Effect of Surfactants on the Immobilization of 4-(2-Pyridylazo)resorcinol on Silochroms

The effect of cationic surfactants (cetyltrimethylammonium bromide, cetylpyridinium bromide, and tetrabutylammonium perchlorate) and a nonionic surfactant (OP-7) on the conditions of the immobilization of 4-(2-pyridylazo)resorcinol (PAR) on three types of silica gel (Silochrom S-120 (200–350 m), Silochrom S-120 (315–500 m), and Silochrom S-80 (200–350 m)) was studied. It was found that OP-7 does not affect the adsorption of surfactants. The effect of cationic surfactants increases in the order tetrabutylammonium perchlorate < cetyltrimethylammonium bromide < cetylpyridinium bromide. The adsorption activity of silica gels increases in the order Silochrom S-120 (315–500 m) < Silochrom S-80 (200–350 m) < Silochrom S-120 (200–350 m). Cetylpyridinium bromide provides full immobilization of PAR on silica gel Silochrom S-120 (200–350 m) in the pH range 2–9.     

Ozone Production in the Positive DC Corona Discharge: Model and Comparison to Experiments

A numerical model of ozone generation in clean, dry air by positive DC corona discharges from a thin wire is presented. The model combines the physical processes in the corona discharge with the chemistry of ozone formation and destruction in the air stream. The distributions of ozone and nitrogen oxides are obtained in the neighborhood of the corona discharge wire. The model is validated with previously published experimental data. About 80% of the ozone produced is attributed to the presence of excited nitrogen and oxygen molecules. A parametric study reveals the effects of linear current density (0.1–100 A/cm of wire), wire radius (10–1000 m), temperature (300–800 K) and air velocity (0.05–2 m/s) on the production of ozone. The rate of ozone production increases with increasing current and wire size and decreases with increasing temperature. The air velocity affects the distribution of ozone, but does not affect the rate of production.     

Influence of nonishothermicity on drag coefficient of a spherical Al particle in a plasma

Experimental results of drag coefficient measurements of spherical Al particles with diameter 100–300 m in an electric-arc argon plasma for Re ynolds numbers 0.4-10, Mach numbers 0.05 in a plasmatron channel with an intersection cavity for an arc current of 75–190A, gas flow rate 0.2–2.75g/.sec, and channel radius 0.75–1.5cm are reported. Plasma flow characteristics obtained using MHD equations are used for treatment of experimental data.     

Depth-structure of airborne microparticles sampled downwind from the city of Karlsruhe in the river Rhine valley

Particulate material from outdoor air collected north of Karlsruhe was analysed with secondary mass spectrometry (SNMS and SIMS) especially to examine the depth distribution within the grains. Two size modes were found, submicron particles in the range of 0.2–0.8 m and coarse particles with diameters of 2–5 m. For both types a shell structure was found. The core of the coarse particles contained geogenic material, which was covered by a double layer structure. The topmost layer (60nm) contained nitrates and ammonium sulfate, while a deeper layer of 400 nm primarily consisted of carbonate and organic carbon compounds. Soot from traffic sources seemed to be the origin of the submicron particles with a core dominated by graphitic and organic carbon, nearly completely covered by a 15 nm thick layer of ammonium sulfate. The latter is of importance for the removal of the soot from the atmosphere since the conversion of the soot surface from originally hydrophobic into hydrophilic behaviour should ease wet precipitation.Dedicated to Professor Dr. Dieter Klockow on the occasion of his 60th birthday     

Preparation of Thick PZT Ceramic Film by an Interfacial Polymerization

The formation of a PZT film of 10–20 m in thickness via an interfacial polymerization of metal-organic precursors has been studied. A commercially available PZT precursor solution developed for dip- or spin-coating was diluted with hexane containing acetylacetone as chelating agent. The solution was poured on water contained in a teflon reaction container of 88 mm inside diameter. A translucent gel film was formed at the interface of the two immiscible liquids. While floating on water it shrank as the evaporation of solvent proceeded until its diameter decreased to about 45% of its initial value. The dried gel film was almost pore free and its thickness was estimated to be about 10 m.     

