WO2015081656A1 - 一种含氯氨吡啶酸和异恶草酮的混合除草剂 - Google Patents

一种含氯氨吡啶酸和异恶草酮的混合除草剂 Download PDF

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WO2015081656A1
WO2015081656A1 PCT/CN2014/076344 CN2014076344W WO2015081656A1 WO 2015081656 A1 WO2015081656 A1 WO 2015081656A1 CN 2014076344 W CN2014076344 W CN 2014076344W WO 2015081656 A1 WO2015081656 A1 WO 2015081656A1
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clomazone
ampicillin
salt
herbicide
mixed herbicide
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PCT/CN2014/076344
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French (fr)
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王建兵
彭永强
甘华军
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南京华洲药业有限公司
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Priority to US15/100,635 priority Critical patent/US9936698B2/en
Publication of WO2015081656A1 publication Critical patent/WO2015081656A1/zh

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2

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  • the invention belongs to the technical field of pesticides, especially in the field of herbicides, and relates to a binary compounding agent of clopyridinic acid and clomazone.
  • the herbicidal composition can be applied to non-cultivated land, orchard, woodland, and corn field and rapeseed field weeding.
  • Aminopyralid chemical name: 4-amino-3,6-dichloropyridine-2-carboxylic acid
  • chlorpyridinic acid is a pyridine herbicide widely used in mountain, grassland, lawn, planting Weed control in gardens and non-cultivated land. It can control one-year or perennial broad-leaved weeds.
  • Isooxalin ( C
  • a pigment-inhibiting pre-emergence herbicide developed by the American company fmc inhibits the production of chlorophyll and chlorophyll-protected pigments in plants, causing plants to die in a short period of time.
  • the effective herbicidal properties of the oxalofenone are converted into non-herbicidal degradation products, so that the soybean plants are protected from the damage.
  • Isooxalin mainly controls broadleaf weeds and grass weeds, and can be used for weeding in cotton, cassava, corn, rape, sugar cane and tobacco fields, in addition to soybean fields.
  • the problem of clopyral acid residues is serious, and has been strictly limited in usage and use in many countries and regions.
  • the chlorpyridinic acid and the oxazinone herbicides are appropriately reduced and mixed to form a mixture, which not only expands the herbicidal spectrum, but also significantly improves the weeding. The effect also avoids the possibility of residual poisoning of the crops.
  • Another object of the present invention is to provide an application of the herbicide in weeding in non-cultivated land, orchard, woodland, corn field and rape field.
  • the herbicide is mainly composed of chlorpyridinic acid and clomazone, and the mass ratio of clopyridinic acid to clomazone is 0.1 ⁇ 80 : 0.1 to 80, preferably, the mass ratio of clopyridic acid to clomazone is ⁇ 60: 1 to 60, and most preferably the mass ratio of clopyridic acid to clomazone is 1 ⁇ 0.5 to 4.
  • the mass percentage of both the clopyralid and the clomazone in the herbicide is 1-85%, and the mass percentage is preferably 10-75%.
  • the mixed herbicide of the present invention wherein the clopyral acid is in the form of a water-soluble salt, and the water-soluble salt includes a sodium salt, a potassium salt, an ammonium salt, an isopropylamine salt, a methylamine salt, a dimethylamine salt, and an ethanol. Ammonium salt, triethanolamine salt, triisopropanolamine salt, etc. Water soluble salts.
  • a conventional surfactant and a thickener which are allowed on the pesticide preparation may be added.
  • Additives such as solvents or solid fillers are formulated into any of the dosage forms allowed on the pesticide. It is preferably processed into an emulsifiable concentrate, a suspending agent, an aqueous emulsion, a microemulsion, a soluble liquid, a wettable powder, and a water-dispersible granule.
  • the invention relates to the application of the mixed herbicide containing chlorpyridin and valerate in the weeding of non-cultivated land, orchard, woodland, corn field and rape field, especially in the prevention of cultivated land, orchard, woodland, corn field and
  • the application of various broadleaf weeds in rapeseed fields has a significant effect.
  • the mixed herbicide of the invention has the advantages of quick effect, wide herbicidal spectrum, long holding period, thorough weeding, low residue, low toxicity, safety and environmental protection, etc., and is high quality non-cultivated land, orchard, woodland, corn field and rape field Chemical herbicide.
  • clopyral acid is present as an isopropylamine salt.
  • the water is made up to 100%, and is formulated into an aqueous emulsion having a mass percentage of 30% according to a conventional formulation method.
  • chlorpyridyl acid exists in the form of a sodium salt.
  • clopyral acid exists in the form of a methylamine salt.
  • chlorpyridyl acid exists in the form of a sodium salt.
  • Example 5 10% of oxalofenone, 10% of chlorpyridinic acid, 5% of sodium dodecylbenzenesulfonate, 3% of nonylphenol ethoxylate, 5% of ammonium sulfate, 100% of kaolin, according to conventional preparation methods Formulated as a wettable powder with a mass percentage of 30%.
  • chlorpyridyl acid exists in the form of a sodium salt.
  • the formulation method is formulated into a water-dispersible granule having a mass percentage of 75%.
  • chlorpyridyl acid exists in the form of a potassium salt.
  • chlorpyridyl acid exists in the form of a sodium salt.
  • clopyral acid exists in the form of a triisopropanolamine salt.
  • a soluble liquid agent having a mass percentage of 10% is formulated according to a conventional formulation method.
  • chlorpyridyl acid exists in the form of a sodium salt.
  • Test method The seeds of the quantitative Amaranthus were separately sown in 9cm disposable cups, and 10 ⁇ 15 seeds were sown in each cup, and cultured in a light incubator. When the A. philoxeroides was 3 ⁇ 6 leaves, in the track Spray treatment on the crop spray. After treatment, the culture was continued in the greenhouse. The weed control effect of each treatment was observed regularly. After 30 days, the fresh weight of weeds after each treatment was weighed. According to the method proposed by Sun Yunpei et al. in I960, the virulence regression curve and co-toxicity coefficient were calculated. . The co-toxicity coefficient is greater than 100, indicating that the two effective substances have synergistic effects, and the co-toxicity coefficient is less than 100, indicating that the two effective substances have antagonistic effects. The measurement results are shown in Table 1. Table 1 Indoor activity measurement results
  • Test agent Four kinds of binary compound herbicides in Examples 1 to 4.
  • Control agent 48% clomazone emulsifiable concentrate (commercially available), 30% chlorpyridinic acid aqueous solution (commercially available).
  • Control crops corn.
  • Control objects weeds such as comfrey, bristle, alfalfa, alfalfa, leeks, and purslane.
  • Test method According to the area of the test plot, accurately weigh all kinds of medicaments, and after dilution with water, use a knapsack sprayer to evenly spray.
  • the nozzles use fan-shaped nozzles for herbicides. When spraying, it is necessary to spray the liquid evenly into the test area, so that there is no leakage or multiple spray.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

