JPS60171261A - Manufacture of incombustible gypsum board - Google Patents
Manufacture of incombustible gypsum boardInfo
- Publication number
- JPS60171261A JPS60171261A JP2558784A JP2558784A JPS60171261A JP S60171261 A JPS60171261 A JP S60171261A JP 2558784 A JP2558784 A JP 2558784A JP 2558784 A JP2558784 A JP 2558784A JP S60171261 A JPS60171261 A JP S60171261A
- Authority
- JP
- Japan
- Prior art keywords
- gypsum
- weight
- parts
- water
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000010440 gypsum Substances 0.000 title claims description 139
- 229910052602 gypsum Inorganic materials 0.000 title claims description 139
- 238000004519 manufacturing process Methods 0.000 title claims description 20
- 238000000034 method Methods 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
- 239000000835 fiber Substances 0.000 claims description 22
- 239000008235 industrial water Substances 0.000 claims description 18
- 238000000465 moulding Methods 0.000 claims description 14
- 239000010425 asbestos Substances 0.000 claims description 10
- 229910052895 riebeckite Inorganic materials 0.000 claims description 10
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 6
- 229910052751 metal Chemical class 0.000 claims description 6
- 239000002184 metal Chemical class 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000004575 stone Substances 0.000 claims description 6
- 235000002906 tartaric acid Nutrition 0.000 claims description 6
- 239000011975 tartaric acid Substances 0.000 claims description 6
- 230000036571 hydration Effects 0.000 claims description 3
- 238000006703 hydration reaction Methods 0.000 claims description 3
- 229920003043 Cellulose fiber Polymers 0.000 claims 1
- 239000002994 raw material Substances 0.000 description 18
- 239000000047 product Substances 0.000 description 17
- ZOMBKNNSYQHRCA-UHFFFAOYSA-J calcium sulfate hemihydrate Chemical compound O.[Ca+2].[Ca+2].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZOMBKNNSYQHRCA-UHFFFAOYSA-J 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- 239000002002 slurry Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 7
- 150000003862 amino acid derivatives Chemical class 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000005452 bending Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004568 cement Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- 235000011116 calcium hydroxide Nutrition 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 239000010893 paper waste Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 241001239379 Calophysus macropterus Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000282341 Mustela putorius furo Species 0.000 description 1
- 241000283220 Odobenus rosmarus Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- JHXCINJSAAFBDH-UHFFFAOYSA-N [Ca].O[Si](O)(O)O Chemical compound [Ca].O[Si](O)(O)O JHXCINJSAAFBDH-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000011507 gypsum plaster Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- -1 polypropylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/14—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
- C04B28/145—Calcium sulfate hemi-hydrate with a specific crystal form
- C04B28/146—Calcium sulfate hemi-hydrate with a specific crystal form alpha-hemihydrate
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 本発明は、不燃性石膏板の製造方法に関する。[Detailed description of the invention] The present invention relates to a method for manufacturing noncombustible gypsum board.
さらに詳しく述べれば、水和性石膏50〜85重量部お
よび工水石膏5御50
なる粉末状石膏に所定量の繊維、凝結遅延剤および所要
の水からなる混合物を成形、硬化および乾燥させる高品
質の鎖板の製造方法に関する。More specifically, a mixture of a predetermined amount of fibers, a set retarder, and the required amount of water is molded into a powdered gypsum of 50 to 85 parts by weight of wettable gypsum and 50 parts by weight of industrial water gypsum, hardened, and dried. The present invention relates to a method of manufacturing a chain plate.
石膏板は、無機質不燃性建築材料の中では、経済的に利
用でき、耐火性、遮音性、断熱性、寸法安定性および被
施工性にすぐれているため、特に内装材として広く使用
されている。石膏板製造技術の基本は、工水石膏を加熱
脱水した焼石膏に水を加えて成形硬化させ、所定形態の
板状物を得るのである。したがって石膏として硬化性を
もたない工水石膏は原則として使用できず、若しも焼石
膏中に僅か数%でも工水石膏が混在すると成形品の強度
が著しく低下するのみならず、紙(=Jき石膏ボードの
場合紙との接着性も失われる。その他、工水石膏は石・
麻の凝結を促進するのでその作用を緩和するため凝結遅
延剤の配合量が増加するなど焼石膏と工水石膏の混合使
用は否定されていた。Among inorganic noncombustible building materials, gypsum board is widely used as an interior material because it is economically usable and has excellent fire resistance, sound insulation, heat insulation, dimensional stability, and workability. . The basic gypsum board manufacturing technology is to add water to calcined gypsum, which is made by heating and dehydrating engineered water gypsum, and then forming and hardening it to obtain a plate-like product of a predetermined shape. Therefore, as a general rule, industrial water gypsum, which does not have hardening properties as plaster, cannot be used. If even a few percent of industrial water gypsum is mixed into the calcined gypsum, the strength of the molded product will not only decrease significantly, but also paper ( = In the case of J type gypsum board, the adhesion with paper is also lost.
The mixed use of calcined gypsum and industrial gypsum was denied, as it promoted the setting of hemp, so the amount of setting retardant was increased to alleviate the effect.
(特公昭57−49004号)、従って、若しも焼石膏
の中の相当割合を工水石膏に置換した粉末状石膏で公知
の石・挽板と同等のものが製造できれば、工水石膏から
焼石膏を製造するための莫大な熱エネルギーを節約する
ことが可能になる。(Special Publication No. 57-49004). Therefore, if powdered gypsum equivalent to known stone and sawn board could be produced by replacing a considerable proportion of calcined gypsum with industrial water gypsum, then It becomes possible to save a huge amount of thermal energy for producing calcined gypsum.
他方、焼石膏を使用せず、工水石膏のま一使用して成形
硬化させる石膏板若しくはその製法についてもいくつか
の提案がある。しかし、それらは、例えば、■300k
g/cm’以上のような極度の高圧加圧を要するに拘ら
ず、得られる石膏板の曲げ強度は10〜35kg/cm
’程度しか得られず(特公昭48−31012号)若し
くは、■比較的低イ10〜250kg/Cm’ような圧
力でプレス成型できるが、得られる製品の曲げ強度は、
著しく低く5〜30kg/am”程度2に止まり (特
公昭55〜348号)いづれも建材としての実用に供し
t;すないものしか得られていない。On the other hand, there are also several proposals regarding gypsum boards and methods for manufacturing the same, which do not use calcined gypsum but instead use industrial gypsum to form and harden. However, they are, for example, ■300k
Even though extremely high pressure such as g/cm' or more is required, the bending strength of the resulting gypsum board is 10 to 35 kg/cm.
