JPH09263958A - Pre-treatment of metallic base material surface - Google Patents

Pre-treatment of metallic base material surface

Info

Publication number
JPH09263958A
JPH09263958A JP9595696A JP9595696A JPH09263958A JP H09263958 A JPH09263958 A JP H09263958A JP 9595696 A JP9595696 A JP 9595696A JP 9595696 A JP9595696 A JP 9595696A JP H09263958 A JPH09263958 A JP H09263958A
Authority
JP
Japan
Prior art keywords
base material
metallic base
solution
pretreatment
treatment
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
Application number
JP9595696A
Other languages
Japanese (ja)
Inventor
Yasuyuki Mizushima
康之 水嶋
Katsuya Yamagiwa
勝也 山際
Masahiko Okuyama
雅彦 奥山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Niterra Co Ltd
Original Assignee
NGK Spark Plug Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by NGK Spark Plug Co Ltd filed Critical NGK Spark Plug Co Ltd
Priority to JP9595696A priority Critical patent/JPH09263958A/en
Publication of JPH09263958A publication Critical patent/JPH09263958A/en
Pending legal-status Critical Current

Links

Landscapes

  • Chemical Treatment Of Metals (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a pre-treating method for easily wetting the surface of a metallic base material by a remarkably simple operation that the metallic base material is brought into contact with an aq. solution, containing an alkali compound or hydrogen peroxide, or a hot water or steam. SOLUTION: The metallic base material is dipped into the aq. solution containing 10mol/l alkali compound such as sodium hydroxide, potassium hydroxide or hydrogen peroxide, for example, for 3hr in the boiling state and by the pre-treatment, the contact angle particularly of an aq. solution or the like to the surface of the metallic base material is lowered to improve the wettability. A coating film composed of a calcium phosphate based sintered compact is formed on the surface of the metallic base material by applying an aq. solution containing calcium phosphate, heat treating and sintering. Particularly if the metallic base material is used for a in-vivo hard tissue substitutive member, the in-vivo hard tissue substitutive member having excellent strength and bioactivity is obtained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、液状原料を用い
て、金属基材の表面に被膜を形成する場合に、均質且つ
その表面が平滑であって、金属基材表面との密着性に優
れる被膜を得るための、金属基材表面の前処理方法に関
する。本発明の前処理方法は、金属基材表面に溶液、ス
ラリー、ゾルゲル法によって得られるゾル等を塗布し、
熱処理、焼成等することにより被膜を形成する場合など
に利用することができる。
TECHNICAL FIELD The present invention relates to a method of forming a coating film on the surface of a metal base material using a liquid material, which is homogeneous and has a smooth surface and is excellent in adhesion to the surface of the metal base material. The present invention relates to a method for pretreating a surface of a metal substrate to obtain a coating. The pretreatment method of the present invention, a solution, a slurry, a sol obtained by a sol-gel method is applied to the surface of a metal substrate,
It can be used when forming a film by heat treatment, baking, or the like.

【0002】[0002]

【従来の技術】セラミックスは耐食性、耐薬品性等に優
れており、種々の用途に用いられている。しかし、上記
の優れた特性を有する反面、靱性に欠け、割れ易いとい
う欠点がある。そこで、例えば、生体内硬組織代替部材
として、金属等の靱性の大きな、割れ難い材料が使用さ
れることも多いが、金属は生体不活性である。そのた
め、その表面に生体活性な素材をコーティングして改質
することが試みられている。このコーティングの方法と
しては、溶液、ゾル等を塗布した後、熱処理、焼成等を
行って被膜を形成する方法が一般的である。
2. Description of the Related Art Ceramics are excellent in corrosion resistance, chemical resistance, etc. and are used for various purposes. However, although it has the above-mentioned excellent properties, it has the drawbacks of lacking toughness and being easily cracked. Therefore, for example, as a hard tissue substitute member in vivo, a material such as a metal having high toughness and which is difficult to break is often used, but the metal is inactive in the body. Therefore, it has been attempted to coat the surface with a bioactive material for modification. As a method of this coating, a method of applying a solution, sol or the like and then performing heat treatment, firing or the like to form a film is generally used.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、溶液、
ゾル等の塗布において、特にその溶液等が水系である場
合は、金属に対する濡れに劣り、はじかれてしまうた
め、均一なコーティングができないという問題がある。
そこで、この濡れを向上させるため、溶液、ゾル等の中
に界面活性剤などを添加する方法、或いは金属基材を予
め熱処理して、その表面に酸化被膜を形成する方法等が
試みられている。しかし、界面活性剤などを添加した場
合は、溶液等の変性又は残炭の問題を生ずることがあ
る。また、金属基材を熱処理した場合は、酸化による着
色、光沢の減少、及び表面の荒れ、劣化等、種々の問題
がある。
However, the solution,
When applying a sol or the like, particularly when the solution or the like is water-based, there is a problem in that it is inferior in wettability with a metal and is repelled, and uniform coating cannot be performed.
Therefore, in order to improve this wetting, a method of adding a surfactant or the like to a solution, a sol or the like, or a method of preliminarily heat treating a metal base material to form an oxide film on the surface thereof has been attempted. . However, when a surfactant or the like is added, the problem of denaturation of the solution or residual carbon may occur. Further, when the metal base material is heat-treated, there are various problems such as coloring due to oxidation, reduction of gloss, and surface roughness and deterioration.

