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Amine absorber

Fluorine systems, e.g., BF3, Freon Moderate foaming, e.g., oil absorbers, amine and. 90... [Pg.304]

Medium MW hydrocarbons Mineral oil absorbers Amines, glycols... [Pg.169]

This process helps to correctly balance the gas mixture but now there will be too much carbon dioxide which must be stripped out using absorbing amine or hot bicarbonate solution. [Pg.547]

Moderate foaming, as in oil absorbers, amine, and glycol regenerators 0.85 Heavy foaming, as in amine and glycol absorbers 0.73... [Pg.1018]

Light Absorbing Amines Upon light exposure, such an amine (10.38) can be directly excited and then react with an acrylate monomer (see Ref. [2c]). A radical is thus created on the monomer (the monomer acts as an electron acceptor) an alkyl radical is obviously formed on the amine. [Pg.367]

Initiator No Wavelength (nm) Amine Absorbance Amine Wavelength (nm) Absorbance... [Pg.78]

Solvent incorrect] incorrect concentration of active ingredient for amine absorbers [amine concentration too high or too low] for glycol dehydration solvent concentration TEG < specifications/[solvent stripping inadequate] /[solvent feed temperature too hot] /[solvent contaminated]. ... [Pg.112]

Figure 7.18 shows selected DRIFTS spectra of the quartz treated for 1 h in solutions of C12-ACI and C -AAc. (The spectrum of untreated quartz is shown in Fig. 7.14.) All spectra display typical bands in the 3000-2800-cm range due to the vCH vibrations of alkyl chains. A broad structural band centered at 3250-3000 cm is attributed to H bonded vN+H, vOH, and vNH stretching vibrations. A close inspection of these spectra reveals that twice the position of this band shifts abruptly and bathychromically at a concentration close to the CHC and when the bulk amine precipitates (vide infra). It is well known [445] that a red shift of any H bonded stretching mode indicates an increase in H bond strength. In all the spectra a negative 3745-cm band for free surface silanols is observed, suggesting that the silanols interact with absorbed amine. This interaction is likely H bonding between a proton of the head group of amine cations and the SiOH oxygen. In addition, adsorption of the C12-ACI at Cfe = Cpr > 2 X 10 M results in appearance of a series of new bands at 3330,... Figure 7.18 shows selected DRIFTS spectra of the quartz treated for 1 h in solutions of C12-ACI and C -AAc. (The spectrum of untreated quartz is shown in Fig. 7.14.) All spectra display typical bands in the 3000-2800-cm range due to the vCH vibrations of alkyl chains. A broad structural band centered at 3250-3000 cm is attributed to H bonded vN+H, vOH, and vNH stretching vibrations. A close inspection of these spectra reveals that twice the position of this band shifts abruptly and bathychromically at a concentration close to the CHC and when the bulk amine precipitates (vide infra). It is well known [445] that a red shift of any H bonded stretching mode indicates an increase in H bond strength. In all the spectra a negative 3745-cm band for free surface silanols is observed, suggesting that the silanols interact with absorbed amine. This interaction is likely H bonding between a proton of the head group of amine cations and the SiOH oxygen. In addition, adsorption of the C12-ACI at Cfe = Cpr > 2 X 10 M results in appearance of a series of new bands at 3330,...
Condensation of carboxylated carbohydrates with UV-absorbing amines in the presence of carbodiimide ... [Pg.1029]

The imaging of thicker films of poly(amic esters) could also be carried out using a long wavelength absorbing amine photogenerator. The o-nitrobenzyl carbamate derivatives when substituted with electron donating substituents have... [Pg.421]


See other pages where Amine absorber is mentioned: [Pg.38]    [Pg.213]    [Pg.278]    [Pg.236]    [Pg.294]    [Pg.79]    [Pg.154]   
See also in sourсe #XX -- [ Pg.154 ]




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Absorber solution, amines

Photoinitiators-Light Absorbing Amines

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