scholarly journals Stoichiometry and Kinetics of Sequential Dimethacrylate Enzymolysis

2019 ◽  
Vol 98 (9) ◽  
pp. 1037-1044
Author(s):  
S. Frukhtbeyn ◽  
K. Van Dongen ◽  
J. Sun
Keyword(s):  
Quantum Coherence ◽  
High Performance ◽  
Kinetic Studies ◽  
Cholesterol Esterase ◽  
Resonance Spectroscopy ◽  
Stoichiometric Analysis ◽  
Dental Restorations ◽  
Alternative Approaches ◽  
Kinetics Of ◽  
Berkeley Madonna

The increasing use of methacrylate-based materials in tissue engineering and dental restorations demands detailed evaluation of enzymolysis of these materials due to toxicity, durability, and biocompatibility concerns. The objective of this study is to develop tools for assessing and ranking the enzymolysis kinetics of dimethacrylate (DMA) compounds. Triethyleneglycol DMA and diurethane DMA are employed as model DMAs for kinetic studies of 2-step enzymolysis by 2 esterases, pseudocholine esterase and cholesterol esterase. In addition, the intermediate hydrolysis products, mono-methacrylates (mono-MAs), are prepared via esterases. The kinetics of DMA enzymolysis are evaluated per the concentrations of DMA. The enzymolysis products are quantified by high-performance liquid chromatography. Additionally, stoichiometric analysis and a Berkeley Madonna model are employed to compare the efficacy of esterases in DMA enzymolysis. The chemical structure of mono-MAs is verified by proton and heteronuclear single quantum coherence (2D 1H-13C) nuclear magnetic resonance spectroscopy and mass spectrometry. In evaluating the ratio of sequential and simultaneous degradations of DMA and mono-MA, the stoichiometric analysis draws the same conclusions without using [mono-MA] as the experimental observation using [mono-MA]. The majority of the 4 esterase-DMA combinations undergo the sequential enzyme-catalyzed hydrolysis, from DMA to mono-MA to diol. However, cholesterol esterase is more effective than pseudocholine esterase in maintaining sequential degradation until >90% of DMA is decomposed. Both enzymolysis steps are first-order reactions. The mono-MAs are more hydrolysis resistant than DMAs. Moreover, esterase efficacy and selectivity on DMA enzymolysis are presented. The stoichiometric analysis provides valuable tools in assessing DMA enzymolysis when mono-MA is difficult to be obtained. The resistance of mono-MAs to enzymolysis suggests a need for thorough toxicity evaluations of these intermediate compounds. It also advocates the alternative approaches in designing and developing durable and biocompatible materials.

Superionic Lithium Intercalation through 2 nm x 2 nm Columns in the Crystallographic Shear Phase Nb18W8O69

2019 ◽  
Author(s):  
Kent Griffith ◽  
Clare Grey
Keyword(s):  
High Performance ◽  
Rate Capability ◽  
Block Size ◽  
Lithium Intercalation ◽  
Resonance Spectroscopy ◽  
Complex Metal Oxides ◽  
Battery Electrode ◽  
Crystallographic Shear ◽  
Battery Material ◽  
First Time

Nb18W8O69 (9Nb2O5×8WO3) is the tungsten-rich end-member of the Wadsley–Roth crystallographic shear (cs) structures within the Nb2O5–WO3 series. It has the largest block size of any known, stable Wadsley–Roth phase, comprising 5 ´ 5 units of corner-shared MO6 octahedra between the shear planes, giving rise to 2 nm ´ 2 nm blocks. Rapid lithium intercalation is observed in this new candidate battery material and 7Li pulsed field gradient nuclear magnetic resonance spectroscopy – measured in a battery electrode for the first time at room temperature – reveals superionic lithium conductivity. In addition to its promising rate capability, Nb18W8O69 adds a piece to the larger picture of our understanding of high-performance Wadsley–Roth complex metal oxides.

scholarly journals Hydrothermal Ageing and Its Effect on Fracture Load of Zirconia Dental Implants

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 3103
Author(s):  
Laurent Gremillard ◽  
Agnès Mattlet ◽  
Alexandre Mathevon ◽  
Damien Fabrègue ◽  
Bruno Zberg ◽  
...  
Keyword(s):  
Dental Implants ◽  
Fracture Load ◽  
Accelerated Ageing ◽  
Dental Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dental Restorations ◽  
Different Temperatures ◽  
Mechanical Performances ◽  
Kinetics Of

