Call number: LD2668 .T4 1979 R65 / Master of Science

Thesis submitted in fulfilment of the requirements for the Degree of Masters of Technology: Organic Chemistry, Durban University of Technology, 2011. / One of the greatest medical challenges facing mankind is the Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome (HIV/AIDS) which has now become a major epidemic with more than 40 million people infected worldwide. Of equal concern is its implication in high mortality and the onset of a number of opportunist mycobacterial infections, principally tuberculosis. In spite of the discovery of some relatively effective antiretroviral (ARV) drugs such as Azido Thymidine (AZT), Nevirapine (NVP) and Efavirenz (EFV), its’ application as either a single or combinational form causes side effects by harming the bone marrow. Drug resistance is a key cause of failure for treatment of HIV infection. Hence greater interdisciplinary efforts, involving both natural and social sciences, are needed urgently to combat this HIV/AIDS pandemic. Heterocyclic nitrogen based compounds, obtained from either natural sources or synthesis are adequately documented to have increased biological activity against several diseases. Recently a study of drugs containing the naphthyridine scaffold has acquired increasing attention because of its potential against HIV/AIDS. Generally, naphthyridines demonstrate good potency in both the enzyme and cellular systems and this prompted our interest in the synthesis of naphthyridine derivatives from simple and readily available starting compounds. Furthermore we wanted to form an intermediate quinolone moiety since it has good biological potential. In this study we report the synthesis of three naphthyridine derivatives, i.e. 6-phenyl-dibenzo [b, h] [1, 6] naphthyridine, 4-methyl-6-phenyl-dibenzo [b, h] [1, 6] naphthyridine and 2- methyl-6-phenyl-dibenzo [b, h] [1, 6] naphthyridine from easily available chemicals such as aniline, ortho-toludine, para-toluidine and ethyl benzoylacetate via a five step reaction scheme using either conventional reflux, microwave irradiation or both methodologies. It was found that microwave irradiation was several folds faster than conventional reflux methodology and the yield of the product was higher. The first step of the reaction scheme is a simple condensation reaction: three acrylate derivatives, viz. ethyl-3-aniline-3-phenyl acrylate, ethyl-3-phenyl-3-(ortho-tolylamino) acrylate and ethyl-3-phenyl-3-(para-tolylamino) acrylate were synthesized by refluxing ethyl benzoylacetate in an acidified ethanolic solution with aniline, ortho-toluidine and paratoluidine respectively for three hours; the yields were 95, 87.5 and 80 % respectively. Page v In the second step, thermal cyclisation was achieved for the synthesis of three quinoline derivatives, viz. 2-phenylquinoline-4(1H)-one, 8-methyl-2-phenylquinoline-4(1H)-one and 6- methyl-2-phenylquinoline-4(1H)-one from their respective acrylates under microwave irradiation for 5 minutes at 180 °C and 250 watts; the yields were 92, 84 and 80 % respectively. In the third step of the reaction, synthesis of 4-chloro-2-phenylquinoline, 4- chloro-8-methyl- 2-phenylquinoline and 4- chloro-6-methyl-2-phenylquinoline was achieved from a mixture of POCl3 and their respective quinolines via microwave irradiation for 3 minutes at 75 °C and 150 watts and via conventional reflux for 5 hours. It was found that under microwave irradiation, the reaction occurred nearly 100 fold faster but the % yield of the product was marginally higher. The fourth step of the reaction resulted in the formation of three schiff’s base, viz. 4-(Nphenyl)- 2-phenyl-4-aminoquinoline, 8-methyl-4-(N-phenyl)-2-phenyl-4-aminoquinoline and 6-methyl-4-(N-phenyl)-2-phenyl-4-aminoquinoline from their respective quinolines via microwave irradiation for 20 minutes at 180 °C and 180 watts and via conventional reflux for 2 hours. It was found that under microwave irradiation, the reaction occurred nearly 6 fold faster and the % yield of the product was over 10 % higher. The final step of the reaction was achieved by a Vilsmeir Haack reaction and in situ base catalyzed thermal cyclisation: 6-phenyl-dibenzo [b, h] [1, 6] naphthyridine, 4-methyl-6- phenyl-dibenzo [b, h] [1, 6] naphthyridine and 2-methyl-6-phenyl-dibenzo [b, h] [1, 6] naphthyridine were synthesized from their respective schiffs base via microwave irradiation for 20 minutes at 75 °C at 120 watts and via conventional reflux for 21 hours. It was found that under microwave irradiation, the reaction occurred over 60 fold faster and the % yield of the product was over 20 % higher.The outline for the five step synthesis of the three naphthyridines is presented graphically below: Page vi Key: (a) R1= H; R2=H (b) R1 = H; R2 = CH3 (c) R1 = CH3; R2 =H Reaction Conditions: 1) conc.HCl, EtOH, 3hrs, 50 °C; 2) conc. HCl, hand stirring 10 min; 3) 180 °C, MWI, 250 watts, 5 min; 4) POCl₃, MWI, 75 °C, 150 watts, 2 min; 5) POCl₃, 100 oC, 5 hrs; 6) aniline, t-BuOH, MWI, 180 °C, 180 watts, 20 min; 7) aniline, t-BuOH, 80 °C, 3 hrs; 8) DMF, POCl₃, MWI, 75 °C,120 watts 20 minute; 9) DMF, POCl3, 100 oC, 21 hrs.

