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百菌清(chlorothalonil)在水中的光化学降解 被引量:19
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作者 李学德 花日茂 +3 位作者 岳永德 李瑛 汤锋 唐俊 《应用生态学报》 CAS CSCD 北大核心 2006年第6期1091-1094,共4页
研究了光源种类、溶液pH、水温和表面活性剂对百菌清光解的影响.结果表明,百菌清水溶液在高压汞灯、紫外灯和太阳光照射下的光解半衰期分别为22.4、82.5和123.8min;在太阳光和高压汞灯照射下,百菌清在碱性溶液中比中性和酸性溶液中光解... 研究了光源种类、溶液pH、水温和表面活性剂对百菌清光解的影响.结果表明,百菌清水溶液在高压汞灯、紫外灯和太阳光照射下的光解半衰期分别为22.4、82.5和123.8min;在太阳光和高压汞灯照射下,百菌清在碱性溶液中比中性和酸性溶液中光解快;随着水温的升高,百菌清光解速率加快,水温平均每升高10℃,光解速率大约增大1倍.表面活性剂十二烷基磺酸钠、Tween60和Span20对百菌清的光解表现出显著的光敏化效应,十六烷基三甲基溴化铵对百菌清光解有强烈的光猝灭效应. 展开更多
关键词 百菌清 光源 PH 水温 表面活性剂 光化学降解.
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Degradation of chlorpyrifos alone and in combination with chlorothalonil and their effects on soil microbial populations 被引量:16
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作者 CHU Xiaoqiang FANG Hua PAN Xuedong WANG Xiao SHAN Min FENG Bo YU Yunlong 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2008年第4期464-469,共6页
In practice, pesticides are usually applied simultaneously or one after another for crop protection, and this type of pesticide application often leads to a combined contamination of pesticide residues in the soil env... In practice, pesticides are usually applied simultaneously or one after another for crop protection, and this type of pesticide application often leads to a combined contamination of pesticide residues in the soil environment. A laboratory study was conducted to investigate the influence of chlorothalonil on chlorpyrifos degradation and its effects on soil bacterial, fungal, and actinomycete populations. Under the experimental conditions here, the half-lives of chlorpyrifos alone, and in combination with chlorothalonil, at the recommended and double dosages, were measured to be 3.24, 2.77, and 2.63 d, respectively. Chlorpyrifos degradation was not significantly altered by its combination with chlorothalonil. However, the inhibitory effect of chlorpyrifos on soil microorganisms was increased by its combination with chlorothalonil, and the increase was related to the levels of chlorothalonil added. Compared to those in the controls, the populations of bacteria, fungi, and actinomycetes were significantly reduced by 44.1%, 61.1%, and 72.8%, respectively, on the first day after treatment (DAT) by chlorpyrifos alone. With the addition of chlorothalonil, the inhibition was increased to 55.2%, 79.3%, and 85,8% at the recommended dosage, and 86.0%, 94.1%, and 90.8% at the double dosage, at one DAT, respectively. The results suggested that combined effects should be taken into account to assess the actual impacts of pesticide applications. 展开更多
关键词 PESTICIDE soil microorganism CHLORPYRIFOS chlorothalonil COMBINATION
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Effects of chlorothalonil and carbendazim on nitrification and denitrification in soils 被引量:14
