CN116965414A - 一种包含嘧啶甲酰基肟衍生物的除草组合物及其应用 - Google Patents
一种包含嘧啶甲酰基肟衍生物的除草组合物及其应用 Download PDFInfo
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- CN116965414A CN116965414A CN202210420582.3A CN202210420582A CN116965414A CN 116965414 A CN116965414 A CN 116965414A CN 202210420582 A CN202210420582 A CN 202210420582A CN 116965414 A CN116965414 A CN 116965414A
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- oxime derivative
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- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- VLCQZHSMCYCDJL-UHFFFAOYSA-N tribenuron methyl Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 VLCQZHSMCYCDJL-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- 235000001019 trigonella foenum-graecum Nutrition 0.000 description 1
- IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
- 229960001082 trimethoprim Drugs 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
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- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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- 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
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
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Abstract
本发明属于农药领域,具体涉及一种包含嘧啶甲酰基肟衍生物的除草组合物及其应用。所述组合物包括除草有效量的活性成分A和活性成分B,其中,活性成分A为
Description
技术领域
本发明属于农药领域,具体涉及一种包含嘧啶甲酰基肟衍生物的除草组合物及其应用。
背景技术
化学除草是农田杂草防除中最为经济、有效的手段,但长期连续高剂量地使用单一品种或单一作用方式的化学除草剂,容易造成杂草耐药和抗性演化等问题。除草剂化合物的合理复配或混配具有扩大杂草谱、提高防除效果、延缓杂草耐药性和抗药性的发生与发展等优点,是解决上述问题的最为有效的方法之一,而生产上仍需开发安全性高、杀草谱广、能够产生增效作用并解决抗性杂草问题的除草组合物品种。
发明内容
为解决现有技术中存在的上述问题,本发明提供一种包含嘧啶甲酰基肟衍生物的除草组合物及其应用。该组合物能有效控制/防除禾本科及阔叶杂草等,具有扩大杀草谱、减少施用量、能够产生增效作用并解决抗性杂草等特点。
一种包含嘧啶甲酰基肟衍生物的除草组合物,包括除草有效量的活性成分A和活性成分B,其中,
活性成分A为或其盐;
活性成分B选自以下化合物及其酸/盐/酯中的一种或多种:
(1)HPPD抑制剂:双唑草酮(CAS号:1622908-18-2)、环吡氟草酮(CAS号:1855929-45-1);
(2)PDS抑制剂:吡氟酰草胺(CAS号:83164-33-4)、氟吡酰草胺(CAS号:137641-05-5)、Beflubutamid-M(CAS号:113614-09-8);
(3)DOXP抑制剂:二氯异噁草酮(CAS号:81777-95-9)、
(4)ALS抑制剂:苯磺隆(CAS号:101200-48-0)、苄嘧磺隆(CAS号:83055-99-6)、双氟磺草胺(CAS号:145701-23-1)、噻吩磺隆(CAS号:79277-27-3)、甲基二磺隆(CAS号:208465-21-8)、啶磺草胺(CAS号:422556-08-9)、氟唑磺隆(CAS号:181274-17-9);
(5)ACCase抑制剂:精噁唑禾草灵(CAS号:113158-40-0)、炔草酯(CAS号:105512-06-9)、唑啉草酯(CAS号:243973-20-8);
(6)PPO抑制剂:苯嘧磺草胺(CAS号:372137-35-4)、 三氟草嗪(CAS号:1258836-72-4);
(7)PSⅡ抑制剂:嗪草酮(CAS号:21087-64-9)、氨唑草酮(CAS号:129909-90-6)、绿麦隆(CAS号:15545-48-9)、异丙隆(CAS号:34123-59-6)、辛酰溴苯腈(CAS号:1689-99-2);
