CN106035358A - 一种灭幼脲杀虫组合物 - Google Patents
一种灭幼脲杀虫组合物 Download PDFInfo
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- CN106035358A CN106035358A CN201610506300.6A CN201610506300A CN106035358A CN 106035358 A CN106035358 A CN 106035358A CN 201610506300 A CN201610506300 A CN 201610506300A CN 106035358 A CN106035358 A CN 106035358A
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- Prior art keywords
- ichlorbenzuron
- pyrazoles
- indanyl
- chlorbenzuron
- pyrazoles indanyl
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- 239000000203 mixture Substances 0.000 title claims abstract description 13
- YPSCQJTUAKNUNF-UHFFFAOYSA-N 2-chloro-n-[(4-chlorophenyl)carbamoyl]benzamide Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl YPSCQJTUAKNUNF-UHFFFAOYSA-N 0.000 title abstract description 26
- 230000000749 insecticidal effect Effects 0.000 title abstract description 5
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- 235000013311 vegetables Nutrition 0.000 claims abstract description 4
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- 150000003217 pyrazoles Chemical class 0.000 claims description 47
- DBGKPDNKZZGWOM-UHFFFAOYSA-N n-(2,3-dihydro-1h-inden-1-yl)formamide Chemical compound C1=CC=C2C(NC=O)CCC2=C1 DBGKPDNKZZGWOM-UHFFFAOYSA-N 0.000 claims description 45
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- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 5
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- DMAXMXPDVWTIRV-UHFFFAOYSA-N 2-(2-phenylethyl)phenol Chemical compound OC1=CC=CC=C1CCC1=CC=CC=C1 DMAXMXPDVWTIRV-UHFFFAOYSA-N 0.000 description 3
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- RRTCFFFUTAGOSG-UHFFFAOYSA-N benzene;phenol Chemical compound C1=CC=CC=C1.OC1=CC=CC=C1 RRTCFFFUTAGOSG-UHFFFAOYSA-N 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
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- 150000001408 amides Chemical class 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
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- MREIFUWKYMNYTK-UHFFFAOYSA-N 1H-pyrrole Chemical class C=1C=CNC=1.C=1C=CNC=1 MREIFUWKYMNYTK-UHFFFAOYSA-N 0.000 description 1
