JPS6054265B2 - inorganic molding material - Google Patents
inorganic molding materialInfo
- Publication number
- JPS6054265B2 JPS6054265B2 JP51071406A JP7140676A JPS6054265B2 JP S6054265 B2 JPS6054265 B2 JP S6054265B2 JP 51071406 A JP51071406 A JP 51071406A JP 7140676 A JP7140676 A JP 7140676A JP S6054265 B2 JPS6054265 B2 JP S6054265B2
- Authority
- JP
- Japan
- Prior art keywords
- molding material
- weight
- glass
- molding
- binder
- 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
- 239000012778 molding material Substances 0.000 title claims description 19
- 239000011521 glass Substances 0.000 claims description 27
- 239000011230 binding agent Substances 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 10
- 239000011256 inorganic filler Substances 0.000 claims description 5
- 229910003475 inorganic filler Inorganic materials 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000009835 boiling Methods 0.000 description 13
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 238000002156 mixing Methods 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 238000009413 insulation Methods 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- 239000010452 phosphate Substances 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- -1 metaborate) Chemical compound 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000010137 moulding (plastic) Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 241000975357 Salangichthys microdon Species 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- ZPPSOOVFTBGHBI-UHFFFAOYSA-N lead(2+);oxido(oxo)borane Chemical compound [Pb+2].[O-]B=O.[O-]B=O ZPPSOOVFTBGHBI-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
Landscapes
- Glass Compositions (AREA)
- Compositions Of Oxide Ceramics (AREA)
Description
【発明の詳細な説明】
本発明は耐熱性、耐水性に優れた無機成形材料に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an inorganic molding material with excellent heat resistance and water resistance.
既存のプラスチック成形材料は優れた性能を有し広範に
利用されているが、耐熱性、不燃性という点においてか
なり改良はなされているもののまだ充分とは云い難く、
特に、最近の火災時の発生ガスの問題や安全性からの耐
熱性に対する要求に応えるのは難しい。Existing plastic molding materials have excellent performance and are widely used, but although considerable improvements have been made in terms of heat resistance and nonflammability, they are still far from satisfactory.
In particular, it is difficult to meet the recent problem of gas generated during fires and the demand for heat resistance for safety reasons.
一方、耐熱、不燃という観点から無機系の成形材料ある
いは成形体としてセラミック、ガラス、セメント、けい
酸塩、りん酸塩などが知られているが、セラミックは高
温での焼成が必要なために収縮が大きく寸法精度が悪い
こと、あるいは金属を成形と同時に組込むことができな
いなどの欠点がある。On the other hand, ceramics, glass, cement, silicates, phosphates, etc. are known as inorganic molding materials or molded bodies from the viewpoint of heat resistance and nonflammability, but ceramics shrink due to the need for firing at high temperatures. There are disadvantages such as the large size and poor dimensional accuracy, and the inability to assemble the metal at the same time as molding.
セメント、けい酸塩、りん酸塩を用いたものは耐水性が
悪いので高湿時の絶縁性の低下が著るしいという欠点が
ある。また、ガラスは700〜800℃の高温で成形し
なければならないので金型の耐熱性に問題がある。古く
からホウ酸鉛系の低融点ガラスを結合剤としこれにマイ
カ粉末を配合し、450〜600℃で成形できる成形材
料又は成形体として「マイカレツクス」があるが、これ
はガラス原料として鉛化合物を使用するのて毒性という
点から好ましくない。以上述べたような欠点を改良する
目的で本発明はなされたものである。Products using cement, silicates, and phosphates have poor water resistance, so they have the disadvantage that their insulation properties are significantly reduced in high humidity. Furthermore, since glass must be molded at a high temperature of 700 to 800°C, there is a problem with the heat resistance of the mold. For a long time, there is a molding material or molded object called "mica rex" which is made by using lead borate-based low melting point glass as a binder and blending it with mica powder, and which can be molded at 450 to 600 degrees Celsius. It is not preferable to use it from the viewpoint of toxicity. The present invention has been made for the purpose of improving the above-mentioned drawbacks.
すなわち、鉛等の毒性を有する物質を含まない低融点ガ
ラスを結合剤としこれに無機充填材を配合してなる耐熱
性、耐水性の成形材料を提供するものである。本発明に
よりJ成形材料は無機物主体であるので不燃であるとい
う特徴を有する。以下さらに詳細に本発明を説明する。
本発明の低融点ガラス結合剤とは水を除く餡重量%(以
下%と略す)以上の組成がNa。That is, the present invention provides a heat-resistant and water-resistant molding material made by using low-melting point glass as a binder, which does not contain toxic substances such as lead, and incorporating an inorganic filler therein. According to the present invention, the J molding material has the characteristic that it is nonflammable because it is mainly composed of inorganic substances. The present invention will be explained in further detail below.
The low melting point glass binder of the present invention has a composition in which the weight of the bean paste excluding water is at least % (hereinafter abbreviated as %) or more.
Oとして; 7.5〜14%、ZnOとして20〜50
%、B。03として0〜35%、P2O5として35〜
65%のガラス組成物である。As O; 7.5-14%, as ZnO 20-50
%,B. 0-35% as 03, 35-35% as P2O5
65% glass composition.
以上の組成において各数値限定がなされた理由は以下の
通りである。The reason why each numerical limitation was made in the above composition is as follows.
Na2Oが7.5%未満ではガラスの軟化温度が高く、
従つて成形温度も高くなる。When Na2O is less than 7.5%, the softening temperature of the glass is high;
Therefore, the molding temperature also increases.
14%を越えると耐水性が低下する傾向が生じる。If it exceeds 14%, water resistance tends to decrease.
ZrlOが20%未満では耐水性が著しく低下し、50
%を越えると結晶化しやすくなり軟化温度も高くなる。
B.O3は軟化温度を下げ、流動しやすくする傾向があ
るが35%を超えると耐水性が低下する。P2O5は3
5%未満では軟化温度が高くなり、成形性の点から好ま
しくない。65%を超えると耐水性が著しく悪くなる。If the ZrlO content is less than 20%, the water resistance decreases significantly, and 50%
%, crystallization tends to occur and the softening temperature increases.
B. O3 tends to lower the softening temperature and make it easier to flow, but if it exceeds 35%, water resistance decreases. P2O5 is 3
If it is less than 5%, the softening temperature becomes high, which is not preferable from the viewpoint of moldability. When it exceeds 65%, water resistance deteriorates significantly.
以上の組成のガラス結合剤を得るための原料としては上
記の酸化物を成す元素を含み、焼成(熔融)により上記
ガラス結合剤配合中の酸化物になるような化合物であれ
ば使用可能である。As a raw material for obtaining the glass binder having the above composition, any compound can be used as long as it contains the elements forming the above oxide and becomes the oxide in the glass binder formulation when fired (melted). .
例えば炭酸ソーダ、りん酸ソーダ(正りん酸塩、縮合り
ん酸塩)、硝酸ソーダ、ホウ酸ソーダ(メタホウ酸塩を
含む)酸化亜鉛、水酸化亜鉛、炭酸亜鉛、(正りん酸塩
、縮合りん酸塩)ホウ酸亜鉛、りん酸、りん酸アンモニ
ウム、ホウ酸などが用いられる。以上の各原料を用いて
目的のガラス結合剤を得るには、各原料を所定の割合で
配合し、常温で、必要であれば加熱して充分粉砕混合す
る。For example, soda carbonate, sodium phosphate (orthophosphate, condensed phosphate), sodium nitrate, sodium borate (including metaborate), zinc oxide, zinc hydroxide, zinc carbonate, (orthophosphate, condensed phosphate), Acid salts) Zinc borate, phosphoric acid, ammonium phosphate, boric acid, etc. are used. In order to obtain the desired glass binder using each of the above raw materials, the raw materials are blended in a predetermined ratio and thoroughly pulverized and mixed at room temperature and heated if necessary.
この混一合物を800〜1300℃て1〜4時間熔融さ
せる。必要があればば途中て攪拌する。炭酸塩、アンモ
ニウム塩あるいは水を含むものを原料として用いる場合
は原料混合後150〜500℃で1〜3時間前焼成して
揮発分を除去した後、熔融したほうがるつぼ!からふき
こぼれなどが起らず安全かつ好都合である。熔融したガ
ラスは水中に投じるか厚い鉄板上に流して急冷する。得
られたガラスをボール・ミルあるいは振動ミルなど適当
な装置で微粉砕する。粒径は細かいほど充填材との混合
に好都合で5ある。限定するものではないが150μ以
下に微粉砕するほうが好ましい。こうして得られるガラ
ス結合剤は軟化温度290〜490℃のものである。本
発明て使用する無機充填材とは一般のプラスチック成形
材料に使用されるものと同様なもの4で、例えば炭酸カ
ルシウム、アルミナ、石英、珪石、硅砂、硅藻土、石綿
、ガラス繊維、ガラス・パウダー、ガラス●バルーン、
シラス●バルーン、雲母、タルク、クレーなど天然物、
合成物あるいは粒状、板状、繊維状、中空球状、棒状い
づれも使用可能でこれらは単独又は2種以上混合して使
用してもよい。これら無機充填材の使用量は前記ガラス
結合剤に対し0.1〜2.5倍量(重量)である。0.
1倍量より少なくても充分成形可能で耐水性、耐熱性か
らは、目的とするものは得られるが、強度の点でもろい
ために実用面から好ましいものではない。This mixture is melted at 800-1300°C for 1-4 hours. Stir in between if necessary. When using carbonate, ammonium salt, or water-containing raw materials as raw materials, it is better to pre-calcine them at 150-500℃ for 1-3 hours after mixing the raw materials to remove volatiles, and then melt them in a crucible! It is safe and convenient, as no boiling over occurs. The molten glass is thrown into water or poured onto a thick iron plate to cool it quickly. The resulting glass is pulverized using a suitable device such as a ball mill or a vibratory mill. The finer the particle size, the more convenient it is to mix with the filler. Although not limited to this, it is preferable to finely pulverize to 150 μm or less. The glass binder thus obtained has a softening temperature of 290-490°C. The inorganic fillers used in the present invention are similar to those used in general plastic molding materials, such as calcium carbonate, alumina, quartz, silica, silica sand, diatomaceous earth, asbestos, glass fiber, glass, etc. Powder, glass balloon,
Whitebait ●Natural products such as balloons, mica, talc, clay, etc.
Compounds, particles, plates, fibers, hollow spheres, and rods can be used, and these may be used alone or in combination of two or more. The amount of these inorganic fillers used is 0.1 to 2.5 times (by weight) the amount of the glass binder. 0.
Even if the amount is less than 1 times the amount, it can be sufficiently molded and the desired properties can be obtained in terms of water resistance and heat resistance, but it is not preferred from a practical point of view because it is brittle in terms of strength.
2h倍量を超えると流れが悪くなり緻密な成形品が得ら
れず耐水性、強度の点で実)用的でない。If the amount exceeds 2 hours, flow becomes poor and a dense molded product cannot be obtained, which is not practical in terms of water resistance and strength.
ガラス結合剤と充填材はボール・ミル、らいかい機など
適当な装置を用いて混合する。こうして得られた成形材
料をガラス結合剤の軟化温度以上に加熱して加圧成形す
る。The glass binder and filler are mixed using suitable equipment such as a ball mill or a mill. The molding material thus obtained is heated to a temperature equal to or higher than the softening temperature of the glass binder and then pressure molded.
成形方法と・しては圧縮成形、トランスファー成形、射
出成形いづれの方法でもよい。成形条件は成形方法、成
形品の形状などによつて異なるが圧縮成形の場合を例に
示すと350〜500℃、100〜1000k9/Cl
tll〜1紛の条件である。こうして成形したものは耐
水性は良好で300℃以上の耐熱性を有し絶縁性、機械
的強度も良好である。The molding method may be compression molding, transfer molding, or injection molding. Molding conditions vary depending on the molding method, shape of the molded product, etc., but in the case of compression molding, for example, 350-500℃, 100-1000k9/Cl
This is a condition of tll to 1 minute. The molded product has good water resistance, heat resistance of 300° C. or more, and good insulation and mechanical strength.
また成形時に金属を組み込むことも可能である。無機物
が主体であるので不燃性であることは当然である。した
がつて本発明による無機成形材料は耐熱性、不燃性を要
求される構造材料、絶縁材料としての応用が考えられる
。以下に実施例を示す。It is also possible to incorporate metal during molding. Since it is mainly composed of inorganic substances, it is natural that it is nonflammable. Therefore, the inorganic molding material according to the present invention can be used as a structural material or an insulating material that requires heat resistance and nonflammability. Examples are shown below.
実施例1
重りん酸亜鉛〔Zn(H2PO4)2・2H20〕33
7g炭酸ソーダ〔Na2cO3〕54.7g1酸化亜鉛
〔ZnO〕38.1gを混合し、350℃で1時間前焼
成し、次に電気炉にて1100〜1200℃にて1時間
溶融後、鉄板上に流して急冷した。Example 1 Zinc heavy phosphate [Zn(H2PO4)2.2H20] 33
7g Soda carbonate [Na2cO3] 54.7g 1 Zinc oxide [ZnO] 38.1g were mixed, pre-fired at 350℃ for 1 hour, then melted in an electric furnace at 1100-1200℃ for 1 hour, and then placed on an iron plate. I rinsed it off and cooled it down quickly.
室温に冷却後、微粉砕し100メッシュ全通にした。得
られたガラスの軟化温度は340℃であつた。このガラ
ス結合剤粉末60gとアルミナ40gを振動ミルにて3
紛間混合し目的とする成形材料を得た。この成形材料1
6gを50WL/7nΦ円板成形用金型に投入し、36
0′C9OOk9/Cltl5分の条件で成形し厚さ2
.40771./Trl,の円板を得た。After cooling to room temperature, it was finely pulverized to a 100-mesh powder. The softening temperature of the obtained glass was 340°C. 60g of this glass binder powder and 40g of alumina were mixed in a vibration mill.
The desired molding material was obtained by powder mixing. This molding material 1
Put 6g into a 50WL/7nΦ disc mold, and
Molded under the conditions of 0'C9OOk9/Cltl for 5 minutes to a thickness of 2
.. 40771. /Trl, was obtained.
比重3.37、煮沸吸水率0%、煮沸後の外観変化はな
く、また300゜Cで4m間熱処理しても何ら変化なか
つた。絶縁抵抗は常態で1014Ω、煮沸後1012Ω
であつた。The specific gravity was 3.37, the boiling water absorption was 0%, there was no change in appearance after boiling, and there was no change at all even after heat treatment at 300°C for 4 m. Insulation resistance is 1014Ω under normal conditions and 1012Ω after boiling.
It was hot.
実施例2
実施例1で得たガラス結合剤60gと硅石粉末(325
メッシュ全通品)40gを振動ミルで3紛間混合し成形
材料を得た。Example 2 60 g of the glass binder obtained in Example 1 and silica powder (325
A molding material was obtained by mixing 3 powders of 40 g of all mesh products in a vibrating mill.
実施例1と同様な条件50n1/mΦの円板を成形した
。A disk having a diameter of 50 n1/mΦ was molded under the same conditions as in Example 1.
厚み280rn/m1比重2.87、煮沸吸水率0.0
1%、煮沸後の外観変化なく300℃、北時間の熱処理
後も何ら変化なかつた。絶縁抵抗は常態で1014Ω、
煮沸後1012Ωであつた。実施例3
実施例1のガラス結合剤60gと雲母粉末40gを振動
ミルで3紛混合して得た成形材料を同様に成形して厚さ
2.807TI./TrLl比重2.88の円板を得た
。Thickness 280rn/m1 Specific gravity 2.87, boiling water absorption rate 0.0
1%, there was no change in appearance after boiling, and no change occurred after heat treatment at 300°C, Northern Time. Insulation resistance is normally 1014Ω,
It was 1012Ω after boiling. Example 3 A molding material obtained by mixing 60 g of the glass binder of Example 1 and 40 g of mica powder in a vibration mill was similarly molded to a thickness of 2.807 TI. /TrLl A disk with a specific gravity of 2.88 was obtained.
煮沸吸水率0.6%、煮沸後および300℃、北時間の
熱処理後も何ら変化なかつた。絶縁抵抗は常態で101
4Ω、煮沸後1010Ωてあつた。実施例4
重りん酸亜鉛〔Zn(H2PO4)2・2H20〕37
9g1無水ほう砂28.7g1炭酸ソーダ53.3g1
酸化亜鉛58.9gを混合し350℃で1時間前焼成し
次に電気炉にて1100〜1200℃にて1時間溶融後
鉄板上に流して急冷した。The boiling water absorption rate was 0.6%, and there was no change after boiling and after heat treatment at 300° C., Northern Time. Insulation resistance is normally 101
4Ω, and after boiling it was 1010Ω. Example 4 Zinc heavy phosphate [Zn(H2PO4)2.2H20] 37
9g1 anhydrous borax 28.7g1 soda carbonate 53.3g1
58.9 g of zinc oxide was mixed and pre-fired at 350°C for 1 hour, then melted in an electric furnace at 1100-1200°C for 1 hour, and then poured onto an iron plate to be rapidly cooled.
