A comparative study of two approaches for supporting optimal network location queries

Given a set S of sites and a set O of weighted objects, an optimal location query finds the location(s) where introducing a new site maximizes the total weight of the objects that are closer to the new site than to any other site. With such a query, for instance, a franchise corporation (e.g., McDonald’s) can find a location to open a new store such that the number of potential store customers (i.e., people living close to the store) is maximized. Optimal location queries are computationally complex to compute and require efficient solutions that scale with large datasets. Previously, two specific approaches have been proposed for efficient computation of optimal location queries. However, they both assume p-norm distance (namely, L₁ and L₂/Euclidean); hence, they are not applicable where sites and objects are located on spatial networks. In this article, we focus on optimal network location (ONL) queries, i.e., optimal location queries in which objects and sites reside on a spatial network. We introduce two complementary approaches, namely EONL (short for Expansion-based ONL) and BONL (short for Bound-based ONL), which enable efficient computation of ONL queries with datasets of uniform and skewed distributions, respectively. Moreover, with an extensive experimental study we verify and compare the efficiency of our proposed approaches with real world datasets, and we demonstrate the importance of considering network distance (rather than p-norm distance) with ONL queries.     

ProDA: An End-to-End Wavelet-Based OLAP System for Massive Datasets

ProDA employs wavelets to support exact, approximate, and progressive OLAP queries on large multidimensional datasets, while keeping update costs relatively low. ProDA not only supports online execution of ad hoc analytical queries on massive datasets, but also extends the set of supported analytical queries to include the entire family of polynomial aggregate queries as well as the new class of plot queries.     

Neodymium(III)-PVC membrane sensor based on a new four dentate ionophore

A new selective Nd(III) sensor has been made by using N,N′-bis(quinoline-2-carboxamido)-4,5-dimethylbenzene (H₂L₄) as a suitable ionophore. The sensor exhibits Nernstian response to Nd(III) ions in the concentration range of 5.0 × 10^− 6 to 1.0 × 10^− 2 M. It displays a Nernstian slope of 19.5 ± 0.4 mV/decade in the pH range of 2.9-9.2. The proposed sensor also exhibits a fast response time of < l0 s. The detection limit of the proposed sensor is 4.8 × 10^− 6 M, and it can be used over a period of 10 weeks without significant changes in its response. Furthermore, the electrode showed high selectivity toward Nd(III) ion respect to all other lanthanide ions tested. The practical utility of the sensor was demonstrated by using it as an indicator electrode in the potentiometric determination of Nd(III) ions in certified reference material and spiked water samples.     

Multi-walled carbon nanotubes (MWCNTs) and room temperature ionic liquids (RTILs) carbon paste Er(III) sensor based on a new derivative of dansyl chloride

Solution studies showed the strong interaction of [5-(dimethylamino) naphthalene-1-sulfonyl 4-phenylsemicarbazide] (NSP) with Er(III) ions. NSP was used as a sensing material during construction of carbon paste Er(III) sensors. The electrodes were modified with 1-n-butyl-3-methylimidazolium tetrafluoroborate, [bmim]BF₄, as room temperature ionic liquid (RTIL) and multi-walled carbon nanotube (MWCNT). Potentiometric sensors constructed with [bmim]BF₄ and MWCNTs show better sensitivity, selectivity, response time, and response stability compared to Er(III) carbon paste sensors. The best performance for the modified sensor was obtained with an electrode composition of 20% [bmim]BF₄, 20% NSP, 45% graphite powder and 15% MWCNT. This particular sensor formulation exhibits a Nernstian response (19.8 ± 0.3 mV decade⁻¹) toward Er(III) ions in the range of 1.0 × 10⁻⁷ to 1.0 × 10⁻¹ mol L⁻¹ with a detection limit of 5.0 × 10⁻⁸ mol L⁻¹. The proposed modified Er(III) sensor can be used over the pH range from 3.5 to 9.0.     

New food safety challenges of viral contamination from a global perspective: Conventional,emerging, and novel methods of viral control

Food- and waterborne viruses, such as human norovirus, hepatitis A virus, hepatitis E virus, rotaviruses, astroviruses, adenoviruses, and enteroviruses, are major contributors to all foodborne illnesses. Their small size, structure, and ability to clump and attach to inanimate surfaces make viruses challenging to reduce or eliminate, especially in the presence of inorganic or organic soils. Besides traditional wet and dry methods of disinfection using chemicals and heat, emerging physical nonthermal decontamination techniques (irradiation, ultraviolet, pulsed light, high hydrostatic pressure, cold atmospheric plasma, and pulsed electric field), novel virucidal surfaces, and bioactive compounds are examined for their potential to inactivate viruses on the surfaces of foods or food contact surfaces (tools, equipment, hands, etc.). Every disinfection technique is discussed based on its efficiency against viruses, specific advantages and disadvantages, and limitations. Structure, genomic organization, and molecular biology of different virus strains are reviewed, as they are key in determining these techniques effectiveness in controlling all or specific foodborne viruses. Selecting suitable viral decontamination techniques requires that their antiviral mechanism of action and ability to reduce virus infectivity must be taken into consideration. Furthermore, details about critical treatments parameters essential to control foodborne viruses in a food production environment are discussed, as they are also determinative in defining best disinfection and hygiene practices preventing viral infection after consuming a food product.     