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作者 LANG Man, CAI Zucong State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences,Nanjing 210008, China 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2009年第4期458-467,共10页
The effects of chlorothalonil and carbendazim on nitrification and denitrification in six soils in upland and rice paddy environments were investigated. Laboratory aerobic (60% water holding capacity) and anaerobic ... The effects of chlorothalonil and carbendazim on nitrification and denitrification in six soils in upland and rice paddy environments were investigated. Laboratory aerobic (60% water holding capacity) and anaerobic (flooded) conditions were studied at 25℃ and fungicide addition rates of 5.5 mg/kg A. I. (field rate, FR), 20 times (20FR) and 40 times (40FR) field rate, respectively. The results indicated that chlorothalonil at the field rate had a slight inhibitory effect on one soil only, and that soil did not nitrify much in the first place. But chlorothalonil at higher rates inhibited nitrification significantly in all soils. For soils JXP and JXU with a pH of less than 5.0, chlorothalonil almost completely stopped their nitrification at 20FR and 40FR during the whole 14 d incubation period. For soils HNP and HNU with a pH of greater than 8.0, chlorothalonil also significantly inhibit nitrification at 20FR and 40FR (p 〈 0.05). However, NH4+ that was added to the soil was also almost completely nitrified by the end of the incubation period in these two soils. The effects of chlorothalonil at 20FR and 40FR on the nitrification of JSP and JSU soils, with a pH of 5.4 and 7.2, respectively, were intermediate between the other soil types. Chlorothalonil had no effect on denitrification at the field rate and had little effect at the higher rates of application in some soils. Carbendazim had essentially no effect on nitrification and denitrification in soils assessed. 展开更多
关键词 FUNGICIDE NITRIFICATION DENITRIFICATION chlorothalonil CARBENDAZIM
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Synthesis of Novel Benzoylphenylurea Chitin Inhibitors from Chlorothalonil 被引量:4
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作者 JunLIN ShengJiaoYAN +3 位作者 DeShouMAO RongXU LiJuanYANG FuChuLIU 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第12期1219-1222,共4页
Twenty-six novel benzoylphenylurea chitin inhibitor derivatives have been synthesized in over 30~50% yield from chlorothalonil 1 via sequential fluorine exchange, aminolysis, hydrolysis, decarboxylation and acylation ... Twenty-six novel benzoylphenylurea chitin inhibitor derivatives have been synthesized in over 30~50% yield from chlorothalonil 1 via sequential fluorine exchange, aminolysis, hydrolysis, decarboxylation and acylation reactions. 展开更多
关键词 Benzoylphenylureas chitin inhibitor chlorothalonil.
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Synthesis of Novel Benzoylphenylurea Chitin Inhibitors From Chlorothalonil(Ⅱ) 被引量:1
