CN113235093A - Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof - Google Patents

Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof Download PDF

Info

Publication number
CN113235093A
CN113235093A CN202110549542.4A CN202110549542A CN113235093A CN 113235093 A CN113235093 A CN 113235093A CN 202110549542 A CN202110549542 A CN 202110549542A CN 113235093 A CN113235093 A CN 113235093A
Authority
CN
China
Prior art keywords
acid
zinc
powder
microetching
alloy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202110549542.4A
Other languages
Chinese (zh)
Inventor
詹吉隆
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shenzhen Gaoxinchang Technology Co ltd
Original Assignee
Shenzhen Gaoxinchang Technology Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shenzhen Gaoxinchang Technology Co ltd filed Critical Shenzhen Gaoxinchang Technology Co ltd
Priority to CN202110549542.4A priority Critical patent/CN113235093A/en
Publication of CN113235093A publication Critical patent/CN113235093A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F3/00Brightening metals by chemical means
    • C23F3/02Light metals
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F3/00Brightening metals by chemical means
    • C23F3/04Heavy metals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • ing And Chemical Polishing (AREA)

Abstract

The invention relates to the field of metal surface treatment processes, in particular to bright dipping powder for galvanizing and zinc alloy and aluminum alloy and a preparation method thereof. Bright dipping powder for galvanizing and zinc alloy and aluminum alloy and a preparation method thereof; the formula of the brightening agent is powder, and no liquid acid is used, so that the brightening agent does not have the problems of high corrosivity and fuming. Replacing nitric acid with a dry acid salt, wherein the dry acid salt is composed of sodium nitrate, sodium fluoride, sulfamic acid and citric acid; the organic acid provides hydrogen ions, reduces the acidity in the liquid medicine to meet the requirement of light emission, and other substances are buffer substances, so that the liquid medicine has the function of stabilizing the liquid medicine and reduces the microetching difference of high and low current regions. The buffering agent exists in the formula, so that the thickness difference of the microetching light on zinc and zinc alloy on the workpiece and the thickness difference of aluminum and aluminum alloy can be reduced, the surface of the workpiece is smoother and finer, the treatment capacity of acid exhaust can be reduced, and the corrosion inhibitor is more nontoxic and harmless compared with liquid acid in the production process.

