Xaxim agroecológico.

bitstream/item/93481/1/2011-203-FOTOLIVRO-XAXIMv3-06-02-2012.pd

Step-type and step-density influences on CO adsorption probed by reflection absorption infrared spectroscopy using a curved Pt(1 1 1) surface

In comparison to flat single crystals, the continuous variation of structure provided by curved crystals offers many benefits for the study of physical and chemical processes at surfaces. However, the curvature of the surface also creates experimental challenges. For infrared spectroscopy, in particular, adsorbates on metal samples are typically probed by grazing-incidence reflection-absorption infrared spectroscopy (RAIRS). In this geometry, a convex crystal acts as a strongly diverging mirror. The authors describe how the experimental difficulties introduced by a cylindrical surface can be resolved for RAIRS. A complementary mirror, placed directly downfield of the curved crystal within the vacuum chamber, minimizes the divergence created by the sample. By simply translating the infrared focus across the sample, the authors probe adsorbate vibrational spectra as a function of local step-type and step-density with high sensitivity and spatial resolution. Time-consuming sample exchange, and the concomitant sample-to-sample experimental errors, are eliminated. The authors apply this new technique to carbon monoxide adsorption on a curved Pt(1 1 1) crystal and use it to resolve the influence of step-type and step-density on the CO stretch vibration as a function of coverage.</p

Microcavity-like exciton-polaritons can be the primary photoexcitation in bare organic semiconductors.

Strong-coupling between excitons and confined photonic modes can lead to the formation of new quasi-particles termed exciton-polaritons which can display a range of interesting properties such as super-fluidity, ultrafast transport and Bose-Einstein condensation. Strong-coupling typically occurs when an excitonic material is confided in a dielectric or plasmonic microcavity. Here, we show polaritons can form at room temperature in a range of chemically diverse, organic semiconductor thin films, despite the absence of an external cavity. We find evidence of strong light-matter coupling via angle-dependent peak splittings in the reflectivity spectra of the materials and emission from collective polariton states. We additionally show exciton-polaritons are the primary photoexcitation in these organic materials by directly imaging their ultrafast (5 × 106 m s-1), ultralong (~270 nm) transport. These results open-up new fundamental physics and could enable a new generation of organic optoelectronic and light harvesting devices based on cavity-free exciton-polaritons.EPSRC (EP/R025517/1), EPSRC (EP/M025330/1), ERC Horizon 2020 (grant agreements No 670405 and No 758826), ERC (ERC-2014-STG H2020 639088), Netherlands Organisation for Scientific Research, Swedish Research Council (VR, 2014-06948), Knut and Alice Wallenberg Foundation 3DEM-NATUR (no. 2012.0112), Royal Commission for the Exhibition of 1851, CNRS (France), US Department of Energy, Office of Science, Basic Energy Sciences, CPIMS Program, Early Career Research Program (DE-SC0019188)

Thermally-activated shape memory effect on biodegradable nanocomposites based on PLA/PCL blend reinforced with hydroxyapatite

[EN] In this work, the effect of the addition of different amount of nanosized hydroxyapatite (nHA) on the shape memory behavior of blends based on poly (lactic acid) (PLA) and poly (epsilon-caprolactone) (PCL) has been studied. In particular PLA/PCL blend with 70 wt % PLA has been reinforced with 0.5, 1 and 3 wt % nHA. Moreover, the relationship between the morphology and the final properties of the nanocomposites has been investigated by field emission scanning electron microscopy, confocal Raman spectroscopy and atomic force microscopy. In particular, PeakForce has been used to study quantitative nanomechanical properties of the multifunctional materials leading to conclusion that nHA increase the phase separation between PLA and PCL as well as act as reinforcements for the PCL-rich phase of the nanocomposites. Furthermore, excellent thermally-activated shape memory response has been obtained for all the nanocomposites at 55 degrees C. Finally, the disintegration under composting conditions at laboratory scale level was studied in order to confirm the biodegradable character of these nanocomposites. Indeed, these materials are able to be used for biomedical issues as well as for packaging applications where both thermally-activated shape memory effect and biodegradability are requested.Authors thank the Spanish Ministry of Economy, Industry and Competitiveness, MINEICO, (MAT2017-88123-P) and the Regional Government of Madrid (S2013/MIT-2862) for the economic support. M.P.A. and L.P. acknowledge the Juan de la Cierva (FJCI-2014-20630) and Ramon y Cajal (RYC-2014-15595) contracts from the MINEICO, respectively. The authors also thanks CSIC for the I-Link project (I-Link1149).Peponi, L.; Sessini, V.; Arrieta, MP.; Navarro-Baena, I.; Sonseca Olalla, Á.; Dominici, F.; Giménez Torres, E.... (2018). Thermally-activated shape memory effect on biodegradable nanocomposites based on PLA/PCL blend reinforced with hydroxyapatite. Polymer Degradation and Stability. 151:36-51. https://doi.org/10.1016/j.polymdegradstab.2018.02.019S365115

