Academic literature on the topic 'Chimica verde'
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Journal articles on the topic "Chimica verde"
Ballini, Roberto. "La chimica verde." PRISMA Economia - Società - Lavoro, no. 2 (March 2012): 65–73. http://dx.doi.org/10.3280/pri2011-002006.
Full textPactat, Inès. "Le recyclage du verre au temps des Romains, des Francs et des Byzantins." Reflets de la physique, no. 74 (December 2022): 16–21. http://dx.doi.org/10.1051/refdp/202274016.
Full textJuéry, Pascal. "Ces grands sites industriels qui ont besoin d’électricité." Revue Générale Nucléaire, no. 2 (March 2018): 23–25. http://dx.doi.org/10.1051/rgn/20182023.
Full textGroves, Peter. "What, if anything, is a caesura? The ontology of the ‘pause’ in English heroic verse." Language and Literature: International Journal of Stylistics 28, no. 3 (June 6, 2019): 263–79. http://dx.doi.org/10.1177/0963947019854001.
Full textNoel, Laurent, Amine Khitous, Quentin Kirscher, Céline Molinaro, Dominique Berling, and Olivier Soppera. "Écriture laser de materiaux fonctionnels inorganiques preparés par voie sol-gel." Photoniques, no. 112 (2022): 43–47. http://dx.doi.org/10.1051/photon/202211243.
Full textTymofieiev, Oleksii, Marta Sokoliuk, Viktoriia Ripa, Diana Havlytiuk, and Lesia Kolisnichenko. "Prevention of Inflammatory Complications after Atypical Tooth Removal." Journal of Diagnostics and Treatment of Oral and Maxillofacial Pathology 6, no. 6 (June 30, 2022): 86–91. http://dx.doi.org/10.23999/j.dtomp.2022.6.3.
Full textHamilton, Chris A. "Tarantulas: Breeding Experience & Wildlife. By Frédéric Cléton, Yannick Sigwalt, and Jean-Michel Verdez. Frankfurt am Main (Germany): Edition Chimaira. €39.80. 231 p.; ill.; no index. ISBN: 978-3-89973-302-9. [Available in the U.S. from ECO Publishing, Rodeo, New Mexico.] 2015." Quarterly Review of Biology 92, no. 1 (March 2017): 111–12. http://dx.doi.org/10.1086/690894.
Full textEnsminger, David Allen. "Populating the Ambient Space of Texts: The Intimate Graffiti of Doodles. Proposals Toward a Theory." M/C Journal 13, no. 2 (March 9, 2010). http://dx.doi.org/10.5204/mcj.219.
Full textDissertations / Theses on the topic "Chimica verde"
Venditti, Giampaolo. "Applicazioni innovative della risonanza magnetica nucleare alle matrici alimentari. Uno studio sul caffè verde." Doctoral thesis, Università degli studi di Padova, 2011. http://hdl.handle.net/11577/3422016.
