JPS595535B2 - Method for manufacturing glass molded bodies - Google Patents
Method for manufacturing glass molded bodiesInfo
- Publication number
- JPS595535B2 JPS595535B2 JP10986280A JP10986280A JPS595535B2 JP S595535 B2 JPS595535 B2 JP S595535B2 JP 10986280 A JP10986280 A JP 10986280A JP 10986280 A JP10986280 A JP 10986280A JP S595535 B2 JPS595535 B2 JP S595535B2
- Authority
- JP
- Japan
- Prior art keywords
- release agent
- mold release
- phosphate
- glass molded
- 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.)
- Expired
Links
- 239000011521 glass Substances 0.000 title claims description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 238000000034 method Methods 0.000 title claims description 12
- 230000001050 lubricating effect Effects 0.000 claims description 37
- 239000006082 mold release agent Substances 0.000 claims description 34
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- 239000010439 graphite Substances 0.000 claims description 20
- 229910002804 graphite Inorganic materials 0.000 claims description 20
- 230000002378 acidificating effect Effects 0.000 claims description 18
- 229910001463 metal phosphate Inorganic materials 0.000 claims description 14
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 12
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 12
- 238000000465 moulding Methods 0.000 claims description 11
- 239000006060 molten glass Substances 0.000 claims description 9
- 239000003085 diluting agent Substances 0.000 claims description 6
- 239000012535 impurity Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 3
- 239000002075 main ingredient Substances 0.000 claims description 3
- 229910000151 chromium(III) phosphate Inorganic materials 0.000 claims description 2
- IKZBVTPSNGOVRJ-UHFFFAOYSA-K chromium(iii) phosphate Chemical compound [Cr+3].[O-]P([O-])([O-])=O IKZBVTPSNGOVRJ-UHFFFAOYSA-K 0.000 claims description 2
- QQFLQYOOQVLGTQ-UHFFFAOYSA-L magnesium;dihydrogen phosphate Chemical compound [Mg+2].OP(O)([O-])=O.OP(O)([O-])=O QQFLQYOOQVLGTQ-UHFFFAOYSA-L 0.000 claims description 2
- 229940035053 monobasic magnesium phosphate Drugs 0.000 claims description 2
- 229910000159 nickel phosphate Inorganic materials 0.000 claims description 2
- JOCJYBPHESYFOK-UHFFFAOYSA-K nickel(3+);phosphate Chemical compound [Ni+3].[O-]P([O-])([O-])=O JOCJYBPHESYFOK-UHFFFAOYSA-K 0.000 claims description 2
- 229910000166 zirconium phosphate Inorganic materials 0.000 claims description 2
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 claims description 2
- 238000007496 glass forming Methods 0.000 claims 1
- 239000011248 coating agent Substances 0.000 description 21
- 238000000576 coating method Methods 0.000 description 21
- 239000010408 film Substances 0.000 description 14
- 239000011230 binding agent Substances 0.000 description 6
- 235000011007 phosphoric acid Nutrition 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- -1 aliphatic amines Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 230000037303 wrinkles Effects 0.000 description 3
- 229910001018 Cast iron Inorganic materials 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000007664 blowing Methods 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
- 230000001680 brushing effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-N diphosphoric acid Chemical compound OP(O)(=O)OP(O)(O)=O XPPKVPWEQAFLFU-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Landscapes
- Re-Forming, After-Treatment, Cutting And Transporting Of Glass Products (AREA)
- Lubricants (AREA)
Description
【発明の詳細な説明】
本発明はガラス成形体の製造方法に関し、さらに詳しく
は高性能の潤滑離型剤を塗布、焼付した金型に溶融ガラ
スを投入して、ガラス成形体を製造する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a glass molded body, and more specifically, a method for manufacturing a glass molded body by pouring molten glass into a mold coated with a high-performance lubricating mold release agent and baked. Regarding.
