Sunlight caused interference in outdoor N, N-diethyl-p-phenylenediamine colorimetric measurement for residual chlorine and the solution for on-site work.

Chlorination is the most common method to control water qualities, in some case on-site outdoor measurements are required to measure easily-decaying residual chlorine concentration appropriately without delay. In this study sunlight-induced unexpected colour development (UCD) of N, N-diethyl-p-phenylenediamine (DPD) colorimetric measurement was studied under several sun exposure conditions. The colour development level was evaluated with reference to chlorine concentration (mg/L) and relationships between colour development rate (mg/L min) and intensities of solar were investigated. UCD was found to be related to both exposure intensity and time. By means of exposure experiment under specific wavelength of ultraviolet (UV), it was confirmed that both middle and short wavelength of UV radiation being responsible for such an unexpected measurement. Consequently, a simple device was designed using three commercially available anti-UV films, one of which could effectively prevent the UCD from direct sun exposure.

Impact of tryptophan on the formation of TCNM in the process of UV/chlorine disinfection.

Low-pressure (LP) UV treatment after chlorine disinfection was associated with enhanced formation of trichloronitromethane (TCNM), a halonitromethane disinfection by-product (DBP), due to the chlorination of tryptophan. Evidence was found that the concentration of TCNM from tryptophan increased quickly to the maximum for the first instance. Moreover, the increase of TCNM under UV exceeded 10 times than under dark. Then, it was found to have an obvious decrease in the formation of TCNM, even finally hardly disappear. In order to elucidate reasons for this phenomenon, the effects of light intensity, initial tryptophan concentration, free chlorine concentration, pH, and tert-butanol (TBA) on the formation of TCNM were investigated under UV/chlorine treatment. Finally, the effects of tryptophan on the formation of TCNM and the direct photodegradation of TCNM under LP UV irradiation were studied for analyzing the possible pathways of TCNM formation from amino acid. Since amino acids are very common in water sources, further research into chemical oxidation of these species by LP UV and chlorine is recommended. It can help us to find the precursors of TCNM formation and reduce the risk of TCNM formation for drinking water and wastewater utilities.

Wavelength-dependent chlorine photolysis and subsequent radical production using UV-LEDs as light sources.

UV-LEDs are considered as the most promising UV light sources, because it has the potential to replace conventional UV lamps in some water treatment applications in the foreseeable future. In this study, UV-LEDs at four wavelengths in the UV-C or near UV-C range (i.e., 257.7, 268, 282.3, and 301.2 nm) were used to investigate the wavelength-dependency on chlorine photolysis and its subsequent radical formation. The fluence-based photodecay rates of hypochlorous acid (HOCl) and hypochlorite (OCl-) were monotonically correlated to their molar absorption coefficients and quantum yields, and the chlorine photodecay rates were much more significantly affected by molar absorption coefficients (ß â€¯= 0.949) than quantum yields (ß â€¯= 0.055). An empirical model that incorporated the chlorine photodecay rate constants, quantum yields, and molar absorption coefficients of HOCl and OCl- was established, validated and then used to predict the chlorine photodecay rate at any wavelength (257.7-301.2 nm) and pH (5-10). The modelling results suggested that the maximum fluence-based rate constant (1.46 × 10-4 m2 J-1) was obtained at 289.7 nm and pH 9.95. The wavelength dependency was larger at alkaline pH than at acidic pH, and the pH dependency was the largest at the longest wavelength. The formation of hydroxyl radicals (HO·) and reactive chlorine species (RCS) decreased with increasing wavelength at pH 6, and increased with increasing wavelength at pH 7. More HO· was formed at pH 6 than pH 7, but RCS showed the opposite pH-dependency. The findings in this study provide the fundamental information in selecting UV-LEDs with specific wavelength for enhancing/optimizing chlorine photodecay and/or its radical generation at different pHs in real-world applications.

Degradation of lipid regulators by the UV/chlorine process: Radical mechanisms, chlorine oxide radical (ClO•)-mediated transformation pathways and toxicity changes.

