Superplasticity of fine-grained Mg-10Li alloy prepared by severe plastic deformation and understanding its deformation mechanisms

The superplastic behavior and associated deformation mechanisms of a fine-grained Mg-10.1 Li-0.8Al-0.6Zn alloy(LAZ1011)with a grain size of 3.2μm,primarily composed of the BCCβphase and a small amount of the HCPαphase,were examined in a temperature range of 473 K to 623 K.The microstructural refinement of this alloy was achieved by employing high-ratio differential speed rolling.The best superplasticity was achieved at 523 K and at strain rates of 10^(-4)-5×10^(-4)s^(-1),where tensile elongations of 550±600%were obtained.During the heating and holding stage of the tensile samples prior to tensile loading,a significant increase in grain size was observed at temperatures above 573 K.Therefore,it was important to consider this effect when analyzing and understanding the superplastic deformation behavior and mechanisms.In the investigated strain rate range,the superplastic flow at low strain rates was governed by lattice diffusion-controlled grain boundary sliding,while at high strain rates,lattice diffusion-controlled dislocation climb creep was the rate-controlling deformation mechanism.It was concluded that solute drag creep is unlikely to occur.During the late stages of deformation at 523 K,it was observed that grain boundary sliding led to the agglomeration of theαphase,resulting in significant strain hardening.Deformation mechanism maps were constructed forβ-Mg-Li alloys in the form of 2D and 3D formats as a function of strain rate,stress,temperature,and grain size,using the constitutive equations for various deformation mechanisms derived based on the data of the current tests.

Achieving high-strain-rate and low-temperature superplasticity in an ECAP-processed Mg-Y-Er-Zn alloy via Ag addition

The effect of adding a small amount of Ag on the microstructure evolution and superplastic properties of Mg-Y-Er-Zn(WEZ612) alloys was systematically studied.The basal texture of the refined WEZ612 alloy produced by equal channel angular pressing was altered to a non-basal structure upon the addition of Ag.Ag addition also refined the grain size and promoted the formation of a large number of nano-14H-long period stacking ordered phases.Using high-resolution transmission electron microscopy,many nano-precipitated phases were detected on the basal plane of the Mg-Y-Er-Zn-1Ag(WEZ612-1Ag) alloy,The nano-precipitated phases on the basal plane improved the thermal stability of the alloy,lowered the deformation activation energy(Q),and improved the stress sensitivity index(m).At 523 K with a strain rate of 10^(-2) s^(-1),the Q value of WEZ612 was higher than that of WEZ612-1Ag(299.14 and 128.5 kJ mol^(-1),respectively).In contrast,the m value of the WEZ612 alloy(0.16) was lower than that of the WEZ612-1Ag alloy(0.46).At 623 K with a tensile rate of 10^(-2) s^(-1),the WEZ612 and WEZ612-1Ag alloys were elongated by 182% and 495%,respectively,with the latter exhibiting high-strain-rate and low-temperature superplasticity.The improved superplasticity of the WEZ612-1Ag alloy is attributed to the nano-precipitated phases,which effectively limit the cavity extension during superplastic deformation.

Influence of High-Robustness Polycarboxylate Superplasticizer on the Performances of Concrete Incorporating Fly Ash and Manufactured Sand

Using ethylene glycol monovinyl polyoxyethylene ether,2-acrylamido-2-methylpropane sulfonic acid(AMPS)and acrylic acid as the main synthetic monomers,a high robustness polycarboxylate superplasticizer was prepared.The effects of initial temperature,ratio of acid to ether,amount of chain transfer agent,and synthesis process on the properties of the superplasticizer were studied.The molecular structure was characterized by GPC(Gel Permeation Chromatography)and IR(Infrared Spectrometer).As shown by the results,when the initial reaction temperature is 15℃,the ratio of acid to ether is 3.4:1 and the acrylic acid pre-neutralization is 15%,The AMPS substitution is 10%,the amount of chain transfer agent is 8%,and the performance of the synthesized superplasticizer is the best.Compared with commercially available ordinary polycarboxylate superplasticizer in C30 concrete prepared with manufactured sand and fly ash,the bleeding rate decreases by 52%,T50 decreases by 1.2 s,and the slump time decreases by 1.1 s.In C60 concrete prepared with fly ash and river sand,the bleeding rate decreases by 46%,T50 decreases by 0.8 s,and the slump time decreases by 3.2 s.