【0004】本発明は、上記問題点を解決するものであ
り、チタン等からなる金属基材の表面に被膜を形成する
場合に、予め、その表面を、アルカリ性化合物等を含む
水溶液、又は熱水若しくは水蒸気と接触させて処理する
方法を提供するものである。この前処理によって、均質
且つ平滑で、金属基材との密着性に優れた被膜を形成す
ることができる。
The present invention is intended to solve the above-mentioned problems, and when a coating film is formed on the surface of a metal substrate made of titanium or the like, the surface thereof is previously treated with an aqueous solution containing an alkaline compound or hot water. Alternatively, it provides a method of treating by contacting with steam. By this pretreatment, it is possible to form a film which is homogeneous and smooth and has excellent adhesion to the metal substrate.

【0005】[0005]

【課題を解決するための手段】第1発明の金属基材表面
の前処理方法は、液状原料を用いて、金属基材の表面に
被膜を形成する場合に、該表面を、予め、(1) アルカリ
性化合物及び過酸化水素のうちのいずれか一方を含む水
溶液、又は(2) 熱水若しくは水蒸気と接触させることを
特徴とする。
A method for pretreating a surface of a metal substrate according to a first aspect of the present invention is such that when a film is formed on the surface of the metal substrate using a liquid raw material, the surface is preliminarily treated in accordance with (1 ) A contact with an aqueous solution containing one of an alkaline compound and hydrogen peroxide, or (2) hot water or steam.

【0006】上記「液状原料」としては、溶媒に、上記
「被膜」を形成するための化合物等を溶解、分散、懸濁
等させたものを使用することができる。その性状は、溶
液、スラリー、ゾル、エマルジョン等いずれであっても
よい。上記の溶媒としては、水、又はアルコール、ケト
ン等の有機溶媒など、特に限定されず、いずれも使用す
ることができる。また、溶媒が水である場合、通常、金
属表面への濡れに劣り、塗布が容易ではないが、本発明
では、第2発明のように、「液状原料が水系」であって
も、何ら問題なく塗布することができる。
As the above-mentioned "liquid raw material", it is possible to use a solvent in which a compound for forming the above "coating" is dissolved, dispersed or suspended. The property may be any of solution, slurry, sol, emulsion and the like. The above-mentioned solvent is not particularly limited, such as water or an organic solvent such as alcohol or ketone, and any of them can be used. Further, when the solvent is water, it is usually inferior in wettability to the metal surface and coating is not easy. However, in the present invention, even if the "liquid raw material is aqueous" as in the second invention, there is no problem. Can be applied without.

【0007】尚、上記の「水系」とは、主たる溶媒又は
分散媒として水を使用している系を意味する。例えば、
水のみ、或いは水と水溶性の溶媒(メタノール、エタノ
ール、アセトン等)との混合溶媒を用いた溶液、スラリ
ーなどが挙げられる。水系では、主として有機溶媒を用
いる系に比べて、取り扱い易く、引火性、毒性等がな
く、且つ蒸気を吸い込んで中毒を起こすというようなこ
ともない。
The above "aqueous system" means a system using water as a main solvent or dispersion medium. For example,
Examples thereof include a solution and a slurry using only water or a mixed solvent of water and a water-soluble solvent (methanol, ethanol, acetone, etc.). Compared to a system mainly using an organic solvent, an aqueous system is easy to handle, has no flammability and toxicity, and does not cause intoxication by inhaling vapor.

【0008】本発明において、金属基材の表面と接触し
て、その表面を処理する処理液としては、水に「アルカ
リ性化合物」又は「過酸化水素」を溶解した水溶液を使
用することができる。また、「熱水若しくは水蒸気」を
用いることもできる。この熱水若しくは水蒸気は、特別
の処理をしていない上水をそのまま用いて加熱し、気化
させて生成させてもよいし、蒸留水等を使用してもよ
い。尚、本発明において、熱水の温度は50℃以上、特
に60℃以上とすることが好ましく、さらには70℃以
上とすることが、より好ましい。
In the present invention, as the treatment liquid for contacting the surface of the metal base material and treating the surface, an aqueous solution in which "alkaline compound" or "hydrogen peroxide" is dissolved in water can be used. Also, "hot water or steam" can be used. This hot water or steam may be produced by heating and vaporizing the tap water that has not been subjected to any special treatment as it is, or using distilled water or the like. In the present invention, the temperature of hot water is preferably 50 ° C. or higher, particularly 60 ° C. or higher, and more preferably 70 ° C. or higher.

