This creative project was a study of combining large-scale ceramics and polymer resin (Brandname: Bondo) vessels. This project came out of an earlier experiment combining metals and resin, and therefore the interest in combining clay and resin was a natural transition for me, since ceramics was my major focus. I had a definite interest in the challenge of marrying two very different materials; clay and resin, and by using this combination I would make vessels that were visually successful and engaged the viewer.The technical basis for all of the ceramic elements of the vessels is wheel throwing. The molds made for the resin parts of the piece were wheel thrown as well. This project was very unique and there was little documented technical information for me to rely on other than personal experimentation and ceramic knowledge.The visual elements of clay with its opaqueness, and resin with its translucent qualities offered great visual contrast. The use of color contrast between warm and cool colors became an important element of the pieces.From an expressive standpoint, I feel the form of the vessels is viewed as solid and confrontational, yet very compelling. The smooth surfaces and the lush vibrant colors compel the viewer to examine the forms. The pieces are commanding in size and strength, so the viewer is somewhat hesitant to view for too long. There is a visual push/pull, a contrast between these simple yet over-scaled layered forms that evokes an emotional push/pull as well. / Department of Art

A microwave assisted methodology was developed to modify Merrifield resins (1-2% cross-linked containing 1.0-3.5 mmol Cl-/g) with different nominal molecular weights PEG (200-1000). The synthesis was also carried out by conventional heating to assess the differences between the two procedures. The most efficient synthesis was achieved by using microwave and by using PEG with molecular weight 200 and MR 2% crosslinked containing 1.25 mmol Cl -/g. The structural elucidation was carried out using Fourier transform infrared (FTIR) spectroscopy and elemental analyses. Upon pyrolsis-GC/MS analysis of the PEGylated MR, the PEG showed the tendency to undergo thermal degradation by the loss of a smaller PEG fragments. This observed degradation of PEG was less prominent during microwave assisted synthesis compared to conventional heating, in addition to faster reaction rates and higher yields. As expected, the PEGylated MR showed improved swelling properties in polar solvents. The chemical reactivity of the PEGylated Merrifield resin was confirmed by the esterification with pyruvic acid and by the substitution of hydroxyl group using thionyl chloride. In addition, the PEGylated MR was converted into (1) polymer-supported acid/base or redox indicator by the attachment of a blue organic dye - 2,6-dichloroindophenol (DCIP) through a nucleophilic substitution reaction and (2) beta-cyclodextrin trap, a water insoluble inclusion-complex, by immobilization of beta-cyclodextrin through cross-linking with 1,6-hexamethylene diisocyanate reagent.

Thesis (M.Eng.). / Written for the Dept. of Mechanical Engineering. Title from title page of PDF (viewed 2008/01/14). Includes bibliographical references.

Thesis (M.S.)--Virginia Polytechnic Institute and State University, 1993. / Vita. Abstract. Includes bibliographical references (leaves 85-87). Also available via the Internet.

Thesis (M.S.)--Oregon State University, 2005. / Printout. Includes bibliographical references (leaves 66-72). Also available on the World Wide Web.

Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2017. / Certain resins used in ion-exchange separation techniques have become very expensive. Although ion-exchange is an economical method to soften water it is important to keep the cost low during the process. Any exorbitant costs will make a process unattractive and eventually obsolete. Bio-Rad AG MP-50 macroporous resin (supplied by Bio-Rad Laboratories, Ltd.) at present costs approximately R20000 (twenty thousand rand) for 500 g compared to Amberlyst 15 R840.00 for 500 mL and Dowex Marathon MSC R312.34 macroporous resin for 500 mL (both supplied by Dow, Rohm and Haas Co). This motivated the research to determine by a comparative study if there is any difference in the efficiency and effectiveness in the quantitative analysis of trace elements when these resins are used. The following elements will be used to determine distribution coefficients for the elements on these resins: Mn, Fe(III), Co, Ni, Cu, Zn, Al, Ag, Cd, In, Ga, Tl, Pb and Bi in 0.1, 0.2, 0.5, 1.0, 2.0, 3.0, 4.0 M nitric acid solutions. Another question is whether there is a difference or a preference when selecting either a microporous or a macroporous resin for the ion-exchange separation. Determination of distribution coefficients for 46 elements had been done by Strelow (Strelow F. W., 1984) in nitric acid on Bio-Rad AG 50W-X8. The results obtained in this study will be compared with the distribution coefficients obtained by Strelow. The Bio-Rad, Amberlyst and Dowex resins were stirred for approximately 30 minutes in deionised water and then packed in a column. Impurities in the resin column were eluted with 5 M HCl and the resin was then rinsed with deionised water to remove the acid. Thereafter the resins was rinsed out of the column with deionised water, filtered off and then dried under vacuum in an oven at 60 0C for approximately 24 hours. Stock solutions of the elements were prepared as 0.1 M solutions and then diluted with deionised water to obtain solutions having the respective concentrations of 0.1, 0.2, 0.5, 1.0, 2.0, 3.0, and 4.0 M. Quadruplicate reference standards of each element were prepared. Distribution coefficients of the elements on each resin were determined as described by Strelow (Strelow F. W., Distribution coefficients and ion exchange behaviour of some chloride complex forming elements with Bio Rad AG50W - X8 cation exchange resin in mixed Nitric-Hydrochloric acid solutions, 1989). From the distribution coefficients, obtained from the ICP-OES data, a selectivity series for the 14 elements, mentioned above, was arranged in the decreasing order for each resin’s affinity for the elements. The distribution coefficients also give an indication whether the elements can be quantitatively separated by the cation exchangers in nitric acid media. Elution curves for some elements were done to establish the experimental conditions for quantitative separations of the elements by column cation exchange chromatography.

