ISO 12742:2007
(Main)Copper, lead, and zinc sulfide concentrates — Determination of transportable moisture limits — Flow-table method
Copper, lead, and zinc sulfide concentrates — Determination of transportable moisture limits — Flow-table method
ISO 12742:2007 specifies a flow-table method for the determination of the transportable moisture limit (TML) of copper, lead and zinc sulfide concentrates, which may liquefy during transport. ISO 12742:2007 is applicable to the determination of the TML of concentrates containing 10 % to 80 % (mass fraction) of lead, or 10 % to 65 % (mass fraction) of zinc, or 10 % to 55 % (mass fraction) of copper. It is applicable to TMLs in the range 3 % to 28 % (mass fraction).
Concentrés sulfurés de cuivre, de plomb et de zinc — Détermination des limites d'humidité transportable — Méthode de la table d'écoulement
General Information
Relations
Standards Content (Sample)
INTERNATIONAL ISO
STANDARD 12742
Second edition
2007-07-01
Copper, lead, and zinc sulfide
concentrates — Determination of
transportable moisture limits —
Flow-table method
Concentrés sulfurés de cuivre, de plomb et de zinc — Détermination
des limites d'humidité transportable — Méthode de la table
d'écoulement
Reference number
ISO 12742:2007(E)
©
ISO 2007
---------------------- Page: 1 ----------------------
ISO 12742:2007(E)
PDF disclaimer
This PDF file may contain embedded typefaces. In accordance with Adobe's licensing policy, this file may be printed or viewed but
shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In
downloading this file, parties accept therein the responsibility of not infringing Adobe's licensing policy. The ISO Central Secretariat
accepts no liability in this area.
Adobe is a trademark of Adobe Systems Incorporated.
Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-creation
parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies. In
the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below.
COPYRIGHT PROTECTED DOCUMENT
© ISO 2007
All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any form or by any means,
electronic or mechanical, including photocopying and microfilm, without permission in writing from either ISO at the address below or
ISO's member body in the country of the requester.
ISO copyright office
Case postale 56 • CH-1211 Geneva 20
Tel. + 41 22 749 01 11
Fax + 41 22 749 09 47
E-mail copyright@iso.org
Web www.iso.org
Published in Switzerland
ii © ISO 2007 – All rights reserved
---------------------- Page: 2 ----------------------
ISO 12742:2007(E)
Contents Page
Foreword. iv
Introduction . v
1 Scope .1
2 Normative references .1
3 Principle.1
4 Apparatus .1
5 Sampling and sample preparation.2
5.1 General.2
5.2 Laboratory sample.3
5.3 Sample preparation .3
6 Procedure .3
6.1 General.3
6.2 Preparation of test portions.4
6.2.1 General.4
6.2.2 Filling the mould .4
6.2.3 Tamping pressure.4
6.2.4 Tamping procedure .5
6.2.5 Removal of the mould .5
6.2.6 Dropping the flow table.5
6.3 Identification of the flow state.5
6.4 Preliminary flow moisture point.7
6.4.1 Preparation of test portion.7
6.4.2 Determination of preliminary flow moisture point .7
6.4.3 Addition of water for preliminary flow moisture point test .8
6.5 Main flow moisture point determination .8
6.5.1 Preparation of test portions.8
6.5.2 Determination of main flow moisture point .8
6.5.3 Addition of water for main flow moisture point determination.8
6.6 Graphical method .8
6.6.1 Preparation of test portions.8
6.6.2 Determination of flow moisture point.9
6.7 Moisture determination .9
7 Expression of results .9
7.1 Main flow moisture point .9
7.2 Flow moisture point determined by the graphical method .9
8 Validation of main flow moisture point .10
9 Test report .10
Annex A (normative) Description of equipment used to determine TML.11
Bibliography .18
© ISO 2007 – All rights reserved iii
---------------------- Page: 3 ----------------------
ISO 12742:2007(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies
(ISO member bodies). The work of preparing International Standards is normally carried out through ISO
technical committees. Each member body interested in a subject for which a technical committee has been
established has the right to be represented on that committee. International organizations, governmental and
non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the
International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
The main task of technical committees is to prepare International Standards. Draft International Standards
adopted by the technical committees are circulated to the member bodies for voting. Publication as an
International Standard requires approval by at least 75 % of the member bodies casting a vote.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. ISO shall not be held responsible for identifying any or all such patent rights.
ISO 12742 was prepared by Technical Committee ISO/TC 183, Copper, lead, zinc and nickel ores and
concentrates.
This second edition cancels and replaces the first edition (ISO 12742:2000), which has been technically
revised.
iv © ISO 2007 – All rights reserved
---------------------- Page: 4 ----------------------
ISO 12742:2007(E)
Introduction
ISO 12742:2000 was published as a guidance document because there had been insufficient test programme
participants to allow precision data to be derived. However, it had been agreed that ISO/TC 183/WG 11 be
kept in existence, as there was likelihood that a precision test programme could be held at a later time.
Revision of ISO 12742 was commenced in 2005, on the basis that changes to the procedure were necessary,
and there were then sufficient participants to allow a test programme to be conducted.
In the final analysis, insufficient participants were identified. However, the International Standard has been
revised for a further edition as a guidance document.
© ISO 2007 – All rights reserved v
---------------------- Page: 5 ----------------------
INTERNATIONAL STANDARD ISO 12742:2007(E)
Copper, lead, and zinc sulfide concentrates — Determination of
transportable moisture limits — Flow-table method
WARNING — This International Standard may involve hazardous materials, operations and equipment.
It is the responsibility of the user of this International Standard to establish appropriate health and
safety practices and determine the applicability of regulatory limitations prior to use.
1 Scope
This International Standard specifies a flow-table method for the determination of the transportable moisture
limit (TML) of copper, lead and zinc sulfide concentrates, which may liquefy during transport.
This International Standard is applicable to the determination of the TML of concentrates containing 10 % to
80 % (mass fraction) of lead, or 10 % to 65 % (mass fraction) of zinc, or 10 % to 55 % (mass fraction) of
copper. It is applicable to TMLs in the range 3 % to 28 % (mass fraction).
2 Normative references
The following referenced documents are indispensable for the application of this document. For dated
references, only the edition cited applies. For undated references, the latest edition of the referenced
document (including any amendments) applies.
ISO 10251, Copper, lead, zinc and nickel concentrates — Determination of mass loss of bulk material on
drying
ISO 12743, Copper, lead, zinc and nickel concentrates — Sampling procedures for determination of metal and
moisture content
3 Principle
The moisture content of the sample is adjusted by mixing with water. The mixture is converted to a conical
shape using a mould and tamper. The sample is placed on the flow table and the mould is removed. The flow
characteristics are determined by repeated dropping of the flow table, while observing the behaviour of the
sample. When sufficient water has been added to the sample so that plastic deformation occurs during the
dropping of the flow table, the sample is considered to be at its flow moisture point.
The TML is calculated as 90 % of the flow moisture point.
4 Apparatus
Copper, lead and zinc concentrates may gain or lose moisture rapidly when exposed to air. The laboratory
should be designed so that excessive temperatures, direct sunlight, air currents and humidity variations are
avoided.
4.1 Flow table and frame, as specified in Annex A.
The flow-table mounting shall be as specified in Figure A.1.
© ISO 2007 – All rights reserved 1
---------------------- Page: 6 ----------------------
ISO 12742:2007(E)
4.2 Mould, as specified in Figure A.1.
4.3 Tamper.
The required tamping pressure may be achieved by using calibrated, spring-loaded tampers or some other
suitable design of tamper that allows a controlled pressure to be applied via a 30 mm diameter tamper head
as specified in Figure A.2.
4.4 Calliper ruler.
4.5 Balance, top loading, having the sensitivity specified in Table 1.
Table 1 — Sensitivity of balance and precision of weighing
Mass of sample plus tray Precision of balance
and weighing
g g
100 0,01
200 0,02
300 0,03
400 0,04
500 0,05
4.6 Measuring cylinder, of capacity 50 ml to 200 ml.
4.7 Burette, of capacity 10 ml.
4.8 Mixing bowl, hemispherical, of diameter approximately 30 cm.
NOTE It is advisable to use an automatic mechanical mixer having a mixing bowl as described, as this leads to
improved precision.
4.9 Rubber gloves.
4.10 Drying trays or pans, having dimensions that permit the sample to be spread to a thickness of less
than 30 mm.
The trays shall be made of corrosion-resistant and heat-resistant material, such as stainless steel, glass or
enamel plate.
4.11 Drying oven, ventilated, with forced circulation of air or inert gas, regulated at a temperature of
105 °C ± 5 °C.
4.12 Airtight containers.
5 Sampling and sample preparation
5.1 General
TML figures are required to be updated on a periodic basis, usually six monthly, or when there is a known
change to the process used to produce the material. The reported figure should be the mean of samples taken
during the period.
2 © ISO 2007 – All rights reserved
---------------------- Page: 7 ----------------------
ISO 12742:2007(E)
To ensure that the TML result is representative, increments of the material shall be taken either
a) while a stockpile is being built up or broken down, or
b) while loading or discharging a vessel.
These increments are combined to form the sample used to determine TML.
The sample used to determine TML should not be used to determine moisture.
Stationary sampling of stockpiles should never be used for the determination of TML. This method of sampling
can only be used to provide an indicative moisture value for use during the planning of shipping schedules.
5.2 Laboratory sample
Samples for the determination of TML shall be taken in accordance with ISO 12743. The laboratory sample
shall not weigh less than 12 kg. To minimize changes to the flow characteristics of the sample, it shall not be
oven dried or ground during its preparation.
5.3 Sample preparation
Homogenize the laboratory sample as quickly as possible to prevent losses. Take nine test samples as
follows:
a) Sample 1
Take not less than 1 kg, which is to be used for determining the moisture content of the sample “as
received”, from the laboratory sample and place on a drying tray or pan.
b) Sample 2
Take approximately 1,2 kg from the laboratory sample. This sample is to be used for the preliminary TML
test. Store this sample in an appropriately labelled airtight container.
c) Samples 3 to 6
Take four samples of approximately 1,2 kg from the laboratory sample. These samples are to be used for
the main TML test. Store these samples in appropriately labelled airtight containers.
d) Samples 7 to 9
Take three samples of approximately 1,2 kg from the laboratory sample. These samples are to be used
for confirmation of TML by the graphical method. Store these samples in appropriately labelled airtight
containers.
6 Procedure
6.1 General
Copper, lead and zinc concentrates may undergo rapid changes in moisture when exposed to air, so all
stages of the test should be accomplished in the shortest time period and shall definitely be completed within
the day of commencement. Where possible, sample containers should be covered with plastic film or any
other suitable airtight cover.
The moisture result from Sample 1 provides information about how far the material under test is from the flow
moisture point.
© ISO 2007 – All rights reserved 3
---------------------- Page: 8 ----------------------
ISO 12742:2007(E)
As more accurate results are obtained when the moisture of the test portion is close to the flow moisture point,
a preliminary test is carried out (Sample 2). The result of this test is used to adjust the moisture of the final test
portion to 1 % to 2 % below (Samples 3 and 4) and above (Samples 5 and 6) the flow moisture point.
To check the main flow moisture point graphically, three more samples (Samples 7 to 9), having moisture
values higher than the flow moisture point, are tested. The flow moisture point is the extrapolation to zero of
the linear adjustment of the seven test portions. The value obtained this way will be used to validate the main
flow moisture point.
6.2 Preparation of test portions
6.2.1 General
Sample 1 is prepared in accordance with ISO 10251. Proceed to 6.7.
Samples 2 to 9 are prepared in accordance with 6.2.2 to 6.2.6.
6.2.2 Filling the mould
Place the mould on the centre of the flow table and fill it in three stages with the test portion as follows:
a) the first charge, after tamping, shall aim to fill the mould to approximately one-third of its depth;
b) the second charge, after tamping, shall fill the mould to about two-thirds of its depth;
c) the third and final charge, after tamping, shall reach to just below the top of the mould (see Figure 1).
The quantity of test portion required to achieve each of these stages will vary from one material to another, but
is readily established after experience has been gained on the packing characteristics of the material being
tested.
6.2.3 Tamping pressure
The aim of tamping is to simulate the amount of compaction prevailing at the bottom of a shipboard cargo for
the material being tested. The correct pressure to be applied via the tamper is calculated as follows:
p=×ρdg× (1)
TD max
where
p is the tamping pressure, in pascals;
T
ρ is the bulk density, in kilograms per cubic metre;
D
d is the maximum depth of the cargo, in metres;
max
2
g is the acceleration due to gravity (= 9,81 m/s ).
If, when calculating the tamping pressure, there is no information available concerning the cargo depth, use
the maximum likely depth.
Alternatively, the pressure may be estimated from Table 2.
4 © ISO 2007 – All rights reserved
---------------------- Page: 9 ----------------------
ISO 12742:2007(E)
a
Table 2 — Tamping pressures (kPa) for selected concentrates
Typical Bulk density
concentrate Maximum cargo depth
3
type
kg/m
2 m 5 m 10 m 20 m
Copper 2 000 39 [2,8] 98 [6,9] 196 [13,9] 392 [27,7]
Lead 2 100 41 [2,9] 103 [7,3] 206 [14,6] 412 [29,1]
Zinc 1 950 38 [2,7] 96 [6,8] 192 [13,5] 384 [27,1]
a
Values in square brackets are equivalent kilogram-force (kgf) when applied via a 30 mm diameter tamper head.
6.2.4 Tamping procedure
The number of tamping actions (applying the correct, steady pressure each time) should be about 35 for the
bottom layer, 25 for the middle layer and 20 for the top layer. Tamping shall be performed successively over
the complete a
...
Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.