APPARATUS AND METHOD FOR UPGRADING COAL
    1.
    发明申请
    APPARATUS AND METHOD FOR UPGRADING COAL 审中-公开
    用于升级煤的装置和方法

    公开(公告)号:US20140054503A1

    公开(公告)日:2014-02-27

    申请号:US13595685

    申请日:2012-08-27

    Abstract: A method of upgrading coal is disclosed, the method comprising: subjecting the coal to a hydrothermal dewatering process at a temperature and a pressure above ambient conditions to produce dewatered coal; removing ash tailings from the dewatered coal to produced reduced ash dewatered coal; and producing a coal water slurry with the reduced ash dewatered coal. An apparatus for upgrading coal is also disclosed, the apparatus comprising: a hydrothermal dewatering reactor connected to receive coal and output dewatered coal; an ash separator connected to receive dewatered coal from the hydrothermal dewatering reactor and output reduced ash dewatered coal; a slurrifier connected to receive reduced ash dewatered coal from the ash separator and output a coal water slurry.

    Abstract translation: 公开了一种升级煤的方法,该方法包括:在高于环境条件的温度和压力下对煤进行水热脱水处理以产生脱水煤; 从脱水煤中除去灰尾渣,生产还原灰脱水煤; 并用还原灰脱水煤生产煤水浆料。 还公开了一种用于升级煤的装置,该装置包括:连接以接收煤并输出脱水煤的水热脱水反应器; 一个灰分分离器,用于接收来自水热脱水反应器的脱水煤,并输出还原灰脱水煤; 一种除渣器连接以从灰分离器中接收还原灰脱水煤并输出煤水浆料。

    Process for preparation of gabapentin
    2.
    发明申请
    Process for preparation of gabapentin 失效
    加巴喷丁的制备方法

    公开(公告)号:US20050119503A1

    公开(公告)日:2005-06-02

    申请号:US10497899

    申请日:2002-11-18

    CPC classification number: C07C227/42 C07C229/28

    Abstract: A process for producing Gabapentin, (1-(anminomethyl)-1-cyclohexaneacetic acid) from Gabapentin hydrochloride salt. In the process the Gabapentin hydrochloride is converted to Gabapentin using inorganic base such as Barium hydroxide. Gabapentin hydrochloride is converted to Gabapentin sulfate which in turn is converted to free base using Barium hydroxide. The process is directed to improvement in the manufacture of Gabapentin which would be industrially feasible and effective Gabapentin obtained following the process of the invention is suitable as a drug especially in the treatment of cerebral diseases such as epilepsy. The above process involves simple steps and avoid the problems of the known art. In particular the process avoids severe conditions and/or complexities and can be readily adopted for industrial application. The process provides for good yield and does not involve lengthy extended process steps. It is cost-effective and can be carried out involving simple ingredients and steps of manufacture.

    Abstract translation: 从加巴喷丁盐酸盐制备加巴喷丁(1-(氨基甲基)-1-环己烷乙酸)的方法。 在该过程中,使用无机碱如氢氧化钡将盐酸加巴喷丁转化为加巴喷丁。 将加巴喷丁盐酸盐转化为硫酸氢巴比坦,然后使用氢氧化钡将其转化为游离碱。 本发明涉及在工业上可行且有效的加巴喷丁的制造方面的改进。本发明方法获得的加巴喷丁适合作为特别是治疗脑疾病如癫痫的药物。 上述过程涉及简单的步骤并且避免了已知技术的问题。 特别地,该方法避免了苛刻的条件和/或复杂性,并且可以容易地用于工业应用。 该方法提供良好的产率,并不涉及冗长的扩展工艺步骤。 它具有成本效益,可以进行简单的成分和制造步骤。

    Manufacture of phenyl ethylamine compounds, in particular venlafaxine
    3.
    发明申请
    Manufacture of phenyl ethylamine compounds, in particular venlafaxine 失效
    制造苯乙胺化合物,特别是文拉法辛

    公开(公告)号:US20050228198A1

    公开(公告)日:2005-10-13

    申请号:US10508930

    申请日:2002-06-13

    Abstract: A process for the preparation of hydroxy(cycloalkane/cyclokene)phenylethyl of the general formula (III) comprising alkylation of its precursor amine of general formula (II) which is in turn produced by an effective reduction process from its precursor cyanide having the general formula (I) using Raney Nickel (CORMIII) as catalyst where, either of R5 and R6 independently could be in meta or para position and R5, R6 are independently hydrogen, hydroxyl, alkyl, alkanoyloxy, cyano nitro, alkylmercapto, amino, alkylamino, alkanamido, halo, trifluoromethyl, or taken together methylenedioxy, n is 0, 1, 2, 3, 4; R7 is hydrogen of alkyl of 1-7 carbon atom, R1 IH or alkyl of 1-3 carbon atom and R2 is alkyl 1-3 carbon atom, the dotted line represents optional unsaturation. Compounds of formulae IV, V and VI are respectively derivatives of compounds I, II and III respectively.

    Abstract translation: 制备通式(III)的羟基(环烷烃/环烯)苯乙基的方法,包括其通式(II)的前体胺的烷基化反应,其通过有效的还原方法从其具有通式(II)的前体氰化物 (I)使用阮内镍(CORIII)作为催化剂,其中R 5和R 6中的任一个可以独立地为间位或对位,R 5,R 6独立地为氢,羟基,烷基,烷酰氧基,氰基硝基,烷基巯基,氨基,烷基氨基,烷酰氨基 ,卤素,三氟甲基或亚甲二氧基取代,n为0,1,2,3,4; R7是1-7个碳原子的烷基,R1H或1-3个碳原子的烷基,R2是烷基1-3个碳原子的氢,虚线代表任选的不饱和键。 式IV,V和VI的化合物分别是化合物I,II和III的衍生物。

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