TW200907042A - Wear reducing agent for low sulphur fuel oil - Google Patents

Wear reducing agent for low sulphur fuel oil Download PDF

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TW200907042A
TW200907042A TW96129212A TW96129212A TW200907042A TW 200907042 A TW200907042 A TW 200907042A TW 96129212 A TW96129212 A TW 96129212A TW 96129212 A TW96129212 A TW 96129212A TW 200907042 A TW200907042 A TW 200907042A
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Taiwan
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acid
fuel oil
low
sulfur
reducing agent
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TW96129212A
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Chinese (zh)
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TWI391480B (en
Inventor
Nobuhiro Ao
Tuyoshi Yuki
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Sanyo Chemical Ind Ltd
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Abstract

A wear reducing agent for low sulphur fuel oil, and a composition of a low sulphur fuel oil containing the wear reducing agent are provided. The wear reducing agent can have a good wear reducing property even when an adding amount of the wear reducing agent is low. The wear reducing agent for low sulphur fuel oil of the invention includes a compound (A) contains saturated carboxylic acids of C14 to 22 and unsaturated carboxylic acid. Kinematic viscosity of the compound (A) ranges from 15 to 21 mm2/s at 40DEG C. The compound (A) comprises saturated monocarboxylic acid (a1) of C14 to 22, monounsaturated monocarboxylic acid (a2) of C14 to 22, diunsaturated monocarboxylic acid (a3) of C14 to 22 and unsaturated monocarboxylic acid (a4) of C14 to 22. In the total weight of the compound (A), the content of (a1) ranges from 1. 5 to 8. 0 wt%, while that of (a2) and (a3) ranges from 84. 0 to 96. 5 wt% and that of (a4) ranges from 2. 0 to 8. 0 wt%.

Description

200907042 九、發明說明: 【發明所屬之技術領域】 、、由έ且^月Γ有關於低硫石黃燃料油用降低磨損劑以及域粗 上述==:=_及燃料油組成物 ==的磨損、進而具備防止由凝結水引4ί 【先前技術】 各國=於對地球環境問題越來越重視,故而在世λ 的降低^油車排放控制的強化以及柴油中之硫續含二 油的硫磺含量,必須 马降低柴 同時去除了此w 材進行深度脫硫,該過程中 :美=:潤滑性物質,導致潤滑性能降低。: £人吴诸國報告過下述事例:柴 ! ‘、 自 噴射栗是藉由柴油而進行ρ ( ^ eilgme)之機料 針對上鍋旋轉不良° 予以應對,然而;===柴油引擎之零件方面 今。 i自燃财面予以應對,從而研究至 ’現在對柴油添加各種降 合物系添加細際公開請⑽號小 ==;=:化合物系添加,本專利 然而,先前添加之降低磨損劑並不能產生充分之防磨 200907042 損性,:¾增加使用量則常常導致燃料油之氧化穩定性等出 現問題。因此,希望有一種低硫磺燃料油用降低磨損劑, 此降低磨損W即使疋不會使燃料油之氧化穩定性出現問題 之低添加量,亦可發揮優良之防磨損性。 【發明内容】 本發明之目的在於提供一種即使添加量低亦具有優良 之降低磨損性的低硫石黃燃料油用降低磨損劑,進而提供包 含該降低磨損劑之低硫磺燃料油組成物。 本發明者們經過專心研究,結果發現具有特定之動黏 度的缓s义可知:供優良之低硫績降低磨損劑,從而完成本發 明。 【實施方式】 以下說明本發明之實施形態。 本發明中’碳數14〜22之飽和羧酸以及不飽和羧酸的 混合物(A)含有至少1種碳數14〜22之飽和羧酸以及至少 1.種不飽和賴。並且,(A)於攸下之動黏度(—C viscosity)為15〜21 mm2/s、較好的是16〜2〇麵2/5。若⑷ 於40 C下之動黏度小於15 mm2/s,則對低硫磺燃料油之降 低f損效果並不充分;若超過21 mm2/s,則低溫下之黏度 增问^故而難以操作。(A)於4〇。〇下之動黏度可利用Jis κ 2283原油以及石油製品一動黏度試驗方法」進行測定。 作為(Α)中所包含之羧酸,可列舉:碳數14〜22之飽 ^元瘦酸㈣、碳數14〜22之單不飽和-元魏酸(a2)、 厌數14 22之—不飽和一元叛酸(a3)、石岌數14〜22之三 200907042 不飽和一元叛酸(a4)。 碳數14〜22之飽和一元羧酸(al)可列舉:肉豆蔻酸 (myristic acid)、十五酸(Pentadecylic acid)、棕桐酸(palmitic acid)、十七酸(margaric acid)、硬脂酸(stearic acid)、花生 酸(arachidic acid)以及二十二酸(behenic acid)等。(al)中, 較好的是碳數為16〜18之飽和一元羧酸,尤其好的是棕櫚 酸、硬脂酸以及將它們併用。併用棕櫊酸以及硬脂酸之情 形時,其重量比較好的是(標櫚酸/硬脂酸)是1/1〜1/2.5, 更好的是1/1〜1/2。 碳數14〜22之單不飽和一元羧酸(a2)可列舉:肉豆錢 油酸(myristoleic acid)、棕櫊油酸(palmitoleic acid)、岩芽酸 (petroselinic acid)、油酸(oleic acid)、反油酸(elaidic acid)、 順-11 -十八碳稀酸(asclepinic acid)、反-11 -十八石炭稀酸 (vaccenic acid)、順-9-二十碳烯酸(gadoleic acid)、順-11-二 十碳烯酸(gondoic acid)、鯨油酸(cetoleic acid)、芬酸(erucic acid)以及芸苔酸(brassidic acid)等。(a2)中,較好的是碳數 為14〜20之單不飽和一元魏酸’尤其好的是油酸。若碳數 小於14或者超過22 ’則存在對柴油燃料油之溶解性不足、 或者提高潤滑性能力不足之情形。 石反數14〜22之一不飽和一元叛酸(a3)可列舉:亞麻油 酸(linoleic acid)、反-2-癸二烯酸、順-4-癸二稀酸、反_1〇· 十八碳二烯酸以及反_12·十八碳二烯酸等。(a3)中,較好的 是碳數為14〜20之二不飽和一元緩酸,尤其好的是亞麻、'由 酸。200907042 IX. Description of the invention: [Technical field to which the invention belongs], and by έ and ^月Γ have reduced wear agent for low-sulfur yellow fuel oil and the domain coarse ==:=_ and fuel oil composition == Wear and, in turn, prevent the introduction of condensed water. [Prior Art] Countries are paying more and more attention to the global environmental problems. Therefore, the reduction of the emission control of the oil gamma in the world λ and the sulfur content of the sulphur in the diesel oil contain two oils. It is necessary to remove the wood and remove the w material for deep desulfurization. In the process: US =: Lubricating substance, resulting in reduced lubrication performance. : The people of Wu Zhuguo reported the following examples: Chai! ‘The self-injection pump is made of diesel oil and the ρ (^ eilgme) machine is used to deal with the poor rotation of the upper pot. However, === parts of the diesel engine. i Spontaneous fuel economy to deal with, so to study to 'now add various compounds to the diesel system to add fineness, please open (10) small ==; =: compound is added, this patent, however, the previously added reducing wear agent can not produce Full wear resistance 200907042 Damage, 3⁄4 increase in usage often leads to problems such as oxidative stability of fuel oil. Therefore, it is desirable to have a low-sulfur fuel oil reducing wear agent, which reduces wear and tear, and exhibits excellent wear resistance even if the enthalpy does not cause a problem of oxidative stability of the fuel oil. DISCLOSURE OF THE INVENTION An object of the present invention is to provide a low-sulphur fuel oil-reducing agent for low-sulfur yellow fuel oil which has excellent wear resistance even when added in a low amount, and further provides a low-sulfur fuel oil composition containing the wear-reducing agent. The inventors of the present invention have conducted intensive studies and found that the specific kinetic viscosity is known to reduce the wear agent for an excellent low sulfur content, thereby completing the present invention. [Embodiment] Hereinafter, embodiments of the present invention will be described. In the present invention, the mixture (A) of the saturated carboxylic acid having 14 to 22 carbon atoms and the unsaturated carboxylic acid contains at least one saturated carboxylic acid having 14 to 22 carbon atoms and at least one kind of unsaturated lysine. Further, (A) the dynamic viscosity (-C viscosity) under the armpit is 15 to 21 mm 2 /s, preferably 16 to 2 mm 2/5. If (4) the dynamic viscosity at 40 C is less than 15 mm2/s, the effect of reducing the low-fracture of low-sulfur fuel oil is not sufficient; if it exceeds 21 mm2/s, the viscosity at low temperature is increased and it is difficult to operate. (A) at 4〇. The dynamic viscosity of the underarm can be measured by using Jis κ 2283 crude oil and a petroleum product one-viscosity test method. The carboxylic acid contained in (Α) may, for example, be a saturated aliphatic acid (four) having a carbon number of 14 to 22, a monounsaturated-fluoric acid (a2) having a carbon number of 14 to 22, and an anorexia 14 22- Unsaturated unary tarenic acid (a3), sarcophagus number 14~22 three 200907042 Unsaturated one dollar rebel acid (a4). The saturated monocarboxylic acid (al) having a carbon number of 14 to 22 may, for example, be myristic acid, pentadecylic acid, palmitic acid, margaric acid or stearic acid. Stearic acid, arachidic acid, and behenic acid. Among the (al), a saturated monocarboxylic acid having a carbon number of 16 to 18 is preferred, and palmitic acid, stearic acid, and the like are preferably used in combination. When palmitate and stearic acid are used, the weight is preferably 1/1 to 1/2.5, more preferably 1/1 to 1/2. The monounsaturated monocarboxylic acid (a2) having a carbon number of 14 to 22 may be exemplified by myristoleic acid, palmitoleic acid, petroselinic acid, and oleic acid. ), elaidic acid, asclepinic acid, vaccenic acid, gadoleic acid ), gondoic acid, ceteleic acid, erucic acid, and brassic acid. Among the (a2), a monounsaturated monobasic acid having a carbon number of 14 to 20 is preferred, and oleic acid is particularly preferred. If the carbon number is less than 14 or exceeds 22 Å, there is a case where the solubility in diesel fuel oil is insufficient or the lubricity is insufficient. One of the reverse number of stones 14~22 is one of the unsaturation ones (a3): linoleic acid, trans-2-decadienoic acid, cis-4-anthracene acid, anti-_1〇· Octadecadienoic acid and anti-12·octadecadienoic acid. In (a3), it is preferred that the carbon number is from 14 to 20% of the unsaturated monobasic acid, and particularly preferred is flax, 'from acid.