Full textLa qualità del caffè verde rappresenta il principale requisito per la realizzazione di una bevanda apprezzata a livello commerciale. Attualmente tra i vari campi interessati dalla produzione scientifica sulla qualità del caffè verde vi sono lo sviluppo di metodologie per garantire l’autenticità e lo studio delle metodiche più appropriate per la quantificazione dell’acqua. Nel primo caso la necessità di metodi rapidi per l’autenticazione del caffè è divenuta in tempi recenti un’esigenza sempre più pressante a causa della crescente diffusione di pratiche di adulterazione nella filiera commerciale di questo prodotto. Tuttavia sono ancora limitati i metodi formulati per la determinazione dell’origine geografica; inoltre, la bassa numerosità di campioni analizzati nei lavori compiuti in tale ambito rende i risultati trovati non sufficientemente significativi. Rimane infine ambiguità sui possibili markers da utilizzare nella discriminazione. Occorrono da un lato quindi metodi adatti ad analisi routinarie per il controllo del maggior numero possibile di campioni, e dall’altro una scelta univoca di possibili markers per la discriminazione geografica delle varie qualità di caffè. Nell’ambito degli studi compiuti sull’acqua rimane ancora aperta la problematica della distribuzione dell’acqua stessa all’interno della matrice. La comprensione di questo fenomeno è di notevole importanza in quanto è stata osservata ad esempio in letteratura la correlazione fra il grado di idratazione e le proprietà meccaniche del chicco verde. La ricerca presentata in questo dottorato ha cercato di dare una risposta alle problematiche aperte appena descritte con il ricorso alla Risonanza Magnetica Nucleare, recentemente utilizzata con successo in ambito alimentare. In questo lavoro sono stati sviluppati infatti due metodi per la determinazione dell’origine geografica del caffè verde, rispettivamente con l’NMR nel dominio dei tempi, e con l’NMr ad alta risoluzione, quest’ultimo in combinazione con l’analisi statistica multivariata. Il primo metodo, basato sull’NMR nel dominio dei tempi, è stato realizzato per mezzo di uno spettrometro operante alla frequenza di 20 MHz (Bruker Minispec Mq20), e permette la determinazione simultanea delle percentuali di acqua e olio di un elevato numero di campioni in maniera rapida e riproducibile tramite l’utilizzo della sequenza spin echo. I valori delle percentuali di acqua e olio nei campioni sottoposti ad analisi è stato ricavato utilizzando due differenti calibrazioni per l’acqua e per l’olio. Le percentuali di acqua e olio ottenute dall’applicazione del metodo su 500 campioni di caffè verde sono stati sottoposti ad analisi statistica (ANOVA). I risultati ottenuti indicano che una buona discriminazione dei continenti di provenienza dei campioni è possibile utilizzando il valore di percentuale di olio come marker. Per quantificare correttamente le componenti acqua e olio con la sequenza spin echo è stata necessaria l’analisi preliminare dei tempi di rilassamento trasversale (T2) nel chicco verde con l’NMR nel dominio dei tempi mediante l’applicazione della sequenza CPMG. Le distribuzioni continue di tempi di rilassamento trasversale sono state ricavate invertendo con la trasformata di Laplace con l’aiuto del software Upen le curve CPMG ottenute. L’assegnazione preliminare della popolazioni di T2 relative alla fase acqua nella regione compresa fra 0.1 e 3 ms è stata realizzata confrontando i profili di rilassamento di una serie di chicchi verdi con i corrispondenti profili ottenuti per essicazione in stufa. La regione di T2 relativa alla componente lipidica dei chicchi verdi è stata invece assegnata sia confrontando i profili di rilassamento di una serie di chicchi a diversi livelli di idratazione sia confrontando le distribuzioni di T2 nel chicco con quella dell’olio estratto dallo stesso. Allo scopo di far luce sulla distribuzione dell’acqua nel caffè verde la regione della distribuzione di T2 attribuita all’acqua è stata studiata in dettaglio con una serie di esperimenti sistematici di reidratazione graduale di chicchi precedentemente essiccati. Le distribuzioni di T2 ottenute da chicchi essiccati e reidratati manualmente fino al 35% (su base secca) sia con H2O che con D2O e, alternativamente, per esposizione in atmosfera di umidità controllata, sono state confrontate con quelle di chicchi verdi tal quali. I dati ottenuti indicano che fino a circa 10% l’acqua incorporata nel chicco manifesta una mobilità ridotta, in quanto probabilmente adsorbita o legata con le pareti cellulari mediante ponti idrogeno. La reidratazione con acqua deuterata ha evidenziato inoltre il contributo dello scambio protonico al segnale della distribuzione osservato. L’analisi dei profili di distribuzioni dell’acqua ha inoltre portato all’osservazione che questo risulta determinato dalla convoluzione di due popolazioni di mobilità protonica, rispettivamente centrate a circa 0.5 e 1 ms. Sia nel chicco verde che in quelli reidratati è stato trovato che a contenuti di acqua fino a 4% delle due popolazioni è visibile solo quella a mobilità inferiore, mentre a percentuali intermedie sono presenti entrambe. Con riferimento all’articolo di Pittia e collaboratori, la componente a rilassamento rapido potrebbe essere associata all’effetto di antiplasticizzazione dell’acqua, mentre la popolazione caratterizzata da rilassamento