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Continuous Cooling Transformation of Undeformed and Deformed High Strength Crack-Arrest Steel Plates for Large Container Ships

  • Yongfeng Qi , Jing Li EMAIL logo , Chengbin Shi and Qintian Zhu
Published/Copyright: September 4, 2018

Abstract

The phase transformation behavior of crack-arrest steel during continuous cooling either with or without deformation at high temperatures was investigated. By carefully examining the microstructures of continuous cooled samples, we found that pearlite, quasi-polygonal ferrite (QPF), acicular ferrite (AF), granular bainite (GB), upper bainite, lath-like bainite and martensite/austenite will exist depending on cooling rates and transformation temperatures in both conditions of deformation and without deformation after austenization. The transformation curves of AF and GB moved toward the left in deformation condition in comparison with that of without deformation condition, which indicated that deformation promoted the formation of QPF and AF; meanwhile, deformation inhibited the formation of bainite. Finer bainite and the accompanying M/A could be obtained by reducing the bainite nucleation activation energy as follows: (i) increasing the undercooling by increasing the cooling rate; (ii) increasing the stored energy by deformation of the austenite.

Introduction

With the growth of world economy and transportation volume, the need for building large container ships has been expanded for the purpose of reducing cost and improving transportation efficiency. Dead weight has a major influence on transportation efficiency so that weight saving is a key factor for building large container ships [1]. To reduce the plate thickness, more advanced plates with high strength and good toughness are required.

In recent years, the 60 mm thick plates with 460 MPa yields strength class have been developed by JFE steel to replace conventional 80 mm plates for energy conservation. The thermo-mechanically controlled process (TMCP) technology combined with accelerated cooling as an effective method for microstructure control during production of steels has been widely employed to achieve high strength steel plates used in large container ships [2,3]. This imposes a requirement for shipbuilding steel to develop optimal microstructure, which should offer the potential for improving the strength and toughness. Steels that are hot rolled and cooled to exhibited high strength and good toughness often require acicular ferrite (AF) and bainite microstructure [4]. Developing optimal microstructure is not an independent factor, which is related to chemical composition, hot deformation processing and accelerated cooling rate. Some alloy elements, such as aluminum, chromium, niobium, copper, titanium and molybdenum, are often added to achieve the satisfied microstructure and accordingly improve the strength and toughness [5, 6, 7]. During the process of alloy design, carbon equivalent (Ceq) and cold cracking susceptibility (Pcm) should be considered, in which the two parameters are calculated by eqs. (1) and (2) [8, 9] so that optimal balance between the properties of the base plate and welded joint could be achieved.

(1)Ceq=C+Mn+Si/6+Cu+Ni/15+Cr+Mo+V/5
(2)Pcm=C+Si/30+(Mn+Cu+Cr)/20+Mo/15+V/10+Ni/60+5B

The main factors to control TMCP are hot deformation strain, hot deformation temperature and subsequently cooling rate. These parameters are essential in controlling microstructure formation based on phase transformation theory. In engineering application, a continuous cooling transformation (CCT) diagram is powerful to display the phase transformation behavior in TMCP processing which can also be used to predict the constitution of microstructure.

In this work, the phase transformation of low-carbon high strength steel used as shipbuilding plate was investigated in the non-deformed and deformed conditions. The object is to clarify the rule of AF and bainite formation by investigating the effects of hot deformation and deformation temperature on the behavior of phase transformation, then plot the CCT curves in two different conditions. It would be beneficial to practical application of TMCP processing to product high performance shipbuilding steels.

Experimental procedure

The chemical compositions of the experimental materials cut from an industrial hot rolled sheet are shown in Table 1. The value of Ceq and Pcm is 0.47 and 0.208, respectively. Samples were prepared as ϕ8 mm×80 mm with effective testing length of 15 mm in the center region to carry out thermomechanical simulation tests under undeformed and deformed conditions.

Table 1:

Chemical compositions of the tested steels (wt%).

