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  • Chemistry and Pharmacology  (433)
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  • 1
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    Springer
    Journal of thermal analysis and calorimetry 47 (1996), S. 135-142 
    ISSN: 1572-8943
    Keywords: complexes ; IR ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Dithiomalonamide [H2A, CH2(CSNH2)2] and 2,2-dimethyldithiomalonamide [H2B, C(CH3)2(CSNH2)2] can act as bidentate ligands and form stable, cationic 1∶2 complexes with general formula M2(H2L)2X2 [M=Ni2+, Pd2+, Pt2+;X=C1, Br, I; H2L=H2A, H2B] in strong acidic medium. An elaborate thermal study is presented, based on results from elemental analyses and vibrational studies (IR and Raman spectroscopy). The H2A complexes start to decompose by releasing two HX molecules whereafter a stable intermediate M(HA)2 is formed. The H2B complexes degrade in a different way; the metal-sulphur bond is broken and the ligand is expelled as a whole. Influences of the metal ion and of the halogenide counterions are investigated.
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  • 2
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    Journal of thermal analysis and calorimetry 47 (1996), S. 399-406 
    ISSN: 1572-8943
    Keywords: ion-exchange procedure ; montmorillonite ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ion-exchange of transition metal ions into montmorillonite was investigated using two different ion-exchange procedures. Performing ion-exchange from aqueous solution of the respective metal ion leads to material possessing measurable BrØnsted acidity, while the solid-state exchange materials show predominantly Lewis acidity. Measurements by means of a derivatograph allowed us to construct a feasible reaction mechanism for solid-state ion exchange. Satisfactory correlation was found between the results calculated from the reaction steps assumed and the measurements by means of a derivatograph.
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  • 3
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    Journal of thermal analysis and calorimetry 47 (1996), S. 543-557 
    ISSN: 1572-8943
    Keywords: compensation effect ; DSC ; kinetics ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Four computer programs as well as one demo-version for non-linear evaluation of kinetic data in thermal analysis and calorimetry, were presented. The multi-task program TA-kin meets all mathematical requirements for solving the numerical assignments. It is shown that the so-called compensation effect is due to the mathematical structure of the Arrhenius equation. Several applications of TA-kin to a lot of DSC- and TG-measurements and isoperibolic batch experiments as well as adiabatic semi batch experiments realized by precision calorimetry have been discussed.
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  • 4
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    Journal of thermal analysis and calorimetry 47 (1996), S. 685-695 
    ISSN: 1572-8943
    Keywords: DSC ; polymers ; resins ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The paper describes the co-curing studies of ethynyl and ethenyl end-capped imide resins. The effect of composition and chemical structure of ethenyl end-capped resins (nadicimides) on thermal behavior of ethynyl end-capped resins was evaluated using DSC and thermogravimetric analysis. An increase in char yield was observed on co-curing of few resin formulations. A mechanism has been proposed to account for this observation.
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  • 5
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    Journal of thermal analysis and calorimetry 48 (1997), S. 83-92 
    ISSN: 1572-8943
    Keywords: DTA ; ETA ; smectite clay minerals ; TG ; X-ray
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The dehydration and dehydroxylation of the smectites, beidellite and montmorillonite (dioctahedral) and saponite and laponite (trioctahedral), were investigated by ETA, DTA, TG and X-ray diffractions. There are differences between the behaviors of di- and trioctahedral clays which are due to the differences in the ability of the exchangeable cations to migrate into hexagonal holes of the SiO4 network and due to the fact that the dehydroxylation and recrystallization of dehydroxylated trioctahedral smectites occur simultaneously, whereas there is a temperature gap of about 300°C between the dehydroxylation and the recrystallization of dioctahedral smectites.
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  • 6
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    Journal of thermal analysis and calorimetry 48 (1997), S. 135-139 
    ISSN: 1572-8943
    Keywords: dilatometry ; DTA ; mica ; TG ; thermal transformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The following criteria can be used for differential diagnosis of mica mineral group: weight loss 〈 350°C; weight loss during dehydroxylation (500–1000°C); peak temperature of structural decomposition and formation of high temperature phases; course of dilatometric curves during dehydroxylation and structural decomposition interval (Fig. 1). Using the single criteria by stepwise comparing a complete thermal differentiation is possible between the members of mica mineral group.
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  • 7
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    Journal of thermal analysis and calorimetry 48 (1997), S. 585-596 
    ISSN: 1572-8943
    Keywords: DTA ; high temperature superconductors ; phase diagrams ; TG ; thermal analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract With the discovery of high temperature superconductivity an extraordinary field for investigations on new materials containing up to (more than) 8 or 9 components has been open. But, in addition to problems specifically related to superconductivity, we are faced with a prelimary difficulty: the preparation of well defined compounds which may have reproducible properties. This difficulty is smoothed out when the phase relations in the relevant systems are known. Differential Thermal Analysis (DTA) contributes to their establishment. However, in multicomponent systems, an isopletic line is expected to intercept various boundary surfaces and the analysis is obviously complicated, compared to low order systems. In addition, by the nature of high temperature superconductors the oxygen partial pressure used for their preparation is an important thermodynamic parameter which contributes to fix the oxygen content in the solid state. During heat treatments, the composition of the systems may change, due to oxygen or volatile oxides (Tl2O3, PbO2 or HgO) release. A permanent composition control then requires thermogravimetric (TG) measurements associated to DTA. This paper attempts to demonstrate the efficiency of the assembly DTA/TG for the study of high temperature superconductors. Going beyond the frame of preparation and quality control, the system is also particularly useful for kinetic studies. Examples will be principally in the (Tl,Pb)-(Ba,Sr)-Ca-Cu-O systems.
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  • 8
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    Journal of thermal analysis and calorimetry 48 (1997), S. 709-716 
    ISSN: 1572-8943
    Keywords: ZrO2-Zr3N4 ; DTA ; TG ; high-temperature XRD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Annealing of ZrO2 in a nitrogen atmosphere leads to a nitrogen containing phase called Β″ phase having a trigonally distorted fluorite structure with ordered anion vacancies. DTA/TG investigations indicated that the Β″ phase decomposes intom-ZrO2 above 500
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  • 9
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    Journal of thermal analysis and calorimetry 48 (1997), S. 819-834 
    ISSN: 1572-8943
    Keywords: composites of cuprates ; DTA ; mixture of oxalates ; TG ; XRD
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Composites of cuprates of La(III) and Ba(II) were obtained by decomposing mixtures of oxalates of La(III), Ba(II) and Cu(II) prepared in 1∶1∶1 and 1∶2∶3 mol proportions respectively and sintering the oxide products at 1173 K. Reactions studied by TG, DTA and XRD techniques revealed the following features: (i) Decomposition of oxalates of La(III) and Ba(II) is drastically affected in mixtures. Decomposition temperature of organic part in the former (1∶1∶1) is shifted by ∼100 K while that of BaCO3 in the case of latter (1∶2∶3) is shifted by ∼400 K towards lower temperature side. (ii) All exothermic peaks on DTA traces of both the mixtures are allotted to the decomposition of oxalates to Cu2O, La2O2CO3 and BaCO3 phases while endothermic peaks around 863 and 1083 K are assigned for BaCuO2 and La2CuO4 phases respectively in the case of former (1∶1∶1) and endothermic peaks at about 1068, 1136 and 1213 K are correlated with BaCuO2, a composite of La2O3, La2CuO4 and La0.5Ba0.5CuO3−δ (δ→0.5) phases and LaBa2Cu3O7−δ (δ→0) phase respectively in the case of latter (1∶2∶3) and (iii) Lines of all cuprate compounds appear in XRD patterns of those samples preheated at temperatures ≥873 K. The following reaction is proposed in the case of 1∶2∶3 mixture:
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  • 10
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    Journal of thermal analysis and calorimetry 48 (1997), S. 989-996 
    ISSN: 1572-8943
    Keywords: sol-gel ; TG ; thermal decomposition ; Y-Ba-Cu superconductors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A precursor of Y-Ba-Cu oxides was prepared by a modified alkoxide sol-gel method and its thermal decomposition in air was studied by on-line coupled TG-FTIR and High Resolution Thermogravimetric measurements. A continuous more or less stepwise weight loss was observed between room temperature and 600°C at which all organic compounds had evolved and were progressively oxidized as the temperature increased leaving only Y and Cu oxides and bariumcarbonate. Between 700 and 800°C a final weight loss was observed due to the decomposition of bariumcarbonate into oxide.
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  • 11
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    Journal of thermal analysis and calorimetry 46 (1996), S. 5-14 
    ISSN: 1572-8943
    Keywords: cadmium phenoxyacetate ; complexes ; DSC ; mercury(II) phenoxyacetate ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Solid cadmium and mercury(II) phenoxyacetates were prepared and investigated by DSC and TG techniques. The cadmium salt decomposed in two steps with the loss of 1.5 water molecules at first and the successive formation of CdCO3 as final product. Δdeh H * associated with the loss of one water molecule was compared with the corresponding values obtained for other phenoxyacetates previously studied and the obtained results were discussed. Anhydrous mercury(II) phenoxyacetate gave, on heating, HgCO3 which successively decomposed with the formation of gaseous products and a little amount of solid residue.
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  • 12
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    Journal of thermal analysis and calorimetry 46 (1996), S. 55-65 
    ISSN: 1572-8943
    Keywords: silica-poly(vinyl acetate) ; sol-gel composites ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermogravimetric analyses of sol-gel derived silica and silica-poly(vinyl acetate) (PVAc) materials show that the loss in weight between 35 and 900°C can be attributed to three distinct reactions. Samples were prepared by dissolving the reactants tetraethyl orthosilicate (TEOS), poly(vinyl acetate) (PVAc), and water in mixtures of ethanol and formamide. The lowest temperature weight loss is due to the decomposition/removal of the solvents, while the intermediate weight loss corresponds to decomposition of the PVAc. The highest temperature weight loss is related to the dehydroxylation of the silica surface. The relative amounts of ethanol and formamide have a considerable effect on processing time, drying behavior, and the resulting thermal behavior of the gels.
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  • 13
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    Journal of thermal analysis and calorimetry 49 (1997), S. 177-182 
    ISSN: 1572-8943
    Keywords: bismaleimide resin ; CTBN ; curing behaviour ; DSC ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Bismaleimide resin (Compimide 353) was modified with the liquid elastomer carboxyl-terminated acrylonitrile butadiene (CTBN). The prereaction synthesis and curing of the CTBN-bismaleimide resin is discussed. The structure of the modified resin was identified by IR and NMR spectroscopy. The basic curing mechanism is also discussed. DSC and TG were used to study the curing behaviour and kinetic parameters, viz. the order of reaction, energy of activation and preexponential factor. Adhesive properties such as lap shear strength and peel strength at room temperature and elevated temperature were evaluated and are discussed.