Description

Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof
Technical Field
The invention relates to the field of metal surface treatment processes, in particular to bright dipping powder for galvanizing and zinc alloy and aluminum alloy and a preparation method thereof.
Background
At present, nitric acid is used for surface treatment of zinc and zinc alloy, nitric acid with different concentrations is used according to various requirements, consumption is high, concentrated acid-removing liquid and vapor have high corrosivity, and the problem of fuming also causes harm to the environment and health inspection.
The nitric acid has strong corrosivity to zinc and zinc alloy, the micro-etching rate of the zinc and the zinc alloy is not easy to control, and particularly, a workpiece in an electroplating process has a high-low current region, so that the stability of the process is low, and the workpiece is easy to generate poor quality due to excessive micro-etching at a thin part.
Disclosure of Invention
In order to solve the problems, the invention provides the glazing powder for the zinc plating, the zinc alloy, the aluminum plating and the aluminum alloy and the preparation method thereof, which have no high corrosivity and fuming problems, ensure that the surface of a workpiece is smoother, meticulous and can reduce the treatment amount of acid exhaust, and have no toxicity and harm compared with liquid acid in the production process. Under the same frequency of use, can reduce the change frequency of changing liquid medicine, increase life.
In order to achieve the purpose, the invention adopts the technical scheme that: the brightening powder for galvanizing and zinc alloy and aluminum alloy comprises the following components in percentage by weight: 50-80% of sodium nitrate, 1-10% of halogen salt, 10-20% of organic acid and 10-20% of sulfonic acid.
Further, the halogen salt comprises one or more of sodium fluoride, sodium chloride, potassium chloride, sodium bromide, potassium bromide and potassium iodide.
Further, the organic acid comprises one or more of citric acid, oxalic acid, formic acid, acetic acid and malic acid.
Further, the sulfonic acid comprises one or more of sulfamic acid, methanesulfonic acid and alkylsulfonic acid.
The application also provides a preparation method of the bright dipping powder for the zinc and zinc alloy plating and the aluminum and aluminum alloy plating, which comprises the following steps:
step 1: weighing sodium nitrate, halogen salt, organic acid and sulfonic acid according to the proportion;
step 2: and (3) uniformly mixing the raw materials weighed in the step (1), wherein the mixing time is 1-5 minutes.
Further, the raw materials weighed in the step 2 were uniformly mixed at 25 ℃. .
The invention has the beneficial effects that: the formula of the brightening agent is powder, and no liquid acid is used, so that the brightening agent does not have the problems of high corrosivity and fuming. Replacing nitric acid with a dry acid salt, wherein the dry acid salt is composed of sodium nitrate, sodium fluoride, sulfamic acid and citric acid; the organic acid provides hydrogen ions, reduces the acidity in the liquid medicine to meet the requirement of light emission, and other substances are buffer substances, so that the liquid medicine has the function of stabilizing the liquid medicine and reduces the microetching difference of high and low current regions. The buffering agent exists in the formula, so that the thickness difference of the microetching light on zinc and zinc alloy on the workpiece and the thickness difference of aluminum and aluminum alloy can be reduced, the surface of the workpiece is smoother and finer, the treatment capacity of acid exhaust can be reduced, and the corrosion inhibitor is more nontoxic and harmless compared with liquid acid in the production process. Under the same frequency of use, can reduce the change frequency of changing liquid medicine, increase life.
Drawings
FIG. 1 is an SEM image of a metal surface after a conventional micro-etching agent treatment.
FIG. 2 is an SEM image of the metal surface after the new micro-etching agent treatment.
Fig. 3 is a comparison of the arithmetic mean deviation Ra of the profile after the new microetching and the conventional microetching treatment.
Fig. 4 is a comparison of the microscopic unevenness ten-point height Rz after the new microetching treatment and the conventional microetching treatment.
Fig. 5 is a graph showing the relationship between the activity of the novel microetching agent and the standing time.
Detailed Description
Referring to fig. 1-5, the present invention relates to a bright dipping powder for zinc and zinc alloy and aluminum alloy, which comprises the following components by weight: 50-80% of sodium nitrate, 1-10% of halogen salt, 10-20% of organic acid and 10-20% of sulfonic acid.
Further, the halogen salt comprises one or more of sodium fluoride, sodium chloride, potassium chloride, sodium bromide, potassium bromide and potassium iodide.
Further, the organic acid comprises one or more of citric acid, oxalic acid, formic acid, acetic acid and malic acid.
Further, the sulfonic acid comprises one or more of sulfamic acid, methanesulfonic acid and alkylsulfonic acid.
Specific example 1: the brightening powder for galvanizing and zinc alloy and aluminum alloy comprises the following components in percentage by weight: 50% of sodium nitrate, 10% of sodium fluoride, 20% of citric acid and 20% of methanesulfonic acid.
Specific example 2: the brightening powder for galvanizing and zinc alloy and aluminum alloy comprises the following components in percentage by weight: 60% of sodium nitrate, 8% of sodium fluoride, 12% of citric acid and 20% of sulfamic acid.
Specific example 3: the brightening powder for galvanizing and zinc alloy and aluminum alloy comprises the following components in percentage by weight: 70% of sodium nitrate, 5% of sodium fluoride, 10% of oxalic acid and 15% of methanesulfonic acid.
