CA1122231A

CA1122231A - Expansive cement compositions

Info

Publication number: CA1122231A
Application number: CA000311342A
Authority: CA
Inventors: Wendell W. Moyer, Jr.; Robert Smith-Johannsen
Original assignee: Raychem Corp
Current assignee: Raychem Corp
Priority date: 1977-09-19
Filing date: 1978-09-14
Publication date: 1982-04-20
Also published as: IT7827769A0; IE781869L; SE7809821L; GB2004529A; DE2840572A1; FI63735B; IL55575A0; NO145232B; DK411178A; FI782851A; IE47357B1; ES473348A1; SE434733B; BE870477A; IT1098856B; JPS5493020A; GB2004529B; FR2403311A1; NO783104L; NO145232C

Abstract

Abstract of the Disclosure The invention relates to expansive cement compositions and to expansion agents containing free lime for use in such composition.
Novel expansion agents are prepared according to the invention by heating lime of particle size less than 250 microns in an atmosphere comprising water vapor at 100 to 400°C. or carbon dioxide at 350 to 850°C., or by heating a partially hydrated lime at a temperature of at least 100°C.
The encapsulated limes produced in this way are useful as expansion agents in hydratable cement compositions, the amount thereof generally being less than 30%, preferably 3 to 10%, based on the weight of the cement and the additive.
Cement compositions containing the novel expansion agents are useful in a wide variety of uses where shrinkage of the composition on drying has to be prevented or reduced.

Description

~R.~2~3~

This invention relates to expansive cement compositions.

Co~,positions which contain hydratable cements (generally Portland cement) tend to shrink on drying. It is known to counteract this undesirable tendency by including in the composition an expansion additive which expands at the correct stage during the drying of the composition [see for example Gen. Civ. 109, 285 (1936, H. Lossier), U.C. SESM
Report No. 72-13 tl973, G. Komendant et al.), Plan. Bau 2, 351 (1951, H. Bickenbach), Concrete Technology and Practice, 3rd Edn, 359 (1969, W.H. Taylor) and U.S. Patents Nos.
3,519,449, 3,649,317, 3,801,339, 3,883,361, 3,a84,710, 3,947,288 and 4,002,483~. In many of the known expansion additives, the active ingredient is free lime (CaO), also known as quicX lime, which expands by about 100% in volume when hydrated, the other ingredients being présent to prevent the h~dration taking place until the desired stage in the drying of the cement composition. Free lime is one of the ingredients of Portland cement, but an excess of it i8 normally regarded as undesirable, and the addition of free lime to cement compositions is avoided. Free lime does not serve as an expansion additive because it is very rapidly hydrated and therefore expands far too early in the setting process to be effective. It is also known (see for example U.Sc Patent No. 3,106,453 and German Patent No.
1,216,753~ to subject free lime to certain specific treatments with water and/or CO2 to produce a lime which hydrates at a slower rate, but the products obtained are ineffective as expansion additives. ~ik~wise the products obtained by exposing lime to the atmosphere, which products contain Ca(OH)2 and CaCO3, are ineffective as expansion additives. ~t has also been proposed in U.S.
Patent No. 1,732,409 to make ~uicX-setting lime products which contain a high proportion of lime, at least some of the lime being in the form of a product obtained by heating ~.~3~

finely divlded lime in an atmosphere containing CO2 at a temperature of 500 to 850C until the increase in weight is 3 to 40~ based on the weight of the starting material.

We have now discovered that excellent expansion additives for cement compositions can be made by heating particles comprising CaO in the presence of water vapor and/or CO2, or simply by heating particles comprising CaO
and a sufficient amount of calcium hydroxide which has been formed by absorption of water vapor.

In one aspect, the invention provides a pulverulent composition which is useful as an expansion additive for hydratable cement compositions; which consists essentially of particles (a) having a size less than 250 microns and (b) comprising a core of calcium oxide and a protective coating around said core of calcium hydroxide or calcium carbonate or both; which contains 36 to 95% by weight of calcium oxide; and which exhibits an Expansion Factor (as hereinafter defined) of at least 0.06%. Such compositions can be made by a process which comprises heating particles (a) having a size less than 250 microns and (b) comprising at least 36% by weight of CaO, with the remainder (if any) preferably consisting essentially of Ca(OH)2 and/or CaCO3, the particles being maintained at a temperature of at least 100C and, if the particles initially contain less than ~% by weight of Ca(OH)2, the particles being maintained at a temperature of 100 to 40~C in an atmosphere which comprises water vapor or at a temperature of 350~ to 850C. in an atmosphere which comprises carbon dioxide, said heating being carried out under conditions such that the product contains 36 to 95% by weight of CaO and exhibits an Expansion Factor (as hereinafter defined) of at least 0.06~.

