TY - CONF A1 - Alić Stolar, Jasna T1 - Harnessing Mechanochemistry to Combat PFAS Contamination N2 - For over 70 years, the uncontrolled production, use, and disposal of per- and polyfluoroalkyl substances (PFAS) have led to widespread global contamination, necessitating the rapid development of innovative and efficient remediation technologies. State-of-the-art strategies rely on energy-intensive incineration, which releases greenhouse gases and smaller, volatile PFAS derivatives. Here, we present a fast, simple, and sustainable method for the complete degradation of PFAS leveraging mechanochemistry to break down the persistent carbon-fluorine bonds. Our findings indicate that liquid-assisted grinding conditions accelerate the degradation of perfluorooctanoic acid compared to neat grinding conditions, resulting in a significant reduction in energy consumption. Moreover, the fluoride released during the process binds to inorganic additives, allowing fluorine recovery as crystalline salts and preventing the formation of secondary toxic waste. The method has strong potential for scaling up and offers a green and viable solution for real-world application in PFAS decontamination. T2 - International Conference on Sustainable Chemistry for Net Zero (ICSC-NZ) CY - St. Andrews, Scotland DA - 10.06.2025 KW - Mechanochemistry KW - PFAS KW - Remediation PY - 2025 AN - OPUS4-63971 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Karafiludis, Stephanos A1 - Stawski, Tomasz T1 - Deciphering the non-classical Crystallization of transition metal phosphates (TMP) N2 - A crucial aspect of ensuring sustainable raw material utilization to meet global demand lies in the efficient recovery and reuse of critical elements and compounds. Phosphate, PO43-, and many transition metals e.g. Ni and Co are listed as critical raw materials (CRMs) due to their indispensable role in numerous industrial processes. However, these elements can also exert harmful environmental impacts, with phosphorus being a major contributor to anthropogenic eutrophication and transition metal ions acting as toxic pollutants, particularly in ground- and wastewaters. Typically, separate pathways have been considered to extract hazardous substances such as transition metals or phosphate, independently from each other. Here, we report the crystallization pathways of transition metal phosphate (TMP) compounds, M-struvite and M-phosphate octahydrate with M = Ni2+, Co2+, NixCo1-x2+, NH4MPO4∙6H2O, M3(PO4)2∙8H2O from aqueous solutions. The co-precipitation of these particular TMP compounds from industrial and agricultural wastewaters has high potential as a P- and 3d metal recovery route. For efficient extraction and transformation of the TMPs, a comprehensive understanding of their nucleation and crystallization pathways from aqueous solutions is required. While the crystallization mechanisms of magnesium or calcium phosphate-bearing phases have been researched for many decades (e.g. struvite, apatite), investigations into TMP materials are relatively scarce and often focus on the adsorption of transition metals on the surface instead of their actual incorporation in minerals. In our study, we investigated in detail the precipitation process of several Co and Ni phosphates using ex- and in-situ spectroscopic-, spectrometric- and diffraction-/scattering-based techniques. We show that the crystallization behavior of TMPs, indeed deviates from a classical crystallization paradigm and follows a non-classical multi-step pathway. Our work extends the understanding of TMP crystallization by elucidating the formation of amorphous precursors preceding the final crystalline phase This time-dependent transition of the transition metal precursor phases can be observed by electron-imaging/tomography depicting a progressively changing amorphous solids until their ultimate reconfiguration to a crystal (Figure 1). Here, the two-metallic NixCo1-x-mixtures deviated anomalously in their reaction kinetics, crystallization outcome and participation of both metals from their pure endmembers. By measuring the crystallization with in-situ X-ray scattering and pH using a flow-through setup geometry, a complex prolonged interplay among nucleating entities e.g. and amorphous or crystalline solids could be observed in the metal phosphate mixtures reaching equilibrium after almost two and a half hours (Figure 2). Our results provide a holistic perspective on the crystallization behavior of transition metal phosphate