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Query: UMLS:C0027960 (mole)
 21,279 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A sensitive spectrophotometric method has been developed for the determination of gold in copper, silver, lead, blister copper, copper concentrate and anode slime. Optimal conditions have been established for the extraction and determination of gold. Gold is extracted as its bromo complex with tri-n-octylamine and determined photometrically with 4,4'-bis(dimethylamino)thiobenzophenone; the absorbance of the organic phase is measured at 540 nm and the apparent molar absorptivity is about 1.2 x 10(5) 1.mole(-1). cm(-1). As little as 0.1 or 0.2 ppm of gold in these materials can be determined.
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PMID:Extraction-spectrophotometric determination of traces of gold in copper in silver, lead, blister copper, copper concentrate and anode slime with 4,4'-bis(dimethylamino)-thiobenzophenone. 1896 61

A simple and rapid ultraviolet spectrophotometric method is proposed for the determination of trace amounts of tungsten(VI) with ammonium 1-pyrrolidinecarbodithioate (APDC). The method is based on measurement of the absorbance of the tungsten APDC complex in fairly concentrated hydrochloric acid medium; no extraction is required. The complex is formed at an initial acidity of 6M hydrochloric acid and has an absorption maximum at 250 nm. The high absorption of the reagent blank at 250 nm disappears on decomposition of excess of reagent by heating. Beer's law is obeyed over the range 0.43-3.2 ppm of tungsten(VI). The molar absorptivity of the complex is 4.5 x 10(4) l.mole(-1) .cm(-1) at 250 nm. Tenfold amounts of aluminium, magnesium, calcium, cobalt, iron(II), lead, silver, sodium and titanium do not interfere in the determination of 50 mug of tungsten (VI).
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PMID:Ultraviolet spectrophotometric determination of tungsten(VI) with ammonium 1-pyrrolidinecarbodithioate. 1896 50

The optimum conditions for preparation of stable solutions of ruthenate and osmate, after alkaline fusion of ruthenium(IV) compounds, ruthenium metal and osmium metal in a silver crucible, have been determined. The molar absorptivities of ruthenate and osmate are 1.74 x 10(3) 1. mole(-1).cm(-1) at 465 nm (Ru) and 2.75 x 10(3) 1.mole(-1).cm(-1) at 340 nm (Os) in 2M sodium hydroxide. A differential spectrophotometric method has been developed for determination of ruthenium in ruthenium dioxide, lead ruthenite and bismuth pyroruthenate. Simultaneous spectrophotometric determination is proposed for ruthenium and osmium. The other platinum metals interfere seriously only when present in > 1:1 w/w ratio to Ru.
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PMID:Spectrophotometric determination of ruthenium and osmium. 1896 3

A sensitive and selective spectrophotometric method for silver has been established by reacting silver(I) with 2-(3,5-dibromo-2-pyridylazo)-5-diethylaminophenol (3,5-diBr-PADAP) in the presence of an anionic surfactant, sodium lauryl sulphate. The molar absorptivity is 7.7 x 10(4) l.mole(-1).cm(-1) at 570nm. The molar ratio of silver to 3,5-diBr-PADAP is 1:2. Beer's law is obeyed from 0.1 to 1 ppm of silver. With EDTA as masking agent, common ions do not interfere. The method has been applied to the determination of silver in waste water.
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PMID:Spectrophotometric determination of silver with 2-(3,5-dibromo-2-pyridylazo)-5-diethyl-aminophenol in the presence of anionic surfactant. 1896 88

A highly sensitive and selective procedure for spectrophotometric determination of silver has been developed. At pH 9.2, in the presence of Triton X-100, silver forms a dark red-violet complex with cadion 2B which has an absorption maximum at 565 nm. The molar absorptivity is 1.0 x 10(5) l.mole(-1).cm(-1). Beer's law is obeyed for silver in the range 0.02-0.8 mug ml . The colour reaction, if EDTA is used as a masking agent, is free from interference by the 20 cations and 19 anions investigated. Only Cl(-), Br(-), I(-), S(2-) and CN(-) interfere and must be absent. This method has been used to determine silver in waste-water.
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PMID:Spectrophotometric determination of silver with cadion 2B and triton X-100. 1896 45

Silver(I), copper(II) and nickel(II) can be reduced to the metallic state by formaldehyde at pH 11, chromium(II) in 2.5M sulphuric acid, and borohydride at pH 5.5-6.0, respectively. Reoxidation of these metals with iron(III) in the presence of Ferrozine enables their determination at concentration below 1 mug/ml by measurement of the absorbance of the iron(II)-Ferrozine complex at 562 nm, with a precision better than 3%. The apparent molar absorptivities for silver, copper and nickel are 2.78 x 10(4), 5.56 x 10(4) and 5.58 x 10(4) l.mole(-1).cm(-1), respectively. The average thickness of silver films on glass surfaces can be determined in the way.
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PMID:Chemical reduction and spectrophotometric determination of silver, copper and nickel. 1896 40

