CA1273368A - Durable and highly stable moulded construction parts - Google Patents
Durable and highly stable moulded construction partsInfo
- Publication number
- CA1273368A CA1273368A CA000553411A CA553411A CA1273368A CA 1273368 A CA1273368 A CA 1273368A CA 000553411 A CA000553411 A CA 000553411A CA 553411 A CA553411 A CA 553411A CA 1273368 A CA1273368 A CA 1273368A
- Authority
- CA
- Canada
- Prior art keywords
- construction
- cement
- construction part
- part according
- binder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000010276 construction Methods 0.000 title claims abstract description 56
- 239000004035 construction material Substances 0.000 claims abstract description 42
- 239000000203 mixture Substances 0.000 claims abstract description 39
- 239000012779 reinforcing material Substances 0.000 claims abstract description 23
- 239000003513 alkali Substances 0.000 claims abstract description 22
- 239000000872 buffer Substances 0.000 claims abstract description 21
- 239000002253 acid Substances 0.000 claims abstract description 17
- 230000036571 hydration Effects 0.000 claims abstract description 7
- 238000006703 hydration reaction Methods 0.000 claims abstract description 7
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 6
- 239000000725 suspension Substances 0.000 claims abstract description 6
- 239000007900 aqueous suspension Substances 0.000 claims abstract description 5
- 230000015556 catabolic process Effects 0.000 claims abstract description 5
- 238000006731 degradation reaction Methods 0.000 claims abstract description 5
- 239000004568 cement Substances 0.000 claims description 56
- 239000011230 binding agent Substances 0.000 claims description 49
- 239000011398 Portland cement Substances 0.000 claims description 29
- 229920003043 Cellulose fiber Polymers 0.000 claims description 26
- 239000000463 material Substances 0.000 claims description 24
- 239000000306 component Substances 0.000 claims description 23
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 22
- 229920002678 cellulose Polymers 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 10
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 claims description 8
- 239000002893 slag Substances 0.000 claims description 8
- 239000003365 glass fiber Substances 0.000 claims description 7
- 235000012239 silicon dioxide Nutrition 0.000 claims description 7
- 239000010893 paper waste Substances 0.000 claims description 6
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 6
- 239000000395 magnesium oxide Substances 0.000 claims description 5
- 230000002787 reinforcement Effects 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 4
- 239000010881 fly ash Substances 0.000 claims description 4
- 239000001175 calcium sulphate Substances 0.000 claims 6
- 235000011132 calcium sulphate Nutrition 0.000 claims 6
- 239000000126 substance Substances 0.000 claims 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052593 corundum Inorganic materials 0.000 claims 1
- 229910001845 yogo sapphire Inorganic materials 0.000 claims 1
- 238000005452 bending Methods 0.000 description 30
- 239000010425 asbestos Substances 0.000 description 23
- 229910052895 riebeckite Inorganic materials 0.000 description 23
- 239000011159 matrix material Substances 0.000 description 14
- 230000007774 longterm Effects 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000002131 composite material Substances 0.000 description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 8
- 238000005260 corrosion Methods 0.000 description 8
- 230000007797 corrosion Effects 0.000 description 8
- 239000011507 gypsum plaster Substances 0.000 description 6
- 239000004571 lime Substances 0.000 description 6
- 230000009467 reduction Effects 0.000 description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 235000011941 Tilia x europaea Nutrition 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 235000012245 magnesium oxide Nutrition 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- 244000198134 Agave sisalana Species 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 235000012241 calcium silicate Nutrition 0.000 description 3
- JHLNERQLKQQLRZ-UHFFFAOYSA-N calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 3
- 229910052918 calcium silicate Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000003546 flue gas Substances 0.000 description 3
- 239000010440 gypsum Substances 0.000 description 3
- 229910052602 gypsum Inorganic materials 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 229920002748 Basalt fiber Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012062 aqueous buffer Substances 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229940106135 cellulose Drugs 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000011518 fibre cement Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/14—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B18/00—Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B18/04—Waste materials; Refuse
- C04B18/18—Waste materials; Refuse organic
- C04B18/24—Vegetable refuse, e.g. rice husks, maize-ear refuse; Cellulosic materials, e.g. paper, cork
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/91—Use of waste materials as fillers for mortars or concrete
Abstract
ABSTRACT OF THE DISCLOSURE
Durable molded construction parts are disclosed, which are prepared from the hydration products of a settable construc-tion material comprising a hydraulically hardening mixture and at least one reinforcing material subject to degradation under alkaline conditions. The construction material has an alkali buffer capacity which does not exceed 0.005 acid equivalents per 100 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation.
Durable molded construction parts are disclosed, which are prepared from the hydration products of a settable construc-tion material comprising a hydraulically hardening mixture and at least one reinforcing material subject to degradation under alkaline conditions. The construction material has an alkali buffer capacity which does not exceed 0.005 acid equivalents per 100 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation.
Description
3~
DURABLE AND HIGHLY STABLE MOULDED CONSTRUCTION PARTS
.
The present invention relates to durable moulded construction parts which in particular are in the form of a plate and consist of hydration products of a cement or a cement-like binder together with alkali sensitive reinforcing materials, in particular ligno-celluloses and, when necessary, further compon-ents.
In the past, durable moulded construction parts of this kind were usually produced from asbestos cement. In this con-struction material, asbestos fibres are usually added to thecement as reinforcing material at a mixing ratio by weight of 1:6 to 1:10. These asbestos reinforced moulded cement parts have properties which are in many respects advantageous and they can be manufactured economically. However, the production and processing of these asbestos-reinforced moulded cements parts involves a high health risk for the people who work with this material. There-fore, for some time now there have been efforts to replace the asbestos fibres in asbes-tos cement construction materials with other fibres serving as reinforcement. In some cases inorganic fibres were used for this purpose, such as glass fibres, basalt fibres and slag fibres. Other examples involve the substitution of the asbestos fibres with fibres of an organic nature, such as synthetic fibres and ligno cellulose-like fibres. For this pur-pose, ligno-cellulose-like fibres such as bamboo fibres, cotton fibres and sisal fibres have been suggested. Whereas the examination of construction materials containing inorganic fibres as reinforcing material produced mostly unsatisfactory results, the use of ligno-celluloses as reinforcing materials produced good preliminary strength results. ~owever, if the long term behaviour is taken into consideration here, a constant decrease in the preliminary strength is observed.
The decrease in the bending strength of ligno-cellulose-reinforced cement materials, which is dependent on the time factor, is due to the high alkalinity of a cement matrix. It is assumed that the ligno-celluloses are not stable in an alkaline medium. With glass-fibre-reinforced cements there is also a considerable reduction in the bending strength due to the corro-sion of the glass caused by the alkali. In the relevant litera-ture, there are therefore different suggestions for improving the properties of ligno-cellulose-reinforced or glass-fibre-reinforced cement materials. The essential problem of a sufficient reduction of the alkalinity, however, is not discussed.
Consequently, all known suggestions for the cement modi-fication can at best only reduce the corrosion of alkali-sensitive fibres, not prevent the corrosion entirely - which would be necessary for the unlimited utilization of such a material combination.
The modification of conventional Portland cements with active pozzolanic materials, in particular of a silicate nature such as silica gel, thus increasing the durability of the ligno-celluloses in the cement matrix is, for example, already known.
In the published European patent application 68 742 it was sug-gested in this respect that a substitute for asbestos cement be produced from 50% to 90~ of cement - whereby it can be gathered from the context that Portland cement is meant here - 5% to 40% of highly active pozzolanic silica, and 5% to 15% of cellulose fibres. In order to improve the activity of the pozzolanic mater-ial, it is necessary that it has a specific surface of at least 15,000 m2/kg; an even better value, however, would be at least 25,000 m2/kg.
