JPH036216B2 - - Google Patents

Info

Publication number
JPH036216B2
JPH036216B2 JP12713886A JP12713886A JPH036216B2 JP H036216 B2 JPH036216 B2 JP H036216B2 JP 12713886 A JP12713886 A JP 12713886A JP 12713886 A JP12713886 A JP 12713886A JP H036216 B2 JPH036216 B2 JP H036216B2
Authority
JP
Japan
Prior art keywords
thermal expansion
coefficient
cast iron
carbon
low
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
JP12713886A
Other languages
Japanese (ja)
Other versions
JPS62284038A (en
Inventor
Takuo Handa
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 CASTING CO Ltd
Original Assignee
NIPPON CASTING 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 NIPPON CASTING CO Ltd filed Critical NIPPON CASTING CO Ltd
Priority to JP12713886A priority Critical patent/JPS62284038A/en
Publication of JPS62284038A publication Critical patent/JPS62284038A/en
Publication of JPH036216B2 publication Critical patent/JPH036216B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Treatment Of Steel In Its Molten State (AREA)

Description

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

〔産業上の利用分野〕 本発明は、高ニツケル鋳鉄を基本とし、炭素、
シリコンの含有量を一定範囲に限定することによ
り、熱膨張係数を従来の高ニツケル低熱膨張鋳鉄
より低くした低熱膨張率のオーステナイト鋳鉄に
関するものである。 〔従来の技術〕 従来、低熱膨張鋳鉄としては、ASTM−A436
タイプ5及びASTM−A439タイプD5が知られて
いる。 これらの低熱膨張鋳鉄の平均熱膨張率αは、20
〜100℃の温度で、普通鋳鉄や普通鋼の約1/2〜1/
3(α=5〜6×10-6/℃)であり、熱変位抑制
の目的で用いられて来た。 然し、この低熱膨張鋳鉄の利用分野における高
精度化の要求に対しては不十分であり、更に一層
熱膨張率の低い材料の出現が望まれていた。 これに対し、特公昭60−51547号公報の低熱膨
張鋳鉄には、炭素0.8〜3.0%、シリコン1.0〜3.0
%、ニツケル30.0〜34.0%、コバルト4.0〜6.0%、
マンガン2.0%以下、イオウ1.0%以下、リン1.5%
以下、マグネシウム1.0%以下、残部は不純物を
含む鉄よりなるオーステナイト系の低熱膨張鋳鉄
が開示されている。 然し、この低熱膨張鋳鉄は極めて高価格で、且
つ供給不安の高いコバルトを含有し、低熱膨張率
は達成される半面、コスト高を伴う問題があつ
た。 〔発明の解決すべき問題点〕 本発明は、前述の従来の低熱膨張鋳鉄より更に
低熱膨張率のオーステナイト鋳鉄を、コバルトを
全く含まず、従来の低熱膨張鋳鉄と同価格で提供
することを目的とするものである。 〔問題点を解決するための手段〕 本発明は、重量基準にて、C:0.6〜1.4%、
Si:0.5〜1.0%、Mn:1.0%以下、Ni:34.0〜36.0
%、S:0.5%以下、P:0.5%以下、Mg又はCa
のうち一種又は二種を0.05〜0.5%、残部不可避
不純物を含む鉄からなり、C及びSiの含有率が次
式 (C+0.4×Si)≦1.6% の範囲にあることを特徴とする低熱膨張鋳鉄であ
る。 〔作用〕 低熱膨張鋳鉄等の合金における低熱膨張率の機
構は、強磁性合金における磁気変態点以下の温度
で生ずる自発磁化歪みが、格子の熱振動を相殺す
ることで説明されている。 鋼系材料では、インバー(アンバー)、スーパ
ーインバー(スーパーアンバー)が実用化されて
おり、これらの熱膨張率αは、0〜1.5×10-6
℃で非常に小さい。一方、35%ニツケル鋳鉄の熱
膨張率αは5〜6×10-6/℃で鋼系の低熱膨張率
材料と比べ相当の隔たりがある。 本発明者は、黒鉛鋳鉄の組織が、低炭素のオー
ステナイト基地と黒鉛の混合組織であることか
ら、基地組成の熱膨張率αに及ぼす影響に着目し
本発明を達成したものである。 即ち、35%前後のニツケルを含むオーステナイ
ト中への炭素の固溶度は、本来0.2%以下とされ
ている。(Metals Handbook第8版vol.8、P413)
これに対して、本発明者が炭素0.2%、ニツケル
36%を含む鋳鋼の熱膨張率αを測定した結果、α
=2.4×10-6/℃を得た。この値を用いて、全炭
素2%、(黒鉛1.8%)、36%ニツケルの鋳鉄の熱
膨張率αを次式で計算すると、 〔普通鋳鉄鋳物(日刊工業新聞社発行第67頁)〕
α=〔基地のα〕×〔基地の容積率〕+〔黒鉛のα〕×
〔黒鉛の容積率〕の次式に 〔基地のα〕 αM=2.4×10-6/℃ 〔基地の容積率〕 VM=0.94 〔黒鉛のα〕 αG=8.0×10-6/℃ 〔黒鉛の容積率〕 VG=0.06、 を夫々代入してαを求めるとα=2.7×10-6/℃
となり、実際のαに比べて約1/2の値となつた。 この結果から、従来の低熱膨張鋳鉄の基地中炭
素が0.2%以上含まれていることが考えられた。
これは、前記の36%ニツケル鋳鋼において、固溶
炭素が0.1%増すとαが約0.6×10-6/℃増加する
と言う知見に基づいて本発明はなされたものであ
る。 そこで、走査型電子顕微鏡(EPMA)を用い
て基地中の炭素量を測定したところ、約0.4%固
溶していることが確認された。この値で計算する
とα=3.9×10-6/℃となり、実際の値に近づく
が、なお計算値は1.0×10-6/℃以上小さい。 この原因として、鋳鉄において多量に添加され
るシリコンに着目し、シリコン量とαとの関係を
調べた結果、後述する実施例に示す如くシリコン
が1%増とαが約1.3×10-6/℃増加することを
見出した。 以上の実験と考察から、後述する実施例の第1
図に示す如く全炭素量を低くして基地中炭素の低
下とシリコン添加量を制限することにより従来の
低熱膨張鋳鉄より低い熱膨張率が得られることが
判つた。 即ち、前述の本発明の低熱膨張鋳鉄により20〜
50℃の平均熱膨張率α3.0〜4.0×10-6/℃が得ら
れる。 次に本発明の低熱膨張鋳鉄の成分の限定理由に
ついて述べる。 C:炭素オーステテナイト基地中に固溶すると
熱膨張率αの著しい増大を招くが、黒鉛として析
