WO2001045932A1 - Strengthened, light weight construction board and method and apparatus for making the same - Google Patents

Strengthened, light weight construction board and method and apparatus for making the same

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Publication number
WO2001045932A1
WO2001045932A1 PCT/US2000/035176 US0035176W WO0145932A1 WO 2001045932 A1 WO2001045932 A1 WO 2001045932A1 US 0035176 W US0035176 W US 0035176W WO 0145932 A1 WO0145932 A1 WO 0145932A1
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WO
Grant status
Application
Patent type
Prior art keywords
board
composition
water
solution
construction board
Prior art date
Application number
PCT/US2000/035176
Other languages
French (fr)
Inventor
Joseph S. Luongo
Original Assignee
Luongo Joseph S
Priority date (The priority date 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 date listed.)
Filing date
Publication date

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B13/00Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material
    • B32B13/04Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B13/08Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of paper or cardboard
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS, SLAG, OR MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B11/00Apparatus or processes for treating or working the shaped or preshaped articles
    • B28B11/24Apparatus or processes for treating or working the shaped or preshaped articles for curing, setting or hardening
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS, SLAG, OR MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B15/00General arrangement or layout of plant Industrial outlines, plant installations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS, SLAG, OR MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B19/00Machines or methods for applying the material to surfaces to form a permanent layer thereon
    • B28B19/0092Machines or methods for applying the material to surfaces to form a permanent layer thereon to webs, sheets or the like, e.g. of paper, cardboard
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS, SLAG, OR MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B23/00Arrangements specially adapted for the production of shaped articles with elements wholly or partly embedded in the moulding material; Production of reinforced objects
    • B28B23/0081Embedding aggregates to obtain particular properties
    • B28B23/0087Lightweight aggregates for making lightweight articles
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B26/00Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
    • C04B26/02Macromolecular compounds
    • C04B26/28Polysaccharides or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/14Compositions 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
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04CSTRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C2/00Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
    • E04C2/02Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
    • E04C2/04Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres
    • E04C2/043Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres of plaster
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/10Inorganic fibres
    • B32B2262/101Glass fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2305/00Condition, form or state of the layers or laminate
    • B32B2305/70Scrap or recycled material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/30Properties of the layers or laminate having particular thermal properties
    • B32B2307/306Resistant to heat
    • B32B2307/3065Flame resistant or retardant, fire resistant or retardant
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2607/00Walls, panels
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2607/00Walls, panels
    • B32B2607/02Wall papers, wall coverings
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00612Uses not provided for elsewhere in C04B2111/00 as one or more layers of a layered structure
    • C04B2111/0062Gypsum-paper board like materials

Abstract

A novel construction board composition is disclosed comprising a unique combination of synthetic binders selected for their ability to establish a strengthened permanent bond in the final dry state for use in a construction board composition comprising primarily gypsum, and in a construction board composition comprising an expanded mineral such as Perlite which largely reduces the amount of gypsum over current gypsum construction board formulations, thus reducing the weight while maintaining the strength of the construction board structure. The composition comprises an expanded mineral, calcium sulfate and a synthetic binder selected from a vinyl acetate emulsion, an acrylic emulsion and a polyrethane emulsion. In a preferred embodiment, the lightweight, strengthened gypsum construction board of the present invention also comprises an optional covering veneer that is applied to provide increased strength, moisture resistance, and fire retardancy, and the back paper top ply is treated to provide increased flexural strength.

Description

STRENGTHENED, LIGHT WEIGHT CONSTRUCTION BOARD AND METHOD AND APPARATUS FOR MAKING THE SAME

Technical Field This invention relates to new compositions and methods that are useful in the manufacture of boards or panels for use in construction applications. More particularly, this invention is directed to a novel construction board or panel composition comprising a unique combination of synthetic binders selected for their ability to establish a strengthened permanent bond in the final dry state, in combination with gypsum and an expanded mineral such as Perlite. Utilizing such synthetic binders provides an increased strength to the construction board core, enabling lighter- weight Perlite to replace at least a portion of the heavier gypsum traditionally used in construction board compositions. Moreover, the synthetic binders disclosed herein uniquely cross-link with the expanded mineral to form a much stronger bond between the constituent components of the construction board core material than that which has been available in previously utilized or known construction board products. In a preferred embodiment, the lightweight, strengthened construction board of the present invention also comprises a covering veneer of paper or fiber that is treated to further the fire retardant and moisture resistance of the product. Additionally, this invention relates to the unique manufacturing process and apparatus to produce the construction board composition of the present invention in order to create a lightweight, strengthened, moisture resistant, and fire retardant panel to be used in construction applications.

Background Art It is well known in the art to use planar panels or sheets formed from inorganic materials in the construction of walls, ceilings, floors, exterior sheathing, and similar construction elements, instead of applying wet plaster to such surfaces. Such panels may be applied to stud work comprising the walls, ceilings, floors, and exteriors of building structures in the form of wallboard. lath, sheathing, and the like, using nails, screws, or other fastening means. The use of calcium sulfate hemihydrate CaS04*2H20 in the manufacture of such construction panels has predominately been unchanged for over half a century. In general, these panels comprise essentially a core of set interlaced gypsum crystals disposed between fibrous, especially paper, liner sheets. After the gypsum slurry has set (i.e.. reacted with the water from the aqueous slurry) and dried, the sheet is cut into standard board sizes. Unfortunately, however, traditional gypsum construction boards can be quite heavy. causing quick fatigue to installers and delayed construction schedules, as well as large transportation costs. Likewise, traditional construction boards often realize significant increases in weight when particular construction applications require stronger construction panels, thus making their use even more problematic. Attempts to modify the composition of traditional gypsum panels in order to provide a lighter weight construction panel have been made, but with little success or commercial viability. For example, the addition of synthetic binders has very recently been attempted as disclosed in U.S. Patent No. 5.879.825 to Burke et al.: however, the engineering and chemical research in various combinations of complex chemical formulations and combinations thereof has been quite limited. Additionally. Burke et al. fails to address the environmental concerns of noxious fumes under fire engineering standard ASTM testing El 19. Still further, cost considerations limit the amount of acrylic polymer present in the Burke et al. composition to 1 to 2 percent, but the fact that such acrylic polymer in Burke et al. employs a less than 10% solids ratio results in a polymer having a minimal cross-linking performance with the other constituent elements. Further, while the use of Perlite as an antidessicant to prevent the dehydration of gypsum crystals formed during setting of the core composition is disclosed, no consideration is gi\ en to introducing an expanded mineral, such as perlite. as a substitute for gypsum as one of the structural foundations of the board core and as a strengthening agent when combined with appropriate other constituent elements (as set forth below), nor the specific need for a synthetic binder composition for establishing a complete cross-linking between the constituent elements of the core in order to create a molecular change within the strengthening agent, which molecular change is in turn required to completely bond a reduced amount of gypsum with the other components of a construction board core. It would therefore by highly advantageous to provide an improved, high strength, lightweight construction panel product which reduces the need for gypsum in the panel composition by means of displacing some of the normal amount of gypsum utilized with the expanded mineral perlite. and which utilizes a synthetic binder composition that enables a complete cross-linking of the constituent elements of the lighter construction panel core to form a rigid structure with the structural integrity to withstand the structural requirements of traditional construction panels. Such construction panels should meet industry requirements, and likewise have a strength at least equal to previously known construction panels while reducing the weight of the finished panel.