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作者 LIN Jun MAO De-shou +4 位作者 XU Rong YAN Sheng-jiao YANG Li-juan LI Jun-feng LIU Fu-chu 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2004年第4期429-432,共4页
Six novel benzoylphenylurea chitin inhibitor derivatives were synthesized in the yields of 30%_50% from the readily available starting material chlorothalonil 1 viasequential fluorine exchange, aminolysis, hydrolysis ... Six novel benzoylphenylurea chitin inhibitor derivatives were synthesized in the yields of 30%_50% from the readily available starting material chlorothalonil 1 viasequential fluorine exchange, aminolysis, hydrolysis and acylation reactions. 展开更多
关键词 Benzoylphenylureas Chitin inhibitor chlorothalonil
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Residue Dynamics of Chlorothalonil and Its 4-Hydroxy Metabolite in Scallion 被引量:1
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作者 Ying CHENG Chenchen WANG Jun TANG 《Agricultural Biotechnology》 CAS 2018年第5期219-221,237,共4页
[Objectives] This study was conducted to explore the dissipation dynamics of chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) in scallion.[Methods] The level of residue and the dissipation of chlorothalonil and... [Objectives] This study was conducted to explore the dissipation dynamics of chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) in scallion.[Methods] The level of residue and the dissipation of chlorothalonil and its main metabolite 4-hydroxy-2,5,6-trichloroisophthalonitrile in scallion in Beijing and Jiangsu experimental bases were determined via acetonitrile extraction and ultra-performance liquid chromatography coupled with ultraviolet detection (UPLC-UV).[Results] The dissipation of chlorothalonil in scallion followed the first-order kinetic model and the half-life of chlorothalonil in scallion was 3.5-4.1 d. The final residue of chlorothalonil in scallion decreased over time after the last application. After chlorothalonil was applied at 1 050 or 1 575 g a.i./hm 2 3 or 4 times, the maximum residue level of chlorothalonil was 1.48, 1.21, 0.72 and 0.45 mg/kg 5, 7, 10 and 14 d after the last application, while that of its 4-hydroxy metabolite was 0.25, 0.19, 0.13 and 0.09 mg/kg, respectively.[Conclusions] The results may provide experimental evidence for evaluating the safety of the use of chlorothalonil in scallion. 展开更多
关键词 chlorothalonil Scallion RESIDUE Dissipation rate
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Determination of Residual Chlorothalonil in Textiles
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作者 Chengyun Wang Junfeng Lin +2 位作者 Tangtang Xie Huiping Zou Yalei Shen 《Journal of Materials Science and Chemical Engineering》 2020年第4期106-114,共9页