~2Z~3~

The invention also includes the use of such lime-containing compositions as expansion additives in hydratable cement compositions, in particular cement compositions comprising a Portland cement, water and a lime-containing composition as defined above in amount less than 30%, based on the combined weight of the cement and the lime-containing composition. The invention further includes a method of making a shaped article which comprises casting a cement composition as defined above.

Except where otherwise noted, parts and percentages in this specification are by weight. The Expansion Factor of a lime-containing composition is defined herein as the % increase in length of a test prism (test bar) which has been cured in water for 7 days after casting, according to ASTM C490-70 and C157-69T, from a mortar prepared according to ASTM C305-65 and containing 0.1 part of the lime-containing composition, 0.9 part of Type III
Portland cement, 2 parts of No. 20 washed sand, and 0.4 part of water. The Expansion Factor of the treated limes of the invention is at least 0.06%, generally 0.07 to 2.5%, preferably 0.07 to 0.4%. The Expansion Factor is a measure of the effectiveness of the protective coating in delaying access of water to the calcium oxide core, and nter alia also of the calcium oxide content of the composition.

The larger is the particle size of the treated lime, the greater is its lime content for a given thickness of the protective coating. For this reason the particle size is generally at least 1 micron. On the other hand, if particles of size greater than 250 microns are used, they cause an undesirable reduction in strength. Larger particle sizes also make it more difficult to obtain a uniform distribution of the treated lime in a cement 23i composition. The treated limes preferably have a particle size of 1 to 100 microns, especially 5 .o 60 microns.

The starting materials used in this invention comprise at least 36% of CaO, with the remainder preferably consisting essentially of Ca(OH)2 and/or CaCO3. The term "consisting essentially of" is used to indicate that the starting material may contain minor amounts, generally less than 10%, of other ingredients which do not prevent formation of an effective protective coating, e.g.
impurities such as silicates and oxides of iron, magnesium and aluminum. When the treated lime is prepared by heating the starting material in the presence of water vapor and/or carbon dioxide, the starting material preferably contains at least 80%, especially at leas~ 90%, of CaO. Thus dolomitic limes, which contain lesser quantities of CaO, are not preferred starting materials.

When the atmosphere comprises water vapor, but no carbon dioxide, the temperature should be 100 to 400C., preferably 150 to 400C., especially 150 to 250C. For a given residual CaO content, the higher the temperature of the treatment, the higher the expansion activity of the product. At temperatures below 100C., the lime becomes hydrated but no effective protective coating is formed. At temperatures above 400~C, calcium hydroxide is not formed, or if present initially is at least partially decomposed.
To ensure an adequate p~otective coating, heating in an atmosphere comprising water vapor should preferably be continued for a time such that the particles increase in weight by at least 2~, e.g. 2 to 16%, particularly 4 to 12%, especially 5 to 11%, based on the weight of the starting material. ~or a starting material which consists essentially of CaO, these weight increases will result ,23~

in a product which contains at most 92%, e.g. 92 to 36%, particularly 84 to 50~, especially 84 to 50% of residual active lime as the core and a protective coating which consists essentially of calcium hydroxide.

When the atmosphere comprises carbon dioxide, a temperature of 350 to 850C. is needed in order to convert the CaO to CaCO3. At temperatures below 350C. the reaction between CaO and CO2 is very slow, and no effective protective coating is formed. At temperatures above 850C.
CaCO3 is not formed or if present initially is decomposedr To ensure an adequate protective coating, heating in an atmosphere comprising CO2 should preferably be continued for a time such that the particles increase in weight by at least 2%, e.g. 2 to 28~, particularly 4 to 16~, especially 5 to 16%, based on the weight of the starting material. For a starting material which consists essentially of CaO, these weight increases will result in a product which contains at most 95~, e.g. 36 to 95%, particularly 64 to 91%, especially

2~ 64 to 89~, of residual active lime as the core and a protective coating which consists essentially of calcium carbonate.