(Japanese Patent Publication No. 48-31012) or ■Comparatively low pressure of 10 to 250 kg/cm.
It is extremely low at only about 5 to 30 kg/am''2 (Special Publication No. 55-348), and only a few have been obtained for practical use as building materials.
本発明者等は、上述の公知技術に係る問題点の解決すな
わち、石膏板の製造に工水石膏を利用することによる原
料面での省エネルギーの達成、工水石膏利用製品の製造
条件の緩和及び強度の向上につき鋭意研究した。その結
果、意外にも、繊維入り石膏板について使用する粉末状
石膏の5〜50重量部の工水石膏を使用し、残部の85
〜50重量部について焼石膏を使用するときは、石膏板
の実用的強度として100%焼石膏を使用したものに劣
らず、かつ、製造工程はより円滑能率的に実施し得るこ
とを知見し、この知見に基づいて本発明を完成した。The present inventors have solved the problems related to the above-mentioned known technologies, namely, achieved energy saving in terms of raw materials by using industrial gypsum in the production of gypsum boards, eased the manufacturing conditions for products using industrial gypsum, and We conducted extensive research on improving strength. As a result, it was surprisingly found that 5 to 50 parts by weight of industrial water gypsum was used in the powdered gypsum used for fiber-filled gypsum boards, and the remaining 85 parts by weight
It has been found that when using ~50 parts by weight of calcined gypsum, the practical strength of the gypsum board is as good as that using 100% calcined gypsum, and the manufacturing process can be carried out more smoothly and efficiently, The present invention was completed based on this knowledge.
以上の記述から明らかなように本発明の目的は、新規な
石膏板の製造方法を提供することであり、より詳しくは
、原料石膏粉末として焼石膏と工水石膏の併用を可能に
し、製造法として円滑能率的で実用可能な製品の強度が
得られる該製造方法を提供することである。As is clear from the above description, the purpose of the present invention is to provide a new method for manufacturing gypsum board, and more specifically, it is possible to use both calcined gypsum and engineered water gypsum as raw material gypsum powder, and the manufacturing method The object of the present invention is to provide a manufacturing method that is smooth, efficient, and has a strength that can be used for practical purposes.
本発明は、下記の主要構成を有する。The present invention has the following main configurations.
水和性石膏50〜95重量部と二人石膏5〜50重量部
よりなる粉末状石膏100重量部に対し、0.5〜30
重量部の繊維、該水和石膏に対し0.1〜2.0重峨%
の凝結遅延剤および水からなる混合物を該水和性石膏が
水和する前に成形し、硬化乾燥せしめることを特徴とす
る不燃性石膏板の製造方法。0.5-30 parts by weight for 100 parts by weight of powdered gypsum consisting of 50-95 parts by weight of wettable gypsum and 5-50 parts by weight of Futari gypsum.
Fiber in weight part, 0.1 to 2.0% by weight based on the hydrated gypsum
1. A method for producing a noncombustible gypsum board, which comprises forming a mixture of a set retarder and water before the hydrated gypsum is hydrated, and hardening and drying the mixture.
本発明の構成と効果につき以下に詳述する。The structure and effects of the present invention will be explained in detail below.
本発明の方法に係る原料的特徴は、水和性石膏と工水石
膏を実質的に併用する点にある。使用する水和性石膏と
しては、工水石膏を公知方法で加熱処理して得られるα
型半水石膏、β型半水石膏若しくは可溶性無水石膏のい
づれか1種若しくは2種以上の混合物である。使用する
水和性石膏の粉末度は、好ましくはブレーン比表面積値
で5000cm’/g以下である。The raw material characteristic of the method of the present invention is that hydratable gypsum and water gypsum are substantially used together. The hydratable gypsum used is α, which is obtained by heat-treating industrial water gypsum using a known method.
It is any one of type hemihydrate gypsum, β type hemihydrate gypsum, and soluble anhydrite, or a mixture of two or more types. The fineness of the hydrated gypsum used is preferably 5000 cm'/g or less in Blaine specific surface area value.
この値を著しく超えるような細かい粉末度のものは、本
発明に係る前述の混合物からの成形品の硬化時間が不都
合に短縮される傾向を生じこれを是正するために凝結遅
延剤の添加量が増大し好ましくない。A fineness of fineness which significantly exceeds this value tends to disadvantageously shorten the curing time of molded articles from the above-mentioned mixtures according to the invention, and in order to rectify this the addition of set retarder may be necessary. Increased and undesirable.
逆に該粉末度が粗すぎる場合は、得られる硬化体すなわ
ち石膏板の強度が低下する。従って、該粉末度は、最大
粒径として500 g以下であり、がっ、ブレーン比表
面積値が1000cm’/g以上であることが好ましい
。なお、本発明に係る成形方法として抄造法を採用する
場合は、該比表面積値は、5000ctn’/g以下で
あることが好ましい。何故なら使用された水和性石膏粉
末の濾水中への逸失を最小限に止めることが可能となる
からである。On the other hand, if the fineness is too coarse, the strength of the resulting cured product, that is, the gypsum board, will decrease. Therefore, the fineness is preferably 500 g or less as the maximum particle size, and the Blaine specific surface area value is preferably 1000 cm'/g or more. In addition, when employ|adopting the paper-making method as a shaping|molding method based on this invention, it is preferable that this specific surface area value is 5000 ctn'/g or less. This is because it becomes possible to minimize the loss of the used hydrated gypsum powder into the filtrate.
他方、工水石膏についてはその粒径が500 #以下で
あれば、その出所又は製法の如何を問わない。周知のよ
うに工業原料としての工水石膏には、天然品の外に多種
類の化学工業(的副生)製ある。塊状品例えば天然石膏
は、上述の粒度まで粉砕する必要があり、その点で他の
化学石膏の方が利用し易い。その反面、該工水石膏は、
その粉末度が過度に細かくなると共存する水和性石膏(
半水石膏および/または可溶性無水石膏)の凝結を著し
く促進する。これを防止するため石膏板製造用程合物に
添加すべき凝結遅延剤の量を増加しなくてはならないと
いう不利が在る。したがって、該工水石膏の粉末度は、
プレーン比表面積値で5000crrf/g以下である
ことが好ましい。工水石膏は、使用にあたり、繊維の離
解の際に混合して分散させておくことが好ましい。On the other hand, as for water gypsum, as long as its particle size is 500# or less, its source or manufacturing method does not matter. As is well known, industrial water gypsum, which is used as an industrial raw material, includes many types of chemical industrial (by-product) products in addition to natural products. Bulky products such as natural gypsum must be ground to the above-mentioned particle size, and other chemical gypsums are easier to use in this respect. On the other hand, the industrial water gypsum is
Hydrateable gypsum (
significantly accelerates the setting of gypsum hemihydrate and/or soluble anhydrite). The disadvantage is that in order to prevent this, the amount of set retarder to be added to the formulation for making gypsum board must be increased. Therefore, the fineness of the industrial water gypsum is
It is preferable that the plane specific surface area value is 5000 crrf/g or less. Before use, it is preferable that the gypsum be mixed and dispersed during disintegration of the fibers.