Superplastic behavior of a fine-grained Mg-Gd-Y-Ag alloy processed by equal channel angular pressing

An extruded Mg-6Gd-3Y-1.5Ag(wt%) alloy was processed by 6 passes of equal channel angular pressing(ECAP) at 553 K using route Bc to refine the microstructure. Electron back-scattered diffraction(EBSD) analysis showed a fully recrystallized microstructure for the extruded alloy with a mean grain size of 8.6 μm. The microstructure of the ECAP-processed alloy was uniformly refined through dynamic recrystallization(DRX). This microstructure contained fine grains with an average size of 1.3 μm, a high fraction of high angle grain boundaries(HAGBs), and nano-sized Mg_(5)Gd-type particles at the boundaries of the DRXed grains, detected by transmission electron microscopy(TEM). High-temperature shear punch testing(SPT) was used to evaluate the superplastic behavior of both the extruded and ECAP-processed alloys by measuring the strain rate sensitivity(SRS) index(m-value). While the highest m-value for the extruded alloy was measured to be 0.24 at 673 K, the ECAP-processed alloy exhibited much higher m-values of 0.41 and 0.52 at 598 and 623 K, respectively,delineating the occurrence of superplastic flow. Based on the calculated average activation energy of 118 kJ mol^(-1) and m-values close to 0.5, the deformation mechanism for superplastic flow at the temperatures of 598 and 623 K for the ECAP-processed alloys was recognized to be grain boundary sliding(GBS) assisted by grain boundary diffusion.

Study on the Hydration and Physical Properties of Cement by M18 Polycarboxylate Superplasticizer Modified Graphene Oxide

Graphene oxide(GO)as a new nano-enhancer in cement-based materials has gained wide attention.However,GO is easy to aggregate in alkaline cement mortar with poor dispersibility.This hinders its application in practical infrastructure construction.In this work,GO-M18 polycarboxylate compound superplasticizer(GM)were obtained by compounding the M18 polycarboxylate superplasticizer with GO solution at different mass ratios.The dispersion of GM in alkaline solution was systematically studied.The phases and functional groups of GM were characterized by XRD and FTIR.The effects of GM on the cement mortar hydration and the formation of microstructure were investigated by measuring the heat of hydration,MIP,TG/DSC,and SEM.The results show that the long-chain structure of the M18 polycarboxylate superplasticizer can increase the interlayer spacing of GO and weaken the force between GO sheets.The modified GO can be uniformly dispersed in the cement slurry.GM can accelerate the early hydration process of cement,which can increase the content of Ca(OH)2 and decrease the grain size.It can optimize the pore size distribution of cement-based materials,increase the density of harmless and less harmful pores,thereby improving mechanical properties.Such methods can transform traditional cement-based materials into stronger,more durable composites,which prolong the life of cement-based materials and reduce the amount of cement used for later maintenance.This provides an idea for achieving sustainability goals in civil engineering.

MICROSTRUCTURAL EVOLUTION AND MECHANISMS OF SUPERPLASTICITY IN LARGE GRAINED IRON ALUMINIDES

The superplastic behavior has been found in Fe 3Al and FeAl alloys with grain sizes of 100～600 μm. The large grained Fe 3Al and FeAl alloys exhibit all deformation characteristics of conventional fine grain size superplastic alloys. However, superplastic behavior was found in large grained iron aluminides without the usual prerequisites for the superplasticity of a fine grain size and grain boundary sliding. The metallographic examinations have shown that average grain size of large grained iron aluminides decreased during superplastic deformation. Transmission electron microscopy (TEM) observations have shown that there were a great number of subgrain boundaries which formed a network and among which the proportion of low and high angle boundaries increased with the increase of strain. The observed superplastic phenomenon is explained by continuous recovery and recrystallization. During superplastic deformation, an unstable subgrain network forms and these subboundaries absorb gliding dislocations and transform into low and high angle grain boundaries. A dislocation gliding and climb process accommodated by subboundary sliding, migration and rotation, allows the superplastic flow to proceed.

