IEC 60811-601:2012
(Main)Electric and optical fibre cables - Test methods for non-metallic materials - Part 601: Physical tests - Measurement of the drop point of filling compounds
Electric and optical fibre cables - Test methods for non-metallic materials - Part 601: Physical tests - Measurement of the drop point of filling compounds
IEC 60811-601:2012 specifies the test procedure for measuring the drop point of filling compounds. IEC 60811-601:2012 cancels and replaces Clause 4 of IEC 60811-5-1:1990, which is withdrawn. Full details of the replacements are shown in Annex A of IEC 60811-100:2012. There are no specific technical changes with respect to the previous edition, but see the foreword to IEC 60811-100:2012.
This publication is to be read in conjunction with IEC 60811-100:2012.
Câbles électriques et à fibres optiques - Méthodes d'essai pour les matériaux non-métalliques - Partie 601: Essais physiques - Mesure du point de goutte des matières de remplissage
La CEI 60811-601:2012 précise les méthodes d'essai à employer pour mesurer le point de goutte des matières de remplissage. La CEI 60811-601:2012 annule et remplace l'Article 4 de la CEI 60811-5-1:1990, qui est supprimée. L'ensemble des informations relatives aux remplacements figure dans l'Annexe A de la CEI 60811-100:2012. Aucune modification technique n'a été effectuée par rapport à l'édition précédente; voir cependant l'avant-propos de la CEI 60811-100:2012.
Cette publication doit être lue conjointement avec la CEI 60811-100:2012.
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Standards Content (Sample)
IEC 60811-601 ®
Edition 1.0 2012-03
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
Electric and optical fibre cables – Test methods for non-metallic materials –
Part 601: Physical tests – Measurement of the drop point of filling compounds
Câbles électriques et à fibres optiques – Méthodes d’essai pour les matériaux
non-métalliques –
Partie 601: Essais physiques – Mesure du point de goutte des matières de
remplissage
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IEC 60811-601 ®
Edition 1.0 2012-03
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
Electric and optical fibre cables – Test methods for non-metallic materials –
Part 601: Physical tests – Measurement of the drop point of filling compounds
Câbles électriques et à fibres optiques – Méthodes d’essai pour les matériaux
non-métalliques –
Partie 601: Essais physiques – Mesure du point de goutte des matières de
remplissage
INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
PRICE CODE
INTERNATIONALE
CODE PRIX M
ICS 29.035.01; 29.060.20 ISBN 978-2-88912-994-2
– 2 – 60811-601 IEC:2012
CONTENTS
FOREWORD . 3
INTRODUCTION . 5
1 Scope . 6
2 Normative references . 6
3 Terms and definitions . 6
4 Test method . 6
4.1 General . 6
4.2 Method A (reference method) . 6
4.2.1 Apparatus . 6
4.2.2 Test procedure . 7
4.2.3 Expression of results . 7
4.3 Method B . 7
4.3.1 Apparatus . 7
4.3.2 Test procedure . 8
4.3.3 Expression of results . 8
5 Test report. 8
Bibliography . 13
Figure 1 – Cup (Method A) . 9
Figure 2 – Assembled apparatus (Method A) . 10
Figure 3 – Cup (Method B) . 11
Figure 4 – Thermometer and sleeve . 11
Figure 5 – Case . 11
Figure 6 – Assembled apparatus (Method B) . 12
60811-601 IEC:2012 – 3 –
INTERNATIONAL ELECTROTECHNICAL COMMISSION
____________
ELECTRIC AND OPTICAL FIBRE CABLES –
TEST METHODS FOR NON-METALLIC MATERIALS –
Part 601: Physical tests –
Measurement of the drop point of filling compounds
FOREWORD
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all national electrotechnical committees (IEC National Committees). The object of IEC is to promote
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8) Attention is drawn to the Normative references cited in this publication. Use of the referenced publications is
indispensable for the correct application of this publication.
9) Attention is drawn to the possibility that some of the elements of this IEC Publication may be the subject of
patent rights. IEC shall not be held responsible for identifying any or all such patent rights.
International Standard IEC 60811-601 has been prepared by IEC technical committee 20:
Electric cables.
This Part 601 of IEC 60811 cancels and replaces Clause 4 of IEC 60811-5-1:1990, which is
withdrawn. Full details of the replacements are shown in Annex A of IEC 60811-100:2012.