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  • 14
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    Journal of thermal analysis and calorimetry 49 (1997), S. 361-366 
    ISSN: 1572-8943
    Keywords: disposable ; evolved gases ; FT-IR spectroscopy ; polymers ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermogravimetric analysis (TG) provides information regarding mass changes in the sample resulting from heat treatment under controlled environment. However, it does not provide any chemical information regarding the gases evolved during the thermal degradation. Using FT-IR spectrometry in combination with TG, it is often possible to identify the evolved gases, and also monitor their evolution profiles during thermal degradation. In this study, we present the TG/FT-IR combined analysis of incineration and pyrolysis of some common plastics such as high density polyethylene (HDPE), polyvinyl chloride (PVC), polyethylene terephthalate (PET), and polystyrene (PS). This study demonstrates the utility of such combined analysis in providing useful information regarding the use of thermal treatment for recycling or incineration.
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  • 15
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    Journal of thermal analysis and calorimetry 49 (1997), S. 399-405 
    ISSN: 1572-8943
    Keywords: DSC ; polyimide fiber ; TMA ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A commercially available polyimide fiber was investigated as a possible precursor for the formation of carbon fibers. The thermal response of the fiber was thoroughly investigated using DSC, TMA and TG. These responses were dependent on the atmosphere and tension during scanning. The fiber was stabilized at high temperatures both in inert and oxidative environments and the effect of these stabilization treatments on the structure and properties of the fiber was carefully followed. During heating, the fiber showed shrinkage tendency at small tensions, but at higher tensions the fibers could be stretched. Among the two environments investigated, air was more effective than nitrogen in getting a more stable fiber.
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  • 16
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    Journal of thermal analysis and calorimetry 49 (1997), S. 657-661 
    ISSN: 1572-8943
    Keywords: carbonaceous products ; DTA ; material characterization ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermogravimetry and differential thermal analysis, using only a combustion step with oxygen, were used to characterize carbonaceous products. Binary composition of alumina and wood charcoal, coke, carbon black, petroleum coke or carbon graphite were prepared containing 5 wt% of each. They were characterized by the burnout onset and DTA and DTG peak temperatures, which range from 476°C for wood charcoal to 790°C for carbon graphite. Complementary characterization of each product was also performed by estimating the ash content from the TG curves, and the calorific value from the DTA curves. The results indicate that these thermal analysis techniques, with only one oxygen burnout step, can be applied both for quality control of each raw material, and to determine the appropriate processing temperatures of the ceramic compositions in which they are used.
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  • 17
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    Journal of thermal analysis and calorimetry 49 (1997), S. 809-816 
    ISSN: 1572-8943
    Keywords: dehydration ; drying method ; DSC ; lactitol ; lactitol monohydrate ; TG ; X-ray powder diffraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The purpose of this study is to find out the effect of the crystal water content on the crystal structure of lactitol monohydrate. Crystal water was removed by drying over silicagel at 40°C and by using phosphorus pentoxide as drying agent at 20°C. The amouts of water removals were identified by thermogravimetry, the melting points and the heat of fusions were calculated from the results of differential scanning calorimetry measurements and the structure of samples were identified by X-ray powder diffraction method. Over 23 w/w% of total water content could removed by gently drying until significant structural changes could be detected. The melting point of anhydrous lactitol obtained by drying lactitol monohydrate was 120°C and the melting enthalpy was 102 J g−1 when measured with heating rate 10°C min−1 by DSC.
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  • 18
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    Journal of thermal analysis and calorimetry 48 (1997), S. 177-202 
    ISSN: 1572-8943
    Keywords: DTA ; mineral synthesis ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Differential thermal analysis (DTA) and thermogravimetry (TG) are applied to various fields of mineral science. The present work illustrates the importance of the application of thermal analysis to mineral synthesis, to the determination of the mechanism and optimum temperature of synthesis and the thermal behaviour of minerals and starting materials. Selected examples of applications in this field are given. These include DTA studies of the synthesis of topaz, cryptohalite, wulfenite, perovskite, scheelite and the refractory materials, baddeleyite and corundum. Thermal analysis is proved to be an important and valuable tool in mineral synthesis.
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  • 19
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    Journal of thermal analysis and calorimetry 48 (1997), S. 473-483 
    ISSN: 1572-8943
    Keywords: dosage form ; drug products ; DSC ; identification ; quantitation ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal analysis techniques, DSC and TG can advantageously be used in quality control of drug products. The methods are commonly used in preformulation for the study of polymorphism and for the study of the interactions drug substance-excipients, since these physical interactions can be the basis of the dosage form performance. For routine control of the drug products, DSC and TG methods which are quick, which require only few mg of the samples and which are automated, are very attractive for routine analysis of drug products. A single scan can give several qualitative and quantitative informations. DSC offer analytical possibilities only if the drug substance and the excipients do not have physical interactions or limited interactions (e.g. eutectic behaviour). About twenty marketed products have been analyzed by DSC and TG. In most of them identification of drug substance is easy. Several excipients could be identified in a tablet. Quantitations are demonstrated for some drug substances and excipients. DSC purity calculations have been applied to acetyl salicylic acid, paracetamol, cimetidine, pindolol, ibuprofen.
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  • 20
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    Journal of thermal analysis and calorimetry 48 (1997), S. 885-891 
    ISSN: 1572-8943
    Keywords: complexes ; DTA ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal behaviour of M(OH)2(8-HQ)2 (M=Ni, Cu and Zn; 8-HQ=8-hydroxyquinoline) has been studied by dynamic TG and DTA methods in nitrogen atmosphere. The percent weights lost in different temperature range was calculated from TG curves. The mode of decomposition has been supported by endotherms observed in DTA curves of the respective compounds.
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  • 21
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    Journal of thermal analysis and calorimetry 50 (1997), S. 7-17 
    ISSN: 1572-8943
    Keywords: cellulose ; starch ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The degradation of cellulose and starch samples in air and nitrogen has been investigated by thermal analysis techniques. The techniques employed were differential thermal analysis, rising temperature and temperature jump thermogravimetry. Rate data were obtained from these experiments and Arrhenius parameters calculated from these values. This data was used to determine the mechanism by which the cellulose and starch samples degraded. The Arrhenius parameters were also calculated. The behavior of starch and cellulose upon thermal analysis were compared and are reported.E act for corn starch was found to be 474 kJ mol−1 and for a cellulose 242 kJ mol−1.
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  • 22
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    Journal of thermal analysis and calorimetry 50 (1997), S. 587-592 
    ISSN: 1572-8943
    Keywords: coordination compounds ; CRTA ; quasi-equilibrium ; TG ; thermodynamics ; volatility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Quasi-equilibrium thermogravimetry (variant of CRTA) is utilized as a thermoanalytical screening method for volatile compounds, standard Q-derivatograph sample holders (platelike holder, open crucible, crucible with lid, and conical holder) were calibrated against the partial pressures of metal β-diketonate vapor (in sublimation and evaporation processes) in the range 0.0006–0.11 atm. The mathematical relationship between the vapor partial pressure, the holder construction, the vapor molecular mass, and the mutual diffusion coefficient of the gas was derived and considered. It is possible to obtain a roughp-T relationship for volatile compounds by using stabilized temperatures of sublimation (evaporation) processes in four pressure-calibrated sample holders.
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  • 23
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    Journal of thermal analysis and calorimetry 52 (1998), S. 863-870 
    ISSN: 1572-8943
    Keywords: calcium hydroxide ; hydration ; limestone cement ; non evaporable water ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Subject of this paper is to investigate the hydration process of Portland limestone cement containing 10-35% limestone. Cements, produced by co-grinding of clinker, limestone and gypsum, were hydrated for periods 6 h to 28 d and were studied by means of TG and XRD. The Ca(OH)2 content of the cements containing limestone is higher than in pure cements, specifically for 10% limestone content and ages more than 1 day. These results are in accordance with the strength development of the studied cements. In earlier ages the Ca(OH)2 content is slightly lower in the limestone cements and independent of the limestone content. After 1 day curing, the increase of limestone addition causes a relative increase of the non evaporable water. The XRD patterns indicated the presence of carboaluminates in the hydrated limestone cements.
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  • 24
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    Journal of thermal analysis and calorimetry 53 (1998), S. 71-85 
    ISSN: 1572-8943
    Keywords: DSC ; enantiomer ; IR ; powder X-ray diffractometry ; racemate ; TG ; thermomicroscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The physicochemical characterization of the solid-state enantiomers and racemate of efaroxan hydrochloride (C13H17N2O+Cl-, M=252.5 g mol-1) was performed by thermoanalytical methods (differential scanning calorimetry, thermogravimetry and thermomicroscopy) and spectral methods (infrared spectrometry and X-ray diffractometry). The efaroxan enantiomers and racemate were shown to be unstable near the melting point. At the beginning of the decomposition, a loss of hydrogen chloride was observed. However when sealed pans were used, the compounds decomposed at higher temperature, allowing a precise evaluation of the melting enthalpies by means of differential scanning calorimetry. The nature of the racemate and its thermal stability were assessed by evaluating its free formation enthalpy. An enantiotropic solid-solid transformation (II→I) was noted for the racemate; the reverse process (I→II) follows zero-order kinetics.
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  • 25
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    Journal of thermal analysis and calorimetry 53 (1998), S. 365-374 
    ISSN: 1572-8943
    Keywords: compositional analysis ; event separation ; heating rate ; MaxRes ; softening ; TG ; TMA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Conventional thermogravimetric analysis (TG) uses constant heating rates to determine decomposition rates of a material and compositional analysis. Often, the decomposition steps can not be separated clearly enough due to parallel or consecutive reactions. If the reaction rates and the respective activation energies are enough different the TG resolution can be much enhanced by lowering the heating rate during the decomposition steps. The automated discrete adjustment of the heating rate is controlled by a set of parameters, such as threshold values, waiting times and rate factors. This technique, called MaxRes, allows for faster compositional analysis without loss of resolution. The same technique is also applicable to thermomechanical analysis (TMA) if time/temperature dependent events such as softening are to be separated.