phases, shedding light on their unique nucleation and growth kinetics involving structural and chemical transformations of the intermediate phases. T2 - Granada Münster Discussion Meeting 2023 CY - Münster, Germany DA - 29.11.2023 KW - Non-classical crystallization theory KW - Transition metals KW - Phosphates PY - 2023 AN - OPUS4-59007 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Roy, Arkendu T1 - Hydroxide Based High Entropy MOF for Oxygen Evolution Reaction N2 - The energy crisis becomes more prominent in higher altitude countries like Germany, with higher annual energy demand. Thus, the generation of higher energy density fuel like hydrogen from renewable resources become the only way to solve the zero-emission energy system while avoiding the expensive batteries as an energy storage option. Therefore, water electrolysis cells to produce hydrogen and oxygen by storing of solar/wind energy in chemical bonds is a fruitful alternative for renewable and long-term energy generation. Thus, designing inexpensive water-splitting electrocatalyst material becomes a field of research of utmost importance. High entropy metal hydroxide organic frameworks (HE-MHOFs) are composed of high entropy hydroxide layer inside MOFs, resulting in a high degree of structural complexity and diversity than conventional MOFs. The concept of ‘high entropy’ refers to multiple types of metal ions (Metal = TM) in a near equimolar ratio in the same framework, creating a high degree of disorder and many possible structural configurations. Here, the HE-MHOF successfully synthesized by a conventional solvothermal process, crystallizes in the single phase with significant lattice distortion. A special-quasi-random (SQS) structure was simulated with equimolar compositions (~20% TM = Mn, Co, Ni, Cu and Zn) and a comparison was made with the ICP-AES (inductively coupled plasma atomic emission spectroscopy), XANES (X-ray absorption near edge structure) and XAFS (X-ray absorption fine structure) observations. Further, the elemental mapping (Energy dispersive Spectroscopy) of HE-MHOF shows the presence of all five different metals in the same crystallite to substantiate the ‘high entropy’ state of the MOF. The HE-MHOF offers improved thermal stability than mono-metallic MHOF and exhibit unique properties compared to traditional monometallic (Ni2+) MOF variants. Firstly, to elucidate the effect of the multimetallic system on the catalytic performance, we have performed density functional theory (DFT) calculations to investigate pre-redox cycles involved in the catalytic activation of HE (and Ni)-MOFs. HE-MHOF is further investigated as an electrocatalyst for oxygen evolution reaction (OER) due to its special high entropy hydroxide layered structure and electronic properties. Our DFT results have examined the traditional proton-coupled electron transfer (PCET) steps involving the single transition-metal site. The scrutiny of d-band centers and their behaviour in catalytic upgradation is investigated with density of states (DOS) analysis. It exhibits outstanding performance towards oxygen evolution reaction (OER) comparable to the experimental findings, which is also comparable to state-of-the-art OER catalysts based on precious metals such as iridium oxide and platinum carbon. We have considered different electrolyte solutions to elucidate the fast kinetics oxygen evolution reaction in the presence of various external nucleophilic anions. In hydroxyl-based MOFs, electrolytes' influence can substantially enhance catalytic activities. Here, with the help of DFT simulations, we have investigated the effect of the nucleophilicity of anion on each elementary reaction involved in the PCET mechanism of OER. T2 - EuroMOF 2023 CY - Granada, Spain DA - 24.09.2023 KW - Metal-organic Framework KW - High Entropy Materials KW - Electrocatalysis PY - 2023 AN - OPUS4-58971 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gugin, Nikita T1 - Optimizing the Green Synthesis of ZIF-8 by Reactive Extrusion Using In Situ Raman Spectroscopy N2 - ZIF-8 is a prominent member of the zeolitic imidazolate frameworks (ZIFs) subfamily of MOFs which possesses high thermal, chemical, and mechanical stabilities. Different routes have been explored to achieve the large-scale production of ZIF-8. However, these synthetic procedures are often inconsistent with the principles of sustainable chemical manufacturing. Aimed at developing scalable and greener production of ZIF-8, we adapted our previously reported