JPS6348394A - Ash adhesion inhibitor for coal/oil mixture - Google Patents

Ash adhesion inhibitor for coal/oil mixture

Info

Publication number
JPS6348394A
JPS6348394A JP19182186A JP19182186A JPS6348394A JP S6348394 A JPS6348394 A JP S6348394A JP 19182186 A JP19182186 A JP 19182186A JP 19182186 A JP19182186 A JP 19182186A JP S6348394 A JPS6348394 A JP S6348394A
Authority
JP
Japan
Prior art keywords
coal
amine
oil mixture
ethylene oxide
inhibitor
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
JP19182186A
Other languages
Japanese (ja)
Other versions
JPH0762144B2 (en
Inventor
Yasunobu Mizuno
水野 康伸
Nobuhiro Ueshima
伸宏 上嶋
Yoshikazu Ogura
義和 小倉
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.)
Neos Co Ltd
Original Assignee
Neos Co Ltd
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 Neos Co Ltd filed Critical Neos Co Ltd
Priority to JP61191821A priority Critical patent/JPH0762144B2/en
Publication of JPS6348394A publication Critical patent/JPS6348394A/en
Publication of JPH0762144B2 publication Critical patent/JPH0762144B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide the title inhibitor capable of inhibiting formation of a grayish white deposit that precipitates in a pipe when a coal/oil mixture is circulated for re-use, which comprises an amine as an active ingredient. CONSTITUTION:A coal/oil mixture having a water content of <=5wt% is compounded with an ash adhesion inhibitor (e.g., triethylamine) which is an amine, pref. having a 2-18C alkyl group, selected from among a prim. amine, a sec. amine, a tert. amine, a nitrogen-contg. heterocyclic compds., an alkanolamine and a quat. ammonium compds., in an amt. of 0.001-2wt%, pref. 0.005-0.5wt% relative to the coal/oil mixture. Moreover, 1pt.wt. dispersant for a coal/oil mixture may be mixed with 0.01-1pt.wt. aforesaid inhibitor, followed by compounding with the coal/oil mixture.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は混炭用天分付着防止剤に関する。[Detailed description of the invention] Industrial applications The present invention relates to a natural adhesion prevention agent for mixed coal.

従来技術および問題点 従来混炭油相分散安定剤としては種々の界面活性剤が提
案されている。その主なものはアルキルベンゼンスルホ
ン酸ソーダ、ジアルキルスルホサクシネート、ナフタレ
ンスルホン酸ソーダホルマリン縮合物等のアニオン界面
活性剤、アルキルフェノールの酸化エチレン付加物、高
吸アルコールの酸化エチレン付加物等のノニオン界面活
性剤を主成分とするもの等が知られている。
Prior Art and Problems Various surfactants have been proposed as conventional dispersion stabilizers for mixed coal and oil phases. The main ones are anionic surfactants such as sodium alkylbenzene sulfonate, dialkyl sulfosuccinate, sodium naphthalene sulfonate formalin condensate, and nonionic surfactants such as ethylene oxide adducts of alkylphenols and ethylene oxide adducts of high-absorbent alcohols. Those containing as the main component are known.

しかしながら従来の分散安定剤は無煙炭、歴青炭、特に
粘結炭、強粘結炭等の比較的石炭含量の高いものに対し
ては効果的であるが、非石炭成分、例えば粘土質や未炭
化成分の多い石炭では効果が不十分で混炭油の輸送配管
、燃焼装置中に沈着して輸送効率や燃焼効率の低下をき
たすことが多い。
However, conventional dispersion stabilizers are effective for relatively high coal content such as anthracite and bituminous coal, especially coking coal and strongly coking coal, but they are effective against non-coal components such as clay and coal. Coal with a high carbonization content is insufficiently effective and often deposits in mixed coal oil transport piping and combustion equipment, resulting in a decrease in transport efficiency and combustion efficiency.

