The present invention discloses a quantitative evaluation method for sensitivity of welding transverse cold cracks in a typical joint of a jacket, including following steps: S1, performing macroscopic analysis, metallographic analysis, fracture analysis and hardness analysis on cracks of a failed component to obtain main causes of cold crack failure; and S2, designing and processing a dedicated sample, and performing rigid restraint crack tests on the dedicated sample at different preheating temperatures to obtain a cracking/non-cracking critical restraint stress σ1cr of the sample. According to the method, a rigid restraint crack test is applied to evaluation of sensitivity of welding transverse cracks, so that external restraint conditions borne by a welding joint can be accurately simulated, a stress state of the welding joint in an actual working condition can be truly reflected, the overall evaluation precision is greatly improved, and a foundation is laid for accurately evaluating sensitivity of welding cold cracks in a tube joint. Furthermore, a welding technology (base material, welding material, welding process and restraint level) is designed to restrain cold cracks from cracking, and the method has important theoretical significance and engineering value.

The present invention discloses a quantitative evaluation method for sensitivity of welding transverse cold cracks in a typical joint of a jacket, including following steps: S1, performing macroscopic analysis, metallographic analysis, fracture analysis and hardness analysis on cracks of a failed component to obtain main causes of cold crack failure; and S2, designing and processing a dedicated sample, and performing rigid restraint crack tests on the dedicated sample at different preheating temperatures to obtain a cracking/non-cracking critical restraint stress σ1cr of the sample. According to the method, a rigid restraint crack test is applied to evaluation of sensitivity of welding transverse cracks, so that external restraint conditions borne by a welding joint can be accurately simulated, a stress state of the welding joint in an actual working condition can be truly reflected, the overall evaluation precision is greatly improved, and a foundation is laid for accurately evaluating sensitivity of welding cold cracks in a tube joint. Furthermore, a welding technology (base material, welding material, welding process and restraint level) is designed to restrain cold cracks from cracking, and the method has important theoretical significance and engineering value.

An apparatus comprising an ion selecting device; an individual ion counter device; and an interface device integral with the ion selecting device and downstream of an ion separating chamber of the ion selecting device. The interface device comprises a tagging particle generator and a tagging chamber. Sample gas containing ions of a selected mobility enters the tagging chamber from the ion selecting device and is exposed to uncharged neutral tagging particles from the tagging particle generator. The ions collide with the tagging particles to form a mixture of tagged ions and uncharged neutral tagging particles which is then separated in a tagged ions separator forming part of the individual ion counting device before the separated tagged ions are counted.

An apparatus comprising an ion selecting device; an individual ion counter device; and an interface device integral with the ion selecting device and downstream of an ion separating chamber of the ion selecting device. The interface device comprises a tagging particle generator and a tagging chamber. Sample gas containing ions of a selected mobility enters the tagging chamber from the ion selecting device and is exposed to uncharged neutral tagging particles from the tagging particle generator. The ions collide with the tagging particles to form a mixture of tagged ions and uncharged neutral tagging particles which is then separated in a tagged ions separator forming part of the individual ion counting device before the separated tagged ions are counted.

A pulse shaping circuit for a spectrometer comprises a circuit input terminal for receiving detector pulses from an analog ion detector, a flip-flop for receiving detector pulses from the circuit input terminal, a delay unit for receiving output pulses from the flip-flop and feeding delayed output pulses to a reset input terminal of said flip-flop, and a circuit output terminal for supplying the output pulses or the delayed output pulses to a counter. The duration of the output pulses and the minimum duration of the interval between the output pulses is determined by the delay unit. The pulse shaping circuit may comprise at least one Schmitt trigger.

A pulse shaping circuit for a spectrometer comprises a circuit input terminal for receiving detector pulses from an analog ion detector, a flip-flop for receiving detector pulses from the circuit input terminal, a delay unit for receiving output pulses from the flip-flop and feeding delayed output pulses to a reset input terminal of said flip-flop, and a circuit output terminal for supplying the output pulses or the delayed output pulses to a counter. The duration of the output pulses and the minimum duration of the interval between the output pulses is determined by the delay unit. The pulse shaping circuit may comprise at least one Schmitt trigger.

A first liquid raw material and a second liquid raw material are reacted with each other by a reactor of a reaction device, so that a reaction product is produced. The reaction product is analyzed by an analyzer. In the controller, the reference value is acquired by the reference value acquirer from the chromatogram obtained from the result of the analysis by the analyzer. An upper limit value and a lower limit value with respect to the reference value are set by an allowable range setter. At least one of a residence time of the first liquid raw material, a residence time of the second liquid raw material, a reaction temperature, and a reaction pressure in the reactor is dynamically changed as a control target by a reaction controller such that the reference value falls between the upper limit value and the lower limit value.

The present invention relates to a separation method comprising: i) providing an aqueous solution comprising a target compound; ii) applying a separation step to the aqueous solution, thereby providing a plurality of fractions of the aqueous solution: iii) determining a concentration parameter indicating a concentration of the target compound in at least part of the fractions; iv) determining a nuclear magnetic resonance (NMR) parameter by applying an NMR measurement to the fractions, the NMR parameter indicating a nuclear magnetic spin relaxation in said at least part of the fractions; and v) determining a target parameter of said at least part of the fractions based on the concentration parameter and the nuclear magnetic resonance parameter. The present invention further relates to separation systems, uses, preparations, and methods related thereto.

The present invention relates to a separation method comprising: i) providing an aqueous solution comprising a target compound; ii) applying a separation step to the aqueous solution, thereby providing a plurality of fractions of the aqueous solution: iii) determining a concentration parameter indicating a concentration of the target compound in at least part of the fractions; iv) determining a nuclear magnetic resonance (NMR) parameter by applying an NMR measurement to the fractions, the NMR parameter indicating a nuclear magnetic spin relaxation in said at least part of the fractions; and v) determining a target parameter of said at least part of the fractions based on the concentration parameter and the nuclear magnetic resonance parameter. The present invention further relates to separation systems, uses, preparations, and methods related thereto.

A portable gas analysis device having a separating column and a detector. The separating column is composed as a multi-capillary unit from parallel individual capillaries and, depending on the length, is bent into a compact shape, preferably even wound into multiple turns. A thermally conductive casing and a thermal stabilizing device are provided for the multi-capillary unit. The thermal stabilizing device comprises a temperature sensor, a heating element and control electronics. The casing protects the sensitive multi-capillary unit from mechanical actions; it acts as a protective space. The temperature-controlled casing also forms a space in which uniform and controlled conditions prevail and which in particular is isolated from the temperature and humidity of the environment, allowing reliable measurements outside a laboratory environment, in the field. This double effect of the casing for the capillaries in conjunction with the compact dimensions forms the true essence of the invention.