Post Cryopreservation Growth Kinetic and Photosynthetic Assessment of an Acid Tolerant Strain of Stichococcus bacillaris

Preserving microbial diversity has become a strategic undertaking. Thus, ex situ microalgal culture conservation results in strategic and functional resource in both biodiversity protection and application domains. Cryopreservation of microalgae has been practiced since the 1960s and is now considered the optimal preservation strategy. Furthermore, the overall monitoring during growth of cultures after freezing/thawing protocols was hardly investigated and there is poor evaluation related to preserve especially the photosystem apparatus. The present study focuses on Stichococcus bacillaris as case study for short-term cryopreservation at −80 °C storage. Various freezing pretreatments using cryoprotective agents, and two thawing methods were compared introducing a novel variable to evaluate viability recovery and assessing growth kinetics of cultures immediately after thawing and after a series batch cultivation. Photosynthetic rate and pigments assessment were proposed to evaluate hidden metabolic cell damage. Results underline cryoprotective agents can increase the kinetic recovery of preserved cells in terms of reduction of lag phase during batch cultivation tests: the use of dimethyl sulfoxide and glycerol granted a growth comparable to unpreserved cells when sudden thawing occurs after 24 hours of storage, but recovery after preservation is less sensitive to cryoprotective agents when gradual thawing and 1 month of storage is considered. However, cells are always able to restore their physiological pathways even without agents, so their kinetic effect has been proved and quantified. Interestingly, both the photosynthetic efficiency and the ratio between total chlorophyll and carotenoids are comparable (0.75 Fv/Fm, 2.2 ± 0.25 g/g) to unpreserved cells and they are unsensitive to chosen agents, but the ratio between chlorophyll a and chlorophyll b was clearly altered (up to 10 times), suggesting that photoactive pigments relative proportions can result in similar growth kinetic performances. Long-term studies will be carried out to assess whether the differences found could cause chronic damage to photosystem efficiency of S. bacillaris cultures.

Microstructure,Properties,and Grain Growth Kinetics of Mo-5Ta Refractory Sputtering Targets Prepared by SPS

Mo-5Ta targets were prepared by the spark plasma sintering(SPS)technology under the sintering temperatures of 1400-1600℃,the holding times of 0-20 min,and the axial pressure of 30 MPa.The microstructure,performance,and grain growth kinetics of Mo-5Ta sputtering targets were studied.With the increase of sintering temperatures and times,Ta can more dissolve in Mo and form a Mo(Ta)solid solution.The grain sizes of Mo-5Ta targets remain unchanged at low temperatures(1400-1500℃)while increasing significantly at high temperature(1600℃)with the extension of the holding time.In addition,the densities and Vickers hardness(HV_(0.5))first ascend and then decrease with sintering proceeding.The thermal conductivity is positively correlated with the grain size and density,as a result of their joint action.Based on the comprehensive analysis,the grain growth is dominated by the combination of boundary diffusion and volume diffusion.When n=2,the activation energies of grain growth under holding times of 5,10,20 min are calculated as 762.70,617.86,and 616.52 kJ/mol,respectively.

Effect of Si on growth kinetics of intermetallic compounds during reaction between solid iron and molten aluminum

The effect of Si on the growth kinetics of intermetallic compounds during the reaction of solid iron and molten aluminum was investigated with a scanning electron microscope coupled with an energy dispersive X-ray spectroscope, and hot-dip aluminized experiments. The results show that the intermetallic layer is composed of major Fe2Al5 and minor FeAl3. The Al-Fe-Si ternary phase, rl/rg, is formed in the Fe2Al5 layer. The tongue-like morphology of the Fe2Als layer becomes less distinct and disappears finally as the content of Si in aluminum bath increases. Si in the bath improves the prohibiting ability to the growth of Fe2Als and FeAl3. When the contents of Si are 0, 0.5%, 1.0%, 1.5%, 2.0% and 3.0%, the activation energies of Fe2Al5 are evaluated to be 207, 186, 169, 168, 167 and 172 kJ/mol, respectively. The reduction of the activation energy might result from the lattice distortion caused by Si atom penetrating into the Fe2Al5 phase. When Si atom occupies the vacancy site, it blocks easy diffusion path and results in the disappearance of tongue-like morphology.

