Aim: To examine the reaction of extreme preterm infants with regarding to body temperature and transepidermal water loss during skin-to-skin care according to Kangaroo Mother Care (KMC) during the infant’s first week of life. Method: This was a descriptive quantitatively designed study, which was a pilot study within the framework of a larger project. Nine children, with a median gestational age of 24.91 weeks, were examined by measuring body temperature (axilla and skin temperature) as well as transepidermal water loss before, during and after KMC. Results: The study showed that skin temperature tended to rise during KMC, especially for those children who were nursed with KMC for more than 60 minutes. Eight out of nine children had, after completing KMC, a normal axilla temperature. As was expected, transepidermal water loss was elevated when measured both pre and post test. Despite this, the children showed normal body temperature. Conclusion: The results of the study support that KMC can create a micro-climate that, for at least one hour, makes it possible for even extreme preterm infants to maintain a body temperature within the normal range during their first week of life.

<p>The visible light photon counter (VLPC) is a high quantum efficiency (QE), Si-based, single-photon detector with high gain, low-noise multiplication, low timing jitter, and photon number resolution. While the VLPC has high QE in the visible wavelengths, the QE in the ultraviolet and infrared is low due to minimal absorption within the active layers of the device. In the ultraviolet, the absorption coefficient of Si is high and most of the incident photons are absorbed within the top contact of the device, whereas, in the infrared, Si is practically transparent. A number of applications in quantum information science would benefit from use of the VLPC if the QE was improved in the ultraviolet (e.g., state detection of trapped ions) and the infrared (e.g., long-distance quantum cryptography). This thesis describes the development of the ultraviolet photon counter (UVPC) and the infrared photon counter (IRPC), which are modified versions of the VLPC with increased QE in the ultraviolet and infrared wavelengths, respectively. The UVPC has a transparent metal Schottky contact to reduce absorption within the top contact of the VLPC, resulting in an increase in the QE in the ultraviolet by several orders of magnitude. The IRPC is a proposed device that has an InGaAs absorption layer that is wafer-fusion bonded to the VLPC. The band alignment of the resulting InGaAs/Si heterojunction is measured and shows a large discontinuity in the valence band that impedes carrier transport at the interface. A ultra-high vacuum wafer-bonding system was developed to understand the impact of the surface chemistry of the bonded wafers on the band alignment of the InGaAs/Si heterojunction of the IRPC.</p> / Dissertation

No description available.

No description available.

In an approach to creating molecular-scale structures on glass surfaces via self assembly, a strongly-dimerizing ureido-[2-(4-pyrimidone)] (UPy) quadruple hydrogen-bonding array was chemically immobilized on silica surfaces by way of a triethoxysilane functionality. The unreacted surface silanols were then thoroughly passivated with a monofunctional organosilane, resulting in isolated UPy binding sites on the glass surface. These binding sites were found to selectively bind the strongly fluorescent perylenediimide (PDI) functionalized UPy molecules from solution, thus non-covalently linking the fluorophore to the surface. The association between the self-complementary molecules was exceptionally strong, both in solution and at the surface, such that effective hydrogen-bonding was retained after most solvent treatments. The binding was also reversible, however, so that washes with polar protic and dipolar aprotic solvents with high hydrogen-bonding capabilities, such as water, alcohols, and DMSO, resulted in the removal of the non-covalently bound fluorophore-tagged UPy. The UPy:UPy dimer system was also investigated in solution, using pyrene intramolecular excimer formation as a monitor of the dissociation of the pyrene heterodimers into homodimers incapable of forming excimers at micromolar concentrations. In addition, the energy transfer process in solution between pyrene and perylenediimide fluorophores linked through UPy dimerization was studied, with the intention using FRET-based measurements on the surface at single-molecule levels in order to determine the distances between UPy binding sites. Energy transfer was found to occur, but the observed photophysical behavior was complicated by possible secondary processes, which steady-state fluorescence measurements were unable to elucidate. The benefit of using this UPy system for attaching molecules to a surface lies in its reversibility of binding and versatility in manner of molecules which van be retained on the modified surface with a strong association. In this way molecular-scale features could conceivably be constructed on a surface by self-assembly, with the option of further chemical reactions to lock them in place, thus creating structures beyond the accessibility range of the conventional lithographic methods.