Due to growing demand for metal-free dental restorations, dental ceramics, especially dental zirconia, represent an increasing share of the dental implants market. They may offer mechanical performances of the same range as titanium ones. However, their use is still restricted by a lack of confidence in their durability and, in particular, in their ability to resist hydrothermal ageing. In the present study, the ageing kinetics of commercial zirconia dental implants are characterized by X-ray diffraction after accelerated ageing in an autoclave at different temperatures, enabling their extrapolation to body temperature. Measurements of the fracture loads show no effect of hydrothermal ageing even after ageing treatments simulated a 90-year implantation.

scholarly journals Kinetic Studies of Cs+ and Sr2+ Ion Exchange Using Clinoptilolite in Static Columns and an Agitated Tubular Reactor (ATR)

2021 ◽  
Vol 5 (1) ◽  
pp. 9
Author(s):  
Muhammad Yusuf Prajitno ◽  
Mohamad Taufiqurrakhman ◽  
David Harbottle ◽  
Timothy N. Hunter
Keyword(s):  
Adsorption Capacity ◽  
Tubular Reactor ◽  
Process Intensification ◽  
Kinetic Studies ◽  
Breakthrough Curves ◽  
Maximum Adsorption Capacity ◽  
Batch Studies ◽  
Shear Mixing ◽  
Natural Clinoptilolite ◽  
Kinetics Of

Natural clinoptilolite was studied to assess its performance in removing caesium and strontium ions, using both static columns and an agitated tube reactor (ATR) for process intensification. Kinetic breakthrough curves were fitted using the Thomas and Modified Dose Response (MDR) models. In the static columns, the clinoptilolite adsorption capacity (qe) for 200 ppm ion concentrations was found to be ~171 and 16 mg/g for caesium and strontium, respectively, highlighting the poor material ability to exchange strontium. Reducing the concentration of strontium to 100 ppm, however, led to a higher strontium qe of ~48 mg/g (close to the maximum adsorption capacity). Conversely, halving the column residence time to 15 min decreased the qe for 100 ppm strontium solutions to 13–14 mg/g. All the kinetic breakthrough data correlated well with the maximum adsorption capacities found in previous batch studies, where, in particular, the influence of concentration on the slow uptake kinetics of strontium was evidenced. For the ATR studies, two column lengths were investigated (of 25 and 34 cm) with the clinoptilolite embedded directly into the agitator bar. The 34 cm-length system significantly outperformed the static vertical columns, where the adsorption capacity and breakthrough time were enhanced by ~30%, which was assumed to be due to the heightened kinetics from shear mixing. Critically, the increase in performance was achieved with a relative process flow rate over twice that of the static columns.

scholarly journals Biochar Chemistry in a Weathered Tropical Soil: Kinetics of Phosphorus Sorption

Agriculture ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 295
Author(s):  
Marina Moura Morales ◽  
Nicholas Brian Comerford ◽  
Maurel Behling ◽  
Daniel Carneiro de Abreu ◽  
Iraê Amaral Guerrini
Keyword(s):  
Mineral Soil ◽  
Soil Surface ◽  
Kinetic Studies ◽  
Inorganic Phosphorus ◽  
Initial Reaction ◽  
Phosphorus Sorption ◽  
P Sorption ◽  
Published Research ◽  
Kinetics Of

The phosphorus (P) chemistry of biochar (BC)-amended soils is poorly understood. This statement is based on the lack of published research attempting a comprehensive characterization of biochar’s influence on P sorption. Therefore, this study addressed the kinetic limitations of these processes. This was accomplished using a fast pyrolysis biochar made from a mix of waste materials applied to a highly weathered Latossolo Vermelho distrofico (Oxisol) from São Paulo, Brazil. Standard method (batch method) was used. The sorption kinetic studies indicated that P sorption in both cases, soil (S) and soil-biochar (SBC), had a relatively fast initial reaction between 0 to 5 min. This may have happened because adding biochar to the soil decreased P sorption capacity compared to the mineral soil alone. Presumably, this is a result of: (i) Inorganic phosphorus desorbed from biochar was resorbed onto the mineral soil; (ii) charcoal particles physically covered P sorption locations on soil; or (iii) the pH increased when BC was added SBC and the soil surface became more negatively charged, thus increasing anion repulsion and decreasing P sorption.

