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Taina Yli-Juuti

Bio: Taina Yli-Juuti is an academic researcher from University of Eastern Finland. The author has contributed to research in topics: Aerosol & Particle. The author has an hindex of 22, co-authored 56 publications receiving 2834 citations. Previous affiliations of Taina Yli-Juuti include Max Planck Society & University of Helsinki.


Papers
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Journal ArticleDOI
Joao Almeida1, Joao Almeida2, Siegfried Schobesberger3, Andreas Kürten2, Ismael K. Ortega3, Oona Kupiainen-Määttä3, Arnaud P. Praplan4, Alexey Adamov3, António Amorim5, F. Bianchi4, Martin Breitenlechner6, A. David1, Josef Dommen4, Neil M. Donahue7, Andrew J. Downard8, Eimear M. Dunne9, Jonathan Duplissy3, Sebastian Ehrhart2, Richard C. Flagan8, Alessandro Franchin3, Roberto Guida1, Jani Hakala3, Armin Hansel6, Martin Heinritzi6, Henning Henschel3, Tuija Jokinen3, Heikki Junninen3, Maija Kajos3, Juha Kangasluoma3, Helmi Keskinen10, Agnieszka Kupc11, Theo Kurtén3, Alexander N. Kvashin12, Ari Laaksonen10, Ari Laaksonen13, Katrianne Lehtipalo3, Markus Leiminger2, Johannes Leppä13, Ville Loukonen3, Vladimir Makhmutov12, Serge Mathot1, Matthew J. McGrath14, Tuomo Nieminen3, Tuomo Nieminen15, Tinja Olenius3, Antti Onnela1, Tuukka Petäjä3, Francesco Riccobono4, Ilona Riipinen16, Matti P. Rissanen3, Linda Rondo2, Taina Ruuskanen3, Filipe Duarte Santos5, Nina Sarnela3, Simon Schallhart3, R. Schnitzhofer6, John H. Seinfeld8, Mario Simon2, Mikko Sipilä15, Mikko Sipilä3, Yuri Stozhkov12, Frank Stratmann17, António Tomé5, Jasmin Tröstl4, Georgios Tsagkogeorgas17, Petri Vaattovaara10, Yrjö Viisanen13, Annele Virtanen10, Aron Vrtala11, Paul E. Wagner11, Ernest Weingartner4, Heike Wex17, Christina Williamson2, Daniela Wimmer2, Daniela Wimmer3, Penglin Ye7, Taina Yli-Juuti3, Kenneth S. Carslaw9, Markku Kulmala15, Markku Kulmala3, Joachim Curtius2, Urs Baltensperger4, Douglas R. Worsnop, Hanna Vehkamäki3, Jasper Kirkby1, Jasper Kirkby2 
17 Oct 2013-Nature
TL;DR: The results show that, in regions of the atmosphere near amine sources, both amines and sulphur dioxide should be considered when assessing the impact of anthropogenic activities on particle formation.
Abstract: Nucleation of aerosol particles from trace atmospheric vapours is thought to provide up to half of global cloud condensation nuclei(1). Aerosols can cause a net cooling of climate by scattering sun ...

738 citations

Journal ArticleDOI
TL;DR: In this paper, atmospheric aerosol particles influence global climate as well as impair air quality through their effects on atmospheric visibility and human health Ultrafine, which is a mixture of ozone and ultrafine.
Abstract: Atmospheric aerosol particles influence global climate as well as impair air quality through their effects on atmospheric visibility and human health Ultrafine (

357 citations

Journal ArticleDOI
TL;DR: In this paper, a synthesis of research indicates that the mechanisms controlling this growth depend on the size of the growing particle, and that dependence of particle growth mechanisms on particle size needs to be investigated more systematically.
Abstract: The growth of the smallest atmospheric particles to sizes at which they may act as seeds for cloud droplets is a key step linking aerosols to clouds and climate. A synthesis of research indicates that the mechanisms controlling this growth depend on the size of the growing particle. Aerosols have a strong, yet poorly quantified, effect on climate. The growth of the smallest atmospheric particles from diameters in the nanometre range to sizes at which they may act as seeds for cloud droplets is a key step linking aerosols to clouds and climate. In many environments, atmospheric nanoparticles grow by taking up organic compounds that are derived from biogenic hydrocarbon emissions. Several mechanisms may control this uptake. Condensation of low-volatility vapours and formation of organic salts probably dominate the very first steps of growth in particles close to 1 nm in diameter. As the particles grow further, formation of organic polymers and effects related to the phase of the particle probably become increasingly important. We suggest that dependence of particle growth mechanisms on particle size needs to be investigated more systematically.

320 citations

Journal ArticleDOI
TL;DR: Compounds with equilibrium vapor pressures in this range will exhibit the greatest sensitivities in terms of their gas to particle partitioning to uncertainties in their saturation vapor pressures, with consequent impacts on the ability of explicit and semiexplicit chemical models to simulate secondary organic aerosol formation.
Abstract: There are a number of techniques that can be used that differ in terms of whether they fundamentally probe the equilibrium and the temperature range over which they can be applied. The series of homologous, straight-chain dicarboxylic acids have received much attention over the past decade given their atmospheric relevance, commercial availability, and low saturation vapor pressures, thus making them ideal test compounds. Uncertainties in the solid-state saturation vapor pressures obtained from individual methodologies are typically on the order of 50-100%, but the differences between saturation vapor pressures obtained with different methods are approximately 1-4 orders of magnitude, with the spread tending to increase as the saturation vapor pressure decreases. Some of the dicarboxylic acids can exist with multiple solid-state structures that have distinct saturation vapor pressures. Furthermore, the samples on which measurements are performed may actually exist as amorphous subcooled liquids rather than solid crystalline compounds, again with consequences for the measured saturation vapor pressures, since the subcooled liquid phase will have a higher saturation vapor pressure than the crystalline solid phase. Compounds with equilibrium vapor pressures in this range will exhibit the greatest sensitivities in terms of their gas to particle partitioning to uncertainties in their saturation vapor pressures, with consequent impacts on the ability of explicit and semiexplicit chemical models to simulate secondary organic aerosol formation.