前述の水和性石膏と工水石膏の使用割合は、両者の合計
量 10(1重量部に対し、前者が50〜95重量部、
後者が5〜50重量部である。前者が50重量部未満で
は成形品の強度が不十分となり、85重量部を超えると
水和性石膏の節約という本発明の目的に反する。他方、
後者を50重量部以上配合した場合は、成形品の強度低
下が著しく、最終的に得られる石膏板の実用性が失われ
る。工水石膏の混合割合と石膏板強度の関係を例示する
と下表のとおりである。The usage ratio of the above-mentioned hydratable gypsum and industrial water gypsum is the total amount of both 10 (1 part by weight, 50 to 95 parts by weight of the former,
The latter is 5 to 50 parts by weight. If the former is less than 50 parts by weight, the strength of the molded article will be insufficient, and if it exceeds 85 parts by weight, it will go against the purpose of the present invention, which is to save hydrated gypsum. On the other hand,
When the latter is added in an amount of 50 parts by weight or more, the strength of the molded product is significantly reduced, and the practicality of the final gypsum board is lost. The table below shows an example of the relationship between the mixing ratio of industrial gypsum and the strength of gypsum board.
表 二水石す゛:゛泥合−χ合と石膏&強度(kg/c
m″)本発明に使用する繊維は、例えば石綿若しくはガ
ラスm維のような無機質mM1または、セルa−ズ繊維
、ビニロン繊維、ポリプロピレン繊維若しくはポリアミ
ドt@維のような天然又は合成の有機質繊維の一種若し
くは二種以上を組合わせて使用できる。これらの中で特
に石綿繊維及びセルローズm 11は、石膏(硬化物)
との接着力が強いので使用する繊維中にこれらのいづれ
かを使用し若しくは混合使用することが好ましい。Table Dihydrite: ゛Mud - χ and gypsum & strength (kg/c
The fibers used in the present invention are, for example, inorganic fibers such as asbestos or glass fibers, or natural or synthetic organic fibers such as cell-A's fibers, vinylon fibers, polypropylene fibers, or polyamide fibers. One type or a combination of two or more types can be used.Among these, asbestos fiber and cellulose M11 are especially suitable for use in gypsum (hardened product).
It is preferable to use one or a mixture of these in the fibers used because of their strong adhesive strength.
本発明に係る石膏板製造用の混合物に前述のような繊維
質を配合することは、得られる石膏硬化体の脆さを改善
し、併せて耐衝撃強度、耐曲げ強度を向上させ柔軟性を
良好にする。該混合物において繊維の使用量は、粉末状
石膏100重量部に対し、好ましくは0.5〜30重量
部である。0.5重量部未満では、上述の諸効果の発現
が不十分であり、30重量部を超えて配合しても該効果
は向上せず、経済的でない。反って、一部の物性につい
ては低下するおそれがある。Incorporating the above-mentioned fibers into the mixture for producing gypsum board according to the present invention improves the brittleness of the resulting hardened gypsum body, and also improves impact strength and bending strength, and improves flexibility. make it good. The amount of fiber used in the mixture is preferably 0.5 to 30 parts by weight per 100 parts by weight of powdered gypsum. If it is less than 0.5 parts by weight, the above-mentioned effects are insufficiently expressed, and even if it exceeds 30 parts by weight, the effects will not improve and it is not economical. On the other hand, some physical properties may deteriorate.
本発明に係る前述の混合物に使用する水量は、限定され
ず、また、成形方法によって異なる。しかしながら、人
以外の該混合物量に対して15〜2.500重量%混合
することにより成形し易い該混合物が得られる。必要な
最小限の水量は、水和性石膏が完全に水和するのに必要
な水量である。The amount of water used in the above-mentioned mixture according to the invention is not limited and varies depending on the forming method. However, by mixing 15 to 2.500% by weight based on the amount of the mixture other than humans, the mixture can be easily molded. The minimum amount of water required is the amount of water required for the hydratable gypsum to be completely hydrated.
本発明に使用する石膏の凝結遅延剤は、グリセリン、ア
ルコール、リン酸塩、カルボン酸、オキシカルボン酸若
しくはそれらの塩類およびアミノ酸誘導体等公知の物質
のいづれも使用できる。しかしながら、本発明のように
粉末状石膏100重量部中に5〜50重量部のように大
量の工水石膏が積極的に配合されている場合にあっては
、特に■少41の添加で凝結遅延効果が大であり、■得
られる石・g硬化体の強度を低下させないという条件を
満足させる必要がある。以上の見地から、本発明者等が
見出した最善の〃延剤は、酒石酪若しくはその金属塩ま
たはより好ましくはそれらの一以上と7ミノ#銹導体の
組合せである。該金属塩層の金属としてはアルカリ金属
が好ましい。As the gypsum setting retarder used in the present invention, any of known substances such as glycerin, alcohol, phosphate, carboxylic acid, oxycarboxylic acid or their salts, and amino acid derivatives can be used. However, when a large amount of industrial water gypsum (5 to 50 parts by weight) is actively blended into 100 parts by weight of powdered gypsum as in the present invention, especially when a small amount of 41 is added, solidification occurs. It is necessary to satisfy the conditions that the retardation effect is large and (1) the strength of the obtained stone/g hardened body is not reduced. From the above viewpoint, the best spreading agent found by the present inventors is a combination of tartaric acid or a metal salt thereof, or more preferably one or more thereof, and a 7 min. rust conductor. The metal of the metal salt layer is preferably an alkali metal.
凝結遅延剤の使用量は、本発明の方法の目的とする石膏
板の成形方法によって異なるが標準的には、使用する水
和性石膏100重量部に対して0.1〜2重M部を必要
とする。(1,1重量部未満では。The amount of the setting retarder to be used varies depending on the method of forming the gypsum board that is the object of the method of the present invention, but it is typically 0.1 to 2 parts by weight per 100 parts by weight of the wettable gypsum used. I need. (Less than 1.1 parts by weight.
