scholarly journals Crystallization kinetics of amorphous calcium carbonate in confinement

2019 ◽  
Vol 10 (19) ◽  
pp. 5039-5043 ◽  
Author(s):  
Jack Cavanaugh ◽  
Michael L. Whittaker ◽  
Derk Joester
Keyword(s):  
Steady State ◽  
Calcium Carbonate ◽  
Crystal Nucleation ◽  
Amorphous Calcium Carbonate ◽  
Emulsion Droplets ◽  
Individual Crystal ◽  
Upper Limit ◽  
Kinetics Of

In situ observation of amorphous calcium carbonate (ACC) confined in ∼500 pL emulsion droplets allows determination of the timing of individual crystal nucleation events. Statistical analysis of events in hundreds of droplets establishes an upper limit for the steady-state nucleation rate of 1.2 cm−3 s−1 for the crystallization from ACC.

scholarly journals Determination of the steady-state turnover rates of the metabolically active pools of phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate in human erythrocytes

1989 ◽  
Vol 259 (3) ◽  
pp. 893-896 ◽  
Author(s):  
C E King ◽  
P T Hawkins ◽  
L R Stephens ◽  
R H Michell
Keyword(s):  
Steady State ◽  
Rate Constants ◽  
Human Erythrocytes ◽  
Turnover Rates ◽  
Metabolic Fluxes ◽  
Metabolic Pool ◽  
Phosphatidylinositol 4 ◽  
Kinetics Of ◽  
Phosphate Groups

When intact human erythrocytes are incubated at metabolic steady state in a chloride-free medium containing [32P]Pi, there is rapid labelling of the gamma-phosphate of ATP, followed by a slower labelling of the monoester phosphate groups of phosphatidylinositol 4-phosphate (PtdIns4P) and phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] [King, Stephens, Hawkins, Guy & Michell (1987) Biochem. J. 244, 209-217]. We have analysed the early kinetics of the labelling of these phosphate groups, in order to determine: (a) the steady-state rates of the interconversions of phosphatidylinositol, PtdIns4P and PtdIns(4,5)P2; and (b) the fractions of the total cellular complement of PtdIns4P and PtdIns(4,5)P2 that participate in this steady-state turnover. The experimental data most closely fit a pattern of PtdIns4P and PtdIns(4,5)P2 turnover in which one-quarter of the total cellular complement of each lipid is in the metabolic pool that participates in rapid metabolic turnover, with rate constants of 0.028 min-1 for the interconversion of PtdIns and PtdIns4P, and of 0.010 min-1 for the PtdIns4P/PtdIns(4,5)P2 cycle. These rate constants represent metabolic fluxes of approx. 2.1 nmol of lipid/h per ml of packed erythrocytes between PtdIns and PtdIns4P and of approx. 5.7 nmol/h per ml of cells between PtdIns4P and PtdIns(4,5)P2.

Measurement of leucine metabolism in man from a primed, continuous infusion of L-[1-3C]leucine

1980 ◽  
Vol 238 (5) ◽  
pp. E473-E479 ◽  
Author(s):  
D. E. Matthews ◽  
K. J. Motil ◽  
D. K. Rohrbaugh ◽  
J. F. Burke ◽  
V. R. Young ◽  
...  
Keyword(s):  
Steady State ◽  
Continuous Infusion ◽  
Co2 Production ◽  
Human Beings ◽  
Priming Dose ◽  
Leucine Metabolism ◽  
Kinetics Of ◽  
13Co2 Enrichment

Leucine metabolism in vivo can be determined from a primed, continuous infusion of L-[1-13C]leucine by measuring, at isotopic steady state, plasm [-13C]leucine enrichment, expired 13CO2 enrichment, and CO2 production rate. With an appropriate priming dose of L-[1-13C]leucine and NaH13CO3, isotopic steady state is reached in less than 2 h, and the infusion is completed in 4 h. The method can determine rates of leucine turnover, oxidation, and incorporation into protein with typical relative uncertainties of 2, 10, and 4%, respectively. The method requires no more than 1 ml of blood and uses stable isotope rather than radioisotope techniques. Thus, the method is applicable to studies of human beings of all ages. L-[1-13C]leucine may be infused with a second amino acid labeled with 15N for simultaneous determination of the kinetics of two amino acids.

Measurements of adsorption for membranes in situ with the use of time-lags and steady state flows

1979 ◽  
Vol 365 (1722) ◽  
pp. 267-281 ◽  
Keyword(s):  
Steady State ◽  
Standard Procedure ◽  
Time Lag ◽  
Sorption Isotherms ◽  
Time Lags ◽  
Carbon Membrane ◽  
Differential Diffusion ◽  
Use Of Time ◽  
Kinetics Of

Isotherms, steady state flows, the four time-lags, the kinetics of sorption and of the approach to the steady state of flow have been measured and analysed to investigate the properties of a graphitized carbon membrane. Sorption isotherms determined on the membrane in situ by a kinetic pro­cedure involving the time-lags and steady state flows were in agreement with isotherms determined by a standard procedure. Analysis of the time-lag and other results left the possibility of a small dependence of the diffusion coefficient, D , upon positional coordinate or upon time, but the dominant influence upon D was its dependence upon concentration, C . Differential diffusion coefficients increased very rapidly with C outside the range of the Henry law. Uptakes of diffusant in the steady state of flow, measured directly, through time-lag measurements and from steady state concentration contours across the membrane were in good agreement.

scholarly journals Analysis of Nucleation and Glass Formation by Chip Calorimetry

2021 ◽  
Vol 11 (16) ◽  
pp. 7652
Author(s):  
Meng Gao ◽  
Chengrong Cao ◽  
John H. Perepezko
Keyword(s):  
Differential Scanning Calorimetry ◽  
Crystal Nucleation ◽  
Transformation Behavior ◽  
Scanning Calorimetry ◽  
Heating And Cooling ◽  
Chip Calorimetry ◽  
In Situ Formation ◽  
Materials Behavior

The advent of chip calorimetry has enabled an unprecedented extension of the capability of differential scanning calorimetry to explore new domains of materials behavior. In this paper, we highlight some of our recent work: the application of heating and cooling rates above 104 K/s allows for the clear determination of the glass transition temperature, Tg, in systems where Tg and the onset temperature for crystallization, Tx, overlap; the evaluation of the delay time for crystal nucleation; the discovery of new polyamorphous materials; and the in-situ formation of glass in liquid crystals. From these application examples, it is evident that chip calorimetry has the potential to reveal new reaction and transformation behavior and to develop a new understanding.

In situ determination of adsorption kinetics of proteins in a finite bath

2005 ◽  
Vol 1069 (1) ◽  
pp. 23-30 ◽  
Author(s):  
Anne Tscheliessnig ◽  
Rainer Hahn ◽  
Alois Jungbauer
Keyword(s):  
Adsorption Kinetics ◽  
Kinetics Of
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