JPS606393B2 - Method for producing a mixture of stabilized petroleum and coal powder - Google Patents

Method for producing a mixture of stabilized petroleum and coal powder

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Publication number
JPS606393B2
JPS606393B2 JP3218878A JP3218878A JPS606393B2 JP S606393 B2 JPS606393 B2 JP S606393B2 JP 3218878 A JP3218878 A JP 3218878A JP 3218878 A JP3218878 A JP 3218878A JP S606393 B2 JPS606393 B2 JP S606393B2
Authority
JP
Japan
Prior art keywords
mixture
coal powder
petroleum
acid
alkenyl
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
JP3218878A
Other languages
Japanese (ja)
Other versions
JPS54124008A (en
Inventor
好伸 中村
忠夫 後藤
泰 高橋
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.)
TOHO KAGAKU KOGYO KK
Original Assignee
TOHO KAGAKU KOGYO 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
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Application filed by TOHO KAGAKU KOGYO KK filed Critical TOHO KAGAKU KOGYO KK
Priority to JP3218878A priority Critical patent/JPS606393B2/en
Publication of JPS54124008A publication Critical patent/JPS54124008A/en
Publication of JPS606393B2 publication Critical patent/JPS606393B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は石油類に混合する石炭粉末の比率を大にして熱
効率の高い混合物を火力発電用、鉄鋼乗用、セメント工
業用等の燃料として供給することを目的とする安定化さ
れた石油類と石炭粉末との混合物の製法に関するもので
ある。
Detailed Description of the Invention The present invention aims to supply a highly thermally efficient mixture as a fuel for thermal power generation, steel passenger vehicles, cement industry, etc. by increasing the ratio of coal powder mixed with petroleum. The present invention relates to a method for producing a mixture of distilled petroleum and coal powder.

従来、石油類特に重油と石炭粉末とを夫々異なるバーナ
ーから噴出させ混暁させることによって火力発電が行わ
れているが、重油と石炭粉末との比率は8:2程度であ
る。
Conventionally, thermal power generation has been performed by ejecting petroleum, especially heavy oil, and coal powder from different burners and mixing them, but the ratio of heavy oil to coal powder is about 8:2.

そこでこの混合比率を大にして熱効率を高くしようと試
みられているが種々の欠点があり実用化に至っていない
。本発明者等は鋭意研究努力した結果、本発明に到達し
たものである。
Attempts have therefore been made to increase the mixing ratio to increase thermal efficiency, but these have various drawbacks and have not been put to practical use. The present inventors have arrived at the present invention as a result of diligent research efforts.

即ち本発明は、N−アルキル(又はアルケニル)ポリア
ルキレンポリアミンと炭素数8〜22の脂肪酸と反応さ
せて得られるN−アルキル(又はアルケニル)−N′−
アルカノイル(又はアルケノイル)ポリアルキレンポリ
アミンにエチレンオキサイド又は(及び)プロピレンオ
キサイドを付加反応させて得られるN−ポリオキシアル
キレン−Nーアルキル(又はアルケニル)−N′ーアル
カノイル(又はアルケノイル)ポリアルキレンポリァミ
ンにカチオン化剤を加えて反応させるか鉱酸又はアリー
ルスルホン酸を加え熟成させ次いでエチレンオキサイド
又はプロピレンオキサイドを導入することにより付加反
応させるかして得られる第4級アンモニウム塩型カチオ
ン界面活性剤を、石油類と石炭粉末との総量に対して0
.05〜1.の重量%添加することを特徴とする安定化
された石油類と石炭粉末との混合物の製法である。
That is, the present invention provides N-alkyl (or alkenyl)-N'- obtained by reacting an N-alkyl (or alkenyl) polyalkylene polyamine with a fatty acid having 8 to 22 carbon atoms.
N-polyoxyalkylene-N-alkyl (or alkenyl)-N'-alkanoyl (or alkenoyl) polyalkylene polyamine obtained by addition reaction of ethylene oxide or (and) propylene oxide to alkanoyl (or alkenoyl) polyalkylene polyamine. A quaternary ammonium salt type cationic surfactant obtained by adding a cationizing agent and reacting, or adding a mineral acid or arylsulfonic acid, aging it, and then introducing ethylene oxide or propylene oxide to perform an addition reaction, 0 for the total amount of petroleum and coal powder
.. 05-1. This is a method for producing a mixture of stabilized petroleum and coal powder, which is characterized by adding % by weight of coal powder.

