IS 2932:2003
Wt’(1%1 ~11*
‘q-aw-?r, +-f%-m, W1-s8 : (*) Wlch‘i (Q) mwufkfafm (dh’mljp?)m) Indian Standard ENAMEL, SYNTHETIC, EXTERIOR : (a) UNDERCOATING (b) FINISHING — SPECIFICATION ( Third Revision)
ICS 87.040
(3 BIS 2003
BUREAU MANAK
December 2003
OF BHAVAN,
INDIAN
STANDARDS
9 BAHADUR SHAH NEW DEL1{I 110002
ZAFAR
MARG
Price Group 7
Paints, Varnishes
and Related Products Sectional Committee,
CHD 20
FOREWORD This Indian Standard (Third Revision) was adopted by the Bureau of Indian Standards, after the draft finalized by the Paints, Varnishes and Related Products Sectional Committee had been approved by the Chemical Division Council. Composition requirement has been simplified making it more performance oriented; requirement for freedom from unsaponifiable synthetic hydrocarbon resin has been deleted. Also, changes made in this standard through various amendments have been amalgamated in this revised version. Through Annex G, a testing programme
has been added in this revision, for the guidance of purchasers.
For satisfactory results, it is desirable that primer, undercoating same manufacturer. The composition
of the Committee
and the finishing enamel are obtained from the
responsible. for the preparation
of this standard is given in Annex H.
For the purpose of deciding whether a particular requirement of this standard is complied with, the final value, observed or calculated, expressing the result of a test or analysis, shall be rounded off in accordance with IS 2: 1960 ‘Rules for rounding off numerical values (revise~’. The number of significant places retained in the rounded off value should be the same as that of the specified value in this standard.
IS 2932:2003
Indian Standard ENAMEL, SYNTHETIC, EXTERIOR : (a) UNDERCOATING (b) FINISHING — SPECIFICATION (’Third Revision) 1 SCOPE
modifications in any form when tested in accordance with IS 101 (Part 9/See 2). In case of disputes, test to be carried out as prescribed in Annex B. It shall be of such a composition as to satisfy the requirements of this standard.
This standard prescribes requirements, methods of sampling and test for the material commercially known as enamel, synthetic, exterior: (a) undercoating (b) finishing, colour as required used in painting system for protection and decoration.
6.1.2 Total Non-volatile
2 REFERENCES
Content
The total non-volatile matter including pigments, extenders and vehicles, when tested as per IS 101 (Part 8/See 2) shall not deviate by more than+ 2 units by mass from the recorded data of ed sample. This applies to both undercoating and finishing enamels.
The standards listed in Annex A contain provisions which through reference in this text, constitute provisions of this standard. At the time of publication, the editions indicated were valid. All standards are subject to revision and parties to agreements based on this standard are encouraged to investigate the possibility of applying the most recent editions of the standards indicated in Annex A.
6.2 Condition
in Container
6.2.1 At Delivery
3 TERMINOLOGY
At the time of delivery the paint shall be in such a condition that manual stirring readily produces a uniform product.
3.1 For the purpose of this standard, the definitions given in IS 1303 and that given below shall apply. 3.1.1 ed Sample — Sample supplied in advance by a prospective supplier and ed by the testing agency, atler testing as per all requirements of this standard. A complete record of its performance shall be kept in respect of all tests.
During the 12 months storage period, the rating for degree of settling shall not drop to O, when tested as per IS 101 (Part 6/See 2).
4 CLASSES
6.3 Freedom
The material shall be supplied in brushing consistency but shall be suitable for application by brushing and air spraying thinning with petroleum hydrocarbon solvent to grade 145/205 low aromatic grade (see IS 1745) or suitable thinner as agreed to between the purchaser and the supplier.
The paint shall be free from coarse aggregates, suspended particles of gel and foreign matter, when tested as per IS 101 (Part l/See 2).
5 COLOUR
6.2.2 During Storage
from Coarse
Particles
6.4 Skin Formation The paint shaIl show no skin formation, examined visually at the time of delivery.
CATEGORIES
For the purpose of registration of the samples of the material, the colour categories given in Table 1 shall be employed.
when
6.5 Thinning Properties The paint shall be capable of being readily mixed with the petroleum hydrocarbon, solvent grade (see IS 1745) or with a suitable thinner as agreed to between the purchaser and the supplier, without showing any precipitation.
6 REQUIREMENTS 6.1 Composition 6.1.1 General
6.6 Application
The material shall be based on synthetic alkyd resin, free from natural rosin or its derivatives or its
Properties
The paint shall normally 1
be supplied
in a condition
IS 2932:2003 Table 1 Colour Categories and Wet Opacity Requirements (Clause 5) Colour Category No.
