JPH03103461A - Porous epoxy resin molded article - Google Patents
Porous epoxy resin molded articleInfo
- Publication number
- JPH03103461A JPH03103461A JP1240171A JP24017189A JPH03103461A JP H03103461 A JPH03103461 A JP H03103461A JP 1240171 A JP1240171 A JP 1240171A JP 24017189 A JP24017189 A JP 24017189A JP H03103461 A JPH03103461 A JP H03103461A
- Authority
- JP
- Japan
- Prior art keywords
- water
- resin molded
- curing
- epoxy compound
- mold
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 title claims description 9
- 229920000647 polyepoxide Polymers 0.000 title claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000011324 bead Substances 0.000 claims abstract description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 239000004593 Epoxy Substances 0.000 claims abstract description 14
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 239000000839 emulsion Substances 0.000 claims abstract description 11
- 239000000945 filler Substances 0.000 claims abstract description 11
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 9
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 8
- 229920005989 resin Polymers 0.000 claims description 13
- 239000011347 resin Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 9
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract description 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 abstract description 3
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract description 3
- -1 sorbitan fatty acid ester Chemical class 0.000 abstract description 3
- 238000004381 surface treatment Methods 0.000 abstract description 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 2
- 229930195729 fatty acid Natural products 0.000 abstract description 2
- 239000000194 fatty acid Substances 0.000 abstract description 2
- 239000012528 membrane Substances 0.000 abstract 1
- 238000007569 slipcasting Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 8
- 238000005266 casting Methods 0.000 description 6
- 238000001914 filtration Methods 0.000 description 3
- 239000011505 plaster Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- 238000005273 aeration Methods 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000006082 mold release agent Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Landscapes
- Filtering Materials (AREA)
- Aeration Devices For Treatment Of Activated Polluted Sludge (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野コ
本発明は、型材、濾過材、散気材、隔膜等の広範な用途
に使用可能な多孔質エポキシ樹脂或形物に関し、特に高
圧鋳込み用成形型としての使用に適した通水量を有する
多孔質エポキシ樹脂成形物に関する。Detailed Description of the Invention [Field of Industrial Application] The present invention relates to a porous epoxy resin or molded product that can be used in a wide range of applications such as mold materials, filtration materials, air diffusers, diaphragms, etc., particularly for high-pressure casting. The present invention relates to a porous epoxy resin molded product having a water flow rate suitable for use as a mold.
[従来技術および発明が解決しようとする課題]型材、
濾過材、散気材、隔膜等に使用する多孔質体としては、
金属粉末、熱可塑性樹脂粉末、無機物粉末等の焼結体や
石膏、セメント類の水和硬化物、多孔質合成樹脂等が挙
げられるが、寸法精度、気孔分布の均一性、耐久性等の
観点から、多孔質合成樹脂が好適に使用される。[Prior art and problems to be solved by the invention] Profile material,
Porous materials used for filtration media, air diffusers, diaphragms, etc.
Examples include sintered bodies of metal powder, thermoplastic resin powder, inorganic powder, etc., hydrated hardened bodies of plaster and cement, porous synthetic resins, etc., but from the viewpoint of dimensional accuracy, uniformity of pore distribution, durability, etc. Therefore, porous synthetic resins are preferably used.
多孔質合戊樹脂としては、例えば特開昭63−188O
f)3号公報において、エポキシ化合物、硬化剤、乳化
剤、水または水と表面活性剤との混合物、および充填剤
から或る混a溶液を硬化して得られる多孔質エポキシ樹
脂成形物が開示されており、前記表面活性剤としてフッ
素系表面活性剤が例示されている。As the porous synthetic resin, for example, JP-A-63-188O
f) Publication No. 3 discloses a porous epoxy resin molded product obtained by curing a certain mixed aqueous solution from an epoxy compound, a curing agent, an emulsifier, water or a mixture of water and a surfactant, and a filler. The above-mentioned surfactant is exemplified by a fluorine-based surfactant.