ここにガラス成形体とは、細口びんあるいは広口ひん等
の組型および仕上型を使用してプレス−ブロー法、ある
いはブロー・ブロー法によって製造される成形体、およ
び皿等のプレス型のみを用いて製造される成形体等を相
称する。Here, the term "glass molded object" refers to a molded object produced by a press-blow method or a blow-blow method using a set mold and a finishing mold such as a narrow-mouth bottle or a wide-mouth bottle, and a molded object manufactured using only a press mold such as a plate. The molded bodies manufactured by
通常、約1100〜1200℃に溶融したガラス塊所謂
ゴブ(gob )を金型に投入して、これをプレスある
いはブローしてガラス成形体を成形するさいに、金型内
面と溶融ガラス間の摩擦抵抗を小さくすることによって
、成形体の表面に皺等の欠陥が発生するのを防止し、か
つ成形の終了した成形体の金型からの分離を容易にする
ため、金型内面に潤滑離型剤を塗布している。Usually, a gob of glass melted at about 1,100 to 1,200°C is put into a mold and pressed or blown to form a glass molded object, and the friction between the inner surface of the mold and the molten glass Lubrication is applied to the inner surface of the mold to prevent defects such as wrinkles on the surface of the molded object by reducing the resistance, and to make it easier to separate the molded object from the mold after molding. The agent is being applied.
これらの潤滑離型剤として従来広く使用されていたもの
は、油性の液体に粉末黒鉛を分散させたものであるが、
この種の潤滑離型剤は成形のさい高温に晒されるための
酸化あるいはガラス成形体への転着等による損耗が甚し
く、通常1回の塗布で50〜100回程度の成形作業し
か行えなかった。The lubricating mold release agent that has been widely used in the past is one in which powdered graphite is dispersed in an oil-based liquid.
This type of lubricating mold release agent is exposed to high temperatures during molding, so it is subject to significant wear and tear due to oxidation or adhesion to glass molded objects, and one application can only be used for around 50 to 100 molding operations. Ta.
このような油性潤滑離型剤の耐久性が悪いという欠点を
解消するため、本発明者の一人はさきに、特開昭52−
150422号において黒鉛と金属の酸性燐酸塩ならび
に酸性水溶液を含む潤滑離型剤を提案した。In order to overcome the drawback of poor durability of oil-based lubricating mold release agents, one of the inventors of the present invention previously published a patent application in Japanese Patent Application Laid-open No.
No. 150,422 proposed a lubricating mold release agent containing graphite and a metal acid phosphate and an acidic aqueous solution.
この種の潤滑離型剤は1回の塗布による成形回数(ゴブ
のショツト数)が作業条件によっては約3万回も可能で
あるという優れた耐久性を有する。This type of lubricating mold release agent has excellent durability and can be molded approximately 30,000 times (number of gob shots) with one application depending on the working conditions.
しかしこれを常温Oこて金型に塗布すると、酸性である
ため塗布後金型(鋳鉄製の場合が多い)材料と反応して
水素ガスを発生し、塗膜と金型面間に気泡が生成して、
塗膜が剥れるという問題があった。However, when this is applied to a mold with an O trowel at room temperature, it reacts with the mold material (often made of cast iron) after application because it is acidic and generates hydrogen gas, causing air bubbles between the coating film and the mold surface. Generate and
There was a problem with the paint film peeling off.
さら(こ酸性であるため容器の選択その他取扱いが厄介
であるという問題があった。Furthermore, because it is acidic, it is difficult to select a container and handle it.
前者の問題を防止するため(こは、金型を約80〜20
0°Cに予熱してから塗布すればよいのであるが、(水
素ガスが発生する前に塗膜を乾燥させるため)、この場
合には塗膜の焼付けのための再加熱を含めて2度の加熱
を必要とし、工程が増えるという別の問題が生ずる。In order to prevent the former problem (in this case, the mold is approximately 80 to 20
It is best to preheat to 0°C before applying the coating, but in this case, the coating must be heated twice (including reheating to bake the coating) (to dry the coating before hydrogen gas is generated). Another problem arises in that heating is required, which increases the number of steps.
本発明は、以上に述べた従来技術の問題点の解消を図る
ことを目的とするものである。The present invention aims to solve the problems of the prior art described above.
