CN111334054A - Anti-aging composition for stable regenerated oil - Google Patents
Anti-aging composition for stable regenerated oil Download PDFInfo
- Publication number
- CN111334054A CN111334054A CN201811560187.5A CN201811560187A CN111334054A CN 111334054 A CN111334054 A CN 111334054A CN 201811560187 A CN201811560187 A CN 201811560187A CN 111334054 A CN111334054 A CN 111334054A
- Authority
- CN
- China
- Prior art keywords
- parts
- component
- amount
- phosphite
- composition according
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 31
- 230000003712 anti-aging effect Effects 0.000 title claims abstract description 28
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 31
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 28
- 239000007788 liquid Substances 0.000 claims abstract description 24
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 150000001412 amines Chemical class 0.000 claims abstract description 12
- 239000004611 light stabiliser Substances 0.000 claims abstract description 10
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims abstract description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 claims description 6
- XDDLRVYDQACVBC-UHFFFAOYSA-N 10-oxo-10-(1,2,2,6,6-pentamethylpiperidin-4-yl)oxydecanoic acid Chemical compound CN1C(C)(C)CC(OC(=O)CCCCCCCCC(O)=O)CC1(C)C XDDLRVYDQACVBC-UHFFFAOYSA-N 0.000 claims description 3
- GAODDBNJCKQQDY-UHFFFAOYSA-N 2-methyl-4,6-bis(octylsulfanylmethyl)phenol Chemical compound CCCCCCCCSCC1=CC(C)=C(O)C(CSCCCCCCCC)=C1 GAODDBNJCKQQDY-UHFFFAOYSA-N 0.000 claims description 3
- ADRNSOYXKABLGT-UHFFFAOYSA-N 8-methylnonyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC(C)C)OC1=CC=CC=C1 ADRNSOYXKABLGT-UHFFFAOYSA-N 0.000 claims description 3
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 claims description 3
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims description 3
- QEDNBHNWMHJNAB-UHFFFAOYSA-N tris(8-methylnonyl) phosphite Chemical compound CC(C)CCCCCCCOP(OCCCCCCCC(C)C)OCCCCCCCC(C)C QEDNBHNWMHJNAB-UHFFFAOYSA-N 0.000 claims description 3
- 235000010290 biphenyl Nutrition 0.000 claims description 2
- 239000004305 biphenyl Substances 0.000 claims description 2
- 125000006267 biphenyl group Chemical group 0.000 claims description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 2
- 150000008301 phosphite esters Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 10
- 238000003860 storage Methods 0.000 abstract description 6
- 230000000087 stabilizing effect Effects 0.000 abstract description 4
- 238000002845 discoloration Methods 0.000 abstract description 3
- 239000003921 oil Substances 0.000 description 38
- 239000000047 product Substances 0.000 description 18
- 229910052799 carbon Inorganic materials 0.000 description 6
- SQKUFYLUXROIFM-UHFFFAOYSA-N 2-[2-[carboxymethyl-[[3-hydroxy-2-methyl-5-(phosphonooxymethyl)pyridin-4-yl]methyl]amino]ethyl-[[3-hydroxy-2-methyl-5-(phosphonooxymethyl)pyridin-4-yl]methyl]amino]acetic acid Chemical compound CC1=NC=C(COP(O)(O)=O)C(CN(CCN(CC(O)=O)CC=2C(=C(C)N=CC=2COP(O)(O)=O)O)CC(O)=O)=C1O SQKUFYLUXROIFM-UHFFFAOYSA-N 0.000 description 5
- -1 carbon alcohol esters Chemical class 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- YHEPZZFDBQOSSN-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate;1-o-methyl 10-o-(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound COC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1.C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 YHEPZZFDBQOSSN-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000001172 regenerating effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 230000032683 aging Effects 0.000 description 3
- 238000005286 illumination Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 208000034301 polycystic dysgenetic disease of parotid salivary glands Diseases 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 2
- DQXKOHDUMJLXKH-PHEQNACWSA-N (e)-n-[2-[2-[[(e)-oct-2-enoyl]amino]ethyldisulfanyl]ethyl]oct-2-enamide Chemical compound CCCCC\C=C\C(=O)NCCSSCCNC(=O)\C=C\CCCCC DQXKOHDUMJLXKH-PHEQNACWSA-N 0.000 description 1
- PXMJCECEFTYEKE-UHFFFAOYSA-N Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, methyl ester Chemical compound COC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 PXMJCECEFTYEKE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 239000010720 hydraulic oil Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
The present invention relates to a composition comprising a reclaimed oil and a liquid age resistor comprising (a) a hindered phenolic primary antioxidant; (b) phosphite-based secondary antioxidants; (c) hindered amine light stabilizers. The invention provides an anti-aging agent product for stabilizing reclaimed oil for the first time, the product is a liquid formula, is convenient to produce and use, and can effectively solve the problem of discoloration in the process of storage and transportation of the reclaimed oil.
