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Comparison of the Particle Size Distribution and Vapor Phase of Electronic Nicotine Delivery Systems Using Two Impactors Cover

Comparison of the Particle Size Distribution and Vapor Phase of Electronic Nicotine Delivery Systems Using Two Impactors

Open Access
|Sep 2023

Figures & Tables

Figure 1.

ELPI®+ custom dilution system consisting of two 3/8″ diameter Swagelock® stainless steel “Y”s with airflow connections.

Table 1.

ELPI®+ dilution system measurements and calculations.

ProductReplicateSet by mass flow controllerMeasuredCalculations
ELPI®+ flowrate (L/min)Zero air dilution (L/min)Laboratory air entering dilution system (L/min)Puff volume (cm3)Range of percent of puff sampled by ELPI®+ aPuff dilution ratio b
Mango 5.0% (nicotine by weight)19.8599.8290.03055.45.1 – 12.8329
29.8269.7920.03455.65.8 – 13.4289
39.8179.7940.02355.63.9 – 11.6427
49.9139.8900.02355.63.9 – 11.6431
59.9159.8780.03755.66.3 – 14.0268
69.9399.9110.02855.44.8 – 12.5355
Mean ± SD9.878 ± 0.0519.840 ± 0.0650.029 ± 0.00655.5 ± 0.16.0 ± 1.0 – 12.7 ± 1.0350 ± 68
Mint 5.0% (nicotine by weight)19.9129.9770.03555.46.0 – 13.7283
29.9529.9130.03955.46.7 – 14.3255
39.9629.9280.03455.55.8 – 13.5293
49.9599.9080.05155.28.7 – 16.5195
59.9619.9140.04755.68.0 – 15.6212
610.0249.9840.04055.66.8 – 14.5251
Mean ± SD9.962 ± 0.0369.937 ± 0.0340.041 ± 0.00755.5 ± 0.27.0 ± 1.1 – 14.7 ± 1.2248 ± 39

SD = standard deviation

a Range of percent of puff sampled = amount of laboratory air sampled over the 8 s exhaust of the pump with and without the 6 cm3 volume from the exhaust arm of dilution system divided by the total puff flow and multiplied by 1 minus aerosol deposition efficiency within the puffing machine piston. Measured aerosol deposition within the puffing machine piston was 29.045% so 1 minus deposition efficiency = 70.955 % of the puff aerosol mass was available for sampling.

b Ratio of ELPI®+ flowrate set by mass flow controller (column 3) divided by measured amount of laboratory air entering the dilution system (column 5), which is also the amount of the puff that was sampled for the 8 s exhaust from the puffing machine.

Table 2.

Measurement of Particle Size Distribution and Recovery Efficiency Calculations.

ProductReplicateImpactor
Mini MOUDI™ELPI®+
MMAD (μm)GSDRecovery %MMAD (μm)GSDRecovery range (%) a
Mango 5.0% (nicotine by weight)10.831.4879.11.131.6962.9 – 157.0
20.901.5477.31.131.6959.8 – 138.6
30.781.4677.01.141.6751.3 – 152.2
4NPNPNP1.171.6753.3 – 158.1
5NPNPNP0.981.6659.4 – 132.4
6NPNPNP1.211.7254.6 – 142.6
Mean ± SD0.84 ± 0.061.49 ± 0.0477.8 ± 1.11.13 ± 0.081.68 ± 0.0256.8 ± 4.5 – 146.8 ± 10.5
Mint 5.0% (nicotine by weight)11.041.5079.81.041.6556.2 – 128.7
21.101.4079.30.961.5865.0 – 139.0
31.021.4882.91.091.6662.0 – 144.9
4NPNPNP0.811.6269.4 – 130.6
5NPNPNP0.851.6568.8 – 134.2
6NPNPNP1.071.6763.0 – 134.3
Mean ± SD1.05 ± 0.41.46 ± 0.0580.7 ± 1.90.97 ± 0.121.64 ± 0.0364.1 ± 4.9 – 135.3 ± 5.9

GSD = geometric standard deviation; MMAD = mass median aerodynamic diameter; NP = not performed; SD = standard deviation

a Based upon percent puff sampled range from Table 1.