上記目的を達成するため、本発明は金型を用いて溶融ガ
ラスの塊を成形してガラス成形体を製造する方法Oこお
いて、上記成形のきいに上記溶融ガラスが接触すべき上
記金型の面には、粉末黒鉛、酸性金属燐酸塩、脂肪族ア
ミンおよび水および/または溶剤よりなる希釈剤を主た
る配合成分とする潤滑離型剤の塗布、焼付被膜が形成さ
れていることを特徴とするガラス成形体の製造方法を提
供するものである。In order to achieve the above object, the present invention provides a method of manufacturing a glass molded body by molding a lump of molten glass using a mold, wherein the molten glass is to be brought into contact with the mold during the molding. The surface is coated with a lubricating mold release agent whose main ingredients are powdered graphite, an acidic metal phosphate, an aliphatic amine, and a diluent made of water and/or a solvent, forming a baked film. The present invention provides a method for manufacturing a glass molded body.
以下本発明について詳細lこ説明する。The present invention will be explained in detail below.
本発明に用いられる潤滑離型剤は、潤滑作用を有する粉
末黒鉛、前記粉末黒鉛に対する粘結剤として作用する酸
性金属燐酸塩、前記酸性金属燐酸塩のpHを上昇させ、
望ましくは該塩をほぼ中和させるための脂肪族アミンお
よび塗布性を向上させるための水および/または溶剤よ
りなる希釈剤を主たる配合成分となっている。The lubricating mold release agent used in the present invention includes powdered graphite that has a lubricating effect, an acidic metal phosphate that acts as a binder for the powdered graphite, and an acidic metal phosphate that increases the pH of the acidic metal phosphate.
Preferably, the main ingredients are an aliphatic amine to substantially neutralize the salt, and a diluent consisting of water and/or a solvent to improve coating properties.
本発明に用いられる潤滑離型剤の粘結剤としては、水溶
液が粘着性を有し、しかも焼付固化膜の耐熱(少なくと
も約400〜600℃における)強度が高く、かつ溶融
ガラスと反応し難い酸性金属燐酸塩が使用される。The binder for the lubricating mold release agent used in the present invention is one that has adhesive properties in its aqueous solution, has high heat resistance (at least at about 400 to 600°C) strength of the baked solidified film, and is difficult to react with molten glass. Acidic metal phosphates are used.
かかる酸性金属燐酸塩としては、第1燐酸アルミニウム
、第1燐酸クロム、第1燐酸マグネシウム、第1燐酸ニ
ツケルまたは第1燐酸ジルコニウム等の単独あるいはこ
れらの混合物、もしくはさらにこれらに燐酸(オルト燐
酸、メタ燐酸、ピロ燐酸等を含む)を添加したもの等が
例示される。Such acidic metal phosphates include monobasic aluminum phosphate, monobasic chromium phosphate, monobasic magnesium phosphate, monobasic nickel phosphate, monobasic zirconium phosphate, etc., singly or in mixtures thereof, or in combination with phosphoric acid (orthophosphoric acid, methacrylate). Examples include those to which phosphoric acid, pyrophosphoric acid, etc.) are added.
特に後者の燐酸の適量の添加は耐熱強度の上昇Oこ貢献
する。In particular, the addition of an appropriate amount of the latter phosphoric acid contributes to an increase in heat resistance strength.
以上の酸性金属燐酸塩の溶液は比較的強い酸性(pH約
15〜2.0)を呈する。The above acidic metal phosphate solution exhibits relatively strong acidity (pH about 15 to 2.0).
従ってこのままでは前述のような問題を有する。Therefore, if left as is, the above-mentioned problems will occur.
従って金型と容易に反応しない程度にまで、すなわち約
pH6以上にまでpHを上昇させる必要がある。Therefore, it is necessary to raise the pH to a level that does not easily react with the mold, that is, to about pH 6 or higher.
この手段として先づ考えられるのは、K OH、NaO
H、NHa等の無機アルカリ剤の添加であるが、本発明
者等の研究によれば、このような方法によって中和した
場合、粘結剤の粘稠性が失われ、乾燥膜強度および耐熱
強度が低下し、従ってかかる粘結剤を使用した潤滑離型
剤の耐久性も低く、一回の塗布により可能なショツト数
も著るしく減少することが判明した。The first possible means for this are KOH, NaO
However, according to research by the present inventors, when neutralized by such a method, the viscosity of the binder is lost and the dry film strength and heat resistance are reduced. It has been found that the strength is reduced and therefore the durability of lubricating mold release agents using such binders is also reduced and the number of shots possible with a single application is significantly reduced.
