JPH0433735B2 - - Google Patents
Info
- Publication number
- JPH0433735B2 JPH0433735B2 JP5153686A JP5153686A JPH0433735B2 JP H0433735 B2 JPH0433735 B2 JP H0433735B2 JP 5153686 A JP5153686 A JP 5153686A JP 5153686 A JP5153686 A JP 5153686A JP H0433735 B2 JPH0433735 B2 JP H0433735B2
- Authority
- JP
- Japan
- Prior art keywords
- glass
- foam
- layer
- shell layer
- specific gravity
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000011521 glass Substances 0.000 claims description 55
- 239000011494 foam glass Substances 0.000 claims description 46
- 239000002994 raw material Substances 0.000 claims description 34
- 239000006260 foam Substances 0.000 claims description 29
- 230000005484 gravity Effects 0.000 claims description 27
- 239000000843 powder Substances 0.000 claims description 20
- 239000001023 inorganic pigment Substances 0.000 claims description 6
- 239000008187 granular material Substances 0.000 claims description 3
- 239000002245 particle Substances 0.000 description 40
- 239000000463 material Substances 0.000 description 15
- 230000035515 penetration Effects 0.000 description 14
- 238000005520 cutting process Methods 0.000 description 10
- 229910000831 Steel Inorganic materials 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000010959 steel Substances 0.000 description 8
- 238000005452 bending Methods 0.000 description 7
- 238000010304 firing Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000005469 granulation Methods 0.000 description 4
- 230000003179 granulation Effects 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 206010039509 Scab Diseases 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 235000019353 potassium silicate Nutrition 0.000 description 3
- 239000005361 soda-lime glass Substances 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 238000009415 formwork Methods 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 239000006061 abrasive grain Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000005354 aluminosilicate glass Substances 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 239000010431 corundum Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000007589 penetration resistance test Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
Landscapes
- Glass Compositions (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は主に建築物の内、外装材、外壁材等に
用いられる泡ガラスに関し、特に耐衝撃性や切削
加工性に優れるとともに耐加傷性にも優れた発泡
層と皮殻層からなる泡ガラスに関するものであ
る。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to foam glass that is mainly used for interior, exterior, and wall materials of buildings, and has particularly excellent impact resistance and machinability as well as load resistance. This invention relates to foam glass consisting of a foam layer and a shell layer, which has excellent scratch resistance.
従来泡ガラスの発泡層に皮殻層を形成させるこ
とは知られている。特開昭50−123108号にはガラ
スあるいはセラミツクス発泡層とガラス質皮殻層
からなる泡ガラス、セラミツクスの製法に関し、
モールドの底に皮殻層を形成するためのガラス片
および該ガラス片間を満たすガラス微粉を敷きつ
め、その上に発泡層を形成すべき材料を充填し加
熱して泡ガラス、セラミツクスとなすことが開示
されている。また、特開昭60−166239号には気孔
率1〜30vol%の皮殻層と気孔率70〜95vol%の多
孔質層を一体に接合し積層泡ガラスとなすこと、
前記皮殻層はガラス微粉を主体とする原料を造粒
して島状となし、一方ガラス微粉を主体とする他
の原料を粉末状のまま前記島状部分の間を充填す
るようにして形成させることが開示されている。
It is conventionally known to form a shell layer on the foam layer of foam glass. JP-A-50-123108 describes a method for producing foam glass and ceramics consisting of a glass or ceramic foam layer and a vitreous shell layer.
Glass pieces for forming a skin layer and glass fine powder to fill between the glass pieces are placed on the bottom of the mold, and a material to form a foam layer is filled on top of the mold and heated to form foam glass or ceramics. Disclosed. In addition, JP-A-60-166239 discloses that a shell layer with a porosity of 1 to 30 vol% and a porous layer with a porosity of 70 to 95 vol% are integrally bonded to form laminated foam glass.
The shell layer is formed by granulating a raw material mainly consisting of fine glass powder into island shapes, while filling the spaces between the island-like parts with other raw materials mainly consisting of fine glass powder in powder form. It is disclosed that
概して皮殻層を形成させることにより、曲げや
引張り等の強度を増大させることができる。しか
し、前記公知技術において、前者は泡ガラス体を
分割、切断しようとするときは泡ガラス製造時に
予め切断予定ラインに沿つて皮殻層を除いておか
なければならない程緻密に皮殻層を形成させたも
のであり、後者は気孔率30vol%以下、すなわち
ガラスの真比重が2.5であるのに対し見掛比重が
1.75以上のやはり緻密な皮殻層を形成させたもの
である。このように皮殻層を緻密にすることによ
り、剛性には富むものの外部から局部的な衝撃を
受けた場合、該部に亀裂が発生するとともに亀裂
はその周辺部に発達し、時として泡ガラス全体の
崩壊を招く。
Generally, by forming a shell layer, strength such as bending and tensile strength can be increased. However, in the above-mentioned known technology, when attempting to divide or cut a foam glass body, the skin layer is formed so densely that the skin layer must be removed in advance along the line to be cut during foam glass production. The latter has a porosity of 30 vol% or less, that is, the true specific gravity of glass is 2.5, while the apparent specific gravity is
It also has a dense skin layer of 1.75 or higher. By making the skin layer denser in this way, it is highly rigid, but if it receives a local impact from the outside, cracks will occur in that area and the cracks will develop in the surrounding area, sometimes resulting in bubble glass. leading to total collapse.
言うまでもなく切削加工性においても劣り、切
断過程で切断ラインを外れた亀裂を生じ易く、生
産歩留を著しく低下させる。 Needless to say, it is inferior in machinability and tends to cause cracks that deviate from the cutting line during the cutting process, significantly reducing production yield.
したがつて皮殻層のかさ比重はこれら公知例よ
りより低くし、外部衝撃力を吸収し得るような気
孔性をもたせる必要があつた。 Therefore, it was necessary to make the bulk specific gravity of the shell layer lower than those of these known examples, and to provide it with porosity capable of absorbing external impact force.
一方、皮殻層のかさ比重を低くすると表面硬度
が必らずしも充分ではなくなり、たとえばナイフ
エツジ等により比較的容易に加傷されるといと新
たな問題が生じた。 On the other hand, when the bulk specific gravity of the skin layer is lowered, the surface hardness is not necessarily sufficient, and a new problem arises in that it is relatively easily damaged by, for example, a knife edge.
本発明は耐衝撃性および切削加工性に優れると
共に、表面硬度にも優れ、よつて耐加傷性を付与
した泡ガラスを提供することを目的とする。 An object of the present invention is to provide foam glass that has excellent impact resistance and cutting workability, and also has excellent surface hardness and thus has scratch resistance.
本発明は発泡層とその少なくとも片面を覆うよ
り高かさ比重の皮殻層より一体的に形成され、該
皮殻層はガラス微粉またはガラス微粉と無機顔料
微粉が相互に融接してなる基相に粒径0.5〜5.2
mm、皮殻層中の含有量が15〜30vol%のガラス粒
が散在するようにした泡ガラスを提供するもので
ある。
The present invention is formed integrally from a foam layer and a shell layer having a higher bulk specific gravity covering at least one side of the foam layer, and the shell layer is formed of a base phase formed by fusion of glass fine powder or glass fine powder and inorganic pigment fine powder. Particle size 0.5~5.2
The present invention provides foam glass in which glass grains having a shell layer with a content of 15 to 30 vol% are scattered therein.
本発明において発泡層の原料として粒径150mm
以下、真比重2.5前後の着色あるいは無色の通常
のガラス、たとえばソーダ石灰ガラス、ホウ珪酸
ガラス、アルミノ珪酸系ガラス等の微粉に石灰
石、苦灰石、カーボン等の発泡剤微粉末、さらに
無機顔料を加え、または加えずして混合、調製し
たものを用いる。これらはさらに水ガラス等の結
合剤を加え通例の造粒手段により粒径1/10mm〜数
mm程度に造粒する。 In the present invention, the particle size is 150mm as the raw material for the foam layer.
Below, fine powder of a colored or colorless ordinary glass with a true specific gravity of around 2.5, such as soda lime glass, borosilicate glass, aluminosilicate glass, etc., is mixed with fine powder of a blowing agent such as limestone, dolomite, or carbon, and further an inorganic pigment. Mix and prepare with or without addition. These are further added with a binder such as water glass and processed by conventional granulation methods to produce particles with a particle size of 1/10 mm to several
Granulate to about mm.
皮殻層の基相を形成する原料として前記同様の
ガラス粉末に適宜必要に応じ無機顔料、発泡剤の
微粉末を添加混合したものを用い、前記同様造粒
する。 As a raw material for forming the base phase of the shell layer, a mixture of the same glass powder as described above and fine powders of an inorganic pigment and a blowing agent as required is used and granulated in the same manner as described above.
皮殻層の他の原料として粒径0.5〜5.2mmの着色
あるいは無色の通常のガラス粒が用いられる。該
ガラス粒は前記造粒原料に対して後述する容積割
合の範囲で均一に混合し、これを皮殻層形成原料
とする。 As another raw material for the shell layer, ordinary colored or colorless glass particles with a particle size of 0.5 to 5.2 mm are used. The glass particles are uniformly mixed with the granulation raw material in a volume ratio range described below, and this is used as a raw material for forming a shell layer.
これら発泡層、皮殻層のかさ比重は発泡剤の種
類や量、ガラスの軟化温度、無機顔料の種類や
量、あるいは皮殻層におけるガラス粒の混入量、
焼成条件等の選択により適宜調整し得る。 The bulk specific gravity of these foam layers and shell layers depends on the type and amount of foaming agent, the softening temperature of glass, the type and amount of inorganic pigment, or the amount of glass grains mixed in the skin layer.
It can be adjusted as appropriate by selecting firing conditions and the like.
なお、発泡層において非造粒原料を用いた場
合、それは極めてかさ高で内に多量の混入空気を
有するが、焼成工程において混入空気が残留、膨
張することによる粗泡、空洞の発生、皮殻層との
界面が平担でなく波状となること、さらには発泡
層が局所的に皮殻層をつき抜けて表面に露呈する
等の弊害があるが、造粒原料を用いることにより
そのような弊害は解消される。 When a non-granulated raw material is used in the foam layer, it is extremely bulky and contains a large amount of air mixed in. However, during the firing process, the mixed air remains and expands, resulting in coarse foam, the formation of cavities, and the formation of crusts. There are disadvantages such as the interface with the foam layer becoming wavy instead of flat, and furthermore, the foam layer locally penetrates the skin layer and is exposed on the surface, but by using granulated raw materials, such problems can be avoided. The harm will be eliminated.
また、製品は非造粒原料を用いた場合は連通気
泡を形成する傾向が大きいが造粒原料を用いた場
合殆どが独立気泡となり、ために耐吸水性、耐透
水性は格段と向上する。 Furthermore, when a non-granulated raw material is used, the product has a strong tendency to form open cells, but when a granulated raw material is used, most of the cells become closed cells, and therefore the water absorption resistance and water permeability resistance are significantly improved.
皮殻層の基相を形成するうえにおいて造粒原料
を用いると前記と同様な理由で非造粒原粒を用い
た場合のような不均一に焼結されることによる局
部的に脆弱な部分が無くなり均質な皮殻層の基相
が形成され、散在するガラス粒とも均一かつ堅固
に付着する。 When granulated raw materials are used to form the base phase of the crust layer, for the same reason as mentioned above, locally weak areas may occur due to non-uniform sintering, unlike when non-granulated raw granules are used. is eliminated, and a homogeneous base phase of the crust layer is formed, which evenly and firmly adheres to the scattered glass grains.
さらにこれら造粒原料やガラス粒は流動性に富
むため、後工程での型枠等への投入が容易でかつ
平担層を形成し易い。 Furthermore, since these granulation raw materials and glass particles have high fluidity, they can be easily charged into a mold or the like in a subsequent step, and a flat layer can be easily formed.
これら泡ガラス原料の焼成には各種の手段を採
用し得る。 Various means can be employed for firing these foam glass raw materials.
たとえばスチール製型枠に発泡層形成、原料を
所望の厚さになるように投入、敷設し次いでその
上に皮殻層形成用原料を所望の厚さになるように
充填し、加熱炉内で700℃〜1000℃の範囲の適宜
温度で焼成発泡させることにより、あるいはさら
に焼成とともにまたは焼成直後に適宜圧力を負荷
させることにより同時一体的に泡ガラスを形成し
得る。 For example, a foamed layer is formed in a steel formwork, the raw material is poured and laid to the desired thickness, and then the raw material for forming the skin layer is filled on top of it to the desired thickness, and the material is placed in a heating furnace. Foamed glass can be simultaneously and integrally formed by firing and foaming at an appropriate temperature in the range of 700° C. to 1000° C., or by further applying appropriate pressure during or immediately after firing.
あるいは上記同様の加熱手段により、発泡層と
皮殻層を別個に製造して後、これらを積層し、加
熱融着させることにより一体的に泡ガラスを形成
し得る。 Alternatively, a foamed layer and a shell layer may be separately manufactured using the same heating means as described above, and then laminated and heat-fused to integrally form foam glass.
さらには上下一対の走行する耐熱ベルト間の下
位に発泡層形成原料、上位に皮殻層形成原料を充
填し連続的に加熱炉に導びいて焼成、発泡させる
等の手段を講ずれば容易かつ経済的に、同時一体
的かつ連続的に泡ガラスを形成し得る。 Furthermore, it is easy to do so by filling the lower part between the upper and lower running heat-resistant belts with the material for forming the foam layer, and filling the upper part with the raw material for forming the shell layer, and then continuously introducing the material into a heating furnace for firing and foaming. Foam glass can be formed economically, simultaneously, integrally and continuously.
このようにして形成される泡ガラスの全体の厚
みは大略30mm〜125mmの範囲が好ましい。すなわ
ち30mm未満であると泡ガラスの特徴とする機能す
なわち断熱性を有効に発現し得ない。125mm程度
であれば通常の建築物において熱を遮断するのに
充分な厚さであつてそれ以上は必要としないし、
それ以上の厚みとなると泡ガラスといえども重量
が増加し建築物の軽量高層化の趨勢に悖り、かつ
取扱施工を困難とする。 The total thickness of the foam glass thus formed is preferably in the range of approximately 30 mm to 125 mm. That is, if the thickness is less than 30 mm, the characteristic function of foam glass, that is, the heat insulation property cannot be effectively exhibited. If it is around 125mm, it is thick enough to block heat in normal buildings, and no more than that is necessary.
If the thickness is greater than that, the weight increases even though it is foam glass, which goes against the trend of lighter and higher-rise buildings and makes handling and construction difficult.
発泡層のかさ比重は0.3〜0.6の範囲が好まし
い。0.3未満では建築物の内、外装材、外壁材と
して使用するうえで脆弱であるし、0.6を超える
と断熱性を損ない、軽量性を阻害して取扱施工性
に劣るものとなる。 The bulk specific gravity of the foam layer is preferably in the range of 0.3 to 0.6. If it is less than 0.3, it will be too weak to be used as interior, exterior, or exterior wall materials for buildings, and if it exceeds 0.6, it will impair heat insulation, reduce lightness, and be inferior in handling and workability.
皮殻層のかさ比重は0.8〜1.7の範囲が、また厚
さは1.5〜20mmが好適である。 The bulk specific gravity of the skin layer is preferably in the range of 0.8 to 1.7, and the thickness is preferably in the range of 1.5 to 20 mm.
前記かさ比重において0.8未満であると緻密性
に劣るため曲げ強度等の機械的強度が不足し、こ
とに外部衝撃により欠けや凹みを発生し易い。
1.7を超えると剛性は向上するが外部からの局部
的な衝撃により該部より亀裂が発生、発達し易く
泡ガラス全体の崩壊を誘起する場合がある。 If the bulk specific gravity is less than 0.8, the density will be poor and mechanical strength such as bending strength will be insufficient, and in particular, chips and dents will easily occur due to external impact.
When it exceeds 1.7, the rigidity improves, but cracks are likely to occur and grow from localized external impacts, which may induce collapse of the entire foam glass.
また、発泡層と皮殻層とのかさ比重の差に関連
し、両層の差が大きいと徐冷を均一に行なうこと
が困難で両層間に歪が発生し、曲げあるいは衝撃
等の外力に対して両層の界面での亀裂が生じ易い
ため、好ましくはその差を1.2以内とすべきであ
る。 In addition, related to the difference in bulk specific gravity between the foam layer and the shell layer, if the difference between the two layers is large, it is difficult to perform slow cooling uniformly, and distortion occurs between the two layers, causing external forces such as bending or impact to occur. On the other hand, since cracks are likely to occur at the interface between both layers, the difference should preferably be within 1.2.
皮殻層の総厚は泡ガラス全体の厚みと関連し、
泡ガラスの断熱性、軽量性、取扱施工性等を損な
わないためには泡ガラス全体の厚みの1/4以下と
すべきである。また前記皮殻層のかさ比重とも関
係するが、たとえばかさ比重1.2の皮殻層の場合
4mmないしその前後の厚みが耐衝撃性が良好であ
り、それより低かさ比重の場合はより厚い方が、
それより高かさ比重の場合はより薄い方が耐衝撃
に効果的な傾向にあり、総じて1.5〜20mm、好適
には2〜9mmの範囲が適当である。 The total thickness of the skin layer is related to the total thickness of the foam glass,
The thickness should be 1/4 or less of the total thickness of the foam glass in order not to impair its insulation properties, light weight, ease of handling, etc. It is also related to the bulk specific gravity of the skin layer, for example, in the case of a skin layer with a bulk specific gravity of 1.2, a thickness of 4 mm or around that has good impact resistance, and if the bulk specific gravity is lower than that, the thicker the better. ,
If the bulk specific gravity is higher than that, the thinner the material, the more effective the impact resistance tends to be, and the appropriate range is generally 1.5 to 20 mm, preferably 2 to 9 mm.
皮殻層はガラス微粉あるいはさらに無機顔料が
相互に融接した基相にガラス粒が散在するように
し、よつて表面硬度を向上させ耐加傷性を付与さ
せる。 The shell layer has glass grains scattered in a base phase in which fine glass powder or inorganic pigments are fused together, thereby improving surface hardness and imparting scratch resistance.
ガラス粒は粒径0.5〜5.2mmのものを皮殻層中に
15vol%〜30vol%の範囲で含有させる。 Glass particles with a particle size of 0.5 to 5.2 mm are placed in the skin layer.
It is contained in a range of 15vol% to 30vol%.
概して皮殻層中のガラス粒の混入割合が大きけ
れば表面硬度が向上し耐加傷に有効であるが泡ガ
ラスの切削加工が困難となるので30vol%以下と
しなければならない。 Generally speaking, if the proportion of glass grains mixed in the shell layer is large, the surface hardness will improve and it will be effective for scratch resistance, but since it becomes difficult to cut foam glass, it must be kept at 30 vol% or less.
貫入抵抗試験において、たとえば比重0.6の
ALCの場合貫入抵抗Rは30〜40Kg/cm3程度と低
く、すなわち表面硬度が低いためナイフエツジ等
により容易に傷が発生する。ナイフエツジを比較
的強く当接しても殆ど傷が認められない程度の表
面硬度を維持するためには120Kg/cm2以上が必要
であるが、そのためには皮殻層中のガラス粒の混
入割合が15vol%以上でなければならない。 In penetration resistance tests, for example,
In the case of ALC, the penetration resistance R is as low as about 30 to 40 kg/cm 3 , that is, the surface hardness is low, so scratches are easily caused by knife edges and the like. In order to maintain a surface hardness to the extent that almost no scratches are observed even when the knife edge is brought into contact with a relatively strong force, a hardness of 120 kg/cm2 or more is required. Must be at least 15vol%.
また、ガラス粒の粒径が5.2mmを超えると泡ガ
ラスの切断時にガラス粒界に沿つた亀裂が生じ易
く、切断予定ラインに沿つた切断を困難とする。
O.5mm未満では前記必要とする表面硬度が得られ
ない。ただし上記条件を満足したうえで0.5mm未
満のガラス粉を併存させることは何等支障なく、
本発明を逸脱するものでないことは容易に理解さ
れよう。 Furthermore, if the particle size of the glass particles exceeds 5.2 mm, cracks are likely to occur along the glass grain boundaries when cutting the foam glass, making it difficult to cut along the planned cutting line.
If it is less than 0.5 mm, the required surface hardness cannot be obtained. However, after satisfying the above conditions, there is no problem in coexisting glass powder of less than 0.5 mm.
It will be readily understood that this does not depart from the invention.
勿論ガラス粒は0.5〜5.2mmの粒径範囲内でバラ
ツキがあつてもよく、これら粒径、あるいはガラ
ス粒の色調を変化させることにより雅趣に富んだ
ものとすることができる。 Of course, the glass particles may vary in particle size within the range of 0.5 to 5.2 mm, and by changing the particle size or the color tone of the glass particles, it can be made elegant.
本発明の範囲であれば衝撃強度、曲げ強度等に
加え耐加傷性に優れかつ切削加工性も良好である
ので建築物の内、外装材、外壁材等として好適で
ある。 Within the scope of the present invention, it has excellent impact strength, bending strength, etc., as well as excellent scratch resistance and good machinability, and is therefore suitable for use as interior, exterior, and exterior wall materials for buildings.
本発明の一態様においては、泡ガラスの皮殻層
または発泡層の一方または双方に予め接着付与剤
を被覆した金属線、金属網、パンチングメタル等
の少なくとも1種により補強するようにすればさ
らに効果的である。これら金属材料は泡ガラスを
製造するに際し予め型枠に配設しておくことによ
り、あるいは連続製造において上、下のベルト間
の原材料中に挿通し走行させることにより特異な
手段を要せずして容易に泡ガラスと一体化し得
る。 In one embodiment of the present invention, one or both of the shell layer and foam layer of the foam glass is reinforced with at least one of metal wire, metal mesh, punched metal, etc. coated with an adhesion promoter in advance. Effective. These metal materials can be placed in a formwork in advance when manufacturing foam glass, or they can be inserted into the raw material between the upper and lower belts during continuous manufacturing without the need for special means. can be easily integrated with foam glass.
従来、泡ガラスを金属材料で補強するにおいて
相互の熱収縮の差あるいは、金属の酸化等により
相互の接着性が悪いことが指摘されているが、予
め接着付与剤すなわちガラス粉を混合した水ガラ
スまたはアクリル等の樹脂、シリカ系酸化物粉等
を金属材料に被覆したものを用いることにより接
着力は格段と増大し補強効果は飛躍的に向上す
る。しかして特に建築物の外壁材として好適なも
のとなる。 Conventionally, when reinforcing foam glass with metal materials, it has been pointed out that mutual adhesion is poor due to differences in mutual thermal shrinkage or oxidation of the metal. Alternatively, by using a metal material coated with resin such as acrylic, silica-based oxide powder, etc., the adhesive strength is significantly increased and the reinforcing effect is dramatically improved. Therefore, it is particularly suitable as an exterior wall material for buildings.
本発明の別の態様として泡ガラスの発泡層の両
面に皮殻層を形成するようにしてもよい。これら
は泡ガラスを製造するに際して型枠に皮殻層形成
原料、発泡層形成原料、さらに皮殻層形成原料の
順に投入することにより、あるいは連続製造にお
いて下位より上記原料の順に投入、積層すること
により既述したような製造手段を適用しこれら三
層より一体的に形成された泡ガラスとすることが
でき、特に外壁材として充分なものとなし得る。 In another embodiment of the present invention, a shell layer may be formed on both sides of the foam layer of the foam glass. When manufacturing foam glass, these materials can be introduced into a mold in the order of the raw material for forming the shell layer, the raw material for forming the foam layer, and then the raw material for forming the shell layer, or in continuous production, the above raw materials can be introduced and laminated in the order from the lowest level. By applying the above-mentioned manufacturing means, it is possible to obtain a foam glass integrally formed from these three layers, which is particularly suitable as an exterior wall material.
本発明はさらに別の態様として泡ガラスの発泡
層の全面を皮殻層で覆うようにしてもよいことは
容易に理解されよう。 It will be readily understood that, as a further embodiment of the present invention, the entire surface of the foam layer of the foam glass may be covered with a shell layer.
すなわち、例えば前記した手段でまず両面皮殻
層で被われた泡ガラス体を製造し、次いで皮殻層
の形成されていない面を上下に保持して型枠内に
皮殻層形成原料、泡ガラス体、さらに皮殻層形成
原料の順で投入し加熱炉内で相互に融着させ、さ
らに他の面についてもこの操作を繰り返すことに
より全面が皮殻層で被覆する。 That is, for example, a foam glass body covered with a skin layer on both sides is first manufactured by the above-mentioned method, and then the surfaces on which the skin layer is not formed are held vertically and the raw material for forming the skin layer and the foam are placed in the mold. The glass body and then the raw material for forming the shell layer are charged in this order and fused together in a heating furnace, and this operation is repeated on other surfaces so that the entire surface is covered with the shell layer.
泡ガラスの連続製造においても同様な手法によ
りまず両面皮殻層で被われた泡ガラス体を製造
し、次いで上、下の耐熱ベルト間に泡ガラス体の
皮殻層が形成されていない面を上下に保持して皮
殻層形成原料、前記泡ガラス体、さらに皮殻層形
成原料の順で下位より順次連続的に投入して加
熱、相互融着させ、さらに他の面についてもこの
操作を繰り返すことにより全面を皮殻層で被覆
し、きわめて堅固な泡ガラス体とすることができ
る。 In the continuous production of foam glass, a similar method is used to first produce a foam glass body covered with a skin layer on both sides, and then to cover the surface of the foam glass body with no skin layer formed between the upper and lower heat-resistant belts. Holding them above and below, the raw material for forming the shell layer, the foam glass body, and the raw material for forming the shell layer are successively introduced from the bottom in this order, heated and fused together, and this operation is repeated for other surfaces as well. By repeating this process, the entire surface is covered with a shell layer, resulting in an extremely strong foam glass body.
また、皮殻層、発泡層の少なくとも何れかの一
方に表面凹凸を配設すれば外装材として壁面に接
着するに際して接着面積が増大してその効果を高
めるし、前記表面凹凸を幾何模様状にし外面とし
て使用すれば美観上好ましいものとなる。 Furthermore, if surface irregularities are provided on at least one of the shell layer and the foam layer, the adhesive area will increase and the effect will be enhanced when adhering to a wall surface as an exterior material, and the surface irregularities can be formed into a geometric pattern. If used as an external surface, it will be aesthetically pleasing.
これら表面凹凸の刻設は予め型枠の底部等に凹
凸を配しておくことにより、あるいは連続製造に
おいてメツシユ跡を形成すべくメツシユ状耐熱ベ
ルトを用いたり、プレス用蓋面に凹凸を配してお
くことによりきわめて容易に為し得る。 These surface irregularities can be carved by placing irregularities on the bottom of the mold in advance, or by using a mesh-like heat-resistant belt to form mesh marks during continuous manufacturing, or by placing irregularities on the press lid surface. This can be done very easily by keeping it in place.
以下に実施の1例として発泡層のかさ比重0.4、
全体の厚み50mmまたは100mmとし、皮殻層のかさ
比重0.9〜1.6、皮殻層の厚み2〜20mm、皮殻層中
のガラス粒の粒径0.1〜6.7mm、ガラス粒の含有量
5〜50vol%の泡ガラスについて鋼棒の貫入抵抗
による表面硬度試験、および切断試験を行なつた
結果を詳述する。
As an example of implementation below, the bulk specific gravity of the foam layer is 0.4,
The total thickness is 50 mm or 100 mm, the bulk specific gravity of the skin layer is 0.9 to 1.6, the thickness of the skin layer is 2 to 20 mm, the particle size of glass grains in the skin layer is 0.1 to 6.7 mm, and the content of glass grains is 5 to 50 vol. % foam glass was subjected to a surface hardness test using penetration resistance of a steel rod and a cutting test.The results are detailed below.
供試料;通常のソーダ石灰ガラス屑を粒径
150μm以下に粉砕したものに発泡剤としての炭酸
カルシウム150μm以下の粉末0.7wt%を添加混合
し、さらに結合剤としての水ガラスを若干量加え
て混合したものを転動造粒し粒径0.5〜2mmの発
泡層用造粒原料を得た。 Sample: Regular soda lime glass waste with particle size
Add and mix 0.7wt% of calcium carbonate powder of 150μm or less as a foaming agent to the powder crushed to 150μm or less, and then add a small amount of water glass as a binder and mix.The mixture is rolled and granulated to obtain particles with a particle size of 0.5~ A granulated raw material for a 2 mm foam layer was obtained.
次にソーダ石灰ガラス屑を粒径150μm以下に粉
砕したものに着色剤としての弁柄1wt%を添加混
合し、結合剤としての水ガラスを若干量添加混合
したうえ転動造粒して粒径0.5〜2mmの皮殻層の
基相を形成するための造粒原料を得た。 Next, 1wt% of Bengara as a coloring agent was added to and mixed with soda lime glass waste crushed to a particle size of 150 μm or less, and a small amount of water glass was added and mixed as a binder, and the particles were granulated by rolling. A granulated raw material for forming a base phase of a shell layer of 0.5 to 2 mm was obtained.
さらに粒径0.1〜6.7mmのガラス粒を準備し、前
記造粒原料と混合して皮殻層中のガラス粒が0〜
50vol%となるように配合割合を調整して皮殻層
用原料とした。 Furthermore, glass particles with a particle size of 0.1 to 6.7 mm are prepared and mixed with the granulation raw material to reduce the glass particles in the shell layer to 0 to 6.7 mm.
The blending ratio was adjusted to 50 vol% and used as a raw material for the skin layer.
次にスチール製型枠に発泡層用造粒原料および
その上に皮殻層用原料をそれぞれ所望の厚さにな
るように投入して後加熱炉内で750〜900℃、20分
〜40分適宜焼成し、徐冷することにより発泡層の
かさ比重0.4、皮殻層のかさ比重0.6〜1.9の泡ガラ
スを得た。 Next, the granulated raw material for the foam layer and the raw material for the shell layer are placed in a steel mold to the desired thickness, and then heated in a heating furnace at 750-900℃ for 20-40 minutes. By appropriately firing and slowly cooling, a foam glass having a foam layer with a bulk specific gravity of 0.4 and a shell layer with a bulk specific gravity of 0.6 to 1.9 was obtained.
得られた泡ガラスについて以下の試験を実施し
た。 The following tests were conducted on the obtained foam glass.
鋼棒貫入試験;巾15cm、長さ15cm、厚み50mmおよ
び100mmの泡ガラス試験片を皮殻層を上面にして
保持したものに上方より4mmφの鋼棒を5mm/分
の速度で貫入させそのときの最大抵抗を測定し
た。Steel rod penetration test: A steel rod of 4 mmφ was penetrated from above at a speed of 5 mm/min into a foam glass specimen with a width of 15 cm, a length of 15 cm, and a thickness of 50 mm and 100 mm, which was held with the skin layer facing upward. The maximum resistance was measured.
切断試験;巾40cm、長さ40cm、厚み50mmおよび
100mmの泡ガラス試験片をコランダムを砥粒とす
るレジノイド切断砥石で切断しその時の欠けや亀
裂の発生状況を観察し良好なものから不良なもの
までA〜Dに段階づけした。 Cutting test; width 40cm, length 40cm, thickness 50mm and
A 100 mm foam glass test piece was cut with a resinoid cutting wheel containing corundum as an abrasive grain, and the occurrence of chips and cracks was observed and graded from A to D from good to bad.
結果を第1〜3図、第1表に示す。 The results are shown in Figures 1 to 3 and Table 1.
第1図は全体の厚み50mm、皮殻層のかさ比重
1.0、厚み8mmの泡ガラスにおいて皮殻層中に粒
径1mmおよび1.7mmのガラス粒を各種容積比率で
含有させたものについての鋼棒貫入抵抗を示した
グラフである。貫入抵抗はガラス粒15vol%付近
までは急激に増加し以降もその量に従がい漸次増
加している。この屈曲傾向は他のガラス粒径にお
いても類似しており、総じてガラス粒の皮殻層中
の含有量が15vol%以上において貫入抵抗Rが120
Kg/cm2以上に達し、したがつて耐加傷性に優れる
ことが判る。 Figure 1 shows the total thickness of 50mm and the bulk specific gravity of the skin layer.
1.0, a graph showing the steel rod penetration resistance of foam glass with a thickness of 8 mm in which glass particles with particle diameters of 1 mm and 1.7 mm were contained in the shell layer at various volume ratios. The penetration resistance increases rapidly up to around 15vol% of glass particles, and thereafter increases gradually as the amount of glass particles increases. This bending tendency is similar for other glass particle sizes, and in general, when the content of glass particles in the shell layer is 15 vol% or more, the penetration resistance R is 120
Kg/cm 2 or more, which indicates that the scratch resistance is excellent.
第2図は全体の厚み50mm、皮殻層のかさ比重
1.0および1.2、厚み8mmの泡ガラスについて皮殻
層中にガラス粒を20vol%含有させ、ガラス粒径
を各種変動させたもの、および皮殻層のかさ比重
1.0でガラス粒30vol%のものを同様にガラス粒径
を変動させたものの鋼棒貫入抵抗を示したグラフ
であつて、ガラス粒径が0.5mm付近までは貫入抵
抗が急激に増加し、以降も漸増傾向にある。な
お、ガラス粒含有量を各種変えた場合においても
同様な屈曲傾向が明白であり、総じてガラス粒径
が0.5mm以上において貫入抵抗Rが120Kg/cm2を超
え、したがつて耐加傷性に優れることが明らかで
ある。 Figure 2 shows a total thickness of 50 mm and bulk specific gravity of the skin layer.
1.0 and 1.2, foam glass with a thickness of 8 mm, containing 20 vol% of glass grains in the skin layer, and varying the glass grain size, and the bulk specific gravity of the skin layer.
This is a graph showing the penetration resistance of a steel bar when the glass particle size is similarly varied with 1.0 and 30 vol% glass particles.The penetration resistance increases rapidly until the glass particle size reaches around 0.5 mm, and after that, it continues to increase. It is on a gradual increase. A similar bending tendency is also evident when the glass particle content is varied, and in general, the penetration resistance R exceeds 120 kg/cm 2 when the glass particle diameter is 0.5 mm or more, and therefore the scratch resistance decreases. It is clear that it is superior.
第3図は全体の厚み50mm、皮殻層中のガラス粒
径1mmおよび1.7mm、ガラス粒の含有量20vol%、
皮殻層のかさ比重を1.0とした場合の皮殻層の厚
みと貫入抵抗との関係を示しているが、皮殻層の
厚みの増加に従がい貫入抵抗の単純な増加傾向が
認められる。 Figure 3 shows a total thickness of 50 mm, glass particle diameters of 1 mm and 1.7 mm in the shell layer, and a glass particle content of 20 vol%.
The relationship between the thickness of the skin layer and the penetration resistance is shown when the bulk specific gravity of the skin layer is 1.0, and a simple tendency for penetration resistance to increase as the thickness of the skin layer increases is observed.
