![]() Method of producing bis-(2-ethylamino-4-diethylamino-5-triazine-6-yl) tetra-sulfide
专利摘要:
The invention relates to a process for the preparation of a new triazine-bis- (2-ethylamino-4-diethylamino-5-triazin-6-yl) tetrasulphide derivative (Y 480), which can be used as an additive to vulcanizates. The purpose of the invention is to obtain a new triazine derivative, which gives the vulcanizates higher resistance to reversion than the known structural analogue - the corresponding disulfide. The essence of the invention is that an aqueous alkaline solution of 2-ethylamino-4-diethylamino-6-mercapto-triazine is reacted at 0-5 ° C with a solution of 2CL 2 in a light gasoline environment (bp 80-110 ° C) . 公开号:SU1473712A3 申请号:SU853964938 申请日:1985-10-17 公开日:1989-04-15 发明作者:Шварце Вернер;Вольфф Зигфрид;Реммель Ханс;Ламбертц Хорст 申请人:Дегусса Аг (Фирма); IPC主号:
专利说明:
one The invention relates to a process for the preparation of a novel triazine-bis- (2-ethylamino-4-diethylamino-5-triazin-6-yl) tetrasulfide derivative (480), which can be used as an additive to vulcanizates. The purpose of the invention is to obtain a new triazine derivative, which gives the vulcanizates higher resistance to reversion than the known structural analogue - the corresponding disulfide. Example 1. 454 g of 2-diethylamino-4-ethylamino-5-mercaptotriazine is dissolved in a sodium hydroxide solution prepared from 84 g sodium hydroxide and 1.5 liters of water. The solution is placed in a three-neck flask with a capacity of 4 liters, 1.5 liters of light gasoline is added (so kip. 80-110 ° C), cl with after which the mixture is cooled to ~ C with vigorous stirring. Then a solution of 137 g of S2C12 in 100 ml of gasoline is added over 20 minutes, and the temperature should not exceed + 5 ° C. Tetrasulfide is precipitated. At the end of the reaction, the mixture was further stirred for 5 minutes. The product is filtered and washed. The snow-white fine powder is dried under a vacuum of 12 mm Hg. at 40-45 ° C. Obtain 499.5 g of the target product (97.1% of theory.), So pl. 149-150 ° C, mol. Mass 516. Calculated,%: C 41.9; H 6.2; N 27.1; S 24.8. C 18 H32.NfoS4 Found,%: C 41.8; H 6.5; N 26.8} S 24.8. 4i GO one ND CM 314 Physical tests were performed at room temperature: tensile strength (DIN 53506, MPa); elongation at break and tensile modulus on discs 6 mm thick; tensile strength of the specimen with a notch (DIN 53507, N / mm); rebound elasticity (DIN 53512,%); A-Shore hardness (DIN 53505); Mooney test, ML4 (DIN 53524); Goodrich flexometer (ASTM, ° C); determination of heat generation - HeaL build-up S (D 623-62); Firestone - Ball Rebound (A D 20245). In the examples concerning the application, the names and abbreviations are used: RSS - Ribbed Smoked Sheet (natural rubber); Corax N 220 - carbon black, surface (BET) 120 m2 / g (Degussa); Naphtholen LD - plasticizer from hydrocarbons; Ingralen 450 - plasticizer from aromatic hydrocarbons; ingrplast NS - plasticizer from naphthenic hydrocarbons; Vulcanox 4010 N A - M-isopropyl-N-phenyl-p-phenylenediamine; volcanox HS - poly-2,2,4-trimethyl-1,2-dihydroquinoline; mesamol - esters of alkyl sulfonic acids, phenol and cresol; G35 protector - antiozonant wax; MOL - V-morpholine-2-ben zothiazole sulfenamide; volcacit mercapto - 2-mercaptoben zothiazole; thiuram vulkacit — tetramethylthiurammonosulfide; C-M-cyclohexyl-2-benzothiazole sulfenamide; volcano E - (N-trichloromethylthiophenylsulfonyl) -benzene; PV 1 - N-cyclohexylthiophthalimide; Ultrasil VN3 Gran. - precipitated silicic acid (Degussa), granulate; V 143 - bis- (2-ethylamino-4-diethylamino-5-triazin-6-yl) disulfide „ Example 2. Resistance to reversion with U 480 as a substance crosslinking a macromolecule (carbon black as a filler). , ML4 67 with N 220 zinc RS one 100 50 5 2 100 50 5 3 100 50 five Max MIN at 170 ° C,% 30.0 8.5 2.3 Thus, when applying At 480 without sulfur durability is reached to reversion. j PRI me R 3. The dependence of the ability to reversion on temperature (soot - silicic acid as Mixtures in which carbon black has been partially replaced by silicic acid are especially prone to reversion. In 480 in mixture 6, the substance used as a crosslinking macromolecule, i.e. without sulfur, gives the vulcanizate, even at the highest temperature of vulcanization, a very high resistance to reversion. PRI me R 4. Stability kanizat when overheating, temperature 170 ° C. lowering substance tqsyo; immediately after this, additional heating was performed for 50 min. (t (+ 50 Example5. Resistance to reversion when using U 480 as an accelerator at a vulcanization temperature of 170 C. The strength at break of the sample with notch Firestone Wa 1 Rebound 28 54.9 52.8 53, 51.3 51.7 53, With an increase in reversion at overheating, namely 50/170 ° C, the physical characteristics of the vulcanizates decrease. In this example, the 480 is compared to a semi-Et system, which is considered in accordance with the prior art as a reversion resistance. 95% of the volcano interacted following the example8 15 20 2fr thirty 3.5 3.2 P SSI, ML4 67 Corax N 220 Zinc Oxide RS Stearic acid Naphtholen LD Vulcanox 4010 NA Vulcanox HS G 35 protector Vulkatsit MOL 480 Sulfur D mox R | Tsoie bo 1% / WOKC Tensile strength when stretched Stretching module 300% Elongation at break Firestone-Ball Rebound Combination 1.5 hours. 46.5 45.9 480 with 0.8 h. sulfur, in comparison with the corresponding sulfenamide, remains at 170 ° C completely resistant to reversion, with t, y ./ ", an almost equal level of values is maintained. Example 6. The effect of the amount of sulfur on the properties of U 480 as accelerator (vulcanization temperature 170 ° C). t 10% 3.8 80 20% 1.4 Characteristics of the vulcanizates at MW ": Stretching module 300% 11.5 Shore 63 hardness An increase in sulfur content in excess of 0.8 is possible, and this leads to an increase in modulus without a very strong increase in reversion, in this case. subtitled contraction 67 NA never 2 de 0%) neither 18 100 50 five nineteen 100 50 five 2021 100,100 5050 55 - 1,2 21.5 8.0 17.5 21.0 3.8 2.8 3.8 4.1 10.5 11.0 8.8 13.7 Example Overcoming subvolumeization and modulus enhancement with RSS 1, ML (1 + 4) 67 Corax N 220 Zinc oxide RS Stearic acid Naphtholen LD Vulcanox 4010 NA Vulcanox HS G 35 protector Vulkatsit MOL 480 Vulkalent ESER1, 5 0,8 change that E. M 1,4 3.1 2.9 2.9 2.8 1.6 1.6 1.5 1.5 2.1 6 10 11.4 63 12.1 63 12.5 64 13.1 65 15 Nizko, which can be increased by applying the volcanthus E (see example 7). Example. The effect of a conventional moderator on scorch time and reversion when applied to a 480. 2021 100,100 5050 55 changes in the combination of U 480 and vulkalente E. 25 100 50 five 2 3 2.5 1.5 1 1.5 0.8 0.8 26 100 50 5 2 3 2.5 1.5 1 1.5 1.2 0.8 Scorch time at 13 ° C, min (increase by 2 dividing the scale) Time scorch at 170 ° C (t 10%), min 300% stretch module PRI me R 9. The increase in the time of vulcanization under the action of volc RSS 1, ML (1 + 4) 67 Corax N 220 Ultrasil VN 3 gran. Zinc Oxide RS Stearic Acid Naphetolen LD Vulcanox 4010 Na Vulcanox HS Protector G 35 Vulkacite MOL U 480 PV1 Vulkalent A Vulkalent V Vulkalent E Sulfur Time scorch at 130 ° C, min (increase by 2 dividing the scale) Scorch time at 170 ° C - - 1.5 29.5 4.5 5.3 When a mixture of carbon black and silicic acid is used, the volcano E is effective. When adding 1.5 hours. At 480.0.8 hours gray 1.2 hours of volcanic E, MOL podulcanization time is reached. The moderator does not have an adverse impact resistance: SBR 1712 Corax N 339 Zinc oxide RS Stearinova Protector G 35 Vulcanox 4010 Vulkacite D Vulkacit CL U 480 Sulfur .-G..R- (max -1-6O D AD014S MIN at 165 ° C,% Strength at stretch 21.5 8.0 ten 12.5 16.7 21.0 2.8 3.1 11.0 11.8 3.7 4.1 12.7 13.7 E tape with vulcanization in the presence of Y 480. 33 1.5 - -1.2 -1, 2 1.5 0.80.8 0.8 29.5 16,128.5 30.0 3.6 6.4 4.2 6.4 4.7 8.6 I significant influence on the propensity to reversion during vulcanization in the presence of V 480, as well as on the physical characteristics of the vulcanizate. Example 10. At 480 as an accelerator when using SBR. 31 32 33 37.5 137.5 137.5 60 60 60 3 2 one 1.5 0.5 0.5 1.45 -. 