本発明において石油類とは、原油、重油、軽油又は燈油
若しくはこれらの混合物で燃料として用いられるもので
あり、経済的には原油又は重油が好ましい。また、石炭
粉末は石炭を粉砕してその粒径が100メッシュより小
さい粒径のものが好ましい。
In the present invention, petroleum refers to crude oil, heavy oil, light oil, kerosene, or a mixture thereof, which is used as a fuel, and economically preferred is crude oil or heavy oil. Further, the coal powder is preferably one obtained by pulverizing coal and having a particle size smaller than 100 mesh.

本発明で用いられる化合物の添加量は石油類と石炭粉末
との総量に対して0.05重量%以上であれば有効であ
り、1の重量%を越えると効果としては差しつかえない
が経済的に好ましくない。石油類と石炭粉末との混合物
に本発明で用いられる化合物を添加する方法の相違又は
石油類と石炭粉末との混合方法の相違によっては本発明
の目的とする効果に影響しない。
It is effective if the amount of the compound used in the present invention is 0.05% by weight or more based on the total amount of petroleum and coal powder, and if it exceeds 1% by weight, the effect is acceptable but it is not economical. unfavorable to Differences in the method of adding the compound used in the present invention to a mixture of petroleum and coal powder or differences in the method of mixing petroleum and coal powder do not affect the intended effects of the present invention.

例えば本発明で用られる化合物を石油類に添加した後、
燈辞しつ)石炭粉末を混合する方法、石油類と石炭粉末
とを混合した後に灘拝しつ)本発明で用いられる化合物
を添加する方法、石油類中で石炭を粉砕しつ)本発明で
用いられる化合物を添加する方法又は石油類中で石炭を
粉砕した後に燈拝しつ)本発明で用いられる化合物を添
加する方法による相違では本発明の効果は変らない。本
発明において用いられる第4級アンモニウム塩型カチオ
ン界面活性剤を得る出発原料のN−アルキル(又はアル
ケニル)ポリアルキレンポリアミンは一般式RNH〔(
CQ)mNH〕nH (但し、Rは炭素数8〜22のアルキル基又はアルケニ
ル基、mは2又は3の整数、nは1〜5の整数を示す。
For example, after adding the compound used in the present invention to petroleum,
Method of mixing coal powder, Adding the compound used in the present invention after mixing petroleum and coal powder, Grinding coal in petroleum) In the present invention The effect of the present invention does not change depending on the method of adding the compound used in the present invention (or the method of adding the compound used in the present invention after pulverizing coal in petroleum). The starting material N-alkyl (or alkenyl) polyalkylene polyamine for obtaining the quaternary ammonium salt type cationic surfactant used in the present invention has the general formula RNH [(
CQ)mNH]nH (wherein, R is an alkyl group or alkenyl group having 8 to 22 carbon atoms, m is an integer of 2 or 3, and n is an integer of 1 to 5.

)にて表わされる化合物であって次の如く例示すること
ができる。RNHC2日4NH2,RNHC3日6NH
2,RNHC2日4NHC2比NH2,RNHC2日4
NHC34NH2,RNHC3日6NHC3日GNH2
RNHC2日4NHC2はNHC2比NH2,RNHC
2日4NHC2日NHC2はNHC2日4NHC2日4
N&RNHC2日4NHC2日NHC2比NHC3日6
NH2,RNHC2日4NHC2氏NHC2比NHC2
日4NH2、但し、上記例示においてRは炭素数8〜2
2のアルキル基又はアルケニル基を示す。
) and can be exemplified as follows. RNHC 2 days 4NH2, RNHC 3 days 6NH
2, RNHC 2 days 4NHC2 ratio NH2, RNHC 2 days 4
NHC34NH2, RNHC3days6NHC3daysGNH2
RNHC2day4NHC2 is NHC2 ratio NH2, RNHC
2 days 4 NHC 2 days NHC 2 is NHC 2 days 4 NHC 2 days 4
N&RNHC 2 days 4NHC 2 daysNHC2 ratioNHC 3 days 6
NH2,RNHC2day4NHC2Mr.NHC2ratioNHC2
However, in the above example, R has 8 to 2 carbon atoms.
2 represents an alkyl group or an alkenyl group.

