Extraction bismuth

Some basic dyes form ion-associates with Bib that can be used in sensitive methods for determining bismuth. Extractable compounds are formed with Rhodamine B, Butylrhodamine B, and Rhodamine 6G (benzene, e = 1.1-10 ) [52], and with the azo dye (formula 10.1, e = 9.2-10 ) [53]. The ion-associate of the bromide complex of Bi with Rhodamine 6G has been floated with DIPE and then dissolved in ethanol (e =1.5-10 ) [54]. 

The experience of the USA and Japan has revealed that equipping copper-smelting, tungsten and lead plants with dust-catching and dust-utilizing systems can essentially enhance bismuth extraction and has great significance for the environment. 

The application area of OSBS process is much wide than the Vanyukov process, which includes lead, antimony and bismuth extraction. Future application of this technology may include refractory gold, complex Cu-Pb-Zn ore processing. Moreover, the process might be used to smelt oxide ore, oxide-sulfide mixed ore, industrial solid waste and living garbage rather than sulfide ore only. 

Sodium bismuthate (oxidation of manganese) heat 20 parts of NaOH nearly to redness in an iron or nickel crucible, and add slowly 10 parts of basic bismuth nitrate which has been previously dried. Add 2 parts of sodium peroxide, and pour the brownish-yellow fused mass on an iron plate to cool. When cold break up in a mortar, extract with water, and collect on an asbestos filter. 

In the Betterton-KroU process the dezinced lead is pumped to the debismuthizing kettie, in which special care is taken to remove drosses that wastefuUy consume the calcium and magnesium. The skimmed blocks from the previous debismuthizing kettie are added to the bath at 420°C and stirred for a short time to enrich the dross with the bismuth being extracted from the new charge. This enriched dross is skimmed to blocks and sent to the bismuth recovery plant. 

Many nonferrous metals can be extracted by reduction smelting, eg, copper, tin, nickel, cobalt, silver, antimony, and bismuth. Blast furnaces are sometimes used for the smelting of copper or tin, but flash and reverberatory furnaces are more common for metals other than lead. 

The first successflil production method for the separation of Pu from U and its fission products was the bismuth phosphate process, based on the carrying of Pu by a precipitate of BiPO (126). That process has been superseded by Hquid-Hquid extraction (qv) and ion exchange (qv). In the Hquid-Hquid... 

Selective solution of the aluminum from the ahoy using a volatile metal, such as mercury, lead, bismuth, cadmium, magnesium, or zinc, has been investigated. After extracting the aluminum from the original ahoy into the volatile metal, the volatile metal is distilled, leaving pure aluminum. Neither electrolysis nor volatile metal extraction can extract aluminum from iron aluniinide [12004-62-3J, EeAl, titanium aluniinide [12004-78-3] TiAl, or Al C. ... 

Triphenylbismuth (bismuth triphenyl) [603-33-8] M 440.3, m 75-76 , 77-78 , 78.5 , d 4 1.6427(melt). Dissolve in EtOH, ppte with H2O, extract with Et20, dry and evaporate when the residue crystallises. It has been recrystd from EtOH and Et20-Et0H and is a stable compound. [J Chem Soc suppl pl21 I949 Chem Ber 37 4620 1904 J Am Chem Soc 62 665 1940 UV J Chem Phys 22 1430 1954.]... 

Kurchi bark is principally used in India as a remedy for amoebic dysentery, and in recent years there has been a revival of medical interest in the drug in this eonneetion. It is generally used in the form of a bark extract but, in imitation of emetine bismuth iodide, kurchi bismuth iodide, consisting of the bismuth iodides of the mixed alkaloids of the bark, has also been used. On the pharmaceutical side Datta and Bal have studied the pharmacognosy of the bark and a method of alkaloidal assay has been devised by Schroff and Dhir, who have also described a process for the preparation of kurchi bismuth iodide, a product for which they, and also Mukherjee and Dutta, have provided methods of assay. 

The reaction is a sensitive one, but is subject to a number of interferences. The solution must be free from large amounts of lead, thallium (I), copper, tin, arsenic, antimony, gold, silver, platinum, and palladium, and from elements in sufficient quantity to colour the solution, e.g. nickel. Metals giving insoluble iodides must be absent, or present in amounts not yielding a precipitate. Substances which liberate iodine from potassium iodide interfere, for example iron(III) the latter should be reduced with sulphurous acid and the excess of gas boiled off, or by a 30 per cent solution of hypophosphorous acid. Chloride ion reduces the intensity of the bismuth colour. Separation of bismuth from copper can be effected by extraction of the bismuth as dithizonate by treatment in ammoniacal potassium cyanide solution with a 0.1 per cent solution of dithizone in chloroform if lead is present, shaking of the chloroform solution of lead and bismuth dithizonates with a buffer solution of pH 3.4 results in the lead alone passing into the aqueous phase. The bismuth complex is soluble in a pentan-l-ol-ethyl acetate mixture, and this fact can be utilised for the determination in the presence of coloured ions, such as nickel, cobalt, chromium, and uranium. 