しかし、上記樹脂成形物は、通水量が少ない等の課題を
有し、高圧鋳込み用成形型として使用することはできな
い。However, the resin molded product has problems such as a small amount of water passing through, and cannot be used as a mold for high-pressure casting.
そこで、本発明は、型材、濾過材、散気材、隔膜等に使
用可能であり、特に高圧鋳込み用成形型として使用する
場合に必要とされる通水ユを有する多孔質エポキシ樹脂
成形物を提供することを目的とする。Therefore, the present invention provides a porous epoxy resin molded product that can be used as a molding material, a filtering material, an aeration material, a diaphragm, etc., and that has a water passageway that is particularly required when used as a mold for high-pressure casting. The purpose is to provide.
[課題を解決するための手段]
本発明者等は上記目的を達成するために、鋭意研究を行
ったところ、シランカップリング剤によって表面処理を
施したアクリルビーズを充填剤として用いることにより
、多孔質エポキシ樹脂の通水量等が向上するという知見
を得て、本発明に至ったものである。[Means for Solving the Problems] In order to achieve the above object, the present inventors conducted intensive research and found that by using acrylic beads surface-treated with a silane coupling agent as a filler, porous The present invention was developed based on the knowledge that the amount of water passing through a high-quality epoxy resin is improved.
すなわち本発明は、エポキシ化合物、硬化剤、乳化剤、
水および充填剤から成るエマルジョン溶液を硬化して得
られる多孔質エポキシ樹脂成形物であって、前記充填剤
がシランカップリング剤によって表面処理を施したアク
リルビーズであることを特徴とする前記樹脂成形物であ
る。That is, the present invention provides an epoxy compound, a curing agent, an emulsifier,
A porous epoxy resin molded product obtained by curing an emulsion solution consisting of water and a filler, wherein the filler is acrylic beads surface-treated with a silane coupling agent. It is a thing.
エポキシ化合物としては、一般にはビスフェノールA型
ジグリシジルエーテル、ビスフェノールF型ジグリシジ
ルエーテル等が好適に使用される。As the epoxy compound, bisphenol A type diglycidyl ether, bisphenol F type diglycidyl ether, etc. are generally suitably used.
前記化合物は単独で用いても良いし、必要に応じて複数
種類を併用しても良い。The above-mentioned compounds may be used alone or in combination of multiple types as required.
硬化剤としては、ジエチレントリアミン(DETA)、
トリエチレンテトラミン(TETA)等が好適に使用さ
れる。これらの硬化剤は単独で用いても良いし、必要に
応じて複数種類を併用しても良い。硬化剤の添加量はエ
ポキシ化合物100重量部に対して好ましくは25〜4
5重量部、最も好ましくは35重量部である。As a curing agent, diethylenetriamine (DETA),
Triethylenetetramine (TETA) and the like are preferably used. These curing agents may be used alone, or in combination if necessary. The amount of curing agent added is preferably 25 to 4 parts by weight per 100 parts by weight of the epoxy compound.
5 parts by weight, most preferably 35 parts by weight.
乳化剤としては、ソルビタン脂肪酸エステル、ポリオキ
シエチレンオレイルエーテル等が用いられる。これらの
乳化剤は単独で用いても良いし、必要に応じて複数種類
を併用しても良い。As the emulsifier, sorbitan fatty acid ester, polyoxyethylene oleyl ether, etc. are used. These emulsifiers may be used alone or in combination if necessary.
水の添加量はエポキシ化合物および硬化剤の合計量10
0重量部に対して30〜50重量部が好ましい。The amount of water added is the total amount of epoxy compound and curing agent 10
It is preferably 30 to 50 parts by weight relative to 0 parts by weight.
充填材としては、アクリルビーズが使用され、平均粒径
80〜120μmのものが好ましい。アクリルビーズの
添加量はエポキシ化合物100重量部に対して80〜1
20重量部が好ましい。As the filler, acrylic beads are used, preferably having an average particle size of 80 to 120 μm. The amount of acrylic beads added is 80 to 1 per 100 parts by weight of the epoxy compound.
