Ambient air quality - Standard method for the determination of total gaseous mercury

This European Standard specifies a standard method for determining total gaseous mercury (TGM) in ambient air using cold vapour atomic absorption spectrometry (CVAAS), or cold vapour atomic fluorescence spectrometry (CVAFS). This European Standard is applicable to background sites that are in accordance with the requirements of Directive 2004/107/EC and to urban and industrial sites. The performance characteristics of the method have been determined in comparative field validation tests carried out at four European locations: two background and two industrial sites. The method was tested for two months at each site over a period of twelve months using automated equipment currently used in Europe for determination of TGM in ambient air. The working range of the method covers the range of ambient air concentrations from those found at background sites, typically less than 2 ng/m3, up to those found at industrial sites where higher concentrations are expected. A maximum daily average up to 300 ng/m3 was measured during the field trials. Results are reported as the average mass of TGM per volume of air at 293,15 K and 101,325 kPa, measured over a specified time period, in nanograms per cubic metre.

Außenluftbeschaffenheit - Standardisiertes Verfahren zur Bestimmung des gesamten gasförmigen Quecksilbers

Die vorliegende Europäische Norm beschreibt ein standardisiertes Verfahren zur Bestimmung des gesamten
gasförmigen Quecksilbers (TGM) in der Außenluft mit der Kaltdampf-Atomabsorptionsspektrometrie (CVAAS)
oder der Kaltdampf-Atomfluoreszenzspektrometrie (CVAFS).
Diese Europäische Norm ist anwendbar auf Hintergrundstationen, die den Anforderungen der Richtlinie
2004/107/EG entsprechen, und auf Stadtgebiete sowie Gebiete mit Industrieeinfluss.
Die Verfahrenskenngrößen wurden mit vergleichenden Feldversuchen zur Validierung bestimmt, die an vier
europäischen Standorten durchgeführt wurden: zwei Hintergrundstationen und zwei Industriestandorte. Das
Verfahren wurde an jedem Standort für zwei Monate über einen Zeitraum von 12 Monaten mit automatisierten
Geräten geprüft, die derzeit in Europa zur TGM-Bestimmung in der Außenluft angewendet werden.
Der Messbereich des Verfahrens umfasst Außenluftkonzentrationen von kleiner 2 ng/m3, wie sie üblicherweise
an Hintergrundstationen anzutreffen sind, bis hin zu höheren Konzentrationen, wie sie in Gebieten mit
Industrieeinfluss erwartet werden. Bei den Feldversuchen wurde ein maximaler Tagesmittelwert von bis zu
300 ng/m3 gemessen.
Die Ergebnisse sind in ng/m3 als Mittelwert der über einen festgelegten Zeitraum bei 293 K und 101,325 kPa
bestimmten Masse an TGM je Luftvolumen angegeben.

Qualité de l'air ambiant - Méthode normalisée pour la détermination du mercure gazeux total

La présente Norme européenne spécifie une méthode normalisée pour la détermination du mercure gazeux
total (TGM) dans l’air ambiant par spectrométrie d’absorption atomique de vapeur froide (SAAVF) ou
spectrométrie de fluorescence atomique de vapeur froide (SFAVF).
La présente Norme européenne s’applique aux sites de fond conformes aux exigences de la
Directive 2004/107/CE et aux sites urbains et industriels.
Les caractéristiques de performance de la méthode ont été déterminées par des essais comparatifs de
validation sur le terrain réalisés sur quatre sites en Europe : deux sites de fond et deux sites industriels. La
méthode a été vérifiée pendant deux mois sur chaque site sur une période de douze mois à l’aide
d’équipements automatisés couramment utilisés en Europe pour la détermination du TGM dans l’air ambiant.
L’étendue de mesure de la méthode couvre la plage des concentrations dans l’air ambiant allant de celles
observées sur les sites de prélèvement de fond, généralement inférieures à 2 ng/m3, à celles observées sur
les sites industriels où des concentrations plus élevées sont attendues. Une moyenne journalière maximale
jusqu’à 300 ng/m3 a été mesurée au cours des essais sur le terrain.
Les résultats sont exprimés en masse moyenne de TGM par volume d’air à 293,15 K et 101,325 kPa,
mesurée sur une période de temps spécifiée, en nanogrammes par mètre cube (ng/m3).

