CN106591547A - Quenching oil composition and manufacturing method thereof - Google Patents

Quenching oil composition and manufacturing method thereof Download PDF

Info

Publication number
CN106591547A
CN106591547A CN201510674623.1A CN201510674623A CN106591547A CN 106591547 A CN106591547 A CN 106591547A CN 201510674623 A CN201510674623 A CN 201510674623A CN 106591547 A CN106591547 A CN 106591547A
Authority
CN
China
Prior art keywords
group
straight
branched alkyl
hydrogen
formula
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
CN201510674623.1A
Other languages
Chinese (zh)
Other versions
CN106591547B (en
Inventor
苏朔
段庆华
张辉
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.)
Beijing General Fine Chemical Technology Development Co ltd
Sinopec Research Institute of Petroleum Processing
China Petroleum and Chemical Corp
Original Assignee
Sinopec Research Institute of Petroleum Processing
China Petroleum and Chemical Corp
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 Sinopec Research Institute of Petroleum Processing, China Petroleum and Chemical Corp filed Critical Sinopec Research Institute of Petroleum Processing
Priority to CN201510674623.1A priority Critical patent/CN106591547B/en
Publication of CN106591547A publication Critical patent/CN106591547A/en
Application granted granted Critical
Publication of CN106591547B publication Critical patent/CN106591547B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/56—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering characterised by the quenching agents
    • C21D1/58—Oils

Abstract

The invention relates to a quenching oil composition. The quenching oil composition comprises a shielding phenol compound, a cooling accelerant, a brightening agent, an antirusting agent and a main amount of lubricating oil foundation oil; the structure of the shielding phenol compound is expressed by a formula (I); and in the formula (I), each radical is defined as the specification. The quenching oil composition can satisfy the increasingly harsh requirements on oxidation resistance by present higher-specification products, and shows excellent clean dispersion performance, corrosion resistance and rust resistance.

