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1.
Polymers (Basel) ; 11(6)2019 Jun 20.
Article in English | MEDLINE | ID: mdl-31226802

ABSTRACT

Poly(furfuryl alcohol) (PFA) is a bioresin synthesized from furfuryl alcohol (FA) that is derived from renewable saccharide-rich biomass. In this study, we compounded this bioresin with polycaprolactone (PCL) for the first time, introducing new functional polymer blends. Although PCL is biodegradable, its production relies on petroleum precursors such as cyclohexanone oils. With the method proposed herein, this dependence on petroleum-derived precursors/monomers is reduced by using PFA without significantly modifying some important properties of the PCL. Polymer blend films were produced by simple solvent casting. The blends were characterized in terms of surface topography by atomic force microscopy (AFM), chemical interactions between PCL and PFA by attenuated total reflection-Fourier transform infrared (ATR-FTIR), crystallinity by XRD, thermal properties by differential scanning calorimetry (DSC), and mechanical properties by tensile tests and biocompatibility by direct and indirect toxicity tests. PFA was found to improve the gas barrier properties of PCL without compromising its mechanical properties, and it demonstrated sustained antioxidant effect with excellent biocompatibility. Our results indicate that these new blends can be potentially used in diverse applications ranging from food packing to biomedical devices.

2.
ACS Omega ; 3(10): 13484-13493, 2018 Oct 31.
Article in English | MEDLINE | ID: mdl-31458057

ABSTRACT

A photoresponsive microstructured composite is fabricated through the impregnation of cellulosic filter paper (FP) with a spiropyran-modified acrylic polymer. The polymer enwraps uniformly each individual cellulose fiber, increases the thermal stability of cellulose, and ensures the preservation of the composite functionalities even upon removal of the surface layers through mechanical scratching. The photochromic spiropyran moieties of the polymer, even while embedded in the cellulosic sheet, can reversibly interconvert between the colorless spiropyran and the pink merocyanine isomeric states upon irradiation with UV and visible light, respectively. Moreover, the photochromic polymer presents a faster photochromic response and a higher resistance to photodegradation, with an outstanding reusability for more than 100 switching cycles when it is incorporated in the cellulose network. Most importantly, the acidochromism of the modified FP, attributed to the spiropyran molecules after UV activation, allows the real-time optical and visual detection of acidity changes and spoilage in food products, such as wine and milk. Spoilage due to bacterial degradation and oxidation processes generates acidic vapors that induce the protonation of the merocyanine. This results in a visually detectable chromic transition from pink to white of the treated cellulose fibers, corresponding to a blue shift in the absorption spectrum. The developed photoresponsive cellulose composite can serve as cost-effective robust optical component in integrated functional platforms and consumer-friendly indicators for smart food packaging, as well as portable on demand acidoresponsive interfaces for gas monitoring in industrial and environmental applications.

3.
ACS Appl Mater Interfaces ; 9(46): 40707-40715, 2017 Nov 22.
Article in English | MEDLINE | ID: mdl-29120601

ABSTRACT

Photochromic spiropyran-doped silk fibroin poly(ethylene oxide) nanofibers which combine the attractive properties and biocompatibility of silk with the photocontrollable and reversible optical, mechanical, and chemical response of the spiropyran dopants are herein presented. As proved, the reversible variation of the absorption and emission signals of the mats and of their Young's modulus upon alternate UV and visible light irradiation is ascribed to the reversible photoconversion of the spiropyran form to its polar merocyanine counterpart. Most importantly, the interactions of the merocyanine molecules with acidic vapors as well as with heavy metal ions dispersed in solution produce analyte-specific spectral changes in the emission profile of the composite, accompanied by a characteristic chromic variation. Because of the high surface-to-volume ratio of the nanofibrous network, such interactions are fast, thus enabling both an optical and a visual detection in a 30-60 s time scale. The sensing platform can be easily regenerated for more than 20 and 3 cycles upon acid or ion depletion, respectively. Overall, the photocontrolled properties of the silk composites combined with a straightforward preparation method render them suitable as porous materials and scaffolds with tunable compliance and reusable nanoprobes for real time optical detection in biomedical, environmental, and industrial applications.

4.
Langmuir ; 31(22): 6072-7, 2015 Jun 09.
Article in English | MEDLINE | ID: mdl-26017025

ABSTRACT

Grasslike compliant micro/nano crystals made of diarylethene (DAE) photochromic molecules are spontaneously formed on elastomer films after dipping them in a solution containing the photochromic molecules. The frictional forces of such micro- and nanofibrillar surfaces are reversibly tuned upon ultraviolet (UV) irradiation and dark storage cycles. This behavior is attributed to the Young's modulus variation of the single fibrils due to the photoisomerization process of the DAE molecules, as measured by advanced atomic force microscopy (AFM) techniques. In fact, a significant yet reversible decrease of the stiffness of the outer part of the fibrils in response to the UV light irradiation is demonstrated. The modification of the molecular structure of the fibrils influences their mechanical properties and affects the frictional behavior of the overall fibrillar surfaces. These findings provide the possibility to develop a system that controllably and accurately generates both low and high friction forces.


Subject(s)
Ethylenes/chemistry , Friction , Microscopy, Atomic Force , Particle Size , Photochemical Processes , Surface Properties , Ultraviolet Rays
5.
Langmuir ; 30(10): 2896-902, 2014 Mar 18.
Article in English | MEDLINE | ID: mdl-24564574

ABSTRACT

Technologies that are able to handle microvolumes of liquids, such as microfluidics and liquid marbles, are attractive for applications that include miniaturized biological and chemical reactors, sensors, microactuators, and drug delivery systems. Inspired from natural fibrous envelopes, here, we present an innovative approach for liquid encapsulation and manipulation using electrospun nanofibers. We demonstrated the realization of non-wetting soft solids consisting of a liquid core wrapped in a hydrophobic fibrillar cloak of a fluoroacrylic copolymer and cellulose acetate. By properly controlling the wetting and mechanical properties of the fibers, we created final architectures with tunable mechanical robustness that were stable on a wide range of substrates (from paper to glass) and floated on liquid surfaces. Remarkably, the realized fiber-coated drops endured vortex mixing in a continuous oil phase at high stirring speed without bursting or water losses, favoring mixing processes inside the entrapped liquid volume. Moreover, the produced cloak can be easily functionalized by incorporating functional particles, active molecules, or drugs inside the nanofibers.


Subject(s)
Biomimetics/methods , Drug Delivery Systems/methods , Hydrophobic and Hydrophilic Interactions , Nanofibers
6.
ACS Appl Mater Interfaces ; 5(15): 7253-7, 2013 Aug 14.
Article in English | MEDLINE | ID: mdl-23875812

ABSTRACT

We present a method to create, align, and locate magnetic wires throughout and on the surface of patterned polymer matrices, following the magnetophoretic transport and self-assembly of ferromagnetic nanoparticles under a static magnetic field during laser photopolymerization of monomer/nanoparticle casted solutions. The resulting films have the ability to attract and immobilize small quantities of magnetic nanomaterials locally on the ferromagnetic wires, as proved by a detailed topography study. Magnetic studies on the films before and after the spontaneous deposition, demonstrate that the deposited nanomaterials alter significantly the magnetic character of the system, making thus possible their macroscopic identification. This offers the possibility to realize sensing devices based on hybrid materials with magnetic properties.

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