• 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:
    Provided are zinc phosphate treatment liquid and zinc phosphate treatment method without sludge generation. That is, zinc phosphate treatment liquid in which the molar concentrations [Zn], [H 3 PO 4 ], and [HNO 3 ] of Zn, H 3 PO 4 and HNO 3 satisfy the following formula. [Zn] 0.3 [H 3 PO 4 ] + 0.5 [HNO 3 ]. The zinc phosphate treatment liquid contains, as an additive, one or two or more additives selected from nitrous acid, permanganic acid, persulfuric acid, hydrogen peroxide, chloric acid, perchloric acid, nitrobenzenesulfonic acid, hydroxylamine, starch phosphate ester, and fluorine compound. desirable. In the present invention, the target metal member is subjected to the cathode electrolytic treatment in the zinc phosphate treatment liquid. Alternatively, the target metal member is brought into contact with a weak alkaline colloid aqueous solution containing titanium oxide, titanium hydroxide and zinc phosphate, followed by cathodic treatment in the zinc phosphate treatment solution.
    公开号:KR20010006711A
    申请号:KR1020000009778
    申请日:2000-02-28
    公开日:2001-01-26
    发明作者:가와구치쥰；이시쿠라가즈히로；만미도모유키
    申请人:사또미 유따까；니혼 파커라이징 가부시키가이샤；
    IPC主号:
    专利说明:

    Zinc phosphate treatment solution and zinc phosphate treatment method without sludge generation {A PROCESS FOR ZIRO-PHOSPHATE TREATMENT OF METALLIC MATERIALS WITHOUT GENERATING SULDGE AND TREATMENT SOLUTION USED THEREFOR}
    The present invention relates to a zinc phosphate treatment liquid without sludge generation used to form a zinc phosphate coating on the surface of a metal material and a treatment method using the same.
    In general, the phosphate treatment is a temporary antirust treatment of steel, as well as a steel (or galvanized steel material) or aluminum under coating, and the plastic processing lubrication of the steel, or a sliding lubrication treatment. It is widely used. This is due to the fact that the phosphate coating provides antirusting property to metal materials as passivation coating, and gives excellent adhesion between these and the surface of the metal material because of excellent affinity between organic materials such as resins and fats and oils. do. In other words, the phosphate film has the most basic characteristics as a surface treatment film of rust resistance and adhesion.
    There are several kinds of phosphate coatings such as iron phosphate, zinc phosphate, zinc phosphate, zinc phosphate, and manganese phosphate depending on the type of the counter metal. The greatest demand for the formation of zinc phosphate or zinc phosphate coatings for plated steel materials (usually a composite film of zinc phosphate and zinc phosphate is formed on the steel surface).
    The phosphate treatment liquid used in such a case is an acidic aqueous solution composed of phosphoric acid, nitric acid and zinc as essential components, in addition to several kinds of additives, and a chemical film is formed by, for example, contacting steel materials for a few minutes. An example of small reaction in this case is shown below.
    Fe → Fe 2+ + 2e (1)
    2H + + 2e → H 2 (2)
    3Zn 2+ + 6H 2 PO 4 - → Zn 3 (PO 4) 2 4H 2 O + 4H 3 PO 4 (3)
    2Zn 2+ + Fe 2+ + 6H 2 PO 4 - → Zn 2 Fe (PO 4) 2 4H 2 O + 4H 3 PO 4 (3 ')
    Fe 2+ → Fe 3+ + e (4)
    Fe 3+ + H 2 PO 4 - → FePO 4 + 2H + (5)
    In an acidic treatment liquid such as the phosphate treatment liquid, the steel material is dissolved as shown in the formula (1), and the electrons released at that time are consumed in the discharge of hydrogen ions as shown in the formula (2) to cause an increase in the pH of the material surface. As the pH rises, the dissociation equilibrium of phosphoric acid shifts, and some of the ferrous ions dissolved from zinc ions or the material become insoluble, and zinc phosphate or phosphoric acid is applied to the surface of the material as shown in equations (3) and (3 '). A film of zinc iron is formed.
