JPS59124991A - Refining and reforming of oil - Google Patents

Refining and reforming of oil

Info

Publication number
JPS59124991A
JPS59124991A JP22991882A JP22991882A JPS59124991A JP S59124991 A JPS59124991 A JP S59124991A JP 22991882 A JP22991882 A JP 22991882A JP 22991882 A JP22991882 A JP 22991882A JP S59124991 A JPS59124991 A JP S59124991A
Authority
JP
Japan
Prior art keywords
oil
molten metal
reaction vessel
water
hydrogen
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
JP22991882A
Other languages
Japanese (ja)
Other versions
JPS6329919B2 (en
Inventor
Tadayuki Yoshida
吉田 忠幸
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.)
Sankyo Yuki KK
Original Assignee
Sankyo Yuki KK
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 Sankyo Yuki KK filed Critical Sankyo Yuki KK
Priority to JP22991882A priority Critical patent/JPS59124991A/en
Publication of JPS59124991A publication Critical patent/JPS59124991A/en
Publication of JPS6329919B2 publication Critical patent/JPS6329919B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)

Abstract

PURPOSE:To obtain refined and reformed oil readily at low cost, by feeding oil and water into the bottom of a reaction vessel packed with molten metal at high temperature, taking out formed gas from the top of the reaction vessel and separating liquefied components. CONSTITUTION:Oil to be refined (e.g. crude oil) and water, preferably in emulsion, are fed by means of a feeder 4 into the bottom of a reaction vessel 1 packed with molten metal (e.g. lead) at 300-800 deg.C to cause reaction of the oil with water under heat and pressure in the presence of the molten metal 2. The reaction reduces molecular weight, removes impurities and gasify the oil. The gasified oil is taken out through an unloading aperture 6, led into a cooler 7 for cooling and liquefaction and is collected in an oil container 8. The non- liquefied gas component is led into a gas container 9 for recovery. Carbide coming up on the surface of the molten metal 2 is carried out of the system on a discharging conveyer 5.

Description

【発明の詳細な説明】 本発明は、油の不純物を除去したり、粘度や引火点等を
調整する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for removing impurities from oil and adjusting its viscosity, flash point, etc.

従来、油の精製改質方法としては、水素精製法が知られ
てている。これは水素添加分解反応を利用したもので、
圧力約50気圧、温度350〜450°Cにて油と水素
を接触させ、油の不飽和結合へ水素を付加すると共に、
飽和結合を切断し、それによって生じた分解生成物へ水
素を添加して行くものである。
BACKGROUND ART Conventionally, a hydrogen refining method is known as a method for refining and reforming oil. This uses a hydrogenolysis reaction,
Oil and hydrogen are brought into contact at a pressure of about 50 atmospheres and a temperature of 350 to 450°C, and hydrogen is added to the unsaturated bonds of the oil,
This method involves breaking saturated bonds and adding hydrogen to the resulting decomposition products.

しかしながら、上記方決では、油と水素とを加熱加圧下
で接触させるための高圧釜を必要とし、設備が高価につ
く欠点がある。また、油と接触させるべき水素を別途用
意しなければならず、水素の製造をも加えると、手間、
装置及び経費に多大の負担が加わっている。
However, the above method requires a high-pressure cooker for bringing the oil and hydrogen into contact under heating and pressure, which has the disadvantage that the equipment is expensive. In addition, hydrogen must be prepared separately to be brought into contact with oil, and when hydrogen production is also added, it is time-consuming and time-consuming.
This adds a significant burden to equipment and costs.

本発明は、簡便な装置で、また別途水素等を用意するこ
となく油の精製改質を行なうことができるようにするこ
とを目的とする。
An object of the present invention is to make it possible to refine and reform oil using a simple device and without separately preparing hydrogen or the like.

即ち、本発明は、300〜800°Cの溶融金属の入っ
た反応容器の下部に油と水を供給して、溶融金属による
加熱加圧下で油と水を接触させ、発生ガスを反応容器上
部より取出して冷却し、液化成分を分離取得することを
特徴とする油の精製改質方法を提供するものである。
That is, in the present invention, oil and water are supplied to the lower part of a reaction vessel containing molten metal at 300 to 800°C, the oil and water are brought into contact with each other under heating and pressure by the molten metal, and the generated gas is transferred to the upper part of the reaction vessel. The present invention provides a method for refining and reforming oil, which is characterized in that the oil is extracted from the oil, cooled, and the liquefied components are separated and obtained.

