Modeling of feeding behavior of solidifying Al-7Si-0.3Mg alloy plate casting

The systematic change of riser size, together with the variation of geometries of solidifying Al-7Si-0.3Mg plate castings, was tested by thermal analysis to model the interdendritic feeding behavior based on Darcy’s law. This law, however, is found to be only applicable to certain thermal conditions in the solidifying casting. The applicability of Darcy’s law depends on the regime of solidification time. A new feeding efficiency parameter integrating all individual ther-mal variables, denoted as(G · t ^2/3)V_s (whereG is the thermal gradient,t is local solidification time, and V_{s i} is solidus velocity), is found satisfactory to predict the formation of porosity. The combined geometries of a casting and its riser size exert a great influence on the thermal vari-ables of Al-7Si-0.3Mg alloy in a complicated way. Together, these thermal variables synergize to govern the feeding behavior of the casting.     

Kinetics and mechanistic aspects of As(III) oxidation by aqueous chlorine, chloramines, and ozone: relevance to drinking water treatment

Kinetics and mechanisms of As(III) oxidation by free available chlorine (FAC-the sum of HOCl and OCl-), ozone (O3), and monochloramine (NH2Cl) were investigated in buffered reagent solutions. Each reaction was found to be first order in oxidant and in As(III), with 1:1 stoichiometry. FAC-As(III) and O3-As(III) reactions were extremely fast, with pH-dependent, apparent second-order rate constants, k'app, of 2.6 (+/- 0.1) x 10(5) M(-1) s(-1) and 1.5 (+/- 0.1) x 10(6) M(-1) s(-1) at pH 7, whereas the NH2Cl-As(III) reaction was relatively slow (k'app = 4.3 (+/- 1.7) x 10(-1) M(-1) s(-1) at pH 7). Experiments conducted in real water samples spiked with 50 microg/L As(III) (6.7 x 10(-7) M) showed that a 0.1 mg/L Cl2 (1.4 x 10-6 M) dose as FAC was sufficient to achieve depletion of As(III) to <1 microg/L As(III) within 10 s of oxidant addition to waters containing negligible NH3 concentrations and DOC concentrations <2 mg-C/L. Even in a water containing 1 mg-N/L (7.1 x 10(-5) M) as NH3, >75% As(III) oxidation could be achieved within 10 s of dosing 1-2 mg/L Cl2 (1.4-2.8 x 10(-5) M) as FAC. As(III) residuals remaining in NH3-containing waters 10 s after dosing FAC were slowly oxidized (t1/2 > or = 4 h) in the presence of NH2Cl formed by the FAC-NH3 reaction. Ozonation was sufficient to yield >99% depletion of 50 microg/L As(III) within 10 s of dosing 0.25 mg/L O3 (5.2 x 10(-6) M) to real waters containing <2 mg-C/L of DOC, while 0.8 mg/L O3 (1.7 x 10(-5) M) was sufficientfor a water containing 5.4 mg-C/L of DOC. NH3 had negligible effect on the efficiency of As(III) oxidation by O3, due to the slow kinetics of the O3-NH3 reaction at circumneutral pH. Time-resolved measurements of As(III) loss during chlorination and ozonation of real waters were accurately modeled using the rate constants determined in this investigation.     

Perfect-reconstruction filter banks having linear-phase FIR filterswith equiripple response

The design of equiripple linear-phase analysis and synthesis FIR filters of two-channel perfect-reconstruction (PR) filter banks is formulated as the minimization of a weighted peak-error under both linear inequality (arising from the desired responses of the analysis filters) and nonlinear equality (PR) constraints. The effectiveness of a proposed method to solve the design problem (a modified dual-affine scaling variant of Karmarkar's (1989) algorithm and an approximation scheme) is illustrated through several design examples     

Visualizing the effect of gold nanocages on absorption, imaging, and lower critical solution temperature phase transition of individual poly(NiPAM)-based hydrogel particles by near infrared multispectral imaging microscopy