Colour Shade
ISC No. as per Is 5
Shade Recommneded for Registration of Samples
Wet Opacity Requirement, Min, m2/10 Iitre
(1)
(2)
(3)
(4)
(5)
1
White
—
White
130
2
Black
—
Black
260
3
Dark violet
796
Dark violet
4
i) ii)
Turquoise
iii)
Oriental
iv)
Light iral grey
697
v) vi)
Phirozi
176
Satin blue
177
i) ii)
Eau-de-nil
216
Opaline
275
iii)
Apple green
281
iv)
Bus green
299
i) ii)
Peacock blue
103
Azure blue
104
iii)
Traffic
169
5
6
7
Sky blue
13
1’4
Ii 16
17
green
blue
Oxford blue
105 106
French blue
12
I 74
Navy blue
Aircraft
II
102
i)
8
10
blue
blue
ii)
9
blue
Apple green
210
Traffic blue
200
Oxford blue
100
170
Aircratl
French blue
150
217
Sea green
170
Sage green
160
Traffic green or Grass green
I 50
Middle
220
i) ii)
Sage green
219
Light olive green
278
iii)
Aircraft
283
O
Grass green
218
ii)
Traffic
267
iii)
India green
iv)
Brilliant
i) ii)
Light brunswick Middle
iii)
Deep brunswick
blue
280
grey green
green
284
green
221 green
brunswick
green
green
225 226
iv)
I.incoln
green
276
Cypress green
277
Forest green
282
i) ii)
Olive green
220
Light bronze green
222
iii)
Middle
223
iv)
Deep bronze green
224
v) vi)
Steel furniture green
279
Scamic
294
vii)
Olive drab
298
bronze green
brunswick
227
v) vi)
Canary yellow
160
108
i) ii)
green
Turquoise blue
166
Sea green Verdigris
80
101
Olive green
220
309
Canary yellow
100
O ii)
Lemon
355
Golden yellow
100
Golden yellow
356
i)
Pale cream
352
ii)
Deep cream
353
iii)
L.igbt stone
361
iv)
Portland stone
364
v)
Vellum
365
Pale cream or
110
vi)
Light straw
384
deep cream
vii)
Light biscuit
385
IS 2932:2003 Table 1 (Corzchde~ (1)
(2) viii)
Champagne
386
ix)
Sunshine
387
x) xi)
Beige
388
Jasmine yellow
397
xii)
Light salmon pink
442
xiii)
Salmon pink
443
18
Primrose
19
Light buff
20
i) ii)
Deep buff
360
iii)
Middle
362
i) ii)
Dark stone
363
Light brown
410
iii)
Middle
brown
411
iv)
Golden brown
414
v) vi)
India brown
415
Leaf brown
489
i) ii)
Dark brown
412
Orange brown
439
iii)
Venetian
445
iv)
Red oxide
446
v) vi)
Deep Indian red
448
Light purple brown
449
vii)
Gulf red
473
viii)
Beech brown
490
i)
Nut brown
413
ii)
Chocolate
451
iii)
Service brown
449
21
22
23
24 25
Middle
buff
(5)
354
Primrose
100
358
Light buff
160
Deep bufY
200
Light brown
140
Gulf red
200
Net brown
220
359
stone
red
Terra cotta
444
i) ii)
Fire red
536
Signal red
537
iii)
Post oflice red
538
Post office red
iv)
Crimson
540
or signal red
v)
International
orange
Maroon
27
i) ii)
Traffic
Light orange
557
iii)
‘fraftic
570
iv)
Deep orange
541 yellow red
Maroon
130
Deep orange
120
India saffron
120
200
591
India saffron
29
i)
Silver grey
ii)
Quaker grey
629
iii)
French grcy
630
574 628
iv)
Light grey
63 [
v) vi)
Dark iral grey
632
Light grey or
Smoke grey
692
aircrafi grey
vii)
Aircraft
693
viii)
Dove grey
694
i) ii)
RAF blue grey
633
S Iate
634
iii)
Lead
iv)
Middle
v)
Dark blue grey
635 graphite
60
368
28
grey
Terra cotta
592
26
30
(4)
(3)
RAF blue grey
671 695
3
230
160
IS 2932:2003 suitable
for application
by brushing,
either
Annex E, shall not show signs of disintegration or change of colour to a rating not less than 8, taking the original coIour as 10. The loss of gloss shall not be more than 50 per cent of the original gloss.
as supplied
or when thinned with not more than 5 percent by volume of petroleum hydrocarbon solvent (see IS 1745) or with another suitable thinner as agreed to between the purchaser and the supplier. The paint may also be supplied in a condition suitable for spraying when thinned with not more than 20 percent by volume of the aforementioned thinner.
6.10 The material shall also requirements given in Table 2. 7 PACKING
6.7 Durability 6.7.1 ed
Sample
AND MARKING
7.2 Marking 7.2.1 Each following:
6.7.1.3 QUV apparatus may be used as an alternative when tested with an approved sample for a period of ~oo }1. that (Iw outdoor exposure test (see C-3) and the
be marked
with
a)
Name and type of the material;
b)
Indication of the source of manufacture;
c)
Volume of the material;
d)
Lot number or batch otherwise; and
e)
Month and year of manufacture.
number
in code
the
or
The container may also be marked with the Standard Mark.
6.7.2 %inp]e,fioin Bulk SUPPIY The characteristics of a film of the material prepared from a representative sample of the bulk supply as prescribed in C-2 tested in the accelerated weathering apparatus (see C-4) and examined every third day for a period of 21 days shall not deviate more than the limits specified in 6.7.2.1 and 6.7.2.2.
7.2.2.1 The use of the Standard Mark is governed by the provisions of Bureau ofIndian Standar& Act, 1986 and the Rules and Regulations made thereunder. The details of conditions under which the Iicence for the use of the Standard Mark may be granted to manufacturers or producers maybe obtained fi-om the Bureau of Indian Standards.
6.7.2. I Gloss (specular 60”) retention of bulk supply shall be within + 10 units of that of the recorded data of ed sample.
8 SAMPLING
6.7.2.2 The results of observation on characteristics of the colour, cracking, checking, spotting etc, of the bulk supply sample shall not be less than rating of 8 when evaluated as per C-3.2.
8.1 Preparation
of Test Samples
8.1.1 For Registration The sample shall be submitted in three different containers each containing not less than 500 ml of the material.
to Acid (for Finishing Only)
A film of the material, when tested as prescribed in Annex D, shall not show signs of disintegration or change of colour to a rating not less than 8, taking the original colour as 10. The loss of gloss shall not be more than 50 percent of the original gloss.
8.1.1.1 As testing to the requirements of this standard covers a period of more than 12 months, the supplier is advised to submit samples for registration sufficiently in advance within the period from October to December of the year, so that outdoor exposure test can be started during the period stipulated in C-3.1.
to Alkali (for Finishing Only) when tested as prescribed
shall
7.2.2 BIS Cert~jication Marking
accelerated weathering test (see C-4) are carried out in duplicate,
A film of the material,
container
7.2.1.1 The material when intended for defence purposes, shall be marked in accordance with IS 5661.
NOTE — As ~ prccaation against inadvertent accidents, it is
6.9 Resistance
the
Unless otherwise agreed to between the purchaser and the supplier, the enamel shall be packed in suitable metal containers (see IS 1407 and IS 2552).