Effects of an AMPS-Modified Polyacrylic Acid Superplasticizer on the Performance of Cement-based Materials

A self-made AMPS-modified polyacrylic acid superplasticizer and two others of the same type but with different molecular structures, which are commercially available, are used in this study to investigate the effect of a 2-acrylamide-2-methyl propylene sulfonic （AMPS）-modified polyacrylic acid superplasticizer on the properties of cement-based materials. In the experiments, initial fluidity, 1 and 2 h fluidity over time after admixtion, bleeding rate of the net cement mortar, and adsorption capacity and rate of cement particles are determined by adding different dosages of the three superplasticizers into the cement paste to characterize the dispersivity and the dispersion retention capability of each superplasticizer. Water-reducing rates of three kinds of mortars are simultaneously determined to characterize the water-reducing capacity of each superplasticizer, as well as the 3 and 28 d compressive strengths to characterize the compression resistance. Results show that water-reducing effect and fluidity better maintain the capability of the AMPS-modified polyacrylic acid superplasticizer than the two commercially available polyacrylic acid superplasticizers, and the compressive strengths after 3 and 28 d show significant growth. In conclusion, the effects of water reduction and strengthening of the AMPS-modified polyacrylic acid superplasticizer are evidently better than those of the two commercially available polyacrylic acid superplasticizers.

Activation Energy for Superplastic Flow Above Critical Temperature of Die Steels

Some commercial cold working die steels C.,Cr15 and CrWMn with ultra fine grain size were chosen as tested materials to research the activation energy for superplastic flow at different temperatures and strain rates above critical temperature. Based on the Arrhenius equation, the activation energy for superplastic flow is evaluated. The activation energy at constant strain rate is estimated by the logσ, vs 1/T relationship. The results show that the ac tivation energy is usually small under the conditions of optimal flow. The characteristics of superplastic deformation of steels above the critical temperature were also analyzed.

Superplasticity and Diffusion Bonding of Ti_3AI Intermetallic Compounds

The superplasticity of Ti_3Al intermetallic compounds has been investigated in this paper.The Ti-14Al-21Nb ternary alloy showed 477% elongation at the strain rate of 1.49×10^(-5) s^(-1) and 950℃.The elongation of Ti-14Al-21 Nb-3Mo-1V quinary alloy approached to 573% at the strain rate of 4.52×10^(-5) s^(-1) and the same temperature,and it was found that the elongation value in- creased to 1096.4%as temperature was raised up to 980℃ at the same strain rate.Ti_3Al base al- loys were bonded by diffusion bonding technology and good joints were created,the simulated specimens were performed by SPF/DB process.

Superplasticity in Aluminium Brass(HAl 66-6-3-2)

1.IntroductionSuperplasticity is not merely a specialphenomenon for certain specific alley,but isone of the intrinsic properties of metallicmaterials[1].When the internal and externalconditions are suitable,superplasticity ofmetal materials will be presented.

Regularity of Structural Superplasticity of Hypoeutectoid Steel

The curve of the relation between fracture elongation and temperature for unltrafine grained low alloy hypoeutectoid steels generally shows that three peaks occur at temperatures just below A_ c1, between A_ c1 and A_ c3, and just above A_ c3, When these steels are subjected to superplastic tensile test at different temperatures, the value of the last one is the lowest and the other two peaks are different one from another depending on components, microstructures and deformation conditions of the steels.

Synthesis of a Macromer, MPEGAA, Used to Prepare an AMPS-modified Polyacrylic Acid Superplasticizer

A macromer, methoxypolyethylene glycol acrylate （MPEGAA）, was synthesized by direct esterification using methoxypolyethylene glycol （MPEG-1200） and acrylic acid （AA） as the main materials. MPEGAA was then used to prepare a polyacrylic acid superplasticizer modified with 2-acrylamido-2- methylpropane sulfonic acid （AMPS）. A single-factor test was performed to investigate the effects of the molar ratio of acid to alcohol （n（AA）/n（MPEG））, inhibitor amount, catalyst amount, temperature, and time of esterification on the synthesis of MPEGAA. The experimental results showed that the optimal esterification conditions were as follows： n（AA）/n（MPEG）, 3.5：1; amount of hydroquinone （as an inhibitor）, 1.2%; amount of para-toluenesulfonic acid （as a catalyst）, 5.5%; reaction temperature, 95 ~C; and reaction time, 6 h. The AMPS- modified polyacrylic acid superplasticizer prepared under the optimal esterification conditions enabled the achievement and maintenance of high cement dispersibility. At an admixture amount of 0.15%, the cement paste fluidity was initially as high as 300 mm, and then decreased to 315 mm after 1 h and to 290 mm after 2 h.

