ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
Keywords
  • 1
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. The volatility and hygroscopicity of nascent SSA was determined with a volatility and hygroscopicity tandem differential mobility analyser (VH-TDMA) (Johnson et al., 2004: doi:10.1016/j.jaerosci.2003.10.008, 2008: doi:10.1016/j.jaerosci.2008.05.005). A diffusion drier was used to dry the sample flow to 20 ± 5 % RH prior to characterisation by the VH-TDMA. The VH-TDMA used two TSI 3010 condensation particle counters. The aerosol sample flow rate for each scanning mobility particle sizer was 1 L/min, resulting in a total inlet flow of 2 L/min, the sheath flow for the pre-DMA, V-DMA and H-DMA were 11, 6 and 6 L/min, respectively. The dependence of HGF on RH at ambient temperature was measured for one water sample (workboat 9) to provide the deliquescence relative humidity (DRH). All VH-TDMA data were inverted using the TDMAinv algorithm (Gysel et al., 2009: doi:10.1016/j.jaerosci.2008.07.013). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; ccn; Chatham Rise; DATE/TIME; Depth, description; FTIR; functional groups; Humidity, relative; Humidity, relative, maximum; Humidity, relative, minimum; Hygroscopic growth factor; Hygroscopic growth factor, raw counts; hygroscopicity; IBA; ion beam; Particle, geometric median diameter; PTFE bottle, 5L; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; Temperature, water; volatility; Volatility-Hygroscopicity Tandem Differential Mobility Analyser (VH-TDMA); WB9
    Type: Dataset
    Format: text/tab-separated-values, 42292 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. Filters were collected for compositional analysis using transmission Fourier Transform Infra Red (FTIR) and Ion Beam analysis (IBA). The nascent SSA was sampled through a 1 μm sharp cut cyclone (SCC 2.229PM1, BGI Inc., Waltham, Massachusetts) and collected on Teflon filters, with the sample confined to deposit on a 10 mm circular area. Back filter blanks were used to characterise the contamination during handling, and before analysis samples were dehydrated to remove all water, including SSA hydrates, as described in (Frossard and Russell, 2012: doi:10.1021/es3032083). Filter samples underwent simultaneous particle induced X-ray emission (PIXE) and gamma ray emission (PIGE) analysis (Cohen et al., 2004: doi:10.1016/j.nimb.2004.01.043). Si was the only compound with blank measurements above the IBA detection limit. The measured S mass was used to calculate the SO4 mass, all S was assumed to be in the form of SO4. The filter exposed area (0.785 cm2) was used to convert inorganic areal concentrations into total mass. The inorganic mass (IM) was computed as the sum of Na, Mg, SO4, Cl, K, Ca, Zn, Br and Sr. The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; Bromine per total inorganic mass fraction; Calcium per total inorganic mass fraction; ccn; Chatham Rise; Chloride per total inorganic mass fraction; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; FTIR; functional groups; hygroscopicity; IBA; Inorganic mass, total; ion beam; Latitude of event; Longitude of event; Magnesium per total inorganic mass fraction; Potassium per total inorganic mass fraction; PTFE bottle, 5L; sea spray; Simultaneous particle induced X-ray emission (PIXE) and gamma ray emission (PIGE) analysis; SOAP; SOAP (Surface Ocean Aerosol Production); Sodium per total inorganic mass fraction; SSA; Strontium per total inorganic mass fraction; Sulfate per total inorganic mass fraction; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9; Zinc per total inorganic mass fraction
    Type: Dataset
    Format: text/tab-separated-values, 213 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. The volatility and hygroscopicity of nascent SSA was determined with a volatility and hygroscopicity tandem differential mobility analyser (VH-TDMA) (Johnson et al., 2004: doi:10.1016/j.jaerosci.2003.10.008, 2008: doi:10.1016/j.jaerosci.2008.05.005). A diffusion drier was used to dry the sample flow to 20 ± 5 % RH prior to characterisation by the VH-TDMA. The VH-TDMA was also used to calculate the organic volume fraction (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). The VH-TDMA used two TSI 3010 condensation particle counters. The aerosol sample flow rate for each scanning mobility