Description
Technical Field
The invention belongs to the field of high polymer material functional additives, and particularly relates to a liquid anti-aging agent composition which is applied to the field of reclaimed oil and can effectively ensure the storage and processing stability of the reclaimed oil.
Background
The regenerated oil is reused oil product produced with edible oil, mechanical oil, gear oil, gasoline, diesel oil, etc. and through washing, decolorizing, deodorizing, blending and other steps. The reclaimed oil is aged due to the influence of temperature and illumination in the production, storage and transportation processes, so that the stability of the reclaimed oil is reduced, the product is obviously discolored, and the service performance of the product is limited finally.
The prior art has more descriptions about the regeneration method of used oil products, for example, patent 201710629123.5 describes a method for regenerating waste transformer oil; patent 201410087216.6 describes a method of regenerating used turbine oil; patent 201710116537.8 describes a method for regenerating used lubricating oil; patent 201110152853.3 describes a method of regenerating waste hydraulic oil. However, in the patents and literature available, there is no relevant method or product for improving the stability of the reclaimed oil. The applicant is aware of practical research that no measures are taken by the reclaimed oil manufacturers to improve the stability of the reclaimed oil during the production and processing of the reclaimed oil.
Therefore, there is a need to develop products/methods for stabilizing reclaimed oils, improve the discoloration of reclaimed oils, and stabilize the service properties of reclaimed oils.
Disclosure of Invention
The invention aims to solve the problems in the prior art and provides an anti-aging product applied to reclaimed oil so as to solve the problem of color change of the reclaimed oil caused by temperature and illumination in production, storage and processing. Through a large number of experimental researches and comparative tests, the inventor provides an anti-aging composition for the reclaimed oil, which can remarkably improve the storage, processing and use stability of the reclaimed oil and well protect the color of the reclaimed oil under the conditions of heat aging and illumination. Specifically, the technical scheme adopted by the invention is as follows:
a composition comprising a reclaimed oil and a liquid age resistor, the liquid age resistor comprising: (a) a hindered phenolic primary antioxidant; (b) phosphite-based secondary antioxidants; (c) hindered amine light stabilizers.
The components (a), (b) and (c) are all liquid products. The primary antioxidant and the secondary antioxidant synergistically protect the heat resistance of the reclaimed oil, and the secondary antioxidant and the hindered amine light stabilizer synergistically protect the light stability of the reclaimed oil.
Preferably, the hindered phenolic antioxidant of component (a) is selected from 4, 6-bis (octylthiomethyl) o-cresol, or one or more compounds of formula I:
in the general formula I, R is C8-18Alkyl group of (1).
Preferably, in the general formula I, R is selected from C8、C9、C10、C11、C12、C13、C14、C15、C16、C17、C18At least one of alkyl groups. Or, in the general formula I, R is selected from C12-18，C13-15，C14-16，C12-17，C12-16，C13-16，C12-14，C16-18At least one of mixed alkyl groups.
More preferably, the compound of the general formula I is one selected from octyl 3, 5-di-tert-butyl-4-hydroxy phenylpropionate (antioxidant 1135R), 13-15 carbon alcohol esters of 3, 5-di-tert-butyl-4-hydroxy phenylpropionate (compound I-1), 14-16 carbon alcohol esters of 3, 5-di-tert-butyl-4-hydroxy phenylpropionate (compound I-2), and 12-18 carbon alcohol esters of 3, 5-di-tert-butyl-4-hydroxy phenylpropionate (compound I-3).