scholarly journals Porous Carbon Architecture Assembled by Cross-Linked Carbon Leaves with Implanted Atomic Cobalt for High-Performance Li–S Batteries

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Ruirui Wang ◽  
Renbing Wu ◽  
Chaofan Ding ◽  
Ziliang Chen ◽  
Hongbin Xu ◽  
...  
Keyword(s):  
Active Sites ◽  
High Performance ◽  
Specific Capacity ◽  
Three Dimension ◽  
Zeolitic Imidazolate Framework ◽  
Shuttle Effect ◽  
Promising Solution ◽  
Fading Rate ◽  
Kinetics Of ◽  
Sulfur Cathodes

AbstractThe practical application of lithium–sulfur batteries is severely hampered by the poor conductivity, polysulfide shuttle effect and sluggish reaction kinetics of sulfur cathodes. Herein, a hierarchically porous three-dimension (3D) carbon architecture assembled by cross-linked carbon leaves with implanted atomic Co–N4 has been delicately developed as an advanced sulfur host through a SiO2-mediated zeolitic imidazolate framework-L (ZIF-L) strategy. The unique 3D architectures not only provide a highly conductive network for fast electron transfer and buffer the volume change upon lithiation–delithiation process but also endow rich interface with full exposure of Co–N4 active sites to boost the lithium polysulfides adsorption and conversion. Owing to the accelerated kinetics and suppressed shuttle effect, the as-prepared sulfur cathode exhibits a superior electrochemical performance with a high reversible specific capacity of 695 mAh g−1 at 5 C and a low capacity fading rate of 0.053% per cycle over 500 cycles at 1 C. This work may provide a promising solution for the design of an advanced sulfur-based cathode toward high-performance Li–S batteries.

Hollow structure engineering of FeCo alloy nanoparticles electrospun in nitrogen-doped carbon enables high performance flexible all-solid-state zinc–air batteries

2020 ◽  
Vol 4 (4) ◽  
pp. 1747-1753 ◽  
Author(s):  
Yuanyuan Ma ◽  
Wenjie Zang ◽  
Afriyanti Sumboja ◽  
Lu Mao ◽  
Ximeng Liu ◽  
...  
Keyword(s):  
Active Sites ◽  
High Performance ◽  
Hollow Structure ◽  
Active Surface ◽  
Oxygen Electrode ◽  
Active Surface Area ◽  
Active Components ◽  
Nitrogen Doped Carbon ◽  
Structure Engineering ◽  
Kinetics Of

Hollow structuring of active components is an effective strategy to improve the kinetics of oxygen electrode catalysts, arising from the increased the active surface area, the defects on the exposed surface, and the accessible active sites.

INHOMOGENEOUS LARGE DEFORMATION KINETICS OF POLYMERIC GELS

2013 ◽  
Vol 05 (01) ◽  
pp. 1350001 ◽  
Author(s):  
WILLIAM TOH ◽  
ZISHUN LIU ◽  
TENG YONG NG ◽  
WEI HONG
Keyword(s):  
Large Deformation ◽  
Soft Matter ◽  
Inner Core ◽  
Kinetic Studies ◽  
Fe Model ◽  
One Dimensional ◽  
Simplified Approach ◽  
Deformation Kinetics ◽  
Polymeric Gels ◽  
Kinetics Of

This work examines the dynamics of nonlinear large deformation of polymeric gels, and the kinetics of gel deformation is carried out through the coupling of existing hyperelastic theory for gels with kinetic laws for diffusion of small molecules. As finite element (FE) models for the transient swelling process is not available in commercial FE software, we develop a customized FE model/methodology which can be used to simulate the transient swelling process of hydrogels. The method is based on the similarity between diffusion and heat transfer laws by determining the equivalent thermal properties for gel kinetics. Several numerical examples are investigated to explore the capabilities of the present FE model, namely: a cube to study free swelling; one-dimensional constrained swelling; a rectangular block fixed to a rigid substrate to study swelling under external constraints; and a thin annulus fixed at the inner core to study buckling phenomena. The simulation results for the constrained block and one-dimensional constrained swelling are compared with available experimental data, and these comparisons show a good degree of similarity. In addition to this work providing a valuable tool to researchers for the study of gel kinetic deformation in the various applications of soft matter, we also hope to inspire works to adopt this simplified approach, in particular to kinetic studies of diffusion-driven mechanisms.

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