200907042 碳數14〜22之三不飽和—-μ · 兀竣酸(a4)可列舉:α_桐酸 (α-eleostearic acid)、β-桐酸、石物减 γ .. ./ 夂石榴酸(jnimdcacid)、次亞麻 ^.(hnolemc acid),^ ^ + ^觀她ndc acid)以及二十石炭三稀酸(dc〇satri⑽化娜 荨=4)中’較好的是碳數為14〜2g之三不飽和—元缓酸, 尤其好的是次亞麻油酸。 —故些叛酸可藉由精製椰子油、掠搁油、落花生油、大 丑油、撖禮油、i麻油、蔡花子油、米糠油、菜軒油、牛 油以及㈣等天然油脂喊得,藉由翔或者混合這些叛 酸可任意變更(al)〜(a4)之比。 (A)中的(al)〜(a4)的各自較好的含量是:以⑷之重量 來計算,⑻為1>5〜8.G重量百分比(wt%)、(a2)以及㈣ 的總計為84.0〜96.5 wt%、並且(a4)為2 〇〜8 〇 wt%。 更好的是(al)為1.5〜4.5 wt%、(a2)以及(a3)之總計為 88.5〜96.5\^%、(这4)為2.0〜7.0加〇/〇。若含量為上述範圍, 則作為降低磨損劑之氧化穩定性更加良好,且抗乳化性良 好0 為提高氧化穩定性或者低溫下之操作性,本發明的降 低磨損劑除上述(A)以外,可含有選自抗氧化劑⑴)、濁點 降低劑(C)以及稀釋劑(D)中的1種或者}種以上。 抗氧化劑(B) ’可列舉·胺系化合物(萘胺(naphthylamine) 系化合物、二笨基胺(diphenylamine)系化合物以及對苯二 胺(P-phenylenediamine)系化合物等),以及酚系化合物等。 私糸化合物中之—苯基胺系化合物,可列舉:對(對曱 200907042 苯·續醒胺>二笨基胺、4,4'-(α,αι_二曱基苄基)二苯基胺、 4,4'-二辛基二苯基胺、4_單辛基二苯基胺、二苯基胺與丙 酮(acetone)之高溫反應物、二苯基胺與丙酮之低溫反應 物、一苯基胺與苯胺與丙酮之低溫反應物、二苯基胺與二 異丁烯之反應生成物以及辛基化二苯基胺之混合物等。200907042 Carbon number 14~22 three unsaturation--μ · Tannic acid (a4) can be cited as: α-eleostearic acid, β-tung acid, stone minus γ .. . / 夂 punicic acid (jnimdcacid), sub-linen ^. (hnolemc acid), ^ ^ + ^ view her ndc acid) and 20 charcoal tribasic acid (dc〇satri (10) Na Na = 4) 'better is the carbon number is 14~ 2g of the three unsaturated - elemental acid, especially good linoleic acid. - Therefore, some of the treason can be shouted by natural coconut oil such as refined coconut oil, grazing oil, peanut oil, big ugly oil, eucalyptus oil, i sesame oil, cole seed oil, rice bran oil, vegetable oil, butter and (four). By Xiang or mixing these traitors, the ratio of (al) to (a4) can be arbitrarily changed. The preferred content of each of (al) to (a4) in (A) is: calculated as the weight of (4), (8) is 1 > 5 to 8. G weight percent (wt%), (a2), and (d) total It is 84.0 to 96.5 wt%, and (a4) is 2 〇 to 8 〇 wt%. More preferably, (al) is 1.5 to 4.5 wt%, (a2) and (a3) are 88.5 to 96.5% by weight, and (4) is 2.0 to 7.0 plus 〇/〇. When the content is in the above range, the oxidative stability as a reducing wear agent is further improved, and the emulsification resistance is good. 0 To improve oxidative stability or workability at low temperature, the wear reducing agent of the present invention may be in addition to the above (A). One or more kinds selected from the group consisting of antioxidant (1)), cloud point reducing agent (C), and diluent (D) are contained. Examples of the antioxidant (B) include an amine compound (naphthylamine compound, a diphenylamine compound, a P-phenylenediamine compound, and the like), and a phenol compound. . The phenylamine-based compound in the compound of the private compound can be exemplified by: (p. 200907042 Benzene·anhydroxylamine>dimethyleneamine, 4,4′-(α,αι_didecylbenzyl)diphenyl) Low temperature reactants of alkamine, 4,4'-dioctyldiphenylamine, 4_monooctyldiphenylamine, diphenylamine and acetone, low temperature reactant of diphenylamine and acetone a low-temperature reaction product of monophenylamine with aniline and acetone, a reaction product of diphenylamine with diisobutylene, and a mixture of octylated diphenylamine.

酚系化合物可列舉:對壬酚等烷酚(alkylphenol)、2,4-一甲基-6-第三丁基苯酚、2,6_二第三丁基苯酚、2,6_二第三 丁,-對甲酚、第三丁基羥基甲氧苯、4,4•亞曱基雙—(2,3_ 一第二丁基苯酚)以及N_丁基_對胺基苯酚等。 攻些抗氧化劑中較好的是對(對甲苯磺醯胺二苯基 胺、4,^(α,α'_二甲基节基)二笨基胺、4,4,_二辛基二苯基 胺、4-單辛基二苯基胺、⑥驗以及2,4_二甲基_6_第三丁基 苯酚等。 抗氧化劑(Β)之添加量,相對於(Α)為1〇〇重量份,通 常為小於等於0.5重量份、較好的是G1〜G 3重量份。 濁點降低劑(C),可列舉:作為聚(曱基)丙稀酸醋系流 動點降低劑(C1)、乙烯-乙酸乙烯酯(ethyiene_vi_c敝, VA)系饥動點降低劑(C2)、以及稀基號轴酸(业㈣ 系流動點降低劑(C3)等之自先前所使用 之下述化合物。 聚(甲基)丙烯酸酯系流動點降低劑 甲基)丙,烧基_為必須構成單體之聚合物該(; f丙烯酸絲I旨財魏U之錢或者核 基)丙稀酸烧基醋,例如可列舉:(甲基㈣酸甲_、(甲基) 】0 200907042 丙烯酸癸酯(decyl methacryiate)、(甲基)丙烯酸十二酯、(甲 基)丙婦酸十三酯、(甲基)丙烯酸十四酯、(甲基)丙烯酸十 =¾、(甲基)丙烯酸十六酯以及(甲基)丙烯酸十八酯等。聚 合物例如,可列舉日本專利公開公報2〇〇丨—35498〇號中所 ' 記载之聚合物等。 EVA系流動點降低劑(C2),可列舉:乙烯-乙酸乙烯酯 共聚物以及乙烯-乙酸乙烯酯-2-乙基己酸乙烯酯三元共聚 Ο 物、以及日本專利公開公報平11 — 240905所記載之聚合物 等。 ASA系流動點降低劑(C3),可列舉:烯基的碳數為8 50 的加基j虎j自酿胺(aikenyisuccinarnide)等。 自易於调整為任意結晶化開始溫度的觀點而言,(C) 中較好的是聚(甲基)丙烯酸酯系流動點降低劑(C1)。濁點 降低劑(C)的添加量,相對於(A)為1〇〇重量份,通常為小 於等於丨.0重量份、較好的是0.1〜0.5重量份。 , 稀釋劑(D)可列舉烴系溶劑。 ^ 烴系溶劑的具體例,例如可列舉:埃克森美孚(Exxon M〇bll)化學(有)製造的「Pegasol 3040」、「pegas〇l AN-45」、 Pegasol AS-100」以及「Exxs〇1 D4〇」等溶解度參數(sp • 值)為6 8之知肪無糸洛劑;埃克森美孚(£χχ〇η M〇bn)化Examples of the phenolic compound include an alkylphenol such as p-nonphenol, 2,4-methyl-6-tert-butylphenol, 2,6-di-t-butylphenol, and 2,6-third. D-, p-cresol, tert-butylhydroxymethoxybenzene, 4,4-indenyl bis-(2,3-di-butylphenol), and N-butyl-p-aminophenol. Among the antioxidants, it is preferred to (p-toluenesulfonamide diphenylamine, 4,^(α,α'_dimethylbenzyl)diphenylamine, 4,4,_dioctyl Phenylamine, 4-monooctyldiphenylamine, 6-test, and 2,4-dimethyl-7-t-butylphenol, etc. The amount of antioxidant (Β) added is 1 relative to (Α) The 〇〇 by weight is usually 0.5 parts by weight or less, preferably G1 to G 3 parts by weight. The cloud point reducing agent (C) may, for example, be a poly(indenyl) acrylate vinegar-based pour point depressant. (C1), ethylene-vinyl acetate (ethyiene_vi_c敝, VA) is an hunger-reducing agent (C2), and a dilute-based acid (the (4)-based pour point depressant (C3), etc. have been used previously. The compound (poly) (meth) acrylate is a pour point depressant, methyl propyl, ketone _ is a polymer which must constitute a monomer. (; f acrylic acid I is the money of Wei Wei or nuclear base) propylene Examples of the acid-base vinegar include (methyl(tetra) acid A-, (methyl) 】 0 200907042 decyl methacryiate, dodecyl (meth)acrylate, (methyl) propyl fosinate thirteen Ester, (meth) propylene Tetradecyl ester, (meth)acrylic acid dec = 3⁄4, hexadecyl (meth) acrylate, octadecyl (meth) acrylate, etc. Examples of the polymer include Japanese Patent Laid-Open Publication No. H-35-498. EVA-based pour point depressant (C2), examples thereof include ethylene-vinyl acetate copolymer and ethylene-vinyl acetate-2-ethylhexanoate ethylene terephthalate copolymer And the polymer described in Japanese Laid-Open Patent Publication No. Hei 11-240905. The ASA-based pour point depressant (C3) may, for example, be an alkenyl group having a carbon number of 8 50, a k-j-self-brewed amine (aikenyisuccinarnide) From the viewpoint of easy adjustment to an arbitrary crystallization starting temperature, (C) is preferably a poly(meth)acrylate-based pour point depressant (C1). The addition amount of the cloud point reducing agent (C) With respect to (A), it is usually 小于.0 parts by weight, preferably 0.1 to 0.5 parts by weight, based on 1 part by weight of (A). The diluent (D) may be a hydrocarbon solvent. Specific examples include, for example, "Pegasol 304" manufactured by Exxon M〇bll Chemical Co., Ltd. Solubility parameters (sp • value) such as “0”, “pegas〇l AN-45”, Pegasol AS-100” and “Exxs〇1 D4〇” are 6 8 of the fat-free agent; Exxon Mobil (£ Χχ〇η M〇bn)

