Soft NanocompositesFrom Interface Control to Interphase Formation
We report measurements of structure, mechanical properties, glass transition temperature, and contact angle of a novel nanocomposite material consisting of swellable silsesquioxane nanoparticles with grafted poly(ethyl methacrylate) (PEMA) brushes and PEMA matrices with varying molecular weight. We...
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Published in | ACS applied materials & interfaces Vol. 7; no. 23; pp. 12380 - 12386 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
17.06.2015
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Abstract | We report measurements of structure, mechanical properties, glass transition temperature, and contact angle of a novel nanocomposite material consisting of swellable silsesquioxane nanoparticles with grafted poly(ethyl methacrylate) (PEMA) brushes and PEMA matrices with varying molecular weight. We measured the interparticle distance at the surface of the composites using scanning probe microscopy (SPM) and in the bulk of ∼0.5 μm thick films by grazing incidence small angle X-ray scattering (GISAXS). For a given molecular weight of the brush unstable dispersions at high molecular weight of the matrix indicate an intrinsic incompatibility between polymer-grafted-nanoparticles and homopolymer matrices. This incompatibility is affirmed by a high contact angle between the polymer-grafted-nanoparticles and the high molecular weight matrix as measured by SPM. For unstable dispersions, we measured a decreased glass transition temperature along with a decreased plateau modulus by dynamic mechanical thermal analysis (DMTA) which indicates the formation of a liquid-like layer at the brush–matrix interface. This proves the ability to decouple the structural and mechanical properties from the potential to be swollen with small molecules. It opens a new area of use of these soft nanocomposites as slow release materials with tailored mechanical properties. |
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AbstractList | We report measurements of structure, mechanical properties, glass transition temperature, and contact angle of a novel nanocomposite material consisting of swellable silsesquioxane nanoparticles with grafted poly(ethyl methacrylate) (PEMA) brushes and PEMA matrices with varying molecular weight. We measured the interparticle distance at the surface of the composites using scanning probe microscopy (SPM) and in the bulk of ∼0.5 μm thick films by grazing incidence small angle X-ray scattering (GISAXS). For a given molecular weight of the brush unstable dispersions at high molecular weight of the matrix indicate an intrinsic incompatibility between polymer-grafted-nanoparticles and homopolymer matrices. This incompatibility is affirmed by a high contact angle between the polymer-grafted-nanoparticles and the high molecular weight matrix as measured by SPM. For unstable dispersions, we measured a decreased glass transition temperature along with a decreased plateau modulus by dynamic mechanical thermal analysis (DMTA) which indicates the formation of a liquid-like layer at the brush-matrix interface. This proves the ability to decouple the structural and mechanical properties from the potential to be swollen with small molecules. It opens a new area of use of these soft nanocomposites as slow release materials with tailored mechanical properties. We report measurements of structure, mechanical properties, glass transition temperature, and contact angle of a novel nanocomposite material consisting of swellable silsesquioxane nanoparticles with grafted poly(ethyl methacrylate) (PEMA) brushes and PEMA matrices with varying molecular weight. We measured the interparticle distance at the surface of the composites using scanning probe microscopy (SPM) and in the bulk of ∼0.5 μm thick films by grazing incidence small angle X-ray scattering (GISAXS). For a given molecular weight of the brush unstable dispersions at high molecular weight of the matrix indicate an intrinsic incompatibility between polymer-grafted-nanoparticles and homopolymer matrices. This incompatibility is affirmed by a high contact angle between the polymer-grafted-nanoparticles and the high molecular weight matrix as measured by SPM. For unstable dispersions, we measured a decreased glass transition temperature along with a decreased plateau modulus by dynamic mechanical thermal analysis (DMTA) which indicates the formation of a liquid-like layer at the brush–matrix interface. This proves the ability to decouple the structural and mechanical properties from the potential to be swollen with small molecules. It opens a new area of use of these soft nanocomposites as slow release materials with tailored mechanical properties. |
Author | Butt, Hans-Jürgen Emmerling, Sebastian G. J Pihan, Sascha A Berger, Rüdiger Gutmann, Jochen S |
AuthorAffiliation | Johannes Gutenberg Universität Mainz Max Planck Institute for Polymer Research |
AuthorAffiliation_xml | – name: Max Planck Institute for Polymer Research – name: Johannes Gutenberg Universität Mainz |
Author_xml | – sequence: 1 givenname: Sascha A surname: Pihan fullname: Pihan, Sascha A – sequence: 2 givenname: Sebastian G. J surname: Emmerling fullname: Emmerling, Sebastian G. J – sequence: 3 givenname: Hans-Jürgen surname: Butt fullname: Butt, Hans-Jürgen – sequence: 4 givenname: Rüdiger surname: Berger fullname: Berger, Rüdiger email: berger@mpip-mainz.mpg.de – sequence: 5 givenname: Jochen S surname: Gutmann fullname: Gutmann, Jochen S email: jochen.gutmann@uni-due.de |
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CitedBy_id | crossref_primary_10_1021_acs_langmuir_7b00723 crossref_primary_10_1016_j_polymer_2021_123525 crossref_primary_10_1021_acs_macromol_1c02382 crossref_primary_10_1021_acsanm_0c00401 crossref_primary_10_1021_acsomega_7b01355 |
Cites_doi | 10.1021/la061136z 10.1021/ma021197d 10.1016/j.polymer.2007.12.030 10.1002/polb.20926 10.1016/j.polymer.2008.10.019 10.1557/mrs2007.229 10.1016/S0168-3659(97)00191-0 10.1021/ma101240j 10.1021/ma990549m 10.1021/ma901755v 10.1177/1045389X9300400414 10.1021/jp800474t 10.1063/1.2245310 10.1140/epje/i2004-10078-0 10.1016/j.compscitech.2007.01.015 10.1007/s00396-008-1949-0 10.1103/PhysRevE.61.R53 10.1002/polb.21251 10.1021/ma071770z 10.1021/ma001192l 10.1103/PhysRev.131.2010 10.1021/ma201714u 10.1021/ma00046a063 10.1016/j.polymer.2008.05.040 10.1039/B814714K 10.1016/0168-3659(90)90138-J 10.1016/j.compscitech.2009.04.005 10.1021/ma902072d 10.1021/ma00099a024 10.1063/1.1826031 10.1098/rsif.2005.0065 10.1021/la7027516 10.1021/la047193e 10.1021/ma9600116 10.1007/12_068 10.1016/j.wear.2011.05.040 10.1016/j.physa.2004.03.058 10.1021/la026338j 10.1002/3527602127 10.1016/j.progpolymsci.2008.01.002 |
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