TY - JOUR A1 - Hemmann, Felix A1 - Agirrezabal-Telleria, Iker A1 - Kemnitz, E. A1 - Jäger, Christian T1 - Probing slow chemical exchange of pyridine molecules at acid magnesium hydroxide fluoride surfaces by 15N NMR N2 - 15N NMR of pyridine has been used to study Lewis and Brønsted sites at the acid surface of magnesium hydroxide fluoride at two different pyridine loadings with ratios of excess pyridine compared to pyridine molecules bound to Lewis and Brønsted sites of about 1:1 (highly loaded) and 0.15:1 (low loaded), respectively. The Lewis and Brønsted sites can be distinguished by the 15N chemical shift of pyridine at about –100 ppm (LPy) and –175 ppm (BPy). In both samples a very broad 15N resonance is found around –88 ppm assigned to weakly adsorbed (excess) pyridine molecules via hydrogen bridges (HPy). Additionally, another signal at about –49 ppm is observed in the highly loaded sample only representing physisorbed pyridine (PPy). A slow chemical exchange process of strongly bound LPy and BPy molecules with excess HPy and PPy molecules can be monitored using 15N exchange NMR. It takes place on a time scale of about 50–100 ms at room temperature. All pyridine molecules have the same 15N T1 and its value increases from 800 ms (highly loaded sample) to 5.3 s (low loading) hinting on changed pyridine mobility depending on the loading level. KW - Catalysis KW - Acid surfaces KW - 15N NMR KW - Chemical exchange KW - Pyridine PY - 2014 DO - https://doi.org/10.1021/jp405213x SN - 1932-7447 SN - 1089-5639 VL - 117 IS - 28 SP - 14710 EP - 14716 PB - Soc. CY - Washington, DC AN - OPUS4-30439 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jeromenok, J. A1 - Böhlmann, W. A1 - Jäger, Christian A1 - Weber, J. T1 - Carbon dioxide adsorption in Betulin-based micro- and macroporous polyurethanes N2 - Separation of CO2. Microporous polyurethane networks were prepared based on a renewable resource. Betulin, extracted from birch bark, is used as a structure-directing diol monomer in A3-B2 monomers. The resulting microporous networks show very promising CO2/N2 selectivities. The state of adsorbed CO2 is analyzed by in situ NMR spectroscopy, and pure physisorption is proven. The preparation of monolithic materials is demonstrated as well. KW - Carbon dioxide KW - Gas adsorption KW - Microporous polymers KW - Renewable resources KW - Solid state NMR spectroscopy PY - 2013 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-304431 DO - https://doi.org/10.1002/open.201200045 SN - 2191-1363 VL - 2 IS - 1 SP - 17 EP - 20 PB - Wiley-VCH-Verl. CY - Weinheim AN - OPUS4-30443 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Agirrezabal-Telleria, Iker A1 - Hemmann, Felix A1 - Jäger, Christian A1 - Arias, P. L. A1 - Kemnitz, E. T1 - Functionalized partially hydroxylated MgF2 as catalysts for the dehydration of d-xylose to furfural N2 - Among the furan-based compounds, furfural (FUR) shows interesting properties as building-block or industrial solvent. It is produced from pentosan-rich biomass via xylose cyclodehydration. The current FUR production uses homogeneous catalysts and steam. According to recent studies, the reaction mechanism is different in the presence of Lewis (L) or Brønsted (B) sites. In this work, partially hydroxylated MgF2 catalysts, containing bifunctional Lewis and Brønsted properties, were further functionalized using different fluorosulfonic precursors. Its main objective was to test these solids as catalysts for xylose conversion to furfural. Extensive characterization techniques using TG–MS, 19F-MAS-NMR, or pyridine adsorption confirmed the substitution of surface OH groups by stronger Brønsted sites. The activity data showed a considerable change of the reaction kinetics and a final furfural selectivity of 90% at 160 °C in water/toluene for optimized L/B ratios by the one-step grafting technique. Moreover, the reaction analyses and the change of conversion