(8)微观组装抑制剂:二甲戊灵(CAS号:40487-42-1);
(9)合成激素类抑制剂:氯氟吡氧乙酸(CAS号:69377-81-7)、氯氟吡氧乙酸异辛酯(CAS号:81406-37-3)、2-甲基-4-氯苯氧乙酸(CAS号:94-74-6)、2甲4氯异辛酯(CAS号:26544-20-7)、2,4-二氯苯氧基乙酸(CAS号:94-75-7)、麦草畏(CAS号:1918-00-9)、氟氯吡啶酯(CAS号:943831-98-9)、
(10)VLCFA抑制剂:氟噻草胺(CAS号:142459-58-3)、砜吡草唑(CAS号:447399-55-5)、精异丙甲草胺(CAS号:87392-12-9)、乙草胺(CAS号:34256-82-1);
(11)脂类合成(非乙酰辅酶A羧化酶)抑制剂:苄草丹(CAS号:52888-80-9);
(12)EPSPS抑制剂:草甘膦(CAS号:1071-83-6);
(13)GS抑制剂:草铵膦(CAS号:77182-82-2);
(14)其他抑制剂:环庚草醚(CAS号:87818-31-3);
其中,所述除草组合物中A、B的重量比为1:800~50:1、1:600~20:1、1:300~10:1、1:200~8:1、1:180~5:1、1:150~2:1、1:120~1:1、1:100~1:2、1:80~1:4、1:60~1:5、1:50~1:8、1:30~1:10或1:20~1:15。
所述除草组合物中A、B的质量百分含量占总量的1-95%,优选10-80%。
所述除草组合物中还包含常规助剂,所述常规助剂包括载体和/或表面活性剂。
本文中的术语“载体”表示一种有机或无机、天然或合成的物质。它们有助于活性成分的施用,该载体一般是惰性的且必须是农业上可接受的,特别是被处理的植物所接受。载体可以是固体的,如陶土、天然或合成的硅酸盐、二氧化硅、树脂、蜡、固体肥料等;或者液体的,如水、醇类、酮类、石油馏分、芳烃或蜡烃、氯代烃、液化气等。
表面活性剂可包括乳化剂、分散剂或润湿剂,它可以是离子型或非离子型的。可提及的实例是聚丙烯酸的盐、木质素磺酸盐、苯酚磺酸或萘磺酸的盐、环氧乙烷与脂肪族醇或与脂族酸或与脂肪族胺与取代苯酚(特别是烷基苯酚或芳基苯酚)的聚合物、磺基琥珀酸盐、牛磺酸衍生物(特别是牛磺酸烷脂)及醇的磷酸酯或多羟乙基化的苯酚的磷酸酯、烷基磺酸盐、烷基芳基磺酸盐、烷基硫酸盐、月桂基醚硫酸盐、脂肪醇硫酸盐,以及硫酸化十六-、十七-和十八烷醇以及硫酸化脂肪醇乙二醇醚,此外还有萘或萘磺酸与苯酚和甲醛的缩合物、聚氧乙烯辛基苯基醚、乙氧基化异辛基酚、辛基酚或壬基酚、烷基苯基聚乙二醇醚、三丁基苯基聚乙二醇醚、三硬脂基苯基聚乙二醇醚、烷基芳基聚醚醇、醇和脂肪醇/氧化乙烯缩合物、乙氧基化蓖麻油、聚氧乙烯烷基醚、乙氧基化聚氧丙烯、月桂醇聚乙二醇醚缩醛、山梨醇酯、木素亚硫酸盐废液,以及蛋白质、变性蛋白、多糖(例如甲基纤维素)、疏水改性淀粉、聚乙烯醇、聚羧酸盐、聚烷氧基化物、聚乙烯胺、聚乙烯吡咯烷酮及其共聚物。至少需要一种表面活性剂存在,以有利于活性成分在水中的分散并有利于使它们能正确地施用于植物。
上述组合物也可含有各种其他的组分,如保护胶体、粘合剂、增稠剂、触变剂、渗透剂、稳定剂、螯合剂、染料、着色剂和聚合物。
另外,本发明的组合物可以与以下活性物质混合,例如《世界农药新品种技术大全》,中国农业科学技术出版社,2010.9和这里引用的文献中的已知物质。例如以下提到的除草剂活性物质,(备注:化合物的名称,或者为根据国际标准化组织(ISO)的普通名称,或者为化学名称,适当的时候有代号):乙草胺、丁草胺、甲草胺、异丙草胺、异丙甲草胺、精异丙甲草胺、丙草胺、毒草胺、克草胺、萘丙酰草胺、R-左旋萘丙酰草胺、敌稗、苯噻酰草胺、双苯酰草胺、吡氟酰草胺、杀草胺、氟丁酰草胺、溴丁酰草胺、二甲噻草胺、高效二甲噻草胺、乙氧苯草胺、氟噻草胺、甲氧噻草胺、吡草胺、异恶草胺、高效麦草伏甲酯、高效麦草伏丙酯、二丙烯草胺、烯草胺、丁酰草胺、环丙草胺、氟磺酰草胺、庚酰草胺、异丁草胺、丙炔草胺、特丁草胺、二甲苯草胺、二甲草胺、落草胺、三甲环草胺、氯甲酰草胺、炔苯酰草胺、戊酰苯草胺、卡草胺、新燕灵、三环赛草胺、丁烯草胺、牧草胺、苄草胺、醌萍胺、苯氟磺胺、萘丙胺、乙酰甲草胺、萘草胺、噻草胺、吡氰草胺、苯草多克死、草克乐、氯酞亚胺、丁脒胺、氟吡草胺、莠去津、西玛津、扑草净、氰草净、西草净、莠灭净、扑灭津、异丙净、氟草净、特丁净、特丁津、三嗪氟草胺、环丙津、甘扑津、草达津、扑灭通、西玛通、叠氮净、敌草净、异戊乙净、环丙青津、灭莠津、另丁津、仲丁通、特丁通、甲氧丙净、氰草净、抑草津、可乐津、莠去通、灭草通、甘草津、三聚氰酸、Indaziflam、氯磺隆、甲磺隆、苄嘧磺隆、氯嘧黄隆、苯磺隆、噻磺隆、吡嘧黄隆、甲基二磺隆、甲基碘磺隆钠盐、甲酰氨基嘧磺隆、醚磺隆、醚苯磺隆、甲嘧磺隆、烟嘧磺隆、胺苯磺隆、酰嘧磺隆、乙氧嘧磺隆、环丙嘧磺隆、砜嘧磺隆、四唑嘧磺隆、啶嘧黄隆、单嘧磺隆、单嘧磺酯、氟唑磺隆、氟啶嘧磺隆、氟吡嘧磺隆、环氧嘧磺隆、唑吡嘧磺隆、氟嘧磺隆、丙苯磺隆、三氟丙磺隆、磺酰磺隆、三氟啶磺隆、氟胺磺隆、三氟甲磺隆、甲磺隆钠盐、氟吡磺隆、甲硫嘧磺隆、嘧苯胺磺隆、Propyrisulfuron(丙嗪嘧磺隆)、嗪吡嘧磺隆、三氟羧草醚、氟磺胺草醚、乳氟禾草灵、乙羧氟草醚、乙氧氟草醚、草枯醚、苯草醚、氯氟草醚乙酯、甲羧除草醚、三氟甲草醚、甲氧除草醚、三氟硝草醚、氟化除草醚、氟呋草醚、除草醚、甲草醚、二甲草醚、氟酯肟草醚、氟草醚酯、Halosafen、绿麦隆、异丙隆、利谷隆、敌草隆、莎扑隆、氟草隆、苯噻隆、甲基苯噻隆、苄草隆、磺噻隆、