An effective method was established to determine the content of residual chlorothalonil in textiles by gas chromatography/mass spectrometry-selected ion monitoring coupled with ultrasonic extraction technique. Residua... An effective method was established to determine the content of residual chlorothalonil in textiles by gas chromatography/mass spectrometry-selected ion monitoring coupled with ultrasonic extraction technique. Residual chlorothalonil in textiles was ultrasonically extracted using ethyl acetate as the extraction solvent. The extract was condensed and analyzed by gas chromatography/mass spectrometry in selected ion monitoring mode (GC/MS-SIM). The concentration of chlorothalonil was calibrated by the external standard method. Good linearity existed between the peak area and the mass concentration of chlorothalonil in the mass concentration range from 0.2 μg/mL to 42.8 μg/mL. The equation was A = 95,399ρ ? 50,848, with a correlation coefficient of 0.9999. The limit of detection was 0.1 mg/kg for chlorothalonil. The blank samples were spiked at three concentration levels, and the spiked average recoveries changed from 81.9% to 95.4% while the relative standard deviation (RSD) changed from 1.8% to 5.2%. The proposed method was simple, rapid, sensitive and the limit of detection could meet the limit requirements of relevant regulations. Commercially available textiles were measured by this method, and chlorothalonil at different concentration levels was detected in some samples. 展开更多
关键词 chlorothalonil TEXTILE ULTRASONIC EXTRACTION GC/MS-SIM
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Synthesis and Fungicidal Activity of Chlorothalonil Derivatives
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作者 Han Jintao Li Jintao +1 位作者 Wang Yingxiu Jiang Aizhong 《Plant Diseases and Pests》 CAS 2020年第3期15-17,27,共4页
[Objective]The paper was to develop a novel fungicide with high efficacy and low toxicity.[Method]Chlorothalonil was used as the parent structure,and its 4-position substituent was converted to amino group.Totally 12 ... [Objective]The paper was to develop a novel fungicide with high efficacy and low toxicity.[Method]Chlorothalonil was used as the parent structure,and its 4-position substituent was converted to amino group.Totally 12 amide compounds not reported in the literature were designed and synthesized.Their structures were conformed by 1H NMR.[Result]The preliminary bioassay test showed that compounds JTCN-01,JTCN-05 and JTCN-07 had good control effect on corn rust at the concentration of 200 mg/L,and the control effect of compound JTCN-05 reached 95%.[Conclusion]Some chlorothalonil derivatives had the potential for further development. 展开更多
关键词 chlorothalonil Novel compound SYNTHESIS Fungicidal activity
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Degradation of chlorothalonil by ultrasonic irradiation:Kinetics and impact factors 被引量:2
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作者 郭洪光 高乃云 +2 位作者 黎雷 金玄雄 陈喆 《Journal of Central South University》 SCIE EI CAS 2011年第4期1068-1073,共6页