Electroless plating and growth kinetics of Ni-P alloy film on SiC_p/Al composite with high SiC volume fraction

After Sn/Pd activating, the SiCp/Al composite with 65% SiC (volume fraction) was coated by electroless Ni?P alloy plating. Surface morphology of the composite and its effect on the Ni?P alloy depositing process and bonding action of Ni and P atoms in the Ni?P alloy were studied. The results show that inhomogeneous distribution of the Sn/Pd activating points results in preferential deposition of the Ni?P alloy particles on the Al alloy and rough SiC particle surfaces and in the etched caves. The Ni?P alloy film has an amorphous structure where chemical bonding between Ni and P atoms exists. After a continuous Ni?P alloy film formed, electroless Ni?P alloy plating is not affected by surface morphology and characteristics of the SiCp/Al composite any longer, but by the electroless plating process itself. The Ni?P alloy film follows linear growth kinetics with an activation energy of 68.44 kJ/mol.

Growth kinetics and mechanism of microarc oxidation coating on Ti-6Al-4V alloy in phosphate/silicate electrolyte

Microarc oxidation(MAO)is an effective surface treatment method for Ti alloys to allow their application in extreme environments.Here,binary electrolytes consisting of different amounts of sodium phosphate and sodium silicate were designed for MAO.The surface morphology,composition,and properties of MAO coatings on Ti-6Al-4V alloy treated in 0.10 mol/L electrolyte were investigated to reveal the effect of PO_(4)^(3-)and SiO_(3)^(2-)ray diffraction,and potentiodynamic polarization.The results showed that PO_(4)^(3-)is beneficial for generating microarcs and forming pores within the coating,resulting in a thick but porous coating.SiO_(3)^(2-)eration of microarcs,resulting in a thin dense coating.The thickness,density,phases content,and polarization resistance of the MAO coatings are primarily affected by the intensity of microarcs for low SiO_(3)^(2-)ciently high.The thickness of MAO coatings obtained in P/Si electrolytes shows a piecewise linear increase with increasing process time during the three stages of microarc discharge.SiO_(3)^(2-)discharge,but slows down the growth of the coating formed in the next stage.

Influence of anions in phosphate and tetraborate electrolytes on growth kinetics of microarc oxidation coatings on Ti6Al4V alloy

The growth kinetics of microarc oxidation(MAO)coatings on Ti6Al4V alloy was studied by designing an electrolyte with low PO_(4)^(3−)content and high B_(4)O_(7)^(2−)content,using scanning electron microscopy,transmission electron microscopy,X-ray diffraction,and potentiodynamic polarization.The results showed that B_(4)O_(7)^(2−)increased the spark intensity and dissolved most of the oxides at high temperatures.Then,a thicker barrier layer at the coating/substrate interface was produced,which increased the polarization resistance of the coating.PO_(4)^(3−)at a low concentration also promoted the uniform growth of the MAO coating and the formation of hat-shaped holes in the outer deposition layer.The thickness of the MAO coatings obtained in Na_(2)B_(4)O_(7) electrolytes exhibited an exponential increase with time at spark discharge stage,while that of the MAO coating obtained in phosphate–tetraborate electrolytes showed a linear trend as the PO_(4)^(3−)content increased.

Isothermal Growth Kinetics of Ultra-fine Austenite Grains in a Nb-V-Ti Microalloyed Steel

Ultra-fine austenite grains with size of i-3 μm were prepared in a Nb-V-Ti steel through repetitive treatment of rapid heating and quenching. A model for the growth kinetics of these ultra-fine austenite grains was successfully created through successive 2 processes, and the activation energy Q for growth was estimated to be about 693.2 kJ/mol, which directly shows the inhibition effect of microalloy elements on the growth of ultra-fine austenite grains.