しかしながら脂肪族アミンにより中和した場合は、粘稠
性が失われることなく、従って高い乾燥膜強度、耐熱強
度が維持でき、かかる粘結剤を使用した潤滑離型剤の耐
久性は著るしく高いことが判明し、本発明tこ到達した
。However, when neutralized with an aliphatic amine, the viscosity is not lost, and therefore high dry film strength and heat resistance can be maintained, and the durability of lubricating mold release agents using such a binder is significantly improved. It has been found that the present invention has achieved this goal.
上記のように粘稠性が失われないことの理由は必ずしも
明らかでないが、酸性燐酸塩と脂肪族アミンがキレート
を作り易い現象と関連あるものと推測される。Although the reason why the viscosity is not lost as described above is not necessarily clear, it is presumed that it is related to the phenomenon in which acidic phosphates and aliphatic amines tend to form chelates.
かかる脂肪族アミンさしては、ブチルアミン、ジプロピ
ルアミン、トリエチルアミン、エチレンジアミン、モノ
エタノールアミン、ジェタノールアミン、トリエタノー
ルアミン、プロパツールアミン等が例示される。Examples of such aliphatic amines include butylamine, dipropylamine, triethylamine, ethylenediamine, monoethanolamine, jetanolamine, triethanolamine, propatoolamine, and the like.
脂肪族アミンの添加量は酸性金属燐酸塩のpHを約6〜
8に高める程度であることが望ましい。The amount of aliphatic amine added is such that the pH of the acidic metal phosphate is approximately 6-6.
It is desirable to increase the number to 8.
上記pHが約6より低いと、常温で塗布された潤滑離型
剤の塗膜と金型表面間での反応により水素ガスを発生し
て、該塗膜が金型面から剥離し易くなり、一方pHが約
8以上になるように過剰の脂肪族アミンを添加すること
は、上記剥離防止の見地から無意味であり、逆に焼付(
通常約250〜300℃で行なわれる)後も多量に残留
して、塗膜の強度の低下を招くおそれがある。When the pH is lower than about 6, hydrogen gas is generated due to the reaction between the lubricating mold release agent coating applied at room temperature and the mold surface, making it easy for the coating to peel off from the mold surface. On the other hand, adding an excess of aliphatic amine to raise the pH to about 8 or higher is meaningless from the standpoint of preventing peeling, and conversely, it causes baking (
(usually carried out at about 250 to 300°C), a large amount remains, which may lead to a decrease in the strength of the coating film.
粉末黒鉛は通常のもの(不純物含有量的0.5〜3重量
%)を使用してもよいが、不純物含有量が0.002重
量%以下の特に精製された高純度粉末黒鉛を使用すると
、潤滑離型剤の耐熱性が一段と向上することを見出した
。Ordinary powdered graphite (0.5 to 3% by weight in terms of impurity content) may be used, but if particularly refined high-purity powdered graphite with an impurity content of 0.002% by weight or less is used, It has been found that the heat resistance of the lubricating mold release agent is further improved.
すなわち通常の粉末黒鉛を配合した本発明による潤滑離
型剤を塗布した金型を使用した場合、金型内面温度が5
00℃以下のときの潤滑離型膜の摩耗は極めて僅かであ
り、1回塗布による可能ショット回数は非常Oこ大きい
。That is, when using a mold coated with the lubricating mold release agent of the present invention containing ordinary powdered graphite, the inside temperature of the mold is 5.
At temperatures below 00°C, the wear of the lubricating release film is extremely small, and the number of shots possible with one application is extremely large.
しかし上記内面温度を500°Cより高くする(成形体
表面の肌を平滑にするのに効果がある)と、急激に上記
消耗が激しくなって、上記可能ショット回数も急減する
。However, if the inner surface temperature is increased above 500°C (effective for smoothing the surface of the molded product), the wear and tear will rapidly increase, and the number of possible shots will also sharply decrease.
しかし上記高純度粉末黒鉛を使用した場合、全型内面温
度が600℃になっても500℃の場合Oこ近い可能シ
ョット回数を示すことが判明した。However, it has been found that when the above-mentioned high-purity powdered graphite is used, even if the inner surface temperature of the entire mold reaches 600°C, the possible number of shots is close to 0 at 500°C.