Factors on degradation of chlorothalonil(CLT) in water by high frequency ultrasonic irradiation were investigated.The effects of initial concentration of chlorothalonil,dosages of tertiary butyl alcohol,humic acid and... Factors on degradation of chlorothalonil(CLT) in water by high frequency ultrasonic irradiation were investigated.The effects of initial concentration of chlorothalonil,dosages of tertiary butyl alcohol,humic acid and initial pH value on degradation of chlorothalonil,as well as the reaction mechanism were studied.The results reveal that chlorothalonil could be effectively degradated by ultrasonic irradiation.The reaction constant value kapp decreased from 0.014 1 to 0.010 2 min-1 with the initial concentration increasing from 50 to 400 μg/L during 180 min irradiation.Tertiary butyl alcohol had negative effect on chlorothalonil degradation,while lower concentration of humic acid promoted the sonolysis,and kapp declined with the further concentration increasing.The kapp varied little when the pH value ranged from 3.10 to 10.28.It may be concluded that mechanical and pyrolysis process played main roles on the degradation of chlorothalonil in ultrasonic irradiation rather than ·OH attack.The electrical energy per order(EEo) values for sonolysis degradation of CLT were also calculated to evaluate the cost of the process. 展开更多
关键词 超声波照射 辐照降解 百菌清 影响因素 动力学 初始PH值 初始浓度 反应机理
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Biosorption of Chlorothalonil on Fique's Bagasse (Furcraea sp.): Equilibrium and Kinetic Studies 被引量:1
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作者 Adriana Maria Quinchfa-Figueroa Margarita Enid Ramfrez-Carmona Geovanna Tafurt-Garcfa 《材料科学与工程(中英文版)》 2010年第6期1-8,共8页
关键词 甘蔗渣 吸附 百菌清 动力学 傅立叶变换红外光谱 扫描电子显微镜 平衡
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同时快速检测蔬菜中百菌清和多菌灵的胶体金免疫层析法
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作者 许奂源 梁植雯 +6 位作者 许景皓 黄苇 尹青春 李斌 江林峰 郭美媛 徐振林 《食品研究与开发》 CAS 2024年第8期139-148,共10页
该研究制备分别特异性识别百菌清、多菌灵的两种单克隆抗体,并建立一种同时快速检测蔬菜中百菌清和多菌灵的胶体金免疫层析法。在最适工作条件下,所建立的方法对百菌清、多菌灵的检测限分别为0.08 ng/mL和1.95 ng/mL,线性范围分别为0.08... 该研究制备分别特异性识别百菌清、多菌灵的两种单克隆抗体,并建立一种同时快速检测蔬菜中百菌清和多菌灵的胶体金免疫层析法。在最适工作条件下,所建立的方法对百菌清、多菌灵的检测限分别为0.08 ng/mL和1.95 ng/mL,线性范围分别为0.08~10.00 ng/mL和1.95~250.00 ng/mL。黄瓜、番茄、包菜3种样品加标回收率为79.2%~112.1%(百菌清)和63.3%~97.5%(多菌灵),变异系数均低于18.9%,试纸条所需检测时间为20 min,可应用于蔬菜中百菌清、多菌灵残留的现场高通量快速筛查。 展开更多
关键词 百菌清 多菌灵 单克隆抗体 胶体金免疫层析 同时检测
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香草醛异[口恶]唑衍生物的设计合成及杀菌活性
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作者 刘伟童 朱长恒 +1 位作者 蒋禹 赵汗青 《化学试剂》 CAS 2024年第3期16-23,共8页
为了寻找结构新颖、杀菌活性更好的绿色农药。选用天然产物香草醛作为基本原料,引入五元杂环异[口恶]唑结构,首次设计并合成了28个香草醛异[口恶]唑类衍生物。结构经核磁共振氢谱、碳谱及高分辨质谱分析确认。测试了所有目标衍生物对烟... 为了寻找结构新颖、杀菌活性更好的绿色农药。选用天然产物香草醛作为基本原料,引入五元杂环异[口恶]唑结构,首次设计并合成了28个香草醛异[口恶]唑类衍生物。结构经核磁共振氢谱、碳谱及高分辨质谱分析确认。测试了所有目标衍生物对烟草灰霉病菌(Botrytis cinerea)、层出镰刀菌(Fusarium proliferatum)、木贼镰刀菌(Fusarium equiseti)、玉米圆斑病菌(Bipolaris zeicola)、胶胞炭疽菌(Colletotrichum gloeosporioides)、草茎点霉菌(Phoma herbarum)6种广谱菌的杀菌活性。杀菌活性测定结果显示:在50μg/mL质量浓度下,部分化合物对6种真菌的菌丝生长均具有一定抑制作用,2-甲氧基-4-(5-苯基异[口恶]唑-3-基)苯乙酸酯对6种真菌的抑菌活性整体良好,对玉米圆斑病菌等3种菌的抑菌活性超过对照组百菌清;2-甲氧基-4-(5-(4-乙基苯基)异唑-3-基)苯酚对烟草灰霉病菌的抑菌活性最高,抑菌率可以达到93%。初步构效关系表明,对活性片段香草醛上的酚羟基进行乙酰化衍生,有助于提高化合物对6种病原菌的抑菌活性,为后续的生物活性研究提供了参考。 展开更多
