2013
DOI: 10.1016/j.clay.2012.10.009
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Nanohybrids of phenolic antioxidant intercalated into MgAl-layered double hydroxide clay

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Cited by 41 publications
(37 citation statements)
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“…Hence peak shiftedslightly towards lower diffraction angle (Chakraborty et al, 2014). This also indicatesthe expansion in the interlayer distance and these planes also show the characteristic peaks of Mg/Al based LDH (Lonkar et al, 2013;Zazoua et al,2014).The XRD patterns (Fig. 1d)of the as-prepared LDH@GO hybrid NSshowamorphous nature,but nocharacteristic peak of GO was observedin hybrid layered NS ofLDH@GO.The peaksat34.0 0 and 60.0 0 , at (012) and (110) intensitiescorrespond to LDH.…”
Section: Structural and Crystallinity Analysismentioning
confidence: 95%
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“…Hence peak shiftedslightly towards lower diffraction angle (Chakraborty et al, 2014). This also indicatesthe expansion in the interlayer distance and these planes also show the characteristic peaks of Mg/Al based LDH (Lonkar et al, 2013;Zazoua et al,2014).The XRD patterns (Fig. 1d)of the as-prepared LDH@GO hybrid NSshowamorphous nature,but nocharacteristic peak of GO was observedin hybrid layered NS ofLDH@GO.The peaksat34.0 0 and 60.0 0 , at (012) and (110) intensitiescorrespond to LDH.…”
Section: Structural and Crystallinity Analysismentioning
confidence: 95%
“…The bands at 1216 and 1063 cm −1 are ascribed to the symmetric vibration of sulfate from SDS, respectively (Chakraborty et al, 2014;Jain et al, 2016).The other low frequency regions(800 cm -1 ) are attributed to metal-oxygen and metal-hydroxyl vibration modes present in the lattice of LDH. .The broad band in the range of 3200-3700 cm −1 may be due to presence of O-H stretching vibration of hydrogen bonded metal hydroxide layer and interlayer water molecules (Lonkar et al, 2013;Chakraborty et al, 2014;Zazoua et al,2014). The band observed near 1637 cm -1 is assigned to the bending vibration of water molecules.…”
Section: Functional Groupanalysismentioning
confidence: 99%
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“…Similarly, trans-cinnamic derivatives (ferulic acid, cafeic acid, hydroxycinnamic acid), known as AOs and UV blockers, have been successfully entrapped between LDH layers for cosmetic use as UV sunscreens and UV stabilizers [28]. Recently, 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid, containing the 2,6-di-tert-butylphenol functional group that is one of the most used AO in industry, has been intercalated within LDH galleries through co-precipitation [29] and regeneration method [30,31]. The modified LDH has been dispersed in polypropylene (PP) [29,30].…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…The radical scavenging activity of AO species and AO-LDHs was determined according to the DPPH method [34,24,29,31]. A 25 mL methanol stock solution of DPPH (60 µM M and 4 x 10 -6 M) were prepared by diluting the appropriate aliquots of the stock.…”
Section: Assessment Of the Antioxidant Activity Of Ao-ldhsmentioning
confidence: 99%