Extreme pressure anti-corrosion addictive of benzo triazole polysulfide and preparation method thereof
Technical field:
The present invention relates to a kind of organic compound and preparation method thereof, a kind of benzo triazole polysulfide and preparation method thereof particularly, it is used for the lubricating grease extreme pressure anti-corrosion addictive.
Background technology:
Sulphur be additive be the earliest, effect lubricating oil extreme-pressure additive preferably.Sulfide isobutene wherein, thiophosphatephosphorothioate and polysulfide etc. are that to use more sulphur be additive.US4204969 has narrated a kind of extreme-pressure additive that adopts the sulfide isobutene of sulfur monochloride and isobutene reaction preparation as lubricating oil.US5324440 discloses a kind of employing basic surface promoting agent, contains the extreme-pressure anti-friction additive of boron derivative synthetic polysulfide as lubricating grease, its synthetic method more complicated, and also this polysulfide additive has corrodibility.
Nitrogen heterocyclic ring and derivative thereof are the lubricating oil and grease additives of a class excellent property, have good anticorrosively, and anti-oxidant and metal causes functions such as blunt.US2002/0058594 A1 discloses a kind of dimer of thiadiazoles as lubricating oil additive, have very high supporting capacity, but solvability is limited in lubricating oil.US4626368 has narrated the product that a kind of phosphorous acid ester, aldehyde, benzotriazole reaction obtain, and have good high-temperature abrasion resistance and the power of carrying into equally, but phosphoric easily makes the poisoning of catalyst in the automobile exhaust gas processing apparatus, so is restricted.
Summary of the invention:
The object of the present invention is to provide a kind of benzo triazole polysulfide that contains heterocycle structure, this compound has the good extreme pressure property of peculiar erosion resistance of heterocycle structure and polysulfide.Another object of the present invention provides the method for simple synthetic above-claimed cpd, its preparation process condition gentleness.
The chemical name of benzo triazole polysulfide of the present invention be two (1-(benzotriazole base-l-alkyl) polysulfide, its chemical structural formula is as follows:
R in the formula
1Be H, C
1-C
20The straight or branched alkyl; S
xExpression contains the polythioalkane chain of 2 to 6 S atoms.
The concrete preparation method of benzo triazole polysulfide of the present invention is as follows:
Thermometer is being housed, in the three-necked bottle of agitator and prolong, is adding 1-chlorine alkyl benzotriazole and reaction medium, dripping the aqueous solution of the alkali metals polysulfide of 30wt%~44wt% then; The mol ratio of 1-chlorine alkyl benzotriazole and alkali metals polysulfide is 2.0: 0.9~1.3; 1-chlorine alkyl benzotriazole mole number: reaction medium milliliter number is 1: 50~10000; Reacted 2~12 hours down at 25 ℃~150 ℃; Suction filtration removes and desalts, and filtrate is concentrated, uses acetic acid ethyl dissolution, and anhydrous magnesium sulfate drying is used in washing again, filters, and the filtrate decompression distillation removes desolvates, and gets pale brown look thick liquid, is two (1-(benzotriazole base-1-alkyl) polysulfides.
The chemical structural formula of the 1-chlorine alkyl benzotriazole that the present invention uses is as follows;
R in the formula
1Be H, C
1-C
20The straight or branched alkyl; 1-chloromethyl benzo triazole is wherein arranged, 1-chlorine n-propyl benzo triazole, 1-chloro-n-butyl benzotriazole, 1-chlorine isobutyl-benzo triazole, 1-chlorine n-heptyl benzo triazole, the positive decyl benzotriazole of 1-chlorine, 1-chlorine dodecyl benzotriazole etc.
The chemical structural formula of the alkali metals polysulfide that the present invention uses is as follows:
Me
2Sx
Me is Na in the formula
+, K
+Or NH
4 +S
xExpression contains the polythioalkane chain of 2 to 6 S atoms; Sodium disulfide is wherein arranged, three sodium sulphite, sodium tetrasulfide, sodium pentosulfide, three potassium sulphides, four potassium sulphides, five potassium sulphides, three ammonium sulfides or five ammonium sulfides etc.
The reaction medium that the present invention uses is tetrahydrofuran (THF), acetone, water, methyl alcohol, ethanol, n-propyl alcohol, Virahol, propyl carbinol, N, dinethylformamide, dimethyl sulfoxide (DMSO) or 1,4 dioxane.