學(有)製造的「Solvessol〇〇」以及曰本能源gAPAN ENERGY)(股)製造的「CAC丁us s〇LVENt 5〇」等 Sp 值為8.5 = 0的鬲沸點芳香族系工業用溶劑;以及sp值為 8左右且含有芳香族烴以及環烷烴的環烷烴系溶劑等。這 200907042 =系溶劑通常可單獨使用,亦可混合2種或者2種以上 .士稀釋劑⑼的添加量,相對於⑷為100重量份,通當 ^小於等於U重量份、較好的是小於等於0.5重量份^ 若超出該範圍則引火點較低。 本發明的降低磨損劑中,(AHD)成分的各自含量其 於降低磨損劑之重量,通常⑷為97 5〜100 0 wt%、較ς Ο 的是9δ.0〜"·7 Wt%,⑼為小於等於0.5 wt%、較好的θ 0.1〜0.3 Wt°/。’(C)為小於等於丨〇 wt%、較好的是〇」〜 = wt% ’(D)為小於等於1.〇 wt%、較好的是〇卜以研〇/。。 車乂理想的疋本發明的降低磨損劑的濁點為1 〜 _10°C、較好的是8〜-8°c、更好的是7〜-7t:,流動點為 〜-u.5t、較好的是5.〇〜_10.0ac、更好的是;5〜 10.0 C,且引火點為大於荨於2〇〇°c、較好的是大於等於 21〇°C。若濁點、流動點以及引火點超出該範圍,則以大於 , ' 等於1〇C的溫度進行保管之情形時,會引起羧酸之結晶析 U 出、或者降低磨損劑操作性不良。 本發明之降低磨損劑可藉由均勻混合(A)、以及視需要 之(B)〜(D)而獲得。另外,可分別添加構成(A)的2種或者 2種以上的羧酸。 本發明的低硫礦燃料油組成物是含有低硫續燃料油以 及20〜300 ppm之上述降低磨損劑而構成。上述低硫磺燃 料油具有蒸餾初沸點(IBP)為140〜200°C、10%餾出溫度為 170〜260°C、50%餾出溫度為240〜310°C、90%餾出溫度 12 200907042 為310〜35(TC、蒸餾終點(EP)為340〜38〇ΐ的蒸餾性狀, 密度(15C)為0.8200〜0.8400 g/cm3,-l(TC的蠟析出量為 1 ·0〜4.0%,硫石黃含量為1〜5〇〇 ppm。 用於本發明的低硫確燃料油,可列舉視需要將下述癖 油摻合2種或者2種以上而獲得之JIS1號柴油、玎幻號_ 油、JIS3號柴油以及JIS特3號柴油。上述柴油是:低戚 石頁原油(例如,米納斯原油(minas crude)等南方系原、、由)之自 常壓蒸餾裝置所獲得之直餾柴油、以減壓蒸餾裝置處理自 常壓瘵餾裝置所獲得之直餾重油或者殘渣油而獲得之滅廖 柴油、以氫化精製裝置氫化處理直餾柴油或者減壓柴油而 獲得之氫化精製柴油、以比氫化精製更苛刻之條件實施氮 化脫硫而獲得之氫化脫硫柴油、進而氫化分解上述柴油參 材而獲得之氫化分解柴油。 ~ 上述中較好的是使用大於等於5〇 wt〇/〇之氫化精製择 油以及氫化脫硫柴油而製造的JIS1號柴油、JIS2號柴油, JIS3號柴油以及JIS特3號柴油。 ^ 本發明的低硫磺柴油的蒸餾性狀較理想的是如下戶斤 示。Sol 鬲 芳香族 芳香族 Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol Sol And a cycloalkane solvent containing an aromatic hydrocarbon or a cycloalkane having an sp value of about 8. This 200907042 = solvent can be used alone or in combination of two or more. The amount of the diluent (9) added is 100 parts by weight relative to (4), and is less than or equal to U parts by weight, preferably less than Equal to 0.5 parts by weight ^ If the range is exceeded, the ignition point is lower. In the wear reducing agent of the present invention, the respective contents of the (AHD) component are reduced in the weight of the abrasive agent, and generally (4) is 97 5 to 100 0 wt%, and more than 9 δ.0 to < 7 Wt%. (9) is 0.5 wt% or less, preferably θ 0.1 to 0.3 Wt ° /. '(C) is 小于 wt% or less, preferably 〇"~ = wt% ′ (D) is less than or equal to 1. 〇 wt%, preferably 〇 以 〇 。. . The turbidity of the rutting agent of the present invention is 1 to _10 ° C, preferably 8 to -8 ° C, more preferably 7 to -7 t:, and the flow point is ~-u. 5t. Preferably, it is 5. 〇 ~_10.0 ac, more preferably 5 to 10.0 C, and the ignition point is greater than 〇〇 ° ° C, preferably greater than or equal to 21 〇 ° C. When the cloud point, the flow point, and the ignition point are outside the range, when the temperature is greater than or equal to 1 〇C, the crystallization of the carboxylic acid may be caused to occur, or the wear agent may be deteriorated. The wear reducing agent of the present invention can be obtained by uniformly mixing (A) and, if necessary, (B) to (D). Further, two or more kinds of carboxylic acids constituting (A) may be added separately. The low sulfur ore fuel oil composition of the present invention comprises a low sulfur fuel oil and 20 to 300 ppm of the above-mentioned reduced wear agent. The low sulfur fuel oil has an initial boiling point (IBP) of 140 to 200 ° C, a 10% distillation temperature of 170 to 260 ° C, a 50% distillation temperature of 240 to 310 ° C, and a 90% distillation temperature of 12 200907042. It is a distillation property of 310 to 35 (TC, distillation end point (EP) of 340 to 38 Torr, density (15C) is 0.8200 to 0.8400 g/cm3, -l (the wax precipitation amount of TC is 1 · 0 to 4.0%, The content of the sulphuric acid is 1 to 5 〇〇 ppm. The low-sulfur fuel oil of the present invention may be JIS No. 1 diesel or yaw, which is obtained by blending two or more of the following eucalyptus oils as needed. _ Oil, JIS No. 3 diesel and JIS Special No. 3. Diesel oil is obtained from an atmospheric distillation unit of low shale crude oil (for example, Minas crude, etc.) Straight-run diesel, hydrocrefoil obtained by treating a straight-run heavy oil or a residual oil obtained from a normal-pressure retorting apparatus with a vacuum distillation apparatus, and hydrogenating a straight-distilled diesel or a vacuum diesel oil by a hydrorefining apparatus Diesel oil, hydrogenated desulfurized diesel oil obtained by nitriding desulfurization under more severe conditions than hydrogenation refining, and further hydrogenation Hydrogenated diesel oil obtained by dissolving the above diesel fuel material. ~ The above is preferably JIS No. 1 diesel oil, JIS No. 2 diesel oil, JIS3 manufactured by hydrorefining oil selection and hydrogenation desulfurization diesel oil of 5 〇wt〇/〇 or more. No. diesel and JIS special No. 3 diesel. ^ The distillation property of the low sulfur diesel of the present invention is preferably as shown below.

蒸餾初沸點(IBP) = 140〜200°CDistillation initial boiling point (IBP) = 140~200°C

10%餾出溫度=170〜260°C10% distillation temperature = 170~260 °C

50%餾出溫度= 240〜310°C50% distillation temperature = 240~310 °C

90%餾出溫度= 310〜350 °C90% distillation temperature = 310~350 °C

蒸餾終點(EP) = 340〜380°C 此處,蒸館性狀是利用JIS K2254「石油製品—蒸權 13 200907042 試驗法」而測定的值。 3本明的低硫磺柴油之密度(丨5艺)為 0.8200 〜0.8400 =在此 1 好ίί是Q.825Q〜Q.835G g/cm3。若低硫績柴油的 二又 11内,則柴油引擎的耗油量、引擎功率、以及 冋狐的起動卜生良好。此處,密度(15。〇是利用JISK2249「原 油以及石油製π口〜十Λ θ λ% σ岔度.貝置.容量換算表」而測定的值。 f m>/本^明的低硫磺柴油的_1〇°C之蠟析出量為〜 咖較好的是U〜3‘0%。若-l〇〇C之堪析出量在該範圍 ’則低硫石黃柴油的低溫流動性方面良好。 蠟析出量以下述方法而峡。 〇之 、將20 ml的柴油冷卻至比濁點大約高坨之溫度,於 ,溫恆溫槽内的過濾器中進而冷卻至。並且,拙 氣過濾將,出之壞捕集於過滤器(細孔徑:5障、直^ : # “丁酮清洗該過濾、器,加以乾燥後,測定 過濾器重量的增量,定量蠟量。 、 降低磨損劑之含量通常為20〜300 、 〜·ρ抑、更好的是50〜170ppm。若小於;;= 防止磨祕不充分;若超過3GG ppm,則添加 、 損及經濟性。 良’ 本發明的低硫磺燃料油組成物的耐磨損性評價, 由用於柴_料油等之潤滑性評價的通t之摩擦磨 : 5工:堂試驗法實施評價。例如,可藉由如下試驗進行4 1貝.使用Falex Brock on ring摩擦磨損試驗 ° 用b〇cle試驗機之試驗(ASTMD5〇〇1)、使用^試驗^ 14 200907042 (德國歐潤寶(OPTIMOL)公司製造)之試驗、以及高頻往广 試驗(HFRR試驗)等。這些t尤其藉由高触復試驗(英: PCS INSTRUMENTS公司製造)的評價與實際之柴油燃料 油的燃料泵之磨損的關聯性較高,故而使用該試驗機干 評價較好。 本發明的低硫續燃料油組成物適合於用於柴油引擎戋 者鍋爐等之硫磺含量為1〜500 ppm的低硫磺燃料油 油)、或者用於飛機等之喷射引擎的燃料油等。 ’、 [實施例] 以下藉由實施例詳細說明本發明,然而本發明並不限 於這些貫施例。 [降低磨損劑的調製] 實施例1〜12以及比較例1〜5 以,下述表1所示之調配組成而調配,作為羧酸混合物 (A)的(A-1)〜(A-5)、作為抗氧化劑⑻的4_單辛基二苯 基胺、作為濁點降低劑之(CHHcq以及作為稀釋劑⑼ 的日本能源(股)製造之Γ CACTUS S〇LVENT ρ·丨5〇」,從而 調製降低磨損劑。 (A—1)〜(A —5)之組成如表2所示,利用JIS κ 2283 原油以及;5 /由製品—動黏度試驗方法」*測定的仙。◦下 的動黏度示於表2。 (C-1)以及(C-2)之組成以及製造例如下述製造例1以 及2所述。 另外,利用JIS Κ 2269「原油以及石油製品之流動點 15 200907042 以及石油製品濁點試驗方法」測定這些降低磨損劑之濁點 以及流動點,結果示於表1。 表1.降低磨損劑之組成、濁點以及流動點Distillation end point (EP) = 340 to 380 ° C Here, the steaming property is a value measured by JIS K2254 "Petroleum Products - Steaming Rights 13 200907042 Test Method". 3 The density of the low sulfur diesel (this art) is 0.8200 ~ 0.8400 = here 1 Good ίί is Q.825Q ~ Q.835G g / cm3. If the low-sulphur diesel is in the second and second, the diesel engine's fuel consumption, engine power, and the start-up of the fox are good. Here, the density (15. 〇 is a value measured by using JISK2249 "crude oil and petroleum π port to ten Λ θ λ% σ . 贝 贝 . 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量 容量The amount of wax precipitated in diesel oil is 〜1°C, and it is preferably U~3'0%. If the amount of precipitation of -l〇〇C is in this range, the low-temperature fluidity of low-sulfur yellow diesel oil Good. The amount of wax precipitated in the following way. Gently, 20 ml of diesel oil is cooled to a temperature higher than the turbidity point, and then cooled in a filter in a thermostatic bath. Moreover, helium gas filtration will , the damage is trapped in the filter (pore size: 5 barrier, straight ^: # "butanone cleaning the filter, the device is dried, the weight of the filter is measured, the amount of wax is quantified. The content is usually 20 to 300, ≤ ρ, more preferably 50 to 170 ppm. If less than;; = to prevent insufficient grinding; if more than 3 GG ppm, add, damage economic. Evaluation of the abrasion resistance of the sulfur fuel oil composition, the friction mill for the lubricity evaluation of the diesel oil, etc.: 5 : Evaluation of the test method. For example, the test can be carried out by the following test. Using the Falex Brock on ring friction test. Using the b〇cle test machine (ASTMD5〇〇1), using the test ^ 14 200907042 ( Tests by Germany ORT (OPTIMOL), and high-frequency test (HFRR test), etc. These t, especially by high-reaction test (English: PCS INSTRUMENTS) evaluation and actual fuel of diesel fuel oil The wear of the pump is highly correlated, so it is better to use the tester for dry evaluation. The low-sulfur fuel oil composition of the present invention is suitable for use in a diesel engine, such as a boiler, etc., having a sulfur content of 1 to 500 ppm. Fuel oil), or fuel oil for an injection engine of an airplane or the like. ', [Embodiment] Hereinafter, the present invention will be described in detail by way of examples, but the invention is not limited to these examples. Preparations Examples 1 to 12 and Comparative Examples 1 to 5 were prepared by using the compounding compositions shown in the following Table 1 as (A-1) to (A-5) of the carboxylic acid mixture (A) as an antioxidant. (8) 4_monooctyldiphenylamine, The cloud point reducing agent (CHHcq and 日本CACTUS S〇LVENT ρ·丨5〇 manufactured by Japan Energy Co., Ltd. as a diluent (9)) modulate and reduce the wear agent. (A-1)~(A-5) The composition is as shown in Table 2, and the dynamic viscosity measured by JIS κ 2283 crude oil and 5/product-dynamic viscosity test method* is shown in Table 2. (C-1) and (C-2) The composition and manufacture are as described in the following Production Examples 1 and 2. In addition, the cloud point and the flow point of these reducing wear agents were measured by JIS Κ 2269 "Pour point of crude oil and petroleum products 15 200907042 and the cloud point test method of petroleum products", and the results are shown in Table 1. Table 1. Reducing the composition of the abrasive, cloud point and pour point

