CN104502719A - Method for testing electrophoresis wet paint film resistance - Google Patents

Method for testing electrophoresis wet paint film resistance Download PDF

Info

Publication number
CN104502719A
CN104502719A CN201410752405.0A CN201410752405A CN104502719A CN 104502719 A CN104502719 A CN 104502719A CN 201410752405 A CN201410752405 A CN 201410752405A CN 104502719 A CN104502719 A CN 104502719A
Authority
CN
China
Prior art keywords
electrophoresis
paint film
wet paint
testing
workpiece
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
CN201410752405.0A
Other languages
Chinese (zh)
Inventor
张澍
宋华
赵冉
庞虹
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.)
FAW Group Corp
Original Assignee
FAW Group Corp
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 FAW Group Corp filed Critical FAW Group Corp
Priority to CN201410752405.0A priority Critical patent/CN104502719A/en
Publication of CN104502719A publication Critical patent/CN104502719A/en
Pending legal-status Critical Current

Links

Landscapes

  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Testing Resistance To Weather, Investigating Materials By Mechanical Methods (AREA)

Abstract

The invention relates to a method for testing electrophoresis wet paint film resistance. The method is characterized in that a direct-current power supply device on which an electrophoresis power supply is connected with an electrophoresis groove is connected in series with a current meter A; during electrophoretic painting according to a standard method, a current value at the last second of electrophoresis is read; the painting voltage is a voltage at which the paint film thickness meets a standard requirement; the painting time is 3 minutes; during electrophoresis, a workpiece is submerged into the electrophoresis groove by 10 centimeters; when the electrophoresis wet paint film resistance is given, pre-treatment processes of the workpiece need to be marked: ternary zinc phosphating and phosphorus-free film transformation; the electrophoresis wet paint film resistance is computed according to a computation formula. Through testing of the resistance of the wet paint film, the magnitude of the electrophoretic paint throwing power can be judged more intuitively. As proved by a large quantity of test results, when the resistance value of the wet paint film is higher, the film forming capability of the inner cavity of the workpiece is higher.