CMnSiSPAlCuNiCrMoNbTiFeCeqPeq
0.0541.510.140.0020.0040.0340.990.980.16<0.0050.240.0098Bal.0.470.208

The thermomechanical experiments were conducted on a Gleeble 3800 thermomechanical simulator (Dynamic System Inc., Poestenkill, NY) in order to plot static (without hot deformation) CCT diagrams and the dynamic (with hot deformation) CCT diagrams. The critical temperature for deformation within austenite phase region is T95 (completely recrystallized temperature) and T5 (recrystallization-stop temperature) [10]. Deformation above T95 leads to complete recrystallization of austenite, which is also accompanied with grain refinement at the same time. Deformation below T5 results in high densities of substructure and dislocation, which increases the nucleation sites of AF and bainite, and it is regarded as a desirable microstructure prior to final cooling. Deformation between T95 and T5 leads to mixed grain and poor final microstructure and properties. Therefore, the temperature for deformation within the later region should be avoided. The critical temperature for deformation in dynamic CCT tests was T95, 1,323 K (1,050°C), and T5, 1,173 K (900°C), respectively, which were determined in a separate experiment for the steel used in these experiments [4]. The schematic diagram for the continuous cooling experiments are shown in Figure 1 and detailed experimental process are as follows:

  1. All specimens in static simulate experiments were first austenitized for 5 min at 1,200°C and then cooled to ambient temperature at the cooling rates of 0.1, 0.5, 2, 5, 10, 20, 30 and 40°C s−1, respectively.

  2. All specimens in dynamic simulate experiments were first austenitized for 5 min at 1,200°C and subsequently deformed by approximately 40 % at 1,050°C and then cooled to ambient temperature at the cooling rates of 0.1, 0.5, 2, 5, 10, 20, 30 and 40°C s−1, respectively.

  3. To investigate the effect of hot deformed temperature on microstructure transformation, deformation at 900°C was carried out to be compared with results in experiment 2. Three specimens were austenitized for 5 min at 1,200°C and subsequently deformed by approximately 40 % at 900°C and then cooled to ambient temperature at the cooling rates of 2, 10 and 40°C s−1, respectively.

Figure 1: Schematic diagrams for the continuous cooling experiments: (a) Static simulation; (b) Dynamic simulation.
Figure 1:

Schematic diagrams for the continuous cooling experiments: (a) Static simulation; (b) Dynamic simulation.

Specimens for metallographic examination were cut on wire cutting machine paralleled to the length direction at the center part. All the specimens were mechanically polished and etched with a 4 % Nital solution and then observed with an optical microscopy (LEICA DM2500M, OM) and scanning electron microscope (FEI MLA250, FEI, Hillsboro, OR, USA, SEM). Vickers microhardness measurement was employed on a THV-1MDX tester using a 200-g load and holding for 10 s. The microhardness was taken average of five points measurement in each specimen. Then, static and dynamic CCT curves were plotted based on the analyzing of measuring temperature, dilatation curves, microstructure and microhardness.

Results and discussion

Effects of cooling rates on transformation microstructures

Optical micrographs of the specimens under different cooling rates in the static and dynamic simulate tests are shown in Figures 24, respectively, which reveals the microstructure evolution with cooling rate increased from 0.1 to 40°C s−1. Microstructure evolution in CCT specimens was almost composed of pearlite (P), quasi-polygonal ferrite (QPF), AF, granular bainite (GB), upper bainite (UB), lath-like bainite (LB) and corresponding martensite/austenite constitute (M/A island) depending on different cooling rates and transformation temperatures.

Figure 2: Optical microstructure of specimens at different cooling rates (static CCT): (a) 0.1 ℃ s–1; (b) 0.5 ℃ s–1; (c) 2 ℃ s–1; (d) 5 ℃ s–1; (e) 10 ℃ s–1; (f) 20 ℃ s–1; (g) 30 ℃ s–1; (h) 40 ℃ s–1.
Figure 2:

Optical microstructure of specimens at different cooling rates (static CCT): (a) 0.1 ℃ s–1; (b) 0.5 ℃ s–1; (c) 2 ℃ s–1; (d) 5 ℃ s–1; (e) 10 ℃ s–1; (f) 20 ℃ s–1; (g) 30 ℃ s–1; (h) 40 ℃ s–1.