più lento può essere correlata all’effetto plasticizzante dell’acqua. In questo senso i nostri dati forniscono una conferma ed un’interpretazione in termini di mobilità protoniche al co-siddetto effetto di antiplasticizzazione, scoperto a livello macroscopico. La distribuzione dei tempi di rilassamento trasversale dei T2 della regione associata ai lipidi (cioè quella compresa fra circa10 ms e circa 300 ms) mostra un profilo multimodale, che suggerisce la presenza di tre diverse mobilità protoniche. Tale osservazione è stata confermata sia con lo studio della dipendenza dalla temperatura delle mobilità protoniche, compiuto sia per la fase lipidica all’interno dei chicchi, sia per l’olio fresco isolato mediante estrazione soxhlet, sia dal confronto con dati di letteratura. Questa osservazione ha trovato inoltre conferma nei dati di letteratura. Un metodo per la discriminazione geografica è stato infine elaborato mediante l’analisi statistica multivariata delle risonanze NMR sia degli estratti organici che acquosi di 48 campioni di caffè verde di diversa provenienza. I dati ottenuti indicano che nell’estratto organico gli acidi grassi sembrano essere efficaci nel discriminare i campioni africani da tutti gli altri analizzati, mentre le componenti minoritarie sono efficaci nella differenziazione tra i campioni con diversa provenienza. In particolare il Kahweolo correla positivamente con i campioni del Brasile, mentre la caffeina e i composti minoritari differenziano i campioni centro americani da quelli del sud America, e altri componenti minoritari non identificati che caratterizzano i campioni africani e quelli asiatici. La caratterizzazione dell’estratto acquoso mediante esperimenti bidimensionali ha permesso inoltre l’identificazione di sistemi di spin caratteristici degli estratti protonici del campioni di caffè brasiliano, quali zuccheri minoritari e isomeri dell’acido clorogenico. Esperimenti di diffusione DOSY condotti sull’estratto acquoso dei campioni di origine africana hanno inoltre avvalorato l’ipotesi di una possibile interazione caffeina/ acidi clorogenici. In particolare i dati ottenuti fanno supporre che nell’estratto acquoso del campione africano analizzato, la caffeina è presente in soluzione sia in forma libera che complessata con l’acido clorogenico.
CERIANI, CHIARA. "Organic Materials for (Opto)electronics introducing Sustainability in Design, Synthesis and Manufacturing." Doctoral thesis, Università degli Studi di Milano-Bicocca, 2022. http://hdl.handle.net/10281/369035.
Full textThe research focuses on the development of new synthetic routes for the preparation of printable organic semiconductors, devised to be suitable for industrial scaling up. As such, a novel synthetic method for facile, cheap, and environmentally friendly production of π-extended organic semiconductors is explored. The concept sustainability is becoming a very important issue for chemical industries which are approaching green chemistry to reduce the environmental impact of chemical processes. In this frame, micellar catalysis has been demonstrated to be profitably performed in water under very mild conditions in the presence of a bit surfactant. Firstly, a self-emulsifying system L-α-Lecithin-Tween 80 mixture (TL82) is explored for the preparation of organic small molecules. The unique characteristic of this surfactant’s mixture offers a new environment for carrying out common cross coupling reactions such as Suzuki-Miyaura, Sonogashira and Heck cross-couplings in a reproducible up-scale way. The versatility of this approach is verified through the synthesis of complex organic semiconductors such as π-extended insoluble pigments. The emphasis on sustainability is not only applied to the synthesis but also to the processing of the active materials into the final target devices. Indeed, an innovative process is introduced enabling the preparation of high-performance thin film devices starting from waterborne dispersions of p- and n-type organic semiconductors. The TL82 self-emulsifying surfactant’s mixture is used both as the synthesis and processing medium. This method allows the preparation of Organic Field Effect Transistor using exclusively water in all steps with performances comparable to those synthesized and processed using common organic solvents. From the standpoint of the design of innovative materials, additional guidelines beside those aiming at achieving high performances are introduced. Original small molecules and polymers are designed selecting low-cost raw materials, severely the limiting the use of toxic and hazardous chemicals and designing all processes with up-scaling already in mind. These materials find an application in the field of (opto)electronics. An example of a good compromise between a simple design-good performance of a class of materials was investigated. In detail, a good part of the work was dedicated to the technology of luminescent solar concentrators devices, where the performances of the newly designed intrinsically sustainable materials are compared with those commercially available luminophores having similar spectral features. In the overall, we demonstrate comparable performance, but greatly improved sustainability and scalability. The final project was dedicated to the presentation of the first example of D-A regioregular polythiophene with an ambipolar character.