Disclosure of Invention It is therefore an object of the instant invention to provide an improved, light weight, strengthened gypsum construction board product that overcomes the disadvantages of the prior art. This and other objects are achieved through a composition consisting essentially of a unique combination of synthetic binders selected for their ability to establish a permanent bond in the drv state, combined with an expanded mineral (e.g.. Perlite and crushed Perlite), organic binding adhesives. drying agents, crystal growth enhancers, and gypsum with a sufficient amount of water to form an aqueous slurry, all contained within a covering of treated moisture and heat resistant paper material, which produces an improved lighter- weight, strengthened gypsum construction board product. The technology of the present invention utilizes an expanded mineral which fuses with the calcined gypsum mineral and physically becomes part of the composite matrix due to the complex formulation of binders and gypsum attaching themselves to the expanded mineral, instead of the expanded mineral only acting as a filler. Perlite (expanded) can be graded by density in pounds per cubic foot, and classified by product number or trade name for producer and user identification. The expanded product can weigh as little as 2 pounds per cubic foot, but the most widely used bulk-density grade range is from 7 to 15 pounds per cubic foot. The range of expanded Perlite utilized in the construction board composite core of the present invention is 3 to 10 pounds per cubic foot, with 4 pounds per cubic foot being preferred. It has been found that the more friable cryogenic and micro-sphere grades in the 3 to 4 pound range are favorable, with 4 pounds being the most preferred, over the heavier grades ranging from 5 to 10 pounds per cubic foot. Grades typical to this heavier range include concrete, plaster, and cavity fill or masonry, which can also be utilized, but are not as preferable as the lighter previously mentioned grades. The particle size ranges from 100 to 2,000 microns, and preferably from 200 to 1000 microns. Preferably, the expanded Perlite will have a particle size ranging from no larger than 10 mesh sieve size and no smaller than 200 mesh sieve size measured on standard screen scale. The particle size of the preferred expanded Perlite is directly related to the strength of the construction board core in the aspect of fusion. Particles that are too large tend to space gypsum crystal growth too far apart, and particles that are too small do not allow enough area for the gypsum crystal to fuse onto. The particle size is not directly related to the expansion method but can be controlled by means of properly sizing the Perlite ore prior to expansion. It was determined to be advantageous to use a polyvinyl acetate emulsion or vinyl acetate homopolymer emulsion or water based non-V.O.C. acrylic or polyurethane emulsion for use in the binder of the instant invention. While vinyl acetates of all types were found to be less costly and performed well, vinyl acetate emulsions with 0.10% to 30% polyvinyl alcohol were further preferred and found to provide unforeseen benefits over powdered polyvinyl acetates. First, vinyl acetate emulsions containing polyvinyl alcohol are available at far less cost (approximately one third) than powdered polyvinyl acetates. Further, vinyl acetate emulsions when properly added and diluted for quick dispersion in the metered water or water solution feeds, prior to entrance into the gypsum slurry mixer, dispersed and performed better than powdered polyvinyl acetates, thus simplifying the manufacturing process and reducing costs caused by flawed boards. Better results in terms of reactivity, dispersion, and ease of mixing occurred in test samples when the vinyl acetate emulsions were strengthened and stabilized with polyvinyl alcohol. It was discovered that the optimum molecular weight of the preferred polyvinyl alcohol selected to strengthen and stabilize the vinyl acetate emulsion is a function of the type of gypsum stucco prepared, and the length of time the final vinyl acetate emulsion needed to be stabilized. In final prepared gypsum stuccos that had higher percentages of certain clays (i.e.. above 1 % of clays commonly found in some gypsum deposits) naturally occurring in or with the gypsum ore. lower molecular weight polyvinyl alcohols, preferably between 20 and 5000. exhibited better results with less initial thickening of the wet gypsum slurry mix. It has also been determined that the addition of small amounts of accelerators or strengthening agents described below can be added to the' final polyvinyl acetate emulsion to increase strength and final composite set performance. To describe this macroscopically. the binder is diluted in the processed water to disperse throughout the wet gypsum and perlite slurry in the pin mixer. An accelerator or strengthening agent is added to the back side of the gypsum slurry pin mixer, to begin to chemically increase the set of the binder once the formed construction board is proceeding downstream to the rotary knife. Optimally, the initial set time of the board is decreased such that the board can be cut in less time. Thus, the board line can be run faster, producing more construction board in a shorter period of time. Potassium or other alkali elements or compounds can be added at 0.001 % to 3% of the total board wet weight at the last stages to increase the rate of the set time of the binder and ultimately decrease the initial set of the construction board. While Potassium Sulfate has been utilized to decrease the initial set time of the green construction board prior to the knife. too high or too small amounts can actually burn the gypsum crystals and create a "'punky" or powdery final construction board that has lost its strength. The binder (vinyl acetate emulsion, or water based non V.O.C. acrylic or polyurethane emulsion) reacts with the accelerator (potassium sulfate) to retard or even eliminate the burning of the gypsum crystals. Optionally, reinforcing fibers, fire retardants. water repellents, and other water proofing materials may be part of the composition. More particularly, current gypsum construction board core formulations, once dried, have common micro-cracks, form more brittle core composites, and exhibit less tolerant processed board flexibility. Paper fibers, or other synthetic fibers, have been utilized more in the past to hold the core composite together, yet have been insufficient to stop board drying over time, and increase short and long term micro-cracking and ultimate core breakdown or spot load failure. Thus, the development of the synthetic adhesive technology of the instant invention has developed critical improvements to board flexibility, moisture retention, and long term, sustained and improved strength. Actual plant manufacturing test runs of the construction board compositions described herein were conducted for several hours each, and using a variety of gypsum ore and gypsum stucco preparation methods. The test runs showed improved ASTM test results at each run. The process of introducing and adding sufficient amounts of the synthetic binder into the final gypsum stucco was successfully completed during each test run. However, improved results occurred when the binder was diluted in the metered water or other prepared water solutions, for direct feed prior to the gypsum slurry mixer. Higher ASTM lab test results occurred when utilizing the optimum design combinations and percentages set forth in the examples below of vinyl acetate and water based non-V.O.C. acrylic or polyurethane emulsions, with each particular type of gypsum stucco supplied during the test runs. Thus, by optimizing the final polyvinyl acetate homopolymer or water based non-V.O.C. acrylic or urethane polymer emulsion, optimum test results were achieved in both the test lab and in actual manufacturing test samples. Thus, the test run results showed that the construction board composition of the instant invention provides a number of benefits over previously known construction board products. First, the present invention allows for a construction board composition that is significantly lighter in weight (up to fifty percent lighter) than current traditional heavy gypsum construction board formulations. This reduced weight also results in transporting lighter loads, in turn reducing transportation costs. Further, job site labor costs are reduced by enabling the workers to handle lightened loads, such that the installation process is made easier and less costly. Similarly, the potential for heavy board related injury accidents to the tradesmen that install the construction board product is reduced. Further, the construction board composition of the instant invention exhibits equal or greater strength than current heavy gypsum construction board, with improvements in moisture resistance and flame resistance that exceeds current industn standards. This lightweight and strength factor equates to decreased structural support load bearing and lessens the total support strength required in any project, in turn further reducing overall construction costs. Yet another benefit of the strengthened construction board of the instant invention is the reduction in the amount of board breakage (and in the amount of airborne particulates associated with such breakage) and losses due to manual or machine transport to the installation site, due to the fact that the composition of the instant invention provides the construction board with greater flexibility than has been known in previous construction board compositions. Yet another benefit of the composition utilized in the instant invention is the "clean- snap" characteristics exhibited by a finished construction board when the board is cut with a utility knife. The attempted addition of synthetic binders in the past to construction board compositions have reduced the ability to cut the finished construction board sheet during installation with a utility knife. However, the composition of the instant invention was developed after extensive testing and analysis of numerous chemical combinations, with extensive chemical technical research and testing to realize a brittle cross-linking complex polymer that combines and fuses with the mineral and expanded mineral, that is easily cut and snapped with a utility knife as applied in standard construction industry use. The specific binders described below as a constituent element of the compositions used herein also provide specific benefits related to the characteristics and manufacturing economics of the construction board of the instant invention. Water based vinyl acetate, non- V.O.C acrylic and non-V.O.C. polyurethane emulsions tested were selected and preferred over other petrochemical-based emulsions or liquid plastics for several specific reasons. First, the most crucial practical factors in selecting the preferred type of adhesive are performance of the adhesive in binding the construction board core, and cost relative to that performance, and the compatibility of the particular emulsion w ith the other specific constituents of the sheathing core. Such cost factors include both the cost of the base components, such as vinyl acetate monomer (VAM) (which today is preferably produced from ethylene) that make up the adhesive, and the cost to make the final product. It was found that vinyl acetates provide the lowest cost, while water based non-V.O.C. acrylic and polyurethane polymers provided non-toxic and environmentally safe high performance at a slightly higher but not unreasonable cost, while all three maintained assurance of high adherence and coherence capabilities to attach to the minerals in the construction board core, namely, gypsum and/or perlite. Also, a deliberate effort was made to determine and utilize a low cost, final stage, brittle-type plastic in emulsion or liquid initial state, that when hardened would have the ease of a clean snap when cut with a utility knife. It was discovered that the vinyl acetate adhesive family and the non-V.O.C. acrylic and polyurethane families performed superior to sodium silicates in meeting these requirements, even though sodium silicates were lower in overall cost. Regarding the compatibility of the emulsion with the other constituents of the construction board core, test results proved that water solubility of the adhesives and ease of dispersion into the final core composite was crucial to fabricating the construction board without paper blows and peels due to insufficient or improper re-hydration of the calcined gypsum. In all of the tests performed, results showed favorably toward the latex water based emulsions for the best compatibility and ease of dispersion when added into the system with no adverse affect on hydration. The preferred polymer systems of the instant invention provided for complete hydration of the gypsum as well as improving upon the paper to core bond in everv instance of its use. The latex water based emulsions also worked best at the drier end of the line (in the kiln) as they didn't react poorly or inhibit evaporation due to filming and/or agglomeration and blistering due to improper dispersion into the slurry. Also, it was discovered that board flexibility during actual board installation, or during the manufacture of the board as it travels over rollers and curved rises in and out of the drying kilns, was improved through the use of more plastic adhesives (such as vinvl acetate and non-V.O.C. acrylic and polyurethanes) as the binder. Yet another benefit of the binder formulations utilized in the construction board of the instant invention lies in their ability to easily cross link with the other constituent elements of the formulations provided below. Vinyl acetates were found to react well and cross-link in the presence of boron with starches to create a final tack)' binder, at the proper percentages set forth below, that forms a brittle plastic excellent for binding the core of the construction board product in such a way as to maintain superior strength characteristics while reducing the overall weight of the board. The improved, strengthened core material of the instant invention also provides increased compression, shear, and tension loading test results in comparison with the conventional non-reinforced gypsum construction board. ASTM Test Standard C79 standard specifications for gypsum construction board require that specimens shall surpass an average surface water absorption of not more than 1.6g after 2 hours of elapsed time (Section 5.1.7). While gypsum construction board is required to meet the above ASTM standards, moisture resistance and adverse weather conditions have been long-term problems with gypsum board. The improved gypsum board of the instant invention comprises an improved moisture resistant cover and core material that far surpasses ASTM C79-5.1 .7. Thus, the present invention improves the structural strength, moisture resistance, and weight factors in the design of a new improved gypsum board to be utilized as a construction material. Gypsum board manufacturing is a complex process from the collection of the gypsum rock to the production of the completed construction board. However, the improved gypsum construction board product of the instant invention, as described more fully in the examples below, offers yet another benefit over previously known construction board products, in that it provides increased production capacity from a given gypsum supply over traditional gypsum products and methods of manufacture. More particularly, the technology of the present invention allows for decreased set times from the pin mixer to the knife in laboratory testing, which in turn increases boardline manufacturing speeds far beyond what is currently being realized. As manufacturing speeds increase, so does production, enabling greater amounts of construction board to be produced to meet the current demand. This complex formulation of binders can be seen to be utilized in a wide variety of other building materials as well. Yet another improvement of the gypsum construction board product of the present invention comprises the environmental improvements realized through the use of the specific binders recited herein. Environmental factors must be evaluated when selecting the preferred adhesive, such as noxious fumes emitted in burning test samples and kiln stack emissions while heating and drying the board during the manufacturing process. Plant operational environmental concerns and plant kiln stack emissions are critical factors for manufacturers to consider in evaluating the use of synthetic adhesives. Petrochemical-based acrylics exhibited higher stack emissions, noxious fumes in burn tests, and presented more environmental operational concerns over similar percentages of vinyl acetate emulsions and water based non-V.O.C acrylics and polyurethanes. Further, the specific adhesives used in the construction board product of the instant invention provide a reduced half-life over commonly used adhesives. The adhesives used in the construction board product of the instant invention decompose very quickly and easih'. Thus, the improved construction board of the present invention provides a lightweight, strengthened, fire retardant. whitish-covered Perlite and gypsum construction board with environmental improvements that is competitively priced to traditional gypsum construction board products. A preferred embodiment of the invention is further directed to a method and apparatus for producing expanded Perlite and gypsum construction boards of a thickness not less than V inch and not greater than 1 inch comprising the steps of: adding starch, boric acid, foamer, gypsum, and a latex polymer emulsion of vinyl acetate or water based non V.O.C. acrylic or polyurethane, with water to expanded Perlite to form a composition; enveloping the aqueous slurry between two high quality paper cover sheets comprised of recycled virgin pulp and forming the same into a board; directing the continuous board away from the forming apparatus to a cutting knife where it is cut to desired length: and finally drying the board in a high temperature kiln at temperatures ranging from 75°C to 325°C. Optionally, the process further includes the steps of forcing hot air to an encapsulated section of board line, starting the curing process prior to the board reaching the board cutting knife.