~t is also possible to form a protective coating comprising both CaCO3 and Ca(OH)2 by heating the starting material in an atmosphere comprising CO2 and water, preferably at a temperature of ~50 to 400C. Under such conditions, the heating should preferably be continued for a time such that the particles increase in weight by 4 to 14%, especially 5 to 12%, these weight increases corresponding to (for a starting material which consists essentially of CaO) final products containing 91 to 40~, especially ~0 to 50~ of residual active lime.

3~

As noted above, limes which have been partially hydra~ed and/or carbonated at temperatures below 100C. do not have an effective protective coating thereon and are not useful as expansion additives. Useful expansion additives can be obtained from such partial~y hydrated and/or carbonated limes by using them as starting materials in the processes described above which involves heating in an atmosphere comprising water vapor and/or CO2, provided that the product has an adequate residual calcium oxide content.
However, we have discovered that partially hydrated limes can also be converted into useful expansion additives by heating them at temperatures of at least 100C., preferably less than 500C, e.g. 200 to 400C, in an atmosphere which ,15 contains no water vapor or carbon dioxide; in this embodiment of the invention, the starting material can comprise 8 to 64%, preferably 16 to 50%, of Ca(OH)2, with the balance preferably consisting essentially of CaO. For a given CaO content, the higher is the temperature of the treatment and the longer its duration, the greater is the expansion activity of the product.

Treated limes which already have some expansion activity can be further treated by one of the processes described above to make them more active. However, it should be noted that such further treatment, especially when carried out in an atmosphere comprising water vapor at relatively low temperatures, e.g. below 200C., especially below 15GC., can reduce the residual CaO content of the treated lime to an extent such that activity is reduced.

The heat treatments described above can be carried out in any convenient way which does not involve grinding of the particles which would disrupt the protective coating.
For small quantities of product, the starting material can ~ ~ ~4 Z ~ 3 ~

simply be spread out on a pan. For larger quantities fluidised bed procedures may be used.

The novel expansion additives can be incorporated into hydratable cement compositions in any convenient way, but we have found that optimum expansion activity is obtained if the additive is added to a mixture of at least part of the cement and at least part of the water. The cement compositions can of course contain sand, aggregate and other conventional additives, but the presence of additional quicklime, hydrated lime or carbonated lime is preferably avoided. The novel additives exhibit a delayed reactivity with water, measured by ASTM Test C110-71, Section 9, of up to 100 minutes, but this does not account for the fact that in cement compositions they show a much greate~ delayed reactivity. It is thought that this unexpectedly delayed reactivity is due to some form of interaction between the protective coating and components present in the cement slurry. The amount of the additive used will depend inter alia on its CaO content and the strength and expansion deslred in the final product, and will generally be 3 to 30%, preferably 3 to 10%, especially 5 to 7%, based on the combined weight of the hydratable cement and the additive.
Especially when the treated limes have been thoroughly treated, their presence has little or no deleterious effect on such important properties of the cement composition as water re~uirements, consistency, open time, and tendency to "false setn.

' 3~

The invention is illustrated in the following Examples. The expansion activities of the various samples prepared in Examples 1-7 are shown in Table 1, which shows the % increase in length of test prisms (i.e. test bars) which (except where otherwise noted) were cured in water after casting according to ASTM C490-70 and C157-69T from mortars prepared according to ASTM C305-65 and containing 1 part of a mixture of the treated lime sample and a Type III
B lo Portland cement (Norcem~Rapid)~ 2 parts of No 20 washed Monterey sand, and 0.4 parts of water. The amount of the treated lime sample in the test prism and the number of days of curing are given in parentheses after each % expansion figure. The samples with a "C" after the sample number in Table 1 are comparative examples, not in accordance with the invention.

Example 1 Portions of CaCO3 having a particle size less than 44 microns were heated in a muffle oven at 1000C. for the time necessary to produce samples comprising CaO in amount 100~ (Sample 1), 93.6~ ~Sample 2), 90.2% (Sample or 72.3~
~Sample 4). Portions of Sample 1 were heated in a muffle oven at 580C in an atmosphere of CO2 until the CaO content was 94.5~ (Sample 5), 89.8% (Sample 6) and 80.5% (Sample 7).
Portions of a commercially available lime (Flintkote) having a particle size less than 44 microns were heated in a muffle oven at 580C in an atmosphere of CO2 until the CaO content was 94.8% (Sample 8),87.5% (Sample 9) or 74.8% (Sample 10).