pathways were studied. KW - Hydroxylated MgF2 KW - Functionalization KW - Fluorosulfonic acid KW - Lewis KW - Brønsted KW - Xylose KW - Furfural PY - 2013 DO - https://doi.org/10.1016/j.jcat.2013.05.005 VL - 305 SP - 81 EP - 91 AN - OPUS4-30444 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hieu, D.T. A1 - Kosslick, H. A1 - Riaz, M. A1 - Schulz, A. A1 - Springer, A. A1 - Frank, M. A1 - Jäger, Christian A1 - Minh Thu, N.T. A1 - Son, L.T. T1 - Acidity and Stability of Bronsted Acid Sites in Green Clinoptilolite Catalysts and Catalytic Performance in the Etherification of Glycerol N2 - Natural zeolite clinoptilolite CLIN with a framework ratio of Si/Al ≥ 4 containing mainly potassium and calcium ions in its internal channel system was used as a starting material. The acidic HCLIN catalysts were prepared under soft conditions avoiding the use of environmental less benign mineral acids. The starting material was ion exchanged using a 0.2 M aqueous ammonium nitrate solution at a temperature 80 ◦C for 2 h. The obtained NH4CLIN was converted into the acid HCLIN catalyst by calcination at 300–600 ◦C. The obtained samples were characterized by XRD, FTIR, SEM/TEM, AAS, and EDX element mapping. The state of aluminium and silicon was studied by 27Al- and 29SiMAS NMR spectroscopy. The textural properties of the catalysts were investigated by nitrogen adsorption and desorption measurements. The Brønsted acidity of the HCLIN catalysts was studied by temperature-programmed decomposition of the exchanged ammonium ions releasing ammonia as well as 1H MAS NMR, {1H–27Al} Trapdor, and {1H–27Al} Redor experiments. The strongly agglomerated samples were crystalline and thermally stable up to >500 ◦C. Although a part of the clinoptilolite framework is maintained up to 600 ◦C, a loss of crystallinity is already observed starting from 450 ◦C. The specific surface areas of the starting CLIN and ammonium exchanged NH4CLIN are low with ca. 26 m2/g. The pores are nearly blocked by the exchangeable cations located in the zeolite pores. The thermal decomposition of the ammonium ions by calcination at 400 ◦C causes an opening of the pore entrances and a markable increase in the specific micropore area and micropore volume to ca. 163 m2/g and 0.07 cm3/g, respectively. It decreases with further rising calcination temperature indicating some structural loss. The catalysts show a broad distribution of Brønsted acid sites (BS) ranging from weak to strong sites as indicated the thermal decomposition of exchanged ammonium ions (TPDA). The ammonium ion decomposition leaving BS, i.e., H+ located at Al–O–Si framework bridges, starts at ≥250 ◦C. A part of the Brønsted sites is lost after calcination specifically at 500 ◦C. It is related to the formation of penta-coordinated aluminium at the expense of tetrahedral framework aluminium. The Brønsted sites are partially recreated after repeated ammonium ion exchange. The catalytic performance of the acidic HCLIN catalysts was tested in the etherification of glycerol as a green renewable resource with different C1 -C4 alcohols. The catalysts are highly active in the etherification of glycerol, especially with alcohols containing the branched, tertiary alkyl groups. Highest activity is observed with the soft activated catalyst HCLIN300 (300 ◦C, temperature holding time: 1 min). A total of 78% conversion of glycerol to mono and di ether were achieved with tert-butanol at 140 ◦C after 4 h of reaction. The mono- and di-ether selectivity were 75% and 25%, respectively. The catalyst can be reused. KW - Etherification KW - Glycerol KW - Zeolite KW - Clinoptilolite KW - Bronsted acidity KW - Dehydroxylation PY - 2022 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-546982 DO - https://doi.org/10.3390/catal12030253 VL - 12 IS - 3 SP - 1 EP - 24 PB - MDPI AN - OPUS4-54698 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Wanner, C. A1 - Poethig, R. A1 - Carrero, S. A1 - Fernandez-Martinez, A. A1 - Jäger, Christian A1 - Furrer, G. T1 - Natural occurrence of nanocrystalline Al-hydroxysulfates: Insights on formation, Al solubility control and As retention N2 - Nanocrystalline basaluminite [Al4OH10(SO4)(H2O)3–5] and Aggregation of the e-Keggin polyoxocation [Al12(AlO4)(OH)24(H2O)12]7+, referred to as Al13, have both been described to form in acid mine Drainage environments. Although the chemical composition is quite similar, their crystalline varieties significantly differ, demonstrating that various types of Al-hydroxysulfates can form under similar conditions and that their respective formation is not fully understood yet. Here, we report the occurrence of nanocrystalline precipitates that form naturally in a small alpine catchment in Switzerland where an acidic mountainous stream (pH 4) is neutralized successively after mixing with several neutral tributaries. The stepwise neutralization in conjunction with the large amount of precipitates provide an ideal setting for obtaining new insights into (i) the structure of naturally forming Al-hydroxysulfates, (ii) their formation mechanism, (iii) their role in controlling the solubility of Al, and (iv) their ability to lower the mobility of As. Synchrotron-based high-energy X-ray diffraction and subsequent pair distribution function analyses demonstrate that these precipitates are structurally identical to basaluminite samples obtained from acid mine drainage sites. In contrast, only minor amounts of tetrahedrally coordinated Al, as present in Al13, were identified by nuclear magnetic resonance spectroscopy. The precipitates are further characterized by elevated As concentrations up to 600 lg/g, whereas other heavy metals are at background concentrations only. Given the low As concentrations in the stream from which precipitation occurs (<0.03 mg/L), high As concentrations confirm that basaluminite serves as a highly efficient As sink, which is attributed to its high anion-exchange capacity. Chemical analysis of streamwater samples in combination with geochemical modeling show that precipitation occurs instantaneously upon mixing with neutral streams. Moreover, our data reveal that the precipitation of basaluminite exerts a strong solubility control on dissolved Al concentrations as manifested by the quasi-constant basaluminite ion activity product observed during neutralization from pH 5 to pH 5.9. We hypothesize that in our field system, high fluoride and sulfate concentrations on the order of 100 and 1–2 mg/L, KW - Basaluminite KW - Al13 KW - Acid rock drainage KW - Arsenic retention KW - Aluminum KW - Anion exchange PY - 2018 DO - https://doi.org/10.1016/j.gca.2018.06.031 SN - 0016-7037 SN - 1872-9533 VL - 238 SP - 252 EP - 269 PB - Elsevier Ltd. AN - OPUS4-46164 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jäger, Christian A1 - Hemmann, Felix T1 - EASY: A simple tool for simultaneously removing background, deadtime and acoustic ringing in quantitative NMR spectroscopy. Part II: Improved ringing suppression, application to quadrupolar nuclei, cross polarisation and 2D NMR N2 - A simple experiment for Elimination of Artifacts in NMR SpectroscopY (EASY) was introduced in Part I, and it was shown that NMR probe background signals, spectral distortions due to deadtime effects, and acoustic ringing can be eliminated simultaneously from solid-state NMR spectra. In this Part II, it is shown that acoustic ringing suppression can be improved up to one order of magnitude compared to the original EASY pulse sequence by inserting a delay τ between the two data acquisition scans of the EASY pulse sequence. The achievable ringing suppression depends on the length of this delay and is limited by the spin-lattice relaxation time T1. Furthermore, EASY is considered in conjunction with NMR of quadrupolar nuclei. For strong second-order broadening, EASY can be used to acquire either