Mechanical characteristics of self-compacting concretes with different filler materials, exposed to elevated temperatures

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    O R I G I N A L A R T I C L E

    Mechanical characteristics of self-compacting concretes

    with different filler materials, exposed to elevatedtemperatures

    N. Anagnostopoulos K. K. Sideris A. Georgiadis

    Received: 7 April 2008 / Accepted: 11 December 2008 / Published online: 24 December 2008

    RILEM 2008

    Abstract In this paper, the studies concern the

    influence that different fillers have on the properties

    of SCC of different strength classes when exposed to

    high temperatures. A total of six different SCC and

    two conventional concrete mixtures were produced.

    The specimens produced are placed at the age of

    180 days in an electrical furnace which is capable of

    reaching 300C at half an hour and 600C at 70 min.

    The maximum temperature is maintained for an hour.

    Then the specimens are let to cool down in the

    furnace. The hardened properties measured after fireexposures are the compressive strength, splitting

    tensile strength, water capillary absorption and the

    ultrasonic pulse velocity. Explosive spalling occurred

    in most cases when specimens of higher strength

    class are exposed to high temperatures. The spalling

    tendency is increased for specimens of higher

    strength class C30/37 irrespective of the mixture

    type (SCC or NC) and the type of filler used.

    Keywords Filler materials Glass filler

    Mechanical characteristics Self-compacting concrete Slag Temperature

    1 Introduction

    1.1 General

    An SCC is due to its various advanced properties

    most useful regarding to the structure industry. The

    ability to self compact without the use of any vibrator

    allows SCC to pass through dense reinforcement and

    fill in restricted sections, guaranteeing time superior

    quality of the cast structure at the same. Moreover the

    fact that the compaction takes place while casting,without any further delay, ensures a tight and

    accurate construction schedule. The feature of self

    consolidation is partly based on a new method for the

    production and quality control of SCC [1] which

    involves lower water to binder ratio, accumulates the

    use of filler materials and the addition of superplast-

    icizer in order to achieve the desired workability.

    Many scientists have reported the similarity of SCC

    with high performance concrete (HPC), which is also

    produced with decreased water to cement ratio and

    certain chemical admixtures [2, 3]. The problem thatoccurs is the behavior of such concrete mixtures

    when exposed to high temperatures.

    In general, concrete as a building material has a

    reasonably good fire resistance. But when SCC or

    HPC is used there are some complications. These

    complications concern microstructure changes which

    grow along with the increasing temperature [4]. At

    certain temperatures there is apparent deterioration

    mostly due to the dehydration of CSH gel and the

    N. Anagnostopoulos K. K. Sideris (&) A. GeorgiadisLaboratory of Building Materials, Democritus University

    of Thrace, P.O. Box 252, Xanthi 67100, Greece

    e-mail: [email protected]

    Materials and Structures (2009) 42:13931405

    DOI 10.1617/s11527-008-9459-6

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    increasing pore water pressure. The finer pore

    distribution along with the poor pore connectivity

    that characterizes SCC and HPC keeps the free and

    chemically bound water trapped inside the structure,

    leading to growing pore pressure [2, 3, 5]. When high

    temperature and high heating rate are applied, the

    concretes fire resistance is most likely to decreaseand thus spalling to occur.

    1.2 Objective

    Considering that SCC is a newer type of concrete

    compared to the traditional concrete or even HPC, the

    research performed on SCC after fire exposure is yet

    limited. As reported in [2] the SCC mixtures which

    are subjected to fire have an explosive spalling

    tendency which is evident in concrete mixes of higher

    strength classes, while SCC of lower strength classeshas a rather good fire resistance. In this contribution

    the efforts are focused on producing SCC of different

    strength classes which incorporate different filler

    materials, in order to investigate their performance

    after exposure at gradually up scaled temperature.

    2 Materials and methods

    2.1 Materials and mixtures

    A total of six SCC and two NC mixes are produced

    for this study. The same class of blended cement

    (CEM II 42, 5 N) is used in all cases to produce

    strength classes such as C25/30 and C30/37, accord-

    ing to EN206-1 [6]. Coarse aggregates consisting of

    crushed granite and limestone sand are used. A high

    range water reducing carboxylic either polymer

    admixture is added in different dosages to achieve

    slump of 190 mm in the case of NC, or self

    compactibility in the case of SCC. The filling

    materials used for the production of all SCC mixesare respectively: limestone filler, slag and glass filler.

