• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The method for improving the initial activity of activated hydrazine, is used as corrosion protection for reservoir drinking water and for the wet preservation of installation parts, which are no longer being used. It is the goal of the invention to improve the initial activity of hydrazine solutions, which are activated with complexes of trivalent cobalt, with respect to oxygen dissolved in water, and to lower the activator concentration; the object of the invention being to use a suitable coactivator. The object is accomplished in that the activator-rich hydrazine solution additionally contains 2-amino-4-nitrophenol or 2-acetamino-4-nitrophenol or mixtures thereof as coactivator.
    公开号:SU1359255A1
    申请号:SU837772898
    申请日:1983-03-18
    公开日:1987-12-15
    发明作者:Фукс Вильфрид；Рихтер Хорст；Кобер Роланд；Кауфман Венделин；Мюллер Кристиан
    申请人:Феб Леуна-Верке "Вальтер Ульбрихт" (Инопредприятие)；
    IPC主号:
    专利说明:

    The invention relates to methods of oxygen from water and can be used in the preparation of feed water, its preservation, while protecting tanks, pipelines, heat exchangers, steam boilers from corrosion.
    To remove dissolved oxygen from water, various reducing agents are used.
     It is known to use hydrazine as an oxygen reducing agent in the presence of activators, in which quinoid, dinenees, aromatic diamines, aminophenols, sulfonic acids and heterocyclic compounds are used (German Patent No. 1521749, class 48d 11/14, 1970, German patent No. 2,115,463, Cl. 4 “d 11/14, 1974).
    The disadvantage of these methods is the need to use high concentrations of the activator and the observance of the ultrasonic pH range of 10.0-10.4.
    It is known to use manganese, copper, cobalt or vanadium compounds as an activator (US Patent No. 4,022,711, CL 252-389, 1977, US Patent No. 4,079,018, CL 252-389, 1978), the disadvantages of which are low activity, as well as the ability to cause corrosion and decomposition of hydrazine.
    The closest to the proposed technical essence and the achieved result is the method of removing NIN from water of dissolved oxygen by reducing it with hydrazine in the presence of an activator — a cationic or anionic complex of cobalt (III) with inorganic ligands — pentamine cobalt (III) chloride or sodium hexane – nitrite cobalt ( III) and co-J activators - trivalent phenols and pyrogallol (owner. GDR patent No. 160314, cl. C 23 F 11/08, 1980),
    The disadvantage of this method is the low activity of the coactivators used and the high consumption of the activator.
    The aim of the invention is to increase the degree of removal of oxygen.
    The goal is achieved
    In addition, in the case of anticorrosion protection of the process, there is a synergistic effect leading to a decrease in the degree of corrosion, as a result of which
    a method for removal of dissolved oxygen from water, including the reduction by comparison with the prototype by one span of its hydrazine in the presence of lok values of the best anticorrosive activator — cationic or anionic protection.
    of a cobalt (III) complex with non-orga-Optimal amounts of activator nigands — amine-cobalt are an order of magnitude lower than
    0
    five
    0
    (III) chloride or sodium hexanitrite-cobalt (III), taken in the amount of (0.1-0.5) g / l solution of hydrazine and coactivator - 2-amino-4-nitrophenol and / or 2-acetamino-4-nitrophenol, addition in the amount of (0.05-0.25) g / l solution of hydrazine.
    The method is carried out by treating water with a solution of hydrazine containing an activator in an amount of (0.1-0.5) g / l of a solution of hydrazine and co-activator in an amount of (0.05-0.25) g / l of a solution of hydrazine.
    Example. 1 ml of an aqueous solution of hydrazine containing 220 g of hydrazine per liter containing 0.05-0.5 g / l sodium hexanitrite-cobalt (III) or cobalt (111) hexammine chloride as an activator and 0.05-0.25 g / l of 2-amino-4-nitrophenol or 2-acetamino-4-nitrophenol or a mixture of both compounds as a co-activator, is fed into 1 liter of oxygen-containing water with an oxygen content of 6.5 mg / l. The pH value was 10.4, the decomposition of oxygen was measured after 10 min of treatment, the process temperature was 293 K.
    The table presents the results of the decomposition of oxygen after a reaction time of 10 minutes. depending on the activators and co-activators used and their concentrations.
