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1.
为评价氯胺嘧草醚的环境安全性,采用批量平衡法测定了氯胺嘧草醚在5种土壤中的吸附-解吸行为,并运用数学模型对其吸附-解吸特性及移动性能进行了分析。结果表明:氯胺嘧草醚在5种土壤中的等温吸附-解吸曲线符合Freundlich模型,吸附常数(Kf值)范围在6.991~18.49之间;不同土壤对其的吸附作用强弱依次为:黑土 > 水稻土 > 褐土 > 潮土 > 红土。氯胺嘧草醚在5种土壤中的有机碳吸附常数(KOC)范围在704.4~1 579之间,推测其在土壤中具有低移动性;薄层层析试验也表明,氯胺嘧草醚在土壤中的移动性较弱。氯胺嘧草醚在5种土壤中的吸附自由能绝对值均小于40 kJ/mol,表明其吸附机理主要是物理吸附。其Kf值与土壤有机质含量、黏粒含量呈正相关,而与土壤pH值呈负相关。解吸试验表明,氯胺醚在其中3种土壤中的解吸过程存在滞后现象。研究表明,在正常使用情况下,氯胺嘧草醚不易对地表水或地下水造成污染风险。  相似文献   

2.
吡嘧磺隆在水稻中的残留消解及膳食风险评估   总被引:1,自引:0,他引:1  
本文建立了超高效液相色谱-串联质谱法(UPLC-MS/MS)测定糙米、稻壳、稻田水、土壤和水稻植株中吡嘧磺隆残留的分析方法,并对我国不同人群的膳食暴露风险进行评估。样品经甲酸乙腈提取,超纯水稀释10倍,UPLC-MS/MS检测。结果表明:在添加水平为0.000 5~1mg/kg范围内,吡嘧磺隆在稻田水、土壤、糙米、稻壳和水稻植株中平均回收率为73.7%~113.6%,相对标准偏差(RSD)为1.5%~12.5%。2014年-2015年北京、安徽和广西田间规范残留试验表明,吡嘧磺隆在水稻植株、土壤和稻田水中的消解符合一级动力学方程,半衰期分别为0.8~2.9d,4.4~5.2d和0.9~5.9d。膳食摄入风险评估显示:我国各类人群的吡嘧磺隆国家估计每日摄入量(NEDI)为0.002 2~0.005 3μg/kg,风险商值(RQ)为5.1×10~(-5)~1.23×10~(-4),表明吡嘧磺隆在糙米中的残留水平不会对人类健康造成不可接受的慢性中毒风险。  相似文献   

3.
不同种类化肥对塿土吸附解吸铅、镉行为的影响   总被引:1,自引:0,他引:1  
通过塿土对重金属Pb和Cd的吸附解吸试验,研究了5种不同类型氮、磷化肥对重金属Pb、Cd的吸附解吸特性的影响。结果表明:在吸附过程中,添加不同种类肥料能够改变塿土对Cd的吸附量,对Pb影响不大;土壤对Pb~(2+)的等温吸附曲线用Langmuir方程拟合效果好,对Cd的吸附曲线用Freundlich和Langmuir方程拟合均能达到显著水平(P0.01);由Langmuir方程拟合得到的最大吸附量可以看出,除磷酸二氢钾促进了土壤Cd的吸附,其余肥料的添加均抑制了土壤对Pb、Cd的吸附量。在解吸过程中,Pb的解吸过程受肥料影响显著,含磷肥料能促进铅解吸率的增大,解吸率最高可达90%以上。由于添加不同类型的肥料影响了土壤对Pb、Cd的吸附和解吸过程,因此,在已经受到Pb、Cd污染的农田进行耕作时,应谨慎选择施用对Pb、Cd影响强烈的磷肥,以避免增加Pb、Cd的迁移对作物造成危害。  相似文献   

