TY - JOUR AB - This study investigates the combustion characteristics and efficiency of six distinct lignite samples, comparing their untreated and treated forms. The experimental approach employs simultaneous thermogravimetry coupled with multiple ion detection (TG–DTG–MID) as well as differential and pressurized scanning calorimetry (DSC–PDSC) techniques. This integrated methodology provides a thorough understanding of the combustion mechanisms involved. The experiments are conducted under a controlled heating rate of 10 °C min−1 across a broad temperature range of 25 to 650 °C. Additionally, PDSC assessments are performed under varying pressure conditions, ranging from 100 to 300 psig, while maintaining the same heating rate. Distinct reaction phases such as evaporation, primary carbonization, and mineral matter decomposition are identified through detailed analyses of the untreated and treated lignite samples. Key combustibility indices, including reactivity and the ignition–combustion index, are systematically evaluated for both untreated and treated specimens. These metrics offer valuable insights into the combustion behavior and efficiency of the lignite samples under different treatment conditions. AU - Kök, M.V.* AU - Matuschek, G. AU - Varfolomeev, M.A.* AU - Nurgaliev, D.K.* C1 - 74077 C2 - 57328 CY - Van Godewijckstraat 30, 3311 Gz Dordrecht, Netherlands TI - Combustion characteristics and efficiency of raw and clean lignite samples by thermal analysis techniques: TG–DTG–MID, DSC, and PDSC applications. JO - J. Therm. Anal. Calorim. PB - Springer PY - 2025 SN - 1388-6150 ER - TY - JOUR AB - In the present study the thermal behavior of phosphorus- and phosphorus/nitrogen-containing functional polymers was studied. The polymers were synthesized via oxidative chlorophosphorylation reaction of butadiene rubber and were subsequently subjected to hydrolysis, aminolysis and/or alcoholysis in order to introduce appropriate functionalities. The successful modifications of the polymer and presences of the respective functional groups were determined using Fourier transform infrared spectroscopy. It was found that the product of hydrolysis of the modified butadiene rubber contains acidic groups in its structure while the products of aminolysis and alcoholysis contain both acidic and amine and/or alcohol-derived moieties. The kinetic analyses of the thermal decomposition reaction were evaluated using thermogravimetric analysis and subsequently Friedman and Ozawa–Flynn–Wall methods revealing three-stage degradation process. Calorimetric measurements were performed for the studied polymers, and mass spectrometric analyses were used to identify the decomposition products for phosphorus-containing polymer. The overall results allowed to reveal the influence of the attached phosphorus- and phosphorus/nitrogen-containing functional groups to the thermal degradation of the cross-linked polymers. AU - Alosmanov, R.* AU - Wolski, K.* AU - Matuschek, G. AU - Magerramov, A.* AU - Azizov, A.* AU - Zimmermann, R. AU - Aliyev, E.* AU - Zapotoczny, S.* C1 - 51346 C2 - 43193 CY - Dordrecht SP - 799–812 TI - Effect of functional groups on the thermal degradation of phosphorus- and phosphorus/nitrogen-containing functional polymers. JO - J. Therm. Anal. Calorim. VL - 130 IS - 2 PB - Springer PY - 2017 SN - 1388-6150 ER - TY - JOUR AB - In this study, thermal analysis coupled with soft ionization mass spectrometry was used for the speciation of sulfur vapor. Its investigation is still a challenge, since it exhibits a complex molecular composition. A thermal analysis–mass spectrometry system was equipped with a single-photon ionization time-of-flight mass spectrometer. Single-photon ionization is a soft ionization method which produces less or no fragments. Ionization is performed with vacuum