JPS6028876B2 - Mixture of stabilized petroleum and coal powder - Google Patents

Mixture of stabilized petroleum and coal powder

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Publication number
JPS6028876B2
JPS6028876B2 JP3605178A JP3605178A JPS6028876B2 JP S6028876 B2 JPS6028876 B2 JP S6028876B2 JP 3605178 A JP3605178 A JP 3605178A JP 3605178 A JP3605178 A JP 3605178A JP S6028876 B2 JPS6028876 B2 JP S6028876B2
Authority
JP
Japan
Prior art keywords
compound
mixture
coal powder
petroleum
added
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
JP3605178A
Other languages
Japanese (ja)
Other versions
JPS54129007A (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
Publication date
Application filed by TOHO KAGAKU KOGYO KK filed Critical TOHO KAGAKU KOGYO KK
Priority to JP3605178A priority Critical patent/JPS6028876B2/en
Publication of JPS54129007A publication Critical patent/JPS54129007A/en
Publication of JPS6028876B2 publication Critical patent/JPS6028876B2/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、鉄鋼業用、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し
た石油類と石炭粉末との混合物に関するものである。
[Detailed Description of the Invention] The purpose of the present invention is to increase the ratio of coal powder mixed with petroleum to supply a mixture with high thermal efficiency as a fuel for thermal power generation, the steel industry, the cement industry, etc. It concerns a mixture of stabilized 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
ーから噴出させ混焼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 co-firing 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 the thermal efficiency, but they 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.

本発明は、アンモニア、モノェタノールアミン、ジエタ
ノールアミン、トリエタノールアミン等のモノアミン類
にエチレンジオキサィドを付加反応させて得られる下記
一般式(但し、x、y及びzは夫々1以上の整数であっ
て、かつx+y十z=3〜30の範囲の数を示す)にて
表される化合物1モルに対し炭素数12〜18の脂肪酸
を1〜1.5モル加えてェステル化反応させてェステル
化合物を得たのち、次いで臭化メチル、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
化剤を反応させて得られる第4級アンモニウム化合物を
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、安定化した石油類と石
炭粉末との混合物との製造方法である。
The present invention is based on the following general formula (where x, y, and z are each an integer of 1 or more) obtained by adding ethylene dioxide to monoamines such as ammonia, monoethanolamine, diethanolamine, and triethanolamine. 1 to 1.5 moles of a fatty acid having a carbon number of 12 to 18 are added to 1 mole of a compound represented by x + y + z = 3 to 30, and an esterification reaction is carried out. After obtaining the ester compound, a quaternary ammonium compound obtained by reacting with a cationizing agent such as methyl bromide, methyl chloride, dimethyl sulfate, jetyl sulfate, penzyl chloride, etc. is added to the total amount of petroleum and coal powder. This is a method for producing a stabilized mixture of petroleum and coal powder, characterized in that 0.05 to 1.0% by weight of coal powder is added.

上記の但し書き中、x+y+zの範囲が5〜20になる
ようにエチレンオキサイドを付加させる場合が効果の上
で特に好ましい。
In the above proviso, it is particularly preferable to add ethylene oxide so that the range of x+y+z is 5 to 20 in terms of effectiveness.

また、炭素数12〜18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
レィン酸等をあげることができるが、ラウリン酸および
オレィン酸が効果の上で特に好ましい。
Further, examples of fatty acids having 12 to 18 carbon atoms include lauric acid, myristic acid, palmitic acid, stearic acid, and oleic acid, but lauric acid and oleic acid are particularly preferred in view of their effects.

そして、トリ(ポリオキシアルキレン)アミンと高級脂
肪酸とのェステル化反応は、好ましくは窒素ガスの如き
不活性ガスの存在下180〜220qoに加熱し脱水反
応させる。
The esterification reaction between the tri(polyoxyalkylene)amine and the higher fatty acid is preferably carried out by heating to 180 to 220 qo in the presence of an inert gas such as nitrogen gas to cause a dehydration reaction.

