Abstract: A vehicle body front part structure has an apron side panel 5 joined to an apron side member 4 extending along the vehicle longitudinal direction, and a tray 14 for battery supported on the apron side member 4. In the front part structure, a leg part 16 is provided in an tray body part 15, a lower end part 16K of the leg part 16 is fixed to the apron side member 4 with a fixing member B, and the leg part 16 is formed of a plate material so that the deformation of the apron side member 4 is allowed when a vehicle longitudinal force is applied to the apron side member 4.
Abstract: A cover 1b of a battery pack case has an intake port and an exhaust port 31. With in the battery pack case, battery accommodation sections respectively accommodate battery modules and a junction box accommodation section. A supply flow path and an exhaust flow path are provided at ends of each of the battery accommodation section. A guide is provided between the cover and the battery modules accommodated in the battery accommodation portions. The guide and a lower surface of the cover define a distribution flow path. The air introduced from the intake port flows to the exhaust port through the distribution flow path, supply flow paths, clearances between battery cells, exhaust flow paths, and exhaust port. The battery cells are efficiently cooled.
Type:
Application
Filed:
June 5, 2012
Publication date:
December 13, 2012
Applicants:
SUZUKI MOTOR COPORATION, Lithium Energy Japan
Abstract: A pillar structure of a vehicle body includes a pillar that forms a closed cross-sectional structure made up of an outer panel and an inner panel and that extends substantially along the vertical direction. The inner panel defines an opening and a reinforcing member is joined to a part including at least the periphery of the opening in the inner panel of the pillar.
Abstract: A protein derived from human plasminogen which has amino acids 355-791 of human plasminogen are purified. A method for purifying said protein and angiostatin comprises the steps of fractionating said protein by Lysine-Sepharose chromatography to separate plasminogen in Form 1 and Form 2 and applying separately each of them to a Lysine-Sepharose column in order.