ultraviolet photons generated by an electron beam-pumped excimer lamp and a deuterium lamp. The applicability of the developed system was demonstrated for the determination of sulfur vapor composition. Several allotropic modifications were detected in the gas phase depending on temperature. Since the ionization energies of the species are between 8.6 and 9.7 eV, soft ionization is crucial for this reason. Thermogravimetric and DSC data deliver additional information to the mass spectrometric data and enable the detection of allotropic transitions in solid and liquid phase. AU - Varga, J. AU - Wohlfahrt, S. AU - Fischer, M. AU - Saraji-Bozorgzad, M.R.* AU - Matuschek, G. AU - Denner, T.* AU - Reller, A.* AU - Zimmermann, R. C1 - 49127 C2 - 41655 CY - Dordrecht SP - 955-960 TI - An evolved gas analysis method for the characterization of sulfur vapor. JO - J. Therm. Anal. Calorim. VL - 127 IS - 1 PB - Springer PY - 2017 SN - 1388-6150 ER - TY - JOUR AB - The applicability of thermogravimetry (TG) coupled to single photon ionization time-of-flight mass spectrometry (TG-SPI-TOFMS) for evolved gas analysis (EGA) of coffee is demonstrated in this study. Coffee is a chemically well-known complex food product of large scientific and commercial interest. The roasting process of single green coffee beans (Arabica, Robusta) was simulated in the TG-SPI-TOFMS device, and the chemical composition of the evolved roasting gases was monitored on-line. Additionally, roasted and ground coffee powders of different types and brands as well as instant coffee were successfully investigated. For example, the diterpenes cafestol and kahweol can be detected among many other roasting products. These compounds can be of particular interest for quality control of coffee. It is shown that kahweol can be used as a tracer compound to discriminate arabica coffee species from robusta species. AU - Fischer, M. AU - Wohlfahrt, S. AU - Varga, J. AU - Saraji-Bozorgzad, M.* AU - Matuschek, G. AU - Denner, T.* AU - Zimmermann, R. C1 - 31646 C2 - 34615 CY - Dordrecht SP - 1461-1469 TI - Evolved gas analysis by single photon ionization-mass spectrometry. JO - J. Therm. Anal. Calorim. VL - 116 IS - 3 PB - Springer PY - 2014 SN - 1388-6150 ER - TY - JOUR AB - Thermal processes are part of many industrial treatments; therefore, it is of great interest to gain more insight of these processes. Evolved gas analysis (EGA) is the most straightforward way to make chemical reactions in thermal processes accessible for on-line investigations. The sample matrix of evolved off gas e.g., from coffee roasting is a permanently changing and complex mixture of a multitude of substances that have to be analyzed simultaneously for real on-line investigations without any sample trapping or separation device. Therefore, a measurement system as an ion trap mass spectrometer (ITMS) with soft ionization is required with its tandem mass spectrometry capability to provide distinct substance identification unperturbed by the remaining matrix. The presented novel system setup is based on a thermogravimetric device (TG) to simulate the thermal treatment as in industrial processes combined with an ITMS with soft single photon ionization (SPI) to achieve the required substance information. Hence it is possible to gain single mass spectrometric information of expected substances for process control. More comprehensive than that are the two-dimensional MS data which are required for research and process development purposes though. The conducted analyses show that this novel setup is able to provide distinct substance identification in evolved gas of roast and ground coffee powder. To our knowledge, this is the first TG-SPI-ITMS setup with successful application in verifying the identity of different mass traces within a single run. AU - Hölzer, J. AU - Fischer, M. AU - Gröger, T.M. AU - Streibel, T. AU - Saraji-Bozorgzad, M.