Characterisation of natural organic matter from the Nordic typing project water samples by chemometric analysis of their near infrared spectral profiles

Natural organic matter (NOM) from nine different water sources located in the southern part of Norway selected for the “NOM typing project” was characterised by using near infrared spectroscopy and multivariate data analysis.

The near infrared profiles of these NOM samples were corrected for multiple scattering effect and differentiated twice before subjecting them for multivariate data analysis. The preprocessed profiles were first subjected to multivariate calibration using partial least squares (PLS) technique against earlier determined values of four different biopolymer input (carbohydrates, N-acetyl amino sugars, proteins and polyhydroxy aromatics) of the NOM as dependent variables. The profiles were then classified using principal component analysis (PCA).

The PLS calibration models obtained demonstrate that the biopolymer input of the NOM samples can be predicted with acceptable precision.

The PCA reveals that the samples fall into three different groups. This classification agrees with earlier classifications carried out by using variables that were determined by alternative expensive and time-consuming analytical techniques.     

混凝-粉末活性炭吸附-超滤工艺去除砂滤池反洗水溶解性有机物

通过混凝-粉末活性炭(PAC)吸附-浸没式超滤膜(UF)组合工艺去除砂滤池反洗水(FBWW)中溶解性有机物(DOM),以降低后续回用过程中消毒副产物(DBPs)生成量。试验对3种混凝药剂——聚合硫酸铁(PFS)、三氯化铁(FeCl3)、聚合氯化铝(PACl)处理FBWW的效果进行了比较,探讨其对UV254和水溶性有机物(DOC)的去除效果。结果表明,PFS对有机物去除效果优于PACl和FeCl3;PFS与粉末活性炭混合投加可增加有机物去除率,粉末活性炭为20mg/L,PFS为8mg/L时出水浊度为0.85NTU,UV254和DOC去除率分别为43%和31%;采用混凝-PAC吸附-超滤膜(UF)处理FBWW对UV254和DOC去除率分别达到51%和41%,出水浊度为0.19NTU,UV254为0.031cm-1,DOC为2.76mg/L.此工艺可有效降低反冲洗水中DOM含量,达到重新利用净水厂废水的目标.     

Evaluation of disinfection by-products formation during chlorination and chloramination of dissolved natural organic matter fractions isolated from a filtered river water

Dissolved natural organic matter (DOM) in a filtered river water was isolated and fractionated into six different fractions. Trihalomethanes (THMs) and haloacetic acids (HAAs) formed from these isolated DOM fractions during chlorination and chloramination were determined. Results show that the hydrophobic acid, hydrophilic acid, hydrophilic base and hydrophobic neutral are major precursors of THMs and HAAs. There exist good correlations between the values of specific ultraviolet absorbance at 254nm of the individual DOM fractions and their disinfection by-products formation potential, indicating that aromatic moieties are responsible for disinfection by-products formation for both hydrophobic and hydrophilic DOM fractions. Chloramination of the DOM fractions yields much less THMs and HAAs than chlorination. For the dominant DOM fraction (i.e. hydrophobic acid) in the water, the yields of THMs and HAAs increase more significantly in chlorination than those in chloramination with the increase of disinfectant dosage, contact time and dissolved organic carbon content.     

FTIR evaluation of functional groups involved in the formation of haloacetic acids during the chlorination of raw water

This work investigated the formation potential of haloacetic acid (HAA) compounds in the raw water for the Bangkhen water treatment plant (Bangkok, Thailand). The resin adsorption technique (with three different types of resins, i.e. DAX-8, AG-MP-50 and WA-10) was employed to characterize the organic content in the raw water into six fractions, i.e. hydrophobic neutral (HPON), hydrophobic acid (HPOA), hydrophobic base (HPOB), hydrophilic neutral (HPIN), hydrophilic acid (HPIA) and hydrophilic base (HPIB). Hydrophilic species appeared to be the predominant organic species in this water source (approximately 60%) with the neutral fraction being the most abundant (approximately 40%). Hydrophobic species, on the other hand, played the most important role in the formation of haloacetic acids as they contributed to as much as approximately 56% of total HAA formation potential. Among the three hydrophobic species, the hydrophobic base exhibited the highest specific HAA formation with 208mugHAAs/mg of dissolved organic carbon (DOC). Each organic fraction was examined for its associated functional groups by Fourier transform infrared (FTIR). The investigation of the formation of HAAs was achieved by tracking the changes in the FTIR results of the same water sample before and after the chlorination reaction. Based on the results obtained from this study, carboxylic acids, ketone, amide, amino acids and aromatic characteristic organics seemed to be the main precursors to HAA formation.     

Metal sorption on soils as affected by the dissolved organic matter in sewage sludge and the relative calculation of sewage sludge application

To evaluate the influences of sewage sludge-derived organic matters on metal sorption and on the resultant sludge loading estimates, a batch experiment was conducted to compare the sorption of Ni, Cu and Pb in sewage sludge filtrates (1:20 sewage sludge to water) on eight soils and the adsorption of metals in a reference solution which had the same matrix as the sewage sludge filtrate except dissolved organic material (henceforth referred to as reference solution). Metal sorption could be well fitted by linear isotherm and the dissolved organic matter in sludge significantly depressed the sorption (p<0.01). The main factor controlling sorption of Ni on different soils was dominated by soil cation exchange capacity (CEC) and sorption of Cu and Pb was by soil organic matter (SOM). The parameters obtained from the sorption isotherm equations were then used to estimate sludge loadings into the soils. When the sorption parameters derived from the reference solution were used for calculation, that is the effect of dissolved organic matter was not considered, the calculated safe application rates are approximately 47.8, 51.4, 34.2, 31.3, 21.7, 46.3, 187.1 and 27.6 t-sludge/ha for the Beijing, Jiangxi, Xiamen, Jilin, Guangdong, Wuhan, Gansu and Xinjiang soils, respectively. However, when the sorption parameters derived from the dissolved organo-metallic complexes are used for calculation, the corresponding application rates are reduced to approximately 6.0, 3.4, 1.9, 10.0, 6.3, 3.6, 7.3 and 3.5 t-sludge/ha, respectively. By this study we can get a conclusion that the effect of sewage sludge derived dissolved organic matter on heavy metal sorption and soil properties should be considered in the course of regulating the safe application rates of sewage sludge to soil.     

Seasonal variations of chemical and physical characteristics of dissolved organic matter and trihalomethane precursors in a reservoir: a case study

Dissolved organic matter (DOM) and its potential to form disinfection by-products (DBPs) during water treatment are of great public health concern. Understanding the seasonal changes in DOM composition and their reactivity in DBP formation could lead to a better treatment of drinking water and a more consistent water quality. DOM from the East-Lake, a reservoir in the south-China, was fractionated and characterized by XAD resin adsorption (RA) and ultrafiltration (UF) techniques during different seasons within a year. The properties of chemical fractions (isolated by RA) appeared more stable than those of physical fractions (separated by UF) throughout the sampling period. The relative contribution of each chemical fraction to the total dissolved organic carbon (DOC), UV(254) absorbance and trihalomethane formation potential (THMFP) remained relatively constant across the sampling period. However, the physical (molecular weight) fractions of the DOM exhibited large seasonal changes in UV(254) and THMFP. Compared to the parameter of DOC, the THMFP and specific THMFP (STHMFP) of either chemical or physical fractions were more variable. In terms of DOC concentration, the hydrophobic acids (HoA) and hydrophilic matter (HiM) dominated in the DOM in most of the seasons; while the components with molecular weight of 10-30 kDa and less than 1 kDa were the predominant physical fractions.     

Influence of hydrogen bonds on the colloidal and fluorescent properties of detonation nanodiamonds in water,methanol and ethanol

This paper presents the results of research of influence of hydrogen bonds with different strength on fluorescence and colloidal properties of detonation nanodiamonds with surface carboxylic groups in the solvents. It is established that the colloidal properties of detonation nanodiamonds are almost independent on hydrogen bonds strength in water, methanol and ethanol. The fluorescent properties of detonation nanodiamonds are dependent on the type of solvent: the more intensive fluorescent properties correspond to weaker hydrogen bonds in solvents.     

低水多变环境下玉米叶片的光合与反射光谱特征

采用盆栽试验,以玉米品种苏玉19为试材,在每次复水第7天同时测定不同处理植株的生物量、根冠比、叶绿素荧光、气体交换以及光谱特征等指标。结果表明,持续干旱处理抑制植株生长,增加根冠比,并通过气孔限制和非气孔限制因素抑制光合作用。持续干旱处理幼苗的mSR705、chlNDI和REP均显著小于对照,但对SIPI的影响不显著。多变低水环境下玉米幼苗生长明显受到抑制,但根冠比、叶绿素荧光、气体交换以及光谱特征等指标与正常供水没有差异。可见,生物量分配、光合作用和光谱特征的维持可能是玉米适应多变低水环境的重要生理机制。     

Degradation of natural organic matter in surface water using vacuum-UV irradiation

The use of vacuum-UV (VUV) radiation to degrade natural organic matter (NOM) and the main variables affecting the efficiency of this process were investigated using an annular photoreactor. After 180 min of irradiation with VUV, the total organic carbon (TOC) decreased from 4.95 ppm to 0.3 ppm. Also, decadic absorption coefficients of the water at 185 nm and 254 nm decreased from 3.2 cm(-1) to 2.85 cm(-1), and 0.225 cm(-1) to 0 cm(-1), respectively. The reactor operation was kinetically controlled for Reynolds numbers greater than 600, changes of pH between 5 and 9 had little effect, and increases in alkalinity decreased the process efficacy. Additionally, H(2)O(2)/VUV and VUV processes were compared to H(2)O(2)/UV and UV processes, where the formers showed greater effectiveness with complete mineralization of NOM as opposed to partial oxidation with H(2)O(2)/UV, and no mineralization with UV alone. Modeling and analysis of the photon flux and absorption in the reactor showed that 99% of the 185 nm radiation was absorbed by the water in the reactor. In comparison, only 48% of the 254 nm radiation was absorbed by the water. The overall quantum efficiency of the mineralization for VUV was 0.10 for 50% TOC reduction.     

