Studio di nuovi processi catalitici per la produzione di Acido Adipico

Adipic Acid (AA) is one of the most important chemicals in the actual worldwide Industrial Chemistry, because of his environmental and economical issues a lot of research challenge are open in this context. The main issue is regarding the substitution of Nitric Acid as oxidant in the last step of the industrial synthesis. This step, in fact, cause the production of various kind of nitrogen oxides that are gaseous pollutant and must be removed from the emissions. The substitution of Nitric Acid with molecular Oxygen or air as oxidant can avoid the production of nitric oxides reducing, in this way, the environmental and economic sustainability of the process. In this work is presented an alternative pathway for the synthesis of the AA. This concern a first step of oxidation with hydrogen peroxide that involve the transformation of ciclohexene into trans-1,2-cyclohexanediole than, the latter, is transformed into AA through a catalyzed oxidative cleavage with molecular Oxygen as oxidant. The first step has been already optimized by a work did in the past. This thesis is focused on the second step, here is presented an experimental work based on the study of the catalytic activity of three kind of catalyst, a Keggin heteropoliacid Mo-V, a Ru - based catalyst and an Au NP - based catalyst.

Oxodiperoxomolybdenum catalyzed olefin epoxidation: the role of Ionic Liquids

Ionic Liquids (ILs) constituted by organic cations and inorganic anions are particular salts with a melting point below 100°C. Their physical properties such as melting point and solubility can be tuned by altering the combination of their anions and cations. In the last years the interest in ILs has been centered mostly on their possible use as “green” alternatives to the traditional volatile organic solvents (VOCs) thanks to their low vapour pressure and the efficient ability in catalyst immobilization. In this regard, the subject of the present thesis is the study of the oxodiperoxomolybdenum catalyzed epoxidation of olefins in ILs media with hydrogen peroxide as the oxidant. In particular N-functionalized imidazolium salts, such as 1-(2-t-Butoxycarbonylamino-ethyl)-3-methylimidazolium (1), were synthesized with different counterions [I]-, [PF6]-, [NO3]-, [NTf2]- and [ClO4]– and tested as reaction solvents. The counterion exchange with [Cl]-, [NTf2]- and [NO3]- was also performed in unfuctionalized imidazolium salts such as 3-butyl-1-methylimidazol-3-ium (3). All the prepared ILs were tested in catalytic epoxidation of olefins exploiting oxodiperoxomolybdenum complexes [MoO(O2)2(C4H6N2)2] (4) and [MoO(O2)2(C5H8N2)2] (5) as catalysts. The IL 3[NTf2] and the catalysts 5 give rise to the best results leading to the selective formation of the epoxide of cis-cyclooctene avoiding hydrolysis side reaction. A preliminary study on the synthesis of novel NHC oxodiperoxomolybdenum complexes starting from imidazolium salts was also developed.

α-ossidazione asimmetrica organocatalizzata di aldeidi ramificate con dibenzoil perossido

In this thesis, the development of an enantioselective oxidation of α-branched aldehydes using covalent organocatalysis is described. At state of the art, the asymmetric organocatalysis approach, gave often serous difficulties for these kind of substrate respect “classic” aldehydes. We have used a primary cinchona alkaloid derived amine (specially the 9-epi-NH2-CDA) to develop the reaction in combinations with additives. With benzoyl peroxide as oxidant and 2-phenylpropionaldehyde as reference substrate, we have tried to optimize this system but we not found great results about enantiomeric excess.

Sviluppo di un metodo elettrochimico per la determinazione della capacità antiossidante

