JPH036334A - Method for briquetting granular metal - Google Patents

Method for briquetting granular metal

Info

Publication number
JPH036334A
JPH036334A JP14116989A JP14116989A JPH036334A JP H036334 A JPH036334 A JP H036334A JP 14116989 A JP14116989 A JP 14116989A JP 14116989 A JP14116989 A JP 14116989A JP H036334 A JPH036334 A JP H036334A
Authority
JP
Japan
Prior art keywords
flour
resin
organic natural
thermosetting resin
resins
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.)
Granted
Application number
JP14116989A
Other languages
Japanese (ja)
Other versions
JP2732898B2 (en
Inventor
Kyoichi Ueda
上田 恭市
Katsushi Watabe
渡部 克士
Kosuke Kono
河野 幸輔
Hiroshi Mitsue
満江 博
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP14116989A priority Critical patent/JP2732898B2/en
Publication of JPH036334A publication Critical patent/JPH036334A/en
Application granted granted Critical
Publication of JP2732898B2 publication Critical patent/JP2732898B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

PURPOSE:To facilitate briquetting and to provide water resistance by adding specific amounts of organic natural material or thermosetting resin to a granular metal, mixing the above, and subjecting the resulting mixture to pressure molding and to heating treatment. CONSTITUTION:A mixture is prepared by adding, by weight, 0.1-10% organic natural material or 0.1-5% thermosetting resin to a granular metal, which is mixed and pressure-molded, followed by heating treatment at about 50-200 deg.C. As the organic natural material, wheat flour, barley flour, rye flour, flying-out flour, starch powder, etc., are used. The thermosetting resin is selected from urea resin, melamine resin, phenolic resin, and copolycondensation resins thereof. By this method, high-degree water resistance can be provided to the resulting molded materials, and outdoor storage is made possible. Further, strength under normal conditions directly after molding can be improved, and improvement in yield in post-process can be expected.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、鉄鉱石の粉粒状体や各種スラグから回収され
る微細な金属粉粒等を製銑、製鋼の原料その他に有効利
用するために耐水性を付与した取扱い易い形態となす方
法に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention is intended to effectively utilize fine metal powder, etc. recovered from iron ore powder and various slags as a raw material for iron making, steel making, etc. The present invention relates to a method for making a material into a form that is easy to handle and has water resistance.

〔従来の技術〕[Conventional technology]

繊維状、線状の材料はそれを単に圧縮成型すれば塊成化
できるために取扱いが容易であるが、もっと細かい粉粒
状金属はそのまま単に圧縮しても塊成化はできない。
Fibrous and linear materials are easy to handle because they can be agglomerated simply by compression molding, but finer powder-like metals cannot be agglomerated by simply being compressed.

このような微細な粉粒状金属を塊成化する方法として一
般に次のような方法が用いられている。
The following method is generally used to agglomerate such fine powdery metal.

即ち、 ■セメントやベントナイト等の無機バインダーを用いる
方法。
Namely, ■A method using an inorganic binder such as cement or bentonite.

■ポリビニルアルコールやカルボキシメチルセルローズ
を用いる方法。
■Method using polyvinyl alcohol or carboxymethyl cellulose.

■デンプンを用いる方法。■Method using starch.

■糖密、タール、エチレンボトムを用いる方法。■Method using molasses, tar, and ethylene bottom.

■ポリウレタン系の熱硬化性樹脂を用いる方法。■Method using polyurethane thermosetting resin.

■フェノール系樹脂を用いる方法。■Method using phenolic resin.

等がある。etc.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

上記■〜■の方法は種々の問題点を持っていて、その改
善が強く望まれていた。
The above methods (1) to (2) have various problems, and their improvement has been strongly desired.

