SIST EN ISO 6144:2006
(Main)Gas analysis - Preparation of calibration gas mixtures - Static volumetric method (ISO 6144:2003)
Gas analysis - Preparation of calibration gas mixtures - Static volumetric method (ISO 6144:2003)
This International Standard specifies a method for the preparation of calibration gas mixtures by a static volumetric method and provides a procedure for calculating the volumetric composition of the mixture. It can be used either with binary gas mixtures (containing one calibration component in a complementary gas, which is usually nitrogen or air [1, 2] ) or with mixtures containing more than one component in the complementary g as. This International Standard also specifies how the expanded uncertainty in the volume fraction of each calibration component in the mixture is determined by a rigorous evaluation of all the measurement uncertainties involved, including those associated with the apparatus used for the preparation of the gas mixture and those associated with the experimental procedure itself.
Gasanalyse - Herstellung von Prüfgasen - Volumetrisch - statisches Verfahren (ISO 6144:2003)
Die vorliegende Internationale Norm legt ein Verfahren zur Herstellung von Prüfgasen mittels eines volumetrisch statischen Verfahrens fest und stellt ein Verfahren zur Berechnung der volumetrischen Zusammensetzung des entsprechenden Gasgemisches vor. Es kann entweder mit Binärgasgemischen verwendet werden (die eine Beimengung in einem Grundgas enthalten, üblicherweise Stickstoff oder Luft[1, 2]) oder mit Gemischen, die mehr als eine Beimengung im Grundgas enthalten. Diese Internationale Norm legt außerdem fest, wie die erweiterte Unsicherheit im Volumenanteil einer jeden Beimengung im Gemisch durch ausführliche Bewertung sämtlicher Messunsicherheiten bestimmt wird, einschließlich der Unsicherheiten der für die Herstellung des Gasgemisches verwendeten Apparatur und der Unsicherheiten der Versuchsdurchführung selbst.
ANMERKUNG 1 Diese Internationale Norm gilt im Allgemeinen für die Herstellung von Prüfgasen, die Beimengungen mit Volumenkonzentrationen zwischen 10 ´ 10-9 (10 ppb parts per billion) bis 50 ´ 10-6 (50 ppm parts per million) enthalten. Die Gasgemische können jedoch mit größeren oder kleineren Volumenanteilen hergestellt werden, sofern die bei der statischen Verdünnung verwendeten Komponenten entsprechend gewählt werden.
ANMERKUNG 2 Eine relative erweiterte Unsicherheit von nicht mehr als ± 1 % bei einem Vertauensniveau von 95 % ist bei diesen Konzentrationen unter folgenden Voraussetzungen erreichbar:
- die Reinheit der Ausgangsgase wurde durch Analyse bestimmt, und signifikante Verunreinigungen sowie die Unsicherheiten bei der Konzentrationsmessung dieser Verunreinigungen wurden berücksichtigt;
- zwischen den gasförmigen Bestandteilen und den Innenflächen der Apparatur treten keine signifikanten Adsorptionswirkungen oder chemischen Reaktionen auf, und zwischen den gasförmigen Komponenten, d. h. zwischen den Beimengungen und dem Grundgas oder zwischen den Beimengungen selbst, kommt es zu keinerlei Reaktionen;
Analyse des gaz - Préparation des mélanges de gaz pour étalonnage - Méthode volumétrique statique (ISO 6144:2003)
Analiza plinov – Priprava kalibrirnih plinskih zmesi – Statična volumetrijska metoda (ISO 6144:2003)
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 6144:2006
01-november-2006
$QDOL]DSOLQRY±3ULSUDYDNDOLEULUQLKSOLQVNLK]PHVL±6WDWLþQDYROXPHWULMVND
PHWRGD ,62
Gas analysis - Preparation of calibration gas mixtures - Static volumetric method (ISO
6144:2003)
Gasanalyse - Herstellung von Prüfgasen - Volumetrisch - statisches Verfahren (ISO
6144:2003)
Analyse des gaz - Préparation des mélanges de gaz pour étalonnage - Méthode
volumétrique statique (ISO 6144:2003)
Ta slovenski standard je istoveten z: EN ISO 6144:2006
ICS:
71.040.40 Kemijska analiza Chemical analysis
SIST EN ISO 6144:2006 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 6144:2006
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SIST EN ISO 6144:2006
EUROPEAN STANDARD
EN ISO 6144
NORME EUROPÉENNE
EUROPÄISCHE NORM
August 2006
ICS 71.040.40
English Version
Gas analysis - Preparation of calibration gas mixtures - Static
volumetric method (ISO 6144:2003)
Analyse des gaz - Préparation des mélanges de gaz pour Gasanalyse - Herstellung von Prüfgasen - Volumetrisch -
étalonnage - Méthode volumétrique statique (ISO statisches Verfahren (ISO 6144:2003)
6144:2003)
This European Standard was approved by CEN on 21 July 2006.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the Central Secretariat or to any CEN member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the Central Secretariat has the same status as the official
versions.
CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania,
Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36 B-1050 Brussels
© 2006 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 6144:2006: E
worldwide for CEN national Members.
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SIST EN ISO 6144:2006
EN ISO 6144:2006 (E)
Foreword
The text of ISO 6144:2003 has been prepared by Technical Committee ISO/TC 158 "Analysis
of gases” of the International Organization for Standardization (ISO) and has been taken over
as EN ISO 6144:2006 by Technical Committee CEN/SS N21 "Gaseous fuels and combustible
gas", the secretariat of which is held by CMC.
This European Standard shall be given the status of a national standard, either by publication
of an identical text or by endorsement, at the latest by February 2007, and conflicting national
standards shall be withdrawn at the latest by February 2007.
According to the CEN/CENELEC Internal Regulations, the national standards organizations of
the following countries are bound to implement this European Standard: Austria, Belgium,
Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary,
Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland,
Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Endorsement notice
The text of ISO 6144:2003 has been approved by CEN as EN ISO 6144:2006 without any
modifications.
2
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SIST EN ISO 6144:2006
INTERNATIONAL ISO
STANDARD 6144
Second edition
2003-02-01
Gas analysis — Preparation of calibration
gas mixtures — Static volumetric method
Analyse des gaz — Préparation des mélanges de gaz pour
étalonnage — Méthode volumétrique statique
Reference number
ISO 6144:2003(E)
©
ISO 2003
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SIST EN ISO 6144:2006
ISO 6144:2003(E)
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ii © ISO 2003 — All rights reserved
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SIST EN ISO 6144:2006
ISO 6144:2003(E)
Contents Page
Foreword .iv
1 Scope.1
2 Normative references.1
3 Terms and definitions .1
4 Principle .2
5 Apparatus.2
6 Procedure for preparing the calibration gas mixture .4
7 Calculation of the volume fraction of the calibration component in the gas mixture.7
8 Determination of the uncertainty in the concentration of the calibration component in the
gas mixture .9
Annex A (informative) Example of an apparatus suitable for the preparation of calibration gas
mixtures by the static volumetric method.12
Annex B (informative) Example of determination of the volume of metering syringes .15
Annex C (informative) Example of the determination of the uncertainty in the concentration of a
calibration gas mixture prepared by the static volumetric method.17
Annex D (informative) Example of the determination of the stability, as a function of time, of
prepared calibration gas mixtures .22
Bibliography.29
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SIST EN ISO 6144:2006
ISO 6144:2003(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 6144 was prepared by Technical Committee ISO/TC 158, Analysis of gases.
This second edition cancels and replaces the first edition (ISO 6144:1981), which has been technically
revised.
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SIST EN ISO 6144:2006
INTERNATIONAL STANDARD ISO 6144:2003(E)
Gas analysis — Preparation of calibration gas mixtures —
Static volumetric method
1 Scope
This International Standard specifies a method for the preparation of calibration gas mixtures by a static
volumetric method and provides a procedure for calculating the volumetric composition of the mixture. It can
be used either with binary gas mixtures (containing one calibration component in a complementary gas, which
[1, 2]
is usually nitrogen or air ) or with mixtures containing more than one component in the complementary gas.
