JPH0380867B2 - - Google Patents
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- Publication number
- JPH0380867B2 JPH0380867B2 JP10736287A JP10736287A JPH0380867B2 JP H0380867 B2 JPH0380867 B2 JP H0380867B2 JP 10736287 A JP10736287 A JP 10736287A JP 10736287 A JP10736287 A JP 10736287A JP H0380867 B2 JPH0380867 B2 JP H0380867B2
- Authority
- JP
- Japan
- Prior art keywords
- corrosion resistance
- less
- weight
- corrosion
- steel
- 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
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- 238000005260 corrosion Methods 0.000 description 54
- 230000007797 corrosion Effects 0.000 description 54
- 229910000831 Steel Inorganic materials 0.000 description 12
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 12
- 239000010935 stainless steel Substances 0.000 description 12
- 229910001220 stainless steel Inorganic materials 0.000 description 12
- 239000010959 steel Substances 0.000 description 12
- 238000007792 addition Methods 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 229910052797 bismuth Inorganic materials 0.000 description 8
- 239000002131 composite material Substances 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 229910052718 tin Inorganic materials 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000004310 lactic acid Substances 0.000 description 6
- 235000014655 lactic acid Nutrition 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000010828 elution Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910018487 Ni—Cr Inorganic materials 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000002436 steel type Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 229910000997 High-speed steel Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 229910001566 austenite Inorganic materials 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000001247 metal acetylides Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 229910016338 Bi—Sn Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- -1 TiC Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Prevention Of Electric Corrosion (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
<産業上の利用分野>
この発明は、Ni−Cr系SUS304ステンレス鋼を
ベースとしてその耐食性と被削性を改善し、特に
食品用機器の材料として好ましく利用することが
できるNi−Cr系ステンレス鋼に関するものであ
る。
<従来の技術>
JISに定められたSUS304の化学成分は表1の
とおりである。
<Industrial Application Field> The present invention is based on Ni-Cr stainless steel SUS304, which improves its corrosion resistance and machinability, and which can be particularly preferably used as a material for food equipment. It is related to. <Prior art> The chemical components of SUS304 specified by JIS are shown in Table 1.
【表】
SUS304は耐食性材料として広く用いられてい
るが、被削加工性が非常に悪い。快削性が要求さ
れる場合には、従来、耐食性を大幅に犠牲にして
意図的に硫化物系介在物(MnS)を生成させる
方法が一般的に採られている。しかし、耐食性を
特に重視して、強腐食環境(例えば、塩化物環境
や酸性飲料環境等)にも対応させるようするに
は、さらにMnSの主成分である鋼中のS及びMn
の組成比Mn/S比を低下させ、MnS中の固溶Cr
量を多くすることが有効とされている(「鉄と
鋼」、70(1984)、p.741)。
<発明が解決しようとする問題点>
上記したMnSの生成およびMn/S比の低下を
バランスよく調整することによつて耐食性を損わ
ず被削性を改善することはある程度可能である
が、未だ充分満足できるものではなかつた。
そこてこの発明は、SUS304をベースとして、
耐食性と被削性の両方がさらに優れたNi−Cr系
ステンレス鋼を提供することを目的としてなされ
たものである。
<問題点を解決するための手段および作用>
この発明による耐食性および被削性を改善した
Ni−Cr系ステレス鋼は、SUS304ステンレス鋼を
基本成分としてこれを一部変更した次のような化
学組成を有するものである:C0.08重量%以下、
Si1.0重量%以下、Mn0.7重量%以下、P0.04重量
%以下、S0.005重量%以下、Ni8.0〜12.0重量%、
Cr17.0〜20.0重量%、Mo0.40〜0.80重量%、
Cu0.3重量%以下、Bi0.03〜0.1重量%、Sn0.03〜
0.2重量%、および残部がFe。
Biは被削性を改善する元素であつて、0.03重量
%以下では被削性改善効果が少なく、一方0.1重
量%以下では鍛造性を害し、さらには孔食を発生
し易くなり耐食性に悪影響を及ぼす。そのためこ
の発明においては0.03〜0.1重量%の範囲でBiを
使用する。
Snは被削性を改善するだけでなく、耐全面腐
食性、耐隙間腐食性を改善する。特にSnとBiと
を複合して添加したこの発明のステンレス鋼は、
Biのみの添加と比べて耐全面腐食性、耐孔食性、
耐隙間腐食性を改善できる。また、希硫酸水溶液
中では、Snが鋼表面に析出して水素過電圧を大
きくし、耐硫酸性(この場合、耐全面腐食性)を
改善する。上述したようなSn添加による耐食性
改善効果は、0.03重量%以下では効果が少なく、
一方0.2重量%以上添加した場合には鍛造割れを
生じ加工材としての利用は不可能となる。
またMoおよびCuは耐食性全般において改善効
果があるが、Cuが多すぎると耐有機酸腐食性を
低下させることがある。しかし、この発明のよう
にCuを0.3重量%以下に抑えることで耐有機酸腐
食性を高めることができる。またMoは0.40重量
%以下では耐食性に無効となる場合があり、また
0.80重量%以下では耐食性改善への効果が添加量
の割には少なくなり、さらにコスト高となるた
め、この発明における0.40〜0.80重量%が最適で
ある。
SおよびMnについては、前述したようにこれ
らの量を低減すると耐食性が改善されるが、反面
において被削加工性を低下させる。この発明にお
いてはSを0.005重量%以下、Mnを0.7重量%以
下として耐食性を改善する一方、被削性の低下は
BiとSnとを複合添加することによつて補うこと
ができる。
Niはオーステナイト(γ)系ステンレス鋼の
基本元素で、γ相を安定にする。強度面では靭性
の改善に寄与する。低Niではγ相が不安定とな
り加工によりマルテンサイトを誘発し、硬化して
靭性を低下させる。NiはFe、Crに比較して電気
化学的に貴であるため、活性態域での腐食を抑制
する。また、中性塩化物溶液や非酸化性酸による
腐食に対して、顕著な抵抗性を与え、かつ不働態
を強化する。この発明では、フエライト生成元素
であるSnを添加しているため、SUS304規格より
もNiを多くしてγ相を安定にしている。
Crはステンレス鋼の基本成分で、酸化性環境
下においてステンレス鋼の不働態化に寄与する。
すなわち、ステンレス鋼の耐食性はこの不働態皮
膜によつて維持されるものであり、Crはステン
レス鋼にとつて必須の元素である。
Cの値に関しては、JISにも規定されているよ
うに、材料の金属組織的安定性、機械的性質、耐
食性、製造コスト等の面から重要な意味がある。
すなわち、Cは強力なオーステナイト生成元素で
あり、侵入型に固溶して強度を増大させるために
固溶限範囲内で多く添加する必要がある。しか
し、C量を過度に多くすると熱処理、溶接等の熱
的影響を受けた場合、Cr23C6、Cr7C3、NbC、
TiC等の炭化物を形成し、耐食性の低下につなが
る。特にCr炭化物が形成されるとマトリツクス
中のCr量を低減させ、耐食性を極端に低下させ
ることから、ある一定量以下に抑える必要があ
る。さらに、最も多く生産されているSUS304に
合わせてC量を決めた方が安価に製造できる点も
考慮して、C量は0.08重量%以下とする。
Siの値も、製造性、機械的性質、製造コスト等
の面で重要な意味がある。Si添加により引張強
さ、弾性限が増大し、また耐食性に関しても
SiO2皮膜を形成し、耐食性が向上する。一方、
Siは強力なフエライト生成元素であり、オーステ
ナイトを不安定にさせる。圧延工程においてもSi
が多いと割れを生じる等の問題がでてくる。こう
したことを考慮すると、Si量はJISで規定されて
いる1.0重量%以下に抑えることが種々の材料特
性、製造コストの両面から最良となる。
Pは有害な作用の多い元素である。Pが増加す
ると孔食感受性が増大し、さらにオーステナイト
の結晶粒界に偏折して粒界腐食の原因となる。ま
た応力腐食割れ性を害することから極力少ない方
が良い。しかし、製鋼過程において極低P化する
ことは技術的にも難しい問題であり、コストも非
常に高くつく。こうした点を考慮すると、P量は
JISで規定されている0.04重量%以下とするのが
性能、コスト両面から最良となる。
<実施例>
表2に示した化学組成をもつこの発明の実施例
の試料2(Bi、Sn複合添加鋼種)および比較用の
試料1(Biのみ添加鋼種)を調製した。[Table] SUS304 is widely used as a corrosion-resistant material, but its machinability is very poor. When free machinability is required, conventional methods have generally been adopted in which sulfide-based inclusions (MnS) are intentionally generated at the expense of significant corrosion resistance. However, in order to place special emphasis on corrosion resistance and make it compatible with strongly corrosive environments (e.g., chloride environments, acidic beverage environments, etc.), it is necessary to
By lowering the composition ratio Mn/S ratio of MnS, solid solution Cr in MnS
It is said that increasing the amount is effective ("Tetsu to Hagane", 70 (1984), p. 741). <Problems to be Solved by the Invention> Although it is possible to some extent to improve machinability without impairing corrosion resistance by adjusting the above-described production of MnS and reduction of the Mn/S ratio in a well-balanced manner, I still wasn't completely satisfied. Therefore, this invention is based on SUS304,
This was done with the aim of providing a Ni-Cr stainless steel with even better corrosion resistance and machinability. <Means and effects for solving the problems> Corrosion resistance and machinability have been improved by this invention.
Ni-Cr stainless steel is a basic component of SUS304 stainless steel with some modifications, and has the following chemical composition: C0.08% by weight or less,
Si 1.0% by weight or less, Mn 0.7% by weight or less, P 0.04% by weight or less, S 0.005% by weight or less, Ni 8.0 to 12.0% by weight,
Cr17.0~20.0wt%, Mo0.40~0.80wt%,
Cu0.3wt% or less, Bi0.03~0.1wt%, Sn0.03~
0.2% by weight, and the balance is Fe. Bi is an element that improves machinability, and if it is less than 0.03% by weight, it has little effect on improving machinability, while if it is less than 0.1% by weight, it impairs forgeability, and furthermore, it tends to cause pitting corrosion, which has a negative impact on corrosion resistance. affect Therefore, in this invention, Bi is used in a range of 0.03 to 0.1% by weight. Sn not only improves machinability but also general corrosion resistance and crevice corrosion resistance. In particular, the stainless steel of this invention with a combination of Sn and Bi added,
Overall corrosion resistance, pitting corrosion resistance, compared to the addition of Bi only.
Can improve crevice corrosion resistance. In addition, in a dilute sulfuric acid aqueous solution, Sn precipitates on the steel surface, increases hydrogen overvoltage, and improves sulfuric acid resistance (in this case, general corrosion resistance). The corrosion resistance improvement effect of Sn addition as described above is less effective at 0.03% by weight or less;
On the other hand, if it is added in excess of 0.2% by weight, forging cracks will occur, making it impossible to use it as a processed material. Furthermore, although Mo and Cu have the effect of improving corrosion resistance in general, too much Cu may reduce organic acid corrosion resistance. However, as in the present invention, by suppressing Cu to 0.3% by weight or less, organic acid corrosion resistance can be improved. Furthermore, if Mo is less than 0.40% by weight, it may become ineffective in corrosion resistance.
If it is less than 0.80% by weight, the effect on improving corrosion resistance will be small compared to the amount added, and the cost will increase, so 0.40 to 0.80% by weight is optimal in this invention. Regarding S and Mn, as described above, reducing these amounts improves corrosion resistance, but on the other hand, machinability is reduced. In this invention, corrosion resistance is improved by setting S to 0.005% by weight or less and Mn to 0.7% by weight, while machinability decreases.
This can be supplemented by adding Bi and Sn in combination. Ni is the basic element of austenitic (γ) stainless steel and stabilizes the γ phase. In terms of strength, it contributes to improving toughness. With low Ni, the γ phase becomes unstable, which induces martensite during processing, which hardens and reduces toughness. Since Ni is electrochemically more noble than Fe and Cr, it suppresses corrosion in the active state region. It also provides significant resistance to corrosion by neutral chloride solutions and non-oxidizing acids, and enhances passivity. In this invention, since Sn, which is a ferrite-forming element, is added, the γ phase is stabilized by adding more Ni than the SUS304 standard. Cr is a basic component of stainless steel and contributes to passivation of stainless steel in oxidizing environments.
That is, the corrosion resistance of stainless steel is maintained by this passive film, and Cr is an essential element for stainless steel. Regarding the value of C, as specified in JIS, it has an important meaning from the viewpoints of metallographic stability, mechanical properties, corrosion resistance, manufacturing cost, etc. of the material.
That is, C is a strong austenite-forming element, and in order to increase the strength by interstitial solid solution, it is necessary to add a large amount within the solid solubility limit. However, if the amount of C is excessively increased, and when subjected to thermal effects such as heat treatment or welding, Cr 23 C 6 , Cr 7 C 3 , NbC,
Forms carbides such as TiC, leading to decreased corrosion resistance. In particular, when Cr carbide is formed, the amount of Cr in the matrix is reduced and the corrosion resistance is extremely deteriorated, so it is necessary to keep the amount below a certain level. Furthermore, considering the fact that it can be manufactured at a lower cost if the C content is determined according to SUS304, which is the most commonly produced material, the C content is set to 0.08% by weight or less. The value of Si also has important meaning in terms of manufacturability, mechanical properties, manufacturing cost, etc. The addition of Si increases tensile strength and elastic limit, and also improves corrosion resistance.
Forms a SiO 2 film, improving corrosion resistance. on the other hand,
Si is a strong ferrite-forming element and destabilizes austenite. Si is also used in the rolling process.
If there is too much, problems such as cracking will occur. Taking these things into consideration, it is best to suppress the amount of Si to 1.0% by weight or less as stipulated by JIS in terms of various material properties and manufacturing costs. P is an element that has many harmful effects. As P increases, susceptibility to pitting corrosion increases, and P is also polarized at grain boundaries of austenite, causing intergranular corrosion. In addition, since it impairs stress corrosion cracking properties, it is better to have as little as possible. However, achieving extremely low P in the steelmaking process is technically difficult and extremely costly. Considering these points, the amount of P is
It is best from both performance and cost standpoints to keep the amount below 0.04% by weight as stipulated by JIS. <Example> Sample 2 (steel type with composite addition of Bi and Sn) of the present invention and comparative sample 1 (steel type with only Bi added) having the chemical compositions shown in Table 2 were prepared.
【表】
(1) 耐全面腐食性の改善
第1図は試料1、2の希塩酸(0.8%塩酸、
沸騰)中での腐食速度を示す。Bi、Sn複合添
加鋼種の腐食速度はBiのみ添加鋼種のそれの
1/3以下であり、耐食性が向上している。
第2図は、試料1、2の希硫酸(5%硫酸、
沸騰)中及び〔乳酸+食塩〕溶液(5%乳酸+
1%食塩、沸騰)中での腐食速度を示す。どち
らの溶液中においても、Bi、Sn複合添加鋼種
の腐食速度はBiのみ添加鋼種の場合よりも小
さく、耐食性が向上している。
(2) Fe、Cr溶出量からの評価
第3図は、試料1、2を〔乳酸+食塩〕溶液
(10%乳酸+0.3%食塩)中に浸漬させ、40℃で
55日間放置した後でFe、Cr溶出量を測定した
結果を示す。Fe溶出量において、試料1は
150ppm以上の溶出量であるが、Bi、Sn複合添
加鋼種は試料1の1/10以下の溶出量である。ま
たCr溶出量においても、試料2は試料1の1/1
0程度となつている。このように、Bi、Sn複合
添加鋼種は、Fe、Cr溶出量から評価して、耐
食性が著しく向上している。
(3) 耐孔食性の改善
第4図は、試料1、2の食塩溶液(3%食
塩、30℃)中における孔食発生電位(V′c100)
を測定した結果である。一般にこの値の高い方
が、孔食を発生しにくいことを意味する。Bi、
Sn複合添加鋼種のV′c100はBiのみ添加鋼種の
V′c100より平均値で50mVも貴であり、Bi、
Sn複合添加が耐孔食性を向上させることがわ
かる。
(4) 耐隙間腐食性の改善
第5図は、試料1、2の食塩溶液(3%食
塩、30℃)中における再不働態化電位(ER)
を測定した結果である。一般にこの値は高い方
が隙間腐食が停止し易いことを示す。第5図に
よれば、Bi、Sn複合添加鋼種のERはBiのみ添
加鋼種のそれよりも高く、Bi、Sn複合添加が
耐隙間腐食性を改善させることがわかる。
(5) 被削性の改善
第6図は、試料1、2に対して高速度鋼
(SKH−51(φ4))によりドリル穴あけ加工をし
た場合の工具寿命を示している。Bi、Sn複合
添加鋼種に対する工具寿命は、Biのみ添加鋼
種に対するそれより大きく、快削性元素Bi、
Snを複合添加加すると、Bi単独添加の場合よ
り被削性を改善することがわかる。
<発明の効果>
以上の説明からわかるようにこの発明のステン
レス鋼は、SUS304ステンレス鋼の耐食性と被削
性の両方を大幅に改善でき、耐食性を重視する食
品用機器の材料といて特に好ましく使用できるも
のである。[Table] (1) Improvement in general corrosion resistance
This shows the corrosion rate in boiling water. The corrosion rate of Bi and Sn composite added steel is less than 1/3 of that of Bi only added steel, indicating improved corrosion resistance. Figure 2 shows samples 1 and 2 of dilute sulfuric acid (5% sulfuric acid,
boiling) and [lactic acid + salt] solution (5% lactic acid +
Corrosion rate in 1% salt (boiling) is shown. In both solutions, the corrosion rate of the steel with Bi and Sn composite additions was lower than that of the steel with only Bi added, indicating improved corrosion resistance. (2) Evaluation from the amount of Fe and Cr eluted Figure 3 shows samples 1 and 2 immersed in a [lactic acid + salt] solution (10% lactic acid + 0.3% salt) and heated at 40℃.
