Abstract:In this study, effects of surface modification of calcium carbonate (CaCO3) nanoparticles with a single-layer of stearic acid were investigated on dispersion in polypropylene (PP) matrix. Two kinds of CaCO3 nanoparticles (monolayer-coated and uncoated) were used to investigate this effect. All combinations were mixed in a co-rotating twin screw extruder and then were injection molded. After breaking the injection molded parts in liquid nitrogen, effect of surface modification of nanoparticles on their dispersi… Show more
“…However, the compounds with modified bentonite and stearic acid in the hopper of the extruder showed the best dispersion state (Figure 4). 23 The extra addition of this fatty acid as an additive to the formulation improved the interactions between the polymer and the filler even more because of interfacial modifications. This means that the surface treatment with stearic acid significantly reduced the filler surface free energy and particle-particle interaction; this led to better dispersion of the particles in the polymer matrix and reduced the filler agglomerates.…”
In this study, we present a study of polypropylene/bentonite composites where stearic acid was used as both a surface and interface modifier during the compounding of composites. The concentration of bentonite was 1.5, 2.5, 5.0, and 10 parts per hundred. The composites were characterized by impact resistance and tensile tests, rheological analysis, the dispersion state of the filler observed by optical microscopy, and interaction between bentonite and stearic acid, as analyzed by Fourier transform infrared spectroscopy. No chemical interaction was found between bentonite and stearic acid. Composites with modified bentonite and stearic acid used as interface modifiers increased the elongation at break; these samples also showed better dispersion of the filler in comparison with the other compounds. In addition, stearic acid acted as a lubricant, favoring the interaction of the polymer with the filler and decreasing the viscosity of the compounds.
“…However, the compounds with modified bentonite and stearic acid in the hopper of the extruder showed the best dispersion state (Figure 4). 23 The extra addition of this fatty acid as an additive to the formulation improved the interactions between the polymer and the filler even more because of interfacial modifications. This means that the surface treatment with stearic acid significantly reduced the filler surface free energy and particle-particle interaction; this led to better dispersion of the particles in the polymer matrix and reduced the filler agglomerates.…”
In this study, we present a study of polypropylene/bentonite composites where stearic acid was used as both a surface and interface modifier during the compounding of composites. The concentration of bentonite was 1.5, 2.5, 5.0, and 10 parts per hundred. The composites were characterized by impact resistance and tensile tests, rheological analysis, the dispersion state of the filler observed by optical microscopy, and interaction between bentonite and stearic acid, as analyzed by Fourier transform infrared spectroscopy. No chemical interaction was found between bentonite and stearic acid. Composites with modified bentonite and stearic acid used as interface modifiers increased the elongation at break; these samples also showed better dispersion of the filler in comparison with the other compounds. In addition, stearic acid acted as a lubricant, favoring the interaction of the polymer with the filler and decreasing the viscosity of the compounds.
“…Calcium carbonate or calcite (CaCO 3 ) is one of the most favorite fillers used in polymer composites owing to its low cost, availability, easy manufacturing, whiteness, reinforcing properties, and contribution to improvements in mechanical properties such as strength, modulus, and toughness. [3][4][5][6][7][8] Calcite is an important rock-forming mineral in sedimentary environments. It is mined and ground to micron-sized particles and is called ground calcium carbonate (GCC).…”
Section: Introductionmentioning
confidence: 99%
“…[9] The incompatibility between the hydrophilic, polar, high-energy surfaces of the calcite grains and hydrophobic, nonpolar, low energy polymer surfaces is a problem that must be solved prior to compound production. [3,10,11] Fine-grained calcite grains tend to agglomerate owing to their high surface area and high surface energy. In addition, the risk of agglomeration increases further, as they are added to composites at high rates owing to the above-mentioned positive contributions of calcite to the composite.…”
Section: Introductionmentioning
confidence: 99%
“…[15] In the literature, the properties of the surface modified CaCO 3 in powder form have been analyzed by various techniques such as brunauer-emmett-teller method (BET), fourier transform Infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA), and differential scanning calorimetry (DSC). [3,4,16] However, while these analyzes provide information on surface energy and hydrophobicity of CaCO 3 particles, these properties cannot fully explain the quality of the dispersion in a thermoplastic polymer matrix. The authors think that tests that can measure the behavior and dispersion of the surface-modified calcium carbonate in the thermoplastic polymer will yield clearer results.…”
Section: Introductionmentioning
confidence: 99%
“…The effect of surface modification of calcium carbonate on dispersions of thermoplastic polymer composites was tested in previous studies mostly by morphological and mechanical analysis. [3,4,[16][17][18][19] The study where the rheological behavior is measured for this purpose on the surface-modified CaCO 3 /PP composites is limited. [20,21] Since the screen pack analysis or filter test is usually applied in pigments, no study has been found by the authors including filter test demonstrating the effect of surface modification on dispersion of CaCO 3 in CaCO 3 /PP composites.…”
The excellent properties of the composites distinctly depend on the filler particles dispersion, which has close relationship with the surface treatment of filler particles. To improve the compatibility between the filler particles and the matrix, the surface of filler particles is generally treated with coating agents, which can be classified as “dispersants” and “coupling agents.” Coating calcite (CaCO3) with dispersants is called a nonreactive treatment. The surface modification of CaCO3 with coupling agents is called reactive treatment. In this study, physical, chemical, morphological, rheological, and mechanical analyses were conducted to determine the effect of reactive and nonreactive surface treatment agents on the dispersion of CaCO3 in polypropylene/CaCO3 composites. Both agents successfully made the surface of CaCO3 hydrophobic. The results of this study revealed that, although stearic acid (SA) establishes stronger bonds with the calcite surface, isopropyl tristearyl titanate, unlike SA, improves the properties of the final product composite, which forms a bond at the polymer/filler interface.
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