The aim of the present thesis, carried out at the Analytical Group of the Faculty of Industrial Chemistry in Bologna, is to develop a new electrochemical method for the determination of the Antioxidant Capacity (AOC). The approach is based on the deposition of a non-conducting polymeric film on the working electrode surface and the following exposition to the radicals OH· produced by H2O2 photolysis. The strongly oxidant action of hydroxyl radicals degrades, causing an increase of the Faradic current, relevant to the redox couple [Ru(NH3)6]2+/3+ monitored by cyclic voltammetry(CV); the presence of an antioxidant compound in solution slows down the radical action, thus protecting the polymeric film and blocking the charge transfer. The parameter adopted for the quantification of the AOC, was the induction time, called also lag phase, which is the time when the degradation of the film starts. Five pure compounds, among most commonly antioxidant, were investigated : Trolox®(an analogue water-soluble of vitamin E), (L)-ascorbic acid, gallic acid, pyrogallol and (-)- epicatechin. The AOC of each antioxidant was expressed by TEAC index (Trolox® Equivalent Antioxidant Capacity), calculated from the ratio between the slope of the calibration curve of the target compound and the slope of the calibration curve of Trolox®. The results from the electrochemical method, have been compared with those obtained from some other standardized methods, widely employed. The assays used for the comparison, have been: ORAC, a spectrofluorimetric method based on the decrease of fluorescein emission after the attack of alkylperoxide radicals, ABTS and DPPH that exploit the decoloration of stable nitrogen radicals when they are reduced in presence of an antioxidant compound and, finally, a potentiometric method based on the response of the redox couple [Fe(CN)6]3-/ [Fe(CN)6]4-. From the results obtained from pure compounds, it has been found that ORAC is the methodology showing the best correlation with the developed electrochemical method, maybe since similar radical species are involved. The comparison between the considered assays, was also extended to the analysis of a real sample of fruit juice. In such a case the TEAC value resulting from the electrochemical method is higher than those from standardized assays.

Stabilizzazione del Blu di Prussia con film politiofenici depositati per via elettrochimica

Hydrogen peroxide (H2O2) is a powerful oxidant which is commonly used in a wide range of applications in the industrial field. Several methods for the quantification of H2O2 have been developed. Among them, electrochemical methods exploit the ability of some hexacyanoferrates (such as Prussian Blue) to detect H2O2 at potentials close to 0.0 V (vs. SCE) avoiding the occurrence of secondary reactions, which are likely to run at large overpotentials. This electrocatalytic behaviour makes hexacyanoferrates excellent redox mediators. When deposited in the form of thin films on the electrode surfaces, they can be employed in the fabrication of sensors and biosensors, normally operated in solutions at pH values close to physiological ones. As hexacyanoferrates show limited stability in not strongly acidic solutions, it is necessary to improve the configuration of the modified electrodes to increase the stability of the films. In this thesis work, organic conducting polymers were used to fabricate composite films with Prussian Blue (PB) to be electro-deposited on Pt surfaces, in order to increase their pH stability. Different electrode configurations and different methods of synthesis of both components were tested, and for each one the achievement of a possible increase in the operational stability of Prussian Blue was verified. Good results were obtained for the polymer 3,3''-didodecyl-2,2':5',2''-terthiophene (poly(3,3''-DDTT)), whose presence created a favourable microenvironment for the electrodeposition of Prussian Blue. The electrochemical behaviour of the modified electrodes was studied in both aqueous and organic solutions. Poly(3,3''-DDTT) showed no response in aqueous solution in the potential range where PB is electroactive, thus in buffered aqueous solution is was possible to characterize the composite material, focusing only on the redox behaviour of PB. A combined effect of anion and cation of the supporting electrolyte was noticed. The response of Pt electrodes modified with films of the PB /poly(3,3''-DDTT) composite was evaluated for the determination of H2O2. The performance of such films was found better than that of the PB alone. It can be concluded that poly(3,3''-DDTT) plays a key role in the stabilization of Prussian Blue causing also a wider linearity range for the electrocatalytic response to H2O2.

Oxidative properties of the Iron - Thymine-1-acetic acid - Hydrogen peroxide catalytic system

