2010
DOI: 10.1080/15440470903579275
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Infrared Spectroscopy of Fiber Flax

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Cited by 20 publications
(16 citation statements)
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“…In addition, the band at 1735 cm −1 has not been observed for any man-made fiber samples, but appeared in several natural fiber samples (flax, hemp, sisal), and can be related to their pectin content. 37 , 38 A strong band in IR spectra of natural fibers at 1425 cm −1 assigned to CH 2 or O–C–H bending appears weak and shifted to 1420 cm −1 for man-made fibers, which is in accordance with prior reports. 39 Further, absorption bands at 1105 and 1051 cm −1 assigned to the antisymmetric and symmetric C–O–C stretching modes, respectively, show high intensity for natural fibers but merely appear as shoulders in man-made fiber samples.…”
Section: Resultssupporting
confidence: 91%
“…In addition, the band at 1735 cm −1 has not been observed for any man-made fiber samples, but appeared in several natural fiber samples (flax, hemp, sisal), and can be related to their pectin content. 37 , 38 A strong band in IR spectra of natural fibers at 1425 cm −1 assigned to CH 2 or O–C–H bending appears weak and shifted to 1420 cm −1 for man-made fibers, which is in accordance with prior reports. 39 Further, absorption bands at 1105 and 1051 cm −1 assigned to the antisymmetric and symmetric C–O–C stretching modes, respectively, show high intensity for natural fibers but merely appear as shoulders in man-made fiber samples.…”
Section: Resultssupporting
confidence: 91%
“…The lack of absorption bands in considered wavelength is characteristic of CF [57]. For FF fiber, several absorption bands were denoted, including 3337 and 3296 cm −1 (O-H stretching band), overlapping 2900 and 2896 cm −1 (C-H stretching and C-H 2 symmetrical stretching), 1713 cm −1 (C=O carbonyl stretching of hemicellulose), 1620 cm −1 (water absorbed in cellulose), 1432 and 1372 cm −1 (-CH 3 asymmetric and C-H symmetric deformations from lignin), 1335 cm −1 (aromatic ring of the cellulose), 1101 cm −1 (C-O-C symmetric glycosidic stretch), 1052 cm −1 (C-OH stretching vibration of cellulose backbone), and 896 cm −1 (phase ring stretching from the cellulose backbone) [58][59][60]. Figure 4 shows the characteristic spectra for epoxy-based composition after curing.…”
Section: Resultsmentioning
confidence: 99%
“…Single flax fiber is formed by fibrils which are bonded together with weak pectin and lignin interphase. 10,15,19 Therefore, when the surface of the untreated flax fiber (Figure 8(a)) was investigated, a heterogeneous structure such as waxes, fats, hemicellulose and lignin was clearly seen on the surface. APPlJ caused increase of fibrillation (Figure 8(b)) due to the removal of impurities in the microstructure.…”
Section: Sem Resultsmentioning
confidence: 99%
“…By the help of molecular bond characterization, the functional groups in the structure of the solid, liquid, gas or solution organic compounds, whether the two compounds are the same, the state of the bonds in the structure, bonding sites and whether the structure is aromatic or aliphatic can be determined. 15 In this case, ATR-FITR was used to determine the differences of molecular bond of untreated and APPlJ-treated flax fibers. The IR spectra of the fibers were obtained using by an IR spectrometer (Perkin-Elmer spectrum BX, Perkin-Elmer Canada).…”
Section: Mechanical Characterizationmentioning
confidence: 99%