{"id":82631,"date":"2024-04-06T01:08:56","date_gmt":"2024-04-05T23:08:56","guid":{"rendered":"https:\/\/obera.fr\/our-advice\/composes-organiques-volatiles-cov-impacts-gestion-industrie\/"},"modified":"2025-12-08T13:22:19","modified_gmt":"2025-12-08T11:22:19","slug":"composes-organiques-volatiles-cov-impacts-gestion-industrie","status":"publish","type":"post","link":"https:\/\/obera.fr\/en\/our-tips\/composes-organiques-volatiles-cov-impacts-gestion-industrie\/","title":{"rendered":"Volatile Organic Compounds (VOCs): Impacts and Management in Industry"},"content":{"rendered":"\n<p>On an industrial site, Volatile Organic Compounds, VOCs, <strong>are among the ambient air pollutants<\/strong>, both indoor and outdoor. The term VOC encompasses a multitude of chemical substances. <\/p>\n\n<p>What do they have in common? They are composed of carbon and hydrogen, and under ambient conditions, they are either in a gaseous phase or in a liquid phase that will easily evaporate. VOCs impact air quality with consequences for <a href=\"https:\/\/obera.fr\/sante\/\">human health<\/a>, the environment, and the economy. They are therefore subject to an official definition at the European level, which is then transposed nationally. Understanding the physicochemical properties of VOCs helps in taking appropriate preventive measures. Here is a <strong>quick overview<\/strong> that will familiarize you with the physical and chemical characteristics of VOCs that impact air quality.     <\/p>\n\n<h2 class=\"wp-block-heading\">Regulatory definition of VOCs<\/h2>\n\n<figure class=\"wp-block-image alignright size-large is-resized\"><img decoding=\"async\" width=\"1024\" height=\"1024\" src=\"https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1-1024x1024.jpg\" alt=\"design sans titre 8 1\" class=\"wp-image-30144\" style=\"width:382px;height:auto\" srcset=\"https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1-1024x1024.jpg 1024w, https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1-300x300.jpg 300w, https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1-150x150.jpg 150w, https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1-768x768.jpg 768w, https:\/\/obera.fr\/wp-content\/uploads\/2024\/04\/design-sans-titre-8-1.jpg 1200w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n\n<p>Article 2, \u00a716 and \u00a717 of Council Directive 1999\/13\/EC of March 11, 1999 on &#8221; <em>the limitation of emissions of volatile organic compounds due to the<a href=\"https:\/\/obera.fr\/en\/our-tips\/cov-aspiration-vapeurs-solvants\/\">use of organic solvents <\/a>in certain activities and installations<\/em> &#8221; gives the following two definitions:<\/p>\n\n<p><strong>Organic compound:<\/strong> &#8220;any compound which, excluding methane, contains carbon and hydrogen, which can be substituted by other atoms such as halogens (<em>e.g., fluorine, chlorine, bromine, iodine),<\/em> oxygen, sulfur, nitrogen, or phosphorus, with the exception of carbon oxides (<em>e.g., CO<\/em><em><sub>2<\/sub><\/em>) and carbonates (<em>e.g.: CO<\/em><em><sub>3<\/sub><\/em><em><sup>2-<\/sup><\/em>) and bicarbonates<em>(e.g. HCO<\/em><em><sub>3<\/sub><\/em><em><sup>&#8211;<\/sup><\/em>) <strong>.<\/strong> &#8221;  <\/p>\n\n<p><strong>Volatile organic compound (VOC) <\/strong>: any organic compound having a vapour pressure of 0.01 kPa or more at a temperature of 293.15 K<em>(20\u00b0C)<\/em> or having a corresponding volatility under the particular conditions of use.<\/p>\n\n<p>The directive has been transposed into French law in the Environmental Code, article R224-48. It defines a VOC as &#8220;any organic compound whose initial boiling point, measured at a standard pressure of 101.3 kPa, is less than or equal to 250\u00b0C.&#8221;<\/p>\n\n<h2 class=\"wp-block-heading\">Volatile? Yes, but to varying degrees! Physical Classification of VOCs<\/h2>\n\n<p>To understand the <strong>extent of VOC emissions<\/strong> degrading <a href=\"https:\/\/obera.fr\/en\/recycling-en\/\">ambient air quality<\/a>, we seek to determine their concentration. To do this, we rely on a physical characteristic: volatility. <\/p>\n\n<p>Volatility is the ability of a substance to evaporate at ambient temperature and pressure.  <\/p>\n\n<p>VOCs are volatile, but to varying degrees. Since the volatility of a VOC depends on its vapor pressure, the effective saturation concentration ???????? (in \u00b5g.m<sup>-3<\/sup>) can be used as a <strong>classification criterion<\/strong>. Furthermore, volatility decreases as the molecular weight of the VOC increases. VOCs can also be classified according to the number of carbon atoms in their structure. <\/p>\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>volatility to non-volatility<\/strong><\/td><td><strong>no. of carbon atoms<\/strong><\/td><td><strong>effective saturation concentration <\/strong><strong>????????<\/strong><\/td><\/tr><tr><td>VOC Very volatile to volatile<\/td><td>nb C \u2264 11<\/td><td>???????? &gt; <sup>106 \u03bcg <\/sup>.<sup>m-3<\/sup><\/td><\/tr><tr><td>VOC-IVolatility Intermediate<\/td><td>12 \u2264 nb C \u2264 18<\/td><td><sup>103<\/sup> \u03bcg.<sup>m-3<\/sup> &lt;???????? \u2264<sup>106<\/sup> \u03bcg.<sup>m-3<\/sup><\/td><\/tr><tr><td>COSVSemi Volatil<\/td><td>18 &lt; nb C \u2264 32<\/td><td><sup>10-1<\/sup> \u03bcg.<sup>m-3<\/sup> &lt;???????? \u2264<sup>103<\/sup> \u03bcg.<sup>m-3<\/sup><\/td><\/tr><tr><td>CONV Non-volatile at room temperature (particle)<\/td><td>nb C &gt; 32<\/td><td>???????? &lt; <sup> 10-1<\/sup> \u03bcg.<sup>m-3<\/sup><\/td><\/tr><\/tbody><\/table><\/figure>\n\n<p>Note that non-volatile organic compounds at room temperature (CONV) will evaporate under specific conditions of use, <a href=\"https:\/\/obera.fr\/en\/our-tips\/cov-processus-industriels-quelle-strategie-attenuation\/\">linked to industrial processes<\/a>, or in the event of an accident (fire, explosion).<\/p>\n\n<p>Another classification of VOCs takes boiling temperature as a criterion.  <\/p>\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>Volatility  <\/strong><\/td><td><strong>Boiling temperature<\/strong><\/td><\/tr><tr><td>Highly volatile  <\/td><td>&lt; (50 &#8211; 100 \u00b0C)<\/td><\/tr><tr><td>Volatile<\/td><td>(50 &#8211; 100 \u00b0C) to (240 &#8211; 260 \u00b0C)<\/td><\/tr><tr><td>Semi-volatile  <\/td><td>(240 &#8211; 260 \u00b0C) to (380 &#8211; 400 \u00b0C)<\/td><\/tr><\/tbody><\/table><\/figure>\n\n<h2 class=\"wp-block-heading\">VOCs and odors<\/h2>\n\n<p>Some VOCs are odorless (butane, propane). Other VOCs may have more or less characteristic odors. Sulfur compounds, amines, oxygenated compounds (ketones, aldehydes), and certain aromatic compounds are particularly odorous. <\/p>\n\n<h2 class=\"wp-block-heading\">Classification of VOCs by chemical structure<\/h2>\n\n<p><strong>VOCs constitute a vast class of chemical compounds<\/strong>, exhibiting a wide diversity of structures and properties. It is their common impact as air, water, and soil pollutants that groups them into this class. However, their structures, particularly the presence of atomic groups other than C and H, influence their chemical properties, and thus on the <strong>specific nature of their toxicity<\/strong> for humans and nature; and consequently, on the resulting economic effects. <\/p>\n\n<h3 class=\"wp-block-heading\">VOC structural criteria<\/h3>\n\n<p>VOCs are distinguished according to several non-exclusive structural criteria, each contributing to the nature and degree of their polluting properties:  <\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>cyclic<\/strong><em>(chain of carbon atoms closing in a circle<\/em>) versus <strong>non-cyclic<\/strong><em>(non-closed carbon chain,<\/em> <em>C atoms link together in a linear fashion<\/em>);<\/li>\n\n\n\n<li><strong>aromatic<\/strong><em>(a specific hexagonal carbon chain, called a benzene ring, composed of 6 carbon atoms each linked to a hydrogen atom<\/em>) versus <strong>non-aromatic<\/strong><em>(a chain without this special