JPH03122053A - Production of graphite crucible for oxygen and nitrogen analysis - Google Patents
Production of graphite crucible for oxygen and nitrogen analysisInfo
- Publication number
- JPH03122053A JPH03122053A JP1258231A JP25823189A JPH03122053A JP H03122053 A JPH03122053 A JP H03122053A JP 1258231 A JP1258231 A JP 1258231A JP 25823189 A JP25823189 A JP 25823189A JP H03122053 A JPH03122053 A JP H03122053A
- Authority
- JP
- Japan
- Prior art keywords
- crucible
- oxygen
- analysis
- graphite crucible
- nitrogen
- 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
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 229910002804 graphite Inorganic materials 0.000 title claims abstract description 23
- 239000010439 graphite Substances 0.000 title claims abstract description 23
- 229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 14
- 238000004458 analytical method Methods 0.000 title claims abstract description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 12
- 239000001301 oxygen Substances 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000011347 resin Substances 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 16
- 238000000465 moulding Methods 0.000 claims abstract description 8
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 239000012298 atmosphere Substances 0.000 claims abstract description 5
- 230000001590 oxidative effect Effects 0.000 claims abstract description 5
- 238000004898 kneading Methods 0.000 claims abstract 2
- 238000010304 firing Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 abstract description 12
- 239000005011 phenolic resin Substances 0.000 abstract description 6
- 125000001743 benzylic group Chemical group 0.000 abstract description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract 1
- 230000020169 heat generation Effects 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 238000001746 injection moulding Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 229910021383 artificial graphite Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007770 graphite material Substances 0.000 description 2
- 229910021385 hard carbon Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- -1 phenol compound Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000011329 calcined coke Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000007849 furan resin Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 238000004901 spalling Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
Landscapes
- Ceramic Products (AREA)
- Carbon And Carbon Compounds (AREA)
- Crucibles And Fluidized-Bed Furnaces (AREA)
- Devices For Use In Laboratory Experiments (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は金属、セラミックスに含まれる酸素、窒素の分
析に用いられ、安定した信頼性の高い、測定結果が得ら
れる黒鉛るつぼの製造法に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a method for manufacturing a graphite crucible that is used to analyze oxygen and nitrogen contained in metals and ceramics, and that provides stable and reliable measurement results. .
従来、金属またはセラミックス中の酸素、窒素を分析す
るには、黒鉛材を、旋盤、ボール盤などで加工成形され
た黒鉛るつぼが用いられている。Conventionally, to analyze oxygen and nitrogen in metals or ceramics, a graphite crucible made of graphite material processed and formed using a lathe, a drill press, or the like has been used.
しかしながら、上記分析用黒鉛るつぼは1試料毎の使い
捨てで、黒鉛るつぼによって標準試料を分析すると、そ
れぞれ使用するるつぼによって測定値が安定せず、ばら
つく問題があった。However, the graphite crucible for analysis is disposable for each sample, and when a standard sample is analyzed using the graphite crucible, there is a problem in that the measured values are not stable and vary depending on the crucible used.
本発明者らは、上記問題について種々検討した結果、る
つぼを加工成形する際の肉厚、重量などが一定せず、そ
れに伴なって電気抵抗等にばらつきを生じ、黒鉛るつぼ
全体を通電加熱した場合、それぞれのるつぼによって加
熱される温度がばらつくことが原因となっていると考え
る。As a result of various studies on the above-mentioned problems, the inventors of the present invention found that the thickness, weight, etc. of the crucible were not constant during processing and molding, resulting in variations in electrical resistance, etc., and that the entire graphite crucible was electrically heated. In this case, it is thought that the cause is variation in the temperature heated by each crucible.
本発明は上記の考えに基づいてなされたもので、金属ま
たはセラミックス中の酸素、窒素の量を正しく測定する
ことが出来る、酸素、窒素分析用黒鉛るつぼの製造法を
提供することを目的とする。The present invention was made based on the above idea, and aims to provide a method for manufacturing a graphite crucible for oxygen and nitrogen analysis, which can accurately measure the amount of oxygen and nitrogen in metals or ceramics. .