【0009】上記のアルカリ性化合物としては、水酸化
ナトリウム、水酸化カリウム、水酸化カルシウム及び水
酸化マグネシウム等の、アルカリ金属或いはアルカリ土
類金属の水酸化物などを使用することができる。この
他、過酸化水素のナトリウム塩、カリウム塩等の、過酸
化水素のアルカリ金属塩などを用いることもできる。こ
れらの中では、第3発明のように、特に表面処理効果の
大きい「ナトリウム、カリウム及びマグネシウム」の水
酸化物及び過酸化水素塩などの化合物がより好ましい。
As the above alkaline compound, hydroxides of alkali metals or alkaline earth metals such as sodium hydroxide, potassium hydroxide, calcium hydroxide and magnesium hydroxide can be used. In addition, alkali metal salts of hydrogen peroxide such as sodium salt and potassium salt of hydrogen peroxide can also be used. Among these, as in the third invention, compounds such as "sodium, potassium and magnesium" hydroxides and hydrogen peroxides, which have particularly large surface treatment effects, are more preferable.

【0010】上記「水溶液」中の、アルカリ性化合物及
び過酸化水素の濃度は、特に限定はされない。通常、そ
の濃度は1〜20モル/リットル、特に3〜17モル/
リットル、さらには7〜14モル/リットル程度とする
ことができる。この水溶液の濃度が1モル/リットル未
満では、十分な処理効果を得るためには長時間を要し、
実用的ではない。また、20モル/リットルを越えて高
濃度としても、それ以上あまり時間を短縮することはで
きない。また、特にアルカリ性化合物では、過度に高濃
度とした場合は、前処理後、金属基材表面から除去する
のに面倒な手間を要する。
The concentrations of the alkaline compound and hydrogen peroxide in the above "aqueous solution" are not particularly limited. Usually, the concentration is 1 to 20 mol / liter, especially 3 to 17 mol / liter.
It may be liter, more preferably about 7 to 14 mol / liter. If the concentration of this aqueous solution is less than 1 mol / liter, it takes a long time to obtain a sufficient treatment effect,
Not practical. Further, even if the concentration is higher than 20 mol / liter, the time cannot be further shortened. Further, particularly in the case of an alkaline compound, if the concentration is excessively high, it is troublesome to remove it from the surface of the metal substrate after the pretreatment.

【0011】金属基材の表面と水溶液又は熱水とは、通
常、水溶液又は熱水中へ金属基材を浸漬することにより
「接触」させる。接触の方法としては、この浸漬方法
が、装置が簡易であり、且つ操作が容易であって好まし
い。しかも、金属基材の処理を要する全表面を確実に、
且つ均等に処理することができる。尚、水蒸気の場合
は、水蒸気を充満させた密閉容器中に金属基材を静置し
てもよいし、基材の表面に連続的に水蒸気を吹き付ける
方法等であってもよい。
The surface of the metal substrate and the aqueous solution or hot water are usually brought into "contact" by immersing the metal substrate in the aqueous solution or hot water. As the contact method, this dipping method is preferable because the apparatus is simple and the operation is easy. Moreover, it ensures that all surfaces that require treatment of the metal substrate are
And it can be processed evenly. In the case of water vapor, the metal base material may be left standing in a closed container filled with water vapor, or a method of continuously spraying water vapor on the surface of the base material may be used.

【0012】また、前処理の温度及び時間は、処理効果
を確認しながら適宜設定すればよい。この処理温度、処
理時間は、水溶液と熱水若しくは水蒸気とでは異なる
し、水溶液の場合、その濃度によっても変える必要があ
る。この接触は、第4発明のように、水溶液又は熱水を
「沸騰」させて実施することが好ましく、これによって
処理時間を大幅に短縮することができる。例えば、アル
カリ性化合物又は過酸化水素の濃度が10モル/リット
ルの水溶液の場合、3時間の処理で十分な効果が得られ
る。しかし、熱水の場合は、70℃であっても5時間程
度と比較的長時間を要するため、この点を考慮して使用
する必要がある。
Further, the temperature and time of the pretreatment may be set appropriately while checking the treatment effect. The treatment temperature and the treatment time are different between the aqueous solution and hot water or steam, and in the case of an aqueous solution, it needs to be changed depending on the concentration. This contact is preferably carried out by "boiling" an aqueous solution or hot water as in the fourth aspect of the invention, which can significantly reduce the processing time. For example, in the case of an aqueous solution having an alkaline compound or hydrogen peroxide concentration of 10 mol / liter, a sufficient effect can be obtained by treating for 3 hours. However, in the case of hot water, even at 70 ° C., it takes a relatively long time of about 5 hours, so it is necessary to consider this point before using.

