Synergistic herbicidal compositions and method
    81.
    发明公开
    Synergistic herbicidal compositions and method 失效
    协奏曲Zusammensetzungen und Verfahren。

    公开(公告)号:EP0218271A1

    公开(公告)日:1987-04-15

    申请号:EP86201403.2

    申请日:1986-08-08

    Inventor: Salmon, Brian N.

    CPC classification number: A01N47/12 A01N47/18 A01N39/02 A01N2300/00

    Abstract: A synergistic herbicidal composition comprising a mixture of
    (a) an herbicidally effective amount of a thiolcarbamate of the formula

    in which X is hydrogen, chlorine or bromine; and R¹ and R² are independently selected from the group consisting of C₁-C₆ alkyl and C₅-C₇ cycloalkyl, and (b) an herbicidally effective amount of a propionic acid derivative compound having the formula

    wherein R³ is hydrogen or an agriculturally acceptable salt-forming cation selected from the group consisting of diethanolamine, diethylamine, dimethylamine, sodium and potassium; at a weight ratio of (a) to (b) of from about 1:1 to about 4:1.

    Abstract translation: 一种协同除草组合物,其包含(a)除草有效量的式CHEM的硫代氨基甲酸酯的混合物,其中X是氢,氯或溴; 和R 1和R 2独立地选自C 1 -C 6烷基和C 5 -C 7环烷基,和(b)除草有效量的具有式CHEM的丙酸衍生物化合物,其中R 3是氢或选自二乙醇胺,二乙胺,二甲胺,钠和钾的农业上可接受的成盐阳离子; (a)至(b)的重量比为约1:1至约4:1。

    Racemization of optically active compounds having a bromine substituted chiral carbon atom
    82.
    发明公开
    Racemization of optically active compounds having a bromine substituted chiral carbon atom 失效
    含有由溴取代的Chiralkohlenstoffatom旋光活性化合物的外消旋化。

    公开(公告)号:EP0216196A2

    公开(公告)日:1987-04-01

    申请号:EP86112008.7

    申请日:1986-08-29

    Inventor: Dahod, Samun K.

    CPC classification number: C07B55/00

    Abstract: Optically active compounds having a chlorine atom attached to the chiral carbon atom such as 2-bromoaliphatic acids can be racemized without by-product formation by heating an acidified solution of the organic acid at a temperature sufficient to accomplish racemization, the solution being substantially devoid of ionized halogen other than bromine ions. The preferred acidifying agent is hydrobromic acid. The use of hydrochloric acid causes extensive by-product formation.

    Method and apparatus for the chemical vapour deposition of III-V semiconductors utilizing organometallic and elemental pnictide sources
    83.
    发明公开
    Method and apparatus for the chemical vapour deposition of III-V semiconductors utilizing organometallic and elemental pnictide sources 失效
    方法以及用于III-V族半导体的Gasplattieren装置,并且被用作原料时,有机金属化合物和elementärepnictides。

    公开(公告)号:EP0212910A2

    公开(公告)日:1987-03-04

    申请号:EP86306055.4

    申请日:1986-08-06

    CPC classification number: C30B25/02 C23C16/301 C30B29/40

    Abstract: A method of chemical vapour deposition characterised in that it comprises:

    (A) producing a first gas stream comprising a Group III organometallic gas and a carrier gas;
    (B) producing a second gas stream comprising an elemental Group V metal gas from an elemental source and a carrier gas; and
    (C) supplying said gas streams to a reactor where they react to form a III-V semiconductor; and, optionally
    (D) supplying hydrogen gas to said reactor is disclosed.

    A chemical vapour deposition apparatus characterised in that it comprises:

    (A) first means (8) for producing a first gas stream comprising a Group III organometallic gas and a carrier gas;
    (B) second means (6) for producing a second gas stream comprising an elemental Group V metal gas from an elemental source and a carrier gas; and
    (C) a reactor (4) to which said gas streams are supplied where they react to form a III-V semiconductor; and, optionally,
    (D) third means for supplying hydrogen gas to said reactor is also disclosed.