The results of measuring the amount of Fe and Cr eluted after being left for 55 days are shown. In terms of Fe elution amount, sample 1 is
The amount of elution is 150 ppm or more, but the amount of elution for steel with Bi and Sn composite addition is less than 1/10 of that of sample 1. Also, in terms of Cr elution amount, sample 2 is 1/1 of sample 1.
It is about 0. In this way, Bi and Sn composite additive steel types have significantly improved corrosion resistance, as evaluated from the amounts of Fe and Cr eluted. (3) Improvement in pitting corrosion resistance Figure 4 shows the pitting corrosion occurrence potential (V'c100) of samples 1 and 2 in a salt solution (3% salt, 30℃).
This is the result of measuring. Generally, a higher value means that pitting corrosion is less likely to occur. Bi,
The V′c100 of Sn composite added steel is the same as that of Bi only added steel.
The average value is 50 mV nobler than V′c100, and Bi,
It can be seen that Sn composite addition improves pitting corrosion resistance. (4) Improvement of crevice corrosion resistance Figure 5 shows the repassivation potential (E R ) of samples 1 and 2 in a salt solution (3% salt, 30°C).
This is the result of measuring. Generally, the higher this value, the easier it is to stop crevice corrosion. According to FIG. 5, the E R of the Bi- and Sn-added steel is higher than that of the Bi-only added steel, indicating that the Bi-Sn combined addition improves the crevice corrosion resistance. (5) Improvement in machinability Figure 6 shows the tool life when drilling holes in samples 1 and 2 using high-speed steel (SKH-51 (φ4)). The tool life for steels with Bi and Sn composite additions is greater than that for steels with only Bi additions;
It can be seen that the combined addition of Sn improves machinability compared to the case of adding Bi alone. <Effects of the Invention> As can be seen from the above explanation, the stainless steel of the present invention can significantly improve both the corrosion resistance and machinability of SUS304 stainless steel, and is particularly preferably used as a material for food equipment where corrosion resistance is important. It is possible.
第1図は、希塩酸中における試料1、2と腐食
速度との関係図である。第2図は、希硫酸、〔乳
酸+食塩〕の各溶液中における試料1、2と腐食
速度との関係図である。第3図は、〔乳酸+食塩〕
溶液中における試料1、2とFe、Cr溶出量との
関係図である。第4図は、食塩溶液中における試
料1、2と孔食発生電位(V′c100)との関係図
である。第5図は、食塩溶液中における試料1、
2と再不働態化電位(ER)との関係図である。
第6図は、試料1、2に対して高速度鋼によりド
リル穴あけをした場合の試料1、2と工具寿命と
の関係図である。
FIG. 1 is a diagram showing the relationship between Samples 1 and 2 and the corrosion rate in dilute hydrochloric acid. FIG. 2 is a diagram showing the relationship between Samples 1 and 2 and the corrosion rate in dilute sulfuric acid and [lactic acid + salt] solutions. Figure 3 shows [lactic acid + salt]
FIG. 2 is a diagram showing the relationship between Samples 1 and 2 and the amounts of Fe and Cr eluted in the solution. FIG. 4 is a diagram showing the relationship between Samples 1 and 2 in a saline solution and the pitting corrosion occurrence potential (V'c100). Figure 5 shows sample 1 in saline solution,
2 and the repassivation potential (E R ).
FIG. 6 is a diagram showing the relationship between Samples 1 and 2 and tool life when holes are drilled using high-speed steel.