Formation mechanism and growth kinetics of TiAl_(3) phase in cold-rolled Ti/Al laminated composites during annealing

Cold-rolled Ti/Al laminated composites were annealed at 525−625℃for 0−128 h,and the interfacial microstructure evolution was investigated.The results indicate that only the TiAl_(3) phase was formed at the Ti/Al interface;most of TiAl_(3) grains were fine equiaxed with average sizes ranging from hundreds of nanometers to several microns and the TiAl_(3) grain size increased with increasing annealing time and/or temperature,but the effect of annealing temperature on the TiAl_(3) grain size was far greater than that of annealing time.The growth of the TiAl_(3) phase consisted of two stages.The initial stage was governed by chemical reaction with a reaction activation energy of 195.75 kJ/mol,and the reaction rate constant of the TiAl_(3) phase was larger as the Ti/Al interface was bonded with fresh surfaces.At the second stage,the growth was governed by diffusion,the diffusion activation energy was 33.69 kJ/mol,and the diffusion growth rate constant of the TiAl_(3) phase was mainly determined by the grain boundary diffusion owing to the smaller TiAl_(3) grain size.

Growth Kinetics of Nanocrystals and Nanorods by Employing Small-angle X-ray Scattering (SAXS) and Other Techniques

In this article, we report the results of our detailed investigations of the growth kinetics of zero-dimensional nanocrystals as well as one-dimensional nanorods by the combined use of small angel X-ray scattering （SAXS）, transmission electron microscopy （TEM） along with other physical techniques. The study includes growth kinetics of gold nanocrystals formed by the reduction of HAuCl4 by tetrakis（hydroxymethyl） phosphonium chloride in aqueous solution, of CdSe nanocrystals formed by the reaction of cadmium stearate and selenium under solvothermal conditions, and of ZnO nanorods formed by the reaction of zinc acetate with sodium hydroxide under solvothermal conditions in the absence and presence of capping agents. The growth of gold nanocrystals does not follow the diffusion-limited Ostwald ripening, and instead follows a Sigmoidal rate curve. The heat change associated with the growth determined by isothermal titration calorimetry is about 10 kcal·mol^-1 per I nm increase in the diameter of the nanocrystals. In the case of CdSe nanocrystals also, the growth mechanism deviates from diffusion-limited growth and follows a combined model containing both diffusion and surface reaction terms. Our study of the growth kinetics of uncapped and poly（vinyl pyrollidone） （PVP）-capped ZnO nanorods has yielded interesting insights. We observe small nanocrystals next to the ZnO nanorods after a lapse of time in addition to periodic focusing and defocusing of the width of the length distribution. These observations lend support to the diffusion-limited growth model for the growth of uncapped ZnO nanorods. Accordingly, the time dependence on the length of uncapped nanorods follows the L3 law as required for diffusion-limited Ostwald ripening. The PVP-capped nanorods, however, show a time dependence, which is best described by a combination of diffusion （L^3） and surface reaction （L^2） terms.

Liquid State Undercoolability and Crystal Growth Kinetics of Ternary Ni-Cu-Sn Alloys

The liquid state undercoolability and crystal growth kinetics of ternary Ni-5%Cu-5%Sn and Ni-10%Cu-10%Sn alloys are investigated by the glass fluxing method. In these two alloys, experimental maximum undercoolings of 304 K （0.18TL ） and 286K （0.17TL ） are achieved and the dendritic growth velocities attain 39.8 and 25.1 m/s, respectively. The transition of morphology from coarse dendrite into equiaxed structure occurs and the grain size of the a （Ni） phase decreases remarkably when the undercooling increases. Both the lattice constant and microhardness increase obviously with the enhancement of undercooling. The enrichment of Cu and Sn solute contents reduces the dendritic growth velocity, while enhances the lattice constant and microhardness of a （Ni） phase.