6.7.1.2 A film of the sample for registration shall be prepared and tested in accelerated weathering apparatus using carbonlxenon arc, as prescribed under C-4. It shall be examined every third day for a period of 21 days and a complete record of its performance maintained.
6.8 Resistance
with
7.1 Packing
6.7.1.1 When prepared and tested as prescribed under C-3 up to a period of 12 months preferably at National Test House, Kolkata , a film prepared from the sample for registration of the material shall satisfy the requirements of the test.
rccommeodcd
comply
in 4
IS 2932:2003 Table 2 Requirements for Enamel, Synthetic, (a) Undercoating (b) Finishing
Exterior
(Clause 6.10)
S1
Methods of Test
Requirements —
Characteristics
No.
/
-
.
Undercoating
Finishing
Refto IS 101
(3)
(4)
(5)
Annex/Other Standard
(1) O
(2)
Smooth, uniform and suitable for brushing without
a) Consistency
(6)
Visual
—
(Part l/See 5)
—
(Part l/See 7)
—
appreciable drag on the brush b) Viscosity by ford cup
80-120 S
80-120 S
11.5
9.0
No. 4 at 27 + 2°C ii)
Mass, in lig/10 Iitres, Mirr
iii)
Drying time, h, Max a)
(Part 3/See 1)
2 8 24
Surface dry
b) Hard dry c) Tack free iv)
a) Finish
4 12 24 Smooth and glossy
(Part 3/See 4)
—
o to 20
Above 71
(Part 4/See 1)
—
Not more than 50
Not more than 15
(Part 3/See 5)
—
microns
microns (Part 4/See 2)
—
Smooth and matt to egg shell gloss
b) (dOSS 60° v) vi)
Fineness of grind
Approximate
Colour
with
match
[SC No.
385
or
match
to
the
an agreed colour
635 vii)
Close
specified 1S eolour or to
No such scratch as to show bare metal
Scratch hardness after 48 h air
Clause 3 of (Part 5/See 1)
drying (1 000 g) viii)
Flexibility
and adhesion
ix)
Flash point
x)
Composition: a)
No visible
damage or
No
visible
damage
or
detachment atler 48 h
detachment after 96 h of
of air drying
air drying
Not below 30”C
Not below 30°C
Volume solids percent, Min
b) Phthaliic anhydride
Clause 2 of (Part 5/See 2)
(Part l/See 6)
40
35
(Part 8/See 6)
20
20
.
— Clause 11 of
cootent of non-volatile
Is 354 (Part 2)
vehicle, percent by mass, Mirr xi)
Accelerated
storage stability
test,
—
Shall the test
Shall the test
Not less than one year
Not less than one year
from date of manufac-
from date of manufac-
turing
turing
Annex F
at 60”C, 96 h xii)
Keeping properties
8.1.2 Tender Sample
(Part 6/See 2)
requirements of this standard if the test results of the composite samples satisfy the requirements as prescribed in 6.
The supplies may dispense with sending a tender sample standard provided that he declares that the material, for which the tender is given, of the same quality as the sample previously ed in his name.
9 TEST METHODS
Representative samples of the materials shall be drawn and treated as prescribed in IS 101 (Part 1/See 1),
9.1 Test shall be conducted as prescribed in various parts of IS 101 and various Annexes to this standard. References to the relevant clauses of these standards are given in CO15 of Table 2, 6.1, 6.2 and 6.3.
8.2 Criteria
9.2 Quality of Reagents
8.1.3 Bulk Supply Sample
A lot shall
for Conformity be declared
as conforming
Unless
to the 5
specified
otherwise,
pure
chemicals
and
IS 2932:2003 test to be not inferior to the approved
distilled water (see 1S 1070) shall be employed in tests. NOTE
— ‘Pure chemicals’
shall mean chemicals that do not
10.2.2 Alternatively, the vendor may give following information and may declare compliance with ed sample:
contain impurities which affect the results of analysis.
9.3 Comparison with the performance of the ed sample shall be carried out on the basis of records maintained for the ed samples (see 6.7. 1). 9.4 For match against Indian Standard shall be used. 10 GENERAL
colours, IS 5
PROVISIONS
a)
Description
of paint,
b)
Vendor’s product reference,
c)
Lot identification,
d)
Quantity in lot, and
e)
Date of manufacture.
10.2.3 A certificate/declaration one lot.
10.1 supply Unless otherwise agreed by the purchaser, the paint supplied shall not differ significantly from the ed sample in either composition or performance. 10.2 Vendor’s
sample.
may relate to more than
10.3 Tests 10.3.1 The frequency and procedure to establish compliance of the paint material with this specification may vary depending on the agreement between the purchaser and the supplier.
Certificate
10.2.1 When required by the purchaser, the vendor shall certify that each batch of the paint supplied has been manufactured to the same formula as the ed sample and/or that it has been indicated by
10.3.2 The kind of testing programme Annex G, maybe taken for guidance, appropriate.
as indicated in where thought
ANNEX A
(Clause 2) LIST OF REFERRED Title
IS No.