Table 3.

Chemicals identified in impactor air blank samples.

Mini MOUDI™ELPI®+
QuantitativeSemi-quantitativeQuantitativeSemi-quantitative
ChemicalQuantity (ng)ChemicalQuantity (ng)ChemicalQuantity (μg)ChemicalQuantity (μg)
Acetone77Diethylene glycol100Acetone*5.9Propylene + propane0.3
Methylene chloride22C6-C8 Hydrocarbon230Methylene chloride *14Dichlorodifluoro methane0.1
Hexane11Acetic acid130Hexane1.4Isobutane0.2
Acetonitrile59Acetonitrile0.1Butane0.4
Ethylacetate7.8Ethylacetate0.05Acetaldehyde0.9
Carbon disulfide15Carbon Disulfide0.92-Methylbutane0.7
Ethanol0.4Trichlorofluoro methane0.4
Toluene0.1Pentane0.4
1,1,2-Trichloro-1,2,2-trifluoroethane0.09Isoprene0.4
Isopropanol1.23-Methylpentane0.3
Carbon tetrachloride0.042-Methyl-2-propenal0.2
Isopropylbenzene0.06Methylcyclopentane0.4
Cyclohexane0.02Butanal0.09
Isooctane0.3Methyl ethyl ketone0.1
Chloroform0.05Pentanal0.1
Benzene0.04Propylene glycol0.4
4-Methyl-2-pentanone0.006Hexanal0.2
m,p-Xylene0.03α-Pinene0.1
o-Xylene0.02Octanal0.1
1,2,4-Trimethylbenzene0.009Nonanal0.3
Ethylbenzene0.007Decanal0.4
Naphthalene0.006Undecanal0.1
Diethyl ether*5.9Tetradecane0.2
Dodecanal0.1
Pentadecane0.1
2-Dodecanone0.3
2-Tridecanone0.4
2,6-Ditertbutylphenol0.1
Siloxane0.1
C13-C15 Hydrocarbon0.1
C15-C17 Hydrocarbon0.1

* Value exceeded calibration range by more than a factor of 10.

Table 4.

Quantitative and semi-quantitative analysis of vapor phase constituents from the Mini MOUDI™ Impactor. Unless otherwise noted chemicals listed were found in all three replicate samples.