Furthermore, it is known from the International Publi-cation ~o. WO 85/03700 that binder mixtures consisting of 75~ to 40% of Portland cement and 25% to 60% of amorphous silica can be used for producing cement-bound moulded wood fibre bodies. More-over, it may be gathered from this printed specification that the activity of the pozzolan increases with the fineness of the grain.
The preferred range of grain size (15 to 25 m2/g) is completely identical with that of the afore-mentioned published European patent application 68 742. United Kingdom Patent 1 588 938 also describes a process for manufacturing moulded fibre-cement bodies.
According to this patent, glass fibres in a proportion of of 0.5%
to 20~, referring to the binder weight, are added as reinforcing material. The glass fibres added have to be substantially
DURABLE AND HIGHLY STABLE MOULDED CONSTRUCTION PARTS
.
The present invention relates to durable moulded construction parts which in particular are in the form of a plate and consist of hydration products of a cement or a cement-like binder together with alkali sensitive reinforcing materials, in particular ligno-celluloses and, when necessary, further compon-ents.
In the past, durable moulded construction parts of this kind were usually produced from asbestos cement. In this con-struction material, asbestos fibres are usually added to thecement as reinforcing material at a mixing ratio by weight of 1:6 to 1:10. These asbestos reinforced moulded cement parts have properties which are in many respects advantageous and they can be manufactured economically. However, the production and processing of these asbestos-reinforced moulded cements parts involves a high health risk for the people who work with this material. There-fore, for some time now there have been efforts to replace the asbestos fibres in asbes-tos cement construction materials with other fibres serving as reinforcement. In some cases inorganic fibres were used for this purpose, such as glass fibres, basalt fibres and slag fibres. Other examples involve the substitution of the asbestos fibres with fibres of an organic nature, such as synthetic fibres and ligno cellulose-like fibres. For this pur-pose, ligno-cellulose-like fibres such as bamboo fibres, cotton fibres and sisal fibres have been suggested. Whereas the examination of construction materials containing inorganic fibres as reinforcing material produced mostly unsatisfactory results, the use of ligno-celluloses as reinforcing materials produced good preliminary strength results. ~owever, if the long term behaviour is taken into consideration here, a constant decrease in the preliminary strength is observed.
The decrease in the bending strength of ligno-cellulose-reinforced cement materials, which is dependent on the time factor, is due to the high alkalinity of a cement matrix. It is assumed that the ligno-celluloses are not stable in an alkaline medium. With glass-fibre-reinforced cements there is also a considerable reduction in the bending strength due to the corro-sion of the glass caused by the alkali. In the relevant litera-ture, there are therefore different suggestions for improving the properties of ligno-cellulose-reinforced or glass-fibre-reinforced cement materials. The essential problem of a sufficient reduction of the alkalinity, however, is not discussed.
Consequently, all known suggestions for the cement modi-fication can at best only reduce the corrosion of alkali-sensitive fibres, not prevent the corrosion entirely - which would be necessary for the unlimited utilization of such a material combination.
The modification of conventional Portland cements with active pozzolanic materials, in particular of a silicate nature such as silica gel, thus increasing the durability of the ligno-celluloses in the cement matrix is, for example, already known.
In the published European patent application 68 742 it was sug-gested in this respect that a substitute for asbestos cement be produced from 50% to 90~ of cement - whereby it can be gathered from the context that Portland cement is meant here - 5% to 40% of highly active pozzolanic silica, and 5% to 15% of cellulose fibres. In order to improve the activity of the pozzolanic mater-ial, it is necessary that it has a specific surface of at least 15,000 m2/kg; an even better value, however, would be at least 25,000 m2/kg.
Furthermore, it is known from the International Publi-cation ~o. WO 85/03700 that binder mixtures consisting of 75~ to 40% of Portland cement and 25% to 60% of amorphous silica can be used for producing cement-bound moulded wood fibre bodies. More-over, it may be gathered from this printed specification that the activity of the pozzolan increases with the fineness of the grain.
The preferred range of grain size (15 to 25 m2/g) is completely identical with that of the afore-mentioned published European patent application 68 742. United Kingdom Patent 1 588 938 also describes a process for manufacturing moulded fibre-cement bodies.
According to this patent, glass fibres in a proportion of of 0.5%
to 20~, referring to the binder weight, are added as reinforcing material. The glass fibres added have to be substantially
2~ resistant to alkali and thus a reduction of the alkalinity in the medium surrounding the glass fibres is not considered. Under this prerequisite, however, a substitution of the glass fibres with cellulose fibres or wood fibres will inevitably produce the above-mentioned negative long-term behaviour due to the alkalinity of the medium.
In contrast to the known moulded asbestos cement construction parts, the Austrian Patent 3~57/12 relates to a fire-~ 2~33~
proof and incompressible asbestos cement construction material consisting of a mixture of asbestos, cement and materials contain-ing silicic acid whereby the fibres should be resistant to corro-sion in an alkaline medium. Here it is assumed that the fibre materials considered have to be regarded as alkali-resistant.
Finally, in an extensive examination carried out by H.E. Gram in 1983 (H.E. Gram, "Durability of natural fibers in concrete"; Swedish Cement and Concrete Research Institute, S-100 44 Stockholm) it was found that sisal fibres become brittle when they are in contact with aqueous buffer solutions with a pH-value of above 12. Other ligno-celluloses were not examined for embrit-tlement in alkaline solutions. In the Gram report, in which the literature regarding "ligno-celluloses in the cement ~atrix" is evaluated very critically, it is concluded that when certain materials, which cause a reduction in the pH-value of the binder cement, are added to the cement, this can also increase the dur-ability of ligno-celluloses in the cement matrix. Thus, for example, an improvement of the durability of ligno-celluloses is a cement matrix is obtained when the binder cement is partially substituted with silicate materials such as amorphous silicic acid (e.g. fumed silica). The partial substitution of Portland cement with alumina cement also results in an improved fibre durability of the sisal fibres embedded in a cement matrix.
All the suggestions for improving the fibre durability made in the state of the art merely retard the damaging of the fibres. In the usual expected life span of construction materials of this kind, however, fibre corrosion takes place to an ~z~
2636~-13 increasing extent. It is not yet possible to prevent fibre corrosion entirely.
Up until now it has been assumed that the damaging of the fibres was only due to the alkalinity of the surrounding matrix, which is defined by the pH-value. According to the state of the art thus either alkali-resistant reinforcing materials were used, which, however, can only be used to a limited extent due to their specific properties, or it was proposed to reduce the pH-value of the binder matrix.
In spite of extensive research in particular in the past few years it has not been possible so far to provide durable moulded construction parts which on the one hand contain alkali-sensitive fibres serving as reinforcing material and on the other hand contain alkaline binder systems.
The present invention seeks to provide moulded construc-tion parts in which fibres of ligno-celluloses or other alkali-sensitive fibres are embedded as a long-term durable reinforcement for increasing the strength of the construction material.
This invention is based on the concept that the damaging 20 of ligno-cellulose fibres in the cement matrix is due to the alka-line buffer capacity of the produced construction material rather than to the pH-value of the binder used. Accordingly, the present invention proposes that the alkaline buffer capacity of the con-struction material, which is variable and sufficiently low, does not exceed 0.005 acid equivalents/lOOg of construction material is a defined aqueous test suspension 24 hours after its production.
This invention is also based on the concept that a cer-tain buffer capacity has to be reached in order to prevent fibre corrosion. The significance of the buffer capacity as a decisive influencing factor has not been recognize~ in the state of the art up until now so that the requirements which the present solution according to the invention puts on the binder system have not been taken into consideration in the cements or cement modifications suggested so far.
