186 research outputs found
Gamifying Project Procurement for Better Goal Incorporation
Many services that we use daily, like healthcare, infrastructures, public transport, education, and others, are provided by the public sector. These services are provided using the project procurement process. In most cases, this process has a highly complex and dynamic interaction. It leads to issues, such as information asymmetry, over-specified tenders, not efficient feedback loops, etc. As a result, projects can rarely match to the objectives of organizations. This work explores the use of participatory simulation to help holistically investigate a project procurement process to incorporate better goals of organizations. Based on case studies from the Swedish road construction field, it can be concluded that participatory simulation is an effective approach to experiment with the effects of project procurement
Loading Stark-decelerated molecules into electrostatic quadrupole traps
Beams of neutral polar molecules in a low-field seeking quantum state can be
slowed down using a Stark decelerator, and can subsequently be loaded and
confined in electrostatic quadrupole traps. The efficiency of the trap loading
process is determined by the ability to couple the decelerated packet of
molecules into the trap without loss of molecules and without heating. We
discuss the inherent difficulties to obtain ideal trap loading, and describe
and compare different trap loading strategies. A new "split-endcap" quadrupole
trap design is presented that enables improved trap loading efficiencies. This
is experimentally verified by comparing the trapping of OH radicals using the
conventional and the new quadrupole trap designs
Operation of a Stark decelerator with optimum acceptance
With a Stark decelerator, beams of neutral polar molecules can be
accelerated, guided at a constant velocity, or decelerated. The effectiveness
of this process is determined by the 6D volume in phase space from which
molecules are accepted by the Stark decelerator. Couplings between the
longitudinal and transverse motion of the molecules in the decelerator can
reduce this acceptance. These couplings are nearly absent when the decelerator
operates such that only every third electric field stage is used for
deceleration, while extra transverse focusing is provided by the intermediate
stages. For many applications, the acceptance of a Stark decelerator in this
so-called mode significantly exceeds that of a decelerator in the
conventionally used () mode. This has been experimentally verified by
passing a beam of OH radicals through a 2.6 meter long Stark decelerator. The
experiments are in quantitative agreement with the results of trajectory
calculations, and can qualitatively be explained with a simple model for the 6D
acceptance. These results imply that the 6D acceptance of a Stark decelerator
in the mode of operation approaches the optimum value, i.e. the value
that is obtained when any couplings are neglected.Comment: 13 pages, 11 figure
Deceleration and electrostatic trapping of OH radicals
A pulsed beam of ground state OH radicals is slowed down using a Stark
decelerator and is subsequently loaded into an electrostatic trap.
Characterization of the molecular beam production, deceleration and trap
loading process is performed via laser induced fluorescence detection inside
the quadrupole trap. Depending on details of the trap loading sequence,
typically OH () radicals are trapped at a density
of around cm and at temperatures in the 50-500 mK range. The 1/e
trap lifetime is around 1.0 second.Comment: 4 pages, 3 figure
Direct measurement of the radiative lifetime of vibrationally excited OH radicals
Neutral molecules, isolated in the gas-phase, can be prepared in a long-lived
excited state and stored in a trap. The long observation time afforded by the
trap can then be exploited to measure the radiative lifetime of this state by
monitoring the temporal decay of the population in the trap. This method is
demonstrated here and used to benchmark the Einstein -coefficients in the
Meinel system of OH. A pulsed beam of vibrationally excited OH radicals is
Stark decelerated and loaded into an electrostatic quadrupole trap. The
radiative lifetime of the upper -doublet component of the level is determined as ms, in good
agreement with the calculated value of ms.Comment: 4 pages, 3 figures, submitted to Phys. Rev. Let
Multiple packets of neutral molecules revolving for over a mile
The level of control that one has over neutral molecules in beams dictates
their possible applications. Here we experimentally demonstrate that
state-selected, neutral molecules can be kept together in a few mm long packet
for a distance of over one mile. This is accomplished in a circular arrangement
of 40 straight electrostatic hexapoles through which the molecules propagate
over 1000 times. Up to 19 packets of molecules have simultaneously been stored
in this ring structure. This brings the realization of a molecular low-energy
collider within reach
Optical pumping of trapped neutral molecules by blackbody radiation
Optical pumping by blackbody radiation is a feature shared by all polar
molecules and fundamentally limits the time that these molecules can be kept in
a single quantum state in a trap. To demonstrate and quantify this, we have
monitored the optical pumping of electrostatically trapped OH and OD radicals
by room-temperature blackbody radiation. Transfer of these molecules to
rotationally excited states by blackbody radiation at 295 K limits the
trapping time for OH and OD in the state to
2.8 s and 7.1 s, respectively.Comment: corrected small mistakes; added journal reference
Reflection of OH molecules from magnetic mirrors
We have reflected a Stark-decelerated beam of OH molecules under normal
incidence from mirrors consisting of permanent magnets. Two different types of
magnetic mirrors have been demonstrated. A long-range flat mirror made from a
large disc magnet has been used to spatially focus the reflected beam in the
longitudinal direction ("bunching"). A short-range curved mirror composed of an
array of small cube magnets allows for transverse focusing of the reflected
beam.Comment: 10 pages, 5 figure
Electrostatic trapping of metastable NH molecules
We report on the Stark deceleration and electrostatic trapping of NH
() radicals. In the trap, the molecules are excited on the
spin-forbidden transition and detected via
their subsequent fluorescence to the ground state. The 1/e
trapping time is 1.4 0.1 s, from which a lower limit of 2.7 s for the
radiative lifetime of the state is deduced. The spectral
profile of the molecules in the trapping field is measured to probe their
spatial distribution. Electrostatic trapping of metastable NH followed by
optical pumping of the trapped molecules to the electronic ground state is an
important step towards accumulation of these radicals in a magnetic trap.Comment: replaced with final version, added journal referenc
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