Reaction equation of the present invention is as follows:
Of the present invention pair (1-(benzotriazole base-1-alkyl) polysulfide can add mineral oil, synthetic oil, vegetables oil to, synthetic ester, polyethers, hydrogenated oil, use in the lubricating greases such as lithium saponify, can obtain the good extreme pressure and the lubricating system of abrasion resistance, also have corrosion resistance simultaneously.
Of the present invention two (1-(benzotriazole base-1-alkyl) polysulfide extreme pressure anti-corrosion addictive, the extreme pressure anti-corrosion addictive that can be used as lubricating grease use separately or and the compound use of other lubricating oil and grease additive, its addition is 0.1wt%~15wt%.
Of the present invention pair (1-(benzotriazole base-1-alkyl) polysulfide possesses the good extreme pressure property of peculiar erosion resistance of heterocycle structure and polysulfide, its synthetic technological condition gentleness, obtain two (1-(benzotriazole base-1-alkyl) polysulfide makes an addition to has good extreme pressure and corrosion resistance in the lubricating grease.Adding 1.0wt%, two (1-(benzotriazole base-1-normal-butyl) polysulfide is in rapeseed oil, and its extreme pressure value is 1.9 times of pure rapeseed oil, and this oil sample is the 1A level at 100 ℃ of following constant temperature 3h to the corrosion of copper sheet.When two (when 1-(benzotriazole base-1-normal-butyl) polysulfide carries out composite use with many sulfuration Trimethylmethanes, when also being 0.6/0.4 and 0.5/0.5 with ratio, have good extreme pressure and antiwear behavior, and can significantly improve the corrosive nature of many sulfuration Trimethylmethanes.
Description of drawings:
Fig. 1 is infrared (IR) of two 1-(benzotriazole base-1-normal-butyl) polysulfides
Fig. 2 be two 1-(benzotriazole base-1-normal-butyl) polysulfides nucleus magnetic resonance (
1H-NMR)
Fig. 3 is the thermogravimetric analysis figure (TG) of two 1-(benzotriazole base-1-normal-butyl) polysulfides
Embodiment:
In order to understand technical scheme of the present invention better, below be described in further detail by specific embodiment.
Embodiment 1:
Take by weighing 0.1mol 1-chloro-n-butyl benzotriazole and 100 milliliters of tetrahydrofuran (THF)s join in the three-necked flask that thermometer, whipping appts, reflux condensing tube are housed, stirred 1 hour.The three sulfuration sodium water solutions that take by weighing 0.055mol 35wt% then slowly are added drop-wise in the three-necked flask, 50 ℃ of reactions 5 hours, are chilled to stirring at room reaction 7 hours then.After reaction finished, suction filtration was removed the salt of generation, and filtrate concentrates, and uses acetic acid ethyl dissolution again, washes with water 3 times, then uses anhydrous magnesium sulfate drying.Filter, filtrate decompression boils off solvent, promptly obtains two 1-(benzotriazole base-1-normal-butyl) the polysulfide 16.67g of pale brown look thickness oily matter, and productive rate is 75.2% (is benchmark with 1-chloro-n-butyl benzotriazole).
Fig. 1 is infrared (IR) spectrogram of two 1-(benzotriazole base-1-normal-butyl) polysulfides, as can be seen: IR (KBr) 3064,1612,1590,1452,782,746cm-1 is the absorption peak of benzotriazole group, 664, and 1092cm-1 is the absorption peak of C-S, 576,615cm-1 is the absorption peak of S-S.
Fig. 2 be two 1-(benzotriazole base-1-normal-butyl) polysulfides nucleus magnetic resonance (
1H-NMR) spectrogram,
1H-NMR (CDCl
3, 400MHz) δ (CDCl wherein
3) 8.08 (d, 2H), 7.76 (d, 2H), 7.57 (t, 2H), 7.42 (t 2H) is all hydrogen on the phenyl ring, 6.70 (s, 2H, N-CH-S) 2.32~2.24 (m, 4H, 2CH
2), 1.52~1.38 (m, 4H, 2CH
2), 0.97 (t, 6H, 2CH
3)
Fig. 3 is the thermogravimetric analysis figure (TG) of two 1-(benzotriazole base-1-normal-butyl) polysulfides, and as can be seen, the temperature of initial decomposition of compound is 216.02 ℃, illustrates that product has thermal stability preferably, can be used as lubricating oil and grease additive.