    The cement-filler material chemical compositions as

    well as the aggregate grading curves are listed in

    Tables 1, 2 respectively. In all cases the water/

    cement ratios as well as the cement content are kept

    relatively the same for each strength class. Moreover

    the slump flow tests and slump tests with reference to

    SCC and NC correspondingly were attempted to be of

    the same order of value and thus to present respective

    properties while in fresh state. The mix proportions of

    all concretes are presented in Table 3.

    2.2 Specimens and temperatures

    The mixing is carried out in a pan mixer according tothe European Guidelines for SCC [7]. Right after the

    mixing is completed the SCC is tested accordingly as

    instructed in EFNARC specifications [8]. A number

    of 150-mm cubes are prepared in order to assess the

    compressive strength and the water capillary absorp-

    tion at the age of 28 days. The water capillary

    absorption is measured according to the procedure

    described by RILEM TC116 [9]. The 150-mm cubes

    are tested for compressive strength after a period of

    Table 1 Chemical composition of cement and filling materials

    (%)

    Sample CEMII-A/M

    42.5 N

    Limestone

    filler

    Ladle

    furnace slag

    Glass

    filler

    SiO2a 23.85 1.8 32.5 62.1

    Al2

    O3

    5.22 0.45 2.5 1.6

    Fe2O3 4.13 0.08 0.1

    FeO 1.72

    CaO 58.2 54.8 54.1 18

    MgO 3.2 0.68 5.55 2.4

    SO3 3.3 0.05 0.2

    K2O 0.68 0.04 0

    Na2O 0.32 0.34 12.4

    TiO2 0.24 0.17

    P2O5 0.06 0.02 0.1

    SrO 0.03

    Cr2O3 0.02 ZnO 0.01

    LoIb 1.57 40.5 3.19 0.4

    SGc (g/cm3) 3.1 2.65 2.59 2.51

    a All the samples are expressed by weigh percentageb Loss of ignitionc Specific gravity

    Table 2 Composition of materials used (%)

    Aggregate passing 0.25 0.5 1 2 4 8 16 32Limestone sand 6 18 56 81 100 100 100 100

    Coarse aggregates 0 0 0 0 12 57 100 100

    All fine materials pass through the 0.125-mm sieve

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    28 days of moist curing (20 2C, RH C 95%), as

    the mean value of three specimens. Fire resistance is

    measured on 100-mm cubes and 150 9 300-mm

    cylinders. Those specimens also go through moist

    curing for 28 days and are then left at ambience

    (20 2C, RH C 65%), and not tested till the age of

    fire tests (180 days).

    Right before fire exposure at the age of 180 days

    three 100-mm cubes of each mixture are dried to

    constant mass at 105C. Table 4 shows the moisture

    content that is afterwards determined as following:

    W= (m0 - md)/mdmd = mass of the test specimen after drying at

    105C

    m0 = mass of the specimen before drying

    At the age of 180 days the specimens which meant

    to be exposed to high temperatures are heated in an

    Table 3 Mix design proportions and fresh properties of self-compacting concretes (SCC) and normal concretes (NC)

