Bismuth temperature

Lead bismuth temperature in primary circuit, °C core inlet 482 ... 

BUmuth was pumped by NlaPA in 1950 [26]. The system was operated for 37 hr, the maximum flow rate measured wa,s 2 gpm, the maximum head developed w as 66 psi, and the maximum bismuth temperature reached was 1765°F. The pump was a modified Browne and Sharpe No. 206, machine-tool-coolant pump. 

Arsenic and antimony resemble phosphorus in having several allotropic modifications. Both have an unstable yellow allotrope. These allotropes can be obtained by rapid condensation of the vapours which presumably, like phosphorus vapour, contain AS4 and Sb4 molecules respectively. No such yellow allotrope is known for bismuth. The ordinary form of arsenic, stable at room temperature, is a grey metallic-looking brittle solid which has some power to conduct. Under ordinary conditions antimony and bismuth are silvery white and reddish white metallic elements respectively. 

Very small quantities of bismuthine are obtained when a bismuth-magnesium alloy, BijMgj, is dissolved in hydrochloric acid. As would be expected, it is extremely unstable, decomposing at room temperature to bismuth and hydrogen. Alkyl and aryl derivatives, for example trimethylbismuthine, Bi(CHj)3, are more stable. 

Early catalysts for acrolein synthesis were based on cuprous oxide and other heavy metal oxides deposited on inert siHca or alumina supports (39). Later, catalysts more selective for the oxidation of propylene to acrolein and acrolein to acryHc acid were prepared from bismuth, cobalt, kon, nickel, tin salts, and molybdic, molybdic phosphoric, and molybdic siHcic acids. Preferred second-stage catalysts generally are complex oxides containing molybdenum and vanadium. Other components, such as tungsten, copper, tellurium, and arsenic oxides, have been incorporated to increase low temperature activity and productivity (39,45,46). 

There is often a wide range of crystalline soHd solubiUty between end-member compositions. Additionally the ferroelectric and antiferroelectric Curie temperatures and consequent properties appear to mutate continuously with fractional cation substitution. Thus the perovskite system has a variety of extremely usehil properties. Other oxygen octahedra stmcture ferroelectrics such as lithium niobate [12031 -63-9] LiNbO, lithium tantalate [12031 -66-2] LiTaO, the tungsten bron2e stmctures, bismuth oxide layer stmctures, pyrochlore stmctures, and order—disorder-type ferroelectrics are well discussed elsewhere (4,12,22,23). 

In the vapor phase, acetone vapor is passed over a catalyst bed of magnesium aluminate (206), 2iac oxide—bismuth oxide (207), calcium oxide (208), lithium or 2iac-doped mixed magnesia—alumina (209), calcium on alumina (210), or basic mixed-metal oxide catalysts (211—214). Temperatures ranging... 

Alaska, Washington, and Nevada. Ores of the Southeast Missouri lead belt and extensive deposits such as in Silesia and Morocco are of the replacement type. These deposits formed when an aqueous solution of the minerals, under the influence of changing temperature and pressure, deposited the sulfides in susceptible sedimentary rock, usually limestone and dolomites. These ore bodies usually contain galena, sphalerite, and pyrite minerals, but seldom contain gold, silver, copper, antimony, or bismuth. 

Low Melting Alloys. Lead ahoys having large amounts of bismuth, tin, cadmium, and iadium that melt at relatively low (10—183°C) temperatures are known as fusible or low melting ahoys. The specifications of many of these ahoys are Hsted ia ASTM B774-87 (7). 

MAA and MMA may also be prepared via the ammoxidation of isobutylene to give meth acrylonitrile as the key intermediate. A mixture of isobutjiene, ammonia, and air are passed over a complex mixed metal oxide catalyst at elevated temperatures to give a 70—80% yield of methacrylonitrile. Suitable catalysts often include mixtures of molybdenum, bismuth, iron, and antimony, in addition to a noble metal (131—133). The meth acrylonitrile formed may then be hydrolyzed to methacrjiamide by treatment with one equivalent of sulfuric acid. The methacrjiamide can be esterified to MMA or hydrolyzed to MAA under conditions similar to those employed in the ACH process. The relatively modest yields obtainable in the ammoxidation reaction and the generation of a considerable acid waste stream combine to make this process economically less desirable than the ACH or C-4 oxidation to methacrolein processes. 

Solders are alloys that have melting temperatures below 300°C, formed from elements such as tin, lead, antimony, bismuth, and cadmium. Tin—lead solders are commonly used for electronic appHcations, showing traces of other elements that can tailor the solder properties for specific appHcations. 