20 parts by weight is preferred.
シランカップリング剤としては、3−アミノブロピルト
リエトキシシラン、3−グリシドオキシプ口ピルトリエ
トキシシラン等が好ましい。前記化合物は単独で用いて
も良いし、必要に応じて複数種類を併用しても良い。シ
ランカップリング剤の添加量はアクリルビーズl00重
量部に対して0.5〜2重量部が好ましい。As the silane coupling agent, 3-aminopropyltriethoxysilane, 3-glycidoxypyltriethoxysilane, etc. are preferred. The above-mentioned compounds may be used alone or in combination of multiple types as required. The amount of the silane coupling agent added is preferably 0.5 to 2 parts by weight per 100 parts by weight of acrylic beads.
本発明の樹脂或形物は、上記のエポキシ化合物、硬化剤
、乳化剤、水、およびシランカップリング剤で表面処理
したアクリルビーズから成るエマルジョン溶液を硬化し
て得られるものである。The resin shaped product of the present invention is obtained by curing an emulsion solution consisting of acrylic beads surface-treated with the above-mentioned epoxy compound, curing agent, emulsifier, water, and silane coupling agent.
エマルジョン溶液を硬化する方法は特に限定されないが
、以下に一例を挙げる。Although the method of curing the emulsion solution is not particularly limited, an example is given below.
目止め用の樹脂を塗布し、さらに疏水性の離型剤を塗布
した樹脂石膏型に上記エマルジョン溶液を流し込み50
℃に加熱して半硬化させ脱型する。Pour the emulsion solution into a resin plaster mold coated with a sealing resin and further coated with a hydrophobic mold release agent for 50 minutes.
Heat to ℃ to semi-cure and demold.
次に、この半硬化された混合物を水中に入れ真空脱泡機
で水洗いすることにより、混合物中に残留している乳化
剤等を洗いおとす。Next, this semi-hardened mixture is placed in water and washed with water using a vacuum deaerator to wash away the emulsifier and the like remaining in the mixture.
さらに、水洗された混合物を60℃に加熱して完全に硬
化させて、樹脂成形物を得る。Furthermore, the water-washed mixture is heated to 60° C. to completely cure it to obtain a resin molded product.
[実施例コ
以下、本発明を実施例および比較例に基づいて具体的に
説明する。なお、以下の記載において、部は重量部を意
味する。[Examples] Hereinafter, the present invention will be specifically explained based on Examples and Comparative Examples. In addition, in the following description, parts mean parts by weight.
実施例1〜9
(アクリルビーズの表面処理)
水75部中に、第1表に示す量のアクリルビーズ(粒径
100μm1商品名;ダイヤナールBRレジンBR−8
7 、三菱レーヨン■社製)を添加し、さらに第1表に
示すシランカップリング剤(チッソ株社製)をアクリル
ビーズ100部に対して1部添加する。Examples 1 to 9 (Surface treatment of acrylic beads) Into 75 parts of water, acrylic beads (particle size 100 μm 1, trade name: Dianal BR Resin BR-8) were added in an amount shown in Table 1.
7, manufactured by Mitsubishi Rayon ■ Co., Ltd.), and further added 1 part of the silane coupling agent shown in Table 1 (manufactured by Chisso Co., Ltd.) per 100 parts of acrylic beads.
その後、上水を捨て、前記アクリルビーズを60〜80
℃に約12時間保持して乾燥させた後、42メッシュの
ふるいに通して分級して、アクリルビーズの表面処理を
終了する。After that, discard the tap water and add 60 to 80 acrylic beads.
After drying by keeping at a temperature of about 12 hours, the beads are classified through a 42-mesh sieve to complete the surface treatment of the acrylic beads.
(エマルジジン溶液の調製)
水20部中に、変性エポキシ化合物(商品名;インキャ
ストTR−100、アイエヌテクニカルラボ■社製)1
00部を添加し、約1分間攪拌して均一なエマルジョン
溶液aを調製する。(Preparation of emulzidine solution) In 20 parts of water, add 1 part of a modified epoxy compound (trade name: Incast TR-100, manufactured by NI Technical Lab ■).