【0013】本発明の金属基材表面の前処理方法は、金
属基材或いは被膜の種類、得られる被覆品の用途等、何
ら特定はされない。そして、水溶液又は熱水若しくは水
蒸気によって前処理を実施するため、被膜を形成するた
めの液状原料も水系である場合に、特に大きな効果が奏
され、均質、且つ金属基材との密着性に優れた被膜を形
成することができる。そのような液状原料としては、例
えば、第5発明のように、「少なくともリンとカルシウ
ムとを含んでいるもの」などが挙げられる。
The method of pretreatment of the surface of the metal substrate of the present invention is not specified at all in terms of the type of the metal substrate or the coating, the use of the resulting coated article and the like. Since the pretreatment is carried out with an aqueous solution or hot water or steam, a particularly large effect is exhibited when the liquid raw material for forming the coating is also an aqueous system, and it is homogeneous and has excellent adhesion to a metal substrate. A coated film can be formed. Examples of such a liquid raw material include "a material containing at least phosphorus and calcium" as in the fifth invention.

【0014】上記の液状原料を金属基材に塗布した後、
300〜550℃程度の温度で熱処理し、溶媒及び有機
物を除去し、その後、焼成することにより被膜を形成す
ることができる。金属基材に対する液状原料の塗布は、
流延、噴霧、ディッピング、スピニング等の種々の方法
によって実施することができる。そして、熱処理後、不
活性雰囲気下、600〜1300℃、特に800℃程度
で焼成することにより、金属基材表面にリン酸カルシウ
ム系焼結体からなる被膜が形成された被覆品とすること
ができる。このような被覆品は、金属基材が、予め、人
口骨、人口歯根、人口関節等の生体内硬組織代替部材の
形状に成形されたものである場合に、特に有用である。
After applying the above liquid raw material to the metal substrate,
A film can be formed by performing heat treatment at a temperature of about 300 to 550 ° C. to remove the solvent and organic substances, and then firing. Applying the liquid raw material to the metal substrate,
It can be carried out by various methods such as casting, spraying, dipping and spinning. Then, after the heat treatment, it is fired at 600 to 1300 ° C., especially at about 800 ° C. in an inert atmosphere to obtain a coated article in which a coating film made of a calcium phosphate-based sintered body is formed on the surface of the metal base material. Such a coated article is particularly useful when the metal base material is previously formed into the shape of an in-vivo hard tissue replacement member such as an artificial bone, an artificial tooth root, or an artificial joint.

【0015】上記の生体内硬組織代替部材の場合、金属
基材としては、第6発明のように、「チタン、チタン合
金又はステンレス鋼からなる基材」が好ましい。特に、
強度が大きく、生体に対する毒性が低く、且つ耐食性に
優れるチタン及びチタン合金は、生体内硬組織代替部材
として好適である。また、金属基材としては、ステンレ
ス鋼からなるものも使用し得るが、Na+ 、K+ などの
イオンの多い生体内ではステンレス鋼は耐食性が不十分
な場合も考えられるため、チタン及びその合金がより好
ましい。
In the case of the above-mentioned in-vivo hard tissue substitute member, the metal base material is preferably a "base material made of titanium, titanium alloy or stainless steel" as in the sixth invention. Especially,
Titanium and titanium alloys, which have high strength, low toxicity to the living body, and excellent corrosion resistance, are suitable as an in-vivo hard tissue substitute member. Further, as the metal base material, one made of stainless steel may be used, but titanium and its alloys may be insufficient in corrosion resistance in the living body where a lot of ions such as Na + and K + are present. Is more preferable.

【0016】チタン、チタン合金、ステンレス鋼等の金
属からなる生体硬組織代替部材は、強度が大きく、毒性
もないが、生体活性はない。一方、リン酸カルシウム系
焼結体からなる生体硬組織代替部材は、強度は小さい
が、生体活性に優れる。従って、上記のような被膜を形
成すれば、強度、生体活性ともに優れた生体硬組織代替
部材が得られる。本発明の前処理方法によって、生体内
硬組織代替部材の形状に成形されたチタン等からなる金
属基材の表面を処理した後、その表面に、リン酸カルシ
ウム系焼結体からなる被膜を形成した場合、均質であっ
て、且つ密着性に優れた被膜とすることができる。
A biohard tissue substitute member made of a metal such as titanium, titanium alloy, or stainless steel has high strength and is not toxic, but is not bioactive. On the other hand, the biohard tissue replacement member made of a calcium phosphate-based sintered body has low strength but excellent bioactivity. Therefore, by forming the coating film as described above, it is possible to obtain a bio-hard tissue replacement member having excellent strength and bioactivity. When the surface of a metal base material made of titanium or the like formed into the shape of an in-vivo hard tissue substitute member is treated by the pretreatment method of the present invention, and then a coating film made of a calcium phosphate-based sintered body is formed on the surface It is possible to obtain a film that is homogeneous and has excellent adhesion.