Description

A kind of quenching oil compound and its manufacture method
Technical field
The present invention relates to a kind of quenching oil compound.Specifically, the present invention relates to a kind of tool There is the grade quench fluid composition that excellent thermal oxidation stability, coking are few.
Background technology
With the development of mechanotronic, national defense industry and aerospace industry, to metal The quenching technique of material requires more and more higher.To solve precision component and large module gear Quenching distortion problem, developed country develops the isothermal hardening using temperature at 120～200 DEG C Oil, hierarchical quenching oil.Because hierarchical quenching oil is to use at high temperature, high-temperature oxydation is pacified It is qualitative to have very high requirement.For this purpose, main in hierarchical quenching oil add 2,6- di-tert-butyls The antioxidant such as phenol, alkylated diphenylamine.But add the hierarchical quenching oil of above-mentioned antioxidant, its Thermal oxidation stability is still not ideal enough.If quenching oil can not be substantially prevented from oxidation, its oxidation Product can form deposit in quenching workpiece, cause coking serious, can not only shorten quenching The service life of oil, and rear manufacturing procedure can be had a strong impact on.
Seek the hierarchical quenching oil of more efficiently antioxidant additive and exploitation novel high-performance, The target that always those skilled in the art make great efforts.
United States Patent (USP) US 5304314 is disclosed and a kind of is suitable as the sulfur-bearing that antioxidant is used With the phenolic compounds of arylamine.United States Patent (USP) US 2006/0189824A1 discloses a kind of being adapted to As the shielding phenolic compounds containing secondary aromatic amine that antioxidant is used.
Chinese patent CN1078489 discloses a kind of grade quench fluid composition, the classification Quenching oil compound includes high-temperature antioxidant, urges cryogen, antirust agent, brightener and base oil. Wherein, high-temperature antioxidant is 4,4- methylene -2,6- DI-tert-butylphenol compounds.
But, the compound of these prior arts when used in quenching oil, the high temperature of oil product Can still there is room for improvement in antioxygenic property, detergent-dispersant performance.In addition, except deposition Beyond the adverse effect of thing, corrosion can also have a strong impact on the following process of workpiece.Prior art Concern to rustless property is also far from enough.
Therefore, prior art is still required for a kind of quenching oil compound, and it is not only able to meet The requirement increasingly harsh to high-temperature oxidation resistance of current more high standard product, and also show Go out excellent detergent-dispersant performance energy and rustless property.
The content of the invention
The present invention relates to the content of following aspect.
1. a kind of quenching oil compound, including shielding phenolic compounds, urge cryogen, brightener, Antirust agent and major amount of lube base oil；
It is described shielding phenolic compounds structure be：
In logical formula (I), each group R is same to each other or different to each other, be each independently selected from hydrogen, C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn is polyolefin-based for 300-3000), the group shown in logical formula (II) and logical formula (III) Shown group, on condition that at least one group R is the group shown in logical formula (II)；Respectively Group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight or branched alkane Base (is preferably each independently selected from hydrogen and C1-4Straight or branched alkyl),
In aforementioned each logical formula (II), (III) and (IV), each group L is mutually the same or not Together, it is independently of one another groupWherein group R " is selected from hydrogen, C1-20Hydrocarbon Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, preferably Selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl；Each group R2It is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl, The group shown in group and logical formula (V) shown in logical formula (IV) is (preferably independently of one another Selected from hydrogen, C1-10Group shown in straight or branched alkyl and logical formula (IV))；Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20Straight or branched alkyl is (excellent Choosing is each independently selected from hydrogen and C1-10Straight or branched alkyl)；Each group RcPhase each other It is same or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Straight chain Or branched alkyl epoxide (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and C1-10Straight or branched alkyl epoxide, is more preferably in cyclic groupUpper nitrogen-atoms Contraposition)；Y is 0 to 3 integer (preferably 0 or 1)；Z be 0 to 3 integer it is (excellent Select 0 or 1)；N is 1 to 8 integer (preferably 1 or 2)；N' be 0 to 7 integer it is (excellent 0,1 or 2) is selected, on condition that n'+n≤8 (preferred n'+n=1 or n'+n=2)；Each group Rd It is same to each other or different to each other, is each independently selected from hydrogen and the group shown in logical formula (V) is (excellent Select hydrogen)；Each cyclic groupIt is same to each other or different to each other, is each independently selected from phenyl ring With naphthalene nucleus (preferred phenyl ring), wherein two adjacent cyclic groupsOptionally lead to each other Cross additional S atom and bridge the N atoms of the two rings and form phenthazine ring, and/or, Two adjacent cyclic groupsEach other optionally by additional group (wherein group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen and C1-10Straight or branched alkyl) and Bridge the N atoms of the two rings and form 9,10- acridan rings,
In logical formula (V), each group R is same to each other or different to each other, be each independently selected from hydrogen, C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn is the polyolefin-based of 300-3000), the group shown in logical formula (II) and logical formula (III) institute The group for showing (is preferably each independently selected from hydrogen and C1-300Straight or branched alkyl)；Each base Group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight or branched alkyl (preferably it is each independently selected from hydrogen and C1-4Straight or branched alkyl)；Group L is groupWherein group R " is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight chain is propped up Alkyl group) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain is propped up Alkyl group and C3-10Straight or branched miscellaneous alkyl；A be 0 or 1, and two group R and One group-(S)a- L- occupies respectively three positions of residue on phenyl ring,
Wherein, the straight or branched miscellaneous alkyl is in straight or branched alkyl molecular structure One or more (such as 1 to 4,1 to 3,1 to 2 or 1) in portion Group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight or branched alkyl) One of the substituting group group that directly substitutes and obtain and straight or branched alkyl molecule One or more (such as 1 to 3,1 to 2 or 1) bases of inside configuration Group-CH<By substituting group-N<The group for directly substituting and obtaining, wherein the shielding phenolate Compound at least one group R in its whole molecular structuredIt is hydrogen.
2. according to the shielding phenolic compounds described in any preceding aspect, selected from following tool The mixture of body compound or its arbitrary proportion：
3. a kind of quenching oil compound, including shielding phenolic compounds, urge cryogen, brightener, Antirust agent and major amount of lube base oil, the manufacture method of the shielding phenolic compounds Exist including phenolic compounds and the amines shown in formula (Y) shown in logical formula (X) is made First reacted in the presence of aldehyde compound (preferred formaldehyde) shown in formula (Z) Step, optionally also includes making the product and vulcanizing agent (preferred sulphur) of the first step Reaction and/or the extra step with aldehyde compound (preferred formaldehyde) reaction shown in formula (Z) Suddenly,
In logical formula (X), each group R0It is same to each other or different to each other, is each independently selected from Hydrogen ,-SH and C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or Number-average molecular weight Mn is polyolefin-based for 300-3000's), on condition that at least one group R0 It is-SH；Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-20Straight chain Or branched alkyl (is preferably each independently selected from hydrogen and C1-4Straight or branched alkyl),
In formula (Y), group R'2Selected from hydrogen, C1-20Straight or branched alkyl and groupEach group RbIt is same to each other or different to each other, is each independently selected from hydrogen And C1-20Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-10Straight chain is propped up Alkyl group)；Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20 Straight or branched alkyl and C1-20Straight or branched alkyl epoxide (is preferably selected independently of one another From hydrogen, C1-10Straight or branched alkyl and C1-10Straight or branched alkyl epoxide, more preferably In cyclic groupThe contraposition of upper nitrogen-atoms)；Y be 0 to 3 integer (preferably 0 or 1)；Z is 0 to 3 integer (preferably 0 or 1)；N1 be 1 to 8 integer it is (excellent Select 1 or 2)；Each cyclic groupIt is same to each other or different to each other, is each independently selected from Phenyl ring and naphthalene nucleus (preferred phenyl ring),
In formula (Z), group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight chain or Branched alkyl) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain or Branched alkyl and C3-10Straight or branched miscellaneous alkyl,
Wherein, the straight or branched miscellaneous alkyl is in straight or branched alkyl molecular structure One or more (such as 1 to 4,1 to 3,1 to 2 or 1) in portion Group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight or branched alkyl) One of the substituting group group that directly substitutes and obtain and straight or branched alkyl molecule One or more (such as 1 to 3,1 to 2 or 1) bases of inside configuration Group-CH<By substituting group-N<The group for directly substituting and obtaining.
4. according to the manufacture method described in any preceding aspect, wherein in the first step In, the phenolic compounds shown in the logical formula (X) and the amination shown in the formula (Y) The mol ratio of compound is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, it is described Phenolic compounds shown in logical formula (X) rubs with the aldehyde compound shown in the formula (Z) You are than being 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, in the extra step In rapid, the amines shown in the formula (Y) is with the mol ratio of the vulcanizing agent 1:1-10, preferably 1:1.2-6.0, more preferably 1:1.5-3.0, the amine shown in the formula (Y) Compound is 1 with the mol ratio of the aldehyde compound shown in the formula (Z):0.1-10, it is excellent Select 1:0.5-5.0, more preferably 1:0.8-2.0.
5. in the quenching oil compound described in any preceding aspect, the shielding phenolate is closed Thing accounts for the 0.001%-30% of the quenching oil compound gross weight, preferred 0.05%-20%, More preferably 0.1%-10%；
It is described to urge cryogen to be selected from sulfonate, polyisobutene succinimide and polyolefin In one or more.The sulfonate can be selected from sulfoacid calcium, sulfonic acid magnesium, barium sulfonate With one or more in sodium sulfonate, such as can select petroleum sodium sulfonate, synthesis sulfonic acid Sodium, barium mahogany sulfonate, synthesis barium sulfonate, dinonyl naphthalene sulfonate barium, dinonylnaphthalene sulfonic acid Calcium and synthesis sulfonic acid magnesium etc., such as can select the production of Jinan Bo Ao Chemical Co., Ltd.s T701, T702, T705, the T106 of the emerging petroleum additive Co., Ltd production in Jinzhou Deng.The polyisobutene succinimide can be sub- from monosubstituted polyisobutene succinyl Amine, disubstituted polyisobutene succinimide, polysubstituted polyisobutene succinimide and One or more in boronation polyisobutene succinimide, wherein polyisobutene (PIB) Partial number-average molecular weight be 800-4000, preferably preferred 900-3000,1000-2400, T151, T161 of the production of Suzhou specialty oil factory, Jinzhou Petrochemical Company point can such as be selected T154, T161A, T161B of additive factory of company production, the big chemical industry of Shanghai Bohai Sea is limited The T154B of company's production, the LZLl57 of Lu Borun Lan Lian additives Co., Ltd production, LZ6418, LZ6420 of Lubrizol Corp.'s production, the Hitec646 of Afton Chemical Corp.'s production Deng.The polyolefin can be selected from polypropylene, polyisobutene and ethylene-propylene copolymer In one or more, such as can select great Lin companies of Korea production PB1300, PB1400、PB2400。
It is described to urge cryogen to be preferably selected from sulfonate and/or polyisobutene succinimide.It is described Cryogen is urged to account for the 0.01%-30% of the quenching oil compound gross mass, preferred 0.05%-20%, More preferably 0.1%-10%.
The brightener can selected from imidazoline, imidazoline oleate, methyl terpene resin, One or more in sorbitol monooleate and binary of fatty acids.The di-fatty Alcohol can be selected from C2-12Alkyl binary of fatty acids, preferred adipic acid, pimelic acid, nonyl two One or more in acid, decanedioic acid, M-phthalic acid and terephthalic acid (TPA).
The brightener is preferably selected from imidazoline oleate and/or sorbitol monooleate. The brightener accounts for the 0.01%-10% of the quenching oil compound gross mass, preferably 0.05%-5%, more preferably 0.1%-3%.
The antirust agent can be selected from alkyl imidazolidine derivatives, benzotriazole derivative and thiazolinyl One or more in butanedioic acid derivative.The alkyl imidazolidine derivatives can be selected from hydrocarbon Base imidazoline alkenyl succinate and/or alkyl phosphoric acid imidazoline salt, such as can select upper T703 of dried shrimps De Jiaerde Chemical Co., Ltd.s production etc..The benzotriazole derivative can With in BTA, methyl benzotriazazole and BTA fatty amine salt Plant or various, such as can select the T706 of Shandong Zibo Hui Hua Chemical Co., Ltd. production Deng.The alkenyl succinic acid derivative can be selected from alkenyl succinic acid and/or alkenyl succinic acid Ester, such as dodecenylsuccinic acid, dodecenylsuccinic acid ester, can select Shanghai Mead T746 and T747 of the production of jar (unit of capacitance) moral Chemical Co., Ltd. etc..
The antirust agent is preferably selected from alkenyl succinic acid derivative.The antirust agent accounts for described quenching The 0.001%-10% of kerosene composition gross mass, preferred 0.005%-5%, more preferably 0.01%-1%.
The lube base oil, can be moistened from API I, II, III, IV and V class One or more in lubricant base oil, such as can be selected from mineral lubricating oil and synthesis profit One or more in lubricating oil, in preferred II, III and IV class lubricating oil base oil Plant or various, most preferably IV class lubricating oils base oil.
Antioxidant, detersive can also be added in the quenching oil compound of the present invention, is divided Powder, pour-point depressant, viscosity index improver, metal corrosion inhibitor, friction improver, One or more in anti emulsifier and anti-foaming agent other lube oil additives.These additions Agent can be used alone, it is also possible to which combination of two or more is used, and its consumption is from this The conventional amount used in field, is not particularly limited.
6. the manufacture method of the quenching oil compound of any preceding aspect, described including making Shielding phenol, the step for urging the mixing of cryogen, brightener, antirust agent and the lube base oil Suddenly.
Technique effect
Shielding phenolic compounds of the invention, phosphorus element-containing and metallic element, are not difficult to produce Raw ash content, is environmentally friendly antioxidant.
Shielding phenolic compounds of the invention, the compound phase ratio with prior art shows Go out the high-temperature oxidation resistance (heat endurance) for significantly improving, can effectively improve such as (high temperature) oxidation stability of lubricating oil.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing While excellent high-temperature oxidation resistance, excellent rustless property is also exhibited further. This is not available for prior art compound.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing While excellent high-temperature oxidation resistance, excellent cleansing performance is also exhibited further (i.e. deposit generation rejection).This is not available for prior art compound.
Shielding phenolic compounds of the invention, in a preferred embodiment, is showing While excellent high-temperature oxidation resistance, excellent corrosion resistance is also exhibited further. This is not available for prior art compound.
The quenching oil compound of the present invention shows excellent antioxygenic property, detergent-dispersant performance Energy, corrosion resistance and rustless property, fully meet the requirement of grade quench oil product.
Specific embodiment
The specific embodiment of the present invention is described in detail below, however it is necessary that point out It is that protection scope of the present invention is not limited to these specific embodiments, but by attached Claims of record are determining.
All publications, patent application, patent and other bibliography that this specification is mentioned All draw in this for reference.Unless otherwise defined, all technologies used by this specification and section Technics all has the implication that those skilled in the art routinely understand.In case of conflict, It is defined by the definition of this specification.