00 parts and stirred for about 1 minute to prepare a uniform emulsion solution a.
一方、水20部中に、硬化剤である変性脂肪族ポリアミ
ン(商品名;インキャストTI−104、アイエヌテク
ニカルラボ■社製)をエポキシ化合物100部に対して
35部添加し、約1分間攪拌して均一なエマルジョン溶
液bを調製する。Meanwhile, 35 parts of modified aliphatic polyamine (trade name: Incast TI-104, manufactured by NI Technical Lab), which is a curing agent, was added to 20 parts of water per 100 parts of the epoxy compound, and the mixture was stirred for about 1 minute. Prepare a uniform emulsion solution b.
さらに、前記溶液aと前記溶液bとを混合し、約1分間
攪拌して均一なエマルジョン溶液Cを調製する。Further, the solution a and the solution b are mixed and stirred for about 1 minute to prepare a uniform emulsion solution C.
溶液aおよび溶液bの調製において用いた水の総量は4
0部であり、これはエポキシ化合物と硬化剤の合計ユを
100部とした場合、30部である。The total amount of water used in preparing solution a and solution b is 4
This is 30 parts when the total amount of the epoxy compound and curing agent is 100 parts.
(エマルジョン溶液と充填剤とから成る混合物の硬化)
前記溶液Cに、表面処理を施したアクリルビーズを加え
、約1分間攪拌して均一な混合物とし、直ちにこれを離
型剤を塗布した石膏ケース型へ注入する。(Curing of a mixture consisting of an emulsion solution and a filler) Surface-treated acrylic beads were added to the solution C, stirred for about 1 minute to form a homogeneous mixture, and immediately mixed into a plaster case coated with a mold release agent. Pour into mold.
注入した混合物を乾燥機内に50℃で3峙間保持した後
、脱型し、水中に入れ、真空脱泡機で約6分間脱泡し、
水洗する。水洗した混合物を乾燥機内に60℃で4時間
以上保持する。The injected mixture was kept in a dryer at 50°C for 3 hours, then demolded, placed in water, and defoamed for about 6 minutes with a vacuum defoamer.
Wash with water. The water-washed mixture is kept in a dryer at 60° C. for 4 hours or more.
上記操作において、エポキシ化合物、硬化剤、充填剤お
よび水は常温より5℃以上高温にしておく 。In the above operation, the epoxy compound, curing agent, filler, and water are kept at a temperature 5° C. or more higher than room temperature.
得られた樹脂成形物を厚さ20111+1,直径80m
の円板状に加工し、これに4 Kg / cdの加圧水
を負荷させて通水量を測定し、その結果を第1表および
第1図に示した。The resulting resin molded product has a thickness of 20111+1 and a diameter of 80 m.
The material was processed into a disk shape, and 4 kg/cd of pressurized water was loaded onto it to measure the water flow rate. The results are shown in Table 1 and Figure 1.
また、樹脂戊形物を厚さ10all1%幅10鷹、長さ
90mに加工して、引張強度も測定し、その結果を第1
表および第2図に示した。In addition, we processed the resin moldings to a thickness of 10all 1%, a width of 10m, and a length of 90m, and measured the tensile strength.
It is shown in the table and FIG.
比較例1〜3
アクリルビーズの表面処理をしない以外は実施例1〜3
と同様にして、第1表に示すアクリルビーズを用いてエ
ポキシ樹脂成形物を得た。Comparative Examples 1-3 Examples 1-3 except that the acrylic beads were not surface treated
In the same manner as above, epoxy resin molded products were obtained using the acrylic beads shown in Table 1.
