ALLOY FOR GRAIN REFINING OF COPPER MATERIALS
    1.
    发明申请
    ALLOY FOR GRAIN REFINING OF COPPER MATERIALS 审中-公开
    铜合金材料精炼

    公开(公告)号:WO1989007660A1

    公开(公告)日:1989-08-24

    申请号:PCT/EP1988000099

    申请日:1988-02-10

    CPC classification number: C22C9/00 C22C1/03

    Abstract: An alloy for grain refining of copper materials consists of copper or a copper alloy containing (a) 0.01 to 25 % calcium, (b) 0.01 to 15 % boron. The alloy permits remarkably uniform and efficient grain refining of copper materials, and no large foreign nuclei are left behind in the relevant material.

    Abstract translation: 一种用于铜材晶粒细化的合金由铜或铜合金组成,含有(a)0.01〜25%的钙,(b)0.01〜15%的硼。 该合金允许铜材料的显着均匀和有效的晶粒细化,并且在相关材料中不留下大的外来核。

    PROCESS FOR PRODUCING FINE-PARTICLE TRANSITION METAL CARBIDES
    2.
    发明申请
    PROCESS FOR PRODUCING FINE-PARTICLE TRANSITION METAL CARBIDES 审中-公开
    生产细颗粒过渡金属碳化物的方法

    公开(公告)号:WO1989005776A1

    公开(公告)日:1989-06-29

    申请号:PCT/EP1988001175

    申请日:1988-12-19

    CPC classification number: C01B32/949 C01B32/907 C01B32/914 C01P2004/62

    Abstract: In a process for producing fine-particle transition metal carbides of vanadium, niobium, tantalum und tungsten or mixtures thereof, a) a complex compound of the transition metal or mixtures thereof containing a metal are reacted with a polymer compound containing carbon, b) the reaction product from step a) is dried and pyrolysed to yield the fine particle transition metal and carbon, c) the pyrolysis products of step b) are converted to the corresponding carbides at 1200 to 1600°C. The transition metal carbides of vanadium, niobium, tantalum and tungsten so obtained are characterized by the extreme fineness of their particles.

    PROCESS FOR PRODUCING AROMATIC NITRILES
    4.
    发明申请
    PROCESS FOR PRODUCING AROMATIC NITRILES 审中-公开
    方法制备芳族腈

    公开(公告)号:WO1996036593A1

    公开(公告)日:1996-11-21

    申请号:PCT/EP1996002127

    申请日:1996-05-17

    CPC classification number: C07C253/28 C07C255/50

    Abstract: The description relates to a process for producing aromatic nitriles from their corresponding aldehydes, in which the latter are caused to react with ammonia at temperatures of 200 to 500 DEG C in the gas phase in the presence of a catalyst based on molybdenum nitride of the general formula MoNxOy in which x = 0.25 to 1.0 and y = 0 to 1.0. It is thus possible to produce aromatic nitriles from the corresponding aldehydes with yields and selectivities of up to 98 % with conversions of up to 100 %.

    Abstract translation: 本发明提供了一种用于从这些相应的醛制备芳族腈所描述的,与氨在200温度下,在催化剂的存在下根据通式MoNxOy,钼氮化物被反应到500℃,在气相中,其中x = 0.25 和1.0和y = 0〜1.0即可。 以这种方式,芳香腈高达100%的可从与收率和选择性高达98%的转化在相应的醛制备。

    CONDENSATION PRODUCTS BASED ON AMINO-S-TRIAZINES AND THE USE OF THE SAID PRODUCTS
    5.
    发明申请
    CONDENSATION PRODUCTS BASED ON AMINO-S-TRIAZINES AND THE USE OF THE SAID PRODUCTS 审中-公开
    依据氨基酸-S三嗪以及它们的使用缩合产物

    公开(公告)号:WO1996030423A1

    公开(公告)日:1996-10-03

    申请号:PCT/EP1996001403

    申请日:1996-03-29

    CPC classification number: C04B24/223 C04B2103/30 C08G12/40

    Abstract: In the proposed condensation product based on amino-s -triazines with at least two amino groups, formaldehyde and sulphite, the molar ratio of amino-s-triazine, formaldehyde and sulphite is 1 : 2.5 - 6.0 : 1.51 - 2.0 and the formiate content is less than 0.3 wt %. The condensation product is obtained by a) heating amino-s-triazine, formaldehyde and a sulphite in the molar ratio 1 : 2.5 - 6.0 : 1.51 - 2.0 in an aqueous solution at a temperature of 60-90 DEG C and a pH level of between 9.0 and 13.0 until the sulphite can no longer be detected; b) continuing the condensation at a pH level of between 3.0 and 6.5 and a temperature of 60-80 DEG C until the condensation product has a viscosity of 5-50 mm/s at 80 DEG C; and c) adjusting the pH level of the condensation product to 7.5-12.0 or carrying out thermal secondary treatment at a pH level of >/= 10.0 and a temperature of 60-100 DEG C. The product can be used as an additive for inorganic binders such as cement.

