2020
DOI: 10.1002/open.201900369
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One‐step Synthesis of End‐Functionalized Hydrogenated Nitrile‐Butadiene Rubber by Combining the Functional Metathesis with Hydrogenation

Abstract: End‐functionalized hydrogenated polymers obtained from nitrile‐butadiene rubber (NBR) yield new materials with suitable properties for a number of applications as sealing material and adhesives. We investigated the one‐step synthesis of ester end‐functionalized hydrogenated nitrile‐butadiene rubber (EF‐HNBR) by combining the functional metathesis with the hydrogenation of NBR in the presence of the 2nd generation Grubbs catalyst and a functionalized olefin as a chain transfer agent (CTA). We established the op… Show more

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Cited by 16 publications
(9 citation statements)
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“…The mixture solutions comprising MF copolymers and HNBR in DMSO also produced physical interactions, as shown in the 1 H NMR spectra (Figure S3). Pristine HNBR showed peaks at around 2.95 and 1.2 ppm, corresponding to a proton adjacent nitrile group and alkyl chain repeating units of the hydrogenated part, respectively. , Upon addition of MF copolymers during high-shear mixing, the peak at 2.95 ppm originated from protons adjacent to CN functional groups are almost the same with that after 20 min (2.94 ppm). One peak from the alkyl chains (1.19 ppm) may also have shifted and overlapped with a butanol peak at approximately 1.21 ppm during mixing.…”
Section: Results and Discussionmentioning
confidence: 82%
“…The mixture solutions comprising MF copolymers and HNBR in DMSO also produced physical interactions, as shown in the 1 H NMR spectra (Figure S3). Pristine HNBR showed peaks at around 2.95 and 1.2 ppm, corresponding to a proton adjacent nitrile group and alkyl chain repeating units of the hydrogenated part, respectively. , Upon addition of MF copolymers during high-shear mixing, the peak at 2.95 ppm originated from protons adjacent to CN functional groups are almost the same with that after 20 min (2.94 ppm). One peak from the alkyl chains (1.19 ppm) may also have shifted and overlapped with a butanol peak at approximately 1.21 ppm during mixing.…”
Section: Results and Discussionmentioning
confidence: 82%
“…The peaks of 1.0–2.5 ppm are assigned to the saturation protons. The peak at 2.53 ppm indicates the proton of –CN [ 5 , 25 ]. The successful grafting reactions are confirmed by the presence of the new peak at 4.2 ppm, which is ascribed to the proton of –COOCH 2 − [ 29 , 30 ].…”
Section: Resultsmentioning
confidence: 99%
“…However, due to the existence of unsaturated bonds on the molecular chain, it shows poor aging resistance. Hydrogenated nitrile rubber (HNBR) is the product of selective hydrogenation of NBR, which retains the original excellent performances of NBR and improves the ability of heat resistance, acid and alkali resistance and aging resistance [ 4 , 5 , 6 , 7 ]. However, HNBR is easy to crystallize due to the nearly ordered polyethylene structure of main chain [ 8 , 9 ], which causes an increase of T g .…”
Section: Introductionmentioning
confidence: 99%
“…The spectra obtained on the NBR and NBR waste/10% PDMS in relation to the virgin NBR rubber (Figure 1), highlight specific groups, namely: the bands from 2918, 2849 and 1450 cm -1 (stretching and deformation vibration of the -C-H bond), the band from 2238 cm -1 (stretching vibration of the -CN bond), the band from 1539 cm -1 (the stretching vibration of the -CN bond, from the additives added into the rubber). The band from 967 cm -1 comes from the -C=C-double bond (1.4 trans) (Liu et al, 2020;Samantarai et al, 2019). Additionally in the spectrum of NBR waste (not modified) intense bands at 1078 cm -1 originated from the Si-O-Si group (silicon dioxide) can be observed.…”
Section: Primary Identification Process (Ftir Analysis)mentioning
confidence: 98%