configuration<\/em>);  <\/li>\n\n\n\n<li><strong>monocyclic<\/strong><em>(a single cyclic carbon chain<\/em>) versus <strong>polycyclic<\/strong><em>(several identical rings linked by one or two carbon atoms in common<\/em>)<\/li>\n\n\n\n<li><strong>homocyclic<\/strong><em>(a ring formed solely of C<\/em>) versus <strong>heterocyclic<\/strong><em>(a ring containing carbon and other carbon-substituting atoms<\/em>);<\/li>\n\n\n\n<li><strong>saturated<\/strong> (<em>presence only of<\/em> <em>single carbon bonds<\/em>) versus <strong>unsaturated<\/strong> (<em>double or triple carbon bonds<\/em>). Unsaturation confers increased reactivity to VOCs, impacting their toxicity. Aromatic structures are all unsaturated.<\/li>\n\n\n\n<li><strong>unbranched <\/strong>versus<strong> branched<\/strong><em>(the main carbon chain has one or more branches formed either from groups of C and H atoms alone, or incorporating other atoms which then give them a characteristic reactivity [functional group])<\/em>.  <\/li>\n<\/ul>\n\n<h3 class=\"wp-block-heading\">VOC classification<\/h3>\n\n<p>There are two main categories of VOCs: <strong>aromatic VOCs<\/strong> and <strong>aliphatic<\/strong> (= non-aromatic) <strong>VOCs<\/strong>.  <\/p>\n\n<p><strong>Aromatic<\/strong> VOCs have a benzene <strong>ring<\/strong> (= benzene ring) as their basic skeleton. They are divided into several subcategories:<\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong> Monocyclic<\/strong> Aromatic Hydrocarbons, including BTEX (short for Benzene, Toluene, Ethylbenzene, Xylene), all of which are toxic and ecotoxic.<\/li>\n\n\n\n<li>Polycyclic <strong>Aromatic<\/strong> Hydrocarbons (PAHs) with carcinogenic properties. They are synthesized during the <a href=\"https:\/\/obera.fr\/en\/chemicals-petrochemicals-para-chemicals\/\">formation of fossil fuels<\/a> (petroleum, coal) or during the incomplete combustion of organic matter (fuel heating, forest fires, etc.). <\/li>\n\n\n\n<li>aromatic <strong>heterocyclic<\/strong> compounds, or aromatic heterocycles, in which one or more C atoms of the benzene ring are substituted by other atoms (or groups of atoms) such as those listed in the above definition.  <\/li>\n<\/ul>\n\n<p><strong>Aliphatic <\/strong> VOCs (=<strong> non-aromatic<\/strong> VOCs) include molecules with :<\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>saturated<\/strong>: <strong>alkanes<\/strong>; example: hexane C<sub>6<\/sub>H<sub>14<\/sub>, which is used in glues, adhesives, degreasing liquids, and is present in gasoline vapors. It can enter the body through respiratory and percutaneous routes. Its effects by inhalation range from dizziness to loss of consciousness. Skin contact causes dermatitis.<\/li>\n\n\n\n<li><strong>insatur\u00e9e<\/strong> aux propri\u00e9t\u00e9s plus polluantes&nbsp;:\n<ul class=\"wp-block-list\">\n<li><strong>alkenes<\/strong> (double carbon bond); example: ethylene C<sub>2<\/sub>H<sub>4<\/sub>, released by most fruits and vegetables as a ripening agent, emitted by exhaust pipes, propane forklifts, and plastic bags under the action of light. By inhalation, it can cause dizziness, headache, loss of consciousness, and contributes to the greenhouse effect; <\/li>\n\n\n\n<li><strong>alkynes<\/strong> (triple carbon bond); example: ethyne or acetylene<sub>C2H2<\/sub><sub>; <\/sub><sub> <\/sub> extremely flammable and explosive, it is used as a fuel for welding or in certain analysis equipment.<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n<p><strong>Alkanes, alkenes and alkynes<\/strong> also incorporate :  <\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>non-cycliques,<\/strong> les <strong>aliphatiques acycliques<\/strong>, qui sont constitu\u00e9es de cha\u00eenes&nbsp;:\n<ul class=\"wp-block-list\">\n<li>either linear. Example: <em>n<\/em>-hexane.<\/li>\n\n\n\n<li>or branched.  <\/li>\n<\/ul>\n<\/li>\n\n\n\n<li><strong>cycliques (<\/strong>cycles non-aromatiques<strong>)<\/strong>, les <strong>alicycliques<\/strong> (= <strong>ali<\/strong>phatiques <strong>cycliques<\/strong>)&nbsp;: cycloalcanes, cycloalc\u00e8nes, cycloalcynes.