Reinforcing efficiency and compatibilizing effect of sol–gel derived in situ silica for natural rubber/chloroprene rubber blends

RSC Advances ◽  
2014 ◽  
Vol 4 (102) ◽  
pp. 58816-58825 ◽  
Author(s):  
Bharat P. Kapgate ◽  
Chayan Das

The strong CR/in situ silica interaction causes filler accumulation at the interphase and enhances the compatibility and reinforcement in the NR/CR blend.

2009 ◽  
Vol 52 (2) ◽  
pp. 219-227 ◽  
Author(s):  
Benjawan Chaichua ◽  
Pattarapan Prasassarakich ◽  
Sirilux Poompradub

2011 ◽  
Vol 58 (2) ◽  
pp. 407-418 ◽  
Author(s):  
Natchamon Watcharakul ◽  
Sirilux Poompradub ◽  
Pattarapan Prasassarakich

2016 ◽  
Vol 80 (2) ◽  
pp. 548-559 ◽  
Author(s):  
Naresh D. Bansod ◽  
Bharat P. Kapgate ◽  
Chayan Das ◽  
Amit Das ◽  
Debdipta Basu ◽  
...  

2001 ◽  
Vol 74 (1) ◽  
pp. 16-27 ◽  
Author(s):  
S. Kohjiya ◽  
K. Murakami ◽  
S. Iio ◽  
T. Tanahashi ◽  
Y. Ikeda

Abstract The sol—gel reaction of tetraethoxysilane produced the fine and well-dispersed in situ silica particles in the “green” natural rubber (NR) matrix before curing. This new method was developed for a NR/silica composite material, and a good reinforcement effect of in situ silica was observed on the NR vulcanizate. The method is expected to be an industrially practical technique. The in situ silica did not much inhibit the accelerated sulfur curing. Thus, it is estimated that the concentration of silanol groups on the in situ silica surface was smaller than those on the conventional silica surface. The silica—silica interaction of in situ silica seems to be weaker to result in better dispersion in the rubber matrix compared with the conventional silica. Atomic force microscopy suggested that the wettability of NR onto in situ silica was higher than that onto conventional silica. The hardness, modulus at 50% elongation and the storage modulus at room temperature of in situ silica-filled NR vulcanizate were smaller than those of conventional silica-filled NR vulcanizate, although the crosslinking density of the former was larger than that of the latter and their silica contents were comparable. These unique characteristics of in situ silica-filled vulcanizate seem to be ascribed to the fine and well-dispersed in situ silica particles in the NR matrix. These observations suggest that NR (a renewable resource)/in situ silica composite has much potential as an ecologically “green” material in the rubber industry.


2010 ◽  
Vol 93-94 ◽  
pp. 525-528 ◽  
Author(s):  
Torpong Sittiphan ◽  
Pattarapan Prasassarakich ◽  
Sirilux Poompradub

In situ silica filling of styrene grafted natural rubber (ST-g-NR) was carried out by using sol-gel reaction of tetraethoxysilane (TEOS). The effects of concentration of catalyst and reaction temperature on the in situ silica content were investigated. ST-g-NR was synthesized via an emulsion polymerization using cumene hydroperoxide (CHPO) and tetraethylene pentamine (TEPA) as initiators. The synthesized ST-g-NR was characterized by a Fourier Transform Infrared Spectroscopy (FTIR) and Proton Nuclear Magnetic Resonance Spectroscopy (1H NMR). The content of in situ silica generated in ST-g-NR matrix was determined by Thermogravimetry Analysis (TGA). In situ silica up to 50 parts per hundred rubbers by weight (phr) was successfully filled in the ST-g-NR matrix. The silica content increased with the increase of n-hexylamine concentration. However, the effect of reaction temperature was insignificant to silica content.


2014 ◽  
Vol 181 ◽  
pp. 39-45 ◽  
Author(s):  
Torpong Sittiphan ◽  
Pattarapan Prasassarakich ◽  
Sirilux Poompradub

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.


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