出させることにより、鋳鋼に比べて切削性、鋳造
性を改善出来る。0.6%未満では黒鉛量が少なく、
切削性が鋳鋼インバーに近づき、また溶解温度の
上昇により製造が難しくなる。1.4%を超えると
所望の低熱膨張率が得られなくなるのでその範囲
を0.6〜1.4%と定めた。 Si:シリコンは0.5%未満では基地中の炭素溶
解度が増し、低熱膨張率αの低減効果が失われ、
1.0%を超えると所望の低熱膨張率が得られない
ので、その範囲を0.5〜1.0%と定めた。 更に、炭素とシリコンの量比は、上記の範囲内
においても、第1図の発明の範囲に示す如く、
(C+0.4×Si)=1.6%を超えると低熱膨張率が得
られなくなるので、CとSiの含有率が(C+0.4
×Si)=1.6%となるように定めた。 Mn:マンガンは、偏析を生じ易く、且つ炭化
物の生成を促進して熱膨張率αの増大を招き、
1.0%を超えるとその影響が無視出来なくなるの
で1.0%以下とした。 Ni:ニツケルは、熱膨張率αに最も影響を与
える元素で、34.0%未満、36.0%を超えると熱膨
張率αの著しい増大を招くため34.0〜36.0%とし
た。 Mg、Ca:マグネシウム又はカルシウムは、黒
鉛の球状化を図るために添加するもので、これに
より機械的性質の向上が得られる。このためには
Mg又はCaのうち一種又は二種を0.05〜0.5%添加
することが必要である。 P、S:リン及びイオウは不可避的に混入する
元素であり、0.5%を超えると脆化が著しいので
0.5%以下とした。 残部は不可避不純物を含む鉄より構成される。 次に本発明の実施例について述べる。 〔実施例〕 実施例 1 30KVA高周波電気炉により、第1表に示す組
成の材料を溶解しCO2珪砂型でJISG−5122B号テ
ストピースを鋳造し、φ9×L50mmの熱膨張率測定
用テストピースを加工し、示差熱膨張率計を用い
て20〜200℃の熱膨張率αを測定した。 機械的性質は、JISG−0567号による高温引張
テストピース(平行部φ10)にて0.2%耐力、引張
強さ及び伸びを測定した。 第1表に組成及び試験結果並びに第1図に炭
素、シリコン組成と熱膨張率αとの関係グラフを
示す。
[Industrial Application Field] The present invention is based on high nickel cast iron, and contains carbon,
This invention relates to an austenitic cast iron with a low thermal expansion coefficient that is lower than that of conventional high nickel low thermal expansion cast irons by limiting the silicon content to a certain range. [Conventional technology] Conventionally, ASTM-A436 was used as a low thermal expansion cast iron.
Type 5 and ASTM-A439 type D5 are known. The average coefficient of thermal expansion α of these low thermal expansion cast irons is 20
At a temperature of ~100℃, it is about 1/2 to 1/2 that of ordinary cast iron or ordinary steel.
3 (α=5 to 6×10 -6 /°C), and has been used for the purpose of suppressing thermal displacement. However, this method is insufficient to meet the demand for high precision in the field of application of low thermal expansion cast iron, and there has been a desire for a material with an even lower coefficient of thermal expansion. In contrast, the low thermal expansion cast iron disclosed in Japanese Patent Publication No. 60-51547 contains 0.8 to 3.0% carbon and 1.0 to 3.0% silicon.
%, Nickel 30.0-34.0%, Cobalt 4.0-6.0%,
Manganese 2.0% or less, sulfur 1.0% or less, phosphorus 1.5%
The following discloses an austenitic low thermal expansion cast iron consisting of 1.0% or less of magnesium and the remainder of iron containing impurities. However, this low thermal expansion cast iron is extremely expensive and contains cobalt, whose supply is highly unstable, and while a low thermal expansion coefficient can be achieved, there is a problem in that it is accompanied by high costs. [Problems to be Solved by the Invention] The purpose of the present invention is to provide an austenitic cast iron having a coefficient of thermal expansion even lower than that of the conventional low thermal expansion cast iron described above, which does not contain any cobalt and at the same price as the conventional low thermal expansion cast iron. That is. [Means for solving the problems] The present invention provides C: 0.6 to 1.4% on a weight basis;
Si: 0.5-1.0%, Mn: 1.0% or less, Ni: 34.0-36.0
%, S: 0.5% or less, P: 0.5% or less, Mg or Ca