There are no specific technical changes with respect to the previous edition, but see the
foreword to IEC 60811-100:2012.
– 4 – 60811-601 IEC:2012
The text of this standard is based on the following documents:
FDIS Report on voting
20/1310/FDIS 20/1359/RVD
Full information on the voting for the approval of this standard can be found in the report on
voting indicated in the above table.
This publication has been drafted in accordance with the ISO/IEC Directives, Part 2.
This part of IEC 60811 shall be used in conjunction with IEC 60811-100.
A list of all the parts in the IEC 60811 series, published under the general title Electric and
optical fibre cables – Test methods for non-metallic materials, can be found on the IEC
website.
The committee has decided that the contents of this publication will remain unchanged until
the stability date indicated on the IEC web site under "http://webstore.iec.ch" in the data
related to the specific publication. At this date, the publication will be
• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
60811-601 IEC:2012 – 5 –
INTRODUCTION
The IEC 60811 series specifies the test methods to be used for testing non-metallic materials
of all types of cables. These test methods are intended to be referenced in standards for
cable construction and for cable materials.
NOTE 1 Non-metallic materials are typically used for insulating, sheathing, bedding, filling or taping within cables.
NOTE 2 These test methods are accepted as basic and fundamental and have been developed and used over
many years principally for the materials in all energy cables. They have also been widely accepted and used for
other cables, in particular optical fibre cables, communication and control cables and cables for ships and offshore
applications.
– 6 – 60811-601 IEC:2012
ELECTRIC AND OPTICAL FIBRE CABLES –
TEST METHODS FOR NON-METALLIC MATERIALS –
Part 601: Physical tests –
Measurement of the drop point of filling compounds
1 Scope
This Part 601 of IEC 60811 specifies the test procedure for measuring the drop point of filling
compounds.
2 Normative references
The following documents, in whole or in part, are normatively referenced in this document and
are indispensable for its application. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any
amendments) applies.
IEC 60811-100:2012, Electric and optical fibre cables – Test methods for non-metallic
materials – Part 100: General
3 Terms and definitions
For the purposes of this document, the terms and definitions given in IEC 60811-100 apply.
4 Test method
4.1 General
This part of IEC 60811 shall be used in conjunction with IEC 60811-100.
Unless otherwise specified, tests shall be carried out at room temperature.
The drop point test may be used as an indication of the maximum temperature to which a
filling compound can be exposed without complete liquefaction or excessive oil separation.
In case of dispute, method A shall be used as reference method.
4.2 Method A (reference method)
4.2.1 Apparatus
The apparatus consists of the following parts:
a) A chromium plated brass cup conforming to the dimensions shown in Figure 1.
b) A heat-resistant glass test tube conforming to the dimensions shown in Figure 2 with three
indentations to support the cup.
c) Thermometers with a range – 5 °C to 300 °C (76 mm immersion) marked in degrees
Celsius with a scale accuracy of 1 °C. The bulb lengths shall be 10 mm to 15 mm, and the
bulb diameters shall be 5 mm to 6 mm.
60811-601 IEC:2012 – 7 –
d) An oil bath consisting of a 400 ml beaker and suitable oil, a ring stand and ring for the
support of the oil bath, clamps for the thermometers, two corks as shown in Figure 2, a
polished metal rod 1,2 mm to 1,6 mm in diameter and 150 mm in length, and a suitable
means for heating and stirring the oil bath.
4.2.2 Test procedure
Place the corks on one of the thermometers as shown in Figure 2 and adjust the position of
the upper cork so that the tip of the thermometer bulb is about 3 mm above the bottom of the
cup when the apparatus is assembled for test. Suspend a second thermometer in the oil bath
so that its bulb is at approximately the same level as the bulb of the thermometer in the test
tube.
Fill the cup by presenting its larger opening into the filling compound until the cup is filled,
taking care to avoid working the filling compound as far as possible. Cut away any excess
compound. The cup shall be held in a vertical position with its smaller opening at the bottom
while it is gently pressed down over the metal rod until the rod protrudes about 25 mm above
the larger opening. Press the rod against the cup in such a manner that the rod makes
contact with both the upper and lower peripheries of the cup. Maintain this contact while
rotating the cup around its axis and simultaneously moving the cup down the rod until the cup
passes over the lower end of the rod. This spiral-like motion will cause the compound to
adhere along the rod leaving a conical void of compound in the cup and a compound coating
having reproducible geometry on the inside of the cup.
