TY - CONF A1 - Schlegel, Moritz-Caspar T1 - In-situ SyXRD Analysis of Cement Hydration on the ms-Scale T2 - Chemistry of Construction Materials CY - Berlin, Germany DA - 2013-10-07 PY - 2013 AN - OPUS4-29829 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Fischer, Franziska T1 - Synthesis and strustural Characterization of a Theophylline:Nicotinamide Cocrystal T2 - Adlershofer Forschungszentrum CY - Berlin, Germany DA - 2013-11-12 PY - 2013 AN - OPUS4-29855 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Joester, Maike T1 - Raman micro-spectroscopy in combination with scattering methods to study silica in plant materials T2 - Adlershofer Forschungsforum CY - Berlin, Germany DA - 2013-11-12 PY - 2013 AN - OPUS4-29836 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Stroh, Julia T1 - Investigations of Degradation of Cementitious Materials by in-situ Structure Analysis T2 - Adlershofer Forschungsforum CY - Berlin, Germany DA - 2013-11-12 PY - 2013 AN - OPUS4-29828 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wilke, Manuel T1 - Verfolgung mechanochemischer Synthesen durch in situ Röntgendiffraktometrie T2 - Adlershofer Foschungsforum CY - Berlin, Germany DA - 2013-11-12 PY - 2013 AN - OPUS4-29854 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gnutzmann, Tanja T1 - In situ characterization of crystallization processes T2 - Adlershofer Forschungsforum CY - Berlin, Germany DA - 2013-11-12 PY - 2013 AN - OPUS4-29831 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Why shaken, not stirred, makes the difference: insights into mechanochemical reactions from in situ investigations N2 - Mechanochemistry is an effective, environmentally benign, and facile method for the synthesis of new multicomponent crystal systems. Different milling parameters are known to affect the mechanisms and rates of product formation: milling frequency, milling time, filling degree of the milling jar, ball diameter and vessel size, degree of milling ball filling, and material of jars. The increasing interest in mechanochemistry is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Different analytical methods and their combinations have been developed for the time resolved in situ monitoring of mechanochemical transformations, including powder X-ray diffraction, X-ray adsorption spectroscopy, NMR, Raman spectroscopy, and thermography. Here we will discuss our recent results investigating the formation of (poly-morphic) cocrystals[1,3], metal-organic compounds, and salts, thereby elucidating the influence of milling parameters and reaction sequences on the formation mechanism and kinetics. For the mechanochemical chlorination reaction of hydantoin normalizing the kinetic profiles to the volume of the milling ball showed clearly that milling reaction kinetics are conserved. Here physical kinetics dominate reaction rates in a ball-milling transformation. Attempting to interpret such kinetics in purely chemical terms risk misinterpreting the results. Our results indicate that time-resolved in situ investigation of milling reactions offer a new approach to tune and optimize mechanochemical processes. T2 - GdCh Vortrag Universität Potsdam CY - Potsdam, Germany DA - 05.06.2023 KW - Mechanochemistry KW - In Situ PY - 2023 AN - OPUS4-58982 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Mechanochemical formation of multicomponent crystal systems: Mechanism & Kinetics N2 - Mechanochemistry is an effective, environmentally benign, and facile method for the synthesis of new multicomponent crystal systems. Different milling parameters are known to affect the mechanisms and rates of product formation: milling frequency, milling time, filling degree of the milling jar, ball diameter and vessel size, degree of milling ball filling, and material of jars. The increasing interest in mechanochemistry is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Different analytical methods and their combinations have been developed for the time resolved in situ monitoring of mechanochemical transformations, including powder X-ray diffraction, X-ray adsorption spectroscopy, NMR, Raman spectroscopy, and thermography. Here we will discuss our recent results investigating the formation of (poly-morphic) cocrystals, metal-organic compounds, and salts, thereby elucidating the influence of milling parameters and reaction sequences on the formation mechanism and kinetics. For the mechanochemical chlorination reaction of hydantoin normalizing the kinetic profiles to the volume of the milling ball showed clearly that milling reaction kinetics are conserved. Here physical kinetics dominate reaction rates in a ball-milling transformation. Attempting to interpret such kinetics in purely chemical terms risk misinterpreting the results. Our results indicate that time-resolved in situ investigation of milling reactions offer a new approach to tune and optimize mechanochemical processes. T2 - 25th International Conference on the Chemistry of the Organic Solid State (ICCOSS XXV) CY - Ohrid, Macedonia DA - 03.07.2022 KW - Mechanochemistry