    On the other hand, the dissolution of the material of formula (1) is an energy source for these film-forming reactions, but most of the ferrous ions dissolved are so-called reaction wastes, and thus, the diffusion reaction of zinc ions or phosphate ions is lowered, and the reaction rate of the film-forming reaction is lowered. It must be removed out of the system. Generally, an oxidizing agent such as nitrite ion is used as an additive to oxidize to ferric ions as shown in formula (4) and precipitated as insoluble iron phosphate as shown in formula (5).
    The impurity produced in such a chemical reaction system can be removed out of the system as a solid precipitate, making it possible to use the treatment liquid semi-permanently only by supplying short components, which greatly contributed to the industrial success of the phosphate treatment. However, due to the complicated maintenance of water-containing solids (sludge) or the rising cost of treatment of sludge discharged as industrial wastes, phosphate treatment without sludge generation has been particularly demanded in recent years.
    As a countermeasure, there is a method of performing phosphate treatment using a cathode electrolysis method. Unlike the phosphate treatment using the chemical conversion method described above, the cathode electrolysis method requires a dissolution reaction of a material such as the formula (1) because the reaction of the formula (2) can be directly caused by electrical energy using an external power source. Therefore, the formation of iron phosphate sludge can be avoided. However, since the actual sludge contains about 10 to 25% of zinc phosphate in addition to iron phosphate, it is impossible to almost eliminate sludge generation simply by applying a cathode electrolysis method.
    Actually, some conventional techniques have been disclosed as phosphate treatments by cathodic electrolysis, including Japanese Patent Application Laid-Open Nos. 64-21095, 4-36498, and 6-506263. . Japanese Unexamined Patent Publication No. 64-21095 aims at high corrosion resistance and high adhesion for coating underlay, but sludge generation cannot be avoided because trivalent iron ions are contained in the treatment liquid. Japanese Unexamined Patent Publication No. 4-36498 aims to form a dense zinc phosphate film at high speed, but the zinc to phosphoric acid is high and the production of zinc phosphate sludge is expected. Japanese Unexamined Patent Publication No. 6-506263 describes that nickel and cobalt, which are indispensable for the performance of the phosphate coating for coating underlay, are expensive and toxic, so that the concentration of these in the treatment liquid can be reduced by using an electrolytic method. have. Therefore, they cannot be said to have any characteristics in comparison with the treatment liquid composition used in the chemical conversion method, and any advantage of the electrolytic method is in the densification of the film (high corrosion resistance) or high speed film formation, and in terms of the reduction of sludge generation amount. Is not mentioned.
    As described above, in the conventional phosphate treatment technique, sludge generation can hardly be eliminated. Accordingly, an object of the present invention is to provide a zinc phosphate treatment liquid that does not involve sludge generation and a zinc phosphate treatment method using the same.
    As a result of intensive studies to solve the above problems, the present inventors newly discovered that zinc phosphate treatment liquid without sludge generation can be obtained by specifying molar concentrations of phosphoric acid, nitric acid and zinc in zinc phosphate treatment liquid.
    That is, the zinc phosphate treatment liquid without sludge generation of the present invention is an aqueous solution containing at least phosphoric acid, nitric acid and zinc, and their molarity (mol / L) [H 3 PO 4 ], [HNO 3 ] and [Zn ] Is characterized by the following relationship.
    [Zn] 0.3 [H 3 PO 4 ] + 0.5 [HNO 3 ]
    Furthermore, the zinc phosphate treatment liquid of the present invention includes one or two or more selected from nitrous acid, permanganic acid, persulfate, hydrogen peroxide, chloric acid, perchloric acid, nitrobenzenesulfonic acid, hydroxylamine, starch phosphate ester and fluorine compound as additives. Or it is preferable that these salts are contained.
    The zinc phosphate treatment method without sludge generation of the present invention is characterized in that the target metal member is cathode treated in the zinc phosphate treatment liquid.
    In the zinc phosphate treatment method of the present invention, the metal member is preferably contacted with a weak alkaline colloid aqueous solution containing titanium oxide, titanium hydroxide and zinc phosphate prior to the cathode electrolytic treatment of the target metal member.
    EMBODIMENT OF THE INVENTION Hereinafter, this invention is demonstrated in detail.
