Mechanochemical devulcanization of natural rubber vulcanizate by dual function disulfide chemicals

被引:83
作者
Ghorai, Soumyajit [1 ]
Bhunia, Satyaban [2 ]
Roy, Madhusudan [2 ]
De, Debapriya [1 ]
机构
[1] MCKV Inst Engn, Dept Chem, Liluah 711204, Howrah, India
[2] Saha Inst Nucl Phys, Surface Phys & Mat Sci Div, Kolkata 700064, India
关键词
Natural rubber; Mechanochemical devulcanization; Crosslink density; Mechanical property; Thermal behavior; RENEWABLE RESOURCE MATERIAL; GROUND TIRE RUBBER; MICROBIAL DESULFURIZATION; STATISTICAL-MECHANICS; WASTE RUBBER; MATERIAL RRM; RECLAMATION; ULTRASOUND; ASPHALT;
D O I
10.1016/j.polymdegradstab.2016.03.024
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Devulcanized natural rubber (DeVulcNR) was produced from NR vulcanizate in an open roll mixing mill by using bis(3-triethoxysilyl propyl) tetrasulfide (TESPT), a novel devulcanizing agent. The versatility of the proposed devulcanizing agent TESPT is that it acts as a devulcanizing agent during devulcanization and as a coupling agent during dispersion of silica filler in devulcanize rubber compound. The extent of devulcanization was monitored through the measurements of sol content, gel content, crosslink density, molecular weight between crosslinks, Mooney viscosity of devulcanized rubber and degree of devulcanization as a function of devulcanization time and the concentration of TESPT. The study of extent of devulcanization by monitoring the above mentioned parameters clearly indicate that the optimum concentration of TESPT is 6 mL. Therefore, for further study DeVulcNR is prepared using 6 mL TESPT and designated as DeVulcNR-6 to optimize the devulcanization time. Determination of the fraction of immobilized polymer chains of DeVulcNR-6 by differential scanning calorimetry (DSC) study indicates that with sol content the fraction of immobilized polymer chains decreases due to increasing molecular weight between crosslinks. To get an idea about the application of DeVulcNR in product formulation revulcanization characteristics in the presence of silica filler were studied. The optimum cure time decreases whereas cure rate increases with devulcanization time. The mechanical properties e.g., modulus at 50% and 100% elongation, tensile strength and elongation at break increases with devulcanization time upto 40 min. To see the reinforcement of silica filler, the mechanical properties of ReVulcNR-6 with silica is compared to that of the ReVulcNR-6 without silica. The mechanical property and thermal behavior data clearly indicates that the optimum time for devulcanization is 40 min. Scanning electron microscopy (SEM) studies further show the coherency and homogeneity of DeVulcNR-6 in the revulcanizate when devulcanization is carried out by optimum TESPT concentration 6 mL and devulcanization time 40 min. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:34 / 46
页数:13
相关论文
共 29 条
[1]   Reclamation and recycling of waste rubber [J].
Adhikari, B ;
De, D ;
Maiti, S .
PROGRESS IN POLYMER SCIENCE, 2000, 25 (07) :909-948
[2]   Influence of hygrothermally degraded polyester-urethane on physical and mechanical properties of chloroprene rubber [J].
Aprem, AS ;
Jose, S ;
Thomas, S ;
Barkoula, NM ;
Kocsis, JK .
EUROPEAN POLYMER JOURNAL, 2003, 39 (01) :69-76
[3]   Reclaiming of ground rubber tire (GRT) by a novel reclaiming agent [J].
De, D ;
Das, A ;
De, D ;
Dey, B ;
Debnath, SC ;
Roy, BC .
EUROPEAN POLYMER JOURNAL, 2006, 42 (04) :917-927
[4]  
De D, 1997, J POLYM MATER, V14, P333
[5]  
De D, 1999, J APPL POLYM SCI, V73, P2951, DOI 10.1002/(SICI)1097-4628(19990929)73:14<2951::AID-APP19>3.3.CO
[6]  
2-2
[7]  
De D, 2000, J APPL POLYM SCI, V75, P1493, DOI 10.1002/(SICI)1097-4628(20000321)75:12<1493::AID-APP8>3.0.CO
[8]  
2-U
[9]   Reclamation of waste tyre rubber with nitrous oxide [J].
Dubkov, K. A. ;
Semikolenov, S. V. ;
Ivanov, D. P. ;
Babushkin, D. E. ;
Panov, G. I. ;
Parmon, V. N. .
POLYMER DEGRADATION AND STABILITY, 2012, 97 (07) :1123-1130
[10]   Statistical mechanics of cross-linked polymer networks II Swelling [J].
Flory, PJ ;
Rehner, J .
JOURNAL OF CHEMICAL PHYSICS, 1943, 11 (11) :521-526