 本发明公开了一种含氯氨吡啶酸与异恶草酮的混合除草剂,属于农药技术领域。该除草剂以氯氨吡啶酸与异恶草酮为主要有效成分,氯氨吡啶酸与异恶草酮的质量比为0.1~80: 0.1~80。本发明混合除草剂在非耕地、果园、林地、玉米田和油菜田除草中的应用,具有见效快、杀草谱宽,持效期长、除草彻底、残留低、低毒、安全环保等优点,是优质的非耕地、果园、林地、玉米田和油菜田化学除草剂。

Description

说 明 书
种含氯氨吡啶酸和异恶草酮的混合除草剂 技术领域
本发明属于农药技术领域, 尤其是除草剂领域, 涉及氯氨吡啶酸与异恶草酮的二元复配 剂。 该除草剂组合物可应用于非耕地、 果园、 林地和、 玉米田和油菜田除草。
背景技术
氯氨吡啶酸 (aminopyralid ) , 化学名称: 4-氨基 -3,6-二氯吡啶 -2-羧酸, 氯氨吡啶酸是 一种吡啶类除草剂, 广泛用于山地、 草原、 草坪、 种植园和非耕地的杂草防治。 可以防治一 年生或多年生阔叶杂草。
异恶草酮 (C|0maz0ne) , 属于恶唑类除草剂, 化学名称: 2- ( 2-氯苄基) -4, 4-二 甲基 -3-异恶唑酮。 由美国 fmc 公司幵发的一种色素抑制芽前类的除草剂, 在植物体内抑制 叶绿素及叶绿素保护色素的产生, 使植物在短期内死亡。 但当它被大豆吸收后, 经过代谢作 用, 异恶草酮的有效杀草性质会转变为无杀草能力的降解产物, 使大豆植株免受其害。 异恶 草酮主要防除阔叶杂草和禾本科杂草, 除大豆田外, 还可以用于棉花、 木薯、 玉米、 油菜、 甘蔗和烟草田等的除草。
目前氯氨吡啶酸残留问题严重, 在很多国家和地区已经被严格限制使用量和使用方法。 为了在减少残留药害的同时, 确保药剂的除草效果, 将氯氨吡啶酸与异恶草酮两种除草剂 适当减量后配成合剂使用, 这样既扩大了杀草谱, 明显提高了除草效果, 也避免了对后茬作 物产生残留毒害的可能性。
发明内容
本发明的目的是提供一种含氯氨吡啶酸与异恶草酮的混合除草剂。
本发明的另一目的是提供该除草剂在非耕地、 果园、 林地、 玉米田和油菜田除草中的应 用。
一种含氯氨吡啶酸与异恶草酮的混合除草剂, 该除草剂以氯氨吡啶酸与异恶草酮为主要 有效成分, 氯氨吡啶酸与异恶草酮的质量比为 0.1〜80: 0.1〜80, 优选氯氨吡啶酸与异恶草 酮的质量比为〗〜 60: 1〜60, 最优选氯氨吡啶酸与异恶草酮的质量比为 1 ·· 0.5〜4。
在混合除草剂中, 氯氨吡啶酸与异恶草酮二者在除草剂中的质量百分含量为 1~85%, 优 选质量百分含量为 10~75%。
本发明的混合除草剂, 其中氯氨吡啶酸以水溶性盐的形式存在, 所述的水溶性盐包括钠 盐、 钾盐、 铵盐、 异丙胺盐、 甲胺盐、 二甲胺盐、 乙醇铵盐、 三乙醇胺盐、 三异丙醇胺盐等 水溶性盐类。
本发明的氯氨吡啶酸与异恶草酮的二元复配制剂中, 除了氯氨吡啶酸与异恶草酮有效成 分外, 还可以添加农药制剂上允许的常规表面活性剂、 增稠剂、 溶剂或固体填料等助剂配制 成农药上允许的任意一种剂型。 优选加工成乳油、 悬浮剂、 水乳剂、 微乳剂、 可溶性液剂、 可湿性粉剂、 水分散粒剂。
