Thermal compression bonding is a straightforward, inexpensive and widely used method for enclosing open microchannels in thermoplastic microfluidic devices. It is advantageous over adhesive, solvent and grafting bonding methods in retaining material homogeneity. However, the trade-off between high bond strength and low microchannel deformation is always a crucial consideration in thermal compression bonding. In this study, an effective method for improving bond strength while retaining the microchannel integrity with negligible distortion is proposed and analyzed. Longitudinal ultrasonic actuation was applied to the preheated cyclic olefin copolymer (COC) substrates to achieve accelerated and enhanced bonding with an ultrasonic welding system. Intimate contact between the bonding surfaces before the ultrasonic actuation was found to be an important prior condition. With improper contact, several bonding defects would occur, such as voids, localized spot melting and edge melting. Under auxiliary ultrasonic vibration, within 10 s, the bond strength developed at the bonding interface could be dramatically improved compared with those achieved without ultrasonic actuation. The enhanced bond strength obtained at a preheating temperature of 20 degrees C lower than its T-g could be comparable to the strength for pure thermal compression at 5 degrees C higher than its T-g. It is believed that the ultrasonic energy introduced could elevate the interfacial temperature and facilitate the interdiffusion of molecular chain segments at the interface, consequently resulting in rapidly enhanced bonding. Also, the microchannel distortion after ultrasonic actuation was found to be satisfactory-another important requirement. From dynamic mechanical analysis, the glass transition temperature of COC was found to increase with increasing frequency, and the temperature of the bulk polymer under ultrasonic actuation was still well under T-g; therefore the deformation is minor under ultrasonic actuation.
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Univ Paris 05, Sorbonne Paris Cite, Fac Sci Pharmaceut & Biol, UTCBS,CNRS,UMR 8258,Inserm,U1022, F-75006 Paris, FranceParis Saclay Univ, CNRS, UMR9001, Ctr Nanosci & Nanotechnol, F-91460 Paris, France
Salmon, Hugo
Loisel, Fanny
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Univ Paris Sud, Inserm 1197, Res Unit, F-94807 Villejuif, Paris Saclay, France
Paris Saclay Univ, Marie Lannelongue Hosp, INSERM, UMR S 999,Res & Innovat Unit,Univ Paris Sud, F-92350 Le Plessis Robinson, Paris, FranceParis Saclay Univ, CNRS, UMR9001, Ctr Nanosci & Nanotechnol, F-91460 Paris, France
Loisel, Fanny
Arouche, Nassim
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Univ Paris Sud, Inserm 1197, Res Unit, F-94807 Villejuif, Paris Saclay, FranceParis Saclay Univ, CNRS, UMR9001, Ctr Nanosci & Nanotechnol, F-91460 Paris, France
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Univ Paris Sud, Inserm 1197, Res Unit, F-94807 Villejuif, Paris Saclay, FranceParis Saclay Univ, CNRS, UMR9001, Ctr Nanosci & Nanotechnol, F-91460 Paris, France
Uzan, Georges
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Mercier, Olaf
Veres, Teodor
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Natl Res Council Canada, 75 Mortagne Blvd, Boucherville, PQ J4B 6Y4, CanadaParis Saclay Univ, CNRS, UMR9001, Ctr Nanosci & Nanotechnol, F-91460 Paris, France