Submitted by Rosivalda Pereira (mrs.pereira@ufma.br) on 2017-12-05T19:27:25Z No. of bitstreams: 1 AquilesAbreu.pdf: 1827634 bytes, checksum: d2d7ee078cf8878dfe676a53e1e8bdf0 (MD5) / Made available in DSpace on 2017-12-05T19:27:25Z (GMT). No. of bitstreams: 1 AquilesAbreu.pdf: 1827634 bytes, checksum: d2d7ee078cf8878dfe676a53e1e8bdf0 (MD5) Previous issue date: 2017-10-30 / CAPES / Biofilms based on sodium alginate (AS) crosslinked with cationic polyacrylamide (PAMc) of high molar mass were made by the casting technique. In this study, the central rotational compound design (DCCR) was used and 11 trials were performed. The biofilms produced were characterized with respect to moisture (ω), water solubility (S), water vapor permeability (PVA), thickness (σ), absorption spectroscopy in the infrared region with Fourier transform (FTIR), microscopy scanning (SEM) and mechanical properties. The experimental results showed that biofilms with lower glycerol contents obtained lower moisture content. It was observed that for the solubility and permeability to water vapor, the lower values observed were influenced by the concentrations of PAMc. Assay 5 (AS 6.0g, GLI 1.0g, PAMc 2.5%) presented lower values of ω and PVA, with possible application as food coatings and assay 10 (AS 6.0g, GLI 3.0g; PAMc 2.5%) higher S, and can be applied in biodegradable packages. The results obtained through FTIR confirmed the chemical interaction between AS and PAMc. Morphological analyzes showed that biofilms showed heterogeneity when the concentrations of MAP were increased. Regarding the mechanical properties, tensile strength (TR) and Young's modulus (E) were found to increase when the PAMc concentrations were higher and the deformation decreased when glycerol concentrations were high. Trial 11 (AS 6.0g, GLI 3.0g, PAMc 2.5%) showed higher TR (14.06 MPa) and E (21.17 MPa), with potential for applications as biodegradable bags. / Biofilmes à base de alginato de sódio (AS) reticulados com poliacrilamida catiônica (PAMc) de alta massa molar foram confeccionados pela técnica casting. Nesse estudo foi utilizado o delineamento composto central rotacional (DCCR) realizando-se 11 ensaios. Os biofilmes produzidos foram caracterizados com relação à umidade (ω), solubilidade em água (S), permeabilidade ao vapor de água (PVA), espessura (σ), espectroscopia de absorção na região do infravermelho com transformada de Fourier (FTIR), microscopia eletrônica de varredura (MEV) e propriedades mecânicas. Os resultados experimentais mostraram que os biofilmes com menores teores de glicerol obtiveram menores teores de umidade. Observou-se que para a solubilidade e permeabilidade ao vapor de água, os menores valores observados foram influenciados pelas concentrações de PAMc. O ensaio 5 (AS 6,0g; GLI 1,0g; PAMc 2,5%) apresentou menores valores de ω e PVA, com possível aplicação como coberturas de alimentos e o ensaio 10 (AS 6,0g; GLI 3,0g; PAMc 2,5%) maior S, podendo ser aplicado em embalagens biodegradáveis. Os resultados obtidos através FTIR confirmaram a interação química entre o AS e a PAMc. As análises morfológicas mostraram que os biofilmes apresentaram heterogeneidade quando as concentrações de PAMc foram aumentadas. Quanto às propriedades mecânicas, verificou-se que a tensão à ruptura (TR) e o módulo de Young (E) aumentaram quando as concentrações de PAMc foram maiores e a deformação diminuiu quando as concentrações de glicerol foram elevadas. O ensaio 11 (AS 6,0g; GLI 3,0g; PAMc 2,5%) apresenta maiores TR (14,06 MPa) e E (21,17 MPa), com potenciais para aplicações como sacolas biodegradáveis.