- XCGBHLLWJZOLEM-UHFFFAOYSA-N 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide Chemical compound CC1CC(C)(C)C(C(=CC=2)F)=C1C=2NC(=O)C1=CN(C)N=C1C(F)F XCGBHLLWJZOLEM-UHFFFAOYSA-N 0.000 description 1
- NASPPUKURYESFJ-UHFFFAOYSA-N C(C)C1=C(C=CC=C1)O.C1=CC=CC=C1 Chemical compound C(C)C1=C(C=CC=C1)O.C1=CC=CC=C1 NASPPUKURYESFJ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
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- 108090000364 Ligases Proteins 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
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- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
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- NWGKJDSIEKMTRX-MDZDMXLPSA-N Sorbitan oleate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OCC(O)C1OCC(O)C1O NWGKJDSIEKMTRX-MDZDMXLPSA-N 0.000 description 1
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- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
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- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
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- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
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- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- 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
本发明涉及农用领域一种杀虫剂组合物,具体地说是以灭幼脲为主体复配而成的一种二元杀虫复合物。吡唑茚满基甲酰胺(或衍生物)与灭幼脲有效成分重量百分比含量为5~80%,吡唑茚满基甲酰胺(或衍生物)与灭幼脲的比例为5:1到1:20。其中最优比例为1/1~1/10可以加工成的剂型包含悬浮剂、可分散油悬浮剂、可湿性粉剂、干悬浮剂、水分散性颗粒剂;二元复合物中的辅助成分包括可以接受的有分散剂、润湿剂、渗透剂、填料等。该组合物复配用来防治甘蓝、苹果、水稻、十字花科蔬菜、棉花、马铃薯等蔬菜及作物上的多种害虫,增效效果显著。
Description
技术领域:
本发明涉及农用领域一种杀虫剂组合物,具体地说是以灭幼脲为主体复配而成的一种二元杀虫复合物。
背景技术:
灭幼脲:
商品名称:灭幼脲三号、扑蛾丹、蛾杀灵、劲杀幼
化学名称:1-(邻氯苯甲酰基)-3-(4-氯苯基)脲;
分子量:308.0;
分子结构式:C14H10N2Cl2O2;
熔点:199℃-201℃;
结构式:
吡唑茚满基甲酰胺类化合物作为一种新型活性成分,有杀菌、杀虫、杀病毒有活性及调节作物生产的作用。其化学名称:3-二氟甲基-N-(7-氟-1,1,3-三甲基-4-茚满基)-1-甲基-4-吡唑甲酰胺,后续简称吡唑茚满基甲酰胺;其分子结构式如下(Me代表甲基-CH3):
目前并没有他们混用情况的报道和记载,发明人在试验中发现,该两类药效混用可以起到明显的增效作用和持效性。
发明内容
本发明基于吡唑茚满基甲酰胺和灭幼脲的特性进行进一步研究,发现并证明以吡唑茚满基甲酰胺及其衍生物和灭幼脲为有效成份进行的混配,可以产生明显的增效效果,提高了速效性和持效期,且扩大了防治谱,降低了使用成本,同时还有降低作物发病,提高作物长势的作用。
为了实现上述目的,本申请所采用的技术方案如下:
一种灭幼脲杀虫组合物,有效成分重量百分比含量为5%~80%,吡唑茚满基甲酰胺或其衍生物与灭幼脲的质量比为5:1~1:20。
优选的,吡唑茚满基甲酰胺或其衍生物与灭幼脲的质量比为1:1~1:10;
灭幼脲属苯甲酰脲类昆虫几丁质合成抑制剂,为昆虫激素类农药。通过抑制昆虫表皮几丁质合成酶和尿核苷辅酶的活性,来抑制昆虫几丁质合成从而导致昆虫不能正常蜕皮而死亡,该药是我国独创产品,国外登记注册很少;在将吡唑茚满基甲酰胺或其衍生物与灭幼脲混用后,有惊人发现:混用后明显加重了灭幼脲的中毒现象,提高了防治效果,起到明显的增效作用。