Hyperbolic Method to Analyze the Electrical Resistivity Curve of Portland Cements with Superplasticizer

Electrical measurement was employed to investigate the early hydration characteristics of cement pastes with different dosages of superplasticizer in the same W/C ratio. The hyperbolic method was applied to analyze the electrical resistivity development. The peak point （Ph） on the hyperbolic curve could be easily read. The time （th） to reach the point Ph had strong relations with the setting time. th was delayed with the increment of the dosage of superplasticizer. The time th was used to plot the relationship between the initial setting time and final setting time. The hyperbolic equation was established to predict the ultimate resistivity. The retardation effect of the superplasticizer was confirmed in the same W/C ratio by setting time and isothermal heat evolution.

Effect of Competitive Adsorption between Sodium Tripolyphosphate and Naphthalene Superplasticizer on Fluidity of Cement Paste

The adsorption amount, ξ-potential of cement particles and fluidity of cement paste were tested to research the competitive adsorption between naphthalene superplasticizer （FDN） and STPP. The experimental results showed that the presence of STPP could significantly improve the fluidity of cement paste and reduce the fluidity loss with FDN. There existed a competitive adsorption between STPP and FDN. STPP and calcium ions formed complexes; they preferentially adsorbed onto surface of cement particles and preempt adsorption points of FDN; and it reduced adsorption amount of FDN. In the absence of STPP, saturation adsorption amount of FDN was 5.93 mg/g; but when the dosage of STPP was 0.1%, it reduced to 4.3 mg/g （about 72.5%）. The adsorption amount of FDN was reduced by STPP, but ξ-potential of cement particles enhanced and fluidity of cement paste increased because of strong negative charge effect of the complexes. Adsorption of the complexes would delay Ca^2＋ into liquid and inhibit formation of active adsorption points. Then, content of FDN in liquid increased with the addition of STPP and ξ-potential of cement particles became stable. In this way, fluidity loss of cement paste reduced.

Synthesis and Properties of an AMPS-Modified Polyacrylic Acid Superplasticizer

A 2-acrylamide-2-methyl propylene sodium sulfonic （AMPS）-modified polyacrylic acid superplasticizer was synthesized using aqueous solution polymerization with the major monomers including the self-made active macromers polyethylene glycol mono-methyl ether acrylate acrylic （MPEGAA）, acrylic acid （AA）, AMPS, and sodium methyl allyl sulfonate （SMAS）. The ratios of the monomers were determined using an orthogonal experiment. This research focused on the effects of the dosages of different macromers, the polymerization conditions, and the length of MPEGAA side chains on the properties of the AMPS-modified polyacrylic acid super-plasticizer. The best polymerization conditions of the AMPS-modified polyacrylic acid superplasticizer are when （n（MPEGAA）：n（SMAS）：n（AMPS）：n（AA） equals 0.1：0.1：0.2：0.65, the molecular weight of monomethoxypolyethylene glycol is 1 200, the initiator ammonium persulfate accounts for 5% of the total mass of the polymerized monomers, the polymerization temperature is 80 ~C, and the reaction time is 4 h. The AMPS-modified polyacrylic acid superplasticizer synthesized in the best conditions exhibited excellent dispersivity and dispersion retainability. When the dosage ratio was 0.24%, the initial fluidity was 400 mm and the fluidity had nearly no loss after 1 h.