175 citations


Cited by
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01 Jan 2007
TL;DR: The Third edition of the Kirk-Othmer encyclopedia of chemical technology as mentioned in this paper was published in 1989, with the title "Kirk's Encyclopedia of Chemical Technology: Chemical Technology".
Abstract: 介绍了Kirk—Othmer Encyclopedia of Chemical Technology(化工技术百科全书)(第五版)电子图书网络版数据库,并对该数据库使用方法和检索途径作出了说明,且结合实例简单地介绍了该数据库的检索方法。

2,666 citations

Journal ArticleDOI
TL;DR: A copy of the Guangbo jiemu bao [Broadcast Program Report] was being passed from hand to hand among a group of young people eager to be the first to read the article introducing the program "What Is Revolutionary Love?".
Abstract: A copy of Guangbo jiemu bao [Broadcast Program Report] was being passed from hand to hand among a group of young people eager to be the first to read the article introducing the program "What Is Revolutionary Love?" It said: "… Young friends, you are certainly very concerned about this problem'. So, we would like you to meet the young women workers Meng Xiaoyu and Meng Yamei and the older cadre Miss Feng. They are the three leading characters in the short story ‘The Place of Love.’ Through the description of the love lives of these three, the story induces us to think deeply about two questions that merit further examination.

1,528 citations

Journal ArticleDOI
27 Feb 2014-Nature
TL;DR: It is found that a direct pathway leads from several biogenic VOCs, such as monoterpenes, to the formation of large amounts of extremely low-volatility vapours, helping to explain the discrepancy between the observed atmospheric burden of secondary organic aerosol and that reported by many model studies.
Abstract: Forests emit large quantities of volatile organic compounds (VOCs) to the atmosphere. Their condensable oxidation products can form secondary organic aerosol, a significant and ubiquitous component of atmospheric aerosol, which is known to affect the Earth's radiation balance by scattering solar radiation and by acting as cloud condensation nuclei. The quantitative assessment of such climate effects remains hampered by a number of factors, including an incomplete understanding of how biogenic VOCs contribute to the formation of atmospheric secondary organic aerosol. The growth of newly formed particles from sizes of less than three nanometres up to the sizes of cloud condensation nuclei (about one hundred nanometres) in many continental ecosystems requires abundant, essentially non-volatile organic vapours, but the sources and compositions of such vapours remain unknown. Here we investigate the oxidation of VOCs, in particular the terpene α-pinene, under atmospherically relevant conditions in chamber experiments. We find that a direct pathway leads from several biogenic VOCs, such as monoterpenes, to the formation of large amounts of extremely low-volatility vapours. These vapours form at significant mass yield in the gas phase and condense irreversibly onto aerosol surfaces to produce secondary organic aerosol, helping to explain the discrepancy between the observed atmospheric burden of secondary organic aerosol and that reported by many model studies. We further demonstrate how these low-volatility vapours can enhance, or even dominate, the formation and growth of aerosol particles over forested regions, providing a missing link between biogenic VOCs and their conversion to aerosol particles. Our findings could help to improve assessments of biosphere-aerosol-climate feedback mechanisms, and the air quality and climate effects of biogenic emissions generally.

1,340 citations

01 Dec 2006
TL;DR: This paper showed that reactive anthropogenic VOCs (AVOCs) produce much larger amounts of SOA than these models predict, even shortly after sunrise, and a significant fraction of the excess SOA is formed from first-generation AVOC oxidation products.
Abstract: [1] The atmospheric chemistry of volatile organic compounds (VOCs) in urban areas results in the formation of ‘photochemical smog’, including secondary organic aerosol (SOA). State-of-the-art SOA models parameterize the results of simulation chamber experiments that bracket the conditions found in the polluted urban atmosphere. Here we show that in the real urban atmosphere reactive anthropogenic VOCs (AVOCs) produce much larger amounts of SOA than these models predict, even shortly after sunrise. Contrary to current belief, a significant fraction of the excess SOA is formed from first-generation AVOC oxidation products. Global models deem AVOCs a very minor contributor to SOA compared to biogenic VOCs (BVOCs). If our results are extrapolated to other urban areas, AVOCs could be responsible for additional 3–25 Tg yr−1 SOA production globally, and cause up to −0.1 W m−2 additional top-of-the-atmosphere radiative cooling.

947 citations

Journal ArticleDOI
TL;DR: Nucleation and Growth of Nanoparticles in the Atmosphere Renyi Zhang,* Alexei Khalizov, Lin Wang, Min Hu, and Wen Xu.
Abstract: Nucleation and Growth of Nanoparticles in the Atmosphere Renyi Zhang,* Alexei Khalizov, Lin Wang, Min Hu, and Wen Xu Department of Atmospheric Sciences andDepartment of Chemistry, Center for Atmospheric Chemistry and Environment, Texas A&M University, College Station, Texas 77843, United States Department of Environmental Science & Engineering and Institute of Global Environment Change Research, Fudan University, Shanghai 200433, China State Key Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing, 100871, China

920 citations