Title
Colours for ready mixed paints and enamels ~ourth revision) Methods of sampling and test for paints, varnish and related products: Test on liquid paints (general and physical), Section 1 Sampling (third revision) Test on liquid paints (general and physical), Section 2 Preliminary examination and preparation of samples for testing (third revision) and Test on liquid paints (general
(Part 2/See 1): 1988
Test on liquid paints (chemical examination), Section 1 Water content (third revision) Tests on paint film formation, Section 1 Drying time (t~ird revision) Tests on paint film formation, Section 4 Finish (third revision) Tests on paint film formation, Section 5 Fineness of grind (third revision) Optical tests on paint films, Section 1 Opacity (third revision) Optical tests on paint films, Section 2 Colour (third revision) Optical tests on paint films, Section 3 Light fastness test (third revision) Optical tests on paint films, Section 4 Gloss (third revision) Mechanical tests on paint films, Section 1 Hardness tests (third revision)
IS No. 5:1994 101 (Part
l/See
1):
1986
(Part l/See 2): 1987
(Part l/See 3): 1986 (Part l/See 5): 1989 (Part l/See 6): 1987
INDIAN STANDARDS
physical),
Section
3 Preparation
s (third revision) Test on liquid paints physical),
Section
(third revision) Test on liquid physical),
(Part 3/See 4): 1987 (Part 3/See 5): 1987 (Part 4/See 1): 1988 (Part 4/See 2): 1989 (Part 4/See 3): 1988
of
(general
and
5 Consistency
paints
Section
(Part 3/See 1): 1986
(general 6
(third revision) (Part 1/See 7) : Test on liquid paints physical), Section 7 1987 litres (third revision)
Flash
(general Mass
and
(Part 4/See 4): 1988 (Part 5/See 1): 1988
point
and
per 10
6
IS 2932:2003 Title
(Part 5/See 2): 1988
Mechanical tests on paint films, Section2 Flexibility and adhesion (third revision) Durability tests on paint films, Section 1 Resistance to humidity under conditions of condensation (third revision) Durability tests on paint films, Section 2 Keeping properties (third revision) Durability tests on paint films Section 4 Degradation of coatings (pictorial aids for evaluation) Tests for pigments and other solids Section 2 Pigments and non-volatile matter (third revision) Tests for pigments and other solid Section 6 Volume solids Test for lacquers and varnish, Section 2 Rosin test Sulphuric acid (secorrd revision) Laundry soaps (third revision)
(Part 6/See 1): 1988
(Part 6/See 2): 1989 (Part
6/See
4)
1991
(Part
8/See
2):
1990
(Part 8/See 6): 1993 (Part 9/See 2) 1993 266:1993 285:1992
:
Title
IS No.
/S No
296:1986 354 (Part 2) : 1986
513:1994 1017:1983 1070:1992 1303:1983 1407:1980 1745:1978 2074:1992
2552:
989
5661:
970
Sodium carbonate, anhydrous (third revision) Methods of sampling and test for resins for paints : Part 2 Special test methods for alkyd resins (second revision) Cold-rolled low carbon steel sheets and strips ~ourth revision) Chamois leather (second revision) Reagent grade water (third revision) Glossary of relating to paints (second revision) Rpund paint tins (second revision) Petroleum hydrocarbon solvents (second revision) Ready mixed paint, air drying, red oxide-zinc chrome, priming (second revision) Steel drums (galvanized and ungalvanized) (third revision) Code of practice for packing and marking of packages of paints, enamels, varnishes and allied products
ANNEX B
(Clause 6.1.1) TEST METHOD
FOR TOTAL ROSIN ACIDS CONTENT
Libermann storch test for Halphen-Hicks test for detection of rosin also gives coloration with bleeding pigments (for example, Post Office Red) which may be confused with the presence of rosin. If the rosin content estimated by method described below is less than I percent, the paint sample should be considered free from rosin. The proposed method covers the determination of total rosin acids content of rosin esters, varnishes and alkyd resins, unmodified by such materials as maleic or fumaric acid or phenols. Total rosin acids determined include free rosin, esterified rosin and metallic salts of rosin. is primarily
dcsigrwd
containing 0.5 to 5 percent rosinon non-volatile
VEHICLES
with potassium hydroxide-ethylene glycol reagent and acidified with hydrochloric acid. Heat is applied to hydrolyze metallic driers. This is necessary when metallic rosinates are present.
B-O GENERAL
NOTE –- This method
OF COATING
B-O.1.2 The mixture described in B-O. L 1 is extracted with toluene. The rosin and fatty acids and unsaponifiables into the toluene layer. The aqueous layer will contain certain dibasic acids, polyhydric alcohol and other water-soluble products of saponification. B-O.I.3 The toluene is removed by evaporation, the residue weighed and the rosin acids are determined by a selective esterification and titration method.
for material basis.
B-1 APPARATUS
B-O.I Outline of the Method
B-1.1 Air condenser taper t.
B-O.1.1 The sample of separated vehicle is saponified 7
700 mm, with a 24/40 standard
1S 2932:2003 B-1.2 Burette — Automatic type having a capacity of 25 ml, for the standard potassium hydroxide solution, fitted with soda-lime trays to protect against absorption of atmospheric carbon dioxide.
according to details shown 12.7 mm asbestos tape. B-1.7 Pipette — Automatic,
Moisture
Funnels — Three of 1 litre capacity.
Collection
50-ml capacity.
B-2.1 Toluene B-2.2 Butyl Alcohol Sulphuric Acid Esterification Reagent — Add 500 ml of n-butyl alcohol, 500 ml of toluene and 3.3 ml (6 g) of sulphuric acid to a 2-litre round bottom flask with ground t, connect to a moisture trap and condenser and reflux on a hot plate
B-1.5 Steam Bath — Located in a fume hood for evaporation of volatile solvents. B-1.6
Trap — Constructed
E2!-.l *
70*3
1. Wrap with
B-2 REAGENTS
B-1.3 Erlenmeyer Flasks — 250 and 500 ml capacity with 24/40 ground ts. B-1.4 Separating
in Fig.
O/l) 22 APPROX
I 24 /40 GROUND
All dimensions
in millimetres,
FIG. 1 MOISTURECOLLECTIONTRAP 8
IS 2932:2003 inert gas to volume of approximately 20 ml. Add 5 ml of anhydrous ethyl alcohol and evaporate to dryness, to remove any water present by azeotropic distillation.
for 30 min to distil out the water and to form butylsulphuric acid. Cool and store in a glass stoppered bottle. B-2.3 Ethyl Alcohol B-2.4 Hydrochloric
B-3.5 Cool and weigh to the nearest 0.001 g. To avoid oxidation, do not try in an oven, also the retention of a small amount of toluene does not affect the final calculation.
Acid — Concentrated (sp gr 1. 19).
B-2.5 Potassium Hydroxide — Ethylene Glycol Solution (132 g/1)—Dissolve 132 g of potassium hydroxide pellets in 1 Iitre of ethylene glycol in a 2-litre Erlenmeyer flask. Insert a thermometer and boil to eliminate water until the temperature of the liquid reaches 190 to 195°C. Cool and store in a rubber stoppered bottle.
