Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aerosol formation, influence

A liquid release offers the potential for the formation of an aerosol (mist). Aerosol formation is influenced by mechanical force (acceleration) and fluid properties, such as the material s surface tension. Additionally, in some systems the pressure, because of static head, may be adequate to cause some aerosol formation and must be considered. Examples of liquid releases include an accidentally opened storage tank drain valve, a pipeline failure downstream of a pump, a damaged nozzle at the base of a liquid knockout drum, or the failure of a loading hose. [Pg.15]

An understanding of the influence that aerosols have on climate has become increasingly important over the last several decades [3]. Primary and secondary aerosols can affect the Earth s radiative balance by scattering and absorbing light directly and can act indirectly as cloud condensation nuclei and therefore influence the distribution, duration, precipitation processes, and radiative properties of clouds. Thus, developing the ability to understand, model, and predict aerosol formation with confidence is essential to determine the impact of aerosol radiative forcing in climate models. [Pg.434]

Aerosol droplet size is influenced by physical variables such as surface tension, viscosity, saturated vapour pressure and temperature. A decrease in the first three decreases droplet size. Because a decrease in temperature increases all three variables, it also increases the difficulty of aerosol formation. Droplet diameter is related to the US frequency [155] and other physical parameters by the following equation ... [Pg.185]

More simultaneous measurements of NH3 in the ocean and in the atmosphere are needed to reduce the considerable uncertainties of the ocean/atmosphere flux estimates. The ongoing acidification of the ocean will shift the NH3/NH4 equilibrium to NH. On the one hand this might have implication for the atmospheric distribution of NH3, since the uptake capacity of the ocean will be increased with unknown consequences for chemistry of the atmosphere (e.g. the aerosol formation) over the ocean. On the other hand this might have severe implications for the nitrification rates in seawater because they are influenced by the pH. When the pH drops from 8 to 7, nitrification rates can be reduced by 50% (Huesemann et al., 2002). (One explanation for this is that the ammonia monooxygenase enzyme uses rather NH3 than NH4 as substrate.) Most recently it was suggested that atmospheric NH3 serves as a foraging cue for seabirds such as the blue petrel (Nevitt ei a/., 2006) is an excretion product of... [Pg.83]

Aerosol Formation. Aerosol formation from pMDIs is a complex process influenced not only by the propellant as discussed above, but also by properties of the formulation and device design (e.g., valve volume and orifice size). After aerosol droplets form at the exit of the spray nozzle, an aerosol plume begins to expand, and large particles travel along the axis of the actuator. Fig. 7 shows photographs of aerosol formation using a commercially available pMDI. [Pg.2102]

Physical interferences may arise from incomplete volatilization and occur especially in the case of strongly reducing flames. In steel analysis, the depression of the Cr and Mo signals as a result of an excess of Fe is well known. It can be reduced by adding NH4C1. Further interferences are related to nebulization effects and arise from the influence of the concentration of acids and salts on the viscosity, the density and the surface tension of the analyte solutions. Changes in physical properties from one sample solution to another influence the aerosol formation efficiencies and the aerosol droplet size distribution, as discussed earlier. However, related changes of the nebulizer gas flows also influence the residence time of the particles in the flame. [Pg.164]

Chambers were also used in the research on heterogeneous reactions of isoprene and of other atmospheric trace compounds. As already discussed, Czoschke et al. (2003) studied the formation of SOA from products of isoprene oxidation in 500 dm Teflon-bag chambers at UNC. FoUcers et al. (2003a,b,c) studied the partitioning and influence of dicarboxylic acids on aerosol formation in Aerosol Chamber in Julich. Shantz et al. (2003) investigated the growth of aqueous organic particles and cloud condensation nuclei in the CALSPAN chamber, linuma et al. (2004 paper submitted to this book) studied the reaction of a-pinene with ozone on acidic particles in the Leipzig tent-chamber (9 m ). [Pg.273]

Various techniques of particle delivery are used to deduce pulmonary and systemic effects from the wide parameters of potential toxicological influences. The specific techniques that are currently employed in these studies include intratracheal instillation, intratracheal aspiration, and intratracheal inhalation. Of these different delivery techniques, intratracheal installation is a useful technique to assess the potential health effects of different particles efficiently and cost effectively. Intratracheal instillation is characterized by saline suspended particles administered directly into the trachea of the animal being tested. Intratracheal installation provides a relatively easy way to compare the toxicology between different materials. However intratracheal installation is not able to assess particle deposition. Intratracheal aspiration involves droplet administration of suspended particle matter in the form of a puff of air. Intratracheal inhalation is the most relevant for toxicity and risk assessment. Intratracheal inhalation involves nanoparticulate aerosol formation at constant concentrations during the exposure. [Pg.710]

Zhang JY, Hartz KEH, Pandis SN, Donahue NM (2006) Secondary organic aerosol formation from limonene ozonolysis homogeneous and heterogeneous influences as a function of NOx. JPhys Chem A 110(38) 11053-11063... [Pg.141]

Aerosols, including those of biogenic origin, have important impacts on atmospheric radiation, both directly, and indirectly through the nucleation of atmospheric water. The impact of biogenic aerosols on radiation through direct and indirect effects depends on their physical and chemical properties. Table 5 shows the main chemical and physical properties of aerosols that influence their interaction with radiation, and with other atmospheric compounds, resulting in the formation of secondary particles, as well as their influence on cloud formation. Chemical... [Pg.177]

Detection that uses a mass spectrometer requires TFA acid substitution with another acid because the addition of TFA acid causes the attenuation of the signal and prevents efficient aerosol formation due to the high surface tension of the mobile phase. Frequently, this acid is replaced with formic acid, and less frequently with acetic acid. The addition of acid to the mobile phase used in the UHPLC-MS method or UHPLC-MS/MS improves the shape of the peaks, and it also reduces the influence of matrix effects and improves the ionization, which increases the sensitivity of the method (20-24,29-35,37). [Pg.207]

One such feedback is the influence of clouds and water vapor. As the climate warms, more water vapor enters the atmosphere. But how much And which parts of the atmosphere, high or low And how does the increased humidity affect cloud formation While the relationships among clouds, water vapor, and global climate are complicated in and of themselves, the situation is further complicated by the fact that aerosols exert a poorly understood influence on clouds. [Pg.247]

The present sources to the ocean are the weathering of old evaporites (75% of river flux) and CP carried by atmospherically cycled sea-salts (25% of river flux). Loss from the ocean occurs via aerosols (about 25%) and formation of new evaporites. This last process is sporadic and tectonically controlled by the closing of marginal seas where evaporation is greater than precipitation. The oceanic residence time is so long for CP ( 100Myr) that an imbalance between input and removal rates will have little influence on oceanic concentrations over periods of less than tens of millions of years. [Pg.270]


See other pages where Aerosol formation, influence is mentioned: [Pg.195]    [Pg.199]    [Pg.186]    [Pg.2038]    [Pg.2082]    [Pg.51]    [Pg.19]    [Pg.779]    [Pg.5]    [Pg.18]    [Pg.218]    [Pg.892]    [Pg.530]    [Pg.86]    [Pg.184]    [Pg.18]    [Pg.395]    [Pg.1427]    [Pg.2173]    [Pg.224]    [Pg.224]    [Pg.129]    [Pg.659]    [Pg.290]    [Pg.157]    [Pg.111]    [Pg.72]    [Pg.489]    [Pg.210]    [Pg.266]    [Pg.112]    [Pg.315]    [Pg.203]   
See also in sourсe #XX -- [ Pg.2 ]




SEARCH



Aerosol formation

© 2024 chempedia.info