Figure 3: Optical microstructure of specimens at different cooling rates (1050 ℃ deformation): (a) 0.1 ℃ s–1; (b) 0.5 ℃ s–1; (c) 2 ℃ s–1; (d) 5 ℃ s–1; (e) 10 ℃ s–1; (f) 20 ℃ s–1; (g) 30 ℃ s–1; (h) 40 ℃ s–1.
Figure 3:

Optical microstructure of specimens at different cooling rates (1050 ℃ deformation): (a) 0.1 ℃ s–1; (b) 0.5 ℃ s–1; (c) 2 ℃ s–1; (d) 5 ℃ s–1; (e) 10 ℃ s–1; (f) 20 ℃ s–1; (g) 30 ℃ s–1; (h) 40 ℃ s–1.

Figure 4: Optical microstructure of specimens at different cooling rates (900 ℃ deformation): (a) 2 ℃ s–1; (b) 10 ℃ s–1; (c) 40 ℃ s–1.
Figure 4:

Optical microstructure of specimens at different cooling rates (900 ℃ deformation): (a) 2 ℃ s–1; (b) 10 ℃ s–1; (c) 40 ℃ s–1.

The microstructure metallographs in non-deformation condition were shown in Figure 2; it can be seen that QPF is the dominant component with a little P microstructure at the cooling rate of 0.1°C s−1. When the cooling rate ranges from 0.5 to 2°C s−1, QPF and AF become the principal components combined with the increase of AF percent, gradually. And corresponding microhardness increases from HV170 to HV207. UB and GB are initially formed at the cooling rate of 5°C s−1. When the cooling rate is in the ranges of 5–20°C s−1, UB and GB are majority phases, resulting in the microhardness increases to HV250. When the cooling rate ranges from 30 to 40°C s−1, refined LB microstructure formed in prior austenite grain and the corresponding microhardness increased to HV270.

The microstructure metallographs in pre-deformation condition were shown in Figure 3; it can be seen that QPF is the dominant component with a little P microstructure at the cooling rate of 0.1°C s−1 and the corresponding microhardness is HV172. When the cooling rate ranges from 0.5 to 10°C s−1, QPF and AF become the principal components combined with the increase of AF percent, gradually. And corresponding microhardness increases from HV216 to HV227. UB and GB are initially formed at the cooling rate of 20°C s−1. When the cooling rate is in the ranges of 30–40°C s−1, UB and GB are majority phases, resulting in the microhardness increases to HV275. In conclusion, hot deformation could enlarge the formation of AF and QPF from cooling rate of 0.5–2 to 0.5–20°C s−1. Furthermore, the corresponding microstructure could be finer under hot deformation.

The microstructures of deformation at temperature 900°C are shown in Figure 4, with the cooling rates of 2, 10 and 40°C s−1, respectively. The microstructure is mainly occupied by QPF at the cooling rate of 2°C s−1, and the corresponding microhardness is HV205. With cooling rate increasing to 10°C s−1, the microstructure transforms to AF and microhardness increases to HV255. When the cooling rate is 40°C s−1, the microstructure consists of finer AF and GB. It can be seen that microstructure under the three cooling rates is finer compared with which deformed at 1,050°C.

In contrast, the corresponding CCT microstructure in the deformed conditions at a temperature of 1,050 and 900°C is obviously different in shape from those in the undeformed conditions due to hot deformation. Compared the microstructure of Figures 2 and 3 or 4, it can be seen that hot deformation could strongly promote the formation of AF and suppress the formation of GB and UB with the cooling rates ranging from 0.5 to 10°C s−1. At the same time, the corresponding microstructure in deformed conditions is refined and LB cannot be found.

The CCT diagrams

The CCT diagrams are believed to be useful in gaining an insight into microstructure and designing an optimal TMCP during industrial processing of steels. The static and dynamic CCT diagrams of shipbuilding steel are shown in Figures 5(a) and (b), respectively, which exhibit multilayer transformation curves as cooling rate increased from 0.1 to 40°C s−1. Solid points were measured from dilatometric data, and dash lines were determined by metallographic observations of OM and corresponding microhardness.

Figure 5: Continuous cooling transformation curves of steel (CCT diagram): (a) Static CCT; (b) Dynamic CCT.
Figure 5:

Continuous cooling transformation curves of steel (CCT diagram): (a) Static CCT; (b) Dynamic CCT.

