Zinc-Rich Priming Paint (Organic Media) : Specification For
Zinc-Rich Priming Paint (Organic Media) : Specification For
Zinc-Rich Priming Paint (Organic Media) : Specification For
BRITISH STANDARD |
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Specification for |
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Zinc-rich priming paint |
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(organic media) |
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ICS 87.040 |
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NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAW
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BS 4652 : 1995 Issue 2, July 1998
The following body was also represented in the drafting of the standard, through a
subcommittee:
BSI 1998
Amendments issued since publication
First published July 1971
Second edition April 1995 Amd. No. Date Text affected
Contents
Page
Committees responsible Inside front cover
Foreword ii
Specification
1 Scope 1
2 Normative references 1
3 Sampling 1
4 Containers and labelling 1
5 Requirements for the components of the paint 1
6 Composition 1
7 Performance requirements of the paint after mixing 1
Annexes
A (normative) Determination of metallic zinc content 3
B (normative) Preparation of test panels 4
C (normative) Resistance to continuous salt spray 5
D (informative) Advice on handling and use of paint 5
Table
B.1 Blast-cleaned steel with shot abrasives and grit abrasives 4
List of references Inside back cover
i
BS 4652 : 1995 Issue 2, July 1998
Foreword
This British Standard has been prepared under the direction of the Materials and
Chemicals Sector Board. It supersedes BS 4652 : 1971, which is withdrawn.
The first edition of BS 4652, and later published amendments, specified three types of
zinc dust-containing coatings intended for use as anticorrosive primers for the
protection of abrasive blast-cleaned steel surfaces.
Experience in the use of these materials, improvements in the preparation of steel
surfaces, and formulation developments of zinc dust-based primers, have indicated that
simplification of the existing standard can be made by a reduction in the number of
types specified.
The method for determination of metallic zinc content (see annex A) is based upon a
method used by Harcros Chemicals.
| A British Standard does not purport to include all the necessary provisions of a
| contract. Users of British Standards are responsible for their correct application.
Compliance with a British Standard does not of itself confer immunity
from legal obligations.
ii BSI 1998
BS 4652 : 1995
Specification
1) Marking BS 4652 on or in relation to a product represents a manufacturer's declaration of conformity, i.e. a claim by or on
behalf of the manufacturer that the product meets the requirements of the standard. The accuracy of the claim is solely the
claimant's responsibility. Such a declaration is not to be confused with third party certification of conformity, which may also be
desirable.
1
BS 4652 : 1995
2
BS 4652 : 1995
Annexes
A.2.2 Methyl ethyl ketone. A.4.1 Carry out the determination in duplicate.
A.2.3 Acetone. A.4.2 Take a test portion of (1.2 ± 0.1) g of the mixed
paint. Place in a weighed centrifuge tube, M1 (A.3.1).
A.2.4 Iron/copper reagent. Dissolve (100 ± 5) g Immediately weigh the tube and the test portion to the
copper (II) sulfate heptahydrate in 1 l of water (A.2.1). nearest 1 mg, M2.
Add 1250 ml 60 % (m/m) iron (III) sulfate solution and
dilute to 2.5 l. A.4.3 Add about 20 ml of a suitable solvent and stir
thoroughly with a glass rod. Withdraw the rod from the
A.2.5 Potassium dichromate 0.05 M. In an agate tube, washing the rod with a small quantity of the
mortar, powder about 30 g potassium dichromate solvent, and centrifuge the tube until there is a clear
(analytical grade reagent). Place in a clean glass supernatant liquor. Decant and discard the supernatant
evaporating basin and heat in an oven at liquor from the tube.
(105 ± 2) 8C for 2 h. Allow to cool in a desiccator.
Weigh out accurately 29.4 g of the dried salt, to the A.4.4 Add further solvent to the tube and mix as
nearest 0.1 mg, dissolve in water and make up to 2 l in described in A.4.3, taking care to disperse completely
a volumetric flask. Shake well. the solid matter. Repeat the centrifuging and
decantation of the liquor.
The reactor for this reagent:
With the addition of methyl ethyl ketone (A.2.2),
mass taken repeat the centrifuging and decantation for a third
is called the dichromate factor.
29.4190 time. Finally add the acetone (A.2.3) in place of the
Record the factor. initial solvent and mix as described in A.4.3.
Centrifuge and decant the liquor as before.
A.2.6 Sulfuric/phosphoric reagent. Carefully add
250 ml concentrated sulfuric acid (r = 1.18 g/cm3) to 1 l A.4.5 After ensuring that excess acetone has
of water, cool and add 500 ml orthophosphoric acid evaporated, place the centrifuge tube in the oven
(r = 1.65 g/cm3). Dilute to 2.5 l. (A.3.4) maintained at (105 ± 2) 8C. After 24 h transfer
the tube to a desiccator and allow to cool to ambient
A.2.7 Indicator solution. Dissolve 0.2 g sodium temperature. Weight the tube and contents to the
diphenylamine sulfonate in water and dilute to 100 ml. nearest 1 mg, M3.
