Structural and Chemical Modification of Polydiene Latexes by Gel Derived Silica

Latex-silicate compositions and unsupported films (green and vulcanized) were prepared by mixing natural Qualitex and synthetic butadiene-styrene (SKSS) latexes with an aqueous solution of sodium silicate modified with a zinc tetrammine complex. The mechanism and efficiency of the inorganic modification of latex structures were investigated by UV-vis and IR spectrophotometry, rotational viscometry of liquid and gelled mixtures as well as by tensile testing of the prepared films. Measurements showed an increase of elastic modulus and tensile strength with silica concentration for all composite films except for the green SKSS-based ones. The improvement of mechanical properties can be related to the formation of interpenetrating organic and silicate networks linked by Zn atoms that can also participate in the vulcanization process.     

Characterization and determination of benzalmalonitriles using infrared,nuclear magnetic resonance and mass spectrometry

Summary The stretching vibration of the CN groups at 2200–2240 cm^–1 and the singlet signal of the olefinic proton at 7–9 ppm in the IR and NMR spectra of benzalmalonitriles are correlated with Hammett sigma parameter of the substituents and the data obtained are used for their selective characterization. Using the base-line method and KBr technique or dimethylsulfoxide solvent and the integration method, 50–800g/250 mg KBr or 10–100 mg/ml of these compounds are quantitated by IR and NMR, respectively. The average recovery by both methods is 98.3% (st. dev. 1.6%). Fragmentation of these compounds using mass spectrometry gives common products that can be used for their characterization.

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Charakterisierung und Bestimmung von Benzalmalonitrilen mittels Infrarot-, Kernresonanz- und Massenspektrometrie

Zusammenfassung Die Valenzschwingung der CN-Gruppen bei 2200–2240 cm^–1 und das Singulettsignal des olefmischen Protons bei =7–9 ppm in den IR-bzw. NMR-Spektren von Benzalmalonitril wurden mit Hammett Sigma Parametern der Substituenten korreliert und die erhaltenen Daten zur selektiven Charakterisierung herangezogen. Unter Verwendung der Basislinien-methode und der Kaliumbromidtechnik bzw. Dimethylsulfoxid als Lösungsmittel und der Integrationsmethode wurden 50–800g/250 mg KBr bzw. 10–110 mg/ml dieser Verbindungen durch IR-bzw. NMR-Spektroskopie quantifiziert. Die durchschnittliche Wiedergewinnungsrate betrug bei beiden Methoden 98,3% (Standardabweichung 1,6%). Die Fragmentierung dieser Verbindungen mittels Massenspektrometrie ergibt Produkte, die zur weiteren Charakterisierung herangezogen werden können.

     

Determination of Trace Proteins by Rayleigh Light Scattering Technique with Indophenol Blue

The interaction of indophenol blue (IPB) with proteins in aqueous solution has been studied by optical absorption and Rayleigh light scattering (RLS) spectroscopy. At pH 3.8, the weak RLS of IPB is enhanced by proteins. Based on this phenomenon, a novel method for the determination of proteins at nanogram levels using the RLS technique is developed. The method is simple, practical and sensitive. The linear range is 0.25–20.9µgmL^–1 for BSA, and 0.25–17.6µgmL^–1 for HSA. The detection limits (S/N=3) are 23ngmL^–1 for BSA and 22ngmL^–1 for HAS. The results for the determination of proteins in human serum samples are very close to those obtained by an established clinical method. There is very little interference from amino acids, metal ions or other coexisting compounds.     

Acetylsevedine fromKorolkowia sewerzowii

The epigeal part ofKorolkowia sewerzowii Regl. has yielded a new alkaloid — acetylsevedine with mp 189°C (with foaming), []_D –36.6°, C₂₉H₄₇NO₄. On the basis of the IR, PMR, and mass spectra of acetylsevedine, of the products of its transformation, and also a passage to the known alkaloid sevedine, the structure of 6-acetoxy-3, 14-dihydroxycevanine has been established for acetylsevedine.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 352–353, May–June, 1986.     