以下、図面を参照しつつ本発明を更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to the drawings.

第1図は、本発明に係る方法の一例を示す説明図である
FIG. 1 is an explanatory diagram showing an example of the method according to the present invention.

図中1は反応容器で、この反応容器1内には、溶融金属
2が充填されている。また、反応容器1の周囲には、加
熱ジャケント3か取付けられており、反応容器1内の溶
融金属2の温度が保持されている。
In the figure, 1 is a reaction vessel, and this reaction vessel 1 is filled with molten metal 2. Further, a heating jacket 3 is attached around the reaction vessel 1 to maintain the temperature of the molten metal 2 within the reaction vessel 1.

反応容器1の下81;には、油及び水を反応容器1のr
′rX1sに供給するだめの供給機4が連結されている
。反応容器1の上部には、生成される炭化物等を搬出す
るだめの搬出コンベア5と、発生ガスを取出すだめのガ
ス抽出116が設けられている。ガス抽出1−16は、
冷却器7を介して油容器8からカス容器9へと連結され
ている。
At the bottom 81 of the reaction vessel 1, oil and water are added to the bottom 81 of the reaction vessel 1.
A feeder 4 is connected to 'rX1s. At the upper part of the reaction vessel 1, there are provided a carry-out conveyor 5 for carrying out the generated carbide, etc., and a gas extractor 116 for taking out the generated gas. Gas extraction 1-16 is
An oil container 8 is connected to a waste container 9 via a cooler 7.

ます、本発明のノコ法においては、溶融金属2の入った
反応容器1の下部に、供給機4で油と水を供給する。油
と水は、後述する反紀、の迅速化及び確実性を守るため
、エマルジョン化するまで混合して供給することが好ま
しい。また、油と水の供給により、溶融金属2を急激に
冷して固化させてしまうことがないよう、供給すべき油
と水は、あらかじめある程度予熱しておくことが好まし
い。
First, in the saw method of the present invention, a feeder 4 supplies oil and water to the lower part of a reaction vessel 1 containing molten metal 2. It is preferable that oil and water are mixed and supplied until they form an emulsion in order to speed up and ensure reliability of the reaction described below. Further, it is preferable that the oil and water to be supplied be preheated to some extent in advance so that the molten metal 2 is not rapidly cooled and solidified by the supply of oil and water.

供給機4としては、射出成形機の射出機様のものが好適
に使用できる。
As the feeder 4, a device similar to an injection molding machine can be suitably used.

このようにして反応容器1に供給された油と水は、溶融
金属2という極めて大きな比重を有する液体内で外部の
酸素から遮断された状態で、比重差により浮−トされつ
つ溶融金属2内の深さに応じた圧力を受け、同時に加熱
されることになる。即ち、供給された油と水は、溶融金
属2からの加圧と加熱を受けながら外生、と遮断された
状態で溶融金属2内を−1−昇するものである。そして
、この溶融金属2による加熱加圧下において油と水が反
応して7古製改質がなされるものである。
The oil and water supplied to the reaction vessel 1 in this way are kept floating inside the molten metal 2 due to the difference in specific gravity while being shielded from external oxygen within the molten metal 2, a liquid with extremely high specific gravity. It receives pressure according to its depth, and is heated at the same time. That is, the supplied oil and water rise within the molten metal 2 while being pressurized and heated by the molten metal 2 while being cut off from the outside. Then, oil and water react under heating and pressure by this molten metal 2, thereby performing the 7-used product modification.