    In general, in the chemical forming phosphate treatment, the energy of the reaction is obtained from the dissolution of the material, so that it cannot be controlled from the outside. Therefore, in order to allow the film forming reaction to occur as quickly as possible, the treatment liquid composition is adjusted so that the reaction of the formula (3) or (3 ') occurs immediately at least when the pH of the material interface is raised. This condition indicates that zinc phosphate can precipitate in the liquid without treating the material with a slight stimulus from the outside. This is why zinc phosphate is also contained in the actual sludge.
    To avoid this, it is necessary to set an appropriate upper limit zinc concentration so that no precipitation of zinc phosphate occurs for a given phosphate concentration and nitric acid concentration. As a result of experiments with a large number of combinations, the inventors have found that the upper limit of zinc concentration which does not produce precipitation of zinc phosphate at temperatures up to at least 90 ° C is represented by the following simple equation.
    [Zn] = 0.3 [H 3 PO 4 ] + 0.5 [HNO 3 ] (6)
    Where [Zn], [H 3 PO 4 ] and [HNO 3 ] represent the concentrations of zinc, phosphoric acid and nitric acid in mol / L units, respectively.
    Therefore, the zinc phosphate treatment liquid of the present invention should not exceed the concentration obtained by the formula (6) as the zinc concentration. Such a treatment liquid is considered to be an inappropriate treatment liquid because zinc concentration is low in applying the conventional chemical conversion method as is easily expected. That is, the zinc phosphate treatment method of the present invention requires the cathode electrolytic method to be applied to the target metal member. This is by supplying as much controllable electrical energy from the outside as the zinc concentration is deteriorated due to the low zinc concentration, and avoiding dissolution of the metal material as in the above formula (1), for example, in the case where the target metal member is a steel material. It has two meanings that almost no iron phosphate sludge is generated.
    However, Eq. (6) above limits the relationship between phosphoric acid concentration, nitric acid concentration and zinc concentration, but does not explain the absolute value of each concentration. In other words, this condition is sufficient as long as the sludge is avoided, but the phosphoric acid concentration and the nitric acid concentration are preferably 0.1 mol / L or more in order for the zinc phosphate treatment of the present invention to obtain a predetermined film formation amount at an industrially realistic film formation rate. Do. Furthermore, for the same reason, it is preferable that the zinc concentration is 50% of the upper limit concentration calculated by the formula (6). On the other hand, the upper limit of phosphoric acid concentration and nitric acid concentration is not particularly specified, but it is economically desirable at the concentration exceeding 0.6 mol / L as the phosphoric acid concentration and 0.1 mol / L as the nitric acid concentration because the effect of thickening the treatment liquid is saturated. Not. And in the industrialization of this invention, especially when the absolute value of phosphoric acid and zinc concentration is large, and stirring of a process liquid is inadequate, sludge may adhere to a heating tube by local overheating. In order to avoid this, it is safer and more preferable to satisfy the conditions of the following formula again in addition to the conditions of the formula (6).
    [Zn] / [H 3 PO 4 ] 〈0.91 (7)
    By immersing the target metal member in the zinc phosphate treatment solution as described above and electrolyzing the cathode, the zinc phosphate treatment can be performed without causing any sludge. The setting of the electrolytic conditions may be carried out by controlling the amount of energized electricity (current x time) in accordance with the required coating amount, but in order to obtain a normal coating, it is preferable to set the current density within the range of 0.5 to 50 A / dm 2 . Although the temperature of the zinc phosphate treatment liquid is 30 to 90 ° C., it is possible to be in a wide range.
    Since the zinc phosphate treatment liquid of the present invention hardly generates sludge, the upper limit concentration of zinc is limited by the above Equation (6), which explains that the zinc phosphate coating is in a direction for controlling the precipitation of the zinc phosphate coating. This is not a problem as long as the cathode electrolytic method can be used to control the current density and the electric current amount, but the present inventors do not increase the zinc concentration for the purpose of merit of the fast film-forming property of the electrolytic method and the refinement of the film crystal. He also found two ways to improve film formation.
