METHOD FOR PREPARING BUTYRONITRILE RUBBER POWDER-BASED PVC THERMOPLASTIC ELASTOMER AND USE OF BUTYRONITRILE RUBBER POWDER-BASED PVC THERMOPLASTIC ELASTOMER IN PREPARING AUTOMOTIVE PARTS

20230074196 · 2023-03-09

    Inventors

    Cpc classification

    International classification

    Abstract

    A method for preparing a butyronitrile rubber powder-based polyvinyl chloride (PVC) thermoplastic elastomer and a use of the butyronitrile rubber powder-based PVC thermoplastic elastomer in preparing automotive parts are provided. The method includes: activating a wasted nitrile butadiene rubber (NBR) powder; plasticizing one of NBR and chloroprene rubber (CR) to obtain a plasticized rubber; dispersing the activated NBR fine rubber powder with one of PVC and chlorinated polyethylene (CPE) in a kneader evenly to obtain a mixture; adding the mixture and pine tar into the plasticized rubber, then mixing evenly to obtain a mixed plastic; adding various compounding agents into the mixed plastic and dispersing evenly to perform cross-linking reaction, thereby obtaining the butyronitrile rubber powder-based PVC thermoplastic elastomer. By using the wasted NBR powder as a main material, which turns waste into treasure and has low cost, and the butyronitrile rubber powder-based PVC thermoplastic elastomer has excellent comprehensive performance.

    Claims

    1. A method for preparing a butyronitrile rubber powder-based polyvinyl chloride (PVC) thermoplastic elastomer, wherein the butyronitrile rubber powder-based PVC thermoplastic elastomer comprises: raw materials in parts by weight as follows: one of PVC and chlorinated polyethylene (CPE) with 15 to 20 parts by weight; one of nitrile butadiene rubber (NBR) and chloroprene rubber (CR) with 15 to 20 parts by weight; a wasted NBR powder with 60 to 70 parts by weight; a regenerant with 2 parts by weight; pine tar with 15 parts by weight; a compatibilizer with 0.8 to 1.3 parts by weight; a vulcanizing agent with 0.3 parts by weight; a zinc oxide with 5 parts by weight; a steric acid with 0.3 parts by weight; and an antioxidant 1010 with 0.3 parts by weight; wherein the method comprises: adding the regenerant to the wasted NBR powder and activating for 30 min at 200° C. to obtain an activated NBR fine rubber powder; plasticizing the one of the NBR and CR at room temperature for 5 min to obtain a plasticized rubber; dispersing the activated NBR fine rubber powder with the one of the PVC and the CPE in a kneader evenly to obtain a mixture; adding the mixture and the pine tar into the plasticized rubber at a range of 160° C. to 165° C., and then mixing evenly to obtain a mixed plastic; adding the vulcanizing agent, the compatibilizer, the zinc oxide, the stearic acid and the antioxidant 1010 to the mixed plastic and dispersing evenly in a twin-screw extruder at 180° C. to perform cross-linking reaction with a help of a dynamic cross-linking system and a mechanical shear stress, thereby obtaining the butyronitrile rubber powder-based PVC thermoplastic elastomer and molding into sheets.

    2. The method according to claim 1, wherein a particle size of the wasted NBR powder is equal to or greater than 100 meshes.

    3. The method according to claim 1, wherein the one of the PVC and the CPE is powdered.

    4. The method according to claim 1, wherein the vulcanizing agent is sulfur.

    5. The method according to claim 1, wherein the compatibilizer is bis (tert-butyldioxyisopropl) benzene.

    6. The method according to claim 1, wherein a length-to-diameter ratio of a screw of the twin-screw extruder is 26 and a compression ratio of the screw of the twin-screw extruder is 3.

    7. A use of the butyronitrile rubber powder-based PVC thermoplastic elastomer prepared by the method according to claim 1 in preparing automotive parts.

    8. The use according to claim 7, wherein a particle size of the wasted NBR powder is equal to or greater than 100 meshes.

    9. The use according to claim 7, wherein the one of the PVC and the CPE is powdered.

    10. The use according to claim 7, wherein the vulcanizing agent is sulfur.

    11. The use according to claim 7, wherein the compatibilizer is bis (tert-butyldioxyisopropl) benzene.

    12. The use according to claim 7, wherein a length-to-diameter ratio of a screw of the twin-screw extruder is 26 and a compression ratio of the screw of the twin-screw extruder is 3.

    13. An automotive part, wherein the automotive part is made from the butyronitrile rubber powder-based PVC thermoplastic elastomer prepared by the method according to claim 1.

    Description

    DETAILED DESCRIPTION OF EMBODIMENTS

    [0031] The disclosure is further explained in conjunction with specific embodiments.

    [0032] Embodiment 1

    [0033] Adding 0.3 Kg regenerant to 19.5 Kg wasted NBR powder, which is equal to or greater than 100 meshes and activating for 30 min at 200° C.

