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All sourcesNASA NTRSDOE OSTI
NASA NTRSDate not supplied

Monthly Mean DNI and GTI Derived from Monthly Mean GHI and DHI Using Two Methods: Comparisons with the BSRN Data and the Results Derived from the CERES Hourly Data

Monthly mean Global Horizontal Irradiances (GHI) and Diffuse Horizontal Irradiances (DHI) are more widely available than monthly mean Direct Normal Irradiances (DNI) and Global Tilted Irradiances (GTI). Empirical methods have been developed to derive monthly mean DNI and GTI from monthly mean GHI or from GHI and DHI. In this paper, we evaluate two such methods. The first one was the Whitlock Method developed by Charles H. Whitlock (2005) for the NASA POWER project by means of regression of the BSRN data. The method expresses the monthly mean DHI-to-GHI ratio as polynomial functions of monthly mean clearness index, sunset hour angle and noon solar elevation angle on the monthly-average-day. The monthly mean DNI is calculated by dividing the monthly mean GHI-DHI difference, or DirHI, by the cosine of the solar zenith angle at the mid-time between sunrise and solar noon on the monthly-average-day. The second method is the LJCR Method developed by Liu and Jorden (1960) and Collares-Pereira and Rabl (1979), and this method empirically splits monthly mean GHI and DHI into hourly means on the monthly-average-day, and the resulting hourly mean GHI and DHI and their difference, DirHI, can then be used to compute the monthly mean DNI, GTI and the global solar tracker irradiance (GTrI). This method is also used by RETScreen. We recently produced a set of hourly DNI and DHI by bias-correcting the CERES hourly DNI and DHI, and computed hourly GTI and GTrI as well. The data span twenty plus years from March 2000 to near present on a 1 by 1 grid system. The monthly mean CERES GHI and the corrected DHI are used as inputs to the above two methods to compute monthly mean DNI, GTI and GTrI. Through comparisons with the BSRN data, it is found that the Whitlock Method, with slight modification, and the LJCR Method can produce results that are nearly as good as the results derived from the CERES hourly data.

Taiping Zhang↗
NASA NTRSDate not supplied

The Hourly GHI, DHI and DNI: Intercomparison of the CERES-Based Data and the NSRDB Data through Comparison with the Ground-Based BSRN Data

The NASA Clouds and the Earth’s Radiant Energy System (CERES) SYN1deg(Ed4.1) provides hourly global horizontal irradiance (GHI), diffuse horizontal irradiance (DHI) and direct horizontal irradiance (DirHI) at 1-degree latitude by 1-degree longitude resolution, and the time span is from March 2000 to near present. While the GHI agrees well with the ground-based Baseline Surface Radiation Network (BSRN) data, the DHI and DirHI are, respectively, positively and negatively biased against the BSRN data, and so is the direct normal irradiance (DNI) derived simply by dividing the DirHI by the cosine of the hourly solar zenith angle (SZA). We found that the biases tend to be well-defined functions of cos(SZA) and the cloud fraction (CLFR). We thus performed a bias-correction on the hourly DHI and DNI in the latitude-cos(SZA)-CLFR phase space, and therefrom, we derived the hourly global tilted irradiance (GTI) at a number of tilt angles using the isotropic diffuse irradiance model, and the results agree well with the GTI derived from the original BSRN near-instantaneous records. Meanwhile, the National Renewable Energy Laboratory (NREL) has produced the National Solar Radiation Database (NSRDB) with finer spatiotemporal resolution using its Physical Solar Model (PSM) and surface-based measured data, model results and satellite-based data as inputs. Now the NSRDB data covers not only the United States and its neighboring regions, but Europe, Africa, Asia and Oceania. The available temporal resolutions are 5, 10, 15, 30 and 60 minutes and the spatial resolutions are 2, 4 and 10 km, depending on the selected region. In this presentation, we compare both the CERES-based and NSRDB GHI, DHI and DNI with their BSRN counterparts and show how finer spatial resolution may give us an advantage in data accuracy and usability.

Taiping Zhang↗
NASA NTRSDate not supplied

The Use of the BSRN Data as A Benchmark for the POWER Hourly DHI and DNI and In Validating Derived Hourly GTI