B-3.6 Using an automatic pipette, accurately measure 50 ml of the esterification reagent into the flask. Connect the flask to the moisture collections trays and condenser. Place on a hot plate to boiling and reflux for 20 min. At the end of heating period, allow the flask to cool somewhat, then remove and cool to room temperature.
B-2.6 Potassium Hydroxide, Alcoholic Standard Solution (13.3 g/1) — Dissolve 13.3 g of potassium hydroxide pellets in 1 Iitre of alcohol. Standardize against potassium acid phthallate primary standard. B-2.7 Sulphuric
B-3.7 Add 10 drops of thymol blue indicator solution and titrate with the alcoholic potassium hydroxide solution to a blue end-point.
Acid — Concentrated
a blank solution,
titration on 50 ml of the after refluxing in the same
B-2.8 Thymol Blue Indicator Solution (10 g/1) — Mix 1 g of thymol blue indicator with 100 ml of ethyl alcohol.
B-3.8 Make esterification manner.
B-3 PROCEDURE
B-4 CALCULATION
B-3.1 Transfer to a 500 ml Erlenmeyer flask an amount of sample, weighed to the nearest 0.001 g, containing approximately 10 + 1 g of non-volatile material. Add 150 ml of the potassium hydroxide ethylene glycol solution and swirl to disperse the sample. Add a boiling stone, attach a condenser and reflux on a hot plate for 2 h.
B-4.1 In order to apply properly the esterification correction factors to the isolated rosin acids- fatty acids mixture, it is necessary first to calculate the percent of rosin acids in the dried toluene extract, and then to correct this value to the on-volatile sample basis. Rosin acids in dried toluene extract, y = [(A – B) N x 30.24 x 1.018] & 0.3 percent by mass
B-3.2 After refluxing, remove the flask from the hot plate and cool to room temperature under tap water. Add 100 ml of water and while cooling under tap water, add 40 ml of the hydrochloric acid. Place on the hot plate again, reflux for 5 min and cool under tap water.
where
B-3.3 Transfer the sample quantitatively to a 1 Iitre separating funnel with the aid of a total of 150 ml of water, followed by two 25 ml rinse with toluene. Shake, allow the layers to separate, and draw off the lower aqueous layers into a second 1 Iitre separating funnel. Extract with a third 50-ml portion of toluene. Draw off and discard the water layer. Combine the benzene extracts, and wash with three 50 ml portions of water. Measure the pH of the third water wash. If it is less than 3.8, repeat with a fourth water wash. Discard the wash waters.
A=
alcoholic potassium hydroxide solution required for titration of the sample, in m 1;
B=
alcoholic potassium hydroxide solution required for titration of blank, in ml;
N=
normality of potassium hydroxide solution used;
s.
= molecular mass of abietic acid multiplied by 100 and divided by 1 000;
1.018
determined factor to = experimentally correct for slight esterification of resin acid; and
0.3
B-3.4 Transfer the washed toluene extract to a weighed (to the nearest 0.001 g) 250-ml Erlenmey6r flask, with the aid of 25 ml of toluene. Evaporate the toluene on the steam bath, preferably with the aid of a gentle stream of
mass of dried toluene extract, in g;
30.24
determined factor = experimentally correct for unesterified fatty acids.
Rosin acids in alkyd vehicle, non-volatile
9
basis, percent = (S x Y)/(W x ~
to
IS 2932:2003 where
expressed as a decimal; and Y
S
= mass ofdried
W
= mass of original alkyd vehicle taken for analysis, ing;
T
=
non-volatile
toluene extract, ing;
content
of the
= percent extract.
of resin acids in dried toh.rene
NOTE— [f it is desired to express the total rosin acids as commercial rosin, use 35.00 instead of30.24 as the factor in the calculation.
vehicle,
ANNEX C (Clauses 6.7.1 .1,6.7.1.2,6.7.2.2 TEST METHOD
FOR DURABILITY
C-O GENERAL
a)
Apply one coat of ready mixed paint red oxide-zinc chrome primer (conforming to IS 2074) by brushing afler a coat of undercoat;
b)
Rub down lightly with waterproof emery paper No. 280/320, wipe off the surface using a piece of clean and dry soft cloth and then apply the brushing one coat of the under coating enamel conforming to this standard and allow to air-dry for 24 h;
c)
Rub down, wet, with waterproof emery paper No. 280/320, wipe off the surface using a piece of clean and dry soft cloth and then apply the brushing one coat of the finishing enamel conforming to this standard and allow to air-dry for 24 h; and
d)
Rub down, wet, with waterproof emery paper No. 320, wipe off water and, when the surface is dry, apply by brushing a second coat of the finishing enamel and allow to air dry for 7 days before subjecting to exposure test.
C-O.1 Outline of the Method The durability of the material is determined by ascertaining actual behaviour of suitably prepared test s in normal outdoor exposure test for a specified period and evaluating the results of the exposure by a suitable method of rating for various characteristics of the film of the material. Apart from this, the material is also evaluated by an accelerated weathering test wherein a prepared is subjected to controlled exposure to heat, light and water in the artificial weathering apparatus. C-1 TEST S C-1. 1 The shall be mild steel plate, 1.25 mm thick and free from surface defects (see IS 5 13). s for the outdoor exposure test shall be 300 mm x 300 mm in size and for the accelerated weathering test 150 tmm x 75 mm. The s shall be cleaned as prescribed in IS 10i (Part l/See 3) and the back and edges of the s shall be protected with two coats of a suitable paint. C-2 PREPARATION
and 8.1.1.1)
NOTE —The primer, undercoatandthe finishing enamelsshalt be from the samesource.
OF TEST S
C-3 NORMAL
OUTDOOR
EXPOSURE
TEST
C-3.O Subject the samples for registration and the tender samples, if supplied, to normal outdoor exposure test in the manner described under C-3.1.
C-2. 1 In the painting procedure outlined under C-2.2, the air drying of the films shall be done at room temperature and at a relative humidity of not more than 70 percent.