Description

The method of testing of a kind of electrophoresis wet paint film impedance
Technical field
The present invention relates to the method for testing of a kind of electrophoresis wet paint film impedance, in particular to when carrying out electrophoretic painting by standard method, a range that continuous-current plant is connected is the reometer of (1 ~ 2) A, by reading the electrophoresis current value of last 1 second, according to the coating area of application voltage, workpiece, calculate the impedance of electrophoresis wet paint film.
Background technology
Painting dressing automobiles is in environmental protection, today that energy-saving and emission-reduction cry is more and more higher, Pretreatment Technology Before Finishing Harmless (without phosphorus, heavy metal free) becomes development trend, and phosphorization treatment process is about to be replaced by the without phosphorus conversion film technique of environment-friendly type (zirconates process, silane treatment).In addition, in order to improve resource utilization, reduce painting cost, the thickness of cathodic electrophoretic paint there has also been new standard, and namely vehicle body outside surface electrodeposited paint film thickness is reduced to (15 ~ 18) μm from (18 ~ 22) μm.As Japanese Toyota just planned that to the target of electrodeposited paint film be vehicle body outside surface 15 μm, inside surface 10 μm as far back as 2006, namely four pieces of box throwing powers reach 0.67, and weight of coated paint can be made to reduce about 20%, and comprehensive production cost reduces by 10%.At home and abroad motor corporation has formed the gesture that exploitation adopts film-type height throwing power electrophoretic coating at present.
When new environment-friendly type without phosphorus conversion film technique replaces phosphorization treatment process operation application traditional before electrophoresis, find that the throwing power of cathode electro-coating declines, the swimming affecting vehicle body inner chamber is coated with quality.Reason is that the new without phosphorus conversion film of environment-friendly type is very thin, only has about 1/10 of current phosphating coat thickness, has had a strong impact on the throwing power of follow-up electrophoretic painting.Found by lot of experiments, high throwing power electrophoretic coating newly developed must be adopted, just can solve the problem.
Affect a lot of because have of electrophoretic coating throwing power, one of them more crucial factor is the characteristic of electrophoretic coating itself, i.e. the conductivity of electrophoresis groove liquid and wet paint film resistance, and the former guarantees the thickness at position, casket chamber, and the latter controls outside plate thickness.Conductivity is existing method of testing at present, but wet paint film resistance does not also have method of testing at present.
By patent retrieval, do not retrieve the patent about electrophoretic coating wet paint film method for testing resistance.
Summary of the invention
The object of this invention is to provide the method for testing of a kind of electrophoresis wet paint film impedance, it, by the impedance of test wet paint film, more intuitive judgment can go out the height of electrophoretic coating throwing power, show according to many experimental results, wet paint film resistance value is larger, and its workpiece lumen film forming ability is stronger.
Technical scheme of the present invention is achieved in that the method for testing of a kind of electrophoresis wet paint film impedance, it is characterized in that: a range of connecting on the continuous-current plant that electrophoresis power is connected with electrophoresis tank is the reometer A of 1000 mA ~ 2000 mA, degree of accuracy 2mA;
Concrete testing procedure is:
When carrying out electrophoretic painting by standard method, by reading the electrophoresis current value of last 1 second; Voltage when application voltage should select film thickness to be standard-required; Being coated with ETL estimated time of loading is 3 minutes; Workpiece coating area chooses the model of 70 mm × 150 mm, and immerse electrophoresis tank 10cm during electrophoresis, such coating area is 0.014 m 2; The pre-treating technology of workpiece to be indicated: ternary zinc phosphatization, without phosphorus conversion film when providing the impedance of electrophoresis wet paint film; Press computing formula calculate the impedance of electrophoresis wet paint film, in formula:
R: wet paint film impedance, unit is Ohms sq rice, (Ω m 2);
U: application voltage, unit is volt (V);
A: current value when last 1 second, unit is ampere (A);
S: Workpiece coating area, unit is a square metre (m 2).
Good effect of the present invention is its size according to electrophoresis wet paint film, and intuitive judgment goes out the height of electrophoretic coating throwing power, correctly can evaluate the quality of electrophoretic coating.
Accompanying drawing explanation
Fig. 1 is the syndeton of electrophoresis wet paint film testing impedance of the present invention.
Embodiment
Below in conjunction with accompanying drawing and embodiment, the present invention will be further described: as shown in Figure 1, the method of testing of a kind of electrophoresis wet paint film impedance, it is characterized in that: a range of connecting on the continuous-current plant that electrophoresis power 1 is connected with electrophoresis tank 2 is the reometer A of 1000 mA ~ 2000 mA, degree of accuracy 2mA;
Concrete testing procedure is:
When carrying out electrophoretic painting by standard method, by reading the electrophoresis current value of last 1 second; Voltage when application voltage should select film thickness to be standard-required; Being coated with ETL estimated time of loading is 3 minutes; Workpiece coating area chooses the model of 70 mm × 150 mm, and immerse electrophoresis tank 10cm during electrophoresis, such coating area is 0.014 m 2; The pre-treating technology of workpiece to be indicated: ternary zinc phosphatization, without phosphorus conversion film when providing the impedance of electrophoresis wet paint film; Press computing formula calculate the impedance of electrophoresis wet paint film, in formula:
R: wet paint film impedance, unit is Ohms sq rice, (Ω m 2);
U: application voltage, unit is volt (V);
A: current value when last 1 second, unit is ampere (A);
S: Workpiece coating area, unit is a square metre (m 2).
embodiment one
The high throwing power electrophoretic paint that certain coating material production producer H produces:
1, in 4 L electrophoresis tanks, former for electrophoretic paint paint working fluid or on-the-spot tank liquor are adjusted to the standard operating conditions of material.
2, be that the reometer series connection of (1 ~ 2) A is received in the DC power supply circuit of regulation by range, selected range.
3, choose the model of 70 mm × 150 mm, the pre-treating technology of test piece chooses ternary zinc phosphating process, is numbered three pieces of models.
4, model is immersed electrophoresis tank 10cm, carry out electrophoresis by standard conditions.
5, voltage 240V during application voltage selection film thickness (15 ~ 19) μm, electrophoresis time is 3 minutes.
Current value when 6, reading last 1 second of electrophoresis is 23.9mA.
7, be 1405.9 Ω m according to formulae discovery electrophoretic coating wet paint film resistance 2.
embodiment two
The general electrophoresis coating that certain coating material production producer G produces:
1, in 4 L electrophoresis tanks, former for electrophoretic paint paint working fluid or on-the-spot tank liquor are adjusted to the standard operating conditions of material.
2, be that the reometer series connection of (1 ~ 2) A is received in the DC power supply circuit of regulation by range, selected range.
3, choose the model of 70 mm × 150 mm, the pre-treating technology of test piece chooses ternary zinc phosphorization treatment process, is numbered three pieces of models.
4, model is immersed electrophoresis tank 10cm, carry out electrophoresis by standard conditions.
5, voltage 210V during application voltage selection film thickness (20 ~ 21) μm, electrophoresis time is 3 minutes.
Current value when 6, reading last 1 second of electrophoresis is 26.9mA.
7, be 1092.9 Ω m according to formulae discovery electrophoretic coating wet paint film resistance 2.
embodiment three
1, with the throwing power of the high throwing power electrophoretic paint of four pieces of box method test manufacturer H production be
0.64。.
2, the throwing power testing the general electrophoresis paint of manufacturer G production by four pieces of box methods is 0.47..
3, according to thing embodiment one and embodiment two, high throwing power electrophoretic coating compares with general electrophoresis coating, reduces coating consumption 22%.

