JP6605898B2 - Humidity control panel and manufacturing method thereof - Google Patents
Humidity control panel and manufacturing method thereof Download PDFInfo
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- JP6605898B2 JP6605898B2 JP2015189723A JP2015189723A JP6605898B2 JP 6605898 B2 JP6605898 B2 JP 6605898B2 JP 2015189723 A JP2015189723 A JP 2015189723A JP 2015189723 A JP2015189723 A JP 2015189723A JP 6605898 B2 JP6605898 B2 JP 6605898B2
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- 238000004519 manufacturing process Methods 0.000 title claims description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 31
- 239000010440 gypsum Substances 0.000 claims description 27
- 229910052602 gypsum Inorganic materials 0.000 claims description 27
- 239000000741 silica gel Substances 0.000 claims description 22
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- 239000000839 emulsion Substances 0.000 claims description 21
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
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- 238000001125 extrusion Methods 0.000 claims description 7
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- 238000000465 moulding Methods 0.000 claims description 3
- 239000002657 fibrous material Substances 0.000 claims description 2
- 239000011505 plaster Substances 0.000 claims 1
- 239000002245 particle Substances 0.000 description 41
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 27
- 239000000835 fiber Substances 0.000 description 18
- 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 15
- 239000002562 thickening agent Substances 0.000 description 15
- 229910000019 calcium carbonate Inorganic materials 0.000 description 13
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- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 238000010276 construction Methods 0.000 description 4
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- 238000009826 distribution Methods 0.000 description 3
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- 239000000377 silicon dioxide Substances 0.000 description 3
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- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 2
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- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
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- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
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- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
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- 229920000297 Rayon Polymers 0.000 description 1
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- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
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- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic 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
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
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- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Press-Shaping Or Shaping Using Conveyers (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
本発明は調湿パネル及びその製造方法に関する。 The present invention relates to a humidity control panel and a manufacturing method thereof.
従来、石膏を原料とした建築材料が知られている。例えば石膏と特定の湿度域において水蒸気を吸放湿するシリカゲル、珪藻土などの多孔質フィラーを石膏ボード用原紙の間に流し込み、硬化させた調湿性石膏ボードが提案されている。(特許文献1)
また、特許文献2には調湿性能を有しながら、軽量にして施工効率を高めることが可能な調湿材料として、石膏100重量部に対して、炭酸カルシウムとシリカゲルの合計が3〜80重量部の割合で含有されている調湿石膏ボードが開示されている。
更に、特許文献3には焼成された半水石膏にシリカゲルと、必要により増量剤、強度補強剤等からなる混和剤を混入し、板状に成型されてなる調湿性石膏ボードが開示されている。
Conventionally, building materials using gypsum as a raw material are known. For example, a humidity control gypsum board in which a porous filler such as silica gel or diatomaceous earth that absorbs and releases water vapor in a specific humidity range is poured between gypsum board base paper and cured is proposed. (Patent Document 1)
Patent Document 2 discloses a humidity control material that has a humidity control performance and is lightweight and capable of improving the construction efficiency. The total amount of calcium carbonate and silica gel is 3 to 80 weights with respect to 100 parts by weight of gypsum. Humidity-conditioning gypsum board contained in parts is disclosed.
Furthermore, Patent Document 3 discloses a humidity control gypsum board formed by mixing a calcined hemihydrate gypsum with silica gel and, if necessary, an admixture composed of a bulking agent, a strength reinforcing agent, and the like, into a plate shape. .
しかしながら、従来の技術ではボードとしての物性を確保するため石膏ボード用の原紙を表裏に配することが必要であり、さらに使用上の強度を確保するために厚みが12〜21mmと厚い。また、住宅内装材として採用するのは意匠性がなく、原紙表面に塗装を施すことが必要とされ、かつその塗装物も調湿性を有することが求められ、「塗装法」には限界があった。
また、市場で流通している調湿フィラーと粘土を混合して焼成した調湿タイルは、意匠性は優れるものの、施工現場での切削加工において専用の工具が必要とされ、熟練度を要するものであった。
However, in the prior art, it is necessary to arrange the base paper for gypsum board on the front and back sides to secure the physical properties as a board, and the thickness is as thick as 12 to 21 mm in order to ensure the strength in use. In addition, it is not designed to be used as a home interior material, and it is necessary to paint the surface of the base paper, and the coated material is required to have humidity control. It was.