Specific example 4: the brightening powder for galvanizing and zinc alloy and aluminum alloy comprises the following components in percentage by weight: 75% of sodium nitrate, 5% of sodium fluoride, 10% of citric acid and 10% of alkyl sulfonic acid.
The following preparation method of the bright dipping powder for galvanizing and zinc alloy and aluminum alloy comprises the following steps:
step 1: weighing sodium nitrate, halogen salt, organic acid and sulfonic acid according to the proportion;
step 2: the raw materials weighed in the step 1 are uniformly mixed at 25 ℃, and the mixing time is not more than 5 minutes.
In order to verify the reliability of microetching treatment using the gloss powder of the present application, a verification test was performed using the mixed powder prepared in specific example 1; meanwhile, in order to test the accuracy, nitric acid of the traditional technology is selected for microetching treatment for comparison;
1. experimental process
In this embodiment, a comparative experiment was performed on the surface of the same material (zinc alloy in this embodiment) by using the microetching agent of the present application and a conventional microetching agent (nitric acid), and the process flow was as follows: washing- > micro-etching treatment (30S treatment at 25 ℃, micro-etching rate: 0.90 +/-0.05 um/min) - > washing- > passivation- > washing- > sealing- > drying.
Wherein 1 to 5g/L of microetching agent for microetching treatment of the present application is prepared by weighing the present invention in the form of a fine powder and completely dissolving detachable water;
2. laboratory apparatus
Scanning Electron Microscope (SEM) (Hitachi S-3000N)
Optical microscope a (0lympus BX51M)
Roughness measuring instrument (DEKTAK 8Advanced Development Profile from Vecco)
3. Microetching treated surface topography
FIG. 1 is an SEM image of a metal surface treated by a conventional microetching agent, and FIG. 2 is an SEM image of a metal surface treated by a new microetching agent; comparing SEM images of the metal surface treated by the new micro-etching agent and the metal surface treated by the traditional micro-etching agent, it can be seen from the eyes of FIGS. 1-2 that the copper surface treated by the new micro-etching agent is smoother and smoother than that treated by the traditional micro-etching agent.
4. Surface roughness of microetching treatment
FIG. 3 is a comparison of the arithmetic mean deviation Ra of the profile after the new microetching agent and the conventional microetching treatment;
FIG. 4 is a comparison of the microscopic unevenness ten-point height Rz after the new microetching treatment and the conventional microetching treatment;
as can be seen from comparison of the surface phase roughness (ra.rz) in fig. 3 to 4, the surface roughness of the zinc alloy treated with the new microetching agent is smaller than that of the zinc alloy treated with the conventional microetching agent.
By comparing and analyzing the results of FIGS. 1-4, the new microetching agent treatment provides significant polishing and leveling of the surface of the zinc alloy.
5 stability of microetching agent
The conventional microetching agents, particularly peroxide microetching agents, are easily decomposed and unstable in working solution, so that it is inconvenient in actual operation to continuously supplement or strictly control the operating conditions to maintain the activity. FIG. 5 shows the relationship between the activity of the novel microetching agent and the standing time, and the stability of the novel microetching agent can be seen from FIG. 3. The new microetching agent is stable, and the activity of the working solution is kept unchanged after the working solution is placed for several months.
In conclusion, the formula of the brightening agent is powder, and no liquid acid is used, so that the brightening agent does not have the problems of high corrosivity and fuming. The buffering agent exists in the formula, so that the thickness difference of the microetching light on zinc and zinc alloy on the workpiece and the thickness difference of aluminum and aluminum alloy can be reduced, the surface of the workpiece is smoother and finer, the treatment capacity of acid exhaust can be reduced, and the corrosion inhibitor is more nontoxic and harmless compared with liquid acid in the production process. Under the same frequency of use, can reduce the change frequency of changing liquid medicine, increase life.
Microetching agents are widely used in the treatment of metal surfaces in microelectronic products and components. The microetching agent is a new technology for microetching copper surface, and not only has the advantages of traditional microetching agent, but also overcomes the disadvantages of traditional microetching agent. The surface of the new micro-etching agent pair material is subjected to the production of obvious polishing and leveling; the surface of the micro-etched aluminum and aluminum alloy or zinc alloy is protected; meanwhile, the novel microetching agent is stable, the microetching rate can be controlled easily, and the microetching rate of the working solution can be controlled to be 2-5000 nm/min, wherein the mass concentration, the total mass concentration, the concentration of accumulated aluminum ions or zinc ions and the temperature of the microetching agent have different influences on the microetching rate, so that the formula or the operating conditions of the microetching agent can be changed according to different requirements, the working solution with different microetching rates can be obtained, and the microetching agent can be used for microetching metal without influencing the size of the metal.
The above embodiments are merely illustrative of the preferred embodiments of the present invention, and not restrictive, and various changes and modifications to the technical solutions of the present invention may be made by those skilled in the art without departing from the spirit of the present invention, and the technical solutions of the present invention are intended to fall within the scope of the present invention defined by the appended claims.