この様な沈着物(以下、天分と言う)は分野すると石炭
性よりもむしろカオリナイト等の粘度質を主成分とし、
従来のアニオン系やノニオン系の界面活性剤を主成分と
する混炭曲用分散安定剤では沈着を十分に抑制すること
ができない。
In the field, such deposits (hereinafter referred to as natural deposits) are mainly composed of viscous substances such as kaolinite rather than coal.
Conventional dispersion stabilizers for blended carbon containing anionic or nonionic surfactants as main components cannot sufficiently suppress deposition.

本発明は従来の混炭油に単に添加するのみて上記天分の
沈着を効果的に抑制し得る。昆炭浦用灰分付着防止剤を
提供することを目的とする。
The present invention can effectively suppress the deposition of the above-mentioned minerals by simply adding it to conventional mixed coal oil. The purpose of the present invention is to provide an ash adhesion prevention agent for Koncharpo.

問題点を解決するための手段 本発明はアンモニアおよび/またはアミン類を有効成分
とずろ、昆炭浦用天分付着防止剤に関オろ。
Means for Solving the Problems The present invention relates to a natural anti-fouling agent for porridge containing ammonia and/or amines as an active ingredient.

本発明に用い得るアミン類としては第1級アミン、第2
級アミン、第3扱アミン、ポリアミン、含窒素異項環化
合物、アルカノールアミン、第・1級アンモニウ2、化
合物等が例示される。炭素数は限定的ではないが、好ま
しくは2〜18、特に4以上のアルキル基または芳香族
基を有ずろちのが好ましい。
The amines that can be used in the present invention include primary amines, secondary amines,
Examples include primary amines, tertiary amines, polyamines, nitrogen-containing heterocyclic compounds, alkanolamines, primary ammonium 2 compounds, and the like. Although the number of carbon atoms is not limited, it is preferably 2 to 18, particularly preferably 4 or more having an alkyl group or an aromatic group.

第1級アミンとしてはメチルアミンのごとき低級アミン
からステアリルアミンのごとき高級アミンを用いてよく
、ジエチルヘキシルアミンのごとき側鎖を有するアミン
やオレイルアミンのごとき不飽和結合を有するものであ
ってもよい。またアニリンのごとき芳香族アミンであっ
てもよい。−般にはアミン性が強く、かつ鉱物油に対し
て親和性にも優れたアミンが好ましく、炭素数2〜18
、好ましくは4以上の脂肪族アミンまたは芳香族アミン
が適当である。低級アミンは揮発性が強く、高級アミン
は毒性、特に皮膚障害が強いため、それを防ILするた
め、酸化エチレンや酸化プロピレンを1〜2モル程度反
応させて使用し易くしてもよい。
As the primary amine, a lower amine such as methylamine to a higher amine such as stearylamine may be used, and an amine having a side chain such as diethylhexylamine or an unsaturated bond such as oleylamine may be used. It may also be an aromatic amine such as aniline. - In general, amines with strong amine properties and excellent affinity for mineral oil are preferred, and have 2 to 18 carbon atoms.
, preferably 4 or more aliphatic amines or aromatic amines. Lower amines are highly volatile, and higher amines are highly toxic, especially skin damage, so in order to prevent IL, about 1 to 2 moles of ethylene oxide or propylene oxide may be reacted to make them easier to use.

第2級アミンとしてはジメチルアミンのごとき低級アミ
ンから、アルキル基の少なくとも1つが長鎖であるメチ
ルステアリルアミンのごとき長鎖2級アミンであっても
よい。またジフェニルアミンのごとき芳香族アミン、モ
ノエチルアニリンのごときアラルキルアミンであっても
よい。第2級アミンも、好ましくはアルキル基の少なく
とも一つが炭素数2〜18程度の脂肪族アミン、または
芳香族アミンが好ましく、酸化エチレンや酸化プロピレ
ンを1モル程度反応させて、揮発性や毒性を低誠させて
もよい。
The secondary amine may be a lower amine such as dimethylamine or a long chain secondary amine such as methylstearylamine in which at least one of the alkyl groups is a long chain. It may also be an aromatic amine such as diphenylamine or an aralkyl amine such as monoethylaniline. The secondary amine is preferably an aliphatic amine or aromatic amine in which at least one of the alkyl groups has about 2 to 18 carbon atoms, and is reacted with about 1 mole of ethylene oxide or propylene oxide to reduce volatility and toxicity. It's okay to be disrespectful.

第3級アミンも同様であってトリメチルアミン等の低級
アミンからジメチルステアリルアミン等の高級アミン、
ジエチルアニリン等のアラルキルアミンまで使用できる
。好ましくはアルキル基の一つが炭素数2〜I8の脂肪
族アミン、または芳香族アミンである。第3級アミンは
塩酸等の酸触媒の存在下に酸化エチレンや酸化プロピレ
ンを反応させて第4級アンモニウム塩とすることができ
る。これを脱塩して用いてもよい。
The same applies to tertiary amines, ranging from lower amines such as trimethylamine to higher amines such as dimethylstearylamine,
Even aralkylamines such as diethylaniline can be used. Preferably, one of the alkyl groups is an aliphatic amine having 2 to 18 carbon atoms or an aromatic amine. A tertiary amine can be converted into a quaternary ammonium salt by reacting ethylene oxide or propylene oxide in the presence of an acid catalyst such as hydrochloric acid. This may be desalted and used.

ポリアミンとしてはエチレンジアミン、ジエチレントリ
アミン、トリエチレンテトラミン、ペンタエチレンへキ
サミン等のポリアミンであって、その一部が適当な鎖長
、例えば炭素数2〜18、好ましくは4〜18程度の脂
肪酸とアミド化されていてもよい。しかしながら、少な
くとも一つのアミノ基は遊離状態であるのが好ましい。
Examples of polyamines include polyamines such as ethylenediamine, diethylenetriamine, triethylenetetramine, and pentaethylenehexamine, some of which are amidated with fatty acids having a suitable chain length, for example, about 2 to 18 carbon atoms, preferably about 4 to 18 carbon atoms. You can leave it there. However, it is preferred that at least one amino group is in the free state.

またフエニレンノアミンのごとき芳香族アミンであって
もよい。
It may also be an aromatic amine such as phenylenenoamine.

アルカノールアミンとしてはトリエタノールアミン、ジ
ェタノールアミン、モノエタノールアミン、トリプロパ
ツールアミン、モノプロパツールアミン等であってもよ
い。また、アルキルアルカノールアミン、例えばジエチ
ルイソプロパノールアミン等であってもよく、より高級
なアルキル基を有するアルキルアルカノールアミンであ
ってもよい。さらにジェタノールアニリンのごとき芳香
族アルカノールアミンであってもよい。
The alkanolamine may be triethanolamine, jetanolamine, monoethanolamine, triproptoolamine, monoproptoolamine, or the like. Further, it may be an alkylalkanolamine, such as diethylisopropanolamine, or an alkylalkanolamine having a higher alkyl group. Furthermore, aromatic alkanolamines such as jetanolaniline may also be used.

含窒素異項環化合物としてはモルホリン、ビリノン、ト
リアジン、ピロール、ピロリジン、インドール、カルバ
ゾール、イミダゾール、オキサゾール、デアゾール等お
よびそれらの誘導体が例示される。
Examples of the nitrogen-containing heterocyclic compound include morpholine, birinone, triazine, pyrrole, pyrrolidine, indole, carbazole, imidazole, oxazole, deazole, and derivatives thereof.

以上のアミノ化合物はいずれも未中和物または部分中和
物の形で用いるのが好ましい。その理由は必ずしも明ら
かでないが、天分の主成分がカオリン等の層状粘度質物
質であり、上記層間に塩基性基であるアミノ基が捕獲さ
れ、アルキル基や芳香族基等の疎水性基をその表面に配
向し、混炭浦の浦と親和して分散安定化するものと考え
られろ。
All of the above amino compounds are preferably used in unneutralized or partially neutralized form. The reason for this is not necessarily clear, but the main component of Tenno is a layered viscous substance such as kaolin, and the amino groups, which are basic groups, are captured between the layers, and hydrophobic groups such as alkyl groups and aromatic groups are captured. It is thought that it is oriented on the surface and has an affinity with the mixed coal Uranoura, stabilizing its dispersion.