    The first method is to use an additive in combination. That is, the zinc phosphate treatment liquid of the present invention includes one, two or more selected from nitrous acid, permanganic acid, persulfate, hydrogen peroxide, chloric acid, perchloric acid, nitrobenzenesulfonic acid, hydroxylamine, starch phosphate ester and fluorine compound, or It is preferable that these salts are added. These additives are expressed in the form of an acid except for hydrogen peroxide, hydroxylamine, starch phosphate ester and fluorine compound, but the form to be added may be an acid as it is or may be in the form of a salt with an alkali metal or ammonium. In addition, it is preferable to add hydroxylamine in the form of a salt with sulfuric acid etc. normally. As the fluorine compound, hydrofluoric acid, hydrofluoric acid, hydrofluoric acid titanate, hydrofluoric acid zirconic acid, or the like can be used. It is preferable to add an acid or an alkali metal salt or ammonium salt thereof. Furthermore, these concentrations should be selected in a timely manner according to the required film formation rate, and it is usually preferred to add them in the range of 0.0005 to 0.1 mol / L.
    By the way, when the additive is used in combination, ionic species other than phosphoric acid, nitric acid and zinc are mixed in the phosphate treatment liquid of the present invention. In this case, care must be taken in the calculation of Equation (6). (6) Since the concentration of zinc to phosphoric acid and nitric acid as "acid" is defined to the last, when a cation other than zinc exists, a part of all nitrate ions is neutralized by the above-mentioned cation component, and the part Does not act as an "acid". Conversely, when anions other than phosphoric acid and nitric acid are present, the action as "acid" is enhanced.
    Therefore, when formula (6) is calculated using the total nitrate ion concentration [NO 3 − ], c 1 c 1 + 1 , C 2 p 2+ . C n pn + , and anion contained in addition to phosphoric acid and nitric acid is selected from A 1 q1- , A 2 q2- . When A m qm- , the value modified according to Equation (8) below should be used as [HNO 3 ] in Equation (6). Wherein [C 1 p1 + ], [C 2 p2 + ]... [C n pn + ] and [A 1 q1- ], [A 2 q2- ]... [A m qm- ] indicates the molar concentration (mol / L) of each component, p 1 , p 2 . p n and q 1 , q 2 . q m represents the number of ionic values of each component, respectively.
    [HNO 3 ] = [NO 3 - ]-(p 1 [C 1 p1 + ] + p 2 [C 2 p2 + ] +… + p n [C n pn + ]) + (q 1 [A 1 q1- ] + q 2 [A 2 q2- ] +… + q m [A m qm- ]) (8)
    A second method of improving the film-forming property is to bring the target metal member into contact with a weak alkaline colloid aqueous solution containing titanium oxide, titanium hydroxide and zinc phosphate before the zinc phosphate treatment by cathode electrolysis. These colloidal particles are adsorbed onto the surface of the metal member as a target and act as crystal nuclei in forming the next zinc phosphate film. By applying this process, the zinc phosphate film formed by the cathode electrolysis can not only improve its formation efficiency but also control the film crystal grain size extremely finely. And even better results can be obtained by simultaneously applying these first and second methods.
    EXAMPLE
    Hereinafter, although the Example of this invention is demonstrated further more concretely with a comparative example, this invention is not limited by these Examples.
    Example 1
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid such that the phosphoric acid concentration was 0.4 mol / L and the nitric acid concentration was 0.8 mol / L, and the zinc concentration was 0.5 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, the turbidity of the solution was not observed at all and the transparent appearance was always maintained. The zinc concentration of this aqueous solution was lower than the limit zinc concentration (0.52 mol / L) calculated by the above formula (6).
    Comparative Example 1
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid so that the phosphoric acid concentration was 0.4 mol / L and the nitric acid concentration was 0.7 mol / L, and the zinc concentration was 0.5 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, turbidity was observed gradually and finally white precipitate was obtained. The zinc concentration of this aqueous solution was higher than the limit zinc concentration (0.47 mol / L) calculated by said formula (6). After filtering and washing the white precipitate, it was confirmed that the dried powder was zinc phosphate by X-ray diffraction analysis.
