Search results for "efficient"

showing 10 items of 1603 documents

How do policies for efficient energy use in the household sector induce energy-efficiency innovation? : An evaluation of European countries

2017

Abstract Research on innovation induced by climate-mitigation policy has been focused predominantly on the supply side of the energy system. Despite considerable climate-mitigation potential on the demand side, less attention is given to the innovation effect of policies addressing the household sector. Based on a comprehensive data set, including 550 policy measures over 30 years (1980–2009) and covering 21 European countries, we find—based on econometric estimations—that policies targeting efficient energy use in the household sector significantly increase the number of patented energy-efficiency inventions. A comparison of the different policy types reveals a particularly strong influenc…

Demand sideta511Public economicsTechnological change020209 energydemand-pull05 social sciencestechnological changeSubsidy02 engineering and technologyManagement Monitoring Policy and LawSupply sidepolicy evaluationGeneral Energy0502 economics and business0202 electrical engineering electronic engineering information engineeringEconomics050207 economicsEnergy systemenergy efficiencyEfficient energy useEnergy Policy
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Collisional Broadening of Rotational Lines in the Stimulated Raman Pentad Q-Branch of CD4

1992

Self- and argon-broadening coefficients are reported for a number of Raman Q-branch transitions in the nu(1) and nu(2) + nu(4) bands of (C-12)D4 at room temperature (296 K). The coefficients display a variation with j and with C exp n (symmetry species A, E, F) that is essentially independent of collision partner and which is similar to the j- and C exp n-dependence found in previous measurements of the IR line-broadening coefficients. The rotationally inelastic collision rates previously measured by Foy et al. (1988) for (C-13)D4 (V4 = 0, 1) in collision with (C-13)D4 or Ar account for only a part of the Raman broadening rate, suggesting possibly significant contributions to the linewidths…

DephasingInelastic collision02 engineering and technologyLORENTZ WIDTH01 natural sciencesLOW-TEMPERATURESSpectral linesymbols.namesakeNuclear magnetic resonance0103 physical sciencesSPECTRAStimulated ramanPhysicsTUNABLE-DIODE-LASERRadiationSPECTROSCOPY010304 chemical physicsINFRARED DOUBLE-RESONANCESpectral bands021001 nanoscience & nanotechnologyAtomic and Molecular Physics and OpticsSymmetry (physics)METHANE LINESCM-1 REGIONsymbolsSHIFT COEFFICIENTSAtomic physics0210 nano-technologyRaman spectroscopyENERGY-TRANSFER
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Odesse: A New Tool for Simulation and Design of Solar Desiccant Cooling Systems in Energy Efficient Buildings

2010

DesiccantEngineeringArchitectural engineeringSettore ING-IND/11 - Fisica Tecnica Ambientalebusiness.industrysolar desiccant cooling computer simulationProcess engineeringbusinessEfficient energy useProceedings of the EuroSun 2010 Conference
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Photo‐Induced Chemiluminometric Determination of Acrolein in a Multicommutation Flow Assembly

2007

Abstract This paper deals with the determination of acrolein based on a strategy provided with a sensitive detection, the chemiluminescence; a “clean chemical” analyte treatment, the on‐line UV‐irradiation; and, a simple and quick automated system, the emergent multicommutation continuous‐flow methodology. The pesticide solution is irradiated (stopped‐flow) for 30 s; then, the resulting solution is introduced to the flow‐cell after being alternated with segments of the stream formed by potassium permanganate in strong acid solution and ethanol segments. The calibration range, from 1 to 1 mg l−1, resulted in a linear behavior over the range 5–100 µg l−1 and fitting the linear equation: I=75.…

Detection limitAnalyteChromatographyCorrelation coefficientBiochemistry (medical)Clinical BiochemistryFlow (psychology)AcroleinAnalytical chemistryBiochemistryAnalytical Chemistrylaw.inventionPotassium permanganatechemistry.chemical_compoundchemistrylawElectrochemistryCalibrationSpectroscopyChemiluminescenceAnalytical Letters
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Fourier-transform infrared determination of nicotine in tobacco samples by transmittance measurements after leaching with CHCl3

1998

Abstract A new procedure is proposed for the FT-IR spectrometric determination of nicotine in tobacco. The method is based on the extraction of nicotine in CHCl 3 from tobacco samples, wetted with an aqueous solution of NH 3 (0.1 M), and the measurement of absorbance in the stopped-flow mode at 1316 cm −1 , using a spectral baseline correction established from 1334 to 1300 cm −1 . The procedure developed does not requires a complex sample preparation, and provides a limit of detection of 0.045 mg ml −1 nicotine, a sampling frequency of 3.3 h −1 and a coefficient of variation of 0.3% for five independent measurements of a tobacco sample with a nicotine content of 1.5% w/w. The accuracy of th…

Detection limitAqueous solutionChromatographyChemistryCoefficient of variationExtraction (chemistry)Analytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryAbsorbanceNicotinemedicineEnvironmental ChemistrySample preparationSpectroscopymedicine.drugAnalytica Chimica Acta
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Determination of n-alkanes, polycyclic aromatic hydrocarbons and hopanes in atmospheric aerosol: evaluation and comparison of thermal desorption GC-M…