in-batch „mix and wait“ synthesis[2] to continuous extrusion. To optimize the process, in-situ Raman spectroscopy was applied. Finally, we developed a simple and comprehensive approach to evaluating the environmental friendliness and scalability of MOF syntheses in view of their large-scale production. The synthesis of ZIF-8 was performed using a twin-screw extruder ZE 12 HMI equipped with an automatic volumetric feeder ZD 12B (Three-Tec GmbH, Switzerland) and peristaltic pump BT-L (Lead Fluid, China). The process was monitored in six different zones using a Raman RXN1TM analyzer (Kaiser Optical Systems, France) with a non-contact probe head. PMMA screw-in parts, which are transparent to Raman laser radiation, were specially manufactured to provide the laser focus within the barrel. PXRD, TGA, N2 adsorption measurements, and SEM were used as complementary techniques to characterize the extrudates. The batch ‘mix and wait’ synthesis of ZIF-8, consisting of bringing solid basic zinc carbonate and 2-methylimidazole in contact in a closed vial, was successfully adapted to reactive extrusion. The crystalline ZIF-8 continuously forms in the extruder under the mixing of solid reagents in the presence of a catalytic amounts of H2O or EtOH. The temperature, type of liquid, feeding rate, and excess of linker were optimized using in situ Raman spectroscopy. Pure and highly crystalline ZIF-8 was isolated at 40 °C by adding a catalytic amount of EtOH and a linker excess of 25%. The resulting material has excellent porosity with the BET surface area slightly exceeding that of the reference Basolite® Z1200 (1816 vs. 1734 m2 g–1). The reaction could yield ~ 3 kg d–1 assuming a continuous operation, with a space-time yield of ca. 67,000 kg m–3 d–1. The present method was compared to the published pathways based on Green Chemistry principles and proved to have the highest potential for large-scale production of ZIF-8. T2 - 5th European Conference on Metal Organic Frameworks and Porous Polymers (EuroMOF2023) CY - Granada, Spain DA - 24.09.2023 KW - In situ Raman KW - Reactive extrusion KW - Green chemistry KW - Mechanochemistry KW - MOFs KW - Large-scale synthesis PY - 2023 AN - OPUS4-58950 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gugin, Nikita T1 - Chemists have solutions and know how to get rid of them N2 - Metal-organic framework-based biocomposites (MOF-biocomposites) are promising materials for biosensing, biocatalysis, and delivery of biopharmaceuticals. One of the most studied MOFs for bioapplications is ZIF-8 (zeolitic imidazolate framework 8) due to its high surface area, high thermal and chemical stability, and low cytotoxicity. The conventional synthesis of ZIF-8-biocomposites called biomimetic mineralization includes mixing selected biomolecules 2-methylimidazole, and soluble Zn2+ source in water.[3] Despite the high efficiency of the method, it does not allow for large-scale production and is restricted to hydrophilic biomolecules. Aimed at developing a scalable and versatile approach, we adapted our recently-reported ZIF-8 reactive extrusion for biocomposite production. We selected bovine serum albumin (BSA) as an inexpensive model biomacromolecule for the preparation of biocomposites. The synthesis of BSA@ZIF-8 was performed using a twin-screw extruder ZE 12 HMI (Three-Tec Gmbh) at a mild temperature of 40 °C. Automatic volumetric feeder ZD 12B (Three-Tec GmbH) was used to supply the reagent mixture consisting of 2-methylimidazole, zinc source, and BSA. To initiate the reaction, a catalytic amount of EtOH was added using a peristaltic pump BT-L (Lead Fluid, China). Powder X-Ray diffraction (PXRD), thermogravimetric analysis (TGA), FTIR, and N2 adsorption were used to characterize the extrudates. Highly crystalline and pure BSA@ZIF-8 with different BSA loadings was isolated after washing the extrudate with EtOH and sodium dodecyl sulfate. The EtOH feeding rate was optimized by following the protein encapsulation efficiency at a BSA mass fraction of 10%. A continuous extruder operation under optimized conditions showed good reproducibility and capability of producing biocomposites on the kilograms scale. These results provide highly valuable information for cheap and large-scale production of ZIF-8-based biocomposites. Due to the lack of restrictions on molecule size and solubility, our proof-of-concept study may significantly expand the selection of biomolecules for immobilization in ZIF-8, making the method applicable to various