Department of Polymer Engineering (2017 - Present)
Polymer Engineering
Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran
Polymer Engineering
Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran
Polymer Engineering
Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran
Somayeh Ghasemirad completed her academic studies in Polymer Engineering at Amirkabir University of Technology (Tehran Polytechnic, AUT) in 2016. She was the instructor at Physical Chemistry of Polymers Laboratory at Polymer Engineering Faculty at AUT in 2016. After her postdoctoral research at AUT, she joined Chemical Engineering Faculty at Tarbiat Modares University as an assistant professor and faculty member at Polymer Engineering Department. Her research is mainly focused on theoretical and experimental studies on the structure-fracture relationship in polymer systems and nanocomposites both in bulk and at interface (i.e. adhesion) on the one hand and preparation of polymer (nano)colloids on the other hand.
Polymer Engineering Department, Faculty of Chemical Engineering, Tarbiat Modares University, PO Box 14115-114, Tehran, IranResearch subject: In recent years, many attempts have been devoted to industrial usage of biobased adhesives, as a result of fossil resources shortage and unusual increase in oil-based products prices. Adhesion s trength of this category of adhesives, however, needs improvement. Research approach: In the current s tudy, lap-shear s trength of joints made of a natural polymer, Persian gum (PG), exuded from wild almond tree, and three various substrates, glass, poly (ethylene terephthalate), and cellulose fabric, was inves tigated. Furthermore, in order to prepare powder acrylic adhesive and evaluate its adhesion to afore
Inorganic-organic core-shell polysilsesquioxane-poly(butyl acrylate) hybrid latex nanoparticles were synthesized via emulsion polymerization. FTIR spectroscopy and dynamic light scattering (DLS) confirmed core-shell structure of the resultant hybrid latex nanoparticles. Hybrid core-shell nanocomposite film underwent drying in a shorter period of time in comparison with the polysilsesquioxane latex, due to the lower Brownian diffusivity of its latex nanoparticles. It also revealed less hydrophilicity and higher resistance to water whitening, compared to the seed latex film.
The polymerization-induced biphasic nature of an emulsion 30/70?wt.% methyl methacrylate (MMA)/butyl acrylate (BA) copolymer was deeply scrutinized with different techniques as the MMA-rich/BA-rich copolymers blend. Its experimentally found upper critical solution temperature (UCST) was then confirmed by the Sanchez-Lacombe lattice fluid (SLLF) and compressible regular solution (CRS) models. Characterization of soft polymer nanocomposites (SPNs) from the aforementioned system as the matrix and different fractions of mono-size poly(styrene-co-acrylonitrile) soft nanoparticles made of 70?wt.% styrene (SAN70) with dynamic mechanical thermal analysis (DMTA), atomic force microscopy (AFM), and rheometry approved their multi-phase character. Homo
The tear strength of a model methyl methacrylate–butyl acrylate copolymer containing 30 wt% methyl methacrylate (MBC30) and its adhesion strength to poly(ethylene terephthalate) were determined to be 10.2 and 0.26 kN m−1, respectively. The addition of 5 wt% mono-size, 180 nm in diameter, soft nanoparticles of poly(styrene-co-acrylonitrile) with 30 wt% acrylonitrile (SAN70) through latex blending, followed by drying, amplified the adhesion strength while reducing the tear strength. Mild and harsh annealing of the nanocomposite led to partial and full deterioration of work of failure per unit volume (WoF), resulting in augmented adhesion and tear strengths followed by their severe decline, respectively. The G0(1 + ϕ) model-based partitio
Temperature-induced nonlinearity of an upper critical solution temperature (UCST) copolymer blend and its nanocomposites containing 5?wt% mono-size soft nanoparticles (SNPs) were investigated. Mechanical and thermal energies contribution into the nonlinearity of UCST copolymer blend was 8.9 ? 103?Jm−3 and 2.2 ? 103?Jmol−1, respectively. Addition of SNP did not change the system thermal-based nonlinearity, while altered its mechanical contribution at constant heating and solicitation conditions. It diminished to 0.4 ? 103?Jm−3 in the nanocomposite containing nano-size dispersion of aged SNPs. Micron-size agglomeration of the fresh SNPs in the nanocomposite; however, enhanced the required mechanical energy for
A model poly (methyl metacrylate-co-butyl acrylate) pressure sensitive adhesive containing 30 wt% of methyl metacrylate (MBC30) was analyzed rheomechanically as a function of annealing time. The extracted G’and G” curves from dynamic mechanical thermal analysis under applied shear load at frequency of 1 Hz and strain amplitude of 1% represented the behavior of highlyfilled elastomers, Payne effect, probably due to its nanostructuring. The glass transition temperature of butyl acrylate-rich and methyl methacrylate-rich copolymers shifted as much as 50 C and 10 C in comparison to their corresponding results from differential scanning calorimetry,-26 C and 160 C, respectively. Long-term storage of model adhesive film at above its glass tra
Phase behavior of butylacrylate-rich and methyl methacrylate-rich copolymers of an emulsion copolymerized 30/70 methyl methacrylate/butyl acrylate (MBC30) copolymer and its nanocomposite containing 5 wt.% mono-size soft nanoparticles of 70/30 styrene/acrylonitrile copolymer (SAN70) were characterized using time-sweep rheomechanical analysis. The test was conducted at 150 C, the near-critical temperature determined by differential scanning calorimetry, and depicted matrix enhanced storage modulus, G’, followed by a plateau implying criticality. The latex blended and dried nanocomposite, however, represented three orders of magnitude lower G’with a maximum-crossing evolution.
PHASE SEPARATION OF AN ALL-POLYMER NANOCOMPOSITE CONTAINING POLY (METHYL METHACRYLATE-CO-BUTYL ACRYLATE) WITH 30 WT% METHYL METHACRYLATE (MBC30) AS MATRIX AND 5 WT% OF MONO-SIZE POLY (STYRENE-CO-ACRYLONITRILE) SOFT NANOPARTICLE WITH 70 WT% STYRENE (SAN70) WERE INVESTIGATED. RHEOLOGY WAS USED TO DETERMINE THE BINODAL AND SPINODAL PHASE SEPARATION TEMPERATURES BASED ON INFLECTION POINT OF STORAGE MODULUS AND MEAN FIELD THEORY. THE MEASURED TEMPERATURE AGREES VERY WELL WITH THE DSC RESULTS.
The effect of butyl glycol acetate (BGA)/ethyl acetate (EA) mixed solvents com-position on nitrocellulose (NC) solution miscibility and rheological properties with or without non-ionic surfactants was investigated. In addition the emulsification of the solution containing two non-ionic surfactants with weight average hydrophilic/lipophilic balance of 14.75 (oil phase), its colloidal stability and microfilterability were studied. The results showed that oil phase viscosity and surface tension increase by high boiling point solvent (BGA) between 50 and 87.5 wt%, which reduced the colloid particle size from 35 μm down to 10 μm. While surfactant free solution viscosity of NC in the BGA/EA mixed solvents increased to a maximum at 75 wt% of BGA
Phase separation of an all-polymer nanocomposite containing poly (methyl methacrylate-co-butyl acrylate) with 30 wt% methyl methacrylate (MBC30) as matrix and 5 wt% of mono-size poly (styrene-co-acrylonitrile) soft nanoparticle with 70 wt% styrene (SAN70) were investigated. Rheology was used to determine the binodal and spinodal phase separation temperatures based on inflection point of storage modulus and mean field theory. The measured temperature agrees very well with the DSC results.
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