Example 2 Portions of a commercially available lime (Flintkote~ containing about 95~ CaO, with the remainder Ca(OH)2 and a trace of CaCO3, and having a particle size ~ e ~a~h~

less than 44 microns, were exposed to water vapor at 22C
(Sample 11)~ 60C (Sample 12), 100C (Sample 13), 15QC
(Sample 14) or 200C (Sample 15) until the CaO content had been reduced to the level shown in Table 1.

Exam~le 3 A treated lime having expansion activity, containing 60~ CaO, 27% Ca(OH)2 and 13% CaCO3, and having a particle size less than 100 microns (Sample 16) was exposed to water vapor at 22C (Sample 17), 60C (Sample 18), 100C
(Sample 19), 150C (Sample 20) and 200C (Sample 21) until the CaO content was 31~ (Sample 17) or 40% (Samples 18-21).

Example 4 A treated lime having expansion activity, containing 85% CaO, 5% Ca(OH)2 and 10% CaCO3, and having a particle size less than 100 microns, was exposed to water vapor at 110C until the CaO content had been reduced to 64~
(Sample 22). Portions of Sample 22 were heated at 110C for 180 min. (Sample 23), at 200C for 15 min. (Sample 24), at 200C for 60 min. (Sample 25), at 300C for 15 min. (Sample 26), at 340C for 30 min. (Sample 27), at 340C for 50 min.
(Sample 28), at 400C for 90 min. (sample 29) and at 455C
for 15 min. (Sample 30). Samples 29 ~nd 30 lost 2~ and 3~
in weight, respectively, during the heat treatment, due to decomposition of calcium hydroxide. The same treated lime was exposed to water vapor at 200C until the CaO content had been reduced to 64% ~Sample 31). A commercially B availa~le lime (Diamond Springs) consisting essentially of CaO and having a particle size less than 100 microns was exposed to water vapor at 25C until the CaO content was 64%
(Sample 32). A portion of Sample 32 was heated at 340C for 60 minutes (Sample 33~. Another sample of the same commercially available lime was ~xposed to water vapor at ~ f~,J~ ~,,,~

200C until the CaO ~ontent had been reduced to 58% (Sample 34).

Example 5 Portions of a commercially available lime (Flintkote) as used in Example 2 were exposed to water vapor at 260C until the CaO content was 85~ (Sample 35) or 58%
(Sample 36). These Samples were made into mortars as described above except that a Type 1-2 cement (Kaiser 0 Permanente) was used and the amount of water was 0.36 part.
A Control mortar containing no added lime was also prepared.
The prisms cast from these mortars were c~red both in water and in 50~ relative humidity air.

Example 6 A treated lime having expansion activity, containing 84.5~ CaO, 6.2% Ca(OH)2 and 9.3% CaCO3, and having a particle size less than 100 microns was used to prepare mortars containing 0.9 part of a Type 1-2 cement (Kaiser Permanente), 0.1 part of the treated lime, 2 parts Of No. 20 washed Monterey sand and 0.36 part of water. The mortars were prepared by three different methods.
Method 1 (ASTM C305-65) - A. The treated lime and cement were dry mixed. B. The water was added and mixed at slow speed for 30 seconds. C. The sand was added and slow speed mixing continued for another 30 seconds. D. The mixer was increased to medium speed for 30 seconds. E. Pause for 90 seconds. F. Mix at medium speed for 1 min.
Method 2 - A. Mix the cement and water for 30 seconds. 8. Add the treated lime and mix for 30 seconds. C-F. Same as in Method 1.~ Ira~

Method 3 - A. The treated lime and water were mixed for 30 seconds, then the cement was added and mixed for 30 seconds. D-F. Same as in Method 1.
The % expansions of prisms cast from these mortars are shown in Table 1 under Samples 37, 38 and 39 (Methods 1, 2 and 3 respectively).

Example 7 A commercially available lime (Flintkote) was fractionated into a first fraction in which the particles were 45 to 425 microns in size and a second fraction in which the particles were less than 45 microns in size. Both fractions were heated at 950C for 1 hour and then treated with water vapor at 200C until the CaO content was 69.5%
(first fraction, Sample 40) or 73% (second fraction, Sample 41).

