic sieving and chemical affinity quantum sieving of Al(OH)(1,4-NDC) and ZIF-67. By optimizing chromatographic separation conditions, the resolution R reached 2.02 with the separation time t = 7.72 min. The composite also showed satisfactory repeatability and reproducibility.
研究领域:
材料科学
·
分离科学
·
物理化学
·
纳米材料
·
能源化学
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ACS Sensors
·
2025
·
IF 9.1
Xiao Ma,Rong Tan,Hong Chen,Jiawei Zhang,Lei Ge,Tingting Zhao,Xinyu Wang,Kaikai Yuan,Hairui Fang,Dong Wang
Nitrogen dioxide (NO2), the main component of pollutants in atmospheric environments, causes and exacerbates respiratory diseases, especially during outdoor sports even at the 100 ppb level. Currently, environmental gas detection still faces challenges such as high detection limits, low SNR, and low sensitivity. A NO2 sensor based on In(OH)3-α-Fe2O3–ZnO was prepared using a hydrothermal method, featuring an ultralow detection limit of 82 ppt, an exceptionally high SNR of 574,000, and an ultrahigh sensitivity of 252.25 mV/ppm (100 ppb to 1 ppm). And this sensor exhibits excellent response, selectivity, and repeatability. These excellent sensing characteristics come from the adsorbed oxygen on the surface of the material with the formation of n–n heterojunctions. Additionally, a low-power, portable, and cost-effective environmental monitoring system (named Smart Breath Sentinel (SBS)) was designed to intelligently upgrade ordinary masks. SBS enables real-time wireless environmental gas monitoring with integrated humidity compensation to ensure accurate measurements in high-humidity environments. SBS has already been tested in multiple environments, and the test results have proven the feasibility of SBS. This sensor based on In(OH)3-α-Fe2O3–ZnO demonstrates significant potential for applications aimed at enhancing human safety.
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ANALYTICA CHIMICA ACTA
·
2016
·
IF 4.712
Dong Zhu,Zhao Yi Miao,Rui Xiang Yang,Hong Mei Wen,Wei Li,Jun Chen,An Kang,Chen-Xiao Shan,Sheng Yu,Yue Hu
The current widely utilized polymer or C8, C18 end-capped material-based sorbents for solid-phase extraction could not capture alkaloids well only based on “like dissolves like” principle. In this paper, a layer-by-layer functionalized porous Zinc sulfide nanospheres-based solid-phase extraction (SPE) combined with liquid chromatography time-of-flight/mass spectrometry (LC-TOF/MS) and gas chromatography-mass spectrometry (GC-MS) was developed for the specific enrichment and identification of alkaloids from complex matrixes, Crinum asiaticum var. sinicum crude extracts. The functionalized porous Zinc sulfide nanospheres were prepared by the amidation reaction of poly-(acrylic acid) (PAA) homopolymer with amino groups onto the porous ZnS nanospheres. Tandem LC-TOF/MS spectrometry presented that the almost all of the twenty-three main peaks in elution fraction from the SPE could be inferred as alkaloids with ion of mass according to the nitrogen rule and hit formula with Peak View1.2@software from AB SCIEX, and seven alkaloids including two new found chemical entities were directly identified from their GC-MS spectra and retention indices. We believe that this SPE protocol can also be utilized in the future to selectively enrich alkaloids from extracts of other plant species .
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