A pyrolysis

Properties. A high volatile western Kentucky bituminous coal, the tar yield of which by Fischer assay was ca 16%, gave a tar yield of ca 26% at a pyrolysis temperature of 537°C (146—148). Tar yield peaked at ca 35% at 577°C and dropped off to 22% at 617°C. The char heating value is essentially equal to that of the starting coal, and the tar has a lower hydrogen content than other pyrolysis tars. The product char is not suitable for direct combustion because of its 2.6% sulfur content. 

Furthermore, 60—100 L (14—24 gal) oil, having sulfur content below 0.4 wt %, could be recovered per metric ton coal from pyrolysis at 427—517°C. The recovered oil was suitable as low sulfur fuel. Figure 15 is a flow sheet of the Rocky Flats pilot plant. Coal is fed from hoppers to a dilute-phase, fluid-bed preheater and transported to a pyrolysis dmm, where it is contacted by hot ceramic balls. Pyrolysis dmm effluent is passed over a trommel screen that permits char product to fall through. Product char is thereafter cooled and sent to storage. The ceramic balls are recycled and pyrolysis vapors are condensed and fractionated. 

Chemical recovery ia sodium-based sulfite pulpiag is more complicated, and a large number of processes have been proposed. The most common process iavolves liquor iaciaeration under reduciag conditions to give a smelt, which is dissolved to produce a kraft-type green liquor. Sulfide is stripped from the liquor as H2S after the pH is lowered by CO2. The H2S is oxidized to sulfur ia a separate stream by reaction with SO2, and the sulfur is subsequendy burned to reform SO2. Alternatively, ia a pyrolysis process such as SCA-Bidemd, the H2S gas is burned direcdy to SO2. A rather novel approach is the Sonoco process, ia which alumina is added to the spent liquors which are then burned ia a kiln to form sodium aluminate. In anther method, used particulady ia neutral sulfite semichemical processes, fluidized-bed combustion is employed to give a mixture of sodium carbonate and sodium sulfate, which can be sold to kraft mills as makeup chemical. 

American Ligurian, Inc. (Stanford, Connecticut) is marketing a pyrolysis process developed in Italy, which generates steam for hot water, air heating, dryers, kilns, and similar installations. A modular plant produces 8000 kg/h of steam from 1 tih of tires. The pyrolysis process produces 0.9 t of fuel ok, 270 t of steel, and 54 t of ash annually. Gas emissions meet the strictest environmental standards (16). 

In TBP extraction, the yeUowcake is dissolved ia nitric acid and extracted with tributyl phosphate ia a kerosene or hexane diluent. The uranyl ion forms the mixed complex U02(N02)2(TBP)2 which is extracted iato the diluent. The purified uranium is then back-extracted iato nitric acid or water, and concentrated. The uranyl nitrate solution is evaporated to uranyl nitrate hexahydrate [13520-83-7], U02(N02)2 6H20. The uranyl nitrate hexahydrate is dehydrated and denitrated duting a pyrolysis step to form uranium trioxide [1344-58-7], UO, as shown ia equation 10. The pyrolysis is most often carried out ia either a batch reactor (Fig. 2) or a fluidized-bed denitrator (Fig. 3). The UO is reduced with hydrogen to uranium dioxide [1344-57-6], UO2 (eq. 11), and converted to uranium tetrafluoride [10049-14-6], UF, with HF at elevated temperatures (eq. 12). The UF can be either reduced to uranium metal or fluotinated to uranium hexafluoride [7783-81-5], UF, for isotope enrichment. The chemistry and operating conditions of the TBP refining process, and conversion to UO, UO2, and ultimately UF have been discussed ia detail (40). 

Ethyleneamines are used in certain petroleum refining operations as well. Eor example, an EDA solution of sodium 2-aminoethoxide is used to extract thiols from straight-mn petroleum distillates (314) a combination of substituted phenol and AEP are used as an antioxidant to control fouling during processing of a hydrocarbon (315) AEP is used to separate alkenes from thermally cracked petroleum products (316) and TEPA is used to separate carbon disulfide from a pyrolysis fraction from ethylene production (317). EDA and DETA are used in the preparation and reprocessing of certain... 

Figure 3.24 shows the process flowsheet for an ethylene/ethylbenzene plant, Gas oil is cracked with steam in a pyrolysis furnace to form ethylene, low BTU gases, hexane, heptane, and heavier hydrocarbons. The ethylene is then reacted with benzene to form ethylbenzene (Stanley and El-Halwagi, 1995). Two wastewater streams are formed R ... 

In a typical Knof procedure, 3jS-hydroxyandrost-5-en-17-one acetate is epoxidized with perbenzoic acid (or m-chloroperbenzoic acid ) to a mixture of 5a,6a- and 5)5,6)5-epoxides (75) in 99 % yield. Subsequent oxidation with aqueous chromium trioxide in methyl ethyl ketone affords the 5a-hydroxy-6-ketone (76) in 89% yield. Baeyer-Villiger oxidation of the hydroxy ketone (76) with perbenzoic acid (or w-chloroperbenzoic acid ) gives keto acid (77) in 96% yield as a complex with benzoic acid. The benzoic acid can be removed by sublimation or, more conveniently, by treating the complex with benzoyl chloride and pyridine to give the easily isolated )5-lactone (70) in 40% yield. As described in section III-A, pyrolysis of j5-lactone (70) affords A -B-norsteroid (71). Knof used this reaction sequence to prepare 3)5-hydroxy-B-norandrost-5-en-17-one acetate, B-noran-... 