また、上記Rに由来する炭素数8〜22の脂肪酸及びN
ーアルキル(又はアルケニル)ポリアルキレンポリアミ
ンとの反応に用いられる炭素数8〜22の脂肪酸を例示
すると、ラウリン酸、ミリスチン酸、パルミチン酸、ス
テアリン酸、オレイン酸、混合ャシ脂肪酸、リノール酸
、リシノール酸、牛脂脂肪酸等の高級脂肪酸を挙げるこ
とができるが、好ましくはラウリン酸、オレイン酸及び
混合ャシ脂肪酸である。
In addition, fatty acids having 8 to 22 carbon atoms derived from the above R and N
- Examples of fatty acids having 8 to 22 carbon atoms used in the reaction with alkyl (or alkenyl) polyalkylene polyamines include lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, mixed coconut fatty acid, linoleic acid, and ricinoleic acid. , tallow fatty acid, and other higher fatty acids, preferably lauric acid, oleic acid, and mixed chassis fatty acids.

N−アルキル(又はアルケニル)ポリアルキレンポリア
ミンと前記の如き高級脂肪酸との反応は、好ましくは窒
素ガス又は炭酸ガス等の不活性ガスの存在下、温度15
0〜16000において脱水反応させてN−アルキル(
又はアルケニル)−N′−アルカノイル(又はアルケノ
イル)ポリアルキレンポリァミンを得る。
The reaction between the N-alkyl (or alkenyl) polyalkylene polyamine and the higher fatty acid as described above is preferably carried out at a temperature of 15% in the presence of an inert gas such as nitrogen gas or carbon dioxide gas.
N-alkyl (
or alkenyl)-N'-alkanoyl (or alkenoyl) polyalkylene polyamine.

このときN−アルキル(又はアルケニル)ポリアルキレ
ンポリアミンの2級アミノ基がアマイド化され難いこと
から実質的にはNーアルキル(又はアルケニル)ポリア
ルキレンポリアミン1モルに対して高級脂肪酸1モル反
応する。次いで行われるエチレンオキサイド又は(及び
)プロピレンオキサイドの付加反応は、N−アルキル(
又はアルケニル)−N′ーアルカノイル(又はアルケノ
イル)ポリアルキレンポリアミン1分子中のアルキル基
(又はアルケニル基)とアルカノイル基(又はアルケノ
イル基)との総量に対してエチレンオキサイド又は(及
び)プロピレンオキサイド50〜100の重量%であり
、好ましくはエチレンオキサイド200〜50の重量%
の場合及びプロピレンオキサイド100〜30の重量%
とエチレンオキサイド300〜60の重量%との場合が
効果上好ましい。
At this time, since the secondary amino group of the N-alkyl (or alkenyl) polyalkylene polyamine is difficult to be amidated, 1 mole of the higher fatty acid is substantially reacted with 1 mole of the N-alkyl (or alkenyl) polyalkylene polyamine. The subsequent addition reaction of ethylene oxide or (and) propylene oxide is performed on N-alkyl (
or alkenyl)-N'-alkanoyl (or alkenoyl) polyalkylenepolyamine 50 to 100% of ethylene oxide or (and) propylene oxide based on the total amount of alkyl groups (or alkenyl groups) and alkanoyl groups (or alkenoyl groups) in one molecule of polyalkylene polyamine. preferably 200 to 50% by weight of ethylene oxide.
and 100-30% by weight of propylene oxide
and ethylene oxide in an amount of 300 to 60% by weight is preferable in terms of effectiveness.

かくして得られるNーポリオキシアルキレンーN−アル
キル(又はアルケニル)−N′ーアルカノイル(又はア
ルケノイル)ポリアルキレンポリアミンに臭化メチル、
塩化メチル、ジメチル硫酸、ジェチル硫酸、塩化ペンジ
ル等のカチオン化剤を加えて反応させるか塩酸、硫酸、
硝酸等の鉱酸又はベンゼンスルホン酸、トルェンスルホ
ン酸、等のアリールスルホン酸を加えて熟成させ次いで
エチレンオキサイド又はプロピレンオキサイドを付加反
応させるかして第4級アンモニウム塩型カチオン界面活
性剤を得る。
Methyl bromide,
Add a cationizing agent such as methyl chloride, dimethyl sulfate, jetyl sulfate, penzyl chloride, etc. to react, or add hydrochloric acid, sulfuric acid,
A mineral acid such as nitric acid or an arylsulfonic acid such as benzenesulfonic acid or toluenesulfonic acid is added and aged, followed by an addition reaction with ethylene oxide or propylene oxide to obtain a quaternary ammonium salt type cationic surfactant. .

