Abstract

The main objective of this work is to study the effect of hydroxylamine sulfate or stabilizer states (solid vs liquid) on the storage hardening of natural rubber (NR). Several types of natural rubber samples were prepared: unstabilized NR samples and stabilized NR samples: (i) dry NR with 0.2 and 2.0 parts per hundred rubber (phr) of dry hydroxylamine sulfate, and (ii) natural latex with 0.2 and 2.0 phr of liquid hydroxylamine sulfate. The samples were characterized immediately (time 0) and after 12 weeks of storage at room temperature, respectively. We found that the Mooney viscosity, gel content, and Wallace plasticity of NR without a stabilizer increases with storage hardening for 12 weeks. However, two types of stabilized NR samples represent constant values of those three parameters, because hydroxylamine sulfate inhibits network and gel formation in NR. Interestingly, the mixing states (solid vs liquid) between natural rubber and the stabilizer affect the properties of stabilized NR. This could be explained by the better dispersion and homogeneous nature of liquid stabilizers in natural latex (liquid state), and thus the higher loading of the stabilizer in the liquid state. This is important, as the stabilization of NR properties as a function of time is required by rubber industry. This study is a utilization model from theory to application.

Highlights

  • Natural rubber (NR) can be obtained from Hevea brasiliensis plant

  • Concerning to the visual aspect of samples (Figure 1), we found that the control NR without any stabilizer had a dark brown color at 0 weeks

  • We investigated the effects of stabilizer states, concentration of

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Summary

Introduction

Natural rubber (NR) can be obtained from Hevea brasiliensis plant. NR has been widely used across industries for surgical gloves, pillows and mattresses, elastic bands, medical products, and tires, plus many more. NR consists of rubber and non-rubber components, the main component is cis-1,4-polyisoprene [1,2,3,4,5]. The non-rubber fraction consists of proteins (ω-terminal) and phospholipids (α-terminal), which are attached at each end chain of the polyisoprene, and included in the serum [6]. When we stored the NR for a prolonged period of time, proteins and phospholipids at the end chain could promote formation of the NR network through protein-protein interactions at the ω-terminal or phospholipid-phospholipid interactions at the α-terminal. The increased of the branch chain or network of NR as a function of time can be determined by the Mooney viscosity via the storage hardening [7]. The storage hardening of NR can be inhibited by a stabilizer. A recent study [8]

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