When this specification is with prefix " as well known to those skilled in the art ", " prior art " or its class When coming derived materials, material, method, step, device or part etc. like term, the prefix Derived object covers those commonly used in the art when the application is proposed, but also includes mesh It is front to be also of little use, but by become it is art-recognized be suitable for be similar to purpose those.
In the context of the present specification, in addition to the content for clearly stating, do not mention Any matters or item directly be suitable for it is known in the art those and any changing need not be carried out Become.And, any embodiment described herein can be a kind of or many with described herein Plant other embodiment freely to combine, the technical scheme or technological thought for being formed therefrom is regarded For original disclosure of the invention or a part for original description, and it is not considered as herein not The new content for disclosing or being expected, unless those skilled in the art think that the combination is substantially not Reasonably.
In the context of the present invention, state " halogen " and refer to fluorine, chlorine, bromine or iodine.
In the context of the present invention, term " alkyl " has conventionally known in the art Implication, including straight or branched alkyl, straight or branched thiazolinyl, straight or branched alkynyl, Cycloalkyl, cycloalkenyl group, cycloalkynyl radical, aryl or its combination group, wherein it is preferred that straight chain or Alkyl group, straight or branched thiazolinyl, aryl or its combination group.As the alkyl, tool Body can such as enumerate C1-20Alkyl, including C1-20Straight or branched alkyl, C2-20Straight chain Or branched-chain alkenyl, C2-20Straight or branched alkynyl, C3-20Cycloalkyl, C3-20Cycloalkenyl group, C3-20Cycloalkynyl radical, C6-20Aryl or its combination group, wherein it is preferred that C1-20Straight or branched Alkyl, C6-20Aryl or its combination group.As the combination group, such as can be with Enumerate one or more C1-20Straight or branched alkyl (preferably one or more C1-10Directly Chain or branched alkyl) and one or more C6-20Aryl (preferred one or more phenyl Or naphthyl) group that obtained by Direct Bonding.As the combination group, such as One or more C can further be enumerated1-10Straight or branched alkyl phenyl, phenyl C1-10Directly Chain or branched alkyl or one or more C1-10Straight or branched alkyl phenyl C1-10Straight chain is propped up Alkyl group etc., wherein more preferably C1-10Straight or branched alkyl phenyl (such as tert-butyl benzene Base), phenyl C1-10Straight or branched alkyl (such as benzyl) or C1-10Straight chain is propped up Alkyl group phenyl C1-10Straight or branched alkyl (such as t-butylbenzyl).
In the context of the present invention, so-called " straight or branched miscellaneous alkyl ", refers to straight chain Or branched alkyl molecular structure inside is not (including main chain or any side in the alkyl molecule structure The end of chain) one or more (such as 1 to 4,1 to 3,1 to 2 or Person 1) group-CH2- (R' is H or C to be selected from-O- ,-S- and-NR'-1-4Straight chain or Branched alkyl) one of the substituting group group that directly substitutes and obtain or straight chain or Branched alkyl molecular structure inside is not (including main chain or any side chain in the alkyl molecule structure End) one or more (such as 1 to 3,1 to 2 or 1) bases Group-CH<By substituting group-N<The group for directly substituting and obtaining.As the replacement base Group, preferably-O- or-S-, more preferably-S-.It is apparent that from the angle of structural stability For, when having multiple, not Direct Bonding between these substituting groups.In addition, Although the carbon number of the straight or branched alkyl is because group-CH2- or group-CH<Quilt Substitute and accordingly reduce, but in order to state simplicity, still with the replacement as described before straight chain or The carbon number of branched alkyl refers to the carbon number of the straight or branched miscellaneous alkyl.As The straight or branched miscellaneous alkyl, for concrete example, C4Straight chained alkyl is such as(group in formula indicated by arrow is not in molecule Inside configuration, but in the end of main chain) by a substituting group-O- directly substitute by Acquisition-CH2-O-CH2-CH3Or-CH2-CH2-O-CH3, Referred to as C4Linear heteroalkyl group.Or, C4Branched alkyl is such as(group in formula indicated by arrow is not in molecular structure Portion, but in main chain and the end of side chain) by a substituting group-N<Directly substituting will ObtainReferred to as C4Branched heteroalkyl groups.According to the present invention, As the straight or branched miscellaneous alkyl, such as can enumerate C3-20The miscellaneous alkane of straight or branched Base, wherein it is preferred that C3-10Straight or branched miscellaneous alkyl or C3-6Straight or branched miscellaneous alkyl.
In the context of the present specification, expression way " numeral+valency+group " or it is similar Term is referred to from the foundation structure (such as chain, ring or its combination etc.) corresponding to the group It is upper remove the numeral representated by quantity hydrogen atom after obtain group, preferably refer to from On carbon atom (preferred saturated carbon atom and/or non-same carbon atom) contained by the structure The group obtained after the hydrogen atom for removing the quantity representated by the numeral.For example, " 3 Valency straight or branched alkyl " is referred to from straight or branched alkane (i.e. straight or branched alkane Basic chain corresponding to base) on remove 3 hydrogen atoms and the group that obtains, and " divalent is straight Chain or branched heteroalkyl groups " are then referred to from the miscellaneous alkane of straight or branched (preferably from the miscellaneous alkane Contained carbon atom, or further, from non-same carbon atom) on remove 2 hydrogen Atom and the group that obtains.
In the case where not clearly indicating, all percentages for being previously mentioned in this specification, Number, ratio etc. are all on the basis of weight, unless do not met this when on the basis of weight The conventional understanding of art personnel.
In the context of the present specification, in case of no particular description, the equal molecule of number Amount Mn is determined by gel permeation chromatography (GPC).
In the context of the present specification, in case of no particular description, it is any to be related to Gel permeation chromatography (GPC) or the condition determination of GPC spectrograms be：Instrument：The U.S. Waters companies waters2695 type gel osmoticing chromatogram analysis instrument；Mobile phase adopts tetrahydrochysene furan Mutter, flow velocity is 1mL/min, chromatogram column temperature is 35 DEG C, delivery time 40min, sample Mass fraction is 0.16%-0.20%.
According to the present invention, the shielding phenolic compounds being related to shown in a kind of logical formula (I).
According to the present invention, in logical formula (I), when having multiple, each group R is each other It is identical or different, it is each independently selected from hydrogen, C1-300Straight or branched alkyl, logical formula (II) Group shown in shown group and logical formula (III), on condition that at least one group R is Group shown in logical formula (II).
According to the present invention, in logical formula (I), as the C1-300Straight or branched alkyl, C can such as be enumerated1-20Straight or branched alkyl (preferred C1-10Straight or branched alkyl, More preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As described polyolefin-based, It is concrete such as to enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000.Now, As polyolefin-based number-average molecular weight Mn, preferred 500-2000, more preferably 500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is presented For chain alkyl structure), but depending on the polyolefinic species as initiation material or this is poly- It is likely to containing a small amount of alkene in the difference of alkene manufacture method, the polyolefin-based strand Category double bond (is remained such as in polyolefin manufacturing process or introduced), but this has no effect on The realization of effect of the present invention, the present invention also has no intention to carry out clearly the amount, and the present invention Still polyolefin-based classify as this " alkyl ".
, in logical formula (I), there are multiple group R in an embodiment of the invention, One of group R is to lead to the group shown in formula (II), in two other group R It is individual be it is described polyolefin-based, another is hydrogen, C1-20Straight or branched alkyl (preferred C1-10 Straight or branched alkyl) or logical formula (III) shown in group.
An embodiment of the invention, in logical formula (I), when group R is institute When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (I).
According to the present invention, in logical formula (I), when having multiple, each group R' is each other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (I), when having multiple, Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane Base.
According to the present invention, in logical formula (II), group L is
According to the present invention, in logical formula (II), in the definition of group L, group R " Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (II), in determining for group L In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous Alkyl.
According to the present invention, in logical formula (II), group R2Selected from hydrogen, C1-20Straight chain is propped up Group and the group shown in logical formula (V) shown in alkyl group, logical formula (IV).
An embodiment of the invention, in logical formula (II), group R2Selected from hydrogen, C1-10Group shown in straight or branched alkyl and logical formula (IV).
According to the present invention, in logical formula (II), when having multiple, each group RbEach other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl, it is preferably each From independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (II), when having multiple, Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched Alkyl, preferred hydrogen.
According to the present invention, in logical formula (II), when having multiple, each group RcEach other It is identical or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly Chain or branched alkyl epoxide.
An embodiment of the invention, in logical formula (II), when having multiple, Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (II), preferably one group RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding) Contraposition.
According to the present invention, in logical formula (II), y is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in logical formula (II), z is 0 to 3 integer, preferably 0 or 1.
According to the present invention, in logical formula (II), n is 1 to 8 integer, preferably 1 or 2。
According to the present invention, in logical formula (II), when having multiple, each group RdEach other It is identical or different, it is each independently selected from hydrogen and the group shown in logical formula (V), preferred hydrogen.
According to the present invention, in logical formula (II), when having multiple, each cyclic group (being rendered as divalent group in the inside configuration of logical formula (II)) is same to each other or different to each other, respectively From independently selected from phenyl ring, (inside configuration preferably in logical formula (II) is rendered as 1,4- Asias benzene Base) and naphthalene nucleus (inside configuration preferably in logical formula (II) is rendered as 1,4- or 2,6- Asias naphthalene Base), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (II), two adjacent rings GroupCan pass through each other additional S atom (not showing in structural formula) and The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (II), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should Phenthazine ring.
An embodiment of the invention, in logical formula (II), two adjacent rings GroupAdditional group can be passed through each other(in structural formula not Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R " Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (II), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups GroupIn each with another adjacent cyclic groupFormed The acridan ring.
According to the present invention, in logical formula (III), group L is
According to the present invention, in logical formula (III), in the definition of group L, group R " Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (III), in determining for group L In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous Alkyl.
According to the present invention, in logical formula (III), group R2Selected from hydrogen, C1-20Straight chain or Group and the group shown in logical formula (V) shown in branched alkyl, logical formula (IV).
An embodiment of the invention, in logical formula (III), group R2It is selected from Hydrogen, C1-10Group shown in straight or branched alkyl and logical formula (IV).
According to the present invention, in logical formula (III), when having multiple, each group RbThat This is identical or different, is each independently selected from hydrogen and C1-20Straight or branched alkyl, preferably It is each independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (III), when having multiple, Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched Alkyl, preferred hydrogen.
According to the present invention, in logical formula (III), when having multiple, each group RcThat This is identical or different, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20 Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (III), when having multiple, Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (III), preferably one group RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding) Contraposition.
According to the present invention, in logical formula (III), y is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in logical formula (III), z is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in logical formula (III), n is 1 to 8 integer, preferably 1 or 2。
According to the present invention, in logical formula (III), when having multiple, each group RdThat This is identical or different, is each independently selected from hydrogen and the group shown in logical formula (V), preferably Hydrogen.
According to the present invention, in logical formula (III), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of logical formula (III)) is mutually the same Or it is different, (inside configuration preferably in logical formula (III) is presented to be each independently selected from phenyl ring For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in logical formula (III) is rendered as 1,4- Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (III), two adjacent rings GroupCan pass through each other additional S atom (not showing in structural formula) and The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (III), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should Phenthazine ring.
An embodiment of the invention, in logical formula (III), two adjacent rings GroupAdditional group can be passed through each other(in structural formula not Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R " Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (III), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups GroupIn each with another adjacent cyclic groupFormed The acridan ring.
According to the present invention, in logical formula (IV), when having multiple, each group RbThat This is identical or different, is each independently selected from hydrogen and C1-20Straight or branched alkyl, preferably It is each independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in logical formula (IV), when having multiple, Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched Alkyl, preferred hydrogen.
According to the present invention, in logical formula (IV), when having multiple, each group RcThat This is identical or different, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20 Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (IV), when having multiple, Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in logical formula (IV), preferably one group RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding) Contraposition.
According to the present invention, in logical formula (IV), y is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in logical formula (IV), z is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in logical formula (IV), n' is 0 to 7 integer, preferably 0,1 Or 2, on condition that n'+n≤8.An embodiment of the invention, n'+n=1 or n'+n=2. Here, n is identical with the definition in aforementioned formula (II).
According to the present invention, in logical formula (IV), when having multiple, each group RdThat This is identical or different, is each independently selected from hydrogen and the group shown in logical formula (V), preferably Hydrogen.
According to the present invention, in logical formula (IV), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of logical formula (IV)) is mutually the same Or it is different, (inside configuration preferably in logical formula (IV) is presented to be each independently selected from phenyl ring For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in logical formula (II) is rendered as 1,4- Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
An embodiment of the invention, in logical formula (IV), two adjacent rings GroupCan pass through each other additional S atom (not showing in structural formula) and The N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) and form fen Thiazine ring, i.e.,
The embodiment of the invention, in logical formula (IV), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm the phenthazine ring, it is not necessary that require these cyclic groupsIn each with another adjacent cyclic groupBeing formed should Phenthazine ring.
