Preparazione e caratterizzazione di concentratori solari fluorescenti a lastra ed a film sottile polimerico

(1)

Elenco delle immagini con le relative citazioni delle fonti:  Fig. 1.1: https://www.fondazionesvilupposostenibile.org/wp-content/uploads/dlm_uploads/2016/05/PRESENTATIONENERGYOUTLOO K2016.pdf ([2])  Fig. 1.2: https://www.google.com/search?q=am+1.5g+spectrum&hl=it-US&tbm=isch&tbs=rimg:CaUWO_1FhjJweIjieAbH5cosJXlM2i1Yv7MMLkS G5tC2KXr3IiS-O7I1fPYuEPMViquGc1qjsRe46nS2NUUb02XUuJioSCZ4BsflyiwleEcTyBzL EPq1UKhIJUzaLVi_1swwsRlRkc2PvcsTYqEgmRIbm0LYpevRHol-eDynJP7yoSCciJL47sjV89EcbDTAEydExAKhIJi4Q8xWKq4ZwRJ3_1K8xo3 fRsqEgnWqOxF7jqdLRH5Nibjscy0YioSCY1RRvTZdS4mEU2vBPPngR-0&tbo=u&sa=X&ved=0ahUKEwjV9sX_rO3WAhVFVhQKHemCB2YQ9C8I Hw&biw=1366&bih=675&dpr=1#imgrc=sFui_07oCxlWVM:

 Fig. 1.3: A. Goetzberger and V. U. Hoffmann, Photovoltaic solar energy generation, vol. 112. Springer Science & Business Media, 2005. ([4])

 Fig. 1.4: M. Sottile, “Concentratori solari luminescenti a matrice epossidica”. Tesi di laurea magistrale in Chimica industriale-Curriculm materiali,

Università di Pisa, 2015. ([141])  Fig.1.5:https://www.google.it/search?q=banda+elettronica+semiconduttori&rlz =1C1EJFA_enIT688IT688&source=lnms&tbm=isch&sa=X&ved=0ahUKEwi d6ezbq-3WAhWLWRQKHZt7DBAQ_AUICygC&biw=1366&bih=675#imgrc=85W8 MacTmORxUM:  Fig.1.6:https://www.google.it/search?q=bande+di+valenza&tbm=isch&tbs=ri mg:CRvqMSfUi3w7IjhoxZPhMXS78wEuSvIS6G8xMwnZ4fdvuhmeKX0yC- wSDHf8UP1rQRN5y0olByrjYqXJn3b4F6aoHyoSCWjFk- ExdLvzEbN7265giftsKhIJAS5K8hLobzERFmQq4k-27qMqEgkzCdnh92-6GRHIStWf9IdvQSoSCZ4pfTIL7BIMEdyGLl6tKe82KhIJd_1xQ_1WtBE3kR NjVoNS2mROAqEgnLSiUHKuNipRF9ZmL9_1me-vSoSCcmfdvgXpqgfEZzEYd5ygFSF&tbo=u&sa=X&ved=0ahUKEwjdw5vIr O3WAhULtBoKHaoWAYUQ9C8IHw&biw=1366&bih=675&dpr=1#imgrc= Vzpz6VyPsQnIVM:

 Fig. 1.7: elaborazione propria

Università di Pisa, 2015. ([141])  Fig. 1.9: elaborazione propria

(2)

 Da Fig. 1.11 a Fig. 1.3: G. Tomei, “Concentratori solari luminescenti a base di polimetilmetacrilato: metodi di preparazione e confronto delle proprietà ultime di efficienza ottica.” Tesi di laurea magistrale in Chimica

Industriale-Curriculum Materiali, Università di Pisa, 2015.