C-3.1 Expose in the open the test s, prepared in the manner prescribed under C-1 and C-2 in duplicate at an angle of 45° facing South. Commence the exposure not earlier than the third week of January and not later than the first week of April.
C-2.2 The surface of the test s to be exposed shall be prepared as follows, taking care that total dry film thickness of the complete system shall be between 75 and !00 microns:
10
1S 2932:2003 Numerical Value 2tol o
C-3.1.1 Examine the condition of the exposed films at monthly intervals for the first quarter and thereafter quarterly for the rest of the period for the following characteristics:
Type of Colour Change
Rating
Very bad colour change L — Loss of colour Complete colour change
a)
Colour;
b)
Checking,
cracking and flaking;
C-3.2.3 Freedom from Checking
c)
Chalking;
and
d)
Spotting.
Freedom from checking shall be rated as 10 for no checking and Ofor most severe and complete checking. Intermediate ratings of 8, 6, 4 and 2 shall be done by matching with standard photographs.
C-3. 1.2 For the above examinations, wash the right hand half of the surface of the two test s by pouring water and then wiping with a soft cloth or chamois leather (see IS 1017). Adequate time for cooling of the s to room temperature shall be allowed prior to washing examine the same half of the test s at each examination. As an aid in the examination, a magnifying glass may be used, but the evaluation shall be based on an assessment with the unaided eye. At the end of the stipulated period for durability test, examine the two halves of the test s. The sample shall be considered satisfactory if the material surface underneath as wel I as condition of the film in both the halves, the one washed periodically as well as the one washed only for the final examination is satisfactory by the method of evaluation described in C-3.2. Stray film failure, due to extraneous causes other than climate, shall be ignored. C-3.2 Evaluation and Characteristics of Test
Rating
of
C-3.2.4 Freedom from Cracking Freedom from cracking shall be rated as 10 for no cracking and O for most severe and complete cracking. Intermediate ratings of 8, 6,4 and 2 shall be done by matching with standard photographs. C-3.2.5 Freedom from Flaking Freedom from flaking shall berated as 10 for no flaking and O for most severe and complete flaking. Intermediate ratings of 8, 6,4 and 2 shall be done by matching with standard photographs. C-3.2.6 Freedom from Chalking Freedom from chalking shall be rated as 10 for no chalking and O for most severe and complete chalking. Intermediate ratings of 8, 6,4 and 2 shall be done by matching with standard photographs. C-3.2.7 Freedom from Spotting
Film
Freedom from spotting shall be rated as follows: Numerica[ Value 10
C-3.2.1 The test s before and after the specified periods of exposure tests shall be assessed for the various film characteristics as prescribed in C-3.2.2 to C-3.2.8.
9
C-3.2.2 Colour The colour of the test shall be compared against the stipulated shade as given in 1S 5. The initial rating for a good colour match shall be 10. The colour retention on exposure shall be expressed and recorded as the abbreviation of the type of colour change followed by the numerical rating as given below: Rating Numericat Value 10 Good match 9 Satisfactory 8 to 7 Slight colour change 6 to 5 Definite colour change 4 to 3 Bad colour change
No spotting Satisfactory
8-7
Slight spotting
6-5
Definite spotting
4-3
Bad spotting
2-1
Very bad spotting
o
Complete
C-3.2.8 Freedom from Blistering
spotting
and Corrosion
Freedom from blistering shall be rated as 10 for no blistering and O for complete failure in respect of blistering. Intermediate ratings for blister density F, M, MD and D ( few medium, medium-dense and dense) and blister sizes 8,6,4 and 2 shall be done by matching with standard photographs.
Type of Colour Change D— F— B— R—
Rating
Darkening Fading Blueing Reddening
C-3.3 Evaluation
of Exposed Films
C-3.3.1 The requirements of this test shall be taken to have been satisfied if performance in respect of the characteristics as noted in C-3.2 is within the limits specified below:
Y — Yellowing
11
IS 2932:2003
sl No. i)
Characteristic
Exposure
Colour
Requirement
After 3 months
The film shall have a minimum rating of 7 (except for colour categories No. 12, 13, 14, 16, 22, 26 and 27 where the minimum rating shall be 4)
After 6 months
The film shall have a minimum rating of 5 (except for colour categories No. 12, 13, 14, 16,22,26 and 27 where the minimum rating shall be 3)
After 12 months
The film shall have a minimum rating of 4 (except for colour categories No. 12, 13, 14, 16,22,26 and 27 where the minimum rating shall be 2)
Freedom from checking
After 12 months
Minimum rating of 6
iii)
Freedom from cracking
After 12 months
Minimum rating of 8
iv)
Freedom
After 12 months
Minimum rating of 9
ii)
from flaking
v)
Freedom from chalking
After 12 months
Minimum rating of 6
vi)
Freedom from spotting
After 12 months
Minimum rating of 5
C-3.3.2 Freedom from Blisters and Corrosion
used if mutually agreed upon between the purchaser and the supplier. The temperature of water for specimen spray shall be 16 * 5°C. The term cycle is the set of exposure conditions (light, light plus water spray, dark periods) that are repeated.
The film shall remain generally free from blisters and the metal underneath shall show no signs of corrosion on exposure for 12 months. A few isolated blisters without any signs of corrosion underneath as well as one or two localized corrosion andlor rust spots shall not constitute a cause of failure. C-3.4 Protection
C-4.2.3 The exposed film shall be evaluated for gloss and various film properties as prescribed under C-3.2.
Against Corrosion
C-4.2.4 The requirement of this test on a sample from bulk supply shall be taken to have been satisfied if the gloss retention shall be minimum 40 percent of the original and the performance in respect of the other film characteristics is generally similar to that obtained with the ed sample.
