Characterization of α and γ polymorphs of glycine crystallized from water‐ammonia solution

Crystallization of metastable α and stable γ polymorphs of glycine was carried out from aqueous solution in the presence of ammonia. Pure aqueous solution and solution with lower concentration of ammonia yield α nucleation and solution with a critical concentration of ammonia yield γ nucleation. Variation in the solubility of glycine in double distilled water and pH of the resulting solution due to the ammonia incorporation was studied in a range of temperatures. The induction period for the α and γ nucleation in the solution was determined and its variation due to the ammonia incorporation was also studied. Single crystals of both the polymorphs were grown by slow evaporation method. Effect of ammonia concentration and the resultant pH of the solution on the nucleation, growth and morphology of the grown polymorphs were investigated. The unidirectional growth of the γ polymorph along the polar axis was revealed. X‐ray powder diffraction method was employed to distinguish both the polymorphs structurally. Their thermal stability above room temperature was studied by differential scanning calorimetry which revealed that the as‐grown γ polymorph transforms to α at 179.6 °C while the as‐grown α retains its phase until melting. The optical transmittance of the grown γ polymorph was studied in the UV‐Vis‐Near IR region. The second harmonic generation (SHG) efficiency of the grown γ polymorph was studied with a Nd:YAG laser source and is about 6.8% higher than that of the inorganic standard KDP. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Preparation,characterization, and conductivity of YLnTiZrO7 (Ln = La,Nd, Sm,and Eu)

The pyrochlore oxide of composition YLnTiZrO₇ (Ln?=?La, Nd, Sm, and Eu) was prepared by sol–gel method. All the samples were characterized by powder X-ray diffraction (XRD), Raman, X-ray photoelectron spectroscopy (XPS), diffused reflectance spectroscopy, and impedance spectroscopy. The powder XRD and Raman studies reveal that these samples were crystallized in cubic lattice with pyrochlore structure. The Rietveld analysis of the samples was carried out to obtain the unit cell parameters and reliability factors. The broad Raman bands observed for all the samples are due to cation/anion disorder in the lattice and nanosize. The XPS analysis of the samples shows the characteristic peaks belonging to Y³⁺, Ln³⁺ (Ln?=?La, Nd, Sm, and Eu), Ti⁴⁺, and Zr⁴⁺. Electrical conductivity of YLaTiZrO₇ (YLTZ) and YEuTiZrO₇ (YETZ) samples was calculated from the impedance as a function of frequency and temperature. These samples have shown conductivity of the order of 10^?5 scm^?1 at 500 °C.     

A general treatment of two dimensional plane flows,for a micropolar fluid

Summary In this paper we have studied the flow of a micropolar fluid, whose constitutive equations were given byEringen, in two dimensional plane flow. In two notes, we have discussed the validity of the boundary conditionv=a and its effect on the entire flow field. We have restricted our study to the case whenStokes' approximation is valid, i. e.slow motion for it is difficult to uncouple the equations in the most general case.

---

Zusammenfassung Gegenstand dieser Untersuchung ist die zweidimensionale ebene Strömung einer mikropolaren Flüssigkeit, deren rheologische Stoffgleichung vonEringen angegeben worden ist. In zwei Abschnitten werden die Gültigkeit der Randbedingungv=a und die daraus resultierenden Konsequenzen für das gesamte Strömungsfeld diskutiert. Wir haben unsere Untersuchung auf den Anwendungsbereich der Stokesschen Näherung (d. h. auf eine schleichende Strömung) beschränkt, da die Entkoppelung der Gleichungen im allgemeinsten Fall Schwierigkeiten bereitet.

     

Ion cyclotron instabilities in a mildly relativistic hydrogen-deuterium fusion plasma

A dispersion relation for the perpendicular propagation of the electromagnetic ion cyclotron wave around the second harmonic of the deuterium ion gyrofrequency in a mildly relativistic, anisotropic Maxwellian plasma with hydrogen as the majority species and deuterium as the minority component has been derived. The work has been carried out in the frame of reference of the majority hydrogen ions; to these ions the waves at 2Θ_D would be at its own gyrofrequency. Using a small quantityɛ to order all relevant parameters of the plasma, it was possible to derive the dispersion relations in a simple form. To the lowest order the relativistic factors do not enter the dispersion relation. The plasma can now support two modes—one above and the other below the hydrogen gyrofrequency in agreement with the assumptions. This was also verified numerically using a standard root solver thereby justifying the correctness of the ordering scheme. In the next higher order, the dispersion relation is a quartic equation and is sensitively dependent on the relativistic factors. The plasma can now support four modes, both above and below the hydrogen gyrofrequency and consistent with the ordering scheme used. However the modes can now coalesce resulting in complex conjugate roots to the dispersion relation thereby indicating an instability. The advantage of such a scheme is that two dispersion relations — one of which is independent of the relativistic factors and the other which is sensitively dependent on them can be separated out.     