    Mix design proportions (kg/m3) Self compacting concrete Normal concrete

    L-filler Slag Glass filler

    SCC SCC SCC SCC SCC SCC NC NC

    C25/30 LF C30/37 LF C25/30 SL C30/37 SL C25/30 GF C30/37 GF C25/30 NC C30/37 NC

    CEMII-A/M 42.5 N 335 375 340 375 340 380 330 375

    Filler 135 100 0 0 0 0 0 0

    Slag 0 0 135 100 0 0 0 0

    Glass filler 0 0 0 0 130 100 0 0

    Sand 915 900 825 862 845 862 940 870

    Coarse aggregates 800 800 800 800 800 800 927 955

    Water 185 186 188 189 190 194 183 186

    Super plasticizer (%)a 1.63 1.88 1.29 1.74 1.16 1.17 1.0 1.0

    W/C 0.55 0.50 0.55 0.50 0.56 0.51 0.55 0.50

    W/P 0.39 0.39 0.40 0.40 0.40 0.40 0.55 0.50

    Air content (%) 1.70 1.60 1.90 1.70 1.40 1.20 2.10 1.80Slump (cm) 19 20

    Slump flow D (cm) 75.5 75 75.5 75.5 74 73.5

    t50 (s) 2 1.72 4.72 4.25 1.66 1.25

    V funnel 1 (s) 10.5 10 8.49 9.18 4.38 6.06

    V funnel 2 (s) 28 15 14.4 11.25 5.16 13

    J ring H (cm) 0.3 0.3 1 0.9 0.6 0.5

    J ring D (cm) 68 68 67 68 66 68

    LBOX (h2/h1) 0.88 0.88 0.83 0.85 0.82 0.84

    t200 (s) 1 1 2.5 3.41 1.2 1.35

    t400 (s) 2.01 3 5.5 5.1 1.4 2.25

    fc28 (Mpa)b 37.1 54 37.7 53.5 38.3 49 36 52.7

    a SP (super plasticizer) value is measured by % percent by weight of the entire fines amount (cement and filler materials)b

    Compressive strength at the age of 28 days is measured in specimens of 150-mm edge cubes

    Table 4 Moisture content of all the mixtures at the age of 180 days

    Mixture C25/30

    CC-LF

    C30/37

    SCC-LF

    C25/30

    SCC-SL

    C30/37

    SCC-SL

    C25/30

    SCC-GF

    C30/37

    SCC-GF

    C25/30

    NC

    C30/37

    NC

    Moisture content (%)a 4.41 3.39 3.17 3.18 4.01 4.11 3.98 3.93

    a Moisture content is measured in specimens of 100-mm edge cubes

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    electrical furnace Fig. 1. Two peak temperatures are

    examined to determine the specimens fire resistance:

    300 and 600C. The heating rate applied is 10C/min

    until the target temperature is reached, and this is

    maintained for a period of 1 h, Fig. 2. When the

    heating period finishes, the furnace remains sealed for

    24 h in order to cool down the specimens down to theambient temperature. Then the specimens are tested

    to determine properties such as compressive strength,

    splitting tensile strength and pulse velocity.

    2.3 Compressive strength

    The compressive strength is measured according to

    EN 12390-3 [9]. The original compressive strength is

    measured on 150-mm cubes which are tested at the

    age of 28 days in order to specify the concretes

    strength class. Residual compressive strength ismeasured after the fire tests on 100-mm cubes. A

    Buehl & Fabel compression testing machine with

    3000 KN capacity is used in all cases.

    2.4 Splitting tensile strength

    Splitting tensile strength is determined by measuring

    the tensile strength on 150 9 300-mm cylinders at

    different peak temperatures so that the residual

    tensile strength is assessed in each case. According

    to EN 12390-6 [10] a splitting attachment (CON-TROLS Model 50-C9000) is adjusted on the

    laboratory compression testing machine.

    2.5 Water capillary absorption

    The water capillary absorption is measured according

    to the procedure described by RILEM TC116 [11].

    That property is measured on pre-weighted 150-mm

    cubes. Specimens are placed on adjusted plastic

    plates filled with water, so that only one surface of the

    specimen is getting wet. Then the specimens areweighted in regular intervals and the absorbed water

    quantity is estimated.

    2.6 Stressstrain curves

    100-mm cubes are used in order to calculate stress

    strain curves at the age of 180 days. The specimensFig. 1 Indicative seating plan of the specimens in the furnace

    Fig. 2 Temperature development of 300C (left) and 600C (right)

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    are placed on the laboratory compression testing

    machine and stressstrain sensors are adjusted on the

    upper metallic plate of the pressing device. As soon

    as the specimen is loaded, the sensors transmit

    electric signal to the data logger which is converted

    through a computer programme into stressstrain

    curves.

    2.7 Pulse velocity

    Pulse velocity is measured on 100-mm cubes accord-

    ing to the procedure described by EN 12504-4 [12].

    Specimens are tested at the age of 180 days before

    and after fire tests using a PUNDIT ultrasonic pulse

    velocity testing device.