本发明所述的 均为质量百分含量。
本发明所述的含氯氨吡啶酸与喔草酯的混合除草剂在非耕地、 果园、 林地、 玉米田和油 菜田除草中的应用, 特别是在防除非耕地、 果园、 林地、 玉米田和油菜田中各种阔叶杂草中 的应用具有显著效果。
和现有技术相比, 本发明的有益效果:
本发明的混合除草剂, 具有见效快、 杀草谱宽, 持效期长、 除草彻底、 残留低、 低毒、 安全环保等优点, 是优质的非耕地、 果园、 林地、 玉米田和油菜田化学除草剂。
具体实施方案
实施例 1
异恶草酮 20%, 氯氨吡啶酸 5%, 十二垸基苯磺酸钙 5%, 垸基酚聚氧乙烯醚 3%, 150# 溶剂油至 100%, 按照常规的制剂方法配制成质量百分含量为 25%的乳油。 其中氯氨吡啶酸 以异丙胺盐形式存在。
实施例 2
异恶草酮 10%, 氯氨吡啶酸 20%, 垸基酚聚氧乙烯醚 3%, 蓖麻油聚氧乙烯醚 2%, 黄 原胶 0.1%, 二甲苯 20%, 乙二醇 5%, 水至 100%, 按照常规的制剂方法配制成质量百分含 量为 30%的水乳剂。 其中氯氨吡啶酸以钠盐形式存在。
实施例 3
异恶草酮 15%, 氯氨吡啶酸 10%, 垸基酚聚氧乙烯醚磷酸酯 5%, 硅酸镁铝 2%, 白炭 黑 2%, 乙二醇 5%, 水至 100%, 按照常规的制剂方法配制成质量百分含量为 25%的悬浮 剂。 其中氯氨吡啶酸以甲胺盐形式存在。
实施例 4
异恶草酮 25%, 氯氨吡啶酸 50%, 木质素磺酸钠 5%、 十二垸基硫酸盐 2%, 硫酸铵 5% , 高岭土至 100%, 按照常规的制剂方法配制成质量百分含量为 75%的水分散粒剂。 其 中氯氨吡啶酸以钠盐形式存在。
实施例 5 异恶草酮 10%, 氯氨吡啶酸 10%, 十二垸基苯磺酸钠 5%, 垸基酚聚氧乙烯醚 3%, 硫 酸铵 5%, 高岭土至 100%, 按照常规的制剂方法配制成质量百分含量为 30%的可湿性粉 剂。 其中氯氨吡啶酸以钠盐形式存在。
实施例 6
异恶草酮 15%, 氯氨吡啶酸 60%, NNO (亚甲基双荼磺酸钠) 润湿剂 5%、 硫酸铵 3%, 聚乙烯醇 2%, 高岭土至 100%, 按照常规的制剂方法配制成质量百分含量为 75%的水 分散粒剂。 其中氯氨吡啶酸以钾盐形式存在。
实施例 7
异恶草酮 20%, 氯氨吡啶酸 10%, NNO (亚甲基双荼磺酸钠) 6%, 木质素磺酸钠 5%, 高岭土至 100%, 按照常规的制剂方法配制成质量百分含量为 30%的可湿性粉剂。 其中 氯氨吡啶酸以钠盐形式存在。
实施例 8
异恶草酮 9%, 氯氨吡啶酸 1%, 十二垸基苯磺酸钙 5%, 蓖麻油聚氧乙烯醚 5%, 150# 溶剂油 15%, 环己酮 5%, 乙二醇 5%, 水至 100%, 按照常规的制剂方法配制成质量百分含 量为 10%的微乳剂。 其中氯氨吡啶酸以三异丙醇胺盐形式存在。