Extraction-spectrophotometric determination of nickel as Ni-(PAR)2-(CTAB)2 complex in polymetallic sea-bed nodules and steels

A red, water-soluble complex of nickel with PAR can be extracted into chloroform with CTAB at pH 7.0. The system obeys Beer's law upto 0.5 g/ml with a molar absorptivity of 45 200 L·mol^–1·cm^–1 at 540 nm. Job's method of continuous variations revealed that the composition of the extracting species is 1:2:2 for nickel:PAR:CTAB. Based on this extraction, a highly sensitive and selective spectrophotometric method for the determination of nickel in polymetallic sea-bed nodules and in steels, after prior separation of iron and manganese, was developed. The standard deviation was 0.04–0.127 g for 5–25 g of nickel.     

Use of a stopped-flow technique for investigation and determination of thiourea and its <Emphasis Type="Italic">N</Emphasis>-methyl derivatives as inducers of the iodine–azide reaction

A stopped-flow technique has been used to investigate the behaviour of 2-thiourea, 1-methyl-2-thiourea, 1,3-dimethyl-2-thiourea, and 1,1,3,3-tetramethyl-2-thiourea in the induced iodine–azide reaction. This technique enables the progress of the reaction to be followed by monitoring the decrease in the absorbance of the iodine–starch complex at 595 nm. The effect of the concentration of the reagents on the rate of the reaction was investigated and a kinetic method for determination of the compounds is proposed. 2-Thiourea, 1-methyl-2-thiourea, and 1,3-dimethyl-2-thiourea can be determined in the range 3–75 mol L^–1 and 1,1,3,3-tetramethyl-2-thiourea in the range 2–200 mol L^–1.     

Simple Extraction and Rapid Quantitative Analysis of Isoflavones in Soybean Seeds

A simple extraction and rapid HPLC method, suitable to separate and quantify the isoflavonoids in soybean seeds, are proposed and discussed. The method has been applied to the separation and quantification of seed isoflavonoids in five naturally grown soy cultivars; the total amount of isoflavones ranged from 1.83 g kg^–1 to 11.88 g kg^–1 of fresh weight. The detection limits (200 g/kg^–1), evaluated for genistein and daidzein, are presented together with a list of the soy polyphenols analysed by HPLC-DAD and HPLC-MS.     

Photometrische Bestimmung des Ephedrins in Arzneimitteln mit diazotiertem p-Dianisidin

Zusammenfassung Ephedrin wurde mittels diazotiertem p-Dianisidin in wäßriger Lösung bei pH 7 ohne und mit vorhergehender Abtrennung durch Dünnschicht-Chromatographie auf Celluloseschichten photometrisch bestimmt. Die gelbe Farbe wurde bei 424 nm gemessen. Die Methode erlaubt die Bestimmung von Ephedrin im Bereich von 50–200 g mit einer relativen Standardabweichung von ±4%.

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Photometric determination of ephedrine in pharmaceuticals by means of diazotized p-dianisidine

Ephedrine has been determined photometrically using diazotized p-dianisidine in aqueous solutions at pH 7 without and with proceeding separation by thin-layer chromatography on cellulose. The yellow colour has been measured at 424 nm. The method permits the determination of ephedrine in the range of 50–200 g with a relative standard deviation of ±4%.

     

Spectrophotometric determination of nitrite in environmental waters using column preconcentration on biphenyl