所述的,吡唑茚满基甲酰胺衍生物选自3-二氯甲基-N-(7-氯-1,1,3-三甲基-4-茚满基)-1-甲基-4-吡唑甲酰胺或3-二氟甲基-N-(7-氟-1,1-二甲基,3-乙基基-4-茚满基)-1-乙基-4-吡唑甲酰胺。
该组合物的剂型为可湿性粉剂、悬浮剂、可分散油悬浮剂、水分散性颗粒剂和干悬浮剂中的一种。
该组合物可以用来防治治甘蓝、十字花科蔬菜、果树、水稻、棉花、油菜、生生、小麦、玉米、马铃薯、森林等农作物上的多种害虫,如:小菜蛾、甜菜夜蛾、菜青虫、斜纹夜蛾、二化螟、三化螟、棉铃虫、美国白蛾等多种植物害虫,具有高效、低毒、低残留、杀虫谱广、增效作用显著并降低使用成本等特点,特别是其高效性、低毒、低残留,尤其有利于绿色食品的生产。
该组合物可以选用的助剂有:烷基苯磺酸盐、木质素磺酸盐类、烷基硫酸盐、烷基聚氧乙烯醚羧酸盐等脂肪酸盐类,脂防醇聚氧乙烯醚、烷基酚聚氧乙烯醚、EOPO嵌段共聚物、苯乙基酚聚氧乙烯醚等非离子单体,黄原胶、羧甲基淀粉钠、硅酸镁铝、乙二醇、丙三醇、大豆油、玉米油、油酸甲酯、尿素、高岭土、膨润土、凹凸棒土、炭酸钙、萘磺酸盐、聚羧酸盐、拉开粉等助剂。
具体实施方式
下面结合实施例对发明涉及的技术方案进行进一步说明,以便有助于本发明的理解,但不作为对技术方案的限制,除特别提及的以外,组分比例均为重量比例。
实施例一
20%吡唑茚满基甲酰胺·灭幼脲悬浮剂;
以配制100克样品为例时原料组成为:5g吡唑茚满基甲酰胺原药,15g灭幼脲原药,1g拉开粉,0.8g亚甲基双荼磺酸钠,2g十二烷基苯磺酸钙,2g三苯乙基苯酚聚氧乙烯醚,苯乙基酚甲醛树酯聚氧乙烯醚1g,1g白炭黑,硅酸镁铝1.5g,0.15g黄原胶,5g的丙三醇,其余用水补足100g,按常规悬浮剂生产方式配制。
该实施例用于防治甘蓝小菜蛾,将20%吡唑茚满基甲酰胺·灭幼脲悬浮剂1500倍兑水稀释喷雾,药后7d和15d的防治效果分别为90.2%和96.7%,20d时防治效果还达到87.3%。20%灭幼脲悬浮剂800倍,用同样的方法使用,药后7d和15d的防效分别为77.8%、80.3%,20d时的防治效果为70.1%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对甘蓝小菜蛾的防治效果好于单剂,延长持效期明显。
将吡唑茚满基甲酰胺和灭幼脲悬浮剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺SC和20%灭幼脲SC作为对照进行小菜蛾毒力测定,具体情况见表1,共毒系数为130.69~165.4,其中5:1~1:20为147.51~165.4,1:1~1:10为158.7~165.4,增效效果显著。
表1
实施例二
30%吡唑茚满基甲酰胺衍生物·灭幼脲悬浮剂;
以配制100克样品为例,原料组成为:10g吡唑茚满基甲酰胺衍生物,20g灭幼脲原药,1g拉开粉,1g亚甲基双荼磺酸钠,1.2g十二烷基苯磺酸钙,1.1g三苯乙基苯酚聚氧乙烯醚,苯乙基酚甲醛树酯聚氧乙烯醚1g,脂防醇聚氧乙烯醚0.8g,1g白炭黑,硅酸镁铝1.5g,0.12g黄原胶,5g丙三醇,其余用水补足100g,按常规悬浮剂生产方式配制。吡唑茚满基甲酰胺衍生物为:3-二氯甲基-N-(7-氯-1,1,3-三甲基-4-茚满基)-1-甲基-4-吡唑甲酰胺。
该实施例用于防治大豆天蛾,将30%吡唑茚满基甲酰胺衍生物·灭幼脲悬浮剂1500倍兑水稀释喷雾,药后7d和15d的防治效果分别为88.7%和95.6%,20d时的防治效果为86.1%。20%灭幼脲悬浮剂800倍用同样的方法使用,药后7d和15d的防效分别为73.6%、85.7%,20d的防治效果为62.9%;灭幼脲和吡唑茚满基甲酰胺衍生物复配后增效作用明显,对大豆天蛾的防治效果好于单剂.
将吡唑茚满基甲酰胺衍生物和灭幼脲悬浮剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺衍生物SC和20%灭幼脲SC作为对照进行大豆天蛾毒力测定,具体情况见表2,共毒系数为129.5~161.3,其中5:1~1:20为142.2~161.3,1:1~1:10为150.1~161.3,增效效果显著。
表2
实施例三
36%吡唑茚满基甲酰胺·灭幼脲悬浮剂;
以配制100克样品为例,原料组成为:9g吡唑茚满基甲酰胺原药,27g灭幼脲原药,1.2g拉开粉,1g亚甲基双荼磺酸钠,1.7g十二烷基苯磺酸钙,2.3g三苯乙基苯酚聚氧乙烯醚,苯乙基酚甲醛树酯聚氧乙烯醚1.5g,0.8g白炭黑,硅酸镁铝1.2g,0.12g黄原胶,5g的丙三醇,其余用水补足100g,按常规悬浮剂生产方式配制。
该实施例用于防治花生斜纹夜蛾,将36%吡唑茚满基甲酰胺·灭幼脲悬浮剂2000倍兑水稀释喷雾,药后7d和15d的防治效果分别为89.7%和96.4%,20d的防治效果为83.2%。20%灭幼脲悬浮剂800倍用同样的方法使用,药后7d和15d的防效分别为76.9%、79.7%,20d的防治效果为63.4%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对花生斜纹夜蛾的防治效果好于单剂。