In the extraction procedure the yellow solution is allowed to stand for 10 minutes, and then extracted with 3 mL portions of a 3 1 mixture by volume of pentan-l-ol and ethyl acetate until the last extract is colourless. Make up the combined extracts to a definite volume (10 mL or 25 mL) with the organic solvent, and determine the transmittance (460 nm) at once. Construct the calibration curve by extracting known amounts of bismuth under the same conditions as the sample. 

Bismuth in lead Discussion. This method is based upon the extraction of... 

Procedure. Dissolve a suitable weight of the sample of lead in 6M nitric acid add a little 50 per cent aqueous tartaric acid to clear the solution if antimony or tin is present. Cool, transfer to a separatory funnel, and dilute to about 25 mL. Add concentrated ammonia solution to the point where the slight precipitate will no longer dissolve on shaking, then adjust the pH to 1, using nitric acid or ammonia solution. Add 1 mL freshly prepared 1 per cent cupferron solution, mix, and extract with 5 mL chloroform. Separate the chloroform layer, and repeat the extraction twice with 1 mL portions of cupferron solution + 5 mL of chloroform. Wash the combined chloroform extracts with 5mL of water. Extract the bismuth from the chloroform by shaking with two 10 mL portions of 1M sulphuric acid. Run the sulphuric acid solution into a 25 mL graduated flask. Add 3 drops saturated sulphur dioxide solution and 4 mL of 20 per cent aqueous potassium iodide. Dilute to volume and measure the transmission at 460 nm. 

The reason for the ultramicrochemical test was to establish whether the bismuth phosphate would carry the plutonium at the concentrations that would exist at the Hanford extraction plant. This test was necessary because it did not seem logical that tripositive bismuth should be so efficient in carrying tetrapositive plutonium. In subsequent months there was much skepticism on this point and the ultramicrochemists were forced to make repeated tests to prove this point. Thompson soon showed that Pu(Vl) was not carried by bismuth phosphate, thus establishing that an oxidation-reduction cycle would be feasible. All the various parts of the bismuth-phosphate oxidation-reduction procedure, bulk reduction via cross-over to a rare earth fluoride oxidation-reduction step and final isolation by precipitation of plutonium (IV) peroxide were tested at the Hanford concentrations of... 

The original method of phosphate preparation involved extracting the phosphate and reprecipitating it as a bismuth phosphate (Tudge 1960). Alternatively, it is precipitated as a silver phosphate (Wright and Hoering 1989) which involves fewer steps and, more importantly, silver phosphate is not hygroscopic (as is bismuth phosphate) which minimizes the potential for contamination by atmospheric water. 

A 15% nitric acid solution in ethanol was used to clean a bismuth crystal. The solution decomposed violently after this treatment and projected the content of the container into the extraction hood in which it was placed. Mixtures with less than 10% of nitric acid in alcohol are the only ones to remain stable for short periods of time. They should never be stored. In this particular accident, the presence of bismuth suggests a reaction of type (3). 

V. H. Aprahamian and D. G. Demopoulos, The Solution Chemistry and Solvent Extraction Behaviour of copper, iron, nickel, zinc, lead, tin, Ag, arsenic, antimony, bismuth, selenium and tellurium in Acid Chloride Solutions Reviewed from the Standpoint of PGM Refining, Mineral Processing and Extractive Metallurgy Review, Vol. 14, p. 143,1995. 

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 [43]. After about 24 h, the samples were filtered on 0.4 jtm Nuclepore filters. The separated precipitates were dissolved with hydrochloric acid and the solutions 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 AAS (EAAS). The decomposition of organic complexes and other procedures were also examined by EAAS. 

Selenium is extracted as diethyldithiocarbamate complex from the solution containing citrate and EDTA [5]. Ohta and Suzuki [6] found that only a few elements, such as copper, bismuth, arsenic, antimony, and tellurium, are also extracted together with selenium. They examined this for effects of hundredfold amounts of elements co-extracted with the selenium diethyldithiocarbamate complex. An appreciable improvement of interferences from diverse elements was observed in the presence of copper. Silver depressed the selenium absorption in the case of atomisation of diethyldithiocarbamate complex, but the interference of silver was suppressed in the presence of copper. The atomisation profile from diethyldithiocarbamate complex was identical with that from selenide. 