Transition (Mn,Fe) and rare earth (La,Pr) metal doped ceria solid solutions for high performance photocatalysis: Effect of metal doping on catalytic activity

Research on Chemical Intermediates - In this work, various transition and rare earth metal ions (M3+; M = Mn3+, Fe3+, La3+, and Pr3+) doped CeO2 solid solutions were prepared by a...     

RETRACTED ARTICLE: Determination of sulpha drugs and ascorbic acid,individually or in mixture,withN-chlorosuccinimide

New spectrophotometric and titrimetric methods for the determination of sulphonamides withN-chlorosuccinimide (NCS) were developed. The spectrophotometric measurements can be made at 324–395 nm at pH 7.4 at room temperature, the stoichiometry being 1: 2, (p-H₂N-C₆H₄-SO₂NHR): (NCS) forming a dibromination product in presence of acidified potassium bromide. Potentiometrically or visually using methyl red as indicator, sulphonamides are titrated in pharmaceutical preparations by NCS always in presence of acidified potassium bromide. Ascorbic acid is determined alone and also in combinations, by first titrating it using potassium iodide and starch or 2,6-dichlorophenolindophenol as indicator. Acylation or diazotization of the aromatic amino groups that prevents substitution at the two ortho positions, is used as additional prereaction to analyze various binary and ternary mixtures of certain sulphonamides. These methods are accurate, simple, rapid, reproducible, useful at higher concentrations, do not involve any preseparation, and can tolerate several compounds that cause interference in other methods.Paper presented at the Eastern Analytical Symposium, New York, USA, 1985, No. 168     

Measurement of polyunsaturated fatty acids of myocardial lipids by high performance liquid chromatography

Summary This report describes a modified method for the separation and analysis of polyunsaturated fatty acids such as 20:4, 20:5, and 22:6, using HPLC. The results show that these fatty acids are well separated from the saturated acids. Since the unsaturated fatty acids elute earlier than saturated acids, and this method does not require the fractionation of free fatty acids using thin layer chromatography, a necessary step for the gas chromatographic analysis, the recoveries of polyunsaturated fatty acids were significantly higher as compared to those from gas chromatography. Furthermore, HPLC and gas chromatographic methods gave identical results for the acyl chain composition of phosphatidylserine. The advantages of using HPLC over gas chromatography in determining the acyl chain composition of free fatty acids and phospholipids are also discussed.     

Investigation of kinetics of curing of triglycidyl-p-aminophenol with aromatic diamines by differential scanning calorimetry

The kinetics of curing of triglycidyl-p-aminophenol with four different diamines in stoichiometric amounts were investigated by means of differential scanning calorimetry. The results indicated that the curing reaction follows first-order Arrhenius kinetics with an activation energy in the range 40–70 kJ · mol^–1. The effect of the structure of the curing agent on the curing characteristics is discussed on the basis of the curing characteristics and the kinetic parameters. An epoxy fortifier was observed to lower the curing temperature of an epoxy-amine system when incorporated prior to curing.

---

Zusammenfassung Mittels Differential-Scanning-Kalorimetrie wurde die Kinetik der Vernetzung von Triglycidyl-p-aminophenol mit stöchiometrischen Mengen vier verschiedener Amine untersucht. Laut den Ergebnissen verläuft die Vernetzungsreaktion mit einer Arrhenius-Kinetik erster Ordnung, wobei die Aktivierungsenergie im Bereich von 40–70 kJ/mol liegt. Auf Grundlage der Vernetzungscharakteristika und der kinetischen Parameter wird der Einfluss der Struktur des Vernetzungsreagenz auf die Vernetzungskenndaten beschrieben. Mit einem vor der Vernetzung eingebrachten Epoxyfortifyers konnte die Vernetzungstemperatur eines Epoxy-Amin-Systemes heruntergesetzt werden.

---

-- , . , 40–70 ·^–1. . , , , .

---

---

One of the authors (R.D.P.) is grateful to the University Grants Commission, New Delhi, for the award of a Research Associateship under the Special Assistance Programme.     

Studies in spiroheterocycles. Part XIII. Synthesis of a novel spiro system: Spiro[9H-acridine-9,3′-[3h]indol]-2′(1′H)-one and related compounds from new fluorinated spiro[3H-indole-3,9′-[9H]xanthen]-2(1H)-ones

A new spiroheterocyclic system spiro[9H-acridine-9,3′-[3H]indol]-2′(1′H)-one and related compounds have been prepared by the reaction of spiro[3H-indole-3,9′-[9H]xanthen]-2(1H)-ones with aromatic amine or ammonium acetate. The latter were prepared by heating fluorinated indole-2,3-diones with m-/p-cresols or α-naphthol in the presence of sulphuric acid at 230-240°. The synthesized compounds have been characterized on the basis of their elemental analyses, ir, nmr (1_H, 13_C, 19_F) and mass spectral data.