Two Methods for Retrieving UV Index for All Cloud Conditions from Sky Imager Products or Total SW Radiation Measurements

Cloud effects on UV Index (UVI) and total solar radiation (TR) as a function of cloud cover and sunny conditions (from sky images) as well as of solar zenith angle (SZA) are assessed. These analyses are undertaken for a southern‐hemisphere mid‐latitude site where a 10‐years dataset is available. It is confirmed that clouds reduce TR more than UV, in particular for obscured Sun conditions, low cloud fraction (<60%) and large SZA (>60°). Similarly, local short‐time enhancement effects are stronger for TR than for UV, mainly for visible Sun conditions, large cloud fraction and large SZA. Two methods to estimate UVI are developed: (1) from sky imaging cloud cover and sunny conditions, and (2) from TR measurements. Both methods may be used in practical applications, although Method 2 shows overall the best performance, as TR allows considering cloud optical properties. The mean absolute (relative) differences of Method 2 estimations with respect to measured values are 0.17 UVI units (6.7%, for 1 min data) and 0.79 Standard Erythemal Dose (SED) units (3.9%, for daily integrations). Method 1 shows less accurate results but it is still suitable to estimate UVI: mean absolute differences are 0.37 UVI units (15%) and 1.6 SED (8.0%).     

Validation of Ozone Monitoring Instrument UV Satellite Data Using Spectral and Broadband Surface Based Measurements at a Queensland Site

This research reconstructed and validated the broadband UVA irradiances derived from discrete spectral irradiance data retrieved from the Ozone Monitoring Instrument (OMI) satellite from 1 January to 31 December 2009. OMI data at solar noon were compared to ground‐based spectral irradiances at Toowoomba (27°36′ S 151°55′ E), Australia, at 310, 324 and 380 nm for both cloud‐free and all sky conditions. There was a strong relationship between the ground‐based UV spectroradiometer data and satellite‐based measurements with an R² of 0.89 or better in each waveband for cloud‐free days. The data show an overestimate of the satellite‐derived spectral irradiances compared to the ground‐based data. The models developed for the subtropical site data account for this overestimation and are essential for any data correlation between satellite‐ and ground‐based measurements. Additionally, this research has compared solar noon broadband UVA irradiances evaluated with a model and the discrete satellite spectral irradiances for the solar noon values of cloud‐free days to those measured with a ground‐based UVA radiometer. An R² of 0.86 was obtained confirming that for cloud‐free days the broadband UVA can be evaluated from the OMI satellite spectral irradiances.     

All-Weather Comparison between Spectral and Broadband (Robertson-Berger) UV Measurements

Abstract— Spectral measurements of UV irradiance at the Fraunhofer Institute at Garmisch-Partenkirchen, Germany, are intercompared with data from two different Robert-son-Berger-type meters. More than 21000 spectra gathered during 20 months of continuous operation were used for this analysis, sampling a large variety of atmospheric conditions. At low solar zenith angles the agreement (± 10%) was quite satisfactory, whereas at high solar zenith angles the broadband instruments gave systematically lower readings than the erythemally weighted spectral data. The deviation of the spectral response of the broadband instruments from the Commission Internationale de 1'Eclairage (CIE) erythema function and the cosine error provide an explanation of the observed differences that are similar for both broadband meters. Model calculations agree quite well with the observations, if an accurate measurement of the broadband spectral response is available. An analytical fit curve was established for the ratio between broadband and weighted spectral data, as a function of solar zenith angle, enabling quick and easy checks of the stability of the spectrora-diometric system. The relative standard deviation of the data from the fit function was only2–3% in the case of cloudless sky conditions and 5% for all sky conditions, including all types of systematic and instrumental errors.     

Zoospores of Three Arctic Laminariales Under Different UV Radiation and Temperature Conditions: Exceptional Spectral Absorbance Properties and Lack of Phlorotannin Induction

Phlorotannins have often been considered to act as UV-protective compounds in zoospores of brown algae. However, only the absorption characteristics of zoospores under UV exposure have been determined and no data are available on the actual content of phlorotannins or on temperature–UV interactions. Therefore, we determined the absorbance spectra and the phlorotannin contents in zoospore suspensions of three Arctic species ( Saccharina latissima , Laminaria digitata , Alaria esculenta ), and in the media surrounding zoospores after exposure to different radiation (400–700, 320–700, 295–700 nm) and temperature (2–18°C) conditions for 8 h. Absorption typical of phlorotannins with a maximum at 276 nm was monitored in zoospore suspensions as well as in the media surrounding zoospores, but the results depended strongly on radiation treatments and on zoospore densities. Surprisingly, the content of UV-absorbing phlorotannins subsequent to different exposures did not change in any of the three species. The observed exceptional absorption properties could, therefore, not be related to phlorotannin contents. These findings are discussed in light of a strong phlorotannin investment from sporophytes during spore release and a minor UV-protective role of phlorotannins for zoospores of Arctic kelp species.     

Synthesis and Spectral Characterization of 2-Mercaptobenzimidazole Derivatives Using a new Active Phase Transfer Reagent Under PTC Conditions

The phase transfer catalyzed synthesis of 2-Mercaptobenzimidazole derivatives using the new active phase transfer reagent namely, 2-benzilidine-N,N,N,N',N',N'-hexaethyl propane-1,3-dimonium dibromide (Dq-Br) have been described. The structures of all the fifteen compounds have been established by spectroscopic means.     

分光光度法与激光热透镜光谱分析法测定高散射物质光吸收的比较

通过理论和实验比较了分光光度法与激光热透镜光谱分析法在高散射背景下测量物质光吸收的差异。研究了在不同含量纳米TiO2的散射背景下，散射对分光光度法和热透镜光谱分析法测定耐尔蓝溶液含量的影响。结果表明，分光光度法对具有光散射性质试样的测定存在较大误差，而激光热透镜光谱分析法能较好的避免散射影响，测定结果准确。实验结果与理论分析相一致。     

Melamine as a Green and Reusable Catalyst for Knoevenagel Condensation at Room Temperature Under Solvent-Free Conditions

A rapid, efficient, and ecofriendly protocol has been developed for the Knoevenagel condensation of active methylene compounds such as malononitrile or ethyl cyanoacetate with aldehydes in the presence of melamine with good to excellent yields at room temperature without solvent.     

Fixed-Dose Combination Antibiotics Interacting with a Quaternary Ammonium Disinfectant: Insights from Spectral and Chromatographic Measurements

Core–shell architecture of surfactant micelles can act to shield active drug molecules from the adverse environmental conditions and enhance their bioavailability. In the present study the molecular interactions of a fixed dose combination (FDC) containing ofloxacin (OFX) and ornidazole (ORN), with cetyltrimethylammonium bromide (CTAB, a quaternary ammonium surfactant) were investigated under normal physiological pH (pH 7.4?±?0.1). The impact of the cationic micelle on the spectral and physiochemical properties of the FDC components OFX and ORN was systematically examined by electronic spectroscopy. Micellar liquid chromatography and differential spectral methods were used to optimize analysis of the magnitude of binding constants and related Gibbs energies. The results suggest the potential solubilization of drugs in the external part of the micelles, which may prove to be more helpful for their controlled release. These outcomes have been verified by the binding capacities of drug–CTAB combinational system that may be helpful to customize the uptake of drug molecules in cells.     

ETD in a Traveling Wave Ion Guide at Tuned Z-Spray Ion Source Conditions Allows for Site-Specific Hydrogen/Deuterium Exchange Measurements

The recent application of electron transfer dissociation (ETD) to measure the hydrogen exchange of proteins in solution at single-residue resolution (HX-ETD) paves the way for mass spectrometry-based analyses of biomolecular structure at an unprecedented level of detail. The approach requires that activation of polypeptide ions prior to ETD is minimal so as to prevent undesirable gas-phase randomization of the deuterium label from solution (i.e., hydrogen scrambling). Here we explore the use of ETD in a traveling wave ion guide of a quadrupole-time-of-flight (Q-TOF) mass spectrometer with a “Z-spray” type ion source, to measure the deuterium content of individual residues in peptides. We systematically identify key parameters of the Z-spray ion source that contribute to collisional activation and define conditions that allow ETD experiments to be performed in the traveling wave ion guide without gas-phase hydrogen scrambling. We show that ETD and supplemental collisional activation in a subsequent traveling wave ion guide allows for improved extraction of residue-specific deuterium contents in peptides with low charge. Our results demonstrate the feasibility, and illustrate the advantages of performing HX-ETD experiments on a high-resolution Q-TOF instrument equipped with traveling wave ion guides. Determination of parameters of the Z-spray ion source that contribute to ion heating are similarly pertinent to a growing number of MS applications that also rely on an energetically gentle transfer of ions into the gas-phase, such as the analysis of biomolecular structure by native mass spectrometry in combination with gas-phase ion-ion/ion-neutral reactions or ion mobility spectrometry.     

Automated Data Acquisition Setup for Interfacial Tension and Capacitance Measurements at Hg‐Solution Contacts Under LabVIEW Control

A system capable of making highly accurate and reproducible automatic measurements of both interfacial tension and capacitance at Hg‐solution contacts in student and research laboratories is presented, based on the control of an arrangement comprising a lock‐in amplifier, a potentiostat and a three electrode electrochemical cell by means of LabVIEW software.     

Volumetric, Compressibility and UV Spectral Studies on Interactions of Amino Acids with Aqueous Solutions of Potassium Dihydrogen Phosphate at Different Temperatures

Densities, ρ, and speeds of sound, u, for glycine, l-alanine and l-valine have been measured in (0.2, 0.4, 0.6 and 0.8) mol · kg^?1 aqueous solutions of potassium dihydrogen phosphate at temperatures T = (288.15, 293.15, 298.15, 303.15, and 308.15) K. Values of the apparent molar volumes, limiting apparent molar volumes, and transfer volumes have been calculated from the density data. The experimental speeds of sound were used to estimate apparent molar adiabatic compressibilities. The variation of these parameters with temperature is discussed in terms of the role of amino acid and salt in solute–solvent interactions. The UV–visible spectrum has also been used to analyze the results.     

Degradation of Sucrose,Glucose and Fructose in Concentrated Aqueous Solutions Under Constant pH Conditions at Elevated Temperature

ABSTRACT

The degradation of sucrose can decrease sucrose yield, reduce the efficiency of sugar factory and refinery processes, and effect end product quality. Characterization of sucrose degradation under modeled industrial processing conditions will underpin further technological improvements. Effects of constant reaction pH on sucrose degradation were investigated using simulated industrial model systems (100 °C; 65 °Brix [% dissolved solids]; N₂; 0.05-3 mol NaOH titrant; 8 h), with the use of an autotitrator. Reaction pH values ranged from 4.40 to 10.45. Polarimetry and ion chromatography with integrated pulsed amperometric detection (IC-IPAD) were used to quantify sucrose degradation and first-order reaction constants were calculated. Minimum sucrose degradation occurred between pH 6.45 - 8.50, with minimum color formation between pH's 4.40 - 7.00. Polarimetry, often used in U.S. sugar factories and refineries to monitor chemical sucrose losses, was shown not to be viable to measure sucrose degradation under alkaline conditions, because of the formation of fructose degradation products with an overall positive optical rotation. For comparison, fructose and glucose (80 °C; 65 °Brix; N₂; 3 mol NaOH; 2 h) were also degraded at constant pH 8.3 conditions. For sucrose, fructose, and glucose, formation of organic acids on degradation was concomitant with color formation, indicating they are probably produced from similar reaction pathways. For the glucose and fructose degradation reactions, color and organic acid formation also were highly correlated (R²>0.966) with changes in optical rotation values, confirming that these compounds are formed from similar reaction pathways.     