In addition, humidity control tiles that are baked by mixing humidity control fillers and clay that are distributed in the market are excellent in design, but require special tools for cutting at construction sites and require skill. Met.
本発明はかかる状況に鑑み検討されたもので、製造が容易で、仕上がった製品も軽量で、施工しやすい調湿性パネルを得ることを目的とする発明であり、石膏、無機充填材、シリカゲル、中空体、繊維状物質を必須成分として含むことを特徴とする調湿性パネル、また、石膏、無機充填材、シリカゲル、中空体、繊維状物質、適量の水を含み、混錬し、成形することを特徴とする調湿性パネルの製造方法である。 The present invention has been studied in view of such circumstances, and is an invention that is easy to manufacture, is a lightweight finished product, and is an invention aimed at obtaining a moisture-controllable panel that is easy to construct, gypsum, inorganic filler, silica gel, Humidity control panels characterized by containing hollow bodies and fibrous substances as essential components, and also containing gypsum, inorganic filler, silica gel, hollow bodies, fibrous substances, and appropriate amounts of water, kneading and molding Is a method for producing a humidity control panel.
本発明の調湿性パネルは厚みが6mmでも取り扱いが可能な強度を有し、かつ調湿性能もすぐれたものとなる。また、意匠性についても、容易にかつ自在にエンボス模様を付すことができる。
製造方法については流し込み法によるような従来の石膏ボード系の調湿パネルで用いていた原紙が不要である。
更に樹脂中空体を配合することにより、調湿パネルの切断が容易となる。これは、実際の施工時に現場において専用の工具を使用することなく、容易に寸法調整が可能で簡易施工できるといった利点がある。
更にまた、真空押し出し法によって得られる本発明の調湿パネルはち密な組織構造となり、機械的強度に優れたものとなる。
The humidity control panel of the present invention has a strength capable of handling even when the thickness is 6 mm, and has excellent humidity control performance. Moreover, an embossed pattern can be easily and freely given to the design properties.
The production method does not require the base paper used in the conventional gypsum board humidity control panel as in the casting method.
Further, by blending the resin hollow body, the humidity control panel can be easily cut. This has the advantage that the dimensions can be easily adjusted and simple construction can be performed without using a dedicated tool on site during actual construction.
Furthermore, the humidity control panel of the present invention obtained by the vacuum extrusion method has a dense structure and excellent mechanical strength.
本発明に関わる石膏としては、2水石膏又は2水石膏を公知の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、III型無水石膏を用いることができる。また、水和反応が遅いII型無水石膏も硬化促進剤、例えば硫酸カリウム、硫酸アルミニウム、ナトリウム塩類などを用いることにより利用できる。これらの石膏の中でもα型半水石膏、β型半水石膏は焼石膏(CaSO4・1/2H2O)と称され水と速やかに反応して安定な2水石膏(CaSO4・2H2O)に変化して水に難溶の凝結硬化物になるため好ましく、本発明では特にβ型でレーザー回折・散乱法(マイクロトラック法)による平均粒子径が10〜20μmの半水石膏が好ましい。 As the gypsum according to the present invention, α-type hemihydrate gypsum, β-type hemihydrate gypsum, and type III anhydrous gypsum obtained by heat-treating dihydrate gypsum or dihydrate gypsum by a known method can be used. In addition, type II anhydrous gypsum with a slow hydration reaction can be used by using a curing accelerator such as potassium sulfate, aluminum sulfate, sodium salts and the like. Among these gypsums, α-type hemihydrate gypsum and β-type hemihydrate gypsum are called calcined gypsum (CaSO 4 · 1 / 2H 2 O), which reacts quickly with water and is stable dihydrate gypsum (CaSO 4 · 2H 2). O) is preferable because it becomes a coagulated hardened material that is hardly soluble in water, and in the present invention, a β-type hemihydrate gypsum having an average particle diameter of 10 to 20 μm by a laser diffraction / scattering method (microtrack method) is particularly preferable. .