异恶隆、特丁噻草隆、炔草隆、氯溴隆、甲基杀草隆、酰草隆、甲氧杀草隆、溴谷隆、甲氧隆、绿谷隆、灭草隆、环草隆、非草隆、氟硫隆、草不隆、枯草隆、草完隆、异草完隆、环莠隆、噻氟隆、丁噻隆、枯莠隆、对氟隆、甲胺噻唑隆、隆草特、三甲异脲、恶唑隆、Monisouron、Anisuron、Methiuron、Chloreturon、四氟隆、甜菜宁、甜菜宁-乙酯、甜菜安、磺草灵、特草灵、燕麦灵、苯胺灵、氯苯胺灵、二氯苄草酯、灭草灵、氯炔灵、Carboxazole、Chlorprocarb、Fenasulam、BCPC、CPPC、Carbasulam、丁草特、禾草丹、灭草猛、禾草特、野麦畏、哌草丹、禾草畏、稗草丹、环草敌、燕麦敌、菌达灭、乙硫草特、坪草丹、克草猛、苄草丹、仲草丹、硫烯草丹、草灭散、Isopolinate、Methiobencarb、2,4-D异辛酯丁酯、2甲4氯钠、2,4-D异辛酯异辛酯、2甲4氯异辛酯、2,4-D异辛酯钠盐、2,4-D异辛酯二甲胺盐、2甲4氯乙硫酯、2甲4氯、2,4-D异辛酯丙酸、高2,4-D异辛酯丙酸盐、2,4-D异辛酯丁酸、2甲4氯丙酸、2甲4氯丙酸盐、2甲4氯丁酸、2,4,5-涕、2,4,5-涕丙酸、2,4,5-涕丁酸、2甲4氯胺盐、麦草畏、抑草蓬、伐草克、赛松、三氯苯酸、氨二氯苯酸、甲氧三氯苯酸、禾草灵、吡氟禾草灵、精吡氟禾草灵、氟吡甲禾灵、高效吡氟氯禾灵、喹禾灵、精喹禾灵、恶唑禾草灵、精恶唑禾草灵、喔草酯、氰氟草酯、恶唑酰草胺、炔草酯、噻唑禾草灵、炔禾灵、羟戊禾灵、三氟禾草肟、异恶草醚、百草枯、敌草快、安磺灵、乙丁烯氟灵、异丙乐灵、甲磺乐灵、环丙氟灵、氨基丙氟灵、乙丁氟灵、氯乙氟灵、氨基乙氟灵、地乐灵、氯乙地乐灵、Methalpropalin、丙硝酚、草甘膦、莎稗膦、草铵膦、甲基胺草磷、草硫膦、哌草膦、双丙氨膦、地散磷、抑草磷、蔓草磷、伐垅磷、双甲胺草磷、草特磷、咪唑烟酸、咪唑乙烟酸、咪唑喹啉酸、甲氧咪草烟、甲氧咪草烟铵盐、甲咪唑烟酸、咪草酯、氯氟吡氧乙酸、氯氟吡氧乙酸异辛酯、二氯吡啶酸、氨氯吡啶酸、三氯吡氧乙酸、氟硫草定、卤草定、三氯吡啶酚、噻草啶、氟啶草酮、氯氨吡啶酸、氟吡草腙、三氯吡氧乙酸丁氧基乙酯、Cliodinate、稀禾啶、烯草酮、噻草酮、禾草灭、环苯草酮、丁苯草酮、肟草酮、吡喃草酮、Buthidazole、嗪草酮、环嗪酮、苯嗪草酮、乙嗪草酮、Ametridione、Amibuzin、溴苯腈、辛酰溴苯腈、辛酰碘苯腈、碘苯腈、敌草腈、二苯乙腈、双唑草腈、羟敌草腈、Iodobonil、唑嘧磺草胺、双氟磺草胺、五氟磺草胺、磺草唑胺、氯酯磺草胺、双氯磺草胺、啶磺草胺、氟草黄、双草醚、嘧啶肟草醚、环酯草醚、嘧草醚、嘧硫草醚、双环磺草酮、硝磺草酮、磺草酮、Tembotrione、Tefuryltrione、Bicyclopyrone、Ketodpiradox、异恶唑草酮、异恶氯草酮、Fenoxasulfone、Methiozolin、异丙吡草酯、吡草醚、吡唑特、野燕枯、苄草唑、吡草酮、吡氯草胺、Pyrasulfotole、苯唑草酮、Pyroxasulfone、唑草胺、氟胺草唑、杀草强、氨唑草酮、唑啶草酮、氟唑草酮、甲磺草胺、Bencarbazone、双苯嘧草酮、氟丙嘧草酯、除草定、异草定、环草啶、特草定、Flupropacil、吲哚酮草酯、氟烯草酸、丙炔氟草胺、炔草胺、酞苄醚、Flumezin、五氯酚(钠)、地乐酚、特乐酚、特乐酯、戊硝酚、二硝酚、氯硝酚、地乐施、地乐特、丙炔恶草酮、恶草酮、环戊恶草酮、氟唑草胺、嗪草酸甲酯、四唑酰草胺、氟哒嗪草酯、杀草敏、溴莠敏、二甲达草伏、哒草醚、草哒酮、草哒松、哒草伏、Pyridafol、二氯喹啉酸、氯甲喹啉酸、苯达松、哒草特、恶嗪草酮、草除灵、异恶草酮、环庚草醚、异丙酯草醚、丙酯草醚、茚草酮、氯酸钠、茅草枯、三氯醋酸、一氯醋酸、六氯丙酮、四氟丙酸、牧草快、溴酚肟、三唑磺、灭杀唑、呋草酮、呋草磺、乙呋草磺、嘧草胺、氯酞酸、氟咯草酮、稗草稀、丙烯醛、苯草灭、灭草环、燕麦酯、噻二唑草胺、棉胺宁、羟草酮、甲氧苯酮、苯嘧磺草胺、氯酰草膦、三氯丙酸、Alorac、Diethamquat、Etnipromid、Iprymidam、Ipfencarbazone、Thiencarbazone-methyl、Pyrimisulfan、Chlorflurazole、Tripropindan、Sulglycapin、甲硫磺乐灵、Cambendichlor、环丙嘧啶酸、硫氰苯胺、解草酮、解草啶、解草安、解草唑、解草喹、解草腈、解草烷、解草胺腈、解草烯、吡唑解草酯、呋喃解草唑、肟草安、双苯噁唑酸、二氯丙烯胺、氟氯吡啶酯、DOW氯氟吡啶酯、UBH-509、D489,LS 82-556、KPP-300、NC-324、NC-330、KH-218、DPX-N8189、SC-0744、DOWCO535、DK-8910、V-53482、PP-600、MBH-001、KIH-9201、ET-751、KIH-6127和KIH-2023。
所述除草组合物进一步包括至少一种安全剂,其选自:
a)二氯苯基吡唑啉-3-羧酸(S1)类化合物,优选的化合物为例如1-(2,4-二氯苯基)-5-(乙氧基羰基)-5-甲基-2-吡唑啉-3-羧酸乙酯(S1-1,吡唑解草酯(mefenpyr-diethyl),PM,第594-595页),以及记载于例如WO91/07874和PM(第594-595页)中的相关化合物。