In Situ Compatibilization of Biopolymer Ternary Blends by Reactive Extrusion with Low-Functionality Epoxy-Based Styrene Acrylic Oligomer

[EN] The present study reports on the use of low-functionality epoxy-based styrene¿acrylic oligomer (ESAO) to compatibilize immiscible ternary blends made of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), polylactide (PLA), and poly(butylene adipate-co-terephthalate) (PBAT). The addition during melt processing of low-functionality ESAO at two parts per hundred resin (phr) of biopolymer successfully changed the soften inclusion phase in the blend system to a thinner morphology, yielding biopolymer ternary blends with higher mechanical ductility and also improved oxygen barrier performance. The compatibilization achieved was ascribed to the in situ formation of a newly block terpolymer, i.e. PHBVb- PLA-b-PBAT, which was produced at the blend interface by the reaction of the multiple epoxy groups present in ESAO with the functional terminal groups of the biopolymers. This chemical reaction was mainly linear due to the inherently low functionality of ESAO and the more favorable reactivity of the epoxy groups with the carboxyl groups of the biopolymers, which avoided the formation of highly branched and/or cross-linked structures and thus facilitated the films processability. Therefore, the reactive blending of biopolymers at different mixing ratios with low-functionality ESAO represents a straightforward methodology to prepare sustainable plastics at industrial scale with different physical properties that can be of interest in, for instance, food packaging applications.This research was funded by the EU H2020 project YPACK (Reference number 773872) and by the Spanish Ministry of Science, Innovation, and Universities (MICIU) with project numbers MAT2017-84909-C2-2-R and AGL2015-63855-C2-1-R. L. Quiles-Carrillo wants to thank the Spanish Ministry of Education, Culture, and Sports (MECD) for financial support through his FPU Grant Number FPU15/03812. Torres-Giner also acknowledges the MICIU for his Juan de la Cierva contract (IJCI-2016-29675).Quiles-Carrillo, L.; Montanes, N.; Lagaron, J.; Balart, R.; Torres-Giner, S. (2019). In Situ Compatibilization of Biopolymer Ternary Blends by Reactive Extrusion with Low-Functionality Epoxy-Based Styrene Acrylic Oligomer. Journal of Polymers and the Environment. 27(1):84-96. https://doi.org/10.1007/s10924-018-1324-2S8496271Babu RP, O’Connor K, Seeram R (2013) Prog Biomater 2:8Torres-Giner S, Torres A, Ferrándiz M, Fombuena V, Balart R (2017) J Food Saf 37:e12348Quiles-Carrillo L, Montanes N, Boronat T, Balart R, Torres-Giner S (2017) Polym Test 61:421Zakharova E, Alla A, Martínez A, De Ilarduya S, Muñoz-Guerra (2015) RSC Adv 5:46395Steinbüchel A, Valentin HE (1995) FEMS Microbiol Lett 128:219McChalicher CWJ, Srienc F (2007) J Biotechnol 132:296Reis KC, Pereira J, Smith AC, Carvalho CWP, Wellner N, Yakimets I (2008) J Food Eng 89:361Vink ETH, Davies S (2015) Ind Biotechnol 11:167John RP, Nampoothiri KM, Pandey A (2006) Process Biochem 41:759Madhavan Nampoothiri K, Nair NR, John RP (2010) Biores Technol 101:8493Garlotta D (2001) J Polym Environ 9:63Lim LT, Auras R, Rubino M (2008) Prog Polym Sci 33:820Quiles-Carrillo L, Montanes N, Sammon C, Balart R, Torres-Giner S (2018) Ind Crops Prod 111:878Quiles-Carrillo L, Blanes-Martínez MM, Montanes N, Fenollar O, Torres-Giner S, Balart R (2018) Eur Polym J 98:402Witt U, Müller R-J, Deckwer W-D (1997) J Environ Polym Degrad 5:81Siegenthaler KO, Künkel A, Skupin G, Yamamoto M (2012) Ecoflex® and Ecovio®: biodegradable, performance-enabling plastics. In: Rieger B, Künkel A, Coates GW, Reichardt R, Dinjus E, Zevaco TA (eds) Synthetic biodegradable polymers. Springer, Berlin Heidelberg, p 91Jiang L, Wolcott MP, Zhang J (2006) Biomacromol 7:199Brandelero RPH, Yamashita F, Grossmann MVE (2010) Carbohyd Polym 82:1102Muthuraj R, Misra M, Mohanty AK (2014) J Polym Environ 22:336Porter RS, Wang L-H (1992) Polymer 33(10): 2019Koning C, Van Duin M, Pagnoulle C, Jerome R (1998) Prog Polym Sci 23:707Muthuraj