functional applications T2 - SALSA Make and Measure conference CY - Berlin, Germany DA - 13.09.2023 KW - In situ Raman KW - Large-scale processing KW - Reactive extrusion KW - Large-scale production KW - Mechanochemistry PY - 2023 AN - OPUS4-58953 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gugin, Nikita A1 - Schwab, Alexander T1 - Reactive extrusion of a model BSA@ZIF-8 biocomposite: a scalable, continuous and sustainable approach N2 - Metal-organic framework-based biocomposites (MOF-biocomposites) are promising materials for biosensing, biocatalysis, and delivery of biopharmaceuticals. One of the most studied MOFs for bioapplications is ZIF-8 (zeolitic imidazolate framework 8) due to its high surface area, high thermal and chemical stability, and low cytotoxicity. The conventional synthesis of ZIF-8-biocomposites called biomimetic mineralization includes mixing selected biomolecules 2-methylimidazole, and soluble Zn2+ source in water. Despite the high efficiency of the method, it does not allow for large-scale production and is restricted to hydrophilic biomolecules. Aimed at developing a scalable and versatile approach, we adapted our recently-reported ZIF-8 reactive extrusion for biocomposite production. We selected bovine serum albumin (BSA) as an inexpensive model biomacromolecule for the preparation of biocomposites. The synthesis of BSA@ZIF-8 was performed using a twin-screw extruder ZE 12 HMI (Three-Tec Gmbh) at a mild temperature of 40 °C. Automatic volumetric feeder ZD 12B (Three-Tec GmbH) was used to supply the reagent mixture consisting of 2-methylimidazole, zinc source, and BSA. To initiate the reaction, a catalytic amount of EtOH was added using a peristaltic pump BT-L (Lead Fluid, China). Powder X-Ray diffraction (PXRD), thermogravimetric analysis (TGA), FTIR, and N2 adsorption were used to characterize the extrudates. Highly crystalline and pure BSA@ZIF-8 with different BSA loadings was isolated after washing the extrudate with EtOH and sodium dodecyl sulfate. The EtOH feeding rate was optimized by following the protein encapsulation efficiency at a BSA mass fraction of 10%. A continuous extruder operation under optimized conditions showed good reproducibility and capability of producing biocomposites on the kilograms scale. These results provide highly valuable information for cheap and large-scale production of ZIF-8-based biocomposites. Due to the lack of restrictions on molecule size and solubility, our proof-of-concept study may significantly expand the selection of biomolecules for immobilization in ZIF-8, making the method applicable to various functional applications T2 - Tag der Chemie 2023 CY - Berlin, Germany DA - 05.07.2023 KW - Biocomposite KW - MOFs KW - Reactive extrusion KW - Zeolitic imidazolate framework PY - 2023 AN - OPUS4-58949 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dietzmann, Simon A1 - Mehmood, Asad A1 - de Oliveira Guilherme Buzanich, Ana A1 - Emmerling, Franziska A1 - Fellinger, Tim-Patrick A1 - Thomas, A. T1 - Characterization of Solid-State Complexes by XAS N2 - Atomically dispersed metal-nitrogen doped carbons (M-N-C) are promising catalysts for the activation of small molecules such as O2 and CO2. These single atom catalysts (SAC) operate at the interface between homogenous and heterogenous catalysts. Currently, many examples of M-N-C are known with good oxygen reduction reaction activity but lacking a controlled synthesis of the specific active sites of the precatalyst. Recently, our group facilitated the synthesis of pure pyrrolic M-N4 sites using Zn ions as imprinters.[1] These amorphous materials obtained by active site imprinting method are characterized at the BAMline (Bessy II) by X-ray absorption spectroscopy (XAS). In-situ/operando measurements will be crucial in future work for a better understanding of the dynamic changes of the active site. T2 - InSynX Workshop 2023 CY - Sao Paulo, Brazil DA - 06.03.2023 KW - Solid-State Complexes PY - 2023 AN - OPUS4-58933 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gugin, Nikita T1 - Mixing Reactions Enable Green Synthesis of ZIF-8 at Large Scale: Batch and Continuous Modes N2 - We report the scale-up of a batch solid synthesis of zeolitic imidazolate framework-8 (ZIF-8) for reactive extrusion. The crystalline product forms in the extruder directly under the mixture of solid 2-methylimidazole and basic zinc carbonate in the presence of a catalytic amount of liquid. The process parameters such as temperature, liquid