The oxidation of alcohols and olefins is a pivotal reaction in organic synthesis. However, traditional oxidants are toxic and they often release a considerable amounts of by-products. Here, two IronIII-based systems are shown as oxidative catalyst, working in mild conditions with hydrogen peroxide as primary oxidant. An efficient catalytic system for the selective oxidation of several alcohols to their corresponding aldehydes and ketones was developed and characterized, [Fe(phen)2Cl2]NO3 (phen=1,10-Phenantroline). It was demonstrated that the adoption of a buffered aqueous solution is of crucial importance to ensure both considerable activity and selectivity.The Iron - Thymine-1-acetic acid in-situ complex was studied as catalyst in alcohol oxidations and C-H oxidative functionalization, involving hydrogen peroxide as primary oxidant in mild reaction conditions. The catalytic ability in alcohol oxidations was investigated by Density Functional Theory calculations, however the catalyst still has uncertain structure. The system shows satisfactory activity in alcohol oxidation and aliphatic rings functionalization. The Fe-THA system was studied in cyclohexene oxidation and oxidative halogenations. Halide salts such as NBu4X and NH4X were introduced in the catalytic system as halogens source to obtain cyclohexene derivatives such as halohydrins, important synthetic intermediates.The purpose of this dissertation is to contribute in testing new catalytic systems for alcohol oxidations and C-H functionalization. In particular, most of the efforts in this work focus on studying the Iron - Thymine-1-acetic acid (THA) systems as non-heme oxidative model, which present: •an iron metal centre(s) as a coordinative active site, •hydrogen peroxide as a primary oxidant, •THA as an eco-friendly, biocompatible, low cost coordinating ligand.

Waste management in Forlì-Cesena province: Life Cycle Assessment (LCA) of Forlì incinerator

This work assesses the environmental impact of a municipal solid waste incinerator with energy recovery in Forlì-Cesena province (Emilia-Romagna region, Italy). The methodology used is Life Cycle Assessment (LCA). As the plant already applies the best technologies available in waste treatment, this study focuses on the fate of the residues (bottom and fly ash) produced during combustion. Nine scenarios are made, based on different ash treatment disposing/recycling techniques. The functional unit is the amount of waste incinerated in 2011. Boundaries are set from waste arrival in the plant to the disposal/recovery of the residues produced, with energy recovery. Only the operative period is considered. Software used is GaBi 4 and the LCIA method used is CML2001. The impact categories analyzed are: abiotic depletion, acidification, eutrophication, freshwater aquatic ecotoxicity, global warming, human toxicity, ozone layer depletion, photochemical oxidant formation, terrestrial ecotoxicity and primary energy demand. Most of the data are taken from Herambiente. When primary data are not available, data from Ecoinvent and GaBi databases or literature data are used. The whole incineration process is sustainable, due to the relevant avoided impact given by co-generator. As far as regards bottom ash treatment, the most influential process is the impact savings from iron recovery. Bottom ash recycling in road construction or as building material are both valid alternatives, even if the first option faces legislative limits in Italy. Regarding fly ash inertization, the adding of cement and Ferrox treatment results the most feasible alternatives. However, this inertized fly ash can maintain its hazardous nature. The only method to ensure the stability of an inertized fly ash is to couple two different stabilization treatments. Ash stabilization technologies shall improve with the same rate of the flexibility of the national legislation about incineration residues recycling.

Valutazione dell'eco-sostenibilità di un impianto di digestione anaerobica cogenerativo e ipotesi di conversione impiantistica per la produzione di biometano

Considerando l'elevato grado di inquinamento del pianeta e la forte dipendenza delle attività antropiche dai combustibili fossili, stanno avendo notevole sviluppo e incentivazione gli impianti per la produzione di energia elettrica da fonti rinnovabili. In particolare, la digestione anaerobica è in grande diffusione in Italia. Lo studio in oggetto si prefigge l'obiettivo di determinare, mediante analisi di Life Cycle Assessment (LCA), i carichi ambientali di un impianto di digestione anaerobica, e della sua filiera, per valutarne l'effettiva ecosostenibilità. L'analisi considera anche gli impatti evitati grazie all'immissione in rete dell'energia elettrica prodotta e all'utilizzo del digestato in sostituzione dell'urea. Lo studio analizza sei categorie d'impatto: Global warming potential (GWP), Abiotic depletion potential (ADP), Acidification potential (AP), Eutrophication potential (EP), Ozone layer depletion potential (ODP) e Photochemical oxidant formation potential (POFP). I valori assoluti degli impatti sono stati oggetto anche di normalizzazione per stabilire la loro magnitudo. Inoltre, è stata effettuata un'analisi di sensitività per investigare le variazioni degli impatti ambientali in base alla sostituzione di differenti tecnologie per la produzione di energia elettrica: mix elettrico italiano, carbone e idroelettrico. Infine, sono stati analizzati due scenari alternativi all'impianto in esame che ipotizzano la sua conversione ad impianto per l'upgrading del biogas a biometano. I risultati mostrano, per lo scenario di riferimento (produzione di biogas), un guadagno, in termini ambientali, per il GWP, l'ADP e il POFP a causa dei notevoli impatti causati dalla produzione di energia elettrica da mix italiano che la filiera esaminata va a sostituire. I risultati evidenziano anche quanto gli impatti ambientali varino in base alla tipologia di alimentazione del digestore anaerobica: colture dedicate o biomasse di scarto. I due scenari alternativi, invece, mostrano un aumento degli impatti, rispetto allo scenario di riferimento, causati soprattutto dagli ulteriori consumi energetici di cui necessitano sia i processi di purificazione del biogas in biometano sia i processi legati alla digestione anaerobica che, nel caso dello scenario di riferimento, sono autoalimentati. L'eventuale conversione dell'attuale funzione dell'impianto deve essere fatta tenendo anche in considerazione i benefici funzionali ed economici apportati dalla produzione del biometano rispetto a quella del biogas.