即ち、 ■の方法はバインダー量を約10重量%(以下、単に%
と略記する)と多量に用い、且つ水を加えて混練後加圧
成型する方法でバインダー量が人なるために金属の品位
が低下すると共にバイングー中に含まれる硫黄(S)に
より3分が増加する等難点がある上に、油が付着してい
る粉粒状金属の場合にはバインダーの付着が悪く常態固
結強度が上がらないために、予めキルン等を用い油脂骨
の燃焼除去その他の除去作業が必要となる。また、この
■の方法は水和反応で硬化しているためにその落下強度
は小さく、割れたり、粉化し易く取扱いが不便であると
共に、溶湯中に投入すれば瞬間的に粉化し塊成化物とし
た効果が十分発揮されない。
That is, in method (2), the binder amount is approximately 10% by weight (hereinafter simply referred to as %).
) is used in large quantities, and the amount of binder increases due to the method of adding water and kneading and then press-molding, which lowers the quality of the metal and increases the sulfur (S) contained in bangu. In addition, in the case of powdered metal with oil attached, the binder does not adhere well and the normal solidification strength does not increase. Is required. In addition, since the method (2) is hardened by a hydration reaction, its drop strength is low, and it is easily cracked or powdered, making it inconvenient to handle. However, the effect is not fully demonstrated.

次に■の方法は約0.5%のバインダー及び水を添加し
混合成型する方法であるが、油脂骨が付着している場合
には硬化しないので、やはりキルン等を用いた燃焼除去
あるいはその他の手段による油脂骨の除去が必要となる
Next, method (2) involves adding about 0.5% binder and water and mixing and molding, but if oil and fat bones are attached, it will not harden, so it is necessary to burn it off using a kiln or other method. It is necessary to remove the greasy bone by means of.

そして■の方法はβ型デンプンを用いた場合は■の方法
と同じ問題を生ずるが、α型デンプンを用いた場合には
比較的塊成化は出来易く常態固結強度もあるが、耐水性
に乏しいために塊化物の屋外貯蔵が出来ないという難点
がある。
Method (2) causes the same problem as method (2) when β-type starch is used, but when α-type starch is used, it is relatively easy to agglomerate and has good solidification strength, but it has poor water resistance. The problem is that the agglomerates cannot be stored outdoors due to the lack of water.

さらに■の方法は■と同様の問題を抱えている上に、臭
気の点で作業環境を著しく損なう。
Furthermore, method (■) has the same problems as (2) and also seriously impairs the working environment due to its odor.

また■の方法は原料を180〜200°Cに加熱しバイ
ンダーを1〜5%添加し混合成型するものであり、バイ
ンダーが高価な事及び油が付着している原料では加熱時
に油が気化するので、キルン等の特別の装置を用いる必
要がある等の難点がある。
In addition, method (■) heats the raw materials to 180 to 200°C, adds 1 to 5% of binder, and mixes and molds.The binder is expensive, and if the raw materials have oil attached, the oil will vaporize during heating. Therefore, there are drawbacks such as the need to use special equipment such as a kiln.

また、■の方法は加熱処理後の耐水圧壊強度は著しく良
好なるものの、常態強度が弱いために塊成化し難く、塊
成化物のハリ取り機中にて破損し取扱い難い難点がある
In addition, although the method (2) has a markedly good water crushing strength after heat treatment, it has a weak normal strength, making it difficult to agglomerate, and the agglomerated material breaks in a de-firming machine, making it difficult to handle.

(課題を解決するための手段〕 本発明では上述の諸問題を解消し、油脂骨が付着した原
料であっても安価でかつ容易に塊成化可能で、しかも耐
水性をイ」与する方法について鋭意検討を重ねた結果、
有機系天然物と熱硬化型樹脂を添加、混合、加圧成型し
た後加熱処理すれば、より以上の好効果が得られる事が
判り本発明を完成するに至った。
(Means for Solving the Problems) The present invention solves the above-mentioned problems, and provides a method that is inexpensive and can be easily agglomerated even if the raw material has oily bones attached, and that also provides water resistance. As a result of careful consideration,
It was found that more favorable effects can be obtained by adding, mixing, and press-molding an organic natural product and a thermosetting resin, followed by heat treatment, which led to the completion of the present invention.

即ち、本発明者等は粉粒状金属に対して有機系天然物0
.1〜10%もしくは、熱硬化性樹脂0.1〜5%を併
用して、添加、混合、加圧成型した後、加熱処理するこ
とを特徴とする粉粒状金属の塊成化方法に関する。
That is, the present inventors added zero organic natural products to powdered metals.
.. The present invention relates to a method for agglomerating powdery metal, which comprises adding, mixing, press-molding, and heat-treating 1 to 10% or 0.1 to 5% of a thermosetting resin.

〔発明の詳細な開示〕[Detailed disclosure of the invention]

本発明を更に具体的に説明する。 The present invention will be explained more specifically.

本発明で使用する粉粒状金属とは鉄鉱石の粉粒状体や各
種スラグから回収される微細な粉粒状金属をいう。
The granular metal used in the present invention refers to fine granular metal recovered from iron ore powder and various slags.

有機天然物とは成分中に少なくともデンプン質を含有す
るもので該デンプン質の含有量には特に制限されない。
An organic natural product is one that contains at least starch as a component, and the content of the starch is not particularly limited.

このような有機天然物としては小麦粉、大麦粉、ライ麦
粉、飛粉、デンプンの一種あるいはこれ等の混合物でも
差し支えない。
Such organic natural products may be wheat flour, barley flour, rye flour, fly flour, starch, or a mixture thereof.

該有機天然物の添加量は粉粒体金属に対して0.1〜1
0%が適当で、好ましくは0.5〜5%である。0.1
%未満では成型性が悪く、成型物の常態強度が弱いため
にもろく、壊れ易い。逆に10%を越えると耐水性が著
しく低下し、屋外貯蔵中に溶出損失が大きく得策でない
The amount of the organic natural product added is 0.1 to 1 based on the powder metal.
0% is suitable, preferably 0.5-5%. 0.1
If it is less than %, moldability is poor and the molded product has low normal strength, making it brittle and easily broken. On the other hand, if it exceeds 10%, the water resistance will drop significantly and the loss of elution during outdoor storage will be large, which is not a good idea.

次に本発明に使用する熱硬化性樹脂としては、尿素樹脂
、メラミン樹脂、フェノール樹脂とまたはこれ等の共縮
合樹脂を挙げる事が出来る。
Next, examples of thermosetting resins used in the present invention include urea resins, melamine resins, phenol resins, and co-condensed resins thereof.

使用される尿素樹脂はホルムアルデヒド(F)と尿素(
U)のモル比がF/llとして1.0〜3.0の比率で
縮合されたものが、またメラミン樹脂はホルムアルデヒ
ド(F) とメラミン(M)のモル比がF/Mとして2
.0〜3.5の比率で縮合されたものが、またフェノー
ル樹脂はホルムアルデヒド(F)とフェノル(P)のモ
ル比がF/Pとして1.0〜3.0の比率で縮合された
ものが使用される。また、これらの樹脂を共縮合させる
か、ただ単に混合して使用しても構わない。
The urea resin used is formaldehyde (F) and urea (
U) is condensed at a molar ratio of 1.0 to 3.0 (F/ll), and melamine resin has a molar ratio of formaldehyde (F) and melamine (M) of 2 (F/M).
.. Those condensed at a ratio of 0 to 3.5, and phenol resins are those condensed at a molar ratio of formaldehyde (F) and phenol (P) of 1.0 to 3.0 (F/P). used. Further, these resins may be used by co-condensing them or simply by mixing them.

またこれ等のアミノ系樹脂はポリビニルアルコル、カル
ボキシメチルセルローズ、ヒドロキシエチルセルローズ
等の変性剤を用いて変性させたものが好ましい。その理
由は、変性させる事により適度の粘度と粘着性のあるア
ミノ系樹脂が得られるので、変性させたアミノ系樹脂に
より粉粒体金属間に強い常態固結強度を付与する事が出
来るからである。
Further, these amino resins are preferably modified using a modifier such as polyvinyl alcohol, carboxymethyl cellulose, or hydroxyethyl cellulose. The reason for this is that by modifying the amino resin, an amino resin with appropriate viscosity and adhesiveness can be obtained, and the modified amino resin can provide strong solidification strength between powder and granule metals. be.

これ等の樹脂の添加量は樹脂固形分として、粉粒体金属
に対し0.1〜5%が適当で好ましくは0.5〜3%で
ある。0.1%未満では著しい耐水性の低下を招き逆に
 5%を越えると成型直後の成型物強度が弱く破損しや
すくなると共にコスト面で上昇を招き経済的に不利にな
る。なお、樹脂の添加量は固形分換算で行なっている。
The amount of these resins to be added is suitably 0.1 to 5%, preferably 0.5 to 3%, based on the powder metal as the resin solid content. If it is less than 0.1%, the water resistance will be significantly reduced, and if it exceeds 5%, the strength of the molded product immediately after molding will be weak and it will be easily damaged, and the cost will increase, resulting in an economic disadvantage. Note that the amount of resin added is calculated in terms of solid content.

これ等のアミノ系樹脂は単独又は併用する事が出来、該
アミノ系樹脂は通常40〜80%の固形分があるので適
量の市水で希釈しても差支えない。該アミノ系樹脂は樹
脂の保存性から物性中のpH値がpl+メーターで7以
上に保たれており、アルカリ領域にあるために先の有機
天然物と粉粒体金属と共に混練される中で、有機天然物
中のデンプン質がアミノ系樹脂中のアルカリ物性により
糊化される事で更に粘結力を増す事が出来るために成型
性が良く取扱いを容易にすることが可能になる。
These amino resins can be used alone or in combination, and since the amino resin usually has a solid content of 40 to 80%, it may be diluted with an appropriate amount of city water. The pH value of the amino resin is kept at a pH value of 7 or more in terms of PL+meter due to the storage stability of the resin, and since it is in the alkaline region, it is kneaded with the organic natural product and powdered metal. The starch in the organic natural product is gelatinized by the alkaline properties of the amino resin, which further increases the cohesive strength, resulting in good moldability and ease of handling.

本発明では有機天然物と熱硬化性樹脂を併用することが
必須要件であり、この要件を満たすことにより成型性の
みならず成型直後の常態固結強度も著しく向上し、その
後の工程での取扱いロスを小さくする事が出来、経済的
にも大きな効果が期待出来る。
In the present invention, it is essential to use an organic natural product and a thermosetting resin together, and by meeting this requirement, not only the moldability but also the normal solidification strength immediately after molding is significantly improved, making it easier to handle in subsequent processes. Loss can be reduced, and a large economic effect can be expected.

かくして得られたこれ等の混練物は加圧成型された後加
熱処理する事で、更に強固な固着強度を得ることができ
る。
The thus obtained kneaded product can be pressure-molded and then heat-treated to obtain even stronger fixing strength.

加圧成型の圧力は圧縮試験機にて0.1〜5t/c+f
lの圧力をかけて行なうが、1〜3t/c+(の圧力で
行うのが好ましい。加圧成型の圧力が0.1 t/af
1未満では、強固な固着強度が得られず、密度も十分で
はない。また5t/cJを越えると粘着力、密度共に十
分であるが、圧縮試験機の保守上好ましいとは言えず、
経済的にもロスである。
The pressure of pressure molding is 0.1 to 5t/c+f using a compression testing machine.
It is preferably carried out at a pressure of 1 to 3 t/c+(.The pressure of pressure molding is 0.1 t/af).
If it is less than 1, strong adhesion strength cannot be obtained and the density is not sufficient. In addition, if it exceeds 5t/cJ, both adhesive strength and density are sufficient, but it is not preferable in terms of maintenance of the compression tester.
It is also an economic loss.

加圧時間は使用する有機天然物と熱硬化性樹脂の種類、
量及び成型圧力等により左右されるが、通常、1秒〜3
0秒で実施される。
The pressurization time depends on the type of organic natural product and thermosetting resin used,
It depends on the amount and molding pressure, etc., but usually 1 second to 3 seconds.
Executed in 0 seconds.

加熱処理温度は通常50〜200°Cが適当であるが、
好ましくは100〜150°Cで熱処理される。加圧温
度が50°C未満ではアミノ系樹脂の硬化が不十分とな
り十分な耐水強度、固着強度等が得られず、また逆に2
00°Cを越えるとアミノ系樹脂の分解を促進し粘結剤
としての効力を発揮することが出来ない。
The appropriate heat treatment temperature is usually 50 to 200°C, but
Preferably, the heat treatment is performed at 100 to 150°C. If the pressing temperature is less than 50°C, the amino resin will not be sufficiently cured and sufficient water resistance and adhesion strength will not be obtained.
If the temperature exceeds 00°C, the decomposition of the amino resin will be promoted and it will not be able to exert its effectiveness as a binder.

加熱処理時間は加熱処理温度及び加圧成型の圧力によっ
ても左右されるが通常10〜40分で実施される。
Although the heat treatment time depends on the heat treatment temperature and the pressure of pressure molding, it is usually carried out for 10 to 40 minutes.

〔実施例及び比較例〕[Examples and comparative examples]

以下、実施例及び比較例によって本発明を具体的に説明
する。
Hereinafter, the present invention will be specifically explained with reference to Examples and Comparative Examples.

実施例1 1でのステンレス製容器3個を用意して、第1表に示す
様な、粉粒状鉄を各々500重量部(以下、単に部と略
記す)入れ、該粉粒状鉄に対し、小麦粉(日清製粉 赤
花)を各々2.5部、10部及び17.5部を加え良く
混合した後、尿素樹脂(三井東圧化学■製ニーロイドU
−701固形分50%)を各々に7.5部をゆっくりと
加え、約10分量子分に混合して混合物を得た。該混合
物を、直径30闘、高さ60開の鋳型に130g入れ、
圧縮試験機で加圧成型の圧力が1.Ot/c+flとな
るように、上部より20秒間加圧し、該混合物の成型体
を得た。その結果、直径30mm、高さ35mm及び密
度5.2g/−の円柱状供試体を得た 以上の操作を各
々3回繰り返し行ない、同一試験条件で円柱状供試体を
3個、計9個の供試体を得た。該供試体9個を110°
Cの乾燥機中に入れ20分間放置し、加熱処理を行った
後、該乾燥機より取り出し成型物とした。該成型物の諸
物性の評価を行なった結果、第2表に示す通りであった
Example 1 Prepare three stainless steel containers in 1, put 500 parts by weight (hereinafter simply referred to as parts) of granular iron as shown in Table 1 in each, and add the following to the granular iron: After adding 2.5 parts, 10 parts, and 17.5 parts of wheat flour (Nissin Seifun Akahana) and mixing well, add urea resin (Neiloid U manufactured by Mitsui Toatsu Chemical Co., Ltd.).
-701 (solid content 50%) was slowly added to each and mixed for about 10 minutes to obtain a mixture. Put 130 g of the mixture into a mold with a diameter of 30 mm and a height of 60 mm,
A compression tester shows that the pressure of pressure molding is 1. Pressure was applied from the top for 20 seconds to obtain Ot/c+fl to obtain a molded body of the mixture. As a result, a cylindrical specimen with a diameter of 30 mm, a height of 35 mm, and a density of 5.2 g/- was obtained.The above operations were repeated three times each, and three cylindrical specimens were prepared under the same test conditions, for a total of nine specimens. A specimen was obtained. 9 specimens at 110°
It was placed in a dryer (C) and left for 20 minutes to undergo heat treatment, and then taken out from the dryer to form a molded product. The various physical properties of the molded product were evaluated and the results are shown in Table 2.

結果より圧壊、耐水、熱間及び落下強度共申し分なく実
用に十分耐え得るものであった。
The results showed that the material had excellent crushing, water resistance, hot and drop strength, and was sufficiently durable for practical use.

第2表における評価結果の値は、いずれも成型物3個の
平均値の結果である。
The evaluation results in Table 2 are the average values of three molded products.

第1表 実施例2〜4 実施例1の方法に従って、熱硬化性樹脂及び有機天然物
を第2表に示す量を添加、混合して混合物を得た。該混
合物を第2表に示す加熱処理温度及び時間で加熱処理を
行ない成型物を得た。該成型物の諸物性の評価を行った
結果、第2表に示す通りであった。
Table 1 Examples 2 to 4 According to the method of Example 1, the amounts of thermosetting resin and organic natural product shown in Table 2 were added and mixed to obtain a mixture. The mixture was heat treated at the heat treatment temperature and time shown in Table 2 to obtain a molded product. The results of evaluating the various physical properties of the molded product were as shown in Table 2.

結果は実施例1と同様に圧壊、耐水、熱間及び落下速度
共に申し分なく製鋼の原料として実用に十分耐え得るも
のであった。
As with Example 1, the results showed that the crushing, water resistance, hot temperature and falling speed were satisfactory, and the material could withstand practical use as a raw material for steel manufacturing.

比較例1 実施例1と同じ粉粒軟鉄を用い該粉粒軟鉄500部に対
しデンプン(日本コーンスターチ)7.5部と市水5部
を加え混合し、実施例1と同様の方法で、第2表に示す
加熱処理温度及び時間で加熱処理を行ない成型物を得た
。該成型物の諸物性の評価を行なった結果、第2表に示
す通りであった。
Comparative Example 1 Using the same granular soft iron as in Example 1, 7.5 parts of starch (Japan Cornstarch) and 5 parts of city water were added and mixed to 500 parts of the granular soft iron, and a A molded article was obtained by performing heat treatment at the heat treatment temperature and time shown in Table 2. The various physical properties of the molded product were evaluated and the results are shown in Table 2.

比較例2 実施例1と同じ粉粒軟鉄を用い該粉粒状銖500部に対
しフェノール樹脂(IIP−300011) 10部を
加え混合し、実施例1と同様の方法で、第2表に示す加
熱処理温度及び時間で加熱処理を行ない成型物を得た。
Comparative Example 2 Using the same powdered soft iron as in Example 1, 10 parts of phenolic resin (IIP-300011) was added and mixed to 500 parts of the powdered iron, and heated as shown in Table 2 in the same manner as in Example 1. A molded product was obtained by heat treatment at the same treatment temperature and time.

該成型物の諸物性の評価を行なった結果、第2表に示す
通りであった。
The various physical properties of the molded product were evaluated and the results are shown in Table 2.

比較例3 実施例1と同じ粉粒軟鉄を用い該粉粒軟鉄500部に対
し尿素樹脂7.5部、小麦粉(界在)60部を加え混合
し、実施例1と同様の方法で、第2表に示す加熱処理温
度及び時間で加熱処理を行い成型物を得た。該成型物の
諸物性の評価を行った結果、第2表に示す通りであった
Comparative Example 3 Using the same powdered soft iron as in Example 1, 7.5 parts of urea resin and 60 parts of wheat flour (boundary) were added and mixed to 500 parts of the powdered soft iron, and a Heat treatment was performed at the heat treatment temperature and time shown in Table 2 to obtain a molded product. The results of evaluating the various physical properties of the molded product were as shown in Table 2.

比較例1〜比較例3の結果、第2表に示す通り圧壊強度
、熱間強度共に実施例1〜4に比べ小さく、耐水強度も
大きく落ちるのは致命傷となって実用的ではない。
As shown in Table 2, the results of Comparative Examples 1 to 3 show that both the crushing strength and the hot strength are lower than those of Examples 1 to 4, and the water resistance strength is also greatly reduced, which is fatal and is not practical.

14 注−1)成型直後のオルセン万能試験機にて測定した強
度を示す。圧縮強度は圧縮速度6 mm/minで測定
して行なった。以下、同様な測定条件で行なった。
14 Note-1) Indicates the strength measured with an Olsen universal testing machine immediately after molding. Compressive strength was measured at a compression speed of 6 mm/min. The following measurements were conducted under similar measurement conditions.

成型物を3日間室温にて養生後車水中(20’C)に2
4時間浸漬したのち取り出し、オルセン万能試験機にて
測定した圧縮強度。
After curing the molded product at room temperature for 3 days, it was placed in car water (20'C) for 2 days.
The compressive strength was measured using an Olsen universal testing machine after being soaked for 4 hours and then taken out.

成型物を3日間室温にて養生後400 ’Cの電気炉内
に10分間入れ、灼熱したのち取り出し、常温まで冷却
し直ちにオルセン万能試験機にて測定した圧縮強度。
After curing the molded product at room temperature for 3 days, it was placed in an electric furnace at 400'C for 10 minutes, heated, taken out, cooled to room temperature, and immediately measured using an Olsen universal testing machine.

注−4)2mの高さから厚さ20mmの鉄板の上に落下
させ ◎:損傷しないもの ○:鉄板に接した部分が一部損傷 ×:鉄板に接した部分がかなり損傷したり173〜1/
2に割れる。
Note-4) Dropped from a height of 2m onto a 20mm thick iron plate ◎: No damage ○: Part of the part in contact with the iron plate was damaged ×: Part of the part in contact with the iron plate was considerably damaged 173-1 /
Divide into 2.

注−2) 注−3) [発明の効果] 本発明は以上詳細に述べたように、粉粒状金属の塊成化
方法である。本発明は従来の粘結剤に比べ有機系天然物
と熱硬化性樹脂を併用し、さらに加熱処理することのに
よりより高度な耐水性が得られることから屋外貯蔵が可
能となり、倉庫等の建物が不必要となり、大幅な建設費
の節約となるのである。
Note-2) Note-3) [Effects of the Invention] As described in detail above, the present invention is a method for agglomerating powdery metal. Compared to conventional binders, the present invention uses a combination of organic natural products and thermosetting resins, and is further heat-treated to achieve higher water resistance, making it possible to store outdoors and store buildings such as warehouses. is no longer necessary, resulting in significant construction cost savings.

粉粒状金属が、成型直後の常態強度をも著しく向上させ
ることができる優れたものが得られるので、あと工程で
の歩留りの向上が大いに期待できる。
Since the powdered metal is excellent in that its normal strength can be significantly improved immediately after molding, it can be expected to greatly improve the yield in subsequent processes.

また、本発明の方法によって塊成化されたものは強度が
大であると共に、それを直接溶湯中へ投入しても突沸現
象を起こすことなく、かつ表面は樹脂コーティングされ
ているために金属等が錆びる事がないといった効果があ
る。
In addition, the agglomerates obtained by the method of the present invention have high strength, do not cause bumping even when directly poured into molten metal, and have a resin-coated surface, so metals, etc. It has the effect that it does not rust.

Claims (1)

【特許請求の範囲】 1)粉粒状金属に対して有機系天然物0.1〜10重量
%、もしくは熱硬化性樹脂0.1〜5重量%を併用して
、添加、混合、加圧成型した後、加熱処理することを特
徴とする粉粒状金属の塊成化方法。 2)有機系天然物が小麦粉、大麦粉、ライ麦粉、飛粉、
デンプン粉からなる群から選ばれる特許請求の範囲第1
)項記載の方法。 3)熱硬化性樹脂が尿素樹脂、メラミン樹脂、フェノー
ル樹脂及びこれ等の共縮合樹脂からなる群から選ばれる
特許請求の範囲第1)項記載の方法。
[Claims] 1) Addition, mixing, and pressure molding of 0.1 to 10% by weight of an organic natural substance or 0.1 to 5% by weight of a thermosetting resin based on the powdered metal. A method for agglomerating powder and granular metal, which comprises: 2) Organic natural products include wheat flour, barley flour, rye flour, flying flour,
Claim 1 selected from the group consisting of starch powder
) method described in section. 3) The method according to claim 1, wherein the thermosetting resin is selected from the group consisting of urea resins, melamine resins, phenol resins, and co-condensed resins thereof.
JP14116989A 1989-06-05 1989-06-05 Agglomeration method of powdered metal Expired - Lifetime JP2732898B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14116989A JP2732898B2 (en) 1989-06-05 1989-06-05 Agglomeration method of powdered metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14116989A JP2732898B2 (en) 1989-06-05 1989-06-05 Agglomeration method of powdered metal

Publications (2)

Publication Number Publication Date
JPH036334A true JPH036334A (en) 1991-01-11
JP2732898B2 JP2732898B2 (en) 1998-03-30

Family

ID=15285743

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14116989A Expired - Lifetime JP2732898B2 (en) 1989-06-05 1989-06-05 Agglomeration method of powdered metal

Country Status (1)

Country Link
JP (1) JP2732898B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5554207A (en) * 1994-11-25 1996-09-10 Usx Corporation Process of recycling iron oxides and plastics in steelmaking
KR20040019425A (en) * 2002-08-26 2004-03-06 민병창 Compound iron and mineral material including mineral rock and fragment iron as an essential element and method of manufacturing it
JP2014521831A (en) * 2011-07-21 2014-08-28 クラリアント・ファイナンス・(ビーブイアイ)・リミテッド Binder composition for agglomerating fine minerals and pelletizing method
US20160265081A1 (en) * 2013-10-17 2016-09-15 Ambiente E Nutrizione S.R.L. A process for upgrading waste powders from mines, containing iron oxides
WO2018115526A1 (en) * 2016-12-23 2018-06-28 Vito Nv (Vlaamse Instelling Voor Technologisch Onderzoek Nv) Recycling metal-rich fines and powder coating waste material in composite briquettes
JP2022029297A (en) * 2020-08-04 2022-02-17 国立大学法人北海道大学 Non-fired agglomerated ore, method for manufacturing non-fired agglomerated ore and iron manufacturing method using the non-fired agglomerated ore

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004033960A (en) 2002-07-04 2004-02-05 Ricoh Co Ltd Toner recycling method and toner recycling system

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5554207A (en) * 1994-11-25 1996-09-10 Usx Corporation Process of recycling iron oxides and plastics in steelmaking
KR20040019425A (en) * 2002-08-26 2004-03-06 민병창 Compound iron and mineral material including mineral rock and fragment iron as an essential element and method of manufacturing it
JP2014521831A (en) * 2011-07-21 2014-08-28 クラリアント・ファイナンス・(ビーブイアイ)・リミテッド Binder composition for agglomerating fine minerals and pelletizing method
US11124855B2 (en) 2011-07-21 2021-09-21 Clariant International Ltd. Binder composition for the agglomeration of fine minerals and pelletizing process
US20160265081A1 (en) * 2013-10-17 2016-09-15 Ambiente E Nutrizione S.R.L. A process for upgrading waste powders from mines, containing iron oxides
US11168381B2 (en) * 2013-10-17 2021-11-09 Ambiente E Nutrizione S.R.L. Process for upgrading waste powders from mines, containing iron oxides
WO2018115526A1 (en) * 2016-12-23 2018-06-28 Vito Nv (Vlaamse Instelling Voor Technologisch Onderzoek Nv) Recycling metal-rich fines and powder coating waste material in composite briquettes
CN110312809A (en) * 2016-12-23 2019-10-08 佛兰芒技术研究所有限公司 Rich metalliferous fine powder and powdery paints waste material are recycled in composite briquettes
JP2022029297A (en) * 2020-08-04 2022-02-17 国立大学法人北海道大学 Non-fired agglomerated ore, method for manufacturing non-fired agglomerated ore and iron manufacturing method using the non-fired agglomerated ore

Also Published As

Publication number Publication date
JP2732898B2 (en) 1998-03-30

Similar Documents

Publication Publication Date Title
TW474960B (en) Compression molding of abrasive articles using water as a temporary binder
US20020152839A1 (en) Cold bonded iron particulate pellets
EP0243172B1 (en) Process for the manufacture of frictional elements
RU2224007C1 (en) Elevated-strength coal briquette and a method of fabrication thereof
AU2019321069B2 (en) Binder formulation
US3852232A (en) Resin composition and process for bond solid particles
US3285756A (en) Mold or core composition for metal casting purposes
JPH036334A (en) Method for briquetting granular metal
EP0201813B1 (en) Molded brake pad
US5089032A (en) Grinding wheel
US6007765A (en) Method of producing molded articles
US4029630A (en) Process for the manufacture of structural elements
US4430459A (en) Method and composition for a furan-modified phenolic novolak binder system
US3316083A (en) Briquetting of foundry materials
Kamińska et al. The Effect of Additive" B" on the Properties of CO2-Hardened Foundry Sands with Hydrated Sodium Silicate
WO1992017419A1 (en) Vibratable resin-bonded refractory composition
US4348343A (en) Method and composition for a furan-modified phenolic novolak binder system
CA1058883A (en) Agglomerates of silicon and silicon base alloy particles
AU671213B2 (en) High alumina refractory shapes
US2997400A (en) Method and composition for forming precision molds
CN117157415A (en) Pellet ball
JPH0135885B2 (en)
EP1141176B1 (en) Briquetting of powdered fuel
JP3151202B2 (en) Refractory materials
JPS6220835A (en) Method for binding granular iron recovered from slag