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JPS6147909B2 - - Google Patents
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JPS6147909B2 - - Google Patents

Info

Publication number
JPS6147909B2
JPS6147909B2 JP5498278A JP5498278A JPS6147909B2 JP S6147909 B2 JPS6147909 B2 JP S6147909B2 JP 5498278 A JP5498278 A JP 5498278A JP 5498278 A JP5498278 A JP 5498278A JP S6147909 B2 JPS6147909 B2 JP S6147909B2
Authority
JP
Japan
Prior art keywords
sublimable
rust preventive
adamantane
weight
rust
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
Application number
JP5498278A
Other languages
Japanese (ja)
Other versions
JPS54147144A (en
Inventor
Haruhito Sato
Hiroshi Ichikawa
Hiroshi Hayashi
Yoshi Kurisaki
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.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan 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 Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Priority to JP5498278A priority Critical patent/JPS54147144A/en
Publication of JPS54147144A publication Critical patent/JPS54147144A/en
Publication of JPS6147909B2 publication Critical patent/JPS6147909B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は防錆物質を昇華性担体に添加してなる
昇華性防錆剤に関する。 従来、気化性防錆剤は、主として各種アミン類
の安息香酸塩や亜硝酸塩などの結晶性粉末をその
ままあるいは紙に含ませた防錆紙として用いてい
る。一般にこれらの塩類は蒸気圧が低いため、金
属表面に保護膜を形成する前に、ある程度金属が
さびるという欠点があつた。 本発明者らは、上記欠点を解消したすぐれた防
錆剤を開発すべく研究を重ねた結果、防錆能を有
する物質を担持できる無味、無臭、無毒で吸湿性
の小さい昇華性担体を見出し本発明を完成するに
至つた。 すなわち本発明は昇華性炭化水素に防錆物質を
添加してなる昇華性防錆剤を提供するものであ
る。 本発明で使用する昇華性炭化水素としてはアダ
マンタン、エンド−トリメチレンノルボルナン
(以下、TMNと略称する。)、シクロドデカン(以
下、CDと略称する)、トリメチルノルボルナン、
ノルボルナンのような各種化合物がある。 アダマンタンは無毒無臭で水に不溶の昇華性炭
化水素であり、融点が高い(268℃)ので、2種
類以上の結晶性炭化水素を混合しても急激な融点
降下が起らない。このため容易に他の昇華性炭化
水素と混合成形することができる。また成形後の
保形性がよく、他の昇華性炭化水素と配合すれば
その成形体の機械的強度を高めることができる。 アダマンタン以外の昇華性炭化水素は単独では
防錆物質を通常2重量%以下しか含有することが
できずその保留も充分でない。 昇華性炭化水素の選定は、防錆期間、すなわち
担体の必要な昇華速度を目安として行ない。組成
物中のその配合量を決定することが好ましい。例
えばアダマンタンとTMNを併用する場合には、
アダマンタン1〜25重量%に対してTMNを99〜
75重量%の割合で配合する。TMNが75重量%未
満では組成物表面にTMNより昇華速度の遅いア
ダマンタン(TMNの昇華速度の1/8)の粉がふ
き、商品価値が低下するため好ましくない。アダ
マンタンとCDを併用する場合は、アダマンタン
とCDは任意の割合で混合することができる。そ
の理由は、CDの昇華速度がアダマンタンの昇華
速度より遅い(アダマンタンの昇華速度の1/2)
ため、CDが組成物表面に残留するが、CDは融点
が低い(60℃)ので三次元に連続した均一相とな
つており、粉をふくことがないからである。通常
はアダマンタン5〜95重量%に対してCDを95〜
5重量%の割合で配合することが好ましい。 本発明に使用する防錆物質としてはモルホリ
ン、ジイソプロピルアミン、ジシクロヘキシルア
ミン、ジイソブチルアミン、ピペリジンなどの揮
発性アミン類、プロパギルアルコール、2−ブチ
ン−1−オールなどの揮発性アセチレン化合物、
その他防錆能を有する比較的蒸気圧の高い揮発性
化合物がある。 防錆物質の添加割合は特に制限はなく、また添
加する防錆物質の種類により異なり一義的に決め
ることはできないが、一般的には昇華性防錆剤に
対して防錆物質0.1〜20重量%である。また、必
要に応じて香料その他の物質を適宜加えることが
できる。 本発明の昇華性防錆剤において、昇華性炭化水
素を適当に選択することにより、担体なる昇華性
炭化水素の昇華と共に防錆物質が揮散するため、
取扱いが容易となる。 本発明の防錆剤を製造するには、たとえばアダ
マンタンおよび他の昇華性炭化水素を配合し、加
熱溶融した後、前記防錆物質を添加し、冷却、凝
固せしめる。あるいはさらに、粉砕、圧縮成形す
ることにより目的の防錆剤を得ることができる。
かくして得られた防錆剤は機械的強度や外観上の
商品性等にすぐれており、防錆物質が吸湿性の小
さい昇華性組成物に担持されているため利用範囲
が極めて広い。 次に、本発明を実施例により詳しく説明する。 実施例 1 アダマンタン20重量部とTMN80重量部を加熱
溶融して均一に混合した後、モルホリンを2重量
部添加して、直径90mm高さ15mmのシヤーレに流し
込み凝固させ防錆剤を得た。これを室温下空気気
流中にて昇華させその昇華特性を求めた。結果を
第1図に示す。図中のモルホリン濃度は、成形後
の組成物におけるモルホリンの初期濃度を1とす
る相対濃度を示す。 実施例 2 TMN100重量部およびジイソプロピルアミン2
重量部を用いて実施例1と同様の操作を行なつ
た。結果を第2図に示す。 実施例 3 昇華性担体100重量部および防錆物質3重量部
からなる均一溶融混合物を成型器に流入し、直径
20mmφ、厚み10mm、重量2.3gの防錆剤を得た。 この防錆剤を用いて「JIS Z0236−1974(さび
止め油一般試験方法)6.7気化性さび止め性」に
準じて防錆試験を行なつた。結果を第1表に示
す。 比較例 1 昇華性担体又はジシクロヘキシルアミンの亜硝
酸塩のみを用いて実施例1と同様の操作を行なつ
た。結果を第1表に示す。
The present invention relates to a sublimable rust preventive agent which is formed by adding a rust preventive substance to a sublimable carrier. Conventionally, volatile rust preventive agents are mainly crystalline powders such as benzoates and nitrites of various amines used as they are or as rust preventive paper impregnated with paper. Since these salts generally have low vapor pressure, they have the disadvantage that the metal rusts to some extent before a protective film is formed on the metal surface. As a result of repeated research to develop an excellent rust preventive agent that eliminates the above drawbacks, the present inventors discovered a sublimable carrier that is tasteless, odorless, nontoxic, and has low hygroscopicity and can support a substance with rust preventive ability. The present invention has now been completed. That is, the present invention provides a sublimable rust preventive agent made by adding a rust preventive substance to a sublimable hydrocarbon. Examples of sublimable hydrocarbons used in the present invention include adamantane, endo-trimethylenenorbornane (hereinafter abbreviated as TMN), cyclododecane (hereinafter abbreviated as CD), trimethylnorbornane,
