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Infrared spectroscopy aromatic amines

Air Monitoring. The atmosphere in work areas is monitored for worker safety. Volatile amines and related compounds can be detected at low concentrations in the air by a number of methods. Suitable methods include chemical, chromatographic, and spectroscopic techniques. For example, the NIOSH Manual of Analytical Methods has methods based on gas chromatography which are suitable for common aromatic and aHphatic amines as well as ethanolamines (67). Aromatic amines which diazotize readily can also be detected photometrically using a treated paper which changes color (68). Other methods based on infrared spectroscopy (69) and mass spectroscopy (70) have also been reported. [Pg.264]

Infrared radiation, electromagnetic spectrum and, 419, 422 energy of. 422 frequencies of, 422 wavelengths of, 422 Infrared spectroscopy, 422-431 acid anhydrides, 822-823 acid chlorides, 822-823 alcohols. 428, 632-633 aldehydes, 428. 730-731 alkanes, 426-427 alkenes, 427 alkynes, 427 amides. 822-823 amines, 428, 952 ammonium salts, 952-953 aromatic compound, 427-428, 534 bond stretching in, 422... [Pg.1301]

Infrared spectroscopy was used to follow the ageing processes of two epoxy resins. Resin samples were exposed to ionising radiation and the effects at the molecular level, and how the resins modified their hydration mechanisms was discussed. Aromatic amine cured resins are only slightly affected by the radiation, but those cured by alkyl diamines are more sensitive and thus absorb more water.molecules. 14 refs. [Pg.53]

Finally, we call attention to the remarkable stability of the complexes of nitrophenols ° and FAD (entries 48-51, Table II). This stability may be due to protonation of the adenine moiety of FAD by the phenols. Briegleb and Delle ° have detected salt formation in complexes of aromatic amines and picric acid (piT 1.8-10 ). They used infrared absorption spectroscopy and detected a typical salt band at 3.4 ju (2910 cm ). [Pg.135]

Antioxidant and antiozonant types most commonly used are aromatic amines or phenolics, though others are also employed, and can be determined using a variety of techniques such as UV-visible spectrophotometry, FTIR, near-infrared spectroscopy, TEC, GC (if the material can be volatilized), supercritical fluid chromatography, and HPLC. Identification of unknown antioxidants requires a separation technique like chromatography followed by mass spectrometry, NMR, ETIR, X-ray crystallography, etc. Standardized TEC methods are given in ASTM D3156 and... [Pg.3808]

The test is best used to distinguish primary aromatic and primary aliphatic amines from secondary and tertiary amines. It also differentiates aromatic and aliphatic primary amines. It cannot distinguish between secondary and tertiary amines. You will need to use infrared spectroscopy to make the distinction between secondary and tertiary amines. Primary aliphatic amines lose nitrogen gas at low temperatures under the conditions of this test. Aromatic amines yield a more stable diazonium salt and do not lose nitrogen until the temperature is elevated. In addition, aromatic diazonium salts produce a red azo dye when -naphthol is added. Secondary and tertiary amines produce yellow nitroso compounds, which may be soluble or may be oils or solids. Many nitroso compounds have been shown to be carcinogenic. Avoid contact and immediately dispose of all such solutions in an appropriate waste container. [Pg.490]

Thus, Frye and co-workers [47] were able to provide evidence by infrared (IR) spectroscopy [46] and radiochemistry [48] of the insertion of ester groupings from barium, cadmium or zinc-carboxylates into PVC after heat treatment. Tin contents and organic residues of organotin stabilisers in heat-treated PVC are indicated by the same authors [47, 49]. Schlimper [50] and Schroder and co-workers [51] proved the direct reaction between PVC and nitrogen-containing organic stabilisers by elemental analytical examinations and infrared and UV spectrometry. Phenolic antioxidants or their decomposition products in part were re-found in PP after oxidative degradation. With rubber vulcanisates hydrochloric acid-resistant amine-rubber compounds have been reported after thermal oxidation in the presence of aromatic amines [52]. [Pg.90]

Amino groups have also been acetylated with acetic anhydride in dimethylacetamide. Diethylamine was added, and the excess amine was titrated potentiometrically. The sequence distribution of an aromatic polyamide terpolymer prepared under various reaction conditions was determined by nuclear magnetic resonance spectrometry. Infrared spectroscopy and mass spectrometry have been used to estimate the degree of conversion of polyimides, ie. the extent of polyamic acid ring closure. [Pg.35]

Recently/ the crosslinking reactions of tetrafiinctional epoxy resins with aromatic primary diamines was investigated. The crosslinked polymers were characterized by UV visible and fluo> rescence spectroscopies after gelation. The amount of tertiary amine fluorescence intensity of the spectra shows significant amounts of such amines in the finished products. The infrared spectra confirm the overall reaction of epoxides with amines, but also show that ether formation becomes significant only late in the cure. In addition, during the cure, especially in air, some oxidations and degradations occur. This results in color formation. [Pg.342]


See other pages where Infrared spectroscopy aromatic amines is mentioned: [Pg.23]    [Pg.377]    [Pg.409]    [Pg.285]    [Pg.269]    [Pg.58]    [Pg.147]    [Pg.298]    [Pg.441]    [Pg.4]    [Pg.171]    [Pg.97]    [Pg.351]    [Pg.167]    [Pg.366]   
See also in sourсe #XX -- [ Pg.687 , Pg.688 ]




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