Comprehensive investigation of self-assembled monolayer formation on ferromagnetic thin film surfaces

We report a simple, universal method for forming high surface coverage SAMs on ferromagnetic thin (< or =100 nm) films of Ni, Co, and Fe. Unlike previous reports, our technique is broadly applicable to different types of SAMs and surface types. Our data constitutes the first comprehensive examination of SAM formation on three different ferromagnetic surface types using two different surface-binding chemistries (thiol and isocyanide) under three different preparation conditions: (1) SAM formation on electroreduced films using a newly developed electroreduction approach, (2) SAM formation on freshly evaporated surfaces in the glovebox, and (3) SAM formation on films exposed to atmospheric conditions beforehand. The extent of SAM formation for all three conditions was probed by cyclic voltammetry for surfaces functionalized with either (11-thiolundecyl)ferrocene (Fc-(CH2) 11-SH) or (11-isocyanoundecyl)ferrocene (Fc-(CH2) 11-NC). SAM formation was also probed for straight-chain molecules, hexadecanethiol and hexadecaneisocyanide, with contact angle measurements, X-ray photoelectron spectroscopy, and reflection-absorption infrared spectroscopy (RAIRS). The results show that high surface coverage SAMs with low surface-oxide content can be achieved for thin, evaporated Ni and Co films using our electroreduction process with thiols. The extent of SAM formation on electroreduced films is comparable to what has been observed for SAMs/Au and to what we observe for SAMs/Ni, Co, and Fe samples prepared in the glovebox.     

Recent progress in thin film fluorescent probe for organic amine vapour

There are great needs for real-time detection of volatile organic amines(VOA)through low-cost detection methods in public health,food safety,and environmental monitoring area.Organic thin-film fluorescent probe(OTFFP)is expected to become a new and efficient means of detecting VOA because of its fast response,high sensitivity,no contamination to the analyte and ease to prepare a portable instrument.Compared with the mature detection methods in solution,research on solid fluorescence sensing has been less studied.In this article,we review recent progress in OTFFP research for VOA vapour.We mainly focus on the new fluorescent sensing mechanisms applied in solid state in recent years and the design principle of probes for different types of organic amines(such as primary amine,secondary amine,tertiary amine and aromatic amine).We also review the material structures of these probes and the strategies to enhance their sensitivity or selectivity.     

pyVib, a computer program for the analysis of infrared and Raman optical activity

A new program called pyVib has been developed as a tool for the analysis of Gaussian (Gaussian 03, Gaussian Inc., Pittsburgh, PA) outputs of vibrational absorption (IR), Raman as well as vibrational optical activity (VOA) spectra calculations. This program has been designed to help the computational chemistry practitioner in the task of analyzing and visualizing molecular vibrations and cross sections. In particular, the analysis of absorption and scattering cross sections can be done using new tools such as group coupling matrices (GCMs) and atomic contribution patterns (ACPs) as either 2D or 3D representations, respectively (Hug, Chem Phys 2001, 264, 53). It reads the Hessian, the atomic polar tensors (APTs), the atomic axial tensors (AATs) (Nafie, J Chem Phys 1983, 79, 4950), and the gradients of the various polarizability tensors involved in VOA calculations and stored in Gaussian fchk ascii files. pyVib is capable of picking suitably chosen atoms or group of atoms for evaluating the contribution of each atom or defined groups of atoms to the calculated VOA scattered intensities. All the results generated by pyVib can be visualized in real-time but can also be transferred to text editors and electronic spreadsheets, which facilitate a detailed subsequent analysis and the visualization by other graphical user interfaces (GUIs).This program is coded in Python and used the visualization toolkit (VTK) library. It is freely available under the terms of the general GNU public license (GPL) for Linux platforms.     

Rapid radiochemical method for determination of actinides in emergency concrete and brick samples

A new rapid method for the determination of actinides in emergency concrete and brick samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used in emergency response situations or for routine analysis. If a radiological dispersive device (RDD), Improvised Nuclear Device (IND) or nuclear accident occurs, there will be a urgent need for rapid analyses of many different environmental matrices, including building materials such as concrete and brick, to support dose mitigation and environmental clean-up. The new method for actinides in concrete and brick method utilizes a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a column separation process with stacked TEVA, TRU and DGA Resin cartridges. Alpha emitters are prepared using rare earth microprecipitation for counting by alpha spectrometry. The method showed high chemical recoveries and effective removal of interferences. The determination of actinides in concrete and brick sample analysis can be performed in less than 8 h with excellent quality for emergency samples. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory actinide particles are effectively digested.     