Place the cup and the thermometer in the test tube and suspend the test tube in the oil bath
with the oil level within 6 mm of the rim. If the cork holding the thermometer in the test tube
has been properly chosen, the 76 mm immersion mark on the thermometer will coincide with
the lower edge of the cork. The assembly should be immersed to this point.
Stir the oil bath and heat at a rate of 4 K/min to 7 K/min until the bath reaches a temperature
approximately 17 °C below the expected drop point of the compound. Then reduce the rate of
heating so that the temperature in the test tube will be within 2 °C or less of the temperature
in the oil bath before the oil bath temperature increases an additional 2,5 K.
Continue heating at a rate such that the difference between the temperature in the test tube
and in the oil bath is maintained between 1 °C and 2 °C. This condition is established when
the oil bath is heated at a rate of about 1 K/min to 1,5 K/min. As the temperature increases,
material will gradually protrude through the orifice of the cup. When the first drop of material
falls, note the temperature on the two thermometers.
4.2.3 Expression of results
Record the average of the two thermometers as the drop point of the filling compound.
4.3 Method B
4.3.1 Apparatus
The apparatus consists of the following parts:
a) A chromium plated brass cup conforming to the dimensions shown in Figure 3. The cup
may be made from another suitable metal which is not affected by the compound being
tested. The top of the cup and the bottom of the tube forming the orifice are smooth,
parallel to each other, and at right angles to the axis of the cup. The wide part of the cup
has an approximately hemispherical lower portion and an internal depth such that when a
steel ball 7,0 mm in diameter is placed in the cup, the top of the ball is (12,2 ± 0,15) mm
above the bottom of the tube forming the orifice. The bottom edge of the orifice should
have neither chamfer nor radius.
b) A cylindrical metal sleeve, attached to the thermometer, and a metal case which screws to
the sleeve, conforming to the dimensions shown in Figures 4 and 5. The metal sleeve is
– 8 – 60811-601 IEC:2012
fixed to the thermometer so that, when the metal case is screwed on to the sleeve, the
bottom of the thermometer bulb is (8,0 ± 0,1) mm below the rim stop and the thermometer
stem is coaxial with the sleeve and case. The thermometer is fixed to the sleeve with
cement that is suitable for the temperature range of the thermometer.
c) Thermometers with a range of 20 °C to 120 °C (100 mm immersion) marked in degrees
Celsius with a scale accuracy of 1 °C. The bulb length shall be 6 mm maximum with bulb
diameter between 3,35 mm and 3,65 mm.
d) A heat-resistant, glass test tube (110 ± 2) mm long and with a (25 ± 1) mm internal
diameter.
e) A beaker large enough to allow the test tube to be immersed vertically to two-thirds of its
length in the liquid heating medium and with the bottom of the tube being about 25 mm
above the bottom of the beaker.
f) A stirrer to ensure uniformity of temperature throughout the bath.
g) A stand to hold the test tube and the bath thermometer and to support the beaker above
the heat source.
h) A gas burner capable of heating the liquid bath at the specified rate.
NOTE Water is recommended as the heating medium for drop points below 80 °C, and glycerol or white oil for
higher drop point materials.
4.3.2 Test procedure
By means of a spatula, fill the cup with the compound and cut away any excess material.
Take precautions to exclude air bubbles, but do not melt the compound.
Push the cup, without lateral movement, into the metal case as far as the stop and cut away
any excess material squeezed out of the bottom. Take care that the orifices in the side of the
metal case are not blocked. Fit the thermometer, with the cup attached, centrally in the test
tube, through a bored cork having a side notch, so that the bottom of the cup is (25 ± 1,0) mm
above the bottom of the test tube. Then, fix the test tube vertically in the beaker containing
the liquid heating medium, so that two-thirds of its length are immersed and the bottom is
about 25 mm above the bottom of the beaker, as shown in Figure 6.
Heat the liquid bath, keeping it stirred at such a rate that the drop point thermometer shows a
rise in temperature of 1 K/min for 20 °C below the drop point of the sample. Record the
temperature at which the first drop, whatever its composition, falls from the cup or at which
the continuous stream of material, if formed, reaches the bottom of the test tube.
4.3.3 Expression of results
Record the temperature of the drop point thermometer to the nearest 1,0 °C as the drop point
of the filling compound.
5 Test report
The test repo
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