A low-heat product characterized by being made of iron containing 0.05 to 0.5% of one or two of the above, and the remainder containing inevitable impurities, with a C and Si content within the range of the following formula (C + 0.4 x Si) ≦ 1.6%. It is expanded cast iron. [Effect] The mechanism of the low coefficient of thermal expansion in alloys such as low thermal expansion cast iron is explained by the fact that the spontaneous magnetization strain that occurs at temperatures below the magnetic transformation point in ferromagnetic alloys cancels out the thermal vibrations of the lattice. Among steel materials, Invar (Amber) and Super Invar (Super Invar) have been put into practical use, and their coefficient of thermal expansion α is 0 to 1.5×10 -6 /
very small in °C. On the other hand, the coefficient of thermal expansion α of 35% nickel cast iron is 5 to 6×10 −6 /°C, which is quite different from that of steel-based materials with low coefficient of thermal expansion. Since the structure of graphite cast iron is a mixed structure of a low carbon austenite base and graphite, the present inventors focused on the influence of the base composition on the coefficient of thermal expansion α, and achieved the present invention. That is, the solid solubility of carbon in austenite containing around 35% nickel is originally supposed to be 0.2% or less. (Metals Handbook 8th edition vol.8, P413)
On the other hand, the inventor has developed a method using 0.2% carbon and nickel.
As a result of measuring the thermal expansion coefficient α of cast steel containing 36%, α
= 2.4×10 -6 /°C was obtained. Using this value, calculate the coefficient of thermal expansion α of cast iron with 2% total carbon, (1.8% graphite), and 36% nickel using the following formula:
α = [α of base] × [volume ratio of base] + [α of graphite] ×
The following formula for [volume ratio of graphite] is [α of base] α M =2.4×10 -6 /℃ [volume ratio of base] V M =0.94 [α of graphite] α G =8.0×10 -6 /℃ [Volume ratio of graphite] V G = 0.06, and α is calculated by substituting them respectively: α = 2.7×10 -6 /℃
The value was approximately 1/2 of the actual α. From this result, it was considered that the base of conventional low thermal expansion cast iron contained 0.2% or more of carbon.
This invention was made based on the knowledge that in the above-mentioned 36% nickel cast steel, when the solute carbon increases by 0.1%, α increases by about 0.6×10 -6 /°C. When the amount of carbon in the base was measured using a scanning electron microscope (EPMA), it was confirmed that approximately 0.4% of carbon was dissolved in solid solution. When calculated using this value, α=3.9×10 −6 /°C, which is close to the actual value, but the calculated value is still smaller than 1.0×10 −6 /°C. As the cause of this, we focused on silicon, which is added in large amounts in cast iron, and investigated the relationship between the amount of silicon and α.As shown in the example below, when silicon increases by 1%, α becomes approximately 1.3×10 -6 / It was found that ℃ increases. From the above experiments and considerations, we found that the first
