ライフサイエンスコーパス: peracetic acid

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1 n peroxide, bleach, tert-butylhydroperoxide, peracetic acid).

2 trap and a hydroperoxide (either H(2)O(2) or peracetic acid).

3 /Na131I required the presence of the oxidant peracetic acid.

4 Pretreatment of yellow poplar with peracetic acid (300 mM, 2.3 wt%) and dilute sulfuric aci

5 Here we report that the addition of peracetic acid, a strong oxidant, to mild dilute acid pr

6 MDO reacts with cyclohexene much faster than peracetic acid/acetic acid under scrupulously dried cond

7 cular rate constant for the reaction between peracetic acid and CcP and between p-nitroperoxybenzoic

8 hlorite, very modest reactivity with H2O2 or peracetic acid, and no observable transient intermediate

9 dence of the reactions of hydrogen peroxide, peracetic acid, and p-nitroperoxybenzoic acid with CcP p

10 aveguides when exposed to hydrogen peroxide, peracetic acid, and peroxydisulfuric acid.

11 ration of pentavalent iodine compounds using peracetic acid as an oxidant in the presence of catalyti

12 (2)OSiMe(3) were oxidized with excess KF and peracetic acid at room temperature for 48 h to form the

13 Monitoring the reaction of Cld with peracetic acid by rapid-mixing UV-visible spectroscopy,

14 mpound II in a manner that is independent of peracetic acid concentration (k(2) = 170 +/- 20 s(-1)).

15 Thus, the addition of peracetic acid, easily generated from acetic acid and hy

16 By contrast, with peracetic acid, Fe(IV)=O plus a tyrosyl radical were obs

17 ncreased the specificity constant of PFE for peracetic acid formation >100-fold.

18 H dependence of the reaction between CcP and peracetic acid has also been determined.

19 the Mn(III)(salen)-catalyzed epoxidation by peracetic acid have been elucidated by the density funct

20 tures of hydrogen peroxide, acetic acid, and peracetic acid in aqueous solution.

21 l)amine, TPA)(NCCH(3))(2)](2+) with 1 equiv. peracetic acid in CH(3)CN at -40 degrees C results in th

22 e chemical oxidation of these compounds with peracetic acid, m-chloroperbenzoic acid, and OXONE.

23 An isolated higher risk associated with peracetic acid manual reuse in freestanding units (1989-

24 When peracetic acid or H(2)O(2) was used as an alternative ox

25 rmediates in reactions with other peroxides, peracetic acid (PA), and iodosylbenzene.

26 , 2) determine the antimicrobial efficacy of peracetic acid (PAA) and Amplon (blend of sulfuric acid

27 GI and GII reductions during disinfection by peracetic acid (PAA) and monochloramine in secondary was

28 ipal wastewater (MWW) effluent while the use peracetic acid (PAA) has been proposed more recently in

29 predict the Escherichia coli inactivation by peracetic acid (PAA) in municipal contact tanks fed by s

30 Peracetic acid (PAA) is a disinfectant considered for us

31 different disinfection processes (chlorine, peracetic acid (PAA), and ultraviolet light (UV)).

32 Olefin epoxidation with peracetic acid shows the imprinted manganese catalysts h

33 hase cells were more tolerant to the biocide peracetic acid than were biofilms.

34 red that the reverse reaction, hydrolysis of peracetic acid to acetic acid and hydrogen peroxide, occ

35 cAOS reacts rapidly with the oxidant peracetic acid to form heme compound I and intermediate

36 utylammonium fluoride and either H(2)O(2) or peracetic acid to form the corresponding alcohols in 48-

37 high-spin intermediate upon the addition of peracetic acid to the enzyme-substrate complex.

38 (2) has been generated by reaction of excess peracetic acid with a mononuclear iron complex [Fe(II)(C

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