Kakovost zunanjega zraka - Standardna metoda za določevanje celotnega živega srebra v plinasti fazi

Ta evropski standard določa standardno metodo za določevanje celotnega živega srebra v plinasti fazi (TGM) v zunanjem zraku z atomsko absorbcijsko  spektrometrijo hladnih par (CVAAS) ali atomsko fluorescenčno spektrometrijo hladnih par (CVAFS). Ta evropski standard velja za zaledna območja, ki so v skladu z zahtevani Direktive 2004/107/ES, ter za urbana in industrijska območja. Značilnosti delovanja metode so bile določene s primerjalnimi validacijskimi preskusi na terenu, opravljenimi na štirih evropskih lokacijah: dve zaledni in dve industrijski območji. Metoda se je preskušala dva meseca v obdobju dvanajstih mesecev na vsakem območju z avtomatsko opremo, ki se trenutno uporablja v Evropi za določevanje TGM v zunanjem zraku. Delovni razpon te metode zajema razpon koncentracij zunanjega zraka od tistih, ki se nahajajo na zalednih območjih, običajno manjših od 2 ng/m3, do tistih, ki se nahajajo na industrijskih območjih, kjer so pričakovane višje koncentracije. Med preskusi na terenu je bilo izmerjeno maksimalno dnevno povprečje do 300 ng/m3. Rezultati so prikazani kot povprečna masa TGM na volumen zraka pri 293,15 K in 101,325 kPa, merjena v določenem roku v nanogramih na kubični meter.

General Information

Status
Published
Public Enquiry End Date
19-Nov-2008
Publication Date
05-Oct-2010
Technical Committee
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
09-Jul-2010
Due Date
13-Sep-2010
Completion Date
06-Oct-2010

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2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.Außenluftbeschaffenheit - Standardisiertes Verfahren zur Bestimmung des gesamten gasförmigen QuecksilbersQualité de l'air ambiant - Méthode normalisée pour la détermination du mercure gazeux totalAmbient air quality - Standard method for the determination of total gaseous mercury13.040.20Kakovost okoljskega zrakaAmbient atmospheresICS:Ta slovenski standard je istoveten z:EN 15852:2010SIST EN 15852:2010en,fr,de01-november-2010SIST EN 15852:2010SLOVENSKI
STANDARD



SIST EN 15852:2010



EUROPEAN STANDARD NORME EUROPÉENNE EUROPÄISCHE NORM
EN 15852
June 2010 ICS 13.040.20 English Version
Ambient air quality - Standard method for the determination of total gaseous mercury
Qualité de l'air ambiant - Méthode normalisée pour la détermination du mercure gazeux total
Außenluftbeschaffenheit - Standardisiertes Verfahren zur Bestimmung des gesamten gasförmigen Quecksilbers This European Standard was approved by CEN on 5 May 2010.
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 CEN Management Centre 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 CEN Management Centre has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, 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:
Avenue Marnix 17,
B-1000 Brussels © 2010 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 15852:2010: ESIST EN 15852:2010



EN 15852:2010 (E) 2 Contents Page Foreword .41Scope .52Normative references .53Terms and definitions .54Symbols and abbreviated terms .84.1Symbols .84.2Abbreviations . 115Principle . 116Requirements . 126.1Siting criteria . 126.2Method requirements . 126.3Method detection limit . 126.4Field operation and quality control . 127Reagents . 128Apparatus . 138.1Sampling equipment . 138.2Analytical instrumentation . 138.3Calibration equipment . 139Sampling considerations . 149.1Inlet location . 149.2Sampling inlet and sampling line . 149.3Measurement time . 1510Measurement procedure . 1610.1Calibration with AFS/AAS . 1610.2Calibration with Zeeman AAS . 1711Quality control . 1711.1Calibration robustness check . 1711.2Zero gas check . 1811.3Degradation of gold traps . 1811.4Proficiency testing scheme . 1811.5Accreditation . 1811.6Measurement uncertainty . 1812Calculation of results . 1812.1General . 1812.2Calculation of TGM concentrations to reference conditions . 1912.3Method detection limit . 2012.4Repeatability . 2012.5Drift in instrument sensitivity . 2113Estimation of the measurement uncertainty method and performance criteria . 2113.1Introduction . 2113.2Assessment against target measurement uncertainty for individual laboratories . 2213.3Use of uncertainties in reporting of results . 2314Performance characteristics determined in field tests . 2415Interferences . 24SIST EN 15852:2010