その理由は必ずしも明らかでないが、粉末黒鉛中に含ま
れる不純物(灰分)が黒鉛の酸化消耗を促進する触媒と
して作用することによるものと推測される。Although the reason for this is not necessarily clear, it is presumed that impurities (ash) contained in powdered graphite act as a catalyst that promotes oxidative consumption of graphite.
潤滑離型剤中における粉末黒鉛と酸性金属燐酸塩の配合
重量比は1/6〜6であることが望ましい。The blending weight ratio of powdered graphite and acidic metal phosphate in the lubricating mold release agent is preferably 1/6 to 6.
粉末黒鉛の量が上記下限である1/6より少ないと、潤
滑離型性が失なわれて、成形体表面に皺等が発生したり
、離型のさい成形体が金型面に耐着して離型困難となる
等のトラブルを生じ易くなるからである。If the amount of powdered graphite is less than the lower limit of 1/6 above, the lubricating mold release property will be lost, wrinkles etc. will occur on the surface of the molded product, and the molded product will not adhere to the mold surface during mold release. This is because troubles such as difficulty in mold release are likely to occur.
一方上記上限である6より多くなると、粉末黒鉛同士の
結合が失なわれて、塗膜強度が低下して、耐久性が損わ
れるからである。On the other hand, if the amount exceeds the upper limit of 6, the bond between the powdered graphite will be lost, the strength of the coating will decrease, and the durability will be impaired.
希釈剤は水単独、エチルアルコールのような溶剤単独、
あるいは水と溶剤の混合物の状態などで添加される。The diluent is water alone, a solvent such as ethyl alcohol,
Alternatively, it is added in the form of a mixture of water and a solvent.
溶剤は配合される脂肪族アミンの種類に応じて当該脂肪
族アミンに対して溶解性を有するものが選ばれる。Depending on the type of aliphatic amine to be blended, a solvent is selected that has solubility for the aliphatic amine.
希釈剤の配合量は、潤滑離型剤の金型への塗布方法【こ
応じて定められ、例えばスプレー塗布の場合は比較的多
量に、刷毛塗りの場合は比較的少量配合される。The amount of diluent to be blended is determined depending on the method of applying the lubricating mold release agent to the mold; for example, in the case of spray coating, a relatively large amount is blended, and in the case of brush coating, a relatively small amount is blended.
本発明(こ使用される潤滑離型剤は、上記の成分の他に
若干量の他の成分、例えば安定化剤としての硼酸あるい
はすべり性向上に寄与する砂糖や澱粉等の添加を妨げる
ものでない。The present invention (the lubricating mold release agent used herein does not preclude the addition of a small amount of other ingredients, such as boric acid as a stabilizer, or sugar or starch that contributes to improving slipperiness, in addition to the above ingredients). .
以上の潤滑離型剤を使用してガラス成形体は次のよう【
こして製造される。Using the above lubricating mold release agent, the glass molded product is made as follows [
It is produced by straining.
先づ室温のガラス金型(組型、バッフル、u型、底型、
仕上型、プレス型等)の少なくとも成形のさい溶融ガラ
スと接触すべき面に、上記の潤滑離型剤をスプレー法、
刷毛塗り法、あるいは浸漬法等の適宜の方法で、できる
たけ均一に塗布する。First, glass molds at room temperature (set molds, baffles, U-types, bottom molds,
The above-mentioned lubricating mold release agent is sprayed onto at least the surface of the finishing mold, press mold, etc. that is to come into contact with the molten glass during molding.
Apply as evenly as possible using an appropriate method such as brushing or dipping.
塗布量は焼付乾燥後の固形膜厚さが、5〜60μmの範
囲内になるように選ぶことが好ましく、さらに20〜5
0μmの範囲内になるように選ぶことがより望ましい。The coating amount is preferably selected so that the solid film thickness after baking and drying is within the range of 5 to 60 μm, and more preferably 20 to 5 μm.
It is more desirable to select it within the range of 0 μm.
