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Species organically complexed

Chemical Variety. The term species refers to the actual form in which a molecule or ion is present in solution. Eor example, a metal ion may occur in natural waters, as a free metal ion, ie, an aquo complex Me(H20), an inorganic or organic complex, and it may be present in dissolved or... [Pg.217]

In addition to the need for an adequate method for free cyanide and an adequate sample preservation method, a methodology should be developed for the differentiation of species, especially between free (HCN and CM ), metallic complexes, and organic complexes. [Pg.23]

Neutral carriers are organic complexing agents which are capable of sequestering and transporting ionic species in a hydrophobic organic phase. The antibiotics, valino-mycin and nonactin were the first neutral carriers to be incorporated in an ISE These macrocyclic neutral carriers contain a polar internal cavity and an outer hydro-phobic shell. The excellent selectivity exhibited by valinomycin for potassium ions is... [Pg.58]

In aquatic systems dissolved aluminum species are toxic to fish. There exists a vast number of aluminum species, ranging from inorganic monomeric to complex colloidal. polymeric and organic complexes. A major problem, when studying aluminum species in water is that the species quickly convert one into the other (Fairman and Sanz-Medel 1995). [Pg.77]

J. Gerke, Aluminium and iron (III) species in the soil solution including organic complexes with citrate and humic substances. Z. Pflanzenemarhr. Bodenk. 160 421 (1997). [Pg.153]

The collection behaviour of chromium species was examined as follows. Seawater (400 ml) spiked with 10 8 M chromium (III), chromium (VI), and chromium (III) organic complexes labelled with 51Cr was adjusted to the desired pH by hydrochloric acid or sodium hydroxide. [Pg.69]

The collection behaviour of chromium species was examined as follows. Seawater (400 ml) spiked with 10-8 M Crm, CrVI, and Crm organic complexes labelled with 51Cr was adjusted to the desired pH by hydrochloric acid or sodium hydroxide. An appropriate amount of hydrated iron (III) or bismuth oxide was added the oxide precipitates were prepared separately and washed thoroughly with distilled water before use [200]. After about 24 h, the samples were filtered on 0.4 pm nucleopore filters. The separated precipitates were dissolved with hydrochloric acid, and the solutions thus obtained were used for /-activity measurements. In the examination of solvent extraction, chromium was measured by using 51Cr, while iron and bismuth were measured by electrothermal atomic absorption spectrometry. The decomposition of organic complexes and other procedures were also examined by electrothermal atomic absorption spectrometry. [Pg.163]

Sunda and Hanson [247] have used ligand competition techniques for the analysis of free copper (II) in seawater. This work demonstrated that only 0.02 -2% of dissolved copper (II) is accounted for by inorganic species. (i.e., Cu2+, CuC03, Cu(OH)+, CuCl+, etc.) the remainder is associated with organic complexes. Clearly, the speciation of copper (II) in seawater is markedly different from that in fresh water. [Pg.169]

A technique for the determination of free cupric ions in seawater has been described by Sunda and Hanson [332], The method is based on sorption of copper onto Sep-Pak Cis cartridges and internal free cupric ion calibration. Calibration is accomplished by adding cupric ion buffers and EDTA, which competes with natural organic ligands for copper complexation. The method was used to establish that 0-2% of the copper occurs as inorganic species and 98-100% occurs as organic complexes. [Pg.179]

In natural waters, dissolved zinc speciates into the toxic aquo ion [Zn(H20)6]2+, other dissolved chemical species, and various inorganic and organic complexes zinc complexes are readily transported. Aquo ions and other toxic species are most harmful to aquatic life under conditions of low pH, low alkalinity, low dissolved oxygen, and elevated temperatures. Most of the zinc introduced into aquatic environments is eventually partitioned into the sediments. Zinc bioavailability from sediments is enhanced under conditions of high dissolved oxygen, low salinity, low pH, and high levels of inorganic oxides and humic substances. [Pg.725]

System 7, 9, 10. roots-rizosphere (VII) plants (VIII) their biological reactions— metabolism (VIII) soil-soil solution, air (IV) aerosols—atmospheric air (26, 28). In this system, the influence of metal-organic complexes on the plant development and their metabolism is considered. Under deficient or excessive contents of some chemical species, the metabolism may be destroyed (see Figure 2). [Pg.33]

For understanding these tendencies, we will consider the values of the biogeo-chemical coefficient of aqueous migration. This coefficient Cw is the ratio between the content of an element in the sum of water-soluble salts and in geological rocks. The values of Cw for certain chemical species are smaller in Arid ecosystems than those in Forest ecosystems. We can suggest two explanations. First, soils of Forest ecosystems are enriched in water-soluble metal-organic complexes (see Chapter 7). Second, most chemical species are trapped in the transpiration barrier of upper soil layers of Arid ecosystems. [Pg.170]

Free metal ions Inorganic ion pairs complexes Organic complexes chelates Metals species bound to high molecular weight DOM Metals in colloids Metals sorbed onto colloids Precipitates... [Pg.105]

At the pH and ionic strength of seawater, the dominant dissolved species of silicon is orthosilicic acid [H4Si04(aq) or Si(OH)4(aq)]. The speciation of silicic acid is shown in Figure 5.19. At the pH of seawater, a minor amount of dissociation occurs, such that about 5% of the dissolved silicon is in the form of HjSiO faq). Dissolved organic complexes of silicon do not occur naturally. [Pg.404]

This example illustrates a case of considerable analytical importance, especially for the determination of complex formation constants for hydrophilic complexes, as discussed in section 4.12, when the equilibrium constants for the stepwise metal-organic complexes are of secondary interest. values are tabulated in several reference works. is a conditional constant and only valid provided no other species are formed besides the extracted one. [Pg.152]

Mordand MM (1970) Clay-organic complexes and interactions. Adv Agron 22 75-117 Mordamd MM (1986) Mechanism of adsorption of nonhumic organic species by clays. In Huang PM, Schnitzer M (eds) Interaction of soil minerals with natural organics and microbes. Soil Sci Soc Amer, Madison, Wisconsin, pp 59-76... [Pg.405]


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See also in sourсe #XX -- [ Pg.274 ]




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Organic complexation

Organic species

Organically complexed metal species

Species complexes

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