Bismuth vanadate can be produced by chemical precipitation, as weU as by high temperature calciaation methods. In the wet process, the acidic solution of bismuth nitrate, Bi(N02)3, is mixed with the alkaline solution of sodium vanadate, Na VO. The gel formed is filtered off on a filter, pressed, washed, and converted to a crystalline form by calciaation at low temperatures of 200—500°C for 1 h (37,38). 

Al-Pb. Both lead [7439-92-17, Pb, and bismuth [7440-69-9] Bi, which form similar systems (Fig. 17), are added to aluminum ahoys to promote machinahility by providing particles to act as chip breakers. The Al—Pb system has a monotectic reaction in which Al-rich Hquid free2es partiahy to soHd aluminum plus a Pb-rich Hquid. This Pb-rich Hquid does not free2e until the temperature has fahen to the eutectic temperature of 327°C. SoHd solubiHty of lead in aluminum is negligible the products contain small spherical particles of lead which melt if they are heated above 327°C. 

Solders. In spite of the wide use and development of solders for millennia, as of the mid-1990s most principal solders are lead- or tin-based alloys to which a small amount of silver, zinc, antimony, bismuth, and indium or a combination thereof are added. The principal criterion for choosing a certain solder is its melting characteristics, ie, soHdus and Hquidus temperatures and the temperature spread or pasty range between them. Other criteria are mechanical properties such as strength and creep resistance, physical properties such as electrical and thermal conductivity, and corrosion resistance. 

Tin exists in two ahotropic forms white tin (P) and gray tin (a). White tin, the form which is most familiar, crystallizes in the body-centered tetragonal system. Gray tin has a diamond cubic stmcture and may be formed when very high purity tin is exposed to temperatures well below zero. The ahotropic transformation is retarded if the tin contains smah amounts of bismuth, antimony, or lead. The spontaneous appearance of gray tin is a rare occurrence because the initiation of transformation requires, in some cases, years of exposure at —40° C. Inoculation with a-tin particles accelerates the transformation. 

Other. Insoluble alkaline-earth metal and heavy metal stannates are prepared by the metathetic reaction of a soluble salt of the metal with a soluble alkah—metal stannate. They are used as additives to ceramic dielectric bodies (32). The use of bismuth stannate [12777-45-6] Bi2(Sn02)3 5H20, with barium titanate produces a ceramic capacitor body of uniform dielectric constant over a substantial temperature range (33). Ceramic and dielectric properties of individual stannates are given in Reference 34. Other typical commercially available stannates are barium stannate [12009-18-6] BaSnO calcium stannate [12013 6-6] CaSnO magnesium stannate [12032-29-0], MgSnO and strontium stannate [12143-34-9], SrSnO. ... 

Catalytic Oxidation. Catalytic oxidation is used only for gaseous streams because combustion reactions take place on the surface of the catalyst which otherwise would be covered by soHd material. Common catalysts are palladium [7440-05-3] and platinum [7440-06-4]. Because of the catalytic boost, operating temperatures and residence times are much lower which reduce operating costs. Catalysts in any treatment system are susceptible to poisoning (masking of or interference with the active sites). Catalysts can be poisoned or deactivated by sulfur, bismuth [7440-69-9] phosphoms [7723-14-0] arsenic, antimony, mercury, lead, zinc, tin [7440-31-5] or halogens (notably chlorine) platinum catalysts can tolerate sulfur compounds, but can be poisoned by chlorine. 

Betterton-KroIIProcess. MetaHic calcium and magnesium are added to the lead bullion in a melt and form ternary compounds that melt higher than lead and are lower in density. By cooling the lead bath to a temperature close to the melting point of lead, the intermetalHc compounds high in bismuth content soHdify and float to the top where they are removed by skimming. 

The crystallisation process for concentrating bismuth ia lead by squeesiag the eutectic (high ia bismuth) Hquid out of the solidified high lead portion at a temperature within the melting range of the alloy is seldom used. 

Anchoring. Bismuth alloys that expand on solidification are particularly useful for aligning and setting punches in a die plate. It is much easier to melt and pour an ahoy around a punch than to machine the entire die plate and punch at the same time. This method also makes it easier to relocate parts or change dies. The low temperatures involved do not cause distortion. 

Fusible Safety Devices. Low melting bismuth ahoys, especiahy those that are eutectic have found numerous uses in safety devices. These ahoys can be cast into any shape necessary in order to be used in a plug or switch that must function at a given temperature. 

Steel (Quenching. Bismuth and bismuth—lead ahoys are used in the processing of some steel products. The thermal conductivity of bismuth makes it ideal for use in quenching steel. The use of a bismuth—lead ahoy in place of lead alone has the advantage of lowering the operating temperature of the bath as weh as reducing adherence of ahoy to the steel. 