5μmより薄いと塗膜の摩耗が速いため、1回塗布当り
の可能ショット回数が著るしく小さくなり、頻繁な金型
交換を必要とし、一方60μmより厚くなると塗膜が剥
れ易くなり、さらに伝熱が悪くなって塗膜内面の温度が
上昇し過ぎて、成形終了後の成形体の冷却が遅くなって
離型までの時間が長くなる、つまり生産性の低下を招く
などの問題を生ずるからである。If it is thinner than 5 μm, the coating will wear quickly, and the number of shots per coating will be significantly reduced, requiring frequent mold replacement. On the other hand, if it is thicker than 60 μm, the coating will easily peel off, and Heat transfer becomes poor and the temperature of the inner surface of the coating film rises too much, causing problems such as slow cooling of the molded product after molding, lengthening the time to release from the mold, and resulting in a decrease in productivity. It is from.
以上のようOこ潤滑離型剤を塗布された金型を、好まし
くは約250〜350°Cで約1〜2時間例えばオーブ
ン中で加熱して、塗膜を焼付固化する。The mold coated with the lubricating mold release agent as described above is preferably heated at about 250 to 350° C. for about 1 to 2 hours, for example, in an oven to bake and solidify the coating film.
このさい脂肪族アミンの大部分は、希釈剤と共Oこ蒸散
するものと推測される。At this time, it is assumed that most of the aliphatic amine evaporates together with the diluent.
以上のようOこして準備された金型に通常の方法により
例えば1100〜1200℃の溶融ガラス塊、所謂ゴブ
を投入してガラス成形体を成形する。A molten glass lump of, for example, 1100 to 1200° C., a so-called gob, is put into the mold prepared as described above and molded into a glass molded body.
ガラス成形体がびんである場合等のようOこ、ブロー・
ブロ一方式あるいはプレス−ブロ一方式で成形される場
合はブロー仕上型には、組型で形成されたパリソン(内
部は溶融状態で、表面に固形薄膜が形成されている)が
投入される。When the glass molded object is a bottle, etc.
In the case of molding using a blow-finishing mold or a press-blowing mold, a parison formed by a set mold (with a molten state inside and a solid thin film formed on the surface) is placed in a blow-finishing mold.
本発明によれば、ガラス成形体成形用の金型面に耐熱強
度に優れ、耐久性の大きい酸性金属燐酸塩を粘結剤とす
る潤滑離型剤の塗膜が形成されているので、1回塗布当
りのショット可能回数が従来の油性潤滑離型剤を用いた
場合にくらべて格段に大きいという効果を有する。According to the present invention, a coating film of a lubricating mold release agent using an acidic metal phosphate having excellent heat resistance and durability as a binder is formed on the mold surface for molding a glass molded object. It has the effect that the number of shots possible per application is much larger than when conventional oil-based lubricating mold release agents are used.
さらに高純度粉末黒鉛を配合することにより、金型内面
温度が約500〜600℃の場合でも上記の高い耐久性
を保持することができる。Furthermore, by blending high-purity powdered graphite, the above-mentioned high durability can be maintained even when the mold inner surface temperature is about 500 to 600°C.
また上記潤滑離型剤には脂肪族アミンが配合されるが、
上記配合によって粘着性は失われず、従って塗布性は損
なわれない。In addition, an aliphatic amine is blended in the lubricating mold release agent, but
Due to the above formulation, tackiness is not lost and, therefore, coatability is not impaired.
そして潤滑離型剤を室温の金型に塗布しても、焼付工程
等Oこおいて水素ガスが発生しない程度にまで、そのp
Hを脂肪族アミンの配合量によって調節することにより
、塗膜の剥離防止が可能であり、従って金型の予熱とい
う工程を省略でき、さらにその取扱いが容易になるとい
う利点を有する。Even if a lubricating mold release agent is applied to a mold at room temperature, the lubricating mold release agent can be applied to a mold at room temperature to the extent that no hydrogen gas is generated during the baking process.
By controlling H by adjusting the amount of aliphatic amine blended, it is possible to prevent the coating film from peeling off, and therefore the process of preheating the mold can be omitted, and furthermore, it has the advantage of being easier to handle.
以下実施例により本発明を説明する。The present invention will be explained below with reference to Examples.