type, feeding rate, and linker excess were optimized using the setup specifically designed for in situ Raman spectroscopy. Highly crystalline ZIF-8 with a Brunauer–Emmett–Teller (BET) surface area of 1816 m2 g–1 was quantitatively prepared at mild temperature using a catalytic amount of ethanol and a small excess of the linker. Finally, we developed a simple and comprehensive approach to evaluating the environmental friendliness and scalability of metal–organic framework (MOF) syntheses in view of their large-scale production. T2 - 2023 #RSCPoster Twitter Conference CY - Online meeting DA - 28.02.2023 KW - MOFs KW - Green chemistry KW - Reactive extrusion KW - Large-scale production KW - Mechanochemistry KW - Zeolitic imidazolate framework PY - 2023 UR - https://twitter.com/NikitaGugin/status/1630538555675099139 AN - OPUS4-58951 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gugin, Nikita T1 - Large-Scale Synthesis of ZIF-8 for Hydrogen Storage: Batch and Continuous Modes N2 - We report the scale-up of a batch solid synthesis of zeolitic imidazolate framework-8 (ZIF-8) for reactive extrusion. The crystalline product forms in the extruder directly under the mixture of solid 2-methylimidazole and basic zinc carbonate in the presence of a catalytic amount of liquid. Highly crystalline ZIF-8 with a Brunauer−Emmett−Teller (BET) surface area of 1816 m2 g−1 was quantitatively prepared at mild temperature using a catalytic amount of ethanol and a small excess of the linker. Extruded ZIF-8 is an affordable alternative to commercial Basolite Z1200 as a reference material for H2 cryoadsorption. T2 - Metrology for Advanced Hydrogen Storage Solutions (MefHySto) Closing Conference CY - Berlin, Germany DA - 03.07.2023 KW - In situ Raman KW - Large-scale processing KW - Mechanochemistry KW - Twin-screw extrusion (TSE) PY - 2023 AN - OPUS4-58926 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Delißen, Friedmar T1 - Agglomeration of proteins in acoustically levitated droplets T2 - EUROANALYSIS-XIV CY - Antwerp, Belgium DA - 2007-09-09 PY - 2007 AN - OPUS4-15057 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Leiterer, Jork T1 - New experimental setup for on-line monitoring of the synthesis of oxides at the µ-spot Beamline T2 - 26th BESSY Users' Meeting (Berliner Elektronenspeicherring-Gesellschaft für Synchrotronstrahlung mbH) CY - Berlin, Germany DA - 2007-12-06 PY - 2007 AN - OPUS4-16401 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Leiterer, Jork T1 - Akustisch levitierte Tropfen für luftgetragene Analytik T2 - 1. Doktorandentagung - Arbeitskreise Chemometrik und Labordatenverarbeitung, Chemo- und Biosensoren, Prozessanalytik, Qualitätsmanagement und Elektro Analytische Chemie CY - Attendorn, Germany DA - 2007-02-08 PY - 2007 AN - OPUS4-16386 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wolf, S. E. T1 - New evidences for a spinodal CaCO3 formation observed by contact-free in situ scattering techniques T2 - 26th BESSY Users' Meeting (Berliner Gesellschaft für Synchotronstrahlung mbH) CY - Berlin, Germany DA - 2007-12-06 PY - 2007 AN - OPUS4-16400 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Leiterer, Jork T1 - Structure Analysis of Acoustically Levitated Droplets via Synchrotron X-ray Diffraction T2 - EUROANALYSIS-XIV CY - Antwerp, Belgium DA - 2007-09-09 PY - 2007 AN - OPUS4-15052 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Altmann, Korinna T1 - Reference material candidates for microplastic analysis N2 - Every day, there are new headlines in the media about microplastics (1-1000 µm, ISO/TR 21960:2020) and nanoplastics (< 1 µm, ISO/TR 21960:2020) findings all over the planet with high variations in particle number and mass. The challenges in analytics are very complex, e.g. representative sampling, non-destructive sample preparation with concentrated particles and homogeneous distribution and true detection. All together lead to lacks in harmonization and results, which are hardly comparable. On the other hand, monitoring of microplastics is mandatory in the future strictly regulated by the EU commission in the Drinking water and Wastewater Framework Directive. One step to accurate and precise results will be the development of suitable reference materials mimicking particles in the environment. BAM developed test materials, which are produced by mixing a small portion of microplastic particles with a water-soluble matrix. After solid phase dilution and homogenisation small portions are pressed into tablets