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Characterization Data (characterization + data)

Distribution by Scientific Domains

Polymers and Materials Science	50%
Chemistry	37%

Selected Abstracts

Estimation of Ultrafilter Performance Based on Characterization Data

CHEMICAL ENGINEERING & TECHNOLOGY (CET), Issue 8 2007
Reid A. Peterson
Abstract Because of limited availability of test data with actual Hanford tank waste samples, a method was developed to estimate expected filtration performance based on physical characterization data for the Hanford Waste Treatment and Immobilization Plant in Richland, Washington. A test with simulated waste was analyzed to demonstrate that filtration of this class of waste is consistent with a concentration polarization model. Subsequently, filtration data from actual waste samples were analyzed to demonstrate that centrifuged solids concentrations provide a reasonable estimate of the limiting concentration for filtration. [source]

RF MEMS-based tunable filters

INTERNATIONAL JOURNAL OF RF AND MICROWAVE COMPUTER-AIDED ENGINEERING, Issue 5 2001
James Brank
Abstract This paper overviews the application of RF MEMS switches in tunable filters as well as circuit developments for bandpass filters covering 110 MHz to 2.8 GHz. RF MEMS have several desirable features, including small size, low power requirements, and low loss. The basic operation of Raytheon's RF MEMS capacitive membrane switch is described. An overview of the technique used to integrate the switch into a variable capacitor structure with sixteen capacitance states is provided. Variable capacitor structures are used to construct multipole lumped bandpass filter designs, each with sixteen states. Finally, measured data from two representative five- and six-pole bandpass filters are presented. Characterization data demonstrates that the insertion loss for the five-pole filter using on-chip inductors was between 6.6 and 7.3 dB, and between 3.7 and 4.2 dB for the six-pole filter using off-chip inductors. © 2001 John Wiley & Sons, Inc. Int J RF and Microwave CAE 11: 276,284, 2001 [source]

Crystallographic rationalization of the reactivity and spectroscopic properties of (2R)- S -(2,5-dihydroxyphenyl)cysteine

ACTA CRYSTALLOGRAPHICA SECTION C, Issue 4 2010
Gabriele Kociok-Köhn
At 150,K, the title compound, C9H11NO4S, crystallizes in the orthorhombic form as a zwitterion and has a low gauche conformation [, = ,46.23,(16)°] for an acyclic cysteine derivative. A difference in bond length is observed for the alkyl C,S bond [1.8299,(15),Å] and the aryl C,S bond [1.7760,(15),Å]. The ,NH3+ group is involved in four hydrogen bonds, two of which are intermolecular and two intramolecular. The compound forms an infinite three-dimensional network constructed from four intermolecular hydrogen bonds. Characterization data (13C NMR, IR and optical rotation) are reported to supplement the incomplete data disclosed previously in the literature. [source]

Raman spectroscopy for spinline crystallinity measurements.

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008

Abstract The original Doufas,McHugh two-phase microstructural/constitutive model for stress-induced crystallization is expanded to polyolefin systems and validated for its predictive capability of online Raman crystallinity and spinline tension data for two Dow homopolymer polypropylene resins. The material parameters,inputs to the model,are obtained from laboratory-scale material characterization data, that is, oscillatory dynamic shear, rheotens (melt extensional rheology), and differential scanning calorimetry data. The same set of two stress-induced crystallization material/molecular parameters are capable of predicting the crystallinity profiles along the spinline and fiber tension very well overall for a variety of industrial fabrication conditions. The model is capable of predicting the freeze point, which is shown, for the first time, to correlate very well with the measured stick point (i.e., the point in the spinline at which the fiber bundle converts from a solid-like state to a liquid-like state and sticks to a solid object such as a glass rod). The model quantitatively captures the effects of the take-up speed, throughput, and melt flow rate on the crystallization rate of polypropylene due to stress-induced crystallization effects. This validated modeling approach has been used to guide fiber spinning for rapid product development. The original Doufas,McHugh stress-induced crystallization model is shown to be numerically robust for the simulation of steady polypropylene melt spinning over a wide range of processing conditions without issues of discontinuities due to the onset of the two-phase constitutive formulation downstream of the die face, at which crystallization more realistically begins. Because of the capturing of the physics of polypropylene fiber spinning and the very good model predictive power, the approximations of the original Doufas,McHugh model are asserted to be reasonable. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]

Synthesis and properties of new aromatic poly(ester-imide)s derived from 4- p -biphenyl-2,6-bis(4-trimellitimidophenyl) pyridine and various dihydroxy compounds