実施例 1
平均粒径25μmの粉末黒鉛(不純物含有量1.2重量
%)35g、第1燐酸アルミニウム25g1正燐酸30
g、モノエタノールアミン32gおよび水50g1エチ
ルアルコール250gを混合攪拌して潤滑離型剤を調製
した。Example 1 35 g of powdered graphite with an average particle size of 25 μm (impurity content 1.2% by weight), 25 g of primary aluminum phosphate, 30 g of orthophosphoric acid
A lubricating mold release agent was prepared by mixing and stirring 1 g, 32 g of monoethanolamine, 50 g of water, and 250 g of ethyl alcohol.
そのpHは7.0であった。Its pH was 7.0.
この潤滑離型剤を、プレス−ブロー成形用の室温の鋳鉄
製組型の胴側型、底型、口型およびバッフルの内面Oこ
固形膜厚さがほぼ30μm(こなるようにスプレー塗布
した後、オーブン中で300℃×80分加熱して、塗膜
を焼付固化したがその剥離は皆無であった。This lubricating mold release agent was sprayed onto the inner surfaces of the body side mold, bottom mold, mouth mold and baffle of a room temperature cast iron assembly mold for press-blow molding so that the solid film thickness was approximately 30 μm. Thereafter, the coating was baked and solidified by heating in an oven at 300° C. for 80 minutes, but no peeling occurred.
この組型に約1140℃のゴブを投入してパリソンをプ
レス成形した。A gob at about 1140° C. was put into this mold and a parison was press-molded.
なおこのさいの組型内面温度は、約450℃、500℃
、550°Cおよび600℃の4段階に調節した。The internal temperature of the mold at this time was approximately 450°C and 500°C.
, 550°C and 600°C.
そして皺等の欠陥を生ずることなく製造された正常なパ
リソンの数、すなわちショット回数を計数した。The number of normal parisons produced without defects such as wrinkles, ie, the number of shots, was counted.
なお、内面温度は放射温度計によって測定した。Note that the inner surface temperature was measured using a radiation thermometer.
結果を第1表に示す。The results are shown in Table 1.
500℃以下の温度で優れた耐久性を示すことが分る。It can be seen that excellent durability is exhibited at temperatures below 500°C.
実施例 2
不純物含有量が0.001重量%の高純度粉末黒鉛鉛を
配合した以外は、実施例1と同様にしてパリソンを製造
し、正常なパリソンの得られるショット回数を計数した
。Example 2 A parison was produced in the same manner as in Example 1, except that high-purity powdered graphite lead with an impurity content of 0.001% by weight was blended, and the number of shots to obtain a normal parison was counted.
結果を第1表に示す。500℃より高い温度でも優れた
耐久性を示すことが分る。The results are shown in Table 1. It can be seen that excellent durability is exhibited even at temperatures higher than 500°C.
比較例 1
モノエタノールアミンを添付しない点を除いては、実施
例1と同一の配合で潤滑離型剤を調整した。Comparative Example 1 A lubricating mold release agent was prepared using the same formulation as in Example 1, except that monoethanolamine was not added.
そのpHは2.0であった。これを実施例と同一条件で
金型0こ塗布焼付したが、焼付後、塗膜が剥離していて
使用不可能であった。Its pH was 2.0. This was coated on a mold and baked under the same conditions as in the example, but after baking the coating had peeled off and could not be used.