THE INFLUENCE OF CAVITY DAMAGE ON MECHANICAL PROPERTIES OF SUPERPLASTICALLY-DEFORMED MATERIALS AND ITS PREDICTION

Aluminium alloy LY12CZ sheet without any pre-treatment has been used to study the influence of cavity damage on the mechanical properties of the superplastically-deformed materials room temper- ature. The experimental results show that: (1) the lower the rate of cavitation as the superplastic strain increases, the higher the superplasticity is; (2) the mechanical properties of superplastically- deformed materials at room temperature decrease as the superplastically-deformed strain increases, especially, a noteworthy decrease in elasticity modulus, yield strenth and ultimate strength at room temperature begins to appear as the level of cavitation by area comes up to about 4%, while at the same level the reduction in area drops down a very large quantity. Then, a three-layer back- propagation neural network has been developed to predict the machanichl properties of the superplasti- cally-deformed material.The results acquired from the neural network are very inspiring

Effects of Molecular Structure of Polycarboxylate-type Superplasticizer on the Hydration Properties of C_3S

Effects of polycarboxylate-type superplasticizer（PC） molecular structure on the hydration heat of tricalcium silicate（C3S） paste and polymerization degree of hydration products（C-S-H gel） were researched by using TAM AIR isothermal microcalorimetry（TA） and 29Si nuclear magnetic resonance（NMR）.Methoxy polyethylene glycol-methacrylates-based polycarboxylate superplasticizers with different side chain lengths and main chain lengths were employed.PC molecules with shorter main chain or longer side chains caused stronger retardation of C3S early hydration and lesser increase of C3S 3 d hydration degree.NMR measurement indicated that the incorporation of PC increased the hydration degree of C3S paste and the polymerization degree of silicon-oxygen tetrahedron of C-S-H gel.The tendency for C3S 7 d hydration degree to improve was more pronounced while PC molecules with longer main chain or shorter side chain were added.Whereas,PC molecules with longer main chains or longer side chains increased the 7 d polymerization degree of C-S-H gel.

The Synthesis Technique of Polyacrylic Acid Superplasticizer

Using water separation technique,acrylic acid （AA） and polyethylene glycol （PEG） 1000,of which the ratio was 1.5,were esterified and the optimum esterification ratio of 90% could be reached under the condition of 110 ℃×3 h.Using polyoxyethylene acrylate macromonomer （PA） prepared in the esterification,AA and sodium methylacryl sulfonate （MAS） as monomers,a copolymer which could be used as superplasticizer was prepared by free radical coolymerization in n（PA）：n（AA）：n（MAS） of 1：7：3.When the synthesis condition was 80 ℃× 5 h,the optimal dosage of initiator was 3.0%-4.0%,the fluidity of cement paste with the samples could reach 270 mm.By analyzing the effect of the content of residual small molecule sulfonic monomer on the properties of sample,n（MAS）/n（PA） was controlled in a range of 2.5-3.8.

Effect of Crosslink Structure of Bridge Polycarboxylate Superplasticizers on Dispersion Ability

Bridge polycarboxylate superplasticizers（PCs） with crosslink structure were synthesized by using polyethyleneglycol di-acrylate（PEGdA）, replacing partial polyethyleneglycol mono-acrylate （PEGmA） as crosslinking agent. Structures of bridge PCs were analyzed by gel permeation chromatography, and dispersion ability was evaluated by cement paste dispersity variation on time and rheology test. The experimental results showed that, molecular weight（MW） of bridge PCs increased with increase of PEGdA proportion, and MW distribution curve changed from Gaussian to fiat like, which meant notable increase of highly crosslinked copolymer. Bridge PCs led to decreased initial cement paste dispersity and better dispersity retention due to slow releasing. Further research showed that, PEGdA proportion had slight effect on polymerization degree of backbone, MW distribution of backbone deviated from Gaussian distribution and shoulder peaks appeared on distribution curve when PEGdA increased.

Effect of superplastic deformation on the bonding property of 00Cr25Ni7Mo3N duplex stainless steel

The superplastic deformation diffusion bonding of 00Cr25Ni7Mo3N duplex stainless steel was performed on a hot simulator. The microstructure of the bonding interface was characterized by scanning electron microscopy （SEM） and electron backscatter diffraction （EBSD）. The mechanical properties of the specimen were investigated by a shear strength test. The results indicated that the shear strength was improved with the increase of superplastic deformation reduction. When the deformation reduction was up to 50%, the shear strength of the specimen achieved 417 Mpa, approaching to that of the base metal. In addtion, the superplastic diffusion bonding technique was not very sensitive to surface roughness levels. When the surface roughness of the bonding specimen surpassed 0.416 pan （level G2）, the shear strength achieved at least 381 MPa.