particle sizer was 1 L/min, resulting in a total inlet flow of 2 L/min, the sheath flow for the pre-DMA, V-DMA and H-DMA were 11, 6 and 6 L/min, respectively. The SSA volatile fraction was computed by measuring the diameter of preselected SSA upon heating by a thermodenuder up to 500 degree C, in temperature increments of 5 degree C - 50 degree C. After heating the SSA hygroscopic growth factor at 90% RH was measured. All VH-TDMA data were inverted using the TDMAinv algorithm (Gysel et al., 2009: doi:10.1016/j.jaerosci.2008.07.013). The hygroscopic growth factor, semi-volatile organic volume fraction and low volatility organic volume fraction were determined as outlined in (Cravigan et al., 2019: doi:10.5194/acp-2019-797). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: aerosols; Calibrated fluorometer (Perkin-Elmer); ccn; Chatham Rise; Chlorophyll a; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; FTIR; functional groups; Hygroscopic growth factor; hygroscopicity; IBA; ion beam; Latitude of event; Longitude of event; Organic volume fraction, low-volatile; Organic volume fraction, semi-volatile; Particle, geometric median diameter; PTFE bottle, 5L; Sea-salt hydrates, volume fraction; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; Volatility-Hygroscopicity Tandem Differential Mobility Analyser (VH-TDMA); WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9
    Type: Dataset
    Format: text/tab-separated-values, 167 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2023-07-06
    Description: The SOAP voyage examined air-sea interactions over the productive waters of the Chatham Rise, east of New Zealand onboard the RV Tangaroa (New Zealand National Institute of Water and Atmospheric Research, Wellington) from February 12 to March 7 (Law et al., 2017: doi:10.5194/acp-17-13645-2017). 23 seawater samples were collected throughout the voyage for the purpose of generating nascent SSA. Seawater samples were collected from the ocean surface during workboat operations (approximately 10 cm depth) or from the mixed layer (3 - 12 m depth, always less than the measured mixed layer depth) or deep water samples. Surface samples were collected in prewashed 5L PTFE bottles, subsurface measurements were colected in Niskin bottles onboard a CTD rosette. Nascent SSA was generated in-situ in a 0.45 m3 cylindrical polytetrafluoroethylene chamber housing four sintered glass filters with porosities between 16 and 250 μm (Cravigan et al., 2019: https://doi.org/10.5194/acp-2019-797). Dried and filtered compressed air was passed through the glass filters at a flow rate of 15.5 ± 3 L/min and resulting SSA was sampled from the headspace of the chamber. Filters were collected for compositional analysis using transmission Fourier Transform Infra Red (FTIR) and Ion Beam analysis (IBA). The nascent SSA was sampled through a 1 μm sharp cut cyclone (SCC 2.229PM1, BGI Inc., Waltham, Massachusetts) and collected on Teflon filters, with the sample confined to deposit on a 10 mm circular area. Back filter blanks were used to characterise the contamination during handling, and before analysis samples were dehydrated to remove all water, including SSA hydrates, as described in (Frossard and Russell, 2012: doi:10.1021/es3032083). FTIR measurements were carried out according to previous marine sampling techniques (Maria et al., 2003: doi:10.1029/2003jd003703; Russell et al., 2010: doi:10.1073/pnas.0908905107). Filter blanks were under the detection limit for the FTIR. The PM1 organic mass fraction from SSA samples collected on filters was computed from the total organic mass from FTIR analysis and the inorganic mass from ion beam analysis, as in (Cravigan et al., 2019: doi:10.5194/acp-2019-797). The uncertainty in the organic mass measured using FTIR is up to 20 % (Maria et al., 2003: doi:10.1029/2003jd003703; Russell et al., 2010: doi:10.1073/pnas.0908905107). The seawater chlorophyll-a concentration was measured by filtering 2 litres of sample water onto GF/F Whatman filters, with immediate freezing in liquid nitrogen and subsequent analysis within 3 months of collection. Filters were ground and chlorophyll-a extracted in 90 % acetone with concentration determined by a calibrated fluorometer (Perkin-Elmer), with an analytical precision of 0.001 mg/m3 (Law et al., 2011: doi:10.1016/j.dsr2.2010.10.018).