关键词 香草醛 异[口恶]唑 合成 百菌清 杀菌活性
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气相色谱法测定西葫芦中百菌清残留量的不确定度评定
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作者 李盼盼 史晓华 +1 位作者 李嘉业 张慧敏 《中国标准化》 2024年第6期185-191,共7页
参照NY/T 761—2008《蔬菜和水果中有机磷、有机氯、拟除虫菊酯和氨基甲酸酯类农药多残留的测定》,通过建立数学模型,对气相色谱法测定西葫芦中百菌清残留量的不确定度进行评定。分析量化了样品称样量、提取溶液体积、标准溶液配置、回... 参照NY/T 761—2008《蔬菜和水果中有机磷、有机氯、拟除虫菊酯和氨基甲酸酯类农药多残留的测定》,通过建立数学模型,对气相色谱法测定西葫芦中百菌清残留量的不确定度进行评定。分析量化了样品称样量、提取溶液体积、标准溶液配置、回收率、测量重复性、气相色谱仪6个不确定度分量,计算出合成标准不确定度和扩展不确定度。结果表明,西葫芦中百菌清添加量为0.1 mg/kg时,其测定结果为0.1069 mg/kg,扩展不确定度为0.0050 mg/kg。影响不确定度的主要因素是标准溶液配置、回收率、测量重复性和气相色谱仪。 展开更多
关键词 西葫芦 百菌清 不确定度 气相色谱法
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基于胶体金免疫层析法快速检测蓝莓中的百菌清残留 被引量:5
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作者 马琳 赵颖 +1 位作者 陈建波 赵莉 《农药学学报》 CAS CSCD 北大核心 2023年第2期435-443,共9页
为建立蓝莓样品中百菌清残留快速筛查方法,以农药百菌清为目标分析物,系统研究了胶体金标记参数及样品前处理方法对胶体金免疫层析方法(colloidal gold immunochromatographic assay,GICA)的影响。结果表明:以25 nm的胶体金颗粒标记百... 为建立蓝莓样品中百菌清残留快速筛查方法,以农药百菌清为目标分析物,系统研究了胶体金标记参数及样品前处理方法对胶体金免疫层析方法(colloidal gold immunochromatographic assay,GICA)的影响。结果表明:以25 nm的胶体金颗粒标记百菌清单克隆抗体作为检测探针,分别将包被原百菌清-BSA(1 mg/mL)和羊抗鼠IgG抗体(0.1 mg/mL)包被于硝酸纤维膜(NC膜),形成检测线(T线)和质控线(C线),组装成百菌清胶体金免疫层析检测试纸条。蓝莓样品经酸化乙腈提取,双蒸水(dd H_(2)O)稀释后,应用该纸条对蓝莓中百菌清残留肉眼观察检出限(LOD)为0.1 mg/kg(T线完全消线),可实现15 min内蓝莓中百菌清的定性与半定量分析,同时,试纸条对样品中4-羟基百菌清、五氯硝基苯、多菌灵和腐霉利的检测不存在交叉反应。蓝莓中百菌清添加回收试验的胶体金免疫层析检测试纸条测试结果与超高效液相色谱-三重四级杆串联质谱仪(UPLC-MS/MS)方法的检测结果一致。这两种方法都可以成功地应用于蓝莓中百菌清的检测,胶体金免疫层析检测试纸条有助于现场检测,基于UPLC-MS/MS的方法则能提供准确的定量。 展开更多
关键词 胶体金免疫层析 蓝莓 百菌清 残留 快速检测 样品前处理
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气相色谱-质谱法同时测定水性涂料中3种生物杀伤剂的含量 被引量:1
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作者 蒋莹 诸鸿未 赵霞 《理化检验(化学分册)》 CAS CSCD 北大核心 2023年第1期61-64,共4页
提出了气相色谱-质谱法同时测定水性涂料中碘代丙炔基氨基甲酸丁酯、百菌清、三氯生等3种生物杀伤剂含量的方法。称取水性涂料样品1 g,加入1 000 mg·L^(-1)正二十烷(内标)溶液500μL,再用乙酸乙酯稀释至10 mL,混匀,超声提取30 min... 提出了气相色谱-质谱法同时测定水性涂料中碘代丙炔基氨基甲酸丁酯、百菌清、三氯生等3种生物杀伤剂含量的方法。称取水性涂料样品1 g,加入1 000 mg·L^(-1)正二十烷(内标)溶液500μL,再用乙酸乙酯稀释至10 mL,混匀,超声提取30 min,冷却,以4 000 r·min^(-1)转速离心20 min,取上清液待测。各目标化合物在HP-5ms石英毛细管柱上以柱升温程序分离后,用质谱仪进行检测,内标法定量。结果显示:3种目标化合物标准曲线的线性范围均为0.1~100 mg·L^(-1),检出限(3S/N)为0.033~0.098 mg·kg^(-1);对阴性样品进行3个浓度水平的加标回收试验,回收率为87.1%~103%,测定值的相对标准偏差(n=7)均小于5.0%;方法用于10种实际样品分析,百菌清和三氯生均未检出,1种样品中检出碘代丙炔基氨基甲酸丁酯,检出量为760.7 mg·kg^(-1)。 展开更多
关键词 气相色谱-质谱法 水性涂料 碘代丙炔基氨基甲酸丁酯 百菌清 三氯生
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百菌清与丙溴磷混合水溶液的光化学降解 被引量:1
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作者 王鑫 张南 +4 位作者 杨亚威 史陶中 马鑫 吕培 花日茂 《农药学学报》 CAS CSCD 北大核心 2023年第5期1173-1178,共6页
为明确水体中百菌清和丙溴磷的混合光降解行为,利用模拟光源(高压汞灯)研究了百菌清和丙溴磷混合水溶液中的光降解作用和光降解产物。结果表明:在高压汞灯照射下,浓度为3μmol/L的百菌清光降解的半衰期为122.46 min,浓度为3、6和9μmol/... 为明确水体中百菌清和丙溴磷的混合光降解行为,利用模拟光源(高压汞灯)研究了百菌清和丙溴磷混合水溶液中的光降解作用和光降解产物。结果表明:在高压汞灯照射下,浓度为3μmol/L的百菌清光降解的半衰期为122.46 min,浓度为3、6和9μmol/L的丙溴磷光解半衰期分别为87.85、86.11和87.63 min。在3μmol/L的百菌清水溶液中分别添加1、2和3倍(3、6和9μmol/L)的丙溴磷后,百菌清的光降解半衰期分别降至64.54、38.25和33.05 min,光降解速率分别提高了1.90、3.20和3.71倍;而丙溴磷的光降解半衰期分别为85.57、83.51和84.32 min,降解速率均未发生显著变化。表明丙溴磷对百菌清在纯水中的光降解具有明显的促进效应,且降解速率与丙溴磷浓度呈正相关,而百菌清则对丙溴磷的光降解无影响。百菌清水溶液在单独光降解和加入丙溴磷后,其光降解产物均为4-羟基百菌清;而丙溴磷则产生了5种光降解产物,分别为4-溴-2氯苯基磷酸氢乙酯、O-(4-溴-2-氯苯基)-O-乙基-S-氢磷酸、O-(2-氯苯基)-O-乙基-S-丙基硫代磷酸酯、(2-氯-4-羟基苯基)邻乙基-S-丙基硫代磷酸酯和2-氯-4-溴苯酚。百菌清和丙溴磷的混合水溶液在光照下产生了更多的羟基自由基。该研究可为评估百菌清和丙溴磷复合污染对环境的生态毒性提供重要理论支撑。 展开更多
