Synthesis and use of hypothiocyanite
    6.
    发明申请
    Synthesis and use of hypothiocyanite 有权
    硫氰酸钙的合成与应用

    公开(公告)号:US20060018817A1

    公开(公告)日:2006-01-26

    申请号:US11181400

    申请日:2005-07-14

    申请人: Michael Ashby

    发明人: Michael Ashby

    IPC分类号: C01B21/093

    CPC分类号: C01C3/00

    摘要: A method of producing hypothiocyanite by combining a hypohalous acid and thiocyanate.

    摘要翻译: 通过组合次卤酸和硫氰酸盐来生产硫氰酸钙的方法。

    Preparation of potassium cyanoborohydride
    7.
    发明授权
    Preparation of potassium cyanoborohydride 失效
    硫氰酸钾的制备

    公开(公告)号:US3697232A

    公开(公告)日:1972-10-10

    申请号:US3697232D

    申请日:1969-06-16

    申请人: VENTRON CORP

    发明人: WADE ROBERT C

    CPC分类号: C01C3/00 C01B6/00

    摘要: THE INVENTION RELATES TO THE PREPARATION OF POTASSIUM CYANOBOROHYDRIDE. THIS COMPOUND IS PREPARED BY MIXING SUBSTANTIALLY ANHYDROUS HYDROGEN CYANIDE WITH A SUBSTANTIALLY ANHYDROUS POTASSIUM BOROHYDRIDE AT A TEMPERATURE BETWEEN 0*C. AND 100*C. IN SUBSTANTIALLY ANHYDROUS DIMETHYLFORMAMIDE AT ATMOSPHERIC PRESSURE. IF DESIRED TO AVOID LOSS OF HYDROGEN CYANIDE, A PRESSURE OF FROM ABOUT 1 TO 5 POUNDS PER SQUARE INCH MAY BE USED. PREFERABLY, THE PREPARATION IS CARRIED OUT IN TWO STAGES (1) INITIALLY AT A TEMPERATURE BETWEEN ABOUT 10*C. TO ABOUT 35*C. UNTIL SUBSTANTIALLY ALL HYDROGEN HAS CEASED TO BE EVOLVED, AND (2) THEN AT A TEMPERATURE BETWEEN ABOUT 35*C. AND THE BOILING POINT OF THE SOLVENT UNTIL ALL THE INTERMEDIATE PRODUCTS HAVE BEEN CONVERTED TO THE DESIRED CYANOBOROHYDRIDE.

    Preparation of lithium,sodium and quaternary ammonium cyanoborohydrides
    8.
    发明授权
    Preparation of lithium,sodium and quaternary ammonium cyanoborohydrides 失效
    锂,钠和季铵甲氰尿酸的制备

    公开(公告)号:US3667923A

    公开(公告)日:1972-06-06

    申请号:US3667923D

    申请日:1969-06-16

    申请人: VENTRON CORP

    发明人: WADE ROBERT C

    CPC分类号: C01C3/00 C01B6/00

    摘要: THE INVENTION RELATES TO THE PREPARATION OF LITHIUM, SODIUM AND QUATERNARY AMMONIUM CYUANOBROHYDRIDES. THESE COMPOUNDS ARE PREPARED BY MIXING SUBSTANTIALLY ANHYDROUS HYDROGEN CYANIDE WITH A SUBSTANTIALLY ANHYDROUS LITHIUM OR SODIUM OR QUATERNARY AMMONIUM BOROHYDRIDE AT A TEMPERATURE BETWEEN 0*C. AND 100*C. IN A SUBSTANTIALLY ANHYDROUS SOLVENT, SUCH AS TETRAHYDROFURAN, GLYME, DIGLYME, TRIGLME OR DIMETHYL FORMAMIDE OR MIXTURES OF THESE AT ATOMPHERIC PRESSURE. IF DESIRED. TO AVOID LOSS OF HYDROGEN CYANIDE, A PRESSURE OF FROM ABOUT 1 TO 5 POUNDS PER SQUARE INCH MAY BE USED. PREFERABLY, THE PREPARATION IS CARRIED OUT IN TWO STAGES (1) INTIALLY AT A TEMPERATURE BETWEEN ABOUT 10*C. TO ABOUT 35*C. UNTIL SUBSTANTIALLY ALL HYDROGEN HAS CEASED TO BE EVOLVED AND (2) THEN AT A TEMPERATURE BETWEEN ABOUT 35* C. AND THE BOILING POINT OF THE SOLVENT UNTIL ALL THE INTERMEDIATE PRODUCTS HAVE BEEN CONVERTED TO THE DESIRED CYANOBOROHYDRIDE.