Ottimizzazione di un controllo di temperatura per diodi laser

In questo lavoro di tesi si studia un processo sperimentale necessario alla realizza- zione di un esperimento di Fisica Atomica. L’attivit`a svolta consiste nell’ottimizzazione dei paramentri di un algoritmo di con- trollo PI (proporzionale-integrale) atto a stabilizzare la temperatura di un Diodo Laser entro 1mK. Nella branca dell’Ottica Non Lineare (dove la polarizzazione del mezzo ha una rispo- sta non lineare al campo elettrico) si possono presentare casi in cui la birifrangenza del mezzo ha una forte dipendenza dalla temperatura. Questa pu o ` essere control- lata per il raggiungimento delle condizioni di phase matching. Le fluttuazioni di temperatura possono minare tramite la dilatazione termica la precisione di una ca- vit`a Fabry-Perot, utilizzata per controllare e misurare la lunghezza d’onda della luce, dato che nominalmente ∆ν/ν = − ∆L/L. Negli esperimenti di Laser Cooling infi- ne si lavora spesso con transizioni la cui larghezza naturale Γ ∼ 1MHz , mentre la frequenza di un laser pu o ́ dipendere dalla temperatura con coefficienti tipicamente dell’ordine del GHz/K. Questa stabilizzazione risulta dunque fondamentale per una vasta classe di esperi- menti nei quali le derive termiche possono influenzare drammaticamente il processo di misura. La tesi, in particolare, si apre con un capitolo nel quale si tratta brevemente il con- testo matematico di riferimento per i sistemi di controllo a retroazione. Tra questi e ` di particolare interesse la regolazione proporzionale-integrale. Il secondo capitolo si concentra sulla caratterizzazione del sistema in oggetto al fine di trovare la sua funzione di trasferimento ad anello aperto. Nel terzo capitolo infine, si utilizzano gli strumenti matematici descritti precedente- mente per ottimizzare i parametri del regolatore e si discutono i risultati ottenuti e le misure finali.

Defects in thermosensitive colloidal crystals

Poly-N-Isopropylacrylamide (PNIPAM) colloidal particles form crystal phases that show a thermosensitive behaviour and can be used as atomic model systems. This polymer has both hydrophilic and hydrophobic character and has interesting stimuli-responsive properties in aqueous solution, of which the most important is the temperature response. Above a certain temperature, called Lower Critical Solution Temperature (LCST), the system undergoes a volume phase transition (VPT). Above the LCST, the water is expelled from the polymer network and the swollen state at low temperature transforms into a shrunken state at high temperature. The thermoresponsive behaviour of PNIPAM can be influenced by pH and ionic strength, as well as by the presence of copolymers, such as acrylic acid. In a system formed both by particles of PNIPAM and PNIPAM doped with acrylic acid, one can control the size ratio of the two components by changing the temperature of the mixture, while keeping particle interactions relatively the same. It is therefore possible to obtain thermoresponsive colloidal crystal in which temperature changes induce defects whose formation processes and dynamics can be analysed in an optical microscope at a convenient spatial and temporal scale. The goal of this thesis project was to find the conditions in which such a system could be formed, by using characterization techniques such as Static Light Scattering, Dynamic Light Scattering and Confocal Laser Scanning Microscopy. Two PNIPAM-AAc systems were available, and after characterization it was possible to select a suitable one, on the basis of its low polydispersity and the lack of a VPT, regardless of the external conditions (system JPN_7). The synthesis of a PNIPAM system was attempted, with particles of dimensions matching the JPN_7 system and, unlike JPN_7, displaying a VPT, and one suitable candidate for the mixed system was finally found (system CB_5). The best conditions to obtain thermoresponsive crystal were selected, and the formation and healing of defects were investigated with CLSM temperature scans. The obtained results show that the approach is the correct one and that the present report could represent a useful start for future developments in defect analysis and defect dynamics studies.

Crystallization and morphology of the PLLA phase within random poly (L-lactide-ran-ɛ-caprolactone)

This work has mainly focused on the poly (L-lactide) (PLLA) which is a material for multiple applications with performances comparable to those of petrochemical polymers (PP, PS, PET, etc. ...), readily recyclable and also compostable. However, PLLA has certain shortcomings that limit its applications. It is a brittle, hard polymer with a very low elongation at break, hydrophobic, exhibits low crystallization kinetics and takes a long time to degrade. The properties of PLLA may be modified by copolymerization (random, block, and graft) of L-lactide monomers with other co-monomers. In this thesis it has been studied the crystallization and morphology of random copolymers poly (L-lactide-ran-ε-caprolactone) with different compositions of the two monomers since the physical, mechanical, optical and chemical properties of a material depend on this behavior. Thermal analyses were performed by differential scanning calorimetry (DSC) and thermogravimetry (TGA) to observe behaviors due to the different compositions of the copolymers. The crystallization kinetics and morphology of poly (L-lactide-ran-ε-caprolactone) was investigated by polarized light optical microscopy (PLOM) and differential scanning calorimetry (DSC). Their thermal behavior was observed with crystallization from melt. It was observed that with increasing amounts of PCL in the copolymer, there is a decrease of the thermal degradation. Studies on the crystallization kinetics have shown that small quantities of PCL in the copolymer increase the overall crystallization kinetics and the crystal growth rate which decreases with higher quantities of PCL.