An embodiment of the invention, in logical formula (IV), two adjacent rings GroupAdditional group can be passed through each other(in structural formula not Show) and the N atoms of the two rings are bridged (that is, with group RdThe N atoms of bonding) And form 9,10- acridan rings, i.e.,
According to the present invention, in groupIn, group R " it is selected from hydrogen, C1-20Hydrocarbon Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in groupIn, group R " Selected from hydrogen and C1-10Straight or branched alkyl.
The embodiment of the invention, in logical formula (IV), exist two with On cyclic groupWhen, as long as wherein at least two (adjacent) cyclic groupForm 9, the 10- acridans ring, it is not necessary that require these ring groups GroupIn each with another adjacent cyclic groupFormed The acridan ring.
According to the present invention, in logical formula (V), when having multiple, each group R is each other It is identical or different, it is each independently selected from hydrogen, C1-300Straight or branched alkyl, logical formula (II) Group shown in shown group and logical formula (III).
An embodiment of the invention, in logical formula (V), when having multiple, Each group R is same to each other or different to each other, and is each independently selected from hydrogen and C1-300Straight or branched Alkyl.
According to the present invention, in logical formula (V), as the C1-300Straight or branched alkane Base, such as can enumerate C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkane Base, more preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As the polyolefin Base, specifically can such as enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000. Now, as polyolefin-based number-average molecular weight Mn, preferred 500-2000 is more excellent Select 500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is in It is now chain alkyl structure), but depending on the polyolefinic species as initiation material or be somebody's turn to do It is likely to containing a small amount of in the difference of polyolefin production process, the polyolefin-based strand Olefinic double bond (such as in polyolefin manufacturing process remain or introduce), but this not shadow The realization of sound effect of the present invention, the present invention also has no intention to carry out clearly the amount, and this It is bright still polyolefin-based to classify as this " alkyl ".
, in logical formula (V), there are multiple groups in an embodiment of the invention R, one of group R are described polyolefin-based, and another is hydrogen or C1-20Straight chain or Branched alkyl (preferred C1-10Straight or branched alkyl, more preferably C1-4Straight or branched alkane Base).
An embodiment of the invention, in logical formula (V), when group R is institute When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (V).
According to the present invention, in logical formula (V), when having multiple, each group R' is each other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (V), when having multiple, Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane Base.
According to the present invention, in logical formula (V), group L is group
According to the present invention, in logical formula (V), in the definition of group L, group R " Selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) and C3-20Straight chain is propped up Chain miscellaneous alkyl.
An embodiment of the invention, in logical formula (V), in determining for group L In justice, group R " it is selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched is miscellaneous Alkyl.
According to one preferred embodiment of the invention, in logical formula (V), in group L Definition in, group R " selected from hydrogen and C1-10Straight or branched alkyl.
According to the present invention, in logical formula (V), two group R and group-(S)a-L- Three positions of residue in logical formula (V) on phenyl ring are occupied respectively.
According to the present invention, in logical formula (V), a is 0 or 1, preferably 1.
According to the present invention, the shielding phenolic compounds is defined as previously mentioned (such as such as logical formula (I) Or further as shown in logical formula (V)), it is necessary to comprising structureAs phenol unit. According to one preferred embodiment of the invention, the shielding phenolic compounds is in its whole molecule At most 5, at most 3, at most 2 or the at most 1 phenol list are included in structure Unit.
According to the present invention, the shielding phenolic compounds is defined as previously mentioned (such as such as logical formula (II) Or further as shown in logical formula (III) or (IV)), it is necessary to comprising structureAs amine unit.According to one preferred embodiment of the invention, It is described shielding phenolic compounds in its whole molecular structure comprising at most 15, at most 10, At most 8, at most 6, at most 4, at most 3 or the at most 2 amine lists Unit.
According to the present invention, the shielding phenolic compounds in its whole molecular structure preferably at least There is (preferably 2,3 or 4 or a more) group RdIt is hydrogen.It is concrete and Speech, the shielding phenolic compounds is preferably in its whole molecular structure containing selected from following hydrogen amine At least one of unit (1), hydrogen amine unit (2) and hydrogen amine unit (3).At these In hydrogen amine unit, cyclic groupWith group R " with logical formula (II) in definition phase Together.
A preferred embodiment of the invention, the shielding phenolic compounds is whole at its Contain hydrogen amine unit (1) described at least one in molecular structure.
Specifically, shielding phenolic compoundsAs a example by, the compound Comprising 2 phenol units and 2 amine units in its whole molecular structure, and wrap Containing 1 hydrogen amine unit (1).
According to the present invention, as the shielding phenolic compounds, such as can enumerate following The mixture of compound or its arbitrary proportion, but the present invention is not limited to this.
According to the present invention, the shielding phenolic compounds shown in aforementioned formula (I) can be with single In the form of a kind of (pure) compound, manufacture or use, it is also possible to two of which or In the form of various mixtures (in any proportion), manufacture or use, this not shadow The realization of sound effect of the present invention.
According to the present invention, the shielding phenolic compounds shown in aforementioned formula (I) can by with Under manufacture method manufactured, but be not limited to this sometimes.
The manufacture method of the invention, closes including the phenolate shown in logical formula (X) is made Amines depositing in the aldehyde compound shown in formula (Z) shown in thing and formula (Y) The first step reacted under.
According to the present invention, in leading to formula (X), when having multiple, each group R0It is mutually the same or Difference, is each independently selected from hydrogen ,-SH and C1-300Straight or branched alkyl, on condition that At least one group R0It is-SH.
According to the present invention, in logical formula (X), as the C1-300Straight or branched alkane Base, such as can enumerate C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkane Base, more preferably C1-4Straight or branched alkyl) or it is polyolefin-based.As the polyolefin Base, specifically can such as enumerate number-average molecular weight Mn for the polyolefin-based of 300-3000. Now, as polyolefin-based number-average molecular weight Mn, preferred 500-2000 is more excellent Select 500-1500.According to the present invention, polyolefin-based (substantially) is that saturation (is in It is now chain alkyl structure), but depending on the polyolefinic species as initiation material or be somebody's turn to do It is likely to containing a small amount of in the difference of polyolefin production process, the polyolefin-based strand Olefinic double bond (such as in polyolefin manufacturing process remain or introduce), but this not shadow The realization of sound effect of the present invention, the present invention also has no intention to carry out clearly the amount, and this It is bright still polyolefin-based to classify as this " alkyl ".
, in logical formula (X), there are multiple groups in an embodiment of the invention R0, one of group R0It is-SH, two other group R0In one be described poly- Alkylene, another is hydrogen or C1-20Straight or branched alkyl (preferred C1-10Straight chain is propped up Alkyl group).
An embodiment of the invention, in logical formula (X), in group R0It is institute When stating polyolefin-based, the polyolefin-based contraposition for being preferably placed at phenolic hydroxyl group in logical formula (X).
According to the present invention, in logical formula (X), when having multiple, each group R' is each other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl.
An embodiment of the invention, in logical formula (X), when having multiple, Each group R' is same to each other or different to each other, and is each independently selected from hydrogen and C1-4Straight or branched alkane Base.
According to the present invention, as the phenolic compounds shown in the logical formula (X), can be direct Using commercially available product, it is also possible to manufactured by conventionally known in the art method, and Have no particular limits.In addition, as the phenolic compounds shown in the logical formula (X), can With only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, as the manufacture method of the phenolic compounds shown in the logical formula (X), Such as can enumerate in the presence of catalyst for alkylation reaction, make the phenol shown in formula (X') (number-average molecular weight Mn is 300-3000, preferred 500-2000, more for compound and polyolefin It is preferred that 500-1500) occur alkylated reaction method.
According to the present invention, in formula (X'), group R' has and aforementioned formula (X) Middle identical implication.
According to three group R' of presence in the present invention, formula (X')0, one of group R'0It is-SH, another group R'0It is H, the 3rd group R'0Be hydrogen ,-SH or C1-20Straight or branched alkyl (preferred C1-10Straight or branched alkyl).
An embodiment of the invention, in formula (X'), at least one group R'0It is H, and group R'0The contraposition of phenolic hydroxyl group in formula (X').
According to the present invention, the polyolefin preferably passes through ethene, propylene or C4-C10Alpha-olefin Homopolymerization or by polyolefin obtained from two or more copolymerization in these alkene.Make For the C4-C10Alpha-olefin, such as can enumerate n-butene, isobutene, n-pentene, just Hexene, positive octene and positive decene.
According to the present invention, at least 20wt% in these polyolefin (preferably at least 50wt%, More preferably at least 70wt%) polymer chain contain olefinic double bond in its end.The olefinic is double Key is usually in the form of the ethenylidene or vinyl of high reaction activity.
According to the present invention, as the polyolefin, more preferably polybutene.Unless otherwise stated, Term as used herein " polybutene " is broadly included by 1- butylene or isobutylene homopolymerisation The polymer for obtaining, and led to by two or three in 1- butylene, 2- butylene and isobutene Cross copolymerization and obtained polymer.The commercially available prod of such polymer is likely to containing negligible Other olefinic components of amount, but this has no effect on the enforcement of the present invention.
According to the present invention, as the polyolefin, further preferred polyisobutene (PIB), Also referred to as high-activity polyisobutylene.In this kind of polyisobutene, at least 20wt% is (excellent Choosing at least 50wt%, more preferably at least 70wt%) total terminal ethylenic double bond be by methyl What ethenylidene was provided.
As the catalyst for alkylation reaction, such as Lewis acid catalysts can be enumerated, Such as it is selected from alchlor, boron trifluoride, butter of tin, titanium tetrabromide, boron trifluoride benzene One or more in phenol, boron trifluoride alcohol complex and boron trifluoride ether complex, its In preferably boron trifluoride etherate and/or boron trifluoride methanol complex compound.These alkyl Changing catalysts can directly use commercially available product.
According to the present invention, in the alkylated reaction, the polyolefin, the formula (X') Mol ratio between shown phenolic compounds, the catalyst for alkylation reaction such as can be 1：1-3：0.1-0.5, preferably 1：1.5-3：0.1-0.4, most preferably 1：1.5-3：0.2-0.4, But this is not limited to sometimes.
According to the present invention, the reaction time of the alkylated reaction is such as 0.5h-10h, excellent 1h-8h, most preferably 3h-5h are selected, but is not limited to this sometimes.
According to the present invention, the reaction temperature of the alkylated reaction is such as 0 DEG C -200 DEG C, It is preferred that 10 DEG C -150 DEG C, most preferably 20 DEG C -100 DEG C, but this is not limited to sometimes.
According to the present invention, the alkylated reaction can be carried out in the presence of the solvent.As The solvent, such as can enumerate C6-10Alkane (such as hexane, heptane, octane, nonyl Alkane or decane etc.).Wherein, hexane and heptane are preferably used, more preferably using hexane.
According to the present invention, after the alkylated reaction terminates, by conventional methods from final Catalyst for alkylation reaction, unreacted reactant and can are removed in the reactant mixture of acquisition After the solvent that can be used, that is, obtain the phenolic compounds shown in the logical formula (X).
According to the present invention, in formula (Y), group R'2Selected from hydrogen, C1-20Straight chain or Branched alkyl and group
According to the present invention, in formula (Y), when having multiple, each group RbEach other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl, it is preferably each From independently selected from hydrogen and C1-10Straight or branched alkyl.
An embodiment of the invention, in formula (Y), when having multiple, Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-6Straight or branched Alkyl, preferred hydrogen.
According to the present invention, in formula (Y), when having multiple, each group RcEach other It is identical or different, it is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly Chain or branched alkyl epoxide.
An embodiment of the invention, in formula (Y), when having multiple, Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-10Straight or branched Alkyl and C1-10Straight or branched alkyl epoxide.
An embodiment of the invention, in formula (Y), preferably one group RcIn cyclic groupUpper N atoms are (that is, with group RdThe N atoms of bonding) Contraposition.
According to the present invention, in formula (Y), y is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in formula (Y), z is 0 to 3 integer, preferably 0 or 1。
According to the present invention, in formula (Y), n1 is 1 to 8 integer, preferably 1 or 2。
According to the present invention, in formula (Y), when having multiple, each cyclic group(being rendered as divalent group in the inside configuration of formula (Y)) is mutually the same Or it is different, (inside configuration preferably in formula (Y) is presented to be each independently selected from phenyl ring For 1,4- phenylenes) and naphthalene nucleus (inside configuration preferably in formula (Y) is rendered as 1,4- Or 2,6- naphthylene), wherein it is preferred that phenyl ring.
According to the present invention, as the amines shown in the formula (Y), can be direct Using commercially available product, it is not particularly limited.In addition, as the formula (Y) Shown amines, can only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in formula (Z), group R " it is selected from hydrogen, C1-20Alkyl is (excellent Select C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl.
An embodiment of the invention, in formula (Z), group R " selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl.
According to one preferred embodiment of the invention, in formula (Z), group R " Selected from hydrogen and C1-10Straight or branched alkyl.
According to the present invention, as the aldehyde compound shown in the formula (Z), such as can be with Enumerate C1-6Aliphatic aldehyde and benzaldehyde.
An embodiment of the invention, as the C1-6Aliphatic aldehyde, such as may be used To enumerate C1-6Straight or branched saturated aliphatic aldehyde, specifically such as acetaldehyde or formaldehyde, more preferably Formaldehyde.As the formaldehyde, such as can use its aqueous solution, paraformaldehyde or oligomeric first Aldehyde form, is not particularly limited.
According to the present invention, as the aldehyde compound shown in the formula (Z), can only make With one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first In step, the phenolic compounds shown in the logical formula (X) with shown in the formula (Y) The mol ratio of amines is generally 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first In step, the phenolic compounds shown in the logical formula (X) with shown in the formula (Z) The mol ratio of aldehyde compound is generally 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the first step Suddenly can carry out in the presence of the solvent.As the solvent, such as can enumerate C2-10 Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon (such as benzene,toluene,xylene and Isopropylbenzene), C6-10Alkane (such as n-hexane, hexamethylene and petroleum ether), C1-6Aliphatic Alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropanol, n-butanol and ethylene glycol), C2-20 Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride, chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone (such as acetone, butanone and methyl iso-butyl ketone (MIBK)) or C3-10Acid amides (such as dimethyl Formamide, dimethyl acetamide and 1-METHYLPYRROLIDONE) etc..These solvents can be only Using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first In step, catalyst can be added without, it is also possible to add catalyst.As the catalyst, Inorganic acid catalyst and organic acid catalyst can such as be enumerated.As the inorganic acid catalysis Agent, such as can enumerate hydrochloric acid, sulfuric acid and phosphoric acid etc..As the organic acid catalyst, Pyrovinic acid, ethylsulfonic acid, sulfamic acid and p-methyl benzenesulfonic acid etc. can such as be enumerated.
