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Articles by Pierre
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Polymer Processing Aids: With or without fluorinated molecules?
Polymer Processing Aids: With or without fluorinated molecules?
By Pierre Sarazin
Activity
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After years of working on blown film extrusion and seeing different guides and books on this process, I still find Qenos Technical Guide for film…
After years of working on blown film extrusion and seeing different guides and books on this process, I still find Qenos Technical Guide for film…
Liked by Pierre Sarazin
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Thank you AMI for a great conference! #agricultural #plasticmulch #sustainable
Thank you AMI for a great conference! #agricultural #plasticmulch #sustainable
Liked by Pierre Sarazin
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We are thrilled to announce that Shilpa Sankhe-Manjure, Director, Global R&D, has been elected as the Chair for SPE’s Bioplastics & Renewable…
We are thrilled to announce that Shilpa Sankhe-Manjure, Director, Global R&D, has been elected as the Chair for SPE’s Bioplastics & Renewable…
Liked by Pierre Sarazin
Experience & Education
Licenses & Certifications
Publications
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Tunable Porous Hydrogels from Cocontinuous Polymer Blends
Macromolecules
AN Esquirol (1st author), N Virgilio (Corresponding author).
Hydrogels embedded with networks of fully interconnected pores were prepared with microporous polylactide (PLA) molds obtained by extracting the polystyrene (PS) phase in melt-processed cocontinuous blends of PLA and PS. Quiescent annealing of the blends prior to the PS extraction allowed control over the average pore diameter from 1 to 500 μm for the PLA molds. Solutions of agar or alginate were injected within the molds and…AN Esquirol (1st author), N Virgilio (Corresponding author).
Hydrogels embedded with networks of fully interconnected pores were prepared with microporous polylactide (PLA) molds obtained by extracting the polystyrene (PS) phase in melt-processed cocontinuous blends of PLA and PS. Quiescent annealing of the blends prior to the PS extraction allowed control over the average pore diameter from 1 to 500 μm for the PLA molds. Solutions of agar or alginate were injected within the molds and gelled in situ. Porous gels were obtained by extracting the PLA molds and X-ray microtomography was employed to characterize their microstructure. Water removal/uptake cycles were fully reversible with very fast kinetics. Freeze-drying yielded ultraporous materials without modification of the macroscopic dimensions, and rehydration yielded back porous hydrogels. It was possible to scale up the technique by using extrusion and injection molding equipment. This versatile new method allows extensive control over the gels’ porosity parameters and the use of various gel chemistries.Other authorsSee publication -
Ultraporous poly(L-lactide) scaffolds prepared with quaternary immiscible polymer blends modified by copolymer brushes at the interface
Polymer, 52, 1483-1489
The activity of polystyrene-block-poly(l-lactide) (PS-b-PLLA) and polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) diblock copolymer brushes located at a PS/PLLA interface were employed as a route to control the final microstructure of 95% void volume, ultraporous PLLA scaffolds.
Other authorsSee publication -
Towards ultraporous poly(L-lactide) scaffolds from quaternary immiscible polymer blends
Biomaterials, 31, 5719-5728
Ultraporous poly(l-lactide) (PLLA) scaffolds were prepared by melt-processing quaternary ethylene propylene diene rubber/poly(ε-caprolactone)/polystyrene/poly(l-lactide) (EPDM/PCL/PS/PLLA) 45/45/5/5 %vol. polymer blends modified with a PS-b-PLLA diblock copolymer. The morphology consists of a PS + PLLA+copolymer sub-blend layer forming at the interface of the EPDM and PCL phases. Quiescent annealing and interfacial modification using the block copolymer are used to control the blend…
Ultraporous poly(l-lactide) (PLLA) scaffolds were prepared by melt-processing quaternary ethylene propylene diene rubber/poly(ε-caprolactone)/polystyrene/poly(l-lactide) (EPDM/PCL/PS/PLLA) 45/45/5/5 %vol. polymer blends modified with a PS-b-PLLA diblock copolymer. The morphology consists of a PS + PLLA+copolymer sub-blend layer forming at the interface of the EPDM and PCL phases. Quiescent annealing and interfacial modification using the block copolymer are used to control the blend microstructure. The ultraporous structure is subsequently obtained by selectively extracting the EPDM, PS and PCL phases. The PLLA scaffolds modified with the PS-b-PLLA copolymer present themselves as fully interconnected porous networks with asymmetric channel walls, one side being smooth while the other is covered with an array of submicron-sized PLLA droplets. They are prepared with a high degree of control over the pore size, with averages ranging from 5 μm to over 100 μm and a specific surface from 9.1 to 23.1 m2/g of PLLA, as annealing is carried out from 0 to 60 min. The void volume reaches values as high as 95% and in all cases the shape and dimensions of the scaffolds are maintained with a high level of integrity. The proposed method represents a comprehensive approach towards the design and generation of porous PLLA scaffolds based on complex morphologies from melt-processed multiphase polymer systems.
