Purification of Iranian bentonite for organoclay synthesis for use in clay–polymer composites

Author:

Shabani Moghaddam Faraz,Ghanbari HajarORCID,Mirkazemi Seyed Mohammad,Ahmadi FatemehORCID

Abstract

AbstractPolymer-based composites modified with organoclay are economically beneficial candidates for a variety of applications. Different types of impurities accompany montmorillonite phases in various bentonites, which impact the quality and cost of organoclays and final composites. To obtain organoclays for clay composite applications, eight Iranian raw bentonites from different geographical locations were selected as the candidates and characterized by X-ray diffraction (XRD). Sample IB was chosen due to its high purity and lower cristobalite content than the other samples. It was purified by centrifugation or sedimentation methods using a sodium hexametaphosphate (NaHMP) dispersant. The cation-exchange capacity (CEC) was measured for bentonite before and after purification by sedimentation, and it showed a significant increase from 6.944 to 12.128 eq g–1, confirming successful purification. Organoclays were prepared using purified bentonite (sedimentation method) with two surfactants (cetyltrimethylammonium bromide and octadecylamine), and the amount of octadecylamine was optimized. Purified bentonite and organoclay were characterized by XRD, scanning electron microscopy (SEM) and X-ray fluorescence. The results indicate that most of the impurities were removed after purification, and the interlayer space of organoclays increased to 35 Å in the optimized sample prepared with an amount of octadecylamine that was twice the CEC in purified bentonite. The prepared organoclay was used to improve low-density polyethylene (LDPE) polymer properties. The clay–polymer composite properties were studied by field emission SEM, thermogravimetric analysis and tensile strength tests. The organoclay was fully dispersed in the LDPE matrix and in the sample with 5 wt.% of organoclay, where Ti (the temperature at which 10% of the sample is decomposed) and T50% (the midpoint of degradation) were 17°C and 13°C greater than those of polyethylene, respectively. Additionally, the sample residue with 5 wt.% of organoclay at 600°C was 43.4%. The tensile strength of polyethylene increased from 8.67 to 9.03 MPa in the sample with 4 wt.% of organoclay.

Publisher

Mineralogical Society

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