上記油と水の溶融金属2内での細かな挙動は必ずしも明
らかてはないが、本発明者は次のように1((−測して
いる。即ち、溶融金属2内で高温にさらされることによ
って、油の連鎖が切断されて低分子化されると共に、炭
素に結合して油を構成している一部の水素やその他の原
子か分taされ、更に炭素と水素が優先的に結合して再
合成が成されているものと考えられる。−力水は、高温
下において活性化されると共に、油が高温下に置かれる
ことによって生成された炭素と反応して水性カス化しよ
うとし、そのときの水素が溶融金属2による加圧下にお
いて油に作用し、油の連鎖の切断、それによって生じた
分解生成物への水素の添加、硫黄や窒素等の分類等を促
進させていると考えられる。そして、このときに溶融金
属2は、炭素と水素の再合成時の触媒的役割をもなすの
ではないがと考えられる。
Although the detailed behavior of the oil and water in the molten metal 2 is not necessarily clear, the inventor has measured the following. As a result, the chain of the oil is cut and the molecular weight is reduced, and some hydrogen and other atoms that are bonded to carbon and make up the oil are separated, and furthermore, carbon and hydrogen are bonded preferentially. It is thought that resynthesis is achieved through the use of water. - Power water is activated at high temperatures and reacts with the carbon produced when the oil is exposed to high temperatures, attempting to form aqueous scum. , the hydrogen at that time acts on the oil under pressure from the molten metal 2, breaking the chain of the oil, adding hydrogen to the resulting decomposition products, and promoting the classification of sulfur, nitrogen, etc. At this time, it is thought that the molten metal 2 also plays a catalytic role during the resynthesis of carbon and hydrogen.

油の組成に含まれている酸素は、水素と結び付いて水と
なり、他方水の分解により生じる酸素は、油の炭酸ど結
ひ伺いて一酸化炭素や二酸化炭素となって、いずれも炭
素と水素の再合成の阻害費囚となる。しかし、溶融金属
2を溶融状態で酸素と結びイqきやすい金属としておく
ことにより、1、記酸素を金属酸化物どして反応系から
除去することができ、炭素と水素の再合成を助けること
ができる。また、油中の硫黄や窒素等加ひにその他の不
純物は、溶融金属2と化合したり、種々のガス体となっ
て除去されでしまうものと考えられる。このようにして
、反応容器1内て低分子化され、不純物か取除かれた油
は、余剰水分と共にガス化して反応容器1のガス抽出1
」6から取出される。一方、炭化物は、溶融金属2上に
浮上分離されると共に、前述の酸素と結び付いた溶融金
属2を還元することになる。
The oxygen contained in the composition of oil combines with hydrogen to form water, while the oxygen produced by the decomposition of water becomes carbon monoxide and carbon dioxide due to the carbonic acid in the oil, both of which are carbon and hydrogen. The cost of inhibiting the resynthesis of However, by combining the molten metal 2 with oxygen in a molten state and making it a metal that is easily oxidized, 1. Oxygen can be removed from the reaction system as a metal oxide, which helps the resynthesis of carbon and hydrogen. I can do it. Further, it is considered that sulfur, nitrogen, and other impurities in the oil combine with the molten metal 2 or become various gases and are not removed. In this way, the oil that has been reduced in molecular weight and removed from impurities in the reaction vessel 1 is gasified together with excess moisture, and the oil is gasified in the gas extraction stage of the reaction vessel 1.
”6. On the other hand, the carbide is floated and separated on the molten metal 2 and reduces the molten metal 2 combined with the aforementioned oxygen.

反応容器1のカス抽出口6から取出された発生ガスは、
冷却器7に導ひかれ、冶化成分は油容器8に回収される
。この油容器8に回収される液化成分は、水と炭化水素
系の油に大別される。また、残りのガス成分は、油容器
8から更にガス容器9へ5ど導ひかれ、そこに回収され
ることになる。このカス成分1オ、!夜化されなかった
炭化水素系のカスや水素等をEl−E成分とし、可燃性
であるのて、反応容器1の加熱等に用いることができる
The generated gas taken out from the waste extraction port 6 of the reaction vessel 1 is
It is led to a cooler 7 and the oxidizing components are collected into an oil container 8. The liquefied components collected in the oil container 8 are roughly classified into water and hydrocarbon oil. Further, the remaining gas components are further led from the oil container 8 to the gas container 9 and recovered there. This scum ingredient is 1 o! Hydrocarbon scum, hydrogen, etc. that have not been nightized are used as the El-E component, and since they are flammable, they can be used for heating the reaction vessel 1, etc.

−・ブ〕、溶融金属2J:、に浮−L分離された炭化物
は、搬出コンベア5で系外に排出されるものである。
The separated carbide floating in the molten metal 2J is discharged out of the system by the discharge conveyor 5.