Embodiment 2:
Take by weighing 0.1mol 1-chlorine n-heptyl benzo triazole and 120 milliliters of ethanol join in the three-necked flask that thermometer, whipping appts, reflux condensing tube are housed, stirred 1 hour.The three sulfuration aqueous ammoniums that take by weighing 0.05mol 30wt% then slowly are added drop-wise in the three-necked flask, 70 ℃ of reactions 7 hours, are chilled to stirring at room reaction 5 hours then.After reaction finished, suction filtration was removed the salt of generation, and filtrate concentrates, and uses acetic acid ethyl dissolution again, washes with water 3 times, then uses anhydrous magnesium sulfate drying.Filter, filtrate decompression boils off solvent, promptly obtains two 1-(benzotriazole base-1-n-heptyl) the polysulfide 19.02g of pale brown look thickness oily matter, and productive rate is 72.3% (is benchmark with 1-chlorine n-heptyl benzo triazole).
The product that obtains in the above-mentioned example, C, H, N, it is as shown in the table for the S results of elemental analyses, from table 1 results of elemental analyses as can be known, the measured value of the C of all target compounds, H, N, S element conforms to substantially with the theoretical value of calculating by molecular formula, absolute error can determine that the gained compound is a target product in allowed band.
Table 1: the results of elemental analyses of various embodiment (in the bracket is calculated value)
| C% | H% | N% | S% | x |
Embodiment 1 embodiment 2 | 54.50(54.73) 60.02(60.15) | 5.61(5.47) 6.68(6.94) | 18.53(19.15) 15.70(16.19) | 20.55(20.65) 16.79(16.72) | 2.83 2.71 |
The performance evaluation of target product:
According to the GB3142-82 standard, the product that obtains in commodity (zinc dialkyl dithiophosphate) ZDDP and example 1 and the example 2 is dispersed in last non seizure load (P in the commercially available refining rapeseed oil
BValue) carried out measuring (addition is 1wt%).Testing used four-ball tester is English home-made Seta-Shell type EP lubricant test machine.Testing used steel ball is secondary standard steel ball (φ 12.7mm, GCr15 bearing steel, HRc are 59-61).Experiment is at room temperature carried out, and rotating speed is 1450 rev/mins.Measured the 392N load down with above-mentioned four-ball tester simultaneously, experimental period 30min, additive level are 1.0wt.%, and rotating speed is the wear scar diameter (WSD) of 1450rpm, and it the results are shown in the table.Table 2 result shows that such novel benzo triazole polysulfide adds to and has good extreme pressure and abrasion resistance in the plant oil based lubricating oil.
Last non seizure load (the P of table 2 base oil and various additives
BBe worth) and
Wear scar diameter WSD (mm) under 392N
Additive | Concentration (wt%) | P
BValue (N)
| WSD(mm) |
Rapeseed oil ZDDP embodiment 1 embodiment 2 | 100 1 1 1 | 549 1049 1049 980 | 0.667 0.412 0.547 0.514 |
In addition, measured the corrosion resistance of the product of preparation in embodiment 1 and the example 2 by the GB5096-85 standard method.After measured as can be known, embodiment 1 and embodiment 2 production concentrations are that the oil sample of 1.0wt% is the 1A level at 100 ℃ of following constant temperature 3h to the corrosion of copper sheet.The presentation of results benzo triazole polysulfide have a good corrosion resistance.
The decomposition temperature of benzo triazole polysulfide is 216.02 ℃, has higher thermostability, is suitable as lubricating oil and grease additive.
Table 3 embodiment 1 and the composite last non seizure load (P of many sulfuration Trimethylmethanes
BValue),
Wear scar diameter WSD (mm) and copper corrosion performance under 392N
| Proportioning | P
BValue (N)
| WSD(mm) | The copper corrosion rank |
Embodiment |
1 embodiment more than 1/ sulfuration Trimethylmethane embodiment more than 1/ sulfuration Trimethylmethane embodiment more than 1/ sulfuration Trimethylmethanes vulcanize Trimethylmethane more | 1.0/0 0.6/0.4 0.5/0.5 0.4/0.6 0/1.0 | 1049 1049 1117 1117 1117 | 0.547 0.510 0.497 0.546 0.524 | 1A 1A 1B 1B 4A |
When above presentation of results proportioning is 0.6/0.4 and 0.5/0.5 for embodiment more than 1/ sulfuration Trimethylmethanes, demonstrate good synergy.