Rapid fusion method for determination of actinides in fecal samples

A new rapid fusion method for the determination of actinides in fecal samples has been developed at the Savannah River National Laboratory that can be used for emergency response or routine bioassay analyses. If a radiological dispersive device, improvised nuclear device or nuclear accident occur, there will be an urgent need for rapid analyses of environmental, food and bioassay matrices. If an inhalation event occurs and there is confirmed radionuclide activity present via urine analyses of individuals, fecal analyses will typically be required to determine the soluble/insoluble fraction of actinides present as a result of the event to allow a more reliable estimate of radiological dose. The new method for actinides in fecal samples uses accelerated furnace heating, a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a column separation process with stacked TEVA, TRU and DGA resin cartridges. The rapid fusion method provides rugged digestion of any refractory particles present, essential for reliable analysis of actinides in fecal samples. Alpha spectrometry was used to determine the actinide isotopes, but this method can be adapted for assay by inductively-coupled plasma mass spectrometry for actinide isotopes with longer half-lives that have sufficient mass to allow measurement. The method showed high chemical recoveries and effective removal of interferences. The determination of actinides in fecal samples can be performed in less than 12 h in an emergency with excellent quality for emergency samples. The new method, which is much less tedious and time-consuming than other reported methods, can be used for emergency or routine fecal sample analyses. This enables more timely estimates of radiological dose to be performed that utilize soluble/insoluble actinide ratios.     

Rapid determination of actinides in emergency food samples

A new rapid method for the determination of actinides in food samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used for emergency response or routine food samples. If a radiological dispersive device or improvised nuclear device event occurs, there will be a urgent need for rapid analyzes of many different environmental matrices, as well as food samples, to support dose mitigation and protect general populations from radioactivity that may enter the food chain. The recent accident at Fukushima nuclear power plant in March, 2011 reinforces the need to have rapid analyzes for radionuclides in environmental and food samples. The new method to determine actinides in food samples utilizes a furnace ashing step, a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a column separation process with stacked TEVA, TRU, and DGA resin cartridges. The furnace ashing and rapid fusion steps are performed in relatively inexpensive, reusable zirconium crucibles. Alpha emitters are prepared using rare earth micro precipitation for counting by alpha spectrometry. The method showed high chemical recoveries and effective removal of interferences. The determination of actinides in food samples can be performed in less than 8 h for 10 g samples with excellent quality for emergency samples using short count times. Larger food samples (100 g) may be processed in 24 h or less. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory actinide particles are effectively digested. This method can be used to meet the derived intervention level guidelines recommended by the U.S. Food and Drug Administrations.     

Electrochemistry in ultrahigh vacuum: underpotential deposition of Al on polycrystalline W and Au from room temperature AlCl(3)/1-ethyl-3-methylimidazolium chloride melts

The voltammetric characteristics of polycrystalline Au and W electrodes cleaned (thermal annealing at 1100 K) and characterized (Auger electron spectroscopy) in ultrahigh vacuum (UHV) have been examined in ultrapure AlCl(3)/1-ethyl-3-methylimidazolium chloride (EtMeImCl) melts in UHV. These experiments were performed using a custom-designed transfer system that allows for the all-Al electrochemical cell to be filled with EtMeImCl in an auxiliary UHV chamber and later transferred under UHV to the main UHV chamber that houses the Auger electron spectrometer. The results obtained for the underpotential (UPD) and bulk deposition of Al on Au were found to be very similar to those reported in the literature for measurements carried out under 1 atm of an inert gas in a glovebox. For the far more reactive W surfaces, voltammetric features ascribed to the stripping of underpotential-deposited Al could be observed following a single scan from 1.0 V vs Al(3+)/Al to a potential negative enough for bulk deposition of Al to ensue. This behavior is unlike that reported in the literature for experiments performed in a glovebox, which required either extensive potential cycling in the Al bulk deposition and stripping region or excursions to potentials positive enough for chlorine evolution to ensue for Al UPD features to be clearly discerned. These observations open new prospects for fundamental electrochemical studies of well-characterized, highly reactive metals, including single crystals, in a variety of low vapor pressure ionic liquids.     

Hot cell based time-of-flight mass spectrometry

A time-of-flight mass spectrometer has been designed and is presently being installed within a radiological controlled hot cell at Argonne National Laboratory-West. Direct solid sampling is performed by laser ablation or glow discharge sputtering followed by supersonic expansion into the TOFMS source chamber. Once the atom/ion beam enters the source chamber, enhanced ionization can be accomplished by laser ionization or electron impact. An assortment of samples may be analyzed ranging from irradiated nuclear fuel elements and cladding materials to eutectic salts, radioactive waste materials and environmental samples.     

