Liquid-liquid equilibria for four ternary systems containing methanol and cyclohexane

Nagata, I., 1984. Liquid-liquid equilibria for four ternary systems containing methanol and cyclohexane. Fluid Phase Equilibria, 18: 83–92.Liquid-liquid equilibria have been obtained experimentally for the systems methanol-benzene-cyclohexane, methanol-toluene-cyclohexane, methanol-acetone-cyclohexane and methanol-2-propanol-cyclohexane at 298.15 K. The experimental results are compared with predicted values obtained from the UNIQUAC and extended UNIQUAC equations.     

Vapor—liquid equilibria for the ternary Ethanol—2-butanone—benzene system at 298.15 K

Vapor—liquid equilibrium data for the ternary ethanol—2-butanone—benzene system and its constituent binary systems at 298.15 K are presented. The results are correlated with the Wilson, original and modified UNIQUAC equations and the UNIFAC group contribution method.     

Biodegradable network elastomeric polyesters from multifunctional aliphatic carboxylic acids and poly(epsilon-caprolactone) diols

Biodegradable elastomeric network polyesters were prepared from multifunctional aliphatic carboxylic acids such as tricarballylic acid (Yt) or meso-1,2,3,4-butanetetracarboxylic acid (Xb) and poly(epsilon-caprolactone) (PCL) diols with molecular weights of 530, 1,250 and 2,000 g.mol-1. Prepolymers prepared by a melt polycondensation were cast from DMF solution and postpolymerized at 280 degrees C for various periods of times to form a network. The resultant films were transparent, flexible and insoluble in organic solvents. The network polyesters obtained were characterized by IR absorption spectra, WAXS, density measurement, DSC, and tensile test. YtPCL1250, and XbPCL1250 network polyester films showed good elastomeric properties with high ultimate elongation (540-590%), and low Young's modulus (2.5-3.3 MPa). The enzymatic degradation was estimated by the weight loss of network films in a buffer solution with Rhizopus delemar lipase at 37 degrees C. The degree and rate of degradation were significantly affected by the molecular weight of PCL diol, chemical structures of multifunctional aliphatic carboxylic acids and the morphology of network films. The changes in the solid states of network films during the degradation were also estimated by the results of DSC and WAXS. [see text]     

Photoluminescence of SrGa2S4:Sn,Re(=Ce, Gd) phosphors

The photoluminescence (PL) spectra, PL excitation spectra, color coordinates, and X-ray diffraction spectra are reported for SrGa₂S₄:Sn,Re(=Ce and Gd, respectively) phosphors. By mixing SrGa₂S₄:Sn,Ce phosphors with different Ce³⁺ concentrations, white emissions can be obtained under the excitation of a 340-nm UV LED. Emissions in the green to yellow color range can be obtained from SrGa₂S₄:Sn,Gd phosphors. The rare earth ions enhance the green emission band, which peaks at 534 nm, instead of the yellow one. The origin of this enhancement is discussed. The resonant energy transfer rates are estimated in the cases from Ce³⁺ to the green and yellow centers of Sn²⁺ and between the yellow centers and the green centers.     

A non-implication between fragments of Martin’s Axiom related to a property which comes from Aronszajn trees

We introduce a property of forcing notions, called the anti-, which comes from Aronszajn trees. This property canonically defines a new chain condition stronger than the countable chain condition, which is called the property .In this paper, we investigate the property . For example, we show that a forcing notion with the property does not add random reals. We prove that it is consistent that every forcing notion with the property has precaliber ℵ₁ and for forcing notions with the property fails. This negatively answers a part of one of the classical problems about implications between fragments of .     