Column preconcentration methods have been established for the spectrophotometric determination of trace nitrite with sulfanilic acid (SA) orp-aminoacetophenone (AAP) as the diazotizable aromatic amine andN, N-dimethylaniline (DMA) or 1-aminonaphthalene (AN) as the coupling agent, using differention-pairs co-precipitated with biphenyl. Nitrite ion reacts with SA in the pH range 2.0–3.0 and AAP in the pH range 1.7–3.0 in HCl medium to form water-soluble colourless diazonium cations. These cations are subsequently coupled with DMA in the pH range 3.7–6.1 for the SA-DMA system and AN in the pH range 1.7–2.3 for the AAP-AN system to be retained on microcrystalline biphenyl packed in a column. The solid mass is dissolved out from the column with 5 ml of DMF and the absorbance is measured by a spectrophotometer at 420 nm for the SA-DMA system and at 517 nm for the AAP-AN system. The calibration was linear over the concentration ranges 0.3–6.0 g of nitrite in 5 ml of DMF solution (i.e., 0.02–0.40 g/ml in the sample solution) for the SA-DMA system and 0.5–7.0 g of nitrite in 5 ml of DMF solution (i.e., 0.03–0.47 g/ml in the sample solution) for the AAP-AN system. The molar absorptivity and Sandell's sensitivity were respectively 2.63 × 10⁴lmol^–1cm^–1 and 1.75 × 10^–3 g cm^–2 for SA-DMA and 3.28 × 10⁴lmol^–1 cm^–1 and 1.40 × 10^–3 g cm^–2 for AAP-AN. The concentration factors were 4 and 16 for SA-DMA and AAP-AN, respectively. The detection limits were 0.0138 and 0.0175 g/ml NO₂ ^– for SA-DMA and AAP-AN, respectively. Seven replicate determinations of a solution containing 3.5 g of nitrite gave mean absorbances of 0.410 and 0.500 with relative standard deviations of 0.51 and 0.55% for SA-DMA and AAP-AN, respectively. Interference from various foreign ions has been studied and the methods have been applied to the determination of nitrite in environmental samples.     

Spectrophotometric determination of microamounts of thorium with disodium salt of 2-(2-hydroxy-3,6-disulfo-1-naphthylazo)-benzenearsonic acid (Thorin) as a chromogenic reagent

A sensitive spectrophotometric method has been developed for the determination of microamounts of thorium using 0.05% thorin in a 3M perchloric acid solution as a chromogenic reagent and measuring the absorbance at 544 nm. The complex of thorium thus formed, is stable for more than two months with a constant absorbance of ±0.55%. Beer's law is obeyed from 0 to 25 g g^–1 of thorium in a solution with a molar absorptivity (544 nm) = 1.69×10⁴ M^–1 cm^–1 at 26±1 °C. Among the anions tested, only phosphate, acetate and cyanide at >200-fold excess of thorium interfere in the determination, whereas cations like Zn(II), Al(III), Na(I), Mg(II), and Ca(II) do not effect the absorbance. Thorium can be determined in the presence of oxalate, nitrate, tartrate, sulfate, thiosulfate, citrate, and ascorbate. The accuracy of the method has been checked by measuring the known concentration of thorium in the range of 100 g-5 mg g^–1 and found to be in the range of 7.7–0.9%. The method has been applied successfully to determine thorium at g g^–1 level in local ore samples with a precision of ±0.3%. The sensitivity of the method on Sandell's scale is 0.082±0.002 g g^–1 cm^–1.     

Réaction spécifique pour le Palladium et son dosage

Résumé Parmi les dihydrazides des acides dicarboxyliques, le plus intéressant est celui de l'acide malonique qui fournit un réactif qualitatif spécifique du palladium. Le dosage gravimétrique ne s'applique pas, mais la colorimétrie permet d'évaluer de 2 à 10g/ml de palladium, à 285 nm.

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Specific reaction for palladium and its determination

Summary The most interesting of the dihydrazides of dicarboxylic acids is that of malonic acid, which yields a qualitative specific reagent for palladium. The gravimetric determination is not practicable but the colorimetric method permits the evaluation of from 2 to 10g/ml of palladium at 285 nm.

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Zusammenfassung Unter den Dicarbonsäure-Dihydraziden ist das interessanteste das der Malonsäure. Es ist ein für Palladium spezifisches Nachweisreagens. Zur gravimetrischen Bestimmung eignet es sich nicht, aber kolorimetrisch kann man bei 285 nm 2 bis 10g Pd/ml bestimmen.