As shown in Figure 5, it could be found that the major transformation curves lie in the temperature ranges from 450 to 750°C in both static and dynamic CCT diagrams. Moreover, in comparison with the static CCT curve, the dynamic CCT curve moved toward the left side, proving that the AF and QPF areas were enlarged. LB microstructure could be obtained at cooling rate of 30°C s−1 in the static CCT curve, but that could not be observed at cooling rate of 40°C s−1 in the dynamic CCT curve. These results were consistent with the results of effects of deformation on microstructure transformation reported by Jun [11]. In conclusion, deformation could promote the formation of P and QPF in low-carbon HSLA steels.

It is well known that the CCT behavior and the corresponding transformed microstructure are related to prior hot deformation. Figure 6 showed Ar3 and Ar1 temperature of steels in undeformed and deformed conditions at different cooling rates. It could be seen that the deformation effectively improved Ar3 temperatures.

Figure 6: Ar3 and Ar1 temperature of specimens in undeformed and deformed conditions at different cooling rates.
Figure 6:

Ar3 and Ar1 temperature of specimens in undeformed and deformed conditions at different cooling rates.

Grain boundary surface areas per unit volume of austenite (Sv) and nucleation rate (Ns) were increased by austenite grain refinement and deformation below the temperature of non-recrystallization [12]. And that was expected to accelerate the AF and bainite formation and raise Ar3 temperature as reported by other groups [13, 14, 15]. Liu and Solberg [16] results showed that the influence of deformation on the Ar3 temperature decreases with decreasing cooling rate due to static recovery in the deformed austenite during cooling, which agreed with the results in Figure 6. Liang et al. [4] and Cizek et al. [17] indicated that the starting temperature of the bainite transformation was raised when applying deformation, this result was consistent with the observations made in the current studied steel. In conclusion, hot deformation increased transformation start temperature and promoted the formation of QPF and AF.

The hardness of specimens in undeformed and deformed condition at different cooling rates is shown in Figure 7. Figure 7 showed that hardness of specimens with deformation at 1,050°C was lower than that with undeformation in region A, which due to the hardness of microstructure composed of AF and QPF was lower than that consisted of UB and GB. Deformation in crystallization region could lead to the finer grain and higher hardness compared with undeformed condition at different cooling rates in addition to the ranges of region A.

Figure 7: Hardness of specimens in undeformed and deformed conditions at different cooling rates.
Figure 7:

Hardness of specimens in undeformed and deformed conditions at different cooling rates.

Effects of hot deformation and deformed temperature on microstructure transformation

In order to investigate the effects of hot deformation and deformed temperature on microstructure transformation, the SEM micrographs of specimens at the cooling rate of 2, 10 and 40°C s−1 in Figures 24 are shown in Figure 8, respectively.

Figure 8: SEM micrographs of specimens at the cooling rate of 2, 10 and 40 ℃ s–1 in Figure 2, Figue 3 and Figure 4, respectively.
Figure 8:

SEM micrographs of specimens at the cooling rate of 2, 10 and 40 ℃ s–1 in Figure 2, Figue 3 and Figure 4, respectively.

Figure 8 showed that microstructures with deformation at a temperature of 1,050and 900°C were markedly different from those without deformation. In the microstructure of specimens with deformation at temperature 1,050°C, the grain sizes of QPF and AF decreased and corresponding M/A islands became finer and disperse. In addition, in the microstructure of specimens with deformation at temperature 900°C, the oriented M/A islands and the prior austenite grain boundary networks were essentially eliminated. Meanwhile, the grains were distributed in a random manner. The above phenomenon could be explained as follows. When the specimens were deformed at temperature 1,050°C, austenite recrystallization led to the finer grain and small M/A islands. In addition, when the specimens were deformed at temperature 900°C, high densities of substructure and dislocation could be formed in the austenite, which increased the nucleation sites of AF, impeded the growth of the coherent and/or semicoherent γ/α interface and accelerated diffusion of carbon to the γ/α interface. At the same time, if the carbon contents of austenite near the γ/α interface were relatively decreased under deformation conditions, the corresponding M/A islands sizes could be decreased and the degree of dispersion could be increased.