EN 15852:2010 (E) 3 15.1General . 2415.2Mercury analyser based on amalgamation and CVAAS or CVAFS . 2415.3Mercury analyser based on Zeeman AAS . 2516Reporting of results . 25Annex A (informative)
Sampling sites . 26Annex B (informative)
Manual method TGM . 27Annex C (informative)
Summary of field validation tests . 29Annex D (informative)
Characteristics of the mercury vapour source . 34Annex E (informative)
Calibration . 37Annex F (informative)
Assessment against target uncertainty by an individual laboratory . 38Annex G (informative)
Relationship between this European Standard and the Essential Requirements of EU Directives . 44Bibliography . 45 SIST EN 15852:2010



EN 15852:2010 (E) 4 Foreword This document (EN 15852:2010) has been prepared by Technical Committee CEN/TC 264 “Air quality”, the secretariat of which is held by DIN. 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 December 2010, and conflicting national standards shall be withdrawn at the latest by December 2010. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights. This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive(s). According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, 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 the United Kingdom. SIST EN 15852:2010



EN 15852:2010 (E) 5 1 Scope
This European Standard specifies a standard method for determining total gaseous mercury (TGM) in ambient air using cold vapour atomic absorption spectrometry (CVAAS), or cold vapour atomic fluorescence spectrometry (CVAFS).
This European Standard is applicable to background sites that are in accordance with the requirements of Directive 2004/107/EC and to urban and industrial sites.
The performance characteristics of the method have been determined in comparative field validation tests carried out at four European locations: two background and two industrial sites. The method was tested for two months at each site over a period of twelve months using automated equipment currently used in Europe for determination of TGM in ambient air.
The working range of the method covers the range of ambient air concentrations from those found at background sites, typically less than 2 ng/m3, up to those found at industrial sites where higher concentrations are expected. A maximum daily average up to 300 ng/m3 was measured during the field trials.
Results are reported as the average mass of TGM per volume of air at 293,15 K and 101,325 kPa, measured over a specified time period, in nanograms per cubic metre. 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.
ENV 13005, Guide to the expression of uncertainty in measurement CR 14377, Air quality
Approach to uncertainty estimation for ambient air reference measurement methods EN ISO 20988, Air quality
Guidelines for estimating measurement uncertainty (ISO 20988:2007) ISO 5725-2:1994, Accuracy (trueness and precision) of measurement methods and results
Part 2: Basic method for the determination of the trueness of a standard measurement method ISO 8573-1:2010, Compressed air
Part 1: Contaminants and purity classes 3 Terms and definitions For the purposes of this document, the following terms and definitions apply.
3.1 ambient air outdoor air in the troposphere, excluding workplace air
3.2 calibration operation that, under specified conditions, in a first step, establishes a relation between the quantity values with measurement uncertainties provided by measurement standards and corresponding indications with associated measurement uncertainties and, in a second step, uses this information to establish a relation for obtaining a measurement result from an indication SIST EN 15852:2010



EN 15852:2010 (E) 6 NOTE 1 A calibration may be expressed by a statement, calibration function, calibration diagram, calibration curve, or calibration table. In some cases, it may consist of an additive or multiplicative correction of the indication with associated measurement uncertainty. NOTE 2 Calibration should not be confused with adjustment of a measuring system, often mistakenly called "self-calibration", nor with verification of calibration.
NOTE 3 Often, the first step alone in the above definition is perceived as being calibration [ISO/IEC Guide 99:2007 (VIM)]. 3.3
combined standard measurement uncertainty standard measurement uncertainty that is obtained using the individual standard measurement uncertainties associated with the input quantities in a measurement model
NOTE In case of correlations of input quantities in a measurement model, covariances should also be taken into account when calculating the combined standard measurement uncertainty [ISO/IEC Guide 99:2007 (VIM)]. 3.4 coverage factor number larger than one by which a combined standard measurement uncertainty is multiplied to obtain an expanded measurement uncertainty
NOTE A coverage factor is usually symbolized k [ISO/IEC Guide 99:2007 (VIM)]. 3.5 detection limit measured quantity value for which the probability of falsely claiming the absence of a component in a material is β, given a probability . of falsely claiming its presence NOTE IUPAC recommends default values for . and β equal to 0,05.
3.6 expanded standard measurement uncertainty product of a combined standard measurement uncertainty and a factor larger than the number one NOTE 1 The factor depends upon the type of probability distribution of the output quantity in a measurement model and on the selected coverage probability. NOTE 2 The term "factor" in this definition refers to a coverage factor. NOTE 3 Expanded measurement uncertainty is termed "overall uncertainty" in paragraph 5 of Recommendation INC-1 (1980) (see the GUM) and simply "uncertainty" in IEC documents [ISO/IEC Guide 99:2007 (VIM)]. NOTE 4 For the purpose of this document the expanded uncertainty is the combined standard uncertainty multiplied by a coverage factor k = 2 resulting in an interval with a level of confidence of 95 %. 3.7 measurement repeatability measurement precision under a set of repeatability conditions of measurement
[ISO/IEC Guide 99:2007 (VIM)] 3.8 measurement reproducibility measurement precision under reproducibility conditions of measurement
NOTE Relevant statistical terms are given in ISO 5725-1:1994 and ISO 5725-2:1994 [ISO/IEC Guide 99:2007 (VIM)]. SIST EN 15852:2010



