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  • Ph.D. (2016)

    Polymer Engineering

    Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran

  • M.Sc. (2009)

    Polymer Engineering

    Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran

  • B.Sc. (2007)

    Polymer Engineering

    Department of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran

  • Study of Structure-Property Relationship in Nanocomposite Adhesives
  • Polymer (Nano)Colloids

    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.

    Contact

    Curriculum Vitae (CV)

    Introducing water-redispersible powderable acrylic adhesives using Persian gum

    A Ahmadi-Dehnoei, S Ghasemirad
    Journal Paper , , {Pages }

    Abstract

    Designing of desired nanocomposite pressure-sensitive adhesives through tailoring the structural characteristics of polysilsesquioxane-acrylic core-shell nanoparticles

    A Ahmadi-Dehnoei, S Ghasemirad
    Journal Paper , , {Pages }

    Abstract

    Eco-Friendly and Smart Polymer Systems

    H Mirzadeh, AA Katbab
    Journal Paper , , {Pages }

    Abstract

    Preparation and Improvement of Shear Strength of a Water-Redispersible Waterborne Acrylic Adhesive for Making Cellulose Joints

    Ali Ahmadi-Dehnoei, Somayeh Ghasemirad, Reza Shiri
    Journal PaperJournal of Applied Research of Chemical-Polymer Engineering , Volume 3 , Issue 1, 2019 May 10, {Pages 47-57 }

    Abstract

    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

    تهیه و تقویت استحکام برشی چسب اکریلیکی پایه‌آبی با قابلیت بازپراکنش در آب برای ایجاد مفصلهای سلولزی‎

    احمدی دهنوئی, علی, قاسمی راد, شیری‎
    Journal Paper , , {Pages }

    Abstract

    Environmentally Friendly Hybrid Polysilsesquioxane-Poly (Butyl Acrylate) Nanocomposite: Film Properties

    Ali Ahmadi Dehnoei, Somayeh Ghasemirad
    Conference PaperInternational Seminar on Polymer Science and Technology , 2018 November 10, {Pages 170-173 }

    Abstract

    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.

    Concurrent determination of two opposite phase transitions in a soft polymer nanocomposite by rheology and their theoretical evaluations

    Zahra Khoubi-Arani, Naser Mohammadi, Somayeh Ghasemirad
    Journal PaperEuropean Polymer Journal , Volume 84 , 2016 November 1, {Pages 40-53 }

    Abstract

    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

    Active layer thickness across the crack plane and fracture energy consumption in polymer nanocomposites: adhesion against tear strength

    S Ghasemirad, N Mohammadi
    Journal PaperRSC Advances , Volume 5 , Issue 130, 2015 January , {Pages 107642-107651 }

    Abstract

    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

    How do soft nanoparticles affect temperature-induced nonlinearity of a UCST copolymer blend?

    Somayeh Ghasemirad, Naser Mohammadi
    Journal PaperColloid and Polymer Science , Volume 293 , Issue 3, 2015 March 1, {Pages 677-686 }

    Abstract

    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

    Rheomechanical Analysis Of A Model Poly (Methyl Methacrylate-Co-Butyl Acrylate) Pressure Sensitive Adhesive As A Function Of Annealing Time

    S Ghasemirad, N Mohammadi
    Journal Paper , Volume 8 , 2014 January , {Pages }

    Abstract

    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

    LCST over UCST Phase Behavior of a Nanocomposite Determined by Differential Scanning Calorimetry and Rheomechanical Analysis

    S Ghasemirad, N Mohammadi
    Journal Paper , Volume 11 , 2014 October 6, {Pages }

    Abstract

    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.

    RHEOLOGICALLY DETERMINED PHASE BEHAVIOR OF AN ALL-POLYMER NANOCOMPOSITE

    ARANI Z KHOUBI, N MOHAMMADI, S GHASEMIRAD
    Journal Paper , Volume 11 , 2014 January , {Pages }

    Abstract

    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/ETHYL ACETATE MIXED SOLVENTS COMPOSITION ON NITROCELLULOSE SOLUTION EMULSIFICATION: THE STABILITY OF RESULTANT

    Halimeh Javidnia, Naser Mohammadi, SHOUSHTARI SA MOUSAVI, Somayeh Ghasemirad, T FARAJPOUR, Mohammad Reza Ghanbari
    Journal Paper , Volume 19 , Issue 5119, 2010 January 1, {Pages 323-332 }

    Abstract

    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

    The Effect of Butyl Glycol Acetate/Ethyl Acetate Mixed Solvents Composition on Nitrocellulose Solution Emulsification: The Stability of Resultant Colloid and Micro-filterability

    H Javidnia, N Mohammadi, SSA Mousavi, S Ghasemirad, T Farajpour, ...
    Journal Paper , , {Pages }

    Abstract

    Rheologically Determined Phase Behavior of an all-Polymer Nanocomposite

    Z Khoubi-Arani, N Mohammadi, S Ghasemirad
    Journal PaperMacromolecules , Volume 41 , 2008 January , {Pages 3276-3283 }

    Abstract

    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.

    Current Teaching

    • MS.c.

      Principles of Adhesion

    Teaching History

    • MS.c.

      Advanced Physical Chemistry of Polymers

    • 2020
      Parvaz, Amir
      Preparation of a Magnetoresponsive Pressure-Sensitive Adhesive Using Iron Oxide/Acrylic Core/Shell Nanoparticles
    • 2020
      Rajabi, Afsaneh
    • 2021
      Pourbakht, Kimia
    • 2021
      Esmaeili, Shadi
    • 2020
      Ahmadi-Dehnoei, Ali
      Prediction of Dependence of Peel Energy of Pressure-Sensitive Adhesives on their Viscoelastic Behaviour

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