    3 Results and discussion

    3.1 Original compressive strength

    The compressive strength results at the age of

    28 days are presented at Table 3 for all prepared

    concrete mixes. While studying the compressive

    strength results it emerges that in almost all cases

    SCC develop higher values as compared with NC of

    the same strength class. This is attributed to the

    changes of the interfacial transition zone (ITZ)

    caused by the different filler materials [13]. Asreported in Zhu and Bartos [14] ITZ is denser and

    significantly more uniform in SCC than in NC.

    Moreover as Traghard points out, the porosity of ITZ

    is much lower in SCC than in NC of the same w/c

    ratio, as the hydrated phases and unhydrited particles

    appear to be more evenly distributed between the ITZ

    and bulk density of SCC [15].

    In the case of SCC, it appears that there are slight

    variations as it regards their compressive strength

    values. The use of different filler materials for SCC

    mixture production has everything to do with these

    deviations. SCC mixtures which are produced usingladle furnace slag as a filler material have higher

    water absorption than expected, resulting to a viscous

    and rather slow concrete, while in fresh state. On

    the other hand, when limestone filler is used the

    mixture performance is excellent in terms of rheo-

    logical and mechanical characteristics. Similar

    performance is noted in the case of glass filler with

    even better rheological features. As mentioned

    before, all mixtures are produced by keeping the w/c

    ratio relatively the same. That means that in relation to

    their absorption requirements, certain porosity isdeveloped in each case, which is finally reflected in

    the compressive strength values.

    3.2 Residual compressive strength

    What would be of great importance in a fire scenario

    is definitely the state of the concretes mechanical

    properties. The residual compressive strength for all

    SCC and NC mixtures after heating in 300 and 600C

    is presented in Fig. 3. As Chan reports in his

    investigation there are three temperature ranges fromthe point of strength loss: 20400, 400800 and

    8001200C [2, 5]. After exposing to fire HPC

    and NC mixtures prepared with ordinary Portland

    cement, Chan concludes that only a small part of the

    original strength is lost up to 400C, while severe

    Fig. 3 Compressive strength of C25/30 (left) and C30/37 (right) SCC and NC, after heating at different temperatures (300 and

    600C) compared with the compressive strength at room temperature (20C)

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    compressive strength loss occurs within the 400

    800C range. That is mostly the case for the SCC and

    NC mixtures prepared in this contribution, which are

    exposed to slightly different temperature ranges,

    though.

    Regarding the 20300C range, there is a com-

    pressive strength reduction for the SCC 25/30 whichfluctuates between 12% and 15% of its initial value,

    while for the SCC 30/37 the strength loss percentage

    reaches 18%. The corresponding strength loss per-

    centages for the equivalent 25/3030/37 NC are 18%

    and 17.6% respectively. At 600C the reduction in

    compressive strength ranges from 52% to 57% for all

    mixtures and explosive spalling occurs in cylindrical

    specimens in all cases. The phenomenon is more

    intense when ladle furnace slag is used as filler

    material and spalling occurs in 100-mm cubes as

    well. As there was no way for visible inspection,spalling is identified by hearing the series of pop outs,

    happening in most cases when the distinctive tem-

    perature of 300C is overrun.

    The use of different filler materials in the case of

    SCC does not seem to make any difference as it

    regards explosive spalling Fig. 4. During fire the

    humidity of the concrete increases along with tem-

    perature and fluid water is formed [16]. The water is

    transported inwards to the center of the specimen

    where the space is limited [16]. At a certain point the

    region becomes saturated and the entrapped water iseventually released in the form of steam by explosive

    spalling [17, 18]. The filler content used is relatively

    high (150 kg/m3) to ensure low levels of concrete

    moisture and eventually to avoid spalling due to

    steam pressure. The concept of using glass filler is the

    formation of micro-cracks which develop because of

    the thermal expansion of glass that is greater than the

    concretes [16]. Thus greater pore connectivity is

    thought to provide canals for the steam to escape.

    Ladle furnace slag is used as a filler material as itpresents cementitious behavior mainly due to its high

    content in CaO [19]. According to Piasta et al. the

    development of micro-cracks increases beyond

    300C and firstly occurs around calcium hydroxide

    Ca(OH)2 crystals [20]. Hence slag due to its cemen-

    titious properties is expected to ensure the

    development of micro-cracks which will lead to

    greater porosity.