实施例 9
异恶草酮 1%, 氯氨吡啶酸 9%, 十二垸基苯磺酸钠 5%, 垸基糖苷 5%, 异丙醇 15%, 环己酮 5%, 乙二醇 5%, 水至 100%, 按照常规的制剂方法配制成质量百分含量为 10%的可 溶性液剂。 其中氯氨吡啶酸以钠盐形式存在。
实施例 10
1、 室内活性测定试验
利用实施例 1~4中的制剂, 测定其对空心莲子草的共毒系数。
试验方法: 将定量的铁苋菜的种子分别播种于 9cm的一次性纸杯中, 每杯中播种 10~15 粒种子, 在光照培养箱中培养, 待空心莲子草 3~6叶期时, 在履带式作物喷雾剂上进行喷雾 处理。 处理后温室内继续培养, 定期观察各处理对杂草的防除效果, 30d后称量各处理后的 杂草鲜重, 按孙云沛等 I960年提出的方法, 计算其毒力回归曲线和共毒系数。 共毒系数大 于 100, 表明两种有效物质具有增效作用, 共毒系数小于 100, 表明两种有效物质具有拮抗 作用。 测定结果如表 1所示。 表 1 室内活性测定结果
Figure imgf000005_0001
从表 1可以看出, 两种有效物质复配后的共毒系数都大于 100, 说明本发明具有明显的 增效作用。
2、 田间药效试验
供试药剂: 实施例 1〜4中的 4种二元复配除草剂。
对照药剂: 48%异恶草酮乳油 (市售), 30%氯氨吡啶酸水剂 (市售)。
防治作物: 玉米。
防除对象: 鸭跖草、 猪殃殃、 空心莲子草、 荠菜、 马齿苋等杂草。
试验方法: 按照试验小区的面积, 准确称量好各种药剂, 并兌水稀释后, 利用背负式喷 雾器, 进行均匀喷雾, 喷头选用除草剂专用的扇形喷头。 喷雾时, 要注意将药液均匀喷施到 试验小区中, 做到没有漏喷、 多喷的现象。
试验后分别在药后 20d、 40d观察杂草死亡情况, 并比较各种药剂的除草活性。
本发明的实施例制剂除草试验效果见下表 2 (药后 20d) 和表 3 (药后 40d)
田间药效试验结果 (药后 20d) 用 量 鸭跖草 猪殃殃 空心莲子草 处理药剂
(ga.i./亩) 防效 (%) 防效 (%) 防效 (%) 实施例 1 15 92 93 92 实施例 2 15 93 95 94 实施例 3 15 94 95 95 实施例 4 15 93 92 93
30%氯氨吡啶酸水剂 20 90 88 87 48%异恶草酮乳油 15 88 86 84 表 3 田间药效试验结果 (药后 40d) 用 量 鸭跖草 猪殃殃 空心莲子草 处理药剂
(ga.i./亩) 防效 (%) 防效 (%) 防效 (%) 实施例 1 15 85 85 83 实施例 2 15 86 85 83 实施例 3 15 88 87 85 实施例 4 15 85 83 82
30%氯氨吡啶酸水剂 20 77 71 76
48%异恶草酮乳油 15 76 73 71 从表 2和表 3中可以看出, 本发明对阔叶杂草都具有显著的防效, 增效性显著, 而且 效快、 持效期长。

