Three-dimensional MPFEM modelling on isostatic pressing and solid phase sintering of tungsten powders

2019 ◽  
Vol 354 ◽  
pp. 854-866
Author(s):  
Yi Zou ◽  
Xizhong An ◽  
Qian Jia ◽  
Ruiping Zou ◽  
Aibing Yu
Keyword(s):  
Solid Phase ◽  
Three Dimensional ◽  
Isostatic Pressing ◽  
Tungsten Powders

Characterization of Monoclonal Anti-human Factor VII Antibody (B101/B1) that Recognized Three-dimensional Structures near Arg at Position 79 in the First EGF-like Domain

1998 ◽  
Vol 79 (01) ◽  
pp. 104-109 ◽  
Author(s):  
Osamu Takamiya
Keyword(s):  
Monoclonal Antibodies ◽  
Tissue Factor ◽  
Human Factor ◽  
Solid Phase ◽  
Three Dimensional ◽  
Coagulation Factors ◽  
Factor Vii ◽  
Dimensional Structure ◽  
Epidermal Growth

SummaryMurine monoclonal antibodies (designated hVII-B101/B1, hVIIDC2/D4 and hVII-DC6/3D8) directed against human factor VII (FVII) were prepared and characterized, with more extensive characterization of hVII-B101/B1 that did not bind reduced FVIIa. The immunoglobulin of the three monoclonal antibodies consisted of IgG1. These antibodies did not inhibit procoagulant activities of other vitamin K-dependent coagulation factors except FVII and did not cross-react with proteins in the immunoblotting test. hVII-DC2/D4 recognized the light chain after reduction of FVIIa with 2-mercaptoethanol, and hVIIDC6/3D8 the heavy chain. hVII-B101/B1 bound FVII without Ca2+, and possessed stronger affinity for FVII in the presence of Ca2+. The Kd for hVII-B101/B1 to FVII was 1.75 x 10–10 M in the presence of 5 mM CaCl2. The antibody inhibited the binding of FVII to tissue factor in the presence of Ca2+. hVII-B101/B1 also inhibited the activation of FX by the complex of FVIIa and tissue factor in the presence of Ca2+. Furthermore, immunoblotting revealed that hVII-B101/B1 reacted with non-reduced γ-carboxyglutaminic acid (Gla)-domainless-FVII and/or FVIIa. hVII-B101/B1 showed a similar pattern to that of non-reduced proteolytic fragments of FVII by trypsin with hVII-DC2/D4 on immunoblotting test. hVII-B101/B1 reacted differently with the FVII from the dysfunctional FVII variant, FVII Shinjo, which has a substitution of Gln for Arg at residue 79 in the first epidermal growth factor (1st EGF)-like domain (Takamiya O, et al. Haemosta 25, 89-97,1995) compared with normal FVII, when used as a solid phase-antibody for ELISA by the sandwich method. hVII-B101/B1 did not react with a series of short peptide sequences near position 79 in the first EGF-like domain on the solid-phase support for epitope scanning. These results suggested that the specific epitope of the antibody, hVII-B101/B1, was located in the three-dimensional structure near position 79 in the first EGF-like domain of human FVII.

scholarly journals Prandtl Number in Classical Hard-Sphere and One-Component Plasma Fluids

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 821
Author(s):  
Sergey Khrapak ◽  
Alexey Khrapak
Keyword(s):  
Prandtl Number ◽  
Hard Sphere ◽  
Solid Phase ◽  
Freezing Point ◽  
Three Dimensional ◽  
Order Unity ◽  
Strongly Coupled ◽  
Dielectric Fluids ◽  
Weakly Coupled ◽  
Component Plasma

The Prandtl number is evaluated for the three-dimensional hard-sphere and one-component plasma fluids, from the dilute weakly coupled regime up to a dense strongly coupled regime near the fluid-solid phase transition. In both cases, numerical values of order unity are obtained. The Prandtl number increases on approaching the freezing point, where it reaches a quasi-universal value for simple dielectric fluids of about ≃1.7. Relations to two-dimensional fluids are briefly discussed.

