JPS6115907B2 - - Google Patents
Info
- Publication number
- JPS6115907B2 JPS6115907B2 JP8345778A JP8345778A JPS6115907B2 JP S6115907 B2 JPS6115907 B2 JP S6115907B2 JP 8345778 A JP8345778 A JP 8345778A JP 8345778 A JP8345778 A JP 8345778A JP S6115907 B2 JPS6115907 B2 JP S6115907B2
- Authority
- JP
- Japan
- Prior art keywords
- glass powder
- adhesive
- sodium silicate
- powder
- borosilicate glass
- 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
- 239000000843 powder Substances 0.000 claims description 54
- 230000001070 adhesive effect Effects 0.000 claims description 39
- 239000000853 adhesive Substances 0.000 claims description 38
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 19
- 239000004115 Sodium Silicate Substances 0.000 claims description 18
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 18
- 239000005388 borosilicate glass Substances 0.000 claims description 16
- 239000011521 glass Substances 0.000 claims description 15
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 14
- 239000005355 lead glass Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 5
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 description 7
- 229910052573 porcelain Inorganic materials 0.000 description 7
- 239000004568 cement Substances 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910021336 sodium silicide Inorganic materials 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Description
この発明は硬化促進剤を混合したケイ酸ソーダ
系接着剤に関するものである。
従来は一般にケイ酸ソーダの硬化促進剤として
ケイフツ化ソーダ(Na2SiF6)が知られているが
排水がF-イオン等を含むことから公害を起す問
題があつた。
又、特に硬化促進剤無添加のケイ酸ソーダ系接
着剤を耐熱気密封止剤として磁器と金属部との接
着に使用した場合、乾燥処理工程において微細な
亀裂や発泡状の吹出しが生じ接着強度、気密性、
耐熱性、機械的衝撃強度等の低下を起す問題が有
つた。
本発明は以上のような欠点を改良する目的のた
めになされたもので、金属酸化物粉末と1号又は
2号ケイ酸ソーダ(JIS規格に定められている液
状のSiO2:Na2Oが1号では36〜38%:17〜18%
でNa2O・nSiO2のnが2.0であり、2号では34〜
36%:14〜15%でNa2O・nSiO2のnが2.4であ
る)との等量混合物99ないし90重量%(以下重量
を省く)と105μ以下のフリツト1ないし10%と
を混合してなり、該フリツトがソーダガラス粉
末、硼ケイ酸ガラス粉末、鉛ガラス粉末の1種又
は2種以上よりなるものであることを特徴とする
ケイ酸ソーダ系接着剤を提供するものである。
硬化促進剤として添加していたケイフツ化ソー
ダの接着剤は脱水により硬化し、先づ表面の水分
が減少し、ゲル状の水硝子が形成される。該ケイ
フツ化ソーダの代替としてソーダガラス粉末、硼
ケイ酸ガラス粉末、鉛ガラス粉末の1種又は2種
以上を1ないし10%含有せしめると内部からもゲ
ル化が進行し発泡上の吹出しの少ない緻密なも
の、気密性、耐熱性に優れたものとなり、上記フ
リツトはケイ酸ソーダとの化学親和性も良いため
接着力は強く、機械的衝撃にも強い接着剤とな
る。
以下実施例について説明すると5μ以下の粒子
が50%である仮焼粘土粉末に液状の1号ケイ酸ソ
ーダと105μ以下(150メツシユ通過)のソーダガ
ラス粉末、硼ケイ酸ガラス粉末及び鉛ガラス粉末
のうちの1種又は2種以上を第1表に示すように
総量100となる重量割合に配合して、30分間混練
し、その混練粘度が最適な粘度350±50ポイズに
なるよう水を添加して調製する。
次に上記調合物を接着力(ネジリトルク)測定
用及びセメント吹出し調査用として第2図に示す
ような形状即ち外径12mm、内径6mm、長さ20mmの
磁器円筒1の中に径8.5mmと長さ20mmの円柱部2a
と径5.2mmと長さ10mmの円柱部2bよりなる段付
円柱鉄芯2の2b部を長さ10mmに上記の調整され
た接着剤3を塗布し挿入接合する。
該接合試料を室音で10Hr以上自然乾燥后25℃/
Hrの割合で昇温し130℃の温度にて5Hr保持して
加熱乾燥を行つた。
以上にて完成した試料の磁器と金具の境界線4
からのセメント吹出しを目視にて各々1000個につ
き調査し、その試料の各々10個につき磁器部分を
固定し鉄芯にトルクを与え、接着面が破壊に到る
トルクを測定した。その平均値をKg・cmにて示
し、セメント吹出し結果と共に第1表に記入す。
わかりやすくするために第1図に示した。図中実
線は接着力をKg・cmで点線は吹出し品の百分率を
示す。
第1図より本発明のフリツトを含有した接着剤
の接着力は最低96から最高122Kg・cmであり、こ
の値は硬化剤としてケイフツ化ソーダを用いたも
のに劣らず、硬化剤を加えない試料の接着力は85
Kg・cmとなり明らかに顕著な効果があり、かつセ
メント吹出率に於ても本発明の硬化剤の添加効果
は無添加の比較品より最悪の場合でも1/8以下に
減少した。
