By use of a pump light source for repeatedly generating a pump light pulse and a probe light source for repeatedly generating a probe light pulse in a shorter repetition time interval than the pump light pulse, the pump light pulse is repeatedly irradiated on a sample, and the probe light pulse is repeatedly irradiated on the sample every time the pump pulse is irradiated. An intensity of a probe light pulse having passed through the sample is detected. A shift in a delay time of the probe light pulse with respect to the pump light pulse is measured every time the pump light pulse is irradiated. Transient absorption measurement data of the sample is obtained based on the detected data of the probe light pulse intensity obtained in higher time density than repetition time density of the probe light pulse based on the measured shift in the delay time.

By use of a pump light source for repeatedly generating a pump light pulse and a probe light source for repeatedly generating a probe light pulse in a shorter repetition time interval than the pump light pulse, the pump light pulse is repeatedly irradiated on a sample, and the probe light pulse is repeatedly irradiated on the sample every time the pump pulse is irradiated. An intensity of a probe light pulse having passed through the sample is detected. A shift in a delay time of the probe light pulse with respect to the pump light pulse is measured every time the pump light pulse is irradiated. Transient absorption measurement data of the sample is obtained based on the detected data of the probe light pulse intensity obtained in higher time density than repetition time density of the probe light pulse based on the measured shift in the delay time.

A total nitrogen measurement apparatus comprising an ultraviolet lamp comprising: a light emission section and a holding section for holding the light emission section, the holding section being formed of a material not including iron; a reaction vessel having a space where the light emission section is to be inserted and a sample water is to be contained around the light emission section for converting nitrogen compounds in the sample water contained in the reaction vessel into nitrate ions by oxidative decomposition using ultraviolet rays from the light emission section; and a measurement section configured to perform absorbance measurement on the sample water including the nitrate ions.

Systems and methods of in vivo and in vitro radical protein foot-printing using an opto-fluidic array are presented. These teachings may be used to, for example, study three-dimensional protein structure or bio-kinetics. Radical dosimetry including an optional intrinsic standard is used. Real-time feedback based on an internal standard provides comparability between different experiments and in vivo and in vitro analysis results in data that is representative of actual biological conditions.

The present invention provides a photolytic converter for converting reactant molecules in a fluid sample into product molecules by photolytic dissociation with electromagnetic radiation. The converter has a reaction chamber in communication with one or more electromagnetic radiation sources, an inflow conduit for conveying the fluid sample into the reaction chamber, and an outflow conduit for conveying the fluid sample out of the reaction chamber into a receptacle, wherein at least one of the first and outflow conduits extends into the reaction chamber. The receptacle can comprise detection means for generating a signal indicative of a concentration of product molecules in the processed fluid sample.

The present disclosure provides a vacuum ultraviolet (VUV) detector for use with a liquid chromatography (LC) system (otherwise referred to herein as an LC-VUV detector) for the study of liquids. The LC-VUV detector incorporates an ultra-short pathlength flow cell into the LC-VUV detector to render liquid samples at least semi-transparent to VUV light. The ultra-short pathlength flow cell is specifically designed to: (a) interface with a focused beam of VUV light, (b) provide zero dead volume, resulting in perfectly laminar flow through the flow cell, and (c) be modular and removable, allowing flow cells of different pathlength to be used within the LC-VUV detector. Methods for analyzing liquid samples using the LC-VUV detector and flow cell disclosed herein are also provided in the present disclosure.

The present disclosure provides a vacuum ultraviolet (VUV) detector for use with a liquid chromatography (LC) system (otherwise referred to herein as an LC-VUV detector) for the study of liquids. The LC-VUV detector incorporates an ultra-short pathlength flow cell into the LC-VUV detector to render liquid samples at least semi-transparent to VUV light. The ultra-short pathlength flow cell is specifically designed to: (a) interface with a focused beam of VUV light, (b) provide zero dead volume, resulting in perfectly laminar flow through the flow cell, and (c) be modular and removable, allowing flow cells of different pathlength to be used within the LC-VUV detector. Methods for analyzing liquid samples using the LC-VUV detector and flow cell disclosed herein are also provided in the present disclosure.