A.2.8 Ammonium hydrogen carbonate. A.4.6 Measure 50 ml of the iron/copper reagent
A.3 Apparatus (A.2.4) into a 500 ml flask. Add approximately 12 g (a
heaped teaspoon) of ammonium hydrogen carbonate
A.3.1 Centrifuge tubes, 50 ml, of inert material. (A.2.8). Wash down any reagent adhering to the side
A.3.2 Laboratory centrifuge, capable of imparting a of the flask with water.
relative centrifugal acceleration of about 100 km⋅s22. Using a precision balance (A.3.10) weigh accurately
(0.4 ± 0.05) g of dried pigment into a suitable weighing
A.3.3 Mortar and pestle, agate.
boat. Record the weight, M0, to four decimal places.
A.3.4 Air-ventilated oven, capable of being Drop the weighing boat carefully into the flask (A.3.7)
maintained at (105 ± 2) 8C. (taking care to avoid touching the neck of the flask).
Stopper and shake vigorously for about 1 min ensuring
that the stopper is firmly positioned at all times.
BSI 1998 3
BS 4652 : 1995 Issue 2, July 1998
Three-quarters fill the lip of the flask with water. With Annex B (normative)
care, gently release the stopper. Wash down the flask
and stopper with water. Preparation of test panels
Drop a magnetic stirrer bar (A.3.12) into the flask and B.1 General
stir for a minimum of 15 min. Except where otherwise stated, the test panels shall be
Add 50 ml of sulfuric/phosphoric reagent (A.2.6). hot-rolled mild steel having the dimensions of
Wash down the flask and stopper with deionized water. 100 mm 3 150 mm 3 5 mm, free from distortion and
Add approximately 1 ml of indicator solution (A.2.7) abrasive blast-cleaned on the test surface to grade
and titrate with the potassium dichromate (A.2.5) Sa 2¯ of BS 7079 : Part A1.
using the burette (A.3.9) to a permanent purple end Profile assessments of the blast-cleaned steel shall be
point. carried out using a visual comparator in accordance
A.4.7 Perform a blank determination, i.e. repeat the with BS 7079 : Part C1 and BS 7079 : Part C2 and the
procedure in A.4.6 without the pigment sample. profile shall be as given in table B.1.
A.4.8 Determine the content of the non-volatile
Table B.1 Blast-cleaned steel with shot
matter of the paint in accordance with BS 3900 :
abrasives and grit abrasives
Part B18.
Shot abrasives Grit abrasives
A.5 Calculation
Grade coarse (S) Grade medium (G)
The percentage of metallic zinc in the dry film shall be
calculated as follows. Profiles equal to Profiles equal to
segment 3 and up to but segment 2 and up to but
Dichromate factor (A 2 B) (M3 2 M1)
| M0 (M2 2 M1) NV
3 excluding segment 4 excluding segment 3
60 mm to 80 mm 50 mm to 70 mm
3 100 3 0.9806
where B.2 Paint application and dry film thickness
The paint shall be applied in accordance with the
M0 is the mass (in g) of the test portion of the manufacturer's instructions to give the following dry
dried pigment (A.4.6); film thicknesses:
M1 is the mass (in g) of the centrifuge tube Weldable primer: up to 15 mm;
(A.4.2);
Prefabrication primer: (25 ± 5) mm;
M2 is the mass (in g) of the centrifuge tube
Post fabrication/build-up primer: up to 75 mm.
together with the paint sample (A.4.2);
The paint shall be allowed to dry for 7 days at a
M3 is the mass (in g) of the centrifuge tube temperature of (23 ± 2) 8C and a relative humidity of
together with the extracted dried pigment (50 ± 5) % out of direct sunlight and with protection
(A.4.5); from dust. Because it is impracticable to measure the
A is the volume (in ml) of 0.05 M potassium thicknesses of thin films on blast-cleaned surfaces, film
dichromate solution required for the sample thickness measurements shall be made on smooth
(A.4.6); cold-rolled steel panels (or coupons) of minimum
B is the volume (in ml) of 0.05 M potassium thickness 2 mm, placed either side and in the same
dichromate solution required for the blank plane and painted at the same time as the test panels.
(A.4.7); The dry film thicknesses shall be measured by use of
an electronic dry film thickness (DFT) gauge zeroed
NV is the content of non-volatile matter (in %) of and calibrated on the same smooth uncoated panels.
the paint (A.4.8).
B.3 Test conditions
0.9806 is the factor to obtain free zinc content.
Tests shall be carried out at a temperature of
(23 ± 2) 8C and relative humidity of (50 ± 5) % except
Calculate the mean of the two determinations and
where otherwise specified.
report the result to one decimal place. If the two
determinations differ by more than 1 % from the mean,
repeat the procedure (A.4) and disregard the original
results.
4 BSI 1998
BS 4652 : 1995
BSI 1998 5
6 blank
BS 4652 : 1995
Normative references
BSI publications
BRITISH STANDARDS INSTITUTION, London