This invention relates to a sodium silicate adhesive mixed with a curing accelerator. Conventionally, sodium silicate (Na 2 SiF 6 ) has been generally known as a curing accelerator for sodium silicate, but this has had the problem of causing pollution because the wastewater contains F - ions and the like. In addition, especially when a sodium silicate adhesive with no hardening accelerator added is used as a heat-resistant air sealant to bond porcelain and metal parts, fine cracks and foam-like blowouts may occur during the drying process, reducing the bond strength. ,airtightness,
There was a problem that heat resistance, mechanical impact strength, etc. decreased. The present invention was made for the purpose of improving the above-mentioned drawbacks, and it combines metal oxide powder and No. 1 or No. 2 sodium silicate (liquid SiO 2 :Na 2 O specified in JIS standards). 36-38% for No. 1: 17-18%
So, n of Na 2 O・nSiO 2 is 2.0, and in No. 2 it is 34~
36%: A mixture of 99 to 90% by weight (hereinafter omitted by weight) of an equal amount of 14 to 15% Na 2 O. The present invention provides a sodium silicate adhesive characterized in that the frit is made of one or more of soda glass powder, borosilicate glass powder, and lead glass powder. The adhesive made of sodium silicate added as a curing accelerator is cured by dehydration, and the moisture on the surface first decreases, forming gel-like water glass. When 1 to 10% of one or more of soda glass powder, borosilicate glass powder, and lead glass powder is contained as a substitute for the sodium silicide powder, gelation progresses from the inside, resulting in a dense foam with less blow-out. The frit has good chemical affinity with sodium silicate, so it has a strong adhesive force and is resistant to mechanical shock. To explain an example below, calcined clay powder containing 50% of particles of 5μ or less, liquid No. 1 sodium silicate, soda glass powder of 105μ or less (passed through 150 meshes), borosilicate glass powder, and lead glass powder. One or more of them are blended in a weight ratio giving a total amount of 100 as shown in Table 1, kneaded for 30 minutes, and water is added so that the kneading viscosity becomes the optimum viscosity of 350±50 poise. Prepare. Next, the above-mentioned mixture was placed in a porcelain cylinder 1 having a diameter of 8.5 mm and a length of 20 mm, as shown in Fig. Cylindrical part 2a with a length of 20 mm
The 2b portion of the stepped cylindrical iron core 2 consisting of the cylindrical portion 2b with a diameter of 5.2 mm and a length of 10 mm is coated with the above adjusted adhesive 3 to a length of 10 mm and inserted and bonded. After drying the bonded sample naturally for more than 10 hours in a room at 25℃/
The temperature was increased at a rate of 130° C. for 5 hours and dried by heating. Boundary line 4 between the porcelain and metal fittings of the sample completed above
We visually inspected 1000 pieces of cement blowing out of each sample, fixed the porcelain part of each of the 10 samples, applied torque to the iron core, and measured the torque that would cause the adhesive surface to break. The average value is shown in kg/cm and entered in Table 1 along with the cement blowout results.
It is shown in Figure 1 for clarity. In the figure, the solid line indicates the adhesive force in kg·cm, and the dotted line indicates the percentage of the blown product. Figure 1 shows that the adhesive strength of the adhesive containing the frit of the present invention ranges from a minimum of 96 to a maximum of 122 kg cm, and this value is comparable to that of the adhesive using sodium silicate as a hardening agent, and the adhesive strength of the adhesive without a hardening agent. The adhesive strength is 85
Kg·cm, which clearly had a significant effect, and the effect of adding the curing agent of the present invention on the cement blowout rate was reduced to 1/8 or less in the worst case compared to a comparative product without additives.
【表】
又本発明のフリツト含有量10%を越えた場合ソ
ーダガラス粉末、硼ケイ酸ガラス粉末、鉛ガラス
粉末の1種を12%含有した接着剤の接着力は93、
94、94Kg・cmとなり、本発明の上限の10%を含有
した接着剤の接着力の99、104、108Kg・cmより明
らかに低下の傾向を示す。また含有量10%を越え
ると粘度350ポイズの規制に合せるために水の添
加量が多くなり、硬化時間が早くなる。其のため
一定の連続使用の作業性に支障をきたす事になる
ため本発明のフリツト含有量の上限を10%と定め
た。本発明の硬化剤のソーダガラス粉末、硼ケイ
酸ガラス粉末、鉛ガラス粉末による接着剤の接着
力の差違は各硬化剤4%含有の時、ソーダガラス
粉末は108Kg・cm、硼ケイ酸ガラス粉末は118Kg・
cmであり、鉛ガラス粉末は122Kg・cmとなり、又
10%含有の時、ソーダガラス粉末は99Kg・cm、硼
ケイ酸ガラス粉末は104Kg・cm、鉛ガラス粉末で
は108Kg・cmとなり、鉛ガラス粉末、硼ケイ酸ガ
ラス粉末、ソーダガラス粉末の順で優劣の差違が
あつた。
本発明の硬化剤のソーダガラス粉末、硼ケイ酸
ガラス粉末、鉛ガラス粉末のうちの2種又は3種
を混合した硬化剤につき接着剤の接着力を調べる
と2種混合による6%即ちソーダガラス粉末3%
と硼ケイ酸ガラス粉末3%を含有した接着剤
No.10と硼ケイ酸ガラス粉末3%と鉛ガラス粉末
3%とを含有した接着剤No.11の2種類はそれぞ
れ112と117Kg・cmとなり、硼ケイ酸ガラス粉末単
味を6%含有した接着剤の接着力108Kg・cmとよ
り判断して1種類含有のものと2種類含有のもの
との差違は小さく、又3種含有の8%即ちソーダ
ガラス粉末2%と硼ケイ酸ガラス粉末3%と鉛ガ
ラス粉末3%を含有した接着剤No.12につき試験
したところ接着剤の接着力は105Kg・cmとなり第
1表の単味含有の6及び10%の接着剤の接着力
108及び104Kg・cmと比較して2種又は3種を含有
した接着剤の接着力も1種のフリツトを含有した
接着剤と差違があまりないものと判断出来る。
上記の如く本発明に係るケイ酸ソーダ系接着剤
の硬化剤としてのソーダガラス粉末、硼ケイ酸ガ
ラス粉末、鉛ガラス粉末の1種又は2種以上添加
はケイフツ化ソーダに変る硬化促進剤としてFイ
オンを含まないから公害を発生することなく、微
細な亀裂や発泡状の吹出しもなく、接着効果も高
く、耐熱性、気密性や機械的衝撃性にすぐれた添
加剤として利用出来るし、上記の特性を必要とす
る圧電着火装置の電極固定やセンサー素子の固
定、点火栓碍子と中心軸との接着固定等に利用範
囲は広く、有効な添加剤である。
以上の実施例は金属酸化物粉末の1例として仮
焼粘土粉末を選んだが本発明はこれにこだわるこ
となく磁器粉末、耐火物粉末、天然石材粉末が同
等に利用出来る。又フリツトとしてソーダガラス
粉末、硼ケイ酸ガラス粉末、鉛ガラス粉末を用い
たがソーダガラスの替りに他のすべてのガラス粉
末を同等に利用することが出来る。又ケイ酸ソー
ダとして液状の1号ケイ酸ソーダを用いたがこれ
は2号ケイ酸ソーダでも同様に用いるとが出来
る。[Table] Furthermore, when the frit content of the present invention exceeds 10%, the adhesive strength of the adhesive containing 12% of one of soda glass powder, borosilicate glass powder, and lead glass powder is 93,
94, 94 Kg·cm, which clearly shows a tendency to decrease compared to 99, 104, and 108 Kg·cm, which is the adhesive force of the adhesive containing 10% of the upper limit of the present invention. Furthermore, if the content exceeds 10%, the amount of water added will increase to meet the viscosity regulation of 350 poise, and the curing time will become faster. As a result, the upper limit of the frit content in the present invention was set at 10%, since this would impede workability during constant continuous use. The difference in adhesive strength between the hardening agents of the present invention, soda glass powder, borosilicate glass powder, and lead glass powder, is that when each hardening agent contains 4%, the soda glass powder is 108 kg cm, the borosilicate glass powder is 108 kg cm. is 118Kg・
cm, lead glass powder is 122Kg・cm, and
When containing 10%, soda glass powder is 99Kg・cm, borosilicate glass powder is 104Kg・cm, and lead glass powder is 108Kg・cm. Lead glass powder, borosilicate glass powder, and soda glass powder are superior in order. There was a difference. The adhesion strength of the adhesive was examined for the hardening agent of the present invention, which is a mixture of two or three of the following: soda glass powder, borosilicate glass powder, and lead glass powder. powder 3%
Adhesive containing 3% of borosilicate glass powder and
Two types of adhesives No. 10 and No. 11 containing 3% borosilicate glass powder and 3% lead glass powder had weights of 112 and 117 kg・cm, respectively, and contained 6% borosilicate glass powder alone. Judging from the adhesive strength of the adhesive of 108 kg cm, the difference between the one containing one kind and the one containing two kinds is small, and the one containing three kinds, 8%, that is, 2% soda glass powder and 3% borosilicate glass powder. % and adhesive No. 12 containing 3% lead glass powder, the adhesive strength of the adhesive was 105 kg cm, which is the adhesive strength of 6 and 10% adhesives containing single ingredients in Table 1.
Compared to 108 and 104 Kg.cm, it can be judged that the adhesive strength of the adhesive containing two or three types of frits is not much different from that of the adhesive containing one type of frit. As mentioned above, the addition of one or more of soda glass powder, borosilicate glass powder, and lead glass powder as a curing agent to the sodium silicate adhesive according to the present invention is F as a curing accelerator that converts into sodium silicate. Since it does not contain ions, it does not cause pollution, has no microscopic cracks or foam-like blowouts, has a high adhesive effect, and can be used as an additive with excellent heat resistance, airtightness, and mechanical impact resistance. It is an effective additive with a wide range of uses, such as fixing the electrodes of piezoelectric ignition devices that require special characteristics, fixing sensor elements, and adhesive fixing the spark plug insulator and central shaft. In the above embodiments, calcined clay powder was selected as an example of the metal oxide powder, but the present invention is not limited to this, and porcelain powder, refractory powder, and natural stone powder can equally be used. Further, although soda glass powder, borosilicate glass powder, and lead glass powder were used as the frit, any other glass powder can be equally used in place of soda glass. Furthermore, although liquid No. 1 sodium silicate was used as the sodium silicate, it is also possible to use No. 2 sodium silicate in the same manner.
第1図は第1表の添加剤の添加量による接着力
(ネジリトルク)とセメント吹出しについて示し
たものであり、実線は接着力(Kg・cm)で、点線
はセメント吹出し(%)である。第2図は接着力
(ネジリトルク)とセメント吹出し測定用試料の
縦断面図である。
1……磁器円筒、2……段付円柱鉄芯、2a…
…径8.5mm部の円柱鉄芯、2b……径5.2mm部の円
柱鉄芯、3……接着剤、4……磁器と金具の境界
線。
Figure 1 shows the adhesion force (screw torque) and cement blowout depending on the amount of additives shown in Table 1, where the solid line is the adhesive force (Kg cm) and the dotted line is the cement blowout (%). FIG. 2 is a longitudinal cross-sectional view of a sample for measuring adhesive force (screw torque) and cement blowout. 1...Porcelain cylinder, 2...Stepped cylindrical iron core, 2a...