     

Colorimetric determination of vanadium with 5,7-dibromo-8-hydroxyquinoline after paper-chromatographic separation from interfering ions

Summary 5,7-Dibromo-8-hydroxyquinoline is recommended as reagent for the colorimetric determination of vanadium. The absorption is measured at 394 nm. Interfering ions are removed by paper chromatography with a collidine containing solvent. With amounts of 45–120 g of vanadium an error of ± 1 g has been obtained.

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Zusammenfassung Zur colorimetrischen Vanadiumbestimmung wird 5,7-Dibrom-8-hydroxychinolin als Reagens empfohlen. Die Messung erfolgt bei 394 nm. Störende Ionen werden durch Papier-Chromatographie mit einem collidinhaltigen Fliemittel entfernt. Der Fehler betrug ±1 g bei Vanadiummengen von 45–120g.

     

Structure and thermal stability of microencapsulated phase-change materials

A series of microcapsules containing n-octadecane with a urea-melamine-formaldehyde copolymer shell were synthesized by in-situ polymerization. The surface morphology, diameter, melting and crystallization properties, and thermal stability of the microcapsules were investigated by using FTIR, SEM, DSC, TGA and DTA. The diameters of the microcapsules are in the range of 0.2–5.6 m. The n-octadecane contents in the microcapsules are in the range of 65–78wt%. The mole ratio of urea-melamine has been found to have no effect on the melting temperature of the microcapsules. Two crystallization peaks on the DSC cooling curve have been observed. The thermal damage mechanisms are the liquefied n-octadecane leaking from the microcapsule and breakage of the shell due to the mismatch of thermal expansion of the core and shell materials at high temperatures. The thermal stability of materials can be enhanced up to 10 °C by the copolymerization of urea, melamine and formaldehyde in a mole ratio 0.2:0.8:3. The thermal stability of 160 °C heat-treated microcapsules containing 8.8% cyclohexane can be further enhanced up to approximately 37 °C.     

Magnetische Messungen an ternären Fe/Ni-Telluriden mit NiAs-Struktur

The hexagonal NiAs-type phase in the ternary system Fe–Ni–Te was investigated by thermal, X-ray and susceptibility measurements from 100 up to 1000K. The high temperature phase -FeTe (Fe₂Te₃), which is stable only above 520°C was stabilized at lower temperatures by the partial substitution of iron by nickel. Alloys containing less iron than two thirds of the total metal amount were found to be stable even down to room temperature. Due to the continuous addition of iron the weak constant paramagnetism of -NiTe increased and became temperature dependent. The variation of the magnetic susceptibilities with temperature in specimens with a high iron content was indicative of magnetic interactions between iron atoms. It was concluded that at low temperatures Fe₂Te₃ exhibits an antiferromagnetic order which is destroyed somewhere between room temperature and 520°C.     

Spectrofluorimetric flow-injection determination of cerium in carbon and low alloy steels

Cerium can be determined spectrofluorimetrically (_em 350 nm, _ex 260 nm) based on the relatively intense native fluorescence of the cerium(III) aquo-ion. The main potential interference in the analysis of steel from iron(III), cerium(IV) and chromium(VI) are removed by use of a carrier solution containing 2.5% w/v hydroxylammonium chloride. The slight residual interference from iron(II) can be corrected by a matrix matching factor linearly related to the amount of iron present. The calibration graphs are linear over the range 0–7 g ml^–1 based on 250 l injection volumes. The sampling rate was 30 h^–1. The relative standard deviation was 2.0% (n=5) at 3 g ml^–1 cerium. The system has been applied to the determination of cerium in carbon or low alloy steels.     