An explosion in a pyrolysis gas plant in Rumania demolished a cooling tower. It fell on the administration block, killing 162 people. Many people w ho would not build offices close to an operating plant would consider it safe to build them close to a cooling tower. It is doubtful if this is wise. 

Cycloundecanone has been prepared in several ways (a) pyrolysis of the thorium salt of dodecanedioic acid [Dodecanedioic acid, thorium (4 + )salt(2 l)],2 (b) reduction of 2-hydroxycyeloundecanone [Cycloundecanone, 2-hydroxy-],3-4 (c) ring expansion of several lower homologs... 

V sol in acetic acid, ethanol and w. Prepn is by dehydration of propan-2-ol over Al oxide at 330°. It is also obtd as a pyrolysis product of propane and as a fraction of petr well head gases Propene has a Qc of 460.47kcal/mole the expln limits with air are 2.0 to 11.1% (Ref 2) it has an autoign temp of 927°F. Under unusual conditions, such as 955 atms press and... 

A pyrolysis technique was investigated as a method for the chemical recycling of glass fibre-reinforced unsaturated polyester SMC composites. The proeess yielded liquid products and gases and also a solid residue formed in the pyrolysis of glass fibres and fillers. The solid residue was used as a reinforeement/filler in unsaturated polyester BMC composites, and the influenee on mechanical properties was studied in comparison with BMC prepared entirely from virgin materials. 

Details are given of a pyrolysis process developed by BP Chemicals for the recovery of raw materials from plastics waste. 

PBE dendrons coordinate to the surface of II-VI semiconductor nanocrystals (e.g., CdSe [33] and CdSe/ZnS core/shell structure [34, 35]) to modulate the photoluminescence of the nanocrystals [32]. Trioctylphosphine oxide (TOPO)-capped II-VI semiconductor nanocrystals of several-nanometers diameter have been synthesized by a pyrolysis reaction of organometallics in TOPO [33-35]. The capping ligand (TOPO) can be replaced by stronger ligands such as thiol compounds [36], suggesting that dendrons bearing sulfur atom(s) at the focal point replace TOPO as well. 

In the Antek Fluoride Analyzer, a pyrolysis furnace is combined with an ion-specific electrode cell (ISE). Table 8.9 compares this specific analyser to a conventional combustion bomb. 

The basic construction consists of a rectangular or cylindrical steel chamber, lined with refractory bricks. Tubes are arranged around the wall, in either horizontal or vertical banks. The fluid to be heated flows through the tubes. Typical layouts are shown in Figure 12.69a, b and c. A more detailed diagram of a pyrolysis furnace is given in Figure 12.70. 

The photodissociation dynamics of jet-cooled methyl radical produced in a pyrolysis radical beam have been investigated at 193.3 nm using photofragment translational spectroscopy by North and co-workers.112 Only... 

Step 4. Automated sampling and application of cell suspension to a pyrolysis probe tip. 

Instrumental drift results from variations in the physical conditions of a pyrolysis mass spectrometer over time.127 It leads to variation in spectral fingerprints taken from the same material on different occasions. Short-term (<30 days) instrument reproducibility was examined by Manchester et al.57 who used PyMS to differentiate strains of Carnobacterium over a four-week period. Excellent reproducibility was obtained as separation of the five type strains was sustained and spectra did not change significantly over the four weeks. 

Magee, J. T. Yousefi-Mashouf, R. Hindmarch, J. M. Duerden, B. I. A pyrolysis mass spectrometry study of the non-pigmented Prevotella species. I. Med. Microbiol. 1992,37,273-282. 

Both pipe sizes give reactors that are satisfactory from the standpoint of pressure drop and effluent temperature. Although the 4-in. reactor must be longer to achieve the desired conversion, it requires significantly less volume, and this is an important consideration in the design of a pyrolysis furnace. The 6-in. pipe has... 

Mass spectrometry (MS) coupled with pyrolysis has been a key technique in detecting the thermal degradation products of polymers, and thereby elucidating their thermal decomposition pathways [69]. In pyrolysis-MS, a sample is thermally decomposed in a reproducible manner by a pyrolysis source that is interfaced with a mass spectrometer. The volatile products formed can then be analysed either as a mixture by MS or after separation by GC/MS [70]. 

As an example of the form of the information that may be derived from a pyrolysis-MS, Figure 26 [69] shows the structure of the polycarbonate (PC) and the EI-MS spectra of pyrolysis compounds obtained by DPMS of poly(bisphenol-A-carbonate) at three different probe temperatures corresponding to the three TIC (total ion current) maxima shown in Figure 27(b) Figure 27 compares the MS-TIC curve with those obtained from thermogravimetry. (The TIC trace is the sum of the relative abundances of all the ions in each mass spectrum plotted against the time (or number of scans) in a data collection sequence [70].)... 

HALS presents some analytical difficulties. Coulier et al. [18] describe a pyrolysis GC-MS method for identification and HPLC with UV and evaporative light scattering detection methods for quantification in polymer extracts. 

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