Brief Description of Drawings Other objects, features, and advantages of the present invention will become more apparent from the following detailed description of the preferred embodiment and certain modifications thereof when taken together with the accompanying drawings in which: FIGURE 1 is a schematic view of the perlite processing arrangement of the instant invention. FIGURE 2 is a schematic view of the perlite construction board production facility of the instant invention. Best Vlode(s) for Carrying Out the Invention The preferred composition of the improved gypsum construction board product of the present invention comprises a binder especially selected for the property of permanent tackiness in the dry state, preferably a self-crosslinking permanently tacky polymer, and more particularly includes a starch, boric acid, vinyl acetate emulsion or water based non-V.O.C. acrylic or polyurethane emulsion, perlite. and gypsum. It has been found that this combination (in the proportions set forth below) offers the best results for weight, strength. setting and bond of the construction board core. After applying and analyzing a wide variety of adhesives by themselves and in combination with one another, it was determined that a binder having the composition set forth herein would allow the construction board to perform as closely to what is currently used while adding strength and reducing weight. The strengthened core of the improved gypsum construction board of the instant invention contains of the total weight of the slurry gypsum at up to about 60%. and expanded Perlite in the range of 0.5 to 60% volume by weight, and more preferably at up to about 40% volume by weight. The expanded Perlite ranges in sizes from 100 to 2000 microns, and preferably from 200 to 1000 microns. The following is a typical sieve analysis of the preferred grade: 1 1.5% retained on 16. 39.1% retained on 30. 24.3% retained on 50. 12.9% retained on 100. and 2.8% retained on 200. The preferred grade loose density ± 1 pound is 4 pounds per cubic foot and has a compacted density of 5.5 pounds per cubic foot. Hard Perlite ore having a high compaction resistance is a very dense concentric ore located within the inner perlitic dome, while softer, low compaction resistant ores are located in the froth}' pumicious outer surface of the perlitic dome and are very friable. The expanded Perlite utilized in the construction board of the instant invention is preferably derived from classical concentric granular ores from the middle of the perlitic dome, which ores are able to achieve densities in the 4 to 8 pound range, in order to minimize the expanded density and weight of the Perlite used in the composition of the instant invention w hile maximizing its strength. While Perlite has been used in the past in small quantities as a filler or additive in gypsum board compositions, the instant invention utilizes expanded Perlite as part of the composite core, adding strength to the core as the binder grabs onto the Perlite. The combination of starch, borate or boric acid and vinyl acetate emulsion or water based non-V.O.C. acrylic or polyurethane emulsion in itself is sufficient to bond the Perlite together in producing the composite core of the instant invention. 1 Iowever. the combination of gypsum and perlite in the formulation of the improved construction board product of the instant invention, in comparison to other cementious materials, is preferred due to excellent compatibility of the components described herein. It is important to note that the unique adhesiv e technology that is described below is completely new and unobvious to the manufacture of construction board products. This process adds a synthetic variable into an already well-used natural adhesive formulation of starch and borate. When starch is treated with borate. interchange linkages are formed throughout the borate anion structure resulting in modifications of the physical properties of the polymer system. The overall result is a binder which, during the construction board manufacturing process, undergoes a chemical change which provides for complete crosslinking between the starch, borate. and synthetic adhesiv e to form a strengthened web for gripping the gypsum and perlite and forming a rigid core. Starch and borate are often added to the traditional construction board composition in order to protect the delicate gypsum crystals and to ensure proper crystal growth of the gypsum constituent of the construction board core as the board is heat treated in a drying kiln at extreme temperatures. However, as mentioned above, starch and borate also combine to form a natural adhesive. Traditional gypsum compositions do not utilize an additional binder to give the board strength, but rather rely on gypsum crystal growth brought about by heat treatment of the board in its final manufacturing stage. Thus, traditional gypsum construction board compositions do not rely on the adhesive nature of the combination of starch and borate. Borate is not utilized as a standard constituent in all construction board core formulations in the industry, but is preferred by some and is always added to fire rated board formulations as a fire retardant. Other fire retardants may optionally be added to the adhesive to increase the binder's fire rating, i.e.. kaolin or bentonite clay emulsions, or other high carbon emulsions. The construction board composition of the present invention, however, does require an additional binder. It has been found that adding another polymer, namely a vinyl acetate emulsion or water based non-V.O.C. acrylic or polyurethane emulsion, to the starch polymer and boric acid enables a cross-linking to occur between the three constituents. By crosslinking the synthetic polymer chain with the starch and borate polymer chain, more extensive chemical changes are brought about. On a molecular scale, the polymer chain branches extend in all directions, attaching to the gypsum and perlite and increasing the overall strength of the board. Cross-linking of the binder utilized in the present invention with the starch polymer chain is brought about through boron or the use of boric acid. It was originally believed that the commonly used compound boric acid was a sufficient source of boron for the process of the present invention to cross-link the hydroxyl groups of the starch with the vinyl acetate emulsion branch polymer chains. However, large scale test runs of the construction board of the instant invention revealed an occasional high water demand when standard technical grade ortho boric acids were used, especially when introduced into the system in solution as is not uncommon in board production. Laboratory testing revealed that the pH of the boric acid (6.1 in 0.1 % solution) and its low molecular w eight were causing some fluidity decrease or viscosity increase in slurry formation. In these circumstances, the solution is to replace the boric acid with sodium tetraborate pentahydratc ( 5 mol) or sodium tetraborate decahydrate ( 10 mol). the two compounds actually being less costly than the ortho boric acid. The amount of borax or boric acid should be limited in the range of not higher than 0.35%o of the total wet weight of the final slurry or more specifically not more than 0.1 % of the total amount of synthetic binder utilized (by weight), as it has been found that higher concentrations can cause gelling of the polyvinyl acetate emulsion and affect strength. The particular type of board starch utilized is yet another important consideration. Starches, or more specifically unmodified cereal flours and modified corn starches, are commonly utilized in gypsum board production to provide a better interface between the paper and the core and to protect the gypsum crystal during drying of the board, as well as to allow for increased paper bond. A large number of starch grades can be utilized from lower grade cereal flour to high grade very thin boiling starches which are acid treated. Gelling and flow properties as well as compatibility are better in the higher-grade starches produced from dent corn. The quantity utilized in standard construction board production can range anywhere from 5 to 12 pounds per thousand square feet (MSF). Typically this range is from .20 to .50 percent of the wet board weight (MSF). Testing conducted in the laboratory showed better resulting strength development using the formulation of the present invention and starch in the range of 0.30 to 0.75 percent by weight (MSF) in combination with the synthetic binder. Higher grade acid modified starches worked well in combination and to cross-link with the vinyl acetate emulsion. Further testing revealed other types of starches, including oxidized thin boiling starches, worked well if not better than acid modified starches. In some situations, oxidized starches are highly compatible with vinyl acetate emulsions as are acid treated starches. But in situations where the gypsum stucco has clay impurities, the oxidized starch can grab onto the vinyl acetate emulsion and block flocculation of clay particles with the polyvinyl alcohol, virtually eliminating "clay shock" and viscosity problems experienced in formulations w here shock occurs. Although slightly higher in cost, oxidized starches are believed to be the least expensive and simplest solution in these clay situations. The gelling and fluid characteristics of starch play a larger role in the formulation of the present invention than in standard construction board formulations. Instead of the majority of the starch migrating to the face to protect the core to paper bond, much of the starch is retained in the core to chemically combine with the synthetic additive to fuse the minerals together. This cross-linking of the starch and synthetic additive is key to the strength development of the core of the lightweight construction board of the present invention. In all tests, the higher grades, meaning flash dried, wet milled modified starches gave the best results in nail pull and flexural strength ASTM testing procedures over the lower grade, dry milled, belt dried starches requiring less processing than higher grade starches. The use of more intensely processed starches is somewhat a factor to consider in determining the optimum final construction board costs. By introducing vinyl acetate, polyvinyl acetate copolymer. or a vinyl acetate-ethylene copolymer. or water based non-V.O.C. acrylic or polyurethane polymer into the compositions of the construction board of the instant invention, the resultant complex molecule is much larger, extending its various branches in all directions. It is this desirable change in the polymeric structure of the molecule to a more highly branched chain polymer of higher molecular weight that produces an adhesive with increased viscosity, quicker tack, and better fluid properties. These qualities are crucial to the strength of the most preferred embodiment of the invention. Listed below are two main benefits of this polymer adhesive system. First, increased flexural and compressive strength is realized over current gypsum board ASTM standards. Secondly, the unique polymer adhesive composition of the instant invention enables a construction board composition that is up to as much as fifty percent lighter than current gypsum board. The vinyl acetate emulsion used as the binder m one embodiment of the instant invention produces very favorable test samples and test results. The vinyl acetate emulsion is a milky white liquid, with typical characteristics in the range of a melting point of 32°F to 39°F, a vapor pressure of 16 mm Hg to 22 mm Hg (68°F to 70°F). specific gravity of 1.0 to 2.0, vapor density of from less than 1 to 1. a boiling point of from 212°F to greater than 212°F. and the emulsion is water miscible. In general. Vinyl Acetate Polymers ( VAP's) such as the \ inyl acetate emulsion used in one embodiment of the composition of the instant invention are hard, brittle, yet tough resins which are found overall to be favorable to the board installation process which requires that the construction board have the ability of being cut and cleanly snapped with a common utility knife after the board has been scored. Additionally, each of the various vendor- supplied VAP's that were tested, when combined in the unique percentages of gypsum and perlite samples tested, were found to be environmentally friendh' and not noxious during heat testing. Further, each of the VAP formulations available clearly exhibited the cross linking with starch and mineral (through the use of boric acid), whereby a fusion occurred between the minerals and the adhesive composition. It is thus firml believed that a chemical fusion of organic and inorganic elements in the composition of the instant invention occurs, rather than a mere adherence by the binder to the mineral. Thus, a fusion occurs which results in a chemically changed binder combination which, when heated, in turn chemically fuses the board formulation. The characteristics of the final vinyl acetate emulsion depend largely on the characteristics of the polyvinyl alcohol used during the manufacture of the emulsion. Wide ranges of polyvinyl alcohols (PVAl's) which can be made are directly dependent upon the characteristics of the intermediate polyvinyl acetate ( PVA ). especially the PVA's molecular weight and hydrolysis process. PVAl's are general!} classified by the percentage of hydrolysis and their degree of polymerization. All polyvinyl alcohols will work in the instant application which are hydrolyzed in preferable ranges from 80 to 100%. Their degree of polymerization based on viscosity at approximately 20°C of 4% aqueous solution, in the range of 5cP (low viscosity) to 60cP (high viscosity) will work in the application. The degree of polymerization of grades which work are in the range of 500 to approximately 2500. The specific PVAl chosen, including the viscosity of the final polyvinyl acetate emulsion, or the derivative of PVAl chosen, shall be field lab or field trial selected. It is primarily dependent on the chemical composition of the gypsum ore, the chemistry of the metered water, and to a significant extent the overall chemical makeup of the constituent additives together. As the temperature increases in the metered water or plant conditions, solubility increases. The fluidity of the wet gypsum slurry finally produced can be directly effected by the proper selection of the PVAl and the final PVA emulsion. Low molecular weight (ca 70-80%) PVAl hydrolyzed grades dissolve rapidly in water at normal room temperatures. It should be noted that solutions of PVAl's in vinyl acetate emulsions mix and disperse more readily in construction board production. They also perform better against "clay shock," as discussed elsewhere in this specification. High molecular weight PVAl's (ca 95-100%o) hydrolyzed grades will generally exhibit higher tensile strength. Higher molecular weight PVAl's are dissolved by dispersing in cold water and heating to approximately 80-90°C with stirring. Middle range molecular weight (ca 80-95%) grades through hydrolysis are dissolved through slow addition to cold water with stirring, although the temperature can then be raised to 60-80 °C to hasten the process. All VAP's including vinyl acetate homopolymers and copolymers tested were found sufficient to cross-link with starch and boric acid and perform quite satisfactorily in construction board applications. VAP emulsions exhibited preferable mixing ease, dilution and dispersion in the metered process water, and into the final w et gypsum slurry. Homopolymer emulsions were found quite fav orable due to their lowest cost, their rapid setting speed, their good ability to adhere to difficult surfaces, and their ""dried" strength. Emulsion homopolymers and copolymers. containing polyvinyl alcohol ( PVAl) at the right percentages and molecular weight tested (as set forth below ). increase the adhesion and cohesion strength, and increase the stabilization (thus the site storage ability) of the final vinyl acetate polymer. The inventor herein has recently discovered a phenomenon that occurs when polyvinyl acetate (PVA) emulsion is added to beta hemi-hydrate gypsum in the practice of the instant invention, and a solution to correct this phenomenon, as follows. When PVA is introduced into the standard construction board manufacturing apparatus, slurry thickening occurs in the pin mixer as the constituents are combined, in turn causing an increase in viscosity which creates an increased water demand to maintain or regain a proper fluidity in the slurry. The increased water demand is a problem in that more energy is required to drive off the excess moisture, and strength is also compromised. The following is an example of post addition of lower molecular weight PVAl to the PVA emulsion before introduction into the pin mixer under conventional construction board line manufacturing production in order to reduce or altogether eliminate the clay shock or thickening phenomenon. A 10% to 25% solution of PVAl and water (the specific concentration depending upon the severity of the thickening and being easily determined upon inspection during production) is mixed to batch with the PVA emulsion. The 10% to 25% solution of PVAl to water is provided in the amount of approximately 0.1 % to 30% by weight of the PVA emulsion, and can be blended together until a homogenous mix is obtained. The above procedure is practiced prior to the emulsion being utilized in the process of this invention, and the two constituents can be recirculated together to combine once the PVAl is placed into solution. Too much PVAl can affect strength and can cause hydration problems in the system, so the proper ratio is essential. It is particularly of note that due to the siliceous nature of some gypsum deposits. the 10% solution of PVAl may not be sufficient at 0.1 % to 5% of the PVA to solve the thickening issue, such that higher concentrations of PVAl would be required to solve the problem. Again, the precise concentration may be easily determined upon inspection during production of the construction board of the instant invention. In addition, a small amount of Sorbitol (between 0.1% and 5%) in approximate!)' 70% solution can act as a vehicle for the gypsum to attach to instead of attaching to the polyvinyl alcohol contained within the PVA emulsion itself. This is the purpose of post adding the lower molecular weight PVAl to the PVA emulsion, namely, to counteract the reaction causing the thickening allowing more PVAl to react with the gypsum. It is believed that the chemical reaction that occurs when PVA is added to the stucco can be countered with the post addition of the lower molecular weight PVAl. While it would be most preferable to blend the PVA with the lower molecular weight PVAl at the emulsion manufacturing site so as to be ready to use when received at the construction board manufacturing facilities, the current need of evaluating the thickness of the slurry during board production to establish the appropriate concentration requires that the two constituents be combined at the board manufacturing facility. It should also be noted that lower molecular weight PVAl's w orked better in the presence of sizable clay percentage gypsum ores (i.e.. above 1 %). to enable initial less thickening of the final wet gypsum with perlite stucco. Higher molecular weight PVAl's increase the absorption of binder molecules onto the particles of the clay minerals or flocculation of clay particles producing in effect "clay shock." The correction for this phenomenon is to utilize lower molecular weight PVAl's that are partially polymerized and hydrolyzed. Thus in essence, they are less "prepared" PVAl's. Partly hydrolyzed grade PVAl's such as GL-02 polyvinyl alcohols of zero to approximately 35 percent to water concentrations should be utilized or added as an anti-shock agent, where there is a fairly sizable presence ( 1 e abov e 1 %) ol clav s in the gv psum oi in the pi esence ot sizable clav percentages ( I e above 0 1%) in the rec cled consti uction boaid papei being utilized The parth hydiol zed grade PV ΛTs is provided in 10% to 25% solution w ith water which solution in turn is present at approximately 0 1 % to 30% bv weight ot the bindei Thickening of the final gy psum pei hte slum can also be coi rected oi tuither corrected through other methods One simple solution is lo utilize oxidized starch in the presence ot PVAl s or PVA s Further improvements in fluiditv w ill occur w hen waxy oxidized starch is used The type of starch used, or piefeπed is discussed in other parts of this specification Higher-grade starches will produce better leactions and strength results, and should be weighed in terms of total cost in determining the final selected and prepared PVAl and PVA copolymer or homopolymei emulsion utilized It was also found favorable to raise the glass tiansitton temperature (Tg) ot the polymer system for better fire testing lesults of the samples tested A higher fiie rating using VAP's would certainly be preferred in constiuction board applications The Tg range from 28°C to 39°C with higher Tg being preferred in VAP applications, were examined during fire tests, and yet all were found acceptable In older to obtain highei tiansition temperatures (Tg), other copolymers may be prepared and/or pre-added to the emulsion in smaller quantities, such as 2-ethyl hexylacivlate, ethyl aci late dibut l lumuiate vinv l stearate. polymethyl methacrylate or butyl methacrylate Cost should be considered in percentages used as these will generally increase the overall modified polv mei emulsion cost As mentioned abov e it is a significant featuie ot the instant inv ention that the manufactuie ot the sy nthetic adhesiv e binder incorporated into the Examples piovided below is carried out at the constiuction boaid pioduction tacilitv as opposed to being manufactmed offsite and latei tianspoited to the construction boaid pioduction lacihtv Moie particularly . for the examples prov ided below, the base components ot the binder are acetic acid and ethvlene w hich make up a vinyl acetate monomer, liich in turn is polymerized into a vinyl acetate latex emulsion. The process by which this occurs and the equipment needed to accomplish the polymerization of the above-listed constituents is located at the site of the construction board manufacturing facility to significantly reduce costs. The manufacture of the polyvinyl acetate emulsion containing polyvinyl alcohol at the construction board manufacturing facility provides many distinct advantages. The cost of the emulsion is reduced in the weight and transportation cost of the main individual components. PVA emulsions have been made for other applications, but have not previously been used in construction board manufacturing. Accelerators, strengthening agents, percentages of PVA and PVAl's. proper end foam generation controls, additives, and stabilization requirements can be uniquely controlled for optimization in construction board usage. Also, another important factor is reduced cost requirements to stabilize and protect from bacteria the final transported PVA emulsion, because the PVA emulsion created is continuously used in the manufacture of the construction board. Also, a consistent quality controlled source of supply is always readily available. Climate conditions (such as winter freeze problems that adversely affect PVA performance), potential contamination of the product in multiple handling, premature agitation which can effect strength performance, and storage buildup of the dried emulsion can be reduced and therefore lower the overall cost of the PVA emulsion. Further, newer improved manufacturing techniques to make PVA emulsions can be employed and master linked computer controlled to optimize production quality and capacities immediately required for the changes in the board formulations of the various sized and types of construction board products. The making of vinyl acetate (VA). vinyl acetate polymers (VAP's). and vinyl acetate monomers (VAM's) onsite at the board manufacturing facility further lowers the cost at the volume usage demanded for construction board applications. VAM's and the elements that make up VAM's. w hich are key base compounds of VAP's. are determinative factors in the ultimate cost of the board manufacturing process. Thus, using the processes and placing the equipment designed to manufacture VAP's at the construction board manufacturing facility plays a substantial role in lowering the ultimate production cost of VAP's. Still further, the stability of a colloidal suspension of vinyl acetate in emulsion is determined by the length and time the emulsion must sit or be unutilized. The longer the emulsion must be ""stabilized." the higher the cost of the emulsion. Therefore, lower costs are realized through the continuous use of the emulsion promptly- after it is prepared, as in the continuous construction board manufacturing application of the instant invention where the adhesive is manufactured on-site. The manufacture of the final synthetic binder at the production site exhibits significant reduction in production costs. Traditionally, synthetic construction board energy costs are significantly reduced through the industry practice of contracting with power plants to dispose of some of the waste produced by the power plant by using it as a constituent of the synthetic board, in exchange for reduced costs in the supply of electricity. Therefore, the energy costs associated with the manufacture of the adhesives at the site of the construction board manufacturing facility are significantly reduced. Moreover, the presence of manufacturing labor at the construction board manufacturing facility, which labor can likewise manufacture the adhesives. reduces the total number of employees required to manufacture the adhesives. once again reducing the overall manufacturing costs. The additional development or polymerization of other adhesives manufactured on site will additionally reduce production costs. The labor and energy required to transport the amount of adhesive material needed to manufacture mass quantities of construction board from a location other than the site on which the board is manufactured would not be logistically or financially feasible in a large production setting. It has been discovered by the inventor herein that the selected binder can be caused to foam when mixed vigorously enough with processed water. The foamed binder can aid in aerating the board and decrease or even eliminate the need for soap foaming agents currently used to aerate construction board in manufacturing. This in turn reduces the cost of the board manufacturing process by reducing the need for soap foaming agents. It is believed that soap bubbles and soaps in general do notning for and actually tend to diminish the strength of the ground gypsum, perlite particles and/or other dry constituents from bonding or cohering to each other and then to the board paper plies. Soaps used today do not aid in sticking or gluing particulates together but separate or repel them from doing the same. Therefore, the binder need be of proper combination and viscosity to form the proper sized bubbles and remain reasonably constant through the kiln drying process to properly aerate the finished board. Polyvinyl acetate emulsions when mixed properly with water, similar to soaps, will foam and can produce a stronger same size bubble due to their surfactant content. The binder or emulsion can also be slightly altered in viscosity by adding other binders or foaming agents to enhance proper sized bubbles that react similarly, yet firmer, than soap bubbles. Examples of nonionic surfactants which can be useful in this invention are polyethers, e. g., ethylene oxide and propylene oxide condensates which include straight and branched chain alkyl and alkaryl polyethylene glycol and polypropylene glycol ethers and thioethers: alkylphenoxypoly (ethyleneoxy) ethanols having alkyl groups containing from about 7 to about 18 carbon atoms and having from about 4 to about 240 ethyleneoxy units. such as heptylphenoxy-poly (ethyleneoxy) ethanols. octyl-and nonylphenoxy-poly (ethyleneoxy) ethanols: the polyoxy-alkylene derivatives of hexitol (including sorbitans. sorbides. manitans and mannides): partial long chain fatty acid esters, such as the polyoxyalkylene derivatives of sorbitan monolaurate. sorbitan monopalmitate. sorbitan monostearate. sorbitan tristearate, sorbitan monooleate and sorbitan trioleate; the condensates