The satellite-based CERES SYN1deg hourly data is the source data of the POWER GIS solar data that covers 2001 to near present. The SYN1deg(Ed4.1) hourly GHI agrees well with the BSRN data, but the hourly DHI and DirHI (Direct Horizontal Irradiance) are positively and negatively, respectively, biased with appreciable magnitudes. The hourly DNI, derived by dividing the DirHI by cos(SZA), or the cosine of the solar zenith angle, is therefore negatively biased. Based on the statistics of comparisons with the BSRN data, we performed bias corrections on the hourly DHI and DNI. The corrections were executed in the 3-D phase space of latitude, cos(SZA), and cloud fraction (CLFR). The isotropic model is then used to derive the hourly global tilted irradiance (GTI). For validation purpose, we applied the isotropic model to the BSRN data at the original 1-, 2-, 3- or 5-minute interval. The satellite-based hourly GTI shows good agreement with their BSRN counterpart. We also examined two monthly-mean-based methods that empirically derive monthly mean GTI and DNI from monthly mean GHI and from both monthly mean GHI and DHI. The monthly-mean-based results compare favorably with the hourly-mean-based results. The GEWEX SRB (V4-IP) provides POWER with daily mean GHI for the years before the CERES era, and the data were corrected using quantile mapping by referencing the CERES SYN1deg data. We used the Kolmogorov -Smirnov test (K-S test) and Cramer-von Mises test to examine how well the results agree with the BSRN data. We found that if we set the lower limit for the daily mean GHI to 30 W m-2, the data can pass the K-S test at 0.01 significance level and the Cramer-von Mises test at 0.001 significance level. If no lower limit is set on the daily means, the data fail both tests. The satellite-based CERES SYN1deg hourly data is the source data of the POWER GIS solar data that covers 2001 to near present. The SYN1deg(Ed4.1) hourly GHI agrees well with the BSRN data, but the hourly DHI and DirHI (Direct Horizontal Irradiance) are positively and negatively, respectively, biased with appreciable magnitudes. The hourly DNI, derived by dividing the DirHI by cos(SZA), or the cosine of the solar zenith angle, is therefore negatively biased. Based on the statistics of comparisons with the BSRN data, we performed bias corrections on the hourly DHI and DNI. The corrections were executed in the 3-D phase space of latitude, cos(SZA), and cloud fraction (CLFR). The isotropic model is then used to derive the hourly global tilted irradiance (GTI). For validation purpose, we applied the isotropic model to the BSRN data at the original 1-, 2-, 3- or 5-minute interval. The satellite-based hourly GTI shows good agreement with their BSRN counterpart. We also examined two monthly-mean-based methods that empirically derive monthly mean GTI and DNI from monthly mean GHI and from both monthly mean GHI and DHI. The monthly-mean-based results compare favorably with the hourly-mean-based results. The GEWEX SRB (V4-IP) provides POWER with daily mean GHI for the years before the CERES era, and the data were corrected using quantile mapping by referencing the CERES SYN1deg data. We used the Kolmogorov -Smirnov test (K-S test) and Cramer-von Mises test to examine how well the results agree with the BSRN data. We found that if we set the lower limit for the daily mean GHI to 30 W m-2, the data can pass the K-S test at 0.01 significance level and the Cramer-von Mises test at 0.001 significance level. If no lower limit is set on the daily means, the data fail both tests.

Taiping Zhang↗
NASA NTRS1995

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations

Gaseous, ionized polycyclic aromatic hydrocarbons (PAHs) are thought to be responsible for a very common family of interstellar infrared emission bands. Here the near- and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo(e)pyrene, benzo-(ghi)perylene, and coronene, are presented to test this hypothesis. For those molecules that have been studied previously (pyrene, pyrene-d(sub 10), and coronene), band positions and relative intensities are in agreement. In all of these cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeuteriophenanthrene, pyrene, benzo(ghi]perylene, and coronene cations. With the exception of coronene, the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations, the CC stretching and CH in-plane bending modes give rise to bands that are an order of magnitude stronger than those of the neutral species, and the CH out-of-plane bends produce bands that are 5-20 times weaker than those of the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

Hudgins, D. M.↗
NASA NTRS1995

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations: The Members of the Thermodynamically Most Favorable Series through Coronene - Part 2

Gaseous, ionized polycyclic aromatic hydrocarbons (PAHS) are thought to be responsible for a very common family of interstellar infrared emission bands. Here the near- and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo[e]pyrene, benzo-[ghi]perylene, and coronene, are presented to test this hypothesis. For those molecules that have been studied previously (pyrene, pyrene-d(sub 10), and coronene), band positions and relative intensities are in agreement. In all of these cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeuteriophenanthrene, pyrene, benzo[ghi]perylene, and coronene cations. With the exception of coronene, the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations, the CC stretching and CH in-plane bending modes give rise to bands that are an order of magnitude stronger than those of the neutral species, and the CH out-of-plane bends produce bands that are 5-20 times weaker than those of the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

Hudgins, D. M.↗
NASA NTRS1995

Infrared spectroscopy of matrix-isolated polycyclic aromatic hydrocarbon cations. 2. The members of the thermodynamically most favorable series through coronene

Gaseous, ionized polycyclic aromatic hydrocarbons (PAHs) are thought to be responsible for a very common family of interstellar infrared emission bands. Here the near- and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene:phenanthrene, pyrene, benzo[e]pyrene, benzo[ghi]perylene, and coronene, are presented to test this hypothesis. For those molecules that have been studied previously (pyrene, pyrene-d10, and coronene), band positions and relative intensities are in agreement. In all of these cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeuteriophenanthrene, pyrene, benzo[ghi]perylene, and coronene cations. With the exception of coronene, the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations, the CC stretching and CH in-plane bending modes give rise to bands that are an order of magnitude stronger than those of the neutral species, and the CH out-of-plane bends produce bands that are 5-20 times weaker than those of the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

NASA Discipline Exobiology↗
NASA NTRS1994

Infrared Spectroscopy of Polycyclic Aromatic Hydrocarbon Cations: The Members - 3

In spite of the fact that the infrared spectroscopic properties of only a few isolated ionized polycyclic aromatic hydrocarbons (PAHs) are known, gaseous, ionized PAHs are thought to be responsible for a very common family of infrared interstellar emission bands. In order to provide a data base to test this hypothesis and, if borne out, to use this emission band family as a probe of many different interstellar environments, we are carrying out a thorough study of the infrared spectroscopic properties of neutral and ionized PAHs in argon matrices. Here we present the near and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo[e]pyrene, benzo[ghilperylene, and coronene. The properties of naphthalene, the first member of the series, are given elsewhere. The spectra of perdeuterated phenanthrene and pyrene are also reported. For those molecules which have been previously studied (pyrene, d(10)-pyrene, and coronene), band positions and relative intensities are in agreement. In all cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeutero-phenanthrene, pyrene, benzo[ghi]perylene, and coronene cations. With the exception of coronene,the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations the CC stretching and CH in-plane bending modes give rise to bands which are an order of magnitude stronger than for the neutral species, and the CH out-of-plane bends produce bands which are 5-20 times weaker than in the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

Hudgins, D. M.↗
NASA NTRS2005

The Mid-Infrared Absorption Spectra of Neutral PAHs in Dense Interstellar Clouds

Polycyclic aromatic hydrocarbons (PAHs) are common throughout the universe and are expected to be present in dense interstellar clouds. In these environments, some P.4Hs may be present in the gas phase, but most should be frozen into ice mantles or adsorbed onto dust grains and their spectral features are expected to be seen in absorption. Here we extend our previous work on the infrared spectral properties of the small PAH naphthalene (C10H8) in several media to include the full mid-infrared laboratory spectra of 11 other PAHs and related aromatic species frozen in H2O ices. These include the molecules 1,2-dihydronaphthalene, anthracene, 9,1O-dihydroanthracene, phenanthrene, pyrene, benzo[e]pyrene, perylene, benzo(k)fluoranthene, pentacene, benzo[ghi]perylene, and coronene. These results demonstrate that PAHs and related molecules, as a class, show the same spectral behaviors as naphthalene when incorporated into H2O-rich matrices. When compared to the spectra of these same molecules isolated in inert matrices (e.g., Ar or N2), the absorption bands produced when they are frozen in H2O matrices are broader (factors of 3-10), show small position shifts in either direction (usually < 4/cm, always < 10/cm), and show variable changes in relative band strengths (typically factors of 1-3). There is no evidence of systematic increases or decreases in the absolute strengths of the bands of these molecules when they are incorporated in H2O matrices. In H2O-rich ices, their absorption bands are relatively insensitive to concentration over the range of 10 < H2O/PAH < 200): The absorption bands of these molecules are also insensitive to temperature over the 10 K < T < 125 K range, although the spectra can show dramatic changes as the ices are warmed through the temperature range in which amorphous H2O ice converts to its cubic and hexagonal crystalline forms (T > 125 Kj. Given the small observed band shifts cause by H2O, the current database of spectra from Ar matrix-isolated neutral PAHs and related molecules should be useful for the search for these species in dense clouds on the basis of observed absorption band positions. Furthermore, these data permit determination of column densities to better than a factor of 3 for PAHs in dense clouds. Column density determination of detected aromatics to better than a factor of 3 will, however, require good knowledge about the nature of the matrix in which the PAH is embedded and laboratory studies of relevant samples.

Bernstein, M. P.↗
NASA NTRSDate not supplied

An Assessment of and Access to NASA CERES Hourly Solar Irradiance Data Products Using POWER Web Services

The National Aeronautics and Space Administration’s (NASA) Clouds and Earth’s Radiant Energy System (CERES) Mission has been providing surface solar irradiance data products since March 2000. With an emphasis on global climate quality data products, CERES produces a suite of data parameters related to both the inputs and the observed and measured solar irradiance components at the top-of-atmosphere and at the surface. This paper discusses the global CERES SYN1Deg (Synoptic 1x1 degree resolution) solar irradiance data products, shows that the accuracy of the global horizontal irradiance (GHI) at the hourly time scale is <1% for bias and 24% RMS compared to the Baseline Surface Radiation Network (BSRN) measurements. This paper then shows the accuracy of the direct and diffuse components and a proposed “bias” correction based upon the solar zenith angle dependence that provides accuracy useful for solar applications on a global basis for all sunlit conditions. Lastly, a brief description of how to obtain these hourly solar irradiance products based upon SYN1Deg using the NASA’s Prediction of Worldwide Energy Resource (POWER) web services portal is given so users can utilize these estimates for testing and evaluation.

Surface solar irradiance↗