4.
采用高效液相色谱-串联质谱法(HPLC-MS/MS),建立了稻田水、土壤、水稻植株、稻秆、稻壳及糙米基质中吡嘧磺隆和苯噻酰草胺的残留分析方法。样品经20 m L V(乙腈)∶V(水)=70∶30的混合溶液提取,提取液用20 mg石墨化碳黑(GCB)与30 mg乙二氨基-N-丙基硅烷(PSA)净化,HPLC-M S/M S检测。吡嘧磺隆在上述各基质中的添加回收率在76%~107%之间,相对标准偏差(RSD)在1.5%~14%之间,定量限为0.004~0.01 mg/kg;苯噻酰草胺的添加回收率在77%~101%之间,RSD在2.4%~13%之间,定量限为0.001~0.01 mg/kg。实现了对两种除草剂同时简便、快速测定的要求。采用该方法测定了26%吡嘧磺隆·苯噻酰草胺水面扩展粒剂在稻田施用后,其有效成分吡嘧磺隆和苯噻酰草胺在实际样品中的残留量。结果表明,两种除草剂均属于易降解农药,在本试验条件下其在糙米中的残留量均低于我国最大残留限量(MRL)(吡嘧磺隆0.1 mg/kg;苯噻酰草胺0.05 mg/kg)。  相似文献   

5.
建立五氟磺草胺和吡嘧磺隆20%SC在稻田土中的残留分析方法,探讨五氟磺草胺和吡嘧磺隆在稻田土中的贮存稳定性。选用乙腈∶水∶乙酸55∶45∶0.1(V∶V∶V)为流动相,流速为0.8m L/min,在250nm采用外标法对五氟磺草胺和吡嘧磺隆进行高效液相色谱分析,在此方法基础上,研究五氟磺草胺和吡嘧磺隆在-18℃下在稻田土中的贮存稳定性规律。五氟磺草胺和吡嘧磺隆的相对标准偏差分别为0.42%~1.35%和2.9%~5.70%,平均回收率分别为77.34%~104.51%和83.71%~90.24%,线性相关系数分别为0.999 9和0.999 7。五氟磺草胺和吡嘧磺隆在-18℃下在稻田土中贮存60d后,分解率5%,符合FAO/WHO联合标准的等同认定要求。五氟磺草胺和吡嘧磺隆具有良好的稳定性。该方法简单、快捷、准确度和精密度高,可用于五氟磺草胺和吡嘧磺隆的同时测定和分析。  相似文献   

6.
不同玉米品种对氯吡嘧磺隆的耐药性差异及其机制   总被引:2,自引:1,他引:1  
为科学评价氯吡嘧磺隆对玉米的安全性,采用室内盆栽法和酶活力测定法探讨不同玉米品种对氯吡嘧磺隆的耐药性差异及其机制。不同玉米品种对氯吡嘧磺隆的耐药性有较大差异,其中甜玉米耐药性最差,IC10仅为94.87g/hm2(有效成分,余同)。花糯1号、鲁单981、五岳97-1等品种表现出中等耐药性,耐药性倍数为1.51~1.97;五岳21、郑单958、强盛16等耐药性较强,耐药性倍数为2.05~2.43。强盛16、鲁单981和甜玉米对氯吡嘧磺隆的耐药性差异显著,但其靶标酶乙酰乳酸合成酶(ALS)在离体条件下对该药剂的敏感性差异不显著;在活体条件下,三者ALS活力均可很快恢复,且耐药性品种恢复能力较强。与甜玉米相比,经氯吡嘧磺隆处理后强盛16的谷胱甘肽-S-转移酶(GSTs)对氯吡嘧磺隆的反应幅度较大和反应时间较短,第72h相对活力就达到4.2的峰值,而甜玉米变化幅度相对较小,第96 h才达到2.6的峰值。研究表明,不同玉米品种对氯吡嘧磺隆耐药性的差异源于GSTs对氯吡嘧磺隆的代谢差异,而与靶标酶ALS对氯吡嘧磺隆的敏感程度无关。  相似文献   

7.
本文采用液相色谱-质谱联用快速分析方法,来检测吡嘧磺隆在水稻植株、土壤残留动态,探究液相色谱-质谱的灵敏度、准确度和可靠性。本文采用Qu ECHERS方法进行样品快速前处理,样品经乙腈提取,PSA、C18吸附剂净化,C18色谱柱分离,0.2%甲酸水∶乙腈等度洗脱,质谱采用电喷雾正离子(ESI+)模式电离,多反应离子监测模式定性分析,基质标匹配外标法定量。在0.02~0.1mg/kg浓度范围内,在不同基质中的吡嘧磺隆的线性相关系数均0.990 7。在3个浓度添加水平范围内,土壤、水稻植株、稻壳和糙米样品中吡嘧磺隆的平均回收率在78.4%~100.3%之间,相对偏差为1.80%~14.9%。该方法简单、快速、灵敏度高、准确度好,能够满足水稻及土壤中吡嘧磺隆残留量的检测要求。  相似文献   