23 of ethylene oxide with a hydrophobic base, said base being those formed by condensing propylene oxide with propylene glycol; sulfur containing condensates, e. g.. those prepared by condensing ethylene oxide with higher alkyl mercaptans. such as nonyl. dodecyl. or tetradecvl mercaptan. or with alkylthiophenols wherein the alkyl group contains from about 6 to about 16 carbon atoms; ethylene oxide derivative of long chain carboxylic acids, such as lauric palmitic, oroleic acids or mixtures of acids, such as tall or fatty acids: and ethylene oxide derivatives of long chain alcohols such as octyl. decyl. lauryl. of cetyl alcohols. The preferred nonionic surfactants useful to be added to the latex polymer for the purpose of dispersing the latex polymer throughout the gypsum slurry and creating a stronger bubble than can be achieved with the more commonly used construction board foaming agents are higher (greater than C8) aliphatic alcohol alkoxylates. aliphatic acid alkoxylates. higher aromatic alcohol alkoxylates. fatty acid amides of alkanolamines, fatty acid amide alkoxylates, propylene glycol alkoxylates. block or random copolymers of ethylene and propylene oxide, higher (greater than C8) alcohol polyethylene polypropylene block or random adducts and mixtures thereof. Of the above classes of nonionic surfactants, the alcohol ethoxylates and alkaryl ethoxylates are particularly preferred. In practice, the nonionic surfactant to be added to the polymer of the instant invention is preferably provided in a solution comprising a 5%o to 30% solution of nonionic ethoxilated alcohol surfactant to water, the solution being present in an amount of approximately 0.1 % to 30% of the binder. Additionally, the binder or emulsion can be pre-mixed with the starch in solution to further enhance or control the foaming presence. The most important difference however from just using soap foam water is that the final combined binder solution bubbles will grab onto and adhere to the gypsum, perlite or expanded mineral, and other dry ingredients in the pin mixer and then grab onto the board paper to form more bonded, firm, and therefore stronger composite construction board. Additionally . water based non-V.O.C. acrylic or polv urcthane polymer systems can be utilized as the binder in the formulation of the construction board of the present invention either alone or in combination with other polymer systems mentioned herein. The benefit of using a water based non-V.O.C. polymer system in formulating the composite core from an environmental standpoint is a polymer that is completely non-toxic to the workers who work with it as well as having no detrimental effects on the ecosystem surrounding the manufacturing plant where it is being utilized. Being water-based, the system is very compatible with the other constituents that make up the core of the gypsum construction board of the instant invention. The non-V.O.C. polymer system is completely biodegradable and safe to the environment as opposed to petrochemical polymers and worked as well as or better than many of the petrochemical based polymers tested. It has been known to add some type of sugar, such as low cost beet sugar, to the edge sections of de-foamed gypsum stucco to ultimately harden the edges of finished wallboard. The present invention also employs the optional use of a relatively small percentage of specific low cost sugars in the construction board formulation of the instant invention, in order to increase overall core ASTM strength tests and further reduce cost. Further, certain sugar solutions, premixed with the preferred adhesives. provide another option towards determining optimal strength and plasticity of the combined low cost tacky compound. However, the effect of sugar addition was generally found to lower the overall cohesion of the selected adhesives. Therefore, there is a tradeoff of cost versus optimum cohesion performance, which must be determined by the manufacturer. Dryer sugar solutions such as beet sugar, or other typical current construction board sugars utilized today, should be introduced separately from the adhesives in the final stage of the pin mixer, as they tend to react with the adhesive adversely. Making the board composite flexible or more plastic was improv ed over conventional methods, yet not as improved as when utilizing the preferred adhesives. Thus, cost reduction with similar edge or possible nail pull performance remained the main improvements by utilizing sugars of low appropriate percentages, in the presence of the preferred selected adhesives previously mixed with the other construction board ingredients. A compatible fire retardant, such as boric acid, zinc borate. sulfamates. diammonium phosphate, nitrogen compounds, antimony oxide, silica, titanium oxide, zircon and others can be used and comprise from about .15 percent to about 3 percent by weight of the board. These fire retardants can be added to the formulation by powder or solution during the slurry mixing process, and also by spraying onto the paper covering for the purpose of fire retarding the laminate covering paper of the construction board. The examples of applying fire retardants are listed as follows: Example 1 (Fire retardant, moisture resistant system): this system sprays fire retardant solutions directly onto the board as it leaves the cascade sections and enters the take off area of the manufacturing equipment. This is accomplished by using spray heads overhead together with switch activators to trigger the action as the board passes by on the conveyor. Additives are supplied by storage tanks and pressure type discharge systems. The additives are sprayed directly on the face paper. Example 2 (Fire Retardant): another way to apply' a fire retardant quality to the paper is to add it in dry form during the Krafting process of the paper's manufacture. Small particle distribution of fire retardant are added to the pulp slurry prior to extrusion into the paperboard. This allows for the fire retardant to be completely integrated into the paper. This fire retardant could be zinc borate. antimony oxide, nitrogen compounds or sulfamates (sulfur compounds). These are all common fire retardants in paper. Fire Retardant additives to the adhesives. such as the addition of boric acid, reduce the overall flash point of these chemicals and therefore increase the fire rating of the core composite. Under fire rating test samples, the presence of noxious fumes were greatly reduced even to the point of being virtually eliminated as the samples moved a ay from the epoxies and non- water solvent adhesive mixtures. The combination of vinyl acetates with cementious materials also provided a good fire retardant combination without the addition of boric acid. Optionally, an improved construction board cover material consists of a manila colored moisture resistant paper face sheet in the range of 40-50 pounds with an altered top ply. In traditional construction board structures incorporating a cover material composed of recycled paper pulp, the length of fibers in the cover material is between 1/2 and 3/4 inches. The instant invention, however, employs a top ply sheet composed of virgin fibers of 1 inch or greater. While papers incorporating fiber lengths of greater than 1 inch have been produced in the past, to the best of the inventor's knowledge, no such virgin pulp has been applied previously to the top ply cover sheet of a construction board sheet. Thus, the inclusion of such extended length fibers into the construction board cover sheet of the instant invention provides the unforeseen and unobvious benefit of providing a much stronger break strength than previously known construction board structures. The unique application of the optional spec paper cover sheets of the construction board of the present invention is completely formed by any ell known paper forming process. Using 100 percent "virgin stocks" for the top ply of the face paper cover sheet allows for predictable liner strength while also eliminating some of the clays and fillers associated with current completely recycled construction board paper. By integrating a virgin pulp top ply with existing recycled construction board paper plies, increased strength and wet handling characteristics are achieved. First, a paper cover sheet is made generally comprising a multiply sheet manufactured on a cylinder machine. Conventional sizing compounds are added to selected vats such as rosin and alum to internally size some or all plies. The plies are remov ed and laminated to form an essentially unitar) web of paper. After being dried, the paper is coated with a water emulsion of the s) nthetic size of the class consisting of certain substituted succinic acid anhydrides, certain substituted glutaric acid anhydrides and the reaction product of maleic acid anhydrides w ith an internal olefin. This process allows for effective absorption into the bond liner of the core side of the paper to provide a mechanical linking of the paper to the composite core. Alternately, a cover sheet may be utilized comprising a combination of non-wood type or organic fibers such as Kenaf with or without recycled waste paper wood pulp fibers. Utilizing a completely or partially tree-free pulp creates a construction board having a more environmentally friendly cover sheet than traditional construction board products. Typically, recycled wood pulp fibers are shorter in length, by up to half, over their virgin pulp counterparts, and the strength that papers manufactured with virgin pulp fibers achieve cannot be duplicated with recycled fibers. However, papers manufactured with virgin wood pulp fibers are much more costly when compared to the cost of papers manufactured with the recycled wood waste pulp variety. By integrating stronger non-wood type organic fibers into the recycled wood waste pulp during the paper manufacturing process, a much thinner but stronger paper cover sheet is realized, allowing the construction board of the instant invention to more easily meet ASTM and Building Code requirements when very' lightweight core formulations are being utilized. The weight percentage of fiber of a source other than wood can vary from 1 to 100 percent of the pulp formulation depending upon the desired end result. As yet another alternative, the paper cover sheets of the construction board of the instant invention may be reinforced using fiberglass mesh material integrated between the inner face liner of the paper cover sheet and the remaining laminates to produce highly abuse- resistant lightweight construction boards. When utilizing formulations to produce construction boards with densities at under 30 pcf (pounds per cubic foot), flexural strength can be reduced significantly in the core. B) integrating a fiberglass mesh material beneath the inner surface laminate of the paper facer, flexural or paper grain strength can be retained well above ASTM utilizing slurry formulations to produce abuse-resistant construction boards of the instant invention as low as 25 pcf density. As paper is the majority of the strength of gypsum construction board, this fiberglass mesh material also strengthens sheer panel strength of the invention when utilizing lightweight construction board core formulations of the instant invention. The paper facers utilized in the production of gypsum construction board are normally made on cylinder machines from recycled paper in order to produce a porous paper capable of receiving the gypsum crystals that grow from the wet core slurry prior to drying. The placement or integration of the fibers between the inner liner face of the cover sheet and the remaining laminate layers can be achieved during the paper manufacturing process after the paper is formed into a fibrous web from the pulping process. The introduction of a non- woven fiber mesh into the papermaking process is achieved through placement of the mesh between the fibrous sheets during the laminating process, before dewatering. The same sizing compounds can be utilized and the porous properties of the paper remain the same. The fiberglass material or mesh can be oriented in a variety of crisscross patterns or evenly spaced shapes. Optionally, the mesh can be interlinked similar to a chain link fence within the inner laminate of the facer sheet to further increase its strength. The paper facers will still maintain their ability to absorb the slurry and the properties of the fiberglass will be such that the gypsum crystal can also mechanically link to the fiberglass strands as well. The fiberglass strands can be of various lengths, with the preferred length being 2 inches or greater. The fibers will increase the flexural and racking loads that the construction board will be able to withstand both during construction and also once the structure is completed. The fiber integration w ill greatly increase the abuse resistance of the construction board while maintaining lighter weights when compared to abuse resistant boards currently on the market. Even further, the inner liner of the facer sheets can be subjected to an abrasive during the manufacturing process to provide a rough finish, to in turn allow for an improved bonding between the stratum of the gypsum core and the facer sheets. The roughed up liner surface of the facer sheets causes an improved surface for the gypsum slurry crystal growth to adhere with in contrast to the very smooth surfaces found on gypsum construction board paper facers commonly utilized. If bituminous or waxy water-repellent materials are used, they comprise from about 1.0 percent to about 10 percent of the Perlite weight by volume. These materials may be applied to the Perlite from molten states or as emulsions. If silicone emulsions are used, the silicone comprises from about 0.01 to about 2 percent of the Perlite by weight. The silicone emulsions may be applied directly to the Perlite as it exits the expander by means well known in the art.

