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C2H5OH oxidation

Thus, both processes of H202 dissociation and C2H5OH oxidation proceed in two stages general intermediate (Chance) complex formation responsible for chemical conjugation in the system and Oguri complex formation, which induces the one-stage synthesis of the final oxidation products. [Pg.215]

Ethanol C2H5OH oxidizes in a multistep process in solution to acetaldehyde. [Pg.568]

Figure 11.8 (a) SNIFTIR spectra of the species coming from methanol adsorption and oxidation at a Pt/C electrode 0.1 M HCIO4 + 0.1 M CH3OH 25 °C. (h) SNIFTIR spectra of the species coming from ethanol adsorption and oxidation on a Pt/C electrode 0.1 M HCIO4 + 0.1 M C2H5OH 25 °C. [Pg.356]

Figure 11.9 Intensities of the COl ( ) and CO2 ( ) bands as functions of potential, (a, b) From the spectra of the species coming from methanol adsorption and oxidation (0.1 M HCIO4 + O.IM CH3OH, 25 °C) (a) Pt/C electrode (b) Pto.g + RU0.2/C electrode, (c, d) From the spectra of the species coming from ethanol adsorption and oxidation (0.1 M HCIO4 + 0.1 M C2H5OH, 25 °C) (c) Pt/C electrode (d) Pto.pSno.i/C electrode. The dashed curves in (c) and (d) show I E). Figure 11.9 Intensities of the COl ( ) and CO2 ( ) bands as functions of potential, (a, b) From the spectra of the species coming from methanol adsorption and oxidation (0.1 M HCIO4 + O.IM CH3OH, 25 °C) (a) Pt/C electrode (b) Pto.g + RU0.2/C electrode, (c, d) From the spectra of the species coming from ethanol adsorption and oxidation (0.1 M HCIO4 + 0.1 M C2H5OH, 25 °C) (c) Pt/C electrode (d) Pto.pSno.i/C electrode. The dashed curves in (c) and (d) show I E).
Example On oxidation of 50.0 g of ethanol, 59.0 g of ethanoic acid were obtained. Calculate the percentage yield of the product (molar masses ethanol C2H5OH = 46.0gmor, ethanoic acid CH3CO2H = 60. Ogmoh1). [Pg.28]

Example Calculate the standard enthalpy change for the oxidation of ethanol (C2H5OH) to ethanal (CH3CHO), given the following standard enthalpies of combustion ... [Pg.65]

Figure 1.11 Electro-oxidation of ethanol on Pt/C (full line) and different Pt-based (dashed and dotted lines) catalysts with 0.1 mgPtcrn" loading. 0.1 M HCIO4 + 1 M C2H5OH 5 mVs ... Figure 1.11 Electro-oxidation of ethanol on Pt/C (full line) and different Pt-based (dashed and dotted lines) catalysts with 0.1 mgPtcrn" loading. 0.1 M HCIO4 + 1 M C2H5OH 5 mVs ...
An example of propellant tailoring is the fuel used to launch the first U. S. satellite into orbit. The original fuel for the launch vehicle was ethyl alcohol. MAF-4 (also known as hydyne or U-DETA), a mixture of 60% UDMH and 40% diethylenetriamine (DETA), was formulated to simulate the physical properties of C2H5OH but provide the increased propellant performance (using liquid oxyen as the oxidizer) requirements of the mission. [Pg.318]

Fig. 18 CTL spectra during catalytic oxidation of CH3CHO, C2H5OH, and C2H4 on nanosized SrCC>3 [23]... Fig. 18 CTL spectra during catalytic oxidation of CH3CHO, C2H5OH, and C2H4 on nanosized SrCC>3 [23]...
Two-electron oxidation of the substrate (i.e. H202 and C2H5OH) in one stage. [Pg.213]

In the [E—OOH C2H5OH] complex ligand OOH is the electron acceptor particle, whereas ligand C2H5OH (DH2 in the general shape) is the electron donor. Their interaction regenerates active sites of catalase, produces H20 and oxidizes the substrate. [Pg.215]


See other pages where C2H5OH oxidation is mentioned: [Pg.165]    [Pg.167]    [Pg.165]    [Pg.167]    [Pg.219]    [Pg.472]    [Pg.506]    [Pg.22]    [Pg.298]    [Pg.411]    [Pg.113]    [Pg.230]    [Pg.245]    [Pg.80]    [Pg.325]    [Pg.124]    [Pg.368]    [Pg.109]    [Pg.208]    [Pg.194]    [Pg.1388]    [Pg.259]    [Pg.45]    [Pg.95]    [Pg.317]    [Pg.467]    [Pg.202]    [Pg.59]    [Pg.365]    [Pg.115]    [Pg.163]    [Pg.302]    [Pg.377]    [Pg.126]    [Pg.47]    [Pg.83]    [Pg.139]    [Pg.324]    [Pg.221]    [Pg.111]   
See also in sourсe #XX -- [ Pg.833 ]




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C2H5OH

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