Degradation of three lipid regulators, i.e., gemfibrozil, bezafibrate and clofibric acid, by a UV/chlorine treatment was systematically investigated. The chlorine oxide radical (ClO•) played an important role in the degradation of gemfibrozil and bezafibrate with second-order rate constants of 4.2 (±0.3) × 108 M-1 s-1 and 3.6 (±0.1) × 107 M-1 s-1, respectively, whereas UV photolysis and the hydroxyl radical (HO•) mainly contributed to the degradation of clofibric acid. The first-order rate constants (k') for the degradation of gemfibrozil and bezafibrate increased linearly with increasing chlorine dosage, primarily due to the linear increase in the ClO• concentration. The k' values for gemfibrozil, bezafibrate, and clofibric acid degradation decreased with increasing pH from 5.0 to 8.4; however, the contribution of the reactive chlorine species (RCS) increased. Degradation of gemfibrozil and bezafibrate was enhanced in the presence of Br-, whereas it was inhibited in the presence of natural organic matter (NOM). The presence of ammonia at a chlorine: ammonia molar ratio of 1:1 resulted in decreases in the k' values for gemfibrozil and bezafibrate of 69.7% and 7%, respectively, but led to an increase in that for clofibric acid of 61.8%. Degradation of gemfibrozil by ClO• was initiated by hydroxylation and chlorine substitution on the benzene ring. Then, subsequent hydroxylation, bond cleavage and chlorination reactions led to the formation of more stable products. Three chlorinated intermediates were identified during ClO• oxidation process. Formation of the chlorinated disinfection by-products chloral hydrate and 1,1,1-trichloropropanone was enhanced relative to that of other by-products. The acute toxicity of gemfibrozil to Vibrio fischeri increased significantly when subjected to direct UV photolysis, whereas it decreased when oxidized by ClO•. This study is the first to report the transformation pathway of a micropollutant by ClO•.

Growth and Properties of Cl- Incorporated ZnO Nanofilms Grown by Ultrasonic Spray-Assisted Chemical Vapor Deposition.

Pure and Cl- incorporated ZnO nanofilms were grown by the ultrasonic spray-assisted chemical vapor deposition (CVD) method. The properties of the nanofilms were investigated. The effects of growth temperature and Cl- concentration on the crystal structure, morphology, and optical properties of the nanofilms were studied. Temperature plays an important role in the growth mode and morphology of the pure nanofilms. Preferential growth along the c-axis occurs only at modulating temperature. Lower temperature suppresses the preferential growth, and higher temperature suppresses the growth of the nanofilms. The morphologies of the nanofilms change from lamellar and spherical structures into hexagonal platelets, then into separated nanoparticles with an increase in the temperature. Incorporating Cl- results in the lattice contracting gradually along with c-axis. Grains composing the nanofilms refine, and the optical gap broadens with increasing of Cl- concentration in growth precursor. Incorporating Cl- could reduce oxygen vacancies and passivate the non-irradiated centers, thus enhancing the UV emission and suppressing the visible emission of ZnO nanofilms.

Natural solar photolysis of total organic chlorine, bromine and iodine in water.

Municipal wastewater has been increasingly used to augment drinking water supplies due to the growing water scarcity. Wastewater-derived disinfection byproducts (DBPs) may negatively affect the aquatic ecosystems and human health of downstream communities during water reuse. The objective of this research was to determine the degradation kinetics of total organic chlorine (TOCl), bromine (TOBr) and iodine (TOI) in water by natural sunlight irradiation. Outdoor solar photolysis experiments were performed to investigate photolytic degradation of the total organic halogen (TOX) formed by fulvic acid and real water and wastewater samples. The results showed that TOX degradation by sunlight irradiation followed the first-order kinetics with half-lives in the range of 2.6-10.7 h for different TOX compounds produced by fulvic acid. The TOX degradation rates were generally in the order of TOI > TOBr â‰… TOCl(NH2Cl) > TOCl(Cl2). High molecular weight TOX was more susceptible to solar photolysis than corresponding low molecular weight halogenated compounds. The nitrate and sulfite induced indirect TOX photolysis rates were less than 50% of the direct photolysis rates under the conditions of this study. Fulvic acid and turbidity in water reduced TOX photodegradation. These results contribute to a better understanding of the fate of chlorinated, brominated and iodinated DBPs in surface waters.

