392-2020-00314301 - VOC'S Emission - PERLIFOC HP
392-2020-00314301 - VOC'S Emission - PERLIFOC HP
Smedeskovvej 38
EUROFINS PRODUCT TESTING, COSMETICS & PERSONAL CARE SPAIN, S.L.U. 8464 Galten
C/ Ausias March, 148-150 Denmark
08013 Barcelona
SPAIN [email protected]
www.eurofins.com/VOC-testing
Applicant:
Perlita y Vermiculita, S.L.U.
C/Josep Irla i Bosch, 5-7. entreplanta
08034. Barcelona
SPAIN
VOC EMISSION TEST REPORT
Indoor Air Comfort GOLD®
9 September 2020
1 Sample Information
Sample name Perlifoc HP
Batch no. Palet number 42
Production date 01/07/2020
Product type Gypsum based mortar
Sample reception 17/07/2020
French CMR components Pass Regulation of April and May 2009 (DEVP0908633A and
DEVP0910046A)
Italian CAM Edilizia Pass Decree 11 October 2017 (GU n.259 del 6-11-2017)
BREEAM International Exemplary Level BREEAM International New Construction v2.0 (2016)
® BREEAM-NOR New Construction v1.2 (2019)
BREEAM NOR Fail
Full details based on the testing and direct comparison with limit values are available in the following pages
5 Results 5
5.1 VOC Emission Test Results after 3 Days 5
5.2 VOC Emission Test Results after 28 Days 7
7 Appendices 15
7.1 Chromatogram of VOC Emissions after 3 Days 15
7.2 Chromatogram of VOC Emissions after 28 Days 15
7.3 How to Understand the Results 16
7.4 Applied LCI and NIK Values 17
7.5 Description of VOC Emission Test 18
7.6 Quality Assurance 20
7.7 Accreditation 20
7.8 Uncertainty of the Test Method 20
VVOC compounds
None determined
TVVOC <5 <5 <2
SVOC compounds
None determined
TSVOC <5 <5 <2
Carcinogens
Total carcinogens <1 <1 <1
Aldehydes
Formaldehyde 50-00-0 1 3.4 1.2
Acetaldehyde 75-07-0 1 32 11 0.027 0.027
Propionaldehyde 123-38-6 1 <3 <2
Butyraldehyde 123-72-8 1 <3 <2
Acrolein * 107-02-8 1 <5 <2
2-Butenal * 123-73-9 1 <5 <2
Glutaraldehyde * 111-30-8 1 <5 <2
Octanal * 124-13-0 1 <5 <2
The results are only valid for the tested sample(s).
This report may only be copied or reprinted in its entity, parts of it only with a written acceptance by Eurofins .
392-2020-00314301_A_EN Page 5 of 20
CAS No. Retention ID- Specific Toluene Specific RD RB
time Cat Conc. eq. SER
[min] [µg/m³] [µg/m³] [µg/(m²·h)]
VVOC compounds
None determined
TVVOC <5 <5 <2
SVOC compounds
None determined
TSVOC <5 <5 <2
Carcinogens
Total carcinogens <1 <1 <1
TVOC 140 31 50
TVOC - 43 <1500
All identified carcinogenic VOCs are listed; if a carcinogenic VOC is not listed then it has not been detected.
Quantification is performed using the TIC signal and authentic response factors, or the relative response
factors relative to toluene for the individual compounds.
This test only covers substances that can be adsorbed on Tenax TA and can be thermally desorbed. If other
emissions occur, then these substances cannot be detected (or with limited reliability only).
All single substances that are listed with a LCI/NIK value in the latest publications (hereafter referred to as
target compounds) are identified if present. All other appearing VOCs are identified as far as possible.
Quantification of target compounds is done using the TIC signal and authentic response factors, or the
relative response factors relative to toluene. For certain compound groups, which differ significantly in
chemistry from toluene, quantification is performed relative to a representative member of the group for more
accurate and precise results. This can include quantification of for example glycols and acids. In addition to
that, all results are also expressed in toluene equivalents. All non-target compounds, as well as all non-
identified substances, are quantified in toluene equivalents.
The results of the individual substances are calculated in three groups depending on their retention time
when analyzing using a non-polar column (HP-1):
- Volatile Organic Compounds (VOC) are defined as: All substances eluting between and including
n-hexane (n-C6) and n-hexadecane (n-C16)
- Semi-Volatile Organic Compounds (SVOC) are defined as: All substances eluting after
n-hexadecane (n-C16) and before and including n-docosane (n-C22)
- Very Volatile Organic Compounds (VVOC) are defined as: All substances eluting before
n-hexane (n-C6).
Total Semi-Volatile Organic Compounds (TSVOC) is calculated by the summation of all individual SVOCs
expressed in toluene equivalents with a concentration ≥ 5 µg/m³, as defined in EN 16516. VOCs that are
regarded as VOC in line with the above definition, but elute after n-C16 in this test, are not added to the
TSVOC.
Total Very Volatile Organic Compounds (TVVOC) is calculated by the summation of all individual VVOCs
with a concentration ≥ 5 µg/m³ and expressed in toluene equivalents. VOCs that are regarded as VOC in line
with the above definition, but elute before n-C6 in this test, are not added to the TVVOC.
This test only covers substances which can be adsorbed on Tenax TA and can be thermally desorbed. If
emissions of substances outside these specifications occur then these substances cannot be detected (or
with limited reliability only).
This R value is calculated, depending on the purpose of this test, for the European LCI list, for the German
LCI/NIK list (RD), and/or for the Belgian LCI list (RB).
All VOCs without published LCI/NIK value and concentration ≥ 5 µg/m³ are summed up as sum of VOCs
without LCI/NIK if required by the standard or protocol.
The absence of formaldehyde and other aldehydes is stated if UV detector response at the specific
wavelength is lacking at the specific retention time in the chromatogram. Otherwise it is checked whether the
reporting limit is exceeded. In this case the identity is finally checked by comparing full scan sample UV
spectra with full scan standard UV spectra.
Air sampling at the chamber outlet and subsequent analysis is performed in duplicate. Relative humidity,
temperature and air change rate in the chambers is logged every 5 minutes and checked daily. A double
determination is performed on random samples at a regular interval and results are registered in a control
chart to ensure the uncertainty and reproducibility of the method.
The stability of the analytical system is checked by a general function test of device and column, and by use
of control charts for monitoring the response of individual substances prior to each analytical sequence.
7.7 Accreditation
The testing methods described above are accredited on line with EN ISO/IEC 17025 by DANAK (no. 522).
This accreditation is valid worldwide due to mutual approvals of the national accreditation bodies (ILAC/IAF,
see also www.eurofins.com/galten.aspx#accreditation).
Not all parameters are covered by this accreditation. The accreditation does not cover parameters marked
with an asterisk (*), however analysis of these parameters is conducted at the same level of quality as for the
accredited parameters.