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Desenvolvimento de micropartículas de xilana utilizando reticulante não tóxico visando a liberação cólon-específicaCosta, Silvana Cartaxo da 23 May 2014 (has links)
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Previous issue date: 2014-05-23 / The development of a colon-specific delivery system using polymeric microparticles
has received great attention in the pharmaceutical field. An interesting group of
polymers with potential properties in this area are the hemicellulose. Xylan is a
hemicellulose that has the ability to pass through the digestive tract unchanged and its
complex structure requires enzymes that are produced specifically by the human colonic
microflora, which makes it an interesting raw material in the production of target drug
delivery systems. The microparticulate systems can be developed by various techniques.
The interfacial crosslinking polymerization is one of the major techniques to produce
polysaccharide based microparticles. However, the use of highly toxic crosslinkers often
makes the use of this technique limited. The sodium trimetaphosphate (TSTP), a low
toxic crosslinking agent, has no adverse effects reported on human beings. The aim of
this study was to develop xylan microparticles using sodium trimetaphosphate. The
microparticles were characterized by optical microscopy, SEM, XRD and FT -IR. The
influence of different parameters on the diameter of the microparticles was analyzed
during their development. Toxicity studies against Artemia saline Leach were made to
compare the microparticles produced with terephthaloyl chloride and sodium
trimetaphosphate. Xylan microparticles showed to be spherical shape, well
individualized and with a smooth surface. All different parameters influenced the in size
of the microparticles. The FT-IR spectrum of microparticles was similar to xylan, but
with the presence of the peak at 1258 cm
-1
, which is typical of phosphate ester bonds,
that can be attributed to the bond between TSTP and xylan during the crosslinking
process. The xylan microparticles produced in this work showed no toxicity at the
concentration studied. It be concluded that TSTP was able to produce xylan
microparticles with well defined physicochemical characteristics and low toxicity. / O desenvolvimento de um sistema de liberação cólon-específica utilizando
micropartículas poliméricas têm recebido grande atenção no campo farmacêutico. Um
grupo interessante de polímeros com potenciais propriedades nessa área são as
hemiceluloses. A xilana é uma hemicelulose que tem a capacidade de passar através do
trato digestivo inalterada e sua complexa estrutura requer enzimas que são produzidas
especificamente pela microflora colônica humana, o que a torna uma interessante
matéria-prima na área produção de sistemas de liberação de fármacos. Os sistemas
microparticulados podem ser desenvolvidos por várias técnicas. A reticulação
polimérica interfacial é uma das principais técnicas para produção de micropartículas à
base de polissacarídeos. Porém o uso de reticulantes de alta toxicidade muitas vezes
torna o uso desta técnica limitada. O trimetafosfato de sódio (TSTP) é um reticulante de
baixa toxicidade, sem efeitos adversos relatados em seres humanos. Esse trabalho teve
como objetivo desenvolver micropartículas de xilana utilizando TSTP. As
micropartículas foram caracterizadas por microscopia óptica, MEV, DRX e FT-IR.
Estudos de toxicidade frente à artemia salina Leach foram feitos para comparar as
micropartículas produzidas com cloridrato de tereftaloíla e trimetafosfato de sódio. As
micropartículas de xilana apresentaram forma esférica, bem individualizada e com
superfície bem definida. Todos os diferentes parâmetros influenciaram no tamanho das
micropartículas. O espectro de FT-IR das micropartículas foi semelhante ao da xilana,
porém com a presença de um pico em 1258 cm
-1
, que é típico de ligações éster-fosfato,
que pode ser atribuído a ligação entre TSTP e a xilana durante o processo de
reticulação. As micropartículas de xilana produzidas neste trabalho não apresentaram
toxicidade na concentração estudada. Podemos concluir que o TSTP foi capaz de
produzir micropartículas de xilana com cracterísticas fisico-químicas bem definidas e de
baixa toxicidade.
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Studies on Poly(N,N-dimethylaminoethyl methacrylate) Composite Membranes for Gas Separation and PervaporationDu, Runhong January 2008 (has links)
Membrane-based acid gas (e.g., CO2) separation, gas dehydration and humidification, as well as solvent dehydration are important to the energy and process industries. Fixed carrier facilitated transport membranes can enhance the permeation without compromising the selectivity. The development of suitable fixed carrier membranes for CO2 and water permeation, and understanding of the transport mechanism were the main objectives of this thesis.
Poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) composite membranes were developed using microporous polysulfone (PSF) or polyacrylonitrile (PAN) substrates. The PDMAEMA layer was crosslinked with p-xylylene dichloride via quaternization reaction. Fourier transform infrared, scanning electron microscopy, adsorption tests, and contact angle measurements were conducted to analyze the chemical and morphological structure of the membrane. It was shown that the polymer could be formed into thin dense layer on the substrates, while the quaternary and tertiary amino groups in the side chains of PDMAEMA offered a high polarity and hydrophilicity.
The solid-liquid interfacial crosslinking of PDMAEMA led to an asymmetric crosslinked network structure, which helped minimize the resistance of the membrane to the mass transport. The interfacially formed membranes were applied to CO2/N2 separation, dehydration of CH4, gas humidification and ethylene glycol dehydration. The membranes showed good permselectivity to CO2 and water. For example, a CO2 permeance of 85 GPU and a CO2/N2 ideal separation factor of 50 were obtained with a PDMAEMA/PSF membrane at 23oC and 0.41 MPa of CO2 feed pressure. At 25oC, the permeance of water vapor through a PDMAEMA/PAN membrane was 5350 GPU and the water vapor/methane selectivity was 4735 when methane was completely saturated with water vapor. On the other hand, the relative humidity of outlet gas was up to 100 % when the membrane was used as a hydrator at 45oC and at a carrier gas flow rate of 1000 sccm. For used for dehydration of ethylene glycol at 30oC, the PDMAEMA/PSF membrane showed a permeation flux of ~1 mol/(m2.h) and a permeate concentration of 99.7 mol% water at 1 mol% water in feed.
This work shows that the quaternary and tertiary amino groups can be used as carriers for CO2 transport through the membrane based on the weak acid-base interaction. In the presence of water, water molecules in the membrane tend to form a water "path" or water "bridge" which also help contribute to the mass transport though the membrane. In addition, CO2 molecules can be hydrated to HCO3-, which reaction can be catalyzed by the amino groups, the hydrated CO2 molecules can transport through the water path as well as the amino groups in the membrane. On the other hand, for processes involving water (either vapor or liquid) permeation, the amino groups in the membrane are also helpful because of the hydrogen bonding effects.
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Studies on Poly(N,N-dimethylaminoethyl methacrylate) Composite Membranes for Gas Separation and PervaporationDu, Runhong January 2008 (has links)
Membrane-based acid gas (e.g., CO2) separation, gas dehydration and humidification, as well as solvent dehydration are important to the energy and process industries. Fixed carrier facilitated transport membranes can enhance the permeation without compromising the selectivity. The development of suitable fixed carrier membranes for CO2 and water permeation, and understanding of the transport mechanism were the main objectives of this thesis.
Poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) composite membranes were developed using microporous polysulfone (PSF) or polyacrylonitrile (PAN) substrates. The PDMAEMA layer was crosslinked with p-xylylene dichloride via quaternization reaction. Fourier transform infrared, scanning electron microscopy, adsorption tests, and contact angle measurements were conducted to analyze the chemical and morphological structure of the membrane. It was shown that the polymer could be formed into thin dense layer on the substrates, while the quaternary and tertiary amino groups in the side chains of PDMAEMA offered a high polarity and hydrophilicity.
The solid-liquid interfacial crosslinking of PDMAEMA led to an asymmetric crosslinked network structure, which helped minimize the resistance of the membrane to the mass transport. The interfacially formed membranes were applied to CO2/N2 separation, dehydration of CH4, gas humidification and ethylene glycol dehydration. The membranes showed good permselectivity to CO2 and water. For example, a CO2 permeance of 85 GPU and a CO2/N2 ideal separation factor of 50 were obtained with a PDMAEMA/PSF membrane at 23oC and 0.41 MPa of CO2 feed pressure. At 25oC, the permeance of water vapor through a PDMAEMA/PAN membrane was 5350 GPU and the water vapor/methane selectivity was 4735 when methane was completely saturated with water vapor. On the other hand, the relative humidity of outlet gas was up to 100 % when the membrane was used as a hydrator at 45oC and at a carrier gas flow rate of 1000 sccm. For used for dehydration of ethylene glycol at 30oC, the PDMAEMA/PSF membrane showed a permeation flux of ~1 mol/(m2.h) and a permeate concentration of 99.7 mol% water at 1 mol% water in feed.
This work shows that the quaternary and tertiary amino groups can be used as carriers for CO2 transport through the membrane based on the weak acid-base interaction. In the presence of water, water molecules in the membrane tend to form a water "path" or water "bridge" which also help contribute to the mass transport though the membrane. In addition, CO2 molecules can be hydrated to HCO3-, which reaction can be catalyzed by the amino groups, the hydrated CO2 molecules can transport through the water path as well as the amino groups in the membrane. On the other hand, for processes involving water (either vapor or liquid) permeation, the amino groups in the membrane are also helpful because of the hydrogen bonding effects.
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