    [0034] Plasticizing 6.0 Kg NBR at room temperature for 5 min to obtain a NBR plasticized rubber; dispersing the activated NBR fine rubber powder with 4.5 Kg PVC powder in a kneader evenly to obtain a mixture; adding the mixture and 4.5 Kg pine tar into the NBR plasticized rubber at a range of 160° C. to 165° C., and then mixing evenly to obtain a mixed plastic.

    [0035] Adding 0.09 Kg sulfur, 0.33 Kg BIBP, 1.5 Kg zinc oxide, 0.09 Kg stearic acid, 0.09 Kg antioxidant 1010 to the mixed plastic and dispersing evenly in a twin-screw extruder (a length-to-diameter ratio of a screw is 26, compression ratio of the screw is 3) at 180° C. to perform cross-linking reaction with a help of a dynamic cross-linking system and a mechanical shear stress, thereby obtaining a butyronitrile rubber powder-based PVC thermoplastic elastomer and molding into sheets.

    [0036] Embodiment 2

    [0037] Adding 0.3 Kg regenerant to 19.5 Kg wasted NBR powder, which is equal to or greater than 100 meshes and activating for 30 min at 200° C.

    [0038] Plasticizing 4.5 Kg NBR at room temperature for 5 min to obtain a NBR plasticized rubber; dispersing the activated NBR fine rubber powder with 6.0 Kg PVC powder in a kneader evenly to obtain a mixture; adding the mixture and 4.5 Kg pine tar into the NBR plasticized rubber at a range of 160° C. to 165° C., and then mixing evenly to obtain a mixed plastic.

    [0039] Adding 0.09 Kg sulfur, 0.33 Kg BIBP, 1.5 Kg zinc oxide, 0.09 Kg stearic acid, 0.09 Kg antioxidant 1010 to the mixed plastic and dispersing evenly in a twin-screw extruder (a length-to-diameter ratio of a screw is 26, a compression ratio of the screw is 3) at 180° C. to perform cross-linking reaction with a help of a dynamic cross-linking system and a mechanical shear stress, thereby obtaining a butyronitrile rubber powder-based PVC thermoplastic elastomer and molding into sheets.

    [0040] Embodiment 3

    [0041] Adding 0.3 Kg regenerant to 19.5 Kg wasted NBR powder, which is equal to or greater than 100 meshes and activating for 30 min at 200° C.

    [0042] Plasticizing 6.0 Kg CR at room temperature for 5 min to obtain a CR plasticized rubber; dispersing the activated NBR fine rubber powder with 4.5 Kg CPE powder in a kneader evenly to obtain a mixture; adding the mixture and 4.5 Kg pine tar into the CR plasticized rubber at a range of 160° C. to 165° C., and then mixing evenly to obtain a mixed plastic.

    [0043] Adding 0.09 Kg sulfur, 0.33 Kg BIBP, 1.5 Kg zinc oxide, 0.09 Kg stearic acid, 0.09 Kg antioxidant 1010 to the mixed plastic and dispersing evenly in a twin-screw extruder (a length-to-diameter ratio of a screw is 26, a compression ratio of the screw is 3) at 180° C. to perform cross-linking reaction with a help of a dynamic cross-linking system and a mechanical shear stress, thereby obtaining a butyronitrile rubber powder-based PVC thermoplastic elastomer and molding into sheets.

    [0044] Test of performance of the butyronitrile rubber powder-based PVC thermoplastic elastomers respectively made in embodiments 1-3 according to GB/T21874-2008 includes results as follows.

    TABLE-US-00001 TABLE 1 performance of the butyronitrile rubber powder-based PVC thermoplastic elastomer Embodiments Testing items GB/T21874-2008 Embodiment 1 Embodiment 2 Embodiment 3 Shore Hardness 50 ± 5 ≤ Hardness ≤ 70 ± 5 61 67 56 Tensile Strength/MPa ≥3.0 8.05 9.82 4.18 Elongation at Tear/% ≥300 323 301 312 Compression set of ≤25 23.84 22.56 17.68 treating with 23° C. for 72 h/% max and min hardness ±5 +5 +5 +5 changes, max and min ±10 +2.02 −3.59 −0.77 strength change ±15 +0.59 +10.08 +3.34 rates, max and min elongation change rates of thermal and oxygen aging test at 70° C. for 7 days Ozone resistance No cracks when observed No cracks No cracks No cracks under unmagnified conditions Volume change in −1~+8 +7.86 +7.52 +7.92 water at 70° C. for 7 days/% Volume change in −10~+50 +0.45 −0.14 +7.71 No. 1 standard oil at 70° C. for 72 h/%

    [0045] As can be seen from Table 1, performance indexes of the butyronitrile rubber powder-based PVC thermoplastic elastomer made by the method far exceed and meet requirements of the international standard GB/T21874-2008 “Elastomeric seals-Requirements for materials for pipe joint seals used in water and drainage applications-Thermoplastic elastomers”, which indicates that the butyronitrile rubber powder-based PVC thermoplastic elastomer made by the method can be used in producing automotive parts, such as fuel pipe seals.