Liang et al. [4] have attempted to discuss the thermodynamics and kinetics of the transformation of bainite in low-carbon steels. It can be concluded that nucleation rate played an important role in the morphology of ferrite and bainite in low-carbon steel. And nucleation rate was dependent on the driving force, which was mostly related to two factors: the transformation temperature and the cooling rate.

Deformation at 1,050°C resulted in complete recrystallization of the austenite, usually accompanied by grain refinement. And deformation at 900°C led to pancaked austenite grain shapes and an increase in the effective grain boundary area (surface areas per unit volume of austenite, Sv). As analyzed above all, deformed austenite increased Sv and, therefore, produced more nucleation sites for the formation of ferrite and bainite. Supposing the Gibbs free energy of original austenite was Gγ; and after deformation, the stored strain energy was defined as ΔGd; and the volume-free energy was defined as ΔGv. Then, the driving force for ferrite formation could be as shown in eqs. (3) and (4):

(3)ΔGv=GαGγ,undeformedaustenite
(4)ΔGvd=Gα+ΔGdGγ,deformedaustenite

Upon comparing the two eqs. (3) and (4), it can be seen that the driving force for ferrite transformation was higher for the deformed austenite, which increased the nucleation sites of AF and promotes the AF transformation.

With the combined consideration of ferrite and bainite transformed from austenite with and without deformation, it could be concluded that the size and morphology of ferrite and bainite were closely related to the controlled cooling rates. And a schematic diagram of Gibbs free energy changes for ferrite transformed from austenite is shown in Figure 9. In particular, T0 was the temperature at which the two phases (austenite and ferrite) have the same energy. ΔT was signed as an undercooling degree (where ΔT=T0T, where T was the undercooling temperature).

Figure 9: Schematic diagram of free energy changes for ferrite transformed from austenite.
Figure 9:

Schematic diagram of free energy changes for ferrite transformed from austenite.

It can be obtained that the deformation in austenite would increase the free energy of austenite (ΔGd) compared to austenite without deformation at the same undercooling degree (ΔT). And it was also known that a large undercooling degree ΔT could cause a high nucleation rate, which resulted in the smaller size of ferrite or bainite microstructure accompanied with M/A.

Conclusion

  1. The microstructure formed in static and dynamic CCT was pearlite, QPF, AF, GB, UB and the accompanying martensite/austenite constitute (M/A island) depending on cooling rate and transformation temperature. In addition, LB was also formed in static CCT.

  2. The transformation curves of AF and GB moved toward to the left in dynamic CCT in comparison with the static CCT, which indicated that deformation promotes the formation of QPF and AF. Hence, the AF transformation area was enlarged and LB was not formed in dynamic CCT.

  3. As analyzed by thermodynamics and kinetics, finer bainite and the accompanying M/A could be obtained by reducing the bainite nucleation activation energy barrier as follows: (i) increasing the undercooling by increasing the cooling rate; (ii) increasing the stored energy by deformation of the austenite.

Acknowledgments

This work was financially supported by the Project of High-tech Ships of Ministry of Industry and Information Technology of the Peoples Republic of China (Grant Nos. [2014] 508).

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Received: 2018-01-05
Accepted: 2018-06-03
Published Online: 2018-09-04
Published in Print: 2019-02-25

© 2019 Walter de Gruyter GmbH, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 Public License.

