Purpose The purpose of this paper is to prepare stabile emulsions with 0–15% of colloidal silica and high monomer/water ratio and to investigate the influence of silica addition and surface modification on the polyacrylate properties. Design/methodology/approach Improving the properties of the composite can be achieved by optimizing the compatibility between the phases of the composite system with improving the interactions at the matrix/filler interface. Therefore, the silica surface was modified with nonionic emulsifier octylphenol ethoxylate, cationic initiator 2,2'-azobis-(amidinopropane dihydrochloride) and 3-methacryloxypropyltrimethoxysilane and polyacrylate/silica nanocomposites were prepared via in situ emulsion polymerization. Particle size distribution, rheological properties of the emulsions and morphology, thermal properties and mechanical properties of the film prepared from the emulsions were investigated. Findings Polyacrylate/silica systems with unmodified silica, silica modified with nonionic emulsifier and cationic initiator have micrometer, while pure PA matrix and systems with silica modified with silane have nanometer particle sizes. Addition and surface modification of the filler increased emulsion viscosity. Agglomeration of silica particles in composites was reduced with silica surface modification. Silica filler improves thermal stability and tensile strength of polyacrylate. Originality/value This paper provides broad spectrum of information depending on filler surface modification and latex preparation via in situ emulsion polymerization and properties with high amount of filler and monomer/water ratio with the aim that prepared latex is suitable for film formation and final application.
Selektivno lasersko sinteriranje (SLS) jedan je od važnijih postupaka 3D ispisa koji se u današnje vrijeme sve više primjenjuju za dobivanje različitih modela. Najvažniji polimerni materijali koji se upotrebljavaju u tom procesu su poliamidi. Značajan nedostatak tog procesa je velika količina otpadnog polimernog praha. Stoga je cilj ovoga rada bio istražiti utjecaj dodatka nanočestica titanijeva dioksida (TiO<sub>2</sub>) na toplinska i mehanička svojstva otpadnog poliamidnog praha (PA 2200). U ovom radu pripremljeni su nanokompoziti PA/TiO2 u rasponu masenog udjela punila 1 – 5 %, postupkom zamješavanja punila u talinu polimera u gnjetilici Brabender. Aglomerati nanopunila vidljivi su na SEM mikrografiji 5 %-tnog PA/TiO<sub>2</sub> nanokompozita. Rezultati diferencijalne pretražne kalorimetrije (DSC) ukazuju na djelovanje nanočestica TiO<sub>2</sub> kao heterogenih nukleacijskih centara. Također, dodatak nanopunila pospješuje stvaranje stabilnijih i uređenijih kristalnih struktura poliamidne matrice. Termogravimetrijskom analizom (TGA) dokazano je da dodatak TiO<sub>2</sub> nanopunila povećava temperaturu početka razgradnje PA matrice, to jest poboljšava toplinsku postojanost PA matrice i neznatno povećava vrijednosti toplinske vodljivosti nanokompozita u odnosu na čistu polimernu matricu. Ispitivanjem mehaničkih svojstava uzoraka uočeno je smanjenje vrijednosti sekantnog modula te neznatne promjene naprezanja i istezanja u točki popuštanja s povećanjem udjela punila u nanokompozitu.
In this study, the addition of carbon nanotubes (MWCNT) and modified carbon nanotubes (MWCNT-COOH) in the range of 0.5 wt. % to 5 wt. % in polyamide (PA) obtained as a residue upon 3D printing, was investigated. PA and nanocomposite samples were prepared by melt mixing. PA/MWCNT and PA/MWCNT-COOH nanocomposites were characterized by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), THB thermal conductivity determination method, electrochemical impedance spectroscopy (EIS), and tensile test. Results of DSC analysis showed that both types of carbon nanotubes (MWCNTs) acted as nucleation centres of PA matrix, but had no effect on the order of the crystalline structure. Due to the polar nature of the surface and better dispersion, MWCNT-COOH filler accelerated PA crystallization more significantly compared to MWCNT. Due to the presence of nanofiller, the PA chains had limited motion space, which interfered with the crystallization process of the matrix. The thermal stability of the PA matrix increased with the addition of both MWCNT and MWCNT-COOH fillers. Higher thermal conductivity was achieved with the addition of MWCNT-COOH filler compared to the addition of MWCNT. The results of the tensile test showed that with the addition of both types of MWCNT fillers in the PA matrix, the modulus of elasticity and yield stress had reduced, but the yield strain increased. Results of the EIS showed that MWCNT nanofiller had not changed the electrical conductivity regardless of modification.
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