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A random target method for fast MTF inspection is proposed. The setup includes a random target, lens under test and a CCD camera with focus adjustment. The target consists of a random black and white pattern of a flat spectrum. The MTF of the lens is acquired by imaging the random target on the CCD using the lens under test, and then analyzing the spatial frequency content of the image. Frequency range up to about 50 cycles/mm is possible using commonly available CCD imagers. Measurement speed and precision depend on the sample matrix size used in calculation. A matrix of 128*128 samples per measured field point provides better than 2% precision and a few second's total execution time (ordinary PC-computer) per lens including best focus evaluation and the measurement of tangential and sagittal MTF curves of 5 field points. Thus fast MTF inspection of low to medium quality lenses seems possible.

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A time-resolved Raman spectrometer is demonstrated based on a 256×8 CMOS SPAD line sensor and a 573 nm fiber-coupled diamond Raman laser delivering pulses with duration below 100 ps FWHM. The collected back scattered light from the sample is dispersed on the line sensor using a custom volume holographic grating having 1800 lines/mm. Efficient fluorescence rejection in the Raman measurements is achieved due to a combination of time gating on sub-100 ps-time scale and a 573 nm excitation wavelength. To demonstrate the performance of the spectrometer, fluorescent oil samples were measured. For organic sesame seed oil having a continuous wave mode fluorescence-to-Raman ratio of 10.5 and a fluorescence lifetime of 2.7 ns, a signal-to-distortion value of 76.2 was achieved. For roasted sesame seed oil having a continuous wave mode fluorescence-to-Raman ratio of 82 and a fluorescence lifetime of 2.2 ns, a signal-to-distortion value of 28.2 was achieved. In both cases, the fluorescence-to-Raman ratio was reduced by a factor of 24-25 owing to time gating. For organic oil, spectral distortion was dominated by dark counts while for the more fluorescent roasted oil, the main source of spectral distortion was timing skew of the sensor. With the presented post-processing techniques, the level of distortion could be reduced by 88-89 % for both samples. Compared to common 532 nm excitation, approximately 73 % lower fluorescence-to-Raman ratio was observed for 573 nm excitation when analyzing the organic sesame seed oil. Index Terms-Fluorescence rejection, Raman laser, Raman spectrometer, Raman spectroscopy, SPAD sensor, time-correlated single photon counting, time gating, timing skew I. INTRODUCTION AMAN spectroscopy is used in a wide range of fields including food and oil industries, mining industry, medical diagnostics, pharmacy, forensic science and archaeometry [1]