    The present invention provides advantages over the prior art.
    The arsine, phosphine and trimethyl triethyl, or trialkyl arsine or trialkyl phosphine adducts of triethyl or trimethyl indium sources of the prior art are replaced by one or more pnictide (Group V) bubblers; that is, heated sources of elemental pnic- tides through which a carrier gas is allowed to flow. The elemental pnictide gas and the carrier gas are supplied in a stream as are a Group III organometallic gas, a carrier gas, and hydrogen to a chemical vapour deposition reactor where they react to form III-V semiconductors surface layers on a substrate. The carrier gas may be nitrogen, or a noble gas, such as argon. Alternatively, hydrogen may be used as the carrier gas so that the reaction is carried out in an exclusive hydrogen atmosphere. At least some of this hydrogen may be monoatomic hydrogen. The substrate may be a III-C semiconductor or glass. Products include layers of gallium arsenide, indium phosphide and alloys thereof, including gallium indium arsenide and gallium aluminium arsenide. Other ternary and quaternary III-V semiconductors are produced using appropriate combinations of sources of Group III organometallic gases and Group V elemental gases produced by bubblers. The products may be used in semiconductor devices including solar cells.

    Abstract translation: 化学气相沉积DASS它的方法包括:(a)产生一个第一气体流,包括一组III有机金属气体和载气; (b)产生一个第二气体流从气体元素源和载气的元素,其包括第V族金属; 和(C)供应所述气体流的反应器中在那里它们反应以形成III-V族半导体; 和,任选地(D)供给氢气到所述反应器中游离缺失盘。 一种化学气相沉积设备DASS它包括:(a)第一装置(8)用于产生第一气流包含III族的有机金属气体和载气; (B)第二装置(6),用于从气体产生第二气体流,以元素包括第V族金属元素源和载气; 和(C)的反应器(4)其中,所述气体流被提供在那里它们反应以形成III-V族半导体; 因此,和任选,D),用于供给氢气至所述反应器的第三装置是游离缺失盘。 本发明提供优于现有技术的优点。 的现有技术的三乙基或三甲基铟源的胂,膦和三甲基三乙基,三烷基或胂或三烷基膦加合物由一个或多个Pnictides(第V组)起泡器代替; 所做的是,元素的pnictides加热源,通过该载气被允许流动。 元素Pnictides气体和载气供给流中的作为是第III族的有机金属气体,载气和氢气的化学气相沉积反应器在那里它们反应以形成在基板III-V族半导体表面层。 载气可以是氮气,或稀有气体,:如氩气。 可替换地,可以使用氢作为载气,以便做的反应是在不包括氢气氛中进行。 在至少一些这种氢可以是单原子氢。 衬底可以是III-C半导体或玻璃。 产品包括砷化镓,磷化铟层和它们的合金,铟砷化镓包含和镓铝砷。 其它三元和四元III-V半导体使用的III族有机金属气体的来源和通过起泡产生的V族元素的气体适当组合产生的。 该产品可以在包括太阳能电池半导体装置中使用。

    Improved fast-setting cements from ammonium phosphate fertilizer solution
    84.
    发明公开
    Improved fast-setting cements from ammonium phosphate fertilizer solution 失效
    Schnellabbindende Zemente aus磷铵 - Düngemittellösung。

    公开(公告)号:EP0203485A1

    公开(公告)日:1986-12-03

    申请号:EP86106754.4

    申请日:1986-05-16

    CPC classification number: C04B12/02

    Abstract: improved magnesium phosphate fast-setting cements can be prepared by treating ammonium phosphate fertilizer solution with an effective amount of an acidic phosphate additive. This additive can include polyphosphoric acid, orthophosphoric acid, monoammonium phosphate, monomagnesium phosphate and mixtures thereof. The fertilizer solution is treated with sufficient additive to reduce the pyrophosphate content of the fertilizer below 8 weight percent expressed as
    P 2 0 5 . The treated ammonium phosphate fertilizer solution is capable of forming a fast-setting cement at ambient temperatures when mixed with a magnesium-containing compound and an optional aggregate.

    Abstract translation: 通过用有效量的酸性磷酸盐添加剂处理磷酸铵肥料溶液可以制备改进的磷酸镁快速凝固水泥。 该添加剂可以包括多磷酸,正磷酸,磷酸一铵,磷酸一镁及其混合物。 肥料溶液用足够的添加剂处理,以将磷肥的焦磷酸盐含量降低到低于8重量%,表示为P2O5。 处理的磷酸铵肥料溶液在与含镁化合物和任选的聚集体混合时能够在环境温度下形成快速凝固的水泥。

    Synergistic herbicidal compositions
    85.
    发明公开
    Synergistic herbicidal compositions 失效
    协调主义者Zusammensetzungen。

    公开(公告)号:EP0200935A2

    公开(公告)日:1986-11-12

    申请号:EP86104727.2

    申请日:1986-04-07

    Abstract: A synergistic herbicidal composition comprising a mixture of (a) an herbicidally effective amount of a thiolcarbamate of the formula
    in which X is hydrogen, chlorine or bromine; and R' and R 2 are independently selected from the group consisting of C 1 -C 6 alkyl and C 5 -C 7 cycloalkyl, and (b) an herbicidally effective amount of a benzene derivative compound selected from N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-toluidine, N-sec-butyl-4-tert-butyl-2,6-dinitroaniline, N 4 ,N 4- diethyl- a,a,a-trifluoro-3,5-dinitrotoluene-2,4-diamine, N-ethyl-N-(2-methyl-2-propenyl)-2,6-dinitro-4-(trifluoromethyl) benzeneamine, N-(2-chloroethyl)-2,6-dinitro-N-propyl-4-trifluoromethyl)aniline, 4-isopropyl-2,6-dinitro-N,N-dipropyl- aniline, 4-methylsulfonyl-2,6-dinitro-N,N-dipropylaniline, 3,5-dinitro-N4,N4-dipropylsulfanilamide and 4-(cyclopropylmethyl)-α,α,α-trifluoro-2,6-dinitro-N-propyl-p-toluidine, N-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine, at a weight ratio of (a) to (b) of from about 0.05:1 to about 32:1.

    Abstract translation: 一种协同除草组合物,其包含(a)除草有效量的式CHEM的硫代氨基甲酸酯的混合物,其中X是氢,氯或溴; 和R 1和R 2独立地选自C 1 -C 6烷基和C 5 -C 7环烷基,和(b)除草有效量的选自N-丁基-N-乙基 α,α,α-三氟-2,6-二硝基对甲苯胺,N-仲丁基-4-叔丁基-2,6-二硝基苯胺,N 4,N 4 - 二乙基-α ,α,α-三氟-3,5-二硝基甲苯-2,4-二胺,N-乙基-N-(2-甲基-2-丙烯基)-2,6-二硝基-4-(三氟甲基)苯胺, (2-氯乙基)-2,6-二硝基-N-丙基-4-三氟甲基)苯胺,4-异丙基-2,6-二硝基-N,N-二丙基苯胺,4-甲基磺酰基-2,6-二硝基-N, N-二丙基苯胺,3,5-二硝基-N 4,N 4 - 二丙基磺酰胺和4-(环丙基甲基)-α,α,α-三氟-2,6-二硝基-N-丙基对甲苯胺, N-(1-乙基丙基)-3,4-二甲基-2,6-二硝基苯胺,(a)至(b)的重量比为约0.05:1至约32:1。

    Preparation of alkyldiarylphosphines and related compounds
    86.
    发明公开
    Preparation of alkyldiarylphosphines and related compounds 失效
    Herstellung von Alkylphosphinen und Verwandten Verbindungen。

    公开(公告)号:EP0196742A1

    公开(公告)日:1986-10-08

    申请号:EP86300592.2

    申请日:1986-01-29

    CPC classification number: C07F9/5077

    Abstract: A process is disclosed for preparing alkyldiarylphosphines and related compounds. In such process a compound having the structural formula:
    wherein :

