Aerosols in Northern Morocco-2: Chemical Characterization and PMF Source Apportionment of Ambient PM2.5

被引:11
|
作者
Benchrif, Abdelfettah [1 ,2 ]
Tahri, Mounia [1 ]
Guinot, Benjamin [3 ]
Chakir, El Mahjoub [2 ]
Zahry, Fatiha [1 ]
Bagdhad, Bouamar [4 ]
Bounakhla, Moussa [1 ]
Cachier, Helene [5 ]
Costabile, Francesca [6 ]
机构
[1] Natl Ctr Nucl Energy Sci & Technol CNESTEN, Rabat 10000, Morocco
[2] Ibn Tofail Univ, Fac Sci, Kenitra 14000, Morocco
[3] Univ Toulouse, Lab Aerol, UPS, CNRS, F-314000 Toulouse, France
[4] Inst Agron & Vet, Rabat 10000, Morocco
[5] Lab Sci Climat & Environm, F-91190 Gif Sur Yvette, France
[6] CNR, Inst Atmospher Sci & Climate, I-00133 Rome, Italy
关键词
urban aerosols; PM2; 5; chemical characterization; source apportionment; southwestern Mediterranean area; northern Morocco; POSITIVE MATRIX FACTORIZATION; LONG-RANGE TRANSPORT; MASS CLOSURE; PARTICULATE MATTER; ESTIMATING UNCERTAINTY; SEASONAL-VARIATIONS; BACKGROUND SITES; URBAN; PARTICLES; PM10;
D O I
10.3390/atmos13101701
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Insufficient data on the chemical composition of PM2.5 and its emission sources in the southwestern (SW) Mediterranean area has been identified. Ambient PM2.5 samples were collected in an urban area of Tetouan city, northern Morocco. Chemical mass closure calculations and positive matrix factorization were performed for the comprehensive dataset of PM2.5 chemical analyses. Mass closure improved when multipliers (1.2 and 0.23, respectively) were used for the conversion of organic carbon (OC) and calcium ion (Ca2+) into particulate organic matter (POM) and mineral dust masses, respectively. The mass closure model performed well in this SW Mediterranean region, with a significant correlation (r(2) = 0.97) obtained between gravimetrically measured and chemically determined PM2.5 mass. The one-year average concentration of PM2.5 was 17.96 mu g/m(3), and the major chemical components were POM (34%), secondary inorganic aerosol (SIA) (28%), and black carbon (18%), while unidentified mass was 4%. The mass concentration and most of the chemical components of PM2.5 showed clear seasonal variations, with a summer-high and winter-low pattern for SIA, dust, and BC. In the winter months, POM was the dominant component. Source apportionment analysis revealed that PM2.5 emission sources, regarding their typical tracers, were ammonium sulfate (SO42-, NH4+, K+, NO3-), road traffic and biomass burning emissions (OC, BC), fresh sea salt (Cl-, K+, NO3-), aged sea salt (Mg2+, Na+, Ca2+), and oxalate-rich (oxalate, NO3-) factors. Further, it is hoped that these findings help to improve the scientific understanding of SW Mediterranean aerosols.
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页数:21
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