降低磨損劑 的品名 調配組成[〇内為重量比] 濁點 rc] 流動點 PC] 羧酸混合物 ΓΑ) 抗氧化劑 (B) 濁點降低劑 (C) 稀釋劑 (D) 實 例 1 S1 A-1 (99.6) (0.1) C-l (0.3) — -5 0.0 2 S2 A-1 (99.6) (0.1) — (0.3) 7 0.0 3 S3 A — 1 (99.6) — C-l (0.3) (0.1) -5 0.0 4 S4 A—1 (]00.0) — — — 7 0.0 5 S5 A-2(99.5) (0.1) C 一2 (0.3) (0-1) -7 -7.5 6 S6 A — 2 (99.6) (0.1) — (0.3) 0 -7.5 7 S7 A-3 (99.6) (0.1) C —2(0.2) (0.1) -9 -12.5 8 S8 A-3 (99.6) (0.1) — (0.3) -5 -12.5 9 S9 A—4(99.5) (O.i) C-l (0.3) (0.1) -2 2.5 10 S10 Α-4(99·6) (0.1) — (0.3) 8 2.5 11 S11 A-5 (99.5) (0.1) C—1 (0.3) (0.1) 0 5.0 12 S12 A-5 (99.6) (0.1) — (0.3) 9 5.0 比 較 例 1 R1 A-6 (100.0) — — — 15 7.5 2 R2 A-6 (99.6) (0.1) C —2(0.3) — 11 7.5 3 R3 A-6 (99.6) (0.1) — (0_3) 15 7.5 4 R4 A-7 (100.0) — — — -13 -17.5 5 R5 A —7(99.6) (0.1) — (0.3) -13 -17.5Reduce the name of the wear agent. [Inside weight ratio] Cloud point rc] Flow point PC] Carboxylic acid mixture ΓΑ) Antioxidant (B) Cloud point reducer (C) Thinner (D) Example 1 S1 A-1 (99.6) (0.1) Cl (0.3) — -5 0.0 2 S2 A-1 (99.6) (0.1) — (0.3) 7 0.0 3 S3 A — 1 (99.6) — Cl (0.3) (0.1) -5 0.0 4 S4 A—1 (]00.0) — — — 7 0.0 5 S5 A-2(99.5) (0.1) C-2 (0.3) (0-1) -7 -7.5 6 S6 A — 2 (99.6) (0.1 ) — (0.3) 0 -7.5 7 S7 A-3 (99.6) (0.1) C —2(0.2) (0.1) -9 -12.5 8 S8 A-3 (99.6) (0.1) — (0.3) -5 - 12.5 9 S9 A—4(99.5) (Oi) Cl (0.3) (0.1) -2 2.5 10 S10 Α-4(99·6) (0.1) — (0.3) 8 2.5 11 S11 A-5 (99.5) ( 0.1) C-1 (0.3) (0.1) 0 5.0 12 S12 A-5 (99.6) (0.1) — (0.3) 9 5.0 Comparative Example 1 R1 A-6 (100.0) — — — 15 7.5 2 R2 A-6 (99.6) (0.1) C —2(0.3) — 11 7.5 3 R3 A-6 (99.6) (0.1) — (0_3) 15 7.5 4 R4 A-7 (100.0) — — — —13 —17.5 5 R5 A —7(99.6) (0.1) — (0.3) -13 -17.5

16 200907042 表2.缓酸混合物之組成以及机下之動黏度 40°c,下的動黏度 (mm~/s)16 200907042 Table 2. Composition of the slow acid mixture and the dynamic viscosity under the machine 40 °c, the dynamic viscosity (mm~/s)