* AU - Wohlfahrt, S. AU - Matuschek, G. AU - Zimmermann, R. C1 - 31647 C2 - 34614 CY - Dordrecht SP - 1471-1479 TI - Hyphenation of Thermogravimetry and Soft single Photon Ionization-Ion Trap Mass Spectrometry (TG-SPI-ITMS) for evolved gas analysis. JO - J. Therm. Anal. Calorim. VL - 116 IS - 3 PB - Springer PY - 2014 SN - 1388-6150 ER - TY - JOUR AB - A simultaneous thermogravimetry/differential scanning calorimetry device (STA) was coupled to single photon ionization time of flight mass spectrometry (SPI-TOFMS) for evolved gas analysis (EGA). Thermal resolution with thermogravimetric signals (TG/DTG) is delivered by STA. On-line coupled EGA with SPI-TOFMS retains the thermal information from the STA and substantiates these with correlating mass spectra. The application of vacuum ultraviolet (VUV)-photons (8-12 eV) for soft ionization, allows almost fragment-free ionization. Thus, it becomes possible to interpret mass spectra of complex matrices, like natural products evolving simultaneously several molecules, without an additional separation step. The STA-SPI-TOFMS on-line coupling offers the possibility to track subset mass traces during one STA run. Focusing on material-depended mass traces, differentiation of organic matrices is obvious. In this work two types of research cigarettes, 3R4F and CM6 were used. While the 3R4F cigarette is composed of a blend of different tobacco sorts and different curing methods, the CM6 research cigarette consists of pure flue cured tobacco. The advantages of coupling on-line chemical analysis methods to thermal analysis (TA) are in the context of the achieved thermo-molecular signatures. AU - Fischer, M. AU - Wohlfahrt, S. AU - Saraji-Bozorgzad, M.* AU - Matuschek, G. AU - Post, E.* AU - Denner, T.* AU - Streibel, T.* AU - Zimmermann, R. C1 - 27469 C2 - 32685 SP - 1667-1673 TI - Thermal analysis/evolved gas analysis using single photon ionization. JO - J. Therm. Anal. Calorim. VL - 113 IS - 3 PB - Springer PY - 2013 SN - 1388-6150 ER - TY - JOUR AB - A newly developed measurement technique for evolved gas analysis in thermogravimetry, viz. a thermo balance coupled to comprehensive gas chromatography/single photon ionization mass spectrometry (TG-GC x SPIMS), has been applied to investigate the thermal degradation of two polymers (polycarbonate (PC) blended with ABS and PVC). This detection method provides a two-dimensional analysis of the evolved gaseous products. TG relevant data is obtained as well as an improved resolution power to separate isobaric molecular structures without losing any fraction of the samples. In addition, this solution is not associated with any extension of the measurement time. The assignment of the substance pattern to distinct species is improved compared to solely using MS without a preceding separation step. Furthermore, hitherto undetected compounds when compared to applying TG-SPIMS without GC such as benzonitrile and its methylated derivatives have been found in the evolved gases from the thermal degradation of PC/ABS blend. Finally, a first estimation of the limit of detection has been carried out, yielding 400 ppt for styrene and 500 ppt for toluene from the thermal decomposition of PC/ABS blend. AU - Saraji-Bozorgzad, M.R. AU - Streibel, T.* AU - Eschner, M.