Apparatus The apparatus necessary for implementing the above-described method comprises several elements which together take expanded Perlite and combine it with varying reactants, apply the mixture to a paper substrate to form a continuous sheet of laminated Perlite construction board, convey the wet Perlite construction board along a conveyor while subjecting it to an initial heat treatment as the wet board travels towards a rotary cutting knife, transferring the laminated assembly to a board dryer, and finally processing the dried construction board for shipment. As shown more particularly in the schematic Perlite processing arrangement of Figure L a Perlite expander system is provided of conventional design. A preferred Perlite expander is readily commercially available from Silbrico Corporation as model number M-30. although any similarly configured Perlite expander would likewise be sufficient. The Perlite expander system comprises a covered hopper car 1 which delivers Perlite ore that has been crushed to the sieve size enumerated above to a conveyor 2 positioned beneath the hopper car 1. Conveyor 2 delivers the Perlite ore to an elevator 3 which, in turn, transfers the Perlite to an ore storage container 4. When the crushed Perlite is to be processed into expanded Perlite. a reclaim conveyor 5 is used to deliver the crushed Perlite to a Perlite ore surge bin 6. which in turn directs the crushed Perlite ore to an ore feeder 7. Ore feeder 7 directs the crushed Perlite ore via a downwardly oriented elongate chute to a four-way Perlite ore splitter 8. At ore splitter 8. the Perlite ore travels further downward through four elongate tubular passages and into the vertical furnace expanding tube of Perlite expander 9. As the crushed Perlite is introduced into the vertical furnace expanding tube of Perlite expander 9, the crushed Perlite is met by compressed air which is heated between 1000 and 2100 degrees Fahrenheit. This heating process causes the crushed Perlite material to soften while the water bound to the Perlite particles rapidly evaporates, in turn expanding the Perlite ore to between 12 to 20 times its original size and into a light, cellular particle which is commonly referred to as '"expanded Perlite." Once the Perlite has been expanded, the expanded Perlite particles are light enough to travel upward in the air stream within the vertical furnace expanding tube. through a duct 10 at the top portion of the expanding tube, and into a cyclone collector 1 1. Within cyclone collector 1 1. the larger expanded Perlite particles fall downward and settle into a hopper at the lower end of the cyclone collector, while the smaller, fine expanded Perlite particles travel upward from the cyclone collector through a duct and into a dust collector 12 where they settle. Within dust collector 1 . the extremely fine particles (which are generally not useable in the construction board production process) are collected by a fiber filter media within dust collector 12. The remaining fine particles and the larger expanded Perlite particles from the hopper of cyclone collector 1 1 are directed to an expanded Perlite storage silo 200. as described in greater detail below. In a preferred embodiment of the present invention, two independent Perlite expansion systems are utilized in order to prov ide an appropriate supply- quantity- of expanded Perlite to the construction board production apparatus. As shown in the schematic diagram of the Perlite construction board production facility of Figure 2. located at the feed end of each Perlite expansion system 100 is a dense phase pneumatic transport system 400 which moves the expanded Perlite from the Perlite expansion system 100 to a plurality of storage silos 200. A suitable dense phase pneumatic transport system is readily commercially available from Nol-Tec Systems. Inc. of Lino Lakes. Minnesota as Transporter model number 201. although any similarly configured pneumatic transport system would likewise be sufficient. The pneumatic transport system is configured to pneumatically convey expanded Perlite from the Perlite expansion system 100 to the expanded Perlite storage silo 200. and in turn from the storage silos to a secondary feed tank 300 located within the construction board manufacturing facility. The dense phase pneumatic transport system has the ability to fluidize the dry expanded Perlite material using air pressure, and in turn to convey the material to the desired location using sealed pressurized tubes. The transport system utilizes relatively high pressure (above 15 psig), low volume air as the force to transfer the granular bulk solids through a pipeline at low velocity. creating dense packets or slugs of expanded Perlite which travels through the conveyor system without risk of the abrasive expanded Perlite material damaging the interior of the conveyor pipeline. It should be noted that alternate means of conveying the expanded Perlite are available, such as the utilization of a screw type conveyor or similarly configured mechanical conveyance apparatus. However, it has been found that such mechanical conveyance means used in the transport of expanded Perlite in the context of construction board manufacture incurs a substantially higher equipment and maintenance cost. Thus, the use of a dense phase pneumatic transport system for conveyance of expanded Perlite during the construction board manufacturing process provides a substantial improvement over traditional bulk material transport means previously used in the construction board manufacturing process. As mentioned above, the dense phase pneumatic transport system 400 is used to transfer expanded Perlite from the Perlite expansion system 100 to a plurality of storage silos 200 of conventional design for storing the expanded Perlite until needed for new construction board production. Each storage silo is equipped with an airslide of conventional design and known to persons of ordinary skill in the art of dry bulk material handling. The airslide directs expanded Perlite from each of the storage silos to a transition hopper positioned above a second dense phase pneumatic transport system. The second dense phase pneumatic transport system is used to convey expanded Perlite from the storage silos 200 to a secondary feed tank 300 inside of the construction board manufacturing facility. This second dense phase pneumatic transport system is configured nearly identical to the first dense phase pneumatic transport system, the sole variations in the system relating to the conveyance capacity of the respective systems as determined by the construction board production goals of the particular manufacturing facility. It should be apparent to those of ordinary skill in the art that modifications could readily be made to the precise handling capacity of each of the pneumatic transport systems in order to meet the production requirements of the particular facility', such as by modifying the diameters of the pipelines in the conveyor system or by modifying the pressure within the pipeline to in turn change the velocity of the materials being transferred within. Traditional construction board production facilities are plagued with the problem of significant production down-time whenever a problem with the ra material processing and storage equipment located upstream of the actual construction board manufacturing equipment is experienced. Such problems can include air pockets or channels within the storage silos w hich inhibit or prevent the free flow of material, clogged processing lines, and other common material handling problems. In order to prev ent the costly losses that such down time would create, the present inv ention employ s a secondary- expanded Perlite feed tank 300 comprising a steel tank positioned w ithin the construction board manufacturing facility in general proximity to the construction board forming equipment. It is significant that traditional gypsum construction board production facilities have been unable to dispense gypsum from a single feeder container, but instead have been required to direct processed, calcined gypsum to multiple small storage bins of limited supply capacity such that the entire supph' in each bin would be consumed by the production process in a single day. The reason for using such an expensive and inconvenient supply system requiring constant replenishment relies on the fact that calcined gypsum plaster cannot be stored in large quantities as it has a tendency to absorb surrounding moisture, in turn causing premature hardening. Thus, the present improved construction board manufacturing process enables a simplified expanded Perlite supply tank to be utilized as the expanded Perlite lacks the moisture sensitivity and long term storage sensitivity of calcined gypsum. As the Perlite expanders work to fill the storage silo that is least full with expanded Perlite, expanded Perlite from the most full storage silo is drawn out and directed to the secondary feed tank 300. using a programmable logic controller as is well known to those of ordinary skill in the art. By constantly maintaining at least one full silo and by always keeping the secondary feed tank filled with expanded Perlite. the risk of being forced to shut down the board production line due to the above-mentioned equipment problems is at least reduced, if not eliminated altogether. The maintenance of a separate, secondary expanded Perlite feeder tank that is constanth' maintained with a read}' supply of expanded Perlite, and positioned adjacent the board production equipment, enables any such equipment malfunctions in the remaining storage and pre-processing equipment to be resolved before the supply of expanded Perlite has diminished to such a level that it can no longer supply the expanded Perlite to the production equipment. Likewise, in the event that each element in the pre-processing and expanded Perlite storage equipment fails, the supply within the secondary feeder tank may be used to supply the expanded Perlite to the production equipment until such supply is fully consumed or the failure in the pre-processing and storage equipment is resolved. The secondary expanded Perlite feeder tank supplies expanded Perlite to the board fabrication equipment using volumetric feeders to feed the dry ingredients into a continuous auger type blender 550. A suitable volumetric feeder is readily commercially available from Acrison as Model BDF. It is of note, however, that alternate means may likewise be provided for directing the dry Perlite to the board fabrication equipment, including the above- described commercially available dense phase pneumatic transport system. Further, a suitable auger type blender is readily commercially available from Acrison as Model Number 350, although any similarly configured blender will likewise suffice. Blender 550 in turn conveys the dry components of the construction board composition to a pin mixer 600. As explained in greater detail below, the liquid constituents 700 of the adhesives are added into the metered water, or other mixing soap or starch waters, and diluted before being added into the pin mixer 600 along with water and a foaming agent for combining with the dry components of the Perlite construction board. Continuous pin mixer 600 is of a conventional design, and a suitable continuous pin mixer is readily commercially available from Asa Brown Bovari ("ABB") Raymond Elirsam Operations, although any similarly configured pin mixer would suffice. The continuous pin mixer combines the dry components of the board formulation with the foamed adhesives, all of which are metered into mixer 600 al a uniform rate, i lie resulting homogeneous wet gypsum/perlite slurry- free flowing is then discharged from the continuous pin mixer through a rubber-like flat opened end boot or hose 650 (which is normally approximately 6-10 inches wide by ' > to 1 Vz inch rectangular opening or approximately- 2 Vz to 4 inch diameter hose or hoses). Alternately, the slurry may be discharged through a dual hose assembly attached to the pin mixer, thereby dispensing slurry through multiple outlets, and still further through the use of a combination of a flat boot and dual hose assembly. It is preferable to comprise the exit boot or hose(s) of proper latex rubber to handle the larger and coarser Perlite when used and to widen the width of the boot or hose to compensate and more widely spread out the slurry or mixture onto the back side of the face paper. The reason is that the Perlite or expanded mineral is lighter and of lesser density and different viscosity due to the binder than the normal wet gypsum slurry, and therefore behaves slightly different in spreading uniformly and evenly onto the back side of the face paper. The face paper is delivered to the construction board assembly line from paper handling equipment 800 positioned upstream of the pin mixer. The paper handling equipment 800 is likewise of conventional design, and a suitable paper handling equipment arrangement is readily commercially' available from ABB Raymond Ehrsam Operations, although any similarly configured paper handling equipment system would suffice. The paper handling equipment arrangement provides the backing and face paper to the board production line, and generally includes paper roll racks or rotary unwind stands that hold the paper, paper pull rolls that supply' the paper at a constant speed to paper tensioners which in turn automatically' adjust to apply uniform tension to the paper. paper splicing tables where the end of the paper from a new roll is joined to the end of a spent roll, paper guides that automatically align two streams of paper vy ith the boardline and ensure even paper flow downstream, paper heaters to remove any moisture from the paper, and paper creasers to prepare the paper so it folds precisely further downstream. Construction board forming apparatus 810 comprising an adjustable mud dam/edger and an extruder-type forming plate or forming rolls all of conventional design are located just downstream of the pin mixer. The adjustable mud dam/edger folds the already creased face paper being supplied from the paper handling equipment into position to receive the glued backing paper, while establishing the board width and edge configuration. The extruder-type forming plate or rolls determine the thickness of the construction board as it enters the conveyor line, and brings the backing paper into contact with the mixture and gluing it to the folded face paper to create the enclosed envelope that holds the free flowing mixture in the shape of a continuous board. After the free flowing mixture has been applied to the paper, a continuous, wet construction board sheet is formed which proceeds along a board forming line conveyor of conventional design comprising a greenboard forming line section and a live roll section. The greenboard forming line section (shown generally at 900) comprises a flat belt surface with very closely spaced rolls to provide adequate belt support to maintain a flat board structure as the wet board travels along the board forming line, and generally extends approximately two-thirds of the distance between the forming plate or rolls and a cut-off knife 910. The live roll section (shown generally at 950) extends the remaining one -third of the distance, and serves to deliver partially set board to the cut-off knife. The live roll section 950 comprises open rolls which allow exposure of the board face to the air and help the final greenboard set prior to cutting. An aligning device of conventional design is also positioned ahead of the knife which positions the board to assure a square cut. It is important in the construction board manufacturing process to ensure that the greenboard is sufficiently set by the time it reaches the cutting knife so that the knife is able to make a clean cut through the board w ithout picking up excessiv e wet substrate material from the board which in turn could gum up the knile sui tace In the examples set forth below in which gypsum is not used as a setting or hardening agent in the composition, in order to ensure that the construction board of the present inv ention has leached a sufficiently dr} state to prev ent the substrate from collecting on the knife sui tace. the board foiming line is preferably provided with an optional initial heat tieatment means which directs heat towards the wet board as it travels from the forming plate oi rolls to the cut-off knife However, another substantial benefit arises from the heat tieatment ot the et boaid pπoi to cutting, and that is the significant cost reduction realized bv the I eduction in processing times and temperatures required to fully set the board withm the div ing kiln, as explained in greater detail below In a first embodiment of the heat treatment means, a tunnel 920 is provided which encapsulates the board line between the forming plate or lolls and the cut-off knife The tunnel is provided with a series of interconnected air ducts 9 1 along its upper interior surface, air ducts 921 being configured to direct hot an dnecth downward on the wet board as it travels along the board line Heat is supplied to the tunnel using any conventional and readily commercially available air duct system which duects heat horn the hot air recycling system of the drying kiln 1200 (discussed in greater detail below ) to the duct work located at the ceiling ot the heating tunnel Fans are suspended horn the ceiling of the heating tunnel to direct the heated air from the downwardly dnected an ducts to the boaid line In a second embodiment of the heat tieatment means a series of drying hoods are positioned over the board line The hoods are ot cony entional design for a standard ventilation hood, and generally comprise a wide open-mouth an duct opening which faces the surface to be heated (I e . the board line), and a section ot duct vvoik which extends upward from the wide, open-mouth air duct opening and v hich narrov\ s as it rises away from the air duct opening until it reaches the diameter of the remainder of the duct work. Fans are positioned within the air duct to direct the heated air into the ducts and out of the hoods towards the board line. As in the first embodiment, heat is supplied to the individual drying hoods using any conventional and readily commercially available air duct system which directs heat from the hot air recycling system of the drying kiln (discussed in greater detail below) to the drying hoods. After the board has traveled along the belt forming and live roll dewatering sections. the continuous construction board is cut into individual sheets using a rotary cut-off knife 910 of conventional design. A suitable rotary cut-off knife is readily commercially available from ABB Raymond Ehrsam Operations of Abilene. Kansas, although any similarly configured cut-off knife would likewise suffice. The cutting is performed by two knife blades, each mounted on a rotor, one above and one below the board. When cutting, the rotors run slightly faster than the speed of the board line to assure that the knife blades make a straight cut. Following the cutting of the board by the rotary cut-off knife, the individual construction board sheets are directed along a board accelerator section (shown generally at 960) of conventional design. A suitable board accelerator section is readily commercially available from ABB Raymond Ehrsam operations of Abilene. Kansas, although any similarly configured accelerating conveyor section would likewise suffice. The board accelerator section comprises sets of rolls turning at increasing speeds to accelerate the cut boards beyond the cut-off knife in order to provide adequate spacing between boards to allow time for transfer and inversion of the boards to the dryer infeed section of the boardline. At the end of the accelerator section, the boards are received by a board transfer/inverter assembly 1000 of conventional design. A suitable board transfer/ inverter assembly is readily commercially available from ABB Raymond Ehrsam operations of Abilene. Kansas. although, once again, any similarly configured panel transfer/inverter assembly would suffice. The transfer/inverter mov es the boards laterally at c () degrees to the boardline while turning the boards face side up and aligning them side by side before they are introduced into the drying kiln. Once the boards have been inverted and transferred to the dryer infeed section of the boardline. a dryer infeed assembly (shown generally at 1 100) comprising a conveyor directs boards from the board transfer/inverter assembly' to the multideck infeed section of the drying kiln. A suitable dryer infeed assembly is readily commercially available from ABB Flakt Industri Ab of Vaxjδ, Sweden, although any similarly' configured conveyor-type feeder system would suffice. Drying kiln 1200 of the present invention comprises a plurality of tiers, preferably between 12 and 15. of roller conveyors w hich receive construction board at the inlet end of the kiln, convey the board through the multiple heating zone drying section, and discharge the board at the outlet end of the kiln. The basic configuration of the drying kiln is of conventional design and well known to those of ordinary skill in the art. and a suitable board drier kiln is readily commercially available from ABB Flakt Industri Ab of Vaxjό, Sweden. The preferred drying kiln of the present invention comprises a two heating zone kiln of conventional design. It is significant, however, that the use of Perlite as a constituent of the construction board of the present invention and the process of providing an initial heat treatment of the wet board prior to cutting allows the drying process to be carried out at significantly lower operational temperatures within the drying kiln. These lower operational temperatures provide a significant cost savings in both energy- consumed in the drying process and in premature wear in the components of the dryer itself caused by long term exposure to extreme operating temperatures. As mentioned above, the heat supplied to the optional heat treatment assembly over the wet board line is supplied by tapping the hot air recycling system of the drying kiln. As shown in Figure 2. in a conventional board drying kiln configuration, stacks 1210 which comprise a flue or exhaust pipe extending upward from the kiln and through the roof of the manufacturing facility are located at each end of the drying kiln to enable moisture laden hot air to escape from the interior of the kiln. The release of this moisture aids in the evaporation process to drive off the excess water that is present in the construction board product. As the air rises in the stack, a portion of the air is captured through side ducts located in the sidewalls of the stacks. The side ducts are provided with fans which direct at least a portion of the rising air into the ducts which in turn direct the captured air to a condenser. The condenser recaptures the moisture from the air. and the now dry air is returned into the air inlet 1220 of the drying kiln. Such a hot air recycling system is well known to those or ordinary skill. The present invention redirects the heated dry air exiting the condenser through duct work of conventional design to the optional heat treatment apparatus situated above the board line, as explained in depth above. Following the drying stage, the fully set construction board exits the drying kiln via a dryer outfeed system 1300 of conventional design. A suitable dryer outfeed system is readily commercially available from ABB Flakt Industri AB of Vaxjδ, Sweden, although any similarly configured conveyor-type outfeed system would suffice. The dryer outfeed system in turn directs the construction board to dry board handling apparatus, including a transfer- booker 1400, a board bundler 1500. and a board stacker 1600. A suitable transfer-booker 1400 of conventional design is readily commercially available from ABB Raymond Ehrsam Operations of Abilene. Kansas, and is used to move each pair of boards off of the dry end boardline onto a receiving table supported by a plurality of rolls, which rolls drop a ay to allow a series of belts to rotate the board by 90 degrees. Hydraulically actuated arms then lift opposing ends of each pair of boards such that the boards are brought together face to face to protect the smooth outer surfaces of the construction board from damage during handling, storage, and shipping. The paired or "booked" boards are then directed to a board bundler 1500 of conventional design which squares and aligns the pair of boards, trims them to precise finished length, and tapes the ends. A suitable board bundler of conventional design is readily commercially available from ABB Raymond Ehrsam Operations of Abilene. Kansas. Finally-, after the boards have been bundled, the}' are transferred via a board stacker assembly of conventional design to a mechanism which automatically aligns the bundles and places them one upon another such that the bundles may be lifted and carried by a forklift to a storage location. A suitable board stacker assembly of conv entional design is readily commercially available from ABB Raymond Ehrsam Operations of Abilene. Kansas. It is significantly of note that several of the above-identified elements used in the process of manufacturing construction board as set forth in this specification are likewise in use in current gypsum board line equipment. Thus, the present apparatus not only provides a new and unique system for manufacturing construction board, but also provides a means by which an existing gypsum board manufacturing facility may be easily and readily transformed into a manufacturing facility for the construction board of the instant invention. Thus, by making minor modifications to a traditional gypsum board production facility, and by adding the additional equipment listed above (e.g., secondary expanded Perlite feed tank, adhesives storage equipment, mixing equipment, and the optional initial heat treatment tunnel and duct work interconnecting the heat treatment tunnel to the standard kiln air recycling system) to an existing gypsum boardline. an existing gypsum board manufacturing facility may be smoothly and economically transitioned into a manufacturing facility for the improved construction board of the instant invention, w ithout the investment costs of building an entirely new production plant. Examples The following examples employing the instant invention proved to bring very favorable test results.

