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Compositions and methods for ballistic conditioning firearm projectiles, firearms, and firearm components such as bores of barrels, by applying to such items a conditioning composition selected from the group consisting of hexagonal boron nitride, graphite, tungsten disulfide, antimony trioxide, tal

Compositions and methods for ballistic conditioning firearm projectiles, firearms, and firearm components such as bores of barrels, by applying to such items a conditioning composition selected from the group consisting of hexagonal boron nitride, graphite, tungsten disulfide, antimony trioxide, talc, mica, and mixtures thereof, suspended in a carrier comprising a volatile solvent, and a binder selected from the group consisting of cellulosic-, alkyd- and acrylic-resins.

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Compositions and methods for ballistic conditioning firearm projectiles, firearms, and firearm components such as bores of barrels, by applying to such items a conditioning composition selected from the group consisting of hexagonal boron nitride, graphite, tungsten disulfide, antimony trioxide, tal

Compositions and methods for ballistic conditioning firearm projectiles, firearms, and firearm components such as bores of barrels, by applying to such items a conditioning composition selected from the group consisting of hexagonal boron nitride, graphite, tungsten disulfide, antimony trioxide, talc, mica, and mixtures thereof, suspended in a carrier comprising a volatile solvent, and a binder selected from the group consisting of cellulosic-, alkyd- and acrylic-resins. >10,--OCOR10,--SCOR10,--NR8COR10,--CO2R10,--COSR10,--CONR8R10,C1-C4-alkyliminooxy, C1-C4-alkoxyamino, C1-C4-alkylcarbonyl, C1-C4-alkoxy-C2-C6-alkoxycarbonyl, C1-C4-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, benzyl, hetaryl, phenoxy, benzyloxy and hetaryloxy, where the last eight radicals mentioned may in turn be substituted; X is oxygen or NR8; n is 0, 1 or 2; R5is hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C2-C6-alkyl, C3-C6-alkenyl or C3-C6-alkynyl; R6is C1-C6-alkyl or C1-C6-haloalkyl; R7is C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C2-C6-alkyl, C3-C6-alkenyl or C3-C6-alkynyl; R8is hydrogen or C1-C6-alkyl; R9is C1-C6-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, phenyl or benzyl; R10is C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-alkenyl or C3-C6-alkynyl; Q is a cyclohexane-1,3-dione ring attached in position 2 with or without substitution; and agriculturally useful salts thereof. 2. 2-Benzoylcyclohexane-1,3-diones of the formula I as claimed in claim 1 in which Q is a cyclohexane-1,3-dione ring of the formula II attached in position 2 where R11,R12,R14and R16are each hydrogen or C1-C4-alkyl; R13is hydrogen, C1-C4-alkyl or C3-C4-cycloalkyl, where the last two groups may carry one to three of the following substituents: halogen, C1-C4-alkylthio or C1-C4-alkoxy; or is tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl, tetrahydrothiopyran-4-yl, 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-dithian-2-yl, where the last 6 radicals mentioned may be substituted by one to three C1-C4-alkyl radicals; R15is hydrogen, C1-C4-alkyl or C1-C6-alkoxycarbonyl; or R13and R16together form a π-bond or a three- to six-membered carbocyclic ring; or the CR13R14unit is replaced by C=O. 3. 2-Benzoylcyclohexane-1,3-diones of the formula I as claimed in claim 1, where R1is nitro, halogen, cyano, thiocyanato, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, --OR5or --S(O)nR7; R2is hydrogen or one of the radicals mentioned above under R1. 4. 2-Benzoylcyclohexane-1,3-diones of the formula Ia where the variables R1to R4,X and Q are each as defined under claim 1. 5. A process for preparing 2-benzoylcyclohexane-1,3-diones of the formula I as claimed in claim 1, which comprises acylating an unsubstituted or substituted cyclohexane-1,3-dione Q with an activated carboxylic acid IIIα or with a carboxylic acid IIIβ, where the variables R1to R4and X are each as defined under claim 1 and L is a nucleophilically displaceable leaving group, and rearranging the a cylation product in the presence or absence of a catalyst to the compounds I. 6. A composition comprising a herbicidally active amount of at least one compound of the formula I or an agriculturally useful salt of I as claimed in claim 1, and auxiliaries conventionally used in the formulation of crop protection agents. 7. A process for preparing herbicidally active compositions as claimed in claim 6, which comprises mixing the herbicidally active amount of the at least one compound of formula I or the agriculturally useful salt and auxiliaries conventionally used in the formulation of crop protection agents. 8. A method for controlling undesirable vegetation, which comprises allowing a herbicidally active amount of at least one compound of the formula I or an agriculturally useful salt of I as claimed in claim 1 to act on plants, their habitat and/or on seeds. 9. A benzoic acid compound of formula IIIa, wherein R1is nitro, halogen, cyano, thiocyanato, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl or --S(O)nR7; R2is nitro, halogen, cyano, thiocyanato, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, --OR5or --S(O)nR7; R3is hydrogen, cyano, C1-C6-alkyl, C1-C6-haloalkyl, --OR7,--SR7or --NR7R10; R4is C1-C6-alkyl, C3-C6-cycloalkyl, C3-C6-alkenyl, C4-C6-cycloalkenyl, C3-C6-alkynyl, --COR9,--CO2R9,--COSR9or --CONR8R9,where the alkyl, cycloalkyl, alkenyl, cycloalkenyl and alkynyl radicals mentioned and R9of the radicals --COR9,--CO2R9,--COSR9and --CONR8R9may be partially or fully halogenated and/or carry one to three of the following groups: hydroxyl, mercapto, amino, cyano, R10,--OR10,--SR10,--NR8R10,=NOR10,--OCOR10,--SCOR10,--NR8COR10,--CO2R10,--COSR10,--CONR8R10,C1-C4-alkyliminooxy, C1-C4-alkoxyamino, C1-C4-alkylcarbonyl, C1-C4-alkoxy-C2-C6-alkoxycarbonyl, C1-C4-alkylsulfonyl, heterocyclyl, heterocyclyloxy, phenyl, benzyl, hetaryl, phenoxy, benzyloxy and hetaryloxy, where the last eight radicals mentioned may in turn be substituted; X is oxygen or NR8; n is 0, 1 or 2; R5is hydrogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C2-C6-alkyl, C3-C6-alkenyl or C3-C6-alkynyl; R7is C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy-C2-C6-alkyl, C3-C6-alkenyl or C3-C6-alkynyl; R8is hydrogen or C1-C6-alkyl; R9is C1-C6-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, phenyl or benzyl; R10is C1-C6-alkyl, C1-C6-haloalkyl, C3-C6-alkenyl or C3-C6-alkynyl; R17is hydroxyl or a radica l that can be removed by hydrolysis. 10. The compound of formula IIIa as claimed in claim 9, where R17is halogen, hydroxyl or C1-C6-alkoxy.