凝結遅延効果を発現できず2重量部を超えると石・a硬
化体の強度を低下させる。If the amount exceeds 2 parts by weight, the setting retardation effect cannot be expressed, and the strength of the stone/a hardened body is reduced.
本発明にあっては、以上の諸原料を混合して得られる混
合物ないしスラリーのPHを好ましくは7以上に調整す
る。調整方法は該混合物に添加剤として少量の塩基性物
質例えばセメント消石灰等を使用する方法でもよい。こ
のようなPHの調整は硬化遅延剤の効果を高めると共に
、本発明に係る石膏板製造設備に錆若しくはスケールの
発生を防止するのみでなく、製品石膏板についてその使
用時に釘打ちされた釘の防錆等の効果を有する。In the present invention, the pH of the mixture or slurry obtained by mixing the above raw materials is preferably adjusted to 7 or higher. The preparation method may be a method of using a small amount of a basic substance such as cement slaked lime as an additive in the mixture. Such PH adjustment not only enhances the effect of the curing retarder and prevents the formation of rust or scale on the gypsum board manufacturing equipment according to the present invention, but also prevents the production of nails on the product gypsum board during use. It has effects such as rust prevention.
上述のように製造された本発明に係る混合物を用いて石
膏板を製造する成形方法としては、流し込み、脱水、加
圧圧縮若しくは抄造等公知のいづれの成形方法も利用で
きる。しかしながら、いづれの成形方法を採用する場合
も、前記混合物中の水和性石膏が水和する以前に成形し
なければならない。若しも該混合物中の水和性石膏が水
和した後に成形を行うと得られる石膏硬化体の強度は激
減し、実用的強度を保持する石膏板を得ることができな
い。同様の理由で若し該成形工程の一部に加圧圧縮工程
が含まれる場合は、原料混合物中の水利性石膏が水和す
る以前に該工程を終了しなければならない。該加圧時の
圧力は、10〜500 Kg/Cm’で実施する必要が
ある。特に本発明に係る前述の混合物について50Kg
/crn’以上の圧力で圧縮成型した石膏板は、工水石
膏を配合しているに拘らず、粉末石膏として水和性石膏
のみを使用して得られた物に比較して殆ど強度的に劣ら
ないものを得ることができる。成形した石膏板は、水和
が完了した後、乾燥せしめる。乾燥は公知の方法で適宜
の条件で行なえばよい。As a molding method for manufacturing a gypsum board using the mixture according to the present invention manufactured as described above, any known molding method such as pouring, dehydration, pressure compression, or paper forming can be used. However, whichever molding method is employed, the molding must be performed before the hydrated gypsum in the mixture is hydrated. If molding is performed after the hydrated gypsum in the mixture has been hydrated, the strength of the resulting hardened gypsum product will be drastically reduced, making it impossible to obtain a gypsum board that maintains practical strength. For the same reason, if a pressurization process is included as part of the molding process, the process must be completed before the water-friendly gypsum in the raw material mixture is hydrated. The pressure at the time of pressurization needs to be 10 to 500 Kg/Cm'. 50 Kg especially for the aforementioned mixture according to the invention.
/crn' or higher compression molded gypsum board has almost no strength compared to that obtained using only hydrated gypsum as powdered gypsum, even though it contains industrial gypsum. You can get something just as good. After hydration is complete, the formed plasterboard is allowed to dry. Drying may be carried out by a known method under appropriate conditions.
以上にようにして、本発明に係る石膏板が得られるが、
該製造工程中で発生する流出混合物は、そのま\の状態
で循環して使用することができる。また、本発明の方法
にかkる石膏板の形態的な不良製品若しくは整形時の切
断端部等の回収品は、再度粉砕して原料の工水石膏およ
び繊維の一部として再使用できる。これらの循環使用若
しくは回収使用が可能な理由は、これらの再使用原料中
の水和性石膏が、水和して工水石膏に変化しても、これ
らを原料工水石膏として扱い本発明に係る原料の配合割
合を調整できるためであって、粉末石膏として水和性石
膏のみ使用する従来法からは予測し得ない効果といえる
。たぐし、以上の再使用の場合も全原料中の工水石膏の
割合が粉末石膏の50重景%を超えてはならないことは
勿論である0本発明の方法によれば、成形された生板を
複数枚重ね合わせて加圧成形することにより、任意の厚
さの一体化された厚物石膏板を製造することができる。As described above, a gypsum board according to the present invention is obtained,
The effluent mixture generated during the manufacturing process can be recycled and used as is. In addition, morphologically defective products of gypsum boards produced by the method of the present invention, or recovered products such as cut ends during shaping, can be re-pulverized and reused as the raw material industrial water gypsum and part of the fibers. The reason why these recycled or recovered materials are possible is that even if the hydratable gypsum in these reused raw materials hydrates and turns into industrial gypsum, it cannot be treated as raw material industrial gypsum and used in the present invention. This is because the mixing ratio of such raw materials can be adjusted, and this can be said to be an effect that cannot be predicted from the conventional method in which only hydrated gypsum is used as powdered gypsum. In the case of reuse as described above, it goes without saying that the proportion of industrial water gypsum in the total raw materials must not exceed 50% of the powdered gypsum. By stacking a plurality of plates and press-molding them, an integrated thick gypsum board of any thickness can be manufactured.
本発明の方法においては、目的とする石膏板の物性を種
々改善するため公知の各種の添加材を使用できる。それ
らは、例えばウオラスナイト、マイカ、バーミキュライ
ト、けいそう土若しく ltパーライト等であるが、勿
論これ等に限定されない。これらの鉱物質の添加量は、
本発明に係る原料Jt合物中のmla質の使用量の枠内
で決定されることが望ましい、すなわち、該繊維質と該
鉱物質の合計是が粉末状石膏100重量部に対して0.
5〜30m歌部の範囲内で使用することが好結果をもた
らす。In the method of the present invention, various known additives can be used to improve various physical properties of the target gypsum board. These include, for example, walrus night, mica, vermiculite, diatomaceous earth, and lt perlite, but are of course not limited to these. The amount of these minerals added is
It is desirable that the amount of ML used in the raw material Jt compound according to the present invention is determined within the framework of the amount used, that is, the total amount of the fibrous and mineral substances is 0.000 parts by weight per 100 parts by weight of powdered gypsum.
Good results are obtained when used within the range of 5 to 30 m.