そのモル比はトリ(ポリオキシアルキレン)アミン1モ
ルに対し高級脂肪酸1〜1.5モルである。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100メッシュよりも小さい粒径のものがよ
り好ましい。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。
The molar ratio is 1 to 1.5 moles of higher fatty acid to 1 mole of tri(polyoxyalkylene)amine. 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, it is more preferable that the coal powder is obtained by pulverizing coal and has a particle size smaller than 100 mesh. 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; 1. If the weight percentage exceeds , the effect may be acceptable but it is economically unfavorable.

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。例えば本発明において用いられる化合物を石油類
に添加した後、鷹拝しつ)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鷹拝しつ)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)本発明において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蝿拝しつ)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。次に実施例によって本発明を説明す
る。
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. For example, the compound used in the present invention is added to petroleum and then coal powder is mixed. The compound used in the present invention is added after mixing petroleum and coal powder. Differences depending on the method of adding the compound used in the present invention after crushing coal in petroleum, or the method of adding the compound used in the present invention after crushing coal in petroleum. In this case, the effect of the present invention remains unchanged. Next, the present invention will be explained by examples.

実施例 1 モノエタノールアミソ305夕(5モル)をオートクレ
ープに仕込み、縄拝しつ)反応温度150±loo○、
反応圧2〜4kg/のの条件でエチレンオキサィド11
00夕(25モル)を導入し付加反応させた。
Example 1 Monoethanolamiso 305 (5 mol) was charged into an autoclave, and the reaction temperature was 150±loo○.
Ethylene oxide 11 at a reaction pressure of 2 to 4 kg/
00 (25 mol) was introduced to cause an addition reaction.

次に櫨洋装層、窒素ガス導入管、温度計、滴下ロート、
検水管及びコンデンサーを備えたフラスコに上記のエチ
レンオキサィド付加反応生成物281夕(1モル)とオ
レィン酸282夕(1モル)とを仕込み、窒素ガスを導
入しつ)200COに昇温し6時間を要し17.5夕を
脱水させ、ェステル化物を得た。
Next, the Hashiyoso layer, nitrogen gas introduction pipe, thermometer, dropping funnel,
The above ethylene oxide addition reaction product 281 (1 mol) and oleic acid 282 (1 mol) were charged into a flask equipped with a water sample tube and a condenser, and the temperature was raised to 200 CO (while introducing nitrogen gas). It took 6 hours and 17.5 hours to dehydrate to obtain an esterified product.

続いて、フラスコ内のェステル化物の温度を70ooに
調整しつ)ジメチル硫酸126夕(1モル)を滴下ロー
トより1時間を要し徐々に滴下させた後、同温度で1時
間熟成させ、次に示す構造と推定される赤褐色透明砧調
液体(以下化合物Aという)を得た。次に樫洋装層を備
えた3その容器に第3表に示す物性を有する中東重油8
00夕を採取し、油裕上で内容物を燈拝しっ)温度70
±2℃に保ち化合物A2夕を添加し、次いで第4表に示
す物性を有する粉砕されたホンゲィ炭800夕を徐々に
加え良く混合した。
Next, while adjusting the temperature of the esterified product in the flask to 70°C, 126 mmol (1 mol) of dimethyl sulfuric acid was gradually added dropwise from the dropping funnel over a period of 1 hour, and then aged at the same temperature for 1 hour. A reddish-brown transparent brownish liquid (hereinafter referred to as compound A) was obtained, which was assumed to have the structure shown in FIG. Next, a middle eastern heavy oil having the physical properties shown in Table 3 is placed in the container.8
The temperature was 70.
The temperature was maintained at ±2°C, and 2 parts of Compound A were added thereto, and then 800 parts of pulverized Hongyi coal having the physical properties shown in Table 4 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そのシリンダーに探り、これを70±1℃の熱風循
環式恒温機に入れて30日間静暦させた後、上部サンプ
リング口から混合物の上層部300私、下部サンプリン
グ口から中層部400舵‘及び下層部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
1. Sampling ports are located at the 0' and 300' positions at the bottom of the cylinder.The cylinder is placed in a hot air circulation constant temperature machine at 70±1°C and left to stand for 30 days. 300 samples were collected from the upper layer, 400 samples from the middle layer, and 300 samples from the lower layer from the lower sampling port.