将吡唑茚满基甲酰胺和灭幼脲悬浮剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺SC和20%灭幼脲SC作为对照进行斜纹夜蛾毒力测定,共毒系数为149.8~170.1,具体情况见表3,其中5:1~1:20为153.6~170.1,1:1~1:10为162.3~170.1,增效效果显著。
表3
实施例四
50%吡唑茚满基甲酰胺·灭幼脲水分散性粒剂
以配制100克样品为例,原料组成为:10g吡唑茚满基甲酰胺原药,40g灭幼脲原药,,聚羧酸盐分散剂9g、萘磺酸盐分散剂6g、羧甲基淀粉钠10g、十二烷基硫酸钠1g、硫酸铵15g、氧化玉米淀粉补充100g。
配制方式:将上述各物料混合后进行气流粉碎、粉碎后检测细度和含量,检测合格后加水混合,然后按挤压法进行造粒、干燥,检测合格后分装即得成品。
该实施例用于防治大豆造桥虫,将50%吡唑茚满基甲酰胺·灭幼脲水分散性粒剂2000倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为89.1%、96.7%和88.4%。20%灭幼脲悬浮剂600倍用同样的方法使用,药后7d、15d和20d的防效分别为79.1%、88.9%和77.5%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对大豆造桥虫的防治效果好于单剂。
将吡唑茚满基甲酰胺和灭幼脲水分散粒剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺WG和20%灭幼脲WG作为对照进行大豆造桥虫毒力测定,共毒系数为136.9~162.4,具体情况见表4,其中5:1~1:20为146.4~162.4,1:1~1:10为151.5~162.4,增效效果显著。
表4
实施例五
12%吡唑茚满基甲酰胺·灭幼脲可分散油悬浮剂;
以配制100克样品为例,原料组成为:2g吡唑茚满基甲酰胺原药,10g灭幼脲原药,有机膨润土1.7g、气相白碳黑2g、羧甲基淀粉钠1g、脂肪醇聚氧乙烯醚5g、司盘80乳化剂6g、聚乙二醇双油酸酯4g、亚油酸聚乙二醇甘油酯5g、十二烷基苯磺酸钙4g、大豆油补充100g。
配制方式:将上述各物料混合后进行砂磨、研磨后检测,检测合格后分装即得成品。
该实施例用于防治玉米斜纹夜蛾,将24%吡唑茚满基甲酰胺·灭幼脲可分散油悬浮剂800倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为87.2%、95.3%和82.4%。20%灭幼脲悬浮剂800倍用同样的方法使用,药后7天和15天的防效分别为76.4%、79.9%和70.9%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对玉米斜纹夜蛾的防治效果好于单剂。
将吡唑茚满基甲酰胺和灭幼脲悬浮剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺悬浮剂和20%灭幼脲悬浮剂作为对照进行玉米斜纹夜蛾毒力测定,共毒系数为149.8~170.1,具体情况见表5,其中5:1~1:20为153.6~170.1,1:1~1:10为162.3~170.1,增效效果显著。
表5
实施例六
70%吡唑茚满基甲酰胺·灭幼脲可湿性粉剂
以配制100克样品为例,原料组成为:10g吡唑茚满基甲酰胺原药,60g灭幼脲原药,10g亚甲基双荼磺酸钠、7g聚羧酸盐分散剂,2g十二烷基硫酸钠,5g萘磺酸盐分散剂,其余用高岭土补足100g。按常规可湿粉生产方式配制。
该实施例用于防治棉花棉铃虫,将70%吡唑茚满基甲酰胺·灭幼脲可湿性粉剂2000倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为80.8%、94.6%和79.8%。20%灭幼脲悬浮剂500倍用同样的方法使用,药后7d和15d、20d的防治效果分别为75.2%、85.4%和72.1%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对棉花棉铃虫的防治效果好于单剂。
将吡唑茚满基甲酰胺和灭幼脲可湿粉分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺可湿粉和20%灭幼脲可湿粉为对照进行棉铃虫毒力测定,共毒系数为139.5~167.7,具体情况见表6,其中5:1~1:20为146.6~167.7,1:1~1:10为151.3~167.7,增效效果显著。
表6
实施例七
54%吡唑茚满基甲酰胺衍生物·灭幼脲可湿性粉剂
以配制100克样品为例,原料组成:6g吡唑茚满基甲酰胺原药衍生物,48g灭幼脲原药;8g亚甲基双荼磺酸钠、5g聚羧酸盐分散剂,2g十二烷基硫酸钠,10g木质素磺酸钙,其余用高岭土补足100g。吡唑茚满基甲酰胺衍生物为:3-二氟甲基-N-(7-氟-1,1-二甲基,3-乙基基-4-茚满基)-1-乙基-4-吡唑甲酰胺。按常规可湿粉生产方式配制。