    3.3 Moisture content and water absorption

    Since the use of different filler materials is expected

    to alter the porosity of SCC mixtures and thus to

    prevent the effect of spalling, the moisture content

    and the capillary water absorption for all mixtures are

    presented in Tables 4 and 5 respectively. As Bostrom

    et al. points out, SCC has a high probability of

    spalling when exposed to fire compared to conven-

    tional concrete [21]. Considering the low

    permeability of SCC due to its denser structure,

    water vapor is very limited to evaporate out of SCC.

    Lower moisture content is therefore of great signif-icance, since the accumulated pore pressure is

    accordingly minimized.

    The concrete mixtures produced in this investiga-

    tion vary with reference to their capillary water

    absorption since they belong to different strength

    classes. Concrete mixtures of the lower strength

    classC25/30appear to have greater water capillary

    absorption values compared to C30/37. Lower w/c

    ratios as well as the higher cement content that is

    used for the C30/37 production forms a tighter

    structure which eventually results in lower perme-ability. Water capillary absorption values are in all

    cases lower in SCC compared to NC of the same

    strength class, probably due to a more efficient

    packing that is achieved by the use of filler materials.

    Among SCC mixtures the one produced with glass

    filler seems to have greater water absorption values,

    since the w/c ratio in that occasion is somewhat

    higher. SCC produced with ladle furnace slag appears

    to be less permeable than the remaining mixturesFig. 4 Spalled specimens after exposure at high temperature

    (600C)

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    mainly due to its denser microstructure, while

    limestone filler performed similarly. In any occasion

    there is explosive spalling when the peak temperature

    of 600C is maintained when all concretes of both

    strength classes are tested, and this is valid irrespec-

    tive of the strength class and the filler material used.

    3.4 Pulse velocity

    The significant changes which concrete specimens

    undergo as far as their pore structure is concerned,

    when heated at different peak temperature are

    assessed by the pulse velocity test. The results are

    plotted in Fig. 5 where the residual pulse velocity is

    expressed as the ratio of the pulse velocity after

    exposure to each peak temperature to the initial value

    at ambient temperature. Using pulse velocity propa-

    gation is possible to figure out through a non

    destructive method, the extent of deterioration due

    to elevated temperatures or even the presence of

    cracks and voids [22]. A decrease in velocity

    indicates the initiation of cracks in the concrete mass

    and increase in the porosity [2]. According to Piasta

    the development of micro-cracks in cement paste

    increases significantly beyond 300C [20]. Lin et al.

    further confirms that the majority of the cracks and

    the extremely large cracks are formed between 300

    and 500C [23].

    The relative pulse velocity results in this research

    coincide well with the above made statements, as

    there is a slight reduction in the slope up to 300C

    and then the angle of gradient is greater for the

    temperature range of 300600C for all mixtures

    Fig. 5 (C25/30-left and C30/37-right). For the con-

    crete mixtures which belong to the lower strength

    classC25/30the relative pulse velocity is almost

    identical for all mixtures after exposure at 300C. At

    the following temperature range (300600C) more

    severe degradation occurs. After exposure to 600C

    SCC produced with limestone filler have the best

    performance and SCC with ladle furnace slag appear

    to have suffered greater deterioration. That is mostly

    the case for the C30/37 mixtures. After exposure at

    600C all SCC specimens containing slag suffer

    severe deterioration due to explosive spalling. With

    the exception of all mixture produced with slag,

    SCCs of the higher strength class perform slightly

    higher residual values compared to ordinary concrete

    after exposure to 600C.