* AU - Gröger, T.M. AU - Geißler, R. AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 6580 C2 - 28934 CY - Dordrecht SP - 859-866 TI - Investigation of polymers by a novel analytical approach for evolved gas analysis in thermogravimetry. JO - J. Therm. Anal. Calorim. VL - 105 IS - 3 PB - Springer PY - 2011 SN - 1388-6150 ER - TY - JOUR AB - A commercial thermogravimetry-supersonic jet-skimmer quadrupole mass spectrometer system (TG-Skimmer-QMS, Netzsch GmbH, Germany) was successfully converted for soft single photon ionisation time-of-flight mass spectrometric (SPI-TOFMS) detection of organic compounds. VUV light for SPI was generated by an electron beam pumped argon excimer light source (EBEL; E (photon) = 9.8 eV). Furthermore, the versatility of the system was conserved, as high temperature TG and DSC measurements as well as electron ionisation mass spectrometry for the detection of inorganic compounds are still possible. The new system was tested with two polymers and a hydrocarbon mixture (diesel). It was demonstrated that aliphatic and aromatic organic compounds can be detected without fragmentation. Thus the system allows the recording of a readily interpretable organic signature of, e.g. thermal polymer decomposition. The thermal degradation of polystyrene shows a rich signature of the monomer, some oligomers and minor products of irregular cleavings of carbon chains. Polycarbonate exhibits a thermal decomposition fingerprint which is dominated by products of bisphenol A. The bisphenol A monomer, however, is also detectable. AU - Saraji-Bozorgzad, M.R. AU - Streibel, T.* AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 6893 C2 - 29417 CY - Dordrecht SP - 691-697 TI - Detection of organic products of polymer pyrolysis by thermogravimetry-supersonic jet-skimmer time-of-flight mass spectrometry (TG-Skimmer-SPI-TOFMS) using an electron beam pumped rare gas excimer VUV-light source (EBEL) for soft photo ionisation. JO - J. Therm. Anal. Calorim. VL - 105 IS - 2 PB - Springer PY - 2011 SN - 1388-6150 ER - TY - JOUR AB - A variety of crude oil samples have been investigated by the combined methods of thermal analysis and mass spectrometry by means of a newly developed prototype of a thermogravimetry-single photon ionisation time-of-flight mass spectrometer coupling (TG-SPI-TOFMS). Single photon ionisation (SPI) was conducted utilising a novel electron beam pumped argon excimer lamp (EBEL) as photon source, and a TOFMS with orthogonal acceleration has been applied for the detection of the mass to charge signals. The advantage of the soft SPI technique over EI for the analysis of such complex samples could be clearly demonstrated, as the aliphatic hydrocarbons present in crude oil may be detected via their respective molecular ion signals, not showing the intense fragmentation typical for EI spectra of this substance class. The application of SPI revealed furthermore two distinct decomposition regions, dominated by evaporation and pyrolysis processes, respectively. Moreover, different crude oils could be distinguished by TA/SPI mass spectra due to their unique molecular signatures. AU - Geißler, R. AU - Saraji-Bozorgzad, M.R. AU - Streibel, T. AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 497 C2 - 26286 CY - Berlin [u.a.] SP - 813-820 TI - Investigation of different crude oils applying thermal analysis/mass spectrometry with soft photoionisation. JO - J. Therm. Anal. Calorim. VL - 96 IS - 3 PB - Springer PY - 2009 SN - 1388-6150 ER - TY - JOUR AB - The potential of hyphenating thermogravimetry (TG) and soft photo ionisation mass spectrometry (EBEL-SPI-MS) for fundamental and applied research and material analysis has been demonstrated by a newly developed TG-SPI quadrupole MS coupling (TG-SPI-QMS). Thermal decomposition of three common plastics, polyethylene (PE), polystyrene (PS) and polyvinylchloride (PVC) has been studied. While the decomposition of PE and PS in inert atmosphere takes place in a one step process (main mass loss at about 490 and 420 A degrees C, respectively), PVC decomposes in a two step mechanism. The organic signature of the PE decomposition shows homologous series of alkenes and polyenes, while PS is forming mainly styrene mono- and oligomers. In the PVC decomposition, firstly hydrogen chloride (HCl) is eliminated in a hydro-dechlorination reaction (1st mass loss step: 285-305 A degrees C), this is accompanied by the emission of the carbon skeletons of small aromatics (predominately benzene and naphthalene). In the second step (2nd mass loss step: 490-510 A degrees C), the residual cross-linked polyolefin moieties decompose under release of heavily alkylated aromatics, including larger PAH. Chlorinated aromatics are formed only in trace levels. AU - Saraji-Bozorgzad, M.R. AU - Geißler, R. AU - Streibel, T. AU - Sklorz, M.* AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 1223 C2 - 27034 CY - Dordrecht SP - 689-694 TI - Hyphenation of a thermobalance to soft single photon ionisation mass spectrometry for evolved gas analysis in thermogravimetry (TG-EGA). JO - J. Therm. Anal. Calorim. VL - 97 IS - 2 PB - Springer PY - 2009 SN - 1388-6150 ER - TY - JOUR AB - A combined thermogravimetry/differential scanning calorimetry device (TG/DSC) was coupled to single photon ionisation mass spectrometry (SPI-MS) for evolved gas analysis (EGA). Single photon ionisation (SPI) was performed with a new type of VUV light source, the so called electron beam pumped rare gas excimer lamp (EBEL). SPI does not fragment molecules upon the ionisation process. Thus the molecular mass signature of the evolving gases from thermal composition of carbonaceous material can be directly on-line recorded. In this work the thermo-analytical data and the SPI-MS information on the released organics is presented and discussed for various samples. Namely biomass (soft and hard wood), fossil fuel (crude oil and coal) as well as a complex polymer (ABS) are investigated. The general potential of hyphenating thermal analysis and soft photo ionisation mass spectrometry (EBEL-SPI-MS) for fundamental and applied research and material analysis is discussed. AU - Streibel, T. AU - Geißler, R. AU - Saraji-Bozorgzad, M.R. AU - Sklorz, M.* AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 512 C2 - 26284 SP - 795-804 TI - Evolved gas analysis (EGA) in TG and DSC with single photon ionisation mass spectrometry (SPI-MS: Molecular organic signatures from pyrolysis of soft and hard wood, coal, crude oil and ABS polymer. JO - J. Therm. Anal. Calorim. VL - 96 IS - 3 PB - Springer PY - 2009 SN - 1388-6150 ER - TY - JOUR AB - The combined analytical methods of thermal analysis and mass spectrometry have been applied in form of a newly developed prototype of a thermogravimetry - single photon ionisation time-of-flight mass spectrometer coupling (TG-SPI-TOFMS) to investigate the molecular patterns of evolved gases from several biomass samples as well as a crude oil sample. Single photon ionization (SPI) was conducted by means of a novel electron beam pumped argon excimer lamp (EBEL) as photon source. With SPI-TOFMS various lignin decomposition products such as guaiacol, syringol and coniferyl alcohol could be monitored. Furthermore, SPI allows the detection of aliphatic hydrocarbons, mainly alkenes, carbonylic compounds such as acetone, and furan derivatives such as furfuryl alcohol and hydroxymethylfurfural. More alkaline biomass such as coarse colza meal show intense signals from nitrogen containing substances such as (iso-)propylamine and pyrrole. Thermal degradation of crude oil takes place in two steps, evaporation of volatile components and pyrolysis of larger molecular structures at higher temperatures. Due to the soft ionisation, homologue rows of alkanes and alkenes could be detected on basis of their molecular ions. The obtained information from the thermal analysis/photo ionisation mass spectrometry experiments can be drawn on in comparison to the investigation of the primary products from flash pyrolysis of biomass for production of biofuels and chemicals. AU - Streibel, T. AU - Fendt, A.