This International Standard also specifies how the expanded uncertainty in the volume fraction of each
calibration component in the mixture is determined by a rigorous evaluation of all the measurement
uncertainties involved, including those associated with the apparatus used for the preparation of the gas
mixture and those associated with the experimental procedure itself.
NOTE 1 This International Standard is generally applicable to the preparation of calibration gas mixtures containing
−9 −6
calibration components in the concentration range 10 × 10 (10 ppb — parts per billion) to 50 × 10 (50 ppm — parts per
million) by volume. However, gas mixtures may be prepared at larger or smaller volume fractions, provided that the
components used in the static dilution process are selected appropriately.
NOTE 2 A relative expanded uncertainty of not greater than ± 1 % at a level of confidence of 95 % may be achievable
at these concentrations, provided that:
the purities of the parent gases have been determined by analysis and any significant impurities and the uncertainties
in their measured concentrations have been taken into account;
no significant adsorption effects or chemical reactions occur between the gaseous constituents and the internal
surfaces of the apparatus, and there are no reactions between any of the gaseous components, i.e. between the
calibration component and complementary gas or between the calibration components themselves;
all the relevant apparatus used in the preparation of a calibration gas mixture have been calibrated with assigned
measurement uncertainties which are appropriate to calculating the final expanded uncertainty for the calibration gas
mixture prepared.
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 7504, Gas analysis — Vocabulary
3 Terms and definitions
For the purposes of this document, the terms and definitions given in ISO 7504 apply.
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SIST EN ISO 6144:2006
ISO 6144:2003(E)
4 Principle
A calibration gas mixture consists of one of more calibration components in a complementary (diluent) gas,
mixed in a suitable gas-mixing chamber. These calibration components are generally pure gases taken from
cylinders, or from pure, volatile liquids that are allowed to evaporate into the gas-mixing chamber. The gas
mixture is prepared using syringes to inject:
5
either known volumes of gaseous calibration components (each at a pressure of about 1 × 10 Pa);
or known masses or volumes of liquid calibration components;
These are injected into a volume of complementary gas contained in the mixing chamber (which is also at a
5
pressure of about 1 × 10 Pa). Further complementary gas is then added to increase the overall pressure of
the gas mixture to an accurately measured value above ambient atmospheric pressure. This final (above-
atmospheric) pressure is required so that the calibration gas mixture will subsequently flow out of the mixing
chamber and can be used to calibrate a gas analyser, which is usually operated at ambient pressure.
At each stage in the preparation procedure, the mixture is homogenized, usually by means of a suitable
stirring device, and then left to equilibrate to ambient atmospheric temperature.
The volume fraction of each calibration component in the calibration gas mixture is determined by calculation
of the ratio of the volume of the calibration component to the total volume of the mixture.
5 Apparatus
5.1 Gas-mixing chamber, consisting of the components specified in 5.1.1 to 5.1.8.
NOTE An example of a suitable gas-mixing chamber is described in Annex A.
5.1.1 Vessel, comprising the gas-mixing chamber itself, of sufficient internal volume to deliver the amount
of calibration gas mixture required for any subsequent instrumental calibrations, manufactured of a suitable
material that is inert to all the component gases, and designed both to be evacuable and to withstand the
required above-atmospheric operating pressures. It shall also have vacuum/high-pressure flanges to allow
access to the components that are mounted within the mixing chamber.
3 3 5
NOTE 1 Vessels with internal volumes of 0,1 m to 0,5 m , capable of operating up to pressures of about 2 × 10 Pa
2
(2 bar) and of maintaining a vacuum of better than 0,1 × 10 Pa (0,1 mbar), have been found to be suitable (see Annex A).