Formation and Growth Kinetics of Intermediate Phases in Ni-Al Diffusion Couples

Formation and growth of the intermediate phases in the Ni-Al diffusion couples prepared by pouring technique were investigated. Electron probe microanalysis, scanning electron microscopy and X-ray diffraction were used to characterize the product phases in the joints. The results show that two intermediate phases form in the sequence of NiAl3 and Ni2Al3 during solidification. After annealed, Ni2Al3 and NiAl3 still exist in the joints of the couples. The reasons for the formation of Ni2Al3 and NiAl3, as well as the absence of NiAl, Ni5Al3 and Ni3Al were discussed, respectively. The growth kinetics of both product phase layers indicates that their growth obeys the parabolic rate law. The activation energies and frequency factors for NiAl3 and Ni2Al3 phases were also calculated according to the Arrhenius equation.

A Study of Grain Growth Kinetics in Sintered NdFeB Magnets

The Nd2Fe14 B grain growth kinetics in sintered NdFeB magnets with nominal compositions of Nd30+xDy1.5Fe67.08-xAl0.4B1.02 (%, x = 0, 3) was studied. The grain size parameters were determined by means of the linear intercept method on SEM secondary electron images. It is observed that the grain growth process is more sensitive to sintering temperature than to sintering time although the grain size rises with both sintering temperature and time. It is also found that magnets prepared from the pre-alloy powder with a higher oxygen content exhibit a lower grain growth rate and magnets made from the pre-alloy powder with a broader particle size distribution demonstrate a higher grain growth rate. It is believed that the presence of appropriate amounts of Nd oxides effectively impedes the grain growth process and a larger difference in sizes between pre-alloy powder particles significantly accelerates the grain growth process. On the basis of experimental results, the grain growth exponent and the corresponding activation energy were obtained. A possible grain growth mechanism in NdFeB magnets during sintering was briefly discussed.

A growth kinetics model of rate decomposition for Si_(1-x)Ge_x alloy based on dimer theory

According to the dimer theory on semiconductor surface and chemical vapor deposition(CVD) growth characteristics of Si1-xGex, two mechanisms of rate decomposition and discrete flow density are proposed. Based on these two mechanisms, the Grove theory and Fick's first law, a CVD growth kinetics model of Si1-xGex alloy is established. In order to make the model more accurate, two growth control mechanisms of vapor transport and surface reaction are taken into account. The paper also considers the influence of the dimer structure on the growth rate. The results show that the model calculated value is consistent with the experimental values at different temperatures.

Grain Growth Kinetics of BaTiO3 Nanocrystals During Calcining Process

BaTiO3 nanocrystals were synthesized by sol-gel method using barium acetate （Ba（CH3COO2） and tetrabutyl titanate （Ti（OC4H9）4） as raw materials. Xerogel precursors and products were characterized by means of thermogravimetric/differential scanning calorimetry （TG/DSC）, X-ray diffraction （XRD） and transmission electron microscope （TEM）. The influence of the calcination temperature and duration on the lattice constant, the lattice distortion, and the grain size of BaTiO3 nanocrystals was discussed based on the XRD results. The grain growth kinetics of BaTiO3 nanocrystals during the calcination process were simulated with a conventional grain growth model which only takes into account diffusion, and an isothermal model proposed by Qu and Song, which takes into account both diffusion and surface reactions. Using these models, the pre-exponential factor and the activation energy of the rate constant were estimated. The simulation results indicate that the isothermal model is superior to the conventional one in describing the grain growth process, implying that both diffusion and surface reactions play important roles in the grain growth process.

HIGH-TEMPERATURE TEM IN SITU STUDY OF GROWTH KINETICS OF BAINITE IN β BRASS

In situ observation of the growth process of bainitic plate in βbrass by means of high-temper- ature TEM is conducted.The lengthening and thickening kinetics of bainitic plate is analysed with Trivedi's model and Zener-Hillert's model,respectively.It is found that the stacking fault substructure exists just in the growth tip of fresh bainitie plate and so does the shear stress in the matrix around the tip.The measured lengthening rate of bainitic plate is not con- sistent with Trivedi's model.The thiekening process is only macroscopieally controlled by vol- ume diffusion but its nature is a shear process.