本発明の方法は、原料の粉末石・Rとして高価な水和性
面・gのみを使用する必要がなく、その半量まで安価な
工水石膏を併用できるので経済的である。もた、本発明
の方法は、次の諸理由で特に抄造法に適用した場合に有
利に実施できる。すなわち、■スラリーの濾過性が改善
されるので抄造性が向」−シ、使用するm維として必ず
しもアスベストとパルプを併用しなくてもよい。これは
、粉末石膏として工水石膏を混合使用したことに基づ〈
。また、■白水および流水石膏を循環使用する際の安定
的連続運転のため配合される凝結遅延剤を(工水石膏を
配合しない場合に較べて)特に増量する必要がない。ざ
らに■該遅延剤として酒石酸若しくはその金属塩および
アミノ酸誘導体(例えば、市販商品名バフタート)を併
用配合した場合には、遅延剤の添加量が酒石酸又はその
金属塩単味の場合と比べ少量ですみ1本発明方法に係る
抄造後の加圧成形により、成形前に含まれていたアミノ
酸誘導体の大半が濾水中に移動するので該抄造品の水和
効果が促進され、短時間に高強度の/
石・a板が得られる。The method of the present invention is economical because it is not necessary to use only the expensive hydrating face/g as the raw material powder stone/R, and up to half of the amount of inexpensive industrial water gypsum can be used in combination. Furthermore, the method of the present invention can be advantageously implemented particularly when applied to a papermaking method for the following reasons. That is, (1) the filterability of the slurry is improved, so the papermaking properties are improved; (2) it is not necessarily necessary to use asbestos and pulp together as the m-fibers used; This is based on the mixed use of industrial water gypsum as powdered gypsum.
. In addition, (1) there is no need to increase the amount of setting retardant (compared to the case where industrial gypsum is not blended) for stable continuous operation when white water and running water gypsum are used in circulation. ZARANI ■ When tartaric acid or its metal salt and an amino acid derivative (for example, commercially available product name Baftat) are combined as the retardant, the amount of retardant added is smaller than when tartaric acid or its metal salt is used alone. 1. Due to the pressure forming after papermaking according to the method of the present invention, most of the amino acid derivatives contained before forming are transferred into the filtrate, promoting the hydration effect of the paper product, and achieving high strength in a short period of time. / Stones and a-boards are obtained.
また、本発明の方法になる石膏板は、僅か数%の工水石
膏の混在下に製造した従来法の石膏板が、該非混在の場
合に比較して著しく強度が低下していたのに対して、石
膏原料の半量について二本石膏を使用してもその強度低
下は僅かですむという利点がある。さらに本発明の方法
になる石膏板は、従来品と比較した場合、その耐火性、
耐水性については勿論、内装材としての諸物性すなわち
、曲げ強さ、耐衝撃性、寸法安定性、柔軟性。In addition, the strength of the gypsum board produced by the method of the present invention was significantly lower than that of the conventional gypsum board manufactured with only a few percent of industrial water gypsum mixed in, compared to the case where the gypsum board was not mixed. Therefore, there is an advantage that even if double gypsum is used for half of the gypsum raw material, the strength decreases only slightly. Furthermore, the gypsum board produced by the method of the present invention has a higher fire resistance than conventional products.
Not only is it water resistant, but it also has various physical properties as an interior material, such as bending strength, impact resistance, dimensional stability, and flexibility.
加工性および保釘性等についてもより優れている。It also has better workability, nail retention, etc.
以下、抄造法その他の製造法による実施例、比較例を示
す。これらに関する試験法としては下記の方法を採用し
た。Examples and comparative examples using papermaking methods and other manufacturing methods are shown below. The following methods were adopted as testing methods for these.
曲げ強度: JISA 5418(石綿セメントけい酸
カルシウム板)
衝撃強度: JISC: 2210(電気絶縁用石綿セ
メント板)
寸法変化率: JISA 541B(吸水による長さ変
化率)加熱収縮率: JISA 9510(けい酸カル
シウム保温材)に準する。但し、加熱条件は
850℃2時間加熱
不燃性:建設省告示1828号
実施例1〜9.比較例1〜6
下記の原料を用い、後述表−1に示す割合で混合した。Bending strength: JISA 5418 (asbestos cement calcium silicate board) Impact strength: JISC: 2210 (asbestos cement board for electrical insulation) Dimensional change rate: JISA 541B (length change rate due to water absorption) Heating shrinkage rate: JISA 9510 (silicic acid Calcium insulation material). However, the heating conditions are 850°C for 2 hours, non-flammable: Ministry of Construction Notification No. 1828 Examples 1 to 9. Comparative Examples 1 to 6 The following raw materials were mixed in the proportions shown in Table 1 below.
排脱石膏:排煙脱硫法で副生した工水石膏(粒度は、0
.511m/m目篩全通、ブレーン1200 crn’
/g)
リン酸石膏ニリン酸二木石膏(粒度は、0.59mar
s目篩全通、ブレーン900crn’/g)β型半水石
膏:焼石膏市販品
α型半水石膏:型材用α石膏市販品
石綿:アモイサイト石綿をパン型グラインダーで解砕
故紙:新聞故紙パルプ
カラス繊維:Eガラス切断品、長さ 172インチ消石
灰:市販品
酒石醇:市販品
アミノ酸誘導体:パフタード5−02 (味の素■製〕
上記原料の混合方法は、凝結遅延剤である酒石酸および
アミノ酸誘導体のみ、水和性石膏であるβ型半水石膏又
はα型半水石膏に対して外側重量%で使用し、その他は
、内割り重量部(計重量%と仝じ)である。Exhaust gypsum: Industrial gypsum produced as a by-product of the flue gas desulfurization method (particle size: 0
.. 511m/m sieve all through, Brain 1200 crn'
/g) Phosphate gypsum Diphosphogypsum (particle size is 0.59mar
S sieve all through, Brain 900crn'/g) β-type hemihydrate gypsum: Plaster of Paris, commercially available α-type hemihydrate gypsum: α-gypsum for molding, commercially available Asbestos: Amoysite asbestos crushed with a pan-shaped grinder Waste paper: waste newspaper Pulp crow fiber: E-glass cut product, length 172 inches Slaked lime: Commercial product Tartar sauce: Commercial product Amino acid derivative: Pufftard 5-02 (manufactured by Ajinomoto ■)
The method of mixing the above raw materials is to use only tartaric acid and amino acid derivatives, which are setting retardants, at the outside weight percent relative to the hydrated gypsum, β-type hemihydrate gypsum or α-type hemihydrate gypsum. Parts by weight (same as % by weight).