pure central transition MAS patterns or pure satellite transition NMR spectra. Two further modifications to EASY are introduced. One concerns improved ringing artifact suppression in experiments in which the central transition NMR signal is amplified by Rotor Assisted Population Transfer (RAPT). The second EASY modification enables the acquisition of quantitative NMR spectra if signals with different quadrupole coupling constants are present. In addition, acoustic ringing and 11B stator signals are removed. Finally, it is demonstrated that the basic idea of EASY for removing ringing artifacts can be realized for heteronuclear one-dimensional and hetero- and homo-nuclear multi-dimensional NMR experiments using extended phase cycling. 15N{1H} CPMAS and 15N 2D Exchange NMR spectroscopy are considered as examples. KW - Solid State NMR KW - Probe background suppression KW - Ringing suppression KW - Deadtime KW - qNMR of quadrupolar nuclei KW - CPMAS NMR KW - 2D NMR KW - 11B KW - 23Na KW - 25Mg PY - 2014 DO - https://doi.org/10.1016/j.ssnmr.2014.08.001 SN - 0926-2040 SN - 1527-3326 VL - 63-64 SP - 13 EP - 19 PB - Academ. Press CY - Orlando, Fla. AN - OPUS4-32329 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jäger, Christian A1 - Hemmann, Felix T1 - EASY: A simple tool for simultaneously removing background, deadtime and acoustic ringing in quantitative NMR spectroscopy-Part I: Basic principle and applications N2 - Elimination of Artifacts in NMR SpectroscopY (EASY) is a simple but very effective tool to remove simultaneously any real NMR probe background signal, any spectral distortions due to deadtime ringdown effects and -specifically- severe acoustic ringing artifacts in NMR spectra of low-gamma nuclei. EASY enables and maintains quantitative NMR (qNMR) as only a single pulse (preferably 90°) is used for data acquisition. After the acquisition of the first scan (it contains the wanted NMR signal and the background/deadtime/ringing artifacts) the same experiment is repeated immediately afterwards before the T1 waiting delay. This second scan contains only the background/deadtime/ringing parts. Hence, the simple difference of both yields clean NMR line shapes free of artefacts. In this Part I various examples for complete 1H, 11B, 13C, 19F probe background removal due to construction parts of the NMR probes are presented. Furthermore, 25Mg EASY of Mg(OH)2 is presented and this example shows how extremely strong acoustic ringing can be suppressed (more than a factor of 200) such that phase and baseline correction for spectra acquired with a single pulse is no longer a problem. EASY is also a step towards deadtime-free data acquisition as these effects are also canceled completely. EASY can be combined with any other NMR experiment, including 2D NMR, if baseline distortions are a big problem. KW - Solid state NMR KW - MAS KW - Probe background suppression KW - Ringing suppression KW - Deadtime KW - 1H KW - 19F KW - 11B KW - 13C KW - 25Mg PY - 2014 DO - https://doi.org/10.1016/j.ssnmr.2013.11.002 SN - 0926-2040 SN - 1527-3326 VL - 57-58 SP - 22 EP - 28 PB - Academ. Press CY - Orlando, Fla. AN - OPUS4-29839 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bücker, Michael A1 - Jäger, Christian A1 - Pfeifer, Dietmar A1 - Unger, Brita T1 - Evidence of Si-O-C bonds in cellulosic materials modified by sol-gel-derived silica N2 - The present study contributes to the controversial discussion in the literature whether Si–O–C bonds in wood–silica–gel composites exist. 