JPS59180361A - Simple evaluating method of microsegregation in steel - Google Patents

Simple evaluating method of microsegregation in steel

Info

Publication number
JPS59180361A
JPS59180361A JP58052794A JP5279483A JPS59180361A JP S59180361 A JPS59180361 A JP S59180361A JP 58052794 A JP58052794 A JP 58052794A JP 5279483 A JP5279483 A JP 5279483A JP S59180361 A JPS59180361 A JP S59180361A
Authority
JP
Japan
Prior art keywords
segregation
section
steel
micro
lead bath
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
JP58052794A
Other languages
Japanese (ja)
Inventor
Masaaki Murakami
雅昭 村上
Hitoshi Tashiro
均 田代
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP58052794A priority Critical patent/JPS59180361A/en
Publication of JPS59180361A publication Critical patent/JPS59180361A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/20Metals
    • G01N33/204Structure thereof, e.g. crystal structure
    • G01N33/2045Defects

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating And Analyzing Materials By Characteristic Methods (AREA)
  • Investigating Or Analyzing Materials Using Thermal Means (AREA)

Abstract

PURPOSE:To evaluate easily segregation with god reproducibility by placing the surface for evaluating segregation of a high carbon steel contg. a specific amt. or above of C, Si and Mn on the front, subjecting the steel to austenitization at a specific temp. or below then to constant temp. transformation in a lead bath then cooling the steel thereby converting the segregated part to micromartensite. CONSTITUTION:The section of a high carbon steel contg., by wt%, >=0.40 C, >=0.15 Si, >=0.30 Mn is cut out and the section is heated to <=1,200 deg.C to austenitize the steel. The section is then dipped in a lead bath kept at 400-600 deg.C and is quickly cooled and after the section is held for 120-180sec, the section is water or air cooled to convert the segregated part to micromartensite by making use of the delay in the end time of the pearlite transformation occurring in segregation. When the section is polished and is treated with an etching soln. such as nital or picral, the segregated part which are more resistant to etching than the pearlite part provides a gloss and is therefore distinctly and visually identified. The detail in the microsegregated part is detected by using an optical microscope in combination. The evaluation with more than half the previously required time is thus made possible.

Description

【発明の詳細な説明】 本発明は高炭素鋼の簡易ミクロ偏析評価法に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a simple micro-segregation evaluation method for high carbon steel.

普通造塊法、連続鋳造法のいかんにかかわらず材質欠陥
となりうる偏析の評価は重要な問題である。偏析評価の
ために種々の分析機器が開発されてきた。例えば電子ビ
ームを利用して発生する特性x hpを分析するEPM
Aはミクロ偏析を精度よく検出できるが、ザンプルの作
製方法、大きさなどに制約がある。また、真空雰囲気を
必要とする。
Regardless of whether the ordinary ingot method or continuous casting method is used, evaluation of segregation, which can lead to material defects, is an important issue. Various analytical instruments have been developed for segregation evaluation. For example, EPM analyzes the characteristics x hp generated using an electron beam.
Method A can detect micro-segregation with high accuracy, but there are restrictions on the method of preparing samples, the size, etc. It also requires a vacuum atmosphere.

最近の研究により鋼の材質に大きな影響を及ぼすのはミ
クロ偏析であることがわかってきた。従来簡易評価法と
してSプリント、マクロ組織が利用されてきだが、これ
はマクロ偏析に関する情報のみをミクロ偏析については
無効である。それ故、分析機器を使わなくてもミクロ偏
析状況を把圃できる簡易評価法の開発が望まれていた。
Recent research has revealed that microsegregation has a major effect on the material properties of steel. Conventionally, S-print and macrostructure have been used as simple evaluation methods, but this only provides information about macro segregation and is invalid for micro segregation. Therefore, it has been desired to develop a simple evaluation method that can determine the state of microsegregation without using analytical equipment.