b)二氯苯基吡唑羧酸衍生物,优选的化合物为例如1-(2,4-二氯苯基)-5-甲基吡唑-3-羧酸乙酯(S1-2)、1-(2,4-二氯苯基)-5-异丙基吡唑-3-羧酸乙酯(S1-3)、1-(2,4-二氯苯基)-5-(1,1-二甲基-乙基)吡唑-3-羧酸乙酯(S1-4)、1-(2,4-二氯苯基)-5-苯基吡唑-3-羧酸乙酯(S1-5),以及记载于EP-A-333131和EP-A-269806中的相关化合物。
c)三唑羧酸(S1)类化合物,优选的化合物为例如解草唑(fenchlorazole),即1-(2,4-二氯苯基)-5-三氯甲基-(1H)-1,2,4-三唑-3-羧酸乙酯(S1-6)及相关化合物(参见EP-A-174562和EP-A-346620)。
d)5-苄基-或5-苯基-2-异噁唑啉-3-羧酸类或5,5-二苯基-2-异噁唑啉-3-羧酸类化合物,优选的化合物为例如5-(2,4-二氯苄基)-2-异噁唑啉-3-羧酸乙酯(S1-7)或5-苯基-2-异噁唑啉-3-羧酸乙酯(S1-8)及记载于WO91/08202中的相关化合物,或记载于专利申请(WO-A-95/07897)中的5,5-二苯基-2-异噁唑啉-3-羧酸乙酯(S1-9,双苯噁唑酸(isoxadifen-ethyl))或5,5-二苯基-2-异噁唑啉-3-羧酸正丙酯(S1-10)或5-(4-氟苯基)-5-苯基-2-异噁唑啉-3-羧酸乙酯(S1-11)。
e)8-喹啉氧基乙酸(S2)类化合物,优选1-甲基己-1-基(5-氯-8-喹啉氧基)乙酸酯(S2-1,解毒喹(cloquintocet-mexyl),如PM(第195-196页),(1,3-二甲基丁-1-基)(5-氯-8-喹啉氧基)乙酸酯(S2-2),4-烯丙基氧基丁基(5-氯-8-喹啉氧基)乙酸酯(S2-3),1-烯丙基氧基丙-2-基(5-氯-8-喹啉氧基)乙酸酯(S2-4),(5-氯-8-喹啉氧基)乙酸乙酯(S2-5),(5-氯-8-喹啉氧基)乙酸甲酯(S2-6),(5-氯-8-喹啉氧基)乙酸烯丙酯(S2-7),2-(2-亚丙基亚氨基氧基)-1-乙基(5-氯-8-喹啉氧基)乙酸酯(S2-8),2-氧代丙-1-基(5-氯-8-喹啉氧基)乙酸酯(S2-9),以及记载于EP-A-86750、EP-A-94349和EP-A-191736或EP-A-0492366中的相关化合物。
f)(5-氯-8-喹啉氧基)丙二酸类化合物,优选的化合物为例如(5-氯-8-喹啉氧基)丙二酸二乙酯、(5-氯-8-喹啉氧基)丙二酸二烯丙酯、(5-氯-8-喹啉氧基)-丙二酸甲基乙酯和记载于EP-A-0582198中的相关化合物。
g)苯氧基乙酸、苯氧基丙酸或芳族羧酸类活性化合物,例如2,4-二氯苯氧基乙酸(和酯)(2,4-D)、4-氯-2-甲基苯氧基丙酸酯(2-甲-4-氯丙酸(mecoprop))、MCPA或3,6-二氯-2-甲氧基苯甲酸(和酯)(麦草畏(dicamba))。
h)嘧啶类活性化合物,例如“解草啶(fenclorim)”(PM,第386-387页)(=4,6-二氯-2-苯基嘧啶),
i)二氯乙酰胺类活性化合物,其常用作苗前安全剂(作用于土壤的安全剂),例如“二氯丙烯胺(dichloromid)”(PM,第270-271页)(=N,N-二烯丙基-2,2-二氯乙酰胺),“AR-29148”(=3-二氯乙酰基-2,2,5-三甲基-1,3-噁唑烷酮,购自Stauffer),“解草嗪(benoxacor)”(PM,第74-75页)(=4-二氯乙酰基-3,4-二氢-3-甲基-2H-1,4-苯并噁嗪),“APPG-1292”(=N-烯丙基-N[(1,3-二氧戊环-2-基)-甲基]二氯乙酰胺,购自PPGIndustries),“ADK-24”(=N-烯丙基-N-[(烯丙基氨基羰基)-甲基]-二氯乙酰胺,购自Sagro-Chem),“AAD-67”或“AMON4660”(=3-二氯乙酰基-1-氧杂-3-氮杂-螺[4,5]癸烷,购自Nitrokemia或Monsanto),“diclonon”或“ABAS145138”或“ALAB145138”(=(=3-二氯乙酰基-2,5,5-三甲基-1,3-二氮杂双环[4.3.0]壬烷,购自BASF),和“furilazol”或“AMON13900”(参见PM,482-483)(=(RS)-3-二氯乙酰基-5-(2-呋喃基)-2,2-二甲基噁唑烷酮),
j)二氯丙酮衍生物类活性化合物,例如,“AMG191”(CAS登记号96420-72-3)(=2-二氯甲基-2-甲基-1,3-二氧戊环,购自Nitrokemia),
k)氧基亚氨基化合物类活性化合物,其被称为拌种材料,例如,“解草腈(oxabetrinil)”(PM,第689页)(=(Z)-1,3-二氧戊环-2-基甲氧基亚氨基(苯基)乙腈),其在拌种中称为安全剂,以防止异丙甲草胺(metolachlor)的损害,“氟草肟(fluxofenim)”(PM,第467-468页)(=1-(4-氯苯基)-2,2,2-三氟-1-乙酮O-(1,3-二氧戊环-2-基甲基)-肟,其在拌种中称为安全剂,以防止异丙甲草胺(metolachlor)的损害,和“解草胺腈(cyometrinil)”或“A-CGA-43089”(PM,第983页)(=(Z)-氰基甲氧基亚氨基(苯基)乙腈),其在拌种中称为安全剂,以防止异丙甲草胺(metolachlor)的损害,
l)噻唑羧酸酯类活性化合物,其被称为拌种材料,例如“解草安(flurazol)”(PM,第450-451页)(=2-氯-4-三氟甲基-1,3-噻唑-5-羧酸苄酯),其在拌种中被称为安全剂,以防止甲草胺(alachlor)和异丙甲草胺的损害,
m)萘二羧酸衍生物类活性化合物,其被称为拌种剂,例如“萘二甲酸酐”(PM,第1009-1010页)(=1,8-萘二甲酸酐),其在玉米拌种中称为安全剂,以防止硫代氨基甲酸酯除草剂的损害,
