Big Chemical Encyclopedia

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

Articles Figures Tables About

Copper in water

The addition of terminal alkynes to carbon-carbon double bonds has not been explored until recently, possibly because C=C double bonds are not as good electrophiles as C=N or C=0. In 2003, Carreira et al. reported the first conjugate addition reaction of terminal alkynes to C=C catalyzed by copper in water. The reaction proceeded with derivatives of Meldrum s acid in water in the presence of Cu(OAc)2 and sodium ascorbate (Eq. 4.35).59 However, this method was limited to C=C double bonds with two electron withdrawing groups. [Pg.116]

It is worth noting that the Ullmann-Goldberg condensation of aryl halides with phenols and anilines worked efficiently in the presence of copper in water.50 For example, the coupling of 2-chlorobenzoic acid with 4-chlorophenol (K2C03/pyridine/copper powder) gave 2-(4-chlorophenoxy)carboxylic acid (Eq. 6.23).51 The Cu(I)-catalyzed transformation of 2-bromobenzoic acid into salicylic acid has also been studied in aqueous media (Eq. 6.24).52... [Pg.182]

Ecologically, copper is a trace element essential to many plants and animals. However, high levels of copper in soil can be directly toxic to certain soil microorganisms and can disrupt important microbial processes in soil, such as nitrogen and phosphorus cycling. Copper is typically found in the environment as a solid metal in soils and soil sediment in surface water. There is no evidence that biotransformation processes have a significant bearing on the fate and transport of copper in water. [Pg.144]

The ditetrazolium salts (309) have been patented for use in electrochromic electrodes which are used in display devices <89JAP01230026) and tetrazolium salts have also been developed for cell bioassays for neurotoxins active on voltage-sensitive sodium channels <93MI 417-03). Tests for inhibition of corrosion of zinc and brass carried out on 5-aminotetrazole showed it to be ineffective relative to other azoles <86MI 417-01). A number of tetrazoles including the 5-amino, 5-methyl, and 5-phenyl derivatives have been separately incorporated into surfactants used for corrosion inhibition with copper in water <9lMl4l7-07). Photopolymerizable resin compositions which are highly resistant... [Pg.677]

Filipovic-Kova vic, Z. and L. Sipos. 1998. Voltammetric determination of copper in water samples digested by ozone. Talanta 45 843-850. [Pg.101]

Further applications are described for sulfur (Fig. 2.6) and copper in water by reversed-phase or ion-exchange high-performance liquid chromatography . Also anions such as thiosulphate and polythionates were separated from environmental samples by HPLC (anion-exchange) . The sensitive detection was made possible by reaction with Ce(lV) after separation and fluorimetry of Ce(lII) ions. [Pg.184]

True hair is found only in mammals, and there is no such thing as a completely hairless mammal. Hair itself is dead, but is produced in hair follicles by specialized keratinocytes at the base of the hair. The outermost layer of hair is a cuticle, and most hairs have a cortex in which the dead keratinized cells are very densely packed, and an iimer medulla in which they are not as densely packed. The pigmentation in hair, like that of skin, comes from melanocytes. Hair exposure to some chemicals may produce hair discoloration, for example, green hair from copper in water or cosmetics, or blue hair in cobalt workers. [Pg.1286]

Copper in water and plant foods was determined with the use of diethyldithiocarbamate in the presence of EDTA and citrate [1]. The detection limit was 0.2 mg l. l-(2-Pyridylazo)-2-naphthol in the presence of Triton X-100 and AW -diphenylbenz-amidine ( = 520 nm, e = 1.1410 1 mol cm, detection limit of 2 ng ml" ) was applied for the determination of copper in dust and soil [2]. Earlier, the effect of an anionic surfactant on the sensitivity of the determination of Cu with PAN has been examined [3]. [Pg.494]

A.N. Anthemidis, G.A. Zachariadis, J.A. Stratis, On-line solid phase extraction system using PTFE packed column for the flame atomic absorption spectrometric determination of copper in water samples, Talanta 54 (2001) 935. [Pg.430]

The calibration data of an electrode for the selective detection of copper in water samples, where the electrode was prepared by modifying a gold electrode with cysteine, is shown in table 5.6. [Pg.161]

The detection limit of the cysteine-modified electrode for copper in water samples is 1.87 nM. [Pg.163]

Nitric ether, six ounces alcohol, one ounce sulphate of cop i>er (blue vitriol), one and a half ounce muriated tincture of iron, one and a half ounce tincture W gum benzoin, one and a half ounce. Dissolve the sulphate of copper in water, add the other ingredients, previously mixed, and then add three pints of boiling water. [Pg.381]

Chen H, Xu S and Fang Z (1994) Determination of copper in water and rice samples with flow-injection on-line adsorption preconcentration using a knotted reactor. Anal Chim Acta 298 167-173. [Pg.1616]

The chanistry of copper in water and soils is very complex. Potential chemical forms include insoluble organic complexes, sulfide minerals, and solid copper phases. It is clear that changes in soil redox condition (from oxidized to reduced) change the relative distribution of copper in various soil phases. [Pg.493]

The dual-column and single-column ion-exchange precoilcentration flame AAS systems as well as the DDC-Cis sorbent extraction flame AAS and ETAAS systems used for the determination of cadmium were also used for the determination of copper in water samples. The detection limit for the dual-column system was 0.07-0.09 /ig l at 60 samples h [7] for the sorbent extraction preconcentration flame AAS system, 0.2 /xg r at 120 samples h [9] for the sorbent extraction ETAAS system, 0.02 /xg 1 at approximately 20 samples h [10]. The sensitivity of sorption column preconcentration methods with flame AAS detection should be sufficient for the determination of copper in most natural water samples. [Pg.200]

The corrosion rate of copper in water is very low. In drinking water systems, the copper release to the water has to be controlled for hygienic and health reasons. The use of copper in drinking water systems is specified in DIN 50930,... [Pg.101]

The corresponding reactions are shown in the Pourbaix diagram of copper in water as shown Fig. 2.10. [Pg.40]

Sparks DL, Schreurs BG. Trace amounts of copper in water induce beta-amyloid plaques and learning deficits in a rabbit model of Alzheimer s disease. Proc.Natl.Acad.Sci.USA. 2003 100 11065-11069... [Pg.482]


See other pages where Copper in water is mentioned: [Pg.507]    [Pg.7]    [Pg.198]    [Pg.98]    [Pg.198]    [Pg.163]    [Pg.340]    [Pg.1045]    [Pg.204]    [Pg.186]    [Pg.195]    [Pg.11]    [Pg.90]    [Pg.376]    [Pg.193]    [Pg.336]    [Pg.1543]    [Pg.1544]    [Pg.1607]    [Pg.12]    [Pg.11]    [Pg.211]    [Pg.225]    [Pg.187]    [Pg.40]    [Pg.536]    [Pg.371]    [Pg.121]   
See also in sourсe #XX -- [ Pg.4 , Pg.44 , Pg.56 ]

See also in sourсe #XX -- [ Pg.4 , Pg.44 , Pg.56 ]




SEARCH



Copper concentration in, natural waters

Copper in sea-water

Copper in tap water

The Nature of Copper in Water and Wastewater

© 2024 chempedia.info