Claims (6)

1. The light emitting powder for galvanizing and zinc alloy and aluminum alloy is characterized in that: comprises the following components in percentage by weight: 50-80% of sodium nitrate, 1-10% of halogen salt, 10-20% of organic acid and 10-20% of sulfonic acid.
2. A glazing powder for galvanising and zinc alloys and aluminium alloys according to claim 1, characterised in that: the halogen salt comprises one or more of sodium fluoride, sodium chloride, potassium chloride, sodium bromide, potassium bromide and potassium iodide.
3. A glazing powder for galvanising and zinc alloys and aluminium alloys according to claim 1, characterised in that: the organic acid comprises one or more of citric acid, oxalic acid, formic acid, acetic acid, and malic acid.
4. A glazing powder for galvanising and zinc alloys and aluminium alloys according to claim 1, characterised in that: the sulfonic acid comprises one or more of sulfamic acid, methanesulfonic acid and alkyl sulfonic acid.
5. A method for preparing glazing powder for galvanizing and zinc alloy and aluminum alloy according to any one of claims 1 to 4, characterized in that: the method comprises the following steps:
step 1: weighing sodium nitrate, halogen salt, organic acid and sulfonic acid according to the proportion;
step 2: and (3) uniformly mixing the raw materials weighed in the step (1), wherein the mixing time is 1-5 minutes.
6. A glazing powder for galvanization and zinc and aluminum alloys according to claim 5, characterized in that: the raw materials weighed in step 2 were mixed uniformly at 25 ℃.
CN202110549542.4A 2021-05-20 2021-05-20 Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof Pending CN113235093A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110549542.4A CN113235093A (en) 2021-05-20 2021-05-20 Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110549542.4A CN113235093A (en) 2021-05-20 2021-05-20 Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof

Publications (1)

Publication Number Publication Date
CN113235093A true CN113235093A (en) 2021-08-10

Family

ID=77137713

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110549542.4A Pending CN113235093A (en) 2021-05-20 2021-05-20 Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof

Country Status (1)

Country Link
CN (1) CN113235093A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2739129A (en) * 1948-10-02 1956-03-20 Henkel & Cie Gmbh Cleaning composition
US3171765A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Powder composition for bright dipping zinc and cadmium
CN101144164A (en) * 2006-09-12 2008-03-19 长葛市天润有色金属研究所 Method for preparing copper product polishing agent
CN108642496A (en) * 2018-04-20 2018-10-12 吴伟华 A kind of preparation method of stainless steel products special solid polishing agent

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2739129A (en) * 1948-10-02 1956-03-20 Henkel & Cie Gmbh Cleaning composition
US3171765A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Powder composition for bright dipping zinc and cadmium
CN101144164A (en) * 2006-09-12 2008-03-19 长葛市天润有色金属研究所 Method for preparing copper product polishing agent
CN108642496A (en) * 2018-04-20 2018-10-12 吴伟华 A kind of preparation method of stainless steel products special solid polishing agent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
张宏祥,王为编著: "《电镀工艺学》", 30 June 2002 *

Similar Documents

Publication Publication Date Title
JPH11310896A (en) Electroplating method
US20060237326A1 (en) Method for treating surface of magnesium or magnesium alloy
CN110629224B (en) Environment-friendly nickel removing agent and preparation method and use method thereof
JP5201315B2 (en) Electroplating method
CN114232030B (en) PCB methanesulfonic acid tin stripping waste liquid recycling method
JPH06173074A (en) Electroplated alloy of gold, copper and silver
JP3450424B2 (en) Reduction of tin sludge in acid tin plating
CN109609934A (en) Cyanide-free zinc deposition solution integrating aluminum and aluminum alloy chemical replacement and electrodeposition and application thereof
CN110760904A (en) Cyanide-free alkaline cuprous copper plating additive
US20090038950A1 (en) High speed method for plating palladium and palladium alloys
CN113235093A (en) Brightening powder for galvanizing and zinc alloy and aluminum alloy and preparation method thereof
EP3059335B1 (en) Surface modifiers for ionic liquid aluminum electroplating solutions, processes for electroplating aluminum therefrom, and methods for producing an aluminum coating using the same
US5194139A (en) Pretreating solution for silver plating and silver plating treating process using the solution
CN107287629B (en) Non-cyanide Au-Sn alloy plating solution
CN108360029B (en) Method and apparatus for mitigating tin whisker growth on tin and tin-plated surfaces by doping tin with gold
KR20190068046A (en) Immersion Tin Plating Solution Using Ionic Liquid Electrolyte materials
EP3686319A1 (en) Indium electroplating compositions and methods for electroplating indium on nickel
CN114108031B (en) Environment-friendly cyanide-free alkaline copper plating refiner and preparation method thereof
FR2545841A1 (en) ELECTROLYTE FOR THE DEPOSITION OF TRIVALENT CHROME AND METHOD OF USING SAME
JPS6056234B2 (en) Manufacturing method of active anode
US3957669A (en) Metal treatment
WO2022158291A1 (en) Electrolytic silver plating bath and electrolytic silver plating method using same
KR102347903B1 (en) Control of additive turnover in an electrodeposition solution
White The electrolytic corrosion of some metals
KR20230050875A (en) Acidic zincate composition for aluminum or aluminum alloy and zincate treatment method using the same

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20210810

RJ01 Rejection of invention patent application after publication