n)色满乙酸(chromaneaceticacid)衍生物类活性化合物,例如,“ACL304415”(CAS登记号31541-57-8)(=2-84-羧基色满-4-基)乙酸,购自AmericanCyanamid),
o)除了对有害植物具有除草作用外还对植物具有安全剂作用的活性化合物,例如,“哌草丹(dimepiperate)”或“AMY-93”(PM,第302-303页)(=S-1-甲基-1-苯基乙基哌啶-1-硫代羧酸酯),“杀草隆(daimuron)”或“ASK23”(PM,第247页)(=1-(1-甲基-1-苯基乙基)-3-对甲苯基脲),“苄草隆(cumyluron)”=“AJC-940”(=3-(2-氯苯基甲基)-1-(1-甲基-1-苯基-乙基)脲,参见JP-A-60087254),“苯甲酮(methoxyphenon)”或“ANK049”(=3,3'-二甲基-4-甲氧基-二苯甲酮),“CSB”(=1-溴-4-(氯甲基磺酰基)苯)(CAS登记号54091-06-4,购自Kumiai)。
所述安全剂优选双苯噁唑酸(CAS:163520-33-0)、cyprosulfamide(CAS:221667-31-8)、吡唑解草酯(CAS:135590-91-9)、解毒喹(CAS:99607-70-2)、赤霉酸(CAS:7-06-5)、furilazole(CAS:121776-33-8)、metcamifen(CAS:129531-12-0)中的一种或多种。
在本说明书的上下文中,如果使用活性化合物的通用名称的缩写形式,则在每种情况下包括所有的常规衍生物,例如酯和盐,以及异构体,特别是光学异构体,特别是一种或多种市售形式。如果通用名称表示酯或盐,则在每种情况下还包括所有其他的常规衍生物,例如其他的酯和盐、游离酸和中性化合物,以及异构体,特别是光学异构体,特别是一种或多种市售形式。给出的化合物的化学名称表示至少一种被通用名称涵盖的化合物,通常是优选的化合物。在磺酰胺如磺酰脲的情况下,盐还包括通过阳离子与磺酰胺基团中的氢原子交换而形成的盐。例如,2甲4氯衍生物包含但不限于:2甲4氯钠盐、钾盐、二甲铵盐、异丙胺盐等,以及2甲4氯甲酯、乙酯、异辛酯、乙硫酯等;2,4-D衍生物包含但不限于:2,4-D盐如钠盐、钾盐、二甲铵盐、三乙醇铵盐、异丙胺盐、胆碱等,以及2,4-D酯如甲酯、乙酯、丁酯、异辛酯等。
在本发明的上下文中,化合物的盐优选为各自的碱金属盐(如锂、钠和钾盐)、碱土金属盐(如钙和镁盐)、过渡金属盐(如锰、铜、锌和铁盐)、铵盐或其中1-4个氢原子被C1-C4烷基、羟基-C1-C4烷基、C1-C4烷氧基-C1-C4烷基、羟基-C1-C4烷氧基-C1-C4烷基、苯基或苄基替代的取代铵,优选铵、甲基铵、异丙基铵、二甲基铵、二异丙基铵、三甲基铵、庚基铵、十二烷基铵、十四烷基铵、四甲基铵、四乙基铵、四丁基铵、2-羟基乙基铵(醇胺盐)、2-(2-羟基乙-1-氧基)乙-1-基铵(二甘醇胺盐)、二(2-羟基乙-1-基)铵(二醇胺盐)、三(2-羟基乙基)铵(三醇胺盐)、三(2-羟基丙基)铵、苄基三甲基铵、苄基三乙基铵、N,N,N-三甲基乙醇铵(胆碱盐),此外还有鏻离子,锍离子,优选三(C1-C4烷基)锍,如三甲基锍,以及氧化锍离子,优选三(C1-C4烷基)氧化锍,最后还有多元胺如N,N-二(3-氨基丙基)甲基胺和二亚乙基三胺的盐的形式。
在本发明的上下文中,化合物的酯,例如作为烷基酯、烯基酯、炔基酯、烷氧基烷基酯、四氢呋喃基甲基酯以及相应硫酯,优选为C1-C10烷基酯、C2-C10烯基酯、C2-C10炔基酯、C1-C10烷氧基C1-C10烷基酯、(四氢呋喃-2-基)甲基酯以及相应硫酯。优选的C1-C10烷基酯或C1-C10烷硫基酯例如为甲基、乙基、丙基、异丙基、丁基、异丁基、戊基、甲基己基(1-甲基己基)、甲基庚基(1-甲基庚基)、庚基、辛基或异辛基(2-乙基己基)酯。优选的C1-C10烷氧基-C1-C10烷基酯是C1-C4烷氧基乙基酯,例如2-甲氧基乙基、2-乙氧基乙基、2-丁氧基乙基(丁氧乙基)、2-丁氧基丙基或3-丁氧基丙基酯。
本发明的组合物可以由使用者在使用前经稀释或直接使用。其配制可由通常的加工方法制备,即将活性物质与液体溶剂或固体载体混合后,再加入表面活性剂如分散剂、稳定剂、湿润剂、粘合剂、消泡剂等中的一种或几种。
所述除草组合物的具体制剂为可分散油悬浮剂、水悬浮剂、悬乳剂、可湿性粉剂、乳油、水分散粒剂(干悬浮剂)、水乳剂、微乳剂。
简而言之,本发明的组合物可以和现有技术的配方中常规使用的固体和液体添加剂混合。随着外部条件的变化,有效成分的使用量也不同,外部条件为,例如温度、湿度、使用的除草剂的性质等等。它可以有大的变化幅度,例如在0.001到2.0kg/ha之间,或更多的活性物质,但优选在0.003到1.0kg/ha之间,特别是在5到500g/ha之间。
本发明还提供一种所述除草组合物在防治杂草上的应用;以及提供一种防治不想要的植物生长的方法,其包括将所述除草组合物施用于植物、植物部位、植物种子或植物生长的区域。
另外,本发明的组合物可通过喷雾的方法被施用于待处理植物叶片上,即施用于杂草,特别是杂草侵扰或易侵扰影响的表面上。
当施用本发明的除草组合物时,获得了预料不到的增效效果,并且除草活性比使用单个除草剂的活性预期总和,以及单个除草剂的活性更为显著。增效效果表现为施用量减少、更宽的杂草控制谱、除草作用更快、更持久,这些特性是杂草控制实践过程中所需要的。就所描述的特性来说,这些新组合物明显地优越于现有的除草剂,达到减量使用,对环境更友好。
