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Parts per trillion

Scale of Operation Voltammetry is routinely used to analyze samples at the parts-per-million level and, in some cases, can be used to detect analytes at the parts-per-billion or parts-per-trillion level. Most analyses are carried out in conventional electrochemical cells using macro samples however, microcells are available that require as little as 50 pL of sample. Microelectrodes, with diameters as small as 2 pm, allow voltammetric measurements to be made on even smaller samples. For example, the concentration of glucose in 200-pm pond snail neurons has been successfully monitored using a 2-pm amperometric glucose electrode. ... [Pg.531]

Microwave spectroscopy is used for studyiag free radicals and ia gas analysis (30). Much laboratory work has been devoted to molecules of astrophysical iaterest (31). The technique is highly sensitive 10 mole may suffice for a spectmm. At microwave resolution, frequencies are so specific that a single line can unambiguously identify a component of a gas mixture. Tabulations of microwave transitions are available (32,33). Remote atmospheric sensing (34) is illustrated by the analysis of trace CIO, O, HO2, HCN, and N2O at the part per trillion level ia the stratosphere, usiag a ground-based millimeter-wave superheterodyne receiver at 260—280 GH2 (35). [Pg.314]

Carbonyl sulfide is overall the most abundant sulfur-beating compound ia the earth s atmosphere 430—570 parts per trillion (10 ), although it is exceeded by H2S and SO2 ia some iadustrial urban atmospheres (27). Carbonyl sulfide is beheved to origiaate from microbes, volcanoes, and the burning of vegetation, as well as from iadustrial processes. It may be the main cause of atmospheric sulfur corrosion (28). [Pg.130]

Bromine compounds are found ia the atmosphere ia small amounts the sea is a primary source. Rainfall over the Pacific and Indian Oceans has been found to contain 60—80 f-lg/L of bromine (46). Approximately 10 parts per trillion (v/v) of bromine is found ia the stratosphere (47). [Pg.284]

Unbumed Hydrocarbons Various unburned hydrocarbon species may be emitted from hydrocarbon flames. In general, there are two classes of unburned hydrocarbons (1) small molecules that are the intermediate products of combustion (for example, formaldehyde) and (2) larger molecules that are formed by pyro-synthesis in hot, fuel-rich zones within flames, e.g., benzene, toluene, xylene, and various polycyclic aromatic hydrocarbons (PAHs). Many of these species are listed as Hazardous Air Pollutants (HAPs) in Title III of the Clean Air Act Amendment of 1990 and are therefore of particular concern. In a well-adjusted combustion system, emission or HAPs is extremely low (typically, parts per trillion to parts per billion). However, emission of certain HAPs may be of concern in poorly designed or maladjusted systems. [Pg.2383]

Mercury generally is found in low and trace concentrations. So there is need to determine Hg in ranges corresponding to various types of water samples. Detection levels of Hg can be improved by the use of vapour generation technique. This technique allows to sepai ate the analyte from the sample matrix and so to overcome the matrix interference. The fluorescence technique, with its high sensitivity and linearity, in combination with vapour generation, provides for a possibility to detect Hg in parts per trillion per liter regions. [Pg.211]

Down to parts-per-trillion level, depending on impurity species and host... [Pg.29]

S. Lacorte and D. Barcelo, Determination of parts per trillion levels of organophospho-rus pesticides in groundwater by automated on-line liquid- solid extraction followed by liquid chr omatography/atmospheric pressure chemical ionization mass spectrometry using positive and negative ion modes of operation . Anal. Chem. 68 2464- 2470 (1996). [Pg.374]

D. Puig, L. Silgoner, M. Grasserbauer and D. Barcelo, Part-per-trillion level determination of priority methyl-, nirto-, and clilor ophenols in river water samples by automated online liquid/solid exrtaction followed by liquid chr omatography/mass spectr ometry using atmospheric pressure chemical ionization and ion spray interfaces . Anal. Chem. 69 2756-2761 (1997). [Pg.374]

I. Eeirer, M. C. Hennion and D. Barcelo, Immunosorbents coupled on-line with liquid chi omatography/atmospheric pressure chemical ionization/mass specti ometiy for the part per trillion level determination of pesticides in sediments and natural waters using low preconcenti ation volumes . Anal. Chem. 69 4508-4514 (1997). [Pg.375]

There are natural sources of brominated hydrocarbons as well as man-made sources, such as the "halons , which are used in fire extinguishers. Reaction 21 is very fast and generates Cl and Br atoms directly the cycle does not require a photolytic step. Although this cycle occurs with high efficiency, it is less important than the chlorine peroxide cycle because of the much smaller concentrations of bromine compounds in the stratosphere-parts per trillion vs. parts per billion for the chlorine compounds. [Pg.32]

In the presence of sufficient NO (roughly 30 parts per trillion) this oxidation produces ozone. [Pg.330]

The Delaney Clause was introduced to protect the American consumer from dangerous substances. By the if proven toxic, X is forbidden logic that did not include any reference to medical risk, the inexorable progress of instrumental analysis naturally lead to the situation where, in a few years, apple pie would have been declared off limits had the clause not been struck from the books, because it is certain to contain a one part per trillion of some X that is toxic at the kg-per-day level. [Pg.270]

Rainfall samples collected in the Great Lakes area of Canada in 1976 and 1977 contained mean concentrations of 1-2 ng/L (parts per trillion) a-endosulfan and 4—5 ng/L P-endosulfan. Endosulfan was detected in spring and summer rainfall samples but not in samples collected during the fall and winter (Strachan et al. 1980). a-Endosulfan has also been detected in snowpack samples obtained from widely distributed sites in the Canadian Arctic. Endosulfan concentrations in samples collected in the spring of 1986 ranged from 0.1 to 1.34 ng/L (Gregor and Gummer 1989). [Pg.231]

Commercially produced amines contain Impurities from synthesis, thus rigid specifications are necessary to avoid unwanted Impurities In final products. Modern-day analytical capability permits detection of minute quantities of Impurities In almost any compound. Detection In parts per million Is routine, parts per billion Is commonplace, and parts per trillion Is attainable. The significance of Impurities In products demands careful and realistic Interpretation. Nltrosatlng species, as well as natural amines, are ubiquitous In the environment. For example, Bassow (1976) cites that about 50 ppb of nitrous oxide and nitrogen dioxide are present In the atmosphere of the cities. Microorganisms In soil and natural water convert ammonia to nitrite. With the potential for nitrosamine formation almost ever-present In the envlronmeit, other approaches to prevention should Include the use of appropriate scavengers as additives In raw materials and finished products. [Pg.371]


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