比較例1〜3に関する各種測定値を実施例1〜3と同様
に第1表に示した。また、比較例2〜3については、通
水量を第1図に、引張強度を第2図にもそれぞれ示した
。Various measured values regarding Comparative Examples 1 to 3 are shown in Table 1 similarly to Examples 1 to 3. Further, for Comparative Examples 2 and 3, the water flow rate is shown in FIG. 1, and the tensile strength is also shown in FIG. 2, respectively.
第1表に示されるように、実施例1〜9の樹脂成形物は
、高圧鋳込み用成形型に要求される5.Oj/分以上の
通水量を有する。また、引張強度は32K9/C一以上
であり、これも高圧鋳込み用成形型として使用するに充
分な値である。As shown in Table 1, the resin molded products of Examples 1 to 9 meet the requirements of 5. It has a water flow rate of Oj/min or more. Further, the tensile strength is 32K9/C or more, which is also a value sufficient for use as a mold for high-pressure casting.
これに対して、比較,例1〜3の樹脂成形物は、通水量
が2.8〜4.14/分であるため、高圧鋳込み用或形
型に使用することは出来ない。On the other hand, the resin molded products of Comparative Examples 1 to 3 have water flow rates of 2.8 to 4.14/min, and therefore cannot be used in certain molds for high-pressure casting.
また、第1図および第2図に実施例2、3、5、6、8
、9および比較例2、3の樹脂或形物の通水量および引
張強度をグラフ化して、実施例と比較例の対比を容易に
することにより、本発明の樹脂成形物が従来の樹脂成形
物に比して、通水量および引張強度の点で優れているこ
とがより明白になる。In addition, Examples 2, 3, 5, 6, and 8 are shown in FIGS. 1 and 2.
. The superiority of water permeation and tensile strength compared to the above becomes clearer.
[発明の効果]
以上、説明したように、本発明の樹脂成形物は、優れた
通水量および引張強度を有し、型材、濾過材、散気材、
隔膜等の広範な用途に使用可能であり、特に高圧鋳込み
用或形型としての使用に適している。[Effects of the Invention] As explained above, the resin molded product of the present invention has excellent water flow rate and tensile strength, and can be used as a mold material, a filter material, an aeration material,
It can be used in a wide range of applications such as diaphragms, and is particularly suitable for use as a mold for high-pressure casting.
第1図は、実施例2、3、5、6、8、9および比較例
2、3の樹脂成形物の通水,量を示すグラフであり、
第2図は、実施例2、3、5、6、8、9および比較例
2、3の樹脂成形物の引張強度を示すグラフである。FIG. 1 is a graph showing the amount of water passed through the resin molded products of Examples 2, 3, 5, 6, 8, and 9 and Comparative Examples 2 and 3. 5 is a graph showing the tensile strength of resin molded products of Comparative Examples 5, 6, 8, 9 and Comparative Examples 2 and 3.
Claims (1)
から成るエマルジョン溶液を硬化して得られる多孔質エ
ポキシ樹脂成形物であって、前記充填剤がシランカップ
リング剤によって表面処理を施したアクリルビーズであ
ることを特徴とする前記樹脂成形物。1. A porous epoxy resin molded product obtained by curing an emulsion solution consisting of an epoxy compound, a curing agent, an emulsifier, water, and a filler, and the filler is an acrylic bead whose surface has been treated with a silane coupling agent. The resin molded article characterized in that:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1240171A JPH03103461A (en) | 1989-09-18 | 1989-09-18 | Porous epoxy resin molded article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1240171A JPH03103461A (en) | 1989-09-18 | 1989-09-18 | Porous epoxy resin molded article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03103461A true JPH03103461A (en) | 1991-04-30 |
Family
ID=17055538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1240171A Pending JPH03103461A (en) | 1989-09-18 | 1989-09-18 | Porous epoxy resin molded article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03103461A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5242635A (en) * | 1991-08-16 | 1993-09-07 | Toto Ltd. | Method of producing porous material having open pores |
-
1989
- 1989-09-18 JP JP1240171A patent/JPH03103461A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5242635A (en) * | 1991-08-16 | 1993-09-07 | Toto Ltd. | Method of producing porous material having open pores |
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