EXAMPLE 1 A 6 inch by 6 inch by lA inch sample is prepared using the following formulation:

Materials Weight in Ounces Weight bv Percentage Perlite 0.20 1.609% Calcined Gypsum Stucco 5.2 41.851% Starch 0.070 0.563% Ball Mill Accelerator 0.035 0.281% Dextrose 0.005 0.040% Boric acid 0.015 0.120% Vinyl Acetate 0.30 2.414% Soap Water 2.0 16.096% Water 4.6 37.022% Lignosite 0.005 0.0040%

In this example, first the dry ingredients were combined together and blended until a homogenous mix was achieved, these dry ingredients being cryogenic grade Perlite with a loose density of 4 pounds per cubic foot, calcined gypsum stucco of approximately 83% purity, starch, ball mill land plaster accelerator, dextrose, and boric acid. Secondly, the lignosite was combined with the water and blended. Thirdly, the soap water was mixed with the vinyl acetate emulsion until thoroughly blended to a foamy consistency and combined with the water and lignosite mixture. The liquid constituents were then combined with the dry blended ingredients and mixed by hand for about 15 seconds to achieve 100% of a slurry. This slurry was then poured into an envelope insert of standard wallboard paper to make a '/. inch thick wallboard sample measuring 6 inches by 6 inches. The face of the envelope was then seated to the folds of the back of the envelope using a starch based dry wall edge paste. formed, and then removed from the form. The initial set was timed and recorded. After hydration was completed, the sample was placed into a small laborator}' kiln and heated at 275°C for 20 minutes. The heat was then reduced to 1 0°C for 20 minutes, then to 70°C for another 20 minutes, and finally was allowed to cool. Dry weight was recorded and evaporation rate was recorded to assure that the combined water was retained. In some instances with various and differing gypsum deposits, impurities such as clays, limestone, and salts can cause adverse reactions in the viscosity of the adhesive system of the present invention. In these instances, additives such as a solution of lower molecular weight polyvinyl alcohol as described earlier, or surfactants can be included in the formulation to optimize the performance of the adhesive system.

