Abstract: Disclosed is a speed reduction device for a vehicle motor. The speed reduction device includes an output gear connected to an output shaft of the motor, a transmission gear engaged with the output gear, a cam formed to be integrated with the transmission gear, a cycloid inner gear, a pair of wedges compressed against the inner peripheral surface of a through hole of the cycloid inner gear by elastic restoring force of a spring and configured to closely contact the cam, a ring gear partially engaged with the cycloid inner gear when the cycloid inner gear is eccentrically rotated, an end plate, and a final output gear configured to finally output rotational force of the cycloid inner gear, thereby preventing backlash between gears during rotational driving of the motor and reliably preventing movement of a seat after swivel adjustment is completed.

Abstract: A method for preparing a phenolic oligomer antioxidant with a very small residual content of butylated hydroxytoluene (BHT) is provided. Specifically, the method for preparing the phenolic oligomer antioxidant relates to a method which is capable of a BHT-free phenolic oligomer antioxidant or a phenolic oligomer antioxidant containing a trace amount of residual BHT by removing the precursor of BHT as much as possible by performing the concentration under the reduced pressure while injecting an inert gas to an intermediate product and/or removing BHT by performing the concentration under the reduced pressure while injecting an inert gas to the final product.

Abstract: A method for preparing a phenolic oligomer antioxidant with a very small residual content of butylated hydroxytoluene (BHT) is provided. Specifically, the method for preparing the phenolic oligomer antioxidant relates to a method which is capable of a BHT-free phenolic oligomer antioxidant or a phenolic oligomer antioxidant containing a trace amount of residual BHT by removing the precursor of BHT as much as possible by performing the concentration under the reduced pressure while injecting an inert gas to an intermediate product and/or removing BHT by performing the concentration under the reduced pressure while injecting an inert gas to the final product.

Abstract: Provided are novel thio compounds and a method for preparing the same. More particularly, there is provided a novel thio compound prepared by reacting an alkylation product of p-cresol and dicyclopentadiene with mercaptan and paraformaldehyde. Unlike existing antioxidants such as 2,6-di-t-butyl-4-methylphenol (BHT) being harmful to the human body due to the high volatility, the novel thio compounds of the present invention, which have the low volatility because of their high molecular weight, give no harm to the human body. Further, with excellent performances, they are suitable to replace the existing antioxidants.

Abstract: Disclosed are a novel anti-oxidant for rubber and a synthetic rubber including the same. The disclosed anti-oxidant contains a thio compound. The rubber including the anti-oxidant has excellent thermostability at a temperature of 100° C. or higher, and the anti-oxidant shows a low volatility due to its high molecular weight thus being applicable to manufacture environment-friendly rubber.

Abstract: Disclosed are a novel anti-oxidant for rubber and a synthetic rubber including the same. The disclosed anti-oxidant contains a thio compound. The rubber including the anti-oxidant has excellent thermostability at a temperature of 100° C. or higher, and the anti-oxidant shows a low volatility due to its high molecular weight thus being applicable to manufacture environment-friendly rubber.

Abstract: Provided are novel thio compounds and a method for preparing the same. More particularly, there is provided a novel thio compound prepared by reacting an alkylation product of p-cresol and dicyclopentadiene with mercaptan and paraformaldehyde. Unlike existing antioxidants such as 2,6-di-t-butyl-4-methylphenol (BHT) being harmful to the human body due to the high volatility, the novel thio compounds of the present invention, which have the low volatility because of their high molecular weight, give no harm to the human body. Further, with excellent performances, they are suitable to replace the existing antioxidants.