本発明では無機充填材を石膏100重量部に対して40〜250重量部配合する。無機充填材としてはシリカ、炭酸カルシウム、硫酸カルシウム、ケイ酸マグネシウム、珪藻土、タルク、フライアッシュ、ゼオライト、ワラストナイト、マイカなどが挙げられるが切削性に優れ安価な炭酸カルシウムが好ましい。 In the present invention, 40 to 250 parts by weight of the inorganic filler is blended with 100 parts by weight of gypsum. Examples of the inorganic filler include silica, calcium carbonate, calcium sulfate, magnesium silicate, diatomaceous earth, talc, fly ash, zeolite, wollastonite, mica, and the like.
炭酸カルシウムとしては特に制約はなく、重質炭酸カルシウム、軽質炭酸カルシウム(沈降性炭酸カルシウム)などが用いられ、平均粒子径(レーザー回折・散乱法(マイクロトラック法)により検出された粒度分布(体積分布)から算出された算術平均径)が1〜20μmの範囲のものを採用すると、パネルの強度、切削性が優れる。特に比表面積値2,500〜23,000cm2/gの炭酸カルシウムが好ましい。 There are no particular restrictions on calcium carbonate, and heavy calcium carbonate, light calcium carbonate (precipitated calcium carbonate), etc. are used, and the average particle size (particle size distribution (volume) detected by the laser diffraction / scattering method (microtrack method) If the arithmetic mean diameter calculated from the distribution) is in the range of 1 to 20 μm, the strength and machinability of the panel are excellent. In particular, calcium carbonate having a specific surface area value of 2,500 to 23,000 cm 2 / g is preferable.
本発明では調湿材料としてシリカゲルを用いる。特に好ましいシリカゲルはB型シリカゲルであり、A型シリカゲルに比べて気孔が大きく、吸放湿機能が優れている。B型シリカゲルは、レーザー回折・散乱法(マイクロトラック法)による平均粒子径が12〜27μmの範囲のものが好適であり、この範囲であれば均一に分散させることができ、吸放湿機能に優れる。粒子径が下限に満たないと比表面積が増大するため、硬化させるために多くのバインダーを必要となることから適さず、また、上限を超えると材料内の分布が不均一となり、位置ごとの調湿性能にバラつきが生じやすくなる。シリカゲルは石膏100重量部に対して40〜80重量部配合する。この範囲であれば充分な吸放湿機能を発揮し、下限に満たないと吸放湿機能が低下しやすく、上限を超えると調湿パネルの曲げ強度が低下しやすくなる。 In the present invention, silica gel is used as the humidity control material. A particularly preferred silica gel is B-type silica gel, which has larger pores than the A-type silica gel and has an excellent moisture absorption / release function. The B-type silica gel preferably has an average particle diameter in the range of 12 to 27 μm by the laser diffraction / scattering method (microtrack method), and within this range, it can be dispersed uniformly and has a moisture absorption / release function. Excellent. If the particle diameter is less than the lower limit, the specific surface area is increased, so a large amount of binder is required for curing, and if the upper limit is exceeded, the distribution in the material becomes non-uniform, and adjustment at each position is not possible. Variations in humidity performance are likely to occur. Silica gel is blended in an amount of 40 to 80 parts by weight per 100 parts by weight of gypsum. If it is in this range, a sufficient moisture absorbing / releasing function is exhibited, and if the lower limit is not reached, the moisture absorbing / releasing function tends to decrease, and if the upper limit is exceeded, the bending strength of the humidity control panel tends to decrease.