Effect of UV irradiation on the proportion of organic chloramines in total chlorine in subsequent chlorination.

This study investigated the changes of chlorine species and proportion of organic chloramines during the chlorination process after UV irradiation pretreatment in drinking water. It was found that the UV pretreatment could enhance the percentage of organic chloramines by increasing free chlorine consumption in the chlorination of raw waters. The percentage of organic chloramines in total chlorine increased with UV intensity and irradiation time in raw waters. However, for the humic acid synthesized water, the percentage of organic chloramines increased first and then decreased with the increase of UV irradiation time. The value of SUVA declined in both raw and humic acid synthesized waters over the UV irradiation time, which indicated that the decomposition of aromatic organic matter by UV could be a contributor to the increase of free chlorine consumption and organic chloramine proportion. The percentage of organic chloramines during chlorination of raw waters after 30-min UV irradiation pretreatment varied from 20.2% to 41.8%. Total chlorine decreased obviously with the increase of nitrate concentration, but the percentage of organic chloramines increased and was linearly correlated to nitrate concentration.

Enhanced inactivation of Bacillus subtilis spores during solar photolysis of free available chlorine.

Aqueous free available chlorine (FAC) can be photolyzed by sunlight and/or artificial UV light to generate various reactive oxygen species, including HO(•) and O((3)P). The influence of this chemistry on inactivation of chlorine-resistant microorganisms was investigated using Bacillus subtilis endospores as model microbial agents and simulated and natural solar radiation as light sources. Irradiation of FAC solutions markedly enhanced inactivation of B. subtilis spores in 10 mM phosphate buffer; increasing inactivation rate constants by as much as 600%, shortening inactivation curve lag phase by up to 73% and lowering CTs required for 2 log10 inactivation by as much as 71% at pH 8.0 and 10 °C. Similar results were observed at pH 7.4 and 10 °C in two drinking water samples with respective DOC concentrations and alkalinities of 0.6 and 1.2 mg C/L and 81.8 and 17.1 mg/L as CaCO3. Solar radiation alone did not inactivate B. subtilis spores under the conditions investigated. A variety of experimental data indicate that the observed enhancements in spore inactivation can be attributed to the concomitant attack of spores by HO(•) and O3, the latter of which was found to accumulate to micromolar concentrations during simulated solar irradiation of 10 mM phosphate buffer (pH 8, 10 °C) containing [FAC]0 = 8 mg/L as Cl2.

Perchlorate production by photodecomposition of aqueous chlorine solutions.

Aqueous chlorine solutions (defined as chlorine solutions (Cl(2,T)) containing solely or a combination of molecular chlorine (Cl(2)), hypochlorous acid (HOCl), and hypochlorite (OCl(-))) are known to produce toxic inorganic disinfection byproduct (e.g., chlorate and chlorite) through photoactivated transformations. Recent reports of perchlorate (ClO(4)(-)) production-a well-known thyroid hormone disruptor- from stored bleach solutions indicates the presence of unexplored transformation pathway(s). The evaluation of this potential ClO(4)(-) source is important given the widespread use of aqueous chlorine as a disinfectant. In this study, we perform detailed rate analysis of ClO(4)(-) generation from aqueous chlorine under varying environmental conditions including ultraviolet (UV) light sources, intensity, solution pH, and Cl(2,T) concentrations. Our results show that ClO(4)(-) is produced upon UV exposure of aqueous chlorine solutions with yields ranging from 0.09 × 10(-3) to 9.2 × 10(-3)% for all experimental conditions. The amount of ClO(4)(-) produced depends on the starting concentrations of Cl(2,T) and ClO(3)(-), UV source wavelength, and solution pH, but it is independent of light intensity. We hypothesize a mechanistic pathway derived from known reactions of Cl(2,T) photodecomposition that involves the reaction of Cl radicals with ClO(3)(-) to produce ClO(4)(-) with calculated rate coefficient (k(ClO4-)) of (4-40) × 10(5) M(-1) s(-1) and (3-250) × 10(5) M(-1) s(-1) for UV-B/C and UV-A, respectively. The measured ClO(4)(-) concentrations for both UV-B and UV-C experiments agreed well with our model (R(2) = 0.88-0.99), except under UV-A light exposure (R(2) = 0.52-0.93), suggesting the possible involvement of additional pathways at higher wavelengths. Based on our results, phototransformation of aqueous chlorine solutions at concentrations relevant to drinking water treatment would result in ClO(4)(-) concentrations (~0.1 µg L(-1)) much below the proposed drinking water limits. The importance of the hypothesized mechanism is discussed in relation to natural ClO(4)(-) formation by atmospheric transformations.

The decontamination of bleaching effluent by pilot-scale solar Fenton process.

A solar Fenton process was applied as post-treatment to selectively eliminate organic pollutants and toxicants in bleaching effluents of kraft pulp mills. Experiments were conducted to study the effect of system parameters (pH, initial concentration of H2O2, molar ratio of Fe2+/H2O2 and solar-UV irradiance) on the removals of chemical oxygen demand and colour. The results showed 92.8% of COD and 99.6% of colour were removed at pH 3.5, H2O2 30 mM/ L, Fe2+/H2O2 1:100, solar-UV irradiance 11070 mW/m2, reaction time 120 min. The first-order kinetic model was used to study the dependence of the reaction rate on solar-UV irradiance: a linear relationship was shown to exist between reaction rate constants and solar-UV irradiance. The results of gas chromatography mass spectrometry analysis showed that the toxicity of the bleaching effluents was mainly derived from the presence of mononuclear aromatics, polycyclic aromatic hydrocarbons and organochlorides, which were all degraded into harmless organic acids under the attack of hydroxyl radicals generated from the solar Fenton reaction.

Some factors influencing the stability of Sterilox(®), a super-oxidised water.

Super-oxidised waters, particularly Sterilox(®), have been suggested for the disinfection of dental unit water lines and dental impression materials owing to their antimicrobial efficacy. One of the previously suggested characteristics is their short shelf life. The purpose of this investigation was to understand the effect of storage conditions on Sterilox(®)'s stability. Eight bottles (four completely full, four half-full) of freshly prepared solution were divided into four groups and subsequently stored by being either exposed to or protected from sunlight. The chlorine concentration was monitored using chlorine test strips until the concentration reached zero, or until the thirteenth week. Statistically significant differences between the groups exposed to sunlight and the non-exposed groups (p <0.001) were found. The mean loss of chlorine per day for the non-exposed samples was 1.01 mg/L, whilst the mean for the exposed samples was 2.42 mg/L. The presence of air did not affect the chlorine decomposition in the bottles. The results of this investigation indicate that when the solution is exposed to sunlight, the decrease of chlorine starts at day 4, whilst for the groups sheltered from sunlight, the process started after day 14. Therefore, Sterilox(®) solutions appear to be more stable than previously surmised.

Investigation and modeling of solar UV-induced chlorine decay in disinfection contact basins at full-scale wastewater treatment plants.

Residual chlorine loss due to UV sunlight in the chlorine disinfection contact basins (DCBs) was investigated at two full-scale wastewater treatment plants (WWTPs). Chlorine decay due to solar UV-induced photochemical reaction was found to be significant and had diurnal and seasonal variations. The total chlorine loss due to sunlight ranged from 19 to 26% of the total chlorine chemical use at the two plants studied. Covering chlorine contact basins led to more stable chlorine demand regardless of the diurnal and seasonal sunlight intensity. Therefore, covering chlorine contact basins offers more stable, or accurate, chlorine dosage and effluent residual control and requires less effort by plant operators. A mathematical model was developed to calculate the amount of UV-induced chlorine decay. The model developed can be used to estimate the UV-induced chlorine decay rate and total chlorine loss due to sunlight at WWTPs with various basin configurations, flowrates, chlorine dosages, and geographical locations. The model results allow the capital cost of covering needs to be assessed against the chlorine chemical cost savings.

The dynamics of reaction of Cl atoms with tetramethylsilane.

Rotational state distributions and state-selected CM-frame angular distributions were measured for HCl (v' = 0, j') products from the reaction of Cl-atoms with tetramethylsilane (TMS) under single collision conditions at a collision energy, E(coll), of 8.2 +/- 2.0 kcal mol(-1). The internal excitation of these products was very low with only 2% of the total energy available partitioned into HCl rotation. A transition state with a quasi-linear C-H-Cl moiety structure was computed and used to explain this finding. A backward peaking differential cross section was also reported together with a product translational energy (T') distribution with a maximum at T' approximately E(coll). This scattering behaviour is accounted for by reactions proceeding through a tight transition state on a highly skewed potential energy surface, which favours collisions at low impact parameters with a strong kinematic constraint on the internal excitation of the products. The large Arrhenius pre-exponential factor previously reported for this reaction is reconciled with the tight differential scattering observed in our study by considering the large size of the TMS molecule.

Ratio of aerosol and gases of radioactive chlorine and particle size distribution of aerosol formed by high-energy proton irradiation.

To estimate internal doses due to the inhalation of radionuclides produced by the nuclear spallation of the air nuclei in high-energy proton accelerator facilities, the physicochemical properties of radionuclides are very important. Thus, the ratio of aerosol and gases of 38Cl and 39Cl formed by irradiating argon gas-added air with a 48 MeV proton beam has been measured. Radionuclides of 38Cl and 39Cl exist as aerosol, acid gas and non-acid gas. The percentages of activity of 38Cl and 39Cl aerosols are about 80%. The number size distributions of non-radioactive aerosol were characterised by two peaks with diameters of 10-20 nm and larger than 20 nm. As a result predicted by a simple surface model, it was found that the activity size distribution of 38Cl aerosols can be regarded as that having a single peak at 120 nm.

Atomic polarization in the photodissociation of diatomic molecules.

The angular momentum polarization of atomic photofragments provides a detailed insight into the dynamics of the photodissociation process. In this article, the origins of electronic angular momentum polarization are introduced and experimental and theoretical methods for the measurement or calculation of atomic orientation and alignment parameters described. Many diatomic photodissociation systems are surveyed, in order to provide an overview both of the historical development of the field and of the most state-of-the-art contemporary studies.

Infrared-induced reaction of Cl atoms trapped in solid parahydrogen.

The 355 nm photodissociation of Cl(2) trapped in a solid parahydrogen matrix at 2 K leads to the formation of isolated Cl photofragments. At these low temperatures (k(B)T approximately 1.4 cm(-1)), the Cl atoms can not react with the parahydrogen matrix since the reaction Cl + H(2)(v = 0, j = 0) --> HCl(v = 0, j = 0) + H is endothermic by 360 cm(-1). Irradiation of the Cl atom doped parahydrogen solid with broadband infrared radiation from 4000 cm(-1) to 5000 cm(-1) induces reaction of atomic Cl with the parahydrogen matrix to form HCl. The infrared-induced chemistry is attributed to solid parahydrogen absorptions that lead to the creation of vibrationally excited H(2)(v = 1), which supply the necessary energy to induce reaction. The kinetics of this low temperature infrared-induced reaction is studied using Fourier Transform infrared spectroscopy of the HCl reaction product. The HCl formation kinetics is first-order and the magnitude of the effective rate constant for the infrared-induced reaction depends on the properties of the near infrared radiation.