混合順序は、所定量の石綿、故紙若しくはガラス繊Mt
の繊維類、消石灰、工水石膏、酒石酸およびアミノ酸誘
導体と水とを混合したスラリーに、所定量のβ型半水石
膏若しくはα型半水石膏を力。The mixing order is as follows: A predetermined amount of asbestos, waste paper or glass fiber Mt.
A predetermined amount of β-type hemihydrate gypsum or α-type hemihydrate gypsum is added to a slurry of water mixed with fibers, slaked lime, industrial gypsum, tartaric acid, and amino acid derivatives.
えて混合し、全固形分の濃度が該ステ1ノー中で10重
量%となるように水量を調整した。The amount of water was adjusted so that the total solid concentration was 10% by weight in the step no.
かくして得られたスラリーを回転式丸網シリンダーによ
り抄き上げ、エンドレスのフェ1レト上番と取り上げて
薄いフィルムを形成させとものを一8〜10mmHgの
吸引力を有する脱水装置で脱水し、メーキングロール上
に仕上がり目標の6mm厚さlこなるまで積層させたも
のを力・ンターで切断し、生シートを得た。The slurry thus obtained is scooped up using a rotary round net cylinder and taken up with the top layer of an endless ferret to form a thin film.The slurry is then dehydrated using a dewatering device with a suction force of 18 to 10 mmHg, and then made. The material was laminated on a roll until it reached the target finished thickness of 6 mm and was cut using a force machine to obtain a green sheet.
かくして得られた生シートIt、そのす」に含有されて
いる焼石膏が水和される以1iij 1.こ、所定の圧
ブJで加圧・脱水し、該加圧・脱水量を硬イし乾燥させ
て本発明の方法に係る若しくCよ比較例の石膏石膏板を
得た。また、比較例としてtよ、工水石膏を添加しない
以外は同様に実施した。Since the calcined gypsum contained in the raw sheet thus obtained is hydrated, 1. This was pressurized and dehydrated using a predetermined pressure tube J, and the amount of pressurized and dehydrated was hardened and dried to obtain a gypsum gypsum board according to the method of the present invention or as a comparative example. In addition, as a comparative example, the same procedure was carried out except that no industrial water gypsum was added.
以上のようにして得られた製品石膏板に各種の件部試験
を行ない得られた結果を表−2に示した。The product gypsum board obtained as described above was subjected to various surface tests and the results are shown in Table 2.
表−I J!1.料配合割合と成形圧力「
al、 2 kg/Cm’
表−2石膏板物性
実施例10〜18.比較例7〜12
実施例1〜9で使用したものと同一の原料を用い、後述
衣−3の割合で混合し、該混合物すなわち固形分に対し
、10重量倍の水を加えてスラリーとし、該スラリーを
口紙上に流して均一の厚さにひろげ、吸引脱水させた後
同表に示す圧力で加圧成形し、ひきつづき硬化乾燥させ
て石膏板を得てその嵩比重および曲げ強度を測定した。Table-I J! 1. Table 2 Gypsum board physical properties Examples 10 to 18. Comparative Examples 7 to 12 Using the same raw materials as those used in Examples 1 to 9, the following coatings were prepared. 3, and add 10 times the weight of water to the mixture, i.e., the solid content, to form a slurry, pour the slurry onto a slip paper to spread it to a uniform thickness, and after dehydration by suction, the results are shown in the same table. A gypsum board was obtained by pressure molding and subsequent curing and drying, and its bulk specific gravity and bending strength were measured.
結果を同表に示す。The results are shown in the same table.
表−3原料配合割合と成形圧力(その■)と結果註1本
kg/cnf、tl kg/crn’実施例18
(本発明に関連する混合物の濾過性)木材パルプ(針葉
樹)をディスク型リアイナーを用い、カナダ標準フリー
ネス(GSF)値で、50,200,400および 7
00ccの4段階にフィブリル化した。これら4種の試
料者5gと焼石膏45gまたは焼石膏22.5gと排煙
脱値石膏各22.5gの混合物にそれぞれ水を加えて全
量がl又となるように調整し、撹拌してスラリーとした
。Table 3 Raw material blending ratio, molding pressure (■) and results Note 1 kg/cnf, tl kg/crn' Example 18 (Filterability of mixtures related to the present invention) Wood pulp (softwood) was used as a disc-shaped rear liner. using Canadian Standard Freeness (GSF) values of 50, 200, 400 and 7.
Fibrillation was carried out in 4 stages of 00cc. Water is added to a mixture of 5 g of these four types of samples and 45 g of calcined gypsum, or 22.5 g of calcined gypsum and 22.5 g each of flue gas devalued gypsum, the total volume is adjusted to 1 volume, and the mixture is stirred to form a slurry. And so.
これらのスラリーを個別にC3F測定装置の45mes
h網上に投入し、投入時から30秒間の濾水を採取した
。この濾水の容積を測定し、下記表−5に示した。ひき
つづき各の濾水中の粉体固形分の乾燥重量を測定し、粉
体損失量として表−6に示した。These slurries were individually measured at 45 mes using a C3F measuring device.
The water was poured onto a mesh screen, and the filtrate was collected for 30 seconds from the time of injection. The volume of this filtrate was measured and shown in Table 5 below. Subsequently, the dry weight of the powder solid content in each filtrate was measured and shown in Table 6 as the amount of powder loss.
表−5417水量の測定結果(表内は濾水11cc)表
−5に明らかなように同−C5F値の場合、二水石・g
を混用したスラリーの濾水量が、焼石膏単用のそれより
も著しく大きい。Table-5417 Water volume measurement results (filtered water is 11cc in the table) As shown in Table-5, in the case of the same -C5F value, dihydrate/g
The drainage amount of slurry mixed with gypsum is significantly larger than that of calcined gypsum alone.
表−6fa氷水中流出した粉体ロス量の測定結果(表内
は乾燥量J1g)表−6に明らかなように同−CSF値
の場合、工水石膏を混用したスラリーの濾水中の粉体ロ
ス量は、焼石膏単用のそれよりも著しく小さい。Table 6fa Measurement results of the amount of powder loss flowing out in ice water (the dry amount J1g in the table) The amount of loss is significantly smaller than that of calcined gypsum alone.