Submitted in fulfilment of the requirements for the Degree of Master of Technology: Organic Chemistry, Durban University of Technology, 2011. / ortho-Deoxygrisan (38), a spirodienone was synthesised from bisphenol (42) using both conventional and microwave assisted methods. The bisphenol (42) was synthesised from phenol (52) by conventional and microwave assisted methods. Benzophenone (43) was synthesised from compound (49) which in turn was synthesised from compound (53) by chromic acid oxidation in acetic anhydride or acetic acid. Compound (53) was synthesised from bisphenol (42) by mono-acetylation method.Acid-catalysed rearrangement of ortho-deoxygrisan (38) in the absence of light was investigated. Chromatography of the reaction mixture afforded compound (D) as a major component. Attempts to synthesise ortho-grisan (50) from benzophenone (43) were unsuccessful. Microwave assisted selenium dioxide oxidation of compound (53) gave a yellow compound C. The spectra of this compound were very similar to the spectra of ortho-deoxygrisan (38). However, selenium dioxide was reacted with compound (53) in the absence of microwave to give a yellow solid B. The 1H NMR spectral data of this compound led to the proposed structure B for it. / National Research Foundation.

Master of Science / Department of Electrical and Computer Engineering / Punit Prakash / Microwave ablation is a minimally invasive therapeutic modality used for the treatment of cancer in various organs. In this procedure, microwave energy is sent through a thin antenna placed inside the tumor. The microwave energy radiated from the antenna generates heat which kills the tumor cells by necrosis. During multiple-applicator microwave ablation, geometric estimates of treatment outcome are typically obtained by assuming parallel insertion of the applicators. This assumption is based on the guidelines provided in the brochures of antenna manufacturing companies. This assumption is flawed because it is rare to insert the antennas in parallel configuration due to the flexible nature of the antennas and the presence of intervening organs. Furthermore, movement of patients during the treatment procedure alters the position of the antennas. In order to see the effect of non-parallel insertion of antennas, model-based treatment planning may be instructive. Treatment planning can also determine the changes needed to be made for prospective ablation therapy if the antennas are not positioned in their ideal parallel configuration. This thesis provides a detailed computational comparison of the skewed configurations of microwave antennas to their closest parallel configurations. The metric used for com-paring the similarity between the cases is Dice Similarity Coefficient (DSC). Experimental results to validate the computational data are also discussed. Computations were done by using realistic cases of antenna positions obtained from Rhode Island Hospital.