As shown in the figure, it was found that a lower coefficient of thermal expansion than conventional low thermal expansion cast iron could be obtained by lowering the total carbon content, reducing the amount of carbon in the matrix, and limiting the amount of silicon added. That is, the low thermal expansion cast iron of the present invention described above has a
An average coefficient of thermal expansion α3.0 to 4.0×10 −6 /°C at 50°C is obtained. Next, the reasons for limiting the components of the low thermal expansion cast iron of the present invention will be described. C: When carbon is dissolved in the austenite base, the coefficient of thermal expansion α will significantly increase, but by precipitating it as graphite, machinability and castability can be improved compared to cast steel. If it is less than 0.6%, the amount of graphite is small;
Machinability approaches that of cast steel Invar, and manufacturing becomes difficult due to increased melting temperature. If it exceeds 1.4%, the desired low coefficient of thermal expansion cannot be obtained, so the range is set at 0.6 to 1.4%. Si: If silicon is less than 0.5%, the solubility of carbon in the base increases, and the effect of reducing the low coefficient of thermal expansion α is lost.
If it exceeds 1.0%, the desired low coefficient of thermal expansion cannot be obtained, so the range is set at 0.5 to 1.0%. Furthermore, even if the quantitative ratio of carbon to silicon is within the above range, as shown in the scope of the invention in FIG.
If the content of C and Si exceeds (C+0.4×Si)=1.6%, a low coefficient of thermal expansion cannot be obtained.
×Si) = 1.6%. Mn: Manganese tends to cause segregation and promotes the formation of carbides, leading to an increase in the coefficient of thermal expansion α.
If it exceeds 1.0%, the effect cannot be ignored, so it was set to 1.0% or less. Ni: Nickel is the element that most affects the thermal expansion coefficient α, and if it is less than 34.0% and exceeds 36.0%, the thermal expansion coefficient α will significantly increase, so it was set to 34.0 to 36.0%. Mg, Ca: Magnesium or calcium is added to make graphite spheroidal, thereby improving mechanical properties. For this purpose
It is necessary to add 0.05 to 0.5% of one or both of Mg and Ca. P, S: Phosphorus and sulfur are elements that are inevitably mixed in, and if they exceed 0.5%, embrittlement will be significant.
It was set to 0.5% or less. The remainder consists of iron containing unavoidable impurities. Next, examples of the present invention will be described. [Example] Example 1 Materials with the composition shown in Table 1 were melted in a 30KVA high-frequency electric furnace, and a JISG-5122B test piece was cast in a CO 2 silica sand mold to form a test piece for thermal expansion coefficient measurement of φ9 x L50mm. was processed, and the coefficient of thermal expansion α from 20 to 200°C was measured using a differential thermal expansion meter. For mechanical properties, 0.2% proof stress, tensile strength, and elongation were measured using a high-temperature tensile test piece (parallel part φ10) according to JISG-0567. Table 1 shows the composition and test results, and FIG. 1 shows a graph of the relationship between the carbon and silicon compositions and the coefficient of thermal expansion α.