大き々ザンプルを大量にしかも簡単に処理できることは
工業上非常なメリットがある。従来高炭素鋼;除材は引
張強さと伸線性確保のために鉛パテンテイング処理を行
なっていた。これはオーステナイト化後鉛浴中に急冷保
持し、恒温変態させ微恢パーライト組織とするものであ
る。この場合、変態終了に必要な保持時間はTTT曲線
より推定していた。本発明者らはこの鉛パテンテイング
処理に注目し別の視点から簡易ミクロ偏析評価法を発明
した。
The ability to easily process large quantities of large samples has great industrial advantages. Conventionally, high carbon steels were removed using lead patenting treatment to ensure tensile strength and wire drawability. After being austenitized, it is rapidly cooled and held in a lead bath, and isostatically transformed into a micro-strengthened pearlite structure. In this case, the retention time required to complete the transformation was estimated from the TTT curve. The present inventors focused on this lead patenting treatment and invented a simple micro-segregation evaluation method from a different perspective.

以下本発明の詳細な説明する。The present invention will be explained in detail below.

T T T Fm 線の形は成分とオーステナイト化条
件で決まる。オーステナイト化条件を一定にすればT 
T T曲線の変態終了時間は成分により一宿的に定まる
。恒温変態を途中で中断し水冷あるいは空冷することに
より残留オーステナイトをマルテンサイトにすることが
できる。一連の研究の糸吉果、これを応用してミクロ偏
析を簡易評価できることがわかった。また鋳片、鋼片な
との大断面サンプルにも適用可能であることを知見した
。この方法は高価な分析、!7!器を利用することなく
恒昌変態時間をかえたサンプル同志の比11佼、TTT
曲線との比較によりミクロ偏析の半定量把握も可能であ
り工業的メリットが大である。
The shape of the T T T Fm line is determined by the components and austenitization conditions. If the austenitizing conditions are kept constant, T
The time at which the transformation of the T T curve ends is temporarily determined by the components. Residual austenite can be converted to martensite by interrupting isothermal transformation and cooling with water or air. As a result of a series of studies, it was found that microsegregation can be easily evaluated by applying this research. It was also found that the method can be applied to large cross-section samples such as cast slabs and steel slabs. This method is expensive analysis! 7! Sample comrade's ratio 11 who changed Tsunemasa metamorphosis time without using a vessel, TTT
It is also possible to semi-quantitatively understand micro-segregation by comparison with curves, which is a great industrial advantage.

すなわち、本発明は02040%、sr=>o、is係
、崗) 0.30%以上の高炭素鋼(Cおいて偏析評価
面が表面になるようにして、1.200°C以下でオー
ステナイト化後、400〜600°Cの鉛浴に浸漬し、
恒温変態後水冷あるいは空冷し、偏析に起因するパーラ
イト変態終了時間の遅れを利用して偏析部分をミクロマ
ルテンサイトとして検出することを相敵とする鋼の簡易
ミクロ偏析評価法である。
That is, the present invention is made of high carbon steel of 0.30% or more (02040%, sr=>o, is ratio, granite) (at C, the segregation evaluation surface is the surface, and austenite is formed at 1.200°C or less. After curing, immerse in a lead bath at 400-600°C,
This is a simple micro-segregation evaluation method for steel that involves water cooling or air cooling after isothermal transformation, and detecting the segregated portion as micro-martensite by utilizing the delay in the completion time of pearlite transformation caused by segregation.

ここで本発明の特許請求の範囲を決定した理由を説明す
る。
Here, the reason for determining the scope of claims of the present invention will be explained.

対象をC20,40%、S1≧0.15%、Mn上06
0係の高炭素鋼としたのは鉛浴利用の4亘温変態におい
て偏析部分を安定して再現性よくミクロマルテンサイト
として検出するためである。この4u囲をはずれると工
業的に利用できる簡易評1曲法として採用できるほど安
定した判定AXできない。オーステナイト化温度、鉛浴
保持時間の設定カニ極めて困難となる。
Target C20, 40%, S1≧0.15%, Mn above 06
The reason for using high carbon steel with a coefficient of 0 is to stably detect the segregated portion as micro martensite with good reproducibility during 4-temperature transformation using a lead bath. Outside this 4u range, the judgment AX cannot be stable enough to be adopted as a simple evaluation method that can be used industrially. Setting the austenitizing temperature and lead bath holding time becomes extremely difficult.