【0017】[0017]

【発明の実施の形態】以下、実施例によって本発明を詳
しく説明する。各実施例及び比較例においては、前処理
後の金属基材表面に対する水の接触角によって、前処理
の効果の確認を行った。即ち、接触角が小さいほど、液
状原料の金属基材表面に対する濡れが良好であり、均一
な厚さの塗膜とすることができ、焼成後は均質、且つ密
着性に優れた被膜が形成される。尚、以下の各実施例に
おいて、○はその処理を実施した場合、×は処理しなか
った場合を表す。また、接触角の測定は、協和科学株式
会社製の接触角測定機を使用した。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below with reference to Examples. In each of the examples and comparative examples, the effect of the pretreatment was confirmed by the contact angle of water with respect to the surface of the metal substrate after the pretreatment. That is, the smaller the contact angle, the better the wettability of the liquid raw material with respect to the surface of the metal base material, and the coating film having a uniform thickness can be formed. After firing, a coating film that is homogeneous and has excellent adhesiveness is formed. It In each of the following examples, ◯ means that the treatment was performed, and x means that the treatment was not performed. The contact angle was measured using a contact angle measuring device manufactured by Kyowa Kagaku Co., Ltd.

【0018】実施例1 チタンからなる板状体を濃度10モル/リットルの水酸
化ナトリウム(NaOH)水溶液に浸漬し、加熱して昇
温させ、3時間、沸騰状態で接触させて前処理を行っ
た。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 32.2 29.0 28.8 74.4 73.8 72.2 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 1 A plate made of titanium was immersed in an aqueous sodium hydroxide (NaOH) solution having a concentration of 10 mol / liter, heated to raise the temperature, and contacted in a boiling state for 3 hours for pretreatment. It was −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 6 −−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ ○ × × × −−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−−−− Contact angle (°) 32.2 29.0 28.8 74.4 73.8 72.2 −−−−−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−

【0019】実施例2 チタンをTi−6Al−4Vのチタン合金に代えた他
は、実施例1と同様にして前処理した。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 45.4 41.3 72.3 55.8 67.4 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 2 Pretreatment was performed in the same manner as in Example 1 except that titanium was replaced with a titanium alloy of Ti-6Al-4V. −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 −−−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ × × × −−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−− Contact angle (°) 45.4 41.3 72.3 55.8 67.4 −−−−−−−−−−−−−−−−−−−−−−−− −−−−−−−−−−−

【0020】実施例3 NaOHを水酸化カリウムに代えた他は、実施例1と同
様にして前処理した。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 27.8 29.5 30.1 75.5 71.3 72.6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 3 Pretreatment was carried out in the same manner as in Example 1 except that potassium hydroxide was used instead of NaOH. −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 6 −−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ ○ × × × −−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−−−− Contact angle (°) 27.8 29.5 30.1 75.5 71.3 72.6 −−−−−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−

【0021】実施例4 NaOHを過酸化水素に代えた他は、実施例1と同様に
して前処理した。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 26.2 27.9 28.1 75.8 73.7 70.2 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 4 Pretreatment was carried out in the same manner as in Example 1 except that hydrogen peroxide was used instead of NaOH. −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 6 −−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ ○ × × × −−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−−−− Contact angle (°) 26.2 27.9 28.1 75.8 73.7 70.2 −−−−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−

【0022】実施例5 チタンをステンレス鋼に代えた他は、実施例1と同様に
して前処理した。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 29.3 27.1 25.9 78.6 73.1 79.6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 5 Pretreatment was carried out in the same manner as in Example 1 except that titanium was replaced with stainless steel. −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 6 −−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ ○ × × × −−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−−−− Contact angle (°) 29.3 27.1 25.9 78.6 73.1 79.6 −−−−−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−

【0023】実施例6 NaOH水溶液を70℃の熱水に代え、処理時間を5時
間とした他は、実施例1と同様にして前処理した。 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 試験片番号 1 2 3 4 5 6 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 前処理 ○ ○ ○ × × × −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− 接触角(°) 31.2 30.9 29.3 74.2 75.1 73.0 −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−
Example 6 Pretreatment was carried out in the same manner as in Example 1 except that the NaOH aqueous solution was replaced with hot water at 70 ° C. and the treatment time was 5 hours. −−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−−− Test piece number 1 2 3 4 5 6 −−−−−−−− −−−−−−−−−−−−−−−−−−−−−−−−−−− Pretreatment ○ ○ ○ × × × −−−−−−−−−−−−−−− −−−−−−−−−−−−−−−−−−− Contact angle (°) 31.2 30.9 29.3 74.2 75.1 73.0 −−−−−−−−−−−−−−−−−−−−− −−−−−−−−−−−−−−

