JPS6019799B2 - Metal surface treatment agent - Google Patents
Metal surface treatment agentInfo
- Publication number
- JPS6019799B2 JPS6019799B2 JP7276778A JP7276778A JPS6019799B2 JP S6019799 B2 JPS6019799 B2 JP S6019799B2 JP 7276778 A JP7276778 A JP 7276778A JP 7276778 A JP7276778 A JP 7276778A JP S6019799 B2 JPS6019799 B2 JP S6019799B2
- Authority
- JP
- Japan
- Prior art keywords
- treatment agent
- surface treatment
- metal surface
- sodium
- nitrite
- 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
Landscapes
- Lubricants (AREA)
Description
【発明の詳細な説明】
本発明は亜硝酸または亜硝酸塩を含有する金属表面処理
剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a metal surface treatment agent containing nitrite or nitrite.
研削剤、防錆剤、洗浄剤等金属の表面処理に使用される
薬剤には従来亜硝酸または亜硝酸塩(以下亜硝酸類と云
う)が広く配合されている。Conventionally, nitrous acid or nitrites (hereinafter referred to as nitrites) have been widely blended into chemicals used for surface treatment of metals, such as abrasives, rust preventives, and cleaning agents.
しかしながらこの頭硝酸類は該金属表面処理剤中に同時
に配合されるアミン類と反応してNーニトロソ化合物を
形成し、これが極めて高い発塵性を示すために、亜硝酸
類を用いない金属表面処理剤の開発が急がれている。し
かしながら一方では未だ亜硝酸類の使用が避けられない
分野があることも否めない事実であり、暫定的にせよ亜
硝酸類にもとづく発癌・性を抑制する何等かの対策が求
められている。However, these nitric acids react with the amines that are simultaneously blended in the metal surface treatment agent to form N-nitroso compounds, which exhibit extremely high dust-generating properties. The development of drugs is urgently needed. However, on the other hand, it is an undeniable fact that there are still fields where the use of nitrites is unavoidable, and there is a need for some kind of countermeasure, even if only temporarily, to suppress carcinogenesis and toxicity caused by nitrites.
本発明者らは金属表面処理にとって悪影響がな〈しかも
人体に有害でない物質であって、亜硝酸類とアミン類と
の反応によるNーニトロソ化合物の抑制作用を有する物
質を検討するうち、ポリりん酸塩に顕著な効果のあるこ
とを見出し、本発明を完成した。The present inventors investigated a substance that has no adverse effect on metal surface treatment (and is not harmful to the human body, and has the effect of suppressing N-nitroso compounds due to the reaction between nitrites and amines), and discovered that polyphosphoric acid They discovered that salt has a remarkable effect and completed the present invention.
即ち本発明は亜硝酸および/または亜硝酸塩とポリりん
酸塩を含有する金属表面処理剤に関する。That is, the present invention relates to a metal surface treatment agent containing nitrite and/or nitrite and polyphosphate.
本発明においてポリりん酸塩とはトリポリりん酸ナトリ
ウム、トリ〆タりん酸ナトリウム、ウルトラりん酸ナト
リウムから選ばれたものである。In the present invention, the polyphosphate is selected from sodium tripolyphosphate, sodium tritaphosphate, and ultrasodium phosphate.
これらのポリりん酸塩はアミン類と反応し、アミンと亜
硝酸類の反応によるN−ニトロソ化合物の生成を阻害す
るものと考えられる。多くの金属表面処理剤、特に研削
剤、切削剤等のごとく、多量の函硝酸とアミン類を併用
するものにおいては処理剤中でニトロソ化合物を形成す
る場合があり、この様な場合には上記ポIJりん酸塩を
使用するアミンと当量、好ましくは2当量以上用いる。
ポリりん酸は単に函硝酸類やアミン類と共に処理剤中に
混合してももよいが多くのポリりん酸は水によって徐々
に加水分解するため、予め使用アミン類と反応させた後
加えてもよい。特に環状ポリりん酸、ウルトラりん酸等
は水溶液中では極めて不安定であるため予めアミンと反
応させておくのがよい。本発明における典型的な用途は
研削もしくは切削剤である。It is thought that these polyphosphates react with amines and inhibit the formation of N-nitroso compounds due to the reaction between amines and nitrites. Many metal surface treatment agents, especially those that use a large amount of nitric acid and amines together, such as abrasives and cutting agents, may form nitroso compounds in the treatment agent. PolyJ phosphate is used in an equivalent amount, preferably 2 equivalents or more, of the amine used.