The objectives of this study were to (1) determine an intermittent aeration strategy that could be used to conserve nitrogen (N) via nitrification in dairy manure, (2) determine the effect of recycled flush water on the bio-availability of N during nitrification, and (3) determine effective and economical dosages of chemicals to remove phosphorus (P) from liquid dairy manure. Intermittent aeration strategies, defined in terms of time the aerator is on and off (ON h:OFF h), could be used to conserve N in dairy manure. Testing of four treatments (continuous aeration [100%], 1h:0.33h [75%], 1h:0.67h [60%], and 1h:1h [50%]) showed that only treatments using air provided for 100% and 75% of the time could support nitrification. The 100% and 75% aeration treatments conserved an average of 38% and 25% of influent total ammonia nitrogen (TAN) as nitrite-N+nitrate-N, respectively. Less than 2% of influent TAN was conserved using 60% and 50% treatments. The effect of manure handling technique on N bioavailability and nitrification was tested using flushed and scraped dairy manure. Nitrification was inhibited in scraped manure. Four aluminum- and iron-based salts and five cationic polyacrylamide polymers were evaluated for P removal using jar tests. Ferric chloride (FeCl3·6H2O), aluminum sulfate (Al2[SO4]3·13H2O, alum), and Superfloc 4512 were selected for further study. Polymer addition enhanced floc size and improved P removal. Treatment of manure (0.89% total solids) from Tank 2 at Virginia Tech's dairy using either FeCl3 or alum in combination with polymer resulted in more than 90% P removal. Chemical treatment and transport of P-rich sludge from a 2,270 cubic meter storage tank would result in an estimated 40% cost savings over transport of the entire manure volume offsite for land application elsewhere. The manure treatment strategies tested provide some solutions to dairy farmers regarding adjustment of N:P ratios so that manure can be applied to meet nutrient needs of crops while adhering to regulations set forth by nutrient management plans. / Master of Science

Polímeros e copolímeros hidrossolúveis a base de acrilamida e seus derivados são sintetizados e aplicados principalmente como floculantes, auxiliando na remoção de sólidos finos presentes em águas residuais e industriais. As poliacrilamidas, como são assim chamadas, podem se apresentar em sua forma neutra ou contendo diferentes cargas iônicas (positivas ou negativas) em sua composição em função do tipo de aplicação específica. As poliacrilamidas são sintetizadas, em sua grande maioria, através de emulsões inversas via polimerização radicalar, visando à elevada massa molar do polímero formado. A formulação da poliacrilamida catiônica com fração molar de 0,6 do comonômero iônico foi otimizada através de planejamento fatorial experimental, variando-se os principais fatores de processo: concentração do pacote de surfactante para formação da emulsão inversa, tempo de micronização, concentração de VISCOPLEX® e concentração de ácido graxo. Com base nos resultados obtidos a partir do primeiro planejamento, foram estudadas as seguintes variáveis: HLB do sistema de surfactantes e a troca dos surfactantes monoméricos por surfactantes poliméricos. A otimização da formulação levou em conta principalmente o custo-benefício para produção e comercialização em escala industrial. O fator micronização foi elevado em seu máximo e os fatores VISCOPLEX® e ácido graxo foram excluídos da formulação, após conclusão dos estudos. A troca dos surfactantes monoméricos por poliméricos foi vantajosa devido ao ganho de qualidade do produto final, mesmo com maior custo de implementação. Para minimizar os custos de formulação o fator HLB foi utilizado em seu máximo, onde houve incremento do ALKONAT® L 50 para formação da emulsão inversa. / Acrylamide based hydrosoluble polymers and copolymers and their derivatives are synthesized and mainly applied as flocculants, assisting removal of fine solids present in wastewater and industrial wastewater. Polyacrylamides may be present in their neutral form or with different ionic charges (positive or negative) in their composition depending on the type of specific application. Polyacrylamides are synthesized, mostly by inverse emulsions using radical polymerization, aiming polymers with high molecular weight. Cationic polyacrylamide formulation with 0.6 mole fraction of the ionic comonomer was optimized through design of experiments (DOE), varying the major process factors: surfactant package concentration to form inverse emulsion, micronization time, VISCOPLEX® concentration and fatty acid concentration. Based on the responses from the first DOE, a second DOE was performed, where the variables surfactant system HLB and the exchange of monomeric surfactant by polymeric surfactants were investigated. The formulation optimization considered mainly cost-effective production and industrial scale. The micronization factor was set at its maximum and VISCOPLEX® and fatty acid factors were excluded from the formulation, after conclusion of studies. Exchanging monomeric surfactants by polymeric surfactants led to a final product with higher quality, even considering a higher implementation cost. In order to minimize formulation costs HLB factor was used at its maximum, increasing the content of ALKONAT® L50 to form the inverse emulsion.