The products represented by component (a) are either commercially available or can be prepared by synthetic means commonly used in the field of organic chemistry. For example, compound I-1 can be prepared from ADDIVANT available under the trademark ANOX 1315, and compound I-2 can be prepared from chenille available under the trademark ST-1620, and the present invention provides a process for preparing a compound of formula I: with methyl 3- (3, 5-di-tert-butyl-4-hydroxyphenyl) propionate and C8～17And (3) taking carbon alcohol as a raw material to react to obtain the catalyst.
Preferably, the phosphite auxiliary antioxidant of component (b) is one or more selected from triphenyl phosphite (antioxidant TPP), diphenyl isodecyl phosphite (antioxidant DPDP), diphenyl diisodecyl phosphite (antioxidant PDDP) and triisodecyl phosphite (antioxidant TITDP).
Preferably, the hindered amine light stabilizer of component (c) is one or more selected from the group consisting of bis (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate and a mixture of mono (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate (light stabilizer 292), bis (1-octyloxy-2, 2,6, 6-tetramethyl-4-piperidyl) sebacate (light stabilizer 123).
As a preferred technical scheme of the invention, the anti-aging agent in the composition comprises: hindered phenol antioxidant 1135R, phosphite antioxidant DPDP and hindered amine light stabilizer 123.
Preferably, in the aging inhibitor, the component (a) is used in an amount of 30 to 80 parts, the component (b) is used in an amount of 10 to 40 parts, and the component (c) is used in an amount of 10 to 40 parts by weight.
More preferably, component (a) is used in an amount of 40 to 70 parts, and even more preferably 50 to 65 parts, and in particular embodiments, component (a) is used in an amount of 30 parts, 40 parts, 50 parts, 60 parts, 70 parts, 80 parts, 40 to 55 parts, 55 to 70 parts, and the like.
More preferably, component (b) is used in an amount of 15 to 30 parts, and even more preferably 15 to 25 parts, and in particular embodiments, may be used in an amount of 10 parts, 20 parts, 30 parts, 40 parts, 15 parts, 25 parts, 35 parts, and the like.
More preferably, component (c) is used in an amount of 15 to 30 parts, and even more preferably 15 to 25 parts, and in particular embodiments, may be used in an amount of 10 parts, 20 parts, 30 parts, 40 parts, 15 parts, 25 parts, 35 parts, and the like.
Most preferably, the weight ratio of components (a), (b), (c) is 3:1: 1.
In the composition, the dosage of the anti-aging agent is 0.1-1.0 wt% of the reclaimed oil. Preferably 0.3 wt%.
The invention also provides a method for stabilizing the reclaimed oil, which is characterized in that the anti-aging agent is added into the reclaimed oil and uniformly mixed. The anti-aging agent is liquid, is convenient to add and use and is easy to mix uniformly.
The reclaimed oil refers to products with the trade marks of 150SN, 250SN or 350 SN.
The invention also provides a liquid anti-aging composition, which comprises the following components in parts by weight:
(i) 30-80 parts of hindered phenol primary antioxidant
(ii) 10-40 parts of phosphite ester auxiliary antioxidant
(iii) 10-40 parts of hindered amine light stabilizer.
The liquid anti-aging composition is completely the same as the anti-aging agent, namely, the optional product and the using amount of the component (i) are completely the same as the component (a); the optional products and the dosage of the component (ii) are completely the same as the component (b); the optional products and the amount of the component (iii) are the same as those of the component (c), and the details are not repeated herein.
The liquid anti-aging composition can be prepared by simple mixing.
The invention also provides application of any one of the liquid anti-aging compositions in processing and using of the reclaimed oil.
On the basis of the common knowledge in the field, the above preferred conditions can be combined with each other to obtain the preferred embodiments of the invention.
The "weight parts" in the present invention are weight units of mg, g, kg, etc. known in the art, or multiples thereof, such as 1/10, 1/100, 10, etc.
Compared with the prior art, the invention has the following positive effects: the regenerated oil is different from a fresh oil product, belongs to the recycling of waste oil, and is darker in color compared with the colorless and transparent appearance of common base oil, and basically is light yellow to dark yellow. Meanwhile, compared with common base oil products, the regenerated oil is easier to age. The invention provides an anti-aging agent product for stabilizing the reclaimed oil for the first time, and the developed product can effectively improve the problem of discoloration in the storage and transportation processes of the reclaimed oil; the anti-aging agent product is in a liquid formula and is convenient to produce and use.