该实施例用于防治白菜菜青虫,将54%吡唑茚满基甲酰胺衍生物·灭幼脲可湿性粉剂2000倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为88.7%、96.7%和85.8%。20%灭幼脲悬浮剂800倍和5%吡唑茚满基甲酰胺水悬浮剂1000倍,用同样的方法使用,药后7d和15d、20d的防效分别为78.3%、93.7%和79.1%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对白菜菜青虫的防治效果好于单剂,同时用该实施例处理的白菜其长势明显好于对比,对白菜有明显促长作用。
将吡唑茚满基甲酰胺衍生物和灭幼脲可湿粉分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺衍生物可湿粉和20%灭幼脲可湿粉为对照进行菜青虫毒力测定,共毒系数为146.3~174.6,具体情况见表7,其中5:1~1:20为150.5~174.6,1:1~1:10为161.2~174.6,增效效果显著。
表7
实施例八
80%吡唑茚满基甲酰胺·灭幼脲干悬浮剂
以配制100克样品为例,原料组成为:8g吡唑茚满基甲酰胺原药,72g灭幼脲原药,萘磺酸盐分散剂8g、聚羧酸盐分散剂5g、辛基酚聚氧乙烯醚2g、羧甲基淀粉钠补足100g。
配制方式:先在砂磨釜内加入200克水,然后加入上述配方中的各项物料,混匀后进行砂磨,研磨合格后进行喷雾干燥,喷雾干燥后检测,检测合格后分装即得成品。
该实施例用于防治苹果卷叶蛾,将80%吡唑茚满基甲酰胺·灭幼脲可湿性粉剂3000倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为88.8%、95.6%和85.7%。20%灭幼脲悬浮剂800倍用同样的方法使用,药后7d和15d、20d的防效分别为80.2%、92.6%和80.1%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对苹果卷叶蛾的防治效果好于单剂。
将吡唑茚满基甲酰胺和灭幼脲水干悬浮剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以30%吡唑茚满基甲酰胺干悬浮剂和50%灭幼脲干悬浮剂作为对照进行苹果卷叶蛾毒力测定,共毒系数为135.8~162.1,具体情况见表8,其中5:1~1:20为146.1~162.1,1:1~1:10为152.2~162.1,增效效果显著。
表8
实施例九
66%吡唑茚满基甲酰胺衍生物·灭幼脲WDG
以配制100克样品为例,原料组成:6g吡唑茚满基甲酰胺衍生物,60g灭幼脲原药;1g十二烷基苯磺酸钙,5g亚甲基双荼磺酸钠,4g萘磺酸盐甲醛缩合物,6g聚羧酸盐分散剂,10g羧甲基淀粉钠,其余用硫酸铵补足100g,按常规挤压造粒方式配制。吡唑茚满基甲酰胺衍生物为:3-二氯甲基-N-(7-氯-1,1,3-三甲基-4-茚满基)-1-甲基-4-吡唑甲酰胺。
该实施例用于防治大豆甜菜夜蛾,将66%吡唑茚满基甲酰胺衍生物·灭幼脲水分散性颗粒剂2000倍兑水稀释喷雾,药后7d和15d、20d的防治效果分别为88.1%、95.9%和86.3%。20%灭幼脲悬浮剂600倍用同样的方法使用,药后7d和15d、20d的防效分别为77.5%、90.6%和72.3%;灭幼脲和吡唑茚满基甲酰胺复配后增效作用明显,对大豆甜菜夜蛾的防治效果好于单剂。
将吡唑茚满基甲酰胺衍生物和灭幼脲水分散粒剂分别按30/1,25/1,20/1,15/1,10/1,5/1、3/1,1/1,1/3,1/5、1/10/、1/15,1/20、1/25,1/30,比例复配,分别以10%吡唑茚满基甲酰胺衍生物WG和20%灭幼脲WG作为对照进行大豆甜菜夜蛾毒力测定,共毒系数为136.7~165.9,具体情况见表8,其中5:1~1:20为145.4~165.9,1:1~1:10为153.8~165.9,增效效果显著。
表9
Claims (5)
1.一种灭幼脲杀虫组合物,其特征在于,有效成分重量百分比含量为5%~80%,吡唑茚满基甲酰胺或其衍生物与灭幼脲的质量比为5:1~1:20。
2.如权利要求1所述的灭幼脲杀虫组合物,其特征在于,吡唑茚满基甲酰胺或其衍生物与灭幼脲的质量比为1:1~1:10。
3.如权利要求1所述的灭幼脲杀虫组合物,其特征在于,吡唑茚满基甲酰胺衍生物选自3-二氯甲基-N-(7-氯-1,1,3-三甲基-4-茚满基)-1-甲基-4-吡唑甲酰胺或3-二氟甲基-N-(7-氟-1,1-二甲基,3-乙基基-4-茚满基)-1-乙基-4-吡唑甲酰胺。
4.如权利要求1所述的灭幼脲杀虫组合物,其特征在于,该组合物的剂型为可湿性粉剂、悬浮剂、可分散油悬浮剂、水分散性颗粒剂和干悬浮剂中的一种。
5.如权利要求1所述的灭幼脲杀虫组合物的应用,其特征在于,该组合物在防治甘蓝、十字花科蔬菜、果树、水稻、棉花、油菜、生生、小麦、玉米、马铃薯、森林防治虫害上的应用。
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| CN102858172A (zh) * | 2010-04-28 | 2013-01-02 | 住友化学株式会社 | 植物病害组合物及其用途 |
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