13C NMR is a suitable method to proof such bonds. Because of the low concentration of 13C isotopes in natural wood, 13C cellulose was used as 13C-enriched substitute. A tailored sol for the impregnation of that cellulose was chosen by liquid 29Si NMR pre-investigations of various sols whose reactivity and stability were time-dependently analysed. It is based on a sub-stoichiometric hydrolysis of tetraethoxysilane (TEOS) with 1 mol water per mol TEOS. Thermal analyses were performed to show a comparability of the thermal behaviour of wood–silica–gel and cellulose–silica–gel composites. There are two strong hints of the existence of stable Si–O–C bonds: (1) by thermal analysis, a shift in the fire behaviour of 100 K can be observed with a change in pyrolysis behaviour of the composite and (2) the proof by REDOR NMR that a dipolar coupling between 1329Si and 13C nuclei exists. KW - Silica-cellulosic composites KW - Sol-gel derived silica KW - Si-O-C bonds KW - 13C NMR KW - 29Si NMR PY - 2014 UR - http://link.springer.com/article/10.1007/s00226-014-0657-9/fulltext.html DO - https://doi.org/10.1007/s00226-014-0657-9 SN - 0043-7719 SN - 1432-5225 VL - 48 IS - 5 SP - 1033 EP - 1047 PB - Springer CY - Berlin AN - OPUS4-31223 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Müller, Patrick A1 - Morys, Michael A1 - Sut, Aleksandra A1 - Jäger, Christian A1 - Illerhaus, Bernhard A1 - Schartel, Bernhard T1 - Melamine poly(zinc phosphate) as flame retardant in epoxy resin: Decomposition pathways, molecular mechanisms and morphology of fire residues N2 - Synergistic multicomponent systems containing melamine poly(metal phosphate)s have been recently proposed as flame retardants. This work focuses on the decomposition pathways, molecular mechanisms and morphology of the fire residues of epoxy resin (EP) flame retarded with melamine poly(zinc phosphate) (MPZnP) to explain the modes of action and synergistic effects with selected synergists (melamine polyphosphate (MPP) and AlO(OH), respectively). The total load of flame retardants was always 20 wt.%. The decomposition pathways were investigated in detail via thermogravimetric Analysis coupled with Fourier transform infrared spectroscopy. The fire residues were investigated via elemental analysis und solid-state nuclear magnetic resonance spectroscopy. The morphology of intumescent fire residues was investigated via micro-computed tomography and scanning electron microscopy. EP + (MPZnP + MPP) formed a highly voluminous residue that showed structural features of both EP + MPZnP and EP + MPP, resulting in a highly effective protection layer. EP + (MPZnP + AlO(OH)) preserved the entire quantity of phosphorus content during combustion due to the Formation of Zn₂P₂O₇ and AlPO₄. KW - Melamine poly(metal phosphate) KW - Flame retardancy KW - Epoxy resin KW - Solid-state NMR KW - Micro-computed tomography KW - Fire residue PY - 2016 DO - https://doi.org/10.1016/j.polymdegradstab.2016.06.023 SN - 0141-3910 VL - 130 SP - 307 EP - 319 PB - Elsevier AN - OPUS4-36863 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Meißner, G. A1 - Dirican, D. A1 - Jäger, Christian A1 - Braun, T. A1 - Kemnitz, E. T1 - Et3GeH versus Et3SiH: controlling reaction pathways in catalytic C–F bond activations at a nanoscopic aluminum chlorofluoride† N2 - Catalytic C–F bond activation reactions of mono- and polyfluoroalkanes at Lewis acidic amorphous aluminum chlorofluoride (ACF) are presented. The hydrogen sources Et3GeH or Et3SiH control the selectivity of the conversions. The immobilization of Et3GeH at ACF resulted in catalytic dehydrohalogenation reactions to yield olefins under very mild conditions. In contrast, if Et3SiH is immobilized at ACF, C–C coupling occured and the formation of Friedel–Crafts products was observed. MAS NMR spectroscopic studies revealed information about the surface binding of the substrates. KW - Vapor-phase hydrofluorination KW - Carbon-fluorine bonds KW - Vinyl fluoride KW - Phosphine-ligands KW - Room-temperature KW - Building-blocks KW - Etal-complexes KW - Germylium ions KW - Lewis-acids KW - Hydrodefluorination PY - 2017 DO - https://doi.org/10.1039/c7cy00845g SN - 2044-4753 SN - 2044-4761 VL - 7 IS - 15 SP - 3348 EP - 3354 PB - The Royal Society of Chemistry AN - OPUS4-41836 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -