JP3217646B2 - Ceramic sound absorbing material - Google Patents
Ceramic sound absorbing materialInfo
- Publication number
- JP3217646B2 JP3217646B2 JP16753395A JP16753395A JP3217646B2 JP 3217646 B2 JP3217646 B2 JP 3217646B2 JP 16753395 A JP16753395 A JP 16753395A JP 16753395 A JP16753395 A JP 16753395A JP 3217646 B2 JP3217646 B2 JP 3217646B2
- Authority
- JP
- Japan
- Prior art keywords
- absorbing material
- sound absorbing
- binder
- ceramic
- strength
- 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 - Fee Related
Links
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Soundproofing, Sound Blocking, And Sound Damping (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、道路、住宅、ビル
などに使用される吸音材、特に火災等の急熱、急冷の状
態に瀑されても吸音性能の劣化しない吸音材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sound absorbing material used for roads, houses, buildings, and the like, and more particularly to a sound absorbing material which does not deteriorate in sound absorbing performance even when it is subjected to rapid heat or quenching such as fire.
【0002】[0002]
【従来の技術】焼成工程を経ない従来のセラミックス吸
音材の製造方法は、一般的に、セラミックス粒子に樹脂
系バインダーを添加しよく混合し、この混合物をプレス
型に充填してプレス成形させた後、取出し常温で1日以
上乾燥させ強度を発揮させることからなる(図3)。2. Description of the Related Art A conventional method for producing a ceramic sound-absorbing material without a firing step generally involves adding a resin-based binder to ceramic particles, mixing the mixture well, filling the mixture into a press mold, and press-molding the mixture. Thereafter, it is taken out and dried at room temperature for one day or more to exhibit strength (FIG. 3).
【0003】[0003]
【発明が解決しようとする課題】従来の樹脂系バインダ
ーを用いた、高温焼成しないタイプのセラミックス吸音
材は、火災等の高温雰囲気のもとでは樹脂系バインダー
が焼失する為に、製造時の加圧工程に於ける押圧力のみ
で、セラミックス粒子同志が固着されているだけであり
吸音材の強度の著しい低下をもたらす。また、時として
吸音材表面のセラミックス粒子の部分的な脱落も起こ
る。(表1の,)。本発明は、このような従来技術
の問題点を解消して、火災等の高温雰囲気に瀑されても
強度低下やセラミックス粒子の脱落の起こらない改良さ
れた吸音材を提供することを目的とする。A conventional ceramic sound-absorbing material using a resin-based binder, which is not fired at a high temperature, burns out the resin-based binder in a high-temperature atmosphere such as a fire. Only the pressing force in the pressing step causes the ceramic particles to adhere to each other, resulting in a significant decrease in the strength of the sound absorbing material. In some cases, the ceramic particles on the surface of the sound absorbing material also partially fall off. (In Table 1). An object of the present invention is to solve the problems of the prior art and to provide an improved sound absorbing material in which the strength is not reduced and the ceramic particles are not dropped even when the water falls in a high temperature atmosphere such as a fire. .
【0004】[0004]
【課題を解決するための手段】本発明者らは、上記従来
技術の欠点を克服するため種々研究の結果、火災等の急
激な高温雰囲気にさらされても吸音材表面からセラミッ
クス粒子が脱落するのを防止するために、従来からの樹
脂系バインダーばかりではなく、無機系バインダーをバ
インダーとして添加する(図1)ことが有効であるとの
知見を得た。ここで、用いられる無機系バインダーは、
火災の温度約500〜800℃で溶融又は半溶融状態と
なり、またある程度の粘度を有した、粘りのあるのり状
の状態になる必要がある(図2)。The present inventors have conducted various studies to overcome the above-mentioned drawbacks of the prior art. As a result, the ceramic particles fall off the surface of the sound absorbing material even when exposed to a sudden high-temperature atmosphere such as a fire. In order to prevent this, it has been found that it is effective to add not only a conventional resin binder but also an inorganic binder as a binder (FIG. 1). Here, the inorganic binder used is
It must be in a molten or semi-molten state at a fire temperature of about 500 to 800 ° C. and have a sticky, glue-like state having a certain viscosity (FIG. 2).
【0005】すなわち、本発明は、酸化物系セラミック
ス粒体を骨材としてこれに樹脂系バインダーと無機系バ
インダーを添加し得られた混合物を加圧し一体成形して
なるセラミックス吸音材であって、上記無機系バインダ
ーが重量比で PbO :35〜65% SiO 2 :20〜35% B 2 O 3 : 5〜20% ZnO,Al 2 O 3 ,その他:残部 からなる組成を有し、かつ体膨張係数が300×10 -7
以下のホウケイ酸鉛ガラスであること を要旨とする。
又、骨材として用いられる酸化物セラミックス粒子とし
ては、例えば、ムライト等が挙げられ、樹脂系バインダ
ーとしては、一般にエポキシ樹脂等の熱硬化性樹脂が好
ましい。[0005] That is, the present invention is a ceramic sound absorbing material obtained by pressing an admixture obtained by adding a resin binder and an inorganic binder to an oxide ceramic granule as an aggregate, and integrally forming the aggregate . The above inorganic binder
Over the PbO by weight ratio: 35~65% SiO 2: 20~35% B 2 O 3: 5~20% ZnO, Al 2 O 3, other: having the composition and the balance, and volume expansion coefficient of 300 × 10 -7
It is the gist of the following lead borosilicate glass .
The oxide ceramic particles used as the aggregate include, for example, mullite, and the resin binder is generally preferably a thermosetting resin such as an epoxy resin.
【0006】樹脂系バインダーと無機系バインダーの両
者を添加した吸音材が火災に出会った時、急激な温度上
昇が起こり、短時間のあいだに500〜800℃に加熱
されるが、又、通常、短時間のうちに消化又は鎮火され
る。この短時間の昇温の間に樹脂系バインダーは消失す
るが、無機系バインダーは溶融又は半溶融状態になり、
この時、それ自身の強度は高くないが、いわばのり状
(又は溶融ガラス状)となり、吸音材表面からの、セラ
ミックス粒子の脱落を防止する役目を果たす。When a sound-absorbing material to which both a resin-based binder and an inorganic-based binder are added encounters a fire, a sharp rise in temperature occurs and the material is heated to 500 to 800 ° C. for a short time. Extinguished or extinguished within a short time. The resin binder disappears during this short temperature rise, but the inorganic binder becomes molten or semi-molten,
At this time, although the strength of itself is not high, it becomes so-called glue-like (or molten glass-like) and plays a role of preventing ceramic particles from falling off the surface of the sound absorbing material.
【0007】[0007]
【発明の実施の形態】そこで低融点の無機系バインダー
として、リン酸系(P2 O5 系)、ホウ酸系(B2 O3
系)、鉛系(PbO系)及びそれらの混合物を検討し
た。まずリン酸系、例えばSM−5(日本フリット株式
会社製商品名、主成分としてP2 O5 35〜40%含
有)は体膨張系数が高い為に(450×10-7)、特に
急冷の場合に自身にクラックが入り強度の低下が著し
く、バインダーとしては適当でない。BEST MODE FOR CARRYING OUT THE INVENTION As low-melting inorganic binders, phosphoric acid (P 2 O 5 ) and boric acid (B 2 O 3)
), Lead (PbO) and mixtures thereof. First, a phosphoric acid system, for example, SM-5 (trade name, manufactured by Nippon Frit Co., containing 35 to 40% of P 2 O 5 as a main component) has a high body expansion number (450 × 10 −7 ), and is particularly rapidly cooled. In such a case, cracks are formed in the material and the strength is remarkably reduced, so that it is not suitable as a binder.
【0008】次にホウ酸系において、例えばPR520
3(日本フリット株式会社製商品名、主成分としてB2
O3 35〜40%含有、他にAl2 O3 、SiO2 含
有)は体膨張係数がやや高い程度であるが(350×1
0-7)、溶融温度が約800℃と高い為、火災の場合の
り状にならずバインダーの役目を果たさず、又溶融した
としても、急冷の際、クラックが入り易いのでバインダ
ーとしては適さない。Next, in a boric acid system, for example, PR520
3 (Japan frit Co., trade name, B 2 as a main component
35 to 40% of O 3 , other than Al 2 O 3 and SiO 2 ) have a slightly higher body expansion coefficient (350 × 1).
0 -7 ), since the melting temperature is as high as about 800 ° C, it does not form a glue in the case of fire and does not serve as a binder. Even if it is melted, cracks easily occur during rapid cooling, so it is not suitable as a binder. .
【0009】鉛系に於いて、例えば、XM−735L
(日本フリット株式会社製商品名、主成分としてPbO
40〜45%、その他SiO2 ,Al2 O3 含有)は体
膨張系数が170×10-7と低く、溶融後の急冷時のク
ラックは見られない。しかし、溶融温度が800〜90
0℃と高い為に、火災の場合には目的を充分果たさな
い。そこで、体膨張系数の低い鉛系で溶融温度が低い成
分のものを種々テストした。その結果目安として、体膨
張系数が300×10-7以下でかつ軟化温度350℃、
溶融温度400〜600℃のものが、火災のような急
熱、急冷の場合に、無材バインダーとしての効果を果た
すことが判明した。In the lead system, for example, XM-735L
(Product name made by Nippon Frit Co., Ltd., PbO as main component
(40-45%, other containing SiO 2 and Al 2 O 3 ) has a low body expansion coefficient of 170 × 10 −7, and no crack is observed during quenching after melting. However, when the melting temperature is 800-90
Since the temperature is as high as 0 ° C, it does not fulfill its purpose in case of fire. Therefore, various tests were conducted on a lead-based material having a low body expansion coefficient and a component having a low melting temperature. As a result, the body expansion coefficient is 300 × 10 −7 or less and the softening temperature is 350 ° C.
It has been found that a material having a melting temperature of 400 to 600 ° C. has an effect as a materialless binder in the case of rapid heat or rapid cooling such as fire.
【0010】この条件を満足するものとしては、Pb
O,B2 O3 ,SiO2 などから構成されているホウケ
イ酸鉛ガラスが良い。P2 O5 系は膨張係数が高いので
好ましくない。ホウケイ酸鉛ガラスで、体膨張係数を3
00×10-7以下とする為にはB2 O3 20%以下とす
ることが必要であり、また溶融温度を下げる為にはPb
Oが35%以上、B2 O3 5%以上、さらに、これらに
SiO2 ,ZnOが適当に配合されていることが必要で
ある。The condition satisfying this condition is Pb
Lead borosilicate glass composed of O, B 2 O 3 , SiO 2 or the like is preferable. P 2 O 5 is not preferable because of its high expansion coefficient. Lead borosilicate glass with a body expansion coefficient of 3
In order to reduce the melting temperature to 00 × 10 −7 or less, it is necessary to reduce B 2 O 3 to 20% or less.
It is necessary that O is 35% or more, B 2 O 3 is 5% or more, and further, SiO 2 and ZnO are appropriately blended.
【0011】またこのホウケイ酸鉛ガラスの配合量とし
ては、セラミックス粒子:ホウケイ酸鉛ガラス:樹脂バ
インダーを重量%で100:3〜20:2〜10の範囲
とするのが好ましい。ホウケイ酸鉛ガラスが3%以下で
は急冷後の強度アップの効果が期待出来ず、又高温時の
バインダーの効果も低い。また増量するにつれて強度ア
ップは期待できるが、気孔率が低下して来て、吸音性能
に大きな影響を及ぼしてくる。尚、樹脂バインダーは、
吸音材として常時使用する雰囲気である低温時での強度
確保の為に添加するものであるが、2〜10%が好まし
く2%以下では強度不足、また10%を越えると、気孔
率が低下し、吸音性能に影響を及ぼすことが判明してい
る。The compounding amount of the lead borosilicate glass is preferably in the range of 100: 3 to 20: 2 to 10 by weight of ceramic particles: lead borosilicate glass: resin binder. When the content of lead borosilicate glass is 3% or less, the effect of increasing the strength after quenching cannot be expected, and the effect of the binder at high temperatures is low. Further, the strength can be expected to increase as the amount is increased, but the porosity decreases, which has a great influence on the sound absorbing performance. The resin binder is
It is added to ensure strength at low temperatures, which is an atmosphere that is always used as a sound absorbing material. However, 2 to 10% is preferable, strength is insufficient at 2% or less, and porosity decreases when it exceeds 10%. Has been found to affect sound absorption performance.
【0012】[0012]
【実施例】以下本発明を実施例により更に詳細に説明す
る。 (実施例1)セラミックス吸音材の製造 (i) セラミックス粒子(約0.5〜1mm径のムライト粉砕粒子) ・・・・・・5000g (ii)エポキシ樹脂接着剤 ・・・・・・・・100g (iii) ホウケイ酸鉛ガラス(#4370) ・・・・・・・・500g (日本ホ−ロ−釉薬株式会社製) の上記原料をミキサーで約20分よく混合した。得られ
た混合物をプレスの金型(450mm×900mm)に
充填して、約200トンの圧力でプレス成形することに
より450×900×9mm厚のサイズの試料を得た。
これを金型より取出し常温で1日以上乾燥させて、接着
剤の硬化を図り、相当の強度を有した吸音材が得られ
た。(表1の)曲げ強度は140kg/cm2 であっ
た。この配合での吸音率を図4に示す。次に、750℃
に30分加熱した後、急冷し常温に戻した試料について
強度を測定したところ80kg/cm2 を示した(表1
の)。図4中実線は加熱前の試料の吸音率を示し、点
線は750℃×30分加熱処理後、冷却した試料の吸音
率を示す。The present invention will be described in more detail with reference to the following examples. (Example 1) Production of ceramic sound absorbing material (i) Ceramic particles (crushed mullite particles having a diameter of about 0.5 to 1 mm) ... 5000 g (ii) Epoxy resin adhesive ... 100 g (iii) Lead borosilicate glass (# 4370) 500 g (produced by Nippon Hollow Glaze Co., Ltd.) was well mixed with a mixer for about 20 minutes. The obtained mixture was filled in a press die (450 mm × 900 mm) and press-molded under a pressure of about 200 tons to obtain a sample having a size of 450 × 900 × 9 mm.
This was taken out of the mold and dried at room temperature for one day or more to cure the adhesive, and a sound absorbing material having considerable strength was obtained. The flexural strength (of Table 1) was 140 kg / cm 2 . FIG. 4 shows the sound absorption coefficient of this composition. Next, 750 ° C
After heating for 30 minutes, the sample was quenched and returned to room temperature, and the strength was measured. As a result, it was found to be 80 kg / cm 2 (Table 1).
of). In FIG. 4, the solid line indicates the sound absorption coefficient of the sample before heating, and the dotted line indicates the sound absorption coefficient of the sample cooled after the heat treatment at 750 ° C. for 30 minutes.
【0013】(比較例1)ホウケイ酸ガラスを配合しな
いほかは実施例1と同様に処理して得られた試料の曲げ
強度を表1の及びに示す。(Comparative Example 1) The flexural strength of a sample obtained by treating in the same manner as in Example 1 except that no borosilicate glass was blended is shown in Table 1 and in Table 1.
【0014】[0014]
【表1】 [Table 1]
【0015】[0015]
【発明の効果】無機系バインダーとしてホウケイ酸鉛ガ
ラスを用いることにより、焼成工程を経ない吸音材も
火災等の急熱時にもセラミックス粒子の脱落を防止で
きる。 又、消火後の冷却時にも溶融していたのが固
まり、ホウケイ酸鉛ガラスがセラミックス粒子の接合剤
としての役目を果たし、適当な強度を有し、しかも吸音
材として再度使用できるという効果を奏する。By using lead borosilicate glass as the inorganic binder, it is possible to prevent the sound-absorbing material which has not been subjected to the sintering step from falling off of the ceramic particles even in the case of rapid heating such as a fire. In addition, when cooled after extinguishing, the molten material solidifies, and the lead borosilicate glass acts as a bonding agent for the ceramic particles, has an appropriate strength, and has an effect that it can be reused as a sound absorbing material. .
【図面の簡単な説明】[Brief description of the drawings]
【図1】図1は本発明のセラミックス吸音材の一実施態
様を示す模式図である。FIG. 1 is a schematic view showing one embodiment of the ceramic sound absorbing material of the present invention.
【図2】図2は本発明のセラミックス吸音材において用
いられる無機系バインダーが溶融した状態を示す模式図
である。FIG. 2 is a schematic view showing a state in which an inorganic binder used in the ceramic sound absorbing material of the present invention is molten.
【図3】図3は樹脂系バインダーを用いた従来のセラミ
ックス吸音材の一例を示す模式図である。FIG. 3 is a schematic view showing an example of a conventional ceramic sound absorbing material using a resin binder.
【図4】図4は本発明の吸音材の加熱前後の残響室法吸
音率を示すグラフである。FIG. 4 is a graph showing a reverberation chamber method sound absorption coefficient before and after heating of the sound absorbing material of the present invention.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) G10K 11/16 - 11/175 C08J 9/32 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int.Cl. 7 , DB name) G10K 11/16-11/175 C08J 9/32
Claims (1)
これに樹脂系バインダーと無機系バインダーを添加し得
られた混合物を加圧し一体成形してなるセラミックス吸
音材であって、上記無機系バインダーが重量比で PbO :35〜65% SiO 2 :20〜35% B 2 O 3 : 5〜20% ZnO,Al 2 O 3 ,その他:残部 からなる組成を有し、かつ体膨張係数が300×10 -7
以下のホウケイ酸鉛ガラスであることを特徴とする セラ
ミックス吸音材。1. A oxide-based ceramics and granular material a ceramic sound absorbing material comprising this mixture of resin binder and an inorganic binder was obtained by adding pressurized integrally molded as an aggregate, the inorganic binder There PbO by weight ratio: 35~65% SiO 2: 20~35% B 2 O 3: 5~20% ZnO, Al 2 O 3, other: having the composition and the balance, and volume expansion coefficient of 300 × 10 -7
A ceramic sound absorbing material characterized by the following lead borosilicate glass .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16753395A JP3217646B2 (en) | 1995-07-03 | 1995-07-03 | Ceramic sound absorbing material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16753395A JP3217646B2 (en) | 1995-07-03 | 1995-07-03 | Ceramic sound absorbing material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0916180A JPH0916180A (en) | 1997-01-17 |
JP3217646B2 true JP3217646B2 (en) | 2001-10-09 |
Family
ID=15851465
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16753395A Expired - Fee Related JP3217646B2 (en) | 1995-07-03 | 1995-07-03 | Ceramic sound absorbing material |
Country Status (1)
Country | Link |
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JP (1) | JP3217646B2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1180763A3 (en) * | 2000-08-15 | 2003-03-12 | Mitsubishi Heavy Industries, Ltd. | Ceramic sound absorbing material and manufacturing method therefor |
KR20050096483A (en) * | 2004-03-30 | 2005-10-06 | 주식회사 이이엠 | Sound absorbing materials for a building |
CN105332435B (en) * | 2014-08-07 | 2018-04-13 | 正升环境科技股份有限公司 | A kind of combined type particulate muffling unit and the noise reduction building block being combined into by it |
CN104167204A (en) * | 2014-08-07 | 2014-11-26 | 四川正升声学科技有限公司 | Particle board resonance sound absorption structure |
-
1995
- 1995-07-03 JP JP16753395A patent/JP3217646B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH0916180A (en) | 1997-01-17 |
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