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70ooにおける粘
度を測定し、その結果を第1表に示す。
The viscosity at 70 oo of each of the upper layer mixture and lower layer mixture sampled as above was measured using a B-type rotational viscometer, and the results are shown in Table 1.

実施例 2 モノエタノールアミン1モルにエチレンオキサィド10
モルを付加反応させて得られる生成物1モルとラウリン
酸1.5モルとを反応させェステル化合物を得た。
Example 2 1 mole of monoethanolamine to 10 ethylene oxide
An ester compound was obtained by reacting 1 mole of the product obtained by the addition reaction with 1.5 moles of lauric acid.

次いで、このェステル化合物1モルを60〜7000に
調整しながら塩化ペンジル(1モル)を約2時間を要し
て滴下し反応させ、次に示す構造と推定される褐色半占
樹液体(以下化合物Bという)を得た。
Next, pendyl chloride (1 mol) was added dropwise to 1 mol of this ester compound over a period of about 2 hours while adjusting the molecular weight to 60 to 7,000 to cause a reaction. B) was obtained.

(x+y+z=11) の混合物。(x+y+z=11) A mixture of.

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。
A mixture was prepared in the same manner as in Example 1, and the viscosity was measured. The results are shown in Table 1.

実施例 3〜7 実施例1と同様にして次の構造と推定される化合物(以
下化合物C〜Gという)を得、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、その結果を表1に示
す。
Examples 3 to 7 Compounds estimated to have the following structures (hereinafter referred to as compounds C to G) were obtained in the same manner as in Example 1, and a mixture was prepared in the same manner as in Example 1 and the viscosity was measured. are shown in Table 1.

(化合物C) (化合物D) (化合物E) (化合物F) (化合物G) 比較例 1及び2 アルキレンオキサィドの付加モル数以外は実施例と同様
にして合成し、次の構造と推定される化合物(以下比較
化合物1及び2という)を得、以下は実施例と同様にし
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。
(Compound C) (Compound D) (Compound E) (Compound F) (Compound G) Comparative Examples 1 and 2 Synthesized in the same manner as in Examples except for the number of moles of alkylene oxide added, and the following structure was estimated. (hereinafter referred to as Comparative Compounds 1 and 2), a mixture was prepared in the same manner as in the Examples, and the viscosity was measured. The results are shown in Table 1.

(比較化合物1) (比較化合物2) 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即ち
化合物A〜化合物G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。
(Comparative compound 1) (Comparative compound 2) 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 G are added, has a viscosity difference between the upper layer and the lower layer. is small, so the mixture of heavy oil and coal has sufficient stability.

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.

実施例 8 櫨畔装置を備えた3その容器に第3表に示す物性を有す
るミナス重油300夕を採取し、油裕上で内容物を蝿拝
しつ〉温度70±2℃に保ち第4表に示す物性を有する
粉砕された大同炭820夕を徐々に加え良く混合した。
Example 8 Collect 300 tons of Minas heavy oil having the physical properties shown in Table 3 into a container equipped with a canopy device, hold the contents on an oil tank, and maintain the temperature at 70 ± 2°C. 820 grams of crushed Daido coal having the physical properties shown in the table was gradually added and mixed well.