Polyphosphoric acid may be simply mixed into a treatment agent with nitric acid or amines, but since many polyphosphoric acids are gradually hydrolyzed by water, it is also possible to react with the amines used before adding the polyphosphoric acid. good. In particular, cyclic polyphosphoric acid, ultraphosphoric acid, etc. are extremely unstable in an aqueous solution, so it is preferable to react them with an amine in advance. A typical use in this invention is as a grinding or cutting agent.
前記のごとく切削、研削剤はアミン類が配合される場合
が多く、特に発癌性の危険性が指摘されている。本発明
のごとくポリりん酸塩を使用した切削、研削剤ではN−
ニトロソ化合物の生成が箸るしく抑制されるのみならず
切削または研削効果そのものが向上する。以下実施例を
あげて説明する。As mentioned above, cutting and abrasive agents often contain amines, and the risk of carcinogenicity has been particularly pointed out. In cutting and abrasive agents using polyphosphate as in the present invention, N-
Not only is the formation of nitroso compounds significantly suppressed, but the cutting or grinding effect itself is improved. This will be explained below by giving examples.
実施例 1
25mMジメチルアミン塩酸塩水溶液、25mM亜硝酸
ナトリウム溶液および縮合リン酸ナトリウム水溶液(p
H3.5の緩衝溶液に溶解させる)を容量比1:1:2
の割合で混合し、所定時間反応させて検液とする。Example 1 25mM dimethylamine hydrochloride aqueous solution, 25mM sodium nitrite solution and condensed sodium phosphate aqueous solution (p
H3.5 buffer solution) in a volume ratio of 1:1:2
The test solution is prepared by mixing at the following ratio and reacting for a predetermined period of time.
検液5の‘にnーブタノール5の‘、スルフアニルアミ
ド1の【、nーナフチルエチレンジアミン1の【および
塩酸:nーブタノール液(1:2)3の‘を加え、60
−65ooで50分間加溢し、抽出溶媒留去後さらに1
00午0で18分間加熱し呈色させる。Add 5 parts of n-butanol, 1 part of sulfanilamide, 1 part of n-naphthylethylenediamine, and 3 parts of hydrochloric acid:n-butanol solution (1:2) to test solution 5,
-65oo for 50 minutes, and after distilling off the extraction solvent,
Heat at 00:00 for 18 minutes to develop color.
得られた溶液をn−ブタノールで10叫に希釈し、55
2凧山の吸光度を測定する。第3図は各種溶液中でのN
−ジメチルニトロソアミン生成量(吸光度)(縦軸)の
経時変化(反応温度370、pH3.5緩衝液中)を示
す。The resulting solution was diluted with n-butanol to 55%
2. Measure the absorbance of the kite mountain. Figure 3 shows N in various solutions.
- Changes in the amount of dimethylnitrosamine produced (absorbance) (vertical axis) over time (reaction temperature 370, in pH 3.5 buffer) are shown.
図中、1,2および3は綾合りん酸ナトリウム溶液がそ
れぞれ0.9Mトリメタリン酸ナトリウム溶液、50m
Mトリポリリン酸ナトリウム溶液および1.5%ウルト
ラリン酸ナトリウム溶液の場合を示し、4は縮合リン酸
塩無添加の場合を示す。以上の表から明らかなごとくポ
リりん酸に箸るしいN−ニトロソジメチルアミン生成抑
止能があることが理解される。実施例 2
亜硝酸ソーダとトリェタノールアミンの水溶液(JIS
W視瞳2号切削油剤)とこれにポリりん酸を配合した切
削油剤の切削効果を比較する。In the figure, 1, 2 and 3 are 0.9M sodium trimetaphosphate solution and 50m
The cases of M sodium tripolyphosphate solution and 1.5% sodium ultraphosphate solution are shown, and 4 shows the case of no condensed phosphate added. As is clear from the above table, it is understood that polyphosphoric acid has a remarkable ability to inhibit the formation of N-nitrosodimethylamine. Example 2 Aqueous solution of sodium nitrite and trietanoamine (JIS
The cutting effects of a cutting fluid containing polyphosphoric acid and a cutting fluid containing polyphosphoric acid will be compared.