    3.5 Residual tensile strength

    With a close look at the tensile splitting strength in

    Fig. 6 it becomes evident that there is a sharp loss of

    tensile strength compared to a rather smoother declin-

    ing curve which corresponds to the compressive

    Table 5 Capillary water absorption (g/cm2

    )

    Time/mix C25/30

    SCC-LF

    C30/37

    SCC-LF

    C25/30

    SCC-SL

    C30/37

    SCC-SL

    C25/30

    SCC-GF

    C30/37

    SCC-GF

    C25/30

    NC

    C30/37

    NC

    T /10 min 0.1578 0.1022 0.1428 0.1122 0.1569 0.1448 0.1444 0.0933

    T /24 h 0.5133 0.4133 0.5019 0.4003 0.5180 0.4536 0.5444 0.4667

    Fig. 5 Ratio of residual pulse velocity [V(T)] after peak temperature to the pulse velocity at room temperature [V(20C)] of C25/30

    (left) and C30/37 (right) for SCC and NC

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    strength loss at different peak temperatures [2, 5].

    Chan et al. [5] attribute this to the presence of many

    micro or macro cracks that are produced in the

    specimens due to thermal incompatibility.

    The tensile splitting strength results for the C25/30

    mixtures are plotted in Fig. 6 consisting of two

    descending branches, exhibiting the strength loss at

    20300 and 300600C temperature ranges respec-

    tively. All mixtures of this strength class tend to a

    similar decrease from 20 to 300C. SCC with

    limestone filler appear to have the best perfor-

    mance, from 300 to 600C. On the other hand SCC

    with ladle furnace slag in its composition along

    with SCC using glass filler follows similar decline

    with NC and suffers the greater loss of tensilestrength at the range of 300600C. Splitting

    tensile strength results are only plotted from 20

    to 300C regarding to the higher strength class

    concrete, since all the cylinders which belong to

    that strength category spall explosively. SCC with

    limestone filler manage in this case also to

    maintain greater percentage of its original tensile

    strength compared to the rest SCC and NC of the

    same strength class.

    3.6 Stressstrain curves

    The stressstrain curve, representing the deformation

    and mechanical characteristics, is an important

    material characteristic of concrete [24]. It is also

    important to extract results for the concrete attributes

    from the stressstrain curves at elevated tempera-

    tures, although many coexisting effects determine the

    shape of the curve. In this study, an attempt is made

    to observe the difference of the stressstrain curves

    among SCC mixtures prepared with several filler

    materials compared to normal concrete.

    As it is observed in Fig. 7, there is no noticeable

    difference between SCC and NC in the shape of the

    curves, either between SCC with different filler

    materials. Generally, the ascending phase of all the

    curves as the temperature increases becomes

    smoother especially at high temperatures (600C)

    while the peak strain increases and the peak strength

    decreases. It must be mentioned that there could be a

    pronounced concave-up curve at the beginning of

    loading due to the pre-existing cracks caused by

    heating and cooling [25]. Comparing the curves

    between the two strength classes it can be mentioned

    that the higher the strength class, the more rapid theascending phase and the more linear the descending

    one, due to the stiffness softening of the specimens at

    all temperatures respectively. Also, the percent of

    peak strain increasing is for the C25/30 mixtures 12

    15% and for the C30/37 mixtures 710% at 300 and

    at 600C the respective percent is 6065% and 50

    55%. Finally, SL mixtures give the impression of

    having more linear phases and rough curve distribu-

    tion before and after the peak strength compared to

    the GF mixtures that have the smoother distribution.

    3.7 Model suggestion

    The model equations which are proposed in order to

    evaluate the mechanical characteristics for both

    unheated and heated concrete are shown in the

    following equations [25]. In this paper the residual

    mechanic characteristics (only the peak values) are

    evaluated and compared with the values that have

    been produced by the experimental program at

    Fig. 6 Tensile strength of C25/30 (left) and C30/37 (right) for SCC and NC after heating at different temperatures

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    different temperatures (T). In particular the residual

    peak strength value (fcr) is evaluated by Eq. 1 using

    original compressive strength (fc). Equation 2

    expresses the peak strain value (eor) using the

    unheated peak strain. The residual tensile strength

    (ftr) is calculated by Eq. 3 using the experimentally

    measured tensile strength (ft), whilst Eq. 4 evaluates

    the residual modulus of elasticity (Ecr).

    fcr=fc 1:008T

    450ln T5800

    !0:0; 20C\T800C1

    Fig. 7 Stressstrain curves of C25/30 (left) and C30/37 (right) of NC (a, b) and SCC (ch) after heating at different temperatures

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    ftr=ft 1:05 0:025 T;

    0:80;1:02 0:0011 T!0;

    8