Quantitative monitoring of terbium ion by a Tb3+ selective electrode based on a new Schiff's base

Solution study showed N,N′-bis(5-nitrosalicylidene)-2-aminobenzylamin (L) trends toward Tb³⁺ ion. Then, it was used as a suitable ionophore in construction of terbium ion selective electrode. The electrode with composition of 30% PVC, 65% solvent mediator (NB), 3% ionophore (L) and 2% anionic additive (NaTPB) shows the best potentiometric response characteristics. It displays a Nernstian behavior (20.1 mV decade^?1) over the concentration range 1.0 × 10^? 6 to 1.0 × 10^? 2 mol L^?1. The detection limit of the electrode is 6.3 × 10^? 7 mol L^?1. It has a very short response time (~ 10 s) and a useful working pH range of 2.6–9.4 for at least 2 months. The proposed membrane sensor shows excellent discriminating ability towards Tb³⁺ ions with regard to several alkali, alkaline earth, transition and heavy metal ions. To investigate the analytical applicability of the sensor, it was successfully applied to the determination of terbium in certified reference material.     

Neutral N,N′-bis(2-pyridinecarboxamide)-1,2-ethane as sensing material for determination of lutetium(III) ions in biological and environmental samples

The biological properties of the lutetium as well as other lanthanide ions, primarily based on their similarity to calcium, have been the bases for research into potential therapeutic applications of lanthanide series since the early part of the twentieth century. In this research, a Lu(III) potentiometric membrane sensor based on N,N′-bis(2-pyridinecarboxamide)-1,2-ethane (PCAE) is described. The sensor exhibits a Nernstian response over a concentration range of 1.0 × 10^? 6 mol L^? 1–1.0 × 10^? 1 mol L^? 1, with a detection limit of 6.0 × 10^? 7 mol L^? 1. The best performance was achieved with a membrane composition, consisting of 30% PVC, 63% o-nitrophenyl octyl ether (NPOE), 5% PCAE and 2% sodium tetraphenylborate (NaTPB). It was found that at the pH range of 4.0–9.0, the potential response of the sensor was not affected by the pH. Furthermore, the electrode presents satisfactory reproducibility, very fast response time (5 s) and relatively good discriminating ability for Lu(III) ions with respect to many common cations and other lanthanide ions. The sensor has been applied to the determination of Lu(III) in human serum and in some soil samples where domestic devices were stored.     

Europium (III) PVC membrane sensor based on N-pyridine-2-carboxamido-8-aminoquinoline as a sensing material

Conductometric study in acetonitrile solution shows the selectivity of PCQ toward europium ion. Therefore, a new europium PVC membrane electrode was prepared based on N-pyridine-2-carboxamido-8-aminoquinoline (PCQ) as an ion carrier. The electrode has a wide concentration range from 1.0 × 10^− 2 and 1.0 × 10^− 6 mol L^− 1, Nernstian slope of 19.8 ± 0.3 mV per decade and a detection limit of 6.4 × 10^− 7 mol L^− 1. The potentiometric response is pH independent in the range of 2.4-7.4. The proposed sensor has a relatively fast response time less than 10 s and it can be used for at least 2 months without any considerable divergence in its potentials. The proposed electrode revealed good selectivity toward europium ion in comparison with variety of other metal ions. The practical utility of the electrodes has been demonstrated by their use as indicator electrodes in the potentiometric titration of Eu^3 + ions with EDTA and for determination of Eu^3 + ion concentration in mixtures of two and three different ions.     

Gadolinium(III) ion selective sensor using a new synthesized Schiff's base as a sensing material

According to a solution study which showed a selective complexation between N,N′-bis(methylsalicylidene)-2-aminobenzylamine (MSAB) and gadolinium ions, MSAB was used as a sensing element in construction of a gadolinium(III) ion selective electrode. Acetophenon (AP) was used as solvent mediator and sodium tetraphenyl borate (NaTPB) as an anion excluder. The electrode showed a good selectivity towards Gd(III) ions over a wide variety of cations tested. The constructed sensor displayed a Nernstian behavior (19.7 ± 0.3 mV/decade) in the concentration range of 1.0 × 10^? 6 to 1.0 × 10^? 2 mol L^? 1 with detection limit of 5.0 × 10^? 7 mol L^? 1 and a short response time (< 10 s). The working pH range of the electrode was 3.5–10.1 and lifetime of the sensor was at least 10 weeks. Analysis of certified reference materials confirmed the accuracy of the proposed sensor. The electrode was successfully applied as an indicator electrode in gadolinium titration with EDTA.     

Heptadentate Schiff-base based PVC membrane sensor for Fe(III) ion determination in water samples

Tests performed using heptadentate Schiff's base ((tris(3-(thiophenal)propyl)amine (TTA)) toward Fe(III) ions indicated that it could be used as an Fe(III) selective ionophore to be used in a plasticized polymeric membrane sensor. The resulting sensors were found to produce a linear response range of five orders of magnitude with a slope of 19.8 ± 0.3 mV decade^− 1 with a detection limit is 8.3 × 10^− 9 mol L^− 1. The sensor could be used in a pH window of 2.4-4.3 and the response time of the sensor was below 10 s, in addition to its very good Fe(III) selectivity over many mono-,di- and trivalent transition and heavy metal ions. The life time of the electrode was found to be at least 10 weeks.