PubMed Health⌕ Search

PubMed · 8579702

Crash pulse recorder--validation in full scale crash tests.

Abstract

Estimation of the accident severity is a fundamental requirement in accident reconstruction and analysis. Accident severity can be measured in many different ways, but in frontal collisions change of velocity, energy equivalent speed or equivalent barrier speed are frequently used parameters. These parameters are most often estimated from vehicle deformation. It is known, however, that the quality of these estimates is limited if compared with these obtained in laboratory test conditions. To be able to achieve almost the same measurements and measurement accuracy in real-life accidents as in the laboratory, where the acceleration time history is measured, an on-board measurement technique is required. This presentation gives results of tests of a low cost device for measuring the crash pulse for a car involved in an accident, concerning systematic and random error. The device, called the Crash Pulse Recorder (CPR), has been tested previously in several sled tests. The CPR is based on measurement of the movement of the mass in a spring mass system in a collision. A brief description of its construction is also included. The CPR is an integral part of a large accident data collection system including interior and exterior deformation measurements and evaluation of injury outcome. This report presents the results of several full-scale crash tests, undertaken to evaluate the accuracy and precision of the CPR in cars in different impact modes. The tests comprised both offset and angled collisions. Most of the tests were car to car collisions, but barrier tests were also performed. The random error of the CPR was found to be 2.2 km/hr for the delta V measurements and 0.6 g for mean acceleration.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A Kullgren, A Lie, C Tingvall. 1995. Crash pulse recorder--validation in full scale crash tests.. https://doi.org/10.1016/0001-4575(95)00025-u

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

The role of attention in horizontal curves: a comparison of advance warning, delineation, and road marking treatments.

Horizontal curves have been recognized as a significant safety issue for many years, a more important factor than road width or sight distance. The research literature suggests that driver errors associated with horizontal curves result from three inter-related problems: failures of driver attention, misperceptions of speed and curvature, and poor lane positioning. To examine the roles of attentional, perceptual, and lane placement factors in driver behaviour at curves, two groups of curve treatments were identified for testing with a driving simulator. The first group of treatments consisted of four combinations of warning signs designed to alert drivers to the presence of curves and produce a reduction in curve approach speeds. The second group was comprised of several types of road markings designed to affect drivers' speed and lane position as they drove through curves. The results indicated that advance warning signs by themselves were not as effective at reducing speeds as when they were used in conjunction with chevron sight boards and/or repeater arrows. Of the road marking treatments only rumble strips produced any appreciable reductions in speed. A herringbones road marking was found to produce significant improvements in drivers' lane positions, effectively flattening the drivers' paths through the curves. A treatment combining the herringbones treatment with chevron and repeater arrow signs produced both a reliable reduction in speed as well as improved lane positions. The results are interpreted as evidence that treatments that highlight perceptual cues are the most effective means of moderating drivers' curve speeds.

Acceleration↗

Uppsalator's acceleration.

Semiquantitative prediction of the Uppsalator (electroosmotical oscillator developed in Uppsala) under constant voltage is confirmed via numerical solution of exact nonlinear integro-differential equations in partial derivatives (PDE). Critical voltage and characteristic features of pressure and liquid flow velocity as functions of time are reproduced with high precision. In particular, the number of inflection points per period of oscillating velocity increases with growing voltage from two to six. A new feature is demonstrated. For sufficiently high voltages the Uppsalator shows normal deceleration, i.e., the oscillation period grows with voltage. However, in some supercritical range of voltages, acceleration is observed, as expressed by decrease of the oscillation period with growing voltage. Thus, the Uppsalator at constant voltage considered earlier as an impossible phenomenon represents a great challenge for experimental verification.

Acceleration↗

Photodissociation at 193 nm of some singly protonated peptides and proteins with m/z 2000-9000 using a tandem time-of-flight mass spectrometer equipped with a second source for delayed extraction/post-acceleration of product ions.

A tandem time-of-flight mass spectrometer was built for photodissociation (PD) of singly protonated peptides and small proteins generated by matrix-assisted laser desorption/ionization. PD was performed in a second source after deceleration of precursor ions. The delayed extraction/post-acceleration scheme was used for the product ions. For the PD at 193 nm of small singly protonated peptides, the present instrument showed much better sensitivity and resolution for product ions than the previous one (Moon JH, Yoon SH, Kim MS, Bull. Korean Chem. Soc. 2005; 26: 763) even though the overall spectral patterns obtained with the two instruments were similar. The present instrument was inferior in precursor ion selection and background noise level. PD was achieved for precursor ions as large as the singly protonated ubiquitin (m/z 8560.63), indicating that the photoexcitation is capable of supplying a sufficient amount of internal energy to dissociate large singly protonated proteins. As the precursor ion m/z increased, however, product ion signals deteriorated rather rapidly. As in the PD of small peptide ions with m/z around 1000, the types of the product ions generated from singly protonated peptides with m/z in the range 2000-4000 were mostly determined by the positions of arginine residues. Namely, a(n) and d(n) ions dominated when an arginine residue(s) was near the N-terminus while v(n), w(n), x(n) and y(n) dominated when the same residue(s) was near the C-terminus. In addition, d(n), v(n) and w(n) ions were generated according to the correlation rules previously observed in the collisionally activated dissociation. Isoleucine and leucine isomers could be easily distinguished based on the w(n) and d(n) ions.

Acceleration↗