Detailed Description
The following examples are intended to illustrate the invention but are not intended to limit the scope of the invention. The operations referred to in the examples are, unless otherwise specified, all those of ordinary skill in the art.
The preparation method of the liquid antiaging agent composition in the examples is: the components are weighed according to the weight of each embodiment and fully stirred in a stirring kettle, so that the components are uniformly dispersed.
Example 1
A liquid anti-aging composition comprises the following components: 60g of antioxidant 1135R, 15g of antioxidant DPDP, 25g of hindered amine light stabilizer 123,
example 2
A liquid anti-aging composition comprises the following components: 60g of antioxidant 3, 5-di-tert-butyl-4-hydroxy phenylpropionic acid 12-18 carbon alcohol ester, 20g of antioxidant PDDP and 20g of hindered amine light stabilizer 292.
Example 3
A liquid anti-aging composition comprises the following components: 50g of antioxidant 3, 5-di-tert-butyl-4-hydroxy phenylpropionic acid 13-15 carbon alcohol ester, 25g of antioxidant TPP and 25g of hindered amine light stabilizer 292.
Comparative example 1
A liquid anti-aging composition comprises the following components: 50g of antioxidant 1135R, 50g of antioxidant DPDP.
Comparative example 2
A liquid anti-aging composition comprises the following components: 25g antioxidant 1135R, 25g antioxidant DPDP, 50g hindered amine light stabilizer 292.
Effect test
The test oil product is the reclaimed oil 150SN, and the color of the reclaimed oil is recorded before the light aging is measured; then the sample is placed under natural conditions (8 months) for 10 days of continuous exposure, and samples exposed for 5 days and 10 days are respectively taken to observe the color. The results are shown in Table 1.
Table 1: test results of examples and comparative examples
Although the invention has been described in detail hereinabove by way of general description, specific embodiments and experiments, it will be apparent to those skilled in the art that many modifications and improvements can be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.
Claims (10)
1. A composition characterized by: including reclaimed oil and liquid age resister, the liquid age resister includes: (a) a hindered phenolic primary antioxidant; (b) phosphite-based secondary antioxidants; (c) hindered amine light stabilizers.
2. The composition of claim 1, wherein: the component (a) is selected from 4, 6-di (octylthiomethyl) o-cresol or one or more compounds in the general formula I:
in the general formula I, R is C8-18Alkyl groups of (a);
preferably, R is selected from C8、C9、C10、C11、C12、C13、C14、C15、C16、C17、C18One of alkyl, or R is selected from C12-18，C13-15，C14-16，C12-17，C12-16，C13-16，C12-14，C16-18One of mixed alkyl groups.
3. The composition according to any one of claims 1-2, characterized in that: the component (b) is one or more selected from triphenyl phosphite, diphenyl isodecyl phosphite and triisodecyl phosphite; and/or the presence of a gas in the gas,
the component (c) is one or more selected from a mixture of bis (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate and mono (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate, and bis (1-octyloxy-2, 2,6, 6-tetramethyl-4-piperidyl) sebacate.
4. The composition according to any one of claims 1 to 3, characterized in that: in the liquid anti-aging agent, the using amount of the component (a) is 30-80 parts, the using amount of the component (b) is 10-40 parts, and the using amount of the component (c) is 10-40 parts by weight;
preferably, component (a) is used in an amount of 40 to 70 parts, component (b) is used in an amount of 15 to 30 parts, and component (c) is used in an amount of 15 to 30 parts;
further preferably, component (a) is used in an amount of 50 to 65 parts, component (b) is used in an amount of 15 to 25 parts, and component (c) is used in an amount of 15 to 25 parts.
5. The composition according to any one of claims 1 to 4, characterized in that: in the liquid antiaging agent, the weight ratio of the components (a), (b), and (c) is 3:1: 1.
6. The composition according to any one of claims 1 to 5, characterized in that: the weight of the liquid anti-aging agent is 0.1-1.0 wt% of the reclaimed oil.