EXAMPLE 2 A large scale trial run of the formulation by weight percentages of example 1 was run using the weights and percentages listed below as the starting formulation for making 'Λ" regular wallboard:

Materials Weight in Ounces Weight bv Percentage Calcined Gypsum Stucco 891.0 39.292% Perlite 30.0 1 .322% Starch 9.0 0.396% Ball Mill Accelerator 10.0 0.440% Boric Acid 1.0 0.044% Fiber Glass 0.50 0.022% Dispersent (DAXAD 19W) 1.50 0.066% Foaming Agent (THATCHER) 0.70 0.036% Retarder 0.20 0.008% Water 1 170.0 51 .598% Vinyl Acetate 63.693 2.808%) Paper 90.0 3.968% After starting the trial production run at 10:30 a.m.. one gallon of water was added to the slurry, and a wet weight was recorded of 2316 pounds per MSF. Net weight varied from 2422 pounds for a high and 2304 for a low between 10:30 a.m. and 1 1 :04 a.m. At 1 1 :05 a.m.. 10 pounds of stucco were added and 8.5 pounds ( 1 gallon) of water were removed from the mix to adjust the fluidity of the slurry. The board was sampled at the takeoff at 1 1 :40 a.m.. and a dry weight of 1306 pounds was recorded. S-Cut showed excellent bond characteristics, and core development edge hardness was good (22 pounds). At 1 :05 p.m.. the vinyl acetate was reduced to 45.495 pounds per MSF. and the Perlite was reduced to 22.5 lbs. (6 cubic ft). Gypsum stucco remained at 917.5 pounds MSF. and the total water remained at 1 189 pounds MSF. Wet weights recorded of random wet wallboard samples were 2365. 2333 and 2292 pounds between 12:05 p.m. and 2:30 p.m. Dry Weight at the takeoff was recorded at 1296 pounds. Foam was down 60% at 2:30 p.m. Gypsum stucco was raised to 934 lbs., and Perlite was reduced to 15 lbs. MSF (4 cubic ft). Water was reduced to 49 lbs. MSF. with foam back up 60% at 3:00 p.m. Wet weights recorded were 2319 lbs. at 2:42 p.m. and 2338 lbs. at 2:57. and dry weight was recorded at the takeoff of 1348 lbs. At 3:05 p.m., the vinyl acetate was reduced to 25.5 lbs. MSF. All other constituent weights remained the same. The wet weight at 3: 10 p.m. was 2284 lbs., and at 4:00 p.m. was recorded at 2263 pounds. At 3:40 p.m.. the dry weight at the take off was 1322 pounds MSF. and at 4:30 p.m.. the dry weight was 1310 lbs. MSF. The run was completed at 5 : 10 p.m. Test results for this trial run are listed below:

Force in Pounds Time Flexural Strength Against With Edge Grain ( iiain Hardness

Sample 1 1 1 30 am Tace up 151 1 ace up 59 23

Sample 2 2 00 pm Face Down 141 I ace Down 53 7 19

Sample 3 3 30 pm Face up 160 2 1 ace up 58 9 21

Sample 4 4 10 pm Face up 162 face up 63 24

Nail pull improved to bevond passing in samples taken at app oximateh 3 15 p m

EXAMPLE 3 The following is an example of post addition of polv v inyl alcohol to the formulation of the instant invention A 6 inch bv 6 inch bv '/; inch sample is ptepared using the following formulation

Materials Weight in Or, :s Weight bv Pei centage Preferred

Gypsum 5 80 42-50% 45 224%

Perlite 0 30 1-3% 2 339%

Board Starch 0 05 0 3-0 6% 0 389%

Accelerator 0 03 0 1 -0 3% 0 233%

Boric Acid 0 01 0 01 -0 15% 0 077%

Vinyl Acetate 0 30 0 8-4% 2 339%

Polyvinyl Alcohol 0 035 0 1 -0 3% 0 272%

Lignosite (dispersant) 0 10 0 07-0 8% 0 779%

Ethoxvsulfate (soap) 0 10 0 07-0 8% 0 779%

Water 6 10 42-48% 47 569%

First, the dry constituents, gypsum, perlite. board staich. acceleratoi. and boric acid are blended until a homogenous mixture is obtained Next in a sepai ate v essel, the vinyl acetate and polyv inyl alcohol and dispeisant are mixed togethei w ith 20 ot the total water and the remaining 1/3 of the total water is combined w ith the soap foaming agent and blended to achieve 1/4 inch diameter bubbles of foam Finally all ot the constituents aie combined in a laboratoiv mixei and blended until 100% oi a sluirv is obtained The slunv is then poured into a papei env elope comprising the lesistant and watei lepellant construction board cover sheets and formed and sealed. After hydration occurs, the sample is placed into a small laboratory kiln to drive off the excess water and dry- the board example. The test results for this composition passed ASTM C36 specification.

EXAMPLE 4 It has been found that sodium trimetaphosphate may be utilized in the amount of 0.01 % to 10% by weight, and more preferably from 0.01 % to about 0.7% by weight, to increase compressive strength by enhancing cylindrical needle-like crystal growth in the core of the improved strengthened construction board of the instant invention. Sodium trimetaphosphate is a combination of earth metals and is known by the chemical equation (NaP03)3. This compound may be added to the slurry either in solution or in a dry powder state, although in solution is preferred. By adding sodium trimetaphosphate into the system. the favorable long cylindrical crystal growth that adds the most strength to the core of the construction board and also enhances the paper to core bond is greatly- increased, and the result is higher compressive strength. The compound is highly water soluble and dilutes very quickly allowing it to disperse very rapidly. The resultant chemical reaction is not entirely understood, although it is believed that the sodium hydroxide and fluoride in the sodium trimetaphosphate reacts with the calcium in the gypsum and increases the crystal growth. The following is an example of the addition of sodium trimetaphosphate to the formulation of the instant invention. A 6 inch by 6 inch by '/. inch sample is prepared using the following formulation: Materials Weight in Ounces Weight bv Percentage Preferred Gypsum 6.70 42-50% 47.857% Perlite 0.25 1 -3% 1 .785% Board Starch 0.05 0.3-0.6% 0.357%. Ball Mill Accelerator (bma) 0.02 0. 1 -0.3% 0.142%.

44 Boric Acid 0.005 ( i .() l -(). 1 5" n 0.035%

Vinyl Acetate 0. 15 0.8-4% 1 .071 %

Polyvinyl Alcohol 0.03 0. 1 -0.3% 0.214% Sodium Trimetaphosphate 0.095 0.01 -0.7% 0.678%

E hoxysulfate (soap) 0.10 0.07-0.8% 0.714%

Lignosite (dispersant) 0.10 0.07-0.8% 0.714%

Water 6.50 42-48% 46.433%

First, the dry constituents, gypsum. Perlite. board starch, bma. and boric acid are blended until a homogenous mixture is obtained. Next, in a separate v essel, the vinyl acetate and polyvinyl alcohol and dispersant are mixed together w ith 2/3 of the total water and the remaining 1/3 of the total water is combined with the soap foaming agent and the sodium trimetaphosphate and blended to achieve 1/4 inch diameter bubbles of foam. Finally, all the constituents are combined in a laboratory mixer and blended until 100% of a slurry is obtained. The slurry is then poured into a paper envelope comprising fire resistant and water repellant construction board cover sheets and formed and sealed. After hydration occurs the sample is placed into a small laboratory kiln to drive off the excess water and dry the board sample. The test results for this composition satisfied the criteria of ASTM methods C-36 and C-473.

EXAMPLE 5

Materials Weig ht in po Weight bv % Preferred

Perlite 60 1 -3% 2.564%

Calcined gypsum 1 130 42-50% 48.295%

Ball mill accelerato r 7.0 0.1 -0.3% .299%

Starch 9.0 0.3-0.6% .384%

Boric Acid .25 0.01 -0. 15% .015%

Sodium Trimetaphc )sphate .50 0.01 -0.7% .021%,

Fiberglass fibers 1.5 0.1 -0.2% .064%

Dispersant (lignosu lfonate) 2.0 0.07-0.8% .085%

Soap (foamer) 1.5 0.07-0.8% .064%

Vinyl Acetate 28.0 0.8-4% 1 .196%

Water 1 100 42-48% 47.013% This example discloses a composition reflecting the most preferred embodiment of the improved construction board composition of the instant invention, and continues the study of the addition of various percentages of calcium sulfate into the composite core. It is also a test of an adhesive formulation comprising vinyl acetate polymer emulsion, modified starch, and boric acid. In this test, the first step was to mix about 15% of the preferred Perlite of the invention with the remaining dry constituents. The Perlite 15% (by volume) was combined with modified starch, ball mill accelerator, boric acid, and about 25% (by volume) calcium sulfate. Next, about 5% (by volume) vinyl acetate emulsion was added to soap foam, dispersant and about 50% (by volume) water. The wet and dry ingredients are fed by normal board manufacturing line apparatus into a pin mixer for 3 seconds. The slurry is dispersed onto continuous moving paper cover sheets. The construction board is formed and conveyed to the cutting knife. The board set up fairly hard in under three minutes and was then cut to desired lengths. The board was then inverted and run through a kiln at normal drying temperature parameters for about an hour. Once cooled, the sample was weighed and measured and the results were catalogued. Several days later this sample was conditioned and then tested to ASTM C473 standards. Test results confirmed nearly double those of the gypsum core control sample in nail pull resistance, edge hardness, and with improved

flexural strength.

EXAMPLE 6

Materials W eight in 0 Weight bv % Preferred

Gypsum 10.0 48-55% 51.355%

Ball Mill Accelerator .05 0.1 -0.3% .244%)

Starch .08 0.3-0.6% .387%

Boric Acid .02 0.01-0.15% .096%

Potassium sulfate .01 0.05-0.3% .048%

Lignosulfonate(dispersant) .01 0.07-0.8% .048%

Soap (foamer) .02 0.07-0.8% .096%

Vinyl Acetate .35 0.8-4% 1.697% Water 9.5 42-48% 46.029%

This example discloses the addition of the unique adhesive formulation of the instant invention into traditional gypsum board w ithout an expanded mineral added. Calcium sulfate(gypsum). starch, ball mill accelerator, potassium sulfate. and boric acid were combined in the above amounts. Then, lignosulfonate. Ethoxysulfate. vinyl acetate, and water were combined and mixed into a foamy consistenc) and combined with the dry ingredients. The mixture was mixed at high speed and then poured into a 6" by 12" form with a construction board paper insert and sealed and formed into a sheet identical to traditional gypsum board. The sample was then removed from the form and the set was timed. After timing the set and allowing the full hydration set to occur, the sample was then heated in a kiln at 180°F to evaporate excess water. Once dry. these boards were left to cure for two days and then tested. These experiments were conducted to evaluate increased strength in traditional construction board compositions with the addition of the synthetic binder. Nail pull resistance, edge hardness, and flexural strength were increased 150%o in all the samples that were made and tested. This decrease in set time and increase in strength of the construction board can allow for increased operating speeds in current board manufacturing facilities. Varying curing temperatures were applied in this example from 75°C to 352°C with favorable test results, including passing nail pull resistance, flexural breaking loads, edge hardness, and humidified bond according to ASTM C36. However, the preferred curing temperatures ranged from 79°C to 275°C.

EXAMPLE 7 Materials Weight in Ounces Weight bv % Preferred Perlite .40 2.366% Gypsum 8.0 42-50% 47.281% Ball mill accelerator .04 0.1 -0.3% .238% Starch .07 0.3-0.6% .413% Boric acid .015 0.01 -0.15% .088% Potassium sulfate .015 0.05-0.3% .088% Dispersant .02 0.07-0.8% .1 18% Soap (foamer) .01 0.07-0.8% .059% Vinyl Acetate .35 0.8-4% 2.068% Water 8.0 42-48% 47.281% In this example, first the dry ingredients were combined together and blended until a homogeneous mix was achieved, these dry ingredients being plaster grade expanded perlite with a loose density of 6 to 8 pounds per cubic foot, calcined gypsum stucco, starch, ball mill land plaster accelerator, pot ash and boric acid. Secondly, the dry lignosite dispersant was combined with the water and mixed until blended. Thirdly, the soap water and vinyl acetate were combined together and blended with an electric mixer to generate foam or bubbles. The soap water and vinyl acetate foam mix was then added to the lignosite and water and then all the wet ingredients were combined with the dry blended ingredients and mixed by hand for about 15 seconds to achieve 100% of a slurry. The ambient temperature was 82°F and the surrounding humidity was 29%. This slurry was then poured into a fire resistant and water repellant construction board paper insert or envelope to make a 1/2 inch thick board sample measuring 6 inches by 6 inches. The back sheet of the insert was then sealed to the face sheet folds using a starch based drywall edge paste, formed, and then removed from the form, and the initial or snap set was timed and recorded. In a typical drywall manufacturing process there are two different sets, first being the initial or snap set, whereas the continuous board hardens or stiffens sufficiently to be cut into desired lengths downstream at the rotary knife. The secondary or hydration set relates to the complete hydration of the gypsum crystals. meaning the amount of time sufficient to rehydrate the calcined gypsum, replacing the two molecules of H20 removed during the calcining process of land plaster. This secondary hydration set can be from as low as 4.6 minutes to as high as 7 minutes depending on the grind and purity of the land plaster being utilized. At 2 1/2 minutes the sample of the above example was cut cleanly and inspected. The inspection revealed that the slurry had sufficiently set and it is believed that the chemical reaction of the synthetic binder (vinyl acetate) and the calcined gypsum allows the gypsum crystal to rehydrate more rapidly than calcined gypsum rehydrated without the synthetic additive of the present invention. The above process has been duplicated repeatedly in the lab with slight variations in formula achieving the same results. A range of volumes of the preferred synthetic binder (vinyl acetate) were tested with gypsum and consistently set times were reduced over those of the gypsum control samples with no synthetic additives, and consistently stronger samples were obtained over those of the gypsum control samples with no synthetic additives. All procedures including the drying of the samples were consistent with typical drywall manufacturing processes. The excess water in the samples was driven off by placing samples in a laboratory kiln with access to moving heated air at a temperature of between 150°C and 200°C for a period of 50 minutes to 1 hour.

