Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

2,3,6-TBA

The tendency to separate is expressed most often by the cloud point, the temperature at which the fuei-alcohol mixture loses its clarity, the first symptom of insolubility. Figure 5.17 gives an example of how the cloud-point temperature changes with the water content for different mixtures of gasoline and methanol. It appears that for a total water content of 500 ppm, that which can be easily observed considering the hydroscopic character of methanol, instability arrives when the temperature approaches 0°C. This situation is unacceptable and is the reason that incorporating methanol in a fuel implies that it be accompanied by a cosolvent. One of the most effective in this domain is tertiary butyl alcohol, TBA. Thus a mixture of 3% methanol and 2% TBA has been used for several years in Germany without noticeable incident. [Pg.244]

Very Htfle data are available regarding effects of anaboHc steroid implants on the Hpid metaboHsm in growing mminants. Lipogenic enzyme activity and fatty acid synthesis in vitro were elevated in subcutaneous adipose tissue from bulls implanted with estradiol (44), which may account for the increase in fat content of carcasses reported in some studies. TBA implants have no effect on Hpogenesis in intact heifers, and only tend to reduce Hpogenic enzyme activities in ovariectomized heifers (45). [Pg.409]

The cure of novolaks with hexa has been studied with differential scanning calorimetry (dsc) and torsional braid analysis (tba) (46) both a high ortho novolak and a conventional acid-cataly2ed system were included. The dsc showed an exothermic peak indicating a novolak—hexa reaction ca 20°C higher than the gelation peak observed in tba. Activation energies were also calculated. [Pg.299]

Geographical location Chlorohydrin Coproduct—TBA Coproduct—Styrene Total produc-ti capaciP... [Pg.136]

The hydroperoxide process involves oxidation of propjiene (qv) to propylene oxide by an organic hydroperoxide. An alcohol is produced as a coproduct. Two different hydroperoxides are used commercially that result in / fZ-butanol or 1-phenylethanol as the coproduct. The / fZ-butanol (TBA) has been used as a gasoline additive, dehydrated to isobutjiene, and used as feedstock to produce methyl tert-huty ether (MTBE), a gasoline additive. The 1-phenyl ethanol is dehydrated to styrene. ARCO Chemical has plants producing the TBA coproduct in the United States, Erance, and the Netherlands. Texaco has a TBA coproduct plant in the United States. Styrene coproduct plants are operated by ARCO Chemical in the United States and Japan, Shell in the Netherlands, Repsol in Spain, and Yukong in South Korea. [Pg.136]

The tert-huty hydroperoxide is then mixed with a catalyst solution to react with propylene. Some TBHP decomposes to TBA during this process step. The catalyst is typically an organometaHic that is soluble in the reaction mixture. The metal can be tungsten, vanadium, or molybdenum. Molybdenum complexes with naphthenates or carboxylates provide the best combination of selectivity and reactivity. Catalyst concentrations of 200—500 ppm in a solution of 55% TBHP and 45% TBA are typically used when water content is less than 0.5 wt %. The homogeneous metal catalyst must be removed from solution for disposal or recycle (137,157). Although heterogeneous catalysts can be employed, elution of some of the metal, particularly molybdenum, from the support surface occurs (158). References 159 and 160 discuss possible mechanisms for the catalytic epoxidation of olefins by hydroperoxides. [Pg.138]

After epoxidation a distillation is performed to remove the propylene, propylene oxide, and a portion of the TBHP and TBA overhead. The bottoms of the distillation contains TBA, TBHP, some impurities such as formic and acetic acid, and the catalyst residue. Concentration of this catalyst residue for recycle or disposal is accompHshed by evaporation of the majority of the TBA and other organics (141,143,144), addition of various compounds to yield a metal precipitate that is filtered from the organics (145—148), or Hquid extraction with water (149). Low (<500 ppm) levels of soluble catalyst can be removed by adsorption on soHd magnesium siUcate (150). The recovered catalyst can be treated for recycle to the epoxidation reaction (151). [Pg.139]

The / f/-butanol (TBA) coproduct is purified for further use as a gasoline additive. Upon reaction with methanol, methyl tert-huty ether (MTBE) is produced. Alternatively the TBA is dehydrated to isobutylene which is further hydrogenated to isobutane for recycle ia the propylene oxide process. [Pg.139]

Torsional Braid Analyzer (TBA) B 10- -1 Plastics Analysis Instmments, Princeton, N.J. [Pg.196]

Free- Vibration Methods. Free-vibration instmments subject a specimen to a displacement and allow it to vibrate freely. The oscillations are monitored for frequency and damping characteristics as they disappear. The displacement is repeated again and again as the specimen is heated or cooled. The results are used to calculate storage and loss modulus data. The torsional pendulum and torsional braid analy2er (TBA) are examples of free-vibration instmments. [Pg.197]