Other authorsSee publication -
Total 20 publications with more than 700 citations, h-index of 12, according to Web of Science
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Patents
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Porous Nanosheath networks, method of making and uses thereof
Issued US US8,257,624 B2
The method for making a porous material, comprises melt-blending of non-miscible polymers to obtain a co-continuous melt, solidifying the co-continuous melt at 200C to obtain a solid mass, obtaining a quiescent annealing of the solid mass, exchanging the solvent and freeze-drying the porous material, extracting the polymers from the solid mass, depositing precursor layers on the internal surface of a continuous pore network, replicating the internal surface of the pore network, and extracting…
The method for making a porous material, comprises melt-blending of non-miscible polymers to obtain a co-continuous melt, solidifying the co-continuous melt at 200C to obtain a solid mass, obtaining a quiescent annealing of the solid mass, exchanging the solvent and freeze-drying the porous material, extracting the polymers from the solid mass, depositing precursor layers on the internal surface of a continuous pore network, replicating the internal surface of the pore network, and extracting the solid mass without extracting the layers for producing the porous material. The polymer is extracted from the solid mass by creating a pore network within the solid mass, and the pore network has an internal surface. The internal surface of the pore network is replicated within the solid mass by coating the internal surface with successive conductive polymeric layers. The last polymeric layer contains functional chemical groups. The total extraction provides the porous material within the extracted solid mass. The successive layers comprise proteins, cell growth promoters and/or functionalizing agents.
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Microporous articles comprising biodegradable medical polymers, method of preparation thereof and method of use thereof
Issued US US 8,007,823 B2
The present invention relates to a highly controlled method of preparation of a microporous biodegradable polymeric article. Firstly, at least one biodegradable polymer A, one polymer B, biodegradable or not, partially or totally immiscible with A, and a compatibilizer C for A and B are selected. Secondly, the selected polymers are melt-blended, thereby preparing a polymer blend, wherein said polymers A and B have an essentially continuous morphology. Thirdly, after cooling, polymer B and…
The present invention relates to a highly controlled method of preparation of a microporous biodegradable polymeric article. Firstly, at least one biodegradable polymer A, one polymer B, biodegradable or not, partially or totally immiscible with A, and a compatibilizer C for A and B are selected. Secondly, the selected polymers are melt-blended, thereby preparing a polymer blend, wherein said polymers A and B have an essentially continuous morphology. Thirdly, after cooling, polymer B and compatibilizer C are selectively extracted from the polymer blend by dissolution in a solvent that is a non-solvent of polymer A. The resulting polymeric article has an essentially continuous porosity with a void volume between 10 and 90% and a unimodal diameter distribution set to a predefined unimodal peak location. It can be
used in tissue engineering, for controlled release applications or as an implantable medical device.Other inventors -
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Polymer Blends comprising Phase-encapsulated Thermoplastic Starch and Process for making the same
Filed US US 20120283364
New polymer blends are provided. These blends comprise a first polymer, a second polymer and thermoplastic starch, the thermoplastic starch being at least partially encapsulated in the second polymer. The polymer blends may be shaped into articles, for example by extrusion or injection molding.
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Languages
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English
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French
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More activity by Pierre
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Two days rich in debate and exchange of ideas at AMI Agricultural Film North America!🌾 Thank you to everyone who took part in our session on…
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Great kick-off at the AMI Agricultural Films conference in Tampa today! Dr. MiaoMiao Xiao gave a fantastic presentation titled "Development of new…
Great kick-off at the AMI Agricultural Films conference in Tampa today! Dr. MiaoMiao Xiao gave a fantastic presentation titled "Development of new…
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Surprising to see the Biden-Harris administration release this document https://lnkd.in/eBTCvwUR at the very end of its mandate. If this document…
Surprising to see the Biden-Harris administration release this document https://lnkd.in/eBTCvwUR at the very end of its mandate. If this document…
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