and bottled in glass vials (Figure 1). These tablets are well characterized with particle size distribution and SEM images. Additionally, they are tested as reference material candidate according to homogeneity and stability for particle number with µ-IR and µ-Raman as well as on particle mass with Py-GC/MS and TED-GC/MS after ISO Guide 35. Results are promising. The material passed the homogeneity control. No changes are observed within 6 months of storage. The same tested reference material is finally used in sample preparation experiments, where environmental suspended particular matter from surface water or baby milk powders are spiked with the tablets. T2 - ESOPS CY - Berlin, Germany DA - 09.09.2024 KW - Microplastics KW - TED-GC/MS KW - Reference materials KW - Polymer 3R KW - Tablets PY - 2024 AN - OPUS4-61017 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Emmerling, Franziska T1 - In situ investigations of mechanochemical reactions N2 - Presentation of the recent results in the context of in situ investigations of reactions using X-ray diffraction. T2 - Germany Brazil Workshop: New light on mechanisms of chemical reactions CY - Kiel, Germany DA - 31.07.2018 KW - In situ KW - XRD PY - 2018 AN - OPUS4-46991 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gnutzmann, Tanja T1 - Time-resolved investigation of crystallization processes T2 - SMI Symposium CY - Bochum, Germany DA - 2012-03-26 PY - 2012 AN - OPUS4-25677 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schlegel, Moritz-Caspar T1 - First and Last Seconds of a Building´s Life - Applied Chemistry in Build Environment T2 - Doktorandentagung der GDCh CY - Berlin, Germany DA - 2012-02-26 PY - 2012 AN - OPUS4-25712 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wolf, S. E. T1 - IFacing the both sides of a coin by merging biological and nonclassical crystallisation models: is a liquid amorphous precursor involved in the formation of the prismatic layer of the Mediterranean Fan Mussel Pinna nobilis? T2 - Faraday Discussion 159, 23 - 25 July 2012 CY - Leeds, England DA - 2012-07-23 PY - 2012 AN - OPUS4-25715 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Akhmetova, Irina T1 - In situ investigation of mechanochemical syntheses of metal phosphonates N2 - We report on the in situ investigation of mechanochemical syntheses of metal phosphonates. The metal phosphonates are formed in milling reactions starting from a metal acetate and a phosphonic acid. The conversions are observed by synchrotron PXRD and Raman spectroscopy to shed light on the reaction mechanisms including possible intermediates. T2 - 8th HZB User Meeting CY - Berlin, Germany DA - 07.12.2016 KW - Mechanochemistry KW - In situ KW - Metal phosphonates KW - XRD KW - Raman spectroscopy PY - 2016 AN - OPUS4-38780 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Fischer, Franziska T1 - In situ investigation of the mechanochemical formation of cocrystals unsing combined PXRD and Raman spectroscopy N2 - We present an in situ investigation of the mechanochemical formation of cocrystals using synchrotron XRD and Raman spectroscopy. This combination allows to study milling processes on the level of the molecular and crystalline structure thus obtaining reliable data for mechanistic studies. Thereby, mechanochemical syntheses can be optimized to isolate new crystal structures. T2 - Joint BER II and BESSY II User Meeting 2016 CY - Berlin, Germany DA - 07.12.2016 KW - Intermediate KW - Mechanochemistry KW - Cocrystal KW - In situ KW - Milling PY - 2016 AN - OPUS4-38722 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rabin, Ira T1 - Chemical composition of the Temple scroll 11Qa T2 - COST D 42 Qumran meeting CY - Jerusalem, Israel DA - 2010-05-25 PY - 2010 AN - OPUS4-23438 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gnutzmann, Tanja T1 - In situ characterization of crystallization processes applying synchrotron XRD and Raman spectroscopy T2 - International School of Crystallography - 44th Course The Power of Powder Diffraction CY - Erice, Italy DA - 2011-06-02 PY - 2011 AN - OPUS4-23976 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schenk, Jonas T1 - Simultaneous Surface Enhanced Raman Scattering and UV/Vis Spectroscopy on Levitated Silver Nanoparticles T2 - ANAKON 2011 CY - Zurich, Switzerland DA - 2011-03-22 PY - 2011 N1 - Geburtsname von Buurman, Merwe: Albrecht, M. - Birth name of Buurman, Merwe: Albrecht, M. AN - OPUS4-23453 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -