Excitation-emission fluorescence spectra and trihalomethane formation potential in the Tama River, Japan

2002 ◽  
Vol 2 (5-6) ◽  
pp. 481-486 ◽  
Author(s):  
F. Nakajima ◽  
M. Hanabusa ◽  
H. Furumai
Keyword(s):  
River Water ◽  
Fluorescence Intensity ◽  
Laundry Detergent ◽  
Three Dimensional ◽  
Fluorescence Emission ◽  
Fluorescent Intensity ◽  
Formation Potential ◽  
Trihalomethane Formation Potential ◽  
Treated Sewage ◽  
Wide Range

Three-dimensional fluorescence spectroscopy was applied to investigate the water quality in the Tama River, Japan, and the variation of the excitation-emission matrix (EEM) profiles of the river water was discussed with particular reference to trihalomethane formation potential (THMFP). The EEMs of the water downstream of a lake exhibited a small but strong peak at 225 nm (excitation)/295 nm (emission) and a weak one at 270 nm/295 nm, which seemed to be derived from algae. The EEMs of the water receiving treated sewage had a distinctive, large and broad peak at around 345 nm/430 nm and also a strong fluorescence at 240 nm/330-450 nm. From the comparison with EEMs of human urine, humic acid and a laundry detergent with fluorescent whitening agents, the peak at around 345 nm/430 nm on the EEM of treated sewage was also found on the EEM of the laundry detergent. The fluorescence intensity had a good correlation with T-THMFP for a wide range of excitation/emission wavelengths considered. The fluorescence intensity at 255-295 nm/345-385 nm correlated with T-THMFP better than E260, and the maximum value of the determination coefficient was R2 = 0.90 at 260 nm/355 nm, where no distinctive peak was found on the EEMs of the river water samples. The highest correlation coefficient between the fluorescent intensity and DOC was R2 = 0.77 at 280 nm/335 nm. Multiple regression analysis revealed that the fluorescence emission from a unit concentration of THM precursors was 1,000 times or more higher than that of the overall DOC, particularly in the wavelength range of 250-265 nm/325-480 nm, and that the THM precursors in the river water contributed to a much larger degree to the fluorescence than the other DOMs not forming THM.

scholarly journals Preparation of polymer–rare earth complexes based on Schiff-base-containing salicylic aldehyde groups attached to the polymer and their fluorescence emission properties

e-Polymers ◽  
2019 ◽  
Vol 19 (1) ◽  
pp. 15-22 ◽  
Author(s):  
Dingjun Zhang ◽  
Wenjin Zhao ◽  
Zhaoxuan Feng ◽  
Youzhi Wu ◽  
Caixia Huo ◽  
...  
Keyword(s):  
Schiff Base ◽  
Rare Earth ◽  
Fluorescence Intensity ◽  
Butyl Acrylate ◽  
Fluorescence Emission ◽  
Rare Earth Complexes ◽  
Functionalized Polymers ◽  
Molar Ratio ◽  
Side Chains ◽  
Fluorescent Intensity

AbstractIn this study, the salicylaldehyde hydrazone was bonded onto the side chains of poly (styrene-co-butyl acrylate), firstly obtaining a series of novel Schiff base-functionalized polymers. and using the base-containing polymers as macromolecular ligands through further reaction with EuCl3/YbCl3·6H2O, a series of polymer-rare earth complexes based on Eu(III)/Yb(III) ion were successfully prepared. The structures of the schiff base-containing polymers and their corresponding complexes were characterized by means of infrared spectra and UV spectra. The thermal properties of the functionalized polymers and complexes were investigated by TGA, and the fluorescence properties of the complexes were also researched by fluorescence spectrum. The experimental results show that the complexes have fine thermal stability likely because of the bidentate chelate effect of base-containing polymer and the conjugative effect of salicylaldehyde hydrazone group on the side chain of poly (styrene-co-butyl acrylate). More important, the salicylaldehyde hydrazone group on the side chains of poly(styrene-co-butyl acrylate) can efficaciously sensitize the fluorescence emission of the center ion due to effective intramolecular energy transfer. All the Eu(III)/Yb(III) complexes exhibit characteristic photoluminescence peaks in the visible region. The fluorescence excitation spectra of the complexes were obtained by monitoring the emission of Eu3+/Yb3+ ion at 497 nm, and the peak at 433 nm was found to be the optimal excitation peak. The concentration of salicylaldehyde hydrazone group was changed gradually with the variation of the molar ratio between the butyl acrylate and styrene (1:0.5; 1:1; 1:1.5; 1:2; 1:2.5), and the differences in their fluorescent intensity were followed, and the fluorescence intensity was very weak when the molar ratio of the butyl acrylate to styrene is equal to 1:2.5, while the fluorescence intensity reached a maximum value in the molar ratio of 1:1.

Importance of correcting for fluorescence quenching in fluorescence-based prediction of trihalomethane formation potential

2019 ◽  
Vol 19 (6) ◽  
pp. 1677-1685
Author(s):  
K. Saipetch ◽  
C. Yoshimura
Keyword(s):  
Fluorescence Quenching ◽  
Natural Organic Matter ◽  
Fluorescence Intensity ◽  
Mean Absolute Error ◽  
Absolute Error ◽  
Fluorescence Excitation ◽  
Formation Potential ◽  
Ultraviolet Absorbance ◽  
Excitation Emission Matrix ◽  
Trihalomethane Formation Potential

Abstract Fluorescence excitation–emission matrix (EEM) spectroscopy is often used to determine the levels of trihalomethane (THM) precursors in natural organic matter. However, humic substances are known to quench the fluorescence of amino acids and proteins. To date, none of the EEM-based models for predicting THM formation potential (THMFP) have explicitly accounted for these quenching effects. Thus, we investigated the importance of correcting for fluorescence quenching during THMFP prediction. Fluorescence titration experiments revealed that the correction improved the accuracy of THM prediction. EEM-based models using the corrected fluorescence intensity displayed the highest accuracy (R2 > 0.99; mean absolute error 8.1 μg/L and 13.9 μg/L for chloroform and bromoform, respectively) among models using individual parameters of EEM intensity, dissolved organic carbon (DOC), ultraviolet absorbance at 254 nm (UV254), specific UV254 (SUVA254) and differential ultraviolet absorbance at 272 nm (ΔUV272). Thus, EEM-based models require both the fluorescence intensity of a humic-like component and the corrected fluorescence intensity of a protein-like component for accurate THMFP prediction, for both chlorination and bromination processes. We also found it to be unnecessary to combine DOC with EEM intensity in terms of prediction accuracy, as long as the fluorescence quenching correction is applied.

Trihalomethane Formation Potential and Disinfection

1992 ◽  
Vol 27 (1) ◽  
pp. 185-202
Author(s):  
C.R. Erland Jansson
Keyword(s):  
Hydroxyl Radicals ◽  
Giardia Lamblia ◽  
Test Results ◽  
Formation Potential ◽  
Trihalomethane Formation Potential ◽  
Resistant Species ◽  
Low Levels ◽  
High Concentrations ◽  
Operational Data ◽  
Surface Water Supply

Abstract The UVOX process was developed to reduce the high concentrations of trihalomethanes, a potentially hazardous disinfection by-product found in a surface water supply for a community in northeastern Saskatchewan. Pilot plant tests were conducted at a throughput of 1.25 l/s utilizing UV to produce hydroxyl radicals from photolysis of H2O2 with air cooled UV units. These tests continued through 1985 andl986 to provide operational data for all seasons of the year. Test results indicated that the UVOX process was effective in reducing trihalomethane formation potential to very low levels. Recent concerns have also centred on the biocidal effectivenesss of disinfectants, particularly when applied to inactivation of resistant species of microogranisms, such as the cysts of Giardia lamblia. The UVOX process in a single pass configuration slightly enhanced the ability of UV to inactivate Giardia cysts.

Turbulent three-dimensional dielectric electrohydrodynamic convection between two plates

2012 ◽  
Vol 696 ◽  
pp. 228-262 ◽  
Author(s):  
A. Kourmatzis ◽  
J. S. Shrimpton
Keyword(s):  
Spatial Data ◽  
Three Dimensional ◽  
Reynolds Numbers ◽  
Two Dimensions ◽  
Three Dimensions ◽  
Energy Budgets ◽  
Turbulent Regime ◽  
Scalar Flux ◽  
Wide Range ◽  
Scalar Variance

AbstractThe fundamental mechanisms responsible for the creation of electrohydrodynamically driven roll structures in free electroconvection between two plates are analysed with reference to traditional Rayleigh–Bénard convection (RBC). Previously available knowledge limited to two dimensions is extended to three-dimensions, and a wide range of electric Reynolds numbers is analysed, extending into a fully inherently three-dimensional turbulent regime. Results reveal that structures appearing in three-dimensional electrohydrodynamics (EHD) are similar to those observed for RBC, and while two-dimensional EHD results bear some similarities with the three-dimensional results there are distinct differences. Analysis of two-point correlations and integral length scales show that full three-dimensional electroconvection is more chaotic than in two dimensions and this is also noted by qualitatively observing the roll structures that arise for both low (${\mathit{Re}}_{E} = 1$) and high electric Reynolds numbers (up to ${\mathit{Re}}_{E} = 120$). Furthermore, calculations of mean profiles and second-order moments along with energy budgets and spectra have examined the validity of neglecting the fluctuating electric field ${ E}_{i}^{\ensuremath{\prime} } $ in the Reynolds-averaged EHD equations and provide insight into the generation and transport mechanisms of turbulent EHD. Spectral and spatial data clearly indicate how fluctuating energy is transferred from electrical to hydrodynamic forms, on moving through the domain away from the charging electrode. It is shown that ${ E}_{i}^{\ensuremath{\prime} } $ is not negligible close to the walls and terms acting as sources and sinks in the turbulent kinetic energy, turbulent scalar flux and turbulent scalar variance equations are examined. Profiles of hydrodynamic terms in the budgets resemble those in the literature for RBC; however there are terms specific to EHD that are significant, indicating that the transfer of energy in EHD is also attributed to further electrodynamic terms and a strong coupling exists between the charge flux and variance, due to the ionic drift term.

scholarly journals Application of Dendrimers for Treating Parasitic Diseases

Pharmaceutics ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 343
Author(s):  
Veronica Folliero ◽  
Carla Zannella ◽  
Annalisa Chianese ◽  
Debora Stelitano ◽  
Annalisa Ambrosino ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Water Solubility ◽  
Parasitic Infection ◽  
Three Dimensional ◽  
Medical Knowledge ◽  
High Ratio ◽  
Molecular Volume ◽  
Parasitic Infections ◽  
Parasitic Diseases ◽  
Wide Range

Despite advances in medical knowledge, parasitic diseases remain a significant global health burden and their pharmacological treatment is often hampered by drug toxicity. Therefore, drug delivery systems may provide useful advantages when used in combination with conventional therapeutic compounds. Dendrimers are three-dimensional polymeric structures, characterized by a central core, branches and terminal functional groups. These nanostructures are known for their defined structure, great water solubility, biocompatibility and high encapsulation ability against a wide range of molecules. Furthermore, the high ratio between terminal groups and molecular volume render them a hopeful vector for drug delivery. These nanostructures offer several advantages compared to conventional drugs for the treatment of parasitic infection. Dendrimers deliver drugs to target sites with reduced dosage, solving side effects that occur with accepted marketed drugs. In recent years, extensive progress has been made towards the use of dendrimers for therapeutic, prophylactic and diagnostic purposes for the management of parasitic infections. The present review highlights the potential of several dendrimers in the management of parasitic diseases.

scholarly journals An Overview on the Rheology, Mechanical Properties, Durability, 3D Printing, and Microstructural Performance of Nanomaterials in Cementitious Composites

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2950
Author(s):  
Hongwei Song ◽  
Xinle Li
Keyword(s):  
Mechanical Properties ◽  
3D Printing ◽  
Three Dimensional ◽  
Cementitious Materials ◽  
Research Area ◽  
Cementitious Composites ◽  
Split Tensile Strength ◽  
Contour Crafting ◽  
Wide Range ◽  
Active Research

The most active research area is nanotechnology in cementitious composites, which has a wide range of applications and has achieved popularity over the last three decades. Nanoparticles (NPs) have emerged as possible materials to be used in the field of civil engineering. Previous research has concentrated on evaluating the effect of different NPs in cementitious materials to alter material characteristics. In order to provide a broad understanding of how nanomaterials (NMs) can be used, this paper critically evaluates previous research on the influence of rheology, mechanical properties, durability, 3D printing, and microstructural performance on cementitious materials. The flow properties of fresh cementitious composites can be measured using rheology and slump. Mechanical properties such as compressive, flexural, and split tensile strength reveal hardened properties. The necessary tests for determining a NM’s durability in concrete are shrinkage, pore structure and porosity, and permeability. The advent of modern 3D printing technologies is suitable for structural printing, such as contour crafting and binder jetting. Three-dimensional (3D) printing has opened up new avenues for the building and construction industry to become more digital. Regardless of the material science, a range of problems must be tackled, including developing smart cementitious composites suitable for 3D structural printing. According to the scanning electron microscopy results, the addition of NMs to cementitious materials results in a denser and improved microstructure with more hydration products. This paper provides valuable information and details about the rheology, mechanical properties, durability, 3D printing, and microstructural performance of cementitious materials with NMs and encourages further research.

scholarly journals Polymer cyclization for the emergence of hierarchical nanostructures

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Chaojian Chen ◽  
Manjesh Kumar Singh ◽  
Katrin Wunderlich ◽  
Sean Harvey ◽  
Colette J. Whitfield ◽  
...  
Keyword(s):  
Self Assembly ◽  
Three Dimensional ◽  
Hierarchical Structures ◽  
Structural Similarity ◽  
Vital Role ◽  
Nanomaterial Synthesis ◽  
Wide Range ◽  
Linear Poly ◽  
Polymer Folding ◽  
Dynamics Simulations

AbstractThe creation of synthetic polymer nanoobjects with well-defined hierarchical structures is important for a wide range of applications such as nanomaterial synthesis, catalysis, and therapeutics. Inspired by the programmability and precise three-dimensional architectures of biomolecules, here we demonstrate the strategy of fabricating controlled hierarchical structures through self-assembly of folded synthetic polymers. Linear poly(2-hydroxyethyl methacrylate) of different lengths are folded into cyclic polymers and their self-assembly into hierarchical structures is elucidated by various experimental techniques and molecular dynamics simulations. Based on their structural similarity, macrocyclic brush polymers with amphiphilic block side chains are synthesized, which can self-assemble into wormlike and higher-ordered structures. Our work points out the vital role of polymer folding in macromolecular self-assembly and establishes a versatile approach for constructing biomimetic hierarchical assemblies.

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