关键词 百菌清 丙溴磷 光降解 水溶液 羟基自由基
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优化后的QuEChERs方法测定不同基质中百菌清农药残留 被引量:1
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作者 刘贺 张鹏 +4 位作者 孙利东 彭菲 马玲 刘振伟 田国辉 《黑龙江大学自然科学学报》 CAS 2023年第2期193-198,共6页
建立并使用优化后的QuEChERs前处理方法,利用气相色谱-电子捕获检测器(Gas chromatography-electron capture detector,GC-ECD)分析了不同基质中的百菌清农药残留物。通过回收率比对,确定使用1%乙酸乙腈进行提取,15 mg多壁碳纳米管(Mult... 建立并使用优化后的QuEChERs前处理方法,利用气相色谱-电子捕获检测器(Gas chromatography-electron capture detector,GC-ECD)分析了不同基质中的百菌清农药残留物。通过回收率比对,确定使用1%乙酸乙腈进行提取,15 mg多壁碳纳米管(Multi-walled carbon nanotubes,MWCNTs)作为色素吸附剂。结果表明,果蔬中百菌清的检出限、定量限及回收率与基质种类有关,在6个浓度水平下,不同果蔬基质中百菌清在0.00063~0.1 g·mL^(-1)范围内线性关系良好,相关系数在0.99以上。在3个加标水平下(n=6),其回收率为93%~105%,相对标准偏差为1.7%~5.8%,检出限(S/N=3)为0.00063 mg·kg^(-1),定量限(S/N=10)为0.0019 mg·kg^(-1)。与其他检测仪器相比较具有更低的检出限,说明本方法快速简便,灵敏度高,为百菌清农药残留量的检测提供了一种高通量的检测方法。 展开更多
关键词 百菌清 农药残留 果蔬 QUECHERS GC-ECD
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基于阵列式SERS基底快速和高灵敏检测黄瓜中百菌清残留
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作者 杨海帆 胡开颜 +4 位作者 王煦博 钱莹莹 章笔椽 陈安迪 钱亚云 《微纳电子技术》 CAS 北大核心 2023年第12期2020-2027,共8页
基于金纳米花(AuNF)的阵列式表面增强Raman散射(SERS)基底可实现黄瓜中百菌清残留的快速、高灵敏度和高通量检测。首先,通过一步合成法制备AuNF。然后,将AuNF组装在双面离型纸表面,以制备阵列式SERS基底。双面离型纸的疏水特性使AuNF富... 基于金纳米花(AuNF)的阵列式表面增强Raman散射(SERS)基底可实现黄瓜中百菌清残留的快速、高灵敏度和高通量检测。首先,通过一步合成法制备AuNF。然后,将AuNF组装在双面离型纸表面,以制备阵列式SERS基底。双面离型纸的疏水特性使AuNF富集,提供丰富的“热点”。以4-巯基苯甲酸(4-MBA)作为Raman信号分子,评估阵列式SERS基底的SERS增强效应,增强因子为4.28×10^(7)。最后,基于阵列式SERS基底对黄瓜中百菌清残留进行检测。该SERS基底可快速检测黄瓜中百菌清残留,无需进行标记或复杂的前处理,其最低检测限(LOD)为5×10^(-9)mol/L。与新制备基底相比,储存15天基底检测相同浓度百菌清的SERS强度仅下降到92.22%,重现性测试的相对标准偏差(RSD)为1.38%。并且该方法检测实际样品的结果与气相色谱法检测结果对比无明显差异。阵列式SERS基底表现出良好的灵敏度、稳定性、重现性和实用性,可实现黄瓜中百菌清残留的快速、高灵敏度和高通量检测。 展开更多
关键词 金纳米花(AuNF) 表面增强Raman散射(SERS) 阵列式疏水基底 百菌清 黄瓜
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利用气相色谱法同时测定生活饮用水中的百菌清和溴氰菊酯 被引量:2
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作者 李婧 《品牌与标准化》 2023年第4期85-87,共3页
本文采用液液萃取法和固相萃取法对生活饮用水中的百菌清和溴氰菊酯进行萃取,真空浓缩后,用HP-5毛细管柱进行组分分离后经电子捕获检测器(ECD)检测。文中对两种萃取方法进行比较后将固相萃取作为预处理方法。
关键词 百菌清 溴氰菊酯 液液萃取 固相萃取 气相色谱
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气相色谱法测定水中百菌清和溴氰菊酯的含量 被引量:1
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作者 欧蕾 《江西化工》 2023年第1期16-19,共4页
文章从标线、检出限、精密度和准确度等方面验证《水质百菌清和溴氰菊酯的测定气相色谱法》(HJ 698-2014)在本实验室的适应性。试验结果表明,当取样体积为100mL时,测得百菌清的检出限为0.06μg/L,测定下限为0.24μg/L,准确度在106.2%~11... 文章从标线、检出限、精密度和准确度等方面验证《水质百菌清和溴氰菊酯的测定气相色谱法》(HJ 698-2014)在本实验室的适应性。试验结果表明,当取样体积为100mL时,测得百菌清的检出限为0.06μg/L,测定下限为0.24μg/L,准确度在106.2%~118.0%,精密度在1.29%~2.44%;溴氰菊酯的检出限是0.10μg/L,测定下限0.40μg/L,准确度在82.5%~106.2%,精密度在2.85%~6.79%,测定结果满足HJ 698-2014标准方法要求。 展开更多
关键词 百菌清 溴氰菊酯 气相色谱法
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