The paper industry utilizes fillers either to reduce the cost or to provide desired functional or end-use properties of paper products. However, there are disadvantages associated with higher filler loadings beyond a certain level, which reduces paper strength. The present study focused on improving the physical property of filled papers. Three methods of structuring fillers were designed; precipitation with starch, complexation with starch and fatty acid, and regeneration with cellulose. Because cellulose and starch have hydroxyl groups on the chemical structure, the hydrogen bonding between fillers and wood fibers is assumed to be occurred by structuring fillers. For starch application, we used two different approaches; salt precipitation and fatty acid complexation. The cooked starch can be precipitated by certain salt solutions such as (NH4)2SO4. Also, the cooked starch can be complexed with fatty acid to produce an insoluble crystalline structure. When starch composites with clay made by both methods were put into the furnish as fillers, dramatic strength improvement was achieved such as 100-200% gains in tensile strength. This is due to the strong bonding between clay fillers and wood fibers, which is determined by Z-directional tensile strength. One of advantages is that using the starch-fatty acid complex has an inherent water repellent property, sizing effect. For cellulose as a bonding material, N-methylmorpholine-N-oxide was used as a solvent to dissolve the cellulose. The advantage of using this method is that we can use the low grade cellulose. The physical properties of the cellulose coated clay handsheets were significantly improved, but optical properties such as brightness and opacity were inferior to the hadnsheets filled with starch-clay composites due to relatively large particle size. In order to model the strength improvement by the composite filler, BDT theory, which is a modified Pages Equation, was used. After calculating the factors such as surface area and specific bond strength, the model matched well with the experimental results. Using this model, the tensile strength improvement could be predicted in terms of the change of bond strength and composite size.

As some companies in the paper industry struggle to shift from commodity grades to value added products, technical challenges and opportunities have grown tremendously. These new products require more stringent manufacturing specifications and improved performance relative to those of lignocellulosic fibers currently being produced. Hence, topochemical and mechanical modifications of pulp fibers have moved to the forefront of many corporate strategies. Researchers are beginning to develop new tools to help better understand the fundamental mechanisms of fiber modifications and how to most efficiently apply them. Two novel approaches are presented. First, a new method to observe single fiber crossings is developed. It was found that refining reduces the stepheight in the fiber crossing for both hardwood and softwood kraft pulps by increasing the tendency of the fibers to collapse, deform, and assume a lens like shape. The effect of pulp type, bleaching, drying, wet pressing, and fiber charge were also investigated. Graphs of stepheight versus freespan were linear through the origin suggesting that the freespan (flexibility) of the crossing fiber is largely unimportant to the formation of fiber crossings. Quite surprisingly, the ratio of stepheight to freespan remained relatively constant no matter the treatment. Only bleaching and the addition of surface charge via CMC had any independent impact on freespan. The data do not fit bending or shear mechanisms that have been developed in the literature suggesting that another mechanism may be responsible for the deformation behavior of single fiber crossings. Also, a method employing fluorescence microscopy and fluorescence resonance energy transfer is used to image the areas of a fiber-fiber interface while they were bonded. Analysis of the FRET signal from fiber crossings indicate that wet pressing increased the FRET occurring between the two dyed fiber surfaces. The results are consistent with the increased amount of interdiffusion expected with higher levels of wet pressing. Two novel techniques are used to investigate fundamental aspects of fiber deformation behavior and fiber-fiber bond formation. As these methods are further refined and utilized they will provide new avenues for researchers to explore and expand the property space of fibers and paper sheets.

The material properties of fibre networks and fibre reinforced composites are strongly influenced by fibre-fibre interactions. Stress transfer between load bearing elements in such materials is often dictated by the nature of the fibre-fibre interface. Inter-fibre bonding is solely responsible for internal cohesion in paper, because all stresses transferred between fibres operate through fibre-fibre bonds. . The future development of cellulosic fibre materials will require an improved understanding of the fibre-fibre interface. Fluorescence resonance energy transfer (FRET) was proposed as a new tool for the study of fibre interfaces. A protocol for covalent linkage of fluorophores to natural and regenerated cellulosic fibres was developed and the absorptive and emissive properties of these dyes were characterized. The fluorescent response of these dyed fibres in paper sheets was studied using steady-state fluorescence spectroscopy. Fluorescence micrographs of fibre crossings on glass slides were analyzed using the FRETN correction algorithm. Energy transfer from coumarin dyed fibres to fluorescein dyed fibres at the interface was observed. The FRETN surfaces for spruce and viscose rayon fibre crossings were distinctly different. The FRET microscopy method was able to detect statistically significant differences in spruce fibre interface development when fibre fraction and wet pressing were varied. The coalescence of natural cellulosic fibre interfaces during drying was also observed with the technique. Polysaccharide films were employed as model systems for the natural and regenerated cellulose fibre interfaces. It was found that pressing cellulose films did not result in significantly increased FRETN either due to resistance to deformation or the inability to participate in interdiffusion. Conversely, xylan films demonstrated a drastic increase in the FRETN signal with increased wet pressing. These results support the previously observed differences between regenerated cellulose fibres and natural wood fibres. The results of the FRETN analysis of the polysaccharide film model systems suggest that lower molecular weight amorphous carbohydrates are likely to be significant contributors to fibre interface development.

Microfluidics emerged during the early 1990s with channel networks in silicon or glass. Microprocessing of these materials is labor-intensive and time-consuming, it requires sophisticated equipment in a clean room, and often involves hazardous chemicals. The subsequent use of polymer greatly simplified the fabrication of microchips and led to the rapid development of the field. Polymer such as poly(dimethylsiloxane) (PDMS), has other attractive properties, such as being elastic (easy to make efficient microvalves), permeable to gases, and compatible with culturing biological cells. Despite these advantages, applications of PDMS chips are severely limited by a few drawbacks that are inherent to this material: (i) strong adsorption of molecules, particularly large biomolecules, onto its surface; (ii) absorption of nonpolar and weakly polar molecules into PDMS bulk; (iii) leaching of small molecules from PDMS bulk into solutions; and (iv) incompatibility with organic solvents. To overcome all these problems, Teflon plastics seem to be the perfect solution. They are well-known for their superior inertness to almost all chemicals and all solvents; they also show excellent resistance to molecular adsorption and molecule leaching from the polymer bulk to solutions. However, Teflon has a high chemical inertness of the surface, which is restricted the bonding temperature (>260¢XC).It is not conducive to the low-temperature packaging process. This study presents a simple and rapid process for sealing Teflon-based microfluidic chip at a temperature of 140oC which is lower than typical bonding temperature of 260oC. A simple ammonium plasma treatment is used to enhance the surface energy of Teflon substrates such that the bonding temperature can be greatly reduced. Results indicate that the ammonium plasma treated Teflon substrates can be sealed using hot press bonding at a temperature of 140oC for 20 min. The measured iv bonding strength for the Teflon-based microfluidic devices is higher than those bonded at a reported temperature of 260oC for 60 min. It shows the measured contact angle for the Teflon substrates treated with different plasmas. Results indicated that the ammonium hydroxide plasma exhibited the best wettability property and the contact angle reached the minimum value of 45o after 5 min of treatment. The ESCA analysis showed the best Defluorination by ammonium plasma. The fluorine/carbon atomic ratio degraded from 1.96 to 1.10 by 5 minutes. The measured bonding strength for the Teflon substrates bonded with different surface activation protocols. Results showed that the bonding strength was enhanced upto 93% after the plasma treatment. The plasma treatment not only enhanced the bonding strength but also reduced the bonding temperature and time. The measured surface roughness only increased 15¡Ó5 nm (Ra) after the plasma treatment, which is acceptable for most applications in microfluidic systems. Finally, the fluorescence optical architecture and cross-chip successfully detected and isolated £XX-174 fragment of DNA samples confirmed the Teflon substrate for the emerging microfluidic plastic chip. The developed method provides a simple and rapid way to fabricate Teflon-based microfluidic devices.

Three-dimensional (3D) polymer structures are very attractive because the extra structural dimension can provide denser integration and superior performance to accomplish complex tasks. Successful fabrication of 3D multilayer microstructures in thermoplastic polymers using optimized nanoimprint lithography techniques such as layer-transfer and transfer-bonding methods are developed in this dissertation work. The capability and flexibility of the techniques developed here are expected to have deep impact on the applications of soft materials such as polymers including functional polymers in micro- and nanofabricated devices and systems. Although NIL technique is developing rapidly in recent years, there are still issues that need to be addressed for broader adoption of the nanoimprint technique. One of the problems is the residual layer that remains in the polymer pattern after nanoimprint. The conventional approach, oxygen reactive-ion-etching (RIE) process, to remove the residual layers, increases the cost and lowers the overall throughput of the nanoimprint process. More severely, it can degrade or even damage the functional polymers. In order to overcome these problems, new residual layer removal techniques need to be developed. In this dissertation, two methods are newly developed, which do not negatively affect the chemistry of the polymer materials. The techniques are suitable for all thermoplastic polymers, particularly functional polymers. Another advantage of nanoimprint is its ability to directly create functional polymers structures. This is because thermal nanoimprint only needs temperature and pressure for pattern replication, which both are benign to functional polymers. This feature combined with newly developed techniques such as transfer-bonding and residue removal techniques opens up the possibilities in nondestructive functional polymers patterning at the micro- and nanoscale for novel applications in electronics, optoelectronics, photonics and bioengineering. Finally, several applications of 3D multilayer structures fabricated by the techniques developed in this dissertation are demonstrated. The first application is a multilayer metal-dielectric-metal structure with embedded microfluidic channels. This structure can be used as an on-chip tunable filter for integrated microfluidic applications. The second application is a multilayer microfluidic channels in which each layer has a different channel size. This device can be used for particle separation and filtration based on lateral fluid flow.