Polímeros e copolímeros hidrossolúveis a base de acrilamida e seus derivados são sintetizados e aplicados principalmente como floculantes, auxiliando na remoção de sólidos finos presentes em águas residuais e industriais. As poliacrilamidas, como são assim chamadas, podem se apresentar em sua forma neutra ou contendo diferentes cargas iônicas (positivas ou negativas) em sua composição em função do tipo de aplicação específica. As poliacrilamidas são sintetizadas, em sua grande maioria, através de emulsões inversas via polimerização radicalar, visando à elevada massa molar do polímero formado. A formulação da poliacrilamida catiônica com fração molar de 0,6 do comonômero iônico foi otimizada através de planejamento fatorial experimental, variando-se os principais fatores de processo: concentração do pacote de surfactante para formação da emulsão inversa, tempo de micronização, concentração de VISCOPLEX® e concentração de ácido graxo. Com base nos resultados obtidos a partir do primeiro planejamento, foram estudadas as seguintes variáveis: HLB do sistema de surfactantes e a troca dos surfactantes monoméricos por surfactantes poliméricos. A otimização da formulação levou em conta principalmente o custo-benefício para produção e comercialização em escala industrial. O fator micronização foi elevado em seu máximo e os fatores VISCOPLEX® e ácido graxo foram excluídos da formulação, após conclusão dos estudos. A troca dos surfactantes monoméricos por poliméricos foi vantajosa devido ao ganho de qualidade do produto final, mesmo com maior custo de implementação. Para minimizar os custos de formulação o fator HLB foi utilizado em seu máximo, onde houve incremento do ALKONAT® L 50 para formação da emulsão inversa. / Acrylamide based hydrosoluble polymers and copolymers and their derivatives are synthesized and mainly applied as flocculants, assisting removal of fine solids present in wastewater and industrial wastewater. Polyacrylamides may be present in their neutral form or with different ionic charges (positive or negative) in their composition depending on the type of specific application. Polyacrylamides are synthesized, mostly by inverse emulsions using radical polymerization, aiming polymers with high molecular weight. Cationic polyacrylamide formulation with 0.6 mole fraction of the ionic comonomer was optimized through design of experiments (DOE), varying the major process factors: surfactant package concentration to form inverse emulsion, micronization time, VISCOPLEX® concentration and fatty acid concentration. Based on the responses from the first DOE, a second DOE was performed, where the variables surfactant system HLB and the exchange of monomeric surfactant by polymeric surfactants were investigated. The formulation optimization considered mainly cost-effective production and industrial scale. The micronization factor was set at its maximum and VISCOPLEX® and fatty acid factors were excluded from the formulation, after conclusion of studies. Exchanging monomeric surfactants by polymeric surfactants led to a final product with higher quality, even considering a higher implementation cost. In order to minimize formulation costs HLB factor was used at its maximum, increasing the content of ALKONAT® L50 to form the inverse emulsion.