IR spectra of certain methyl -d-glucopyranoside nitrates

Conclusions A study has been made of the IR spectra of methyl--D-glucopyranoside 2-and 3-nitrates, methyl--D-glucopyranoside 6-nitrate, and methyl-4-O-methyl--D-glucopyranoside 2,3-and 3,6-dinitrates and 2,3,6-trinitrate.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1763–1765, August, 1987.     

Investigations of hard elastic polypropylene with respect to the coil-strand-transition model

Hard elastic polypropylene was investigated by x-ray scattering using synchrotron radiation and by performing stress strain measurements in different liquids. It was found that the long period increases with elongation up to 1.3–1.4. Beyond this extension a change in the deformation behavior takes place. In the range from 1.1 to 1.3–1.4 the deformation measurements in the different liquids are in good agreement with the coil-strand-transition model. The proposed linear relationship between the deformation work and the elongation could be confirmed. The same holds for the surface energy. Moreover, the calculated ratio between the surface energy and the deformation work agrees with the measurements.     

Electrochemical Determination of 4-Nitrophenol Using a Single-Wall Carbon Nanotube Film-Coated Glassy Carbon Electrode

A single-wall carbon nanotubes (SWNT) film coated glassy carbon electrode (GCE) was fabricated for the direct determination of 4-nitrophenol (4-NP). The electrochemical behaviors of 4-NP at the SWNT-film coated GCE were examined. In 0.1M phosphate buffer with a pH of 5.0, 4-NP yields a very sensitive and well-defined reduction peak at the SWNT-modified GCE. It is found that the SWNT film exhibits obvious electrocatalytic activity towards the reduction of 4-NP since it not only increases the reduction peak current but also lowers the reduction overpotential. Based on this, an electrochemical method was proposed for the direct determination of 4-NP. The reduction peak current varies linearly with the concentration of 4-NP ranging from 1×10^–8 to 5×10^–6M, and the detection limit is 2.5×10^–9M after 3min of open-circuit accumulation. The relative standard deviation at 2×10^–7M 4-NP was about 6% (n=10), suggesting excellent reproducibility. This new method was successfully employed to determine 4-NP in several lake water samples.     

Lead Zirconate-Titanate Films Prepared from Soluble Powders

Precursor powders for Pb(Zr1 – xTix) O3 (PZT) thin films were produced by the reaction of zirconium-and titanium-n-propoxides with acetylacetone and lead acetate trihydrate. The subsequent complete removal of volatile components yielded powders that can be handled in air. The powders are indefinitely stable under ambient conditions.High molarity (>2m) coating sols were prepared by dissolution of the precursor powders in mixtures of 1,3-propanediol, triethanolamine (TEA) and water. Excess amounts of lead to compensate lead loss during firing were easily introduced into these solutions.The deposition of these sols on steel substrates and firing at 600°C yielded PZT films. Many physical parameters like film thickness, morphology and electrical performance could be influenced by choice of the solvent mixture composition and oxide content of the sols. Depending on the preparation dielectric permittivities, r of up to 840 were measured at 1 kHz. By hysteresis measurements at 50 Hz and a field amplitude of 50 V/m a remanent polarization of about 40 C/cm2 and coercivity of about 8 V/m was obtained. The films were stable against dielectric breakdown up to 70V/m.     

Synthesis, Properties, and Crystal and Molecular Structures of New Ni(II) Complexes with Sterically Hindered Methoxy-β-iminoketones

This paper describes a procedure for the synthesis of two new volatile complexes, C₂₂H₄₀N₂NiO₄ and C₂₀H₃₆N₂NiO₄, based on sterically hindered methoxy--iminoketones. The compounds were investigated by IR spectroscopy and DTA. Full crystal-chemical analysis has been carried out. The structures are molecular. The complexes have close geometrical characteristics; the distances are Ni–O 1.826 and Ni–N 1.842 ; the O–Ni–N chelate angle is 93.2°. The complexes have an intramolecular hydrogen bond N–H...O, estimated at 2.54 (2.08) . In both structures, the packing of complexes is similar to that in nickel(II) dipivalylmethanate.     

