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61.
Pietro Lura Frank Winnefeld Stefanie Klemm 《Journal of Thermal Analysis and Calorimetry》2010,101(3):925-932
Isothermal calorimetry and chemical shrinkage measurements are two independent techniques used to study the development of
hydration in cementitious systems. In this study, calorimetry and chemical shrinkage measurements were combined and simultaneously
performed on hydrating cement paste samples. Portland cement pastes with different water to cement ratios and a cement paste
containing calcium sulfoaluminate clinker and anhydrite were studied. The combined calorimetry/chemical shrinkage test showed
good reproducibility and revealed the different hydration behavior of sealed samples and open samples, i.e., samples exposed
to external water during hydration. Large differences between sealed and open samples were observed in a Portland cement paste
with low water to cement ratio and in the calcium sulfoaluminate paste; these effects are attributed to self-desiccation of
the sealed pastes. Once the setup is fully automatized, it is expected that combined calorimetry/chemical shrinkage measurements
can be routinely used for investigating cement hydration. 相似文献
62.
We introduce an approach to enhance the angular tolerance of resonant waveguide gratings by stacking two resonant structures on top of each other. It is shown that reflectivities close to unity can be retrieved over the entire angular spectrum by a double T-shaped grating configuration. Although a combination of silicon as the high-index and diamond as the low-index material is considered, the principles of our new approach can also be used to realize monolithic silicon structures with similar properties. We illustrate that the functionality of the device can be understood by a decomposition into separated elements. Our approach might have compelling applications as new diffractive-reflective optical components with low-coating thermal noise in the field of high-precision metrology. 相似文献
63.
Laminated paperboard is widely used in packaging products. It usually consists of multiple layers bonded to each other by starch or adhesion. The indentation of fold lines (creasing) plays a crucial role during the whole converting process. It is important to control delamination and other damage effects to arrive at commercial cartons with high quality. Thus, the aim of this study is to describe the material behavior of a laminated paperboard during the creasing process. The paperboard was considered as a laminate of three different layers, and each was modeled separately with an anisotropic elastic-plastic material model while a cohesive zone approach described the opening behavior in between. The initial yielding was given by the Hill's 48 yield criterion, while the isotropic strain hardening was described by a power law hardening function. To calibrate the material parameters, a sequence of tensile and compression tests was conducted for each layer in different directions to account for the material's anisotropy. Finally, the creasing process was investigated using a two-dimensional plane strain finite element model. (© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
64.
Dr. Robert J. Wilson Dr. Lies Broeckaert M. Sc. Fabian Spitzer Priv.‐Doz. Dr. Florian Weigend Prof. Dr. Stefanie Dehnen 《Angewandte Chemie (International ed. in English)》2016,55(39):11775-11780
Reaction of the binary Zintl anion (Sn2Sb2)2? with the β‐diketiminato complex [LCu(NCMe)] (L=nacnac=[(N(C6H3iPr2‐2,6)C(Me))2CH]?) in ethylenediamine or DMF affords the ternary cluster dimer {[CuSn5Sb3]2?}2 ( 1 ) as its [K(crypt‐222)]+ salt. The chemical formulation of 1 is supported by energy‐dispersive X‐ray spectroscopy (EDX) and quantum chemical calculations. Each monomeric part of the dimer represents a trimetallic “[CuSn5Sb3]2?” cluster, with an architecture in between a tricapped trigonal prism and a capped square antiprism. As shown by quantum chemical investigations, the presence of Sb atoms and, in particular, of Cu atoms in the cluster skeleton makes the monomeric unit behave like an inhomogeneous superatom, which clearly prefers to dimerize, thereby producing a relatively short, yet virtually non‐bonding Cu???Cu distance. 相似文献
65.