As the consumption of the catalyst, can directly with reference to the conventional amount used of prior art, It is not particularly limited.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described first The reaction time of step, there is no particular limitation, but generally 0.1h-24h, preferred 0.2h-12h, Most preferably 0.5h-6h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described first There is no particular limitation for the reaction temperature of step, but generally 0 DEG C -250 DEG C, preferably 20 DEG C -180 DEG C, most preferably 60 DEG C -120 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described first After step terminates, by conventionally known separation method (such as evaporation etc.) from this first Remove in the reactant mixture (the hereinafter referred to as reactant mixture of first step) that step is obtained After the volatile materials such as solvent that may be present, you can obtain the product of first step.
An embodiment of the invention, the manufacture method of the shielding phenolic compounds is appointed Choosing also includes making the product of the first step and vulcanizing agent reaction (forming phenthazine ring) Additional step (hereinafter referred to as additional step A).
An embodiment of the invention, the manufacture method of the shielding phenolic compounds is appointed Choosing also includes making the product of the first step and the hydroformylation shown in aforementioned formula (Z) Additional step (the hereinafter referred to as extra step of compound reaction (formed acridan ring) Rapid B).
According to the present invention, in the manufacture method of the shielding phenolic compounds, can only carry out The additional step A, it is also possible to only carry out the additional step B, it is also possible to both carried out institute State additional step A carries out the additional step B again.Both the additional step A is being carried out When carrying out the additional step B again, to the additional step A and additional step B Precedence there is no particular limitation, can first carry out the additional step A, it is attached at this Plus step A terminates to carry out the additional step B again afterwards, or first carry out the extra step Rapid B, after additional step B terminates the additional step A is carried out again.In addition, each There can be product (that is, from the product of previous additional step) point between additional step From step, it is also possible to there is no product separating step, be not particularly limited.
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds In, the additional step A is carried out after the first step terminates.Now, it is described The product of first step is as previously mentioned from the reactant mixture of the first step In separate.Or, the product of the first step can also without the separation, And be directly used to carry out the extra step in the form of the reactant mixture of the first step Rapid A.Or, the additional step A can also be after the additional step B terminates Carry out.When the additional step A after the additional step B terminates when carrying out, institute The product for stating additional step B is as described herein from the anti-of the additional step B Answer in mixture and separate.Or, the product of the additional step B can also Without the separation, and directly used in the form of the reactant mixture of the additional step B In carrying out the additional step A.
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds In, in the additional step A, as the vulcanizing agent, such as can enumerate sulphur and Sulfur dichloride etc., wherein it is preferred that sulphur.As the sulphur, such as can enumerate sulphur or distillation Sulphur.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional In step A, the mol ratio of the amines shown in the formula (Y) and the vulcanizing agent Generally 1:1-10, preferably 1:1.2-6.0, more preferably 1:1.5-3.0.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step Rapid A can be carried out in the presence of the solvent.As the solvent, such as can enumerate C2-10 Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon (such as benzene,toluene,xylene and Isopropylbenzene), C6-10Alkane (such as n-hexane, hexamethylene and petroleum ether), C1-6Aliphatic Alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropanol, n-butanol and ethylene glycol), C2-20 Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride, chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone (such as acetone, butanone and methyl iso-butyl ketone (MIBK)) or C3-10Acid amides (such as dimethyl Formamide, dimethyl acetamide and 1-METHYLPYRROLIDONE) etc..These solvents can be only Using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step Rapid A is typically carried out in the presence of a catalyst.As the catalyst, such as can lift The have technology conventional catalyst for adopting for this purpose, specifically such as iodine.As described The consumption of catalyst, can directly with reference to prior art conventional amount used, not particularly Limit.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional The reaction time of step A, there is no particular limitation, but generally 0.1h-24h, preferably 0.2h-12h, most preferably 0.5h-4h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional There is no particular limitation for the reaction temperature of step A, but generally 60 DEG C -300 DEG C, preferably 120 DEG C -240 DEG C, most preferably 150 DEG C -200 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional After step A terminates, by conventionally known separation method (such as evaporation etc.) from this The volatility thing such as solvent that may be present is removed in the reactant mixture that additional step A is obtained After matter, you can obtain the product of additional step A, or can also be without this Separate, be directly used in follow-up reactions steps (than additional step B as the aforementioned).
An embodiment of the invention, in the manufacture method of the shielding phenolic compounds In, the additional step B can be carried out (as list after the first step terminates Only step), it is also possible to carry out simultaneously with the first step, be not particularly limited. When the additional step B after the first step terminates when carrying out, the first step The separation from the reactant mixture of the first step as previously mentioned of rapid product Out.Or, the product of the first step can also be and straight without the separation To connect be used in the form of the reactant mixture of the first step and carry out the additional step B. Or, the additional step B can also be carried out after the additional step A terminates. It is described additional when the additional step B after the additional step A terminates when carrying out The reaction from the additional step A as described herein of the product of step A mixes Separate in thing.Or, the product of the additional step A can also be without The separation, and be directly used to carry out in the form of the reactant mixture of the additional step A The additional step B.In addition, when simultaneously the additional step B enters with the first step During row, directly in the reaction system of the first step (such as in the first step Start or during the first step is carried out) add institute according to hereinafter provided consumption State the aldehyde compound shown in formula (Z).
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional In step B, as the aldehyde compound shown in the formula (Z), such as can enumerate C1-6Aliphatic aldehyde and benzaldehyde.As the C1-6Aliphatic aldehyde, such as can enumerate C1-6 Straight or branched saturated aliphatic aldehyde, specifically such as acetaldehyde or formaldehyde, more preferably formaldehyde.As The formaldehyde, such as can use its aqueous solution, paraformaldehyde or paraformaldehyde form, and There is no particular limitation.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional In step B, the amines shown in the formula (Y) with the formula (Z) Suo Shi The mol ratio of aldehyde compound be generally 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0。
According to the present invention, in the manufacture method of the shielding phenolic compounds, the extra step Rapid B (when carrying out as independent step) can be carried out in the presence of the solvent.As institute Solvent is stated, such as can enumerate C2-10Aliphatic nitrile (such as acetonitrile etc.), C6-20Aromatic hydrocarbon (such as benzene,toluene,xylene and isopropylbenzene), C6-10Alkane (such as n-hexane, ring Hexane and petroleum ether), C1-6Aliphatic alcohol (such as methyl alcohol, ethanol, normal propyl alcohol, isopropyl Alcohol, n-butanol and ethylene glycol), C2-20Halogenated hydrocarbons (such as dichloromethane, carbon tetrachloride, Chlorobenzene and 1,2- dichloro-benzenes), C3-10Ketone (such as acetone, butanone and methyl iso-butyl ketone (MIBK)) Or C3-10Acid amides (such as dimethylformamide, dimethyl acetamide and N- methylpyrroles Alkanone) etc..These solvents can only using one kind, it is also possible to which combination of two or more is used.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional In step B (when carrying out as independent step), catalyst can be added without, it is also possible to Add catalyst.As the catalyst, such as can enumerate inorganic acid catalyst and organic Acid catalyst.As the inorganic acid catalyst, such as can enumerate hydrochloric acid, sulfuric acid and phosphorus Acid etc..As the organic acid catalyst, such as can enumerate pyrovinic acid, ethylsulfonic acid, Sulfamic acid and p-methyl benzenesulfonic acid etc..As the consumption of the catalyst, can directly reference The conventional amount used of prior art, is not particularly limited.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional The reaction time of step B (when carrying out as independent step), there is no particular limitation, but Generally 0.1h-24h, most preferably preferred 0.2h-12h, 0.5h-6h.
According to the present invention, in the manufacture method of the shielding phenolic compounds, to described additional There is no particular limitation for the reaction temperature of step B (when carrying out as independent step), but Generally 0 DEG C -250 DEG C, preferably 20 DEG C -180 DEG C, most preferably 60 DEG C -120 DEG C.
According to the present invention, in the manufacture method of the shielding phenolic compounds, described additional After step B (when carrying out as independent step) terminates, by conventionally known separation Removing in the reactant mixture that method (such as evaporation etc.) is obtained from additional step B can After the volatile materials such as the solvent that can exist, you can the reaction for obtaining additional step B is produced Thing, or follow-up reactions steps can also be directly used in (before such as without the separation The additional step A for stating).
It is known in the art, aforementioned all of reactions steps (including the first step, The additional step A and additional step B) it is general under the protection of inert gas atmosphere Carry out.As the inert gas, such as nitrogen and argon gas etc. can be enumerated, it is not special Other restriction.
According to the present invention, in the manufacture method of the shielding phenolic compounds, as described the The product of one step, the product of the additional step A or the additional step The product of B, can be a kind of single shielding phenolic compounds (such as aforementioned formula (I) Shown shielding phenolic compounds), or the mixture comprising various shielding phenolic compounds. These product are all that desired by the present invention, the difference of its existence form has no effect on this The realization of invention effect.Therefore, in this specification context these are reacted without distinction Product is collectively termed as the shielding phenolic compounds of the present invention.In consideration of it, according to the present invention, not Presence is further purified these product, or further separates from these product The absolute necessity for going out the shielding phenolic compounds of a certain ad hoc structure.Certainly, the purifying or point It is preferred from being sometimes for the further lifting of Expected Results of the present invention, but Yu Benfa For bright not necessarily.Even so, as the purifying or separation method, such as can be with Enumerate the product is purified by methods such as column chromatography method or preparative chromatographies Or separate etc..
An embodiment of the invention, further relates to according to aforesaid shielding phenol of the invention The shielding phenolic compounds of the manufacture method manufacture of compound.
The present invention's shields phenolic compounds due to showing excellent high-temperature oxidation resistance, because This is particularly suitable as antioxidant and uses, and is used for manufacture especially as antioxidant and expects excellent (high temperature) oxidation stability lubricant oil composite.In consideration of it, of the invention one Individual embodiment, is related to a kind of quenching oil compound, and it includes the aforesaid any screen of the present invention Cover phenolic compounds (or mixture of its arbitrary proportion), urge cryogen, brightener, antirust agent And lube base oil.
Embodiment
Hereinafter the present invention is illustrated in further detail using embodiment, but the present invention is not limited to These embodiments.
Performance in embodiment and comparative example is evaluated as follows.
(1) high-temperature oxidation resistance evaluation
The lubricant oil composite that embodiment or comparative example are manufactured is adopted and added as test specimen Pressure differential scanning calorimetry (PDSC) evaluates the antioxygenic property of the test specimen, to try The oxidation induction period (unit is min) for testing sample is represented.The temperature of PDSC tests is 210 DEG C, Pressure is 0.5MPa, and oxygen gas flow rate is 100mL/min.
(2) deposit generates rejection evaluation
The lubricant oil composite that embodiment or comparative example are manufactured is carried out into mould as test specimen Intend the engine crankcase coking simulated test of piston deposit.The method is by 300ml Test specimen adds coking plate analog meter, 150 DEG C is heated to, using continuation mode to temperature For 310 DEG C of aluminium sheet spilled oil, the burnt amount generated on aluminium sheet is weighed after 6 hours, to deposit Thing amount (unit is mg) expression, simulates the deposit on piston.Coking amount is higher, generation The piston detergency of table this test specimen is poorer.
(3) copper corrosion assessment of performance is suppressed
With reference to ASTM D130 standard methods, the lubricating oil that embodiment or comparative example are manufactured Composition carries out copper strip test as test specimen.The copper sheet for having polished is immersed in into examination In sample, 121 DEG C of test temperature is heated to, is kept for 3 hours, end to be tested, take out copper Piece, it is scrubbed to be compared with Corrosion standards colour table afterwards, determine corrosion level.
(4) rustless property evaluation
According to the standard methods of GB/T 11143, the lubricating oil that embodiment or comparative example are manufactured Composition carries out antiseptic property test as test specimen.By 300mL samples and 30mL Distilled water mixes, and test rod iron is totally immersed into wherein, stirs 24 hours at 60 DEG C, The vestige of viewing test rod iron corrosion and the degree of corrosion after off-test.
Embodiment 1
In the 500ml four-hole boiling flasks equipped with agitator, thermometer, condenser pipe and dropping funel In, add 58.79g (0.323mol) the 2- tert-butyl group -6- mercapto-phenols, 6.88g (0.048mol) BFEE (catalyst for alkylation reaction), 100ml n-hexanes solvent and (Mn=1000, Jilin Chemical group fine chemicals has the polyisobutene of 161.61g (0.162mol) Limit company manufactures), react 2h at 80 DEG C.After reaction terminates, use quality fraction is 5% Potassium hydroxide solution cleaning reactant mixture once, and with hot water be washed to neutrality to remove Catalyst, then vacuum distillation removes solvent and unreacted phenol, obtains polyisobutene sulfydryl Phenol, hydroxyl value is 53.49mgKOH/g.Hydroxy value measuring is with reference in GB/T7383-2007 Acetic anhydride method.
Example reaction equation is as follows：
From the nucleus magnetic hydrogen spectrum spectrum analysis of polyisobutene mercapto-phenol product：Chemical shift It is the characteristic peak of tert-butyl group hydrogen on polyisobutene mercapto-phenol phenyl ring at 1.40；Chemical shift The unimodal characteristic peak for sulfydryl hydrogen on polyisobutene mercapto-phenol phenyl ring at 3.58；Chemical shift The unimodal characteristic peak for hydroxyl hydrogen on polyisobutene mercapto-phenol phenyl ring at 4.84；Chemical shift At 7.12 it is unimodal and 7.20 at it is unimodal be respectively polyisobutene mercapto-phenol phenyl ring on two hydrogen Characteristic peak.It is 1 by the Definitions On Integration of hydroxyl hydrogen on phenyl ring, obtains hydrogen on phenyl ring, sulfydryl The integration of hydrogen and hydroxyl hydrogen compares for 0.95:0.97:1.05:0.94, it is close to theoretical 1:1:1:1:1, From nuclear magnetic spectrogram analysis, the polyisobutene mercapto-phenol alkyl that expected contraposition replaces is synthesized Change product.
Embodiment 2
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 30.58 grams of (156mmol) 2- sulfydryl -4- methyl -6- Methylphenol, 9.29 grams of (112mmol) formaldehyde, 32.38 grams of (176mmol) N- benzene Base p-phenylenediamine and 100mL toluene, rapid stirring, at 100 DEG C 2h is reacted.Question response After end, vacuum distillation removes solvent and a small amount of water for generating, and is obtained by column chromatography for separation To the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.40 (9H), 2.37 (3H), 4.02 (1H), 4.83 (2H), 6.95-7.00 (12H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 21.2,30.1,34.1,49.9,114.3, 118.9,119.4,121.8,122.2,125.8,126.5,129.5,131.8,132.3, 133.5,143.3,150.8；
C24H28N2OS calculated values C 73.43, H 7.19, N 7.14, O 4.08, S 8.17； Measured value：C 73.31, H 7.23, N 7.21, O 3.99, S 8.28.
Embodiment 3
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 31.65 grams of (133mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 1.86 grams of (62mmol) formaldehyde, 28.15 grams of (153mmol) N- phenyl P-phenylenediamine, 0.75 gram of (7.5mmol) hydrochloric acid and 150mL isopropanols, rapid stirring, 24h is reacted at 25 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36-1.54 (18H), 3.75 (1H), 4.80 (2H), 5.32 (1H), 6.80 (2H), 6.97 (5H), 7.17 (2H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,51.2,119.4,121.8, 126.5,129.5,131.4,136.6,144.5,153.4；
C27H34N2OS calculated values C 74.61, H 7.88, N 6.45, O 3.68, S 7.38； Measured value：C 74.52, H 7.84, N 6.51, O 3.73, S 7.40.
Embodiment 4
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 8.57 grams of (36mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 1.24 grams of (15mmol) formaldehyde, 10.14 grams of (39mmol) N, N'- bis- Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring, at 90 DEG C 4h is reacted.Treat anti- After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 5.23 (2H), 6.80-7.02 (10H), 7.17 (2H), 7.26 (4H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,55.2,117.1,121.8, 126.2,129.5,136.6,143.6,153.4；
C33H38N2OS calculated values C 77.60, H 7.50, N 5.48, O 3.13, S 6.28； Measured value：C 77.71, H 7.52, N 5.53, O 3.10, S 6.23.
Embodiment 5
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 20.23 grams of (85mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 9.54 grams of (115mmol) formaldehyde, 18.49 grams of (69mmol) N- (1,3- Dimethylbutyl)-N'- diphenyl-para-phenylene diamines and 150mL benzene, rapid stirring is anti-at 85 DEG C Answer 3h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and leads to Cross the shielding phenol product that column chromatography for separation obtains structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 0.80 (6H), 1.11-1.21 (4H), 1.36 (18H), 1.67 (2H), 3.47 (1H), 4.80 (2H), 5.32 (1H), 6.80 (2H), 6.97 (5H), 7.17 (2H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 17.9,22.4,29.6,34.6,45.2, 52.7,58.6,119.4,121.8,126.2,129.5,131.2,136.6,144.1, 146.1,153.4；
C33H46N2OS calculated values:C 76.40, H 8.94, N 5.40, O 3.08, S 6.18； Measured value：C 76.48, H 8.96, N 5.35, O 3.09, S 6.12.
Embodiment 6
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 3.57 grams of (15mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 5.14 grams of (62mmol) formaldehyde, 21.76 grams of (103mmol) N- phenyl - N '-[4- (phenyl amino) phenyl]-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring, 2h is reacted at 110 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 5.20 (2H), 5.32 (1H), 6.80-7.02 (14H), 7.17 (2H), 7.20 (1H), 7.26 (4H), 7.55(1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,55.5,117.1,120.4, 126.2,129.5,132.3,136.6,142.8,146.1,153.4；
C36H43N3OS calculated values C 77.83, H 7.20, N 6.98, O 2.66, S 5.33； Measured value：C 77.69, H 7.19, N 7.08, O 2.65, S 5.38.
Embodiment 7
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 34.51 grams of (145mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 2.91 grams of (35mmol) formaldehyde, 4.49 grams of (21mmol) 4- amino -4'- Methoxy diphenylamine, 0.26 gram of (2.61mmol) hydrochloric acid and 150mL benzene, rapid stirring, 2h is reacted at 90 DEG C.After question response terminates, it is a small amount of with what is generated that vacuum distillation removes solvent Water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 3.72-3.76 (4H), 4.80 (2H), 5.32 (1H), 6.97-7.06 (8H), 7.17 (2H), 7.20 (1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,51.1,55.5,114.6, 118.9,121.8,124.7,126.5,132.3,136.6,144.5,153.4,154.5；
C28H36N2O2S calculated values C 72.38, H 7.81, N 6.03, O 6.89, S 6.90； Measured value：C 72.37, H 7.69, N 6.12, O 6.80, S 6.83.
Embodiment 8
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add gram 21.66 (91mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 1.35 grams of (9.51mmol) aldehyde C-9s, 6.51 grams of (25mmol) N, N'- bis- Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL benzene, rapid stirring, at 70 DEG C 6h is reacted.Question response After end, vacuum distillation removes solvent and a small amount of water for generating, and is obtained by column chromatography for separation To the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 0.88 (3H), 1.08-1.85 (24H), 5.23 (1H), 5.32 (1H), 6.80 (1H), 6.97 (8H), 7.17 (2H), 7.26 (4H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 14.1,22.6,29.6,31.7,34.6, 41.6,60.8,116.6,119.4,121.8,126.5,129.5,131.4,136.6, 142.8,144.5,146.1,153.4；
C38H48N2OS calculated values C 78.57, H 8.33, N 4.82, O 2.75, S 5.52； Measured value：C 78.62, H 8.25, N 4.75, O 2.81, S 5.42.
Embodiment 9
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 8.33 grams of (35mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 4.23 grams of (51mmol) formaldehyde, 9.61 grams of (31mmol) N, N'- hexichol Base -2,6- naphthylenediamines and 150mL toluene, rapid stirring, at 110 DEG C 4h is reacted.Treat anti- After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 5.25 (2H), 5.32 (1H), 5.80 (1H), 6.99-7.06 (7H), 7.17 (3H), 7.26 (4H), 7.40 (2H), 7.84 (2H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,54.8,106.9,118.6, 123.3,126.2,129.2,136.6,142.8,148.3,153.5；
C37H41N2OS calculated values C 79.24, H 7.19, N 5.00, O 2.85, S 5.72； Measured value：C 79.20, H 7.23, N 5.14, O 2.72, S 5.65.
Embodiment 10
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 6.19 grams of (26mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 9.57 grams of (92mmol) 3- methylthiopropionaldehyde aldehyde, 3.13 grams (17mmol) 4-aminodiphenylamine and 150mL toluene, rapid stirring, at 80 DEG C 2h is reacted.Treat After reaction terminates, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography point From the shielding phenol product for obtaining structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36-1.54 (18H), 2.12-2.80 (7H), 3.47 (1H), 4.97 (1H), 5.32 (1H), 6.97 (7H), 7.17 (2H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 15.2,29.6,31.9,34.6,41.7, 60.2,114.3,119.4,121.8,126.2,129.5,132.4,136.6,144.5, 146.1,153.5；
C30H40N2OS2Calculated value C 70.82, H 7.92, N 5.51, O 3.14, S 12.60； Measured value：C 70.75, H 7.83, N 5.46, O 3.20, S 12.71.
Embodiment 11
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 4.99 grams of (21mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 4.4 grams of (53mmol) formaldehyde, 5.70 grams of (31mmol) N- phenyl pair Phenylenediamine and 150mL ethanol, rapid stirring after reacting 2.5h at 60 DEG C, is down to room temperature, 7.05 grams of (85mmol) formaldehyde are added, 85 DEG C of reaction 2.5h are warming up to.Question response terminates Afterwards, vacuum distillation removes solvent and a small amount of water for generating, and is marked by column chromatography for separation The shielding phenol product of structure shown in topic.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 3.74 (1H), 4.12 (2H), 4.59 (1H), 4.83 (2H), 5.32 (1H), 6.97-7.11 (5H), 7.17 (2H), 7.24 (2H)；
13C NMR (75MHz, CDCl3)：δ 29.6,33.1,34.6,50.6,119.4, 123.3,126.2,126.7,127.9,136.6,140.5,142.9,153.4；
C26H34N2OS calculated values C 75.29, H 7.67, N 6.27, O 3.58, S 7.18； Measured value：C 75.20, H 7.59, N 6.29, O 3.65, S 7.22.
Embodiment 12
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 19.52 grams of (82mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 10.04 grams of (121mmol) formaldehyde, 19.93 grams of (94mmol) 4- amino - 4'- ethyls diphenylamines and 150mL dimethylbenzene, rapid stirring, after reacting 3h at 90 DEG C, Room temperature is down to, 10.11 grams of (316mmol) sulphur and 0.04 gram of (0.35mmol) iodine is added, It is warming up to 150 DEG C of reaction 8h.After question response terminates, vacuum distillation removes solvent with generation A small amount of water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.23 (1H), 1.36 (18H), 2.61 (2H), 3.77 (1H), 4.84 (2H), 5.32 (1H), 5.70 (1H), 6.98 (5H), 7.17 (2H), 7.49 (1H)；
13C NMR (75MHz, CDCl3)：δ 15.60,29.6,34.6,50.7,118.9, 121.8,126.2,129.7,136.6,141.2,146.1,153.4；
C29H36N2OS2Calculated value C 70.69, H 7.36, N 5.69, O 3.25, S 13.02； Measured value：C 70.77, H 7.41, N 5.67, O 3.17, S 12.93.
Embodiment 13
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 10.95 grams of (46mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 3.98 grams of (48mmol) formaldehyde, 13.78 grams of (53mmol) N, N'- bis- Phenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL trimethylbenzenes, rapid stirring, after reacting 1h at 85 DEG C, 3.82 grams of (46mmol) formaldehyde are added, after continuing to react 1h at 85 DEG C, room temperature is down to, 10.11 grams of (316mmol) sulphur and 0.27 gram of (2.11mmol) iodine are added, 180 DEG C are warming up to Reaction 1h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and The shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 4.26 (2H), 5.18 (2H), 5.32 (1H), 6.40 (1H), 6.97 (8H), 7.17 (2H), 7.37 (2H)；
13C NMR (75MHz, CDCl3)：δ 29.6,33.6,34.6,54.3,106.5, 114.4,119.4,121.8,126.2,129.5,136.6,141.9,144.5,153.4；
C34H36N2OS2Calculated value C 73.87, H 6.56, N 5.07, O 2.89, S 11.60； Measured value：C 73.91, H 6.49, N 5.02, O 2.94, S 11.49.
Embodiment 14
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 21.66 grams of (91mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 7.39 grams of (89mmol) formaldehyde, 6.62 grams of (36mmol) N- phenyl pair Phenylenediamine, 0.45 gram of (4.51mmol) NaOH and 150mL isopropanols, stir rapidly Mix, at 80 DEG C 3h is reacted.After question response terminates, vacuum distillation removes solvent with generation A small amount of water, and the shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36-1.54 (36H), 4.82 (4H), 5.32 (2H), 6.97 (7H), 7.17 (4H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,56.5,106.5,119.4, 121.8,126.5,129.5,131.4,136.6,144.5,146.1,153.4；
C42H56N2O2S2Calculated value C 73.64, H 8.24, N 4.09, O 4.67, S 9.36； Measured value：C 73.59, H 8.21, N 4.15, O 4.62, S 9.34.
Embodiment 15
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 6.55 grams of (36mmol) 2- tert-butyl group -4- sulfydryl benzene Phenol, 7.64 grams of (92mmol) formaldehyde, 13.06 grams of (71mmol) N- phenyl are to benzene two Amine and 150mL toluene, rapid stirring, at 90 DEG C 4h is reacted.After question response terminates, subtract Pressure is distilled off solvent and a small amount of water for generating, and is obtained shown in title by column chromatography for separation The shielding phenol product of structure.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (9H), 3.81 (1H), 4.38 (2H), 4.69 (2H), 5.29 (1H), 6.95-7.00 (15H), 7.17 (1H), 7.26 (4H), 7.55 (1H), 8.62 (1H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,43.5,50.8,114.3, 119.4,121.8,125.4,129.5,132.3,136.6,145.2,146.1,149.0, 153.4；
C36H38N4OS calculated values C 75.23, H 6.66, N 9.75, O 2.78, S 5.58； Measured value：C 75.27, H 6.69, N 9.68, O 2.79, S 5.51.
Embodiment 16
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 11.66 grams of (49mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 10.92 grams of (53mmol) 2,6- DI-tert-butylphenol compounds, 7.89 grams (95mmol) Formaldehyde, 11.23 grams of (32mmol) N- phenyl-N '-[4- (phenyl amino) phenyl]-Isosorbide-5-Nitraes- Phenylenediamine and 150mL toluene, rapid stirring, at 100 DEG C 3h is reacted.Question response terminates Afterwards, vacuum distillation removes solvent and a small amount of water for generating, and is marked by column chromatography for separation The shielding phenol product of structure shown in topic.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36-1.54 (36H), 4.91 (2H), 5.22 (2H), 5.32 (2H), 6.97-7.07 (16H), 7.17 (2H), 7.20 (1H), 7.27(4H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.4,55.6,56.9,93.6, 119.4,123.3,126.5,129.2,131.4,136.6,142.8,146.1,153.4；
C54H65N3O2S calculated values C 79.08, H 7.99, N 5.12, O 3.90, S 3.91； Measured value：C 79.15, H 8.03, N 5.01, O 3.87, S 3.85.
Embodiment 17
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 47.16 grams of (45mmol) polyisobutene mercapto-phenols (embodiment 1 is manufactured), 4.23 grams of (51mmol) formaldehyde, 9.75 grams (53mmol) 4-aminodiphenylamine and 150mL benzene, rapid stirring, at 80 DEG C 2.5h is reacted.Treat anti- After should terminating, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography for separation Obtain the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 0.88,0.98,1.02,1.24,1.40, 2.42,4.86,6.97,7.02,7.14,7.26,7.55；
13C NMR (75MHz, CDCl3)：δ 28.2,30.1,32.3,34.5,38.1, 49.8,59.1,114.3,119.4,121.8,122.0,127.3,129.5,132.3, 143.3,146.1,151.3.
Embodiment 18
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 29.34 grams of (28mmol) polyisobutene mercapto-phenols (embodiment 1 is manufactured), 2.91 grams of (35mmol) formaldehyde, 6.24 grams (24mmol) N, N'- diphenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL toluene, rapid stirring, in 90 DEG C of reactions 2h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and by post Chromatography obtains the shielding phenol product of structure shown in title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 0.88,0.98,1.02,1.24,1.40, 2.42,4.00,4.86,5.56,6.97,7.02,7.14,7.26,7.55；
13C NMR (75MHz, CDCl3)：δ 28.2,30.1,32.3,33.1,34.5, 38.1,49.8,59.1,114.3,119.4,121.8,125.2,122.0,127.3,129.5, 132.3,143.3,146.1,151.3.
Comparative example 1
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 20.23 grams of (85mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 7.22 grams of (87mmol) formaldehyde, 14.37 grams of (85mmol) diphenylamines With 150mL methyl alcohol, rapid stirring, at 60 DEG C 2h is reacted.After question response terminates, decompression Solvent and a small amount of water for generating are distilled off, and obtain being tied shown in title by column chromatography for separation The shielding phenol product of structure.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.36 (18H), 5.21 (2H), 5.32 (1H), 6.99 (6H), 7.17 (2H), 7.27 (4H)；
13C NMR (75MHz, CDCl3)：δ 29.6,34.6,55.2,120.4,123.3, 125.9,126.2,129.2,136.6,150.0,153.5；
C27H33NOS calculated values C 77.28, H 7.93, N 3.34, O 3.81, S 7.64； Measured value：C 77.22, H 7.89, N 3.31, O 3.83, S 7.67.
Comparative example 2
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 10.71 grams of (52mmol) 2,6- di-t-butyl -4- Mercapto-phenol, 1.89 grams of (63mmol) formaldehyde, 17.42 grams of (65mmol) N- (1,3- Dimethylbutyl)-N'- diphenyl-para-phenylene diamines and 150mL methyl alcohol, rapid stirring, at 70 DEG C Reaction 4h.After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and The shielding phenol product of structure shown in title is obtained by column chromatography for separation.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 0.80 (6H), 1.11 (3H), 1.29 (1H), 1.36 (18H), 3.45 (1H), 4.53 (2H), 5.32 (2H), 6.97-7.07 (9H), 7.26 (2H), 7.55 (1H)；
13C NMR (75MHz, CDCl3)：δ 17.9,22.40,24.6,30.4,34.3, 45.7,54.5,56.7,116.6,120.4,121.8,125.9,128.9,129.5,135.6, 146.1,153.5,154.8；
C33H46N2O calculated values C 81.43, H 9.53, N 5.76, O 3.29；Measured value： C 81.38, H 9.51, N 5.79, O 3.31.
Comparative example 3
Under nitrogen protection atmosphere, equipped with agitator, thermometer, condenser pipe and dropping funel 250ml four-hole boiling flasks in, add 9.24 grams of (33mmol) 2,6- di-t-butyl -4- (3- Mercaptopropyi) phenol, 3.07 grams of (37mmol) formaldehyde, 11.71 grams (45mmol) N, N'- diphenyl-Isosorbide-5-Nitrae-phenylenediamine and 150mL benzene, rapid stirring, at 80 DEG C 4h is reacted. After question response terminates, vacuum distillation removes solvent and a small amount of water for generating, and by column chromatography The shielding phenol product of structure shown in isolated title.
Characterization of The Products data are as follows：
1H NMR (300MHz, CDCl3)：δ 1.40 (18H), 1.99 (1H), 2.61-2.80 (6H), 4.63 (2H), 5.32 (1H), 6.97-7.02 (12H), 7.26 (4H), 7.55(1H)；
13C NMR (75MHz, CDCl3)：δ 28.7,31.1,34.3,35.7,54.1, 117.1,119.4,123.3,124.8,129.2,131.8,136.0,142.8,144.9, 146.1,151.9；
C36H44N2OS calculated values C 78.22, H 8.02, N 5.07, O 2.89, S 5.80； Measured value：C 78.27, H 7.96, N 4.98, O 2.92, S 5.83.
Comparative example 4～7
The composition of the comparative example 4～7 of antioxidant is shown in Table 1.
Table 1
The embodiment 19～28 of quenching oil and the formula composition of comparative example 8～14 are shown in Table 2,3. Each component in table is added to scale in mediation container, in 45 DEG C of heating stirrings 2 Hour, prepare obtain quenching oil compound respectively.
Some lube oil additives for specifically being used are as follows：
Urge cryogen：Petroleum sodium sulfonate, trade names T702；Disubstituted polyisobutene fourth two Acid imide, trade names T154；Polyisobutene, trade names PB1300；
Brightener：Imidazoline oleate；Sorbitol monooleate；
Antirust agent：Dodecenylsuccinic acid, trade names T746；
Lube base oil：II base oil 100N, II base oil 500N.
Table 2
Table 3
The test result of PDSC tests, coking simulated test, copper strip test and corrosion test is such as Shown in table 4.
Table 4
From table 4, it can be seen that quenching oil compound of the present invention have excellent high-temperature oxidation resistance, Detergent-dispersant performance energy, excellent corrosion resistance and excellent anti-corrosion ability.

