Physical Chemistry Chemical Physics 2011-02-14

The uptake of 2-methyl-3-buten-2-ol into aqueous mixed solutions of sulfuric acid and hydrogen peroxide.

Ze Liu, Maofa Ge, Weigang Wang, Shi Yin, Shengrui Tong

Index: Phys. Chem. Chem. Phys. 13(6) , 2069-75, (2011)

Full Text: HTML

Abstract

Multiphase acid-catalyzed oxidation with hydrogen peroxide (H(2)O(2)) has been suggested recently to be a potential route to SOA formation from isoprene and its gas-phase oxidation products, the kinetics and chemical mechanism of this process have not been well-known yet. In this work, the uptake of 2-methyl-3-buten-2-ol (MBO), an important biogenic hydrocarbon and structurally similar to isoprene, into aqueous mixed solutions of H(2)O(2) and sulfuric acid (H(2)SO(4)) was performed using a rotated wetted-wall reactor coupled to a differentially pumped single-photon ionization time of flight mass spectrometer (RWW-SPI-TOFMS). The reactive uptake coefficients (γ) were acquired for the first time and the reaction pathways were deduced according to products information. The reactive uptake coefficients of MBO into H(2)SO(4)-H(2)O(2) mixed solutions are much greater than that into H(2)SO(4) solutions. Acetaldehyde, acetone and an on-line product, which transformed to isoprene readily in the duration of an off-line experiment, were suggested as products in this process. The further reactions of the carbonyl products can occur in acidic solution, which may play a role in SOA formation. Additionally, in real atmosphere the on-line product is apt to transform to isoprene, an acknowledged precursor of biogenic SOA. Thus, the multiphase acid-catalyzed oxidation of MBO with H(2)O(2) might be a potential contributor to SOA loading.


Related Compounds

Related Articles:

Kinetics and mechanism of chlorine-atom-initiated oxidation of allyl alcohol, 3-buten-2-ol, and 2-methyl-3-buten-2-ol.

2010-04-01

[J. Phys. Chem. A 114(12) , 4224-31, (2010)]

Dose-dependent response and preliminary observations on attraction range of Ips typographus to pheromones at low release rates.

2001-12-01

[J. Chem. Ecol. 27(12) , 2425-35, (2001)]

Biosynthesis of 2-methyl-3-buten-2-ol emitted from needles of Pinus ponderosa via the non-mevalonate DOXP/MEP pathway of isoprenoid formation.

2001-06-01

[Planta 213(2) , 323-6, (2001)]

[The sedative-hypnotic action of hops. 4. Pharmacology of the hop substance 2-methyl-3-buten-2-ol].

1983-06-01

[Planta Med. 48(2) , 120-3, (1983)]

Ion trap mass spectrometry affords advances in the analytical and atmospheric chemistry of 2-hydroxy-2-methylpropanal, a proposed photooxidation product of 2-methyl-3-buten-2-Ol.

2002-05-01

[J. Am. Soc. Mass Spectrom. 13(5) , 530-42, (2002)]

More Articles...