Augmented reality assisted facility layout digitization and planning

Journal of Mechanical Science and Technology - Facility layout planning (FLP) has an important role in manufacturing industries. There are few approaches to solve FLP such as procedural,...     

Discontinuous Galerkin approximation of two-phase flows in heterogeneous porous media with discontinuous capillary pressures

We design and investigate a sequential discontinuous Galerkin method to approximate two-phase immiscible incompressible flows in heterogeneous porous media with discontinuous capillary pressures. The nonlinear interface conditions are enforced weakly through an adequate design of the penalties on interelement jumps of the pressure and the saturation. An accurate reconstruction of the total velocity is considered in the Raviart–Thomas(–Nédélec) finite element spaces, together with diffusivity-dependent weighted averages to cope with degeneracies in the saturation equation and with media heterogeneities. The proposed method is assessed on one-dimensional test cases exhibiting rough solutions, degeneracies, and capillary barriers. Stable and accurate solutions are obtained without limiters.     

Ion-selective supported liquid membranes placed under steady-state diffusion control

Supported liquid membranes are used here to establish steady-state concentration profiles across ion-selective membranes rapidly and reproducibly. This opens up new avenues in the area of nonequilibrium potentiometry, where reproducible accumulation and depletion processes at ion-selective membranes may be used to gain valuable analytical information about the sample. Until today, drifting signals originating from a slowly developing concentration profile across the ion-selective membrane made such approaches impractical in zero current potentiometry. Here, calcium- and silver-selective membranes were placed between two identical aqueous electrolyte solutions, and the open circuit potential was monitored upon changing the composition of one solution. Steady state was reached in approximately 1 min with 25-microm porous polypropylene membranes filled with bis(2-ethylhexyl) sebacate doped with ionophore and lipophilic ion exchanger. Ion transport across the membrane resulted on the basis of nonsymmetric ion-exchange processes at both membrane sides. The steady-state potential was calculated as the sum of the two membrane phase boundary potentials, and good correspondence to experiment was observed. Concentration polarizations in the contacting aqueous phases were confirmed with stirring experiments. It was found that interferences (barium in the case of calcium electrodes and potassium with silver electrodes) induce a larger potential change than expected with the Nicolsky equation because they influence the level of polarization of the primary ion (calcium or silver) that remains potential determining.     

Backside calibration potentiometry: ion activity measurements with selective supported liquid membranes by calibrating from the inner side of the membrane

In direct potentiometry, the magnitude of the measured potentials is used to determine the composition of the sample. While this places rather formidable demands on the required reproducibility of the associated potential measurements, typically on the order of microvolts, in vitro clinical analyses of blood samples are today successfully performed with direct potentiometry using ion-selective electrodes (ISEs). Unfortunately, most other analytical situations do not permit the sensor to be recalibrated every few minutes, as in environmental monitoring or in vivo measurements, and direct potentiometry is often bound to fail as an accurate method in these circumstances. This paper introduces a novel direction for potentiometric sensing, termed backside calibration potentiometry. Chemical asymmetries across thin supported liquid ISE membranes are assessed by determining the direction of potential drift upon changing the stirring rate on either side of the membrane. Disappearance of this drift indicates the disappearance of concentration gradients across the membrane and is used to determine the sample composition if the solution composition at the backside of the membrane and the interfering ion concentration in the sample are known. For practical determinations, the concentration of either the primary or the interfering ion is varied in the reference solution until the stirring effect disappears. The procedure is demonstrated with a Ca2+-selective membrane using Ba2+ as the dominant interfering ion. Another example includes the determination of Pb2+ in environmental samples where the pH is adjusted to a known level. At pH 4.0, H+ turns out to be the dominant interfering ion. The practical applicability of the method is shown with different environmental water samples, for which the results obtained with the novel method are compared with those obtained by traditional calibration using standard additions. The limitations of the novel method in terms of accuracy and applicable concentration ranges are discussed.     

Elimination of undesirable water layers in solid-contact polymeric ion-selective electrodes

This study aimed to develop a novel approach for the production of analytically robust and miniaturized polymeric ion sensors that are vitally important in modern analytical chemistry (e.g., clinical chemistry using single blood droplets, modern biosensors measuring clouds of ions released from nanoparticle-tagged biomolecules, laboratory-on-a-chip applications, etc.). This research has shown that the use of a water-repellent poly(methyl methacrylate)/poly(decyl methacrylate) (PMMA/PDMA) copolymer as the ion-sensing membrane, along with a hydrophobic poly(3-octylthiophene 2,5-diyl) (POT) solid contact as the ion-to-electron transducer, is an excellent strategy for avoiding the detrimental water layer formed at the buried interface of solid-contact ion-selective electrodes (ISEs). Accordingly, it has been necessary to implement a rigorous surface analysis scheme employing electrochemical impedance spectroscopy (EIS), in situ neutron reflectometry/EIS (NR/EIS), secondary ion mass spectrometry (SIMS), and small-angle neutron scattering (SANS) to probe structurally the solid-contact/membrane interface, so as to identify the conditions that eliminate the undesirable water layer in all solid-state polymeric ion sensors. In this work, we provide the first experimental evidence that the PMMA/PDMA copolymer system is susceptible to water "pooling" at the interface in areas surrounding physical imperfections in the solid contact, with the exposure time for such an event in a PMMA/PDMA copolymer ISE taking nearly 20 times longer than that for a plasticized poly(vinyl chloride) (PVC) ISE, and the simultaneous use of a hydrophobic POT solid contact with a PMMA/PDMA membrane can eliminate totally this water layer problem.     

Open magnetic and electric graphic analysis.

The OMEGA software provides an analysis platform for user-independent, fast, and reproducible multimodal data analysis in one single software environment. Synergetic interactions pursued between the two functional imaging techniques fMRI and MEG use the morphological MRI recording as a basis for a common coordinate frame. In this way, direct interchange, comparison, and integration among the results of the different modalities have become feasible. The fMRI data analysis provides information about the localization of functional activity with low temporal resolution, whereas the MEG recording complements the corresponding time evolution with a high temporal resolution. The implementation of OMEGA allows the analyst to receive comprehensive MEG/fMRI results in a matter of minutes after the measurements have been completed. With OMEGA, the clinical researcher gets comprehensive information in a quick and standardized approach about the sites and the time course of neurological activation, which is useful for clinical applications and diagnostics.     

Discrete p-robust $$\varvec{H}({{\mathrm{div}}})$$-liftings and a posteriori estimates for elli ptic problems with $$H^{-1}$$H-1 source terms

We establish the existence of liftings into discrete subspaces of \(\varvec{H}({{\mathrm{div}}})\) of piecewise polynomial data on locally refined simplicial partitions of polygonal/polyhedral domains. Our liftings are robust with respect to the polynomial degree. This result has important applications in the a posteriori error analysis of parabolic problems, where it permits the removal of so-called transition conditions that link two consecutive meshes. It can also be used in the a posteriori error analysis of elliptic problems, where it allows the treatment of meshes with arbitrary numbers of hanging nodes between elements. We present a constructive proof based on the a posteriori error analysis of an auxiliary elliptic problem with \(H^{-1}\) source terms, thereby yielding results of independent interest. In particular, for such problems, we obtain guaranteed upper bounds on the error along with polynomial-degree robust local efficiency of the estimators.