The mechanism through which a charged polymer cationic polyacrylamide (C-PAM) operates to increase the rate of cornstarch hydrolysis was investigated. The main objective was to determine the major factors that affect the mechanism so that these parameters may be adjusted to achieve optimal hydrolysis rates. A combination of analytical methods including dynamic light scattering, optical imaging, and uv-vis spectroscopy were used to study polymer, starch, and enzyme interactions as a function of process conditions. It was found that C-PAM binds strongly to starch granules, increasing solubilization and decreasing onset gelatinization temperature. Granule swelling was unaffected by C-PAM. Both binding of enzyme to cornstarch, and rate of cornstarch hydrolysis were found to increase in the presence of C-PAM. By analogy to previous work on cationic polymer promoted hydrolysis of cellulose, it was proposed that the polymer reduces the charge on the starch surface through a "charge-patch" mechanism. Because both enzyme and substrate are negatively charged, the positively charged polymer reduces the charge repulsion experienced by the approaching enzyme. This leads to stronger enzyme-substrate binding, and faster hydrolysis. There is a mirror image relationship between viscosity of the medium and hydrolysis rate, which allows optimization of these parameters with enzyme and C-PAM dosage. Overall, the polymer addition reduced enzyme dose by 62% depending on the conditions used, so this method could have significant economic impact on the industrial conversion of starch to ethanol.

<p>Denna avhandling presenterar experimentella studier av polyelektrolytadsorption på motsatt laddade ytor, där substrat av både kiseloxid och blekt barrsulfatmassa har använts. Ett huvudsakligt syfte med denna forskning var att karaktärisera konformationen hos adsorberade skikt av katjonisk polyakrylamid (CPAM) i jämförelse med katjonisk dextran (Cdextran) och relatera denna information till inbindningskapaciteten av kolloidal kiselsyra. Ett andra syfte i denna avhandling var att studera kinetiken för sekventiell adsorption av polyamidamin epiklorhydrin (PAE) och karboxymetyl cellulosa (CMC) på massafibrer och att bestämma adsorptionsisotermer för deponering av polyelektrolyter skikt för skikt på massafibrer.</p><p>Adsorptionen av CPAM på kiseloxidytor studeras med stagnationspunkts-reflektometri och kvartskristalls-mikrogravimetri för att bestämma adsorptionskinetiken och mättnadsadsorptionens beroende av polyelektrolytens laddningstäthet, pH och NaCl koncentration. Konformationen hos adsorberade skikt av CPAM och Cdextran bestämdes både före och efter sekundär tillsats av kolloidal kiselsyra (CS) och adsorptionen av CS kvantifierades också som funktion av yttäckningen av polyelektrolyt.</p><p>Resultaten indikerar att laddningstätheten hos CPAM kontrollerar den adsorberade mängden på kiseloxidytor vid låga NaCl koncentrationer. Både adsorptionen av CPAM och Cdextran på kiseloxid visades vara effektiv i NaCl koncentrationer upp till 1 M, vilket indikerar ett signifikant bidrag av icke-jonisk interaktion mellan polyelektrolyterna och kiseloxid. Adsorptionen av CS var högre på föradsorberad CPAM än Cdextran. Konformationen hos de adsorberade skikten efter tillsats av CS sågs expandera signifikant för skikt baserade på CPAM medan skikt av Cdextran vid låga salthalter verkade återta sin konformation efter en temporär expansion.</p><p>I den andra delen av avhandlingen studerades sekventiell adsorption av PAE och CMC på massafibrer. Adsorptionsisotermer skikt för skikt på avkryllad massa visade att PAE adsorberade i större mängd än CMC, både i hänseende av massa och laddning. Adsorptionen av PAE var signifikant långsammare än CMC och adsorptionstiden till 90% av mättnadsadsorptionen bestämdes till 3 respektive 1 minut. Zetapotentialen för kryll bestämdes för adsorption av de två första polyelektrolytskikten och resultaten tydde på att kryllmaterialet omladdade inom en minut efter tillsatserna av polyelektrolyt. Reflektometriförsök inom sekventiell adsorption av PAE och CMC på kiseloxid antydde att den låga molekylviktsfraktionen av PAE störde uppbyggnaden av polyelektrolyt-multiskikten.