According to one aspect of the present invention there is provided durable molded construction part, in cured form, prepared from the hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, wherein said construction material has an alkali buffer capacity which does not exceed 0.005 acid equi valents per lO0 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation.
According to a further aspect of the pr~sent invention there is provided method of manufacturing a durable molded con-~0 struction part from hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, comprising mixing said reinforcing material with a binder mixture selected such thak said construction mater-ial has an alkali buffer capacity which does not exceed 0.005 acid equivalents per lO0 grams of construction material, as -~' ~ 3 ~ ~ 2801g-1 measured in an aqueous suspension of the construction material 24 hours after suspension formation, and adding sufficient water to set said construction material.
In an advantageous embodiment of the invention, cement-bound moulded construction parts containing a durable reinforcing material in the form of ligno-celluloses can be produced by mixing conventional Portland cements, alumina cernents and bellite cements or mixtures thereof at such a gravimetric ratio with active poz-zolan such as amorphous silicic acid, powdered trass and fly ash and, if necessary, with or without adding acids until a sufficient buffer capacity of the material, or a value below it, has been reached.
When acids are added for reducing the buffer capacity as suggested in the invention, the additional effect of accelerated hardening of the binder may, furthermore, be utilized if the acids are chosen according to the acceleration properties of their calcium salts. The addition of 1.0 to 2.5 ml of concentrated hydrochloric acid to lOOg of a binder with Portland cement as its main component, for example, results ir. a considerable reduction in the buffer capacity and acceleration of the hardening process.
With binders having alumina cement as their main component a cimilar effect may be observed when 0.5 to 4.0 ml of concentrated sulfuric acid are added to lOOg of the binder. Depending on the - 6a -~' ~3~
composition of the binder and its use, the addition of other inorganic or organic acids may also produce the desired effect.
Of course, any other binder systems which have the characteris~ic features described herein, are also considered in this invention. Moulded construction parts with glass fibres as reinforcing material also have the desired long~term behaviour when the teaching according to the inven-tion is observed.
In the present invention it is assumed that asbestos fibres or other alkali-resistant fibres and conventional Portland cements were used for the production of moulded construction parts or composites and that this produces excellent results. Thus it is further known that materials made from asbestos cement in their compressed state (material density 1.7 - 2.1 kg/dm3) with bending strengths of 20 - 35 N/mm2 and high long-term durability or weatherproofness have so far been considered beyond all comparison with any other composites. The known composites made from asbes-tos cement optimally fulfilled the requirements of their users.
The production and use of asbestos cement products, however, have to be stopped due to the ecological and physiological problems linked with the material asbestos. For this reason, the substitu-tion of the asbestos fibres has become a problem which has to be solved without delay. As a result of most intensive research work inorganic and organic fibres have been developed which are, above all, resistant to an alkaline medium in a Portland cement matrix.
When these substitutes are used, however, the high bending strengths of asbestos cement cannot be reached. The use of cellu-lose fibres in combination with Portland cement produced ~33~
263~2-13 preliminary strengths which are closest to, but not ldentical to, that of asbestos cement. However, moulded construction parts comprising cellulose fibres as reinforcing material were disappointing in their long-term behaviour since the cellulose fibres proved to be alkali-sensitive and thus fibre corrosion occurred.
All known substitute solutions with alkali-resistant synthetic fibres have the shortcoming that although the production costs for the fibres are high, only relatively low bending strengths of the material can be obtained, or that although good preliminary strengths are obtained when non-alkali-resistant cellulose fibres in combination with Portland cement were used, the long-term strengths are unsatisfactory.
It is, therefore, a further aspect of this invention to improve the initially good reinforcing behaviour of inexpensive and readily available non-alkali-resistant fibres, is particular waste paper fibres and cellulose fibres, which are bound with hydraulically hardening binders so that the long-term behaviour is also satisfactory and the material can be used in industry and thus to make the production of long-term durable and weatherproof composites possible which have bending strengths that are equal to, or higher than, that of asbestos reinforced cement. Further-more, a long~term durability is also to be obtained with materials other than asbestos.
This additional problem is solved according to the invention in that the above described durable moulded construction part which is made from a material comprising a fibre material and ~6362-13 a binder system whereby the binder is a hydraulic binder with a considerably lower lime content and a much higher content of calcium sulfate than that of Portland cement and the fibres are alkali-sensitive fibres, in particular cellulose fibres.
According to the preferred embodiment of this aspect of the invention the binder consists of 60% - 80~ by weight of a latently hydraulic component, e.g. ground blast sand or ground blast slag, 15% - 25% by weight of a calcium sulfate component, e.g. hemi-hydrate gypsum (Plaster of Paris) and 3% - 10% of a conventional cement component, e.g. Portland cement or Portland clinker. The latently hydraulic component should contain 8~ - 15 by weight of amorphous reactive A12O3, 1% - 10~ by weight of amorphous MgO (not in the form of periclase) and 35% - 45~ by weight of CaO.
When mixed with water, the binder hardens, thereby forming water- and weatherproof solid gels and crystalline hardening products.
The A12O3 content ensures a good sulfatic stimulation and - in combination with the other active components - it results in the development of high bonding strengths between the binder matrix and -the cellulose fibre. It is, therefore, possible to even add up to 40~ by weight of cellulose fibres, referring to the binder weight. The optimum amount to be added ranges between 5~ -40~ by weight of cellulose fibres, referring to the binder weight.
The A12O3 promotes the formation of gel and the bonding of CaO and MgO so that the alkalinity is permanently reduced to a value which is not damaging to the cellulose fibres.
In contrast to moulded construction parts comprising conventional fibre composites, the moulded construction parts according to the invention are considerably more effective since they have an even higher strength than the asbestos cements, which had the reputation of being highly strong and stable, and they prodcue extremely advantageous strength-density-ratios. Further-more, their economical effectiveness is increased by the fact that recycling materials (such as blast slag, gypsum obtained from flue gas desulfurisation, and waste paper) can be used which are, as a rule, inexpensive.
The fibres-binder-mixtures, which have the composition according to this invention and which are used for the production of the moulded construction parts, harden out, thus resulting in high bonding strengths between the cellulose fibres and the binder matrix. The reinforcing effect of the cellulose fibre in this binder matrix is durable since due to the special binder composi-tion the alkalies are bound to suc'n an extent that a low alkalin-ity which is not damaging to the cellulose fibre is obtained. The hardened fibre composites have high bending strengths, are to a significant extent durable in the long term, weatherproof and they feature an improved acid resistance compared to products made from Portland cement. In spite of the high bending strengths their elasticity modulus is relatively low/ which suggasts a lower proneness to brittle fracture compared to conventional cement products and a reduction in the clamped stresses due to the inevitable influence of moisture- and temperature gradients in the .. . . . .
. . .
In contrast to the known moulded asbestos cement construction parts, the Austrian Patent 3~57/12 relates to a fire-~ 2~33~
proof and incompressible asbestos cement construction material consisting of a mixture of asbestos, cement and materials contain-ing silicic acid whereby the fibres should be resistant to corro-sion in an alkaline medium. Here it is assumed that the fibre materials considered have to be regarded as alkali-resistant.
Finally, in an extensive examination carried out by H.E. Gram in 1983 (H.E. Gram, "Durability of natural fibers in concrete"; Swedish Cement and Concrete Research Institute, S-100 44 Stockholm) it was found that sisal fibres become brittle when they are in contact with aqueous buffer solutions with a pH-value of above 12. Other ligno-celluloses were not examined for embrit-tlement in alkaline solutions. In the Gram report, in which the literature regarding "ligno-celluloses in the cement ~atrix" is evaluated very critically, it is concluded that when certain materials, which cause a reduction in the pH-value of the binder cement, are added to the cement, this can also increase the dur-ability of ligno-celluloses in the cement matrix. Thus, for example, an improvement of the durability of ligno-celluloses is a cement matrix is obtained when the binder cement is partially substituted with silicate materials such as amorphous silicic acid (e.g. fumed silica). The partial substitution of Portland cement with alumina cement also results in an improved fibre durability of the sisal fibres embedded in a cement matrix.
All the suggestions for improving the fibre durability made in the state of the art merely retard the damaging of the fibres. In the usual expected life span of construction materials of this kind, however, fibre corrosion takes place to an ~z~
2636~-13 increasing extent. It is not yet possible to prevent fibre corrosion entirely.
Up until now it has been assumed that the damaging of the fibres was only due to the alkalinity of the surrounding matrix, which is defined by the pH-value. According to the state of the art thus either alkali-resistant reinforcing materials were used, which, however, can only be used to a limited extent due to their specific properties, or it was proposed to reduce the pH-value of the binder matrix.
In spite of extensive research in particular in the past few years it has not been possible so far to provide durable moulded construction parts which on the one hand contain alkali-sensitive fibres serving as reinforcing material and on the other hand contain alkaline binder systems.
The present invention seeks to provide moulded construc-tion parts in which fibres of ligno-celluloses or other alkali-sensitive fibres are embedded as a long-term durable reinforcement for increasing the strength of the construction material.
This invention is based on the concept that the damaging 20 of ligno-cellulose fibres in the cement matrix is due to the alka-line buffer capacity of the produced construction material rather than to the pH-value of the binder used. Accordingly, the present invention proposes that the alkaline buffer capacity of the con-struction material, which is variable and sufficiently low, does not exceed 0.005 acid equivalents/lOOg of construction material is a defined aqueous test suspension 24 hours after its production.
This invention is also based on the concept that a cer-tain buffer capacity has to be reached in order to prevent fibre corrosion. The significance of the buffer capacity as a decisive influencing factor has not been recognize~ in the state of the art up until now so that the requirements which the present solution according to the invention puts on the binder system have not been taken into consideration in the cements or cement modifications suggested so far.
According to one aspect of the present invention there is provided durable molded construction part, in cured form, prepared from the hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, wherein said construction material has an alkali buffer capacity which does not exceed 0.005 acid equi valents per lO0 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation.
According to a further aspect of the pr~sent invention there is provided method of manufacturing a durable molded con-~0 struction part from hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, comprising mixing said reinforcing material with a binder mixture selected such thak said construction mater-ial has an alkali buffer capacity which does not exceed 0.005 acid equivalents per lO0 grams of construction material, as -~' ~ 3 ~ ~ 2801g-1 measured in an aqueous suspension of the construction material 24 hours after suspension formation, and adding sufficient water to set said construction material.
In an advantageous embodiment of the invention, cement-bound moulded construction parts containing a durable reinforcing material in the form of ligno-celluloses can be produced by mixing conventional Portland cements, alumina cernents and bellite cements or mixtures thereof at such a gravimetric ratio with active poz-zolan such as amorphous silicic acid, powdered trass and fly ash and, if necessary, with or without adding acids until a sufficient buffer capacity of the material, or a value below it, has been reached.
When acids are added for reducing the buffer capacity as suggested in the invention, the additional effect of accelerated hardening of the binder may, furthermore, be utilized if the acids are chosen according to the acceleration properties of their calcium salts. The addition of 1.0 to 2.5 ml of concentrated hydrochloric acid to lOOg of a binder with Portland cement as its main component, for example, results ir. a considerable reduction in the buffer capacity and acceleration of the hardening process.
With binders having alumina cement as their main component a cimilar effect may be observed when 0.5 to 4.0 ml of concentrated sulfuric acid are added to lOOg of the binder. Depending on the - 6a -~' ~3~
composition of the binder and its use, the addition of other inorganic or organic acids may also produce the desired effect.
Of course, any other binder systems which have the characteris~ic features described herein, are also considered in this invention. Moulded construction parts with glass fibres as reinforcing material also have the desired long~term behaviour when the teaching according to the inven-tion is observed.
In the present invention it is assumed that asbestos fibres or other alkali-resistant fibres and conventional Portland cements were used for the production of moulded construction parts or composites and that this produces excellent results. Thus it is further known that materials made from asbestos cement in their compressed state (material density 1.7 - 2.1 kg/dm3) with bending strengths of 20 - 35 N/mm2 and high long-term durability or weatherproofness have so far been considered beyond all comparison with any other composites. The known composites made from asbes-tos cement optimally fulfilled the requirements of their users.
The production and use of asbestos cement products, however, have to be stopped due to the ecological and physiological problems linked with the material asbestos. For this reason, the substitu-tion of the asbestos fibres has become a problem which has to be solved without delay. As a result of most intensive research work inorganic and organic fibres have been developed which are, above all, resistant to an alkaline medium in a Portland cement matrix.
When these substitutes are used, however, the high bending strengths of asbestos cement cannot be reached. The use of cellu-lose fibres in combination with Portland cement produced ~33~
263~2-13 preliminary strengths which are closest to, but not ldentical to, that of asbestos cement. However, moulded construction parts comprising cellulose fibres as reinforcing material were disappointing in their long-term behaviour since the cellulose fibres proved to be alkali-sensitive and thus fibre corrosion occurred.
All known substitute solutions with alkali-resistant synthetic fibres have the shortcoming that although the production costs for the fibres are high, only relatively low bending strengths of the material can be obtained, or that although good preliminary strengths are obtained when non-alkali-resistant cellulose fibres in combination with Portland cement were used, the long-term strengths are unsatisfactory.
It is, therefore, a further aspect of this invention to improve the initially good reinforcing behaviour of inexpensive and readily available non-alkali-resistant fibres, is particular waste paper fibres and cellulose fibres, which are bound with hydraulically hardening binders so that the long-term behaviour is also satisfactory and the material can be used in industry and thus to make the production of long-term durable and weatherproof composites possible which have bending strengths that are equal to, or higher than, that of asbestos reinforced cement. Further-more, a long~term durability is also to be obtained with materials other than asbestos.
This additional problem is solved according to the invention in that the above described durable moulded construction part which is made from a material comprising a fibre material and ~6362-13 a binder system whereby the binder is a hydraulic binder with a considerably lower lime content and a much higher content of calcium sulfate than that of Portland cement and the fibres are alkali-sensitive fibres, in particular cellulose fibres.
According to the preferred embodiment of this aspect of the invention the binder consists of 60% - 80~ by weight of a latently hydraulic component, e.g. ground blast sand or ground blast slag, 15% - 25% by weight of a calcium sulfate component, e.g. hemi-hydrate gypsum (Plaster of Paris) and 3% - 10% of a conventional cement component, e.g. Portland cement or Portland clinker. The latently hydraulic component should contain 8~ - 15 by weight of amorphous reactive A12O3, 1% - 10~ by weight of amorphous MgO (not in the form of periclase) and 35% - 45~ by weight of CaO.
When mixed with water, the binder hardens, thereby forming water- and weatherproof solid gels and crystalline hardening products.
The A12O3 content ensures a good sulfatic stimulation and - in combination with the other active components - it results in the development of high bonding strengths between the binder matrix and -the cellulose fibre. It is, therefore, possible to even add up to 40~ by weight of cellulose fibres, referring to the binder weight. The optimum amount to be added ranges between 5~ -40~ by weight of cellulose fibres, referring to the binder weight.
The A12O3 promotes the formation of gel and the bonding of CaO and MgO so that the alkalinity is permanently reduced to a value which is not damaging to the cellulose fibres.
In contrast to moulded construction parts comprising conventional fibre composites, the moulded construction parts according to the invention are considerably more effective since they have an even higher strength than the asbestos cements, which had the reputation of being highly strong and stable, and they prodcue extremely advantageous strength-density-ratios. Further-more, their economical effectiveness is increased by the fact that recycling materials (such as blast slag, gypsum obtained from flue gas desulfurisation, and waste paper) can be used which are, as a rule, inexpensive.
The fibres-binder-mixtures, which have the composition according to this invention and which are used for the production of the moulded construction parts, harden out, thus resulting in high bonding strengths between the cellulose fibres and the binder matrix. The reinforcing effect of the cellulose fibre in this binder matrix is durable since due to the special binder composi-tion the alkalies are bound to suc'n an extent that a low alkalin-ity which is not damaging to the cellulose fibre is obtained. The hardened fibre composites have high bending strengths, are to a significant extent durable in the long term, weatherproof and they feature an improved acid resistance compared to products made from Portland cement. In spite of the high bending strengths their elasticity modulus is relatively low/ which suggasts a lower proneness to brittle fracture compared to conventional cement products and a reduction in the clamped stresses due to the inevitable influence of moisture- and temperature gradients in the .. . . . .
. . .
3~
2636~-13 plates.
In the following, the invention is explained in examples whereby further details, characteristic features and advantayes of the moulded construction parts according to the invention are emphasizedO Unless otherwise indicated, the composition of the binder and the proportions of fibres are each indicated in weight percentages. The buffer capacity in the examples was determined as follows.
lOg of the material were mixed with 50 ml of distilled water, the mixture was shaken for 24 hours at room temperature, and thereafter subsequently 20 ml of the solution were titrated with 0.1 n HCl to pH=7. The consumption of hydrochloric acid per lOOg of material was converted into acid equivalents.
Example 1 Moulded construction parts are produced from 100 parts of high-lime Portland cement (PZ45F) and 18 parts of ligno-cellulose fibres. The buffer capacity measured after one day is around 0.013 acid equivalents/lOOg of construction material and is thus more than twice as high as the claimed limit value. The bending strength was measured after 14 days and was 21.3 N/mm2.
After 168 days it was measured again and was only 16.9 N/mm2.
Example 2 19 parts of ligno-cellulose fibres were added to 100 parts of a Portland cement with a lower lime content, i.e.
belite-rich cement (PZ35L), and moulded construction parts were produced from this mixture. The buffer capacity was 0.011 acid equivalents/lOOg of construction material after one day and was 3 7~ 8 thus also above the claimed limit value. The bending strength after 14 days was 18.5 N/mm2; after 168 days the bending strength was only 15.7 N/mm2.
Example 3 A moulded construction part made from 60 parts of a Portland cement with a lower lime content, i.e. belite-rich cement (PZ35L), 40 parts of alumina cement and 18 parts of ligno-cellulose fibres has a buffer capacity of O.OOS acid equivalents/lOOg of construction material after one day. This value corresponds to the claimed upper limit value. After 14 days a bending strength of 18.4 ~/mm2 was measured. The measuring of the long-term durability after 168 days produced a bending strength of 20.3 N/mm2, which is an increase in strength.
Example 4 A moulded construction part made from 57 parts of a Portland cement with a lower lime content, i.e. belite-rich cement (PZ35L), 38 parts of alumina cement, 5 parts of amorphous silicic acid and 18 parts of li~no-cellulose fibres after one day has a buffer capacity of 0.005 acid equivalents/lOOg of construction material, which is the claimed limit value. The bending strength after 14 days is 18.1 and the bending strength after 168 days is 18.2 N/mm2.
Example 5 A moulded construction parts is made from 27 parts of lime-rich Portland cement (PZ45F), 40 parts of alumina cement, 29 parts of fly ash and 4 parts of sulphuric acid together with 20 parts of ligno-cellulose fibres. The buffer capacity after one 33'~
day is 0.004 acid equivalents/lOOg of construction material. Thus the buffer capacity is in the claimed range and below the claimed limit value. The bending strength after 14 days was 1~.4 N/mm2 and after 168 days the bending strength was 20.5 N/mm2.
When the five examples are compared, it is clear that when the buffer capacity is in the c~.aimed range the moulded construction parts of different compositions will feature the desired long-term behaviour.
The process according to the invention is further explained by means of a figure.
The figure is a diagram which shows the trend of the bending strength development with comparable density of the con-struction material.
The ordinate is the bending strength in N/mm2 and the abscissa is the age in days. The curves 1, 2 and 3 refer to three different compositions of the construction material. Curve 1 is characteristic for hardening products from conventional Portland cements or binder having the composition according to the inven-tion without fibre reinforcement, the increase in the streng~h of which is first fast due to hydration and then only very slow.
Curve 2 shows moulded construction parts with cellulose reinforcement according to the state of the art which are made from Portland cement as they are mentioned in the above Example 1.
The bending strength of these moulded construction parts decreases steadily due to damaging of the fibres because of alkali after having reached a maximum. The curve seems to approach the value of the matrix strength according to curve 1 asymptotically.
æ~7~
The curve representing the bending strength (curve 3) is typical of a cellulose-Eibre reinforced construction material according to the present invention, for example for moulded con-struction parts according to the above examples 3 to 5. The bend-ing strength at first increases very much until a very high strength value is reached. Then, however, a slight gradual increase of the strength value can be observed in contrast to the moulded construction part according to curve 2. This increase corresponds approximately to the increase which also occurs in curve 1 due to increasing hardening of the matrix. The damaging of the ibres has been avoided is these moulded construction parts according to the invention.
Example 6 A moisture-resistant and weatherproof composite for producing the moulded construction parts was made from:
75 % of blast furnace slag, ground as finely as the binder (Blaine value of at least 3500 cm2/g) 20 % of plaster of Paris according to DIN 1168 (DIN: Deutsche Industrienorm, German Industrial Standard) 5 ~ of Portland cement 45 according to DIN 1164 20 ~ of waste water fibres or cellulose fibres.
The ground blast sand comprises the following com-ponents:
34.44 SiO2, 0.39 Tio2, 12.75 A1203, 1.22 Fe203 (the entire Fe as Fe203), 0.18 MnO, 42.1 CaO, 7.~34 MgO, 0.36 Na20 and 0.6 K20 ~
The composite produced from these components had a dry ~IJ~
density of at least 1.3 kg/dm3 and a minimum strength of 20 N/mm2 .
Example 7 A moulded construction part was produced from 73% of a furnace slag ground as finely as the binder and hav-ing the composition described in Example 1 20~ of plaster o~ Paris according to DI~ 1168 7~ of Portland cement 45 according to DIN 1164 20% of waste paper fibres or cellulose fibres 1~ The composite plates had a dry density of at least 1.5 kg/dm3 and a minimum bending strength of 30 N/mm~
The same results were obtained when gypsum from flue gas desulfurisation was used instead of plaster of Paris.
Example 8 A moulded construction part was produced from the following components:
73% of furnace slag ground as finely as the binder and having the composition of Example 1 20% of plaster of Paris according to DIN 1168 7% of Portlant cement 45 according to DIN 1164 22% of waste paper fibres of cellulose fibres.
The plates produced from this composition had a dry density of at least 1.5 kg/dm3 and a minimum bending strength of 45 N/mm2. When gypsum obtained from flue gas desulfurisation was used instead of plaster of Paris, the construction material had the same properties.
~7~61~
Example 9 A moulded construction part was produced from the following components:
73% of furnace slag of the composition of Example 1 20~ of plaster of Paris according to DIN 1168 7% of Portland cemen-t 45 according to DIN 1164 30~ of waste paper fibres or cellulose fibres.
The binder mixture was most finely ground to a Blaine-value of at least 6,000 cm2/g and preferably to around 7,500 cm2/g.
A moulded construction part produced in this manner has a minimum bending strength of 45 N/mm2 and a dry density of only at least 1.4 kg/dm3. In Table l the bending strength-density ratios of the four examples are shown again.
Table l .. . . .. . . . .
Bending strength-density ratiosExample no.
Ndm mmGkg 15.4 6 20.0 7 30.0 8 32.1 9 In comparison with these construction parts, convention moulded construction parts made from asbestos cement only reach bending strength-density ratio of around 12 or 17 (Ndm3/(mm2kg)).
The given Examples 6 to 9 clearly show that - compared to moulded parts made from asbestos cement - -the moulded construc-tion parts according to the invention have the same or higher ~3;~
bending strengths already with low density of the construction material and they thus feature an essentially improved input-output ratio. The economical effectiveness of the moulded con-struction parts according to the invention is due not only to the high bending strength-density ratios but also in particular to the low raw material prices for the materials used. The moulded construction parts according to the present invention can be produced by means of conventional wet and semi-dry technologies so that time- and money-consuming R ~ D work for new production technologies is avoided.
2636~-13 plates.
In the following, the invention is explained in examples whereby further details, characteristic features and advantayes of the moulded construction parts according to the invention are emphasizedO Unless otherwise indicated, the composition of the binder and the proportions of fibres are each indicated in weight percentages. The buffer capacity in the examples was determined as follows.
lOg of the material were mixed with 50 ml of distilled water, the mixture was shaken for 24 hours at room temperature, and thereafter subsequently 20 ml of the solution were titrated with 0.1 n HCl to pH=7. The consumption of hydrochloric acid per lOOg of material was converted into acid equivalents.
Example 1 Moulded construction parts are produced from 100 parts of high-lime Portland cement (PZ45F) and 18 parts of ligno-cellulose fibres. The buffer capacity measured after one day is around 0.013 acid equivalents/lOOg of construction material and is thus more than twice as high as the claimed limit value. The bending strength was measured after 14 days and was 21.3 N/mm2.
After 168 days it was measured again and was only 16.9 N/mm2.
Example 2 19 parts of ligno-cellulose fibres were added to 100 parts of a Portland cement with a lower lime content, i.e.
belite-rich cement (PZ35L), and moulded construction parts were produced from this mixture. The buffer capacity was 0.011 acid equivalents/lOOg of construction material after one day and was 3 7~ 8 thus also above the claimed limit value. The bending strength after 14 days was 18.5 N/mm2; after 168 days the bending strength was only 15.7 N/mm2.
Example 3 A moulded construction part made from 60 parts of a Portland cement with a lower lime content, i.e. belite-rich cement (PZ35L), 40 parts of alumina cement and 18 parts of ligno-cellulose fibres has a buffer capacity of O.OOS acid equivalents/lOOg of construction material after one day. This value corresponds to the claimed upper limit value. After 14 days a bending strength of 18.4 ~/mm2 was measured. The measuring of the long-term durability after 168 days produced a bending strength of 20.3 N/mm2, which is an increase in strength.
Example 4 A moulded construction part made from 57 parts of a Portland cement with a lower lime content, i.e. belite-rich cement (PZ35L), 38 parts of alumina cement, 5 parts of amorphous silicic acid and 18 parts of li~no-cellulose fibres after one day has a buffer capacity of 0.005 acid equivalents/lOOg of construction material, which is the claimed limit value. The bending strength after 14 days is 18.1 and the bending strength after 168 days is 18.2 N/mm2.
Example 5 A moulded construction parts is made from 27 parts of lime-rich Portland cement (PZ45F), 40 parts of alumina cement, 29 parts of fly ash and 4 parts of sulphuric acid together with 20 parts of ligno-cellulose fibres. The buffer capacity after one 33'~
day is 0.004 acid equivalents/lOOg of construction material. Thus the buffer capacity is in the claimed range and below the claimed limit value. The bending strength after 14 days was 1~.4 N/mm2 and after 168 days the bending strength was 20.5 N/mm2.
When the five examples are compared, it is clear that when the buffer capacity is in the c~.aimed range the moulded construction parts of different compositions will feature the desired long-term behaviour.
The process according to the invention is further explained by means of a figure.
The figure is a diagram which shows the trend of the bending strength development with comparable density of the con-struction material.
The ordinate is the bending strength in N/mm2 and the abscissa is the age in days. The curves 1, 2 and 3 refer to three different compositions of the construction material. Curve 1 is characteristic for hardening products from conventional Portland cements or binder having the composition according to the inven-tion without fibre reinforcement, the increase in the streng~h of which is first fast due to hydration and then only very slow.
Curve 2 shows moulded construction parts with cellulose reinforcement according to the state of the art which are made from Portland cement as they are mentioned in the above Example 1.
The bending strength of these moulded construction parts decreases steadily due to damaging of the fibres because of alkali after having reached a maximum. The curve seems to approach the value of the matrix strength according to curve 1 asymptotically.
æ~7~
The curve representing the bending strength (curve 3) is typical of a cellulose-Eibre reinforced construction material according to the present invention, for example for moulded con-struction parts according to the above examples 3 to 5. The bend-ing strength at first increases very much until a very high strength value is reached. Then, however, a slight gradual increase of the strength value can be observed in contrast to the moulded construction part according to curve 2. This increase corresponds approximately to the increase which also occurs in curve 1 due to increasing hardening of the matrix. The damaging of the ibres has been avoided is these moulded construction parts according to the invention.
Example 6 A moisture-resistant and weatherproof composite for producing the moulded construction parts was made from:
75 % of blast furnace slag, ground as finely as the binder (Blaine value of at least 3500 cm2/g) 20 % of plaster of Paris according to DIN 1168 (DIN: Deutsche Industrienorm, German Industrial Standard) 5 ~ of Portland cement 45 according to DIN 1164 20 ~ of waste water fibres or cellulose fibres.
The ground blast sand comprises the following com-ponents:
34.44 SiO2, 0.39 Tio2, 12.75 A1203, 1.22 Fe203 (the entire Fe as Fe203), 0.18 MnO, 42.1 CaO, 7.~34 MgO, 0.36 Na20 and 0.6 K20 ~
The composite produced from these components had a dry ~IJ~
density of at least 1.3 kg/dm3 and a minimum strength of 20 N/mm2 .
Example 7 A moulded construction part was produced from 73% of a furnace slag ground as finely as the binder and hav-ing the composition described in Example 1 20~ of plaster o~ Paris according to DI~ 1168 7~ of Portland cement 45 according to DIN 1164 20% of waste paper fibres or cellulose fibres 1~ The composite plates had a dry density of at least 1.5 kg/dm3 and a minimum bending strength of 30 N/mm~
The same results were obtained when gypsum from flue gas desulfurisation was used instead of plaster of Paris.
Example 8 A moulded construction part was produced from the following components:
73% of furnace slag ground as finely as the binder and having the composition of Example 1 20% of plaster of Paris according to DIN 1168 7% of Portlant cement 45 according to DIN 1164 22% of waste paper fibres of cellulose fibres.
The plates produced from this composition had a dry density of at least 1.5 kg/dm3 and a minimum bending strength of 45 N/mm2. When gypsum obtained from flue gas desulfurisation was used instead of plaster of Paris, the construction material had the same properties.
~7~61~
Example 9 A moulded construction part was produced from the following components:
73% of furnace slag of the composition of Example 1 20~ of plaster of Paris according to DIN 1168 7% of Portland cemen-t 45 according to DIN 1164 30~ of waste paper fibres or cellulose fibres.
The binder mixture was most finely ground to a Blaine-value of at least 6,000 cm2/g and preferably to around 7,500 cm2/g.
A moulded construction part produced in this manner has a minimum bending strength of 45 N/mm2 and a dry density of only at least 1.4 kg/dm3. In Table l the bending strength-density ratios of the four examples are shown again.
Table l .. . . .. . . . .
Bending strength-density ratiosExample no.
Ndm mmGkg 15.4 6 20.0 7 30.0 8 32.1 9 In comparison with these construction parts, convention moulded construction parts made from asbestos cement only reach bending strength-density ratio of around 12 or 17 (Ndm3/(mm2kg)).
The given Examples 6 to 9 clearly show that - compared to moulded parts made from asbestos cement - -the moulded construc-tion parts according to the invention have the same or higher ~3;~
bending strengths already with low density of the construction material and they thus feature an essentially improved input-output ratio. The economical effectiveness of the moulded con-struction parts according to the invention is due not only to the high bending strength-density ratios but also in particular to the low raw material prices for the materials used. The moulded construction parts according to the present invention can be produced by means of conventional wet and semi-dry technologies so that time- and money-consuming R ~ D work for new production technologies is avoided.
Claims (25)
- THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
l. Durable molded construction part, in cured form, pre-pared from the hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, wherein said construction material has an alkali buffer capacity which does not exceed 0.005 acid equivalents per 100 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation. - 2. Construction part according to Claim 1, wherein said binder mixture comprises at least two components selected from the group consisting of Portland cement, alumina cement, bellite-rich cement, and pozzolanic substances.
- 3. Construction part according to Claim 2, wherein said pozzolanic substances are selected from the group consisting of amorphous silicic acid, powdered trass, fly ash and mixtures thereof.
- 4. Construction part according to Claim 1, wherein said alkali buffer capacity is adjusted by addition of an acid.
- 5. Construction part according to Claim 1, wherein said binder mixture comprises a finely ground, latently hydraulic component, calcium sulphate and Portland cement.
- 6. Construction part according to Claim 5, wherein said binder mixture comprises, by weight, 60 to 80% of a ground latent-ly hydraulic component, 15 to 25% calcium sulphate and 3 to 10%
Portland cement. - 7. Construction part according to Claim 5, wherein said latently hydraulic component comprises, by weight, 8 to 15% of amorphous Al2O3, 30 to 40% amorphous SiO2, 1 to 10% amorphous MgO, and 35 to 45% CaO.
- 8. Construction part according to Claim 5, wherein said latently hydraulic component comprises granulated blast furnaced slag.
- 9. Construction part according to Claim 5, wherein said calcium sulphate component comprises a technical hemihydrate gypsum.
- 10. Construction part according to Claim 1, wherein said binder mixture comprises a finely ground latently hydraulic com-ponent, calcium sulphate and a commercial cement component.
- 11. Construction part according to Claim 1, wherein said binder mixture comprises a finely ground latently hydraulic com-ponent, calcium sulphate and a calcium component.
- 12. Construction part according to Claim 1, wherein said reinforcing material comprises a ligno-cellulose.
- 13. Construction part according to Claim 12, wherein said reinforcement material comprises waste paper fibers.
- 14. Construction part according to Claim 11, comprising 5 to 40% by weight cellulose fibers.
- 15. Construction part according to Claim 1, wherein said reinforcing material is selected from the group consisting of glass fibers, cellulose fibers and mixtures thereof.
- 16. Construction part according to Claim 15, wherein said reinforcing material comprises 5 to 40% by weight of said settable construction material.
- 17. Method of manufacturing a durable molded construction part from hydration products of a settable construction material comprising a hydraulically hardening binder mixture and at least one reinforcing material subject to degradation under alkaline conditions, comprising mixing said reinforcing material with a binder mixture selected such that said construction material has an alkali buffer capacity which does not exceed 0.005 acid equi-valents per 100 grams of construction material, as measured in an aqueous suspension of the construction material 24 hours after suspension formation, and adding sufficient water to set said construction material.
- 18. A method according to Claim 17, wherein said binder mix-ture comprises Portland cement and alumina cement.
- 19. Method according to Claim 17, wherein said mixture com-prises bellite-rich cement, Portland cement and alumina cement.
- 20. Method according to Claim 17, wherein said binder mix-ture comprises Portland cement and pozzolanic substances.
- 21. Method according to Claim 20, wherein said pozzolanic substances are selected from the group consisting of amorphous silicic acid, powdered trass, fly ash and mixtures thereof.
- 22. Method according to Claim 17, wherein said binder mix-ture comprises a finely ground latently hydraulic component, calcium sulphate and Portland cement.
- 23. Method according to Claim 17, wherein said reinforcing material comprises ligno-cellulose.
- 24. Method according to Claim 17, wherein said binder mix-ture and said reinforcing material are finely ground together before the addition of water.
- 25. Method according to Claim 24, wherein said binder mix-ture and reinforcing material are ground until a specific surface area in the range of 5000 cm2/g to 10000 cm2/g is obtained.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3641370.4 | 1986-12-04 | ||
DE19863641370 DE3641370A1 (en) | 1986-12-04 | 1986-12-04 | Long-term resistant construction-material mouldings |
DE19873720134 DE3720134A1 (en) | 1987-06-16 | 1987-06-16 | Durable, high-strength construction-material mouldings |
DEP3720134.4 | 1987-06-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1273368A true CA1273368A (en) | 1990-08-28 |
Family
ID=25850000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000553411A Expired - Fee Related CA1273368A (en) | 1986-12-04 | 1987-12-03 | Durable and highly stable moulded construction parts |
Country Status (10)
Country | Link |
---|---|
US (1) | US5030289A (en) |
EP (1) | EP0270075B1 (en) |
AU (1) | AU604801B2 (en) |
BR (1) | BR8706548A (en) |
CA (1) | CA1273368A (en) |
DE (1) | DE3785307T2 (en) |
ES (1) | ES2040729T3 (en) |
FI (1) | FI875307A (en) |
NO (1) | NO176313C (en) |
NZ (1) | NZ222784A (en) |
Families Citing this family (33)
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GB8904271D0 (en) * | 1989-02-24 | 1989-04-12 | Sandoz Ltd | Improvements in or relating to organic compounds |
DE3927850A1 (en) * | 1989-08-23 | 1991-02-28 | Fraunhofer Ges Forschung | MORTAR FOR SEALING SPRAY ASPECT CEMENT COATINGS |