    Keywords: Acid functional groups per total organic mass fraction; aerosols; Alcohol functional groups per total organic mass fraction; Alkane functional groups per total organic mass fraction; Amine functional groups per total organic mass fraction; Carbonyl functional groups per total organic mass fraction; ccn; Chatham Rise; Chlorophyll a; CTD/Rosette; CTD-RO; Date/Time of event; Depth, description; DEPTH, water; Event label; Fourier transform infrared spectroscopy (FTIR); FTIR; functional groups; hygroscopicity; IBA; ion beam; Latitude of event; Longitude of event; Organic mass, total; Organic mass fraction; PTFE bottle, 5L; sea spray; SOAP; SOAP (Surface Ocean Aerosol Production); SSA; TAN1203; Tangaroa; TDMA; U7505; U7506; U7507; U7508; U7510; U7518; U7520; U7521; U7524; U7528; U7530; U7532; volatility; WB1; WB10; WB4; WB5; WB6; WB7; WB8; WB9
    Type: Dataset
    Format: text/tab-separated-values, 174 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: CoSi2 exhibits the features of low resistivity and stability at elevated temperatures which make it interesting to employ for metallization on GaAs. The interfacial reactions in GaAs samples with thin film overlayers of Si and Co [Si(220 nm)/Co(50 nm)/(〈100〉-GaAs)] were studied using x-ray diffraction, scanning electron microscopy, x-ray photoelectron spectroscopy, and mass and energy dispersive recoil spectrometry. Samples were vacuum furnace annealed for time periods between 1 and 8 h at temperatures ranging from 300 to 700 °C. It was found that a CoSi2 layer formed without observable reaction with the substrate at 500 °C and above. The excess Si (Si/Co atomic ratio of 2.41) remained near the surface as elemental Si and as SiO2 for the 500 and 600 °C annealings. For the 700 °C annealing the excess near-surface Si was not observed. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 62 (1987), S. 1778-1781 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: A scanned electron beam was used to diffuse tin in GaAs from doped emulsions. Rutherford backscattering method was used to investigate the results of the diffusion. The diffusion was greatly enhanced by capping the emulsion with evaporated silicon dioxide.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Interfacial reactions between (100) InP and thin films of the transition metals Cr, Ni, Pt, and Ti have been studied. A thin layer of metal was deposited onto the InP substrates using e-beam evaporation and parts of the samples were then subjected to heat treatment in vacuum for 30 min at several temperatures up to 500 °C. Separate characterizations of the metal, In, and P depth distributions were carried out using mass and energy dispersive recoil spectrometry. The different crystalline phases observed were determined using x-ray diffraction. The near-noble metals (Ni, Pt) formed ternary phases, while Ti and Cr formed phosphides. The phases formed were generally stable up to 500 °C with the major exception being Pt where the ternary phase decomposed to form PtIn2, PtP2, and Pt3In7. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 141 (1967), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1436-5073
    Keywords: elemental analysis ; depth profiling ; surfaces ; interface ; C ; O ; N ; Al ; Si ; S ; P ; Ni ; Zn ; zinc dialkyldithiophosphate ; GaAs ; AlxGa1−x As ; InP ; tribology ; lubricating oils ; boundary lubrication ; ferrous metals ; time-of-flight ; quantum wells ; thin-films ; metallisation ; ion beam analysis ; recoil atoms ; ion accelerators
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Recoil Spectrometry covers a group of techniques that are very similar to the well known Rutherford backscattering Spectrometry technique, but with the important difference that one measures the recoiling target atom rather than the projectile ion. This makes it possible to determine both the identity of the recoil and its depth of origin from its energy and velocity, using a suitable detector system. The incident ion is typically high-energy (30–100MeV)35C1,81Br or127I. Low concentrations of light elements such as C, O and N can be profiled in a heavy matrix such as Fe or GaAs. Here we present an overview of mass and energy dispersive recoil Spectrometry and illustrate its successful use in some typical applications.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    X-Ray Spectrometry 16 (1987), S. 237-241 
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A simple technique for measuring the thickness of ice build-up on the front face of Si(Li) detectors is described. This ice thickness varies with time and significantly modifies the low-energy efficiency of Si(Li) detectors in the 1-5 keV energy range. We also report on the branching ratios for the ten resolvable neptunium M shell X-ray lines from thin 241Am α sources.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...