本発明に用いる油どしては、原油、重質油、廃油、並び
に油脂等であって、これらを単−又は混合して用いる。
The oils used in the present invention include crude oil, heavy oil, waste oil, fats and oils, and these can be used singly or in combination.

本発明で溶融状態て用いる金属としては、アルカリ土類
金属、鉄族金属、ホウ素族金属、炭素族金属、窒素族金
属、酸素族金属並びにこれらの合金等で、好ましくは、
鉛、錫、ビスマス、バリウム、アルミニウム、アンチモ
ン並びにこれらを含む合金である。最適には、溶融状態
で酸素と結び利きやすい鉛、錫、バリウム並びにこれら
を含む合金である。酸素と結び付きゃすい金属であれは
、前述のように炭素と水素の再合成阻害要因である酸素
を金属酸化物として反応系から除去できるためである。
The metals used in a molten state in the present invention include alkaline earth metals, iron group metals, boron group metals, carbon group metals, nitrogen group metals, oxygen group metals, and alloys thereof, and preferably,
Lead, tin, bismuth, barium, aluminum, antimony, and alloys containing these. The most suitable materials are lead, tin, barium, and alloys containing these materials, which easily combine with oxygen in a molten state. The reason why metals that do not easily combine with oxygen is that oxygen, which is a factor inhibiting the resynthesis of carbon and hydrogen, can be removed from the reaction system as a metal oxide, as described above.

また、溶融金属2は、前述のように、酸素と水素の再合
成時の触媒的役割もなしていると見られるので、対象油
に応じて最も効果的に作用し得るものを選択することが
好ましい。
Furthermore, as mentioned above, the molten metal 2 seems to also play a catalytic role during the resynthesis of oxygen and hydrogen, so it is important to select the one that can work most effectively depending on the target oil. preferable.

反応容器1の温度、即ち、溶融金属2の温度は、対象と
なる油や使用する金属によっても異なるが、300〜8
oo0cであることが必要である。温度が低過ぎると十
分な油の分解ができなくなる。逆に温度が高くなり過ぎ
ると、分解が進行して生成される炭化水素が低級化し過
ぎ、冷却しても油として取得できなくなる。十分な量の
精製改質油を得るためには、350°C〜600°Cが
最適である。
The temperature of the reaction vessel 1, that is, the temperature of the molten metal 2, varies depending on the target oil and the metal used, but is between 300 and 80°C.
It needs to be oo0c. If the temperature is too low, sufficient oil decomposition will not be possible. On the other hand, if the temperature becomes too high, the decomposition progresses and the hydrocarbons produced become too low-grade and cannot be obtained as oil even after cooling. In order to obtain a sufficient amount of refined reformate, the optimum temperature is 350°C to 600°C.

また、本発明においては、溶融金属2の温度より高い融
点の金属であって、油の炭素と水の水素との結合に触媒
として機能し得ると考えられるものを、反応容器1内に
介在させることもてきる。
Further, in the present invention, a metal having a melting point higher than the temperature of the molten metal 2 and which is considered to be able to function as a catalyst for the bonding of carbon in the oil and hydrogen in the water is interposed in the reaction vessel 1. It can also happen.

例えは、ニッケルや白金等を網状に形成して、反応容器
1内を上下に仕切るようにして設置しておく等の方法が
考えられる。この触媒用の金属は、反復使用ができるよ
う酸化されにくい金属であることが好ましい。
For example, a method may be considered in which nickel, platinum, or the like is formed into a net shape, and the interior of the reaction vessel 1 is partitioned into upper and lower sections. The metal for this catalyst is preferably a metal that is resistant to oxidation so that it can be used repeatedly.

反応容器1内における油と水の接触反応時の圧力は、使
用金属の比重及びその反応容器1内充填深さによって自
由に定めることができるのて、対象油の種類等に応じて
適宜調節すればよい。また、供給すべき油と水の混合比
は、油によっても相違するが、油100重量部に対して
水を10〜100重量部、最適には30〜60重量部を
加えることが好ましい。水が少な過ぎると十分な最の精
製改質油を回収できなくなり、逆に過量としてもそれほ
ど精製改質油量は増大せず、かえって溶融金属2の熱を
多く奪うことになって熱のロスが大きくなる。
The pressure during the contact reaction between oil and water in the reaction vessel 1 can be freely determined depending on the specific gravity of the metal used and the filling depth of the metal in the reaction vessel 1, so it should be adjusted as appropriate depending on the type of target oil, etc. Bye. Although the mixing ratio of oil and water to be supplied varies depending on the oil, it is preferable to add 10 to 100 parts by weight, most preferably 30 to 60 parts by weight, of water to 100 parts by weight of oil. If there is too little water, it will not be possible to recover enough refined reformed oil, and on the other hand, even if there is too much water, the amount of refined reformed oil will not increase that much, and on the contrary, more heat will be taken away from the molten metal 2, resulting in heat loss. becomes larger.

以」二の説明から明らかなように、本発明は、溶融金属
中に水と混合した油を供給している点に大きな特徴を有
するもので、これらによって次のような利益が得られる
ものである。
As is clear from the following explanation, the present invention has a major feature in that oil mixed with water is supplied into the molten metal, and the following benefits can be obtained by these. be.

■)溶融金属が加圧触媒として作用するので、反応容器
の高さ及び溶融金属の充填深さを調節するだけで容易に
圧力設定ができ、装置が極めて簡便なもので済む。
(2) Since the molten metal acts as a pressurized catalyst, the pressure can be easily set by simply adjusting the height of the reaction vessel and the filling depth of the molten metal, and the equipment can be extremely simple.

2)水素源として水を利用しているため、ことさら別途
水素を用意する必要がなく、水素製造のだめの設(1f
i、手間、経費を省くことができる。
2) Since water is used as a hydrogen source, there is no need to prepare hydrogen separately, and there is no need to install a tank for hydrogen production (1st floor).
i. It saves time and money.

3)廃油の如き不純物の多いものであっても、混在物を
炭化物等として溶融金属上に浮上分離することができる
ので、その処理が極めて容易であ、 る。
3) Even if there are many impurities, such as waste oil, the inclusions can be floated and separated on the molten metal as carbides, so the treatment is extremely easy.

以下に本発明の実施例を示す。Examples of the present invention are shown below.

実施例1 市販のエンジンオイルを用いてその精製改質を行なった
Example 1 A commercially available engine oil was purified and reformed.

反応容器は直径約50mmの筒体とし、また溶融金属と
しては鉛を使用し、反応容器内に50c+nの深さで充
填した。鉛の溶融及び温度保持は、反応容器の周囲に巻
き付けた電気ヒーターによって行なった。
The reaction vessel was a cylinder with a diameter of about 50 mm, and lead was used as the molten metal, and the reaction vessel was filled to a depth of 50c+n. Melting the lead and maintaining the temperature was accomplished by an electric heater wrapped around the reaction vessel.

エンジンオイルに50重量%の水を添加したものを、鉛
を約550°Cに保持して、反応容器の下部に油圧シリ
ンダーて圧入し、反応容器上部から発生ガスを取出して
冷却し、液化成分とガス成分を回収する作業を行なった
Engine oil with 50% water added is pressurized into the lower part of the reaction vessel using a hydraulic cylinder while the lead is maintained at approximately 550°C.The generated gas is taken out from the upper part of the reaction vessel and cooled, and the liquefied components and performed work to recover gas components.

液化成分は、水と油に大別され、この油は石油状の低粘
度静体であり、マツチの炎を近ずけると瞬時に引火燃焼
した。
The liquefied components are broadly divided into water and oil, and this oil is a low-viscosity static solid similar to petroleum, and when brought close to the flame of pine, it instantly ignited and burned.

結果等を第1表に示す。The results are shown in Table 1.

実施例2 水の添加量を100重量%として429g供給し、鉛の
温度を600°Cとした以外は実施例1と全く同様にし
てエンジンオイルの精製改質を行なった。
Example 2 Engine oil was refined and reformed in exactly the same manner as in Example 1, except that the amount of water added was 100% by weight, 429 g was supplied, and the temperature of lead was 600°C.

結果等を第1表に示す。The results are shown in Table 1.

実施例3 7容融金属を錫にしてエンジンオイルの改質を行なった
ところ、実施例1及び2と同様の結果が得られた。
Example 3 7 When engine oil was modified using tin as the molten metal, the same results as in Examples 1 and 2 were obtained.