偏析評価面が表面になるようにするのも1つのポイント
である。これは鉛浴浸漬後、ル踊査面を瞬時に鉛浴温度
にするためである。特にサンプルカニ大きくなるとこの
影響が犬になる。変態1柑始I時間の遅れが防止できサ
ンプルの大きさの影響75:無視できる。このような方
法をとることによりイ虫拐゛などの小サンプルばかりで
なく鋳片、鋼片なとの犬サンプルの評価も可能となり汎
用性力;でた。i,200゛C以下でオーステナイト化
するのは再力日熱の影響を防止するためである。1,2
00’Oをこえると元素の拡散が盛んとなシミクロ偏析
状況が変わるためである。鉛浴温度を400〜6 0 
0 ’Oとしたのはベース成分における変態時間を工業
的に許容できる6分以内におさめるためである。4 D
 O ”O以下でも、600°C以上でも変態時間が長
くな!Sl簡易評価法としては利用できなくなる。この
場合、鉛が最適であるがンルト浴、オイル浴の使用も可
能である。
One point is to ensure that the segregation evaluation surface is the front surface. This is to instantly bring the surface to be inspected to the temperature of the lead bath after being immersed in the lead bath. Especially when the sample crab gets larger, this effect becomes more pronounced on the dog. The delay in time for metamorphosis can be prevented and the influence of sample size 75 can be ignored. By adopting such a method, it is possible to evaluate not only small samples such as caterpillar insects, but also dog samples such as cast slabs and steel slabs, resulting in versatility. The purpose of austenitizing at temperatures below 200°C is to prevent the effects of re-energizing solar heat. 1,2
This is because when the value exceeds 00'O, the state of micro-segregation changes, with active diffusion of elements. Lead bath temperature 400~60
The reason for setting it to 0'O is to keep the transformation time in the base component within 6 minutes, which is industrially acceptable. 4 D
The transformation time is too long even if the temperature is below O ''O or above 600°C!It cannot be used as a simple evaluation method for Sl.In this case, lead is most suitable, but it is also possible to use a wet bath or an oil bath.

鉛浴浸漬後、水冷あるいは空冷するのは偏析に起因する
残留オーステナイトをマルテンサイト化するためである
。焼入性がよい高Mn、合金添加材の場合は空冷でもよ
いが焼入性がよくない低Mn材は水冷が必要である。も
ちろん、水冷であればいずれの成分系でも適用可能であ
る。これによシミクロ偏析部分がミクロマルテンサイト
として検出される。ミクロマルテンサイトを見るにはナ
イタール、ピクラールなどの鋼でよく使用されている腐
食液で十分でちる。
The reason why water or air cooling is performed after immersion in a lead bath is to convert residual austenite caused by segregation into martensite. High Mn and alloy additive materials with good hardenability may be air cooled, but low Mn materials with poor hardenability require water cooling. Of course, any component system can be applied as long as it is water-cooled. As a result, the micro-segregation portion is detected as micro-martensite. To see micromartensite, a corrosive solution commonly used for steels such as nital and picral is sufficient.

パーライト部に比較してミクロマルテンサイト部は腐食
されにくいので偏析部が光沢をはなち目視判定ができる
。光学顕微鏡を併用すればミクロ偏析部の詳細な形状の
把握も可能である。また、このサンプルを用いれば硬度
分布を測定することによシ偏析状況を正確に把握できる
。通常のa s cast材、as rol I材を使
用して測定すると表面と中心部の冷却速度の差の影響が
出て偏析状況は把握できない。本発明法は鋼片、鋼片な
との犬サンプルの処理が可能なのでSプリントやマクロ
組織用サンプルがその′!2ま利用できるのもメリット
の1つでちる。
Since the micromartensite part is less susceptible to corrosion than the pearlite part, the segregated part becomes glossy and can be visually determined. If an optical microscope is also used, it is possible to understand the detailed shape of the micro-segregation area. Furthermore, by using this sample, the segregation situation can be accurately determined by measuring the hardness distribution. When measuring using normal A S cast material or A S ROL I material, the segregation situation cannot be ascertained due to the influence of the difference in cooling rate between the surface and the center. The method of the present invention is capable of processing samples such as steel slabs and slabs, so it is perfect for S-print and macrostructure samples! One of the benefits is that it can be used for 2 hours.

以上述べたように本発明法は工業的メリットの臣めて犬
な簡易ミクロ偏析評価法である。次に実施例で本発明法
の有用性を示す。
As described above, the method of the present invention is a simple micro-segregation evaluation method with industrial merits. Next, Examples will demonstrate the usefulness of the method of the present invention.