切削油剤処方
A:亜硝酸ソーダ 0.5% 水溶液(参トリ
ェタノールアミン 0.5% 照例)B:亜硝酸ソーダ
0.5%
トリェタノールアミン 0.5% 水溶液トリポリりん
酸ソ−ダ 0.5%
C:亜硝酸ソーダ 0.5%
トリェタノールアミン 0.5% 水溶液へキサメタ
りん酸ソーダ 0.5%研削条件:
研削盤 内面研削盤
砥石 WA80KV
材質 SUJ−2
トリシロ 0.3肋
回転教 主軸 120仇pm
砥石 2000仇Pm
試験結果を表−1に示す。Cutting fluid formulation A: Sodium nitrite 0.5% aqueous solution (Reference example: Trietanolamine 0.5%) B: Sodium nitrite 0.5% Trietanoamine 0.5% aqueous solution Sodium tripolyphosphate 0.5 % C: Sodium nitrite 0.5% Trietanoamine 0.5% Aqueous solution Sodium hexametaphosphate 0.5% Grinding conditions: Grinding machine Internal grinding wheel WA80KV Material SUJ-2 Torishiro 0.3 rib rotation spindle 120 Pm grinding wheel 2000 Pm The test results are shown in Table-1.
表−1
(なお防錆性は鋳物のドライ力ッテイング切粉を浸贋後
、液を切りシャーレ‘こ入れて72時間経過した後の発
錆を観察した結果である)以上の結果はポリりん酸の添
加が研削性を向上させるのみならず、それ自体防錆剤と
して有用であることを示している。Table 1 (The rust prevention properties are based on the results obtained by observing rust after 72 hours had elapsed after dipping dry cutting chips from castings, draining the liquid, and placing them in a petri dish.) This shows that the addition of acid not only improves grindability, but is itself useful as a rust inhibitor.
ポリりん酸塩は種類によっては亜硝酸塩、アミン混合物
に溶けにくいものがあるのでアミンを含まない晒硝酸塩
系研削剤を使用し、使用液にポリりん酸を添加してもよ
い。Depending on the type of polyphosphate, some types are difficult to dissolve in nitrite and amine mixtures, so a bleached nitrate-based abrasive that does not contain amines may be used and polyphosphoric acid may be added to the solution used.
第1図は縮合りん酸塩によるN−ニトロソ化合物の生成
抑止効果を示す。
縦軸は吸光度、横軸は時間を示す。1はトリメタリン酸
ナトリウム、2はトリポリりん酸ナトリウム、3はウル
トラリン酸ナトリウムおよび4は縮合りん酸無添加を示
す。
第1図FIG. 1 shows the effect of condensed phosphates on inhibiting the formation of N-nitroso compounds. The vertical axis shows absorbance and the horizontal axis shows time. 1 indicates sodium trimetaphosphate, 2 indicates sodium tripolyphosphate, 3 indicates sodium ultraphosphate, and 4 indicates no addition of condensed phosphoric acid. Figure 1
Claims (1)
トリウム、トリポリりん酸ナトリウムおよびウルトラり
ん酸ナトリウムから選ばれたポリりん酸塩を含有する金
属表面処理剤。 2 金属表面処理剤が切削または研削剤である第1項記
載の処理剤。 3 金属表面処理剤が防錆剤である第1項記載の処理剤
。[Claims] 1. A metal surface treatment agent containing nitrous acid and/or a nitrite and a polyphosphate selected from sodium trimetaphosphate, sodium tripolyphosphate and sodium ultraphosphate. 2. The treatment agent according to item 1, wherein the metal surface treatment agent is a cutting or grinding agent. 3. The treatment agent according to item 1, wherein the metal surface treatment agent is a rust preventive agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7276778A JPS6019799B2 (en) | 1978-06-15 | 1978-06-15 | Metal surface treatment agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7276778A JPS6019799B2 (en) | 1978-06-15 | 1978-06-15 | Metal surface treatment agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54163276A JPS54163276A (en) | 1979-12-25 |
| JPS6019799B2 true JPS6019799B2 (en) | 1985-05-17 |
Family
ID=13498848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7276778A Expired JPS6019799B2 (en) | 1978-06-15 | 1978-06-15 | Metal surface treatment agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6019799B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6071697A (en) * | 1983-09-28 | 1985-04-23 | Hitachi Ltd | Lubricant for plastic working |
-
1978
- 1978-06-15 JP JP7276778A patent/JPS6019799B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54163276A (en) | 1979-12-25 |
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