KW - In situ real-time monitoring KW - Crystal Engineering PY - 2022 AN - OPUS4-55413 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Shaken not stirred: enhancing the flavor of mechanochemistry N2 - compounds and cocrystals. The ever-increasing interest in this method is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Different milling parameters are known to affect the mechanisms and rates of product formation: milling frequency, milling time, filling degree of the milling jar, ball diameter and vessel size, degree of milling ball filling, and material of jars. Time-resolved in situ investigations of milling reactions (Figure 1) provide direct insights into the underlying mechanisms. We recently introduced different setups enabling in situ investigation of mechanochemical reactions using synchrotron XRD and XAS combined with Raman spectroscopy and thermography. The presented setup allows the detection of crystalline, amorphous, eutectic, and liquid intermediates. Furthermore, the chemical composition of the reaction mixture was found to be directly correlated with changes in the temperature profile of the reaction. The resulting deeper kinetic and thermodynamic understanding of milling processes is the key to future optimization of mechanochemical syntheses. In this contribution, we will discuss our recent results investigating the formation of (polymorphic) cocrystals and coordination polymers. Our results indicate that time-resolved in situ investigations of mechanochemical processes are key for tuning and optimizing mechanochemical syntheses allowing to unleash the potential of mechanochemistry for a green materials design. T2 - 2nd National Crystallographic Meeting Lisbon, Portugal CY - Lisbon, Portugal DA - 15.07.2022 KW - Mechanochemistry KW - In situ real-time monitoring KW - Crystal PY - 2022 AN - OPUS4-55415 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Mechanochemical formation of multicomponent crystals systems N2 - Mechanochemistry is an effective, environmentally benign, and facile method for the synthesis of new multicomponent crystal systems. Different milling parameters are known to affect the mechanisms and rates of product formation: milling frequency, milling time, filling degree of the milling jar, ball diameter and vessel size, degree of milling ball filling, and material of jars. The increasing interest in mechanochemistry is contrasted by a limited mechanistic understanding of mechanochemical reactivity and selectivity. Different analytical methods and their combinations have been developed for the time-resolved in situ monitoring of mechanochemical transformations, including powder X-ray diffraction, X-ray absorption spectroscopy, NMR, Raman spectroscopy, and thermography. Here we will discuss our recent results investigating the formation of (polymorphic) cocrystals, metal-organic compounds, and salts, thereby elucidating the influence of milling parameters and reaction sequences on the formation mechanism and kinetics. Our results indicate that time-resolved in situ investigations of milling reactions offer a new approach to tune and optimize mechanochemical processes. T2 - 5ECQUL Forging Bonds CY - Lisbon, Portugal DA - 12.07.2022 KW - Mechanochemistry KW - In situ real-time monitoring KW - N-Chlorination PY - 2022 AN - OPUS4-55414 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - Mechanochemical formation of multicomponent crystal systems: Mechanism & Kinetics N2 - Mechanochemistry is an effective, environmentally benign, and facile method for the synthesis of new multicomponent crystal systems. Different milling parameters are known to affect the mechanisms and rates of product formation: milling frequency, milling time, filling degree of the milling jar, ball diameter and vessel size, degree of milling ball filling, and material of jars. The increasing interest in mechanochemistry is contrasted by a limited mechanistic understanding of the mechanochemical reactivity and selectivity. Different analytical methods and their combinations have been developed for the time resolved in situ monitoring of mechanochemical transformations, including powder X-ray diffraction, X-ray adsorption spectroscopy, NMR, Raman spectroscopy, and thermography.1 Here we will discuss our recent results investigating the formation of (polymorphic) cocrystals2–3 and metal-organic frameworks,4 thereby elucidating the influence of milling parameters and reaction sequences on the formation mechanism and kinetics. For the mechanochemical chlorination reaction of hydantoin normalizing the kinetic profiles to the volume of the milling ball showed clearly that milling reaction kinetics are conserved.6 Here physical kinetics dominate reaction rates in a ball-milling transformation. Attempting to interpret such kinetics in purely chemical terms risk misinterpreting the results. Our results indicate that time-resolved in situ investigation of milling reactions offer a new approach to tune and optimize mechanochemical processes. T2 - 10th International conference on