Claims (10)

1. a kind of quenching oil compound, including shielding phenolic compounds, urge cryogen, brightener, antirust Agent and major amount of lube base oil, the structure of the shielding phenolic compounds is：
In logical formula (I), each group R is same to each other or different to each other, and is each independently selected from hydrogen, C1-300 Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn are 300-3000's is polyolefin-based), the group shown in logical formula (II) and the group shown in logical formula (III), On condition that at least one group R is the group shown in logical formula (II)；Each group R' is mutually the same or not Together, hydrogen and C are each independently selected from1-20Straight or branched alkyl (is preferably each independently selected from hydrogen And C1-4Straight or branched alkyl),
In aforementioned each logical formula (II), (III) and (IV), each group L is same to each other or different to each other, respectively From being independently groupWherein group R " is selected from hydrogen, C1-20Alkyl (preferred C1-20 Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight chain or Branched alkyl and C3-10Straight or branched miscellaneous alkyl；Each group R2It is same to each other or different to each other, each solely On the spot it is selected from hydrogen, C1-20Group and logical formula (V) shown in straight or branched alkyl, logical formula (IV) Shown group (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and logical formula (IV) Shown group)；Each group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20Directly Chain or branched alkyl (are preferably each independently selected from hydrogen and C1-10Straight or branched alkyl)；Each group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20Directly Chain or branched alkyl epoxide (are preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and C1-10 Straight or branched alkyl epoxide, is more preferably in cyclic groupThe contraposition of upper nitrogen-atoms)；y It is 0 to 3 integer (preferably 0 or 1)；Z is 0 to 3 integer (preferably 0 or 1)；N is 1 To 8 integer (preferably 1 or 2)；N' is 0 to 7 integer (preferably 0,1 or 2), on condition that N'+n≤8 (preferred n'+n=1 or n'+n=2)；Each group RdIt is same to each other or different to each other, independently of one another Selected from the group (preferred hydrogen) shown in hydrogen and logical formula (V)；Each cyclic groupIt is mutually the same Or it is different, phenyl ring and naphthalene nucleus (preferred phenyl ring) are each independently selected from, wherein two adjacent ring groups GroupOptionally formed by the S atom for adding and the N atoms for bridging the two rings each other Phenthazine ring, and/or, two adjacent cyclic groupsEach other optionally by additional group(wherein group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkyl) And C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen and C1-10Straight or branched alkyl) and bridge joint The N atoms of the two rings and form 9,10- acridan rings,
In logical formula (V), each group R is same to each other or different to each other, and is each independently selected from hydrogen, C1-300 Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn are 300-3000 It is polyolefin-based), the group shown in logical formula (II) and the group shown in logical formula (III) (preferably each solely On the spot selected from hydrogen and C1-300Straight or branched alkyl)；Each group R' is same to each other or different to each other, each solely On the spot selected from hydrogen and C1-20Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-4Straight chain Or branched alkyl)；Group L is groupWherein group R " is selected from hydrogen, C1-20Hydrocarbon Base (preferred C1-20Straight or branched alkyl) and C3-20Straight or branched miscellaneous alkyl, be preferably selected from hydrogen, C1-10Straight or branched alkyl and C3-10Straight or branched miscellaneous alkyl；A is 0 or 1, and two bases R and group-(S) of groupa- L- occupies respectively three positions of residue on phenyl ring,
Wherein, the straight or branched miscellaneous alkyl is selected from inside straight or branched alkyl molecular structure Individual or multiple (such as 1 to 4,1 to 3,1 to 2 or 1) group-CH2- quilt Selected from-O- ,-S- and-NR'-, (R' is H or C1-4Straight or branched alkyl) one of substituting group One or more inside the group for directly substituting and obtaining and straight or branched alkyl molecular structure (such as 1 to 3,1 to 2 or 1) group-CH<By substituting group-N<Directly replace Generation and obtain group, wherein the shielding phenolic compounds in its whole molecular structure at least one Group RdIt is hydrogen.
2. according to the quenching oil compound described in claim 1, it is characterised in that the shielding Mixture of the phenolic compounds selected from following particular compound or its arbitrary proportion：
3. a kind of quenching oil compound, including shielding phenolic compounds, urge cryogen, brightener, antirust Agent and major amount of lube base oil, the manufacture method of the shielding phenolic compounds includes making formula (X) amines shown in phenolic compounds and formula (Y) shown in is in the aldehyde shown in formula (Z) The first step reacted in the presence of compound (preferred formaldehyde), optionally also includes making described the The product of one step react with vulcanizing agent (preferred sulphur) and/or with the hydroformylation shown in formula (Z) The additional step of compound (preferred formaldehyde) reaction,
In logical formula (X), each group R0It is same to each other or different to each other, is each independently selected from hydrogen ,-SH And C1-300Straight or branched alkyl (preferred C1-10Straight or branched alkyl or number-average molecular weight Mn For the polyolefin-based of 300-3000), on condition that at least one group R0It is-SH；Each group R' is each other It is identical or different, it is each independently selected from hydrogen and C1-20Straight or branched alkyl is (preferably each independent Ground is selected from hydrogen and C1-4Straight or branched alkyl),
In formula (Y), group R'2Selected from hydrogen, C1-20Straight or branched alkyl and groupEach group RbIt is same to each other or different to each other, is each independently selected from hydrogen and C1-20 Straight or branched alkyl (is preferably each independently selected from hydrogen and C1-10Straight or branched alkyl)；Each base Group RcIt is same to each other or different to each other, is each independently selected from hydrogen, C1-20Straight or branched alkyl and C1-20 Straight or branched alkyl epoxide (is preferably each independently selected from hydrogen, C1-10Straight or branched alkyl and C1-10Straight or branched alkyl epoxide, is more preferably in cyclic groupThe contraposition of upper nitrogen-atoms)； Y is 0 to 3 integer (preferably 0 or 1)；Z is 0 to 3 integer (preferably 0 or 1)；n1 For 1 to 8 integer (preferably 1 or 2)；Each cyclic groupIt is same to each other or different to each other, respectively From independently selected from phenyl ring and naphthalene nucleus (preferred phenyl ring),
In formula (Z), group R " it is selected from hydrogen, C1-20Alkyl (preferred C1-20Straight or branched alkane Base) and C3-20Straight or branched miscellaneous alkyl, is preferably selected from hydrogen, C1-10Straight or branched alkyl and C3-10 Straight or branched miscellaneous alkyl,
Wherein, the straight or branched miscellaneous alkyl is selected from inside straight or branched alkyl molecular structure Individual or multiple (such as 1 to 4,1 to 3,1 to 2 or 1) group-CH2- quilt Selected from-O- ,-S- and-NR'-, (R' is H or C1-4Straight or branched alkyl) one of substituting group One or more inside the group for directly substituting and obtaining and straight or branched alkyl molecular structure (such as 1 to 3,1 to 2 or 1) group-CH<By substituting group-N<Directly replace Generation and obtain group.
4. according to the quenching oil compound described in claim 3, it is characterised in that described first In step, the phenolic compounds shown in the logical formula (X) and the amine compounds shown in the formula (Y) The mol ratio of thing is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0, the logical formula (X) Shown phenolic compounds is 1 with the mol ratio of the aldehyde compound shown in the formula (Z):0.1-10, It is preferred that 1:0.5-5.0, more preferably 1:0.8-2.0, in the additional step, formula (Y) institute The amines for showing is 1 with the mol ratio of the vulcanizing agent:1-10, preferably 1:1.2-6.0, more preferably 1:1.5-3.0, the amines shown in the formula (Y) is closed with the hydroformylation shown in the formula (Z) The mol ratio of thing is 1:0.1-10, preferably 1:0.5-5.0, more preferably 1:0.8-2.0.
5. according to the quenching oil compound described in one of claim 1-4, it is characterised in that described Shielding phenolic compounds accounts for the 0.001-30% of the quenching oil compound gross weight；
Described one kind for urging cryogen in sulfonate, polyisobutene succinimide and polyolefin Or it is various, account for the 0.01%-30% of the quenching oil compound gross mass；
The brightener is selected from imidazoline, imidazoline oleate, methyl terpene resin, sorbose One or more in alcohol monoleate and binary of fatty acids, accounts for the quenching oil compound gross mass 0.01%-10%；
The antirust agent is derivative selected from alkyl imidazolidine derivatives, benzotriazole derivative and alkenyl succinic acid One or more in thing, accounts for the 0.001%-10% of the quenching oil compound gross mass；
The lube base oil is in API I, II, III, IV and V class lubricating oil base oils One or more.
6. according to the quenching oil compound described in one of claim 1-4, it is characterised in that described Cryogen is urged selected from sulfonate and/or polyisobutene succinimide；The brightener is selected from imidazoline oil Hydrochlorate and/or sorbitol monooleate；The antirust agent is selected from alkenyl succinic acid derivative.
7. according to the quenching oil compound described in one of claim 1-4, it is characterised in that described Shielding phenolic compounds accounts for the 0.05%-20% of the quenching oil compound gross weight；It is described to urge cryogen to account for The 0.05%-20% of the quenching oil compound gross mass；The brightener accounts for the quenching oil compound The 0.05%-5% of gross mass；The antirust agent accounts for the quenching oil compound gross mass 0.005%-5%.
8. according to the quenching oil compound described in one of claim 1-4, it is characterised in that described Shielding phenolic compounds accounts for the 0.1%-10% of the quenching oil compound gross weight；It is described to urge cryogen to account for The 0.1%-10% of the quenching oil compound gross mass；The brightener accounts for the quenching oil compound The 0.1%-3% of gross mass；The antirust agent accounts for the 0.01%-1% of the quenching oil compound gross mass.
9. according to the quenching oil compound described in one of claim 1-4, it is characterised in that in institute State and add in quenching oil compound antioxidant, detersive, dispersant, pour-point depressant, viscosity index (VI) One kind in modifier, metal corrosion inhibitor, friction improver, anti emulsifier and anti-foaming agent Or it is various.
10. the manufacture method of the quenching oil compound described in one of claim 1-4, including making The step of stating shielding phenol, urge cryogen, brightener, antirust agent and the lube base oil to mix.
CN201510674623.1A 2015-10-19 2015-10-19 A kind of quenching oil compound and its manufacturing method Active CN106591547B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510674623.1A CN106591547B (en) 2015-10-19 2015-10-19 A kind of quenching oil compound and its manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510674623.1A CN106591547B (en) 2015-10-19 2015-10-19 A kind of quenching oil compound and its manufacturing method