There are various compounds such as norbornane. Adamantane is a non-toxic, odorless, sublimable hydrocarbon that is insoluble in water, and has a high melting point (268°C), so even when two or more types of crystalline hydrocarbons are mixed together, the melting point does not drop sharply. Therefore, it can be easily mixed and molded with other sublimable hydrocarbons. In addition, it has good shape retention after molding, and when mixed with other sublimable hydrocarbons, the mechanical strength of the molded product can be increased. Sublimable hydrocarbons other than adamantane alone can usually contain less than 2% by weight of rust preventive substances, and their retention is insufficient. The sublimable hydrocarbon is selected based on the rust prevention period, that is, the required sublimation rate of the carrier. It is preferable to determine its amount in the composition. For example, when using adamantane and TMN together,
TMN from 99% to 1% to 25% by weight of adamantane
Blend at a ratio of 75% by weight. If the TMN content is less than 75% by weight, powder of adamantane, which has a lower sublimation rate than TMN (1/8 of the sublimation rate of TMN), will be scattered on the surface of the composition, which is undesirable because the commercial value will decrease. When adamantane and CD are used together, adamantane and CD can be mixed in any ratio. The reason is that the sublimation speed of CD is slower than that of adamantane (1/2 of the sublimation speed of adamantane)
Therefore, CD remains on the surface of the composition, but since CD has a low melting point (60°C), it forms a three-dimensionally continuous homogeneous phase and does not form powder. Usually 95% to 95% CD to 5% to 95% by weight of adamantane
It is preferable to mix it in a proportion of 5% by weight. The antirust substances used in the present invention include volatile amines such as morpholine, diisopropylamine, dicyclohexylamine, diisobutylamine, and piperidine, volatile acetylene compounds such as propargyl alcohol, and 2-butyn-1-ol;
There are other volatile compounds with relatively high vapor pressure that have antirust properties. There is no particular limit to the ratio of rust preventive substances added, and it varies depending on the type of rust preventive substance added and cannot be determined unambiguously, but in general, the ratio of rust preventive substance to sublimation rust preventive substance is 0.1 to 20% by weight. %. Further, fragrances and other substances can be added as appropriate. In the sublimable rust preventive agent of the present invention, by appropriately selecting the sublimable hydrocarbon, the rust preventive substance evaporates with the sublimation of the sublimable hydrocarbon that is the carrier.
Easy to handle. To produce the rust preventive agent of the present invention, for example, adamantane and other sublimable hydrocarbons are blended, heated and melted, then the rust preventive substance is added, and the mixture is cooled and solidified. Alternatively, the desired rust preventive can be obtained by crushing and compression molding.
The rust preventive agent thus obtained has excellent mechanical strength and commercial appearance, and has an extremely wide range of applications because the rust preventive substance is supported by a sublimable composition with low hygroscopicity. Next, the present invention will be explained in detail with reference to examples. Example 1 After heating and melting 20 parts by weight of adamantane and 80 parts by weight of TMN and uniformly mixing them, 2 parts by weight of morpholine were added, and the mixture was poured into a shear dish with a diameter of 90 mm and a height of 15 mm to solidify to obtain a rust preventive agent. This was sublimated in an air stream at room temperature and its sublimation characteristics were determined. The results are shown in Figure 1. The morpholine concentration in the figure indicates a relative concentration with the initial concentration of morpholine in the composition after molding being 1. Example 2 100 parts by weight of TMN and diisopropylamine 2
The same operation as in Example 1 was carried out using parts by weight. The results are shown in Figure 2. Example 3 A homogeneous molten mixture consisting of 100 parts by weight of a sublimable carrier and 3 parts by weight of a rust preventive substance was poured into a molding machine, and a diameter
A rust preventive agent having a diameter of 20 mm, a thickness of 10 mm, and a weight of 2.3 g was obtained. Using this rust preventive agent, a rust prevention test was conducted in accordance with "JIS Z0236-1974 (General test methods for rust preventive oils) 6.7 Volatile rust prevention properties". The results are shown in Table 1. Comparative Example 1 The same operation as in Example 1 was carried out using only the sublimable carrier or dicyclohexylamine nitrite. The results are shown in Table 1.