8.
建立了高效液相色谱-串联质谱检测糙米、稻壳和秸秆中氯吡嘧磺隆残留的分析方法。样品经乙腈和水提取,C 18吸附剂净化,多反应监测模式检测,外标法定量。结果表明,在0.01~2mg/L范围内,氯吡嘧磺隆的质量浓度与对应的峰面积间呈良好的线性关系,其相关系数为0.9997。在0.01~0.5mg/kg添加水平下,氯吡嘧磺隆在糙米中的平均回收率为95%~98%,相对标准偏差(RSD)为2%~4%。在0.05~5mg/kg添加水平下,氯吡嘧磺隆在稻壳和秸秆中的平均回收率为78%~87%,相对标准偏差(RSD)为1%~5%。氯吡嘧磺隆在糙米中的定量限(LOQ)为0.01mg/kg,在稻壳和秸秆中的定量限(LOQ)为0.05mg/kg。该方法简便、快速、准确。  相似文献   

9.
通过田间小区试验评价了前期筛选的几种适用“播喷同步”的封闭除草剂对水稻的安全性及对直播田杂草的防效, 明确了“播喷同步”技术与常规播后4 d封闭的差异, 以及施药时期×除草剂种类交互作用及对控草效果的影响, 优化水稻直播田杂草防控策略?试验结果表明, 播种当天(播喷同步)或播种后4 d(常规方法)喷施120 g/L噁草酮EC 360 g/hm2+10%苄嘧磺隆WP 30 g/hm2(有效剂量, 下同)?33%嗪吡嘧磺隆WG 74.25 g/hm2+300 g/L丙草胺EC 450 g/hm2?60%丁草胺EC 1 350 g/hm2+10%吡嘧磺隆WP 30 g/hm2?35%吡嘧·嘧草·丙OD 525 g/hm2?300 g/L丙草胺EC 450 g/hm2+10%苄嘧磺隆WP 30 g/hm2, 5组除草剂处理对直播稻均无可见药害, 各“播喷同步”处理的杂草防除效果不低于常规播后4 d用药; 同步喷施33%嗪吡嘧磺隆WG+300 g/L丙草胺EC防效最高, 药后35 d对禾本科?莎草科?阔叶草防效达到98.3%及以上; 水稻直播4 d后喷药, 水稻成苗率提高但 35 d 的禾本科杂草防效低, 33%嗪吡嘧磺隆WG+300 g/L丙草胺EC处理受喷药时间影响小; 复合双因子方差分析表明, 单一因子会对水稻安全性?杂草防效产生显著影响, 用药时期×除草剂种类交互对水稻安全性无显著影响, 对控草效果影响显著?因此, 直播田封闭除草剂宜尽早施药提高防治效果, 同时应选用安全高效的除草剂, 33%嗪吡嘧磺隆WG+300 g/L丙草胺EC处理, 可于播种当天到播种后4 d内用药, 保障直播田杂草防治效果的同时兼顾水稻安全?  相似文献   

10.
为研究三氟苯嘧啶的吸附-解吸附特性,采用振荡平衡法研究了三氟苯嘧啶在采集于吉林通化、江苏扬州、江西萍乡、广西南宁和海南海口等地的5种土壤中的吸附-解吸附行为及其环境影响因素。结果表明:三氟苯嘧啶在土壤中的吸附动力学符合Elovich模型,吸附和解吸附等温线符合Freundlich模型,吸附常数在1.886~7.626。温度的升高更有利于吸附,土壤对三氟苯嘧啶的吸附主要是物理吸附;随着溶液中pH值的升高,土壤对三氟苯嘧啶的吸附能力逐渐下降。除广西南宁黏壤土外,三氟苯嘧啶在5种土壤中的解吸附过程中存在滞后现象,不易在土壤中长期积累,具有一定的迁移特性。  相似文献   