本発明では軽量化を目的に無機中空体、合成樹脂中空体などの中空体を用いても良い。無機中空体としては、シリカバルーン、シラスバルーン、フライアッシュバルーン、発泡パーライト、発泡バーミキュライト、発泡ガラスビーズなどが、合成樹脂中空体としては、例えばアクリロニトリル(共)重合体樹脂、フェノール樹脂、尿素樹脂、ポリスチレン、ポリプロピレンおよびポリ塩化ビニリデンなどを材質とする発泡樹脂中空体が挙げられる。中空体の配合割合は石膏100重量部に対して5〜15重量部配合する。下限に満たないと調湿パネルの軽量化が図りにくく、上限を超えると調湿パネルの曲げ強度が低下しやすくなる。 In the present invention, for the purpose of weight reduction, a hollow body such as an inorganic hollow body or a synthetic resin hollow body may be used. Examples of the inorganic hollow body include silica balloon, shirasu balloon, fly ash balloon, foamed pearlite, foamed vermiculite, and foamed glass beads. Examples of the synthetic resin hollow body include acrylonitrile (co) polymer resin, phenol resin, urea resin, Examples thereof include a foamed resin hollow body made of polystyrene, polypropylene, polyvinylidene chloride, or the like. The blending ratio of the hollow body is 5 to 15 parts by weight based on 100 parts by weight of gypsum. If the lower limit is not reached, it is difficult to reduce the weight of the humidity control panel, and if the upper limit is exceeded, the bending strength of the humidity control panel tends to decrease.
本発明では軽量化を目的に中空体を用いていたが熱可塑性樹脂発泡中空体の方が切削加工性に優れることが分かったことから特に好ましい。これは熱可塑性樹脂発泡中空体が切削時の熱により溶融するためと考えられる。中でもレーザー回折・散乱法(マイクロトラック法)による平均粒子径が35〜55μmで、比重0.08〜0.18g/cm3の熱可塑性樹脂発泡中空体が好ましい。 In the present invention, the hollow body is used for the purpose of reducing the weight, but the thermoplastic resin foam hollow body is particularly preferable because it has been found that it is superior in cutting workability. This is considered because the thermoplastic resin foam hollow body is melted by heat at the time of cutting. Among these, a thermoplastic foam hollow body having an average particle diameter of 35 to 55 μm by a laser diffraction / scattering method (microtrack method) and a specific gravity of 0.08 to 0.18 g / cm 3 is preferable.
更に、耐水性を向上させ、バインダー成分としても作用する熱可塑性樹脂エマルジヨンを配合しても良い。熱可塑性樹脂エマルジヨンとしては、例えば酢酸ビニル系重合体エマルジヨン、アクリル系重合体エマルジヨン、塩化ビニル系重合体エマルジヨン、塩化ビニリデン系重合体エマルジヨン、ウレタン系重合体エマルジヨン等を挙げることができるが特にアクリル樹脂エマルジョンが好ましく、アクリル樹脂エマルジョンはエチルアクリレートとメチルメタアクリレートを主モノマーとし、平均粒子径が200〜300nmのものが分散性の点でより好ましい。なお、平均粒子径は、レーザー光回折・散乱式粒子径測定装置(大塚電子株式会社製ELS−8000)を使用し、レーザーの照射時に検出された散乱光に基づいて計算した値である。熱可塑性樹脂エマルジヨンを配合割合は固形分で石膏100重量部に対して10〜25重量部とすればバインダーとして機能する。
Furthermore, you may mix | blend the thermoplastic resin emulsion which improves water resistance and acts also as a binder component. The thermoplastic resin Emarujiyon, such as vinyl acetate-based polymer Emarujiyon, acrylic polymer Emarujiyon vinyl polymer Emarujiyon chloride, vinylidene chloride polymer Emarujiyon, there may be mentioned a urethane-based polymer Emarujiyon etc. Especially acrylic resin Emulsions are preferable, and acrylic resin emulsions having ethyl acrylate and methyl methacrylate as main monomers and having an average particle size of 200 to 300 nm are more preferable in terms of dispersibility. The average particle diameter is a value calculated based on scattered light detected at the time of laser irradiation using a laser light diffraction / scattering particle diameter measuring apparatus (ELS-8000 manufactured by Otsuka Electronics Co., Ltd.). If the blending ratio of the thermoplastic resin emulsion is 10 to 25 parts by weight with respect to 100 parts by weight of gypsum as a solid content, it functions as a binder.
