Functionalized starch as a novel eco-friendly vulcanization accelerator enhancing mechanical properties of natural rubber

2020 ◽  
Vol 231 ◽  
pp. 115705 ◽  
Author(s):  
Kuncai Li ◽  
Jianhua You ◽  
Yu Liu ◽  
Kaizheng Zhu ◽  
Chengliao Xue ◽  
...  
2012 ◽  
Vol 85 (1) ◽  
pp. 120-131 ◽  
Author(s):  
Md. Najib Alam ◽  
Swapan Kumar Mandal ◽  
Subhas Chandra Debnath

Abstract Several zinc dithiocarbamates (ZDCs) as accelerator derived from safe amine has been exclusively studied in the presence of thiazole-based accelerators to introduce safe dithiocarbamate in the vulcanization of natural rubber. Comparison has been made between conventional unsafe zinc dimethyldithiocarbamate (ZDMC) with safe novel ZDC combined with thizole-based accelerators in the light of mechanical properties. The study reveals that thiuram disulfide and 2-mercaptobenzothiazole (MBT) are always formed from the reaction either between ZDC and dibenzothiazyledisulfide (MBTS) or between ZDC and N-cyclohexyl-2-benzothiazole sulfenamide (CBS). It has been conclusively proved that MBT generated from MBTS or CBS reacts with ZDC and produces tetramethylthiuram disulfide. The observed synergistic activity has been discussed based on the cure and physical data and explained through the results based on high-performance liquid chromatography and a reaction mechanism. Synergistic activity is observed in all binary systems studied. The highest tensile strength is observed in the zinc (N-benzyl piperazino) dithiocarbamate-accelerated system at 3:6 mM ratios. In respect of tensile strength and modulus value, unsafe ZDMC can be successfully replaced by safe ZDCs in combination with thiazole group containing accelerator.


Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1510
Author(s):  
Marek Pöschl ◽  
Shibulal Gopi Sathi ◽  
Radek Stoček ◽  
Ondřej Kratina

The rheometer curing curves of neat natural rubber (NR) and neat chloroprene rubber (CR) with maleide F (MF) exhibit considerable crosslinking torque at 180 °C. This indicates that MF can crosslink both these rubbers via Alder-ene reactions. Based on this knowledge, MF has been introduced as a co-crosslinking agent for a 50/50 blend of NR and CR in conjunction with accelerated sulfur. The delta (Δ) torque obtained from the curing curves of a blend with the addition of 1 phr MF was around 62% higher than those without MF. As the content of MF increased to 3 phr, the Δ torque was further raised to 236%. Moreover, the mechanical properties, particularly the tensile strength of the blend with the addition of 1 phr MF in conjunction with the accelerated sulfur, was around 201% higher than the blend without MF. The overall tensile properties of the blends cured with MF were almost retained even after ageing the samples at 70 °C for 72 h. This significant improvement in the curing torque and the tensile properties of the blends indicates that MF can co-crosslink between NR and CR via the Diels–Alder reaction.


2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Chatree Homkhiew ◽  
Surasit Rawangwong ◽  
Worapong Boonchouytan ◽  
Wiriya Thongruang ◽  
Thanate Ratanawilai

The aim of this work is to investigate the effects of rubberwood sawdust (RWS) size and content as well as the ratio of natural rubber (NR)/high-density polyethylene (HDPE) blend on properties of RWS reinforced thermoplastic natural rubber (TPNR) composites. The addition of RWS about 30–50 wt% improved the modulus of the rupture and tensile strength of TPNR composites blending with NR/HDPE ratios of 60/40 and 50/50. TPNR composites reinforced with RWS 80 mesh yielded better tensile strength and modulus of rupture than the composites with RWS 40 mesh. The TPNR/RWS composites with larger HDPE content gave higher tensile, flexural, and Shore hardness properties and thermal stability as well as lower water absorption. The TPNR/RWS composites with larger plastic content were therefore suggested for applications requiring high performance of thermal, physical, and mechanical properties.


1966 ◽  
Vol 39 (5) ◽  
pp. 1436-1450
Author(s):  
K. J. Smith ◽  
D. Puett

Abstract The birefringence of natural rubber networks at large deformations has been investigated experimentally and compared with the simultaneously determined stress—strain behavior. Our data is analyzed using a statistical theory of flexibly jointed chains, derived herein, which is believed to be more significant for the particular range of deformation used than the theories of Treloar and of Kuhn and Grün. In addition, the experimental data of Saunders is commented on in light of our theoretical development. We find that for network extensions exceeding those of the Gaussian region there is little correlation between the observed and theoretical behavior of the stress and birefringence (based upon the theory of flexibly jointed chains) and this lack of agreement is attributed to the fact that the statistical parameters needed for the description of the optical chain properties differ in magnitude from those required for the mechanical properties. Furthermore, by considering the points of incipient crystallization the strain behavior of the stress-optical coefficient is highly indicative of nonGaussian behavior rather than crystallization, and therefore yields strong support for the position that nonGaussian behavior does exist in rubber networks.


2005 ◽  
Vol 38 (22) ◽  
pp. 9161-9170 ◽  
Author(s):  
Hélène Angellier ◽  
Sonia Molina-Boisseau ◽  
Alain Dufresne

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