Compared with conventional camera, the light field camera takes the advantage of being capable of recording the direction and intensity information of each ray projected onto the CCD (charge couple device) sensor simultaneously. In this paper, a novel method is proposed for reconstructing three-dimensional (3-D) temperature field of a flame based on a single light field camera. A radiative imaging of a single light field camera is also modeled for the flame. In this model, the principal ray represents the beam projected onto the pixel of the CCD sensor. The radiation direction of the ray from the flame outside the camera is obtained according to thin lens equation based on geometrical optics. The intensities of the principal rays recorded by the pixels on the CCD sensor are mathematically modeled based on radiative transfer equation. The temperature distribution of the flame is then reconstructed by solving the mathematical model through the use of least square QR-factorization algorithm (LSQR). The numerical simulations and experiments are carried out to investigate the validity of the proposed method. The results presented in this study show that the proposed method is capable of reconstructing the 3-D temperature field of a flame.
This study evaluated the biodistribution and organ oxidative effects of silver nanoparticles (AgNPs) coated with/without polyvinylpyrrolidone (PVP) (AgNP‐20 and AgNP‐PVP) in mice; these were administered by gavage at a dose of 10‐250 mg/kg body weight per day for 28 days. The results showed that both the AgNPs could induce subacute toxicity and oxidative damage to mice and were mainly accumulated in the liver and spleen and excreted by feces. AgNPs could be absorbed into blood and might cross the blood‐brain barrier, and be distributed extensively in mice. The malondialdehyde content in the liver, lungs and kidneys increased in both AgNP groups, while the content of glutathione decreased, and the activity of superoxide dismutase increased at first and then decreased along with the increased doses. Inflammatory pathological changes in the lung and liver at high dose of both AgNPs were consistent with increases in glutamate pyruvic transaminase, glutamate oxaloacetic transaminase and the total protein in serum detection. The Ag content was detected in organs, with the highest content in the liver, followed by spleen, while the Ag content in feces was about 500 times higher than that in urine. AgNP‐PVP could induce higher oxidative stress and subacute toxicity than AgNP‐20 at the same dose, which might be related to the higher concentrations and more Ag+ ions released in mice after AgNP‐PVP exposure. The data from this research provided information on toxicity and biodistribution of AgNPs following gavage administration in mice, and might shed light for future application of AgNPs in daily life.
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