’蜀點降低劑之製造例 製造例l[(c—1)的製造] 叶、:二It苯投入具備授拌装置、加熱裝置、溫度 溫至=二Γ應器内,將系内設為氮氣環境,並升 '、、〗叙,一邊攪拌反應器中的甲苯,一邊將?50 &amp; 的(甲基)丙燁酸燒基醋混合物(甲基丙婦酸十二醋:甲基^ 烯酸十四酯:甲基丙烯酸十六酯:甲基丙烯酸十八酯=忉: 10 : 40 : 40重量比的調配物)、以及於2〇 g的甲苯中溶解 有1.5 g的2,2f-偶氮雙_2,4-二甲基戊腈的溶液,分別自不 同之滴液漏斗向反應器内以2小時且等速度全部滴下。滴 下結束後於85°C進行2小時聚合反應。反應結束後,於 13(TC下,鶴去甲苯而獲得聚合物’將其作為濁點降低劑(C 一 1)。 製造例2[(C-2)的製造] 除將(甲基)丙烯酸烷基酯混合物設為f基丙烯酸十二 酯:甲基丙烯酸十四酯:曱基丙烯酸十六酯:甲基丙烯酸 十八酯=25 : 25 : 25 : 25重量比之調配物以外,以與製造 17 200907042 例1相同之方式進行聚合而獲得聚合物,將其作為濁點降 低劑(C一2)。 [燃料油組成物之調製與評價] 實施例13〜24以及比較例6〜1〇 於考油燃料油中’分別溶解1 〇〇 ppm的降低磨損劑s j 〜S12或者R1〜R5,從而調製燃料油組成物,上述柴油燃 料油是具有蒸餾初沸點(IBP)為170。(:、10%餾出溫度為 205°C、50%餾出溫度為3〇5。(:、90〇/〇餾出溫度為338t:、 蒸餾終點(EP)為360°C的蒸餾性狀,且密度(15。〇為0.8320 g/cm ’ -10 C之躐析出量為2.3% ’硫續含量為1〇 ppm之 相當於JIS2號的柴油燃料油。 對這些燃料油組成物的耐磨損性、水分離性、氧化穩 定性以及防銹性進行評價。 試驗方法如下所示。試驗結果示於表3。 &lt;耐磨損性&gt; 利用石油學會標準JPI_5S_50_98「柴油一潤滑性試驗 方法」進行尚頻往復試驗(HFRR,High Frequency Keciprocating Rig) ’評價試驗球之磨損痕的大小。裝置是 英國PCS INSTRUMENTS公司製造。 &lt;水分離性&gt; 以JISK2776中所記載的「航空燃料油試驗方法」的 水溶解度試驗方法進行。 於100 ml的附;j:全之量筒中量取8〇 mi的樣品、20 ml 的緩衝液’以既定條件振動混合,測定靜置後的緩衝液部 18 200907042 分的容量變化,目視界面狀態以及分離狀態,根據以下基 準進行評價。 界面狀態之評價點: 1 :透明、清淨之狀態 lb :較小且透明之泡所占面積小於等於界面的50%, 無小片、花邊狀或者膜狀物質之狀態。 分離狀態之評價點: (1) :於兩層或者樣品層上部完全無乳化物或者沈殿物 之狀態 (2) :除於樣品層存在較小之氣泡或者水滴以外,為與 (1)相同之狀態 &lt;氧化穩定性&gt; 藉由可試驗實車中是否產生引擎附著物的ISOT試驗 (Indiana Stirring Oxidation Test) ’ 於、溫度 110°C、旋轉數 700 rpm、試驗時間8小時下,進行試驗。評價基準如下所示。 氧化穩定性之評價點: 1 :器壁上幾乎無附著物 2:器壁上僅產生一點附著物 3:器壁上產生一些附著物 4:器壁上附滿了附著物 〈防銹性&gt; 利用JISK 2510之防銹試驗測定防鎊性。 19 200907042 ipil 表3 所含有的降低磨 損劑的品名 耐磨損性(磨損 痕之大小) (μηι) 水分離性(” 氧化穩 定性 防鎮性 鏽之有無 鏽之程度 實 施 例 13 S1 290 0/1/(1) 1 有 輕微 14 S2 295 0/1/(1) 1 有 輕微 15 S3 300 0/1/(1) 1 有 輕微 16 S4 285 0/1/(1) 1 有 輕微 17 S5 305 0/1/(1) 1 有 輕微 18 S6 290 0/1/(1) 1 有 輕微 19 S7 290 0/1/(1) 1 有 輕微 20 S8 290 0/1/(1) 1 有 輕微 21 S9 305 0/1/(1) 1 有 輕微 22 S10 290 0/1/(1) 1 有 輕微 23 S11 300 0/1/(1) 1 有 輕微 24 S12 290 0/1/(1) 1 有 輕微 空白 600 0/1/(1) 1 有 強度 比 較 例 6 R1 360 0/lb/(2) 1 有 輕微 7 R2 375 0/lb/(2) 1 有 輕微 8 R3 360 0/lb/(2) 1 有 輕微 9 R4 370 0/lb/(2) 3 有 中度 10 R5 380 0/lb/(2) 2 有 中度 (氺)緩衝液部分的容量變化/界面狀態/分離狀態<Production Example of Production of Defecting Agent> Production of [(c-1)] Leaves: Two It benzenes are supplied with a mixing device, a heating device, and the temperature is up to the temperature of the second reactor. Under the nitrogen atmosphere, and raise the ',,〗, while stirring the toluene in the reactor, will? Mixture of (meth)propionic acid ketone vinegar of 50 & (methyl acetoacetate decanoic acid: tetradecyl methacrylate: hexadecyl methacrylate: octadecyl methacrylate = hydrazine: 10 : 40 : 40 weight ratio of the formulation), and 1.5 g of 2,2f-azobis 2,4-dimethylvaleronitrile dissolved in 2 g of toluene, respectively, from different drops The liquid funnel was completely dropped into the reactor at 2 hours and at the same speed. After the completion of the dropwise addition, polymerization was carried out at 85 ° C for 2 hours. After completion of the reaction, the polymer was obtained as a cloud point reducing agent (C-1) at 13 (under TC, toluene). Production Example 2 [Production of (C-2)] In addition to (meth)acrylic acid The alkyl ester mixture is set to f-based dodecyl acrylate: tetradecyl methacrylate: hexadecyl methacrylate: octadecyl methacrylate = 25: 25: 25: 25 by weight of the formulation, in addition to Production 17 200907042 The polymerization was carried out in the same manner as in Example 1 to obtain a polymer, which was used as a cloud point reducing agent (C-2). [Modulation and Evaluation of Fuel Oil Composition] Examples 13 to 24 and Comparative Examples 6 to 1 The fuel oil composition is prepared by dissolving 1 〇〇ppm of the reducing agent sj 〜S12 or R1 〜R5 in the fuel oil, and the diesel fuel oil has an initial boiling point (IBP) of 170. (:, 10% distillation temperature is 205 ° C, 50% distillation temperature is 3 〇 5. (:, 90 〇 / 〇 distillation temperature is 338t: distillation end point (EP) is 360 ° C distillation characteristics, and density ( 15. The enthalpy is 0.8320 g/cm ' -10 C. The amount of bismuth precipitated is 2.3%. The sulphur content of 1 〇ppm is equivalent to JIS No. 2 diesel fuel oil. The fuel oil composition was evaluated for abrasion resistance, water separation property, oxidation stability, and rust resistance. The test methods are as follows. The test results are shown in Table 3. &lt;Abrasion resistance&gt; JPI_5S_50_98 "Diesel-lubricity test method" HFRR (High Frequency Keciprocating Rig) 'Evaluate the size of the wear marks of the test ball. The device is manufactured by PCS INSTRUMENTS, UK. &lt;Water Separability&gt; JISK2776 The water solubility test method of the "Aviation Fuel Oil Test Method" is carried out. In a 100 ml sample; j: a sample of 8 〇mi in a measuring cylinder and 20 ml of a buffer solution are vibrated and mixed under predetermined conditions. The capacity change of the buffer portion 18 after standing at 200907042, the visual interface state and the separation state were evaluated according to the following criteria. Evaluation of interface state: 1 : Transparent, clean state lb: Small and transparent bubble The area is less than or equal to 50% of the interface, and there is no state of small pieces, lace-like or membranous substances. Evaluation points of separation state: (1): on two layers or samples The state of the upper part of the layer is completely free of emulsification or sedimentation. (2): In the same state as (1) except for the presence of small bubbles or water droplets in the sample layer, &lt;oxidative stability&gt; The ISOT test (Indiana Stirring Oxidation Test) for producing engine attachments was tested at a temperature of 110 ° C, a number of revolutions of 700 rpm, and a test time of 8 hours. The evaluation criteria are as follows. Evaluation points of oxidative stability: 1 : There is almost no deposit on the wall 2: only a little attachment is produced on the wall 3: some deposits are formed on the wall 4: the wall is covered with attachments <rust resistance> ; Use the rust proof test of JISK 2510 to determine the anti-pound property. 19 200907042 ipil Table 3 The name of the wear-reducing agent contained in the wear-resistant (the size of the wear marks) (μηι) Water-separable ("Oxidative stability Anti-town rust with or without rust degree Example 13 S1 290 0/ 1/(1) 1 Minor 14 S2 295 0/1/(1) 1 Minor 15 S3 300 0/1/(1) 1 Minor 16 S4 285 0/1/(1) 1 Minor 17 S5 305 0/1/(1) 1 has a slight 18 S6 290 0/1/(1) 1 has a slight 19 S7 290 0/1/(1) 1 has a slight 20 S8 290 0/1/(1) 1 has a slight 21 S9 305 0/1/(1) 1 Minor 22 S10 290 0/1/(1) 1 Minor 23 S11 300 0/1/(1) 1 Minor 24 S12 290 0/1/(1) 1 Yes Slight blank 600 0/1/(1) 1 Strength comparison Example 6 R1 360 0/lb/(2) 1 Minor 7 R2 375 0/lb/(2) 1 Minor 8 R3 360 0/lb/(2 1 1 Minor 9 R4 370 0/lb/(2) 3 Moderate 10 R5 380 0/lb/(2) 2 Capacity change/interface state/separation state with moderate (氺) buffer