EN 15852:2010 (E) 7 3.9 measurement time length of time over which the measurement instrumentation produces a single concentration value, during normal operation NOTE 1 For "trap and desorb" instruments this will be the time period air is sampled across the gold trap prior to each thermal desorption cycle analysis; for direct measurement instruments this will be the time period in which the absorbance is averaged to produce a single value.
NOTE 2 Measurement times during the field trial campaign ranged from 30 s to 30 min.
3.10 measurement uncertainty non-negative parameter characterizing the dispersion of the quantity values being attributed to a measurand, based on the information used NOTE 1 Measurement uncertainty includes components arising from systematic effects, such as components associated with corrections and the assigned quantity values of measurement standards, as well as the definitional uncertainty. Sometimes estimated systematic effects are not corrected for but, instead, associated measurement uncertainty components are incorporated. NOTE 2 The parameter may be, for example, a standard deviation called standard measurement uncertainty (or a specified multiple of it), or the half-width of an interval, having a stated coverage probability [ISO/IEC Guide 99:2007 (VIM)]. 3.11 method detection limit lowest amount of an analyte that is detectable using the method, as determined by sampling and analysis of zero gas 3.12 monitoring period time period over which monitoring is intended to take place, defined in terms of the time and date of the start and end of the period 3.13 monitoring station (for mercury) enclosure located in the field in which an analyser has been installed to monitor TGM concentrations
3.14 monitoring time length of time over which monitoring is intended to take place NOTE For example: an instrument measured TGM using a measurement time of 15 min, over a sampling time of 30 days (producing 2 880 data points). The monitoring period was from 0001 h on 1 April 2008 to 0001 h on 1 May 2008. 3.15 reference conditions ambient temperature of 293,15 K and pressure of 101,325 kPa
3.16 repeatability condition of measurement
condition of measurement, out of a set of conditions that includes the same measurement procedure, same operators, same measuring system, same operating conditions and same location, and replicate measurements on the same or similar objects over a short period of time NOTE 1 A condition of measurement is a repeatability condition only with respect to a specified set of repeatability conditions. SIST EN 15852:2010



EN 15852:2010 (E) 8 NOTE 2 In chemistry, the term "intra-serial precision condition of measurement" is sometimes used to designate this concept [ISO/IEC Guide 99:2007 (VIM)]. 3.17 reproducibility condition of measurement condition of measurement, out of a set of conditions that includes different locations, operators, measuring systems, and replicate measurements on the same or similar objects NOTE 1 The different measuring systems may use different measurement procedures. NOTE 2 A specification should give the conditions changed and unchanged, to the extent practical [ISO/IEC Guide 99:2007 (VIM)]. 3.18 sampling inlet entrance to the sampling system where ambient air is taken from the atmosphere 3.19 standard uncertainty
measurement uncertainty expressed as a standard deviation [ISO/IEC Guide 99:2007 (VIM)] 3.20 total gaseous mercury
TGM elemental mercury vapour (Hg0) and reactive gaseous mercury, i.e. water-soluble mercury species with sufficiently high vapour pressure to exist in the gas phase
[Directive 2004/107/EC] NOTE This definition is taken in this standard to include all gaseous mercury species.
3.21 zero gas gas free from mercury, interfering compounds and particles
NOTE 1 Free from mercury means containing a concentration less than the method detection limit. NOTE 2 Zero gas is used in conjunction to calibration of automatic mercury instruments. It may consist of pure nitrogen or synthetic air from a gas cylinder. Purified air from the surrounding can also be used (see instructions in user manuals). 4 Symbols and abbreviated terms
For the purposes of this document, the following symbols and abbreviated terms apply.
4.1 Symbols A
is a constant with numerical value - 8,134 46; AHg
is the atomic weight of mercury, 0,20059; .
for a given detection limit the probability of a false positive identification occurring; B
is a constant with numerical value 3 240,87;
ß
for a given detection limit the probability of a false negative identification occurring;
SIST EN 15852:2010