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  • 26
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    Journal of thermal analysis and calorimetry 53 (1998), S. 487-492 
    ISSN: 1572-8943
    Keywords: calcite ; calcium polyphosphates ; dolomite ; phase transformation ; TG ; X-ray
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal interactions of dolomite and calcite with calcium polyphosphates up to 1000°C were studied by thermal (dynamic heating and isobaric conditions) and X-ray diffraction methods. It was found that in mixtures with Ca-polyphosphates less than half of the carbonates reacted before decomposition to oxides with the phosphates. The rates of the reactions of phosphates with MgO were much lower than those with CaO. The scheme of the main crystalline phase transformations was constructed.
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  • 27
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    Journal of thermal analysis and calorimetry 55 (1999), S. 67-76 
    ISSN: 1572-8943
    Keywords: activation energy ; DSC ; ethylene-vinyl acetate copolymer ; TG ; TG/IR ; thermal degradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract When ethylene-vinyl acetate copolymer, EVA, is heated, a two-stage thermal degradation occurs following its melting. The vinyl acetate content of the copolymer was determined to be 43.8% by using TA 2950 and TA 2050 thermogravimetric instruments. TG/FTIR was used to detect the evolved gas. Acetic acid and trans-1-R-4-R'-cyclohexane were the main products evolved from EVA in the first and second stage, respectively. The apparent activation energies were determined for both stages by differential methods.
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  • 28
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    Journal of thermal analysis and calorimetry 55 (1999), S. 93-98 
    ISSN: 1572-8943
    Keywords: degradation ; DTA ; flame retardant ; IR ; pyrolysis ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal degradation of cotton cellulose treated with chemical mixtures containing P and N was studied by thermal analysis, infrared spectroscopy, Char yield and limiting-oxygen-index (LOI). Our experiments demonstrated the following facts. The temperatures and activation energies of pyrolysis were lower for cotton cellulose treated with flame retardants than those for untreated samples and the values of Char yield and LOI were greater for treated cotton than those for untreated one.
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  • 29
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    Journal of thermal analysis and calorimetry 55 (1999), S. 841-849 
    ISSN: 1572-8943
    Keywords: cobalt(II)-dothiepin ; kinetics ; TG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The complexes of cobalt(II) with dothiepin (DOT) hydrochloride have been studied for kinetics of thermal degradation by thermogravimetric analysis (TG) and derivative thermogravimetric studies (DTG) in a static nitrogen atmosphere at a heating rate of 10° C min−1. A general mechanism of thermal decomposition is advanced involving dehydration and decomposition process for both organic and inorganic ligands. The thermal degradation reactions were found to proceed in three steps having an activation energy in the range 6.75–170 kJ mol−1. Thermal decomposition kinetics parameters were computed on the basis of thermal decomposition data.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 297-303 
    ISSN: 1572-8943
    Keywords: β-zeolite ; coke ; cumene ; kinetics ; regeneration ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract An accurate description of coke burn off is obtained from a catalyst based on β-zeolite and used for benzene alkylation with propylene giving cumene by using the thermogravimetric technique. A simple empirical kinetic model was successfully applied to interpolate the data of thermogravimetric analysis performed on samples after partial burn off. Different temperatures, partial pressures of oxygen and gas flow rates were the variables studied in order to calculate the apparent rates and the activation energy for the coke oxidation reaction and to outline the best conditions for the industrial regeneration procedure of our proprietary catalyst PBE-1 for cumene synthesis. Combining the unusually long lifetime per reaction cycle with the optimized regeneration procedure leads to an outstanding overall catalyst life.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 337-343 
    ISSN: 1572-8943
    Keywords: DTA ; DTG ; immobilized cinchonidine ; Pt/K-10 montmorillonite ; TG ; thermal stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The characterization of new cinchonidine doped K-10 montmorillonite supported noble metal catalysts is described. Our aim was the mapping of thermal stability of these new catalytic materials by thermogravimetry (TG), differential thermogravimetry (DTG) and differential thermoanalysis (DTA) methods accompanied by X-ray diffraction (XRD) measurements. The catalysts were prepared by various methods including conventional, microwave and ultrasonic treatments. They were characterized first by X-ray diffraction to verify the stability of montmorillonite crystal structure during preparation. Then, TG and DTG methods were applied to determine their stability under the experimental conditions usually applied. The main changes observed were the loss of water and the decomposition of the organic modifiers in the higher temperature region. The catalyst showed the best performance were prepared and characterized using microwaves and ultrasonic irradiation in order to get more insight to the effect of preparation methods on their stability. As a consequence, the catalysts were found to be stable and regenerable under 450-500 K, however, higher temperatures resulted in the complete destruction of the catalysts.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 541-546 
    ISSN: 1572-8943
    Keywords: acetate ; DTA and IR ; halogenoacetates ; Mg(II) ; pyridine ; SCN ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract TG, DTA and other analytical methods were applied to investigate the thermal behaviour and structures of the compounds Mg(ClAc)2(Py)2·2H2O (I), Mg(Cl2Ac)2(Py)·H2O (II), Mg(Cl3Ac)2(Py)·6H2O (III) and Mg(SCN)2(Py)3·2H2O (IV), where ClAc=ClCH2COO−, Cl2Ac=Cl2CHCOO−, Cl3Ac=Cl3CCOO− and Py=Pyridine. The compositions of the complexes and the solid-state intermediates and products of thermolysis were identified by means of elemental analysis. Possible schemes of destruction of the complexes are suggested. The final products of the thermal decompositions were MgO (I–III) and MgS (IV). The IR data suggest unidentate coordination of the carboxylate ions to Mg(II) in complexes I–III. Py is coordinated to the Mg(II) through the nitrogen atom of its heterocyclic ring.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 479-484 
    ISSN: 1572-8943
    Keywords: copper thiocarbamide complex ; DTA ; spray pyrolysis ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Hydrated isostructural 1:3 complexes of copper(I) chloride and bromide with thiourea were synthesised and their thermal decomposition studied by simultaneous TG/DTA complemented by ex situ FTIR and XRD studies. The decomposition of Cu(tu)3Cl·H2O is initiated by dehydration around 100°C, followed by a total multi-step degradation of the structure in the temperature range of 200–600°C. The counter ion has some influence on the temperatures and composition of the solid residue. The results were compared with those obtained with the 1:1 complex Cu(tu)Cl·1/2H2O.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1059-1063 
    ISSN: 1572-8943
    Keywords: dehydration ; miscibility ; NMR ; polymer blend ; poly(2-hydroxyethyl methacrylate) (PHEMA) ; poly(methacrylic acid) (PMAA) ; TG ; TMDSC
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Miscibility and dehydration of poly(2-hydroxyethyl methacrylate) and poly(methacrylic acid) (PHEMA/PMAA) blends were investigated by temperature modulated DSC (TMDSC), TG and solid-state 13C NMR methods. TMDSC spectra and 1H spin-relaxation times showed that the blends are homogeneous on a scale of 5-10 nm for all compositions. From TG and 13C NMR, we elucidated that the mass loss of the blends at 300°C is ascribed to the dehydration between the hydroxyl group of PHEMA and the carboxyl group of PMAA.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1093-1096 
    ISSN: 1572-8943
    Keywords: activation energy ; aromatic polyamide ; benzimidazolyl-substitution ; TG ; thermal stability
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The TG studies are presented for isomers of benzimidazolyl-substituted polyamides (BIPA). The TG data are compared with those polyamides (PA) of identical backbones without substitution, in view of the mechanism of thermal degradation. The TG mass loss curves divided to three temperature ranges reflect the decomposition reactions in the respective temperature ranges: (1) cleavage of single bonds of nitrogen to aromatic ring, (2) random scission of single bonds, (3) condensation of the remained rings. Liberation of benzimidazole rings occurs in the temperature range (2). The final product, char, contains benzimidazole rings. Terephthaloyl-rich BIPA's retard liberation of benzimidazole from the decomposed polymer.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1285-1304 
    ISSN: 1572-8943
    Keywords: amorphous state ; combined techniques ; drug design ; drug product development ; drug substance ; drug technology ; DSC ; excipients ; failure investigations ; hydrates ; MDSC ; microcalorimetry ; pharmaceuticals ; polymorphism ; polymers ; preformulation ; process optimization ; purity ; quality control ; solvates ; stability ; sub-ambient DSC ; TG ; temperature resolved X-ray diffraction ; water interactions ; thermal microscopy ; water sorption-desorption
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Modern thermal analysis, microcalorimetry and new emerging combined techniques which deliver calorimetric, microscopic and spectroscopic data offer a powerful analytical battery for the study of pharmaceuticals. These techniques are very useful in all steps of development of new drug products as well as methods for quality control in production. The characterization of raw materials enables to understand the relationships between polymorphs, solvates and hydrates and to choose the proper development of new drug products with very small amount of material in a very short time. Information on stability, purity is valuable for new entities as well as for marketed drug substances from different suppliers. Excipients which vary from single organic or inorganic entity to complexes matrixes or polymers need to be characterized and properly controlled. The thermodynamic phase-diagrams are the basis of the studies of drug-excipients interactions. They are very useful for the development of new delivery systems. A great number of new formulations need proper knowledge of the behaviour of the glass transition temperature of the components. Semi-liquid systems, interactions in aqueous media are also successfully studied by these techniques.
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    Journal of thermal analysis and calorimetry 57 (1999), S. 61-73 
    ISSN: 1572-8943
    Keywords: amorphous ; combined techniques for polymorphism ; DSC ; MKS 492 ; polymorphism ; purine ; quantitative determination ofamorphous and polymorphs ; solvent mediated transitions ; temperature resolved X-ray diffraction ; TG ; thermodynamic relation between polymorphs ; xanthine
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The polymorphic behaviour of the purine derivative MKS 492 was studied with investigations of suspensions of selected samples in different solvents and of samples obtained by crystallizations. The samples were analyzed by DSC, TG and X-ray diffraction. Six different crystalline modifications called A, B, B’, C, D and E and an amorphous form were identified. Four pure crystalline modifications, A, B, C and D have been manufactured and characterized by DSC, X-ray, IR, solubilities, densities, hygroscopicity and dissolution measurements. The four forms A, C, D and E are monotrop to the form B. The form B is enantiotrop to the form B’, which revealed the highest melting point of all known polymorphs. This form B’ is only stable at high temperature. Temperature resolved X-ray diffraction was very helpful for proper interpretation of the thermal events. The melting peaks of the forms A and C and the endothermic peak corresponding to the enantiotropic transition B into B’ occur in a narrow range of temperature. The form B which is the most stable one at room temperature has been chosen for further development. Quantitative methods to determine the content of the forms A, C and D in samples of form B or to determine the content of form A, B and D in form C have been developed by using X-ray diffraction. Limits of detection are 1 or 2%. For the quantitative determination of the amorphous fraction, X-ray diffraction and microcalorimetry are compared. For high amounts of the amorphous fraction, the X-ray diffraction method is preferred because it is faster. Microcalorimetry is very attractive for levels below 10% amorphous content. The lowest limit of detection is obtained by microcalorimetry, about 1%.