【表】【table】

【表】 * 添加量を示す。
** 石英(+0.5×10−6/℃)補正計算済み値
本発明材料は、熱膨張率αが3.0〜3.7×10-6
℃で、従来の高ニツケル低熱膨張鋳鉄の約3/4〜
1/2であり、非常に低い熱膨張率が得られた。 No.1においては、コバルトを含んだNo.9と同様
の熱膨張率αを示し、低コストで、含コバルト材
並みの熱膨張率αが得られる利点がある。 又、機械的性質はほぼ従来の低熱膨張鋳鉄と同
じレベルであり、材力上の特別の配慮は不用であ
る。 No.3は、従来の低熱膨張鋳鉄より1.9×10-6
℃小さい熱膨張率αで且つ0.2%耐力が5Kgf/
mm2以上高く、実使用において有利である。 実施例 2 実施例1に準じて第2表の組成で第2図に示す
如き実体鋳物を製造し、各位置から第2図に示す
如く、テストピースを切り出し、実施例1に準じ
て熱膨張率αを測定して第3表の結果を得た。 第2図は実体鋳物形状とテストピース採取位置
の説明図で、数字の内( )値は寸法を他は採取
ケ所を示すものである。 尚、鋳造温度は、No.10が1515℃、No.11が1550℃
で鋳造性は良好で、問題となる欠陥は見られなか
つた。
[Table] * Shows the amount added.
** Quartz (+0.5×10 −6 /℃) corrected calculated value The material of the present invention has a thermal expansion coefficient α of 3.0 to 3.7×10 −6 /
℃, approximately 3/4 to 3/4 of conventional high nickel low thermal expansion cast iron
1/2, and a very low coefficient of thermal expansion was obtained. No. 1 exhibits a coefficient of thermal expansion α similar to that of No. 9 containing cobalt, and has the advantage of being low cost and having a coefficient of thermal expansion α comparable to that of cobalt-containing materials. In addition, the mechanical properties are almost at the same level as conventional low thermal expansion cast iron, and no special considerations regarding material strength are required. No. 3 is 1.9×10 -6 / lower than conventional low thermal expansion cast iron.
℃ small thermal expansion coefficient α and 0.2% yield strength 5Kgf/
mm 2 or higher, which is advantageous in actual use. Example 2 A solid casting as shown in FIG. 2 was manufactured with the composition shown in Table 2 according to Example 1, test pieces were cut out from each position as shown in FIG. 2, and subjected to thermal expansion according to Example 1. The rate α was measured and the results shown in Table 3 were obtained. Figure 2 is an explanatory diagram of the actual casting shape and test piece collection locations, where the values in parentheses ( ) indicate dimensions and the others indicate collection locations. The casting temperature is 1515℃ for No.10 and 1550℃ for No.11.
Castability was good and no problematic defects were observed.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

本発明による低熱膨張鋳鉄を、各種精密機械例
えば工作機械、計測器、半導体製造装置、光学機
械等の重要部に適用することにより、従来の低熱
膨張率の高ニツケル鋳鉄と同等のコストで、より
優れた高精度が得られ、関連分野に与える効果は
計り知れない効果を奏するものである。
By applying the low thermal expansion cast iron of the present invention to important parts of various precision machines, such as machine tools, measuring instruments, semiconductor manufacturing equipment, optical machinery, etc., it can be used at the same cost as conventional high nickel cast iron with a low thermal expansion coefficient, and at a higher cost. Excellent high precision can be obtained, and the effects on related fields will be immeasurable.