7. The composition according to any one of claims 1 to 6, characterized in that: the reclaimed oil refers to products with the trade marks of 150SN, 250SN or 350 SN.
8. A liquid anti-aging composition comprises the following components in parts by weight:
(i) 30-80 parts of hindered phenol primary antioxidant
(ii) 10-40 parts of phosphite ester auxiliary antioxidant
(iii) 10-40 parts of hindered amine light stabilizer.
9. The liquid anti-aging composition according to claim 8, characterized in that: the component (I) is selected from 4, 6-di (octylthiomethyl) o-cresol or one or more compounds in the general formula I:
in the general formula I, R is C8-17Alkyl groups of (a);
preferably, R is selected from C8、C9、C10、C11、C12、C13、C14、C15、C16、C17、C18One of alkyl, or R is selected from C12-18，C13-15，C14-16，C12-17，C12-16，C13-16，C12-14，C16-18One of mixed alkyl groups; and/or the presence of a gas in the gas,
the component (ii) is one or more selected from triphenyl phosphite, diphenyl isodecyl phosphite, diphenyl diisodecyl phosphite and triisodecyl phosphite; and/or the presence of a gas in the gas,
the component (iii) is one or more selected from a mixture of bis (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate and mono (1,2,2,6, 6-pentamethyl-4-piperidyl) sebacate, and bis (1-octyloxy-2, 2,6, 6-tetramethyl-4-piperidyl) sebacate.
10. The composition according to any one of claims 8 to 9, characterized in that: the amount of the component (i) is 40-70 parts, the amount of the component (ii) is 15-30 parts, and the amount of the component (iii) is 15-30 parts;
preferably, component (i) is used in an amount of 50 to 65 parts, component (ii) is used in an amount of 15 to 25 parts, and component (iii) is used in an amount of 15 to 25 parts;
further preferably, the weight ratio of components (i), (ii), (iii) is 3:1: 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201811560187.5A CN111334054A (en) | 2018-12-19 | 2018-12-19 | Anti-aging composition for stable regenerated oil |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201811560187.5A CN111334054A (en) | 2018-12-19 | 2018-12-19 | Anti-aging composition for stable regenerated oil |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN111334054A true CN111334054A (en) | 2020-06-26 |
Family
ID=71177671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201811560187.5A Pending CN111334054A (en) | 2018-12-19 | 2018-12-19 | Anti-aging composition for stable regenerated oil |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN111334054A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112342074A (en) * | 2020-12-21 | 2021-02-09 | 山东恒利热载体工程技术有限公司 | Regenerated base oil lubricating oil light-resistant and heat-stabilizing agent |
| CN113174283A (en) * | 2021-04-02 | 2021-07-27 | 安徽中天石化股份有限公司 | High-performance phosphate flame-retardant hydraulic oil |
| CN116218030A (en) * | 2023-03-15 | 2023-06-06 | 上海石化西尼尔化工科技有限公司 | Anti-core burning and anti-oxidation composition and preparation method and application thereof |
| WO2024160242A1 (en) * | 2023-02-03 | 2024-08-08 | 天津利安隆新材料股份有限公司 | Anti-aging agent composition, use thereof, and anti-aging polymer material |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004026857A (en) * | 2002-06-21 | 2004-01-29 | Toray Ind Inc | Polyoxymethylene resin composition |
| CN1715381A (en) * | 2004-06-29 | 2006-01-04 | 中国石油化工股份有限公司 | Lubricating oil composite stabilizer and stable hydrogenated lubricating oil composition |
| CN105440580A (en) * | 2014-08-13 | 2016-03-30 | 中国蓝星（集团）股份有限公司 | Fiber reinforced resin matrix composite weatherability improvement composition and application thereof |
| CN107858182A (en) * | 2017-11-15 | 2018-03-30 | 天津利安隆新材料股份有限公司 | A kind of liquid antioxidant composition and its application |
| CN110028700A (en) * | 2018-01-12 | 2019-07-19 | 天津利安隆新材料股份有限公司 | A kind of liquid antioxidant composition for C5 Petropols |
-
2018
- 2018-12-19 CN CN201811560187.5A patent/CN111334054A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004026857A (en) * | 2002-06-21 | 2004-01-29 | Toray Ind Inc | Polyoxymethylene resin composition |
| CN1715381A (en) * | 2004-06-29 | 2006-01-04 | 中国石油化工股份有限公司 | Lubricating oil composite stabilizer and stable hydrogenated lubricating oil composition |
| CN105440580A (en) * | 2014-08-13 | 2016-03-30 | 中国蓝星（集团）股份有限公司 | Fiber reinforced resin matrix composite weatherability improvement composition and application thereof |
| CN107858182A (en) * | 2017-11-15 | 2018-03-30 | 天津利安隆新材料股份有限公司 | A kind of liquid antioxidant composition and its application |
| CN110028700A (en) * | 2018-01-12 | 2019-07-19 | 天津利安隆新材料股份有限公司 | A kind of liquid antioxidant composition for C5 Petropols |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112342074A (en) * | 2020-12-21 | 2021-02-09 | 山东恒利热载体工程技术有限公司 | Regenerated base oil lubricating oil light-resistant and heat-stabilizing agent |
| CN113174283A (en) * | 2021-04-02 | 2021-07-27 | 安徽中天石化股份有限公司 | High-performance phosphate flame-retardant hydraulic oil |
| WO2024160242A1 (en) * | 2023-02-03 | 2024-08-08 | 天津利安隆新材料股份有限公司 | Anti-aging agent composition, use thereof, and anti-aging polymer material |
| CN116218030A (en) * | 2023-03-15 | 2023-06-06 | 上海石化西尼尔化工科技有限公司 | Anti-core burning and anti-oxidation composition and preparation method and application thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN111334054A (en) | Anti-aging composition for stable regenerated oil | |
| JPS63221141A (en) | Stabilized composition and manufacture | |
| JP6961698B6 (en) | Liquid Antioxidant Composition for Raw Rubber | |
| CN104822805B (en) | THPE ethers | |
| CN101665585A (en) | Method for preparing ternary complex antiager and emulsion and application thereof in neoprene | |
| CN115368630B (en) | Liquid antioxidant composition for raw rubber and application thereof | |
| RU2109027C1 (en) | Mixture of stabilizing agents, glue composition | |
| CN104327389A (en) | Rubber use high dispersing insoluble sulfur pre-dispersion mother colloidal particle and preparation method thereof | |
| CN110305366B (en) | Antioxidant stabilizer composition and modified butadiene rubber | |
| ITVA20080038A1 (en) | LIQUID THERMAL STABILIZERS FOR PVC | |
| CN105924650B (en) | A kind of chain alkyl phenyl modified silicon oil and preparation method thereof | |
| CN104530414B (en) | Preparation and application of silica white dispersing agent for rubber products | |
| US3838080A (en) | Waxy composition for preventing rubbery substance from ozone deterioration | |
| CN111333909B (en) | Application of high-carbon alcohol ester hindered phenol antioxidant in C5 petroleum resin | |
| CN102351905B (en) | Organic sulfobenzyl antimony compound and preparation method thereof | |
| JP6461138B2 (en) | A new class of anti-aging agent for rubber products | |
| DE19900829A1 (en) | Stabilizing elastomers against thermal, oxidative, light or ozone-induced degradation | |
| DE2231672A1 (en) | 3,5-DIALKYL-4-HYDROXYPHENYLALCANIC ACID ESTERS OF HYDROXYALKYLHYDROXYAL CANOATES | |
| JPS58167630A (en) | Liquid stabilizer composition for polymer | |
| US2729671A (en) | Method of inhibiting polymerization and product | |
| US2557921A (en) | Stabilization of edible fats and oils | |
| CN113061345B (en) | Warm-mix pouring type asphalt, mixture containing warm-mix pouring type asphalt, and preparation method and application of warm-mix pouring type asphalt | |
| DE1201350B (en) | Stabilizing organic matter | |
| WO2015110754A1 (en) | Polymer-bitumen primary mixtures that can be used for preparing polymer-bitumen binders, and products obtained from these primary mixtures | |
| US2860066A (en) | Stabilized paraffin wax resistant to discoloration by light |
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 | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20200626 |
|
| RJ01 | Rejection of invention patent application after publication |