EN 15852:2010 (E) 9
is the mass concentration; amb
is the mercury concentration in a certain air volume V (T, P);
d,i
is the daily mass concentration value on day d from instrument i; Hg
is the theoretical mass concentration of mercury vapour samples that can be collected from the
mercury vapour source using a syringe;
Hg, sou is the mercury concentration in the source; Hg, syr
is the mercury concentration in the syringe; MDL
is the method detection limit; ref
is the mass concentration of TGM in reference air at 293,15 K and 101,325 kPa; sam
is the mercury concentration related to a certain air temp (Tsam) and pressure (Psam); γ
is the mean mass concentration over all N days and across all M instruments; d
is the mean mass concentration on day d across all M instruments; D
is a constant with numerical value 3 216 522;
/
is the estimated statistical uncertainty associated with the mercury vapour equation used; /d,i
is the deviation of instrument i from the mean mass concentration on day d; iδ
is the mean deviation of instrument i from the mean mass concentration over all N days; k
is the coverage factor; sam
is the sampling efficiency; mair
is the mass of air under reference conditions; mtrap
is the mass of mercury found on the gold trap;
M
is the number of parallel samplers used in a field trial;
Mair
is the molecular weight of air, 0,029 kg/mol;
n
is the number of measurements; N
is the duration of the field trial in days; PHg
is the vapour pressure of mercury; Pref
is the reference pressure, 101,325 kPa; Psam
is the actual pressure of the sampled air; qv,ave
is the average volume flow rate of ambient air through the trap during the monitoring period;
r2
is the correlation coefficient; SIST EN 15852:2010



EN 15852:2010 (E) 10 rflow
is the flow calibration coefficient,
rsyr
is the volume calibration coefficient;
R
is the ideal gas constant, 8,314 J/K·mol; Rcal
is the instrumental response produced after the injection of a volume of mercury saturated gas; R i
is the instrumental response generated from measurement i; R sam
is the instrumental response following analysis of the sample;
R
is the average of n (n)10≥repeat measurements of iR; 0R
is the instrumental response generated upon the injection of a zero volume of mercury saturated gas; 0R
is the average of n (10≥n) repeat measurements of i0,R; i0,R
is the instrumental response generated upon introduction of zero gas from measurement i; 1i
is the standard deviation of the deviation of instrument i over all N days; 1R
is the relative standard deviation of a set of n measurements; t is the sampling time;
Tsam
is the actual temperature of the sampled air; Tsou is the temperature of mercury source; Tsyr is the temperature of syringe; Tref
is the reference temperature, 293,15 K;
uc ()
is the relative combined standard uncertainty in the TGM concentration in ambient air;
uc,i () is the relative combined standard uncertainty from instrument i;
ui, vol is the uncertainty in the sampled volume for instrument i; ur ()
is the relative random contribution to the uncertainty; ur, i () is the random contribution to the relative combined uncertainty from instrument i; us ()
is the relative non-random contribution to the uncertainty; us, i () is the non-random contribution to the relative combined uncertainty from instrument i; U is the expanded uncertainty;
Vamb
is the volume of ambient air sampled onto the trap;
V (T,P) is a certain air volume;
Vsam(T,P) is the corresponding air volume at the actual temperature Tsam and pressure Psam; SIST EN 15852:2010