Claims (1)
体を製造する方法において、上記成形のさいに上記溶融
ガラスが、接触すべき上記金型の面には、粉末黒鉛、酸
性金属燐酸塩、脂肪族アミンおよび水および/または溶
剤よりなる希釈剤を主たる配合成分とする潤滑離型剤の
塗布、焼付被膜が形成されていることを特徴とするガラ
ス成形体の製造方法。 2 粉末黒鉛中の不純物の含有量が0.002重量%以
下である特許請求の範囲第1項藺載のガラス成形体の製
造方法。 3 酸性金属燐酸塩が、第1燐酸アルミニウム、第1燐
酸クロム、第1燐酸マグネシウム、第1燐酸ニツケルま
たは第1燐酸ジルコニウムの倒れか、ならびに燐酸より
なる特許請求の範囲第1項記載のガラス成形体の製造方
法。 4 潤滑離型剤中に該脂肪族アミンが、該酸性金属燐酸
塩をほぼ中和して該潤滑離型剤のpHを約6〜8にする
に十分な量配合されている特許請求の範囲第1項記載の
ガラス成形体の製造方法。 5 潤滑離型剤中における該粉末黒鉛と該酸性金属燐酸
塩の配合重量比が1/6〜6の範囲内にある特許請求の
範囲第1項記載のガラス成形体の製造方法。 6 潤滑離型剤の塗布、焼付被膜の厚さが5〜60μm
である特許請求の範囲第1項記載のガラス成形体の製造
方法。 7 潤滑離型剤の焼付温度が、250〜350℃である
特許請求の範囲第1項記載のガラス成形体の製造方法。[Claims] 1. In a method of manufacturing a glass molded body by molding a lump of molten glass using a mold, the surface of the mold with which the molten glass comes into contact during the molding includes: A glass molded article characterized in that a lubricating mold release agent containing powdered graphite, an acidic metal phosphate, an aliphatic amine, and a diluent consisting of water and/or a solvent as the main ingredients is coated and a baked film is formed. Production method. 2. The method for producing a glass molded body according to claim 1, wherein the content of impurities in powdered graphite is 0.002% by weight or less. 3. The glass forming according to claim 1, wherein the acidic metal phosphate is composed of monobasic aluminum phosphate, monobasic chromium phosphate, monobasic magnesium phosphate, monobasic nickel phosphate, or monobasic zirconium phosphate, and phosphoric acid. How the body is manufactured. 4. The lubricating mold release agent contains the aliphatic amine in an amount sufficient to substantially neutralize the acidic metal phosphate and bring the pH of the lubricating mold release agent to about 6 to 8. 2. A method for producing a glass molded article according to item 1. 5. The method for producing a glass molded body according to claim 1, wherein the blending weight ratio of the powdered graphite and the acidic metal phosphate in the lubricating mold release agent is within the range of 1/6 to 6. 6 Application of lubricating mold release agent, thickness of baked film is 5 to 60 μm
A method for manufacturing a glass molded body according to claim 1. 7. The method for producing a glass molded body according to claim 1, wherein the baking temperature of the lubricating mold release agent is 250 to 350°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10986280A JPS595535B2 (en) | 1980-08-12 | 1980-08-12 | Method for manufacturing glass molded bodies |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10986280A JPS595535B2 (en) | 1980-08-12 | 1980-08-12 | Method for manufacturing glass molded bodies |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5738339A JPS5738339A (en) | 1982-03-03 |
| JPS595535B2 true JPS595535B2 (en) | 1984-02-06 |
Family
ID=14521073
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10986280A Expired JPS595535B2 (en) | 1980-08-12 | 1980-08-12 | Method for manufacturing glass molded bodies |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS595535B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62124812U (en) * | 1986-01-29 | 1987-08-08 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2817862B2 (en) * | 1992-03-12 | 1998-10-30 | 敷島紡績 株式会社 | Dryer canvas travel guide palm |
| FR2776653B1 (en) * | 1998-03-24 | 2000-04-28 | Promatech | PROCESS FOR LUBRICATING GLASS MOLDS BY COMBUSTION THEREOF OF A LIQUID AMINE OR AMINO-ALCOHOL SUBSTANCE |
| EP0882684A1 (en) * | 1997-06-04 | 1998-12-09 | Promatech | Method of lubrification of glass molds by direct combustion of amine or amino-alcohol solutions therein |
| AU2003904225A0 (en) * | 2003-08-08 | 2003-08-21 | Ripetech Pty Limited | Method for reducing precure during the curing of thermosetting resins |
| JP4502728B2 (en) * | 2004-07-01 | 2010-07-14 | 日本山村硝子株式会社 | Method for producing molding die having seizure lubricant release agent layer |
| JP2010208884A (en) * | 2009-03-10 | 2010-09-24 | Biotope:Kk | Glass molding method |
| CN107384562B (en) * | 2017-07-04 | 2020-05-05 | 富兰克润滑科技(太仓)有限公司 | Aluminum alloy water-based die-casting release agent and preparation method thereof |
| CN108192687B (en) * | 2018-01-12 | 2020-10-30 | 南阳师范学院 | Water-based graphite-based release agent and preparation and use methods thereof |
-
1980
- 1980-08-12 JP JP10986280A patent/JPS595535B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62124812U (en) * | 1986-01-29 | 1987-08-08 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5738339A (en) | 1982-03-03 |
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