</p> / <p>This thesis presents experimental studies of polyelectrolyte adsorption on oppositely charged surfaces, where substrates of both silica and bleached softwood kraft pulp were used. A major aim of this research was to characterise the conformation of adsorbed layers of cationic polyacrylamide (CPAM), in comparison to cationic dextran (Cdextran), and relate this information to the binding capacity of colloidal silica. A second aim in this thesis was to study the kinetics of the sequential adsorption of polyamide epichlorohydrine (PAE) and carboxymethyl cellulose (CMC) on pulp fibres, and to determine the adsorption isotherms for the layer-by-layer deposition of polyelectrolytes on pulp fibres.</p><p>The adsorption of CPAM on silica surfaces was studied using stagnation point adsorption reflectometry and quartz crystal microgravimetry to determine its adsorption kinetics as well as the dependencies of polyelectrolyte charge densities, pH, and NaCl concentration on saturation adsorption. The conformation of adsorbed layers of CPAM and Cdextran, analysed in terms of amount of water and layer thickness, was determined both before and after the secondary adsorption of colloidal silica (CS), and the adsorption of CS was also quantified as a function of the surface coverage of the polyelectrolyte.</p><p>Results indicate that the charge density of CPAM controlled the amount of the polyelectrolyte adsorbed on silica surfaces at low NaCl concentrations. The adsorption of both CPAM and Cdextran on silica was shown to be effective at up to 1 M NaCl concentrations, which indicates that non-ionic interactions between the polyelectrolytes and silica contribute significantly. CS adsorption was higher on pre-adsorbed CPAM than on Cdextran. The conformation of the adsorbed layer after CS addition was seen to expand significantly in CPAM-based layers, while the Cdextran layer appeared to restore its conformation after a temporary expansion at low salt concentrations.</p><p>In the second part of the thesis, the sequential adsorption of PAE and CMC on pulp fibres was determined using the polyelectrolyte titration technique. Layer-by-layer adsorption isotherms derived on fractionated pulp showed that PAE adsorbed in higher amounts than CMC did, both in terms of adsorbed mass and adsorbed charge. The adsorption of PAE was significantly slower compared to CMC, and the adsorption times required to reach 90% of the saturation adsorption were 3 and 1 min, respectively. The zeta potential of pulp fines was determined for the adsorption of the two first polyelectrolyte layers, and data indicated that the fines recharge within one minute after the polyelectrolyte additions. Reflectometry experiments regarding the sequential adsorption of PAE and CMC on silica indicated that the low-molecular-weight fraction of PAE disturbed the formation of polyelectrolyte multilayers.</p>

Denna avhandling presenterar experimentella studier av polyelektrolytadsorption på motsatt laddade ytor, där substrat av både kiseloxid och blekt barrsulfatmassa har använts. Ett huvudsakligt syfte med denna forskning var att karaktärisera konformationen hos adsorberade skikt av katjonisk polyakrylamid (CPAM) i jämförelse med katjonisk dextran (Cdextran) och relatera denna information till inbindningskapaciteten av kolloidal kiselsyra. Ett andra syfte i denna avhandling var att studera kinetiken för sekventiell adsorption av polyamidamin epiklorhydrin (PAE) och karboxymetyl cellulosa (CMC) på massafibrer och att bestämma adsorptionsisotermer för deponering av polyelektrolyter skikt för skikt på massafibrer. Adsorptionen av CPAM på kiseloxidytor studeras med stagnationspunkts-reflektometri och kvartskristalls-mikrogravimetri för att bestämma adsorptionskinetiken och mättnadsadsorptionens beroende av polyelektrolytens laddningstäthet, pH och NaCl koncentration. Konformationen hos adsorberade skikt av CPAM och Cdextran bestämdes både före och efter sekundär tillsats av kolloidal kiselsyra (CS) och adsorptionen av CS kvantifierades också som funktion av yttäckningen av polyelektrolyt. Resultaten indikerar att laddningstätheten hos CPAM kontrollerar den adsorberade