ProductChemicalCAS #Amount (Mean ± SD)
Measured (μg/sorbent tube)Calculated for entire sampled volume (μg)Collected aerosol (μg/mg)
Quantitative analysis Mini MOUDI™
Mango 5.0% (nicotine by weight)Total amount aNA65.5 ± 21.11310 ± 42277.6 ± 25.0
Ethanol64-17-538.2 ± 13.3764 ± 26645.2 ± 15.8
Isopropanol67-63-00.076 ± 0.0151.52 ± 0.30.09 ± 0.02
Toluene108-88-30.007 ± 0.0010.14 ± 0.020.008 ± 0.001
Mint 5.0% (nicotine by weight)Total amount aNA34.8 ± 23.6696 ± 47236.2 ± 24.5
Ethanol b64-17-50.051.00.05
Isopropanol c67-63-00.08 ± 0.021.6 ± 0.40.08 ± 0.02
p-Isopropyltoluene c99-87-60.007 ± 0.0010.14 ± 0.020.14 ± 0.02
Benzene b71-43-20.0080.160.008
Toluene b108-88-30.0080.160.008
m,p-Xylene b108-38-3 or 106-42-30.020.40.02
Semi-quantitative analysis Mini MOUDI™
Mango 5.0% (nicotine by weight)Propylene glycol57-55-627.5 ± 11.9550 ± 23832.6 ± 14.1
Nicotine54-11-50.17 ± 0.123.4 ± 2.40.2 ± 0.1
Menthol89-78-1 or 1490-04-60.098 ± 0.0041.96 ± 0.080.116 ± 0.005
Acetaldehyde75-07-00.83 ± 0.1216.6 ± 2.40.98 ± 0.14
Ethylbutyrate105-54-40.35 ± 0.17.0 ± 2.00.41 ± 0.12
Methylcyclopentane c96-37-70.145 ± 0.0782.90 ± 1.560.17 ± 0.09
Limonene or d-limonene138-86-3 or 5989-27-50.182 ± 0.0453.64 ± 0.90.22 ± 0.05
Decanalc112-31-20.15 ± 0.063.0 ± 1.20.18 ± 0.07
3-Methylpentane b96-14-00.24.00.24
Linalool c78-70-60.09 ± 0.011.8 ± 0.20.11 ± 0.01
Nonanal b124-19-60.091.80.11
3-Hexen-1-ol544-12-70.53 ± 0.1810.6 ± 3.60.62 ± 0.21
Allyl hexanoate b123-68-20.088 ± 0.0131.76 ± 0.260.1 ± 0.02
2-Methyl-4-phenyl-1H-imidazole b13739-48-50.043 ± 0.0120.86 ± 0.240.051 ± 0.014
Mint 5.0% (nicotine by weight)*Propylene glycol57-55-620.1 ± 16.8402 ± 33620.9 ± 17.5
Nicotine c54-11-50.15 ± 0.133.0 ± 2.60.16 ± 0.14
Acetol c116-09-60.070.05 – 0.090.003 – 0.005
Acetaldehyde b75-07-00.81.60.083
3-Octanol b589-98-00.051.00.052
Decanal c112-31-20.2 ± 0.14.0 ± 2.00.21 ± 0.1
Eucalyptol c470-82-60.28 ± 0.15.6 ± 2.00.29 ± 0.1
Menthone c89-80-50.67 ± 0.3913.4 ± 7.80.7 ± 0.4
Menthol c89-78-1 or 1490-04-65.4 ± 3.5108 ± 705.6 ± 3.6
Menthyl acetate c89-48-50.11 ± 0.062.2 ± 1.20.11 ± 0.06
Benzyl alcohol c100-51-60.09 ± 0.011.8 ± 0.20.094 ± 0.01
Nonanal b124-19-60.36.00.3
1,1-Difluorethane75-37-64.00.09 – 8.00.005 – 0.42
2-Methyl-4-phenyl-1H-imidazole c13739-48-50.0450.04 – 0.050.002 – 0.003
Nerylacetone b3879-26-30.091.80.09

NA = not available; SD = standard deviation

* C6-C8 and C9-C11 hydrocarbons found.

a Calculated based upon internal standard, summation of individual chemical levels will not match due to semi-quantitative analysis.

b Found in one of three samples.

c Found in two of three samples (mean ± range).

Table 5.

Quantitative and semi-quantitative analysis of vapor phase constituents from the ELPI®+ Impactor. Unless otherwise noted chemicals listed were found in all six replicate samples.