11.
鱼藤酮在3种土壤中的吸附-解吸附特性   总被引:2,自引:0,他引:2  
为了综合评价鱼藤酮在土壤环境中的吸附-解吸附特性,采用批量平衡法,系统研究了鱼藤酮在砂壤土、黏壤土及壤土3种农业土壤中的吸附-解吸附行为。结果表明,鱼藤酮在3种土壤中的吸附-解吸附行为符合Freundlich模型 (R2≥0.946 8),吸附常数 (Kf-ads) 在1.52~11.39之间,吸附能力为:黏壤土 > 砂壤土 > 壤土;而解吸附常数 (Kf-des) 在1.02~4.55之间,解吸附强弱次序为壤土 > 黏壤土 > 砂壤土。鱼藤酮在砂壤土、黏壤土和壤土3种土壤中有机碳吸附常数 (KOC) 分别为982、101 7和219,而滞后系数 (H) 分别为0.687 3、0.556 9和0.892 3,表明鱼藤酮在黏壤土及砂壤土中移动性较弱,有正迟滞作用,而在壤土中移动性较强,无迟滞作用。该研究将对鱼藤酮的环境风险评估具有一定的理论指导意义。  相似文献   

12.
Flumioxazin adsorption kinetics were described using a Greenville sandy clay loam soil. Adsorption kinetics experiments showed that 72% of total herbicide was absorbed after 1 h of continuous shaking and continued to increase to 78% after 72 h. Flumioxazin adsorption was then tested on seven agriculturally important soils throughout the southern USA. Adsorption isotherms for all soils had K(f) (Freundlich distribution coefficient) values that ranged from 8.8 to 0.4, with many near 1.5. Soil organic matter content was the parameter most highly correlated with flumioxazin adsorption (r(2) = 0.95, P < 0.001). Sorption to clay minerals had K(f) values ranging from 50 for bentonite to 4.7 for kaolinite. However, normalizing K(f) for sorbent surface area revealed that aluminum hydroxide (gibbsite) possessed the greatest flumioxazin sorption per unit area. Sorption to anionic exchange resin (K(f) 676) was greater than cationic exchange resin (K(f) 42). Molecular model calculations were performed to elucidate why sorption was greater to anionic exchangers. These calculations indicated that a region of dense electronegativity exists on the 3-dione moiety of the molecule. This would lead to greater flumioxazin sorption by positively charged surface sites. Desorption isotherms from soil exhibited no effect of hysteresis. Desorption from clay minerals was very rapid and flumioxazin in solution was undetectable after three desorption steps. From these data it was concluded that flumioxazin can become readily available in soil solution with increase in soil water content.  相似文献   

13.
采用静态批次试验法研究西北旱作农田黄土对Pb(Ⅱ)的吸附等温线和动力学特性,通过正交试验揭示Pb(Ⅱ)的解吸行为。结果表明:黄土对Pb(Ⅱ)的吸附过程更好地符合Langmuir等温线方程和准二级动力学方程,拟合系数R2分别为0.9937和0.9964;Langmuir方程计算得出的黄土对Pb(Ⅱ)的最大吸附量qm为17.0068mg/g。吸附过程自发、吸热,反应后体系自由度略有增加。对比极差R值发现:影响解吸过程的主要因素为水土比和解吸时间,在水土比为150mL/g、解吸时间为3 h、解吸液pH值为5和解吸温度为288 K时,Pb(Ⅱ)的平均解吸率r为50.15%。去除有机质农田黄土对Pb(Ⅱ)的吸附量qe仅为6.6814mg/g,推测有机质在Pb(Ⅱ)的去除过程中有重要贡献。  相似文献   

14.
精异丙甲草胺在土壤中的吸附行为及 环境影响因素研究   总被引:1,自引:1,他引:1  
采用平衡振荡法研究了精异丙甲草胺在粘壤土、粘土及砂壤土中的吸附和解吸附行为。结果表明,3种土壤的吸附等温线均属L型并符合Freundlich模型,吸附常数(Kf)分别为4.01、6.15及8.62,且Kf 和1/n(n为经验常数)的乘积与土壤有机质含量呈正相关性。解吸附实验结果表明,精异丙甲草胺在土壤中的解吸附与吸附并不一致,显示出明显的滞后性。温度及pH值等环境因素对吸附影响的结果显示,随温度升高精异丙甲草胺在土壤中的吸附量有所减少,中性环境下土壤吸附量较低。  相似文献   