更に、繊維状物質、例えば麻、木綿、パルプなどの天然繊維や、ロックウール繊維、セラミック繊維、炭素繊維、ガラス繊維、ボロン繊維などの無機繊維、レーヨン、ポリプロピレン、ポリエチレン、ビニロン、ナイロン、ポリエステル、及びアクリル等の合成繊維などを配合してもよく、配合することにより調湿パネルの耐衝撃性が向上する。繊維長は3〜13mm、配合割合は石膏100重量部に対して1〜10重量部配合する。繊維長がこの範囲であれば分散性がよく、調湿パネルのピンホールの発生がなく、配合が下限に満たないと耐衝撃性の効果が少なく、上限を超えると調湿パネルの平滑性が劣りやすくなる。 Furthermore, fibrous materials such as hemp, cotton, pulp and other natural fibers, rock wool fibers, ceramic fibers, carbon fibers, glass fibers, boron fibers and other inorganic fibers, rayon, polypropylene, polyethylene, vinylon, nylon, polyester, In addition, synthetic fibers such as acrylic may be blended, and by blending, the impact resistance of the humidity control panel is improved. The fiber length is 3 to 13 mm, and the blending ratio is 1 to 10 parts by weight per 100 parts by weight of gypsum. If the fiber length is within this range, the dispersibility is good, there is no occurrence of pinholes in the humidity control panel, and if the blending is less than the lower limit, the effect of impact resistance is small. It tends to be inferior.
本発明では増粘剤を加えることにより保型性が向上する。増粘剤としては、ベントナイト、カオリナイト類、ロウ石、シリカエアロジルなどの無機系増粘剤、メチルセルロース、エチルセルロース、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース、アクリルアミド重合体、ポリビニルアルコールなどの有機系増粘剤、膠、カゼイン、澱粉などの天然系増粘剤などが挙げられる。増粘剤を加えることにより押し出し成形に適した粘度になり、板状に成形しやすくなる。配合割合は石膏100重量部に対して0.5〜5重量部配合する。 In the present invention, the shape retention is improved by adding a thickener. Thickeners include inorganic thickeners such as bentonite, kaolinites, wax, silica aerosil, and organic thickeners such as methylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, acrylamide polymer, and polyvinyl alcohol. , Natural thickeners such as glue, casein and starch. By adding a thickener, the viscosity becomes suitable for extrusion molding, and it becomes easy to mold into a plate shape. The blending ratio is 0.5 to 5 parts by weight based on 100 parts by weight of gypsum.
上記の物質は適量の水を加えて混錬ペースト状にされる。混錬後は注型成形、スクリュー式或いはピストン式の真空押し出し成形機で所望の形状に成形される。スクリュー式の場合、単軸であっても多軸であっても良い。特に真空押し出し成形することにより連続で大量生産でき、ダイの形状を適宜変更することにより厚みが6〜12mmと薄い物も容易に製造することができる。しかも、流し込み方式のように石膏ボード用の原紙を必要としない。 The above substances are made into a kneaded paste by adding an appropriate amount of water. After kneading, it is molded into a desired shape with a cast molding, screw type or piston type vacuum extrusion molding machine. In the case of a screw type, it may be uniaxial or multiaxial. In particular, it can be mass-produced continuously by vacuum extrusion molding, and a thin product having a thickness of 6 to 12 mm can be easily manufactured by appropriately changing the shape of the die. Moreover, the base paper for gypsum board is not required unlike the pouring method.
真空度は700〜750mmHgで成形し、ベルトコンベアで搬送し、常温〜60℃の温度で養生、硬化させて調湿パネルを得る。押し出し成形後にエンボスロールで模様を賦与すると意匠性が向上し、エンボスを賦与しない物に比べて見栄えがして商品価値が高まる。 The degree of vacuum is formed at 700 to 750 mmHg, conveyed by a belt conveyor, and cured and cured at a temperature of room temperature to 60 ° C. to obtain a humidity control panel. When a pattern is applied with an embossing roll after extrusion molding, the design is improved, and it looks better than a product without embossing and increases the commercial value.
以下、本発明を実施例にて詳細に説明する。
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル56重量部、平均粒子径5μmの炭酸カルシウム50重量部、平均粒子径45μmの発泡アクリル系樹脂中空体8重量部、平均粒子径230μmのアクリル樹脂エマルジョンを15重量部、平均繊維長6mmのガラス繊維を4重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを2重量部を投入して、15分間混錬した。
Hereinafter, the present invention will be described in detail with reference to examples.
