Supramolecular Soft Adhesive Materials

被引:150
作者
Courtois, Jeremie [1 ]
Baroudi, Imane [1 ]
Nouvel, Nicolas [2 ,3 ]
Degrandi, Elise [1 ]
Pensec, Sandrine [2 ,3 ]
Ducouret, Guylaine [1 ]
Chaneac, Corinne [4 ]
Bouteiller, Laurent [2 ,3 ]
Creton, Costantino [1 ]
机构
[1] UPMC, CNRS, Lab Physicochim Polymeres & Milieux Disperses, ESPCI ParisTech,UMR7615, F-75231 Paris 05, France
[2] Univ Paris 06, UMR 7610, F-75005 Paris, France
[3] CNRS, UMR 7610, F-75005 Paris, France
[4] Univ Paris 06, UMR 7574, F-75005 Paris, France
关键词
PRESSURE-SENSITIVE ADHESIVES; HYDROGEN-BONDING NETWORKS; THERMOPLASTIC ELASTOMERS; CROSS-LINKING; MECHANICAL-PROPERTIES; MOLECULAR-PARAMETERS; DEFORMATION-BEHAVIOR; INTERFACIAL SLIPPAGE; MODEL ADHESIVES; POLYMER MELTS;
D O I
10.1002/adfm.200901903
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The rheological and adhesive properties of bis-urea functionalized low-molecular-weight polyisobutylenes (PIBUT) are investigated. The polymers, which can interact through supramolecular hydrogen bonds, can self-organize over times of the order of days at room temperature. This organized structure has been identified by small angle X-ray scattering (SAXS) and its rheological properties indicate the behaviour of a soft viscoelastic gel. The ordered structure can be disrupted by temperature and shear so that at 80 degrees C, the material behaves as a highly viscoelastic fluid and no SAXS peak is observed. When cooled back at room temperature, the PIBUT retrieves its ordered structure and gel properties after 20 h of annealing. This very slow molecular dynamics gives PIBUT a highly dissipative nature upon deformation, which combined with strongly interacting moieties results in very interesting adhesive properties both on steel surfaces but more importantly on typical low adhesion surfaces such as silicone. A strategy based on the controlled incorporation of supramolecular bonds in a covalently crosslinked network appears promising for the development of a new generation of highly interacting and dissipative soft adhesives.
引用
收藏
页码:1803 / 1811
页数:9
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