Esta tese propõe a síntese e o estudo de uma nova técnica de cavidades de borda aplicada a antenas Vivaldi, com o intuito de melhorar suas características de diretividade. Embora as antenas do tipo Vivaldi possuam características diretivas, elas produzem radiações laterais indesejáveis, o que se reflete nos elevados índices de lóbulos laterais devido a correntes superficiais que fluem ao longo das bordas metalizadas nas laterais da antena. Estas correntes são a origem das radiações laterais que vêm sendo mitigadas pela aplicação de cavidades ressonantes, triangulares ou retangulares, que aprisionam tais correntes e, consequentemente, atenuam os lóbulos laterais, sem o incremento do lóbulo principal, uma vez que toda a energia dos lóbulos laterais é apenas confinada nos ressonadores e por isso literalmente perdida. Ao contrário desses esforços, este trabalho propõe cavidades radiantes tanto na forma de abertura exponencial, como na forma do fractais de Koch, que funcionam como radiadores auxiliares (antenas auxiliares), canalizando as correntes de borda e aproveitando-as para aumentar os níveis do lóbulo principal, mitigando os níveis de lóbulo lateral. A síntese desta nova técnica foi implementada em uma antena Vivaldi antipodal com características de baixa diretividade, como qualquer antena Vivaldi, o que foi corrigido e a aplicação da técnica de cavidades radiantes deu origem a duas novas antenas Vivaldis efetivamente diretivas. Os resultados foram obtidos através de simulações do modelo numérico no CST Microwave Studio e confirmados com medidas de laboratório, o que evidenciou a melhora das características de diretividade da antena pela aplicação da nova técnica de cavidades radiantes. / This work presents a new Slot Edge technique applied to Vivaldi antennas to improve their characteristics of directivity, resulting in two new Vivaldi antennas: the Palm Tree Vivaldi antenna and the Koch Vivaldi antenna. This new technique proposes to add lateral radiators which reduce the side lobe level, increasing the gain of the main lobe in an unprecedented way. This technique is called radiating slot edges, and acts as parasitic antennas, surface currents draining edges of the antenna, and using them to increase the gain in the main lobe. The development was done systematically, starting with an extensive literature review, design and simulation in CST, as well as prototyping and measurements of several antenna designs. All this effort proved the functionality of this technique.

O presente trabalho apresenta um equipamento para o processamento de reduções carbotérmicas sob campo de micro-ondas, permitindo pleno controle da potência fornecida e da medida da energia de micro-ondas efetivamente aplicada à carga em processo de redução podendo assim realizar balanços de energia e determinação de taxa de reação com altos níveis de confiança. O equipamento permite, sobretudo, a medida simultânea de temperatura e de massa do material sob redução, e a fácil reprodutibilidade das condições de ensaio. O protótipo opera com um gerador de micro-ondas de 2.45 GHz e potência variável até 3000 W. A amostra é mantida sob atmosfera de argônio. Nos testes operacionais do protótipo procedeu-se à redução carbotérmica de minério de ferro de Carajás, utilizando coque de petróleo como redutor através de pelotas esféricas com massa de 3,5 g e diâmetro de 15 mm. Obtiveram-se curvas cinéticas de redução de minério de ferro e de consumo de energia durante o processo. Os dados colhidos com este protótipo permitiram realizar uma análise da energia de micro-ondas efetivamente consumida na redução do minério. / This work presents of a device for microwave enhanced carbothermic reductions which permits the full control of microwave power irradiated, the measurement of effectively applied microwave power to the charge in process thus performing a high confidence determination of rate of reaction and energy balance. In particular, the simultaneous records of its temperature and mass loss, and good reproducibility of operation parameters, are obtainable. This prototype works with a 2.45 GHz microwave generator with variable power up to 3000 W. Samples are processes under argon gas atmosphere. Operational tests for Carajás iron ore reduction with petroleum coke were performed using spherical pellets with weight of 3,5 g and diameter of 15 mm. Kinetic curves of iron ore reduction and effective consumption of microwave power curves were determined. These results made possible to perform an analysis of actual energy consumption for enhanced microwave iron ore carbothermic reduction.

Thesis (M.S.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 1980. / MICROFICHE COPY AVAILABLE IN ARCHIVES AND ENGINEERING. / Includes bibliographical references. / by David Bazeley Tuckerman. / M.S.

<p>The aim with this study was to investigate the effects a change of manufacturing process would have on the mechanical properties of drill bits made of a WC/Co composite used for stone cutting. The method used today is sintering, where the material is heated in a conventional sintering oven. The other method was microwave sintering, where the material is heated by radiation in the microwave region. Also an investigation of the manufacturing cost were made.</p><p>The main difference between the two heating methods is that the conventional way is a rather slow process and the microwave method is very fast. The material is also heated homogeniously in the method with mirowaves, aposed to the case with the conventional sintering where the material is heated from the outside in.</p><p>This makes the material harder and more wear resistent. Another positive effect is that the pysical properties of the drill bits is easier to controll, because of the very small grain growth due to the short process time.The cost of manufacturing these drill bits by microwave sintering does not exceed the cost of the conventionall sintering.</p>

Arthur V. Phelps, O.T. Fundingsland [and] Sanborn C. Brown. / "July 23, 1951." / Bibliography: p. 9. / Army Signal Corps Contract No. DA36-039 sc-100 Project No. 3-99-10-022. Dept. of the Army Project No. 3-99-10-022.

by R.A. Rapuano and J. Halpern. / "June 28, 1946." / Includes bibliographical references. / Army Signal Corps Contract No. W-36-039 sc-32037.