    Example 2
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid such that the phosphoric acid concentration was 0.6 mol / L and the nitric acid concentration was 1.0 mol / L, and the zinc concentration was 0.65 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, the turbidity of the solution was not observed at all and the transparent appearance was always maintained. The zinc concentration of this aqueous solution was lower than the limit zinc concentration (0.68 mol / L) calculated by the above formula (6).
    Comparative Example 2
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid such that the phosphoric acid concentration was 0.6 mol / L and the nitric acid concentration was 0.9 mol / L, and the zinc concentration was 0.65 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, turbidity was observed gradually and finally white precipitate was obtained. The zinc concentration of this aqueous solution was higher than the limit zinc concentration (0.63 mol / L) calculated by said formula (6).
    Example 3
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid so that the phosphoric acid concentration was 0.2 mol / L and the nitric acid concentration was 0.4 mol / L, and the zinc concentration was 0.25 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, the turbidity of the solution was not observed at all and the transparent appearance was always maintained. The zinc concentration of this aqueous solution was lower than the limit zinc concentration (0.26 mol / L) calculated by the above formula (6).
    Comparative Example 3
    Zinc carbonate (ZnCO 3 ) was added to the mixed aqueous solution of phosphoric acid and nitric acid so that the phosphoric acid concentration was 0.2 mol / L and the nitric acid concentration was 0.4 mol / L, and the zinc concentration was 0.3 mol / L. When this aqueous solution was heated to 80 degreeC and hold | maintained for 2 hours, turbidity was observed gradually and finally white precipitate was obtained. The zinc concentration of this aqueous solution was higher than the limit zinc concentration (0.26 mol / L) calculated by said formula (6).
    Example 4
    After degreasing the hot rolled material of JIS S45C, a test panel was prepared by removing the surface oxide film by immersing in 5% HCl at room temperature for 30 seconds. Furthermore, it was immersed in the aqueous solution of Example 1 warmed to 80 ° C. and the current density was 10 A / dm.2Cathode electrolysis was carried out so that a zinc phosphate film was formed on this surface. At this time, the electrolytic time was found to be 50% by the zinc phosphate coating on the surface, and the result was 10 seconds. Coverage was measured by SEM observation (50 times). At this time, the crystal size of the zinc phosphate film was a maximum of about 50 µm. So in the aqueous solution of Example 1 sodium nitrite (NaNO2) 0.001 mol / L and the same electrolytic conditions (current density: 10 A / dm2, Electrolytic time: 10 seconds), the zinc phosphate treatment and SEM observation showed that the coverage by the coating was improved to about 90%. At this time, the crystal size of the zinc phosphate film was a maximum of about 40 µm.
    Example 5
    To the aqueous solution of Example 1 was added 0.007 mol / L sodium fluoride (NaF) and hydrofluoric acid (H2SiF6) And 0.04 mol / L of the same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 30 µm.
    Example 6
    Potassium permanganate (KMnO) in the aqueous solution of Example 14) And 0.001 mol / L of the same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 60 µm.
    Example 7
    In the aqueous solution of Example 1 sodium persulfate (Na2S2O8) And 0.01 mol / L of the same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 30 µm.
    Example 8
    Sodium metanitrobenzenesulfonate (C in the aqueous solution of Example 16H4NO2SO30.005 mol / L of Na) was added and the same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 40 µm.
    Example 9
    In aqueous solution of Example 1 hydroxylamine hydroxylamine [(NH2OH)2H2SO4] And the same electrolytic conditions as in Example 4 (current density: 10 A / dm)2, Electrolytic time: 10 seconds), zinc phosphate treatment and SEM observation showed that the coverage by the coating was 85%. At this time, the crystal size of the zinc phosphate film was a maximum of about 60 µm.
    Example 10
    2 g / L of starch phosphate ester sodium was added to the aqueous solution of Example 1, and the same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 60 µm.
    Example 11
    A test panel of JIS S45C, previously degreased and pickled, was immersed in a 3 g / L aqueous solution (titanium colloidal solution) of pureparenZ, a surface regulator of Japanese parkarizing agent, at room temperature for 30 seconds, and immediately in the aqueous solution of Example 1 Same electrolytic conditions as in Example 4 (current density: 10 A / dm2, Electrolysis time: 10 seconds) was observed by SEM after zinc phosphate treatment, the coverage by the film was 100%. At this time, the crystal size of the zinc phosphate film was a maximum of about 15 µm.