EN 15852:2010 (E) 11 calV& is the sensitivity of the analyser, determined by calibration;
0,cal=tV& is the measured sensitivity of the instrument at time t=0;
ttV=,cal& is the measured sensitivity of the instrument at time t;
calV&∆ is the drift in the sensitivity of the measuring system, over a time, t; VHg
is the volume of mercury saturated gas from within the mercury vapour source; Vref
is the reference air volume; x is the mass of mercury; y
is the measurement result; Y is the measurand. 4.2 Abbreviations CVAAS Cold Vapour Atomic Absorption Spectrometry CVAFS Cold Vapour Atomic Fluorescence Spectrometry EMEP Co-operative Programme for Monitoring and Evaluation of the Long-range Transmission of Air pollutants in Europe (European Monitoring and Evaluation Programme) FEP Fluorinated ethylene propylene IUPAC International Union of Pure and Applied Chemistry MFC Mass flow controller MFM Mass flow meter ng Nanogram; 10-9 g PTFE
Polytetrafluoroethylene TGM Total Gaseous Mercury Zeeman AAS Zeeman Atomic Absorption Spectrometry 5
Principle The methods described in this standard are automated methods that involve either:
 adsorption of TGM from a measured air volume on a gold trap, followed by thermal desorption of total mercury from the gold trap and determination as gaseous elemental mercury by CVAAS or CVAFS; or  direct continuous measurement of elemental mercury by Zeeman AAS. SIST EN 15852:2010



EN 15852:2010 (E) 12 6 Requirements
6.1 Siting criteria The siting requirements for TGM measurements are given in Annex A. 6.2 Method requirements The method for the measurement of total gaseous mercury concentrations in ambient air shall be an automated method based on Atomic Absorption Spectrometry or Atomic Fluorescence Spectrometry, as specified in Annex V.III of Directive 2004/107/EC. 6.3 Method detection limit The detection limit of the gold trap analysis method (expressed in nanograms of mercury) shall not exceed 10 % of the lower limit of the working range of the mercury expected to be collected during any measurement period. This will depend on the measurement time and the sampling flow rate. The detection limit of the Zeeman AAS method (expressed in nanograms per cubic metre) shall not exceed 10 % of the lower working range.
6.4
Field operation and quality control
After the installation at the monitoring station, the analyser shall be tested to ensure that it is working correctly.
It is essential that the expanded uncertainty of measurements in the field does not exceed the 50 % according to Directive 2004/107/EC. Requirements and recommendations for quality assurance and quality control are given for the measurements in the field (see Clause 11).
7 Reagents
7.1 Argon, of purity greater than 99,999 %, suitable for use as a carrier gas for CVAAS and CVAFS. 7.2 Nitrogen, of purity greater than 99,999 %, suitable for use as a carrier gas for CVAAS and CVAFS. 7.3 Air, of class 3.3.3 purity or better according to ISO 8573-1:2010. 7.4 Elemental mercury, of purity 99,999 9 %, for preparation of gaseous mercury vapour standard. WARNING — Mercury is toxic by skin absorption and inhalation of vapour. Use suitable personal protective equipment (including gloves, face shield or safety glasses, etc.) and minimize exposure by using a fume hood.
7.5 Water, resistivity greater or equal to 18 M·cm at 298 K. The ultrapure water used in this method is for cleaning purposes only. 7.6 Hydrochloric acid (HCl), concentrated, density ~ 1,18 g/ml, mass fraction 36 % to 38 %. The concentration of mercury shall be less than 0,002 mg/l. WARNING — Concentrated hydrochloric acid is corrosive and hydrochloric acid is an irritant. Avoid contact with the skin and eyes, or inhalation of the vapour. Use suitable personal protective equipment (including gloves, face shield or safety glasses, etc.) when working with hydrochloric acid. SIST EN 15852:2010



EN 15852:2010 (E) 13 Handle open vessels containing concentrated hydrochloric acid in a fume hood. The vapour pressure of hydrochloric acid is high. Therefore beware of pressure build-upin capped vessels when preparing dilute hydrochloric solutions.
7.7 Hydrochloric acid, diluted 1:49 with ultrapure water for cleaning of filter housings, glass manifolds and sampling components.
Add approximately 700 ml of water (7.5) to a 1 000 ml volumetric flask. Carefully add 20 ml of concentrated hydrochloric acid (7.6) to the flask and swirl to mix. Allow to cool, dilute to the mark with water, stopper and mix thoroughly.
8 Apparatus 8.1 Sampling equipment 8.1.1 Polytetrafluoroethylene (PTFE)
...

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