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

第1図は、実施例における炭素、シリコン組成
と熱膨張率αとの関係グラフ、第2図は、同じく
実体鋳物形状とテストピースの採取位置の説明図
である。
FIG. 1 is a graph of the relationship between the carbon and silicon compositions and the coefficient of thermal expansion α in Examples, and FIG. 2 is an explanatory diagram of the solid casting shape and the sampling position of the test piece.

Claims (1)

【特許請求の範囲】 1 重量基準にて、C:0.6〜1.4%、Si:0.5〜1.0
%、Mn:1.0%以下、Ni:34.0〜36.0%、S:0.5
%以下、P:0.5%以下、Mg又はCaのうち一種
又は二種を0.05〜0.5%、残部不可避不純物を含
む鉄からなり、C及びSiの含有率が次式 (C+0.4×Si)≦1.6% の範囲にあることを特徴とする低熱膨張鋳鉄。
[Claims] 1. On a weight basis, C: 0.6 to 1.4%, Si: 0.5 to 1.0
%, Mn: 1.0% or less, Ni: 34.0 to 36.0%, S: 0.5
% or less, P: 0.5% or less, 0.05 to 0.5% of one or both of Mg or Ca, and the remainder consists of iron containing inevitable impurities, and the content of C and Si is as follows: (C + 0.4 × Si) ≦ Low thermal expansion cast iron characterized by a range of 1.6%.
JP12713886A 1986-06-03 1986-06-03 Low thermal expansion cast iron Granted JPS62284038A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12713886A JPS62284038A (en) 1986-06-03 1986-06-03 Low thermal expansion cast iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12713886A JPS62284038A (en) 1986-06-03 1986-06-03 Low thermal expansion cast iron

Publications (2)

Publication Number Publication Date
JPS62284038A JPS62284038A (en) 1987-12-09
JPH036216B2 true JPH036216B2 (en) 1991-01-29

Family

ID=14952554

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12713886A Granted JPS62284038A (en) 1986-06-03 1986-06-03 Low thermal expansion cast iron

Country Status (1)

Country Link
JP (1) JPS62284038A (en)

Also Published As

Publication number Publication date
JPS62284038A (en) 1987-12-09

Similar Documents

Publication Publication Date Title
US7618499B2 (en) Fe-base in-situ composite alloys comprising amorphous phase
US4946644A (en) Austenitic stainless steel with improved castability
US4904447A (en) Low thermal expansion casting alloy having excellent machinability
KR101331322B1 (en) High-rigidity high-damping-capacity cast iron
JPH0321622B2 (en)
WO2011145339A1 (en) Austenitic cast iron, cast product of austenitic cast iron, and process for production of the cast product
JPH039179B2 (en)
US4217136A (en) Corrosion resistant austenitic stainless steel
US3740212A (en) Oxidation resistant austenitic ductile nickel chromium iron
JPH036216B2 (en)
JP2010095747A (en) Method for producing low thermal-expansion cast iron material
JP2585014B2 (en) Free-cutting high-strength low-thermal-expansion cast alloy and method for producing the same
JPH02298236A (en) Low thermal expansion alloy
JPS5845360A (en) Low alloy steel with temper embrittlement resistance
JP4213901B2 (en) Low thermal expansion casting alloy having excellent hardness and strength at room temperature and low cracking susceptibility during casting, and method for producing the same
JPH0586463B2 (en)
JP5475380B2 (en) Austenitic cast iron, its manufacturing method and austenitic cast iron casting
JPH06256890A (en) Heat resistant iron alloy for casting
JPS6254388B2 (en)
JP4253101B2 (en) High vibration damping cast steel with excellent machinability and manufacturing method thereof
KR101151073B1 (en) High-rigidity high-damping-capacity cast iron
JPS628497B2 (en)
JPH07179984A (en) High strength and low expansion cast iron and method of manufacturing the same
JPS61207553A (en) Non-magnetic steel for cryogenic temperatures
JPS63162841A (en) Free cutting alloy having low thermal expandability

Legal Events

Date Code Title Description
LAPS Cancellation because of no payment of annual fees