以 上
時計出願人 小野田セメント株式会社
同 上 朝日石綿工業株式会社
代理人弁理士 野 中 克 彦
手続補正書
昭和59年 3月、? 日
1、事件の表示
昭和59年特許順第25587号
2、発明の名称
不燃性石膏板の製造方法
3、補正をする者
事件との関係 特許出願人
山「1県小野FrJ市大字小野田6276番地(024
) 小野田セメント株式会社
4、代理人
東京都中央区築地4丁目4番15号(〒104)6、補
正により増加する発明の数
な し
7、補正の対象
明細書の「発明の詳細な説明」の欄。Applicant for the watch Onoda Cement Co., Ltd. Same as above Patent attorney for Asahi Asbestos Industries Co., Ltd. Katsuhiko Nonaka Procedural amendment March 1980, ? Day 1, Indication of the case 1982 Patent Order No. 25587 2, Name of the invention Method for manufacturing non-combustible gypsum board 3, Person making the amendment Relationship to the case Patent applicant mountain 6276 Oaza Onoda, Ono FrJ City, Prefecture 1 (024
) Onoda Cement Co., Ltd. 4, Agent 4-4-15 Tsukiji, Chuo-ku, Tokyo (104) 6, No number of inventions increased by amendment 7, “Detailed description of the invention” in the specification to be amended column.
8、補正の内容 明細書をつぎのように訂正する。8. Contents of amendment The specification shall be amended as follows.
(1)第8頁下から144行目「使用する繊維は、」を
[使用する繊維としては、Jに訂正する。(1) On page 8, line 144 from the bottom, ``The fiber used is'' is corrected to [The fiber used is J.
(2)i1o頁下から6行目の「セメント」のつぎにr
、Jを挿入する。(2) r next to “cement” in the 6th line from the bottom of page i1o
, insert J.
”’)@+3頁3頁目行目ウオラスナイト」を「ウオラ
ストナイト」に訂正する。``') @+3, page 3, line 3, ``Wollast Night'' is corrected to ``Wollast Night.''
(4)同頁5行目のFノヘーライトJを「パーライト」
に訂正する。(4) F Nohelite J on the 5th line of the same page is “Pearlite”
Correct.
(5)同頁下から6行目の「もた、」を「また、」に訂
正する。(5) In the 6th line from the bottom of the same page, "Mota," is corrected to "Also."
(8)第17頁6行目の「させとものを」を「させたも
のを」に訂正する。(8) On page 17, line 6, ``Sasetomono'' is corrected to ``Sasetamono''.
(7)同頁下から5行目の「石膏石膏ノを「石膏」に訂
正する。(7) In the fifth line from the bottom of the same page, "gypsum gypsum" is corrected to "gypsum."
(8)同頁下から4ないし3行目の「添加しない以外は
」を「添加せず若しくは50重量%以上使用した以外は
」に訂正する。(8) In the fourth or third line from the bottom of the same page, "Except not added" should be corrected to "Except not added or used at least 50% by weight."
(9)同頁下から2行目の「石膏板に」のつぎにrつき
」を挿入する。(9) On the second line from the bottom of the same page, insert "r" after "on the plasterboard."
(10)第18頁表−1中「石膏の種類」の欄の下の欄
中の「α型半水」を「β型半水」に、「β型半水」をα
型半水」に訂正する。(10) In Table 1 on page 18, in the column below the column for “type of gypsum,” “α-type hemihydrate” is changed to “β-type hemihydrate,” and “β-type hemihydrate” is changed to α
Corrected to ``Kata Hansui''.
(11)第18頁の表−2中最終行(註r // 6
Jの行)中の「寸法変化率%」の欄にr O,0!5J
を同じく「加熱収縮率%」の欄にr3.2 Jを挿入す
る。(11) Last line of Table 2 on page 18 (note r // 6
R O, 0!5J in the "Dimensional change rate %" column in row J)
Similarly, insert r3.2 J in the "heat shrinkage percentage" column.
以 上that's all
Claims (7)
重量部よりなる粉末状石膏100重量部に対し、0.5
〜30重量部の繊維、該水和性石膏に対し0.1〜2.
0重量%の凝結遅延剤および水からなる混合物を該水利
性石・gが水和する前に成形し、硬化乾燥せしめること
を4.¥徴とする不燃性面・a板の製造方法。(1) 50 to 85 parts by weight of hydrated gypsum and 5 to 50 parts by weight of industrial water gypsum
0.5 parts by weight for 100 parts by weight of powdered gypsum
~30 parts by weight of fiber, 0.1-2.
4. Forming a mixture of 0% by weight of a set retarder and water before the hydration stone is hydrated and allowing it to harden and dry. Manufacturing method of non-combustible surface/a-board marked as ¥.
わせを使用する特許請求の範囲第(1)項に記載の方法
。(2) The method according to claim (1), which uses asbestos fibers, cellulose fibers, or a combination thereof.
用する特許請求の範囲第(1)項に記載の方法。(3) The method according to claim (1), wherein tartaric acid or a metal salt thereof is used as the setting retarder.
よび水からなる混合物のPHを7以上調整する特許請求
の範囲第(1)項に記載の方法。(4) The method according to claim (1), wherein the pH of a mixture consisting of hydrated gypsum, dihydrate-*, tam, a setting retarder, and water is adjusted to 7 or more.
の圧力で加圧成形する特許請求の範囲第(1)項に記載
の方法。(5) Iθ~500kg/crn' of the mixture during molding
The method according to claim (1), which comprises press molding at a pressure of .
(1)項に記載の方法。(6) The method according to claim (1), wherein the method is formed by a circular mesh papermaking method.
n’ ノ圧力で、加圧成形する特許請求の範囲第(6)
項に記載の方法。(7) Raw sheet Tk after papermaking 10-500kg/cr
Claim No. 6: Pressure molding is performed at a pressure of n'.