[發明之效果] 〇 根據表3可知,本發明的低硫磺燃料油用降低磨損劑 以及包含該低硫磺燃料油用降低磨損劑的燃料油組成物較 之先前的添加劑,不僅可發揮同等或同等以上的防磨損 性,並且於操作性、氧化穩定性、水分離性方面亦發揮優 良的性能。 【圖式簡單說明】 無 【主要元件符號說明】 無 20[Effects of the Invention] According to Table 3, the fuel oil composition for a low sulfur fuel oil of the present invention and the fuel oil composition for reducing the wear agent for the low sulfur fuel oil are not only equivalent or equivalent to the prior additives. The above abrasion resistance is excellent, and also exhibits excellent performance in terms of workability, oxidation stability, and water separation property. [Simple diagram description] None [Main component symbol description] None 20

Claims (1)

200907042 十、申請專利範圍: 1. 一種低硫磺燃料油用降低磨損劑,其特徵在於:該 降低磨損劑為含有碳數14〜22之飽和羧酸以及不飽和羧 酸的混合物(A)’該(A)於40°C下之動黏度為15〜21 mm2/s。 2. 如申請專利範圍第1項所述之低硫磺燃料油用降低 磨才貝劑,其中上述(A)包括:含碳數14〜22之飽和一元叛 酸(al)、碳數14〜22之單不飽和一元羧酸(a2)、碳數14〜 22之二不飽和一元羧酸(a3)以及碳數14〜22之三不飽和一 元叛酸(a4), 以(A)之總重量來計算,(al)為1.5〜8.0重量百分比、 (a2)以及(a3)之總計為84.0〜96.5重量百分比、(a4)為2.0 〜8.0重量百分比。 3. 如申請專利範圍第2項所述之低硫磺燃料油用降低 磨損劑,其中上述飽和一元羧酸(al)包含棕櫚酸以及硬脂 酸,其重量比(掠櫚酸/硬脂酸)為1/1〜1/2.5。 4. 如申請專利範圍第2項所述之低硫磺燃料油用降低 磨損劑,其中上述單不飽和一元羧酸(a2)為油酸,且上述 二不飽和一元羧酸(a3)為亞麻油酸,且上述三不飽和一元 羧酸(a4)為次亞麻油酸。 5. 如申請專利範圍第丨項所述之低硫磺燃料油用降低 磨損劑,其中該降低磨損劑進/步含有選自抗氧化劑(B)、 濁點降低劑(C)以及稀釋劑(D)中的1種或者1種以上而成。 6. 如申請專利範圍第1項所述之低硫石黃燃料油用降低 磨損劑,其中該降低磨損劑的濁點為C〜-10 C,胤動 200907042 點為5°C〜-12.5°C,且引火點為大於等於210°C。 7.—種低硫磺燃料油組成物,其特徵在於:含有低硫 磺燃料油,以及20〜300 ppm之如申請專利範圍第1項至 第6項中任一項所述之低硫石黃燃料油用降低磨損劑, 上述低硫項燃料油具有蒸館初沸點(IBP)為140〜 200°C、10%餾出溫度為170〜260°C、50%餾出溫度為240 〜310°C、90%餾出溫度為310〜350°C、蒸餾終點(EP)為 340〜380°C的蒸餾性狀,密度(15°C)為0.8200〜0.8400 g/cm3,-10°C之蠟析出量為1.0〜4.0%,硫磺含量為1〜500 ppm。 22 200907042 七、 指定代表圖: (一) 本案指定代表圖為:無。 (二) 本代‘圖之元件符號簡單說明: 益 八、 本案若有化學式時,請揭示最能顯示發明特徵 的化學式: 益200907042 X. Patent application scope: 1. A low-sulfur fuel oil reducing wear agent, characterized in that the reducing wear agent is a mixture of saturated carboxylic acid having a carbon number of 14 to 22 and an unsaturated carboxylic acid (A) (A) The dynamic viscosity at 40 ° C is 15 to 21 mm 2 / s. 2. The method for reducing the sulphur fuel oil according to the first aspect of the patent application, wherein the above (A) comprises: a saturated monobasic acid (al) having a carbon number of 14 to 22, and a carbon number of 14 to 22 The monounsaturated monocarboxylic acid (a2), the carbon number 14 to 22 bis unsaturated monocarboxylic acid (a3), and the carbon number 14 to 22 of the triunsaturated monobasic acid (a4), with the total weight of (A) To calculate, (al) is 1.5 to 8.0 weight percent, (a2) and (a3) are 84.0 to 96.5 weight percent, and (a4) is 2.0 to 8.0 weight percent. 3. The anti-wear agent for a low-sulfur fuel oil according to claim 2, wherein the saturated monocarboxylic acid (al) comprises palmitic acid and stearic acid in a weight ratio (pampic acid/stearic acid) It is 1/1 to 1/2.5. 4. The anti-wear agent for a low-sulfur fuel oil according to claim 2, wherein the monounsaturated monocarboxylic acid (a2) is oleic acid, and the di-unsaturated monocarboxylic acid (a3) is linseed oil. An acid, and the above tri-unsaturated monocarboxylic acid (a4) is linolenic acid. 5. The low-sulfur fuel oil reducing wear agent according to the invention of claim 2, wherein the reducing wear agent further comprises an antioxidant (B), a cloud point reducing agent (C), and a diluent (D). One or more of them are formed. 6. For the low-sulfur yellow fuel oil as described in claim 1, the reducing agent has a cloud point of C~-10 C, and the 200907042 point is 5°C~-12.5°. C, and the ignition point is 210 ° C or more. 7. A low-sulfur fuel oil composition, characterized by comprising a low-sulfur fuel oil, and a low-sulfur yellow fuel according to any one of claims 1 to 6 of 20 to 300 ppm. The oil-reducing wear agent, the low-sulfur fuel oil has an initial boiling point (IBP) of 140 to 200 ° C, a 10% distillation temperature of 170 to 260 ° C, and a 50% distillation temperature of 240 to 310 ° C. The 90% distillation temperature is 310 to 350 ° C, the distillation end point (EP) is 340 to 380 ° C, and the density (15 ° C) is 0.8200 to 0.8400 g/cm 3 , and the wax precipitation amount is -10 ° C. It is 1.0 to 4.0% and has a sulfur content of 1 to 500 ppm. 22 200907042 VII. Designation of representative representatives: (1) The representative representative of the case is: None. (2) The simple description of the symbol of the figure in this generation: Benefits 8. If there is a chemical formula in this case, please reveal the chemical formula that best shows the characteristics of the invention:
TW96129212A 2007-08-08 2007-08-08 Low sulphur fuel oil for reducing wear agent TWI391480B (en)

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