本発明混炭油用灰分付着防止剤は混炭浦に対し、0.0
01〜2重量%、好ましくは0.005〜0゜5重量%
程度用いる。使用法は混炭浦にそのまま配合してもよく
、あるいは混炭油の製造に用いる浦に配合して、あるい
は混炭曲用分散安定剤に配合して用いる。水は用いなく
てよく、好ましくは混炭油中の水分が5重量%以下、よ
り好ましくは2重量%以下である。
The ash adhesion prevention agent for mixed coal oil of the present invention is 0.0
0.01-2% by weight, preferably 0.005-0.5% by weight
Use to a certain degree. It can be used by blending it into a mixed coal pond as it is, by blending it into a pool used for producing mixed coal oil, or by blending it into a dispersion stabilizer for mixed coal mixing. Water may not be used, and preferably the water content in the mixed coal oil is 5% by weight or less, more preferably 2% by weight or less.

本発明天分付着防止剤と併用し得ろ混炭曲用分散剤は限
定的でなく、従来公知の分散剤のいずれとも任意に配合
し得る。具体的には、例えばドデシルベンゼンスルホン
酸等のアルキルベンセンスルホン酸のアルカリ塩、(ア
ルキル)ナフタレンスルホン酸ホルマリン縮合物のアル
カリ塩、高級アルコール硫酸エステルアルカリ塩、ジオ
クチルスルホサクシネート、アルキルフェノールや高級
アルコールの酸化エチレン付加物の硫酸エステル塩等の
アニオン界面活性剤、アルキルフェノールまたはそのホ
ルマリン縮合物の酸化エチレン付加物、高級アルコール
の酸化エチレン付加物、酸化エチレンと酸化プロピレン
の共重合体、ナフトールまたはそのホルマリン縮合物の
酸化エチレン付加物、フェニルフェノール、スチレン化
フェノール等の酸化エチレン付加物、ソルビタンアルキ
レートの酸化エチレン付加物等のノニオン界面活性剤、
各種高分子化合物等の単独または混合物等が例示される
The dispersant for blending mixed carbon that can be used in combination with the anti-fouling agent of the present invention is not limited, and can be blended with any conventionally known dispersant. Specifically, for example, alkali salts of alkylbenzenesulfonic acids such as dodecylbenzenesulfonic acid, alkali salts of formalin condensates of (alkyl)naphthalenesulfonic acids, alkali salts of higher alcohol sulfuric esters, dioctyl sulfosuccinate, alkylphenols and higher alcohols. Anionic surfactants such as sulfate ester salts of ethylene oxide adducts, ethylene oxide adducts of alkylphenols or their formalin condensates, ethylene oxide adducts of higher alcohols, copolymers of ethylene oxide and propylene oxide, naphthol or formalin condensates thereof nonionic surfactants such as ethylene oxide adducts such as phenylphenol and styrenated phenol, ethylene oxide adducts of sorbitan alkylate,
Examples include various polymer compounds, etc., singly or in mixtures.

本発明にとって特に好ましくはブヂルフェノール、ノニ
ルフェノール、オクチルフェノール等のアルキルフェノ
ールまたはそのホルマリン縮合物の酸化エチレン付加物
またはそれに酸化プロピレンを付加し、さらに酸化エチ
レンを付加したノニオン界面活性剤との併用である。上
記ノニオン界面活性剤はアルキルフェノールに予め5〜
100モルの酸化プロピレンを反応させさらに10〜2
50モルの酸化エチレンを反応させたものあるいは単に
アルキルフェノールに10〜200モルの酸化エチレン
を反応させたちのが特に好ましい。
Particularly preferred for the present invention are alkylphenols such as butylphenol, nonylphenol, and octylphenol, or ethylene oxide adducts of formalin condensates thereof, or a combination thereof with propylene oxide and a nonionic surfactant with ethylene oxide added thereto. The above nonionic surfactant is added to the alkylphenol in advance.
100 moles of propylene oxide are reacted and further 10 to 2
Particular preference is given to reacting 50 moles of ethylene oxide or simply reacting an alkylphenol with 10 to 200 moles of ethylene oxide.

混炭曲用分散剤と本発明天分付着防止剤の配合比は前者
1重量部に対し後者0.OI〜]1量部が特に好ましい
The blending ratio of the mixed carbon dispersant and the natural adhesion inhibitor of the present invention is 1 part by weight of the former to 0.0 parts by weight of the latter. OI~] 1 part is particularly preferred.

以下実施例をあげて本発明を説明する。The present invention will be explained below with reference to Examples.

実施例および坂恰桝 サクソンベル炭の微粉末(200メツシュパス84%)
49重量部と重油50重量部をミルで湿式製造した混炭
浦に混炭曲用分散剤0.2重量部を配合し、その500
9をとってホモミキザー(・1000 r、p、m、)
を用いて5分間中分にl昆合し1.昆炭浦を調製した。
Examples and Saxon Bell charcoal fine powder (200 mesh pass 84%)
49 parts by weight and 50 parts by weight of heavy oil were wet-produced in a mill, and 0.2 parts by weight of a dispersant for mixed coal bending was added to the mixed coal, and 500 parts by weight
Take 9 and homomixer (・1000 r, p, m,)
Mix in medium for 5 minutes using 1. Kuntanpo was prepared.

を昆炭油用分散剤 I;ジオクチルスルホサクシネート ■・ ドデシルベンゼンスルホネート ■;ノニルフェノールEO(60モル)付加物TV: 
/−1−ル7工/−ルPO/EO(10/120)付加
物 ■二ノニルフェノールホルマリン縮合物(縮合度3)P
O/EO(35/100)付加物但し、Eoは酸化エチ
レン、POは酸化プロピレンを示す。
Dispersant I for kontan oil; Dioctyl sulfosuccinate ■ Dodecylbenzenesulfonate ■; Nonylphenol EO (60 mol) adduct TV:
/-1-ru 7 engineering/-ru PO/EO (10/120) adduct ■ dinonylphenol formalin condensate (degree of condensation 3) P
O/EO (35/100) adduct Where Eo represents ethylene oxide and PO represents propylene oxide.

さらに上記混炭曲用分散剤にそのlO重爪形に相当する
アミン化合物を配合したものを前記分散剤に代えて0.
2重量部配合し、同様にして混炭、II]を製造した。
Furthermore, an amine compound corresponding to the 1O heavy claw type was blended with the above dispersant for mixed carbon bending in place of the above dispersant.
2 parts by weight were added, and a mixed coal II] was produced in the same manner.

アミン化合物としては下記のものを用いた。The following amine compounds were used.

イ、トリエチルアミン ロ:ラウリルアミン ハ:アニリン ニ・ トリエタノールアミン ホ モルホリン へニラウリルアミン酸化エチレン(2モル)付加物 ト ラウリン酸(1モル)とエチレンジアミン(1モル
)とのアミド チ:オクチルモノエタノールアミン 評価試験 上のごとく調製した混炭油lQをオートクレーブに入れ
、110°C,l Okg/ctn’、窒素雰囲気下で
、ステンレス製2枚羽根を用い、700rpmで20時
間撹拌し、羽根を取り出し、トルエンで洗浄して残った
灰分量を測定した。
B. Triethylamine: laurylamine: aniline, triethanolamine, morpholine, nilaurylamine ethylene oxide (2 mol) adduct, amide of lauric acid (1 mol) and ethylenediamine (1 mol): octyl monoethanolamine evaluation The mixed coal oil lQ prepared as above was put into an autoclave, stirred at 110°C, lOkg/ctn' under a nitrogen atmosphere using two stainless steel blades at 700 rpm for 20 hours, the blade was taken out, and stirred with toluene. The amount of ash remaining after washing was measured.