NOTE 2 Mixing chambers manufactured from borosilicate glass or stainless steel have been found to be suitable for
the commonly used gaseous species (e.g. gas mixtures which contain SO , NO, NO , CO and C H as the calibration
2 2 6 6
components). However, care shall be taken in selecting the materials of the mixing chamber, and of the other components
which come into contact with the gas mixtures, so that they do not affect the mixture's stability adversely — particularly
when more reactive gas mixtures are to be prepared.
5.1.2 Vacuum pump, capable of evacuating the mixing chamber and its associated components to a low
pressure, and including a suitable vacuum shut-off valve. This low pressure shall be defined either so that any
gaseous contamination resulting from the residual low pressure has no effect on the accuracy of the
concentration of the gas mixture prepared, or so that a quantitative correction for the effect of this residual low
pressure may be made to the concentration of the mixture.
NOTE The residual gas pressure is generally due mainly to nitrogen from residual air. However, care must be taken
to ensure that other gases that may react with the constituents of the gas mixture are not present at significant
concentrations in this residual gas (e.g. traces of water vapour when acid gases are being used as calibration
components, or traces of oxygen in the case when nitric oxide calibration mixtures are being prepared).
5.1.3 Gas line, used for the injection of the complementary gas, and including appropriate metering and
shut-off valves.
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5.1.4 Pressure, vacuum and temperature gauges, used to monitor these parameters inside the mixing
vessel.
5.1.5 Septum, enabling a gas or liquid of known volume or mass to be injected into the mixing chamber
from a metering syringe (5.2).
5.1.6 Motor-driven gas-mixing device, e.g. a fan, enabling the gaseous components in the gas-mixing
chamber to be homogenized, and designed to provide satisfactory mixing of all the gaseous components to a
given degree of homogeneity within a specified time. Experimental tests shall be carried out to demonstrate
that the mixing device is able to achieve the required homogeneity within the specified time.
5.1.7 Pressure relief valve, used to ensure that the maximum internal safe working pressure specified for
the mixing vessel and its associated components is not exceeded.
5.1.8 Outlet-gas sampling line, enabling the gas mixture prepared to be used for calibration purposes,
and having a device for equalizing the internal pressure of the gas mixture in the mixing chamber with
atmospheric pressure so as to enable the gas mixture to be determined at ambient pressure for calibration
purposes.
5.2 Calibrated metering syringe, which can be used to inject, by means of a piston, a known volume of
gas or liquid through a needle. The syringe shall have gastight seals to ensure that no significant leakage of
the gas or liquid takes place.
NOTE 1 Glass syringes having polytetrafluoroethene (PTFE) bushings as seals, and with internal volumes of 10 ml,
5 ml, 1 ml, 0,5 ml and 0,1 ml, have been found to be suitable when used with mixing chambers of volumes which are in
practical use, and when used to prepare gas mixtures for the calibration of ambient-air analysers.
NOTE 2 It is recommended that the internal volume of the syringe be measured experimentally with a maximum
relative uncertainty of ± 1 % (at a level of confidence of 95 %). In addition, the syringe should have a maximum leak rate of
2 –2
10 × 10 Pa (10 mbar) per hour after evacuation to 5 Pa (5 × 10 mbar), in order that it has satisfactory leaktightness.
5.3 Apparatus for filling the metering syringe, consisting of the components specified in 5.3.1 to 5.3.9.
NOTE An example of a suitable set-up for filling the syringe is described in Annex A.
5.3.1 Evacuable gas reservoir, capable of containing gas at above-atmospheric pressure so as to enable
the metering syringe to be filled to that pressure, its internal surfaces being made of a material that does not
react with any of the calibration components.
5
NOTE A gas reservoir with an internal volume of about 100 ml, capable of operating up to a pressure of 1,4 × 10 Pa
2
(1,4 bar) and of maintaining a vacuum of better than 0,1 × 10 Pa (0,1 mbar), has been found suitable.
5.3.2 High-pressure gas cylinder, containing the selected pure gas component (or a pre-mixture
containing a higher concentration of gas mixture).