...Cylindrical iron core with a diameter of 8.5 mm, 2b...Cylindrical iron core with a diameter of 5.2 mm, 3...Adhesive, 4...Boundary line between porcelain and metal fittings.
Claims (1)
との等量混合物99〜90重量%と105μ以下のフリ
ツト1ないし10重量%とを混合してなるケイ酸ソ
ーダ系接着剤。 2 上記フリツトがソーダガラス粉末 硼ケイ酸
ガラス粉末、鉛ガラス粉末の1種又は2種以上よ
りなる特許請求範囲第1項記載のケイ酸ソーダ系
接着剤。[Claims] 1. Sodium silicate based mixture of 99 to 90% by weight of an equal mixture of metal oxide powder and No. 1 or No. 2 sodium silicate and 1 to 10% by weight of frits of 105μ or less. glue. 2. The sodium silicate adhesive according to claim 1, wherein the frit is made of one or more of soda glass powder, borosilicate glass powder, and lead glass powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8345778A JPS559674A (en) | 1978-07-07 | 1978-07-07 | Sodium silicate adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8345778A JPS559674A (en) | 1978-07-07 | 1978-07-07 | Sodium silicate adhesive |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS559674A JPS559674A (en) | 1980-01-23 |
JPS6115907B2 true JPS6115907B2 (en) | 1986-04-26 |
Family
ID=13802981
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8345778A Granted JPS559674A (en) | 1978-07-07 | 1978-07-07 | Sodium silicate adhesive |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS559674A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58199761A (en) * | 1982-05-13 | 1983-11-21 | 大塚化学薬品株式会社 | Alkali silicate composition, heat solidified matter and manufacture |
WO2000044686A1 (en) * | 1999-01-27 | 2000-08-03 | Weihua Jin | Artificial stone employing waste glass |
CN103198982B (en) * | 2013-03-07 | 2015-02-18 | 上海电气钠硫储能技术有限公司 | Inorganic gelling agent for fuse for sodium-sulfur cell module and preparation technology thereof |
CN105315900B (en) * | 2015-11-17 | 2017-11-10 | 申梓刚 | A kind of ceramic seal glue and preparation method thereof |
-
1978
- 1978-07-07 JP JP8345778A patent/JPS559674A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS559674A (en) | 1980-01-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5332432A (en) | Inorganic adhesive composition | |
US4017321A (en) | Void free electrical cement-concrete | |
JPS6218494B2 (en) | ||
JPH0726166A (en) | Aqueous heat-resistant paint and heat-resistant coating layer | |
US3389002A (en) | Heat and corrosion resistant coating composition | |
JPS6115907B2 (en) | ||
US3480452A (en) | Cordierite ceramic process and product | |
CN102811968A (en) | Reinforced composite material, method of preparing the same, its use for preparing manufactured products, as well as manufactured products formed in this way and their use | |
CA1196700A (en) | High voltage porcelain insulators | |
JPS6115908B2 (en) | ||
US4073657A (en) | Glass for semiconductors | |
US2103746A (en) | Light weight construction composition | |
CN114804634A (en) | Colored glaze for porcelain insulator and preparation method thereof | |
US3957519A (en) | Acid and heat-resistant mortars for cellular glass compositions and products therefrom | |
US2972544A (en) | Glass composition | |
US2839414A (en) | Low loss ceramic insulators | |
RU1306454C (en) | Composite material for resistance heater | |
US4033776A (en) | Composition of ceramic material | |
JP2839365B2 (en) | Non-combustible cement for electronic components and method for producing the same | |
JPH05311091A (en) | Water-resistant inorganic binder | |
US3320043A (en) | Method for making thin film glass elements | |
JPH07133136A (en) | Glass paste and its production | |
US3278660A (en) | Light-weight structural units and method for producing the same | |
CN115028406B (en) | High-aluminum porcelain insulator for oil smoke purifier and preparation method thereof | |
SU790022A1 (en) | Composition material |