\n<ul class=\"wp-block-list\">\n<li>Molecules can comprise several cycles\n<ul class=\"wp-block-list\">\n<li>either linked by 2 common carbon atoms; example: polycyclic cycloalkanes<\/li>\n\n\n\n<li>or linked by 1 common carbon atom: spirans.  <\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>The ring can include atoms other than carbon (heterocycle)  <\/li>\n\n\n\n<li>A ring can bear a branch. For example, methylcyclohexane (C<sub>6<\/sub>H<sub>11<\/sub>CH<sub>3<\/sub>), used as a base for organic synthesis, a solvent for ethers and cellulose, and <a href=\"https:\/\/obera.fr\/en\/aeronautics\/\">aviation fuel<\/a>. It can irritate the respiratory tract, central nervous system, skin, and eyes.  <\/li>\n<\/ul>\n<\/li>\n<\/ul>\n\n<p>If the <strong>aliphatic or aromatic structure<\/strong> has a branch identified as a functional group (a group of atoms that gives it distinctive chemical properties), such as certain alkane derivatives or some PAHs, for example, the VOC will specifically impact <a href=\"https:\/\/obera.fr\/en\/our-tips\/quels-procedes-ameliorent-qualite-air-eliminant-cov\/\">air quality<\/a>. VOCs are then classified into a particular family:<\/p>\n\n<ul class=\"wp-block-list\">\n<li>Halogenated VOCs, e.g. chloromethane CH\u2083Cl  <\/li>\n\n\n\n<li>Sulfur VOCs, e.g., \u03b2-mercaptoethanol C<sub>2<\/sub>H<sub>6<\/sub>OS, <\/li>\n\n\n\n<li>COV oxyg\u00e9n\u00e9s dont des&nbsp;:\n<ul class=\"wp-block-list\">\n<li>Alcohol VOCs, e.g., ethylene glycol C<sub>2<\/sub>H<sub>6<\/sub>O<sub>2<\/sub>; used as antifreeze, solvent, brake fluids, dyes&#8230; Its inhalation causes cough and headache, its ingestion causes abdominal pain, nausea<\/li>\n\n\n\n<li>Ketone VOCs, e.g., acetone C<sub>3<\/sub>H<sub>6<\/sub>O, a solvent used in the paint, lacquer, rubber, and plastics industries&#8230; Highly volatile, it can be inhaled in large quantities when its concentration in the air is high. It can enter the bloodstream via the lungs and spread throughout the body. Symptoms range from nasal irritation to central nervous system depression.<\/li>\n\n\n\n<li>VOC aldehydes, e.g. <sub>CH2O<\/sub>formaldehyde, emitted to a greater or lesser extent in all industrial sectors and recognized as a carcinogen.<\/li>\n\n\n\n<li>Ether VOCs, e.g., ethylene glycol n-butyl ether (<em>EGBE<\/em>) C<sub>6<\/sub>H<sub>14<\/sub>O<sub>2<\/sub>,<\/li>\n\n\n\n<li>Ester VOCs, e.g., methyl acetate C<sub>3<\/sub>H<sub>6<\/sub>O<sub>2<\/sub>. <\/li>\n<\/ul>\n<\/li>\n\n\n\n<li>Nitrated VOCs, e.g., nitroethane C<sub>2<\/sub>H<sub>5<\/sub>NO<sub>2<\/sub>, irritating to the respiratory tract, it can alter blood, and cause convulsions. <\/li>\n\n\n\n<li>Amino VOCs, e.g. aniline, which adsorb easily to work clothes, walls, machines and worktops.<\/li>\n<\/ul>\n\n<p><strong>Several thousand substances meet the definition of VOCs<\/strong>. They affect air quality in all industrial sectors. Understanding their nature helps to comprehend how they react with gases and dust present in the air of an industrial site. Appropriate preventive measures will thus be taken based on their chemical composition, particularly regarding source capture, filtration, and treatment.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>On an industrial site, Volatile Organic Compounds, or VOCs, are part of the ambient air pollutants, both indoors and outdoors. The term VOC covers a multitude of chemical substances.   <\/p>\n","protected":false},"author":4,"featured_media":81985,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_seopress_robots_primary_cat":"none","_seopress_titles_title":"Volatile Organic Compounds (VOCs): Impacts and Management","_seopress_titles_desc":"On an industrial site, Volatile Organic Compounds, or VOCs, are part of the ambient air pollutants, both indoors and outdoors. The term VOC covers a multitude of chemical substances. 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