Growth Kinetics of Silicon Carbide Film Prepared by Heating Polystyrene/Si（111）

SiC films were prepared by heating polystyrene/Si（111） in normal pressure argon atmosphere at different temperatures. The films were investigated by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and Fourier transform infrared absorption measurements. The thicknesses of SiC films were calculated from FTIR spectra. The growth kinetics of the growth process of SiC films were investigated as well. The thicknesses of the SiC films grown for 1 h with increasing growth temperatures have different trends in the three temperature ranges： increasing slowly （1200-1250 ℃）, increasing quickly （1250- 12.70 ℃）, and decreasing （1270-1300 ℃）. The apparent activation energies of the growth process of SiC films in the three ranges were calculated to be 122.5,522.5, and -127.5 J/mol respectively. Mechanisms of the different growth processes were discussed. The relation between film thicknesses and growth temperatures indicated that the growth process was a 2D mechanism in the first range and 3D mechanism in the second range. In the third range, the thicknesses of SiC films were decreased by the volatility of Si and C atoms.

Grain Growth Kinetics of SnO_2 Nanocrystals Synthesized by Precipitation Method

Monodispersed spheroidal SnO2 nanocrystals with the grain size of 8-30 nm were synthesized by the precipitation method using SnCl4·5H2O （stannic chloride hydrate） as raw materials.Differential scanning calorimetry/thermogravimetry （DSC/TG）,X-ray diffraction （XRD） and transmission electron microscope （TEM） were used to characterize the structure of SnO2 nanocrystals.The influences of the calcination temperature and time on the lattice constant,the lattice distortion and the grain size of SnO2 nanocrystals were discussed based on the XRD results.The grain growth kinetics of SnO2 nanocrystals during calcination process was simulated with a conventional grain growth model which only took into account of diffusion and with a new isothermal model proposed by our group,which took into account of both diffusion and surface reactions.Using conventional model,the grain growth rate constant of SnO2 crystals is 1.55×104nm5/min with a pre-exponential factor of 5 and an activation energy of 108.62 kJ/mol.Compared with the convention model,the new isothermal model is more realistic in reflecting the grain growth behavior of SnO2 nanocrystals during the calcination process.This indicates that the grain growth of SnO2 nanocrystals is controlled by both diffusion and reaction factors,and the effect of surface reactivity on the grain growth of SnO2 nanocrystals could not be ignored.A combined activation energy estimated with the new isothermal model is 53.46 kJ/mol.

Growth Kinetics of γ′ Particles in Incoloy 907

The kinetics of growth of the γ' precipitate in an lncoloy 907 alloy have been studied. The kinetics of particle growth obeyed the tirne law predicted by the Lifshitz-Wagner theory. The distribution of γ'particle sizes was found to be significantly broader than the theoretical distribution of LifshitZ-Wagner theory. It is suggested that this is due to the relatively large lattice parameter mismatch between γ' and the Fe-Ni-Co matrix

The Use of Image Analysis to Simulate Growth Kinetics of Ferrite by Carbon Diffusion in SG Cast Iron

1.IntroductionThe use of the Quantimet 900 imageanalysis system to simulate the growth kine-tics of ferrite by carbon diffusion inspheroidal graphite(SG)cast iron has beendiscussed[1].The results obtained from theQ900 agreed qualitatively with experiment.

Study on the thermodynamics and the growth kinetics of synthesis of the β-SiC whiskers

The thermodynamics and the growth kinetics of synthesis of the SiC whiskers (SiC w ) from rice hulls are studied in this paper. The results show that the intimate contact of SiO 2 with C in the rice hulls resulted in the formation of SiC particle (SiC p ) at lower temperature, and the external ash of the hulls (w (SiO 2 )>98%) is the main silicon source for SiCw growth. The metallic composite catalyst increases the selectivity for SiCw growth and the reaction rate. The growth mechanism of the SiCw can be characterized as the VLS (vapour liquid solid) with the presence of the whisker forming catalyst: from SiC nucleation through enlargement and growing with the <1 1 1> crystallographic orientation in a certain diameter, then the SiC w is a complete single crystal of β SiC. The generation reaction of SiO is the rate determing step for synthesis of SiC w .