We have successfully utilized the near-infrared multispectral imaging (NIR-MSI) microscope to observe and measure directly images and spectra of individual hydrogel particles alone or with added gold nanocages (GNs). The NIR-MSI is suited for this task because it can simultaneously record spectral and spatial information of a sample with high sensitivity (single pixel resolution) and high spatial resolution (～0.9 μm/pixel). Because both images and spectra of the individual particles can be directly and simultaneously measured by the microscope, it is possible to detect any changes in the spectroscopic properties and/or nature (size, volume) of individual hydrogel particles induced by external factors (e.g., temperature and/or pH). These features make it possible to determine lower critical solution temperature (LCST) values based on monitoring either changes in the NIR spectra or the volume of the hydrogel particle in response to variations in temperature. More importantly, the measured volume transition temperature or LCST value is not of a collection of many hydrogel particles, but rather of individual hydrogel particles. GNs were found to significantly affect not only absorption but also images and properties of individual hydrogel particles. Specifically, GNs were found to enhance absorption of individual hydrogel particles, particularly the C-H band at 1716 nm, by about 25%. Of particular interest is the fact that not all individual hydrogel particles were enhanced by GNs; only about 50% of total number of particles were enhanced by GNs. GNs were also found to make it difficult to observe individual hydrogel particles, i.e., it seems that GNs defocused images of hydrogel particles. The defocusing effect by GNs might be due to photothermal generation of heat and vapor bubbles by the GNs. Of particular interest is the effect of GNs on the volume transition temperature of individual hydrogel particles. It seems that individual hydrogel particles lose their LCST in the presence of GNs, i.e., when heated, they undergo a gradual decrease in the volume but do not exhibit any clear and observable discontinued phase transition temperature.     

Simultaneous measurement of one- and two-photon excited fluorescence from a single sample: a detection method for oligonucleotides

A new method has been developed that is based on the use of a single-excitation wavelength from a cw laser to excite simultaneously one-photon and two-photon fluorescence (TPF). Fluorescence bands of a sample containing two oligonucleotides, one labeled with a one-photon fluorescence dye and the other with a TPF dye, can be measured simultaneously. The two fluorescence bands are well separated, because the one-photon excited fluorescence band is redshifted, whereas the TPF band is blueshifted from the excitation wavelength. The spectral separation was found to be as large as 200 nm when ADS 840NCS was used to label one oligonucleotide for one-photon fluorescence and Rhodamine Red-X dye was used for TPF. Spectral overlapping problem that plagues current DNA sequencing techniques can be eliminated effectively with this method.     

Visualizing chemical compositions and kinetics of sol-gel by near-infrared multispectral imaging technique

Kinetics of sol-gel formation were studied using the recently developed near-infrared (NIR) multispectral imaging instrument. This imaging spectrometer possesses all the advantages of conventional spectrometers. It also has additional features that NIR spectrometers cannot offer, namely, its ability to provide kinetic information at different positions within a sample. The high spatial resolution and sensitivity of the InSb camera make it possible for the imaging spectrometer to determine the kinetic from data recorded by a single pixel. Kinetics of sol-gel reactions, determined by this multispectral imaging instrument, show that the initial hydrolysis of the TEOS, MTES, or a mixture of these two alkoxysilanes is relatively inhomogeneous. The inhomogeneity is dependent on the number of pixels used to calculate the spectrum for each spot. Data calculated from a single pixel provide the largest inhomogeneity. No inhomogeneity was observed when an average of a large number of pixels (e.g., 10 x 10) is used for calculation. The inhomogeneities observed for TEOS sol-gels are different from those for the MTES sol-gels, and those for sol-gels prepared from a mixture of TEOS and MTES are relatively larger and more similar to those of the MTES sol-gels. A variety of reasons might account for the observed inhomogeneities including differences in the structure of the TEOS sol-gels and MTES sol-gels and the inability of the TEOS to mix well with MTES with the latter being more hydrophobic.     

Determination of binding constants of cyclodextrins in room-temperature ionic liquids by near-infrared spectrometry

Near-infrared spectrometry has been successfully used to determine association binding constants between phenol and alpha-, beta- and gamma-cyclodextrin (CD) in [butylmethylimidazolium][chloride] room-temperature ionic liquid (RTIL). It was found that adding CD into the RTIL solution of phenol resulted in an enhancement in the absorption coefficient of the stretching overtone of the aromatic C-H groups. However, the enhancement induced by CDs in RTIL is much lower (order of magnitude) than those corresponding in D20. The binding constants in RTIL are also much lower than those in D2O ((11 +/- 2), (16 +/- 2), and (40 +/- 6) M(-1) for phenol and alpha-, beta- and gamma-CD, respectively, as compared to 87 and 214 M(-1) for a- and beta-CD in D2O). The results obtained seem to suggest that in ionic liquid, the main interaction between phenol and CDs may not be inclusion complex formation but rather external adsorption. A variety of reasons may be responsible for relatively weaker interactions and lower binding constants in the ionic liquid, including differences in the polarity and viscosity of RTIL and D20. However, the main reason may be due to the possibility that the 1-butyl-3-methylimidazolium cation of the ionic liquid may form inclusion complexes with CDs either through its imidazolium moiety or its butyl group. Such complex formation would prevent phenol from being included in the cavity of the CDs.     

Absorption of water by room-temperature ionic liquids: effect of anions on concentration and state of water

Near-infrared (NIR) spectrometry was successfully used for the non-invasive and in situ determination of concentrations and structure of water absorbed by room-temperature ionic liquids (RTILs). It was found that RTILs based on 1-butyl-3-methylimidazolium, namely, [BuMIm]+ [BF4]-, [BuMIm]+ [bis((trifluoromethyl)sulfonyl)amide, or Tf2N]- and [BuMIm]+ [PF6]-, are hydroscopic and can quickly absorb water when they are exposed to air. Absorbed water interacts with the anions of the RTILs, and these interactions lead to changes in the structure of water. Among the RTILs studied, [BF4]- provides the strongest interactions and [PF6]- the weakest. In 24 hours, [Bu-MIm]+ [BF4]- can absorb up to 0.320 M of water, whereas [Bu-MIm]+ [PF6]- can only absorb 8.3 x 10(-2) M of water. It seems that higher amounts of water can be absorbed when the anion of the RTIL can strongly interact and hence stabilize absorbed water molecules by forming hydrogen bonds with them or inducing hydrogen bonds among water molecules. More importantly, the NIR technique can be sensitively used for the noninvasive, in situ determination of absorbed water in RTILs, without any pretreatment, and at limits of detection as low as 3.20 x 10(-3) M.     

A portable medical system using real-time streaming transport over 3G wireless networks

The paper proposes architecture for the software implementation of a multimedia, tele-medicine system. It considers video streaming from both video servers in hospitals and webcams localized to patients. It also considers transmission of vital bio-signs, such as heart rates and blood pressure, etc. All these data are transmitted over a 3G-wireless communication system to various client devices (hand-held devices, such as PDAs) used by physicians and nurses. Our video codec is a software implementation of the MPEG-4 standard, compression rate at about 1/24 sizes suited for available transmitting bandwidth. Moreover, our design, which also integrates the processing of heart sounds, supports a 44.1 KHz sampling rate and a 16-bit representation required about 11 kbps bandwidth. At the same time, in the streaming process, we propose a congestion control scheme to reduce packet losses.     

Minimax design of two-channel low-delay perfect-reconstruction FIRfilter banks

The authors deal with the design problem of low-delay perfect-reconstruction filter banks for which the FIR analysis and synthesis filters have equiripple magnitude response. Based on the minimax error criterion, the design problem is formulated in such a manner that the coefficients for the FIR analysis filters can be found by minimising the weighted peak error of the designed analysis filters, subject to the perfect-reconstruction constraints. A design technique based on a modified dual-affine scaling variant of Karmarkar's (1989) algorithm, in conjunction with approximation schemes, is then developed for solving the resulting nonlinear optimisation problem. The effectiveness of the proposed design technique is demonstrated by several simulation examples