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  60. Microstructure and Mechanical Properties of Thick Plate Friction Stir Welds for 6082-T6 Aluminum Alloy
  61. Research Article
  62. Kinetics of oxide scale growth on a (Ti, Mo)5Si3 based oxidation resistant Mo-Ti-Si alloy at 900-1300C
  63. Calorimetric study on Bi-Cu-Sn alloys
  64. Mineralogical Phase of Slag and Its Effect on Dephosphorization during Converter Steelmaking Using Slag-Remaining Technology
  65. Controllability of joint integrity and mechanical properties of friction stir welded 6061-T6 aluminum and AZ31B magnesium alloys based on stationary shoulder
  66. Cellular Automaton Modeling of Phase Transformation of U-Nb Alloys during Solidification and Consequent Cooling Process
  67. The effect of MgTiO3Adding on Inclusion Characteristics
  68. Cutting performance of a functionally graded cemented carbide tool prepared by microwave heating and nitriding sintering
  69. Creep behaviour and life assessment of a cast nickel – base superalloy MAR – M247
  70. Failure mechanism and acoustic emission signal characteristics of coatings under the condition of impact indentation
  71. Reducing Surface Cracks and Improving Cleanliness of H-Beam Blanks in Continuous Casting — Improving continuous casting of H-beam blanks
  72. Rhodium influence on the microstructure and oxidation behaviour of aluminide coatings deposited on pure nickel and nickel based superalloy
  73. The effect of Nb content on precipitates, microstructure and texture of grain oriented silicon steel
  74. Effect of Arc Power on the Wear and High-temperature Oxidation Resistances of Plasma-Sprayed Fe-based Amorphous Coatings
  75. Short Communication
  76. Novel Combined Feeding Approach to Produce Quality Al6061 Composites for Heat Sinks
  77. Research Article
  78. Micromorphology change and microstructure of Cu-P based amorphous filler during heating process
  79. Controlling residual stress and distortion of friction stir welding joint by external stationary shoulder
  80. Research on the ingot shrinkage in the electroslag remelting withdrawal process for 9Cr3Mo roller
  81. Production of Mo2NiB2 Based Hard Alloys by Self-Propagating High-Temperature Synthesis
  82. The Morphology Analysis of Plasma-Sprayed Cast Iron Splats at Different Substrate Temperatures via Fractal Dimension and Circularity Methods
  83. A Comparative Study on Johnson–Cook, Modified Johnson–Cook, Modified Zerilli–Armstrong and Arrhenius-Type Constitutive Models to Predict Hot Deformation Behavior of TA2
  84. Dynamic absorption efficiency of paracetamol powder in microwave drying
  85. Preparation and Properties of Blast Furnace Slag Glass Ceramics Containing Cr2O3
  86. Influence of unburned pulverized coal on gasification reaction of coke in blast furnace
  87. Effect of PWHT Conditions on Toughness and Creep Rupture Strength in Modified 9Cr-1Mo Steel Welds
  88. Role of B2O3 on structure and shear-thinning property in CaO–SiO2–Na2O-based mold fluxes
  89. Effect of Acid Slag Treatment on the Inclusions in GCr15 Bearing Steel
  90. Recovery of Iron and Zinc from Blast Furnace Dust Using Iron-Bath Reduction
  91. Phase Analysis and Microstructural Investigations of Ce2Zr2O7 for High-Temperature Coatings on Ni-Base Superalloy Substrates
  92. Combustion Characteristics and Kinetics Study of Pulverized Coal and Semi-Coke
  93. Mechanical and Electrochemical Characterization of Supersolidus Sintered Austenitic Stainless Steel (316 L)
  94. Synthesis and characterization of Cu doped chromium oxide (Cr2O3) thin films
  95. Ladle Nozzle Clogging during casting of Silicon-Steel
  96. Thermodynamics and Industrial Trial on Increasing the Carbon Content at the BOF Endpoint to Produce Ultra-Low Carbon IF Steel by BOF-RH-CSP Process
  97. Research Article
  98. Effect of Boundary Conditions on Residual Stresses and Distortion in 316 Stainless Steel Butt Welded Plate
  99. Numerical Analysis on Effect of Additional Gas Injection on Characteristics around Raceway in Melter Gasifier
  100. Variation on thermal damage rate of granite specimen with thermal cycle treatment
  101. Effects of Fluoride and Sulphate Mineralizers on the Properties of Reconstructed Steel Slag
  102. Effect of Basicity on Precipitation of Spinel Crystals in a CaO-SiO2-MgO-Cr2O3-FeO System
  103. Review Article
  104. Exploitation of Mold Flux for the Ti-bearing Welding Wire Steel ER80-G
  105. Research Article
  106. Furnace heat prediction and control model and its application to large blast furnace
  107. Effects of Different Solid Solution Temperatures on Microstructure and Mechanical Properties of the AA7075 Alloy After T6 Heat Treatment
  108. Study of the Viscosity of a La2O3-SiO2-FeO Slag System
  109. Tensile Deformation and Work Hardening Behaviour of AISI 431 Martensitic Stainless Steel at Elevated Temperatures
  110. The Effectiveness of Reinforcement and Processing on Mechanical Properties, Wear Behavior and Damping Response of Aluminum Matrix Composites
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