本发明的增效除草组合物还具有下述优点:
(1)本发明的组合物为环境友好型,在环境中均易于降解。
(2)本发明的除草组合物成本低、使用方便,其推广应用有巨大的经济效益和社会效益。
具体实施方式
下列实施例并非限制本发明,而只是用来说明本发明是如何实现的。对于某些杂草,这些实施例显示出特别显著的有效性。举例如下:
A)实施例
1.A+双唑草酮(1+5)乳油
1%A+5%双唑草酮+20%DMAC+3%十二烷基苯磺酸钙+8%苯乙基苯酚聚氧乙烯醚+180#溶剂油补足
2.A+环吡氟草酮(1+22.5)可分散油悬浮剂
1%A+22.5%环吡氟草酮+5%十二烷基苯磺酸钙+10%腰果酚聚氧乙烯醚+3%蓖麻油聚氧乙烯醚+1.0%有机膨润土+5%180#溶剂油+20%豆油+油酸甲酯补足
3.A+吡氟酰草胺(1+25)水悬浮剂
1%A+25%吡氟酰草胺+3%苯乙基苯酚聚氧乙烯醚磷酸酯三乙醇胺盐+1.5%丙二醇嵌段聚醚+2%脂肪醇聚氧乙烯醚+0.14%黄原胶+1.8%硅酸镁铝+4%丙三醇+消泡剂+水
4.A+Beflubutamid-M(1+25)乳油
1%A+25%Beflubutamid-M+8%DMAC+4%十二烷基苯磺酸钙+5%苯乙基苯酚聚氧乙烯醚+180#溶剂油补足
5.A+(1+50)可湿性粉剂
1%A+50%+10%白炭黑+2%十二烷基苯磺酸钠+4%萘磺酸盐分散剂+硅藻土补足
6.A+二氯异噁草酮(1+50)水悬浮剂
1%A+50%二氯异噁草酮+3%苯乙基苯酚聚氧乙烯醚磷酸酯三乙醇胺盐+1.5%聚羧酸盐+1%脂肪醇聚氧乙烯醚+0.06%黄原胶+4%丙三醇+消泡剂+水
7.A+双氟磺草胺(2+2.5)可分散油悬浮剂
2%A+2.5%双氟磺草胺+5%十二烷基苯磺酸钙+8%脂肪酸聚氧乙烯酯+5%蓖麻油聚氧乙烯醚+2.5%有机膨润土+3%气相法白炭黑+5%180#溶剂油+豆油补足
8.A+啶磺草胺(1+2.5)可分散油悬浮剂
1%A+2.5%啶磺草胺(1+2.5)+5%十二烷基苯磺酸钙+9%脂肪酸聚氧乙烯酯+6%蓖麻油聚氧乙烯醚+3%有机膨润土+3%气相法白炭黑+5%180#溶剂油+豆油补足
9.A+甲基二磺隆(1+2.5)可分散油悬浮剂
1%A+2.5%甲基二磺隆+1%稳定剂+5%十二烷基苯磺酸钙+9%脂肪酸聚氧乙烯酯+6%蓖麻油聚氧乙烯醚+3%有机膨润土+3%气相法白炭黑+5%180#溶剂油+5%混合脂肪酸甲酯+豆油补足
10.A+唑啉草酯(1+12.5)乳油
1%A+12.5%唑啉草酯+8%DMAC+8%十二烷基苯磺酸钙+15%腰果酚聚氧乙烯醚+5%磷酸三苯酯+180#溶剂油补足
11.A+辛酰溴苯腈(1+30)乳油
1%A+30%辛酰溴苯腈(1+30)+5%DMAC+4%十二烷基苯磺酸钙+6%腰果酚聚氧乙烯醚+200#溶剂油补足
12.A+氯氟吡氧乙酸异辛酯(1+15)乳油
1%A+15%氯氟吡氧乙酸异辛酯+5%DMAC+8%十二烷基苯磺酸钙+10%十二烷基酚聚氧乙烯醚+200#溶剂油补足
13.A+2甲4氯异辛酯(1+50)乳油
1%A+50%2甲4氯异辛酯+5%DMAC+4%十二烷基苯磺酸钙+5%腰果酚聚氧乙烯醚+180#溶剂油补足
14.乳油
1%A+5%+5%DMAC+6%十二烷基苯磺酸钙+10%腰果酚聚氧乙烯醚+10%180#溶剂油+油酸甲酯补足
15.A+氟氯吡啶酯(2+1.5)可分散油悬浮剂
2%A+1.5%氟氯吡啶酯+5%十二烷基苯磺酸钙+10%脂肪酸聚氧乙烯酯+6%蓖麻油聚氧乙烯醚+3%有机膨润土+3%气相法白炭黑+5%180#溶剂油+5%油酸正丁酯+豆油补足
上述乳油的加工设备:真空泵,配料釜,储罐。
上述乳油的加工过程:将所有物料投入配料釜中,搅拌溶解至完全透明,化验合格后,转移至储罐灌装。
上述可湿性粉剂加工设备:机械粉碎机,气流粉碎机。
上述可湿性粉剂加工过程:将原药、助剂等所有物料投入机械粉碎机中,之后过气流粉碎机,取样化验合格后备用。
上述水悬浮剂加工设备:混料釜、胶体磨、砂磨机、剪切机等。
上述水悬浮剂加工过程:将所有物料投入混料釜中,搅拌混合后过胶体磨,之后进入砂磨机三级砂磨,最后在剪切机中剪切均匀,化验合格后,转移至储罐灌装。
上述可分散油悬浮剂加工设备:混料釜、胶体磨、砂磨机、剪切机等。
上述可分散油悬浮剂加工过程:将所有物料投入混料釜中,搅拌混合后过胶体磨,之后进入砂磨机三级砂磨,最后在剪切机中剪切均匀,化验合格后,转移至储罐灌装。
B)药效试验
苗后茎叶喷雾处理:
1)试验条件
1.1)、供试靶标
杂草采用盆栽法培养,用180х140mm塑料营养钵,摆放于搪瓷盘中,内装从农田采回经风干过筛的表层土壤(4/5处),土壤湿度初期均控制在20%,挑选籽粒饱满均一的杂草种子,用25℃温水浸泡6小时,在28℃生化培养箱(黑暗)中催芽,将刚刚露白的杂草种子均匀摆放在土壤表面,根据种子粒径大小然后覆土0.5-1cm。
1.2)、培养条件
在可控日光温室内进行,温度20~30℃,自然光照,相对湿度55%~75%。土壤类型为壤土,有机质含量为1.63%,pH=7.1,碱解氮84.3mg/kg,速效磷38.5mg/kg,速效钾82.1mg/kg。
1.3)、仪器设备
3WP-2000型行走式喷雾塔,农业部南京农业机械研究所。GA10型万分之一电子天平(德国);ZDR2000智能数据记录仪(杭州泽大仪器有限公司);SPX型智能生化培养箱(宁波江南仪器厂)。
2)试验设计
2.1)、试剂
所需活性成分A参照专利CN108586357A所述方法制备,所需活性成分B由试剂公司购买或采用已知方法制得。原药均采用丙酮作溶剂,用含量0.1%乳化剂吐温-80水溶液稀释,现用现稀释。