The first known incidence of pollution from approved herbicides was identified in 1972 in Essex, where tomato plants grown by commercial producers became malformed. The plants had been watered from public water supplies fed from a reservoir. The reservoir in turn abstracted water from a river supplemented by a water transfer scheme, from the River Cam in Cambridgeshire. Pollution from a factory manufacturing 2,3,6-TBA was identified as the cause and the problem was subsequently resolved by treating the effluent. [Pg.45]

Chemical Designations - Synonyms 2-Aminoisobutane 2-Amino-2-Methylpropane 1,1-Diraethylethylamine TBA Trimethylaminomethane Chemical Formula (CH3)3CNHj Observable Characteristics - Physical State (as normally shipped) Liquid Color Colorless Odor. Like ammonia. [Pg.61]

Tba oil coDiaius a terpent- iiihellaudiein 1), heiuyl liftnzoatu, benzvl ciimamate, and tirnesol. [Pg.485]

Oxygen was added as oxygenated hydrocarbon components methyl tert-butyl ether (MTBE), tert-amyl methyl ether (TAME), ethyl tert-butyl ether (ETBE), di-isopropyl ether (DIPE), ethanol, methanol, and tertiary butyl alcohol (TBA). The properties of oxygenates, as they relate to gasoline blending, are shown in Table 10-1. [Pg.312]

The effects of solvent on reactivity ratios and polymerization kinetics have been analyzed for many copolymerizations in terms of this theory.98 These include copolymerizations of S with MAH,"7 118 S with MAA,112 S with MMA,116 117 "9 121 S with HEMA,122 S with BA,123,124 S with AN,103415 125 S with MAN,112 S with AM,11" BA with MM A126,127 and tBA with HEMA.128 It must, however, be pointed out that while the experimental data for many systems are consistent with a bootstrap effect, it is usually not always necessary to invoke the bootstrap effect for data interpretation. Many authors have questioned the bootstrap effect and much effort has been put into finding evidence both for or against the theory.69 70 98 129 "0 If a bootstrap effect applies, then reactivity ratios cannot be determined by analysis of composition or sequence data in the normal manner discussed in Section 7.3.3. [Pg.431]

A few studies have appeared on systems based on persistent nitrogen-centered radicals. Yamada et al.2"1 examined the synthesis of block polymers of S and MMA initiated by derivatives of the triphenylverdazyl radical 115. Klapper and coworkers243 have reported on the use of triazolinyl radicals (e.g. 116 and 117). The triazolinyl radicals have been used to control S, methacrylate and acrylate polymerization and for the synthesis of block copolymers based on these monomers [S,243 245 tBA,243 MMA,243 245 BMA,245 DMAEMA,24 5 TMSEMA,247 (DMAEMA-Wbc/fc-MMA),246 (DMAEMA-Woc -S)246 and (TMSEMA-6/ocfc-S)247]. Reaction conditions in these experiments were similar to those used for NMP. The triazolinyl radicals show no tendency to give disproportionation with methacrylate propagating radicals. Dispcrsitics reported arc typically in the range 1.4-1.8.2"43 246... [Pg.483]

Many suspension polymerization recipes have been reported/75 Some of the more successful that yield polymers of low dispersity are for MMA with 146, S, BA, MA, tBA and copolymers with 154,j7/ and BMA with I38/21 Important considerations are a catalyst that is both hydrophobic (to limit partitioning into the aqueous phase) and hydrolytically stable. [Pg.498]


See other pages where 2,3,6-TBA is mentioned: [Pg.205]    [Pg.503]    [Pg.134]    [Pg.88]    [Pg.185]    [Pg.185]    [Pg.408]    [Pg.409]    [Pg.409]    [Pg.409]    [Pg.299]    [Pg.136]    [Pg.138]    [Pg.198]    [Pg.198]    [Pg.247]    [Pg.349]    [Pg.358]    [Pg.179]    [Pg.258]    [Pg.258]    [Pg.419]    [Pg.1289]    [Pg.1289]    [Pg.1289]    [Pg.1289]    [Pg.1289]    [Pg.1685]    [Pg.1706]    [Pg.1732]    [Pg.253]    [Pg.312]    [Pg.7]   
See also in sourсe #XX -- [ Pg.65 ]

See also in sourсe #XX -- [ Pg.435 ]

See also in sourсe #XX -- [ Pg.228 , Pg.232 ]

See also in sourсe #XX -- [ Pg.435 ]

See also in sourсe #XX -- [ Pg.210 ]

See also in sourсe #XX -- [ Pg.210 ]

See also in sourсe #XX -- [ Pg.468 ]




SEARCH



Chitosan-TBA conjugate

Generalizations of the TBA

MDA-TBA adduct by HPLC

TBA carboxylates

TBA dicarboxylates

TBA formate

TBA hydroxide

TBA numbers

TBA test

TBA value

TBA-reaction

TbAs 533 susceptibility

© 2024 chempedia.info