Big Chemical Encyclopedia

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

Articles Figures Tables About

Analysis and Toxicity

The simplest method is probably colorimetric, based on its electronic spectrum [215], It can also be determined gravimetrically by addition of diphenylsulfide or ethanol to a solution of RuO this gives RuO which is then reduced to the metal [236], Alternatively addition of 2-propanol to a solution of RuO solution generates RuO. nHp [237], [Pg.10]

Although it has been said [236] that RuO is less harmful to the eyes than is OsO, nevertheless great care should always be taken in handling it. The high vapour pressure of the solid under ambient conditions makes it very dangerous [Pg.10]

As mentioned in 1.2.1 above, there are several reviews on the properties of RuO as an oxidant in organic chemistry, both as a stoicheiometric but also as a catalytic reagent [12, 34-36, 39, 60, 64, 201-203]. It is one of the most important and versatile of Ru oxidants. In the first few years after its properties in the field were realised it was often used for oxidation of alcohol groups in carbohydrates, but its versatility as an oxidant quickly became apparent and its use was extended to a variety of other reactions, notably to alkene cleavage and, more recently, to the c/x-dihydroxylation and ketohydroxylation of alkenes. [Pg.11]

The publication used [239] is relatively obscure, and it was a paper of 1959 which really established the RuO /aq. Na(IO )/CCl system for production of RuO  [Pg.11]

Common procedures for making RuO in situ generally use hydrated RuO or RuClj as starting materials. The dioxide RuO is said to be preferable to RuClj since oxidised chloro impurities are not formed and it may react faster than RuClj [242]) hydrated rather than anhydrous RuO should be used [243, 244]. [Pg.12]


Specifications, Analysis, and Toxicity. Dicyandiamide is identified quaHtatively by paper chromatography and quantitatively by ultraviolet spectrometry of the chromatogram. More commonly, total nitrogen analysis is used as a purity control or the dicyandiamide is converted by hydrolysis to guanylurea, which is determined gravimetrically as the nickel salt (50). Methods based on the precipitation of silver dicyandiamide picrate are sometimes used (51). Dicyandiamide can also be titrated with tetrabutylammonium hydroxide ia pyridine solution. Table 4 gives a typical analysis of a commercial sample. Dicyandiamide is essentially nontoxic. It may, however, cause dermatitis. [Pg.371]

Kannan, K., Tanabe, S., and Borrell, A. et al. (1993). Isomer specific analysis and toxic evaluation of PCBs in striped dolphins affected by an epizootic in the western Mediterranean sea. Archives Environmental Contamination and Toxicology 25, 227-233. [Pg.355]

I. H. Suffet and M. Malalyandi, (Eds.), "Organic Pollutants in Hater. Sampling, Analysis, and Toxicity Testing", American Chemical Society, Washington, D.C., 1987. [Pg.977]

Nematollahi J, Guess WL, Autian J. 1967. Plasticizers in medical application I. Analysis and toxicity evaluation of dialkyl benzenedicarboxylates. J Pharmacol Sci 56 1446-1453. [Pg.123]

The detection of M. aeruginosa toxins is readily achieved by HPLC and ultraviolet absorbance. Provisionally, components with identical retention times are considered identical. Confirmation is made by preparative isolation, amino acid analysis, and toxicity testing. The frequent, but not invariable, presence of toxin-LR as a principal toxin provides a useful HPLC marker. The wavelength used for detection of the toxins, 238 nm, is the principal absorbance maximum of toxin-LR. The 238 nm absorbance is probably... [Pg.408]

Masuda Y, Yoshimura H Chemical analysis and toxicity of polychlorinated biphenyls and dibenzofurans in relation to Yusho. f Toxicol Sci 7(3) 161-175, 1982... [Pg.156]

HV160 Puls R., and J. A. Greenway. Fusario-toxicosis from barley in British Columbia. II. Analysis and toxicity of syspected barley. Can J Comp Med 1976 40(1) 16-19. [Pg.258]

Similarly, simple solutions may not be readily available to the real-life problems of analysis and toxicity testing of environmentally important waters. Many of these samples contain complex mixtures of many organic compounds, some of which may be present at very low concentrations. These aqueous solutions must be concentrated and/or the constituents must be isolated before most of the various organic constituents present can be chemically analyzed. This step is necessary so that a sufficient mass of chemicals can be obtained for separation and identification of individual components. An analogous situation... [Pg.13]

Kopfler, F. C. Ringhand, H. P. Miller, R. G. In Organic Pollutants in Water Sampling, Analysis, and Toxicity Testing Suffet, I. H. Malaiyandi, M., Eds. Advances in Chemistry 214 American Chemical Society Washington, DC, 1986 Chapter 20. [Pg.574]

Baun, A., A. Ledin, L.A. Reitzel, P.L. Bjerg, and T.H. Christensen. 2004. Xenobiotic organic compounds in leachates from ten Danish MSW landfills—chemical analysis and toxicity tests. Water Res. 38 3845-3858. [Pg.218]

De Boer, J., J. Klungsoyr, G. Nesje, et al. 1999. MATT Monitoring, analysis and toxicity of Toxaphene— improvement of analytical methods. Organohalogen Compd. 41 569-574. [Pg.473]

Jaward, F M., Barber, J. L., Booij, K., Jones, K. C. Spatial distribution of atmospheric PAHs and PCNs along a north-south Atlantic transect. Environmental Pollution, 132 173-181 (2004). Kannan, K., Imagawa, T., Blankenship, A. L., Giesy, J. P. Isomer-specific analysis and toxic evaluation of polychlorinated naphthalenes in soil, sediment, and biota collected near the site of a former chlor-alkali plant. Environmental Science and Technology, 32 2507-2514 (1998). [Pg.164]

Environmental contaminants are present as complex mixtures, so that if toxicity is found, procedures known as toxicity identification evaluation may be carried out. This procedure identifies toxic components by systematically treating the effluent, elutrate, or pore water to remove various fractions - hydro-phobic ( fat soluble ) chemicals, metals, acids, volatile compounds, etc. - and retesting the toxicity after each extraction. Loss of toxicity after an extraction implicates the chemical that was extracted. This is confirmed by chemical analysis and toxicity tests on... [Pg.294]

S. Focardi, R. Bargagli, S. Corsolini, Isomer specific analysis and toxic potential evaluation of polychlorinated biphenyls in Antarctic fish, seabirds and Weddel seals from Terra Nova Bay (Ross Sea)... [Pg.271]

Kuruntachalam K, Takashi I (1998) Isomer-Specific Analysis and Toxic Evaluation of Polychlorinated Naphtalenes in Soil, Sediment and Biota Collected near the Site of a Formar Chlor-Alkali Plant. Environ Sci Technol 32, 2507-2514. [Pg.429]


See other pages where Analysis and Toxicity is mentioned: [Pg.373]    [Pg.71]    [Pg.276]    [Pg.10]    [Pg.3]    [Pg.296]    [Pg.62]    [Pg.305]    [Pg.128]    [Pg.2]    [Pg.234]    [Pg.133]    [Pg.611]    [Pg.594]    [Pg.128]    [Pg.368]    [Pg.373]    [Pg.375]    [Pg.375]    [Pg.375]    [Pg.376]    [Pg.376]    [Pg.62]   


SEARCH



Toxic analysis

Toxicant Analysis and Quality Assurance Principles

© 2024 chempedia.info