上記のカチオン化反応においてN−ポリオキシアルキレ
ン−Nーアルキル(又はアルケニル)−N′ーアルカノ
イル(又はアルケノイル)ポリアルキレンポリアミンの
分子中の3級アミノ基の数だけカチオン化剤を反応させ
ることができる。
In the above cationization reaction, a cationization agent can be reacted with the same number of tertiary amino groups in the molecule of the N-polyoxyalkylene-N-alkyl (or alkenyl)-N'-alkanoyl (or alkenoyl) polyalkylene polyamine.

N−アルキル(又はアルケニル)ポリアルキレンポリア
ミンのアミノ基2〜3個の場合は、このアミンに対して
カチオン化剤1:1モル、アミノ基4〜6個の場合はア
ミンに対してカチオン化剤1:1.5〜2.0モルの範
囲が好ましい。次に本発明を実施例によって説明する。
When the N-alkyl (or alkenyl) polyalkylene polyamine has 2 to 3 amino groups, the ratio of cationizing agent to the amine is 1:1 mole, and when the N-alkyl (or alkenyl) polyalkylene polyamine has 4 to 6 amino groups, the ratio of cationizing agent to the amine is 1:1. 1: preferably in the range of 1.5 to 2.0 mol. Next, the present invention will be explained by examples.

実施例 1 濃洋装暦、窒素ガス導入装置、温度計、検水管及びコン
デンサーを備えたフラスコにラウリルジブロピレントリ
アミン299夕(1モル)及びラウリン酸200夕(1
モル)とを仕込み、窒素ガス導入下、温度160こ0に
おいて6時間反応させ179の脱水をさせ、酸価2.5
のアマイド化合物を得た。
Example 1 In a flask equipped with a concentrated Western-style calendar, a nitrogen gas introducing device, a thermometer, a water sample tube, and a condenser, 299 mol of lauryl dibropyrene triamine (1 mol) and 200 mol of lauric acid (1 mol) were added.
mol) and reacted for 6 hours at a temperature of 160°C under nitrogen gas introduction to dehydrate 179% and give an acid value of 2.5.
An amide compound was obtained.

次に上記アマイド化合物481夕(1モル)と酢酸ソー
ダ24夕とをオートクレープに仕込み、蝿梓下、反応温
度160±10qo、反応圧2〜4k9/均においてエ
チレンオキサイド1056夕(24モル:アマイド化合
物のアルキル基と脂肪酸のアシル基(C,.日23CO
)の総量に対して30の重量%)を4時間要して付加反
応させた。次に櫨洋装層、温度計及びガス導入管を備え
たフラスコに上記のエチレンオキサイド付加反応生成物
768.59(0.5モル)を仕込み温度80つ0にお
いて臭化メチルガス47.5夕(0.5モル)をガス導
入管より2時間を要して吹き込みカチオン化反応させた
Next, 481 moles (1 mole) of the above amide compound and 24 moles of sodium acetate were charged into an autoclave, and 1056 moles of ethylene oxide (24 moles: amide The alkyl group of the compound and the acyl group of the fatty acid (C,.day23CO
) was subjected to an addition reaction for 4 hours. Next, 768.59 (0.5 mol) of the above ethylene oxide addition reaction product was charged into a flask equipped with a wax layer, a thermometer, and a gas inlet tube, and at a temperature of 80. 0.5 mol) was blown through the gas introduction tube over a period of 2 hours to cause a cationization reaction.

得られた反応生成物(以下化合物Aという)は褐色粘調
液体であり、次に示す構造の化合物であると推定される
The obtained reaction product (hereinafter referred to as compound A) is a brown viscous liquid, and is estimated to be a compound having the structure shown below.

(但し、p+g+r=4) 次に渡洋装置を備えた3ク容器に第2表に示す物性を有
する中東重油800夕を採取し、これを油俗で内容物を
濃伴しつ)温度70±2℃に保ち化合物A2夕を添加し
、次いで第3表に示す物性を有する粉砕されたホンゲイ
炭800夕を徐々に加え良く混合した。
(However, p + g + r = 4) Next, 800 tons of Middle Eastern heavy oil having the physical properties shown in Table 2 was collected in a 3-kg container equipped with a crossing device, and the contents were thickened with oil at a temperature of 70 ± The mixture was kept at 2° C. and 2 portions of Compound A was added thereto, and then 800 tons of crushed Hongei charcoal having the physical properties shown in Table 3 was gradually added and mixed well.

次に、上記混合物1そを次図に示す如き、即ち上部30
0の‘と下部300の‘の位置にサンプリング口を備え
た1そのシリンダーに採り、これを70q0±1℃の熱
風循環式恒温機に入れて30日間静層させた後、上部サ
ンプリング口から混合物の上層部300の‘を採取し、
下部サンプリング口から中層部400叫を取り出した後
、下層部300叫を採取した。
Next, the above mixture 1 is prepared as shown in the following figure, i.e., the upper part 30
Sample the mixture into a cylinder equipped with sampling ports at the 0' and 300' positions at the bottom, place it in a hot air circulation constant temperature machine at 70q0±1°C, let it stand still for 30 days, and then pour the mixture from the top sampling port. Collect 300' of the upper layer of
After taking out 400 samples from the middle layer from the lower sampling port, 300 samples from the lower layer were collected.

上記の如く採取した上層部の混合物及び下層部の混合物
夫々についてB型回転粘度計で7000における粘度を
測定し、その結果を第1表に示す。実施例 2 バルミチルジプロピレントリアミン1モルとヤシ油脂肋
酸1モルとを反応させて得られたアマイド化合物にエチ
レンオキサイド350重量%を付加反応させ、この生成
物1モルにジメチル硫酸1モルを加えたカチオン化反応
させ、濃褐色粘調液体(以下化合物Bという)を得た。
The viscosity at 7000 was measured using a B-type rotational viscometer for each of the upper layer mixture and lower layer mixture sampled as described above, and the results are shown in Table 1. Example 2 350% by weight of ethylene oxide was added to an amide compound obtained by reacting 1 mole of valmityl dipropylene triamine and 1 mole of coconut oil, and 1 mole of dimethyl sulfate was added to 1 mole of this product. A cationization reaction was performed to obtain a dark brown viscous liquid (hereinafter referred to as compound B).

以下は実施例1と同様にして混合物をつくり粘度を測定
し。その結果を第1表に示す。実施例 3 オレイルテトラエチレンベンタミン1モルとラウリン酸
1モルとを反応させて得られたアマイド化合物にエチレ
ンオキサイド40の重量%を付加反応させ、この生成物
1モルにジェチル硫酸1.5モルを加えカチオン化反応
させ、濃褐色粘認液体(以下化合物Cという)を得た。
In the following, a mixture was prepared in the same manner as in Example 1, and the viscosity was measured. The results are shown in Table 1. Example 3 40% by weight of ethylene oxide was added to an amide compound obtained by reacting 1 mole of oleyltetraethylenebentamine and 1 mole of lauric acid, and 1.5 moles of diethyl sulfate was added to 1 mole of the product. In addition, a cationization reaction was carried out to obtain a dark brown viscous liquid (hereinafter referred to as compound C).

以下は実施例1と同様にして混合物をつくり粘度を測定
しその結果を第1表に示す。比較例 1 濃伴装置を備えた3その容器に第2表に示す物性を有す
る中東重油800夕を採取し、これを油俗で内容物を凝
拝しつ)温度70土2℃に保ちラウリルジメチルアンモ
ニウムクロライド(以下比較化合物1と称す)2夕を添
加し、次いで第3表に示す物性を有する粉砕されたホン
ゲイ炭800夕を徐々に加え良く混合した。
A mixture was prepared in the same manner as in Example 1, and the viscosity was measured. The results are shown in Table 1. Comparative Example 1 In a container equipped with a thickening device, 800 g of Middle Eastern heavy oil having the physical properties shown in Table 2 was collected, and the contents were poured into a container with an oil concentrator and kept at a temperature of 70 °C and 2 °C. Two parts of dimethyl ammonium chloride (hereinafter referred to as Comparative Compound 1) were added, and then 800 parts of crushed Hongei charcoal having the physical properties shown in Table 3 were gradually added and mixed well.