上記の目的を達成するため、本発明に係る酸素、窒素分
析用黒鉛るつぼの製造法においては、炭素粉末100重
量部に熱硬化性樹脂を15〜50重量部添加して混練し
、これをるつぼ形状に成形した後、非酸化性雰囲気下、
2500℃以上の温度で焼成する。In order to achieve the above object, in the method for manufacturing a graphite crucible for oxygen and nitrogen analysis according to the present invention, 15 to 50 parts by weight of a thermosetting resin is added to 100 parts by weight of carbon powder, kneaded, and the mixture is placed in a crucible. After forming into a shape, under a non-oxidizing atmosphere,
Calcinate at a temperature of 2500°C or higher.
本発明の方法に用いる炭素粉末としてはコークス、黒鉛
等の粉末で粒度は500μm以下、特に200μm以下
が好ましい。粒度が500μmを越えると製造したるつ
ぼの緻密さが低下する。The carbon powder used in the method of the present invention is preferably a powder of coke, graphite, etc., and has a particle size of 500 μm or less, particularly 200 μm or less. When the particle size exceeds 500 μm, the density of the produced crucible decreases.
また、熱硬化性樹脂としてはフェノール樹脂、フラン樹
脂等が使用可能であるが、射出成形が容易であることか
ら、特にベンジリックエーテル型フェノール樹脂が好ま
しい。この樹脂は粘度が低く、しかも成形温度に保持さ
れた場合に増粘速度が遅いので安定して成形することが
できる。Further, as the thermosetting resin, phenol resin, furan resin, etc. can be used, but benzylic ether type phenol resin is particularly preferred because injection molding is easy. This resin has a low viscosity and has a slow rate of increase in viscosity when maintained at the molding temperature, so it can be molded stably.
上記ベンジリックエーテル型フェノール樹脂は次のよう
にして作られる。The above benzylic ether type phenol resin is produced as follows.
すなわち、フェノール化合物とRCHO(Rは、H又は
炭化水素基)で表わされるアルデヒドとを1:1〜3程
度の割合に金属塩触媒、例えば亜鉛、コバルト、マンガ
ン、スズ等の塩を触媒にして反応させて得られる。この
樹脂はレゾールと7ボラツクの中間的な性質をもってい
る。That is, a phenol compound and an aldehyde represented by RCHO (R is H or a hydrocarbon group) are mixed in a ratio of about 1:1 to 3 using a metal salt catalyst, such as a salt of zinc, cobalt, manganese, tin, etc. Obtained by reaction. This resin has properties intermediate between resol and 7volac.
これらの樹脂は通常アセトン、エタノール等の溶剤で希
釈して用いられる。These resins are usually used after being diluted with a solvent such as acetone or ethanol.
炭素粉末と樹脂の混合割合は前者100重量部に対し後
者が溶剤を除いた不揮発分として15〜50重量部であ
る。樹脂の量が15重量部未満であると射出成形が難し
くなり、生成形体にヒビ等が発生し易く、50重量部を
越えると焼成中の収縮か大きくなり、焼成後の製品の寸
法安定性に欠けたり、また焼成中にヒビ等が発生し易(
なる。The mixing ratio of carbon powder and resin is 100 parts by weight of the former and 15 to 50 parts by weight of the latter as non-volatile content excluding the solvent. If the amount of resin is less than 15 parts by weight, injection molding becomes difficult and cracks are likely to occur in the formed product, while if it exceeds 50 parts by weight, shrinkage during firing will be large and the dimensional stability of the product after firing will be affected. It is easy to chip or crack during firing (
Become.
炭素粉末と樹脂は通常の加圧ニーグー等で混練する。混
練物は予じめ100℃程度でキュアーし、固化したもの
を解砕して成形に供する。The carbon powder and resin are kneaded using a conventional pressurized kneader or the like. The kneaded material is cured in advance at about 100° C., and the solidified material is crushed and used for molding.
成形方法は、射出成形によって行なうのが好ましく、第
1図に一例を示すように、外底面が平面部1を有するる
つぼ形状に成形される。The molding method is preferably injection molding, and as shown in FIG.
次いで、この生成形体を、窒素等の非酸化性雰囲気下、
2500 ’C以上の温度で焼成し、樹脂を炭化、黒鉛
化する。焼成温度が2500℃未満では、るつぼの耐酸
化性、耐熱スポーリング性、電気伝導性等に問題を生ず
る。温度の上限は特に制限ないが工業的には3000℃
程度が限度である。Next, this formed body is exposed to a non-oxidizing atmosphere such as nitrogen.