Adsorbents from Waste materials

The possibility of using pyrolyzed wastes produced in already working incineration plants, as adsorbents for waste water treatment, was studied. Showing very poor adsorption properties, they were improved by steam activation technique used in the conventional activated carbon manufacturing. It is concluded that various organic waste materials can be converted to carbonaceous final products with a character similar to activated carbon. Their adsorption properties and pore size distribution are determined by the structure of the starting material. Although most of these samples have a low specific surface area, their pore volume is not negligible in the meso-and micropore range. Adsorption tests with model waste waters confirmed that adsorption properties are strongly influenced by the character of the suface. The adsorption capacity of these samples can be utilized for the treatment of strongly polluted industrial waste waters. Considering that the raw material ‘needed’ to manufacture these adsorbent is produced permanently and the adsorbents do not have to be regenerated, it might be worthwhile using these kinds of adsorbents in the primary treatment of industrial waste waters.     

Radiometric detector options to aid in DOE high activity waste tank in situ characterization efforts

Radioactive waste cleanup and subsequent closure of waste storage tanks is currently underway at the Savannah river site, prompting the need to characterize the residual contents (heels) of the tanks. Occasionally, results from laboratory analyses indicate alternative sub-sampling strategies are needed, resulting in repetitive efforts to sample and analyze tank bottoms. The development of a system for in situ tank analyses using a radiometric probe, which could be lowered into a waste tank, could aid in identifying waste structures on tank bottoms requiring further sampling and characterization. Ideally, the probe would provide information for determining which structures were higher in concentrations of actinides and fission products characteristic of DOE high level waste (HLW) heels. Although only a limited set of isotopes can be measured directly without extensive radiochemical separations, the low-energy photon spectra of HLW do offer some intriguing possibilities for characterization using a radiometric probe. One possibility for obtaining a low-energy photon spectrum in the presence of high levels of interfering radiation would be to design a probe primarily based upon recently developed technology from Amptek Inc. Such a detector would be relatively insensitive to the high photon background, which would paralyze conventional gamma probes (i.e. sodium iodide) subjected to the same radiological conditions. The prototype detector is capable of successfully obtaining high resolution measurements at very high count rates (in excess of 500,000 counts per second). An overview of measurements obtained from various HLW samples using the prototype Amptek detector, as well as some additional detector technologies, which could enhance this prototype, will be discussed.     

Photofission for the detection of actinides

Nuclear waste management cost at CEA is a heavy budget share. Therefore, it is important, in order to minimize that cost, to select the most suitable repository for the waste. Significant cost savings are obtained, for example, whenever a medium activity waste drum initially filed to end up in a geological repository can be measured accurately enough to be accepted by the Centre de Stockage de l’Aube (CSA). Photofission can be used as a non-destructive technique to measure the actinide content embedded in a nuclear waste drum. It can even be applied when the waste is packaged in its heavy concrete shielding. It is equally sensitive to non-fissile nuclear material. However, the present state of art suffers from a lack of sensitivity to be able to help redirecting the waste to the proper repository. A new program called INPHO is proposed at CEA Saclay aiming at enhancing the sensitivity sufficiently to be applicable for waste characterization.     

Environmental semivolatiles and nonvolatiles analysis by hyphenated spectral techniques

Environmental sample extracts contain a variety of volatile and nonvolatile organic compounds exhibiting a range of polarities and concentrations. Although gas chromatography/mass spectrometry (GC/MS) is the method of choice thus far for such analyses, this technique used alone cannot adequately characterize the volatiles in such samples and is not amenable to environmental nonvolatiles. A more complete characterization of environmental and hazardous waste samples is required to assess the dangers posed to the nation's groundwater by hazardous waste dumps. Online spectral confirmation by directly linked GC/Fourier transform infrared (FTIR)/MS is shown to provide useful structural information on environmental volatiles in hazardous wastes, even when the analyte's spectrum is not in either spectral database. This information can lead to biological-hazard estimation. The diffuse reflectance Fourier transform infrared (DRIFT) technique, used in conjunction with thermospray MS or fast atom bombardment (FAB) MS, provides confirmed identifications or confirmed compound class assignments of organic nonvolatiles in solid wastes. This is believed to be the first report of spectral confirmation (identification or functionality) of organic volatiles and nonvolatiles in environmental samples.     