* AU - Geißler, R. AU - Kaisersberger, E.* AU - Denner, T.* AU - Zimmermann, R. C1 - 695 C2 - 26803 CY - Dordrecht SP - 615-619 TI - Thermal analysis/mass spectrometry using soft photo-ionisation for the investigation of biomass and mineral oils. JO - J. Therm. Anal. Calorim. VL - 97 IS - 2 PB - Springer PY - 2009 SN - 1388-6150 ER - TY - JOUR AB - Emanation thermal analysis (ETA) and thermogravimetry measured in the range 20-1000 degrees C was used to characterize the thermal behaviour of Na-montmorillonite (Upton Wyoming, USA) and homoionic montmorillonite samples prepared by saturation with cations Li+ , Mg2+, Al3+, respectively. It was confirmed that the presence of cations used for montmorillonite saturation (Li+, Mg2+, Al3+) influenced the thermal behaviour of the samples. The results that indicated the decrease of radon release rate corresponding to a collapse of the interlayer space between the silicate sheets after water release and the crystallization of meta-montmorillonite in the respective temperature intervals were compared. From the ETA results it followed that the thermal stability of intermediate microstructure depends on the type of exchanged cation. A mathematical model was used to evaluate the ETA data. AU - Balek, V.* AU - Benes, M.* AU - Malek, Z.* AU - Matuschek, G. AU - Kettrup, A.* AU - Yariv, S.* C1 - 3988 C2 - 24005 SP - 617-623 TI - Emanation thermal analysis study of Na-montmorillonite and montmorillonite saturated with various cations. JO - J. Therm. Anal. Calorim. VL - 83 IS - 3 PY - 2006 SN - 1388-6150 ER - TY - JOUR AB - Thermal behaviour of different starch derivatives, i.e. starch esters and ethers having degree of substitution (DS) in the range of 0.02-0.18 were studied. Potato, maize and wheat starches were used. Measurements were carried out by coupled thermal analysis/mass spectrometry method (STA-MS) in air atmosphere. The major DTG peak during the investigation for starch derivatives is observed below 300 degrees C. The mass loss up to a temperature of 300 degrees C is about 50%. The most abundant ions found are H2O+ and CO2+. For the studied starch derivatives with a low degree of substitution (DS < 0.18) no correlation was found between thermal stability and the level of substitution regardless of the nature of substitution. AU - Rudnik, E.* AU - Matuschek, G. AU - Milanov, N. AU - Kettrup, A.* C1 - 3987 C2 - 24004 SP - 267-270 TI - Thermal stability and degradation of starch derivatives. JO - J. Therm. Anal. Calorim. VL - 85 IS - 2 PY - 2006 SN - 1388-6150 ER - TY - JOUR AU - Benes, M.* AU - Placek, V.* AU - Matuschek, G. AU - Kettrup, A.* AU - Györyova, K.* AU - Emmerich, W.D.* AU - Balek, V.* C1 - 3594 C2 - 23711 SP - 761-768 TI - Lifetime simulation and thermal characterization of PVC cable insulation materials. JO - J. Therm. Anal. Calorim. VL - 82 PY - 2005 SN - 1388-6150 ER - TY - JOUR AU - Benes, M.* AU - Milanov, N. AU - Matuschek, G. AU - Kettrup, A. AU - Placek, V.* AU - Balek, V.* C1 - 2794 C2 - 22350 SP - 621-630 TI - Thermal degradation of PVC cable insulation studied by simultaneous TG-FTIR and TG-EGA methods. JO - J. Therm. Anal. Calorim. VL - 78 PY - 2004 SN - 1388-6150 ER - TY - JOUR AU - Matuschek, G. AU - Saritas, Y. AU - Karg, E.W. AU - Schröppel, A. C1 - 3415 C2 - 22085 SP - 575-586 TI - Characterisation of aerosol particles using combined thermoanalytical techniques. JO - J. Therm. Anal. Calorim. VL - 78 PY - 2004 SN - 1388-6150 ER - TY - JOUR AU - Li, X.* AU - Matuschek, G. AU - Herrera, M. AU - Wang, H.