ProductChemicalCAS #Mean ± SD (μg/collection)Collected aerosol (μg/mg)
Quantitative analysis ELPI®+
Mango 5.0% (nicotine by weight)Total amount aNA9.5 ± 2.90.07 ± 0.03
1,3-Butadiene b106-99-00.020.00014
Tetrahydrofuran109-99-90.0147 ± 0.00060.0001 ± 0.000004
2-Methyl-1-propanol c78-83-10.0009 ± 0.00010.000006 ± 0.0000007
Methyl tertiary butyl ether f1634-04-40.021 ± 0.0270.00015 ± 0.00019
trans 1,2-Dichloroethene c156-60-50.007 ± 0.0010.00005 ± 0.000007
1,2-Dichloroethane b107-06-20.0065 ± 0.00050.000046 ± 0.000035
Bromodichloromethane b75-27-40.0070.00005
Styrene b100-42-50.0050.000035
Bromoform b75-25-20.0090.00006
1,3,5-Trimethylbenzene b108-67-80.0060.000043
p-Isopropyltoluene b99-87-60.0050.000035
Ethylmethacrylate c97-63-20.006 ± 0.0020.0000436 ± 0.000014
Trichloroethene b79-01-20.0070.00005
Mint 5.0% (nicotine by weight)Total amount aNA15.5 ± 7.60.21 ± 0.1
1,3-Butadiene b106-99-00.030.0004
Tetrahydrofuran109-99-90.023 ± 0.0140.0003 ± 0.0002
trans 1,2-Dichloroethene c156-60-50.014 ± 0.0060.0002 ± 0.00008
Styrene b100-42-50.0090.00012
1,3,5-Trimethylbenzene b108-67-80.0050.000067
p-Isopropyltoluene99-87-60.027 ± 0.0050.00036 ± 0.000067
Tetrachloroethene c127-18-40.0135 ± 0.00650.00018 ± 0.000087
Diethyl ether b60-29-70.060.0008
Naphthalene c91-20-30.0075 ± 0.00050.0001 ± 0.000007
1,2-Dichloroethane b107-06-20.0080.00011
Bromodichloromethane b75-27-40.0070.00009
Semi-quantitative analysis ELPI®+
Mango 5.0% (nicotine by weight) f2-Methyl-1-propene b115-11-70.10.0007
1-Propanol b71-23-80.30.002
Menthol89-78-1 or 1490-04-61.08 ± 0.460.008 ± 0.003
Menthone f89-80-50.138 ± 0.0570.001 ± 0.0002
Ethylbutyrate105-54-42.62 ± 1.580.02 ± 0.1
Limonene or d-limonene138-86-3 or 5989-27-50.3 ± 0.170.002 ± 0.001
Decanoic acid e334-48-50.1 ± 0.00.0007 ± 0.0
Noanaoic acid e112-05-00.125 ± 0.050.0009 ± 0.0004
2-Pentanone107-87-90.182 ± 0.0780.001 ± 0.0006
Propanal e123-38-60.15 ± 0.060.001 ± 0.0004
2-Methylpentane e107-83-50.12 ± 0.050.0009 ± 0.0004
tert-Butanol b75-65-00.10.0007
Methyl vinyl ketone d78-94-40.17 ± 0.060.001 ± 0.0004
4-Methyloctane2216-34-40.1 ± 0.00.0007 ± 0.0
Heptanal111-71-70.183 ± 0.0750.0013 ± 0.0005
Ethylhexanoate e123-66-00.125 ± 0.050.0009 ± 0.0004
Acetic acid b64-19-70.10.0007
Diethylene glycol c11-46-60.15 ± 0.050.001 ± 0.0004
3-Methylbutanol b590-86-30.090.0006
Hexamethylchclotrisiloxane c541-05-90.1 ± 0.00.0007 ± 0.0
Mint 5.0% (nicotine by weight) fLimonene or d-limonene c138-86-3 or 5989-27-50.2 ± 0.00.0027 ± 0.0
Heptane b142-82-50.095 ± 0.0050.001 ± 0.0001
Propanal b123-38-60.10.001
Menthol89-78-1 or 1490-04-66.25 ± 3.710.084 ± 0.05
Menthone89-80-51.82 ± 0.780.024 ± 0.01
Eucalyptol470-82-60.72 ± 0.190.01 ± 0.003
Benzaldehyde c100-52-70.15 ± 0.050.002 ± 0.0007
4-methyloctane e2216-34-40.2 ± 0.00.003 ± 0.0
2-Methyl-1-propene d115-11-70.17 ± 0.120.0023 ± 0.0016
Trimethylsilanol d1066-40-60.1 ± 0.00.001 ± 0.0
2-Methylpentane c107-83-50.2 ± 0.140.003 ± 0.002
tert-Butanol e75-65-00.15 ± 0.060.002 ± 0.0008
Methyl vinyl ketone d78-94-40.2 ± 0.10.003 ± 0.001
2-Pentanone107-87-90.2 ± 0.10.003 ± 0.001
Heptanal e111-71-70.3 ± 0.20.004 ± 0.003
Acetic acid e64-19-70.12 ± 0.50.002 ± 0.007
Hexamethylchclotrisiloxane d541-05-90.097 ± 0.0060.013 ± 0.0001
Chlorodifluormethane b75-45-60.10.001
1,1-Difluoroethane b75-37-60.40.005
Nonanoic acid c112-05-00.45 ± 0.150.006 ± 0.002
2-Methyl-2-propenal b78-85-30.40.005
2-Hexanone b591-52-40.10.001
Pentanoic acid b109-52-40.10.001
3-Octanol b589-98-00.20.003
Heptanoic acid b111-14-80.10.001
Triacetin b102-76-10.10.001