1.5 1.5 3 2 1 1.5 1.6 3 2 1 1.5 1.5 1.5 10.5 7.3 8.3 20 19.2 23.1 111473712 300% stretch module Elongation at break Shore hardness Thus, the U 480 in the resistant to the version of the SBR-mixture additionally increases the resistance to reversion. Example 11. Resistance to the verification of SBR-vulcanizates with 480. 33 34 SBR 1500100 100 Krrax N 22050 50 Zinc Oxide RS 55 Stearic Acid 2 2 Naphtholen LD33, Vulcanox 4010 NA 2.5 2.5 Vulcanox HS1.5 1.5 Protector G 35 11 Vulkatsit CL1,5U 4801 Sulfur1.8 1.8 $ 5 ac. 1l 2 & c ± boO D Max DMHH at 170 ° C,% 12.1 9.1 Characteristics of volcanoes at Ts5u J Strength at stretching 20.2 21.8 Tensile modulus 300% 10.6 11.1 Elongation at break 450 460 The tensile strength of the specimen with a notch 13 14 Shore hardness is 63 64 Thus, the 480 W, when used, the BR 1500, which is slightly prone to reversion, improves the resistance to reversing. Example 12. At 480 in perbunan, nitrile-butadiene rubber). Perbunan N 3307 NS 100 100 Corax N 220 50 50 Zinc Oxide RS 55 Stearic acid 1 1 Ingrated 450 5 5 Mesamol10 10 Vulkatsit CL 1,3- U 480-1,5 Sulfur1.8 1.8 D Ms4s l5iiSja ic tiPlL D max Omni at 170% 9.5 6.9 Characteristics of the vulcanizates: Strength at stretching19.5 18.8 12 10.1 11.4 10.9 480 430 460 63 65 64 9.2 11.3 0 300% stretch module Elongation at break 480 380 Shore hardness 64 65 When applied to 480 instead of sulphinamide in perbunane, an additional 5 each, resistance to reversion is improved. PRI me R 13. At 480 in EPDM. Buna AP 541100 100 Corax N 220 50 50 Zinc Oxide RS 55 0 Stearic acid 1 1 Ingroplast NS 10 10 Vulkatsit thiuram 1 - Vulkatsit mercapto 0.5 - У 480- 2,5 Sulfur1 1 DjjoKo. (MCI K with 460) five D Max -Dj min at 170 ° С,% 3,3 О Characteristics of vul0 kanisates: Strength at stretch 16,0 16,0 Stretching module 300% 14.4 14.0 5 Elongation at break 320 350 Shore hardness 72 69 As a result of applying U 480 to EPDM while maintaining the same In addition, the vulcanizate riser additionally has the possibility of increasing the resistance to reversion. Example 14. Simultaneous application of V 480 and Si 69. RSS1, ML 00 1 00. Corax N 22050 50 RS55 Zinc Oxide Stearic acid2 2 Q Naphtholen LD33 Vulcanox 4010 NA2.5 2.5 Vulcanox HS1,5 1,5 Protector G 35 1 1 480-1,5 5 Si 69-1.5 Sulfur 1.5 0.4 РМОКО Р Сме кс + б / D at 170 ° С,% 29.7 O 13 Characteristics of vulcanization: Strength at stretching25,1 22,0 Modulus of stretching 300% 10.2 10.8 Firestone ball Rebound45.2 44.2 Shore hardness 63 62 Goodrich flexometer If a part of sulfur (0.8 hour) is replaced by a source of sulfur, for example a polysulfide silane, then natural rubber compounds that are reversible and resistant to reversion form. In addition, an unusual decrease in heat generation is observed. Example 15. At 480, crosslinked epoxidized natural rubber using carbon black and silicic acid as a filler. 12 ENR 50100 100 Corax N 330 25 25 Ultrasil VN 3 Gran. 25 25 Zinc oxide RS 55 Stearic acid 2 2 Vulcanox HS 22 W 480-3 Vulkatsit MOL 2,4 - Vulkatsit thiuram 1,6 - Sulfur0.3 0.3 73712 4 Strength at stretch Dispersion of solids Module of stretching 100% The tensile strength of the specimen with notch A-Shore hardness at 23 ° C 15.1 15.6 ten 8.4 82 11.0 eight 89 Example 16. At 480, crosslinked natural rubber 15, seamed, when filled with carbon black. ENR Corax N 220 Zinc Oxide RS Stearic acid Vulcanox HS 480 Vulkatsit MOL Vulkatsit Tiuram Sulfur Strength at stretching Stretching module 300% Breaking Strength specimen notched A-shore hardness at 23 ° C 75 80
权利要求:
Claims (1) [1] METHOD FOR PRODUCING BIS- (2ETHYLAMINO-4-DIETHYLAMINO-5-TRIAZIN- 6-IL) -TETRASULPHIDE, characterized in that the aqueous alkaline solution of 2-ethylamino-4-diethylamino-6mercaptotriazine is introduced into the reaction at a temperature of 0-5 C with a solution of S 2 C1 2 in light gasoline (boil. 80110 ° C).
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同族专利:
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引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 DE1669954C3|1951-01-28|1974-05-22|Degussa| US3923724A|1951-01-28|1975-12-02|Degussa|Processes for improving the processing characteristics of vulcanized elastomers| JPS478134Y1|1967-05-18|1972-03-28| US3635903A|1967-11-02|1972-01-18|Stauffer Chemical Co|Curing system for polymeric rubber materials| DE2848559C2|1978-11-09|1982-01-21|Degussa Ag, 6000 Frankfurt|Rubber mixtures resulting in reversion-free vulcanizates and their use| DE3014717A1|1980-04-17|1981-10-22|Bayer Ag, 5090 Leverkusen|VULCANIZATION SYSTEM, THIS CONTAINING RUBBER MIX, AND A METHOD FOR VULCANIZATION| JPS57175174A|1981-04-22|1982-10-28|Japan Synthetic Rubber Co Ltd|Trithiotriazine compound and vulcanization of rubber using the same| DE3610794C2|1986-04-01|1995-02-09|Degussa|N, N'-substituted bis- tetrasulfides, processes for their preparation and their use in vulcanizable rubber mixtures| DE3630055C2|1986-09-04|1997-04-10|Swan Thomas & Co Ltd|Process for the preparation of sulfur-containing triazine compounds|JPH0627129B2|1985-10-31|1994-04-13|三井石油化学工業株式会社|Chlorinated rubber| DE3610794C2|1986-04-01|1995-02-09|Degussa|N, N'-substituted bis-tetrasulfides, processes for their preparation and their use in vulcanizable rubber mixtures| DE3610811A1|1986-04-01|1987-10-08|Degussa|USE OF SUBSTITUTED N-TRICHLORMETHYLTHIODICARBOXIMIDES IN COMBINATION WITH N; N'-SUBSTITUTED BIS--OLIGOSULFIDES IN VULCANIZABLE RUBBER RUBBERS| DE3630055C2|1986-09-04|1997-04-10|Swan Thomas & Co Ltd|Process for the preparation of sulfur-containing triazine compounds| DE3820969A1|1988-06-22|1989-12-28|Degussa|BISPOLYSULFANE, METHOD FOR THE PRODUCTION THEREOF AND VULCANIZABLE RUBBER MIXTURES CONTAINING THEREOF| US5118546A|1990-08-03|1992-06-02|The Goodyear Tire & Rubber Company|Blend of polychloroprene and epoxidized natural rubber| IL106891A|1992-09-04|1997-07-13|Moore Co|ENR-NR composition| DE4340902C2|1992-12-05|2001-05-31|Phoenix Ag|Use of a rubber compound for the production of rubber springs and rubber couplings| US5396940A|1993-09-17|1995-03-14|The Goodyear Tire & Rubber Company|Sulfur cured rubber composition containing epoxidized natural rubber and silica filler| DE4415720C2|1994-05-05|1997-09-25|Uniroyal Englebert Gmbh|Tire carcass, its manufacture and use| DE4437646C2|1994-10-21|1999-01-14|Uniroyal Englebert Gmbh|Tire comprising lateral cushions| DE19858706A1|1998-12-18|2000-06-21|Pulver Kautschuk Union Gmbh|Rubber powderand process for their preparation| CN102667634B|2009-12-22|2016-02-24|佳能株式会社|Charging member, electronic photographing device and handle box| EP2471851A1|2010-12-29|2012-07-04|LANXESS Deutschland GmbH|Vulcanisable compounds based on nitrile rubbers containing epoxy groups| JP5663455B2|2011-10-26|2015-02-04|住友ゴム工業株式会社|Paper feed roller and rubber composition| JP5855931B2|2011-12-26|2016-02-09|株式会社ブリヂストン|Rubber composition for conveyor belt and conveyor belt| US9238730B2|2012-01-30|2016-01-19|Bridgestone Corporation|Anti-vibration rubber composition, crosslinked anti-vibration rubber composition, and anti-vibration rubber|
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申请号 | 申请日 | 专利标题 DE19843438290|DE3438290A1|1984-10-19|1984-10-19|BIS-TETRASULFIDE, METHOD FOR THE PRODUCTION, USE AND VULCANIZABLE MIXTURES CONTAINING THE SAME| 相关专利
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