第1表Table 1

Claims (1)

【特許請求の範囲】[Claims] 1)30.0〜800°Cの溶融金属の入った反応容器
の下部に油と水を供給して、溶融金属による加熱加圧下
で油と水を接触させ、発生ガスを反応容器上部より取出
して冷却し、液化成分を分離取得することを特徴とする
油の精製改質方法。
1) Oil and water are supplied to the bottom of a reaction vessel containing molten metal at 30.0 to 800°C, and the oil and water are brought into contact under heating and pressure by the molten metal, and the generated gas is taken out from the top of the reaction vessel. A method for refining and reforming oil, which comprises cooling the oil and separating and obtaining liquefied components.
JP22991882A 1982-12-29 1982-12-29 Refining and reforming of oil Granted JPS59124991A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22991882A JPS59124991A (en) 1982-12-29 1982-12-29 Refining and reforming of oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22991882A JPS59124991A (en) 1982-12-29 1982-12-29 Refining and reforming of oil

Publications (2)

Publication Number Publication Date
JPS59124991A true JPS59124991A (en) 1984-07-19
JPS6329919B2 JPS6329919B2 (en) 1988-06-15

Family

ID=16899775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22991882A Granted JPS59124991A (en) 1982-12-29 1982-12-29 Refining and reforming of oil

Country Status (1)

Country Link
JP (1) JPS59124991A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7150822B1 (en) * 2003-09-04 2006-12-19 Dtx Technologies Llc Five degrees for separation
US7241377B2 (en) * 2003-09-04 2007-07-10 Dtx Technologies, Llc Salt bath refining
JP2010510345A (en) * 2006-11-17 2010-04-02 ディーティーエックス テクノロジーズ リミテッド ライアビリティ カンパニー Essential oil treatment

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50139805A (en) * 1974-04-20 1975-11-08

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50139805A (en) * 1974-04-20 1975-11-08

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7150822B1 (en) * 2003-09-04 2006-12-19 Dtx Technologies Llc Five degrees for separation
US7241377B2 (en) * 2003-09-04 2007-07-10 Dtx Technologies, Llc Salt bath refining
JP2010510345A (en) * 2006-11-17 2010-04-02 ディーティーエックス テクノロジーズ リミテッド ライアビリティ カンパニー Essential oil treatment

Also Published As

Publication number Publication date
JPS6329919B2 (en) 1988-06-15

Similar Documents

Publication Publication Date Title
US4681599A (en) Gassification of carbon containing waste, refuse or the like
US4007034A (en) Method for making steel
EP0024139B1 (en) Producing liquid hydrocarbon streams by hydrogenation of fossil-based feedstock
US4344839A (en) Process for separating oil from a naturally occurring mixture
FI68075C (en) SAETTING OVER ANORDING FOR FRAMSTAELLNING AV EN HUVUDSAKLIGEN COOKS OCH VAETGAS INNEHAOLLANDE GAS UR KOL- OCH / ELLER KOLV AEEHALTIGT UTGAONGSMATERIAL
JPH09507068A (en) Organic substance homologation method using organic substance-containing feed material
US4881972A (en) Process for feeding heat energy into a molten metal bath
JPH09507482A (en) Method for producing unsaturated organics from organic-containing feedstock
JPS61119611A (en) Production of molten pig iron
GB2082624A (en) Method of gas production
US2675307A (en) Process for coking-calcining complete smelting charge aggregates
LU83048A1 (en) PROCESS FOR DESULFURIZING FUSED FERROUS METALS
US4304598A (en) Method for producing steel from solid, iron containing pieces
JPS59124991A (en) Refining and reforming of oil
JPS59133314A (en) Steel refinement and device in metallurgical vessel
JPS6397332A (en) Steel-making process
FR2466509A1 (en) PROCESS FOR PRODUCING STEEL FROM SOLID METAL MATERIALS CONTAINING IRON
EP0644788B1 (en) Method and appartus for treating organic waste
US2923615A (en) Process for obtaining metals from their ores
CA2041307A1 (en) Method for disposing of run-down batteries and other waste products made toxic by the presence of heavy metals therein
JPH09507067A (en) Method of modifying organics to produce unsaturated organic compounds with shorter chain lengths
JPS59124989A (en) Liquefaction of coal
US1958754A (en) Treatment of copper and other metals
MXPA02000108A (en) Method for producing melt iron.
US4007108A (en) Converting solid fuels to gaseous and liquid fuels