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    Journal of thermal analysis and calorimetry 58 (1999), S. 355-362 
    ISSN: 1572-8943
    Keywords: Curie temperature ; nanocrystalline ; TG ; TG(M) and DTG(M)
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The σ—T and dσ/dT—T curves of the FeCuNbSiB amorphous alloy, which are the relationship between the total saturated magnetic moment per unit mass σ and temperature, are investigated by magnetic thermogravimetry analysis (TG(M)) technique. It is found that the crystallization process of the samples can be divided into five stages. The studies of samples annealed in temperature range of 480–610°C for 1h show that when the annealing temperature (Ta) is less than 540°C, the quantity of nanocrystalline α-Fe(Si) phase increases evidently with Ta, and the Curie temperature (TC) of residual amorphous phase also increases linearly with Ta, i.e. TC=0.52Ta+91.7°C, with correlation coefficient γ=0.98. The variation of volume fraction of α-Fe(Si) nanocrystalline phase or residual amorphous phase with Ta is measured by TG(M) technique.
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  • 39
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    Keywords: first order autocatalytic reaction ; HNNC ; kinetics ; TG
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    Notes: Abstract The kinetics of the first order autocatalytic decomposition reaction of highly nitrated nitrocellulose (HNNC, 14.14%N) was studied by using thermogravimetry (TG). The results show that the TG curve for the initial 50% of mass-loss of HNNC can be described by the first order autocatalytic equation $$\frac{{{\text{d}}y}} {{dt}} = - 10^{16.4} \exp \left( { - \frac{{210380}} {{RT}}} \right)y - 10^{16.7} \exp \left( { - \frac{{171205}} {{RT}}} \right)y(1 - y)$$ and that for the latter 50% mass-loss of HNNC described by the reaction equations $$\frac{{dy}} {{dy}} = - 10^{16.3} \exp \left( { - \frac{{169483}} {{RT}}} \right)y\quad (n = 1)$$ and $$\frac{{dy}} {{dt}} = - 10^{16.8} \exp \left( { - \frac{{165597}} {{RT}}} \right)y^{2.61} \quad (n \ne 1)$$
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    Journal of thermal analysis and calorimetry 58 (1999), S. 671-675 
    ISSN: 1572-8943
    Keywords: chemically modified zeolite thermochemical properties ; DTA ; emanation thermal analysis ; TG ; zeolite
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Zeolites chemically modified with 1, 4 or 6 M aqueous solutions of NaOH were studied by DTA, TG and ETA (emanation thermal analysis) in the temperature range 201–200°C. The structural changes in the modified zeolites at room temperature and in the modified zeolites annealed at 1000°C were studied by XRD analysis. Thermal analysis demonstrated dehydration, dehydroxylation, structural changes and a glass transition. A gradual loss in crystallinity of the chemically modified zeolites was also observed. XRD analysis revealed structural changes caused by chemical treatment and also by annealing.
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    Journal of thermal analysis and calorimetry 58 (1999), S. 653-662 
    ISSN: 1572-8943
    Keywords: dehydration ; DSC ; TG ; water ; zeolites
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    Topics: Chemistry and Pharmacology
    Notes: Abstract A procedure for measurement of the heat of zeolite dehydration by scanning heating has been designed. Simultaneous data on heat flow (DSC) and mass loss (TG) are required for evaluation. The heating rate depends on the experimental conditions (point-spread function, sample mass, crucible design, and calorimetric reproducibility). Dehydration measurements have three advantages as compared with the sorption procedure: i) one can investigate samples with irreversible dehydration; ii) no approximation model is needed for calculation of the partial molar heat of dehydration; and iii) the procedure is not labor-consuming. The procedure was tested on the natural zeolites heulandite, chabazite and mordenite. The results are close to those measured by the sorption procedure. The partial molar heat of dehydration was found to depend on the water content. It increases from 50 to 87 J mol−1 K−1 for heulandite, from 53 to 81 J mol−1 K−1 for chabazite, and from 51 to 71 J mol−1 K−1 for mordenite. The approximation of the heat of sorption by linear regression was found to be wrong. Detection of a ‘phase transitioN’ after this approximation has no meaning.
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    Journal of thermal analysis and calorimetry 49 (1997), S. 595-599 
    ISSN: 1572-8943
    Keywords: methyl benzoate ; perfumes ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Ingredients used in the manufacture of perfumes can be investigated by thermogravimetry. In this study the evaporation of methyl benzoate was investigated using a simultaneous TG-DTA unit. A rising temperature method of thermal analysis was used for the study. The rate of evaporation of the ingredient was calculated from a simple plot of percentage mass lossvs. time. A derivative plot of the same was used to calculate the coefficient of evaporation in a controlled atmosphere and regulated air flow rate. In a series of programmed temperature runs on the TGDTA unit it was shown that the evaporation process is zero order, and that the evaporation coefficients at each temperature can be fitted into the Arrhenius equation. The energy of activation, Eact can be calculated from the slope of the line. It was found to be 47 kJ mol−1. This value was compared and shown to approach the enthalpy of vaporization as calculated using the Troutons or Clausius Clapeyron equation
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    Journal of thermal analysis and calorimetry 50 (1997), S. 719-726 
    ISSN: 1572-8943
    Keywords: aluminum ; carbon black ; DTA ; indium ; TG ; zinc ; zinc oxalate
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Simultaneous TG-DTA units have a work station which allows plots to be made of temperature against time, as well as the conventional TG and DTA plots. These time-temperature plots and their derivatives can be used to show details of both exothermic and endothermic events. The melting behavior of zinc is used as illustrative of endothermic phase changes. Solid-solid transitions are exemplified by noting the transitions in quartz. Examples of chemical reactions being treated to temperature-time plots are the decomposition's of zinc oxalate in nitrogen (an endothermic event) and the oxidation of carbon black in air (a sustained exothermic event). This wide selection of exothermic and endothermic events serves to illustrate the details which can be drawn from any thermogravimetric plot irrespective of the other associated equipment present, which serves to reinforce the data presented in the present study.
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    Journal of thermal analysis and calorimetry 50 (1997), S. 525-531 
    ISSN: 1572-8943
    Keywords: activation ; carbon ; corn cobs ; SEM ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Corn cobs obtained as waste from the corn industry, were analyzed by a TG-DTA unit in an atmosphere of flowing nitrogen. The carbonaceous products so formed were then produced on a preparative scale and activated chemically using potassium hydroxide. This resulted in the formation of a carbon with a very high surface area. The active carbon produced was then examined using thermal analysis in the temperature jump mode on a thermogravimetry unit. From this data the kinetics of degradation of the active carbon was determined using zero order rate kinetics. The pore structure of the active material was also examined using SEM. TheE a for activated corn cobs was found to be 106 kJ mol−1.
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    Journal of thermal analysis and calorimetry 53 (1998), S. 895-904 
    ISSN: 1572-8943
    Keywords: crosslinking ; differential scanning calorimetry ; polyaniline ; post-polymerization ; relaxation transition ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal behaviour of polyaniline-‘emeraldine base’ (PANI-EB) was studied using thermogravimetric analysis (TG) and differential scanning calorimetry (DSC). We assume that during heating over 150°C three exothermal processes proceed - reorganization and crosslinking between PANI-EB chains followed by post-polymerization. The low temperature relaxation transition for PANI-EB was registered for the first time by DSC. We suppose that it might be due to the motion of polymer chains non-crosslinked during the first heating, chain fragments resulting from high-temperature decomposition over 300°C and chain ends of the already crosslinked polymer.
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    Journal of thermal analysis and calorimetry 54 (1998), S. 63-69 
    ISSN: 1572-8943
    Keywords: DTA ; IR ; K0.5Bi0.5TiO3 ; PbZrO3 ; solid solution ; TG ; XRD
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    Topics: Chemistry and Pharmacology
    Notes: Abstract DTA, TG, XRD and IR methods were used to study the formation of solid solutions in the selected subsolidus range of the PbZrO3-K0.5Bi0.5TiO3 system by heating mixtures prepared using oxide substrates, i.e. PbO, Bi2O3, ZrO2, TiO2 and K2CO3. It was found that solid solutions are formed in the reaction of PbO and ZrO2 with intermediate compound, i.e. K0.5Bi0.5TiO3. PbZrO3 was not found to be formed as an intermediate phase.
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    Journal of thermal analysis and calorimetry 54 (1998), S. 369-379 
    ISSN: 1572-8943
    Keywords: compensation effect ; dimensionless analysis ; DTG ; error levels ; evaluation ; kinetic parameters ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract It follows from an analysis of the error levels of TG evaluation methods that it is a conceptual error to disregard the analogies of mass, energy and momentum streams of subordinate partial processes. This error is bypassed by means of the introduced method of dimensionless analysis and by determining the characteristic, constants-like data of thermal processes by using the measured data directly. These methods are very suitable for increasing the consistency of the calculated results by seeking for similarity, even in comparisons of measurements made under very different conditions and for emphasizing the differences too, quantitatively. With this new interpretation of TG processes, the idea of the kinetic compensation effect becomes only a consequence of the discussed conceptual error.
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  • 48
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    Keywords: activation energies ; degradation behaviour ; epoxy resin ; master curves ; TG
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    Notes: Abstract A study of an epoxy-cycloaliphatic amine system has been realized using a thermogravimetric technique (TG). Isothermal and non-isothermal (dynamic) methods were employed to determine the kinetic data of this system. Five methods were used for determining the activation energies of this system in the dynamic heating experiments. In two of them (Flynn-Wall-Ozawa, and Kissinger) it is not necessary to have a prior knowledge of the reaction mechanism of the degradation behaviour for this system. In the other ones (Coats and Redfern, Horowitz and Metzger, and Van Krevelen et al.) it is necessary to know this reaction mechanism, besides Criado et al. method was used for determining it. The results have shown that good agreement between the activation energies obtained from all methods can be achieved if it is assumed that the degradation behaviour of this system is of sigmoidal-rate type.
