5
International RILEM Conference on Materials, Systems and Structures in Civil Engineering
Conference segment on Service Life of Cement-Based Materials and Structures
22-24 August 2016, Technical University of Denmark, Lyngby, Denmark
Table 3: Characterization of cement compositions.
Nos Cement
compositions Na
2
O – content %, by mass
Al
2
O
3
/ SiO
2
1
portland cement + H
2
O
0.60
0.242
2
portland cement+MK +H
2
O 0.51
0.366
3
portland cement + SG
1.70
0.210
4
portland cement+MK+ SG
1.61
0.325
3.2 Interfacial transition zone
The presence of active Al
2
O
3
intensifies structure formation processes in the interfacial
transition zone “cement stone – aggregate”. This is confirmed by the results of studies of
physico-mechanical characteristics of the interfacial transition zones and visual observation of
changes in it state on the model system “cement–basalt bar”.
Microphotos of the interfacial transition zones show flow of destructive processes in case of
portland cement without metakaolin additive (Fig 1).
Figure 1:
Microphotos of the interfacial transition zone of the model system “cement
stone
basalt bar”: 1 – cement stone; 2 – interfacial transition zone; 3 – basalt bar.
a – cement composition: “portland cement + water”; b – cement composition: “portland
cement + soluble glass (
s
= 2.87; = 1300 kg/m
3
)”
It is clearly seen that the interfacial boundary has lost its geometry and clearness as compared
to its primary state, the edges of basalt are “eaten” (eroded), and the interfacial transition zone
is rather wide and filled with products of corrosion of whitish colour. Microcracks stretching
in the direction perpendicular to basalt aggregate and which are evidently caused by the
increasing pressure in the interfacial transition zone are clearly visualized in the body of
cement stone. The metakaolin additive somewhat changes picture for better (Fig. 2). No
microcracks are seen. The products of corrosion are present but in lower quantities and edges
of the basalt aggregate are more clear and not so heavily eroded (“eaten”) by corrosion, as in
the first case.
6
International RILEM Conference on Materials, Systems and Structures in Civil Engineering
Conference segment on Service Life of Cement-Based Materials and Structures
22-24 August 2016, Technical University of Denmark, Lyngby, Denmark
Figure 2:
Microphotos and elemental distribution in the interfacial transition zone of the
model system “cement stone basalt bar”: 1 – cement stone; 2 – interfacial transition zone; 3
– basalt bar.
a – cement composition: “portland cement + metakaolin + water”; b – cement composition:
“portland cement + metakaolin + soluble glass ( s=2.87; = 1300 kg/m
3
)”
4. Structure formation processes in the interfacial transition zone.
In compliance with the data of X-ray analysis, a phase composition of the hydrated
dispersions in the interfacial transition zone of the concrete made with the cement
composition 1 (Table 2) is represented briefly (Fig. 3, Curve 2), by the following reaction
products:
6
S
3
H (d = 0.335; 0.284; 0.246; 0.237; 0.225; 0.180 nm),
2
SH (d =0.284; 0.270;
0.246; 0.190; 0.180 nm),
3
S
2
H (d = 0.560; 0.284; 0.184 nm),
(
)
2
(d = 0.487; 0.311;
0.261; 0.193; 0.180 nm),
3
(d = 0.303; 0.229; 0.210; 0.193; 0.188 nm). Weak lines of
the phase corresponding to the
2
4
type (d = 0.717; 0.376; 0.266; 0.258; 0.246 nm) were
identified. An X-ray amorphous phase of the calcium silicate gel, which can be formed in the
interfacial transition zone and to weaken it, was not identified in the X-ray pattern. However,
judging by the elemental distribution in the interfacial transition zone and with account of a
relatively high value of expansion (+0.44 mm/m), this possibility may exist and is supported
to a great extent by the increased contents of
and Si in the interfacial transition zone. As it
is seen from the microphotos, the interfacial transition zone is not clear, thus supporting this
assumption.
The use of the alkali activated portland cement (Table 2, Composition 3) results in changes in
the diffraction picture of the model of the interfacial transition zone (Fig. 3, Curve 5). So, the
hydration of the cements deepens, what is seen from the reduction of intensity of the initial
diffraction lines. A re-distribution of the phase formation in the direction of synthesis of the
more low-basic calcium silicate hydrates CSH(I) (d = 0.283; 0.270; 0.247; 0.179 nm),
tobermorite (d = 0.560; 0.307; 0.299; 0.283; 0.227; 0.208; 0.183 nm) types takes place. The
lines corresponding to
(
)
2
are completely absent. This
allowed to make a conclusion