mängden på kiseloxidytor vid låga NaCl koncentrationer. Både adsorptionen av CPAM och Cdextran på kiseloxid visades vara effektiv i NaCl koncentrationer upp till 1 M, vilket indikerar ett signifikant bidrag av icke-jonisk interaktion mellan polyelektrolyterna och kiseloxid. Adsorptionen av CS var högre på föradsorberad CPAM än Cdextran. Konformationen hos de adsorberade skikten efter tillsats av CS sågs expandera signifikant för skikt baserade på CPAM medan skikt av Cdextran vid låga salthalter verkade återta sin konformation efter en temporär expansion. I den andra delen av avhandlingen studerades sekventiell adsorption av PAE och CMC på massafibrer. Adsorptionsisotermer skikt för skikt på avkryllad massa visade att PAE adsorberade i större mängd än CMC, både i hänseende av massa och laddning. Adsorptionen av PAE var signifikant långsammare än CMC och adsorptionstiden till 90% av mättnadsadsorptionen bestämdes till 3 respektive 1 minut. Zetapotentialen för kryll bestämdes för adsorption av de två första polyelektrolytskikten och resultaten tydde på att kryllmaterialet omladdade inom en minut efter tillsatserna av polyelektrolyt. Reflektometriförsök inom sekventiell adsorption av PAE och CMC på kiseloxid antydde att den låga molekylviktsfraktionen av PAE störde uppbyggnaden av polyelektrolyt-multiskikten. / This thesis presents experimental studies of polyelectrolyte adsorption on oppositely charged surfaces, where substrates of both silica and bleached softwood kraft pulp were used. A major aim of this research was to characterise the conformation of adsorbed layers of cationic polyacrylamide (CPAM), in comparison to cationic dextran (Cdextran), and relate this information to the binding capacity of colloidal silica. A second aim in this thesis was to study the kinetics of the sequential adsorption of polyamide epichlorohydrine (PAE) and carboxymethyl cellulose (CMC) on pulp fibres, and to determine the adsorption isotherms for the layer-by-layer deposition of polyelectrolytes on pulp fibres. The adsorption of CPAM on silica surfaces was studied using stagnation point adsorption reflectometry and quartz crystal microgravimetry to determine its adsorption kinetics as well as the dependencies of polyelectrolyte charge densities, pH, and NaCl concentration on saturation adsorption. The conformation of adsorbed layers of CPAM and Cdextran, analysed in terms of amount of water and layer thickness, was determined both before and after the secondary adsorption of colloidal silica (CS), and the adsorption of CS was also quantified as a function of the surface coverage of the polyelectrolyte. Results indicate that the charge density of CPAM controlled the amount of the polyelectrolyte adsorbed on silica surfaces at low NaCl concentrations. The adsorption of both CPAM and Cdextran on silica was shown to be effective at up to 1 M NaCl concentrations, which indicates that non-ionic interactions between the polyelectrolytes and silica contribute significantly. CS adsorption was higher on pre-adsorbed CPAM than on Cdextran. The conformation of the adsorbed layer after CS addition was seen to expand significantly in CPAM-based layers, while the Cdextran layer appeared to restore its conformation after a temporary expansion at low salt concentrations. In the second part of the thesis, the sequential adsorption of PAE and CMC on pulp fibres was determined using the polyelectrolyte titration technique. Layer-by-layer adsorption isotherms derived on fractionated pulp showed that PAE adsorbed in higher amounts than CMC did, both in terms of adsorbed mass and adsorbed charge. The adsorption of PAE was significantly slower compared to CMC, and the adsorption times required to reach 90% of the saturation adsorption were 3 and 1 min, respectively. The zeta potential of pulp fines was determined for the adsorption of the two first polyelectrolyte layers, and data indicated that the fines recharge within one minute after the polyelectrolyte additions. Reflectometry experiments regarding the sequential adsorption of PAE and CMC on silica indicated that the low-molecular-weight fraction of PAE disturbed the formation of polyelectrolyte multilayers. / QC 20101112