The effect of zinc(II) on the formation of 2,2′- and 2,3′-bipyridine complexes of [Ru2II(ttha)]2−(ttha6−=triethylenetetraminehexaacetate)

Ru2II(ttha)(H2O)2]2– (ttha6–= triethylene tetramine hexa-acetate), prepared by the reduction of the ruthenium(III) precursor, reacts with 2,2-bipyridine (2,2-bpy) in a multi-step fashion. The first 2,2-bpy equivalent (1:1) adds with bidentate chelation at one ruthenium(II) site as revealed by separate ruthenium(II)/(III) waves at 0.03 and 0.54V vs. n.h.e. A second equivalent of 2,2-bpy (1:2) is initially stored and retained as the [Zn(2,2-bpy)]2+ complex. Further addition of 2,2-bpy initiates coordination at the second ruthenium(II) site. [Ru2(ttha)-(2,2-bpy)(H2O)]2– forms a strong ion-pair with zinc(II) that is in rapid equilibrium with the Zn(H2O)62+/Zn(2,2-bpy)]2+ pool. The solubility of the ion-pair is low. The ion-pair exhibits a shifted ruthenium(II)/(III) wave at 0.60V. Higher amounts of 2,2-bpy recomplex the zinc(II), solubilizing the complex and returning the E1/2 value to 0.54V. Other ligands which either have a higher affinity for ruthenium(II) centres than for zinc(II) as bidentate donors (1,10-phenanthroline), or ligands that cannot form bidentate zinc(II) complexes [(2-methylpyrazine, 4,4-bipyridine (4,4-bpy), and 2,3-bipyridine (2,3-bpy)] do not exhibit the unusual competition by zinc(II). These ligands all add statistically to the ruthenium(II) centres forming 1:2 complexes with 1:2 stoichiometries. 1H-n.m.r. studies of the Ru(II)polyaminopolycarboxylate complexes [RuII(hedta)(H2O)]– complex, and [Ru2(ttha)(H2O)2]2– itself, reveal that substitution of 2,3-bpy at ruthenium(II) sites occurs with an initial kinetic split between the pyridyl rings of the 3- less-hindered and 2-more-hindered ring. A slower rearrangement occurs, producing the isomer of the more-hindered 2-substituted ring. A process is driven by forming a more -accepting system when ruthenium(II) binds to the 2-ring of 2,3-bpy. Understanding the unusual influence of zinc(II) on the substitution of 2,2-bpy with [Ru2(ttha)(H2O)2]2– clarifies the nature of the 1:1 complex – namely that the 2,2-bpy becomes bidentate at one ruthenium(II) centre rather than serving as a trans-bridging ligand between both ruthenium(II) centres within one [Ru2(ttha)]2– unit.     

Characterization of airborne particulates by laser microprobe mass analysis

Summary Laser microprobe mass analysis (LAMMA) was applied to characterize aerosol particles collected and separated from 16m to 0.06m by a low pressure cascade impactor. Positive ion LAMMA spectra showed characteristic molecular peaks such as PbCl⁺, a series of Si₂O⁺–Si₂O₄ ⁺ and NaAl₂Si₂O₂ ⁺–NaAl₂Si₂O₅ ⁺, and TiO⁺ in 0.06–0.12m, 0.5–1m and 4–8m fraction, respectively. In the negative ion LAMMA spectra, it was observed that the fragment peaks of sulfate ions were deficient above 2m and those of nitrate ions were deficient under 2m. LAMMA allows remarkable insights into the chemical nature of aerosol particles.

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Charakterisierung luftgetragener Teilchen durch Laser-Microprobe-Massenspektrometrie

Zusammenfassung Laser-Microprobe-Spektrometrie (LAMMS) wurde zur Analyse atmosphärischen Aerosols herangezogen, welches im Korngrößenbereich zwischen 16m und 0.06m mit einem Niederdruckkaskadenimpaktor fraktioniert gesammelt wurde. Positive LAMMS-Spektren zeigten charakteristische molekulare Peaks, wie etwa PbCl⁺, eine Serie von Si₂O⁺–Si₂O₄ ⁺ und NaAl₂Si₂O₂ ⁺–NaAl₂Si₂O₅ ⁺, sowie TiO⁺ in der 0,06–0,12-m,- 0,5–1–m- bzw. 4–8-m-Fraktion. In den negativen LAMMS-Spektren konnten über 2m keine Fragmentpeaks für Sulfationen, unter 2m. keine für Nitrationen beobachtet werden. LAMMS ermöglicht eine bemerkenswerte Einsicht in die chemische Natur von Aerosolteilchen.