Mechanochemistry and Mechanical Alloying CY - Cagliari, Italy DA - 06.06.2022 KW - Mechanochemistry KW - In situ real-time monitoring KW - Cocrystal PY - 2022 AN - OPUS4-55421 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Altmann, Korinna T1 - ILC on Laser diffraction - preliminary results N2 - This presentation addresses an interlaboratory comparison on size of polymeric particles (microplastics) measured by laser diffraction. Two microplastic particles were measured separately and once as mixture. Evaluation was done with Fraunhofer and Mie. Here, the first results are presented. T2 - CUSP Annual Meeting CY - Utrecht, Netherlands DA - 12.09.2023 KW - Microplastics KW - Laser diffraction KW - Polymer 3R KW - Size distribution KW - Polymer size PY - 2023 AN - OPUS4-58318 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Stawski, Tomasz T1 - Evolution of mesoporous frameworks from precipitated struvite-structured metal phosphate materials N2 - Mesoporous transition metal phosphates (TMPs) have attracted major interest due to their high (electro-)catalytic activity suitable for H2 generation, supercapacitors or batteries. Typically, mesoporous materials are synthesized via a template-based route. This way is in the case of TMP because the surfactants used are difficult to remove due to the sensitivity of the mesoporous framework. We present a template-free method including the formation of a precursor phase called M-struvite (NH4MPO4•6H2O, M = Mg2+, Ni2+, Co2+, Ni2+xCo2+1-x) to synthesize mesoporous and amorphous metal phosphates. This method relies on the thermal decomposition of crystalline M-struvite precursors to an amorphous and simultaneous mesoporous phase associated with the degassing of NH3 and H2O. The temporal evolution of mesoporous frameworks and the response of the coordination metal coordination environment was followed with diffraction and spectroscopy based in-situ and ex-situ methods. We highlight the systematic differences in absolute surface area, pore shape, pore size, and phase transitions between the chemical systems. In a complex amorphous structure, thermal decomposed Mg-, Ni- and NixCo1-x-struvites exhibit high surface areas and pore volumes for phosphate materials with a spherical to channel-like pore geometry (240 m²g-1 and 0.32 cm-3 g-1 for Mg and 90 m²g-1 and 0.13 cm-3 g-1 for Ni). In addition to this low-cost, environmentally friendly and simple synthesis, M-struvites could grow as a recycling product from industrial and agricultural wastewaters. These waste products could be upcycled through a simple thermal treatment for further applications. T2 - ECCG7, European Conference on Crystal Growth CY - Paris, France DA - 25.07.2022 KW - Transition metals KW - Phosphates KW - Struvite KW - Amorphous phases KW - Mesoporosity PY - 2022 AN - OPUS4-55491 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kraehnert, R. T1 - Size-controlled synthesis of gold-nanoparticles for catalytic applications followed by in-situ SAXS, XANES and UV/Vis T2 - Deutsche Tagung für Forschung mit Synchrotronstrahlung, Neutronen und Ionenstrahlen an Großgeräten CY - Berlin, Germany DA - 2010-02-24 PY - 2010 AN - OPUS4-20176 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Radnik, J. T1 - Simultaneous Synchrotron X-ray Scattering and Optical Spectroscopy: The first fivefold in situ-coupling technique for on-line monitoring of catalyst synthesis T2 - 6th World Congress on Oxidation Catalysis CY - Lille, France DA - 2009-07-05 PY - 2009 AN - OPUS4-19187 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Tuaev, Xenia T1 - In situ Analytik von Nukleations- und Wachstumsprozessen von Silbernanopartikeln am offenen Flüssigkeitsstrahl mittels Röntgenkleinwinkelstreuung T2 - Deutsche Tagung für Forschung mit Synchrotronstrahlung, Neutronen und Ionenstrahlen an Großgeräten CY - Berlin, Germany DA - 2010-02-24 PY - 2010 AN - OPUS4-20180 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Polte, Jörg T1 - In situ studies using SAXS allow new insights in the nucleation and growth processes of nanoparticles T2 - Adlershofer Jubiläumssymposium "Licht-Materialien-Modelle" CY - Berlin, Germany DA - 2009-09-08 PY - 2009 AN - OPUS4-19999 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Matschulat, Andrea T1 - NIR SERS hybrid probes for vitro and in vivo bioanalytics T2 - DGD - Frühjahrstagung CY - Dresden, Germany DA - 2009-03-22 PY - 2009 AN - OPUS4-19199 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Matschulat, Andrea T1 - NIR-SERS probes for in vitro and in vivo bioanalytics T2 - ANAKON CY - Berlin, Germany DA - 2009-03-17 PY - 2009 AN - OPUS4-19209 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Batzdorf, Lisa T1 - Mechanochemical Synthesis of Two 2D Organometallic Structures: [Co(C2O4)(4,4'-bipy)] and [Zn3(C2O4)3(4,4'-bipy)4] T2 - 6. Interdisziplinäres Doktorandenseminar CY - Berlin, Germany DA - 2012-02-26 PY - 2012 N1 - Geburtsname von Batzdorf, Lisa: Tröbs, L. - Birth name of Batzdorf, Lisa: Tröbs, L. AN - OPUS4-25495 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -