CA1225670A - Fire resistant gypsum board containing calcium sulfate anhydrite - Google Patents
Fire resistant gypsum board containing calcium sulfate anhydriteInfo
- Publication number
- CA1225670A CA1225670A CA000469372A CA469372A CA1225670A CA 1225670 A CA1225670 A CA 1225670A CA 000469372 A CA000469372 A CA 000469372A CA 469372 A CA469372 A CA 469372A CA 1225670 A CA1225670 A CA 1225670A
- Authority
- CA
- Canada
- Prior art keywords
- anhydrite
- calcium sulfate
- gypsum
- fire
- board
- 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
Links
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 title claims abstract description 102
- 239000010440 gypsum Substances 0.000 title claims abstract description 68
- 229910052602 gypsum Inorganic materials 0.000 title claims abstract description 68
- 229910052925 anhydrite Inorganic materials 0.000 title claims abstract description 53
- 230000009970 fire resistant effect Effects 0.000 title claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 46
- 239000010455 vermiculite Substances 0.000 claims abstract description 26
- 229910052902 vermiculite Inorganic materials 0.000 claims abstract description 26
- 235000019354 vermiculite Nutrition 0.000 claims abstract description 26
- 239000003365 glass fiber Substances 0.000 claims abstract description 14
- 239000011505 plaster Substances 0.000 claims abstract description 8
- 229910052882 wollastonite Inorganic materials 0.000 claims abstract description 8
- 239000004753 textile Substances 0.000 claims abstract description 7
- 239000010456 wollastonite Substances 0.000 claims abstract description 7
- 238000012360 testing method Methods 0.000 claims description 33
- 239000002002 slurry Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 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 3
- 239000011707 mineral Substances 0.000 claims description 3
- 229940095672 calcium sulfate Drugs 0.000 claims 9
- 235000011132 calcium sulphate Nutrition 0.000 claims 9
- 239000007787 solid Substances 0.000 claims 3
- 229920001410 Microfiber Polymers 0.000 claims 1
- 239000003658 microfiber Substances 0.000 claims 1
- 235000010755 mineral Nutrition 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 27
- 238000004079 fireproofing Methods 0.000 abstract 1
- 239000011162 core material Substances 0.000 description 30
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000002245 particle Substances 0.000 description 10
- 239000000835 fiber Substances 0.000 description 9
- 239000000945 filler Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 238000004901 spalling Methods 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000019610 cohesiveness Nutrition 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000012777 commercial manufacturing Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000009431 timber framing Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Building Environments (AREA)
Abstract
ABSTRACT
FIRE RESISTANT GYPSUM BOARD
CONTAINING CALCIUM SULFATE ANHYDRITE
Increased fire resistant gypsum board core formulations and plaster fireproofing formulations are provided by incorpor-ating calcium sulfate anhydrite into the formulations. Particu-larly fire resistant effects are achieved with a fibrous form of calcium sulfate anhydrite, and with blends of calcium sulfate anhydrite II in particulate or fibrous form. Optionally, the formulations may contain either small amounts of textile glass fiber, wollastonite or vermiculite.
FIRE RESISTANT GYPSUM BOARD
CONTAINING CALCIUM SULFATE ANHYDRITE
Increased fire resistant gypsum board core formulations and plaster fireproofing formulations are provided by incorpor-ating calcium sulfate anhydrite into the formulations. Particu-larly fire resistant effects are achieved with a fibrous form of calcium sulfate anhydrite, and with blends of calcium sulfate anhydrite II in particulate or fibrous form. Optionally, the formulations may contain either small amounts of textile glass fiber, wollastonite or vermiculite.
Description
~S670 FIRE ~ESISTANT GYPSUM BOARD
CONTAINING CALCIUM SULFATE ANHYDRITE
Background of the Invention Field of the Invention This invention relates to improved gypsum formulations, and more particularly to gypsum board formulations whereby increased protection against fire is attained.
Gypsum board products, comprising a monolithic core of set gypsum and a cover sheet (generally paper) encasement, are well known in the art. They are widely used in the construction of interior walls and ceilings and are variously termed gypsum panels, plaster board, gypsum wallboard or the like.
The chemically combined water (about 21% by weight of the gypsum) contributes to the effectiveness of products containing it as a fire barrier in various building and construction products.
When gypsum board or set plaster formulations are exposed to fire, the water is slowly released as steam, retarding heat transmission for a time as the gypsum calcines. The heat resistive properties of various gypsum building materials have been determined by testing facilities on fire testing of assemblies performed in accordance with the American Society for Testing and l~aterials (ASTM) procedures. For example, ASTM C 36 Section 3.3 provides a special fire retardant designation, type X, for gypsum wallboard that provides at least one hour fire retardant rating for boards 5/8 inch (16 millimeters) thick, or 3/4 hour fire retardant rating for boards 1/2 inch (13 mm) thick, when the boards are applied to a test partition in single-layer nailed application on each face of load bearing wood framing members and the assembly tested in accordance with the requirements cf ASTM method E 119.
From studies of the actions of gypsum board when exposed to a fire, such as in a laboratory fire test, it has been generally evident that there is a substantial shrinkage of the board core at sustained high temperature with consequent cracking, which not only contributes to passing excessive heat and hot gases through the test wall but also hastens the disintegration of the board under these adverse conditions. Also, as the gypsum calcines it loses its inherent set strength.
Description of the Prior Art To increase the fire resistant properties of these products it has been conventional to introduce certain fibers and unexpanded vermiculite ores into the slurry of calcium sulfate hemihydrate ~plaster or calcined gypsum or gypsum stucco) and water during the board forming process. This concept is disclosed in U.S. patent numbers 2,526,066; 2,681,861; 2,744,022; 2,803,575; 2,853,394;
3,454,456 and 3,616,173. These patents basically teach the use of certain unexpanded vermiculite to offset the shrinkage of the board core during the heat exposure, the unexpanded vermiculite expanding as the chemically combined water present in the gypsum is driven off. As this heating also tends to degrade the cohesive-ness of the gypsum, reducing the strength and integrity of the core, the fiber component of the core formulation imparts a mechanical binding or matting effect to help hold the calcining gypsum together and l~eep it from disintegrating and falling into the test furnace.
Further, U.S. patent 3,616,173 notes that particular pro-portions of certain small inorganic particles will further improve the overall fire resistant properties of the board cores containing unexpanded vermiculite. Thus certain clays of less than 1 to about 40 micrometer (um) size and either colloidal silica or alumina of less than 1 micrometer size, or mixtures thereof, are said to pro-vide some fire resistant properties in further cooperation with the ore fiber mixture. I).S. patent 3,454,456 indicates that having some proportion of the unexpanded vermiculite present as fine sized particles smaller than 100 mesh (147 um) helps to pre-vent large surface fissures and spalling on the board core. This . . -- . .
~ZZS6~0 patent calls for the use of an unexpanded vermiculite of a par-ticle size which will pass through 50 ~.S. Standard mesh t297 um) and be retained upon a 140 mesh sieve (105 um) for accomplishing low fire shrinkage and low spalling.
Summary of the Invention The present invention was discovered upon retesting a board core sample fire tested a day before, whereupon it was determined that the sample did not shrink at all in the subsequent fire test, but expanded to 0.150 inches (0.038 cm) in a one hour exposure.
Upon further evaluation, it was discovered that during the first test the gypsum of the board core sample had been converted to the anhydrite II form, and this led to the idea of using anhydrite in the core composition. The anhydrite may be regarded as a pre-heat-treated and pre-shrunk gypsum additive which provides improved fire resistant properties.
It is an object of this invention to provide improved fire resistant gypsum board and plaster formulations.
It is another object and advantage of this invention to provide a fire resistant gypsum board core and other calcined gypsum formulations that not only do not shrink as a result of fire exposure but may expand while providing integrity to the heated gypsum material.
The objects of this invention are accomplished basically by incorporating in the gypsum formulation, instead of the customary unexpanded vermiculite, about 2-40 weight % of calcium sulfate anhydrite II, alone or in further combination with small amounts of textile glass fiber or more substantial amounts of unexpanded vermiculite or wollastonite.
Brief Description of the Drawings Figure 1 is a graphic illustration of expansion/shrinkage curves obtained during one hour small scale fire testing of a control and two formulations of the present invention.
' ~ i y ~
~Z~5670 Description of the Preferred Embodiments The major ingredient of the gypsum composition of the invention is set gypsum, i.e. calcium sulfate dihydrate. It is formed by the hydration crystallization of calcined gypsum which has been slurried with water along with conventional additives according to the usual techniques. The calcined gypsum may be either alpha or beta hemihydrate, soluble anhydrite, or mixtures thereof, from natural or synthetic sources. Conventional additives may be added in customary amounts to gypsum formulations to impart desirable properties and to facilitate manufacturing, such as, for example, foaming agents, accelerating agents, retarding agents, dispersing agents, core adhesives, and mixtures thereof.
In the manufacture of gypsum wallboard, the core material is generally made by metering the dry ingredients and water into a mixer and therein generating a foam to control the density of the resultant core material, such as by adding a dilute surface active foaming material solution to the mixer in proportions suitable to form a pourable aqueous slurry. The slurry is dis-pensed through one or more outlets at the bottom of the mixer onto a moving conveyor carrying a cover sheet, such as of a multi-ply paper. Another paper cover sheet is then placed on top of the slurry, so that the slurry is sandwiched between two moving cover sheets which become the facings of the resultant gypsum board.
The thickness of the resultant board is controlled by a forming roll, and the edges of the board are formed by appropriate mechani-cal devices which continuously score, fold and glue the overlapping edges of the paper. Additional guides maintain thickness and width as the setting slurry travels on the moving belt. The board panels are than cut, trimmed and passed to dryers to dry the set but still somewhat wet boards.
~ he improved gypsum board of the present invention is essentially a board core of set gypsum and calcium sulfate anhy-drite II, i.e. the water insoluble form of calcium sulfate in . . .
12;~5~70 contrast to the soluble form which hydrates quickly with the moist air or water.
The core may also contain glass fibers for improved strength and integrity, but it can be made without them. The core formula-tion can include the anhydrite in addition to the customary amounts of gypsum or the anhydrite may be in partial substitution for customary amounts of the gypsum. The gypsum core may also include additional inorganic mineral fillers, particularly of acicular particle shape such as wollastonite (CaSiO3) or about 1-5% by weight of unexpanded vermiculite.
It is preferred that a slowly calcined dead burned anhydrite II, and most preferably of fibrous particle shape having an aspect ratio of greater than 20:1 of length: diameter be used, but slowly or rapidly calcined anhydrite II particles may be used. Dead burned (calcined at greater than 1200C) anhydrite prepared from natural mineral gypsum or gypsum synthesized from industrial pro-cesses may be used as well as natural mineral anhydrite. Mixtures and blends of different anhydrite II forms may be used. The anhy-drite II may be present in an amount ranging from about 2-40~ or more by weight when used by itself. It may also be present in an amount of between about 1% and 10~ by weight particularly where wollastonite, unexpanded vermiculite, and~or glass fiber fillers are present.
The following specific examples will further illustrate various specific embodiments of the compositions and products of the present invention. All amounts are expressed as parts by weight unless specified to tile contrary. Of course, lt is to be understood that these examples are by way of illustration only and are not to be construed as limitations upon the present invention.
EX~IPLE 1 In a first series of evaluations, several formulations were formed into nominal 1.3 cm thick paper covered gypsum board panels on a commercial manufacturing size gypsum board forming line.
.
~ZZ5670 These boards were all made as nearly the same as possible, with substantially identical amounts of set adjusting agents, consis-tency red~cers, binding aids, foam, water and other adjuvants of commercial gypsum boards. Aliquot panel portions measuring 15.25 cm by 25.5 cm were taken from the full si~e panels and submitted ~-small scale fire testing.
For the small scale fire test, the board sample was placed vertically in front of a test furnace composed of fire brick and had a front plenum opening 0.635 cm larger than the board sample.
The furnace was equipped with natural gas burners arranged so that the flames bathed the sample, rather than impinging upon particular spots of the sample, and so that the temperatures along the exposed face of the board sample were essentially uniform.
Temperatures within the furnace and on the exposed face of the sample were measured by thermocouples. In addltlon, the sample was restrained within the brackets of a spring strain gauge to measure the expansion and contraction of the sample during the one hour fire test. For each test the furnace temperature was held as close as possible to the same time-temperature curve.
The furnace fire was started after the panel was set in place, and the temperature raised from ambient to 538C-593C over the first 5 minutes of the test, to 746C-755C at 10 minutes into the test, and maintained at about 755C for the remainder of the hour long test.
Normally, conventional gypsum board core formulations with-out any particular fire resistant additives undergo a thermal expansion of about 0.05-0.06 cm in the first 10 minutes of this test as the paper cover sheets burn off, and then start to shrink as the gypsum in the core calcines. The maximum shrinkage ordi-narily takes place in the first 40 minutes of the test. In this series of tests, the control was a currently preferred fire resistant formulation according to the hereinbefore discussed patents con-cerned with unexpanded vermiculite ore and chopped segments of textile glass fiber. The anhydrite used in samples 2-5 was a . _ . . _ , . _ .
particulate dead burned calcium sulfate anhydrite ground to a mean particle size of 1.5 micrometers. Integrity of the samples was measured by visual observation of the sample during and at the conclusion of the test. In general expansion of the vermicu-lite caused microcracks and weakened the burnt core so it cannot withstand it's own weight. With the anhydrite, smooth burned high integrity cores without visible microcracking were obtained.
Representative results of the fire testing were as follows:
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12256~0 In this example the formulation additions were by weight based on the total composition of the board core ingredients. The results of the control and samples 2 and 3 are graphically pre-sented in FIGURE L. From the FIGURE it may be clearly seen that the anhydrite sample 2 without any unexpanded vermiculite ore and without any glass fiber provided less expansion/shrinkage deviation during the 60 minute test than the standard fire resistant formu-lation. In the FIGURE, sample 3 further shows that the amount of anhydrite may be considerably decreased and fire resistance main-tained with further benefit from including some unexpanded vermicu-lite. Sample 4, not set forth graphically, had equivalent shrinkage performance in the last half hour of the fire test as sample 3 but it had less than half of the anhydrite additive. Sample 5 further shows very good expansion/shrinkage control in an anhydrite formu-lation with low amounts of the anhydrite and without any unexpanded vermiculite.
In a second series of evaluations in accordance with the fire test procedure of Example 1, portions of the hemihydrate used in conventional gypsum board slurry formulations were replaced with various anhydrite materials, and small size paper covered gypsum panels were formed on a laboratory size gypsum board forming line.
The particulate anhydrite II materials used are identified in the data. The FRANKLIN FIBER filler used was a calcium sulfate whisker fiber in anhydrite II form having single crystal average diameters of about 2 um and lengths typically of 50-60 um. For convenience, only the cumulative shrinkage at the end of the one hour tests is reported, with representative results as follows:
.. , .. ~
~2~5670 Sample 1 hour % change in comparison to shrinkage -cmControl A Control Control A - no fire .589, with resistive core large cracks additives in core Control B - 5%
vermiculite ore & 0.3% glass flber .188 Sample ~8 8.3% reground board core from prior testing .188 68~ -Sample #9 8.3% ground anhy-drite rock & 0.3%
glass fiber .165 72% 12%
Sample #10 8.3% commercial SNOW T~ITE~ anhy-drite particulate filler, average 8 micrometers particle size &
0.3% glass fiber .165 72% 12%
Sample #11 30% slow burned particulate anhy-drite, average 9 micrometers particle size ~ 0.3% glass fiber .008 99% 96%
: Sample #12 23% particulate anhy-drite filler, average : particle size 2-2-1/2 micrometers, 5% ver-miculite & 2.25% boric acid +.188 expansion 132% 200%
Sample #13 16.7% particulate anhydrite (2-2-1/2 um), - 5% vermiculite, 2.25~
boric acid +.119 expansion 120% 164%
Sample #14 6.7% anhydrite (2-2-1/2 um) 5%
vermiculite ore .056 91% 70%
PlFRANKLIN FIBER
calcium sulfate filler +.033 expansion106% 118%
Sample #16 3% FRANKLIN FI~ER
calcium sulfate filler .175 70% 7%
,~ Sa3mP3%e FlANKLIN FIEIER
calcium sulfate filler & 3.3% woll- .099 83% 47%
astonite 5~70 From these results it is quite clear that hlghly variable amounts of different forms of anhydrite provide improved fire resistant gypsum board core formulations. With sample B, ground for this example to average particle size of 12 micrometers, and sample 9, ground to average 8 micrometers, shrinkage characteristics equivalent to the use of unexpanded vermiculite ore and glass fiber was obtained. SampLes 12-14 show from equivalent to expansive results with a finely gound anhydrite particular filler; and samples 15-17 show from less shrinkage to expansion with small amounts of an anhydrite whisker fiber.
Full size nominal 1.3 cm thick paper covered gypsum panels were made 1.2 m wide by 3.6 m long on commercial scale gypsum board manufacturing equipment, and the panels submitted to large scale fire testing.
For this fire test a full size non-load bearing wall assembly was erected by screw attaching four panels onto 89 mm steel studs;
and the heat transmission from a test fire monitored by 9 thermo-couples placed in accordance with ASTM E-ll9. This test evaluates the times an assembly can endure a standard fire before (a~ the average temperature readings of a-l tkermocouples attached to the unexposed face of the panel rises 200 degrees Fahrenheit above ambient temperature and (b) an individual thermocouple attached to the unexposed face of the panel rises 125 degrees Fahrenheit above ambient temperature.
A control formulation panel containing 5~ unexpanded vermicu-lite ore and 0.3% textile glass fiber obtained a single point unexposed side failure time at 203Cof 43 minutes and 40 seconds, and an averaged multiple points unexposed side failure time at 162C of 44 minutes. Observation further showed a maximum exposed side opening at a panel edge of 0.635 cm and signs of spalling and hairline cracks on the exposed side.
, ' ~ZZ5670 ~ panel with a core formulation including 3.25% FRANK1IN
FIBER calcium sulfate deadburned anhydrite whisker fiber filler and ~ 3.25% wollastonite as used in ~xample 2 obtained longer exposure times of single point failure at 45 minutes and 30 seconds, and multiple points failure at 46 minutes and 12 seconds. Obser-vation showed maximum deflection of 1.270 cm, maximum opening of 0.159 and one large crack alongside one of the studs.
From the foregoing it is clear that the formulations of the present invention are most useful in the formation of gypsum wall-board cores whereby a markedly improved fire rating for systems employing such wallboard may be obtained. Moreover the for~ulations can be used in the formation of other products based upon a set gypsum core obtained from the mixing of water with a dry calcined gypsum formulation. Thus, dry calcined gypsum plaster mixes based on the formulations of the present invention may be used, for example, in metal casting plasters and in dry plaster mixes which when added to water, can be applied to surfaces such as over steel beams and girders or cast into partition blocks or ceiling tiles and panels to give improved fire protection.
-~:,
CONTAINING CALCIUM SULFATE ANHYDRITE
Background of the Invention Field of the Invention This invention relates to improved gypsum formulations, and more particularly to gypsum board formulations whereby increased protection against fire is attained.
Gypsum board products, comprising a monolithic core of set gypsum and a cover sheet (generally paper) encasement, are well known in the art. They are widely used in the construction of interior walls and ceilings and are variously termed gypsum panels, plaster board, gypsum wallboard or the like.
The chemically combined water (about 21% by weight of the gypsum) contributes to the effectiveness of products containing it as a fire barrier in various building and construction products.
When gypsum board or set plaster formulations are exposed to fire, the water is slowly released as steam, retarding heat transmission for a time as the gypsum calcines. The heat resistive properties of various gypsum building materials have been determined by testing facilities on fire testing of assemblies performed in accordance with the American Society for Testing and l~aterials (ASTM) procedures. For example, ASTM C 36 Section 3.3 provides a special fire retardant designation, type X, for gypsum wallboard that provides at least one hour fire retardant rating for boards 5/8 inch (16 millimeters) thick, or 3/4 hour fire retardant rating for boards 1/2 inch (13 mm) thick, when the boards are applied to a test partition in single-layer nailed application on each face of load bearing wood framing members and the assembly tested in accordance with the requirements cf ASTM method E 119.
From studies of the actions of gypsum board when exposed to a fire, such as in a laboratory fire test, it has been generally evident that there is a substantial shrinkage of the board core at sustained high temperature with consequent cracking, which not only contributes to passing excessive heat and hot gases through the test wall but also hastens the disintegration of the board under these adverse conditions. Also, as the gypsum calcines it loses its inherent set strength.
Description of the Prior Art To increase the fire resistant properties of these products it has been conventional to introduce certain fibers and unexpanded vermiculite ores into the slurry of calcium sulfate hemihydrate ~plaster or calcined gypsum or gypsum stucco) and water during the board forming process. This concept is disclosed in U.S. patent numbers 2,526,066; 2,681,861; 2,744,022; 2,803,575; 2,853,394;
3,454,456 and 3,616,173. These patents basically teach the use of certain unexpanded vermiculite to offset the shrinkage of the board core during the heat exposure, the unexpanded vermiculite expanding as the chemically combined water present in the gypsum is driven off. As this heating also tends to degrade the cohesive-ness of the gypsum, reducing the strength and integrity of the core, the fiber component of the core formulation imparts a mechanical binding or matting effect to help hold the calcining gypsum together and l~eep it from disintegrating and falling into the test furnace.
Further, U.S. patent 3,616,173 notes that particular pro-portions of certain small inorganic particles will further improve the overall fire resistant properties of the board cores containing unexpanded vermiculite. Thus certain clays of less than 1 to about 40 micrometer (um) size and either colloidal silica or alumina of less than 1 micrometer size, or mixtures thereof, are said to pro-vide some fire resistant properties in further cooperation with the ore fiber mixture. I).S. patent 3,454,456 indicates that having some proportion of the unexpanded vermiculite present as fine sized particles smaller than 100 mesh (147 um) helps to pre-vent large surface fissures and spalling on the board core. This . . -- . .
~ZZS6~0 patent calls for the use of an unexpanded vermiculite of a par-ticle size which will pass through 50 ~.S. Standard mesh t297 um) and be retained upon a 140 mesh sieve (105 um) for accomplishing low fire shrinkage and low spalling.
Summary of the Invention The present invention was discovered upon retesting a board core sample fire tested a day before, whereupon it was determined that the sample did not shrink at all in the subsequent fire test, but expanded to 0.150 inches (0.038 cm) in a one hour exposure.
Upon further evaluation, it was discovered that during the first test the gypsum of the board core sample had been converted to the anhydrite II form, and this led to the idea of using anhydrite in the core composition. The anhydrite may be regarded as a pre-heat-treated and pre-shrunk gypsum additive which provides improved fire resistant properties.
It is an object of this invention to provide improved fire resistant gypsum board and plaster formulations.
It is another object and advantage of this invention to provide a fire resistant gypsum board core and other calcined gypsum formulations that not only do not shrink as a result of fire exposure but may expand while providing integrity to the heated gypsum material.
The objects of this invention are accomplished basically by incorporating in the gypsum formulation, instead of the customary unexpanded vermiculite, about 2-40 weight % of calcium sulfate anhydrite II, alone or in further combination with small amounts of textile glass fiber or more substantial amounts of unexpanded vermiculite or wollastonite.
Brief Description of the Drawings Figure 1 is a graphic illustration of expansion/shrinkage curves obtained during one hour small scale fire testing of a control and two formulations of the present invention.
' ~ i y ~
~Z~5670 Description of the Preferred Embodiments The major ingredient of the gypsum composition of the invention is set gypsum, i.e. calcium sulfate dihydrate. It is formed by the hydration crystallization of calcined gypsum which has been slurried with water along with conventional additives according to the usual techniques. The calcined gypsum may be either alpha or beta hemihydrate, soluble anhydrite, or mixtures thereof, from natural or synthetic sources. Conventional additives may be added in customary amounts to gypsum formulations to impart desirable properties and to facilitate manufacturing, such as, for example, foaming agents, accelerating agents, retarding agents, dispersing agents, core adhesives, and mixtures thereof.
In the manufacture of gypsum wallboard, the core material is generally made by metering the dry ingredients and water into a mixer and therein generating a foam to control the density of the resultant core material, such as by adding a dilute surface active foaming material solution to the mixer in proportions suitable to form a pourable aqueous slurry. The slurry is dis-pensed through one or more outlets at the bottom of the mixer onto a moving conveyor carrying a cover sheet, such as of a multi-ply paper. Another paper cover sheet is then placed on top of the slurry, so that the slurry is sandwiched between two moving cover sheets which become the facings of the resultant gypsum board.
The thickness of the resultant board is controlled by a forming roll, and the edges of the board are formed by appropriate mechani-cal devices which continuously score, fold and glue the overlapping edges of the paper. Additional guides maintain thickness and width as the setting slurry travels on the moving belt. The board panels are than cut, trimmed and passed to dryers to dry the set but still somewhat wet boards.
~ he improved gypsum board of the present invention is essentially a board core of set gypsum and calcium sulfate anhy-drite II, i.e. the water insoluble form of calcium sulfate in . . .
12;~5~70 contrast to the soluble form which hydrates quickly with the moist air or water.
The core may also contain glass fibers for improved strength and integrity, but it can be made without them. The core formula-tion can include the anhydrite in addition to the customary amounts of gypsum or the anhydrite may be in partial substitution for customary amounts of the gypsum. The gypsum core may also include additional inorganic mineral fillers, particularly of acicular particle shape such as wollastonite (CaSiO3) or about 1-5% by weight of unexpanded vermiculite.
It is preferred that a slowly calcined dead burned anhydrite II, and most preferably of fibrous particle shape having an aspect ratio of greater than 20:1 of length: diameter be used, but slowly or rapidly calcined anhydrite II particles may be used. Dead burned (calcined at greater than 1200C) anhydrite prepared from natural mineral gypsum or gypsum synthesized from industrial pro-cesses may be used as well as natural mineral anhydrite. Mixtures and blends of different anhydrite II forms may be used. The anhy-drite II may be present in an amount ranging from about 2-40~ or more by weight when used by itself. It may also be present in an amount of between about 1% and 10~ by weight particularly where wollastonite, unexpanded vermiculite, and~or glass fiber fillers are present.
The following specific examples will further illustrate various specific embodiments of the compositions and products of the present invention. All amounts are expressed as parts by weight unless specified to tile contrary. Of course, lt is to be understood that these examples are by way of illustration only and are not to be construed as limitations upon the present invention.
EX~IPLE 1 In a first series of evaluations, several formulations were formed into nominal 1.3 cm thick paper covered gypsum board panels on a commercial manufacturing size gypsum board forming line.
.
~ZZ5670 These boards were all made as nearly the same as possible, with substantially identical amounts of set adjusting agents, consis-tency red~cers, binding aids, foam, water and other adjuvants of commercial gypsum boards. Aliquot panel portions measuring 15.25 cm by 25.5 cm were taken from the full si~e panels and submitted ~-small scale fire testing.
For the small scale fire test, the board sample was placed vertically in front of a test furnace composed of fire brick and had a front plenum opening 0.635 cm larger than the board sample.
The furnace was equipped with natural gas burners arranged so that the flames bathed the sample, rather than impinging upon particular spots of the sample, and so that the temperatures along the exposed face of the board sample were essentially uniform.
Temperatures within the furnace and on the exposed face of the sample were measured by thermocouples. In addltlon, the sample was restrained within the brackets of a spring strain gauge to measure the expansion and contraction of the sample during the one hour fire test. For each test the furnace temperature was held as close as possible to the same time-temperature curve.
The furnace fire was started after the panel was set in place, and the temperature raised from ambient to 538C-593C over the first 5 minutes of the test, to 746C-755C at 10 minutes into the test, and maintained at about 755C for the remainder of the hour long test.
Normally, conventional gypsum board core formulations with-out any particular fire resistant additives undergo a thermal expansion of about 0.05-0.06 cm in the first 10 minutes of this test as the paper cover sheets burn off, and then start to shrink as the gypsum in the core calcines. The maximum shrinkage ordi-narily takes place in the first 40 minutes of the test. In this series of tests, the control was a currently preferred fire resistant formulation according to the hereinbefore discussed patents con-cerned with unexpanded vermiculite ore and chopped segments of textile glass fiber. The anhydrite used in samples 2-5 was a . _ . . _ , . _ .
particulate dead burned calcium sulfate anhydrite ground to a mean particle size of 1.5 micrometers. Integrity of the samples was measured by visual observation of the sample during and at the conclusion of the test. In general expansion of the vermicu-lite caused microcracks and weakened the burnt core so it cannot withstand it's own weight. With the anhydrite, smooth burned high integrity cores without visible microcracking were obtained.
Representative results of the fire testing were as follows:
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12256~0 In this example the formulation additions were by weight based on the total composition of the board core ingredients. The results of the control and samples 2 and 3 are graphically pre-sented in FIGURE L. From the FIGURE it may be clearly seen that the anhydrite sample 2 without any unexpanded vermiculite ore and without any glass fiber provided less expansion/shrinkage deviation during the 60 minute test than the standard fire resistant formu-lation. In the FIGURE, sample 3 further shows that the amount of anhydrite may be considerably decreased and fire resistance main-tained with further benefit from including some unexpanded vermicu-lite. Sample 4, not set forth graphically, had equivalent shrinkage performance in the last half hour of the fire test as sample 3 but it had less than half of the anhydrite additive. Sample 5 further shows very good expansion/shrinkage control in an anhydrite formu-lation with low amounts of the anhydrite and without any unexpanded vermiculite.
In a second series of evaluations in accordance with the fire test procedure of Example 1, portions of the hemihydrate used in conventional gypsum board slurry formulations were replaced with various anhydrite materials, and small size paper covered gypsum panels were formed on a laboratory size gypsum board forming line.
The particulate anhydrite II materials used are identified in the data. The FRANKLIN FIBER filler used was a calcium sulfate whisker fiber in anhydrite II form having single crystal average diameters of about 2 um and lengths typically of 50-60 um. For convenience, only the cumulative shrinkage at the end of the one hour tests is reported, with representative results as follows:
.. , .. ~
~2~5670 Sample 1 hour % change in comparison to shrinkage -cmControl A Control Control A - no fire .589, with resistive core large cracks additives in core Control B - 5%
vermiculite ore & 0.3% glass flber .188 Sample ~8 8.3% reground board core from prior testing .188 68~ -Sample #9 8.3% ground anhy-drite rock & 0.3%
glass fiber .165 72% 12%
Sample #10 8.3% commercial SNOW T~ITE~ anhy-drite particulate filler, average 8 micrometers particle size &
0.3% glass fiber .165 72% 12%
Sample #11 30% slow burned particulate anhy-drite, average 9 micrometers particle size ~ 0.3% glass fiber .008 99% 96%
: Sample #12 23% particulate anhy-drite filler, average : particle size 2-2-1/2 micrometers, 5% ver-miculite & 2.25% boric acid +.188 expansion 132% 200%
Sample #13 16.7% particulate anhydrite (2-2-1/2 um), - 5% vermiculite, 2.25~
boric acid +.119 expansion 120% 164%
Sample #14 6.7% anhydrite (2-2-1/2 um) 5%
vermiculite ore .056 91% 70%
PlFRANKLIN FIBER
calcium sulfate filler +.033 expansion106% 118%
Sample #16 3% FRANKLIN FI~ER
calcium sulfate filler .175 70% 7%
,~ Sa3mP3%e FlANKLIN FIEIER
calcium sulfate filler & 3.3% woll- .099 83% 47%
astonite 5~70 From these results it is quite clear that hlghly variable amounts of different forms of anhydrite provide improved fire resistant gypsum board core formulations. With sample B, ground for this example to average particle size of 12 micrometers, and sample 9, ground to average 8 micrometers, shrinkage characteristics equivalent to the use of unexpanded vermiculite ore and glass fiber was obtained. SampLes 12-14 show from equivalent to expansive results with a finely gound anhydrite particular filler; and samples 15-17 show from less shrinkage to expansion with small amounts of an anhydrite whisker fiber.
Full size nominal 1.3 cm thick paper covered gypsum panels were made 1.2 m wide by 3.6 m long on commercial scale gypsum board manufacturing equipment, and the panels submitted to large scale fire testing.
For this fire test a full size non-load bearing wall assembly was erected by screw attaching four panels onto 89 mm steel studs;
and the heat transmission from a test fire monitored by 9 thermo-couples placed in accordance with ASTM E-ll9. This test evaluates the times an assembly can endure a standard fire before (a~ the average temperature readings of a-l tkermocouples attached to the unexposed face of the panel rises 200 degrees Fahrenheit above ambient temperature and (b) an individual thermocouple attached to the unexposed face of the panel rises 125 degrees Fahrenheit above ambient temperature.
A control formulation panel containing 5~ unexpanded vermicu-lite ore and 0.3% textile glass fiber obtained a single point unexposed side failure time at 203Cof 43 minutes and 40 seconds, and an averaged multiple points unexposed side failure time at 162C of 44 minutes. Observation further showed a maximum exposed side opening at a panel edge of 0.635 cm and signs of spalling and hairline cracks on the exposed side.
, ' ~ZZ5670 ~ panel with a core formulation including 3.25% FRANK1IN
FIBER calcium sulfate deadburned anhydrite whisker fiber filler and ~ 3.25% wollastonite as used in ~xample 2 obtained longer exposure times of single point failure at 45 minutes and 30 seconds, and multiple points failure at 46 minutes and 12 seconds. Obser-vation showed maximum deflection of 1.270 cm, maximum opening of 0.159 and one large crack alongside one of the studs.
From the foregoing it is clear that the formulations of the present invention are most useful in the formation of gypsum wall-board cores whereby a markedly improved fire rating for systems employing such wallboard may be obtained. Moreover the for~ulations can be used in the formation of other products based upon a set gypsum core obtained from the mixing of water with a dry calcined gypsum formulation. Thus, dry calcined gypsum plaster mixes based on the formulations of the present invention may be used, for example, in metal casting plasters and in dry plaster mixes which when added to water, can be applied to surfaces such as over steel beams and girders or cast into partition blocks or ceiling tiles and panels to give improved fire protection.
-~:,
Claims (10)
1. A cast gypsum composition suitable for forming the core of a gypsum board which will provide at least one hour fire resistance by laboratory fire test, which comprises the set gypsum solids from a plaster slurry and about 2-40 weight percent of cal-cium sulfate anhydrite II.
2. The cast gypsum composition of Claim 1 in which said anhydrite II is natural mineral calcium sulfate anhydrite.
3. The cast gypsum composition of Claim 1 in which said anhydrite II is calcined calcium sulfate anhydrite.
4. The cast gypsum composition of Claim 3 in which said calcined anhydrite is dead burned particulate calcium sulfate anhydrite.
5. The cast gypsum composition of Claim 3 in which said calcined anhydrite is dead burned acicular microfiber calcium sul-fate anhydrite having an aspect ratio of length to diameter of greater than 20 to 1.
6. The cast gypsum composition of Claim 1 in which the set solids include by weight about 1-10% calcium sulfate anhy-drite II, about 1-5% unexpanded vermiculite ore and about 0.1-1%
textile glass fiber.
textile glass fiber.
7. The east gypsum composition of Claim 1 in which the set solids include by weight about 1-10% calcium sulfate anhydrite II
and about 1-5% vermiculite.
and about 1-5% vermiculite.
8. A fire resistant gypsum board product comprising a monolithic core of set gypsum and a cover sheet encasement, said core characterized in containing about 2-40 weight percent of cal-cium sulfate anhydrite II effective to maintain integrity of the board and inhibit thermal shrinkage of the board when exposed to the heat of a test fire for 60 minutes.
9. The board product of Claim 8 in which the core further contains about 01-1 weight % textile glass fiber and about 1-5 weight % of a material selected from the group consisting of unexpanded vermiculite and wollastonite.
10. A fire resistant plaster product comprising calcium sulfate hemihydrate, about 1-10% by weight of calcium sulfate anhydrite II and about 0.1-5% by weight of materials selected from the group consisting of textile glass fiber, unexpanded vermiculite, wollastonite and mixtures thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56632883A | 1983-12-28 | 1983-12-28 | |
| US566,328 | 1983-12-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1225670A true CA1225670A (en) | 1987-08-18 |
Family
ID=24262433
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000469372A Expired CA1225670A (en) | 1983-12-28 | 1984-12-05 | Fire resistant gypsum board containing calcium sulfate anhydrite |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS60155558A (en) |
| AU (1) | AU571294B2 (en) |
| CA (1) | CA1225670A (en) |
| NZ (1) | NZ210705A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3221529B1 (en) | 2014-11-17 | 2020-12-23 | Georgia-Pacific Gypsum LLC | Gypsum panels, cores, and methods for the manufacture thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2083321A (en) * | 1935-06-24 | 1937-06-08 | Ici Ltd | Calcium sulphate plaster |
-
1984
- 1984-12-05 CA CA000469372A patent/CA1225670A/en not_active Expired
- 1984-12-18 AU AU36883/84A patent/AU571294B2/en not_active Ceased
- 1984-12-21 NZ NZ21070584A patent/NZ210705A/en unknown
- 1984-12-26 JP JP27351684A patent/JPS60155558A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3221529B1 (en) | 2014-11-17 | 2020-12-23 | Georgia-Pacific Gypsum LLC | Gypsum panels, cores, and methods for the manufacture thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60155558A (en) | 1985-08-15 |
| AU3688384A (en) | 1985-07-04 |
| NZ210705A (en) | 1988-06-30 |
| AU571294B2 (en) | 1988-04-14 |
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