     

Dielectric properties of cleaned and monodisperse polystyrene latexes in microwaves

The dielectric behavior (, ) of three well-cleaned monodisperse polystyrene latexes having the same particle size and the same number of chemically-bound surface groups has been studied at a fixed microwave frequency (9.4 GHz), as a function of temperature and surface group (SO ₄ ^– , COO^–, OH).A large dielectric relaxation was observed in the sulfate-stabilized latex, which has the most polar surface end-group. The anomalous behavior in the thermal dependence of the hydroxyl and carboxyl-stabilized latexes (the OH latex being more pronounced than the COO^– latex) may originate from differences in the experimental conditions used for the preparation of such polymer colloids, or due to the presence of ionic species.On the basis of various dielectric models, the apparent volume fractions of the latexes were calculated. The amount of bound water around the latex particle was quantitatively correlated to the polarity of surface end-group (SO ₄ ^– > COO^– > OH). The differences between the calculated and actual values were not only a reflection of the thickness of vicinal water, but could also be indicative of the presence of oligomeric species in the suspension's medium (serum) of the latex. The permittivities of hydrated particle and of bound water were obtained with a non-linear iterative procedure.     

Analysis for fungicides in paint

Summary Simple methods have been developed for the determination of copper and 8-hydroxyquinoline in paint films. Copper is separated from 8-hydroxy-quinoline by precipitation as copper sulphide and is determined photometrically either by means of diphenylcarbazone (0.1–1g Cu/ml) or benzoin oxime (1 to 10 g Cu/ml). 8-Hydroxyquinoline is determined by measuring the optical density in the ultraviolet region.

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Zusammenfassung Einfache Verfahren zur Bestimmung von Kupfer und 8-Hydroxychinolin in Anstrichfilmen werden beschrieben. Kupfer wird als Sulfid abgetrennt und photometrisch mit Diphenylcarbazon (0,1–1g Cu/ml) oder Benzoinoxim (1–10g Cu/ml) bestimmt. 8-Hydroxychinolin wird durch Messung der UV-Absorption bestimmt.

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Part III: Hoffmann, E., A. Saracz, and B. Bursztyn: Z. analyt. Chem. 208, 431 (1965).     

Determination of Caffeine Using a Simple Graphite Pencil Electrode with Square-Wave Anodic Stripping Voltammetry

A simple commercial graphite pencil electrode (GPE) was utilized for monitoring caffeine using the square-wave anodic stripping voltammetry (SWASV) method. This method was applied to determine the caffeine levels in several tea samples, which yielded a relative error of 1% in the concentrations. Caffeine was deposited at 0.0V (vs. Ag/AgCl), then reduced at +1.40V to strip it on the GPE. Optimal experimental conditions for the analysis were found to be as follows: pH value of 9 for the medium; deposition potential of 0.0V; deposition time of 120s; SW frequency of 25Hz; SW amplitude of 45mV, and step potential of 6mV. Given these optimum conditions, a linear range was observed within the concentration of 0500mgL^–1. At caffeine concentrations of 50.0, 250.0, and 500.0mgL^–1, the relative standard deviations in measured concentrations (n=12) were 0.19, 0.09, and 0.11%, respectively. The detection limit was found to be 9.2mgL^–1, which is comparable with the result obtained using a carbon paste electrode, equivalent to 8.2mgL^–1.     

Cardenolide glycosides ofCheiranthus allioni. XV. Glucocheiranthoside

Another new cardenolide glycoside has been isolated from the plantCheiranthus allioni Hort., and has been named glucocheiranthoside. Its chemical structure has been established as 3-(4-O--D-glucopyranosyl--D-gulmoethylpyranosyloxy)-14-hydroxy-19-oxo-5,14-card-20(22)-enolide.State Scientific Center for Drugs, Ukraine, 310085, Kharkov, USSR. ul. Astronomicheskaya, 33. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 269–271, March–April, 1994.     