In a double-arm kneader, 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g, 56 parts by weight of B-type silica gel with an average particle diameter of 19 μm, and 50 parts by weight of calcium carbonate with an average particle diameter of 5 μm 8 parts by weight of a foamed acrylic resin hollow body having an average particle diameter of 45 μm, 15 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 4 parts by weight of glass fibers having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 2 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
次いで、真空度735mmHgで、幅330mm、高さ6mmのスリットから押し出し成型し、ブロック調のエンボスロールで模様を付し、40℃で12時間、105℃で5時間養生して硬化させた後、300×300mmになるように周囲を切断して目的とするパネルを得た。 Next, after extrusion molding from a slit having a vacuum degree of 735 mmHg, a width of 330 mm and a height of 6 mm, a pattern is applied with a block-like embossing roll, curing at 40 ° C. for 12 hours and 105 ° C. for 5 hours, The target panel was obtained by cutting the periphery to 300 × 300 mm.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル75重量部、平均粒子径5μmの炭酸カルシウム100重量部、平均粒子径45μmの発泡アクリル系樹脂中空体11重量部、平均粒子径230μmのアクリル樹脂エマルジョンを20重量部、平均繊維長6mmのガラス繊維を5重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを3重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader, 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g, 75 parts by weight of B-type silica gel with an average particle diameter of 19 μm, and 100 parts by weight of calcium carbonate with an average particle diameter of 5 μm 11 parts by weight of hollow acrylic resin foam having an average particle size of 45 μm, 20 parts by weight of acrylic resin emulsion having an average particle size of 230 μm, 5 parts by weight of glass fiber having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 3 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル43重量部、平均粒子径5μmの炭酸カルシウム46重量部、平均粒子径45μmの発泡アクリル系樹脂中空体6重量部、平均粒子径230μmのアクリル樹脂エマルジョンを12重量部、平均繊維長6mmのビニロン繊維を2重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを1重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader machine, 43 parts by weight of B-type silica gel with an average particle diameter of 19 μm and 46 parts by weight of calcium carbonate with an average particle diameter of 5 μm per 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g , 6 parts by weight of a foamed acrylic resin hollow body having an average particle diameter of 45 μm, 12 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 2 parts by weight of vinylon fiber having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 1 part by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル56重量部、平均粒子径5μmの炭酸カルシウム50重量部、平均粒子径45μmの発泡アクリル系樹脂中空体8重量部、平均粒子径230μmのアクリル樹脂エマルジョンを15重量部、平均繊維長6mmのビニロン繊維を2重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを2重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader, 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g, 56 parts by weight of B-type silica gel with an average particle diameter of 19 μm, and 50 parts by weight of calcium carbonate with an average particle diameter of 5 μm 8 parts by weight of a foamed acrylic resin hollow body having an average particle diameter of 45 μm, 15 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 2 parts by weight of vinylon fibers having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 2 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル75重量部、平均粒子径5μmの炭酸カルシウム100重量部、平均粒子径45μmの発泡アクリル系樹脂中空体6重量部、平均粒子径230μmのアクリル樹脂エマルジョンを20重量部、平均繊維長6mmのガラス繊維を5重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを3重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader machine, 75 parts by weight of B-type silica gel with an average particle diameter of 19 μm and 100 parts by weight of calcium carbonate with an average particle diameter of 5 μm per 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g , 6 parts by weight of a hollow foamed acrylic resin having an average particle diameter of 45 μm, 20 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 5 parts by weight of glass fibers having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 3 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル48重量部、平均粒子径5μmの炭酸カルシウム100重量部、平均粒子径45μmの発泡アクリル系樹脂中空体3重量部、平均粒子径230μmのアクリル樹脂エマルジョンを13重量部、平均繊維長6mmのガラス繊維を3重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを3重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader, 