Claims

权 利 要 求 书
1、 一种含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于该除草剂以氯氨吡啶酸与 异恶草酮为主要有效成分, 氯氨吡啶酸与异恶草酮的质量比为 0.1〜80: 0.1〜80。
2、 根据权利要求 1 所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于该除草 剂中氯氨吡啶酸与异恶草酮的质量比为 1〜60: 1〜60。
3、 根据权利要求 2 所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在 f该除草 剂中氯氨吡啶酸与异恶草酮的质量比为 1 : 0.5〜4。
4、 根据权利要求 1 所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于氯氨吡 啶酸与异恶草酮二者在除草剂中的质量百分含量为 1~85%。
5、 根据权利要求 4所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于氯氨吡 啶酸与异恶草酮二者在除草剂中的质量百分含量为 10~75%。
6、 根据权利要求 1-5 任一一项所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征 在于所述的氯氨吡啶酸以水溶性盐的形式存在, 所述的水溶性盐包括钠盐、 钾盐、 铵盐、 异 丙胺盐、 甲胺盐、 二甲胺盐、 乙醇铰盐、 三乙醇胺盐、 三异丙醇胺盐。
7、 根据权利要求 1 所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于它以氯 氨吡啶酸与异恶草酮为主要有效成分和农药上允许的助剂配制成任意一种剂型。
8、 根据权利要求 7所述的含氯氨吡啶酸和异恶草酮的混合除草剂, 其特征在于所述的 剂型为乳油、 悬浮剂、 水乳剂、 微乳剂、 可溶性液剂、 可湿性粉剂、 水分散粒剂。
9、 权利要求 1 所述的含氯氨吡啶酸和异恶草酮的混合除草剂在非耕地、 果园、 林地、 玉米田和油菜田除草中的应用。
10、 权利要求 1所述的含氯氨吡啶酸和异恶草酮的混合除草剂在防除非耕地、 果园、 林 地、 玉米田和油菜田中各种阔叶杂草中的应用。
替换页 (细则第 26条)
PCT/CN2014/076344 2013-12-06 2014-04-28 一种含氯氨吡啶酸和异恶草酮的混合除草剂 WO2015081656A1 (zh)

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