In vivo and in vitro effects of antioxidant compounds and PPAR γ modulators on rainbow trout oxidative stress and lipid metabolism.

The aquafeed use of raw plant materials, as protein and lipid sources, has been considered and approved as a sustainable alternative to fish products (fish meal and oils) because the current trend to use high-lipid diets has been shown to induce undesirable increase in fat depots or further physiological alterations, such as induction of oxidative stress. In the aquaculture perspective, the addition of natural substances with antioxidant properties is an emerging strategy for protecting biological systems and foodstuffs from oxidative damage. Among natural substances, hydroxytyrosol (HT) and caffeic acid (CA) have attracted considerable attention as food antioxidant additives and modulators of physiological and molecular pathways involved in energy metabolism and adiposity. The aim of this study was to evaluate the effects of CA and HT on lipid metabolism and oxidative stress of rainbow trout (Oncorhynchus mykiss). In vitro results showed the potential anti-obesogenic effects of the compounds CA and HT on the adipose tissue of the rainbow trout. To support these data, in vitro assays performed (MTT, ORO, immunofluorescence) resulted in accordance among them; only results from proliferating cell nuclear antigen (PCNA) assay were not significant. In vivo results showed a possible anti-obesogenic effect of CA in liver and HT in adipose tissue. Regarding oxidative stress, we could hypothesize a possible anti-oxidant role of CA in liver.

Trattamento plasma assistito di acqua con una sorgente Dielectric Barrier Discharge (DBD): analisi delle specie reattive prodotte e potere battericida

La proliferazione di batteri in liquido è una problematica che riguarda anche le acque di fiumi e mari. In questo progetto di tesi sperimentale si indagherà un trattamento plasma assistito diretto di acqua sintetica riprodotta in laboratorio con l’obiettivo di ottenere un effetto battericida sul liquido contaminato. L’acqua trattata verrà analizzata chimicamente, in particolare si andranno a misurare i TRO (Total Residual Oxidant, composti dell’ossigeno derivanti dalla parziale ozonizzazione dell’acqua) che dovranno essere presenti in quantità minori di 0,1 mg/l. Il dispositivo utilizzato per i test biologici è una sorgente di tipologia DBD (Dielectric Barrier Discharge) indiretto. Gli elettrodi della sorgente sono separati dal solo strato di materiale dielettrico e uno di questi è composto da una rete metallica in acciaio inossidabile. Il plasma si forma tra le maglie della rete e induce la formazione di specie reattive, radiazioni UV, particelle cariche, campi elettromagnetici e calore. Ciò che raggiunge la soluzione contaminata è l’afterglow del plasma, ovvero tutte le specie reattive a lunga vita prodotte dalla ionizzazione dell’aria e dalle radiazioni UV. La sorgente è stata dapprima caratterizzata elettricamente studiando le forme d’onda di tensione e corrente a determinate condizioni operative. Il liquido da trattare è contaminato con il batterio Escherichia coli. è emerso che in tutti i casi testati i livelli degli ossidanti sono entro il limite prestabilito di 0,1 mg/l. Il trattamento plasma in soli 10 secondi è responsabile di una decontaminazione parziale del batterio E. coli. Da ulteriori studi si potranno trovare delle condizioni tali da inattivare totalmente la carica batterica presente date le grandi potenzialità di questo trattamento.