Tran, Quang Nguyen. "Chimie verte sur catalyseurs perovskites." Thesis, Montpellier, Ecole nationale supérieure de chimie, 2019. http://www.theses.fr/2019ENCM0011.
Full textDevelopment of active and stable noble metal-free catalysts is more and more required for environmental applications and valorization of renewable resources. Easy tuning of the reactivity of mixed oxide perovskites by cation and anion substitutions render them a promising field of catalyst innovation. In the thesis, two classes of perovskite materials have been synthesized, characterized and tested in catalysis. Cation substitution of Co and Ga for Al in LaAlO3 has allowed to modify both redox and acid-base properties, whereas partial hydride substitutions for oxygen in LaSrCoO4 has provided a test-bed of hydrogenation activity.Tailoring the redox properties of the LaAlO3 mixed oxide by Co substitution has allowed to develop a multifunctional catalysts dealing with NOx and soot decontamination of diesel exhausts. NOx-assisted soot oxidation involves NO to NO2 conversion and subsequent soot oxidation by the formed NO2 at relatively low temperature. LaAlO3 materials with different degrees of Co substitution for Al were prepared by sol-gel method and their catalytic activity was correlated with crystallinity, redox properties and mobility of lattice oxygen. Among the studied samples LaAl1-xCoxO3 with x 0.75 exhibits superior catalytic activity for both NO to NO2 oxidation and NOx-assisted soot oxidation. The excellent performance is attributed to the synergetic interaction between Al-Co in B-site of the structure and may be linked to the high lattice surface oxygen supported by a well-crystallized perovskite structure.The production of bio-ethanol is one of the staples of the replacement of fossil fuels with renewable biomass-derived resources. Valorisation of bio-ethanol for the production of chemicals requires a fine control of the acid-base properties of catalysts. While most of the research on perovskite catalysts has focused on their redox properties, studies on their acid-base properties have been much less developed. Partial substitution of Co and Ga for Al in LaAlO3 has allowed to tune the acidity and basicity of the material and to control the relative activity of dehydration and dehydrogenation of ethanol, controlling the ratio between ethylene and acetaldehyde. The nature of the introduced cation allowed to form different Lewis acid-base pairs, orienting the reactivity of the acetaldehyde intermediates towards Tishchenko or aldol coupling, allowing to direct the reaction cascade towards the formation of butadiene or acetone and odd-C oxygenates.While most of the literature on perovskite reactivity has focused on their structure/properties modifications by cation substitutions, there is a limited number of works on substitutions in the anion sites. Oxyhydride perovskites, ABO3-xHx, where hydride anions H- can substitute O2- in any sites of the BO6 octahedron, have been reported presenting important hydride mobility, suggesting potential applications in hydrogenation catalysis. Oxyhydrides LaSrCoO3H0.7 and BaTiO3-xHx have been prepared, characterized and tested in a model hydrogenation reaction. The reactivity of hydride species has been tested using chemical titration of toluene at temperatures at which hydrides are expected to be mobile. The results show that LaSrCoO4-xHy exhibited a much higher activity than BaTiO3-xHx, due to the metallic sites formed by partial reduction of LaSrCoO4-xHy,, indicating a possible use of perovskites as support for hydrogenation catalysts
Monnereau, Laure. "Calix[4]arènes fonctionnels pour la chimie verte." Strasbourg, 2010. http://www.theses.fr/2010STRA6037.