Orientador: Altair Antoninha Del Bel Cury / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Odontologia de Piracicaba / Made available in DSpace on 2018-08-17T11:17:25Z (GMT). No. of bitstreams: 1 Fernandes_FredericoSilvadeFreitas_D.pdf: 739091 bytes, checksum: 727731c2061dd20f60d28b6f01753ccf (MD5) Previous issue date: 2011 / Resumo: Os limpadores químicos de prótese têm sido bastante indicados para o controle do biofilme formado sobre próteses removíveis de pacientes com comprometimento motor. Apesar de estudos prévios terem mostrado que uma única imersão nesses agentes é capaz de reduzir os níveis de Candida albicans do biofilme formado sobre próteses removíveis, pouco se sabe sobre o efeito do uso diário desses limpadores sobre o biofilme residual de Candida. Assim, o objetivo desse estudo foi avaliar a eficácia do uso diário de um limpador químico enzimático sobre o biofilme de C. albicans formado sobre a superfície de materiais para confecção de próteses removíveis; bem como a atividade enzimática das células de Candida desse biofilme após exposições diárias a esse limpador de prótese. Foram confeccionados espécimes de resina de polimetilmetacrilato (PMMA) e resina de poliamida, nos quais foi realizada, inicialmente, a padronização da rugosidade de superfície (0,34 ± 0,02 ?m). Após a formação da película adquirida, os espécimes foram divididos aleatoriamente em 12 grupos (n=9) para formação do biofilme de C. albicans por 72 horas. Após esse período, os espécimes foram tratados por 1, 4 ou 7 dias, sendo realizado um tratamento por dia, com um limpador químico enzimático (Polident 3 Minutes) ou com água destilada (controle negativo). Após os respectivos períodos de tratamento, os microrganismos remanescentes foram removidos da superfície dos espécimes por meio de ondas ultra-sônicas (7W por 30s). Em seguida, as unidades formadoras de colônia (UFC) foram calculadas e a atividade enzimática das células remanescentes foi avaliada. Os dados foram submetidos à ANOVA um fator ou dois fatores, seguido do teste de Tukey-Kramer. O biofilme de Candida albicans formado sobre a resina de poliamida apresentou maiores níveis de Candida e uma maior atividade fosfolipásica que o biofilme formado sobre a resina de PMMA (p<0,001). O limpador químico enzimático reduziu significantemente os níveis de Candida albicans em todos os períodos avaliados (p<0,001), entretanto os níveis desse microrganismo aumentaram com o tempo, sendo observada diferença estatisticamente significante entre os períodos avaliados (p<0,001). As exposições diárias a esse limpador químico aumentaram a virulência das células de Candida, no que diz respeito à atividade fosfolipásica. Nas condições desse estudo, conclui-se que o uso diário do limpador químico enzimático não foi capaz de impedir a proliferação de Candida albicans no biofilme residual, apesar de ter interferido no crescimento desse biofilme. / Abstract: Chemical cleansing with immersion in denture cleansers has been indicated for denture biofilm control in patients with limited motor capacity. Although previous studies have shown that a single immersion in those agents is able to substantially reduce Candida albicans biofilm levels, the effect of the routine use of denture cleansers on the Candida residual biofilm is poorly understood. This study evaluated the efficacy of daily use of an enzymatic denture cleanser on C. albicans biofilm formed on denture base materials; and the enzymatic activities of Candida biofilm cells after daily exposure to this cleanser agent. Polymethyl methacrylate (PMMA) and polyamide resins specimens were prepared (n=54), and their surface roughness was standardized (0.34 ±0.02 ?m). Saliva-coated specimens were randomly divided by lottery into 12 groups (n=9) for biofilm assay. C. albicans biofilm was formed for 72 hours, and then specimens were treated for 1, 4 or 7 days, once a day, with an enzymatic cleanser (Polident 3 Minutes), or distilled water (negative control). Remaining adherent microorganisms were removed from the treated specimens by ultrasonic waves at 7 watts for 30 seconds, and then colony-forming units (CFU) were calculated and remaining cells enzymatic activities were determined. Data were analyzed by 1-way or 2-way ANOVA followed by the Tukey-Kramer test. C. albicans biofilm formed on polyamide resin showed significantly higher Candida levels and phospholipase activity (p<0.001) than biofilm formed on PMMA resin. The enzymatic cleanser significantly reduced C. albicans levels in all evaluated periods (p<0.001); however, the number of this microorganism increased with time, showing statistical difference among the treatment periods (p<0.001). The daily exposure to the denture cleanser increased Candida cells virulence, with regard to phospholipase activity. Our study has shown that the enzymatic cleanser daily use did not prevent C. albicans proliferation in residual biofilm; however, this agent reduced this fungus rate of growth. / Doutorado / Protese Dental / Doutor em Clínica Odontológica