~2~1 Ex. Sample No. No. % CaO Expansion (parts of sample in mortar, days) 1 l(C) 100 0.042 (0.1,7) 2(C) 93.6 0.031 ( "
3(C) 90.2 0.031 ( "

4(C) 72.3 0.029 ( "
94.5 0.234 ( "
6 89.8 0.188 ( n 7 80.5 2.3 ( n 8 94.8 0.077 ( n 9 87.5 0.150 ( n 74.8 0.757 ( n 2 ll(C) 49 0.037 12(C) 53 0.043 ( n 13 53 0.125 14 57 0.212 ( n 53 0.347 3 16 60 0.61 (0.1,14) 0.067 (0.04,16) 17(C) 31 0.134 ( " ) 0.046 ( "
18 40 0.186 ( n ) 0.045 ( n 19 40 0.330 ( n ) o ~ 044 ( 0.413 ( n ) 0~058 ( 21 40 2.8 ( n ) O . 092 ( 1~.2'~

_i ~1 o _ _ _ _ ~IJ CO N ~ u~
~ ~0 - - .
C) ~U~ 00_tO
~ _ _ _ _ O ------ O
O O
O
O O`~-- ~ O _ _ O
u~~ co o a~ o ~ n N u~
~ 0 u~ O ~ J N ~ u~ ~ N N 1` N 1~ ~D O _~ N
0 ~ N u ~0 'r t~ ~D O ~:1 ~ N ~1 O ~ O O --1 ~ N r--O O O O O O O O O O O O O O O O O O O O _l O
I I

_ C-- _ ~ ~ Z: s C ~ o t~
.,1_~ O O O ` ~O Z ~s C ~ , . __ o O --I
O ~ r N ~ ~ _~ ~r X ~ N N ~` u7 It~ _ _ _ _ t.) 0 ~ O ~ ~ 01 u~ _I N ~ ~ _I O _I N ~ u~ D O_ ~ I 1~ N U ~.CI ~ ~ ~0 O ~0 ~ N N O O O _1 0 _I ~
......... -........ -..... .. ....
0 0000000000000000000 00~0 _t ~ I
~n JJ

^

rl O O~ O ^ ~
~n . o ~ o _I
O -- _ _ _ _ __ X ~ D N N ~ CO N ~ Il') O N ~ ~ ~ O ~r ~ ~ O 10 ~13 0 0 0 N O O O O O O O ~ O O O O O ~ ~ 1~ 0 0 N O
........... ........................ .
dP OOOOOOOOOOOOOOOOOOOOOOOOOO
l l l V ....

O O
~-I ~ U
O V V V
la N ~ ~P m ~ t` 0 ~ O t N ~ ~ U') ~D O n ~D O 1--CO ~ O ~--1 0 U~ N t~ ~ N N ~ ~ N r~ ~ r~
B
X o Z er u~ ~ l~

Example 8 A commercially available lime (Cementa) was treated with water vapor at 250C until the CaO content was 80%, and was then fractionated into a first fraction in which the particles were less than 74 microns in size and a second fraction in which the particles were 75 to 125 microns in size. The first fraction was used to prepare mortars containing 0.954 part of a Type 1 cement (Norcem PC 300), 0.046 part of the treated lime, 3 parts of No. 20 washed Monterey sand, and 0.5 part of water. The second fraction was used to prepare mortars in the same way except that 0.96 part of the cement and 0.04 part of the treated lime were used. The compressive strength of prisms cast from these mortars was measured after curing in water for the indicated number of days, and is shown in Table 2.

Table 2 Particle Size Compressive Strength (kg/cm2) after 1 day 3 days 7 days 0-74 105.5 240 300 75-125 103.5 195 248 Example 9 Portions o~ a commercially available lime (Flint~ote) as used in Example 2 were treated with water vapor at 200C until the CaO content was 91% (Sample 42), 70 (Sample 43) or 49.5% ( Sample 44) or with CO2 at 580C until the CaO content was 88% (Sample 45) or 68% (Sample 46). Part of Sample 4~ was treated with water vapor at 200C until the CaO content was 54~ (Sample 47). Cement pastes were made by ~0 dry mixing 0.1 part of the sample and 0.9 part of a Type ~-2 cement (Kaiser Permanente); water ~0.36 part) was then added 2;~31 and the mixture was mixed in a Hobart Mixer for 20 seconds at low speed followed by 20 seconds at medium speed. The pastes were placed in a Halliburton Consistometer, and their consistencies, expressed in Halliburton Consistency units, are shown in Table 3 below (which also shows results for a paste containing 1 part of the Type 1-2 cement and no treated lime).