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    Journal of thermal analysis and calorimetry 55 (1999), S. 789-796 
    ISSN: 1572-8943
    Keywords: alkaline earth malonates ; DSC ; DTA ; kinetic parameters ; TG ; thermal decomposition
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal decomposition of strontium and barium malonates has been studied isothermally and non-isothermally employing simultaneous TG-DTG-DTA, DSC, XRD and IR spectroscopic techniques. DSC of these malonates has been recorded both in oxygen and nitrogen atmospheres. The decomposition is a single step process and the end product formed is carbonate. The energy of activation and frequency factor values for the decomposition of strontium malonate are 547 kJ mol−1 and 1041 s−1 respectively. The activation energy and frequency factor values for isothermal dehydration of barium malonate sester-hydrate are 57–111 kJ mol−1 and 107–1012 s−1 respectively and the corresponding values for decomposition from DSC are 499.5 kJ mol−1 and 1044 s−1 respectively. The higher thermal stability of strontium malonate as compared to that of barium salt is ascribed to its being anhydrous so that decomposition proceeds without restructuring. Their thermal stabilities have also been compared with that of respective oxalate salts.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 7-15 
    ISSN: 1572-8943
    Keywords: ALE ; CVD ; DSC ; DTA ; EGA ; EL display ; solar cell ; sol-gel ; spray pyrolysis ; super-conductor ; TG ; thin films
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Processing thin films for advanced applications, for instance in electronics and optoelectronics, involves several steps starting from precursor synthesis and ending up with the devices. Especially when optimizing the first steps of this chain of processes, thermoanalytical techniques play an important role. The review will focus on the main chemical deposition methods (CVD, ALE, spray pyrolysis, sol-gel) giving selected examples of problem-solving by thermal analysis. The techniques discussed are TG, DTA/DSC, EGA and their combinations. High-temperature X-ray diffraction (HTXRD) is also a powerful tool for in situ studies of thin films. The examples are taken from solar cell, superconductor and flat panel electroluminescent display technologies.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 429-435 
    ISSN: 1572-8943
    Keywords: DSC ; nickel sulphide ; TG ; toughened glass ; X-ray diffraction
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Nickel sulphide (NiS) was characterised using X-ray diffraction, thermal gravimetric analysis (TG) and differential scanning calorimetry (DSC). The 'as received' Millerite, stoichiometric NiS, observed to be slightly nickel deficient, was found to readily decompose in a nitrogen atmosphere at elevated temperatures (450°C max.) to the sulphur deficient Godlevskite, Ni7S6. DSC and X-ray measurements demonstrated that the high temperature form of the Godlevskite was readily stabilised at room temperature. The kinetics of the α-β re-transformation in Godlevskite were then investigated using DSC and were observed to be first order.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1389-1396 
    ISSN: 1572-8943
    Keywords: FT-IR ; fuel ; oil ; pyrolysis ; residue ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Although thermogravimetric analysis (TG) has become an indispensable tool for the analysis and characterization of materials, its scope is limited as no information is obtained about the qualitative aspects of the evolved gases during the thermal decomposition. For processes involving mass loss, a powerful technique to provide this missing information is Fourier transform infrared spectroscopy (FT-IR) in combination with TG. It supplies a comprehensive understanding of thermal events in a reliable and meaningful way as data are obtained from a single sample under the same conditions. The coupling TG/FT-IR is used in fuel analysis for the identification of residual volatiles, to determine their sequence of release and to resolve thermogravimetric curves. In this work, the usefulness of TG/FT-IR for characterizing middle distillate fuel residues is illustrated with some typical examples of recent application. A Bio-Rad FTS 25 FT-IR spectrometer coupled with a TA Instruments TGA 2950 thermogravimetric analyzer was used for data aquisition. The results obtained demonstrate the utility of this combined technique in determining the decomposition pathway of tarry materials at various stages of pyrolysis, thereby allowing new insights into the complex thermal behaviour of hydrocarbon residual systems.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1123-1131 
    ISSN: 1572-8943
    Keywords: compatibility ; decomposition ; energetic materials ; peak temperature ; polymers ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Compatibility is an important safety aspect related to the production and storage of energetic materials. To test different combinations of materials a simple test method with clear criteria is advisable. At the last ESTAC the use of microcalorimetry and the vacuum stability test for the compatibility testing of propellants were presented. This paper presents DSC, DTA/TG and (pressure) vacuum stability test results for the same combination. For three polymers (PMMA, PVC and CA) the results for all tests are the same. Only Nylon-6/6 gives a variable result for the different test methods.
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1353-1357 
    ISSN: 1572-8943
    Keywords: DSC ; terpenoids ; TG ; thermal behaviour
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The terpenoids acetyl sitosterol, lupeol, acetyl diosgenin and stigmasterol were studied. Comparison of the thermogravimetric curves and the activation energies of the terpenoids suggested the following sequence of thermal stability: acetyl sitosterol 〈 acetyl diosgenin 〈 lupeol 〈 stigmasterol. The DSC curves allowed determination of the melting points and the degrees of purity. Comparison of the TG and DSC curves revealed the presence of phase transitions without mass loss that were attributed to rearrangements in the terpenoid molecules.
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    Journal of thermal analysis and calorimetry 58 (1999), S. 309-315 
    ISSN: 1572-8943
    Keywords: dispersion threshold value ; Mn2O3/γ-Al2O3 catalyst ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Mn2O3/γ-Al2O3 catalysts were prepared by the impregnation method, and the maximum monolayer dispersion capacity or dispersion threshold value of Mn2O3 on the surface of γ-Al2O3 was determined to be 13.08% from the decomposition mass loss of supported Mn(NO3)2 in the monolayer state. This was compared with the values estimated from a close-packed monolayer model and an interaction model. It was confirmed that the high activities and selectivities of the catalysts for benzoic acid hydrogenation to benzaldehyde are due to the monolayer dispersion of the Mn2O3 on the surface of γ-Al2O3.
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  • 56
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    Journal of thermal analysis and calorimetry 47 (1996), S. 259-262 
    ISSN: 1572-8943
    Keywords: DTA ; hyphenated technique (EGA) ; sample robot ; TG ; thermobalance ; SDTA
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    Topics: Chemistry and Pharmacology
    Notes: Abstract A thermogravimetric unit is described having horizontal furnace arrangement, a temperature range of up to 1100°C and unsurpassed dynamic weighing range from 0 to 2 g at 0.1 μg resolution. Options of the system are sample robot, gas controller, high temperature furnace and hyphenated EGA techniques. In addition to the TG, the SDTATM curve allows the detection of endo-or exothermal effects (analogous to DTA or DSC) to a resolution of 5 mK.
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  • 57
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    Journal of thermal analysis and calorimetry 47 (1996), S. 1121-1140 
    ISSN: 1572-8943
    Keywords: dynamic mechanical thermal analysis ; low density polyethylene ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal behaviour of pineapple leaf fibre (PALF) reinforced polyethylene composites was studied by thermogravimetric and dynamic mechanical thermal analysis. Fibre treatment was carried out using isocyanate, silane and peroxide to improve the interfacial adhesion between fibre and matrix. The effects of fibre loading and surface modification on the thermal properties were evaluated. It was found that at high temperature PALF degrades before the polyethylene matrix. The storage modulus increased with increase of fibre loading and decreased with increase of temperature. The treated fibre composites impart better properties compared to untreated system. Tan δ showed a distinct peak at low temperature ascribed to the glass transition temperature of polyethylene but no peak was observed for PALF fibre. The relative damping increased with fibre loading. Cole-Cole analysis was made to understand the phase behaviour of the composite samples.
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  • 58
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    Journal of thermal analysis and calorimetry 49 (1997), S. 247-254 
    ISSN: 1572-8943
    Keywords: degradation ; kinetic parameters ; microscopy ; miscibility ; PVC/EVA blends ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal stability and degradation processes in PVC/EVA systems were evaluated for a series of EVAs with different vinyl acetate contents. The experimental data revealed a relationship between the thermogravimetric curves and the degree of interaction in the mixtures as compared to the pure polymers, which is consistent with the results of microscopic analysis. Kinetic parameters and lifetime data on the mixtures were also calculated.
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  • 59
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    Journal of thermal analysis and calorimetry 46 (1996), S. 1501-1505 
    ISSN: 1572-8943
    Keywords: Conditioning Houses ; history ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract This paper describes the origins of Conditioning Houses in Manchester and London as an adjunct to early commercial equipment in the UK.
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  • 60
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    Journal of thermal analysis and calorimetry 46 (1996), S. 1541-1550 
    ISSN: 1572-8943
    Keywords: DSC ; FTIR ; grafting ; IDSC ; kinetic parameters ; polymerization ; TG ; thermodynamic parameters
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal polymerization of pentabromobenzyl (mono)acrylate (PBB-MA) on the surface of the inorganic fillers Mg(OH)2 and CaCO3 was studied. FTIR spectroscopy and extraction of the polymer in bromobenzene show that polypentabromobenzyl acrylate (PBB-PA) was mostly grafted on the surface of Mg(OH)2. Thermal analysis (TG, DSC, isothermal DSC (IDSC)) demonstrated an increase in polymerization starting temperature, and differences in polymerization enthalpy and apparent activation energy when an inorganic filler is added. These differences depend on the chemical composition of the filler used.
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  • 61
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    Journal of thermal analysis and calorimetry 47 (1996), S. 93-102 
    ISSN: 1572-8943
    Keywords: cyclic voltammetry ; manganese oxides ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermal decomposition of various synthetic manganese oxides (MnO, Mn3O4, Mn2O3, MnOOH) and a natural manganese dioxide (MnO2) from Gabon was studied with the help of termogravimetry in inert, oxidizing and reducing atmospheres. The compounds were characterized by XRD and electrochemical activity was tested by cyclic voltammetry using a carbon paste electrode. The natural manganese dioxide showed the best oxidizing and reducing capacity, confirmed by the lower temperatures of the transitions, the extent of the reactions and electrochemical performance in cyclic voltammograms.