実施例1 第1表に使用した連続鋳造片の成分と鋳造条件を示す。Example 1 Table 1 shows the components and casting conditions of the continuously cast pieces used.

第  1  表 サンプルはいずれも5WRH82B相当材である。連続
鋳造片の断面サイズは240X 375 mra、、で
ある。
All samples in Table 1 are materials equivalent to 5WRH82B. The cross-sectional size of the continuous cast piece is 240 x 375 mra.

この連続鋳造片よ9幅240×長さ50×厚さ10Tn
mのL断面サンプルを切出した。このvJ片を950°
C15分オーステナイト化後、55す°Cに保持された
鉛浴中に20秒、60秒、120秒保持後空冷した。こ
の後、サンプルを研磨しナイタール腐食し、ミクロマル
テンサイトの発生状況をチェックした。チェック結果を
第2表に示す。鋳造条件、部位毎に明瞭な差が検出でき
た。
This continuous casting piece is 9 width 240 x length 50 x thickness 10Tn
An L cross section sample of m was cut out. This vJ piece is 950°
After being austenitized for 15 minutes, the sample was kept in a lead bath kept at 55 degrees Celsius for 20 seconds, 60 seconds, and 120 seconds, and then air-cooled. After this, the sample was polished and subjected to nital corrosion, and the occurrence of micromartensite was checked. The check results are shown in Table 2. Clear differences could be detected depending on casting conditions and locations.

ミクロマルテンサイト部を含む小サンプルを切り出しB
PMA分析を行なったがミクロマルテンサイト部には明
瞭なSi、Mn、Pのミクロ偏析が検出できた。首た偏
析度はサンプル2よシサンプル1のほうが大であった。
Cut out a small sample containing micro martensite part B
PMA analysis was performed, and clear micro-segregation of Si, Mn, and P could be detected in the micro-martensite portion. The degree of segregation was greater in sample 1 than in sample 2.

サンプル2の中間部と中心部を比較すると中心部のほう
が偏析度が犬であった。
When comparing the middle part and the center part of Sample 2, the degree of segregation in the center part was higher.

それ故、本発明法はミクロ個析頌向を正確に反映できる
ことがわかる。
Therefore, it can be seen that the method of the present invention can accurately reflect the micro-individualization direction.

実施例2 第6表に使用した連続鋳造片の成分と鋳造条件を示す。Example 2 Table 6 shows the components and casting conditions of the continuously cast pieces used.

サンプルはいずれも5WRI−162A相当材である。All samples are materials equivalent to 5WRI-162A.

連続鋳造片の断面サイズは240×375朋である。The cross-sectional size of the continuously cast piece is 240 x 375 mm.

この連続鋳造片よシ幅240×長さ100mmX厚烙1
0龍0L断面サンプルを切出した。この鋳片を1,00
0°C15分オーステナイト化後、500°Cに保持さ
れた鉛浴中に2秒、15秒、30秒保持後空冷した。こ
の後、サンプルを研磨しナイタール腐食し、ミクロマル
テンサイトの発生状況をチェックした。チェック結果を
第4表に示す。鋳造条件、部位でミクロ偏析の差が検出
できた。
This continuous casting piece has a width of 240 mm, a length of 100 mm, and a thickness of 1 mm.
A cross-sectional sample of 0 Dragon 0L was cut out. 1,000 pieces of this slab
After austenitizing at 0°C for 15 minutes, the sample was kept in a lead bath at 500°C for 2 seconds, 15 seconds, and 30 seconds, and then cooled in air. After this, the sample was polished and subjected to nital corrosion, and the occurrence of micromartensite was checked. The check results are shown in Table 4. Differences in microsegregation could be detected depending on casting conditions and locations.

本発明法を使えば、許容できるミクロ偏析限界サンプル
での鉛浴保持時間とミクロマルテンサイト発生の有無の
表を作っておけば、各チャージにおいて簡単に合否判定
できるメリットがある。
The method of the present invention has the advantage that by making a table of the lead bath holding time and the presence or absence of micromartensite generation for samples with acceptable microsegregation limits, it is possible to easily judge pass/fail for each charge.