    The effectiveness of the proposed method in comparison with the prototype lies in a higher degree of oxygen removal and. significantly lower total activator concentration.
    With 1 g sodium hexanitrite cobalt (III) and 0.1 g of pyrogallol per 1 l of hydrazine solution at pH 10.5 according to the prototype, after 10 minutes of treatment only 88% of the available oxygen decomposes. The same decomposition by 88% according to the proposed method is achieved even at 0.1 g of the total activator system. Increasing the concentration of the activator to 0.5 g / l leads to the complete decomposition of oxygen.
    In addition, in the case of anticorrosion protection of the process, there is a synergistic effect leading to a decrease in the degree of corrosion, as a result of which
    0
    five
    0
    5 compared to the prototype by one order - a block of quantities of the best anticorrosive protection.
    31359255
    According to a known method, the activator — cationic or anionic — leads to a more rapid removal of the oxygen of the cobalt (III) complex from the water. The method is simple, works at normal temperature, in a low pH range and achieves the best anticorrosive protection that has been established so far.
    权利要求:
    Claims (1)
    [1]
    Amiccobalt (III) chloride or sodium hexanitrite-cobalt (III) and co-activator — nomic ligands — which, in order to increase the degree of oxygen removal, use 2-amino-4-nitrophenol and /or
    2 acetamino-4-nitrophenol taken in
    A method for removing dissolved acid at a concentration of 0.05-0.25 g / l of a solution of hydrogen from water, including the reduction of hydrazine, the activator is used in hydrazine in the presence of 0.1-0.5 g / l.
    类似技术:
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    同族专利:
    公开号 | 公开日
    DD210407A3|1984-06-06|
    FR2525489A1|1983-10-28|
    US4519997A|1985-05-28|
    DE3309194A1|1983-10-27|
    JPS58186492A|1983-10-31|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    US2780531A|1954-02-23|1957-02-05|Olin Mathieson|Hydrazine recovery|
    US3728281A|1970-04-02|1973-04-17|Fisons Ltd|Corrosion inhibiting composition containing hydrazine and a pyrazolidone or an aminophenol|
    FR2297814B1|1975-01-20|1978-07-21|Ugine Kuhlmann|
    US4022712A|1976-02-24|1977-05-10|Olin Corporation|Catalyzed hydrazine compound corrosion inhibiting composition containing complex of metal salt and amino derivative of carboxylic acid, and its use|
    US4079018A|1976-02-24|1978-03-14|Olin Corporation|Catalyzed hydrazine compositions and methods of their use|
    US4022711A|1976-02-24|1977-05-10|Olin Corporation|Catalyzed hydrazine compound corrosion inhibiting composition containing a complex of metal salt and amino derivative of carboxylic acid, and a quinone compound|
    DD160315A3|1980-10-01|1983-06-01|Wilfried Fuchs|METHOD FOR REMOVING OXYGEN ESTABLISHED IN WATER|
    DD160314A3|1981-01-27|1983-06-01|Wilfried Fuchs|PROCESS FOR IMPROVING THE INITIAL ACTIVITY OF ACTIVATED HYDRAZINE|FR2522522A1|1982-01-27|1983-09-09|Leuna Werke Veb|PROCESS FOR IMPROVING THE INITIAL ACTIVITY OF ACTIVATED HYDRAZINE|
    FR2540854A1|1983-04-22|1984-08-17|Leuna Werke Veb|Process for removing oxygen dissolved in water|
    CA2472069C|2002-01-04|2010-03-09|University Of Dayton|Non-toxic corrosion protection pigments based on cobalt|
    US7235142B2|2002-01-04|2007-06-26|University Of Dayton|Non-toxic corrosion-protection rinses and seals based on cobalt|
    US7294211B2|2002-01-04|2007-11-13|University Of Dayton|Non-toxic corrosion-protection conversion coats based on cobalt|
    US20040011252A1|2003-01-13|2004-01-22|Sturgill Jeffrey A.|Non-toxic corrosion-protection pigments based on manganese|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DD23921782A|DD210407A3|1982-04-22|1982-04-22|PROCESS FOR IMPROVING THE INITIAL ACTIVITY OF ACTIVATED HYDRAZINE|
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