EXAMPLE 8

Materials Weight in 0 Weight by % Prefern

Perlite .30 1-3% 1.816

Gypsum 8.0 42-50% 48.434

Starch .075 0.3-0.6% .454

Ball mill accelerator .037 0.1-0.3% .224

Boric acid .015 0.01-0.15% .090

Dispersant .020 0.07-0.8% .121

Soap (foamer) .020 0.07-0.8% .121

Non-V.O.C. acrylic polymer .35 0.8-4%) 2.119

Water 7.7 42-48% 46.618

This example discloses the other preferred unique adhesive formulation of the instant invention into traditional gypsum board. Calcium sulfate(gypsum). starch, ball mill accelerator, and boric acid were combined in the above amounts. Then, lignosulfonate, Ethoxvsulfate, non-V.O.C. acrylic emulsion, and water were combined and mixed thoroughly and was then combined with the dry ingredients. The mixture as mixed at high speed and then poured into a 6" by 12" form with a construction board paper insert and sealed and formed into a sheet identical to traditional gypsum board. The sample was then removed from the form and the set was timed. After timing the set and allowing the full hydration set to occur, the sample was then heated in a kiln at 180°F to evaporate excess water. Once dry, these boards were left to cure for two days and then tested. These experiments were conducted to evaluate increased strength in traditional construction board compositions with the addition of the synthetic binder. The resulting board samples of this particular example surpassed all ASTM C36 specifications. The test results for this composition satisfied the criteria of ASTM methods C-36 and C-473.

EXAMPLE 9 Materials Weight in Ounces Weight bv % Preferred Gypsum 990.0 42-50% 48.072% Expanded Perlite 50.0 1-3% 2.427% Starch 10.0 0.3-0.6% 0.485% Ball mill accelerator 4.0 0.1-0.3%) 0.194% Potassium sulfate 2.75 0.134% 0.05-0.3% Boric acid 0.25 0.01-0.15% 0.013% Foaming Agent 1.50 0.07-0.8% 0.073% Sodium Trimetaphosphate 0.50 0.01-0.7% 0.024% Ethoxilated Alcohol 0.40 0.01-0.7% 0.019% Vinyl Acetate Emulsion 28.0 0.8-4% 1.359% Diloflo (Naphthalene Sulfonate) 2.0 0.07-0.8% 0.099% Water 970.0 42-49% 47.101% This example discloses the addition of a straight chain linear ethoxilated alcohol, added to the synthetic binder in a blend prior to its introduction into the system of this invention. By adding the nonionic surfactant to the binder, the polymer has greater dispersion capabilities in the slurry and forms strong or strengthened air entrainment into the matrix. The wetting action of the nonionic surfactant when blended with the polymer also decreases the amount of water needed to achieve a workable slurry. This example exemplifies the most preferred formulation of this invention. The system as a whole will achieve construction board weights up to 40 percent lighter and meets all ASTM standards for C36 gypsum wallboard specifications. This formulation is for use in production runs of the invention and is measured in units per thousand square feet typical to industry' practice. The dry ingredients are fed into a mixing conveyor screw from their respectiv e feeders and blended while being conveyed to the pin mixer. The wet ingredients, with the exception of the foam, are blended and fed into the water system upstream of the pin mixer to achieve proper dispersion. The formed construction board is then conveyed on a belt to the knife during which time it has set to a hardness sufficient to be cut at the knife. After being cut into the desired lengths it is inverted and run through a rnulti deck board drying kiln. The resulting dry construction board is stacked and housed for shipment to consumers. All of the construction board of this example met or exceeded nail pull resistance, flexural breaking loads, core and edge hardness, and deflection as well as humidified bond requirements per ASTM C36.

Industrial Applicability For the industrial application of construction board manufacture, it is desirable to provide a composition of and a method and device for manufacturing a construction board product having a strength equal to or greater than traditional construction board products with a coinciding lesser weight than previously known construction board products, and having a lesser amount of gypsum than what has been previously required in construction board compositions. Herein disclosed is a composition of and a method and device for manufacturing such a construction board product comprising a unique combination of synthetic binders selected for their ability to establish a strengthened permanent bond in the final dry state, in combination with an expanded mineral such as Perlite which reduces the amount of gypsum present in the construction board product from what has been required by previous gypsum construction board formulations. Such a reduction in the amount of gypsum present in the board formulation in turn reduces the weight of the board structure while maintaining its strength. Moreover, the synthetic binders uniquely cross-link with the expanded mineral to form a much stronger bond between the constituent components of the construction board core material than that which has been available in previously utilized or known construction board products.

Claims

CLAIMS: I claim: L A composition suitable for use in the manufacture of construction board comprising: an expanded mineral present at up to about 40% by weight: calcium sulfate present at up to about 60% by weight: and a synthetic binder, said synthetic binder being selected from the group consisting essentially of: (i) a vinyl acetate emulsion comprising a homogenous blend of suspended polyvinyl acetate particles in polyvinyl alcohol and water, and a solution comprising a 10%> to 25%o solution of polyvinyl alcohol to water, said solution being present in said composition in an amount of approximately 0.1% to about 30% of said vinyl acetate emulsion; (ii) a water-based non-V.O.C. acrylic emulsion comprising acrylic particles suspended in solution; and (iii) a water-based non-V.O.C. polyurethane emulsion comprising polyurethane particles suspended in solution.
2. The composition of claim 1 , further comprising: sodium trimetaphosphate present at about 0.01 % to about 10% by weight.
3. The composition of claim 1. further comprising: sodium trimetaphosphate present at about 0.01 % to about 0.7% by weight.
4. The composition of claim 1. said binder further comprising: a solution comprising a 5% to 30% solution of nonionic ethoxilated alcohol surfactant to water, said solution being present in said composition in an amount of approximately 0.1 % to 30%) of said binder.
5. A composition suitable for use in the manufacture of construction board comprising: an expanded mineral present at up to about 40% by weight; calcium sulfate present at up to about 60% by weight; and a water-based non-V.O.C. acrylic emulsion comprising acrylic particles suspended in solution.
6. A composition suitable for use in the manufacture of construction board comprising: an expanded mineral present at up to about 40% by weight; calcium sulfate present at up to about 60%) by weight; and a water-based non-V.O.C. polyurethane emulsion comprising polyurethane particles suspended in solution.
7. A composition suitable for use in the manufacture of construction board comprising: a dry powder mineral substrate selected from the group of minerals comprising calcium sulfate, perlite. and combinations thereof; and a synthetic binder, said synthetic binder comprising starch, a boron source, and an emulsion selected from the group consisting essentially of: ( i) a vinyl acetate emulsion comprising a homogenous blend of suspended polyvinyl acetate particles in polyvinyl alcohol and water, and a solution comprising a 10%> to 25% solution of polyvinyl alcohol to water, said solution being present in said composition in an amount of approximately 0.1% to about 30% of said vinyl acetate emulsion; (ii) a water-based non-V.O.C. acrylic emulsion comprising acrylic particles suspended in solution: and (iii) a water-based non-V.O.C. polyurethane emulsion comprising polyurethane particles suspended in solution.
8. The composition of claim 7, further comprising: sodium trimetaphosphate present at about 0.01% to about 10% by weight.
9. The composition of claim 7. further comprising: sodium trimetaphosphate present at about 0.01% to about 0.7% by weight.
10. The composition of claim 7, said binder further comprising: a solution comprising a 5% to 30% solution of nonionic ethoxilated alcohol surfactant to water, said solution being present in said composition in an amount of approximately 0.1% to 30% of said binder.
1 1. The composition of claim 7. said starch being present at about 0.30% to about 0.75% by weight.
12. The composition of claim 7. said boron source being present at up to about 0.35% by weight.
13. The composition of claim 7. wherein said starch is selected from the group comprising corn starch, dent corn starch, oxidized starch, waxy oxidized starch, dextrin, and white-canary dextrin.
14. The composition of claim 7. wherein said boron source is selected from the group comprising borate and boric acid.
15. The composition of claim 7, wherein said boron source is selected from the group comprising sodium tetraborate pentahydrate and sodium tetraborate decahvdrate.
16. A construction board composition comprising: a mineral selected from the group consisting essentially of calcium sulfate, perlite, and combinations thereof; a synthetic binder, said synthetic binder comprising starch, a boron source, and a polymer emulsion; and paper cover sheets sandwiching said mineral and said binder formulation therebetween.
17. The construction board composition of claim 16. wherein said paper cover sheets are formed from a virgin paper pulp comprising fibers having a length of at least one inch.
18. The construction board composition of claim 16. wherein said paper cover sheets are formed from a paper pulp comprising non-wood pulp fibers.
19. The construction board composition of claim 1 8. wherein said paper pulp forming said paper cover sheets further comprises recycled waste paper wood pulp fibers.
20. The construction board composition of claim 16. wherein said paper cover sheets comprise a multi-layer structure, said paper cover sheets further comprising a fiberglass mesh integrated between an inner face liner of said paper cover sheet and remaining layers of said multi-layer structure.
21. The construction board composition of claim 16. said paper cover sheets further comprising a fire retardant agent.
22. The construction board composition of claim 21. wherein said fire retardant agent comprises an agent selected from the group consisting essentially of boric acid, zinc borate, sulfamates, diammonium phosphate, nitrogen compounds, antimony oxide, silica, titanium oxide, and zircon.
23. The construction board composition of claim 22. wherein said fire retardant agent is present at about 0.15% to about 3% by weight of the finished construction board.
24. A method of manufacturing a construction grade construction board product comprising the steps of: (a) forming a first mixture by adding a first emulsion to a stream of metered water, said first emulsion being selected from the group consisting essentially of: (i) a first solution comprising a 10% to 25% solution of polyvinyl alcohol to water added to a vinyl acetate emulsion comprising a homogeneous blend of suspended polyvinyl acetate particles in polyvinyl alcohol and water, such that said first solution is present in said first emulsion in an amount of approximately 0.1 % to about 30% of said vinyl acetate emulsion; (ii) a water-based non-V.O.C. acrylic emulsion comprising acrylic particles suspended in solution: and (iii) a water-based non-V.O.C. polyurethane emulsion comprising polyurethane particles suspended in solution; (b) forming a second mixture by adding a mineral selected from the group consisting essentially of calcium sulfate, perlite, and combinations thereof, to said first mixture; (c) combining said second mixture with an additional amount of water; (d) gradually preparing a slurry by mixing and stirring said second mixture and said water to form said slurry; (e) enveloping said slurry between two paper cover sheets to form a wet board; and (f) drying said wet board at a temperature in the range of 75°C to 325°C.
25. The method of claim 24, further comprising the step of pre-coating an inside face of said paper cover sheets with said first emulsion prior to enveloping said slurry between said paper cover sheets.
26. The method of claim 24, further comprising the step of vigorously mixing said first mixture to foam said first mixture prior to forming said second mixture.
27. The method of claim 24, further comprising the step of adding an accelerating agent after preparing said slurry and prior to enveloping said slurry between two paper cover sheets.
28. The method of claim 27. wherein said accelerating agent comprises an alkali element present at about 0.001% to about 3% by weight.
29. The method of claim 24. further comprising the step of: applying heat to said wet board during its transfer from a board forming apparatus to a drying kiln.
30. The method of claim 24. further comprising the step of: adding starch and borate to said first mixture prior to forming said second mixture.
31. The method of claim 30, in which said starch is selected from the group comprising corn starch, dent corn starch, oxidized starch, axy oxidized starch, dextrin, white-canary dextrin, and combinations thereof.
32. The method of claim 30, in which said starch is present in the amount of about 0.30% to about 0.75% by weight.
33. The method of claim 30. in which said borate is selected from the group comprising sodium tetraborate pentahydrate and sodium tetraborate decahydrate.
34. The method of claim 30. in which said borate is present in the amount of about 0.001% to about 0.35% by weight.
35. The method of claim 24, further comprising the step of adding a solution comprising a 5% to 30% solution of nonionic ethoxilated alcohol surfactant to water to said first solution prior to forming said second mixture.
36. The method of claim 35, wherein said solution comprising a 5% to 30% solution of nonionic ethoxilated alcohol surfactant to water is added to said first solution in an amount of approximately 0.1 % to 30% of said first emulsion.
37. In a wallboard manufacturing facility, apparatus for forming a wallboard comprising an expanded mineral and a binder formulation having at least one self- crosslinking permanently tacky polymer, said apparatus comprising: an expander system for expanding a mineral; a plurality of expanded mineral storage silos; a first transport means for directing an expanded mineral from said expander system to said plurality of storage silos; a secondary expanded mineral feed tank; a second transport means for directing said expanded mineral from said storage silos to said secondary expanded mineral feed tank: blender means receiving said expanded mineral from said secondary expanded mineral feed tank and combining said expanded mineral with remaining dry materials in said wallboard: mixing means for mixing said expanded mineral, said dry materials, liquid components of said wallboard. water, and foaming agents into a slurry, and an elastomeric dispensing means attached to a dispensing outlet on said mixing means for dispensing said slurry from said mixing means; wallboard forming means for sandwiching said slurry between a plurality of paper sheets to form a wet board; conveyor means for conveying said wet board from said wallboard forming means to a wet board cutting means; drying means for drying said wet board: and transfer means for transferring said wet board from said cutting means to said drying means.
38. The apparatus of claim 37, said elastomeric dispensing means further comprising an elastomeric. wide flat hose having a first open end and a second end opposite said first end configured to convey larger expanded mineral particles present in said slurry.
39. The apparatus of claim 37. said elastomeric dispensing means further comprising a plurality of elastomeric hoses, each said hose having a first open end and a second end opposite said first end configured to convey larger expanded mineral particles present in said slurry.
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