Withasteroids ofPhysalis. V. A study of the1H and13C NMR spectra of the withasteroids visconolide and 28-hydroxywithaperuvin C

The PMR and¹³C NMR spectra of new withasteroids — visconolide and 28-hydroxywithaperuvin C, isolated fromPhysalis viscosa L. — have been investigated. A detailed analysis of the spectral characteristics obtained is given. For visconolide is proposed the structure of 4,12,17,28-pentahydroxy-1-oxo-5, 6-epoxy-22R-witha-2,24-dienolide, and for 28-hydroxywithaperuvin C that of 6,14,17,20R, 28-pentahydroxy-l-oxo-22R-witha-2, 4, 24-trienolide.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 657–663, September–October, 1985.     

Catalytic alkylation of benzofurans

The alkylation of benzofuran with tert-butyl chloride in various solvents with a zinc chloride catalyst was studied. It was found that the alkylation proceeds primarily at the 3-position. The ratio of the 2- and 3-tert-butylbenzofurans is 12 regardless of the nature of the solvent.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 156–159, February, 1971.     

Pyridylethylation of some 4-azolidones

N-Pyridylethylated derivatives were obtained by the reaction of- or-vinylpyridines with 4-azolidones and their 5-benzylidene-substituted derivatives. Their IR and UV spectra were studied.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 599–600, May, 1971.     

Iron Catalysis of SO2 Oxidation in the Atmosphere

The mechanisms of SO₂ oxidation catalyzed by iron ions in the droplet phase of the convective cloud in the lower atmosphere were examined. The relations of the catalytic SO₂ decrease to the concentration of the iron ions and to the intensity of fluxes to the droplet of the OH _(g) and HO _2(g) radicals were characterized. The determining role of the replacement of the low-reactive HO _2(g)(O^– _2(aq)) radical by the reactive SO^– _5(aq) radical in the sulfite medium during daytime was revealed. This process occurred due to the coupling of the decay of the radicals and their regeneration in the liquid-phase reactions O^– _2(aq) + FeOH²⁺ _(aq) Fe²⁺ _(aq) + OH^– _(aq) + O_2(aq), HSO^– _5(aq) + Fe²⁺ _(aq) FeOH²⁺ _(aq) + SO^– _4(aq)HSO ₃ ^- _(aq),O_{2 (aq)} SO^– _5(aq).     

Determination of Heavy Metal Ions in Chinese Herbal Medicine by Microwave Digestion and RP-HPLC with UV-Vis Detection

A new method for the simultaneous determination of heavy metal ions in Chinese herbal medicine by microwave digestion and reversed-phase high-performance liquid chromatography (RP-HPLC) has been developed. The Chinese herbal medicine samples were digested by microwave digestion. Lead, cadmium, mercury, nickel, copper, zinc, and tin ions in the digested samples were pre-column derivatized with tetra-(4-chlorophenyl)-porphyrin (T₄-CPP) to form the colored chelates which were then enriched by solid phase extraction with C₁₈ cartridge and eluted from the cartridge with tetrahydrofuran (THF). The chelates were separated on a Waters Xterra RP₁₈ column by gradient elution with methanol (containing 0.05molL^–1 pyrrolidine-acetic acid buffer salt, pH=10.0) and THF (containing 0.05molL^–1 pyrrolidine-acetic acid buffer salt, pH=10.0) as mobile phase at a flow rate of 0.5mLmin^–1 and detected with a photodiode array detector in the range of 350–600nm. In the original samples the detection limits of lead, cadmium, mercury, nickel, copper, zinc and tin are 4ngL^–1, 3ngL^–1, 6ngL^–1, 5ngL^–1, 2ngL^–1, 6ngL^–1, and 4ngL^–1, respectively. This method was applied to the determination of lead, cadmium, mercury, nickel, copper, zinc and tin in Chinese herbal medicine samples with good results.