B 、P M A分析ではサンプル作製から分析結果が
出るモでに半日以上かかるが、本発明法を使用すればミ
分以下の時間ですむ。それ故、従来の8プリンやマクロ
組織と同様に利用できる。
B, PMA analysis takes more than half a day from sample preparation to obtaining analytical results, but using the method of the present invention, it takes less than a minute. Therefore, it can be used in the same way as conventional 8-purine or macrostructure.

手続補正書 昭和58年4月」日 特許庁長官 若 杉 和 夫 殿 1事件の表示 昭和58年特許願第52794号 2発明の名称 鋼の簡易ミクロ偏析評価法 ろ補正をする者 事件との関係 特許出願人 住 所 東京都千代田区大手町2丁目6番ろ号名称 (
665)新日本製鐵株式会社 代表者  武 1)   豊 4代 理 人〒105 置(503)4877住 所 
東京都港区西新#1l−12−1第1森ビル8階5補正
命令の日付  自 発 6補正の対象  明細書の発明の詳細な説明の泗7補正
の内容  別紙の通り 別紙 (1)明細書第3頁7行目において、 「のみを」と「ミクロ」との間に「検出し」る字句を挿
入する。
Procedural Amendment April 1980'' Kazuo Wakasugi, Commissioner of the Japan Patent Office 1 Display of the case 1988 Patent Application No. 52794 2 Name of the invention Simple micro-segregation evaluation method for steel Relationship with the case Patent applicant address: 2-6-6 Otemachi, Chiyoda-ku, Tokyo Name (
665) Nippon Steel Corporation Representative Takeshi 1) Yutaka 4th generation Director Address: (503) 4877, 105
Date of amendment order to 5th Floor, 8th Mori Building, Daiichi Mori Building, #1l-12-1 Nishijin, Minato-ku, Tokyo Subject of voluntary 6th amendment Contents of 07th amendment to the detailed explanation of the invention in the specification Attachment (1) Details as attached On page 3, line 7, insert the word ``detect'' between ``only'' and ``micro''.

(21明細書第3頁下から8行目において、[Ca2.
40%Jの前に「重量係にして」なる字・を挿入する。
(In the 8th line from the bottom of page 3 of the 21 Specification, [Ca2.
40% Insert the characters ``to be in charge of weight'' before J.

(3)  明細書第3頁4行目\において、「Ca2.
40%」の前に「重量係にして」なる字を挿入する。
(3) On page 3, line 4 of the specification, “Ca2.
Insert the words ``by weight'' before ``40%''.

3232

Claims (1)

【特許請求の範囲】[Claims] 重量係にして、C≧040%、Sj≧0.15%、Mn
≧0.60%以上の高炭素鋼において偏析評価面が表面
になるようにして、1,200°C以下でオーステナイ
ト化後、400〜600“Cの鉛浴に浸漬し、恒温変態
後水冷あるいは空冷し、偏析に起因するパーライト変態
終了時間の遅れを利用して、偏析部分をミクロマルテン
サイトとして検出することを特徴とする鋼の簡易ミクロ
偏析評価法。
In terms of weight, C≧040%, Sj≧0.15%, Mn
≧0.60% or more high carbon steel with the segregation evaluation surface facing the surface, austenitized at 1,200°C or less, immersed in a lead bath at 400 to 600"C, and after isothermal transformation, water-cooled or A simple micro-segregation evaluation method for steel, which is characterized by detecting segregated portions as micro-martensite by air-cooling and utilizing the delay in pearlite transformation completion time caused by segregation.
JP58052794A 1983-03-30 1983-03-30 Simple evaluating method of microsegregation in steel Pending JPS59180361A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58052794A JPS59180361A (en) 1983-03-30 1983-03-30 Simple evaluating method of microsegregation in steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58052794A JPS59180361A (en) 1983-03-30 1983-03-30 Simple evaluating method of microsegregation in steel

Publications (1)

Publication Number Publication Date
JPS59180361A true JPS59180361A (en) 1984-10-13

Family

ID=12924738

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58052794A Pending JPS59180361A (en) 1983-03-30 1983-03-30 Simple evaluating method of microsegregation in steel

Country Status (1)

Country Link
JP (1) JPS59180361A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6080986A (en) * 1997-06-09 2000-06-27 Atomika Instruments Gmbh Secondary ion mass spectrometer with aperture mask

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6080986A (en) * 1997-06-09 2000-06-27 Atomika Instruments Gmbh Secondary ion mass spectrometer with aperture mask

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