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Metals copper lead manganese

As mentioned above, approximately 7% of the total sulfur present in lead ore is emitted as S02. The remainder is captured by the blast furnace slag. The blast furnace slag is composed primarily of iron and silicon oxides, as well as aluminum and calcium oxides. Other metals may also be present in smaller amounts, including antimony, arsenic, beryllium, cadmium, chromium, cobalt, copper, lead, manganese, mercury, molybdenum, silver, and zinc. This blast furnace slag is either recycled back into the process or disposed of in piles on site. About 50 to 60% of the recovery furnace output is slag and residual lead, which are both returned to the blast furnace. The remainder of this dross furnace output is sold to copper smelters for recovery of the copper and other precious metals. [Pg.90]

We have studied the toxicokinetics of heavy metals (arsenic, lead, manganese and copper), as well as of organophosphorus and clorinated pesticides. It has been shown that they are all characterized by different... [Pg.144]

Besides the alkali salts, the copper, lead, manganese, and uranium salts were subjected to electrolysis by Dupre,3 Wiedemann,4 Despretz,5 and Smith.6 The metals were precipitated on the cathode, a portion of the manganese and lead in the form of superoxides. [Pg.81]

The analytical results from the precipitation and adsorption tests conducted with Thio-Red II, 5% Na2CS3, and the WI starch xanthate on WPA containing additional cadmium, copper, lead, manganese, and mercury are summarized in Table III. As mentioned previously, addition of TMT-15 to WPA results in the precipitation of trithiocyanuric acid no heavy metals are coprecipitated. [Pg.155]

Rubidium metal alloys with the other alkaU metals, the alkaline-earth metals, antimony, bismuth, gold, and mercury. Rubidium forms double haUde salts with antimony, bismuth, cadmium, cobalt, copper, iron, lead, manganese, mercury, nickel, thorium, and 2iac. These complexes are generally water iasoluble and not hygroscopic. The soluble mbidium compounds are acetate, bromide, carbonate, chloride, chromate, fluoride, formate, hydroxide, iodide. [Pg.278]

Samples Analyzed by Inductively Coupled Plasma (ICP) Metals — Where two or more of the following analytes are requested on the same filter, an ICP analysis may be conducted. However, the Industrial Hygienist should specify the metals of interest in the event samples cannot be analyzed by the ICP method. A computer print-out of the following 13 analytes may be typically reported Antimony, Beryllium, Cadmium, Chromium, Cobalt, Copper, Iron, Lead, Manganese, Molybdenum, Nickel, Vanadium, Zinc. Arsenic — Lead, cadmium, copper, and iron can be analyzed on the same filter with arsenic. [Pg.253]

Precipitation is often applied to the removal of most metals from wastewater including zinc, cadmium, chromium, copper, fluoride, lead, manganese, and mercury. Also, certain anionic species can be removed by precipitation, such as phosphate, sulfate, and fluoride. Note that in some cases, organic compounds may form organometallic complexes with metals, which could inhibit precipitation. Cyanide and other ions in the wastewater may also complex with metals, making treatment by precipitation less efficient. A cutaway view of a rapid sand filter that is most often used in a municipal treatment plant is illustrated in Figure 4. The design features of this filter have been relied upon for more than 60 years in municipal applications. [Pg.246]

Environmental hazards of batteries can be briefly summarized as follows. A battery is an electrochemical device with the ability to convert chemical energy to electrical energy to provide power to electronic devices. Batteries may contain lead, cadmium, mercury, copper, zinc, lead, manganese, nickel, and lithium, which can be hazardous when incorrectly disposed. Batteries may produce the following potential problems or hazards (a) they pollute the lakes and streams as the metals... [Pg.1225]

Gasgnier M (2000) Ultrasound effects on metallic (Fe and Cr) iron sesquioxide (a-, y-Fe203) calcite copper, lead and manganese oxides as powders. Ultrason Sonochem 7 25-39... [Pg.270]

Tominaga et al. [682,683] studied the effect of ascorbic acid on the response of these metals in seawater obtained by graphite-furnace atomic absorption spectrometry from standpoint of variation of peak times and the sensitivity. Matrix interferences from seawater in the determination of lead, magnesium, vanadium, and molybdenum were suppressed by addition of 10% (w/v) ascorbic acid solution to the sample in the furnace. Matrix effects on the determination of cobalt and copper could not be removed in this way. These workers propose a direct method for the determination of lead, manganese, vanadium, and molybdenum in seawater. [Pg.246]

Holzbecker and Ryan [825] determined these elements in seawater by neutron activation analysis after coprecipitation with lead phosphate. Lead phosphate gives no intense activities on irradiation, so it is a suitable matrix for trace metal determinations by neutron activation analysis. Precipitation of lead phosphate also brings down quantitatively the insoluble phosphates of silver (I), cadmium (II), chromium (III), copper (II), manganese (II), thorium (IV), uranium (VI), and zirconium (IV). Detection limits for each of these are given, and thorium and uranium determinations are described in detail. Gamma activity from 204Pb makes a useful internal standard to correct for geometry differences between samples, which for the lowest detection limits are counted close to the detector. [Pg.282]


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