Bismuthides. Many intermetaUic compounds of bismuth with alkafl metals and alkaline earth metals have the expected formulas M Bi and M Bi, respectively. These compounds ate not saltlike but have high coordination numbers, interatomic distances similar to those found in metals, and metallic electrical conductivities. They dissolve to some extent in molten salts (eg, NaCl—Nal) to form solutions that have been interpreted from cryoscopic data as containing some Bi . Both the alkafl and alkaline earth metals form another series of alloylike bismuth compounds that become superconducting at low temperatures (Table 1). The MBi compounds are particularly noteworthy as having extremely short bond distances between the alkafl metal atoms. 

A number of complex bismuth halides are weU-known, eg, disodium bismuth pentachloride [66184-10-9] Na2BiCl sodium dibismuth heptachloride [66184-09-6J, NaBi Cl and trisodium bismuth hexachlotide [66114-82-7J, Na BiCl. The acid, hydrogen dibismuth heptachloride tnhydrate [66124-39-9] HBi Cl 3H20, is a crystalline substance, stable at room temperature, that maybe isolated by cooling a solution of BiCl in concentrated hydrochloric acid to 0°C. 

Bismuth pentafluoride is an active fluorinating agent. It reacts explosively with water to form ozone, oxygen difluoride, and a voluminous chocolate-brown precipitate, possibly a hydrated bismuth(V) oxyfluoride. A similar brown precipitate is observed when the white soHd compound bismuth oxytrifluoride [66172-91 -6] BiOF, is hydrolyzed. Upon standing, the chocolate-brown precipitate slowly undergoes reduction to yield a white bismuth(Ill) compound. At room temperature BiF reacts vigorously with iodine or sulfur above 50°C it converts paraffin oil to fluorocarbons at 150°C it fluorinates uranium tetrafluoride to uranium pentafluoride and at 180°C it converts Br2 to bromine trifluoride, BrF, and bromine pentafluoride, BrF, and chlorine to chlorine fluoride, GIF. It apparently does not react with dry oxygen. 

Bismuth trioxide may be prepared by the following methods (/) the oxidation of bismuth metal by oxygen at temperatures between 750 and 800°C (2) the thermal decomposition of compounds such as the basic carbonate, the carbonate, or the nitrate (700—800°C) (J) precipitation of hydrated bismuth trioxide upon addition of an alkah metal hydroxide to a solution of a bismuth salt and removal of the water by ignition. The gelatinous precipitate initially formed becomes crystalline on standing it has been represented by the formula Bi(OH)2 and called bismuth hydroxide [10361 -43-0]. However, no definite compound has been isolated. 

Bismuth trisulfide has been used as a high temperature lubricant and has been of interest for its photo- and thermoelectric properties. 

Sihcon carbide is comparatively stable. The only violent reaction occurs when SiC is heated with a mixture of potassium dichromate and lead chromate. Chemical reactions do, however, take place between sihcon carbide and a variety of compounds at relatively high temperatures. Sodium sihcate attacks SiC above 1300°C, and SiC reacts with calcium and magnesium oxides above 1000°C and with copper oxide at 800°C to form the metal sihcide. Sihcon carbide decomposes in fused alkahes such as potassium chromate or sodium chromate and in fused borax or cryohte, and reacts with carbon dioxide, hydrogen, ak, and steam. Sihcon carbide, resistant to chlorine below 700°C, reacts to form carbon and sihcon tetrachloride at high temperature. SiC dissociates in molten kon and the sihcon reacts with oxides present in the melt, a reaction of use in the metallurgy of kon and steel (qv). The dense, self-bonded type of SiC has good resistance to aluminum up to about 800°C, to bismuth and zinc at 600°C, and to tin up to 400°C a new sihcon nitride-bonded type exhibits improved resistance to cryohte. 

Among arsenic, bismuth, lead, antimony, and sulfur in the concentration range of 5—26 ppm, bismuth had the greatest unit effect (59). A decrease in the annealing temperature prior to cold deformation led to a decrease in the measured unit effectiveness, indicating that at low temperature bismuth is not in sohd solution. Lead lowered the recrystaUization temperature, provided that the samples were aimealed at 700°C or lower. A precipitation reaction between lead and sulfur was proposed (60). 

Bismuth. Bismuth 2-ethyIhexanoate [72877-97-5] is an auxiliary drier that has been promoted for drying under adverse conditions. Like rare earths, in some coatings it is reported to give better results than zirconium at low temperature and high humidity. 

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