Method for purging paint circuits and waterborne purge cleaner
12428567 ยท 2025-09-30
Assignee
Inventors
- Jose M. Casamor (Barcelona, ES)
- Miguel Angel Jaen Franco (Canovelles, ES)
- Jordi Girbau (Canovelles, ES)
Cpc classification
B08B3/08
PERFORMING OPERATIONS; TRANSPORTING
B08B3/10
PERFORMING OPERATIONS; TRANSPORTING
C11D3/30
CHEMISTRY; METALLURGY
International classification
C11D3/30
CHEMISTRY; METALLURGY
B08B3/08
PERFORMING OPERATIONS; TRANSPORTING
B08B3/10
PERFORMING OPERATIONS; TRANSPORTING
Abstract
Described herein is a method for purging paint circuits coated with a non-cured paint with improved cleaning efficiency and a reduced COD (Chemical Oxygen Demand) in the wastewater, where a paint circuit is brought into contact with a waterborne purge cleaner solution including at least one glycolether and which additionally includes at least one water-soluble amine having at least 7 carbon atoms. Also described herein is a waterborne purge cleaner solution with improved cleaning efficiency and reduced VOC (Volatile Organic Compound) content as well as a concentrate for producing the purge cleaner solution.
Claims
1. A method for purging a paint circuit coated with a non-cured paint, comprising bringing the paint circuit into contact with a waterborne purge cleaner solution comprising at least one glycolether characterized in that it additionally comprises at least one water-soluble amine having 7 to 15 carbon atoms, wherein the waterborne purge cleaner solution does not comprise any organic solvents other than the at least one glycolether and does not comprise any surfactants.
2. The method according to claim 1 characterized in that the at least one glycolether comprises hexylglycol and/or hexyldiglycol.
3. The method according to claim 1 characterized in that the at least one water-soluble amine comprises at least one amine having 7 to 12 carbon atoms.
4. The method according to claim 1 characterized in that the purge cleaner solution comprises a) 0.05 to 0.50% (w/w) of at least one water-soluble amine having 7 to 15 carbon atoms, b) 0.3 to 1.0% (w/w) of hexylglycol, and c) 0.3 to 1.0% (w/w) of hexyldiglycol.
5. The method according to claim 1 characterized in that the at least one amine comprises at least one amine having a conjugated acid with a pKa of at least 8.0.
6. The method according to claim 1 characterized in that the at least one amine comprises at least one tertiary amine having at least one hydroxyalkyl group.
7. The method according to claim 6 characterized in that the at least one tertiary amine has one to three hydroxyalkyl groups.
8. The method according to claim 7 characterized in that the at least one amine comprises at least one amine selected from the group consisting of N-methyldiisopropanolamine, N-octyldiethanolamine, triisopropanolamine and N,N-dibutylethanolamine.
9. The method according to claim 1 characterized in that the at least one glycolether comprises hexyldiglycol.
10. The method according to claim 1 characterized in that the at least one water-soluble amine comprises at least one amine having 7 to 12 carbon atoms.
11. The method according to claim 1 characterized in that the at least one amine comprises at least one amine having a conjugated acid with a pKa of at least 8.3.
12. The method according to claim 6 characterized in that the at least one tertiary amine has one to three hydroxyalkyl groups selected from the group consisting of 2-hydroxyethyl and 2-hydroxypropyl and zero to two alkyl groups, with the proviso that the sum of the hydroxyalkyl groups and the alkyl groups is three.
13. The method according to claim 7 characterized in that the at least one amine comprises at least one amine selected from the group consisting of N-methyldiisopropanolamine, triisopropanolamine and N,N-dibutylethanolamine.
14. The method according to claim 1 characterized in that the at least one glycoether comprises at least one glycoether having an alkyl group with 6 to 10 carbon atoms.
15. The method according to claim 1 characterized in that the solution does not comprise any amines having less than 7 carbon atoms.
Description
EXAMPLES
(1) Test 1: Quantitative 9 Drops Test on Wet Paint 5 Min. at RT:
(2) A waterborne paint layer with a thickness between 40 to 60 m was extended on a glass panel (200200 mm). The layer was then partially dried for 4 minutes at room temperature (RT) and placed at a slope of 45. At a rate of 1 drop per second and from a height of 12 cm, 9 drops of the purge cleaner solution to be tested were added onto the panel.
(3) After 5 minutes at room temperature, the width of the paint-free spot where the drops had hit the panel (open head), in cm was measured. The larger the width, the better the stripping effect, i.e. the cleaning efficiency, of the tested solution.
(4) Test 2: Spray on Wet Paint Test 10 Min. at RT:
(5) A waterborne paint layer with a thickness of approx. 60 m was extended on a glass panel (100200 mm). The layer was then partially dried for 4 minutes at room temperature and placed at a slope of 45. From 30 cm distance, 10 ml of the purge cleaner solution to be tested were sprayed on the panel.
(6) After 10 minutes at room temperature, the stripping effect, i.e. the cleaning efficiency, was evaluated according to the following categories: Bad (), regular (+), good (++) and very good (+++).
(7) Test 3: Quantitative N Drops Test on Dried Paint:
(8) A waterborne paint layer with a thickness between 40 to 60 m was extended on a glass panel (200200 mm). The layer was then dried for 24 h at room temperature and placed at a slope of 45. At a rate of 1 drop per second and from a height of 12 cm, drops of the purge cleaner solution to be tested were added onto the panel until the layer was opened, i.e. until there was a paint-free spot where the drops had hit the panel.
(9) The number of drops (n) added was determined. The lower the number, the better the stripping effect, i.e. the cleaning efficiency, of the tested solution.
(10) Purge Cleaner Solutions and Test Results:
(11) For every amine A, B and C (see below), a mixture of 95 wt.-% of hexyldiglycol and 5 wt.-% of amine was prepared.
(12) Amine A: Triethanolamine (6 carbon atoms) (comparative example)
(13) Amine B: N-methyldiisopropanolamine) (7 carbon atoms) (inventive example)
(14) Amine C: N,N-dibutylethanolamine (10 carbon atoms) (inventive example)
(15) The mixtures were diluted with deionized water to 2 wt.-%.
(16) The Quantitative 9 Drops Test was performed as described above (Test 1) on the wet paint Fller Red (Hemmelrath, Germany).
(17) The results are summarized in the following table wherein the cleaning efficiency was calculated compared to the one with triethanolamine (amine A) which was considered as reference.
(18) TABLE-US-00001 Amine Width of open head in cm Cleaning efficiency in % A 1.45 100 B 1.51 104 C 1.48 102
(19) The Spray Test was conducted as described above (Test 2) on the wet paint Fller Red (Hemmelrath, Germany) as well and showed the following results:
(20) TABLE-US-00002 Amine Cleaning efficiency A + B + to ++ C ++
(21) For amines A and B, the Quantitative N Drops Test was performed as described above (Test 3) on the dried paint Fller Red (Hemmelrath, Germany). The results are summarized in the following table. The cleaning efficiency was calculated compared to the one with triethanolamine (amine A) as a reference.
(22) TABLE-US-00003 Amine Number of drops (n) Cleaning efficiency in % A 20 100 B 9 222
(23) Surprisingly, all tests revealed an improved cleaning efficiency of the inventive purge cleaner solutions containing a water-soluble amine with at least 7 carbon atoms (amines B and C) compared to a purge cleaner solution which contains an amine having 6 carbon atoms (amine A).