Publications (2)

Publication Number Publication Date
CN106591547A true CN106591547A (en) 2017-04-26
CN106591547B CN106591547B (en) 2018-07-31

Family

ID=58554278

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510674623.1A Active CN106591547B (en) 2015-10-19 2015-10-19 A kind of quenching oil compound and its manufacturing method

Country Status (1)

Country Link
CN (1) CN106591547B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108842046A (en) * 2018-05-21 2018-11-20 山东高强紧固件有限公司 A kind of cooling fluid composition of discarded oil renewal of automobile
WO2019006660A1 (en) * 2017-07-04 2019-01-10 江苏鑫露新材料股份有限公司 Overspeed quenching oil composition having excellent cooling rate stability, and preparation method therefor
CN111074045A (en) * 2019-12-30 2020-04-28 南京科润工业介质股份有限公司 Rapid bright quenching oil and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3925113A (en) * 1973-12-21 1975-12-09 Shell Oil Co Quenching oil composition
CN101029349A (en) * 2007-04-05 2007-09-05 南京航空航天大学 Heat-treatment quench oil composite additive and its production
CN101603118A (en) * 2009-05-26 2009-12-16 锦州康泰润滑油添加剂有限公司 Light-color quenching oil complexing agent composition and preparation method thereof
CN102212662A (en) * 2011-06-09 2011-10-12 上海德润宝特种润滑剂有限公司 Ultra quick quenching oil and preparation method thereof
CN103981340A (en) * 2014-05-26 2014-08-13 江苏鑫露新材料股份有限公司 Conveniently-recyclable high-speed quenching oil composition and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3925113A (en) * 1973-12-21 1975-12-09 Shell Oil Co Quenching oil composition
CN101029349A (en) * 2007-04-05 2007-09-05 南京航空航天大学 Heat-treatment quench oil composite additive and its production
CN101603118A (en) * 2009-05-26 2009-12-16 锦州康泰润滑油添加剂有限公司 Light-color quenching oil complexing agent composition and preparation method thereof
CN102212662A (en) * 2011-06-09 2011-10-12 上海德润宝特种润滑剂有限公司 Ultra quick quenching oil and preparation method thereof
CN103981340A (en) * 2014-05-26 2014-08-13 江苏鑫露新材料股份有限公司 Conveniently-recyclable high-speed quenching oil composition and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019006660A1 (en) * 2017-07-04 2019-01-10 江苏鑫露新材料股份有限公司 Overspeed quenching oil composition having excellent cooling rate stability, and preparation method therefor
CN108842046A (en) * 2018-05-21 2018-11-20 山东高强紧固件有限公司 A kind of cooling fluid composition of discarded oil renewal of automobile
CN111074045A (en) * 2019-12-30 2020-04-28 南京科润工业介质股份有限公司 Rapid bright quenching oil and preparation method thereof
WO2021134941A1 (en) * 2019-12-30 2021-07-08 南京科润工业介质股份有限公司 Quick bright quenching oil and preparation method therefor
CN111074045B (en) * 2019-12-30 2021-11-12 南京科润工业介质股份有限公司 Rapid bright quenching oil and preparation method thereof

Also Published As

Publication number Publication date
CN106591547B (en) 2018-07-31

Similar Documents

Publication Publication Date Title
CN106318528B (en) Universal gear lubricating oil composition
CN106318531B (en) Diesel engine lubricating oil composite and its manufacturing method
CN106590829B (en) Railway high speed diesel engine lubricating oil composite and its manufacturing method
CN106591547A (en) Quenching oil composition and manufacturing method thereof
CN106590849A (en) Hydraulic oil composition and production method therefor
CN106590833B (en) Two-stroke engine lubricating oil composition and its manufacturing method
CN106318530B (en) Lubricant composition for gasoline engine and its manufacturing method
CN106590827A (en) Lubricating oil composition for four-stroke motorcycle engine and manufacturing method thereof
CN106590832B (en) Gas engine lubricant oil composite and its manufacturing method
CN106256890B (en) Lubricant composition for gasoline engine
CN106590847A (en) High temperature chain oil composition and production method thereof
CN106590830B (en) A kind of fully synthetic extreme pressure lubricating oil for industrial gears composition and its manufacturing method
CN105130859B (en) A kind of shielding phenolic compounds, its manufacturing method and its application as antioxidant
CN105272892B (en) A kind of shielding phenolic compounds, its manufacturing method and its application as antioxidant
CN106590828A (en) Heavy-load vehicle gear lubricating oil composition and manufacturing method thereof
CN106590831A (en) Heat-conducting oil composition and production method thereof
CN106590826A (en) Steam turbine lubricating oil composition and production method
CN106590848B (en) A kind of automatic drive liquid composition and its manufacturing method
CN106318524B (en) Composition oil of gasoline engine and its manufacturing method
CN105218420B (en) A kind of shielding phenolic compounds, its manufacturing method and its application as antioxidant
CN106318526B (en) Methanol-fueled engine lubricant oil composite and its manufacturing method
CN106590852A (en) Industrial lubricating oil composition and production method therefor
CN106256889B (en) Diesel engine oil composition and its manufacturing method
CN106318529B (en) Universal gear lubricating oil composition and its manufacturing method
CN106318562B (en) Universal gear lubricating oil composition and its manufacturing method

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right

Effective date of registration: 20210701

Address after: 100728 No. 22 North Main Street, Chaoyang District, Beijing, Chaoyangmen

Patentee after: China Petroleum & Chemical Corp.

Patentee after: SINOPEC CORP Research Institute OF PETROLEUM PROCESSING

Patentee after: Beijing General Fine Chemical Technology Development Co.,Ltd.

Address before: 100728 No. 22 North Main Street, Chaoyang District, Beijing, Chaoyangmen

Patentee before: China Petroleum & Chemical Corp.

Patentee before: SINOPEC CORP Research Institute OF PETROLEUM PROCESSING

TR01 Transfer of patent right