The Construction of New Proteins. II. Design, Synthesis and Conformational Studies of Folding Units with βαβ-Topology

1986 ◽  
Vol 41 (10) ◽  
pp. 1315-1322 ◽  
Author(s):  
Manfred Mutter ◽  
Karl-Heinz Altmann ◽  
Thomas Vorherr
Keyword(s):  
Solid Phase ◽  
Three Dimensional ◽  
Chemical Properties ◽  
Spectroscopic Studies ◽  
General Concept ◽  
Dimensional Structure ◽  
Design Synthesis ◽  
Phase Synthesis ◽  
Conformational Studies ◽  
Conformational Effects

The design, synthesis and preliminary conformational studies of two polypeptides exhibiting βαβ-type folding topologies are presented. In the design of the model peptides the general concept for the construction of new proteins developed in the preceeding paper was applied. According to this strategy, amphiphilic helices and β-sheets are linked together via hydrophilic loops to attain three-dimensional structures of higher order (‘supersecondary structures’). Com­puter-assisted molecular modelling served as a valuable tool for minimizing conformational con­straints within the molecules. The 38-residue peptide MI was synthesized using polyethylene glycol (PEG) as solubilizing polymeric support (‘Liquid-Phase synthesis'). Conformationally in­duced changes in the physico-chemical properties of the growing peptide chain stressed the significance of conformational effects in peptide synthesis reported earlier. Similar observations were made during the solid-phase synthesis of the 35-peptide MII. CD and IR spectroscopic studies revealed a high degree of secondary structure for both folding units. The present data strongly support the adoption of a three-dimensional structure for both models.

3D Numerical Simulation of Polydisperse Pressurized Gas-Solid Fluidized Bed

2011 ◽  
Author(s):  
P. Fede ◽  
O. Simonin ◽  
I. Ghouila
Keyword(s):  
Numerical Simulation ◽  
Fluidized Bed ◽  
Ethylene Polymerization ◽  
Solid Phase ◽  
Three Dimensional ◽  
Gas Velocity ◽  
Particle Segregation ◽  
3D Numerical Simulation ◽  
Model Predictions ◽  
The Mean

Three dimensional unsteady numerical simulations of dense pressurized polydisperse fluidized bed have been carried out. The geometry is a medium-scale industrial pilot for ethylene polymerization. The numerical simulation have been performed with a polydisperse collision model. The consistency of the polydisperse model predictions with the monodisperse ones is shown. The results show that the pressure distribution and the mean vertical gas velocity are not modified by polydispersion of the solid phase. In contrast, the solid particle species are not identically distributed in the fluidized bed indicating the presence of particle segregation.

A novel, convenient, three-dimensional orthogonal strategy for solid-phase synthesis of cyclic peptides

1993 ◽  
Vol 34 (10) ◽  
pp. 1549-1552 ◽  
Author(s):  
Steven A. Kates ◽  
Nuria A. Solé ◽  
Charles R. Johnson ◽  
Derek Hudson ◽  
George Barany ◽  
...  
Keyword(s):  
Cyclic Peptides ◽  
Solid Phase Synthesis ◽  
Solid Phase ◽  
Three Dimensional ◽  
Phase Synthesis

Optimization of Laser Hardening Processes for Industrial Parts With Complex Geometry via Predictive Modeling

2009 ◽  
Author(s):  
Neil S. Bailey ◽  
Yung C. Shin
Keyword(s):  
Phase Transformation ◽  
Thermal Model ◽  
Complex Geometry ◽  
Solid Phase ◽  
Three Dimensional ◽  
Laser Hardening ◽  
Temperature History ◽  
Temperature Phase ◽  
Laser Systems ◽  
History Of

A predictive laser hardening model for industrial parts with complex geometric features has been developed and used for optimization of hardening processes. A transient three-dimensional thermal model is combined with a three-dimensional kinetic model for steel phase transformation and solved in order to predict the temperature history and solid phase history of the workpiece while considering latent heat of phase transformation. Further, back-tempering is also added to the model to determine the phase transformation during multitrack laser hardening. The integrated model is designed to accurately predict temperature, phase distributions and hardness inside complex geometric domains. The laser hardening parameters for two industrial workpieces are optimized for two different industrial laser systems using this model. Experimental results confirm the validity of predicted results.

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