第1表は各種泡ガラスについて鋼棒貫入試験、
切断試験の結果を表に付記するランク付けに従が
つて示したものである。貫入抵抗においてかさ比
重0.8〜1.7、厚み2〜20mmの範囲にある皮殻層中
のガラス粒の含有量が15vol%以上、粒径がO.5mm
以上のものが良好である。一方、ガラス粒の増
加、粒径の増大に従がい切断性は漸次劣る傾向に
あるが上記かさ比重、厚み範囲の皮殻層中のガラ
ス粒の含有量が30vol%以下、粒径が5.2mm以下の
範囲において良好であることが明らかである。 Table 1 shows the steel rod penetration test for various types of foam glass.
The results of the cutting test are shown according to the rankings appended to the table. In terms of penetration resistance, the bulk specific gravity is 0.8 to 1.7, the content of glass particles in the shell layer is in the range of 2 to 20 mm, 15 vol% or more, and the particle size is 0.5 mm.
The above are good. On the other hand, as the number of glass grains increases and the grain size increases, cutting performance tends to gradually deteriorate. It is clear that the following ranges are good.
以上のように本発明の泡ガラスは耐衝撃強度、
曲げ強度等に優れると共に耐加傷性にも優れ、切
削加工が容易であるという著効を奏し、建築物の
内、外装剤、外壁材等として有効に適用し得るも
のである。
As described above, the foam glass of the present invention has high impact strength and
It has excellent bending strength, etc., excellent scratch resistance, and is easy to cut, so it can be effectively applied as an interior material, exterior material, exterior wall material, etc. of buildings.
第1〜3図は本発明の実施の一例を示した耐加
傷性に係る貫入抵抗のグラフである。
1 to 3 are graphs of penetration resistance related to scratch resistance showing an example of the implementation of the present invention.
【表】【table】
【表】【table】
【表】【table】
Claims (1)
さ比重の皮殻層より一体的に形成され、該皮殻層
はガラス微粉またはガラス微粉と無機顔料微粉が
相互に融接してなる基相に粒径0.5〜5.2mm、皮殻
層中の含有量15〜30vol%のガラス粒が散在する
ようにしたことを特徴とする泡ガラス。 2 発泡層のかさ比重が0.3〜0.6、皮殻層のかさ
比重が0.8〜1.7からなることを特徴とする特許請
求の範囲第1項記載の泡ガラス。 3 発泡層形成原料、皮殻層の基相形成原料とし
て各々ガラス微粉を主体とする造粒物を使用する
ようにしたことを特徴とする特許請求の範囲第1
項ないし第2項記載の泡ガラス。[Scope of Claims] 1. It is integrally formed of a foam layer and a shell layer having a higher bulk specific gravity covering at least one side of the foam layer, and the shell layer is made of glass fine powder or glass fine powder and inorganic pigment fine powder fused together. A foam glass characterized in that glass grains having a grain size of 0.5 to 5.2 mm and a content of 15 to 30 vol% in a shell layer are scattered in a base phase. 2. The foam glass according to claim 1, wherein the foam layer has a bulk specific gravity of 0.3 to 0.6, and the skin layer has a bulk specific gravity of 0.8 to 1.7. 3. Claim 1, characterized in that granules mainly composed of glass fine powder are used as the raw material for forming the foam layer and the raw material for forming the base phase of the shell layer, respectively.
Bubble glass according to items 1 to 2.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5153686A JPS62212245A (en) | 1986-03-11 | 1986-03-11 | Foam glass |
| GB8705184A GB2188926B (en) | 1986-03-10 | 1987-03-05 | Foam glass having crust layer and method of producing same |
| FR8703179A FR2596386B1 (en) | 1986-03-10 | 1987-03-09 | CELL GLASS HAVING A COAT OF LAYER AND METHOD FOR PRODUCING THE SAME |
| US07/023,854 US4798758A (en) | 1986-03-10 | 1987-03-09 | Foam glass having crust layer and method of producing same |
| DE19873707670 DE3707670A1 (en) | 1986-03-10 | 1987-03-10 | FOAM GLASS WITH CRUST LAYER AND METHOD FOR THE PRODUCTION THEREOF |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5153686A JPS62212245A (en) | 1986-03-11 | 1986-03-11 | Foam glass |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62212245A JPS62212245A (en) | 1987-09-18 |
| JPH0433735B2 true JPH0433735B2 (en) | 1992-06-03 |
Family
ID=12889745
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5153686A Granted JPS62212245A (en) | 1986-03-10 | 1986-03-11 | Foam glass |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62212245A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0238342A (en) * | 1988-07-28 | 1990-02-07 | Central Glass Co Ltd | Decorative glassy cellular substance |
| US6964809B2 (en) * | 2002-02-15 | 2005-11-15 | Pedro M. Buarque de Macedo | Large high density foam glass tile |
| JP2006206380A (en) * | 2005-01-28 | 2006-08-10 | Sekisui House Ltd | Glass building materials |
-
1986
- 1986-03-11 JP JP5153686A patent/JPS62212245A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62212245A (en) | 1987-09-18 |
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