結果を表−1に示す。The results are shown in Table-1.

表−1 発明の効果 本発明混炭曲用スラッジ沈降防止剤を用いると混炭部の
循環使用時にパイプ管内に沈積する灰白色の沈若物の発
生を抑制することができる。
Table 1 Effects of the Invention When the sludge sedimentation prevention agent for mixed coal bending of the present invention is used, it is possible to suppress the generation of gray-white sediments that accumulate in pipes when the mixed coal section is used for circulation.

Claims (1)

【特許請求の範囲】 1、アミン類を有効成分とする混炭油用灰分付着防止剤
。 2、アミン類が炭素数2〜18のアルキル基を有する第
1項記載の防止剤。
[Claims] 1. An ash adhesion inhibitor for mixed coal oil containing amines as an active ingredient. 2. The inhibitor according to item 1, wherein the amine has an alkyl group having 2 to 18 carbon atoms.
JP61191821A 1986-08-15 1986-08-15 Additives for mixed coal oil Expired - Lifetime JPH0762144B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61191821A JPH0762144B2 (en) 1986-08-15 1986-08-15 Additives for mixed coal oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61191821A JPH0762144B2 (en) 1986-08-15 1986-08-15 Additives for mixed coal oil

Publications (2)

Publication Number Publication Date
JPS6348394A true JPS6348394A (en) 1988-03-01
JPH0762144B2 JPH0762144B2 (en) 1995-07-05

Family

ID=16281080

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61191821A Expired - Lifetime JPH0762144B2 (en) 1986-08-15 1986-08-15 Additives for mixed coal oil

Country Status (1)

Country Link
JP (1) JPH0762144B2 (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5372011A (en) * 1976-12-09 1978-06-27 Lion Corp Process for dispersing coal in oil
JPS5372012A (en) * 1976-12-09 1978-06-27 Lion Corp Process for dispersing coal in oil
JPS5382810A (en) * 1976-12-28 1978-07-21 Lion Corp Method for dispersing coal in oil using etheramine derivative
JPS54142208A (en) * 1978-04-25 1979-11-06 Rolfite Co Method of stabilizing suspension of ground coal in fuel oil
JPS5516078A (en) * 1978-07-20 1980-02-04 New England Power Service Coalloil slurry composition
JPS5594995A (en) * 1979-01-10 1980-07-18 Dai Ichi Kogyo Seiyaku Co Ltd Slurry fuel additive
JPS55139495A (en) * 1979-04-16 1980-10-31 Kao Corp Sludge-containing mixed fuel composition
JPS55139494A (en) * 1979-04-16 1980-10-31 Kao Corp Sludge-containing mixed fuel

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5372011A (en) * 1976-12-09 1978-06-27 Lion Corp Process for dispersing coal in oil
JPS5372012A (en) * 1976-12-09 1978-06-27 Lion Corp Process for dispersing coal in oil
JPS5382810A (en) * 1976-12-28 1978-07-21 Lion Corp Method for dispersing coal in oil using etheramine derivative
JPS54142208A (en) * 1978-04-25 1979-11-06 Rolfite Co Method of stabilizing suspension of ground coal in fuel oil
JPS5516078A (en) * 1978-07-20 1980-02-04 New England Power Service Coalloil slurry composition
JPS5594995A (en) * 1979-01-10 1980-07-18 Dai Ichi Kogyo Seiyaku Co Ltd Slurry fuel additive
JPS55139495A (en) * 1979-04-16 1980-10-31 Kao Corp Sludge-containing mixed fuel composition
JPS55139494A (en) * 1979-04-16 1980-10-31 Kao Corp Sludge-containing mixed fuel

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JPH0762144B2 (en) 1995-07-05

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