これを微粉砕し100メッシュ全通にした。得られたガ
ラスの軟化温度は440℃であつた。このガラス結合剤
粉末60gと雲母粉末40gを振動ミルで3紛混合して
目的とする成形材料を得た。この成形材料16gを用い
て480′Cl9OOk9/CFl!、5分の条件で円
板(50n1/mΦ)を成形した。厚さ2.75m/m
、比重2.92、煮沸吸水率0.5%、煮沸後の外観変
化なく、300℃4時間熱処理しても何ら変化なかつた
。常態での絶縁抵抗1013Ω、煮沸後1010Ωであ
つた。実施例5
重りん酸亜鉛〔Zn(H2PO4)2・2H20〕25
2.6g1炭酸ソーダ88.9g1酸化亜鉛172.6
g1を混合し実施例1と同様にして軟化温度390℃の
ガラス結合剤粉末を得た。This was finely pulverized to 100 mesh. The softening temperature of the obtained glass was 440°C. A desired molding material was obtained by mixing 60 g of this glass binder powder and 40 g of mica powder in a vibrating mill. Using 16 g of this molding material, 480'Cl9OOk9/CFl! A disk (50n1/mΦ) was molded under conditions of , 5 minutes. Thickness 2.75m/m
, specific gravity 2.92, boiling water absorption 0.5%, no change in appearance after boiling, no change at all even after heat treatment at 300°C for 4 hours. The insulation resistance was 1013Ω under normal conditions and 1010Ω after boiling. Example 5 Zinc heavy phosphate [Zn(H2PO4)2.2H20]25
2.6g 1 soda carbonate 88.9g 1 zinc oxide 172.6
A glass binder powder having a softening temperature of 390° C. was obtained in the same manner as in Example 1 by mixing G1.
このガラス結合剤50gにアルミナ50gを混合して成
形材料を得た。A molding material was obtained by mixing 50 g of alumina with 50 g of this glass binder.
Claims (1)
し、重量基準で0.1〜2.5倍量の無機充填材を添加
混合したことを特徴とする無機成形材料。 2 組成が、 Na_2O:7.5〜14重量% ZnO:20〜50重量% P_2O_5:35〜65重量% B_2O_3:35重量%以下配合 である低融点ガラス組成物粉末を結合剤とし、れに対し
、重量基準で0.1〜2.5倍量の無機充填材を添加混
合したことを特徴とする無機成形材料。[Claims] 1 A low melting point glass composition powder having the following composition: Na_2O: 7.5 to 14% by weight, ZnO: 20 to 50% by weight, P_2O_5: 35 to 65% by weight is used as a binder, and on the other hand, An inorganic molding material characterized in that an inorganic filler is added and mixed in an amount of 0.1 to 2.5 times on a weight basis. 2 A low melting point glass composition powder having a composition of Na_2O: 7.5 to 14% by weight, ZnO: 20 to 50% by weight, P_2O_5: 35 to 65% by weight, B_2O_3: 35% by weight or less is used as a binder, and An inorganic molding material characterized in that an inorganic filler is added and mixed in an amount of 0.1 to 2.5 times by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51071406A JPS6054265B2 (en) | 1976-06-16 | 1976-06-16 | inorganic molding material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51071406A JPS6054265B2 (en) | 1976-06-16 | 1976-06-16 | inorganic molding material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS52152907A JPS52152907A (en) | 1977-12-19 |
| JPS6054265B2 true JPS6054265B2 (en) | 1985-11-29 |
Family
ID=13459591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51071406A Expired JPS6054265B2 (en) | 1976-06-16 | 1976-06-16 | inorganic molding material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6054265B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62153659U (en) * | 1986-03-20 | 1987-09-29 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0974984B1 (en) * | 1998-07-20 | 2006-10-04 | Littelfuse Ireland Development Company Limited | Manufacture of varistors |
-
1976
- 1976-06-16 JP JP51071406A patent/JPS6054265B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62153659U (en) * | 1986-03-20 | 1987-09-29 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS52152907A (en) | 1977-12-19 |
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