【表】【table】

【表】【table】 【図面の簡単な説明】[Brief explanation of the drawing]

第1図および第2図は本発明の防錆剤の昇華特
性を示すグラフである。
FIGS. 1 and 2 are graphs showing the sublimation properties of the rust preventive of the present invention.

Claims (1)

【特許請求の範囲】 1 昇華性炭化水素に防錆物質を添加してなる昇
華性防錆剤。 2 昇華性炭化水素がアダマンタン、エンド−ト
リメチレンノルボルナン、シクロドデカンから選
ばれた1種又は2種以上の物質である特許請求の
範囲第1項記載の昇華性防錆剤。 3 昇華性炭化水素がアダマンタンとエンド−ト
リメチレンノルボルナンあるいはアダマンタンと
シクロドデカンを組み合せたものである特許請求
の範囲第1項記載の昇華性防錆剤。 4 防錆物質がモルホリン、ジイソプロピルアミ
ン、ジシクロヘキシルアミン、ジイソブチルアミ
ン、ピペリジン、プロパギルアルコール、2−ブ
チン−1−オールから選ばれた1種又は2種以上
の物質である特許請求の範囲第1項記載の昇華性
防錆剤。
[Claims] 1. A sublimable rust preventive agent made by adding a rust preventive substance to a sublimable hydrocarbon. 2. The sublimable rust inhibitor according to claim 1, wherein the sublimable hydrocarbon is one or more substances selected from adamantane, endo-trimethylenenorbornane, and cyclododecane. 3. The sublimable rust inhibitor according to claim 1, wherein the sublimable hydrocarbon is a combination of adamantane and endo-trimethylenenorbornane or adamantane and cyclododecane. 4. Claim 1, wherein the rust preventive substance is one or more substances selected from morpholine, diisopropylamine, dicyclohexylamine, diisobutylamine, piperidine, propargyl alcohol, and 2-butyn-1-ol. Sublimation rust inhibitor as described.
JP5498278A 1978-05-11 1978-05-11 Sublimable rust inhibitor Granted JPS54147144A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5498278A JPS54147144A (en) 1978-05-11 1978-05-11 Sublimable rust inhibitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5498278A JPS54147144A (en) 1978-05-11 1978-05-11 Sublimable rust inhibitor

Publications (2)

Publication Number Publication Date
JPS54147144A JPS54147144A (en) 1979-11-17
JPS6147909B2 true JPS6147909B2 (en) 1986-10-21

Family

ID=12985846

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5498278A Granted JPS54147144A (en) 1978-05-11 1978-05-11 Sublimable rust inhibitor

Country Status (1)

Country Link
JP (1) JPS54147144A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19511340C1 (en) * 1995-03-28 1996-10-02 Hans Michael Hangleiter Process for temporarily sealing or solidifying materials
EP2829328A1 (en) 2013-07-22 2015-01-28 Hans-Michael Hangleiter GmbH Application device for applying at least one sublimatable condensable compound, in particular of condensable cyclododecane, on surfaces of solid substrates or construction parts and device for determining the quality, in particular of the surface of a solid substrate or component
EP2829329A1 (en) 2013-07-22 2015-01-28 Hans-Michael Hangleiter GmbH Method for providing a surface of a solid substrate or component with a coating of at least one sublimatable compound, particularly with a cyclododecane layer, substrate or component manufactured according to the method

Also Published As

Publication number Publication date
JPS54147144A (en) 1979-11-17

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