Full textThe aim of this work was to extend the scope of catalytic applications of ligands based on a calix[4]arene skeleton. The first part of this work focusses on new applications of hemispherical bis-phosphites calix[4]arenes in the rhodium catalysed hydroformylation of α-olefins, either in aqueous medium or under solvent-free conditions. These particular conditions resulted in enhanced activities compared to tests carried out in toluene. The ligands turned out to efficiently drive reactions towards the formation of linear products. The selectivity of the system is mainly controlled by the intrinsic properties of the ligand, which is able to tightly envelope the catalytic centre. In keeping with these observations, the application of solvent-free conditions to the rhodium-catalysed hydroaminovinylation of α-olefins resulted in high linear/branched ratios of enamines/amines (starting from secondary amines) or imines (starting from primary amines). In the following chapters, calix[4]arenes bearing a PPh2 or a N=PPh2 group as the sole functional group anchored at their upper rim were assessed in palladium or nickel-catalysed cross-coupling reactions. With arylbromides, these monodentate ligands led to remarkably high activities. The high performances probably arise from a combination of the bulkiness of the calixarenyl fragment as well as its ability to temporarely entrap metal-(η6-arene) moieties in a supramolecular fashion. Both properties favour the formation of mono-ligand intermediates M(0)L(ArX) (M = Pd, Ni), from which the following oxidative addition step is facilitated with respect to a step involving M(0)L2 species
Barthel, Etienne. "Mécanique de surface du verre et physico-chimie d'interface." Habilitation à diriger des recherches, Université Pierre et Marie Curie - Paris VI, 2006. http://tel.archives-ouvertes.fr/tel-00171154.
Full textest le terrain d'expression de procédés de fonctionnalisation
puissants et souvent peu coûteux. Ces procédés, les propriétés ainsi
obtenues, ou souhaitées, suscitent une grande variété de
développements de nature fondamentale. Parmi ceux-ci, la mécanique
de surface allie physico-chimie de l'interface et réponse mécanique.
Je décris ici un ensemble de projets de recherche que j'ai
développés dans ce domaine. Je traite de la question du couplage
entre surfaces et de leurs interactions à longue portée, de
l'adhésion considérée tant du point de vue macroscopique que
microscopique et enfin de la nécessité de comprendre le matériau à
l'échelle locale pour maîtriser la réponse mécanique de systèmes de
structures complexes.
Tremblay-Morin, Jean-Philippe. "Porphyrines cationiques romées pour la radiothérapie et chimie verte catalysée." Mémoire, Université de Sherbrooke, 2005. http://savoirs.usherbrooke.ca/handle/11143/3864.
Full textHOCDE, SANDRINE. "Fibres optiques en verre infrarouge applications en chimie et biologie." Rennes 1, 2000. http://www.theses.fr/2000REN10067.
Full textTremblay-Morin, Jean-Philippe. "Porphyrines cationiques romées pour la radiothérapie et chimie verte catalysée /." [S.l. : s.n.], 2005.
Find full textBenamara, Nassima. "Intensification de procédés par chauffage micro-ondes pour la chimie verte." Thesis, Normandie, 2017. http://www.theses.fr/2017NORMIR13.