Stefanie K. Nguyen Supaporn Sophonputtanaphoca Eugene Kim Michael H. Penner 《Applied biochemistry and biotechnology》2009,158(2):352-361
A low, but significant, fraction of the carbohydrate portion of herbaceous biomass may be composed of fructose/fructosyl-containing
components (“fructose equivalents”); such carbohydrates include sucrose, fructooligosaccharides, and fructans. Standard methods
used for the quantification of structural-carbohydrate-derived neutral monosaccharide equivalents in biomass are not particularly
well suited for the quantification of fructose equivalents due to the inherent instability of fructose in conditions commonly
used for hemicellulose/cellulose hydrolysis (>80% degradation of fructose standards treated at 4% sulfuric acid, 121°C, 1 h).
Alternative time, temperature, and acid concentration combinations for fructan hydrolysis were considered using model fructans
(inulin, β-2,1, and levan, β-2,6) and a grass seed straw (tall fescue, Festuca arundinacea) as representative feedstocks. The instability of fructose, relative to glucose and xylose, at higher acid/temperature combinations
is demonstrated, all rates of fructose degradation being acid and temperature dependent. Fructans are shown to be completely
hydrolyzed at acid concentrations well below that used for the structural carbohydrates, as low as 0.2%, at 121°C for 1 h.
Lower temperatures are also shown to be effective, with corresponding adjustments in acid concentration and time. Thus, fructans
can be effectively hydrolyzed under conditions where fructose degradation is maintained below 10%. Hydrolysis of the β-2,1
fructans at temperatures ≥50°C, at all conditions consistent with complete hydrolysis, appears to generate difructose dianhydrides.
These same compounds were not detected upon hydrolysis of levan, sucrose, or straw components. It is suggested that fructan
hydrolysis conditions be chosen such that hydrolysis goes to completion; fructose degradation is minimized, and difructose
dianhydride production is accounted for. 相似文献
66.
Organotin–Oxido Cluster‐Based Multiferrocenyl Complexes Obtained by Hydrolysis of Ferrocenyl‐Functionalized Organotin Chlorides
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Zhiliang You Robert Möckel Jakob Bergunde Prof. Dr. Stefanie Dehnen 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(42):13491-13496
Three organotin–oxido clusters were formed by hydrolysis of ferrocenyl‐functionalized organotin chloride precursors in the presence of NaEPh (E=S, Se). [RFcSnCl3?HCl] ( C ; RFc = CMe2CH2C(Me)?N?N?C(Me)Fc) and [SnCl6]2? formed {(RFcSnCl2)3[Sn(OH)6]}[SnCl3] ( 3 a ) and {(RFcSnCl2)3[Sn(OH)6]}[PhSeO3] ( 3 b ), bearing an unprecedented [Sn4O6] unit, in a one‐pot synthesis or stepwise through [(RFcSnCl2)2Se] ( 1 ) plus [(RFcSnCl2)SePh] ( 2 ). A one‐pot reaction starting out from FcSnCl3 gave [(FcSn)9(OH)6O8Cl5] ( 4 ), which represents the largest Fc‐decorated Sn/O cluster reported to date. 相似文献
67.
Jannik Brückmann Dr. Carolin Müller Tamar Maisuradze Dr. Alexander K. Mengele Dr. Djawed Nauroozi Sven Fauth Andreas Gruber Prof. Dr. Stefanie Gräfe Prof. Dr. Kerstin Leopold Dr. Stephan Kupfer Prof. Dr. Benjamin Dietzek-Ivanšić Prof. Dr. Sven Rau 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(51):e202200766
The synthesis and detailed characterization of a new Ru polypyridine complex containing a heteroditopic bridging ligand with previously unexplored metal-metal distances is presented. Due to the twisted geometry of the novel ligand, the resultant division of the ligand in two distinct subunits leads to steady state as well as excited state properties of the corresponding mononuclear Ru(II) polypyridine complex resembling those of prototype [Ru(bpy)3]2+ (bpy=2,2'-bipyridine). The localization of the initially optically excited and the nature of the long-lived excited states on the Ru-facing ligand spheres is evaluated by resonance Raman and fs-TA spectroscopy, respectively, and supported by DFT and TDDFT calculations. Coordination of a second metal (Zn or Rh) to the available bis-pyrimidyl-like coordination sphere strongly influences the frontier orbitals, apparent by, for example, luminescence quenching. Thus, the new bridging ligand motif offers electronic properties, which can be adjusted by the nature of the second metal center. Using the heterodinuclear Ru−Rh complex, visible light-driven reduction of NAD+ to NADH was achieved, highlighting the potential of this system for photocatalytic applications. 相似文献
68.