5.3.3 Pressure regulator, used to enable the pressure of gas in the reservoir to be adjusted to a pre-
defined pressure above that of the ambient atmosphere.
5.3.4 Septum, constructed of appropriate material, enabling the needle of the metering syringe to be
introduced into the gas reservoir.
5.3.5 Vacuum pump, enabling the gas reservoir and its associated components to be evacuated to below
the required vacuum.
NOTE It is important to ensure that any gaseous component which may be hazardous, and which is exhausted by
the vacuum pump to the atmosphere, is vented in a safe way.
5.3.6 Pressure gauge, used to monitor the pressure of the gas in the reservoir during the various stages of
the preparation procedure.
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SIST EN ISO 6144:2006
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5.3.7 Gas shut-off valves, used to isolate the gas cylinder from the reservoir, and the gas reservoir from
the vacuum pump.
5.3.8 Pressure-relief valve, capable of relieving a gas pressure selected to protect the apparatus (typically
5
1,4 × 10 Pa). It should be vented to a safe location.
5.3.9 Suitable vessel, for use when the metering syringe is to be filled with a volatile liquid rather than a
gas, and enabling the syringe to be filled in a manner that prevents the ingress into the syringe of any
components other than the volatile liquid.
6 Procedure for preparing the calibration gas mixture
6.1 Determination of the volume of the gas-mixing chamber
There are a number of ways by which the internal volume of the gas-mixing chamber may be determined in
practice. The major component of this volume will be the internal volume of the empty vessel itself and this is
normally measured by filling it with water, or with another liquid of known density, and then determining the
increase in mass due to this liquid. However, other methods may be used where these have the required
accuracy. Following this, the internal volumes of the components within the gas-mixing chamber shall be
determined by, for example, geometric measurement or liquid displacement. Corrections shall then be made
for the volumes of these additional components when determining the net volume of the chamber. Corrections
for some of the components (e.g. the gas-mixing device) will lead to a smaller volume whereas others (e.g.
the pressure gauge and the outlet pipes leading to the shut-off valves) will lead to an increase in volume.
These measurements of the volumes of the components that make up the total gas-mixing chamber (see 5.1)
may have been carried out at different temperatures. In such cases, corrections shall be made, where
significant, to convert the measured volumes to a common ambient temperature. A further correction may
need to be made if the complete mixing chamber with all its components is used at a different ambient
temperature, provided such a correction is significant.
6.2 Conditioning the gas-mixing chamber before use
A new gas-mixing chamber will normally contain ambient air, and this may contain trace pollutants at levels
that would affect the accuracy of the calibration gas mixture. In addition, the inside surfaces of the chamber
may be contaminated with a surface layer which may react with some species which are put in the mixing
chamber. It is therefore necessary to condition the mixing chamber before use so as to avoid any potential
contamination of the calibration gas from these causes. Do this by evacuating the chamber to a pressure of
2
less than 5 × 10 Pa (5 mbar). Then fill the chamber to above-atmospheric pressure with the complementary
gas which is to be used in the preparation of the calibration gas mixture. Subsequently, connect the outlet
from the mixing chamber to a set of instruments designed to measure air pollutants (e.g. analysers which
monitor SO , NO , CO and hydrocarbons). These shall have sufficient detection sensitivity to determine
2 x
whether significant concentrations of the relevant gaseous impurities exist in the complementary gas in the
mixing chamber at this time. Allow the complementary gas in the mixing chamber to flow into these analysers,
and observe the concentrations of any impurities detected.
Repeat this procedure, involving the evacuation of the mixing chamber followed by re-filling with
complementary gas, several times or until all relevant gaseous impurities are below the concentrations
required to prevent significant contamination of the calibration gas mixtures to be prepared in the chamber. In
circumstances where this cannot be achieved, either clean the mixing chamber by other means so as to
remove the contaminants, or make a suitable correction when calculating the concentration of the calibration
component in the calibration gas mixture so as to allow for such impurities.