Table 3 Sample No. Consistency after indicated time (mins.) 42 XloO 45 45 47 49 53 64 82100 43 40 40 38 38 4~ 42 43 4548 52 58 63 70 XloO 42 40 42 42 43 47 5258 63 70 79 -91 46 56 50 47 45 g5 46 46 5051 53 56 60 67 Control 52 38 36 36 36 36 36 37 . 38 39 40 42 43 x shows "false set"

Claims

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows.

1. A pulverulent composition which is useful as an expansion additive for hydratable cement compositions; which consists essentially of particles having a size less than 250 microns and comprising a core of calcium oxide and a protective coating around said core of calcium hydroxide or calcium carbonate or both, which contains 36 to 95% by weight of calcium oxide, and which exhibits an Expansion Factor of at least 0.06%, the Expansion Factor being the increase in length of a test prism which has been cured in water for 7 days after casting according to ASTM C490-70 and C157-69T from a mortar prepared according to ASTM C305-65 and containing 0.1 part of the composition 0.9 part of Type III Portland cement 2 parts of No. 20 washed sand, and 0.4 part of water.

2. A composition according to Claim 1 which comprises 36 to 92% by weight of calcium oxide and wherein said protective coating consists essentially of calcium hydroxide.

3. A composition according to Claim 2 which comprises 50 to 84% by weight of calcium oxide.

4. A composition according to Claim 1 which comprises 40 to 91% by weight of calcium oxide and wherein said protective coating consists essentially of calcium carbonate.

5. A composition according to Claim 4 which comprises 64 to 91% by weight of calcium oxide.

6. A composition according to Claim 1 wherein said particles have a size of 1 to 100 microns.

7. A composition according to Claim 6 wherein said particles have a size of 5 to 60 microns.

8. A composition according to Claim 1 having an Expansion Factor of 0.07 to 0.4%.

9. A process for the production of a composition as claimed in Claim 1, which process comprises heating particles (a) having a size less than 250 microns and (b) comprising at least 36% by weight of CaO, the particles being maintained at a temperature of at least 100°C. and, if the particles initially contain less than 8% by weight of Ca(OH)2, the particles being maintained at a temperature of 100° to 400°C.
in an atmosphere which comprises water vapor or at a temperature of 350° to 850°C. in an atmosphere which comprises carbon dioxide, said heating being carried out under conditions such that the product contains 36 to 95% by weight of CaO and exhibits an Expansion Factor of at least 0.06%.

10. A process according to Claim 9 wherein said particles initially comprise at least 80% by weight of CaO
and are heated at a temperature of 100 to 400°C in an atmosphere comprising water vapor for a time sufficient to increase the weight of the particles by at least 2%.

11. A process according to Claim 10 wherein the weight of the particles is increased by 4 to 12%.

12. A process according to Claim 11 wherein the weight of the particles is increased by 5 to 11%.

13. A process according to Claim 9 wherein said particles initially comprise at least 80% by weight of CaO
and are heated at a temperature of 350 to 850°C. in an atmosphere comprising CO2 for a time sufficient to increase the weight of the particles by at least 2%.

14. A process according to Claim 13 wherein the weight of the particles is increased by 4 to 16%.

15. A process according to Claim 9 wherein said particles initially comprise at least 80% by weight of CaO
and are heated in an atmosphere comprising CO2 and water vapor for a time sufficient to increase the weight of the particles by 4 to 14%.

16. A process according to Claim 9 wherein said particles initially comprise 8 to 64% by weight of Ca(OH)2 and are heated at a temperature of 100 to 400°C.

17. A process according to Claim 16 wherein said particles initially contain 16 to 50% by weight of Ca(OH)2.

18. A cement composition comprising a Portland cement, water and a lime-containing composition as claimed in Claim 1, 2 or 3, in amount less than 30%, based on the combined weight of the cement and the lime-containing composition.

19. A cement composition comprising a Portland cement, water and a lime-containing composition as claimed in Claim 4, 5 or 6, in amount less than 30%, based on the combined weight of the cement and the lime-containing composition.

20. A cement composition comprising a Portland cement, water and a lime-containing composition which has been prepared by a process as claimed in Claim 10, 13 or 15 in amount less than 30%, based on the combined weight of the cement and the lime-containing composition.