No description available.

Orientador: Frab Norberto Boscolo / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba / Made available in DSpace on 2018-07-22T03:00:44Z (GMT). No. of bitstreams: 1 Almeida_SolangeMariade_D.pdf: 5623908 bytes, checksum: b26c68566d3a5cc890cf18e225a7c0c1 (MD5) Previous issue date: 1997 / Resumo: O presente trabalho teve como finalidade estudar o efeito de baixas doses de radiação de elétrons no processo de reparação tecidual em ratos. Para tanto, os animais sofreram um procedimento cirúrgico, onde foi produzida uma ferida retangular, medindo 2,3 cm por 1,4 cm, na sua região dorsal anterior. No momento da irradiação, as feridas produzidas foram protegidas, sendo irradiada somente uma região corresponde a 1,0 cm lateralmente à cada borda da ferida, com todo o restante do corpo do animal também protegido. A irradiação foi realizada para um grupo de animais, imediatamente após a abertura da ferida. O outro grupo sofreu a irradiação 3 dias após esse procedimento. O processo de reparação tecidual foi estudado aos 2, 4, 7, 11, 14, 17 e 21 dias após o procedimento cirúrgico para o primeiro grupo, enquanto para o segundo grupo de animais, a reparação tecidual foi avaliada 5, 7, 10, 14, 17, 20 e 24 dias também após a abertura da ferida. Cada grupo irradiado foi comparado com. grupos controles correspondentes, os quais não sofreram irradiação. O processo de reparação tecidual foi avaliado pelos seguintes métodos: coloração pela hematoxilina - eosina, que possibilitou avaliar a mortologia do tecido de granulação; reação histoquímica de metacromasia pelo azul de toluidina pH 4, podendo assim ser avaliada a síntese de glicosaminoglicanas e por fim, impregnação argêntica, onde foi observada a síntese de colágeno, através da microscopia de polarização (birrefringência). Os resultados obtidos mostraram que 1,0 Gy de radiação de elétrons com um feixe de 6 MéV, usou um retardo no processo de reparação tecidual, quando aplicado imediatamente e 3 dias após a abertura da ferida, sendo que quando comparados os dois grupos irradiados, para os dias 7, 14 e 17 , o efeito na reparação tecidual foi mais acentuado no grupo que sofreu irradiação 3 dias após a abertura da ferida / Abstract: The present search had the purpose to study the low dose electron irrradiation effect in the process of tissue repair in rats. In such a way, the animais were submitted to a surgical procedure, in which a rectangular wound was performed, measuring 2.3cm X 1.4cm on the fore dorsal area. At the moment of irradiation, the wounds were protected so that only an area near 1.0cm laterally to each b9rder of the wound was i rrad iated , being protected ali the rest ofthe animal body. The irradiation was performed in one group of animais immediately after the wounding procedure. The other group was irradiated three days after wounding. The process of tissue repair was studied at 2, 4, 7, 11, 14, 17 and 21 days after the surgical procedure on the first group, while for the other group of animais, tissue repair was evaluated at 5, 7, 10, 14, 17, 20 and 24 days, also after wounding. Each irradiated group was compared to corresponding control groups, which did not were submited irradiation. The tissue repair process was evaluated by the following methods: staining by haematoxylin-eosin in order to evaluating granulation tissue morphology; histochemical reaction of metachromasia by toluidin pH 4.0, so that it was possible to evaluate the synthesis of glucosaminglucans and at last, the silver impregnation, in which it was studied the collagen synthesis bymeans of polarizing microscopy. The results obtained showed that 1.0 Gy of electron irradiation with a 6 MeV beam caused a delay in the process of tissue repair, when applied immediately after and at three days after wounding. The comparison of both irradiated groups at days 7, 14 and 17, have showed that the effect on tissue repair was stronger on the group that received irradiation 3 days after wounding / Doutorado / Radiologia / Doutor em Odontologia

Thermoplastic Vulcanizates (TPVs) are itself a commercially high valued group of polymer blend. They render technological properties of conventional vulcanized elastomers with the ease of thermoplastic melt (re)processability. With ever growing market, TPVs have got plenty of applications among various fields. Here, the technological properties of these TPVs were tailored according to the purpose by interplaying physical parameters of polymers and advanced high energy electron technology. Electron irradiation, though a well-known technique for cross-linking in polymer industry, is only restricted to final product treatment. We take it to the next level by coupling a conventional internal mixer and a high energy electron accelerator. Polypropylene (PP) and natural rubber (NR) based TPVs have been prepared using this new reactive processing technology, named Electron Induced Reactive Processing (EIReP). Various electron treatment parameters were explored to maximize technological properties of TPVs. Effects of various polyfunctional monomers (PFM) were also studied. In an endeavor to develop a potential method for customization, deep insights of macroscopic and microscopic structure of these TPVs were presented with the help of various advanced scientific characterization techniques. Commonly faced difficulties like viscosity mismatch, cure rate mismatch, and incompatibility due to different molecular structures were furnished along with plausible solutions. Investigation of phase inversion from co-continuous matrix to thermoplastic matrix was dealt with special care as it helps to understand structure property correlation for all TPVs. To make the whole effort relevant, at the end of this thesis a summary of various technological properties has been given for the newly processed and commercially available TPVs.