 Fig. 1.14: A. Goetzberger and W. Greubel, “Solar energy conversion with fluorescent collectors,” Applied Physics A: Materials Science & Processing, vol. 14, no. 2, pp. 123–139, 1977. ([51])

 Fig. 1.16 e Fig. 1.17: C. G. dos Remedios, M. Miki, and J. A. Barden, “Fluorescence resonance energy transfer measurements of distances in actin and myosin. A critical evaluation,” J Muscle Res Cell Motil, vol. 8, no. 2, pp. 97–117, Apr. 1987. ([68])

 Fig. 1.19: C. G. dos Remedios, M. Miki, and J. A. Barden, “Fluorescence resonance energy transfer measurements of distances in actin and myosin. A critical evaluation,” J Muscle Res Cell Motil, vol. 8, no. 2, pp. 97–117, Apr. 1987. ([68])

 Fig. 1.20: G. A. Crosby, R. E. Whan, and R. M. Alire, “Intramolecular energy transfer in rare earth chelates. Role of the triplet state,” The journal of chemical physics, vol. 34, no. 3, pp. 743–748, 1961. ([74])

 Fig. 1.21: A. Visser and O. J. Rolinski, “Basic photophysics,” American Society for Photobiology, 2010. ([86])

 Fig. 1.22: S. Poli, “Preparazione e caratterizzazione di concentratori solari luminescenti a film sottile a base del colorante organico Hostasol Red”. Tesi di laurea triennale in Chimica per l’industria e l’ambiente, Università di Pisa, 2016. ([138])

 Fig. 1.23 e Fig. 1.24: elaborazione propria

Università di Pisa, 2015. ([141])

 Da Fig. 2.4 a Fig. 2.9: elaborazione propria

 Fig. 2.10: F. Vignola, J. Michalsky, and T. Stoffel, Solar and infrared radiation measurements. CRC press, 2012. ([142])

(3)

 Fig. 3.16 e Fig. 3.17: A. Rivaton, “Recent advances in bisphenol-A

polycarbonate photodegradation,” Polymer Degradation and Stability, vol. 49, no. 1, pp. 163–179, 1995. ([155])

 Fig. 3.28: J. Berger and F. Lohse, “Polymerization of p-cresyl glycidyl ether induced by benzyldimethylamine,” European polymer journal, vol. 21, no. 5, pp. 435–444, 1985. ([161])

 Fig. 3.29: L. Shechter, J. Wynstra, and R. P. Kurkjy, “Glycidyl ether reactions with amines,” Industrial & Engineering Chemistry, vol. 48, no. 1, pp. 94–97, 1956. ([167])

 Fig. 3.43 e Fig. 3.44: B. Mailhot, S. Morlat-Thérias, M. Ouahioune, and J.-L. Gardette, “Study of the degradation of an epoxy/amine resin, 1,”

Macromolecular Chemistry and physics, vol. 206, no. 5, pp. 575–584, 2005. ([119]) e A. Rivaton, L. Moreau, and J.-L. Gardette, “Photo-oxidation of

phenoxy resins at long and short wavelengths—II. Mechanisms of formation of photoproducts,” Polymer degradation and stability, vol. 58, no. 3, pp. 333–339, 1997. ([181])  Fig.3.45:https://www.google.it/search?biw=1366&bih=675&tbm=isch&sa=1& q=p-quinone+methide&oq=p-quinone+methide&gs_l=psy-ab.3..0i19k1.755202.767192.0.767388.19.19.0.0.0.0.124.1170.16j1.19.0....0...1 .1.64.psy-ab..0.16.1108.0..0j0i13i10k1j0i30k1j0i10i30k1j0i13i30k1j0i5i30k1j0i8i30i19k 1j0i8i10i30i19k1.50.ZvYwz6djnYw#imgrc=krZ-497p2LfrCM:

 Fig. 3.55: M. Carlotti, G. Ruggeri, F. Bellina, and A. Pucci, “Enhancing optical efficiency of thin-film luminescent solar concentrators by combining energy transfer and stacked design,” Journal of Luminescence, vol. 171, pp. 215–220, 2016. ([59])