Very Facile Polarity Umpolung and Noncovalent Functionalization of Inorganic Nanoparticles: A Tool Kit for Supramolecular Materials Chemistry
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Lukas Zeininger Stefanie Petzi Jörg Schönamsgruber Luis Portilla Prof. Dr. Marcus Halik Prof. Dr. Andreas Hirsch 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(40):14030-14035
The facile assembly of shell‐by‐shell (SbS)‐coated nanoparticles [TiO2?PAC16]@shell 1 – 7 (PAC16=hexadecylphosphonic acid), which are soluble in water and can be isolated as stable solids, is reported. In these functional architectures, an umpolung of dispersibility (organic apolar versus water) was accomplished by the noncovalent binding of ligands 1 – 7 to titania nanoparticles [TiO2?PAC16] containing a first covalent coating with PAC16. Ligands 1 – 7 are amphiphilic and form the outer second shell of [TiO2?PAC16]@shell 1 – 7 . The tailor‐designed dendritic building blocks 3 – 5 contain negative and positive charges in the same molecule, and ligands 6 and 7 contain a perylenetetracarboxylic acid dimide (PDI) core ( 6 / 7 ) as a photoactive reporter component. In the redox and photoactive system [TiO2?PAC16]@shell 7 , electronic communication between the inorganic core to the PDI ligands was observed. 相似文献
69.
Kaggwa GB Froebe S Huynh L Ralston J Bremmell K 《Langmuir : the ACS journal of surfaces and colloids》2005,21(10):4695-4704
The adsorption of a polyacrylamide (MW 14600) and two polysaccharides (MW 9260 and 706 x 10(3)) onto model silica surfaces of different hydrophobicities was investigated. In all cases, adsorption adhered to the Freundlich isotherm, reflecting the heterogeneous character of the solid substrates. The latter strongly influenced the character of the adsorbed polymer, with morphologies from chainlike structures to thin films and patches being observed. Surface roughness, polymer type, and molecular weight also play roles in controlling adsorbed polymer morphology. Surface wettability is strongly influenced by the thickness of the adsorbed layer. 相似文献
70.
Lausten R Smirnova O Sussman BJ Gräfe S Mouritzen AS Stolow A 《The Journal of chemical physics》2008,128(24):244310
In general, many different diagrams can contribute to the signal measured in broadband four-wave mixing experiments. Care must therefore be taken when designing an experiment to be sensitive to only the desired diagram by taking advantage of phase matching, pulse timing, sequence, and the wavelengths employed. We use sub-25 fs pulses to create and monitor vibrational wavepackets in gaseous iodine, bromine, and iodine bromide through time- and frequency-resolved femtosecond coherent anti-Stokes Raman scattering (CARS) spectroscopy. We experimentally illustrate this using iodine, where the broad bandwidths of our pulses, and Boltzmann population in the lower three vibrational levels conspire to make a single diagram dominant in one spectral region of the signal spectrum. In another spectral region, however, the signal is the sum of two almost equally contributing diagrams, making it difficult to directly extract information about the molecular dynamics. We derive simple analytical expressions for the time- and frequency-resolved CARS signal to study the interplay of different diagrams. Expressions are given for all five diagrams which can contribute to the CARS signal in our case. 相似文献