POLYMER INTERNATIONAL, Issue 1 2007
Hossein Behniafar
Abstract A novel class of wholly aromatic poly(ester-imide)s, having a biphenylene pendant group, with inherent viscosities of 0.32,0.49 dL g,1 was prepared by the diphenylchlorophosphate-activated direct polyesterification of the preformed imide-ring-containing diacid, 4- p -biphenyl-2,6-bis(4-trimellitimidophenyl)pyridine (1) with various aromatic dihydroxy compounds in the presence of pyridine and lithium chloride. A reference diacid, 2,6-bis(trimellitimido)pyridine (2) without a biphenylene pendant group and two phenylene rings in the backbone, was also synthesized for comparison purposes. At first, with due attention to structural similarity and to compare the characterization data, a model compound (3) was synthesized by the reaction of compound 1 with two mole equivalents of phenol. Moreover, the optimum condition of polymerization reactions was obtained via a study of the model compound synthesis. All of the resulting polymers were characterized by Fourier transform infrared and 1H NMR spectroscopy and elemental analysis. The ultraviolet ,max values of the poly(ester-imide)s were also determined. All of the resulting polymers exhibited excellent solubility in common organic solvents, such as pyridine, chloroform, tetrahydrofuran, and m -cresol, as well as in polar organic solvents, such as N -methyl-2-pyrrolidone, N,N -dimethylacetamide, N,N -dimethylformamide, and dimethyl sulfoxide. The crystalline nature of the polymers obtained was evaluated by means of wide-angle X-ray diffraction. The resulting poly(ester-imide)s showed nearly an amorphous nature, except poly(ester-imide) derived from 4,4,-dihydroxy biphenyl. The glass transition temperatures (Tg) of the polymers determined by differential scanning calorimetry thermograms were in the range 298,342 °C. The 10% weight loss temperatures (T10%) from thermogravimetric analysis curves were found to be in the range 433,471 °C in nitrogen. Films of the polymers were also prepared by casting the solutions. Copyright © 2006 Society of Chemical Industry [source]

Synthesis and characterization of novel aromatic poly(amide-imide)s derived from 2,2,-bis(4-trimellitimidophenoxy)biphenyl or 2,2,-bis(4-trimellitimidophenoxy)-1,1,-binaphthyl and various aromatic diamines

POLYMER INTERNATIONAL, Issue 7 2003
Ahmad Banihashemi
Abstract New aromatic diimide-dicarboxylic acids having kinked and cranked structures, 2,2,-bis(4-trimellitimidophenoxy)biphenyl (2a) and 2,2,-bis(4-trimellitimidophenoxy)-1,1,-binaphthyl (2b), were synthesized by the reaction of trimellitic anhydride with 2,2,-bis(4-aminophenoxy)biphenyl (1a) and 2,2,-bis(4-aminophenoxy)-1,1,-binaphthyl (1b), respectively. Compounds 2a and 2b were characterized by FT-IR and NMR spectroscopy and elemental analyses. Then, a series of novel aromatic poly(amide-imide)s were prepared by the phosphorylation polycondensation of the synthesized monomers with various aromatic diamines. Owing to structural similarity, and a comparison of the characterization data, a model compound was synthesized by the reaction of 2b with aniline. The resulting polymers with inherent viscosities of 0.58,0.97 dl g,1 were obtained in high yield. The polymers were fully characterized by FT-IR and NMR spectroscopy. The ultraviolet ,max values of the poly(amide-imide)s were also determined. The polymers were readily soluble in polar aprotic solvents. They exhibited excellent thermal stabilities and had 10% weight loss at temperatures above 500 °C under a nitrogen atmosphere. Copyright © 2003 Society of Chemical Industry [source]

Polymerizability, copolymerizability, and properties of cyanoacrylate-telechelic polyisobutylenes II: copolymerization of three-arm star cyanoacrylate- telechelic polyisobutylene with ethyl cyanoacrylate,

POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 10 2007
Yongmoon Kwon
Abstract This research concerned the synthesis and characterization of novel conetworks containing polyisobutylene (PIB) and polyethyl-2-cyanoacrylate [poly(Et-CA)] sequences. The syntheses involved the copolymerization of CA-telechelic three-arm star PIB [Ø(PIB-CA)3] with ethyl-2-cyanoacrylate (Et-CA) mediated by nucleophiles or by living tissue (fresh eggs). The conetworks were characterized by swelling in hexanes, tetrahydrofuran (THF), and acetone, and the results indicate co-continuous PIB and poly(Et-CA) domains. The conetworks exhibit two Tgs indicating phase-separation between PIB and poly(Et-CA). The outstanding oxidative resistance of the conetworks was demonstrated by exposure to concentrated nitric acid. The tensile strengths, moduli, and elongations of a series of conetworks with different overall compositions were investigated and the findings interpreted in terms of covalently linked rubbery and glassy domains. AFM also suggests the presence of phase-separated rubbery and glassy domains. DMTA spectra of a Ø(PIB-CA)3 homonetwork, and Ø(PIB-CA)3/Et-CA conetworks were analyzed and interpreted in terms of coexisting rubbery and glassy domains. Observations made during the exposure of Ø(PIB-CA)3/Et-CA mixtures to proteinaceous tissue, in combination with characterization data, were used to propose a structural model for the conetworks. Copyright © 2007 John Wiley & Sons, Ltd. [source]