【0024】実施例1、3及び4の結果によれば、接触
角は同様に大きく低下し、前処理の効果が明らかであ
る。このように、アルカリ性化合物の種類、又は過酸化
水素による前処理の効果の差はほとんどないことが分か
る。また、実施例5のステンレス鋼の場合も、同様の優
れた効果が奏されているが、実施例2のチタン合金の場
合は、これら各実施例に比べて接触角の低下が小さい。
しかし、それでも前処理によって接触角は相当に低下し
ている。尚、熱水を使用した実施例6では、5時間と長
時間の処理を実施すれば、接触角は十分に低下すること
が分かる。
According to the results of Examples 1, 3 and 4, the contact angle was similarly greatly reduced, and the effect of the pretreatment is clear. Thus, it can be seen that there is almost no difference in the effect of the type of alkaline compound or the pretreatment with hydrogen peroxide. In addition, the same excellent effect is exhibited also in the case of the stainless steel of Example 5, but in the case of the titanium alloy of Example 2, the decrease in contact angle is smaller than that in each of these examples.
However, the contact angle is still considerably reduced by the pretreatment. In addition, in Example 6 using hot water, it can be seen that the contact angle is sufficiently reduced by performing the treatment for a long time of 5 hours.

【0025】実施例7 蒸留水1リットル中に、硝酸カルシウム3.125×1
-2モルを溶解した。この溶液に、エチレンジアミン四
酢酸アンモニウム塩を等モル量添加し、30分間攪拌し
て反応させた。その後、この反応溶液に、リン酸アンモ
ニウムを1.875×10-2モル加えて(リンとカルシ
ウムとの合計モル濃度;0.05モル/リットル)、透
明な溶液となるまで更に攪拌を続けた。次いで、加熱し
て120℃に昇温させ、蒸留水を徐々に除去して10倍
に濃縮した後、pHを4.0に調整した。
Example 7 3.125 × 1 calcium nitrate in 1 liter of distilled water
0 -2 mol was dissolved. An equimolar amount of ethylenediaminetetraacetic acid ammonium salt was added to this solution, and the mixture was reacted by stirring for 30 minutes. Then, 1.875 × 10 -2 mol of ammonium phosphate was added to this reaction solution (total molar concentration of phosphorus and calcium; 0.05 mol / liter), and stirring was continued until a transparent solution was obtained. . Then, the temperature was raised to 120 ° C. by heating, the distilled water was gradually removed and the solution was concentrated 10 times, and then the pH was adjusted to 4.0.

【0026】その後、上記の実施例1において前処理し
たチタンからなる板状体を基材として、この基材を上記
の濃縮溶液中に浸漬して製膜し、5℃/分の速度で昇温
して、525℃の温度で熱処理を行った。この浸漬、製
膜と熱処理とを繰り返し実施した後、アルゴン雰囲気
下、800℃で焼成してリン酸カルシウム系焼結体から
なる被膜を形成した。得られた被膜に亀裂等はなく、そ
の表面は平滑であった。また、ビッカース圧子埋入試験
を行ったが、被膜の剥離は認められず、密着性も良好で
あった。
Then, using the plate-shaped body made of titanium pretreated in Example 1 as a base material, the base material was immersed in the concentrated solution to form a film, and the film was heated at a rate of 5 ° C./min. It was heated and heat-treated at a temperature of 525 ° C. After repeating the immersion, film formation and heat treatment, the film was baked at 800 ° C. in an argon atmosphere to form a film made of a calcium phosphate-based sintered body. The obtained coating had no cracks and the surface was smooth. Further, a Vickers indenter embedding test was conducted, but no peeling of the coating film was observed and the adhesion was good.

【0027】比較例1 実施例7において、前処理していない板状体を使用した
他は、同様にして濃縮溶液を調製し、同様にして浸漬、
製膜と熱処理及び焼成を行って、被膜の形成を試みた。
しかし、前処理をしていない板状体は濡れ難く、濃縮溶
液がはじかれてしまって、均質、平滑な被膜を形成する
ことはできなかった。
Comparative Example 1 A concentrated solution was prepared in the same manner as in Example 7 except that the plate-like body which was not pretreated was used.
An attempt was made to form a film by performing film formation, heat treatment and firing.
However, the plate-shaped body not subjected to the pretreatment was difficult to get wet, and the concentrated solution was repelled, so that a uniform and smooth film could not be formed.

【0028】実施例7と比較例1とを比べれば、本発明
の前処理の効果が実用上も十分であることが分かる。ま
た、この実施例7の結果は、チタンからなる生体内硬組
織代替部材を基材とすれば、強度と生体活性とを併せ有
する優れた性能の生体内硬組織代替部材が得られること
を十分に裏付けるものである。
Comparing Example 7 with Comparative Example 1, it can be seen that the effect of the pretreatment of the present invention is practically sufficient. In addition, the result of this Example 7 is that it is sufficient to obtain an in-vivo hard tissue substitute member having excellent performance having both strength and bioactivity when the in-vivo hard tissue substitute member made of titanium is used as the base material. It is something to support.