在确定的热力学状态下测量气体导热系数与黏度

气体的导热系数和黏度是重要的热物性参数,其数值大小取决于所处的热力学状态。在目前的导热系数和黏度主要测量方法中,待测工质在测量时需经历非定常的过程或处于具有物性梯度的非平衡态之下,使得待测工质的物性在时间或者空间上不处于一个确定的热力学状态。本文利用圆柱定程干涉法,通过分析气体导热系数和黏度导致的声波能量耗散,结合气体输运理论中对稀疏气体的描述,探索了在确定的热力学状态下同时测量气体导热系数和黏度的方法,并以氩(Ar)为例进行了实验验证。测量结果与已有文献一致性较好,初步证实了方法的可行性。     

Measurements of excess enthalpies at high temperature and pressure using a new type of mixing unit

A flow mixing unit (calorimetric cell and auxiliary devices) has been designed for measuring the enthalpy of mixing or reaction of two fluids (gas+liquid or liquid+liquid). The indicator of the heat effect is a differential heat flux calorimeter, SETARAM C-80, allowing measurements at temperatures up to 300°C. The mixing cell is made of a stainless-steel capillary (o.d 1.6 mm, length 2.4m) which is coiled in a cylindrical form and tightly fitted in the thermopile well of the calorimeter. The fluids are delivered from the high pressure piston pumps and circulated through the system at controlled flow rates ranging from 100 to 1500 L-min^–1. The tests were carried out at pressures up to 20 MPa. Special care was taken to allow good thermostatting of fluids entering the mixing cell. Check measurements were made with one liquid-liquid system (C₂H₅OH+H₂O) and one gas-liquid system (CO₂+C₆H₅CH₃); our enthalpies of mixing agreed with the literature values in most cases to 2%. For the system ethanol+water the experiments have been also performed at temperature of 250°C and pressures of 15 and 20 MPa. The endothermal mixing effect was higher than expected indicating an increase in the excess heat capacity.     

Efficient NaOH-Catalyzed Reaction of Aromatic Aldehyde,Cyclic Ketones,and Malononitrile Under Solvent-Free Conditions Using a Grinding Method

An efficient and facile synthesis of 2,6-dicyanoanilines via a one-pot reaction of aromatic aldehydes, malononitrile, and cyclic ketones in the presence of NaOH under solvent-free conditions using a grinding method has been developed. Compared with the classical reaction conditions, the new synthetic method has the advantages of excellent yields, shorter reaction times, and mild reaction conditions.     

Silica Chloride/NaNO 2 as a Novel Heterogeneous System for Production of Thionitrites and Disulfides Under Mild Conditions

Thiols can be readily converted to their corresponding thionitrites with a combination of silica chloride ( I ), wet SiO 2 and sodium nitrite in dichloromethane at room temperature. Disulfides result from the homolytic cleavage of the sulfur-nitrogen bond of the unstable thionitrite and subsequent coupling of the resultant thiyl radicals.     

Preparation of N-Arylsulfonyl Imines from Sulfonamides and Aryl Aldehydes Using Magnesium Oxide as a Heterogeneous and Reusable Catalyst Under Solvent-Free Conditions

An efficient solvent-free procedure for the preparation of N-arylsulfonyl imines from sulfonamides and aryl aldehydes in the presence of a catalytic amount of magnesium oxide and tetrabutylammonium bromide (TBAB) under microwave irradiation is described. The advantages of this method are good to high yields, short reaction times, low cost, and matching with green chemistry protocols.     

Carbon‐Supported Pt Particles as a Catalyst for Electrooxidation of Methanol and Cyclic Voltammetry Studies Under Acidic Conditions

Electrooxidation of methanol on glassy carbon (GC) electrode modified by optimum carbon supported Pt electrocatalyst (Pt‐C/GC) in acid media is investigated. The catalyst is prepared by ultrasonicating Pt/C powders in aqueous media. The activity of prepared Pt‐C/GC electrode is studied in potential range of 0–1000 mV (versus SCE) by cyclic voltammetry. The results showed that the Pt/C dispersed layer at the surface of glassy carbon electrode, behaves as an electrocatalyst for the oxidation of methanol in acid medium by optimum loading of Pt (0.2 mg cm^?2). The electrochemical properties of prepared electrode are studied under various conditions. However the effect of various parameters in the catalytic enhancement of Pt/C, such as platinum loading, sulfuric acid concentration, different scan rates, different final potentials, and medium temperature are considered and examined.