Claims (1)

1. a method of testing for electrophoresis wet paint film impedance, is characterized in that: a range of connecting on the continuous-current plant that electrophoresis power is connected with electrophoresis tank is the reometer A of 1000 mA ~ 2000 mA, degree of accuracy 2mA;
Concrete testing procedure is:
When carrying out electrophoretic painting by standard method, by reading the electrophoresis current value of last 1 second; Voltage when application voltage should select film thickness to be standard-required; Being coated with ETL estimated time of loading is 3 minutes; Workpiece coating area chooses the model of 70 mm × 150 mm, and immerse electrophoresis tank 10cm during electrophoresis, such coating area is 0.014 m 2; The pre-treating technology of workpiece to be indicated: ternary zinc phosphatization, without phosphorus conversion film when providing the impedance of electrophoresis wet paint film; Press computing formula calculate the impedance of electrophoresis wet paint film, in formula:
R: wet paint film impedance, unit is Ohms sq rice, (Ω m 2);
U: application voltage, unit is volt (V);
A: current value when last 1 second, unit is ampere (A);
S: Workpiece coating area, unit is a square metre (m 2).
CN201410752405.0A 2014-12-10 2014-12-10 Method for testing electrophoresis wet paint film resistance Pending CN104502719A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410752405.0A CN104502719A (en) 2014-12-10 2014-12-10 Method for testing electrophoresis wet paint film resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410752405.0A CN104502719A (en) 2014-12-10 2014-12-10 Method for testing electrophoresis wet paint film resistance

Publications (1)

Publication Number Publication Date
CN104502719A true CN104502719A (en) 2015-04-08

Family

ID=52944130

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410752405.0A Pending CN104502719A (en) 2014-12-10 2014-12-10 Method for testing electrophoresis wet paint film resistance

Country Status (1)

Country Link
CN (1) CN104502719A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106290134A (en) * 2016-08-24 2017-01-04 奇瑞商用车(安徽)有限公司 A kind of automobile electrophoretic paint sharp edge covering performance test method
CN107179333A (en) * 2017-06-20 2017-09-19 巴斯夫上海涂料有限公司 Detect method and its application of the electrodeposited paint film to base material side along protective value

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1198192A (en) * 1996-07-23 1998-11-04 日本油漆株式会社 Cationic electrodeposition process and coating composition for cationic electrodeposition
CN1346859A (en) * 2000-10-11 2002-05-01 关西油漆株式会社 Cationic paint composition
JP2004179311A (en) * 2002-11-26 2004-06-24 Seiko Epson Corp Semiconductor substrate and method for manufacturing the same, electrooptical apparatus, and electronic apparatus
CN1712461A (en) * 2004-06-16 2005-12-28 日本油漆株式会社 Cationic electrodeposition coating composition
CN1849416A (en) * 2003-09-11 2006-10-18 日本油漆株式会社 Method for forming cathodic electrodeposition film which forms electric through-hole therein, and cation electrodeposition paint which reliably forms electric through-hole
US20090208733A1 (en) * 2008-02-15 2009-08-20 Woo-Jae Lee Display devices with transparent electrodes containing nanocarbon materials
JP2010129733A (en) * 2008-11-27 2010-06-10 Seiko Epson Corp Thin-film transistor, electro-optical device, and electronic apparatus
CN102768261A (en) * 2012-07-02 2012-11-07 奇瑞汽车股份有限公司 On-site detection device for throwing power of electrophoretic paint and detection method for same