NA = not available; SD = standard deviation

a Calculated based upon internal standard, summation of individual chemical levels will not match due to semi-quantitative analysis.

b Found in one of six samples.

c Found in two of six samples (mean ± range).

d Found in three of six samples.

e Found in four of six samples.

f Found in five of six samples.

g Numerous unidentified hydrocarbons with various number of carbon atoms (C6-C8, C7-C9, C8-C10, C9-C11, C10-C12, C12-C14, C13-C15, C14-C16, and C15-C17) and siloxanes.

Table 6.

Collection efficiency calculated including the measured vapor phase.

ImpactorParameterMango 5.0% (nicotine by weight)Mint 5.0% (nicotine by weight)
Replicate 1Replicate 2Replicate 3Replicate 1Replicate 2Replicate 3
Mini MOUDIDevice mass loss (mg)20.6023.3017.4023.8022.2023.40
Mass collected (mg)*16.3018.0013.4019.0017.6019.40
Calculated mass of volatiles (mg)1.080.621.240.680.080.96
Recovery efficiency (%) a84.479.984.182.779.687.0
Mango 5.0% (nicotine by weight)
Replicate 1Replicate 2Replicate 3Replicate 4Replicate 5Replicate 6
ELPI®+Device mass loss (mg)116.8122.0185.5201.265.1155.4
Mass collected (mg)*73.4 – 183.472.9 – 169.195.1 – 282.4107.2 – 318.238.1 – 86.284.8 – 221.6
Calculated mass range of volatiles (mg)0.06 – 0.160.04 – 0.10.07 – 0.210.12 – 0.360.09 – 0.190.07 – 0.19
Recovery efficiency range (%)62.9 – 157.259.8 – 138.751.3 – 152.453.3 – 158.358.7 – 132.754.6 – 142.7
Mint 5.0% (nicotine by weight)
Replicate 1Replicate 2Replicate 3Replicate 4Replicate 5Replicate 6
Device mass loss (mg)96.571.9113.734.243.489.1
Mass collected (mg)*54.3 – 124.246.8 – 99.970.5 – 164.723.7 – 45.029.9 – 58.356.1 – 119.7
Calculated mass range of volatiles (mg)0.06 – 0.130.10 – 0.210.14 – 0.330.06 – 0.110.08 – 0.160.20 – 0.43
Recovery efficiency range (%)56.3 – 128.865.1 – 139.267.2 – 145.169.5 – 131.969.1 – 134.763.2 – 134.8

* Measured on each stage and final filter of Mini MOUDI™ and only on each stage of ELPI®+ based upon percent of puff sampled.

a Revised mean collection efficiency including calculated volatiles for Mango 5.0% = 84.5 ± 3.2% and for Mint 5.0% = 81.6 ± 7.7%.

Figure 2.

Correlation of ELPI®+ measured MMAD and puff dilution ratio (values from Tables 1 and 2).

DOI: https://doi.org/10.2478/cttr-2023-0012 | Journal eISSN: 2719-9509 (formerly 1612-9237)
Language: English, French, German
Page range: 113 - 126
Submitted on: Apr 7, 2023
Accepted on: Aug 17, 2023
Published on: Sep 28, 2023
Published by: Beiträge zur Tabakforschung GmbH
In partnership with: Paradigm Publishing Services

© 2023 Michael J. Oldham, Lena Jeong, Adam Ozvald, I. Gene Gillman, published by Beiträge zur Tabakforschung GmbH
This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License.