The resin is fired at a temperature of 2500'C or higher to carbonize and graphitize it. If the firing temperature is less than 2500° C., problems will arise in the oxidation resistance, heat spalling resistance, electrical conductivity, etc. of the crucible. There is no particular upper limit on the temperature, but industrially it is 3000℃.
The extent is the limit.
この分析法における黒鉛るつぼの通常の使用温度は、2
400〜2600℃程度であるが、ボロン等の特殊な成
分を測定する場合には、2700〜3000 ’Cで使
用される。そのため上記焼成温度は、特に2700℃以
上であることが好ましい。The normal operating temperature of the graphite crucible in this analytical method is 2
The temperature is approximately 400-2600°C, but when measuring special components such as boron, it is used at 2700-3000'C. Therefore, it is particularly preferable that the firing temperature is 2700° C. or higher.
上記熱硬化性樹脂を炭化したものは硬質炭素である。硬
質炭素は緻密質で、非表面積が小さく、耐酸化性で不浸
透性に優れている。この特性は、黒鉛るつぼにサンプル
を入れ、)m重加熱した場合、その耐性を増大し分析中
途で破損するのを防止する。Carbonized thermosetting resin is hard carbon. Hard carbon is dense, has a small non-surface area, is oxidation resistant, and has excellent impermeability. This property increases the resistance of the sample to a graphite crucible and prevents it from being damaged during analysis when it is heated to 500 mt.
また、射出成形によって成形することにより、各部寸法
のばらつきのない成形体が容易に得られる。この寸法の
ばらつきのないことにより、分析において黒鉛るつぼを
通電加熱した際の発熱量の個々のるつぼ間の差がな(な
り、安定した分析値を得ることが出来る。In addition, by molding by injection molding, a molded article with uniform dimensions of each part can be easily obtained. Due to this lack of variation in dimensions, there is no difference in calorific value between individual crucibles when the graphite crucibles are heated with electricity during analysis, and stable analytical values can be obtained.
次に実施例、比較例を示して本発明を具体的に説明する
。Next, the present invention will be specifically explained by showing Examples and Comparative Examples.
実施例1〜7
先ず、ベンジリックエーテル形フェノール樹脂を次のよ
うにして製造した。Examples 1 to 7 First, a benzylic ether type phenol resin was produced as follows.
すなわち、フェ/−ル1.0モルに対し37wt%の割
合でホルマリン(CH,O換算1.5モル)を加え、触
媒として、無水酢酸亜鉛0.005モルの割合で添加し
て100 ’Cで2時間反応させた。That is, formalin (1.5 mol in terms of CH, O) was added at a ratio of 37 wt% to 1.0 mol of Fer/-, and as a catalyst, 0.005 mol of zinc acetate anhydride was added at 100'C. The mixture was allowed to react for 2 hours.
反応終了後、真空脱水で水分か1wt%になる様に水を
除去しフェ/−ル樹脂を得た。After the reaction was completed, water was removed by vacuum dehydration to reduce the water content to 1 wt % to obtain a Fer/Fell resin.
得られた樹脂の物性は 粘度 12,000 CP 不揮発分 80% 水分 0.9% であった。The physical properties of the obtained resin are Viscosity 12,000 CP Non-volatile content 80% Moisture 0.9% Met.
また炭素粉末として人造黒鉛(昭和電工株式会社製、U
FG)の30μm下粉末(平均粒径:10μm)を用い
、これに上記ベンジリックエーテル型フェノール樹脂を
それぞれの割合で/f!合し、30Q加圧ニーダ−(株
式会社森山製作所製)を使用して加圧圧力1 kg/
cm’、室温で60分間混練した。この混練したペース
トを+00℃で20分間ブレキュアーした後、ハンマー
ミルで解砕し、成彩材料とした。In addition, artificial graphite (manufactured by Showa Denko K.K., U
Using 30 μm powder (average particle size: 10 μm) of FG), the above benzylic ether type phenol resin was added to it in the respective ratios /f! Using a 30Q pressure kneader (manufactured by Moriyama Seisakusho Co., Ltd.), the pressurization pressure was 1 kg/
cm', and kneaded for 60 minutes at room temperature. This kneaded paste was breculated at +00°C for 20 minutes and then crushed in a hammer mill to obtain a coloring material.
成形は、65トンの熱硬化性樹脂射出成形機(株式会社
名機製作所製)を用い、金型温度は190℃1金型締め
圧は総圧50トンの条件で成形した。Molding was carried out using a 65-ton thermosetting resin injection molding machine (manufactured by Meiki Seisakusho Co., Ltd.) under conditions of a mold temperature of 190° C. and a total mold clamping pressure of 50 tons.
成形した生成形体は、第1図に示す形状で各部寸法は、
a:14.6mmφ、b:13mmφ、C゛1.3mm
5d + 20.0mmSe : 6.On+mφ・
f゛3mmとした。The molded product has the shape shown in Figure 1, and the dimensions of each part are as follows.
a: 14.6mmφ, b: 13mmφ, C゛1.3mm
5d + 20.0mmSe: 6. On+mφ・
It was set to f゛3mm.
この生成形体を常法に従って、窒素雰囲気下、約5℃/
hrの昇温速度で昇温し、それぞれのt温度で焼成し黒
鉛るつぼをつくった。This formed body was prepared in a nitrogen atmosphere at a temperature of about 5°C according to a conventional method.
The temperature was raised at a heating rate of hr, and the graphite crucibles were produced by firing at each temperature t.
これらるつぼを各7個つつ用意し、それぞれ酸素、窒素
同時分析装置(LECO社製、TC−436)にセット
し、(票準サンプル(鉄 含有酸素潰9305±5 p
pm、含有窒素量、68±3 ppm)中の酸素、窒素
を分析し、用いたるつぼによる分析値のばらつきを調べ
た。Prepare 7 of these crucibles and set them in a simultaneous oxygen and nitrogen analyzer (manufactured by LECO, TC-436).
pm, amount of nitrogen contained, 68±3 ppm) was analyzed, and variations in analytical values due to the crucible used were investigated.
実施例8.9
人造黒鉛粉末の代りに、仮焼コークス(日本鉱業株式会
社製、ペトロコークス)の最大粒径100μm、平均粒
径、40μmの粉末を用いた以外は、実施例1〜7と同
じにした。Example 8.9 The same as Examples 1 to 7 except that powder of calcined coke (manufactured by Nippon Mining Co., Ltd., Petrocoke) with a maximum particle size of 100 μm and an average particle size of 40 μm was used instead of the artificial graphite powder. Made it the same.
比較f+ 1.2
焼成温度を2300℃とした以外は実施例1〜7と同じ
にした。Comparison f+ 1.2 Same as Examples 1 to 7 except that the firing temperature was 2300°C.
比較例3
焼成l温度を2300℃とした以外は実施例8.9と同
じにした。Comparative Example 3 Same as Example 8.9 except that the firing temperature was 2300°C.
比較例4
市販の黒鉛るつぼ(通常の黒鉛材を機械加工によって成
形したもの、日立化成株式会社製)を用いた以外は実施
例1〜7と同じ測定を行なった。Comparative Example 4 The same measurements as in Examples 1 to 7 were performed except that a commercially available graphite crucible (made by machining a normal graphite material, manufactured by Hitachi Chemical Co., Ltd.) was used.
実施例1〜9、比較例1〜4の結果を一括して第1表に
示す。The results of Examples 1 to 9 and Comparative Examples 1 to 4 are collectively shown in Table 1.
第1表より明かなように、本発明の方法によって作製さ
れたるつぼは、ばらつきが少なく、信頼性の高い分析値
が得られる。As is clear from Table 1, the crucibles produced by the method of the present invention have little variation and can provide highly reliable analytical values.
実施例10
第1表、No5の条件で30ケの実、鉛るつぼをつくり
、第1図に示す生成形体のa、、b、c、dに+f1
”Uする部分の寸法、および重量を測定した。Example 10 A lead crucible was made with 30 nuts under the conditions of No. 5 in Table 1, and +f1 was added to a, b, c, and d of the formed shape shown in Figure 1.
``The dimensions and weight of the U part were measured.
また第2図に示すように、るつぼに20mmφの丸棒よ
りなる銅電極2を当接し、定電流1アンペアの電流を流
して、四端子法により電圧降下を測定した。Further, as shown in FIG. 2, a copper electrode 2 made of a 20 mmφ round bar was brought into contact with the crucible, a constant current of 1 ampere was applied, and the voltage drop was measured by the four-terminal method.
比較例5
市販の酸素、窒素分析用の黒鉛るつぼを用いた以外は実
施例10と同じにして測定を行なった。Comparative Example 5 Measurement was carried out in the same manner as in Example 10, except that a commercially available graphite crucible for oxygen and nitrogen analysis was used.
実施例10.比較例5の結宋を第2表に示す。Example 10. The results of Comparative Example 5 are shown in Table 2.
第
2表
第2表より、本発明の方法によってつくられた黒鉛るつ
ぼの電圧降下の分散は格段に小さいことがわかる。Table 2 It can be seen from Table 2 that the voltage drop variance of the graphite crucible made by the method of the present invention is much smaller.
以上述べたように、本発明に係る黒鉛るつぼの製造法は
、あと加工を行なう必要がなく、市販黒鉛るつぼに比し
寸法精度か高く、電圧降下の分散が大幅に小さいるつぼ
か安価に得られる。As described above, the method for manufacturing a graphite crucible according to the present invention does not require any post-processing, and can be obtained at a low cost with higher dimensional accuracy and significantly smaller variance in voltage drop than commercially available graphite crucibles. .
この分析用るつぼは、金属材料、セラミックス材料、超
電導材料、電子材料等の分野で酸素、窒素の含有量を測
定する際、l試料測定毎に使い捨となっており、その消
費個数は大きく、安価で高性能の分析用黒鉛るつぼの供
給を可能とした本発明は、産業界に寄与することが極め
て大きい。When measuring the content of oxygen and nitrogen in the fields of metal materials, ceramic materials, superconducting materials, electronic materials, etc., this analytical crucible is disposable for each sample measurement, and the number of crucibles consumed is large. The present invention, which makes it possible to supply an inexpensive and high-performance graphite crucible for analysis, will greatly contribute to the industrial world.
第1図は本発明の方法によって成形された生成形体の縦
断面図、第2図はるつぼの電圧降下を測定する方法の説
明図である。FIG. 1 is a longitudinal sectional view of a formed body formed by the method of the present invention, and FIG. 2 is an explanatory diagram of a method for measuring the voltage drop in a crucible.
Claims (1)
部添加して混練し、これをるつぼの形状に成形した後、
非酸化性雰囲気下、2500℃以上の温度で焼成するこ
とを特徴とする酸素、窒素分析用黒鉛るつぼの製造法。After adding 15 to 50 parts by weight of a thermosetting resin to 100 parts by weight of carbon powder and kneading the mixture, molding it into the shape of a crucible,
A method for producing a graphite crucible for oxygen and nitrogen analysis, which comprises firing at a temperature of 2500° C. or higher in a non-oxidizing atmosphere.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1258231A JPH03122053A (en) | 1989-10-03 | 1989-10-03 | Production of graphite crucible for oxygen and nitrogen analysis |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1258231A JPH03122053A (en) | 1989-10-03 | 1989-10-03 | Production of graphite crucible for oxygen and nitrogen analysis |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03122053A true JPH03122053A (en) | 1991-05-24 |
Family
ID=17317339
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1258231A Pending JPH03122053A (en) | 1989-10-03 | 1989-10-03 | Production of graphite crucible for oxygen and nitrogen analysis |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03122053A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004230779A (en) * | 2003-01-31 | 2004-08-19 | Mitsubishi Pencil Co Ltd | Chuck for mechanical pencil |
JP2010248072A (en) * | 2000-12-18 | 2010-11-04 | Toyo Tanso Kk | Low nitrogen concentration graphite material and storage method of the same |
US8616616B2 (en) | 2007-08-13 | 2013-12-31 | Ephicas Patents Bvba | Side skirt for a pulled vehicle |
-
1989
- 1989-10-03 JP JP1258231A patent/JPH03122053A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010248072A (en) * | 2000-12-18 | 2010-11-04 | Toyo Tanso Kk | Low nitrogen concentration graphite material and storage method of the same |
JP2004230779A (en) * | 2003-01-31 | 2004-08-19 | Mitsubishi Pencil Co Ltd | Chuck for mechanical pencil |
US8616616B2 (en) | 2007-08-13 | 2013-12-31 | Ephicas Patents Bvba | Side skirt for a pulled vehicle |
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