After exposure of the film is discontinued, examine for corrosion of the metal surface of the underneath by removing film at 5 different places, one in the centre and one each at 4 different places near the 4 corners about 50 mm away from the edges. The paint film shall be removed by solvent type paint remover. When the film is softened by the paint remover it shall be removed by gently rubbing with cotton swab or waste jute taking care to remove adhering film of primer and/or undercoating. After removal of the film, the exposed metal shall be covered by thick mineral oil or petroleum jelly. Localized corrosion andlor one or two rust spots shall not constitute a cause of failure. To satisfy the requirements of this standard, the metal surface shall be otherwise free from corrosion. C-4 ACCELERATED
WEATHERING
Table 3 Test Cycles Commonly Used for Carbon-Arc Exposure Testing of Paints (Cfause C-4.2.2) Cycle Description
(1) 102 min light
Black Temp, “C
Typical [Jses
(2)
(3)
63 + 2.5 General coatings
18 min light and water spray 18 h using; 102 min light
TEST
General coatings 63*2.5
18 min light and water spray
C-4.1 Accelerated
Weathering
Apparatus
6 h at 95 + 4 percent
An artificial weathering apparatus of the xenonlcarbon arc type for uniform and controlled exposure to the effects of heat, light and water.
75*3
relative humidity with no spray 48 min light
63 + 2,5 Original equipment
12 min light and water spray
C-4.2 Procedure
4 h light
C-4.2. 1 The for this test shall be prepared as described under C-2.2. Samples for registration shall be tested in duplicate in a suitable accelerated weathering apparatus (see C-4.1 ) and samples drawn from the bulk supply shall be tested in a similar manner.
Manufactured
Exterior pigmented
63+ 2.5
Exterior wood stains
4 h water spray 12 h light
coating
63+ 2.5
Paints and clears
12 h water spray 8 h light 10 h light and water spray
C-4.2.2 Commonly used cycles and test conditions are given in Table 3. However, any other cycle may be
6 h water spray
12
63 * 2.5 Marine enamels
IS 2932:2003
ANNEX D
(Clause 6.8) TEST FOR RESISTANCE
D-O GENERAL
TO ACID
with the mass in kg/1 O litres of the material. Protect the edges of the by applying a coat of wax. Allow the to air-dry in a horizontal position for 48 h under specified laboratory drying conditions [see IS 101 (Part 1/See 3)]. Immerse the in a 2 percent (m/v) solution of concentrated sulphuric acid (relative density 1.84) (see IS 266) for 24 h at room temperature. Remove the s, wash in running fresh water and allow to dry for 1 h.
D-O.I Outline of the Method A test coated with the enamel, after specified drying period, is immersed in a definite concentration of sulphuric acid for 24 h after which it is washed, dried and compared in performance with a paneI prepared with the ed sample data. D-1 PROCEDURE
D-1.2 The tested portion shall not show signs of disintegration. The colour shall not vary more than slightly from that of untested portion of the test .
D-1. 1 Apply a coat of the finishing enamel, as specified in2.2of1S 101 (Part 6/See l) ona 150mm x 100mm clean glass to give a dry film mass commensurate
ANNEX E
(Clause 6.9) TEST FOR RESISTANCE
TO ALKALI
of 27 * 2“C. Remove, wash in running water, dry for an hour and examine the film and then subject it to test as prescribed under E-1.2.
E-O GENERAL E-O.1 Outline of the Method The tilm of the material is tested with a solution of laundry soap followed by a solution of sodium carbonate, washed dried and compared in performance with a prepared with the ed sample.
E-1.2 Immerse the in a 2 percent (m/v) solution of sodium carbonate of analytical reagent grade (see 1S 296) for half an hour at a temperature of 27 * 2°C. Remove the , wash in running water, dry for an hour and examine the film.
E-1 PROCEDURE
E-1.3 The tested portion shall not show signs of disintegration. The colour shall not vary more than slightly from that of the untested portion of the test .
E-1.1 Immerse a prepared as prescribed in D-1.1 in a 1 percent (m/v) solution of laundry soap (see Type 1 of IS 285) for half an hour at temperature
13
IS 2932:2003
ANNEX F [Table 2, S1No. (xi)] ACCELERATED
STORAGE
F-1 PROCEDURE F-1.1 Store the paint sample in a closed container and keep at 600C for 96 h.
STABILITY
TEST
original value and there shall be no evidence of seeding. The paint shall meet the drying requirements and produce a film free from streaking, mottling and seeding. Further, for finishing paint, change in gioss value shall not be more than 5 units fi-om that of original value.
500-ml
F-1.2 After the test, paint shall not gel, liver, curdle or increase in viscosity by more than 20 percent of the
ANNEX G
(Clause 10.3.2) TESTING PROGRAMME G-1 When a purchaser orders for supply of paint (conforming to this standard) in lots to be delivered, over a period of time, it is assumed that not all of the tests specified shall be carried out on samples representing of each lot or consignment. The extent and frequency of the tests may vary depending on many factors and on choice of purchaser. The following programme of tests is, however, maybe useful for the guidance of purchasers, particularly in relation to vendor’s certification. It may also provide a usefuI tool to establish a testing programme when an inspecting agency acting on behalf of a purchaser, is required to examine lots of products for compliance to this standard. C-1.1 Programme
f)
Drying time,
g)
Colour,
h)
G1OSS,
j)
Finish, and
k)
Viscosity.
G-1.2 Programme
2
Following tests to be made on first lot and subsequently as and when agreed upon: a)
Flexibility and adhesion,
b)
Scratch resistance,
c)
Acid resistance and alkali resistance.
