Summary: An in‐line method for monitoring the solidification process during injection molding of semicrystalline polymers (demonstrated previously in J. Appl. Polym. Sci. 2003 , 89, 3713) is based on a simple device, where an additional ejector pin is pushed on the injection molded part at different times during the solidification phase. The ‘indentation depth profile’, i.e., residual deformation as a function of time, was obtained and allowed to determine the evolution of the solidification front in the mold as a function of the cooling time. The present work shows the reliability and the powerfulness of the aforementioned method for a large variety of different semicrystalline polymers (PET, PBT, polyamide‐6 PA6, isotactic poly(propylene) iPP) characterized also by different molecular weight and/or nucleating agents. The results show that the indentation test may be considered as a ‘predictive’ tool to qualitatively and quantitatively compare the solidification process of different polymers and polymer grades during injection molding.
Comparison of the solid front propagation during injection molding of different materials. 相似文献
Mass production of microfluidic devices commonly relies on injection molding. Injection molding requires a master surface made using micro or nanofabrication. Conventionally, electroplating from a silicon master is used for mold insert production, but this is expensive and cannot be used with masters produced via the Bosch process as interlocking of the scalloping between polymer and metal insert hinders part ejection. Here, an alternative to the electroplating process is developed by adapting a nanoimprint route to produce flexible micro-structured polymer inserts capable of molding using a Bosch process-produced master. An optimized fabrication approach using silicon masters with smooth sidewalls (produced using the mixed process) is used to characterize the limits of the process. Aspect ratios of 1 and below are successfully replicated. Feature spacings down to 20 µm are successfully produced with minimal variation between repeated parts. Masters produced using two different Bosch etches exhibiting both coarse and fine nanometer scalloping are also studied. Parts are successfully ejected with retained nanometer scalloping in all samples although inlay damage occurred after >10 replicas. A proof-of-concept microfluidic device is successfully produced vindicating the use of this approach as an efficient and cost-effective approach for the rapid prototyping of complex micro-structured designs. 相似文献
The nanometer scale topography of self‐assembling structural protein complexes in animals is believed to induce favorable cell responses. An important example of such nanostructured biological complexes is fibrillar collagen that possesses a cross‐striation structure with a periodicity of 69 nm and a peak‐to‐valley distance of 4–6 nm. Bovine collagen type I was assembled into fibrillar structures in vitro and sedimented onto solid supports. Their structural motif was transferred into a nickel replica by physical vapor deposition of a small‐grained metal layer followed by galvanic plating. The resulting inverted nickel structure was found to faithfully present most of the micrometer and nanometer scale topography of the biological original. This nickel replica was used as a die for the injection molding of a range of different thermoplastic polymers. Total injection molding cycle times were in the range of 30–45 seconds. One of the polymer materials investigated, polyethylene, displayed poor replication of the biological nanotopographical motif. However, the majority of the polymers showed very high replication fidelity as witnessed by their ability to replicate the cross‐striation features of less than 5 nm height difference. The latter group of materials includes poly(propylene), poly(methyl methacrylate), poly(L ‐lactic acid), polycaprolactone, and a copolymer of cyclic and linear olefins (COC). This work suggests that the current limiting factor for the injection molding of nanometer scale topography in thermoplastic polymers lies with the grain size of the initial metal coating of the mold rather than the polymers themselves.