Characterization of precursors to trihalomethanes formation in Bangkok source water

Resin adsorption techniques using three types of resin (DAX-8, AG-MP-50, and WA-10) were employed to characterize the raw water (RW) from the major 3 million m³/day (793 million gal/day) drinking water treatment plant in Bangkok, Thailand. The dissolved organic carbon (DOC) mass distribution sequences of the six organic fractions in raw water, from high to low, were hydrophilic neutral (HPIN), hydrophobic acid (HPOA), hydrophilic acid (HPIA), hydrophobic neutral (HPON), hydrophilic base (HPIB), and hydrophobic base (HPOB). HPIN and HPOA were the two main precursors for trihalomethanes formation (THMFP) in this water source following chlorination. The chlorination of HPON and HPIN fractions only led to the formation of mostly chloroform, while other organic fractions formed both chloroform and bromodichloromethane. The linear dependency between each organic fraction concentration and THMFP indicated that the reactions of each organic fraction with chlorine were first-order.     

卷烟与食品包装材料中挥发性有机化合物的比较分析及其安全性探讨

采用顶空-气相色谱法对卷烟和食品装材料中挥发性有机化合物(VOCs)的含量进行了测定。结果表明:一般来说,同一卷烟商标,条盒比小盒的VOCs含量要高一些,接装纸和内衬纸VOCs含量大大低于条盒和小盒;条盒和小盒VOCs含量随存放时间的增加而不断减少,放置同样的时间条盒中UOCs挥发慢,小盒挥发快。同时对卷烟与食品包装材料VOCs进行了对比分析和安全性探讨,后者被检测有苯系物存在,会给消费者身体造成危害。     

Novel oxidative electrophilic coupling reactions of phenoxazine derivatives with MBTH and their applications to spectrophotometric determination of residual chlorine in drinking water and environmental water samples

Novel, sensitive and rapid spectrophotometric methods, using phenoxazine (PNZ), 2-chlorophe-noxazine (CPN) and 2-trifluoromethylphenoxazine (TPN) as chromogenic reagents for the determination of residual chlorine are proposed. The methods are based on the reduction of chlorine by an electrophilic coupling reagent, 3-methyl-2-benzothiazoline hydrazono hydrochloride hydrate (MBTH) in mild hydrochloric acid medium and subsequent coupling with PNZ, CPN or TPN. The blue color formed in the reaction showed maximum absorbance at 680–690 nm and obeyed Beer's law over the range 0.1–2.2 μg ml⁻¹. The molar absorptivity values with PNZ, CPN and TPN were 2.80 × 10⁴, 2.67 × 10⁴ and 1.91 × 10⁴ l mol⁻¹ cm⁻¹ and Sandell's sensitivity values were 0.028, 0.027 and 0.028 μg cm⁻² respectively. The proposed methods were successfully applied in the determination of residual chlorine in drinking water and environmental water samples. The performance of proposed methods was evaluated in terms of Student's t-test and variance ratio F-test which indicated the significance of proposed methods over the standard spectrophotometric method.     

Enrichment of trace amounts of copper(II) ions in water samples using octadecyl silica disks modified by a Schiff base ionophore prior to flame atomic absorption spectrometric determination

Bis(5-bromo-2-hydroxybenzaldehyde)-1,2-propanediimine is synthesized by the reaction of 5-bromo-2-hydroxybenzaldehyde and 1,2-diaminopropane in ethanol. This ligand is used as a modifier of octadecyl silica disks for preconcentration of trace amounts of copper(II) ions, followed by nitric acid elution and flame atomic absorption spectrometric (FAAS) determination. The effect of parameters influencing the extraction efficiency, i.e. pH of the sample solutions, amount of the Schiff base, type and volume of stripping reagent, sample and eluent flow rates were evaluated. Under optimum experimental conditions, the capacity of the membrane disks modified by 4mg of the ligand was found to be 247.7 (+/-2.1)mug of copper. The detection limit and the concentration factor of the presented method are 2.4ng/l and greater than 400, respectively. The method was applied to the extraction, recovery and detection of copper in different synthetic and water samples.