* AU - Kettrup, A. C1 - 10030 C2 - 21166 SP - 601-612 TI - Investigation of Pyrolysis of Chinese Coals using Thermal Analysis/Mass Spectrometry. JO - J. Therm. Anal. Calorim. VL - 71 PY - 2003 SN - 1388-6150 ER - TY - JOUR AB - he thermal degradation of the aliphatic polyamides 6 and 66 was investigated by means of the combined techniques TA-MS and TA-FTIR. The analyses were performed in three different devices. Sample mass ranged from 13 mg to 1 g and heating rates of 2.6 and 10 K min(-1) were used in both air and nitrogen atmospheres. The most important decomposition products were caprolactam for PA 6 and cyclopentanone for PA 66. Evolution of NH3 and HCN was registered. The findings of the two hyphenated techniques led to the same results and complemented each other well. The evolved products were captured and analyzed off-line by GC/MS for further confirmation of results. AU - Herrera, M. AU - Matuschek, G. AU - Kettrup, A. C1 - 10029 C2 - 19147 SP - 385-394 TI - Thermal degradation studies of some aliphatic polyamides using hypenated techniques (TG-MS, TG-FTIR). JO - J. Therm. Anal. Calorim. VL - 59 PB - Assoc. PY - 2000 SN - 1388-6150 ER - TY - JOUR AU - Balek, V.* AU - Malek, Z.* AU - Yariv, S.* AU - Matuschek, G. C1 - 20894 C2 - 18942 SP - 67-76 TI - Characterization of montmorillonite saturated with various cations. JO - J. Therm. Anal. Calorim. VL - 56 PY - 1999 SN - 1388-6150 ER - TY - JOUR AU - Matuschek, G. AU - Kettrup, A. AU - Prior, A.* C1 - 20895 C2 - 18941 SP - 471-477 TI - EGA/MS investigations on the thermal degradation of diammoniumhexachloroplatinate. JO - J. Therm. Anal. Calorim. VL - 56 PY - 1999 SN - 1388-6150 ER - TY - JOUR AB - Poly(butadiene-alt-1-olefin) copolymers and poly[(butadiene-alt-ethene)-co-(butadiene-alt-1-olefin)] terpolymers, and the hydrogenated products too, has been characterized with the aid of differential scanning calorimetry (DSC). Both the glass transition and the melting behaviour of the partial crystallized products has been investigated. From the peak area the degree of crystalunity has been calculated in a first approximation. The results allow to draw conclusions about the crystallization behaviour in relation to the number and length of the side chains and about the course of the synthesis in question. AU - Reußner, J.* AU - Höhne, G.W.H.* AU - Utschick, H. AU - Arnold, M.* AU - Wegner, T.* AU - Wohlfarth, L.* C1 - 33201 C2 - 35623 SP - 975-992 TI - DSC-Untersuchungen an Butadien/Olefin-CO-und Terpolymeren sowie an ihren Hydrier-Produkten. JO - J. Therm. Anal. Calorim. VL - 47 IS - 4 PY - 1996 SN - 1388-6150 ER - TY - JOUR AU - Matuschek, G. AU - Ohrbach, K.-H. AU - Kettrup, A. C1 - 19129 C2 - 12185 SP - 1141-1155 TI - Simultaneous Thermal Analysis / Mass Spectrometry on Commercial Phosphororganic Pesticide Compounds. JO - J. Therm. Anal. Calorim. VL - 39 PY - 1993 SN - 1388-6150 ER - TY - JOUR AU - Matuschek, G. AU - Cyrys, J. AU - Lenoir, D. AU - Kettrup, A. C1 - 20263 C2 - 13449 SP - 533-535 TI - DSC and TA/MS Studies on Formation and Decomposition of Polychlorinated Dibenzo-p- dioxines and Dibenzofuranes. JO - J. Therm. Anal. Calorim. VL - 40 PY - 1993 SN - 1388-6150 ER - TY - JOUR AB - The effect of oxydation of particulate carbon as a part of fly ash has been studied by mean of differential scanning calorimetry (DSC) and simultaneous thermal analysis/mass spectrometry (TA/MS). The results from different carbon modifications added to fly ash were discussed and compared to those of the pure samples. AU - Matuschek, G.M. AU - Cyrys, J. AU - Lenoir, D. AU - Kettrup, A. C1 - 40302 C2 - 40080 SP - 533-535 TI - DSC and TA/MS studies on formation and decomposition of polychlorinated dibenzo-p-dioxines and dibenzofuranes - Fly ash as reagent and catalyst; oxidation of particulate carbon. JO - J. Therm. Anal. Calorim. VL - 40 IS - 2 PY - 1993 SN - 1388-6150 ER - TY - JOUR AU - Kettrup, A. AU - Ohrbach, K.-H. AU - Matuschek, G. C1 - 19699 C2 - 12829 SP - 1793-1794 TI - Risk Assessment of Volatiles Release from Polymers and Flame Retardants Using off Line and on Line TA Methods. JO - J. Therm. Anal. Calorim. VL - 37 PY - 1991 SN - 1388-6150 ER -