    Abstract translation: 基于氨基-s-三嗪与至少两个氨基基团,甲醛和亚硫酸盐的缩合产物,氨基-s-三嗪与甲醛的摩尔比为亚硫酸盐1:2.5〜6.0,1.51〜2.0, 和甲酸含量小于0.3重量%。 其制备是加热一)氨基-s-三嗪,甲醛和的摩尔比1亚硫酸盐:在60℃至90℃,的温度下在水溶液中1.51〜2.0:2.5〜6.0 pH为9.0〜13.0,直至亚硫酸盐是不再可检测,b)然后将在pH 3.0和6.5和60至80℃的温度之间,缩合的 为只要直到在80℃下5至50毫米/秒,并具有C)然后缩合产物调节到7.5的pH值到12.0或热后处理在pH进行粘度的缩合产物 值> / = 10.0和60〜100℃的温度下 该产品适于作为无机粘合剂的添加剂,特别是水泥。

    QUICKLY SOLUBLE ADDUCT FOR MOLTEN BATH
    6.
    发明申请
    QUICKLY SOLUBLE ADDUCT FOR MOLTEN BATH 审中-公开
    快速溶解润滑剂

    公开(公告)号:WO1988000620A2

    公开(公告)日:1988-01-28

    申请号:PCT/EP1987000387

    申请日:1987-07-16

    CPC classification number: C22C1/026

    Abstract: A quickly soluble adduct for molten baths contains between 2 and 50 weight % of a component A composed of alcaline aluminium fluoride or of a salt containing alcaline aluminium fluoride and a component B composed of one or several alloy metals, the components A and B being intimately mixed. This adduct has an unexpectedly high speed of dissolution also with high contents of alloy metals and at the same time yields completely the alloy metal.

    Abstract translation: 用于熔融浴的快速溶解的加合物含有2至50重量%的由碱金属氟化铝或含有碱金属氟化铝的盐组成的组分A和由一种或多种合金金属组成的组分B,组分A和B是密切的 混合。 该加合物具有意想不到的高溶解速度,同时具有高含量的合金金属,同时完全产生合金金属。

    PROCESS FOR FRACTIONATING VISCOUS SILICONES
    8.
    发明申请
    PROCESS FOR FRACTIONATING VISCOUS SILICONES 审中-公开
    方法进行分馏硅胶VISCOSER

    公开(公告)号:WO1998029474A1

    公开(公告)日:1998-07-09

    申请号:PCT/EP1997007301

    申请日:1997-12-24

    CPC classification number: C08G77/36

    Abstract: In order to fractionate viscous silicones, oily or polymer diorganosilicones with a chain length from 2 to 10.000 are continuously separated with condensed hydrocarbons such as ethane, propane and n- or i-butane or their mixtures into a head and a bottom product, preferably in an extraction column, at temperatures between 25 and 250 DEG C, pressures between 20 and 500 bars and a gas density > 160 kg/m . In order to avoid viscosity-caused problems, an organic solvent in the form of a C5-8-alkane or up to 85 % by weight of the condensed gas (mixture) can be added to the starting materials before the fractionation. This process enables high-grade viscous silicone fractions to be obtained, with a chain length from 200 to 10,000 and/or a viscosity from 100 to 500,000 mPas, as well as a total D4 to D20 oligomer content below 0.05 % by weight.

    Abstract translation: 对于具有链长2-10000状油或聚合物分馏viscoser硅Diorganosilicone与压缩烃如乙烷,丙烷和正 - 或异丁烷或它们的混合物,在25和250℃,20至500巴之间的压力和温度之间的其 的>160公斤/ m的气体密度<3>优选连续在萃取塔分离成顶部和底部产物。 为了规避粘度问题,它可以被添加到到分馏在C 5-8 - 烷的形式是有机溶剂,或至多85重量压缩气体(混合物)的%之前的起始原料。 与获得高品质的粘胶硅氧烷组分,其具有200至10,000和/或100至500000毫帕·秒,并且它们Gesamtoligomerengehalt D4到D20的粘度的链长度的方法是小于0.05重量%。

    DESULPHURATING AGENT FOR CO-INJECTION TREATMENT OF PIG IRON MELTS
    9.
    发明申请
    DESULPHURATING AGENT FOR CO-INJECTION TREATMENT OF PIG IRON MELTS 审中-公开
    脱硫铁液共注射治疗

    公开(公告)号:WO1997021841A1

    公开(公告)日:1997-06-19

    申请号:PCT/EP1996005515

    申请日:1996-12-10

    CPC classification number: C21C1/025

    Abstract: A desulphurating agent is proposed for co-injection treatment of pig iron melts by injection of magnesium granulate and, separately, of the second injection component consisting of a magnesium granulate with a grain size of between 0.1 and 0.8 mm and containing 5-20 wt % calcium carbide with a grain size of

    Abstract translation: 用于共注射治疗生铁的脱硫剂熔化通过注入镁颗粒和,分别在第二次注射部件,包括具有0.1和0.8毫米之间的晶粒尺寸的镁颗粒,含有.- 5〜20重量% 电石与含有粒度

    PROCESS FOR PREPARING CALCIUM CYANAMIDE FROM UREA
    10.
    发明申请
    PROCESS FOR PREPARING CALCIUM CYANAMIDE FROM UREA 审中-公开
    PROCESS一种生产尿素的氰氨化钙

    公开(公告)号:WO1995024358A1

    公开(公告)日:1995-09-14

    申请号:PCT/EP1995000771

    申请日:1995-03-02

    CPC classification number: C01C3/18

    Abstract: The invention concerns a process for preparing calcium cyanamide by reacting urea with an oxygenous calcium compound in at least two steps: a) in a first step the reaction components are reacted by condensation and/or circulation or by applying them to a hot surface at temperatures of between 120 and 500 DEG C until a solid forms; and b) the resultant solid reaction mixture is then calcined at temperatures of between 600 and 900 DEG C. In this way high yields and charges of calcium cyanamide can be obtained without necessitating complicated reprocessing of the reaction product after the first or second step.

    Abstract translation: 通过脲与在至少两个阶段中含有氧气的钙化合物反应生产氰氨化钙的被允许a)在第一步骤中在压力下和/或循环或通过在120温度下,以500℃将其应用到一个热表面,直至固体形成的反应组分 反应,和b)形成的固体的反应混合物随后在600温度下煅烧至900℃ 在这里,高收率和氰氨化钙的流速,可以在不要求第一或第二阶段之后需要将反应产物的复杂的后实现。

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