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  • 62
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    Journal of thermal analysis and calorimetry 49 (1997), S. 589-594 
    ISSN: 1572-8943
    Keywords: decomposition ; parylene ; poly(α,α,α′α′-tetrafluoro-p-xylylene) ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal decomposition of poly(α,α,α′,α′-tetrafluoro-p-xylylene) (parylene AF-4) films with thicknesses of ca. 7.5 and 10 μm has been studied by both dynamic (10°C min−1) and isothermal TG in either nitrogen or oxygen atmospheres. In dynamic studies with nitrogen, gross decomposition occurs between 546.7±1.4 and 589.0±2.6°C, with 26.8±4.4% of the initial mass remaining at 700°C. With oxygen as the purge gas, the onset of decomposition shifts slightly to 530.8±4.2°C. The end of the transition at 587.4±2.6°C is within experimental error of the nitrogen value, but no polymer remains above 600°C. Isothermal data were obtained at 10°C intervals from 420 to 490°C in nitrogen, and from 390 to 450°C in oxygen. Plots of log(Δ%wt/Δt)vs. T−1 are linear throughout the specified range for oxygen and from 420 to 470°C for nitrogen. The calculated activation energies of (147±16) kJ mol−1 and (150±12) kJ mol−1 in N2 and O2, respectively, are equal within experimental error.
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  • 63
    ISSN: 1572-8943
    Keywords: coordination compounds ; CRTA ; TG ; quasi-equilibrium ; thermodynamics ; volatility
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Quasi-equilibrium thermogravimetry (with sample holders specially calibrated for the vapour pressure) was used for thermoanalytical screening of volatile compounds. ‘p-T’ relationships (in the range 0.0006 to 0.11 at) were obtained for acetylacetonates and fluoroacetylacetonates of Al, Cr and Zr. The incorporation of the trifluoromethyl group into the acetylacetone ligand noticeably increases the volatility: the enthalpy of evaporation remains practically constant, but the evaporation entropy changes distinctly.
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  • 64
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    Journal of thermal analysis and calorimetry 52 (1998), S. 145-155 
    ISSN: 1572-8943
    Keywords: acrylates ; DMA ; DSC ; epoxides ; radiation curing ; structure-property relationship ; TG ; thermal analysis
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Thermo-oxidative and thermo-mechanical stabilities of radiation-cured acrylates and epoxides were examined by TG, DMA and DSC. The polymeric trifunctional acrylates PETIA, TMPTA and THEIC displayed the highest temperatures of onset of degradation. The high crosslinking density of the films resulted in an almost temperature-independent complex E-modulus, as measured by DMA. With increasing degree of ethoxylation or propoxylation of the monomers, decreases in thermal stability and strength were found. For difunctional polymeric acrylates and epoxides, the glass transition temperature was measured. The average degree of curing of UV-cured epoxy films can be determined from the temperature of the maximum in the loss modulus (E″max.
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  • 65
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    Journal of thermal analysis and calorimetry 52 (1998), S. 221-233 
    ISSN: 1572-8943
    Keywords: DTA ; DTG ; highly additivated plastics ; MS ; recycling ; soft-PVC waste ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Within a research project, a new process for the recycling of soft-PVC waste has been developed. Additionally to the economic significance, the material is predestined to serve as a model system for plastics with high additive contents.
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  • 66
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    Journal of thermal analysis and calorimetry 53 (1998), S. 649-658 
    ISSN: 1572-8943
    Keywords: calcination ; limestone ; phase analysis ; porosity ; reactivity ; SEM ; sulphation ; sulphur oxide capture ; texture ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The reactions occurring between CaCO3/CaO and SO2/SO3 in oxidizing atmospheres are discussed. Calcination and sulphation were carried out in a thermobalance under conditions relevant to atmospheric fluidized bed combustion. It is suggested that the quality of limestones as potential SO2 sorbents can be assessed on the basis of tests carried out in a TG apparatus adapted for use with corrosive gases. Limestone calcined under different conditions including the treatment with NaCl leads to changes in surface texture. Sulphated samples were examined in a SEM by energy dispersive X-ray and backscattered electron imaging. Two sulphur-bearing solids (CaSO4 and CaS) were identified. The sulphation rate and extent are determined by the product layer diffusion. The amount of CaS present at the end of the process depends on the particle size of the sorbent.
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  • 67
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    Journal of thermal analysis and calorimetry 55 (1999), S. 833-840 
    ISSN: 1572-8943
    Keywords: acidity ; ammonium perchlorate ; basicity ; characterization ; DTG ; metal oxides ; pyrolysis ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Six metal oxide samples were prepared by calcination of the corresponding precursors at 500°C for 5 h in air and were characterized by IR and XRD analyses. Their surface areas were calculated by means of the BET method. The acidities and basicities of these metal oxides were estimated thermogravimetrically by the method of adsorption of pyridine and formic acid as probe molecules. The pyrolyses of pure ammonium perchlorate (AP) and of AP mixed with (10% w/w) metal oxide were studied, in a dynamic atmosphere of N2, by thermogravimetric analysis (TG) and derivative thermogravimetric analysis. A correlation was found between the catalytic activities of the metal oxides during the pyrolysis of AP, and their acidic-basic characters. The activation energies of the non-catalyzed and catalyzed pyrolysis of AP were calculated from the TG results via the Coats-Redfern equation.
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  • 68
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    Journal of thermal analysis and calorimetry 55 (1999), S. 773-777 
    ISSN: 1572-8943
    Keywords: aerogel ; calcination ; hydrophylicity ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Differences in mass loss occurring in the course of dynamic and isothermal heating of SiO2-aerogel and changes of specific surface and hydrophylicity during calcination were studied by thermal analysis. SiO2-aerogel was prepared from tetramethoxysilane (TMOS) hydrolyzed by ammonia solution at 0°C with molar ratio TMOS: H2O:NH4OH 4:1:0.01. Differences are caused mainly by oxidation of organic matter and by diffusion of products of the oxidation. Heat transfer has none or little effect on the differences. Samples calcined at temperatures about 300°C reach maximum hydrophilicity though they still contain small amounts of residual organic matter.
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  • 69
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    Journal of thermal analysis and calorimetry 55 (1999), S. 995-1002 
    ISSN: 1572-8943
    Keywords: benzoic acid ; DTA ; DTG ; hydroxy- and aminobenzoic acids ; o-phthalic acid ; principal component analysis ; sulphanilic acid ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal decomposition of benzoic acid and its derivatives containing —OH, —NH2, —COOH and —SO3H functional groups as substituents in ortho, meta and (or) para position together with sulphanilic acid was investigated. The analyses were performed using derivatograph, sample mass ranged from 50 to 200 mg, heating rates from 3 to 15 K min−1 and static air atmosphere. It has been established that thermal decomposition of these aromatic acids proceeds through three common stages. In the first stage the phase transformations occur. The following two stages are due to the formation of intermediate products of the thermal decomposition and their combustion. Principal component analysis (PCA) was applied for evaluation of the results. Thanks to this method the influence of specific functional groups and their positions on the benzene ring on the thermal decomposition of the compounds under investigation was determined.
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  • 70
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    Journal of thermal analysis and calorimetry 56 (1999), S. 1323-1327 
    ISSN: 1572-8943
    Keywords: chloramphenicol ; DSC ; quality control ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The stability and thermal behaviour of chloramphenicol and various of its mixtures were investigated. The thermogravimetric and stability constant results showed that the chloramphenicol base is thermally more stable than the tablet in the studied formulation. The reduction in stability was attributed to the presence of starch in the formulation. The thermal decompositions of the chloramphenicol base and the tablet obey first-order kinetics.
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  • 71
    ISSN: 1572-8943
    Keywords: coordinationcompounds ; CRTA ; kinetics ; polymerization ; pyrolysis ; quasi-equilibrium ; TG ; thermolysis ; volatility
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Quasi-equilibrium thermogravimetry (variant of CRTA) is put to use as an express method of thermoanalytical screening for volatile compounds. During the experiments for P—T relationship calculations (running with several calibrated standard sample holders) the non-volatile (polymerized) residue is formed (and is decomposed with further temperature rising). Thermogravimetric data are used for the calculation of the kinetic parameters for the polymerization reaction, taking place (concurrently with the evaporation) in the melt of the studied volatile compound.
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  • 72
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    Journal of thermal analysis and calorimetry 58 (1999), S. 301-307 
    ISSN: 1572-8943
    Keywords: acrylamide ; FT-IR ; N,N-dialkylacrylamide ; plasma-initiated polymerization ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract Polyacrylamide (PAM), poly(N,N-dimethylacrylamide) (PDMA) and poly(N,N-diethylacryl-amide) (PDEA) were synthesized by plasma-initiated polymerization. Both wet and dry polymers were prepared. The states of the water absorbed in the wet and dry samples were studied directly by means of TG, and the stabilities of the dry polymers in the process of thermal treatment were investigated by FT-IR. The activation energy of release of the bonded water was calculated by the Kissinger method. The water absorbed in the polymers was found to be in two states, i.e. weakly-bonded water and bonded water, and the absorbed water content varied with the monomer concentration, the plasma duration time and the type of polymer.
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  • 73
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    Journal of thermal analysis and calorimetry 58 (1999), S. 375-381 
    ISSN: 1572-8943
    Keywords: benzene alkylation ; carbondeposition ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract In our invention, FCC (fluid catalytic cracking) dry gas could be used to react with benzene without any special purification, and more than 90% ethylene was converted to ethylbenzene. The phenomenon of carbon deposition over catalyst surface was obvious and leads to a deactivation of catalyst, so it is important to study the behavior of carbon deposition of catalyst during alkylation of benzene. The influence of several factors such as temperature, reaction time, reactant concentration of the amount and the kinetics of carbon deposition were investigated, during which carbon depositing rate equations were obtained for different reactant.
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    Journal of thermal analysis and calorimetry 58 (1999), S. 447-453 
    ISSN: 1572-8943
    Keywords: coal ; combustion reaction ; kinetics ; TG
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    Topics: Chemistry and Pharmacology
    Notes: Abstract The combustion behavior of Shuangya Mountain (SYM) coal dust has been investigated by means of TG in this paper. The reaction fraction α can be obtained from isothermal TG data. The regressions of g(α), an integral function of α vs. t for different reaction mechanisms were performed. The mechanism of nucleation and nuclei growth is determined as the controlling step of the coal dust combustion reaction by the correlation coefficient of the regression, and the kinetic equation of the SYM coal dust combustion reaction has been established.
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    Chromatographia 40 (1995), S. 99-101 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; High temperature open-tubular columns ; Solvent make-up ; Acetophenone oxidation
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    Topics: Chemistry and Pharmacology
    Notes: Summary Acetophnone, a substance stable at room temperature, is readily oxidizes in a high temperature open tubular liquid chromatographic system by the residual oxygen in the mobile phase. The oxidation product is less UV absorptive and detection sensitivity decreases greatly. To prevent the oxidation, through degassing of the mobile phase is necessary.