In circumstances where such an analysis of the impurities present in the complementary gas is the only one
that is carried out, the detection limits of the analysers used shall represent the upper limits for the
concentrations of the impurities which could be present in the calibration gas mixture. In these cases, the
concentrations represented by these detection limits shall be taken into account in the determination of the
expanded uncertainty of the prepared calibration gas mixture. In cases, however, where additional, more
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SIST EN ISO 6144:2006
ISO 6144:2003(E)
sensitive, analyses of impurities are carried out by other means, the results of these analyses shall instead be
incorporated into the expanded uncertainty of the calibration gas mixture.
After the mixing chamber has been pre-conditioned using the above procedure, it is possible that it might not
be used for a significant period. If this is the case, re-fill the mixing chamber with the selected complementary
gas at a pressure that is higher than ambient, so as to minimize further contamination which may arise from
ingress of gaseous pollutants from the ambient atmosphere.
Subsequently, carry out the following steps to prepare the calibration gas mixture.
6.3 Filling the mixing chamber with the complementary gas
First evacuate the mixing chamber, using the vacuum pump (5.1.2), to a residual pressure such that
contamination by components of the residual gas will have no significant effect on the accuracy and stability of
2
the final calibration gas mixture (typically about 5 × 10 Pa). Then fill the chamber with the selected
5
complementary gas through the feed line (5.1.3) to about 0,1 × 10 Pa (0,1 bar) above ambient pressure. The
temperature of the complementary gas in the mixing chamber after filling will normally be above ambient
temperature (due to adiabatic compression). Allow the gas to stand, therefore, so that it equilibrates to the
temperature of the mixing chamber, and to that of the ambient atmosphere.
NOTE A temperature difference of 0,2 °C will introduce an uncertainty in the final volume fraction of a component of
less than 0,1 % (relative) of the value of the concentration. In practice, therefore, it is sufficient to ensure that the
complementary gas temperature and the ambient temperature are within 0,2 °C of each other.
After the temperature of the complementary gas and the external temperature have equilibrated, bring the
pressure of the complementary gas in the mixing chamber to ambient pressure by opening the shut-off valve
connected to the pressure relief valve (5.1.7). Record both the temperature and the pressure of the gas in the
mixing chamber at this point, for use subsequently in the determination of the concentration of the calibration
gas mixture.
6.4 Determination of the calibration component volume required
The required volume of the calibration component which is to be injected into the mixing chamber is calculated
from the required composition of the final gas mixture, the volume of the mixing chamber itself, and the target
value of the final gas pressure in the mixing chamber. Where a liquid is to be injected, it is important to know,
at least approximately, the density of the calibration component in its liquid form so as to obtain the required
concentration in the gaseous state when the final calibration gas mixture is produced.
The accuracy to which the internal volume of the syringe is known, and any leakage to the atmosphere
through the needle or through the seals of the syringe, will make a contribution to the overall accuracy of the
calibration gas mixture. An example of a method used to determine experimentally the volume of gas in the
syringe, to demonstrate the leaktightness of the syringe, and to demonstrate the amount of gas loss through
the needle is given in Annex B.
Select a syringe of appropriate volume so as to provide a final gas mixture with the required uncertainty in its
concentration. In most cases, multiple injections using the selected syringe will be necessary. The uncertainty
in the final volume fraction of the component is usually minimized by using a syringe that gives the minimum
number of injections of calibration component into the mixing chamber. However, the choice of syringe will
also depend, in practice, on the availability of a suitable syringe with the required uncertainty in its volume.
Record the number of injections that are required.
6.5 Filling the syringe with the calibration component
6.5.1 Gaseous calibration components
When gaseous calibration components are employed, use the apparatus described in 5.3 to fill the syringe.
Then proceed using the following procedure.
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ISO 6144:2003(E)
First close the shut-off valve on the cylinder of calibration component. Then use the vacuum pump to
evacuate the whole apparatus, including the reservoir, to a
...
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