Shijo et al. [95] converted bismuth in seawater into its dithiocarbamate complex, and then extracted the complex into xylene prior to determination in amounts down to 0.3 ppt by electrothermal atomic absorption spectrometry. 

Rodionova and Ivanov [667] used chelate extraction in the determination of copper, bismuth, lead, cadmium, and zinc in seawater. The metal complexes of diethyl and dithiophosphates are extracted in carbon tetrachloride prior to determination by atomic absorption spectrometry. 

Bismuth Liquid-liquid extraction into xylene as the ammonium pyrrolidine dithiocarbamate complex Electrothermal AAS 0.3 ppt or 0.0005 xg/l [95]... 

Tsunogai and Nozaki [6] analysed Pacific Oceans surface water by consecutive coprecipitations of polonium with calcium carbonate and bismuth oxychloride after addition of lead and bismuth carriers to acidified seawater samples. After concentration, polonium was spontaneously deposited onto silver planchets. Quantitative recoveries of polonium were assumed at the extraction steps and plating step. Shannon et al. [7], who analysed surface water from the Atlantic Ocean near the tip of South Africa, extracted polonium from acidified samples as the ammonium pyrrolidine dithiocarbamate complex into methyl isobutyl ketone. They also autoplated polonium onto silver counting disks. An average efficiency of 92% was assigned to their procedure after calibration with 210Po-210Pb tracer experiments. 

Tseng et al. [69] determined 60cobalt in seawater by successive extractions with tris(pyrrolidine dithiocarbamate) bismuth (III) and ammonium pyrrolidine dithiocarbamate and back-extraction with bismuth (III). Filtered seawater adjusted to pH 1.0-1.5 was extracted with chloroform and 0.01 M tris(pyrrolidine dithiocarbamate) bismuth (III) to remove certain metallic contaminants. The aqueous residue was adjusted to pH 4.5 and re-extracted with chloroform and 2% ammonium pyrrolidine thiocarbamate, to remove cobalt. Back-extraction with bismuth (III) solution removed further trace elements. The organic phase was dried under infrared and counted in a ger-manium/lithium detector coupled to a 4096 channel pulse height analyser. Indicated recovery was 96%, and the analysis time excluding counting was 50-min per sample. 

Flynn [72] has described a solvent extraction procedure for the determination of 54manganese in seawater in which the sample with bismuth, cerium, and chromium carriers, is extracted with a heptane solution of bis(2-ethylhexyl) phosphate and the manganese back-extracted with 1M hydrochloric acid. After... 

More recently, Robert A. Nelson s collection, Adept Alchemy (1998), continues to assert alchemy s scientific validity and its relationship to modem atomic science. Nelson s anthology intends to help alchemists working in the so-called dry path to transmutation. It includes extracts and summaries of work from the Middle Ages through the late twentieth century by Hermetic alchemists, chemists, and physicists, including the 1980 transmutation of bismuth into gold by scientists at the Lawrence Berkeley lab. (Nelson also includes the more controversial methods of Joe Champion in the 1990s. Champion was convicted of fraud in Arizona because he had not produced the results he claimed for investors.) Across the century, then, followers of occult alchemy have clearly continued to make connections to modern atomic science. 

Pattinson (1) A process for extracting silver from lead by selective crystallization. When molten lead is cooled, the first crystals of lead contain less silver than the residual melt. Repetition of this process a number of times yields a silver concentrate which is further purified by cupellation. Invented in 1833 by H. L. Pattinson. Largely superseded by the Parkes process, except for metals containing bismuth for which the Pattinson is the preferred process. See also Luce-Rozan. 

Willis 93) extracted lead directly from 200 ml of urine with APDC into 1.5 ml of methyl-n-amyl ketone. He was able to determine as little as 0.02 ppm of lead. Kopito and Shwachman 141>, on the other hand, co-precipitate the lead from urine with bismuth nitrate by adding ammonia. The precipitated bismuth hydroxide is dissolved in acid and this solution is aspirated. Coprecipitation of the lead is not quantitative, and so standards should be prepared in the same manner. It should be possible to employ this procedure with protein free filtrates of blood without the necessity of close pH control. 

Willis determined the physiological level of bismuth in urine to be about 0.02 ppm by using the same procedure he described for lead 93). Devoto ls°) dry ashed 100 ml of urine and extracted bismuth with APDC into 5 ml of MIBK. 

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