【0029】[0029]

【発明の効果】本発明によれば、金属基材と処理液とを
接触させるという、極めて簡便な操作によって、金属基
材表面の濡れを向上させることができる。それにより、
水系等の液状原料を使用して、金属基材表面に、均質、
且つ密着性に優れた被膜を容易に形成することができ
る。特に、第5発明のリンとカルシウムとを含む液状原
料を使用して、第6発明の、特にチタン又はチタン合金
からなる生体内硬組織代替部材の表面に、リン酸カルシ
ウム系焼結体からなる被膜を形成した場合は、大きな強
度と優れた生体活性とを併せ有する生体内硬組織代替部
材を得ることができる。
According to the present invention, the wetting of the surface of the metal base material can be improved by a very simple operation of bringing the metal base material and the treatment liquid into contact with each other. Thereby,
Using liquid raw materials such as water, it is possible to
In addition, it is possible to easily form a film having excellent adhesion. In particular, a liquid raw material containing phosphorus and calcium of the fifth invention is used to form a coating film of a calcium phosphate-based sintered body on the surface of the in-vivo hard tissue substitute member of the sixth invention, particularly titanium or titanium alloy. When formed, an in-vivo hard tissue substitute member having both high strength and excellent bioactivity can be obtained.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 液状原料を用いて、金属基材の表面に被
膜を形成する場合に、該表面を、予め、(1) アルカリ性
化合物及び過酸化水素のうちのいずれか一方を含む水溶
液、又は(2) 熱水若しくは水蒸気と接触させることを特
徴とする金属基材表面の前処理方法。
1. When a liquid material is used to form a coating on the surface of a metal base material, the surface is previously formed with an aqueous solution containing one of (1) an alkaline compound and hydrogen peroxide, or (2) A method of pretreating the surface of a metal substrate, which comprises contacting with hot water or steam.
【請求項2】 上記液状原料は水系である請求項1記載
の金属基材表面の前処理方法。
2. The pretreatment method for the surface of a metal substrate according to claim 1, wherein the liquid raw material is water-based.
【請求項3】 上記アルカリ性化合物は、ナトリウム化
合物、カリウム化合物及びマグネシウム化合物のうちの
少なくとも1種である請求項1又は2記載の金属基材表
面の前処理方法。
3. The method for pretreatment of the surface of a metal substrate according to claim 1, wherein the alkaline compound is at least one selected from a sodium compound, a potassium compound and a magnesium compound.
【請求項4】 上記水溶液又は熱水を加熱して沸騰させ
る請求項1乃至3のいずれか1項に記載の金属基材表面
の前処理方法。
4. The method for pretreating the surface of a metal substrate according to claim 1, wherein the aqueous solution or hot water is heated and boiled.
【請求項5】 上記液状原料は、少なくともリンとカル
シウムとを含んでいる請求項1乃至4のいずれか1項に
記載の金属基材表面の前処理方法。
5. The pretreatment method for a surface of a metal base material according to claim 1, wherein the liquid raw material contains at least phosphorus and calcium.
【請求項6】 上記金属基材が、チタン、チタン合金又
はステンレス鋼からなるものである請求項1乃至5のい
ずれか1項に記載の金属基材表面の前処理方法。
6. The pretreatment method for the surface of a metal base material according to claim 1, wherein the metal base material is made of titanium, a titanium alloy or stainless steel.
JP9595696A 1996-03-25 1996-03-25 Pre-treatment of metallic base material surface Pending JPH09263958A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9595696A JPH09263958A (en) 1996-03-25 1996-03-25 Pre-treatment of metallic base material surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9595696A JPH09263958A (en) 1996-03-25 1996-03-25 Pre-treatment of metallic base material surface

Publications (1)

Publication Number Publication Date
JPH09263958A true JPH09263958A (en) 1997-10-07

Family

ID=14151702

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9595696A Pending JPH09263958A (en) 1996-03-25 1996-03-25 Pre-treatment of metallic base material surface

Country Status (1)

Country Link
JP (1) JPH09263958A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002068715A1 (en) * 2001-02-26 2002-09-06 Sumitomo Metal Industries, Ltd. Surface treated steel product, method for production thereof and chemical conversion treatment solution
JP4593682B1 (en) * 2010-02-16 2010-12-08 昭和電工株式会社 Surface-coated cermet member and manufacturing method thereof
JP4593687B1 (en) * 2010-02-26 2010-12-08 昭和電工株式会社 CUTTING TOOL, ITS MANUFACTURING METHOD, AND CUTTING METHOD
JP2011144399A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
JP2011144398A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
JP2011144397A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
WO2011096398A1 (en) * 2010-02-03 2011-08-11 昭和電工株式会社 Treatment solution for forming oxidation-resistant film on surface-coated cermet member
JP2011157621A (en) * 2010-10-12 2011-08-18 Showa Denko Kk Method for manufacturing surface coated cermet member
JP2011167752A (en) * 2010-02-22 2011-09-01 Showa Denko Kk Draw die and method for manufacturing the same, and drawing method
JP2011177716A (en) * 2010-02-26 2011-09-15 Showa Denko Kk Forging die, method for manufacturing the same, and forging method

