Big Chemical Encyclopedia

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

Articles Figures Tables About

Di-butyl phosphate

Many organic reagents have been used successfully in Pu separation processes. The reagents include tri- -butyl phosphate (TBP) methyl isobutyl ketone thenoyl ttifluoroacetone (TTA) ethers, eg, diethyl ether, di- -butyl ether, tetraethylene glycol dibutyl ether trdaurylamine (TT,A) trioctylamine (TOA) di- -butyl phosphate (DBP) hexyl-di(2-ethylhexyl) phosphate (HDEHP) and many others. Of these, TBP is by far the most widely used (30,95). [Pg.201]

Synonyms Dibutyl hydrogen phosphate di- -butyl phosphate... [Pg.217]

Tetra-n-butylammonium di-r-butyl phosphate, [(CH3)3CO]2PON[C4Hg-n]4 (1). Mol. wt. 451.7, m.p. 108-110°. The salt is prepared by reaction of potassium di-(-butyl phosphate with tetra-n-butylammonium hydrogen sulfate in aqueous NaOH-CHjCU (96% yield). [Pg.528]

Whyman, 1970 Chapman et al, 1971). Other surfactants such as Triton X-114 have also been investigated. Anderson and McClure (1973) report a formulation of Triton X-114 in xylene which will accept up to 30% (v/v) aqueous sample and provides up to 47% efficiency for tritium. Another scintillation cocktail dubbed "Plasmasol" is a mixture of xylene, Triton X-100 and mono- and di-butyl phosphate (Wiegman et al, 1975). As the name Plasmasol suggests, it was designed for use with aqueous solutions containing soluble protein and is especially suited for radioimmunoassay. [Pg.494]

Ho, D., Corrosion Inhibition Effectiveness of Green Cerinm-organo Compounds Cerium Salicylate and Cerium Di-butyl Phosphate on AA2024 T3 in Both Aqueous and Epoxy Coating Environments, in Materials Engineering. 2007, Monash University Melbourne. [Pg.142]

New GC and GC-MS methods have been reported for simultaneous determinations of organophosphorus flame retardants in textiles, including a GC method combined with microwave-assisted extraction, and a GC-MS method following ultrasonic extraction, also a phosphate-based flame retardant in textiles by GC-MS, ° and in styrene-based polymers from waste electrical equipment by both GC (NP detector) and GC-MS. ° The gas chromatographic retentions of allq l phosphates on ionic liquid stationary phases have been studied, as well as a comparative study on the determination of di- -butyl phosphate in spent nuclear solvents by both gas- (GC) and ion chromatography (IC) methods/ ... [Pg.441]

Successful strategies for generating complexes of the di(terf-butyl)phosphate ligand primarily focus on the use of H0P(0)(0 Bu)2 as a reagent. As with the related siloxide species, all synthetic manipulations must be performed under inert conditions to avoid hydrolysis of the M - O - P linkages. Complexes of the - 02P(0 Bu)2 ligand are useful precursors to M/P/0 oxide materials. [Pg.84]

The following examples describing the thermolytic behavior of di(ferf-butyl)phosphate complexes serve to demonstrate the utihty of the TMP approach for synthesis of various phosphate materials. [Pg.98]

Di-t-butyl phosphate complexes of zinc were synthesized as precursors for ceramic material formation. A tetrameric zinc complex was characterized from the treatment of zinc acetate with the phosphate resulting in a compound with a bridging oxo at the center, [Zn4(/i4-0)(di-t-butyl phosphate)6]. In the presence of auxiliary donor ligands such as imidazole or ethylenediamine, monomeric complexes are formed, [Zn(di-t-butyl phosphate)2(imidazole)4]. It is also possible to convert the tetramer into the monomer by treating with a large excess of imidazole.41... [Pg.1180]

Various organic extractants may be used, including butyl and amyl alcohols, di-isopropyl ether, tri-n-butyl phosphate, and tri-2-ethylhexyl phosphate. The fluoride remains with the... [Pg.121]

For the preparation of coordination polymers (see above) by rearrangement reactions of di-tert-butyl phosphate complexes containing the M4(//4-0) core (Fig. 4) in the presence of an acid or a base [98, 99] (Scheme 4)... [Pg.161]

Methyl-lH-imidazol-l-yl group, present in a side chain of perhydro-pyrido[2,l-c][l,4]oxazin-6-one skeleton was quaternized by reacting with chloromethyl di-ferf-butyl phosphate in the presence of Nal and Hiining s base in DME at 80 °C for 2 h, followed by treatment TFA in CHCI3 to give methylphosphonic acid derivative (08WOP2008/013213). [Pg.72]

Chart 12. Complexes of Di(ferf-butyl) Phosphate with Aluminum... [Pg.363]


See other pages where Di-butyl phosphate is mentioned: [Pg.486]    [Pg.442]    [Pg.442]    [Pg.486]    [Pg.563]    [Pg.339]    [Pg.154]    [Pg.537]    [Pg.537]    [Pg.133]    [Pg.141]    [Pg.486]    [Pg.442]    [Pg.442]    [Pg.486]    [Pg.563]    [Pg.339]    [Pg.154]    [Pg.537]    [Pg.537]    [Pg.133]    [Pg.141]    [Pg.300]    [Pg.70]    [Pg.84]    [Pg.84]    [Pg.85]    [Pg.86]    [Pg.89]    [Pg.89]    [Pg.98]    [Pg.100]    [Pg.466]    [Pg.300]    [Pg.68]    [Pg.502]    [Pg.362]   
See also in sourсe #XX -- [ Pg.125 , Pg.174 ]




SEARCH



4- butyl phosphates

Di phosphate

Di-n-butyl phosphate

© 2024 chempedia.info