2016
DOI: 10.1063/1.4966762
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Chemical modifications of liquid natural rubber

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Cited by 13 publications
(5 citation statements)
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“…33 In the spectrum of the ENR, new peaks appeared at 1250 cm À1 and 868 cm À1 correspond to the symmetric and asymmetric stretching vibrations of the epoxy ring. 34 It is also clearly seen that the peak of the = C-H group at 841 cm À1 decreases in intensity. This result proves that some C = C double bonds were converted to epoxy rings as intended, and the ENR structure was successfully formed.…”
Section: Atr-ftirmentioning
confidence: 89%
“…33 In the spectrum of the ENR, new peaks appeared at 1250 cm À1 and 868 cm À1 correspond to the symmetric and asymmetric stretching vibrations of the epoxy ring. 34 It is also clearly seen that the peak of the = C-H group at 841 cm À1 decreases in intensity. This result proves that some C = C double bonds were converted to epoxy rings as intended, and the ENR structure was successfully formed.…”
Section: Atr-ftirmentioning
confidence: 89%
“…Modification of NR also may be carried out with LNR. [6,24] LNR may be epoxidized, followed by hydrogenation to form LENR and LENR-OH. Epoxy content of LENR may be very high -till 98%; epoxy group may further hydrolyze and open ring to form diol and carbonyl groups.…”
Section: Epoxidation Of Nrmentioning
confidence: 99%
“…The procedure employed by Azhar et al [17] was utilised to produce liquid natural rubber (LNR) without any modifications. For the synthesis of rubber-based hydrogels, 4 g of maleic anhydride (MaH) in 20 mL toluene and 0.3 g of free radical initiator benzoyl peroxide (BPO) in 20 mL toluene were added into 6 g of LNR solution to produce maleated LNR.…”
Section: Synthesis Of Rubber-based Hydrogelsmentioning
confidence: 99%