The effects of silicone coated heat-exchanger tubes on the water film coefficient of heat transfer and on the formation of gypsum seals were studied. The heat-exchanger tubes consisted of 74 ½-in. sections of 1-in. Nominal diameter standard iron pipe into whose surface were installed six copper-constantan thermocouples for measuring the temperature of the tube well. Silicone resins DC 804 and DC 802 were used for coating the tubes. Silicone resin DC 804 was cured for 16 hours under infra-red heat at 440-450°F to a pencil hardness of 7H; however, due to the fact that it would not withstand the thermal stresses encountered in the heat-exchanger, its use was abandoned. Silicone resin DC 802 was cured for 12 hours under infra-red heat at 440-450°F to a pencil hardness of 2H. The horizontal tube double-pipe heat-exchanger consisted of a 5-ft. section of 2-in. I.D. Pyrex pipe fitted with a reducing tee and a reducing cross as the end-sections. Heat was applied to the heat-exchanger by steam from 15 to 40 psig. In the "Heat Transfer Tests", which were conducted with water at 60°F and at Reynolds numbers from 2500 to 11,000, it was found that the water film coefficients on the silicon surface varied from 810 to 1590 BTu/(hr.)(sq.ft.)(°F); while those on non-coated iron tubes varied from 244 to 670 under the same conditions. In "Accelerated scaling tests", which were conducted at Reynolds numbers of 15,000 and 4,100 using a saturated gypsum solution at l55°F as the scaling medium, it was found that scale formation on the coated and non-coated tubes reduced the film coefficient approximately 50 percent in 3 ½ to 4 ½ hours. A coating of 0.0006-in. Thickness caused the initial water film coefficient to be 70 percent of the coefficient for a non-coated tube at a Reynolds number of 15,000. A coating of 0.0018-in. thickness caused the initial. water film coefficient to be 83 per eent of the initial coefficient for a non-coated tube at a Reynolds number of 4,100. The thermal conductivity of silicone resin DC 802 was found to be 0.096-0.103 Btu/(hr.)(aq.ft.)(°F per ft.) at 150°F. / Master of Science

The objective of this study was to develop tests that could be used to characterize autohesive strength development in amorphous thermoplastic resins and fiber-reinforced thermoplastic prepregs. All tests were performed using polysulfone P1700 thermoplastic resin and AS4/P1700 graphite-polysulfone prepreg. Two test methods were examined to measure autohesion in neat resin samples. These included an interfacial tension test based on the ASTM tensile adhesion test (ASTM D897) and a fracture toughness test using a compact tension (CT) specimen (based on the ASTM toughness test for metals ASTM E399-83). The interfacial tensile test proved to be very difficult to perform and with an unacceptable amount of data scatter. The data obtained using the compact tension test were repeatable and could be correlated with temperature and contact time. Autohesive strength development in fiber-reinforced prepreg samples was measured using a double cantilever beam (DCB) interlaminar fracture toughness test. The fracture mechanisms were determined to be different in the healed DCB specimen than the virgin specimen due to resin flow at the crack plane during the healing tests. The CT test was found suitable for use in determining the autohesive properties and self-diffusion coefficient of neat resin. The DCB test, although not suitable for autohesive testing, indicated that repair of thermoplastic matrix composites is possible; however, the repair will not be as tough as the virgin material. / Master of Science

see document / Master of Science