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  • 76
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Endotoxins ; Lipopolysaccharide ; Aminated poly(γ-methyl L-glutamate) ; Bovine serum albumin
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    Topics: Chemistry and Pharmacology
    Notes: Summary A method is described for the selective removal of endotoxins from various protein solutions using columns packed with aminated poly (γ-methyl L-glutamate) (PMLG-NH2) spheres. The PMLG-NH2 adsorbents showed a high adsorbing activity for endotoxins which had an ionic strength of μ=0.05–1.0 and pH 5.0–9.0. The endotoxin-adsorbing capacity per millitre of the wet adsorbent increased from 0.40 to 1.35 mg (E. coli O111: B4 LPS) at μ=0.2 and pH 7.0 while the aminogroup content of the adsorbent increased from 0.8 to 3.5 meq g−1. The PMLG-NH2-3.5 has an amino-group content of 3.5 meq g−1. This column packing selectively adsorbed endotoxins, without loss of the protein, from a γ-globulin or cytochromec solution which contained endotoxins at μ=0.05 and pH 7.0. On the other hand, when bovine serum albumin (BSA) was present in solution with endotoxins, both the endotoxins and the BSA were adsorbed by the column. The BSA-adsorbing activity increased with increasing amino-group content of the adsorbent. However, this undesirable adsorption was suppressed with increasing ionic strength of the buffer. As a result, when the packing which had an amino-group content of 1.5 meg g−1 was used in conditions of μ=0.2 and pH 7.0, the endotoxins were removed from a BSA-containing solution without affecting the recovery of the BSA.
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    Chromatographia 40 (1995), S. 51-57 
    ISSN: 1612-1112
    Keywords: Column electrophoresis ; Column liquid chromatography ; Phenolic lignin degradation compounds ; Sugar degradation products ; Quantitative analysis
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    Topics: Chemistry and Pharmacology
    Notes: Summary A method for the quantitative analysis of phenolic lignin degradation products by capillary electrophoresis (CE) with on-column UV detection has been developed. The liquid biomass solutions contain low molecular hemicellulosic sugars and phenolic lignin degradation products with various degrees of polymerization. Special attention has been paid to the monomeric phenolic components of lignin degradation fragments, e.g. derivatives of phenolic acids, aldehydes, and alcohols. Uncoated fused silica capillaries and borate-phosphate buffer systems at moderate pH conditions were used in order to separate the compounds of interest. To provide validation of the method, the same samples were analyzed independently by HPLC using gradient elution on a RP-C18 column. As sugar degradation fragment, furan-2-carboxylic acid was detected.
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    Chromatographia 40 (1995), S. 85-90 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Phenolic compounds ; Ion-pair solid phase extraction ; On-line trace enrichment
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    Topics: Chemistry and Pharmacology
    Notes: Summary Two packing materials, C18 and PLRP-S, are studied for on-line trace enrichment of phenolic compounds in water. Various precolumns of different internal diameter are also tested and the addition of an ion-pair reagent to increase retention and thus, breakthrough volumes of phenolic compounds, is studied. Best results are obtained when a PLRP-S precolumn is coupled on-line with a C18 analytical column and DAD detector. Addition of TBA considerably increases breakthrough volumes. In contrast, when a C18 precolumn is used, breakthrough volumes are lower and it is impossible to determine TCP and PCP, under the experimental conditions used, because of interference of other nonpolar compounds in the samples. The performance of the system is evaluated with river and tap water and the preconcentration of 10 ml of sample in a PLRP-S precolumn involves a linear range between 1 μg 1−1 and 20 μl−1 and limits of determination between 0.5 μg l−1 and 1 μg l−1 are obtained.
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    Chromatographia 40 (1995), S. 631-637 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Trace analysis ; Pesticides in tap water ; Aromatic sulphonates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Methodology and instrumentation are described which allow chromatographic screening of water samples under substantially simplified conditions and at reduced cost. A single column is used to accomplish sample extraction, trace enrichment, and separation. The performance of such a system is demonstrated, and the results compared with conventionally used concepts.
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  • 80
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Transchelation ; Zinc pyrithione and related compounds ; Antidandruff formulations
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    Topics: Chemistry and Pharmacology
    Notes: Summary An analytical procedure has been developed for the determination of zinc pyrithione in antidandruff formulations. Zinc pyrithione was converted into a stable copper complex and then analysed by reversed-phase HPLC. The proposed method allows the separation of the analyte from related pyrithiones and therefore is able to verify the compliance of cosmetic preparations with current legislation.
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  • 81
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Benzodiazepines ; Solvent effects ; ACN clusters
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    Topics: Chemistry and Pharmacology
    Notes: Summary Two different methods were used to determine the separation factor α at different temperatures and the Gibbs-Helmholtz parameters (Δ(ΔH), Δ(ΔS)) of two adjacent benzodiazepines on a chromatogram were obtained from plots of lnα versus 1/T. We first studied each factor (fraction of water ϕ in the ACN/water mixture and column temperatureT), which controls the retention mechanism, and then we examined the simultaneous variation of all these factors. The changes in Δ(ΔH) and Δ(ΔS) in relation to a volume fraction of water ϕ in an ACN/water mixture were examined. In the ACN/water system, Δ(ΔH) was fairly constant in the acetonitrile region of ϕ≤0.52 and appears to be a roughly linear function of ϕ for ϕ≥0.52. In this system Δ(ΔS) is approximately a parabolic function of ϕ with an optimum at ϕ≅0.52. The retention mechanism of ten benzodiazepines was found to be significantly different in the methanol/water and ACN/water mixtures. The separation optimization of these ten benzodiazepines was then considered. A fraction of water of 0.43 in the ACN/water mixture and a column temperature of 44°C gave the most efficient separation conditions in the ACN/water mixture.
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  • 82
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polyurethane degradation products ; 2,4- and 2,6-toluendiamine ; Urine analysis ; Breast implants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A reversed-phase HPLC method has been developed for the urinary determination of mutagenic 2,4- and 2,6-toluendiamines. These amines are degradation products of polyurethane, a material used to cover textured silicone breast implants. FMOC-Cl was used as fluorescent derivatising agent in order to obtain a limit of detection of 15 ng/ml in urine. Pre-treatment of urine samples was by liquid/liquid extraction and urine specimens of patients after surgury were analysed.
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    Chromatographia 41 (1995), S. 657-660 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polyphenols ; Flavonoids ; Phenolic acids and aldehydes ; Eucalyptus spp.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Standards of the polyphenols occurring in wood, bark and leaf extracts ofEucalyptus spp. (i.e. flavonoids and phenolic acids and aldehydes) have been analyzed by HPLC using reversed phase columns, gradient elution and diode-array detection. The conditions used are reported.
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    Chromatographia 40 (1995), S. 657-661 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed phases ; Polyencapsulated silica ; Polyacrylates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary By copolymerization of silica modified with vinyl groups and acrylic acid esters in suspension highly efficient, polymeric-encapsulated stationary-phases can be prepared. The suspending liquid has to be selected such that the monomers are at least partially adsorbed on the surface and the polymer formed does not precipitate. Under these conditions stationary phases capable of speedy mass transfer can be prepared, where the reduced plate heights are between 2 and 3. The silica surface shielding is optimized so that basic and acidic solutes elute with symmetrical peak.
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  • 85
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chiral resolution of amino acids ; Pre-column derivatization ; Fluorescent chiral tagging reagents ; Stereochemical purity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Derivatization of amino acid enantiomers with fluorescent chiral Edman-type reagents, 4-(3-isothiocyanatopyrrolidin-1-yl)-7-nitro-2,1,3-benzoxadiazole [R(−)- and S(+)-NBD-PyNCS] and 4-(3-isothiocyanatopyrrolidin-1-yl)-7-(N,N-dimethylaminosulfonyl)-2,1,3-benzoxadiazole [R(−)-and S(+)-DBD-PyNCS], yields corresponding diastereomers separable by reversed-phase HPLC on normal achiral columns. The resolved diastereomers were detected fluorometrically at 530 nm with excitation at 490 nm for the NBD-PyNCS derivatives and at 560 nm with excitation at 450 nm for those derived from DBD-PyNCS reagents. This HPLC-derivatization method was used for evaluation of stereochemical purity for some synthetic commercial peptides. The enantioanalysis was reliable down to 0.05% racemization of the amino acid residues and a quantity of 100 μg peptide sample was usually enough for the analysis. Two acid hydrolysis methods, i.e. the standard procedure with constant-boiling hydrochloric acid (HCl) and a rapid vapor-phase procedure with HCl-trifluoroacetic acid (TFA) mixture, were compared. The later was found to be unsuitable owing to increased racemization of the amino acid residues during the hydrolysis. Judging from the results obtained for proline and leucine residues, most of the tested peptides including biologically active peptides, such as neurotensin, [d-Ala2,d-Leu5]-enkepharin and morphine tolerance peptide, possessed stereochemical purities higher than 98%. Influence of structural features of the peptides on the racemization of the amino acid residues was found to be significant.
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  • 86
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Mass spectrometric detection ; Fast atom bombardment ionization ; Serum bile acid ; Rat bile
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary In order to analyse bile acids in biological matrices, e.g. rat bile and human serum, high performance liquid chromatography (HPLC) was coupled to continuous-flow fast atom bombardment mass spectrometry (CFFAB-MS). A gradient elution system which had already proved to be well suited for the quantitative determination of conjugated bile acids in bile was modified to allow HPLC-CFFAB-MS-coupling. Due to the sensitivity of this coupling method it is possible to obtain more information about the biliary bile acid pattern and species-specific secondary bile acids. Furthermore, we were able to identify obviously unknown bile acid species in rat bile which most likely classify as mono-oxo and di-oxo-taurocholates (MW 513 Da, 511 Da) and mono-oxo-glycocholates (MW 463 Da). In the present study we show that using this system it is possible to determine both conjugated and unconjugated as well as sulfated bile acids, without time consuming group separation and derivatization, from rat bile and human serum. In addition, it is suggested that the method presented here should be considered for use in routine analysis.
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  • 87
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Fluorescence enhancement ; Bovine serum albumin ; Dansylamino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The effects of acetonitrile and bovine serum albumin (BSA) concentrations on the signal intensity and retention behavior of dansylamino acids have been examined by using γ-cyclodextrin-bonded silica gel as the stationary phase in microcolumn liquid chromatography. Fluorescence intensities of dansylamino acids were enhanced by BSA as a mobile phase additive, e.g., detection limits of dansyl derivatives of L-Ala and L-Phe were improved by a factor of 12–18.