2.2)、试验处理
2.2.1)、剂量设置
在确定A与活性成分B配比或含量时,应从两种药剂的作用特点及其毒力等衡量,还要考虑该配方的主要使用目的。本研究在前期预试的基础上,设A、B活性成分单用及混合用量分别见表格。以不含药剂、含相同溶剂及乳化剂的水作为空白对照。
2.2.2)、试验重复
每处理重复4次,每次处理3盆,每盆播种杂草种子20粒,每处理共60株。
2.3)、处理方式
2.3.1)、处理时间和次数
试验共用药1次。待杂草1~1.5叶期,间苗,保持每盆内杂草10株,每处理保留30株,然后继续培养至2.5-4.5叶进行处理。
2.3.2)、使用器械和用药方法
将培养好的试材均匀摆放在面积0.5m2的平台上,用3WP-2000型行走式喷雾塔茎叶喷雾,喷液量按450公斤/公顷计,喷雾压力0.3MPa。待全部药液喷完后,关闭气阀,30秒后,打开喷雾塔门,取出营养钵。然后打开气阀,喷清水50mL,清洗喷液管。
3)试验方法
采用盆栽法。杂草培养见1.1),参照《农药室内生物测定试验准则除草剂》进行。用药方法见2.3.2),采用茎叶处理法。处理后移入温室常规培养。
4)数据调查与统计分析
4.1)、调查方法
采用绝对数调查法,用刀片沿土壤表面切断存活杂草整株幼苗,用分析天平称量杂草鲜重。对于已经死亡的杂草,按鲜重为零计。
4.2)、调查时间和次数
处理后21天调查,共调查1次。
4.3)、数据统计分析
用Gowing法计算各处理混合组合的理论鲜重抑制率(E0=X+Y-X*Y/100),然后与实测抑制率(E)相比较,评价二者混用对杂草的联合作用类型,当E-E0值大于10%为增效作用、小于-10%为拮抗作用、在-10%~10%之间为加成作用。并根据实际防效和除草剂特点、配方的平衡性等因素确定最佳配比。式中X为活性成分A用量为P时的鲜重抑制率;Y为活性成分B用量为Q时的鲜重抑制率。
土壤封闭处理:
1)试验条件
1.1)、培养条件
在可控日光温室内进行,温度20~30℃,自然光照,相对湿度55%~75%。
土壤类型为壤土,有机质含量为1.63%,pH=7.1,碱解氮84.3mg/kg,速效磷38.5mg/kg,速效钾82.1mg/kg。试验土壤定量装至盆钵的3/4处,然后从盆钵底部浇灌,使土壤完全湿润至饱和状态。供试杂草种子催芽处理至露白,然后均匀定量撒播表面,根据种子大小覆土0.5-1cm,播种后72小时备用。
1.2)、仪器设备
GA10型万分之一电子天平(德国);ZDR2000智能数据记录仪(杭州泽大仪器有限公司);SPX型智能生化培养箱(宁波江南仪器厂),移液器等。
2)试验设计
2.1)、试剂
2.1.1)、试验药剂
原药均采用丙酮作溶剂,用含量0.1%乳化剂T-80水溶液稀释,现用现稀释。
2.2)、试验处理
2.2.1)、剂量设置
在确定A与活性成分B各组分配比或含量时,应从两种药剂的作用特点及其毒力等衡量,还要考虑该配方的主要使用目的。本研究在前期预试的基础上,设A、B活性成分单用及混合用量分别见表格。以不含药剂、含相同溶剂及乳化剂的水作为空白对照。
2.2.2)、试验重复
每处理重复4次,每次每处理3盆,每盆播种杂草种子30粒。
2)试验方法
处理前浇灌,保持1-2cm水层。用移液器取定量药液,按照试验设计从低剂量到高剂量分别进行浇灌处理,每次处理4次重复;处理后移入温室常规培养,试验期间始终保持1-2cm水层。
3)数据调查与统计分析
与苗后茎叶喷雾处理相同,故不再赘述。
统计结果见下表1-43,除有明确标记“土壤处理”外,其他均为“苗后茎叶喷雾处理”。
表1A混配双唑草酮对宝盖草的实际防效与联合作用评价
表2A混配环吡氟草酮对宝盖草的实际防效与联合作用评价
表3A混配吡氟酰草胺对野油菜的实际防效与联合作用评价
表4A混配氟吡酰草胺对野油菜的实际防效与联合作用评价
表5A混配Beflubutamid-M对野油菜的实际防效与联合作用评价
表6A混配二氯异噁草酮对稗草的实际防效与联合作用评价
表7A混配对稗草的实际防效与联合作用评价
表8A混配苯磺隆对播娘蒿的实际防效与联合作用评价
表9A混配苄嘧磺隆对播娘蒿的实际防效与联合作用评价
表10A混配双氟磺草胺对播娘蒿的实际防效与联合作用评价
表11A混配噻吩磺隆对播娘蒿的实际防效与联合作用评价
表12A混配甲基二磺隆对播娘蒿的实际防效与联合作用评价
表13A混配啶磺草胺对播娘蒿的实际防效与联合作用评价
表14A混配氟唑磺隆对播娘蒿的实际防效与联合作用评价
表15A混配精噁唑禾草灵对菵草的实际防效与联合作用评价
表16A混配炔草酯对菵草的实际防效与联合作用评价
表17A混配唑啉草酯对菵草的实际防效与联合作用评价
表18A混配苯嘧磺草胺对猪殃殃的实际防效与联合作用评价
表19A混配对猪殃殃的实际防效与联合作用评价
表20A混配对猪殃殃的实际防效与联合作用评价/>
表21A混配三氟草嗪对猪殃殃的实际防效与联合作用评价
表22A混配嗪草酮对麦家公的实际防效与联合作用评价
表23A混配氨唑草酮对麦家公的实际防效与联合作用评价
表24A混配绿麦隆对麦家公的实际防效与联合作用评价
表25A混配异丙隆对麦家公的实际防效与联合作用评价
表26A混配辛酰溴苯腈对麦家公的实际防效与联合作用评价
表27A混配二甲戊灵对鸭舌草的实际防效与联合作用评价(土壤处理)
表28A混配氯氟吡氧乙酸对牛繁缕的实际防效与联合作用评价
表29A混配氯氟吡氧乙酸异辛酯对牛繁缕的实际防效与联合作用评价
表30A混配2-甲基-4-氯苯氧乙酸对牛繁缕的实际防效与联合作用评价
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表31A混配2甲4氯异辛酯对牛繁缕的实际防效与联合作用评价
