Methyl halides (CHCl, CHBr, and CHI) are ozone-depleting substances. Biomass burning (BB) is an important source of methyl halides. The temporal variations and global spatial distribution of BB methyl halide emissions are unclear. Thus, global methyl halide emissions from BB during 2003-2021 were estimated based on satellite data. A significant decreasing trend ( < 0.01) in global methyl halide emissions from BB was found between 2003 and 2021, with CHCl emissions decreasing from 302 to 220 Gg yr, CHBr emissions decreasing from 16.5 to 11.7 Gg yr, and CHI emissions decreasing from 8.9 to 6.1 Gg yr. From a latitudinal perspective, the northern high-latitude region (60-90° N) was the only latitude zone with significant increases in BB methyl halide emissions ( < 0.01). Based on an analysis of the drivers of BB methyl halide emissions, emissions from cropland, grassland, and shrubland fires were more correlated with the burned area, while BB emissions from forest fires were more correlated with the emissions per unit burned area. The non-BB emissions of CHCl increased from 4749 Gg yr in 2003 to 4882 Gg yr in 2020, while those of CHBr decreased from 136 Gg yr in 2003 to 118 Gg yr in 2020 (global total CHI emissions are not available). The finding indicates that global CHCl and CHBr emissions from sources besides BB increased and decreased during 2003-2020. Based on our findings, not only searching for unknown sources is important, but also re-evaluating known sources is necessary for addressing methyl halide emissions.
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http://dx.doi.org/10.1016/j.ese.2022.100228 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
January 2025
Department of Chemistry, Taras Shevchenko National University of Kyiv, Volodymyrska str. 64/13, 01601 Kyiv, Ukraine.
The title compound, {(CHNO)[SnBr]} , is a layered hybrid perovskite crystallizing in the monoclinic space group 2/. The asymmetric unit consists of one HC-O-NH -CH cation (MeHA), one Sn atom located on a twofold rotation axis, and two Br atoms. The Sn atom has a distorted octa-hedral coordination environment formed by the bromido ligands.
View Article and Find Full Text PDFAdv Mater
January 2025
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan, 430070, P. R. China.
Effective modifications for the buried interface between self-assembled monolayers (SAMs) and perovskites are vital for the development of efficient, stable inverted perovskite solar cells (PSCs) and their tandem photovoltaics. Herein, an ionic-liquid-SAM hybrid strategy is developed to synergistically optimize the uniformity of SAMs and the crystallization of perovskites above. Specifically, an ionic liquid of 1-butyl-3-methyl-1H-imidazol-3-iumbis((trifluoromethyl)sulfonyl)amide (BMIMTFSI) is incorporated into the SAM solution, enabling reduced surface roughness, improved wettability, and a more evenly distributed surface potential of the SAM film.
View Article and Find Full Text PDFHeliyon
December 2024
Curia Wisconsin, Inc. D/B/A Siegfried Acceleration Hub, 870 Badger Circle, Grafton, WI, 53024, United States.
Primary and secondary alkyl iodides and primary alkyl bromides were quickly and conveniently converted into their corresponding alkyl chlorides via S2 halide-halide substitution. The resultant alkyl chlorides simultaneously demonstrated increased volatility and stability paired with standard headspace GC-FID methodology. The derivatization was performed on both standard and sample alike and occurred during the headspace oven equilibration phase, eliminating the extra reaction step traditionally performed during many derivatization analyses.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
October 2024
Department of Chemistry and Biochemistry Lamar University, 4400 MLK Blvd Beaumont Texas 77710 USA.
The mercury(II) halide complex [1,3-di--butyl-2,4-bis-(-butyl-amino)-1,3,2λ,4λ-di-aza-diphosphetidine-2,4-diselone-κ ,']di-iodido-mercury(II),-di-methyl-formamide monosolvate, [HgI(CHNPSe)]·CHNO or ()HgI, , containing -[( BuNH)(Se)P(μ-N Bu)P(Se)(NH Bu)] () was synthesized and structurally characterized. The crystal structure of confirms the chelation of chalcogen donors to HgI with a natural bite angle of 112.95 (2)°.
View Article and Find Full Text PDFOrg Lett
December 2024
College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China.
NHC boryl radical mediated halogen atom transfer (XAT) is useful in organic synthesis. Yet, most of the reaction ends only with reducing the halogen to hydrogen, that is, the C-X to C-H. This is especially dominant for electron-deficient alkyl halides, where the formed electrophilic radical reacts rapidly with NHC boranes.
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