1 液体又は気体の圧縮機に用いられるベーンに
おいて、その組成が重量%でC0.7〜3.0%、Si0.1
〜1.5%、Cr2.5〜7.0%、Wと2Moを合計で10.0〜
20.0%、V0.5〜6.0%、Co10.0%以下、残部Feお
よび不可避的不純物よりなる焼結体で、該焼結体
中に最大径が100μ以下の空孔が面積%で1〜10
%有し、基地部硬さがHv800〜1000であり、該基
地中に平均粒径5μ以下のM6CとMC型結晶構造で
示される炭化物が容積%で9〜15%均一に分散し
ていることを特徴とする耐摩耗性、摺動性に優れ
たベーン。
2 液体又は気体の圧縮機に用いられるベーンに
おいて、その組成が重量%でC0.7〜3.0%、Si0.1
〜1.5%、Cr2.5〜7.0%、Wと2Moを合計で10.0〜
20.0%、V0.5〜6.0%、Co10.0%以下、Mn0.3〜
2.0%、S0.2〜0.7%、残部Feおよび不可避的不純
物よりなる焼結体で、該基地中に最大径が100μ
以下の空孔が面積%で1〜10%有し、基地部硬さ
がHv800〜1000であり、該基地中に平均粒径5μ以
下のM6CとMC型結晶構造で示される炭化物が容
積%で9〜15%均一に分散し、更に該基地中に硫
化物系介在物が面積%で0.5〜3.0%均一に分散し
ていることを特徴とする耐摩耗性と摺動性に優れ
たベーン。
1 Vanes used in liquid or gas compressors have a composition of 0.7 to 3.0% C and 0.1% Si by weight.
~1.5%, Cr2.5~7.0%, W and 2Mo total 10.0~
A sintered body consisting of 20.0%, V0.5~6.0%, Co10.0% or less, the balance Fe and unavoidable impurities, and the sintered body has pores with a maximum diameter of 100μ or less in area% of 1~10.
%, the hardness of the base part is Hv800-1000, and in the base, M 6 C with an average particle size of 5μ or less and carbide having an MC type crystal structure are uniformly dispersed in the volume% of 9-15%. Vanes with excellent wear resistance and sliding properties. 2 Vanes used in liquid or gas compressors have a composition of 0.7 to 3.0% C and 0.1% Si by weight.
~1.5%, Cr2.5~7.0%, W and 2Mo total 10.0~
20.0%, V0.5~6.0%, Co10.0% or less, Mn0.3~
A sintered body consisting of 2.0% S, 0.2~0.7% S, the balance Fe and unavoidable impurities, with a maximum diameter of 100μ in the base.
The following pores have an area percentage of 1 to 10%, the hardness of the base part is Hv800 to 1000, and the base has M 6 C with an average grain size of 5μ or less and carbides having an MC type crystal structure by volume. %, and sulfide inclusions are uniformly dispersed in the base by 0.5 to 3.0% in area %.It has excellent wear resistance and sliding properties. Vane.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62107362A JPS63274744A (en) | 1987-04-30 | 1987-04-30 | Ni-cr stainless steel improved in corrosion resistance and machinability |
| KR1019880001510A KR910003482B1 (en) | 1987-04-30 | 1988-02-15 | Ni-Cr stainless steel with improved corrosion resistance and machinability |
| US07/157,265 US4812287A (en) | 1987-04-30 | 1988-02-18 | Nickel-chromium stainless steel having improved corrosion resistances and machinability |
| CA000559581A CA1300406C (en) | 1987-04-30 | 1988-02-23 | Nickel-chromium stainless steel having improved corrosion resistances and machinability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62107362A JPS63274744A (en) | 1987-04-30 | 1987-04-30 | Ni-cr stainless steel improved in corrosion resistance and machinability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63274744A JPS63274744A (en) | 1988-11-11 |
| JPH0380867B2 true JPH0380867B2 (en) | 1991-12-26 |
Family
ID=14457153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62107362A Granted JPS63274744A (en) | 1987-04-30 | 1987-04-30 | Ni-cr stainless steel improved in corrosion resistance and machinability |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63274744A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4906193B2 (en) * | 2000-04-13 | 2012-03-28 | 新日鐵住金ステンレス株式会社 | Ferritic free-cutting stainless steel |
-
1987
- 1987-04-30 JP JP62107362A patent/JPS63274744A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63274744A (en) | 1988-11-11 |
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