表32A混配2,4-二氯苯氧基乙酸对牛繁缕的实际防效与联合作用评价
表33A混配麦草畏对牛繁缕的实际防效与联合作用评价
表34A混配氟氯吡啶酯对牛繁缕的实际防效与联合作用评价
表35A混配对牛繁缕的实际防效与联合作用评价
/>
表36A混配氟噻草胺对马唐的实际防效与联合作用评价(土壤处理)
表37A混配砜吡草唑对马唐的实际防效与联合作用评价(土壤处理)
表38A混配精异丙甲草胺对马唐的实际防效与联合作用评价(土壤处理)
表39A混配乙草胺对马唐的实际防效与联合作用评价(土壤处理)
表40A混配苄草丹对马唐的实际防效与联合作用评价
/>
表41A混配草甘膦对绿狗尾的实际防效与联合作用评价
表42A混配草铵膦对小飞蓬的实际防效与联合作用评价
表43A混配环庚草醚对陌上菜的实际防效与联合作用评价(土壤处理)
C)大田示范
利用上述实施例1-15制得的除草组合物对杂草婆婆纳进行效果试验。
苗后茎叶喷雾处理:于杂草生长至2.5-4.5叶进行手动喷雾,兑水量45公斤/667m2,采用茎叶表面均匀喷雾。
具体试验药剂及剂量详见表44,小区面积20平方米,每处理重复3次。施药后30天调查防除效果见表44。
表44所述复配组合物的大田示范效果情况
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经过大量试验和探索,本发明意外地发现,所述组合物用于防除宝盖草、野油菜、稗草、播娘蒿、菵草、猪殃殃、麦家公、鸭舌草、牛繁缕、马唐、绿狗尾、小飞蓬、陌上菜和婆婆纳等杂草,具有令人惊讶的、意想不到的增效作用,这种增效作用在低剂量下表现更为显著,可降低用药量,降低对环境的污染,且合理复配降低了农用成本,具有很好的应用前景。同时经过测试在小麦田、玉米田、水稻田、花生、甘蔗、高粱、谷子、马铃薯、油菜、大豆、棉花、蔬菜、早熟禾、高羊茅、结缕草等植物显示良好的选择性和优异的增效作用,可以开发成具有广泛市场价值的除草剂混剂。
Claims (10)
1.一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,包括除草有效量的活性成分A和活性成分B,其中,
活性成分A为或其盐;
活性成分B选自以下化合物及其酸/盐/酯中的一种或多种:
(1)HPPD抑制剂:双唑草酮、环吡氟草酮;
(2)PDS抑制剂:吡氟酰草胺、氟吡酰草胺、Beflubutamid-M;
(3)DOXP抑制剂:二氯异噁草酮、
(4)ALS抑制剂:苯磺隆、苄嘧磺隆、双氟磺草胺、噻吩磺隆、甲基二磺隆、啶磺草胺、氟唑磺隆;
(5)ACCase抑制剂:精噁唑禾草灵、炔草酯、唑啉草酯;
(6)PPO抑制剂:苯嘧磺草胺、三氟草嗪;
(7)PSⅡ抑制剂:嗪草酮、氨唑草酮、绿麦隆、异丙隆、辛酰溴苯腈;
(8)微观组装抑制剂:二甲戊灵;
(9)合成激素类抑制剂:氯氟吡氧乙酸、氯氟吡氧乙酸异辛酯、2-甲基-4-氯苯氧乙酸、2甲4氯异辛酯、2,4-二氯苯氧基乙酸、麦草畏、氟氯吡啶酯、
(10)VLCFA抑制剂:氟噻草胺、砜吡草唑、精异丙甲草胺、乙草胺;
(11)脂类合成(非乙酰辅酶A羧化酶)抑制剂:苄草丹;
(12)EPSPS抑制剂:草甘膦;
(13)GS抑制剂:草铵膦;
(14)其他抑制剂:环庚草醚。
2.根据权利要求1所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述除草组合物中A、B的重量比为1:800~50:1、1:600~20:1、1:300~10:1、1:200~8:1、1:180~5:1、1:150~2:1、1:120~1:1、1:100~1:2、1:80~1:4、1:60~1:5、1:50~1:8、1:30~1:10或1:20~1:15。
3.根据权利要求1或2所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述除草组合物中A和B的质量百分含量占总量的1-95%,优选10-80%。
4.根据权利要求1至3任意一项所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述除草组合物中还包括常规助剂。
5.根据权利要求4所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述常规助剂包括载体和/或表面活性剂。
6.根据权利要求1至5任意一项所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述除草组合物进一步包括至少一种安全剂。
7.根据权利要求6所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述安全剂选自双苯噁唑酸、cyprosulfamide、吡唑解草酯、解毒喹、赤霉酸、furilazole、metcamifen中的一种或多种。
8.根据权利要求1至7任意一项所述的一种包含嘧啶甲酰基肟衍生物的除草组合物,其特征在于,所述除草组合物的具体制剂为可分散油悬浮剂、水悬浮剂、悬乳剂、可湿性粉剂、乳油、水分散粒剂、水乳剂或微乳剂。
9.如权利要求1至8任意一项所述包含嘧啶甲酰基肟衍生物的除草组合物在防治杂草上的应用。
10.一种防治不想要的植物生长的方法,其包括将权利要求1至8任意一项所述包含嘧啶甲酰基肟衍生物的除草组合物施用于植物、植物部位、植物种子或植物生长的区域。
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