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1198192A (en) * 1996-07-23 1998-11-04 日本油漆株式会社 Cationic electrodeposition process and coating composition for cationic electrodeposition
CN1346859A (en) * 2000-10-11 2002-05-01 关西油漆株式会社 Cationic paint composition
JP2004179311A (en) * 2002-11-26 2004-06-24 Seiko Epson Corp Semiconductor substrate and method for manufacturing the same, electrooptical apparatus, and electronic apparatus
CN1849416A (en) * 2003-09-11 2006-10-18 日本油漆株式会社 Method for forming cathodic electrodeposition film which forms electric through-hole therein, and cation electrodeposition paint which reliably forms electric through-hole
CN1712461A (en) * 2004-06-16 2005-12-28 日本油漆株式会社 Cationic electrodeposition coating composition
US20090208733A1 (en) * 2008-02-15 2009-08-20 Woo-Jae Lee Display devices with transparent electrodes containing nanocarbon materials
JP2010129733A (en) * 2008-11-27 2010-06-10 Seiko Epson Corp Thin-film transistor, electro-optical device, and electronic apparatus
CN102768261A (en) * 2012-07-02 2012-11-07 奇瑞汽车股份有限公司 On-site detection device for throwing power of electrophoretic paint and detection method for same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106290134A (en) * 2016-08-24 2017-01-04 奇瑞商用车(安徽)有限公司 A kind of automobile electrophoretic paint sharp edge covering performance test method
CN107179333A (en) * 2017-06-20 2017-09-19 巴斯夫上海涂料有限公司 Detect method and its application of the electrodeposited paint film to base material side along protective value
CN107179333B (en) * 2017-06-20 2019-08-16 巴斯夫上海涂料有限公司 Electrodeposited paint film is detected to base material side along the method and its application of protective value

Similar Documents

Publication Publication Date Title
CN103088393B (en) A kind of automobile panel surface treatment method
CN103898447A (en) Stainless steel surface treatment method and shell prepared thereby
CN105586613A (en) Hard chromium plating method and solution formula for piston rod class parts
CN104109891A (en) Method for preparing aluminum alloy anode oxide film by direct-current superposition pulse voltage
CN103243371B (en) Preparation method of zinc anode oxidation film layer
CN104502719A (en) Method for testing electrophoresis wet paint film resistance
CN203415343U (en) Anticorrosive neodymium iron boron magnet
CN104962893A (en) Environmental phosphating solution
CN105386045B (en) A kind of method of Mg alloy surface processing
CN105316741B (en) A kind of method for carrying out surface by micro-arc oxidation processing to aluminium alloy using grading current
CN103726094A (en) Passivating treatment method for surface of copper foil and copper foil thereof
CN102787311A (en) Rare earth-fluorozirconate compounding processing agent technology suitable for catholic electrophoresis pretreatment
CN104962976A (en) Automobile part cathode electrophoresis paint surface quality processing technique
CN104947100A (en) Surface treatment technology of aluminum product
CN101949044B (en) Niobium electro-osmosis method for steel surface in ionic liquid
CN104250737A (en) Phosphatization technology for electrostatic spraying pre-treatment
CN103897584B (en) A kind of offshore drilling tool-joint silane surface inorganic agent
MX2018007193A (en) Electrochemical deposition of elements in aqueous media.
CN103088399A (en) Multi-step electrochemical metal coat removal method
CN104962896A (en) Zinc-system phosphating solution additive and use method thereof
CN101555596A (en) Vacuum plating process and complete equipment
CN204608191U (en) Electrophoresis anolyte controls and voltage control system
CN104032350A (en) Surface coating formula for aluminum alloy product
CN206052152U (en) A kind of device for making high electrode current potential piece surface deposition chemical plating ni-p alloy coating
CN203346510U (en) Paralleling-type multi-head electrolytic polishing gun

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20150408