2019

Organic aerosol (OA) constitutes a large fraction of fine particulate matter (PM) in the urban air. However, the chemical nature and sources of OA are not well constrained. Quantitative analysis of OA is essential for understanding the sources and atmospheric evolution of fine PM, which requires accurate quantification of some organic compounds (e.g., markers). In this study, two analytical approaches, i.e., thermal desorption (TD) gas chromatography mass spectrometry (GC-MS) and solvent extract (SE) GC-MS, were evaluated for the determination of n-alkanes, polycyclic aromatic hydrocarbons (PAHs) and hopanes in ambient aerosol. For the SE approach, the recovery obtained is 89.3 %–101…

Detection limitAtmospheric Science010504 meteorology & atmospheric sciencesCorrelation coefficientlcsh:TA715-787Chemistrylcsh:Earthwork. FoundationsThermal desorptionCoal combustion productsFraction (chemistry)Repeatability010501 environmental sciences01 natural scienceslcsh:Environmental engineeringAerosolEnvironmental chemistrylcsh:TA170-171Gas chromatography–mass spectrometry0105 earth and related environmental sciencesAtmospheric Measurement Techniques
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Automatic in-tube SPME and fast liquid chromatography: A cost-effective method for the estimation of dibuthyl and di-2-ethylhexyl phthalates in envir…

2007

A 80-cm length commercially available capillary coated with 95% polydimethylsiloxane and 5% polydiphenylsiloxane (TBR-5) was employed to carry out on-line extraction and preconcentration of dibuthyl phthalate (DBP) and di-2-ethylhexyl phthalate (DEHP) in the chromatographic system. The coated capillary was placed between the sample injection loop and the injection needle of an autosampler. Variables affecting the automatic in-tube solid-phase microextraction (SPME) were optimized. A Genesis C(18) (5 cm x 4.6 mm i.d., 4 microm particle size) was employed as analytical column. The achieved limits of detection by use of diode array detection were 1 and 2.5 microg L(-1), respectively. The propo…

Detection limitChromatographyCapillary actionCost-Benefit AnalysisCoefficient of variationExtraction (chemistry)PhthalateAnalytical chemistryReproducibility of ResultsSolid-phase microextractionSensitivity and SpecificityBiochemistryDibutyl PhthalateAnalytical Chemistrychemistry.chemical_compoundchemistryDiethylhexyl PhthalateEnvironmental ChemistrySample preparationParticle sizeWater Pollutants ChemicalSpectroscopyAnalytica Chimica Acta
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Analytical strategy photodegradation/chemiluminescence/continuous-flow multicommutation methodology for the determination of the herbicide Propanil

2006

The present paper is dealing with an analytical strategy based on coupling photodegradation, chemiluminescence and multicommutation continuous-flow methodology for the determination of the pesticide Propanil, a common herbicide. The pesticide solution is inserted as small segments sequentially alternated with segments of the solution for adjusting the suitable medium for the photodegradation. Both flow-rates (sample and medium) are adjusted to required time for photodegradation, 2.0 min; and then, the resulting solution is also sequentially inserted as segments alternated with segments of the oxidizing solutions system, 1.00 x 10(-4) mol 1(-1) potassium permanganate in 2.00 mol 1(-1) sulphu…

Detection limitChromatographyChemiluminescenceCorrelation coefficientChemistryAlachlorAnalytical chemistryRepeatabilityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatePhotoreactionlawMulticommutationPropanilQUIMICA ANALITICAPesticidesPhotodegradationChemiluminescence
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Chemiluminometric photo-induced determination of Strychnine in a Multicommutation flow assembly

2007

This paper deals on the determination of Strychnine, a potent and dangerous pesticide and the analytical procedure is based on the photo-induced chemiluminescence of the pesticide by means of the Multicommutation continuous-flow methodology. Small segments of the pesticide solution were sequentially alternated with segments of the solution for adjusting the suitable medium for the photodegradation. The required time of UV irradiation was obtained by stopped-flow during 150 s; then, the resulting solution formed alternated segments with the oxidizing solution containing 5 × 10−3 mol l−1 Ce(IV) in 0.6 mol l−1 nitric acid. The calibration range, from 2 μg l−1 to 50 mg l−1, resulted in a linear…

Detection limitChromatographyCorrelation coefficientAnalytical chemistryStrychnineAnalytical Chemistrylaw.inventionchemistry.chemical_compoundchemistryNitric acidlawOxidizing agentIrradiationPhotodegradationChemiluminescenceTalanta
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Direct vapor generation Fourier transform infrared spectrometric determination of ethanol in blood

1996

Abstract A new procedure is proposed for a direct determination of ethanol in plasma and whole blood. The method is based on the injection of a discrete sample volume of 10 μl into an electrically heated Pyrex glass reactor in which, at a temperature of 90 °C, the ethanol is volatilized and introduced by means of a N 2 carrier flow inside a long-path infrared gas cell and the corresponding flow analysis recording registered as a function of time. The measurement of the area of the flow injection recording, obtained from the absorbance of the transient signal in the range 1150−950 cm −1 , allows the direct quantification of ethanol upto 2 g l −1 , with a limit of detection of 0.020 g l −1 an…

Detection limitChromatographyInfraredChemistryCoefficient of variationDrop (liquid)Analytical chemistryInfrared spectroscopyPlasmaBiochemistryAnalytical ChemistryAbsorbancesymbols.namesakeFourier transformsymbolsEnvironmental ChemistrySpectroscopyAnalytica Chimica Acta
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