    Moreover, in the cathode electrolytic operation of Examples 4 to 11, the treatment liquid was always transparent and no formation of precipitate appeared.
    As apparent from Examples 1 to 3, the zinc phosphate treatment liquid of the present invention having a zinc concentration below the limit zinc concentration represented by Equation (6) described above does not produce precipitation of zinc phosphate even when heated to 80 ° C. Can be. On the other hand, as shown in Comparative Examples 1 to 3, zinc phosphate was precipitated in the zinc phosphate treatment liquid having a zinc concentration exceeding the above-mentioned limit zinc concentration of the formula (6).
    As apparent from Examples 4 to 10, the use of the zinc phosphate treatment solution in combination with the additive of the present invention formed a zinc phosphate coating having good coverage even with a relatively short electrolysis time of 10 seconds.
    As apparent from Example 11, the titanium-based colloidal surface adjustment treatment of the present invention was carried out prior to the electrolytic zinc phosphate treatment to obtain a coating of perfect coverage and to form a coating having extremely dense zinc phosphate crystals.
    By applying the zinc phosphate treatment liquid of the present invention, generation of industrial waste (sludge), which has conventionally been a problem, can be almost eliminated, which can greatly contribute to alleviation of global environmental pollution. In the method of the present invention, since the electrolytic method is used, zinc phosphate treatment can be performed at extremely high speed, and if it is a semiconductor, zinc phosphate treatment can be basically performed on any material, and industrially, a large merit can be provided.
    权利要求:
    Claims (4)
    [1" claim-type="Currently amended] It is an aqueous solution containing at least phosphoric acid, nitric acid and zinc, and their molarity (mol / L), that is, [H 3 PO 4 ], [HNO 3 ] and [Zn], respectively, satisfy the following relationship. Zinc phosphate treatment liquid without sludge generation.
    [Zn] 0.3 [H 3 PO 4 ] + 0.5 [HNO 3 ] [2" claim-type="Currently amended] The method according to claim 1, wherein one or two or more selected from nitrous acid, permanganic acid, persulfuric acid, hydrogen peroxide, chloric acid, perchloric acid, nitrobenzenesulfonic acid, hydroxylamine, starch phosphate ester and fluorine compound Zinc phosphate treatment solution containing no salt containing sludge.
    [3" claim-type="Currently amended] A method of treating zinc phosphate without sludge, characterized by subjecting the subject metal member to a cathode electrolytic treatment in the zinc phosphate treatment liquid according to claim 1.
    [4" claim-type="Currently amended] 4. The method of treating zinc phosphate without sludge according to claim 3, wherein the metal member is contacted with a weak alkaline colloid aqueous solution containing titanium oxide, titanium hydroxide and zinc phosphate prior to the cathode electrolytic treatment.
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    同族专利:
    公开号 | 公开日
    BR0008673A|2002-09-24|
    RU2001126522A|2003-06-27|
    JP3479609B2|2003-12-15|
    CN1180134C|2004-12-15|
    EP1161575A4|2004-08-11|
    AU3510400A|2000-09-21|
    US7422629B1|2008-09-09|
    KR100672189B1|2007-01-19|
    WO2000052227A1|2000-09-08|
    CN1266110A|2000-09-13|
    EP1161575A1|2001-12-12|
    JP2000248368A|2000-09-12|
    CA2363083A1|2000-09-08|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1999-03-02|Priority to JP99-54834
    1999-03-02|Priority to JP05483499A
    2000-02-28|Application filed by 사또미 유따까, 니혼 파커라이징 가부시키가이샤
    2001-01-26|Publication of KR20010006711A
    2007-01-19|Application granted
    2007-01-19|Publication of KR100672189B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP99-54834|1999-03-02|
    JP05483499A|JP3479609B2|1999-03-02|1999-03-02|Sludge-free zinc phosphate treatment liquid and zinc phosphate treatment method|
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