US5366549A (en) * | 1990-11-28 | 1994-11-22 | Kyowa Giken Co., Ltd. | Method for fabricating fiber-reinforced slag gypsum cement-based, lightweight set articles |
DE69318400T2 (en) * | 1992-08-24 | 1998-10-01 | Vontech Int Corp | CEMENT WITH SIMULTANEOUSLY GROUND FIBERS |
US5733671A (en) * | 1992-11-12 | 1998-03-31 | San Diego State University Foundation | Cellulose fiber reinforced cementitious materials and method of producing same |
US5374309A (en) * | 1993-02-26 | 1994-12-20 | Blue Circle America, Inc. | Process and system for producing cementitious materials from ferrous blast furnace slags |
JP3137263B2 (en) * | 1993-03-25 | 2001-02-19 | 三智商事株式会社 | High bending strength hardened cement |
US5503789A (en) * | 1994-04-04 | 1996-04-02 | Hull; Harold L. | Method of forming and making a carvable/moldable material |
US5858083A (en) * | 1994-06-03 | 1999-01-12 | National Gypsum Company | Cementitious gypsum-containing binders and compositions and materials made therefrom |
US5718759A (en) * | 1995-02-07 | 1998-02-17 | National Gypsum Company | Cementitious gypsum-containing compositions and materials made therefrom |
US6250715B1 (en) * | 1998-01-21 | 2001-06-26 | Herman Miller, Inc. | Chair |
US6164034A (en) * | 1998-08-31 | 2000-12-26 | Poly Proximates, Inc. | Fiber-reinforced molded plastic roofing unit and method of making the same |
ATE368017T1 (en) | 2000-03-14 | 2007-08-15 | James Hardie Int Finance Bv | FIBER CEMENT CONSTRUCTION MATERIALS WITH LOW DENSITY ADDITIVES |
PL365829A1 (en) | 2000-10-04 | 2005-01-10 | James Hardie Research Pty Limited | Fiber cement composite materials using sized cellulose fibers |
PL365806A1 (en) | 2000-10-04 | 2005-01-10 | James Hardie Research Pty Limited | Fiber cement composite materials using cellulose fibers loaded with inorganic and/or organic substances |
WO2002033164A2 (en) * | 2000-10-17 | 2002-04-25 | James Hardie Research Pty Limited | Method for reducing impurities in cellulose fibers for manufacture of fiber reinforced cement composite materials |
US20050126430A1 (en) * | 2000-10-17 | 2005-06-16 | Lightner James E.Jr. | Building materials with bioresistant properties |
KR100817968B1 (en) | 2000-10-17 | 2008-03-31 | 제임스 하디 인터내셔널 파이낸스 비.브이. | Fiber cement composite material using biocide treated durable cellulose fibers |
DE60219443T2 (en) * | 2001-03-09 | 2007-12-20 | James Hardie International Finance B.V. | FIBER REINFORCED CEMENT MATERIALS USING CHEMICALLY MODIFIED FIBERS WITH IMPROVED MIXABILITY |
US20070277472A1 (en) * | 2002-04-11 | 2007-12-06 | Sinclair Raymond F | Building block and system for manufacture |
US8215079B2 (en) * | 2002-04-11 | 2012-07-10 | Encore Building Solutions, Inc | Building block and system for manufacture |
US7993570B2 (en) | 2002-10-07 | 2011-08-09 | James Hardie Technology Limited | Durable medium-density fibre cement composite |
US7942964B2 (en) * | 2003-01-09 | 2011-05-17 | James Hardie Technology Limited | Fiber cement composite materials using bleached cellulose fibers |
US20050152621A1 (en) * | 2004-01-09 | 2005-07-14 | Healy Paul T. | Computer mounted file folder apparatus |
US7220001B2 (en) * | 2004-02-24 | 2007-05-22 | Searete, Llc | Defect correction based on “virtual” lenslets |
US7998571B2 (en) | 2004-07-09 | 2011-08-16 | James Hardie Technology Limited | Composite cement article incorporating a powder coating and methods of making same |
EP2010730A4 (en) | 2006-04-12 | 2013-07-17 | Hardie James Technology Ltd | A surface sealed reinforced building element |
US7939156B1 (en) | 2006-07-27 | 2011-05-10 | Slaven Jr Leland | Composite concrete/bamboo structure |
US8209927B2 (en) | 2007-12-20 | 2012-07-03 | James Hardie Technology Limited | Structural fiber cement building materials |
PL2080742T3 (en) * | 2008-01-15 | 2015-05-29 | Heidelbergcement Ag | Sulphate foundry cement |
US10882048B2 (en) | 2016-07-11 | 2021-01-05 | Resource Fiber LLC | Apparatus and method for conditioning bamboo or vegetable cane fiber |
US11175116B2 (en) | 2017-04-12 | 2021-11-16 | Resource Fiber LLC | Bamboo and/or vegetable cane fiber ballistic impact panel and process |
US10597863B2 (en) | 2018-01-19 | 2020-03-24 | Resource Fiber LLC | Laminated bamboo platform and concrete composite slab system |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US723015A (en) * | 1902-10-13 | 1903-03-17 | William H Orr | Wall-plaster. |
GB258665A (en) * | 1925-05-06 | 1926-08-30 | Novocrete And Cement Products | Improvements in or relating to the treatment of loose or fibrous organic materials, and to the manufacture of light forms of concrete therefrom |
US2703289A (en) * | 1950-10-23 | 1955-03-01 | Corwin D Willson | Cement bound lightweight aggregate masses |
GB1537501A (en) * | 1974-12-28 | 1978-12-29 | Matsushita Electric Works Ltd | Compositions for forming hardened cement products and process for producing hardened cement products |
FI64935C (en) * | 1976-08-30 | 1984-02-10 | Partek Ab | FRAMSTAELLNING AV ASBESTFRI BRANDHAERDIG BYGGNADSPLATTA GENOM UPPRULLNINGSFOERFARANDE |
FI64129C (en) * | 1980-05-30 | 1983-10-10 | Partek Ab | FRAMSTAELLNING AV EN BYGGNADSPLATTA ENLIGT UPPRULLNINGSFOERFARANDET |
AU515151B1 (en) * | 1980-07-21 | 1981-03-19 | James Hardie Research Pty Limited | Fibre-reinforced cementitious articles |
EP0047158B2 (en) * | 1980-08-29 | 1989-04-12 | Dansk Eternit-Fabrik A/S | A process for the manufacture of fibre reinforced shaped articles |
GB2117753A (en) * | 1982-04-06 | 1983-10-19 | Printsulate Limited | Compositions |
DE3409597A1 (en) * | 1984-03-15 | 1985-09-26 | Baierl & Demmelhuber GmbH & Co Akustik & Trockenbau KG, 8121 Pähl | ASBEST-FREE BUILDING MATERIAL PARTS AND METHOD FOR THEIR PRODUCTION |
US4600434A (en) * | 1985-07-24 | 1986-07-15 | Armco Inc. | Process for desulfurization of ferrous metal melts |
-
1987
- 1987-12-01 EP EP19870117754 patent/EP0270075B1/en not_active Expired - Lifetime
- 1987-12-01 DE DE8787117754T patent/DE3785307T2/en not_active Expired - Fee Related
- 1987-12-01 ES ES87117754T patent/ES2040729T3/en not_active Expired - Lifetime
- 1987-12-02 FI FI875307A patent/FI875307A/en not_active Application Discontinuation
- 1987-12-02 NZ NZ222784A patent/NZ222784A/en unknown
- 1987-12-03 CA CA000553411A patent/CA1273368A/en not_active Expired - Fee Related
- 1987-12-03 NO NO875061A patent/NO176313C/en unknown
- 1987-12-04 BR BR8706548A patent/BR8706548A/en not_active IP Right Cessation
- 1987-12-04 AU AU82084/87A patent/AU604801B2/en not_active Ceased
-
1990
- 1990-01-19 US US07/465,599 patent/US5030289A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP0270075B1 (en) | 1993-04-07 |
NO176313C (en) | 1995-03-15 |
ES2040729T3 (en) | 1993-11-01 |
US5030289A (en) | 1991-07-09 |
NO875061L (en) | 1988-06-06 |
EP0270075A3 (en) | 1989-01-04 |
AU604801B2 (en) | 1991-01-03 |
NZ222784A (en) | 1991-05-28 |
NO875061D0 (en) | 1987-12-03 |
DE3785307D1 (en) | 1993-05-13 |
AU8208487A (en) | 1988-06-09 |
DE3785307T2 (en) | 1993-07-22 |
BR8706548A (en) | 1988-07-12 |
NO176313B (en) | 1994-12-05 |
FI875307A (en) | 1988-06-05 |
EP0270075A2 (en) | 1988-06-08 |
FI875307A0 (en) | 1987-12-02 |
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