Polypropylene (PP) is a common thermoplastic and frequently adapted permanently with increasing requirements by adding fillers as well as reinforcing materials. Because of incompatibility of non-polar PP and polar inorganic filler, resulting composites are brittle which has a detrimental effect on the desired properties. Improvements in mechanical properties can be reached by compatibilization, creating of chemical couplings between phases and by increasing of inhomogeneity. Thus, maleic anhydride grafted PP is used as well as reactive processing of PP in presence of peroxide radical initiators. The temperature dependence of peroxide decay as well as the dependence of radical generation rate on time are two disadvantages of peroxide induced reactive processing. Modification of polymers with high energy electron treatment is also well known and used to form parts (after) molding as well as raw materials (pellets, powders, fibers) in solid state and at room temperature. The spatially and temporally precise input of energy is used to produce desired material properties on radical-induced chemical reactions. Coupling of high energy electron modification of polymers and melt mixing offers a new possibility of reactive processing. In this case, radical generation is independent of temperature, can be easily controlled by beam current and kept constant over time. Absence of any crystallinity, high reaction rates as well as intensive macromolecular mobility and intensive mixing are reasons to expect novel structures and properties. Electron beam induced reactive processing is a novel technique where chemical reactions are induced by spatial and temporal precise energy input via high energy electrons under dynamic conditions of melt mixing. This method gives the possibility to increase surface energy of polypropylene (PP) effectively as well as to generate chemical couplings between filler and PP. The process was applied to a proved system consisting of PP (38 wt%), magnesium hydroxide (MH) (60 wt%), triallyl cyanurate (TAC) (2 wt%). This composite system was successful tested in peroxide induced conventional reactive processing. Absorbed dose imparted per rotation of rotors is a new parameter controlling mechanical properties of polymer composites. Improved properties were found in tensile strength (150 %), elongation at break (175 %), and impact strength (175 %). It can be shown that chemical couplings are generated during electron induced reactive processing in comparison to only compatibilized material.:1 Einleitung 6 2 Stand der Technik 8 2.1 Werkstoffeigenschaften von Polypropylen-Kompositen 8 2.1.1 Polypropylen 8 2.1.2 Füll- und Verstärkungsstoffe 10 2.1.3 Phasengrenze und Phasenmorphologie 12 2.1.3.1 Füllstoffmodifizierung 15 2.1.3.2 PP-Modifizierung 16 2.1.3.3 Mehrkomponentensysteme 17 2.1.3.4 Ansätze aus anderen Werkstoffsystemen 18 2.2 Reaktive Aufbereitung 19 2.3 Polymermodifizierung mit energiereichen Elektronen 22 2.3.1 Einordnung und Wechselwirkungsmechanismen 22 2.3.2 Einfluss von Polymerstruktur und G-Wert 25 2.3.3 Steuerparameter 26 2.3.3.1 Parameter der chemischen Umgebung 26 2.3.3.2 Parameter der Elektronenmodifizierung 28 2.3.4 Bestrahlung von Polypropylen 32 2.3.5 Bestrahlung von partikelgefüllten Thermoplastkompositen 33 2.3.6 Bestrahlung von Füll- und Verstärkungsstoffen 33 2.4 Zusammenfassung Stand Technik 34 3 Zielstellung 37 4 Aufgabenstellung 39 5 Experimentelles 40 5.1 Anlagentechnik 40 5.1.1 Stationäre Behandlung 40 5.1.2 Elektronen induzierte reaktive Aufbereitung 41 5.1.2.1 Aufbau u. Funktionsweise 41 5.1.2.2 Parameter der Elektronen induzierten reaktiven Aufbereitung 42 5.1.2.3 Dosimetrie 44 5.2 Probenherstellung 45 5.2.1 Materialien 45 5.2.2 Aufbereitung 45 5.2.3 Prüfkörperherstellung 46 5.3 Modifizierungsparameter 47 5.4 Vorgehensweise 49 5.5 Analytische Methoden 51 5.5.1 Zugversuch 51 5.5.2 Schlagbiegeversuch (nach Charpy) 52 5.5.3 Größenausschlusschromatographie (SEC) 54 5.5.4 Dynamische Differenzkalorimetrie (DSC) 55 5.5.5 Laserbeugungsspektrometrie 57 5.5.6 Rasterelektronenmikroskopie (REM) 58 5.5.7 Fourier-Transmissions-Infrarot-Spektroskopie (FTIR) 58 5.5.8 Dynamische Kontaktwinkelmessung 59 5.5.9 Schmelzerheologische Untersuchungen von Polymerschmelzen 60 5.5.9.1 Ungefüllte Polymerschmelzen 62 5.5.9.2 Partikelgefüllte Polymerschmelzen 63 6 Ergebnisse 68 6.1 Mechanische Kompositeigenschaften 68 6.2 Matrixpolymersysteme PP und PPTAC 69 6.3 Partikelgröße und -verteilung 75 6.4 Kompatibilität 77 6.5 Phasenkopplung 82 6.6 Inhomogenität 86 6.7 Einfluss verschiedener Prozessparameter auf die mechanischen Eigenschaften 87 6.7.1 Dosis 88 6.7.2 Elektronenenergie 90 6.7.3 Bestrahlungsdauer 91 6.7.4 Aufbereitungszeit 93 6.7.5 Dosisleistung im Modifizierungsvolumen 96 7 Zusammenfassung 98 8 Ausblick 100 9 Anhang 104 10 Literaturverzeichnis 112 11 Abkürzungsverzeichnis 115