次に上記混合物1そを実施例1で用いた1そのシリンダ
ーに探り、これを70±1℃の熱風循環式恒温機に入れ
て30日間静層させた後、上部サンプリング口から混合
物の上層部300の上を採取し、下部サンプリング口か
ら中層部400の【を取り出した後、下層部300の‘
を採取した。
Next, the above mixture 1 was poured into the cylinder used in Example 1, and after placing it in a hot air circulation constant temperature machine at 70±1°C and allowing it to stand still for 30 days, the upper layer of the mixture was poured from the upper sampling port. After sampling the upper part of 300 and taking out the middle part 400 from the lower sampling port,
was collected.

上記の如くして採取した上層部の混合物及び下層部の混
合物夫々についてB型回転粘度計で7000における粘
度を測定しその結果を第1表に示す。
The viscosity at 7000 was measured using a B-type rotational viscometer for each of the upper layer mixture and lower layer mixture sampled as described above, and the results are shown in Table 1.

比較例 2比較例1と同様にしてステアリルトリメチル
アンモニウムプロマイド(以下比較化合物2と称す)に
ついて比較例1と同機にして混合物をつくり、粘度を測
定し、その結果を第1表に示す。
Comparative Example 2 A mixture of stearyltrimethylammonium bromide (hereinafter referred to as Comparative Compound 2) was prepared in the same machine as Comparative Example 1 in the same manner as in Comparative Example 1, and the viscosity was measured. The results are shown in Table 1.

第1表第1表に示したように、本発明で用いられる化合
物則ち化合物A〜化合物Cを添加した混合物の夫々は上
層部と下層部との粘度差は僅少であり、従って重油と石
炭との混合物はその安定性が十分である。
Table 1 As shown in Table 1, each of the compounds used in the present invention, that is, the mixtures to which Compounds A to C are added, has a small viscosity difference between the upper layer and the lower layer. The stability of the mixture is sufficient.

一方、比較化合物1及び比較化合物2を添加した混合物
の夫々は著しい石炭の沈降がみられ下層部は流動性を失
っており、粘度測定が不可能であつた。
On the other hand, in each of the mixtures to which Comparative Compound 1 and Comparative Compound 2 were added, significant sedimentation of coal was observed and the lower layer lost fluidity, making it impossible to measure the viscosity.

第2表 第3表Table 2 Table 3

Claims (1)

【特許請求の範囲】[Claims] 1 N−アルキル(又はアルケニル)ポリアルキレンポ
リアミンと炭素数8〜22の脂肪酸とを反応させて次い
でエチレンオキサイド又は(及び)プロピレンオキサイ
ドを付加反応させて得られる生成物にカチオン化剤を加
えて反応させるか鉱酸又はアリールスルホン酸の存在下
でエチレンオキサイド又はプロピレンオキサイドを付加
反応させるかして得られる第4級アンモニウム塩型カチ
オン界面活性剤を、石油類と石炭粉末との総量に対して
0.05〜1.0重量%添加することを特徴とする安定
化された石油類と石炭粉末との混合物の製法。
1. A cationizing agent is added to the product obtained by reacting an N-alkyl (or alkenyl) polyalkylene polyamine with a fatty acid having 8 to 22 carbon atoms and then adding ethylene oxide or (and) propylene oxide. A quaternary ammonium salt type cationic surfactant obtained by addition reaction of ethylene oxide or propylene oxide in the presence of a mineral acid or an arylsulfonic acid is added to the total amount of petroleum and coal powder. A method for producing a stabilized mixture of petroleum and coal powder, characterized by adding .05 to 1.0% by weight.
JP3218878A 1978-03-20 1978-03-20 Method for producing a mixture of stabilized petroleum and coal powder Expired JPS606393B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3218878A JPS606393B2 (en) 1978-03-20 1978-03-20 Method for producing a mixture of stabilized petroleum and coal powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3218878A JPS606393B2 (en) 1978-03-20 1978-03-20 Method for producing a mixture of stabilized petroleum and coal powder

Publications (2)

Publication Number Publication Date
JPS54124008A JPS54124008A (en) 1979-09-26
JPS606393B2 true JPS606393B2 (en) 1985-02-18

Family

ID=12351925

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3218878A Expired JPS606393B2 (en) 1978-03-20 1978-03-20 Method for producing a mixture of stabilized petroleum and coal powder

Country Status (1)

Country Link
JP (1) JPS606393B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4696677A (en) * 1986-04-11 1987-09-29 Merck & Co., Inc. Quaternary ammonium salts of anionic gums

Also Published As

Publication number Publication date
JPS54124008A (en) 1979-09-26

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