Full textThe aim of this thesis is the development and characterisation of an intensified continuous microwave reactor for green chemistry. The development of this reactor required, at first, the characterisation of the dielectric and magnetic properties of the used materials. A numerical simulation was then used to predict the field and temperature profiles within the materials. The influence of different parameters on the microwave heating was also studied, such as the influence of the dielectric nature of the reaction medium, the ratio of the fluid in the reactor, the arrangement of the reactor in the applicator and the size and shape of the latter. Hydrodynamics were also taken into account in the simulation to predict the temperature profiles in the reactor. All the numerical results were validated experimentally. Experimental results also made it possible to refine the thermal model of the reactor. In the end, an esterification reaction was carried out and it proved the thermal and chemical efficiency of the designed reactor. Beyond this prototype, this thesis establishes a general scheme for the design of a continuous chemical process under microwaves whilst following the key rules of electromagnetism and optimising the wave propagation and the thermal performance of the reactor
Sartori, Guillaume. "Catalyse dans l'eau appliquée à la synthèse de nucléosides ciblés." Thesis, Compiègne, 2013. http://www.theses.fr/2013COMP2071/document.
Full textMany nucleosides analogues are reported in literature as antitumor, antibacterial or antiviral. Among them, the BVDU, is used as a drug against the herpes virus. In order to synthesize derivates of this compounds, we decided to develop new synthetic routes of 5-aryl-2'-deoxyrudine analogues. The synthesis of such compounds is widely described in literature using cross-coupling reaction with palladium but they often use organic solvents. A methodology to synthesize these analogues using the Suzuki-Miyaura reaction, in water, has been developed. 5-aryluridine and 6-aryluridine derivates were also synthetized using a similar methodology. The relevance of the ligand, commonly used in organo-palladated reactions, was studied. In our hands, the target compounds were obtained in good yiels using a free ligand methodology. Micro-wave activation was also studied. It allowed the synthesis of the nucleosides in good yields within very short reaction times. In collaboration with an Indian laboratory, the synthesis of 5-allyluridine and 5-allyl-2'-deoxyuridine was studied
Books on the topic "Chimica verde"
Santamaria, Clément. Toute la physique dans un verre d'eau. Paris: Ellipses, 2005.
Find full textAdvanced biofuels: Using catalytic routes for the conversion of biomass platform molecules. Oakville, ON: Apple Academic Press, 2016.
Find full textCraddock, Henry. The development and application of green chemistry in the upstream oil and gas industry. Norwich, N.Y.]: Knovel, 2014.
Find full textYaws handbook of properties for environmental and green engineering: Adsorption capacity, water solubility, Henry's law constant ... Houston, Tex: Gulf Pub., 2008.
Find full textSmith, Aisling, Bonnie Reid, and Gavin Yates. Verge 2017: Chimera. Monash University Publishing, 2017.
Find full textSmith, Aisling, Bonnie Reid, and Gavin Yates. Verge 2017: Chimera. Monash University Publishing, 2017.
Find full textSmith, Aisling, Bonnie Reid, and Gavin Yates. Verge 2017: Chimera. Monash University Publishing, 2017.
Find full textApplications in Design and Simulation of Sustainable Chemical Processes. Elsevier, 2019.
Find full textApplications in Design and Simulation of Sustainable Chemical Processes. Elsevier, 2019.
Find full textChallenges in Green Analytical Chemistry. Royal Society of Chemistry, The, 2011.
Find full textBook chapters on the topic "Chimica verde"
Ducamp, Christine. "La chimie verte." In Développement durable et autres questions d'actualité, 145–62. Éducagri éditions, 2011. http://dx.doi.org/10.3917/edagri.legar.2011.01.0145.
Full text"5 Méthodes alternatives en synthèse." In Chimie verte, 339–406. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-006.
Full text"4 Solvants alternatifs." In Chimie verte, 277–338. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-005.
Full text"6 Biomasse." In Chimie verte, 407–50. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-007.
Full text"Frontmatter." In Chimie verte, I—III. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-fm.
Full text"2 Réactions à économie d’atomes optimale." In Chimie verte, 35–132. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-003.
Full text"3 Catalyse." In Chimie verte, 133–276. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-004.
Full text"1 Problématique du développement durable et chimie." In Chimie verte, 1–34. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-002.
Full text"Table des matières." In Chimie verte, VIII—XIII. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-toc.
Full text"Préface." In Chimie verte, IV—VII. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-001.
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