Thermal behavior and structure of liquid-crystalline aromatic-aliphatic polyester/poly(tetramethylene oxide) block copolymers

The thermal behavior and structure of poly(hexamethylene p,p′-biben-zoate) (BB-6)/poly(tetramethyleneoxide) (PTMO) block copolymers (BB-6/PTMO) were studied using differential scanning calorimetry, polarizing optical microscopy, and wide-angle and small-angle x-ray diffractometry. As the PTMO fraction increases, BB-6 liquid crystallinity decreased and two transition temperatures [Tc→M (crystal-mesophase) and Tm→i (mesophase-isotropic melt)] move to lower temperatures. BB-6/PTMO containing less than 20 mol% of PTMO retains liquid crystallinity. The isotropic melt-mesophase transition exotherm of BB-6/PTMO in the cooling process moves to lower temperature with increasing PTMO. Contrary to the isotropic melt-mesophase transition, the mesophase-crystal transition exotherm moves to higher temperature, indicating that PTMO segments favor the molecular mobility of BB-6 segments. As the mole fraction of BB-6 increases, the texture indicative of the smectic liquid crystal is gradually disorganized. BB-6/PTMO containing more than 30 mol% of PTMO no longer forms the texture indicative of smectic liquid crystals.     

Sonochemical degradation of chlorophenols in water

Sonochemical degradation of dilute aqueous solutions of 2-, 3- and 4-chlorophenol and pentachlorophenol has been investigated under air or argon atmosphere. The degradation follows first-order kinetics in the initial state with rates in the range 4.5-6.6 microM min-1 under air and 6.0-7.2 microM min-1 under argon at a concentration of 100 microM of chlorophenols. The rate of OH radical formation from water is 19.8 microM min-1 under argon and 14.7 microM min-1 under air in the same sonolysis conditions. The sonolysis of chlorophenols is effectively inhibited, but not completely, by the addition of t-BuOH, which is known to be an efficient OH radical scavenger in aqueous sonolysis. This suggests that the main degradation of chlorophenols proceeds via reaction with OH radicals; a thermal reaction also occurs, although its contribution is small. The addition of appropriate amounts of Fe(II) ions accelerates the degradation. This is probably due to the regeneration of OH radicals from hydrogen peroxide, which would be formed from recombination of OH radicals and which may contribute a little to the degradation. The ability to inhibit bacterial multiplication of pentachlorophenol decreases with ultrasonic irradiation.     

Radial compression of an antiproton cloud for production of intense antiproton beams

We report here the radial compression of a large number of antiprotons ( approximately 5 x 10(5)) in a strong magnetic field under ultrahigh vacuum conditions by applying a rotating electric field. Compression without any resonant structures was demonstrated for a range of frequencies from the sideband frequency of 200 kHz to more than 1000 kHz. The radial compression achieved is a key technique for synthesizing and manipulating antihydrogen atoms and antiprotonic atoms.     

Stereospecific construction of a trans-1,4-diphosphacyclohexane skeleton

trans-1,4-Diphosphacyclohexanes were successfully synthesized by the stereospecific intramolecular coupling reaction of the optically active bisphosphine. This is a new route for the construction of the trans-1,4-diphosphacyclohexane skeleton. A cis isomer was also prepared along with the trans isomer from a mixture of rac- and meso-bisphosphines. The coordinated boranes were easily removed to afford the corresponding 1,4-diphosphacyclohexanes.     

Structures of [(CO2)n(CH3OH)m](-) (n = 1-4, m = 1, 2) cluster anions

The infrared photodissociation spectra of [(CO 2) n (CH 3OH) m ] (-) ( n = 1-4, m = 1, 2) are measured in the 2700-3700 cm (-1) range. The observed spectra consist of an intense broad band characteristic of hydrogen-bonded OH stretching vibrations at approximately 3300 cm (-1) and congested vibrational bands around 2900 cm (-1). No photofragment signal is observed for [(CO 2) 1,2(CH 3OH) 1] (-) in the spectral range studied. Ab initio calculations are performed at the MP2/6-311++G** level to obtain structural information such as optimized structures, stabilization energies, and vibrational frequencies of [(CO 2) n (CH 3OH) m ] (-). Comparison between the experimental and the theoretical results reveals the structural properties of [(CO 2) n (CH 3OH) m ] (-): (1) the incorporated CH 3OH interacts directly with either CO 2 (-) or C 2O 4 (-) core by forming an O-HO linkage; (2) the introduction of CH 3OH promotes charge localization in the clusters via the hydrogen-bond formation, resulting in the predominance of CO 2 (-).(CH 3OH) m (CO 2) n-1 isomeric forms over C 2O 4 (-).(CH 3OH) m (CO 2) n-2 ; (3) the hydroxyl group of CH 3OH provides an additional solvation cite for neutral CO 2 molecules.