    Z is an atom from group VA of the periodic table;
    Y is any radical that is essentially incapable of reacting with an alkali metal;
    X is any radical that is essentially incapable of reacting with an alkali metal;
    W is a substituted or unsubstituted aryl, alkyl, arylalkyl, or alkylaryl radical or hydrogen; and
    is prepared by reacting a first halide with a molten alkali metal or amalgam thereof in the presence of an inert solvent to form a first reacted mixture which is reacted with a second halide wherein an amount of the alkali metal or amalgam thereof is used in an excess of less than 100% and the yield of the product is greater than 70%. Typically, diphenylphosphinous chloride is reacted in solution with an excess of an alkali metal; and the reaction product reacted with chorohex- ane thereby forming hexyldiphenylphosphine. The improved process produces greater yields, by use of critical amounts of alkali metal; use of a single reactor rather than two reactors; preinitiation of the first stage reaction reduction of temperatures to increase reaction rate under certain conditions; and preferred reactants and physical form thereof. Novel products include behenyldiphenylphosphine.

    Abstract translation: 公开了制备烷基二芳基膦和相关化合物的方法。 在这种方法中,具有以下结构式的化合物:其中:Z是周期表第VA族的原子; Y是基本上不能与碱金属反应的任何基团; X是任何 基本上不能与碱金属反应的基团; W是取代或未取代的芳基,烷基,芳基烷基或烷基芳基或氢; 和... U是氢或... ...或卤素; ...通过使第一卤化物与熔融碱金属或汞齐在惰性溶剂的存在下反应以形成与第二卤化物反应的第一反应混合物 其中使用的碱金属或汞的量超过100%,产物的收率大于70%。 通常,二苯基次氯化物在溶液中与过量的碱金属反应; 反应产物与己烷反应,从而形成己基二苯基膦。 改进的方法通过使用临界量的碱金属产生更高的产率; 使用单个反应器而不是两个反应器; 在某些条件下第一阶段反应降低温度以提高反应速率; 和优选的反应物及其物理形式。 新产品包括二苯基二苯基膦。

    Production of high purity white phosphorus
    87.
    发明公开
    Production of high purity white phosphorus 失效
    生产高纯度白磷

    公开(公告)号:EP0154072A3

    公开(公告)日:1986-07-23

    申请号:EP84304412

    申请日:1984-06-28

    CPC classification number: C01B25/02

    Abstract: A process for the production of high purity phosphorus characterised in that it comprises:
    (A) heating high purity red phosphorus in vacuo to cause it to vaporize; and (B) condensing liquid white phosphorus in vacuo is disclosed. Referring to the accompanying illustrative diagram, red phosphorus may be heated in bulb A and condensed in collective bulb G. The present invention provides advances over the prior art. For example, the clear, colourless phosphorus produced may be utilized as a source of P 4 species for chemical vapour deposition, sputtering, vacuum deposition and molecular beam deposition of phosphorus, polyphosphide and other phosphorus compound films for semiconductor and other applications including insulation and passivation.

    Improved activated preparation of metal alkoxides
    88.
    发明公开
    Improved activated preparation of metal alkoxides 失效
    Aktivierte Herstellung von Metallalkoxyden。

    公开(公告)号:EP0186294A2

    公开(公告)日:1986-07-02

    申请号:EP85308251.9

    申请日:1985-11-13

    CPC classification number: C07C29/70 C07C31/28 C07C31/30 C07C31/32

    Abstract: 57 Improved methods for preparing metal alkoxides from metals and alcohols involve dry-grinding the metal in an inert atmosphere prior to the addition of the alcohol. When an activator is used, it is usually ballmilled with the metal. Higher yields are obtained particularly when the metal and alcohol are not very reactive without an activator. Typical metals are those from Groups 2A, 2B, 3A, and 3B, particularly aluminum, magnesium, and yttrium. Typical alcohols are those which contain up to 16 carbon atoms, particularly those containing 4 or more carbon atoms.

    Abstract translation: 从金属和醇制备金属醇盐的改进方法包括在加入醇之前在惰性气氛中干磨金属。 当使用活化剂时,通常用金属球磨。 特别是当金属和醇在没有活化剂的情况下不是非常活泼的情况下获得更高的收率。 典型的金属是来自2A,2B,3A和3B族的金属,特别是铝,镁和钇。 典型的醇是含有至多16个碳原子的醇,特别是含有4个或更多个碳原子的醇。

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