100 parts by weight of B-type silica gel with an average particle diameter of 19 μm and 100 parts by weight of calcium carbonate with an average particle diameter of 5 μm per 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g 3 parts by weight of a foamed acrylic resin hollow body having an average particle diameter of 45 μm, 13 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 3 parts by weight of glass fiber having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 3 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル77重量部、平均粒子径5μmの炭酸カルシウム223重量部、平均粒子径45μmの発泡アクリル系樹脂中空体6重量部、平均粒子径230μmのアクリル樹脂エマルジョンを21重量部、平均繊維長6mmのガラス繊維を5重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを3重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
In a double-arm kneader, 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g, 77 parts by weight of B-type silica gel with an average particle diameter of 19 μm, and 223 parts by weight of calcium carbonate with an average particle diameter of 5 μm , 6 parts by weight of a foamed acrylic resin hollow body having an average particle diameter of 45 μm, 21 parts by weight of an acrylic resin emulsion having an average particle diameter of 230 μm, 5 parts by weight of glass fiber having an average fiber length of 6 mm, an appropriate amount of water, and hydroxy as a thickener 3 parts by weight of propylmethylcellulose was added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
参考例1
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル25重量部、平均粒子径230μmのアクリル樹脂エマルジョンを10重量部、平均繊維長6mmのガラス繊維を5重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを1重量部を投入して、15分間混錬し、型に乾燥後の厚みが6mmとなるように注型した。
Reference example 1
10 parts of an acrylic resin emulsion having an average particle diameter of 230 μm and 25 parts by weight of B-type silica gel and an average particle diameter of 230 μm per 100 parts by weight of β-type hemihydrate gypsum having a specific surface area of 18,800 cm 2 / g. 5 parts by weight of glass fiber having an average fiber length of 6 mm, an appropriate amount of water, 1 part by weight of hydroxypropylmethylcellulose as a thickener, kneaded for 15 minutes, and the mold thickness after drying is 6 mm It was cast to be
比較例1
双腕型のニーダー機に比表面積18,800cm2/gのβ型半水石膏100重量部に対して、平均粒子径19μmのB型シリカゲル23重量部、平均粒子径230μmのアクリル樹脂エマルジョンを8重量部、平均繊維長6mmのビニロン繊維を1重量部、水を適量、増粘剤としてヒドロキシプロピルメチルセルロースを1重量部を投入して、15分間混錬した。
次いで、実施例1と同様に製造した。
Comparative Example 1
Into a double-arm kneader, 100 parts by weight of β-type hemihydrate gypsum with a specific surface area of 18,800 cm 2 / g, 23 parts by weight of B-type silica gel with an average particle diameter of 19 μm, and 8 acrylic resin emulsions with an average particle diameter of 230 μm 1 part by weight of vinylon fiber having an average fiber length of 6 mm, 1 part by weight of water and 1 part by weight of hydroxypropylmethylcellulose as a thickener were added and kneaded for 15 minutes.
Subsequently, it manufactured similarly to Example 1.
比較例2
実施例1において、ガラス繊維を配合しなかった以外は同様に実施した。
Comparative Example 2
In Example 1, it implemented similarly except not having mix | blended glass fiber.
評価結果を表1に示す。
評価方法を以下に示す。
(1)強度:JIS A 1408建築用ボード類の曲げ試験方法に準拠して測定した。
(2)調湿性能は23℃50%にて重量が安定するまで養生した後、23℃75%にて12時間放置した時の水蒸気吸着量、その状態から湿度を50%にしたときの水蒸気放出量を測定した。
(3)切削性:チップソーによる切削性を確認し、バリや欠けがないものを○、バリや欠けがあるものを×とした。
(4)耐衝撃性:320gの鋼球を500mmの高さから落下させ表面にヒビが生じない場合を○、生じた場合を×とした。
The evaluation method is shown below.
(1) Strength: Measured in accordance with a bending test method for JIS A 1408 building boards.
(2) Humidity adjustment performance is 23 ° C 50% until the weight is stabilized, then water vapor adsorption when left at 23 ° C 75% for 12 hours, water vapor when humidity is 50% The amount released was measured.
(3) Machinability: The machinability with a tip saw was confirmed.
(4) Impact resistance: A case where a 320 g steel ball was dropped from a height of 500 mm and no cracks were generated on the surface was indicated as “◯”, and a case where it occurred was indicated as “X”.
Claims (9)
請求項2又は3いずれか記載の調湿性パネル。The humidity control panel according to claim 2.
請求項7又は8いずれか記載の調湿性パネルの製造方法。The manufacturing method of the humidity control panel in any one of Claim 7 or 8.
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