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  • 88
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Micellar liquid phases ; Octanol-water partition coefficient ; Benzene and naphthalene derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary It is shown that the logarithm of the capacity factor (log k′) for fifteen benzene and naphthalene derivatives in micellar liquid chromatography with forty nine different mobile phases generally correlates better with the logarithm of the octanol-water partition coefficient (log Pow) than the capacity factor (k′). Optimum conditions are established to obtain the best linear correlations of log k′-log Pow.
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  • 89
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Photolysis ; Electrochemical detection ; Drugs with chlorinated aromatic rings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Pharmaceuticals containing a thiazide ring or chlorinated aromatic ring were investigated with respect to enhanced selectivity in determination. Oxidative electrochemical detection coupled with HPLC was used to study the influence of the pH of the mobile phase under conditions of photolysis. To cover a pH range 3.9–12, the employment of a polymer column stable in alkaline media was necessary. The method offers the great advantage of derivatization without chemicals at low operating potentials, thereby providing high selectivity.
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  • 90
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    Chromatographia 40 (1995), S. 296-302 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Structural isomer separation ; Cyclodextrin ; Polymers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Several β-cyclodextrin (CD)-bonded stationary phases for high performance liquid chromatography (HPLC) were prepared, based on silica beads coated with a poly(alkylamine), [poly(ethyleneimine)(PEI)]. In order to obtain stationary phases with a high content of CD and maximum accessibility of the CD cavity, the functionalization was carried out after the coating, using the mono-tosyl derivative of CD as the intermediate. The ability of these supports to separate ortho, meta and para isomers of some disubstituted benzene derivatives was examined. The contribution of the amino groups of the polymer and of the CD cavity to the separation process is discussed. The resolution is mainly based on the difference in the stability of the complexes of the various isomers with CD. The influence of the amount of CD on the height of the theoretical plate is also studied.
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  • 91
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Reversed phase ; Polystyrene ; Pellicular ; Ultra high molecular mass
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Ultra high molecular mass (〉 7 million dalton) polystyrenes are prone to degradation in size exclusion chromatography. In gradient elution reversed phase HPLC they do not elute visibly on small particle size porous supports. However, large diameter C18 pellicular particles were successfully employed for reversed phase study of ultra high molecular mass (15 million dalton) polystyrenes without polymer degradation during elution. Although retention for the lower molecular mass polystyrenes was lower than on small diameter porous particles, the medium high molecular mass polystyrenes (0.5–1 million dalton) showed similar retention. The addition of small diameter porous particles in small quantities, to the large diameter pellicular particles, increased the amount of retention of the low molecular mass polystyrenes without affecting the higher molecular mass polystyrenes.
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  • 92
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Methyl ethyl ketone in urine ; Derivatization ; 3-Methyl-2-benzothiazolinone hydrazone ; Comparison with GC-MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A HPLC method for the determination of methyl ethyl ketone (MEK) in urine after derivatization with 3-methyl-2-benzothiazolinone hydrazone is proposed. The calibration curve for the ketone was linear, ranging between 0.23–10 mg/L, with a detection limit of 0.025 mg/L. The results were compared to those obtained by GC-MS, coupled to the headspace technique. MEK derivatization and the derivative purification processes were verified with respect to the main variables such as reaction temperature, reagent concentration, probable interferences and enrichment phase. The method is simple and reliable and shows a good sensitivity.
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  • 93
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    Chromatographia 40 (1995), S. 382-386 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Sulfonamides in foodstuffs ; Honey ; Milk ; Eggs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A procedure for the simultaneous determination of several sulfonamides in different foods, such as honey, milk and eggs is proposed. The analysis is carried out using reversed phase liquid chromatography with spectrophotometric detection. Optimization of the mobile phase led to good separation and a short analysis time when an initial isocratic step with a 3∶97 acetonitrile: water mixture was used for 5 minutes, followed by a linear gradient up to a 40∶60 mixture over 15 min. The proposed method is suitable for routine quality control analysis to ensure the absence of sulfonamides in foods. Recovery studies yielded good results for all food samples because there were no interferences from the matrices.
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  • 94
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    Chromatographia 40 (1995), S. 411-416 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Particle beam LC/MS interface ; Capillary columns for LC ; Mycotoxins ; Peanut meal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new method for the analysis of aflatoxins in food extracts, based on liquid chromatography/mass spectrometry interfacing, is presented. The chromatographic separation was performed with a reversed phase packed capillary column coupled with a modified particle beam interface capable of handling microliter per minute flow rates. This system allows higher overall sensitivity and easier operation procedures. The method has proved to be particularly suitable for the analysis of the toxins in very complex matrices. The specificity of electron impact ionization allowed positive identification of the aflatoxins with an excellent response linearity for accurate quantitation.
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  • 95
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin-layer chromatography ; Reversed phase ; 2-benzoylbenzoic acids ; Anionic and cationic counter ions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The 2-benzoylbenzoic acid series was investigated by reversed-phase, high-performance, thin-layer and column chromatography using various alkylammonium salts and di(2-ethylhexyl)orthophosphoric acid as polar associating reagents. The effects of the individual substituents on retention were quantified by Δlog k′ and ΔRM values. The compounds investigated differing in molecular structure (hydrophilic and hydrophobic substituents) commonly occurring groups in drugs and biologically active substances provide information on molecular interaction in these ion-pair systems. The combined effects on retention of organic modifier and ion-pair reagent concentration were investigated.
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  • 96
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Two-dimensional separation ; D- and L-amino acids ; Enantioseperation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A two-dimensional, column liquid chromatographic system is used for the determination of the D- and L-enantiomers of amino acids in biological samples. Separation of the amino acids is first on ion-exchange column by gradient elution with a sodium citratesodium chloride buffer. Enantioseparation is by subsequent injection of 3 μl heart-cuts of the individual amino acids onto a second column with a chiral crown ether stationary phase. Finally, fluorescence detection is after post-column labelling of the amino acids using ano-phthalaldehyde-2-mercaptoethanol reagent solution. The high separation power and selectivity of the system allow processing of complex samples with hardly any additional treatment and the determination of small quantities of D-amino acids in the presence of excess L-form. Applicability of the system is illustrated by the determination of D- and L-aspartate, serine, glutamate and alanine in various complex biological samples, such as protein hydrolysates, urine and biotechnological and food samples. Data are given on detectability, repeatability and linearity.
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  • 97
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion pair LC ; Sweeteners, preservatives and antioxidants ; Food additive analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A paired-ion, reversed-phase high-performance liquid chromatographic method was developed for the simultaneous determination of sweeteners (dulcin, saccharin-Na and acesulfame-K), preservatives (sodium dehydroacetate, sorbic acid, salicyclic acid, benzoic acid, succinic acid, methyl-para-hydroxybenzoic acid, ethylpara-hydroxybenzoic acid, n-propyl-para-hydroxybenzoic acid, isopropyl-para-hydroxybenzoic acid, n-butyl-para-hydroxybenzoic acid, and isobutyl-para-hydroxybenzoic acid), and antioxidants (3-tertiary-butyl-4-hydroxyanisole and tertiary-butyl-hydroquinone). A mobile phase of acetonitrile-50 mM aqueous α-hydroxy-isobutyric acid solution (pH 4.5) (2.2 ∶ 3.4 or 2.4 ∶ 3.6, v/v) containing 2.5 mM hexadecyltrimethylammonium bromide and a C18 column with a flow rate at 1.0 mL/min and detection at 233 nm were used. This method was found to be very reproducible with detection limits ranged from 0.15 to 3.00 μg. The retention factor (k) of each additive could be affected by concentrations of hexadecyltrimethylammonium bromide and α-hydroxyisobutyric acid, and pH and ratio of mobile phase. The presence of additives in some food samples was determined.
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  • 98
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Limit of detection ; Precision ; Uncertainty prediction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The precision of integration over noisy instrumental output for quantitative analysis is studied. A probability theory is developed to predict the relative standard deviation (RSD) of integration results over an integration domain from one-point integation (peak height measurement) to entire area integration in HPLC. Common integration modes of horizontal zero line and oblique zero line are taken into account, but no peak overlap is assumed. The question of the analytical superiority of peak height measurement or integration for quantitation is answered. In the HPLC apparatus used, the minimum RSD of measurements is found in the integration domain of ca. ±0.5 σ for analytes [peaks are approximated by the Gaussian signal of width, σ (standard deviation)]. The RSD of integration measurements is also shown to depend on the stochastic properties of back-ground noise (uncorrelated noise and correlated 1/f type noise). The theoretical conclusion is verified by Monte Carlo simulation and HPLC experiments for some aromatic compounds.
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  • 99
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ion-pair and GPC separations ; Amoxicillin oligomers ; β-Lactam ring polymers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Polymeric substances formed from concentrated sodium amoxicillin in an aqueous solution have been separated using two high-performance liquid chromatographic methods. We used a C18 reversed-phase column with tetrabutylammonium chloride as an ion-pairing agent with an acetonitrile gradient and a TSKgel G2500PWxl column with water as the solvent for gel permeation chromatography. The separated materials, ranging in size from the monomer to the tetramer, have been characterized by functional-group chemical analysis, while the identification of the piperazine-2,5-dione was done using a pure standard. A greater number of peaks which were also better defined were obtained using the ion-pair reversed-phase method, and open and closed beta-lactam ring polymer forms could be distinguished. Using the gel permeation method, only a few monomer, piperazine-2,5-dione, dimer, trimer and combined amoxicillin trimer and tetramer peaks were obtained with water, although those obtained were quite well defined. The data on the time-course of formation of the oligomers and the amoxicillin degradation product were virtually identical by both methods.
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  • 100
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; On-column fluorimetric detection ; Gradient elution ; Dansyl amino acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Fluorimetric detection in the presence of a stationary phase has been applied to gradient elution of dansyl amino acids in liquid chromatography. A 1.5 mm ID quartz tube packed with the same materials as the separation column was employed for the flow cell. Conventional-size columns were employed. The peak height of analytes increased with increasing retention owing to focusing and environmental effects of the stationary phase, leading to improvements in sensitivity, which was pronounced for analytes eluting late. The lower the gradient, the larger the improvement in sensitivity achieved. Detection limits were improved by a factor of up to 5.1 by fluorimetric detection using the packed flow cell, compared with those achieved using a common empty flow cell.
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