Fluorimetry compared to spectrophotometry for uranium evaluation in liquid waste

Uranium concentration levels in surface waters are of great importance because uranium presents both chemical and radiological hazard to the environment. The subject of this article is to establish that spectrophotometric method for uranium evaluation in effluents collected from liquid waste treatment generated during fabrication of nuclear fuel elements could be replaced by the optical fluorimetric technique. Both methods are briefly described. The comparison of the two methods was carried out with regard to international standards and national regulations offering from a statistical point of view a useful approach to compare two analytical measurement techniques. This methodology can be applied to any other measurement procedures. A discussion about the compliance of the fluorimetric analytical method with the mandatory discharge level of uranium concentration in surface waters is also presented.     

Alpha/beta indices determination in drinking water using plastic scintillation and evaporation to dryness

Alpha/beta indices are screening parameters that provide a quick approach to the determination of the radioactivity levels of water samples. These indices have commonly been determined by methods involving measurement by proportional counter or liquid scintillation (LS) techniques. However, both of these types of techniques present some limitations. Plastic scintillation (PS) is an alternative technique that does not generate mixed wastes and also provides a solid surface onto which the sample can be evaporated. The objective of this study is to evaluate a new procedure for the determination of alpha/beta indices using PS microspheres and evaporation to dryness. For this purpose, the capabilities of this technique were first compared with those of LS and PS in solution. Various parameters were then optimised: the diameter of the microspheres, the discrimination values and the evaporation system. Next, the calibration procedure was established, and finally, the procedure was validated with the analysis of spiked water samples. The results show that this technique can be applied for alpha/beta indices determination with a simple procedure, high detection efficiency and acceptable uncertainties.     

Waste water analysis by purge and trap capillary GC-FTIR spectrometry

Gas chromatography with Fourier transform infra-red spectroscopic detection (GC-FTIR) is used for the analysis of waste water samples. Compared to GC-MS, this technique offers a more complete identification of organic compounds. Lower concentrations of organic volatiles however require preconcentration techniques such as a Purge and Trap (P&T) preconcentrator. Using this combination, concentrations of organic volatiles in the ppb range can be detected and positively identified.     

一种新的五日生物需氧量分析方法

利用荧光氧传感器连续监测封装在密闭培养皿中的废水溶氧浓度，提出了一种新的ＢＯＤ５分析方法，建立了两套ＢＯＤ５检测装置。实验结果表明，利用荧光氧传感器检测ＢＯＤ５，提高了测量的准确性和精度，可望成为新的标准化检测方法。     

A New Approach for the Determination of Organobromine in Harmful Waste

Determination and estimation of organic sulphur, nitrogen, phosphor and halides in harmful chemical waste and estimation of emission of SO₂, NO_X, HCI, HBr or HI during incineration are the primary task of risk assessment. In our paper we present a new analytical approach for determination of bromine in a heterogeneous sample. The method applied is based on combustion of chemical waste under oxygen atmosphere (pressure 20 bars) and transformation to corresponding anions. These anions can be measured by ion chromatography. Using this method all hetero atoms can be transformed to corresponding anions (except for oxygen) and can be measured by ion chromatography. In this paper we report of determination of bromine content of chemical waste. During the combustion of organobromine compounds different types of inorganic bromine are formed. All types of bromine must be converted to Br^–. To fulfil it the above, ascorbic acid solution was used for absorbing and transforming all types bromine compounds to Br^–. We will discuss all the details about this new approach and give all the parameters to get efficient conversion from organic bromine to bromide anions.This revised version was published online in November 2005 with corrections to the Cover Date.     

An air and thermally stable one- component catalyst for the amination of aryl chlorides

[reaction: see text] In this paper we report a new, highly efficient palladacyclic precatalyst that is air, moisture, and thermally stable and obviates the need to employ a glovebox. We have developed a convenient one-component precatalyst for the amination of aryl chlorides that overcomes many of the limitations of those previously described.     

A method based on microextraction by packed sorbent-programmed temperature vaporizer–fast gas chromatography–mass spectrometry for the determination of aromatic amines in environmental water samples

We report a sensitive method for the determination of 15 aromatic amines in environmental water samples. They have been included in the list of priority pollutants in surface water by the European Union. The method is based on analyte enrichment using microextraction by packed sorbent (MEPS) and later analysis using programmed temperature vaporizer-gas chromatography-mass spectrometry (PTV-GC-MS). All MEPS steps were carried out manually. The detection limits were of the order of nanograms per liter for most of the compounds. The results were compared with those obtained without MEPS using the method exclusively based on direct injection of the sample into the PTV-GC-MS. External calibration in ultrapure water was used in the determination of the compounds studied in five types of water samples (sea, river, tap, influent, and effluent waste water) since no significant matrix effect was found. The results obtained can be considered highly satisfactory and they revealed the presence of aniline in the sea and the influent and effluent waste water samples.