A new spectrophotometric method for the determination of micro amounts of formaldehyde in aqueous and methanol solutions is based on the oxidation of formaldehyde by hydrous silver oxide at pH 11-12.5 and oxidation of the metallic silver produced, with iron(III) in the presence of Ferrozine. The absorbance of the resulting iron(II)-Ferrozine complex at 562 nm is proportional to the amount of formaldehyde and corresponds to an apparent molar absorptivity of 5.58 x 10(4) 1.mole(-1).cm(-1).
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PMID:Spectrophotometric determination of formaldehyde. 1896 88

Gold-silver alloy nanoparticles with a homogeneous size distribution and good stability were synthesized in aqueous solution by one-step reduction with gallic acid as reductant in the absence of other stabilizers for the first time. The absorption spectra of as prepared gold-silver alloy nanoparticles under different reaction temperatures and with various gold-silver mole ratios were studied. The absorption spectra exhibit only one single peak with the maximum wavelength located between the absorption peaks of Au nanoparticles and Ag nanoparticles, however, the absorption spectrum of the physical mixtures of Au nanoparticles and Ag nanoparticles exhibits two absorption peaks coming from their corresponding monometallic metal nanoparticles, suggesting primarily the formation of the alloy nanoparticles. The maximal absorption peaks of alloy nanoparticles showed gradually a blue-shift with the rising of reaction temperature companying with the increase in absorbance and the narrowing of peak shape. The maximum absorption wavelengths of alloy nanoparticles showed a red-shift with increasing Au/Ag molar ratio in a linear fashion, further indicating the formation of alloy nanoparticles. HRTEM images showed that the as-prepared alloy nanoparticles with Ag/Au molar ratio of 1:1 are close to sphere in shape, homogeneous in size distribution and without capping phenomenon. EDX analysis suggested the present of Au and Ag in individual nanoparticles, and the Au/Ag mole ratio value of a sample with a nominal element composition was found to be close to the nominal value.
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PMID:[Synthesis and absorption spectra properties of Au-Ag alloy nanoparticles using gallic acid as reductant]. 1897 89

A striking feature of cellular blue nevus consists in the presence, in its histologic picture, of numerous hypertrophic nerves and nerve-like figures, positive for histochemical and immunohistochemical methods for nerve fibers and myelin sheaths. These findings, first described in Masson's original article and repeatedly highlighted in the past for their possible histogenetic significance, are currently considered as merely coincidental. However, the thin conventional histologic sections, catching only short tracts of the nerves, preclude a correct observation of their route and do not allow us to verify if there is an architectural relationship between them and the nevus as a whole. With this aim, we observed a few specimens of cellular blue nevus on digitally overlapped images of contiguous 25-microm-thick sections, processed with Winkelmann's technique of silver impregnation for nerve fibers, which supplied an overall, 3-dimensional view of the lesions and the nerves running through them. In these images, the lobular form of the nevus could be seen gathering around a branching hypertrophic nerve, whose stem stretched vertically from the depth to the most superficial tract of the lesion. The nevus cell aggregates invested the stem and the limbs individually, and these followed the curvilinear contour of the nevus lobules. Our images represent evidence of a preferential perineural aggregation of cellular blue nevus, at least in its lobular form. This indicates that the numerous nerves and the neuroid figures, observed in detail-but within a limited perspective- in the conventional sections, are not merely coincidental and they could indeed be a sign of neural differentiation and/or a clue to the possible neural origin of the nevus.
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PMID:Perineural pattern of aggregation of cellular blue nevus: probable histoarchitectural reminiscence of histogenesis. 1903 44

Silver(I) oxalate, Ag2(C2O4), reacts with two equivalents of oleylamine (Ag:oleylamine = 1:1 mole/mole) to form an oxalate-bridged silver-oleylamine complex, [(oleylamine)Ag(micro-C2O4)Ag(oleylamine)]. The precursor complex is thermally decomposed at approximately 150 degrees C with CO2 evolution to produce Ag nanoparticles with approximately 11 nm dimension. The Ag nanoparticles contain approximately 12 wt% of oleylamines as the surface stabilizer. In the synthetic mechanism, the oxalate ligand acts as a two-electron reducing agent. The precursor complex is directly transformed into oleylamine-stabilized Ag nanoparticles in high yields of more than 80% without any additional synthetic organic solvents and reducing agents.
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PMID:Direct transformation into silver nanoparticles via thermal decomposition of oxalate-bridging silver oleylamine complexes. 1990 80


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