R, Misra M, Mohanty AK (2017) J Appl Polym Sci 135:45726Ryan AJ (2002) Nat Mater 1:8Wu D, Zhang Y, Yuan L, Zhang M, Zhou W (2010) J Polym Sci Part B 48:756Kim CH, Cho KY, Choi EJ, Park JK (2000) J Appl Polym Sci 77:226Supthanyakul R, Kaabbuathong N, Chirachanchai S (2016) Polymer 105:1Na Y-H, He Y, Shuai X, Kikkawa Y, Doi Y, Inoue Y (2002) Biomacromolecules 3:1179Zeng J-B, Li K-A, Du A-K (2015) RSC Adv 5:32546Xanthos M, Dagli SS (1991) Polym Eng Sci 31:929Sundararaj U, Macosko CW (1995) Macromolecules 28:2647Milner ST, Xi H (1996) J Rheol 40:663Villalobos M, Awojulu A, Greeley T, Turco G, Deeter G (2006) Energy 31:3227Torres-Giner S, Montanes N, Boronat T, Quiles-Carrillo L, Balart R (2016) Eur Polym J 84:693Lehermeier HJ, Dorgan JR (2001) Polym Eng Sci 41:2172Liu B, Xu Q (2013) J Mater Sci Chem Eng 1:9Eslami H, Kamal MR (2013) J Appl Polym Sci 129:2418Loontjens T, Pauwels K, Derks F, Neilen M, Sham CK, Serné M (1997) J Appl Polym Sci 65:1813Ojijo V, Ray SS (2015) Polymer 80:1Frenz V, Scherzer D, Villalobos M, Awojulu AA, Edison M, Van Der Meer R (2008) Multifunctional polymers as chain extenders and compatibilizers for polycondensates and biopolymers. In: Technical papers, regional technical conference—society of plastics engineers, p. 3/1678Utracki LA (2002) Can J Chem Eng 80:1008Al-Itry R, Lamnawar K, Maazouz A (2012) Polym Degrad Stab 97:1898Lin S, Guo W, Chen C, Ma J, Wang B (2012) Mater Des (1980–2015) 36: 604Arruda LC, Magaton M, Bretas RES, Ueki MM (2015) Polym Test 43:27Wang Y, Fu C, Luo Y, Ruan C, Zhang Y, Fu Y (2010) J Wuhan Univ Technol Mater Sci Ed 25:774Wei D, Wang H, Xiao H, Zheng A, Yang Y (2015) Carbohyd Polym 123:275Abdelwahab MA, Taylor S, Misra M, Mohanty AK (2015) Macromol Mater Eng 300:299Sun Q, Mekonnen T, Misra M, Mohanty AK (2016) J Polym Environ 24:23Torres-Giner S, Gimeno-Alcañiz JV, Ocio MJ, Lagaron JM (2011) J Appl Polym Sci 122:914Miyata T, Masuko T (1998) Polymer 39:5515Muthuraj R, Misra M, Mohanty AK (2015) J Appl Polym Sci 132:42189Ren J, Fu H, Ren T, Yuan W (2009) Carbohyd Polym 77:576Torres-Giner S, Montanes N, Fenollar O, García-Sanoguera D, Balart R (2016) Mater Des 108:648Jamshidian M, Tehrany EA, Imran M, Jacquot M, Desobry S (2010) Compr Rev Food Sci Food Saf 9:552Savenkova L, Gercberga Z, Nikolaeva V, Dzene A, Bibers I, Kalnin M (2000) Process Biochem 35:573Costa ARM, Almeida TG, Silva SML, Carvalho LH, Canedo EL (2015) Polym Test 42:115Zhang K, Mohanty AK, Misra M (2012) ACS Appl Mater Interfaces 4:3091Zhang N, Wang Q, Ren J, Wang L (2009) J Mater Sci 44:250Chinsirikul W, Rojsatean J, Hararak B, Kerddonfag N, Aontee A, Jaieau K, Kumsang P, Sripethdee C (2015) Packag Technol Sci 28:741Auras R, Harte B, Selke S (2004) J Appl Polym Sci 92:1790Sanchez-Garcia MD, Gimenez E, Lagaron JM (2008) Carbohyd Polym 71:235Sanchez-Garcia MD, Gimenez E, Lagaron JM (2007) J Plast Film Sheeting 23:133Lagaron JM (2011) Multifunctional and nanoreinforced polymers for food packaging. In: Multifunctional and nanoreinforced polymers for food packaging. Woodhead Publishing, Cambridge, p 

Development of microspheres for biomedical applications: a review

An overview of microspheres manufactured for use in biomedical applications based on recent literature is presented in this review. Different types of glasses (i.e. silicate, borate, and phosphates), ceramics and polymer-based microspheres (both natural and synthetic) in the form of porous , non-porous and hollow structures that are either already in use or are currently being investigated within the biomedical area are discussed. The advantages of using microspheres in applications such as drug delivery, bone tissue engineering and regeneration, absorption and desorption of substances, kinetic release of the loaded drug components are also presented. This review also reports on the preparation and characterisation methodologies used for the manufacture of these microspheres. Finally, a brief summary of the existing challenges associated with processing these microspheres which requires further research and development are presented