Trace and minor elements in four commercial honey brands

Instrumental neutron activation analysis was used to measure the concentrations of 24 elements in four honey brands commercially available in Austin, Texas (USA). The measured elements (and concentration) were: As, (<30 ng/g); Ba, (<2 g/g); Br, (0.24–0.49 g/g); Ce, (<20 ng/g); Co, (9–180 ng/g); Cr, (37–64 ng/g); Cs, (<3–45 ng/g); Fe, (<4–15.9 g/g); Hf, (<3 ng/g); Hg, (1 ng/g); K, (91–230 g/g); La, (<4 ng/g); Na, (20.3–25.3 g/g); Ni, (0.39–0.77 g/g); Rb, (68–340 ng/g); Sb, (13–61 ng/g); Sc, (<0.3–200 ng/g); Se, (<20 ng/g); Sm, (<9 ng/g); Sr, (<2 ng/g); Th, (<4 ng/g); U, (<30 ng/g); Zn, (3.36–4.61 g/g); and Zr, (<0.5–0.84 g/g). The results obtained were compared to the concentration of the same elements in honey produced or commercially available in Turkey, Mexico, El-Salvador, China, Czechoslovakia and Yugoslavia.     

Sol-Gel Synthesis and Microstructural Characterization of Silicon Oxycarbide Glass Sheets with High Fracture Strength and High Modulus

A synthesis route to silicon oxycarbide glass sheets (thickness 40 to 1000 m and area up to 20 × 35 cm2) has been developed for the first time starting from a methyl modified sol containing nano-particulate SiO2 and having a solid content of 70 wt%. The gel sheets obtained by casting and drying of this sol were sintered in N2 atmosphere at temperatures between 900–1650°C. Only by the incorporation of colloidal silica (0.10–0.35 mole per mole alkoxide) to the sol could crack-free, large area glass sheets be obtained. Fracture strength (three point bending) was found to attain a maximum (200–300 MPa) for the sheets sintered at 1000°C. Young's modulus attained a peak value between 120 and 130 GPa for the sheets sintered at 1200°C. HR-TEM studies showed an amorphous and homogeneous matrix up to a sintering temperature of 1200°C, whereas at 1450°C and 1650°C, crystallites of SiC and lamellar graphite were formed. It is concluded that addition of colloidal silica to the sol does not lead to inhomogeneities after sintering and therefore does not decrease the strength and elastic modulus.     

Sol-Gel Processing of Transparent PLZT((Pb,La)(Zr,Ti)O3) Fibers

PLZT((Pb,La)(Zr,Ti)O₃) ceramic fibers were prepared by the sol-gel method from a solution of lead acetate trihydrate, lanthanum isopropoxide, zirconium n-propoxide and titanium isopropoxide containing 2-methoxyethanol as the solvent. The as-drawn gel fibers were pretreated in an autoclave and preheated in flowing H₂O vapor prior to the heat-treatment for crystallization. The effects of autoclaving and preheating in flowing H₂O vapor on the structure and composition of the resultant fibers were investigated. Optically transparent single phase perovskite PLZT fibers of 5–15 m in thickness and 5 cm in length were successfully prepared when the autoclave-treatment and the preheating in flowing H₂O vapor were conducted prior to crystallization. These treatments are thought to promote hydrolysis of the organic groups and polycondensation reaction in the gel fibers, leading to the successful formation of dense, crack-free transparent PLZT fibers.     

Preparation of PZT Thick Films by an Interfacial Polymerization Method

Pb(Zr_0.53Ti_0.47)O₃ (PZT) films of 10 to 50 m in thickness were prepared by a new sol-gel process using an interfacial polymerization technique. The interfacial polymerization process is that an alkoxide precursor solution is poured on the surface of water in a container to form a gel film at the interface between the two immiscible liquids. The precursor solution was prepared by adding PZT alkoxide solution, PZT powders coated with Pb₅Ge₃O₁₁ (PG), and a surfactant into hexane solvent. After the polymerization at the interface, the gel films were gently placed on a silicon substrate by draining the water in the container. The gel films containing PZT powders were sintered at 950°C for 10 min to obtain crystallized PZT films. The remanent polarization of a PZT thick film was 33.1 C/cm². The piezoelectric d ₃₃ constant measured with a Mach-Zehnder interferometer was 225 pm/V and was independent of frequency from 0.2 to 3 kHz.