15.
Isoxaflutole, [4-(2-methanesulfonyl-4-trifluoromethylbenzoyl)-5-cyclopropyl isoxazole] is a relatively new pre-emergence herbicide which undergoes rapid conversion to a diketonitrile metabolite in soil. The half-life of isoxaflutole is very short but the half-life of diketonitrile is much longer and hence, diketonitrile remains for a extended period of time in soil. Sorption-desorption studies were conducted with five soils varying in physical and chemical properties. The batch equilibration technique was used for the sorption experiments, while completely mixed batch reactor systems with the decant and refill method was used for the desorption experiments. Four subsequent desorptions were examined after the sorption process in each soil with an equilibration period of seven days. An apparent sorption-desorption hysteresis was observed in all five soils. Organic matter content and the clay content of the soils were the two determining factors for hysteresis. In soils with high organic matter content, the sorption-desorption hysteresis was mainly governed by organic matter content, but in soils with low organic matter clay content played an important role. With the exception of the Chelsea soil, which had a very high organic matter content (57.4%), all other soils exhibited a high correlation between the clay content and hysteresis index (HI) values calculated at 0.75 ( r 2 = 0.960), 25 ( r 2 = 0.934) and 150 mg L−1 ( r 2 = 0.928). In conclusion, the potential for leaching through soil and crop injury due to isoxaflutole and its metabolite would decrease as soil organic matter and clay content increases.  相似文献   

16.
Adsorption-desorption of the herbicide flufenacet (FOE 5043) has been studied in five soils from different locations in India (Delhi, Ranchi, Nagpur, Kerala and Assam) varying in their physicochemical properties. The organic matter (OM) content varied from 0.072 to 0.864%, clay content from 2.5 to 43.7% and pH from 4.45 to 8.35. The adsorption studies were carried out using a batch equilibration technique. Ten grams of soil were equilibrated with 20 ml of aqueous 0.01 M CaCl2 solution containing different concentrations (0-30 mg litre-1) of flufenacet. After equilibration, an aliquot of supernatant was taken out for analysis. During desorption, the amount withdrawn for analysis was replenished with fresh 0.01 M CaCl2 solution and further equilibrated. Desorption studies were carried out with the 30 mg litre-1 concentration of flufenacet only. The adsorption studies revealed that there was moderate to high adsorption of flufenacet considering the comparatively low organic carbon content in the five test soils. Average Kd values ranged from 0.77 to 4.52 and Freundlich KF values from 0.76 to 4.39. The highest adsorption was observed in Kerala soil (OM 0.786%; clay 25%; pH 4.45) followed by Ranchi, Nagpur and Delhi soils, and the lowest in Assam soil (OM 0.553%; clay 2.5%; pH 6.87). The trend in adsorption could be attributed to the chemical nature of flufenacet and the physicochemical properties of the soil such as pH, OM and clay contents. OM and clay contents were positively correlated whereas pH was negatively correlated. Soils having low pH, high OM and high clay contents showed higher adsorption. Desorption studies revealed that there was a hysteresis effect in all the soils. Hysteresis coefficient values (ratio of n(ad) and n(des)) varied from 0.09 to 0.45. The study implies that, because of its moderate to high adsorption, flufenacet is likely to persist in soil for some time. However, the possibility of its movement by leaching or surface run off is less.  相似文献   

17.
七种农药在3种不同类型土壤中的吸附及淋溶特性   总被引:5,自引:3,他引:2  
采用振荡平衡法和土柱淋溶法研究了2,4-滴酸、丁噻隆、毒草胺、炔草酸、氟环唑、甲基磺草酮和烯啶虫胺7种农药在江西红壤、太湖水稻土及东北黑土3种不同理化性质土壤中的吸附及淋溶特性,探讨了农药性质及土壤理化性质对供试农药在土壤中吸附、淋溶行为的影响。结果表明:农药的水溶性越大,其在土壤中的吸附性越弱,淋溶性越强;农药在土壤中的吸附性与土壤pH值、有机质含量以及阳离子交换量之间有较好的相关性。土壤pH值、有机质含量以及农药性质是影响农药在土壤中淋溶及迁移的主要因素。  相似文献   

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