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6756092B2 (en) 2001-02-26 2004-06-29 Sumitomo Metal Industries, Ltd. Surface treated steel material, a method for its manufacture, and a chemical conversion treatment liquid
US8333847B2 (en) 2001-02-26 2012-12-18 Sumitomo Metal Industries, Ltd. Chemical conversion treatment liquid
WO2002068715A1 (en) * 2001-02-26 2002-09-06 Sumitomo Metal Industries, Ltd. Surface treated steel product, method for production thereof and chemical conversion treatment solution
US7918945B2 (en) 2001-02-26 2011-04-05 Sumitomo Metal Industries, Ltd. Method for manufacturing surface treated steel material using a chemical conversion treatment liquid
JP2011144397A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
JP2011144399A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
JP2011144398A (en) * 2010-01-12 2011-07-28 Showa Denko Kk Treatment liquid for forming oxidation-resistant film on surface-coated cermet member
WO2011096398A1 (en) * 2010-02-03 2011-08-11 昭和電工株式会社 Treatment solution for forming oxidation-resistant film on surface-coated cermet member
JP2011157611A (en) * 2010-02-03 2011-08-18 Showa Denko Kk Treatment solution for depositing oxidation-resistant film of surface coated cermet member
JP2011168802A (en) * 2010-02-16 2011-09-01 Showa Denko Kk Surface covered cermet member and method of manufacturing the same
JP4593682B1 (en) * 2010-02-16 2010-12-08 昭和電工株式会社 Surface-coated cermet member and manufacturing method thereof
JP2011167752A (en) * 2010-02-22 2011-09-01 Showa Denko Kk Draw die and method for manufacturing the same, and drawing method
JP4593687B1 (en) * 2010-02-26 2010-12-08 昭和電工株式会社 CUTTING TOOL, ITS MANUFACTURING METHOD, AND CUTTING METHOD
JP2011177716A (en) * 2010-02-26 2011-09-15 Showa Denko Kk Forging die, method for manufacturing the same, and forging method
JP2011177804A (en) * 2010-02-26 2011-09-15 Showa Denko Kk Cutting tool, method of manufacturing the same, and cutting method
JP2011157621A (en) * 2010-10-12 2011-08-18 Showa Denko Kk Method for manufacturing surface coated cermet member

Similar Documents

Publication Publication Date Title
Galliano et al. Sol-gel coatings on 316L steel for clinical applications
Zeng et al. Progress and challenge for magnesium alloys as biomaterials
Izman et al. Surface modification techniques for biomedical grade of titanium alloys: oxidation, carburization and ion implantation processes
Hryniewicz et al. Magnetoelectropolishing for metal surface modification
SE464415B (en) PROCEDURE FOR THE PREPARATION OF A COMPOSITION MATERIAL COATED WITH CALCIUM PHOSPHATE SOCIETY, AS USEFUL AS AN IMPLANT
JPH09263958A (en) Pre-treatment of metallic base material surface
JP5360660B2 (en) Method for producing biocompatible implant
KR101737358B1 (en) Surface treated Method of Dental implants using plasma electrolytic oxidation
EP1975277A1 (en) Surface treatment method of titanium or titanium alloy
JPH0312159B2 (en)
JP5951478B2 (en) Implant surface treatment method, implant treated by the method, and electrolyte solution used in the method
US20080086211A1 (en) Titanium implant and a process for the preparation thereof
JP2003235954A (en) Bone conductive biomaterial and manufacturing method therefor
Shanaghi et al. Enhanced corrosion resistance and reduced cytotoxicity of the AZ91 Mg alloy by plasma nitriding and a hierarchical structure composed of ciprofloxacin‐loaded polymeric multilayers and calcium phosphate coating
Valanezhad et al. Novel ceramic coating on titanium with high mechanical properties
JP2000093498A (en) Bone substitution material and its production
JP3129041B2 (en) Implant and manufacturing method thereof
JPS6399869A (en) Production of composite material coated with calcium phosphate
JP3670755B2 (en) Method for forming calcium phosphate coating
JPH0139787B2 (en)
JPH11323570A (en) Method of forming hydroxyapatite film
SU1560621A1 (en) Method of applying protective coatings
JP3846817B2 (en) Method for producing calcium phosphate coating
JPH0747115A (en) Implant and its manufacture
Al-Khafaji et al. Evaluation of Corrosion Resistance of Laser-Treated and PEKK-Coated Titanium