G-1.3 Programme
1
and
3
Following tests to be made on first lot alone:
Following tests to be made on first lot and on every subsequent lot:
Durability, Keeping qualities,
a)
Non-volatile
b)
Mass per 10 Iitre,
c)
Volume solids percent,
Condition
d)
Phthallic anhydride content of non-volatile vehicle, percent by mass, and
e)
Flash point.
c)
content,
a) b)
in container,
d)
Fineness of grind,
e)
Thinning properties,
14
IS 2932:2003
ANNEX H (F’orewwd) COMMITTEE
COMPOS1TION
Paints, Varnishes and Related Products Sectional Committee, Representative
Organization (14, Orion,
In personal capacity
CHD 20
Oorner Park, Bhulabhai
Desai Road,
SHN RAW ~ARPHAnA
(s)
(Chairman)
,Mumhai 400026) Addisons Paint & Chemicals Asian Paints (India)
SHRI R. SRtNIVASAN
Ltd, Chennai
SHRI A. B. MENON
Ltd, Mumbai
DR B. P. MALJK (Alternate) Bajaj Auto Limited,
REPfti3E~A~
Pune
Bcrger Paints India Ltd, Howrah
SHRI K. NIRMALKUMAR
Bharat Heavy Electrical
SHRI M, SOMU
SHRIN. K. RAY (Alternate)
Central Building
Ltd, Tiruchirapalli
DR L. K. AGARWAL
Research Institute, Roorkec
DR K. K. ASTHANA(Alternate) Central Poblic Works Department, Colour-Chem
Limited,
REPRESEFWATIW
New Delhi
SHRI R. R. VAIDYA
Thane
Consumer Unity & ‘rurst Society (CUTS),
Jaipur
Strru SANOEEPSINGH
Continental
Coatings Pvt Ltd, Chennai
SHRI M. B. SATVANARAYANA
Directorate
Gcnmal
REPRESENTAITVE
of Supplies & Disposals, New Delhi
Export Inspection
Council
Goodlass Nerolac
Paints Ltd, Mumbai
Hindustan Shipyard
REPRESENTATIVE
of India, Ncw Delhi
SHRI S. V, PORWAL SHRI P. V. RAMANAMURTHY
Ltd, Visakhapatmrm
SHRI A. P. CH. N. PRASAD(Alternate) ICI (India)
ltd.
REPRESENTATIVE
Kolkata
[ndian Institute ot’ Chem Technology, Indian Paints Association,
DR K. V. S. N. RAIU
Hyderabad
DR M, B. GUHA
Kolkata
SHRI V. M. NATU (Ahernate) Indian Petrochemicals
Indian Small Scale Paint Association, Jensen & Nicholson Maruti
REPRESEmATIVE
Corp Ltd, Vadodra
(India)
REPRESENTATIVE
Mumbai
Ltd, Gorifa,
24 Pargtmas (N), West Bengal
SHRIT. K. BANERJEE
Lldyog Ltd, Gurgaon
Ministry
REPRE.5E~A~E
of Defence (DGQA),
SHRI M. S. SULTANtA
Kanpur
SHRI L. S. MISHRA(A/[ernate) Ministry
of Environment
Ministry
of Industry,
Mumbai
Paints Limited,
REPREsE~Amw
& Forest, New Delhi
SHFOP. K. JAIN
New Delhi
SHIUN. C. TIWAtU (Ahernate) REPmsE~,4~
Mumbai
National
Organic Chemical
National
Test House (ER),
Industries Ltd, Mumbai
DR B. V. BAPAT DR B. B. PAL
Kolkata
DR SUNtLKUMARSAHA (Ahernafe) Ollice
of the DevIopment
office
of the Scientific
Commissioner (SS1), New Delhi
Adviser
to Chief Naval
Oil and Natural Gas Corporation Oil ‘Technologists Association
StatY, New Delhi
Ltd, New Delhi
of India, Kanpur
SHSOY. S. BHATNAGAR SHRI A. K. JAIN (Alternate) SHRI R, K. SEHGAL REPRESENTATIVE REPRESENTAWE
(Corrfinued on page 16)
IS 2932:2003 (Continued jrom page
15) Representative(s)
Organization Punjab Paint Colour
and Varnish
Works,
Research Designs & Standards Organization, Resins & Plastics Limited,
REPREsE14TATlvE
Lucknow
SHRI M. C. CHOKSI
Mumbai
Shriram institute forlndustrial Sudarshan Chemicals
SHRI G. N. TIWARI
Kanpur
Research, Delhi Ssuu SUDHIRH. HARSULE
hrdustries Ltd, Pune
Smu MAHESHD. METTELLDO(Alternate) Tata Engineering
& Locomotive
The Indian Turpentine Travancore
Titanium
REPRESE~A~
Co Ltd, Jamshedpur
SHRI R. C. BASSI
& Rosin Co Ltd, Bariely
SHRI V. S. BASHIR
Products Ltd, Triruvananthapuram
DR K. GOPINATHAN NAIR (Ahernate) U. K. Paints industries, BIS Directorate
SHRI V. K. NAYYAR
New Delhi
SHRI S. K. CHAUDHORI,Director&
General
Head (CHD)
[Representing Director General (Ex-off7cio)]
Member Secretary SHRIN. K. BANSAL t Director (CHD),
16
BIS
Bureau of Indian Standards institution established under the Bureau 131S is a statutory harmonious development of the activities of standardization, and attending to connected matters in the country.
of Zndian Standards Act, 1986 to promote marking and quality certification of goods
Copyright Bl S has the copyright of all its publications. No part of these publications may be reproduced in any form without the prior permission in writing of BIS. This does not preclude the free use, in the course of implementing the standard, of necessary details, such as symbols and sizes, type or grade designations. Enquiries relating to copyright be addressed to the Director (Publications), BIS. Review of’ Indidn Standards Amendments are issued to standards as the need arises on the basis periodically; a standard along with amendments is reaffirmed when needed: if the review indicates that changes are needed, it is taken should ascertain that they are in possession of the latest amendments ‘BIS Catalogue’ and ‘Standards: Monthly Additions’. This Inciian Standard has been developed
from Doc : No. CHD 20 (946).
Amendments Amend No.
of comments. Standards are also reviewed such review indicates that no changes are up for revision. s of Indian Standards or edition by referring to the latest issue of
Issued Since Publication Date of Issue
Text Affected
BUREAU OF INDIAN STANDARDS Headquarters
:
Manak Bhavan, 9 Bahadur Shah Zafar Marg, New DeIhi 110002 Telephones :23230131,23233375,2323 9402 Regional Offices :
Telegrams : Manaksanstha (Common to all offices) Telephone
Central
: Manak Bhavan, 9 Bahadur Shah Zafar Marg NEW DELHI 110002
Eastern
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