The method described in section.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2558784A JPS60171261A (en) | 1984-02-14 | 1984-02-14 | Manufacture of incombustible gypsum board |
US06/698,674 US4645548A (en) | 1984-02-14 | 1985-02-05 | Process for producing non-combustible gypsum board and non-combustible laminated gypsum board |
BR8500668A BR8500668A (en) | 1984-02-14 | 1985-02-13 | PROCESS FOR THE PRODUCTION OF NON-COMBUSTIBLE PLASTER BOARD AND LAMINATED PLASTER BOARD |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2558784A JPS60171261A (en) | 1984-02-14 | 1984-02-14 | Manufacture of incombustible gypsum board |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60171261A true JPS60171261A (en) | 1985-09-04 |
JPH0476943B2 JPH0476943B2 (en) | 1992-12-07 |
Family
ID=12170044
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2558784A Granted JPS60171261A (en) | 1984-02-14 | 1984-02-14 | Manufacture of incombustible gypsum board |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60171261A (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6241747A (en) * | 1985-08-13 | 1987-02-23 | 太平洋セメント株式会社 | Manufacture of incombustible gypsum board |
US5155959A (en) * | 1989-10-12 | 1992-10-20 | Georgia-Pacific Corporation | Firedoor constructions including gypsum building product |
US5171366A (en) * | 1989-10-12 | 1992-12-15 | Georgia-Pacific Corporation | Gypsum building product |
US5305577A (en) * | 1989-10-12 | 1994-04-26 | Georgia-Pacific Corporation | Fire-resistant structure containing gypsum fiberboard |
US5347780A (en) * | 1989-10-12 | 1994-09-20 | Georgia-Pacific Corporation | Gypsum fiberboard door frame |
US5482551A (en) * | 1993-09-20 | 1996-01-09 | Armstrong World Industries, Inc. | Extruded fire resistant construction and building products |
US5632848A (en) * | 1989-10-12 | 1997-05-27 | Georgia-Pacific Corporation | Continuous processing equipment for making fiberboard |
US5945182A (en) * | 1995-02-14 | 1999-08-31 | G-P Gypsum Corporation | Fire-resistant members containing gypsum fiberboard |
JP2001327941A (en) * | 2000-05-23 | 2001-11-27 | Yoshino Gypsum Co Ltd | Gypsum building material |
JP2002097058A (en) * | 2000-09-19 | 2002-04-02 | Nitto Boseki Co Ltd | Method for recycling construction waste material including gypsum board |
JP2002114559A (en) * | 2000-10-02 | 2002-04-16 | Nitto Boseki Co Ltd | Method for recycling building waste material containing gypsum board |
JP2016121048A (en) * | 2014-12-25 | 2016-07-07 | チヨダウーテ株式会社 | Gypsum member, gypsum board, and method for producing gypsum member |
JP2019135099A (en) * | 2013-10-07 | 2019-08-15 | クナウフ ギプス カーゲー | Manufacturing method of gypsum plaster board |
JP2020528868A (en) * | 2017-08-04 | 2020-10-01 | クナウフ ギプス コマンディトゲゼルシャフト | Improved stucco characteristics by aging at high temperature and high humidity levels |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0811585A4 (en) * | 1995-02-24 | 1998-05-20 | Chichibu Onoda Cement Corp | Composite gypsum board |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS509622A (en) * | 1973-05-29 | 1975-01-31 | ||
JPS5027823A (en) * | 1973-07-12 | 1975-03-22 | ||
JPS5396030A (en) * | 1977-02-02 | 1978-08-22 | Okura Industrial Co Ltd | Accelerative agent for setting of plaster of paris |
JPS55236A (en) * | 1978-06-19 | 1980-01-05 | Kanden Hankiyuu Shoji Kk | Extruding molding method of dihydric gypsum |
JPS57205351A (en) * | 1981-06-09 | 1982-12-16 | Nihon Cement | Manufacture of gypsum board |
JPS589855A (en) * | 1981-07-02 | 1983-01-20 | 日産自動車株式会社 | Formation of high expansion gypsum formed article |
-
1984
- 1984-02-14 JP JP2558784A patent/JPS60171261A/en active Granted
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS509622A (en) * | 1973-05-29 | 1975-01-31 | ||
JPS5027823A (en) * | 1973-07-12 | 1975-03-22 | ||
JPS5396030A (en) * | 1977-02-02 | 1978-08-22 | Okura Industrial Co Ltd | Accelerative agent for setting of plaster of paris |
JPS55236A (en) * | 1978-06-19 | 1980-01-05 | Kanden Hankiyuu Shoji Kk | Extruding molding method of dihydric gypsum |
JPS57205351A (en) * | 1981-06-09 | 1982-12-16 | Nihon Cement | Manufacture of gypsum board |
JPS589855A (en) * | 1981-07-02 | 1983-01-20 | 日産自動車株式会社 | Formation of high expansion gypsum formed article |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6241747A (en) * | 1985-08-13 | 1987-02-23 | 太平洋セメント株式会社 | Manufacture of incombustible gypsum board |
US6299970B1 (en) | 1989-10-12 | 2001-10-09 | Georgia-Pacific Gypsum Corporation | Fire-resistant gypsum fiberboard |
US5155959A (en) * | 1989-10-12 | 1992-10-20 | Georgia-Pacific Corporation | Firedoor constructions including gypsum building product |
US5171366A (en) * | 1989-10-12 | 1992-12-15 | Georgia-Pacific Corporation | Gypsum building product |
US5305577A (en) * | 1989-10-12 | 1994-04-26 | Georgia-Pacific Corporation | Fire-resistant structure containing gypsum fiberboard |
US5347780A (en) * | 1989-10-12 | 1994-09-20 | Georgia-Pacific Corporation | Gypsum fiberboard door frame |
US5632848A (en) * | 1989-10-12 | 1997-05-27 | Georgia-Pacific Corporation | Continuous processing equipment for making fiberboard |
US5945208A (en) * | 1989-10-12 | 1999-08-31 | G-P Gypsum Corporation | Fire-resistant gypsum building materials |
US5482551A (en) * | 1993-09-20 | 1996-01-09 | Armstrong World Industries, Inc. | Extruded fire resistant construction and building products |
US5945182A (en) * | 1995-02-14 | 1999-08-31 | G-P Gypsum Corporation | Fire-resistant members containing gypsum fiberboard |
JP2001327941A (en) * | 2000-05-23 | 2001-11-27 | Yoshino Gypsum Co Ltd | Gypsum building material |
JP2002097058A (en) * | 2000-09-19 | 2002-04-02 | Nitto Boseki Co Ltd | Method for recycling construction waste material including gypsum board |
JP2002114559A (en) * | 2000-10-02 | 2002-04-16 | Nitto Boseki Co Ltd | Method for recycling building waste material containing gypsum board |
JP4639454B2 (en) * | 2000-10-02 | 2011-02-23 | 日東紡績株式会社 | Recycling method of building waste including gypsum board |
JP2019135099A (en) * | 2013-10-07 | 2019-08-15 | クナウフ ギプス カーゲー | Manufacturing method of gypsum plaster board |
JP2016121048A (en) * | 2014-12-25 | 2016-07-07 | チヨダウーテ株式会社 | Gypsum member, gypsum board, and method for producing gypsum member |
JP2020528868A (en) * | 2017-08-04 | 2020-10-01 | クナウフ ギプス コマンディトゲゼルシャフト | Improved stucco characteristics by aging at high temperature and high humidity levels |
JP2022078070A (en) * | 2019-03-04 | 2022-05-24 | クナウフ ギプス カーゲー | Method for producing gypsum plaster board |
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