次に上記混合物の総量に対し実施例1で得られた化合物
AO.02重量%添加した混合物をつくり、以下は実施
例1と同様にして粘度を測定し第2表に示す。次に化合
物Aの添加量を夫々0.05重量%、0.1重量%及び
0.3重量とした以外は前記と同様にして粘度を測定し
第2表に示す。
Next, the compound AO obtained in Example 1 was added to the total amount of the above mixture. A mixture containing 0.02% by weight was prepared, and the viscosity was measured in the same manner as in Example 1 and is shown in Table 2. Next, the viscosity was measured in the same manner as above except that the amounts of Compound A added were 0.05% by weight, 0.1% by weight, and 0.3% by weight, respectively, and are shown in Table 2.

比較例 3 実施例8と同様にして得られたミナス重油と大同炭との
混合物の総量に対し比較例1で得た比較化合物1を0.
5重量%添加した混合物をつくり、以下は実施例1と同
様にして粘度を測定し第2表に示す。
Comparative Example 3 Comparative Compound 1 obtained in Comparative Example 1 was added to 0.0% of the total amount of the mixture of Minas heavy oil and Daido coal obtained in the same manner as in Example 8.
A mixture containing 5% by weight was prepared, and the viscosity was measured in the same manner as in Example 1 and is shown in Table 2.

次に比較化合物1の添加量を夫々1.0重量%及び2.
の重量%添加した以外は前記と同様にして粘度を測定し
第2表に示す。
Next, the amounts of Comparative Compound 1 added were 1.0% by weight and 2.0% by weight, respectively.
The viscosity was measured in the same manner as described above, except that 2% by weight was added, and the results are shown in Table 2.

第2表 第2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AO.3重量%以上添加すれば混合物の上層部と
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 2 As shown in Table 2, the compounds used in the present invention, namely the compound AO. If 3% by weight or more is added, the difference in viscosity between the upper and lower parts of the mixture will be small, and therefore the mixture of heavy oil and coal will have sufficient stability.

一方、比較化合物1の添加量を増加しても混合物の夫々
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った。
On the other hand, even when the amount of Comparative Compound 1 was increased, significant sedimentation of coal was observed in each of the mixtures, and the lower layer lost fluidity, making it impossible to measure the viscosity.

第3表第4表Table 3 Table 4

Claims (1)

【特許請求の範囲】 1 一般式 ▲数式、化学式、表等があります▼ (但し、x、y及びzは夫々1以上の整数であつて、か
つx+y+z=3〜30の範囲)にて表わされる化合物
1モルに対し炭素数12〜18の飽和もしくは不飽和高
級脂肪酸を1〜1.5モル反応させたのちカチオン化し
て得られる化合物を、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
定化した石油類と石炭粉末との混合物の製造方法。
[Claims] 1. Represented by the general formula ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (However, x, y, and z are each integers of 1 or more, and x+y+z=3 to 30) The compound obtained by reacting 1 to 1.5 mol of saturated or unsaturated higher fatty acids having 12 to 18 carbon atoms per 1 mol of the compound and then cationizing the compound is 0.05 mol based on the total amount of petroleum and coal powder. A method for producing a stabilized mixture of petroleum and coal powder, characterized by adding ~1.0% by weight.
JP3605178A 1978-03-30 1978-03-30 Mixture of stabilized petroleum and coal powder Expired JPS6028876B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3605178A JPS6028876B2 (en) 1978-03-30 1978-03-30 Mixture of stabilized petroleum and coal powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3605178A JPS6028876B2 (en) 1978-03-30 1978-03-30 Mixture of stabilized petroleum and coal powder

Publications (2)

Publication Number Publication Date
JPS54129007A JPS54129007A (en) 1979-10-06
JPS6028876B2 true JPS6028876B2 (en) 1985-07-06

Family

ID=12458906

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3605178A Expired JPS6028876B2 (en) 1978-03-30 1978-03-30 Mixture of stabilized petroleum and coal powder

Country Status (1)

Country Link
JP (1) JPS6028876B2 (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
JPS54129007A (en) 1979-10-06

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