温度对海水微絮凝-超滤工艺的影响

采用微絮凝-超滤工艺处理不同温度的海水,研究了温度对有机物的去除效果、絮体特性以及超滤膜通量的影响规律.以三氯化铁为絮凝剂,分析了微絮凝-超滤对海水UV254、DOC及三维荧光光谱的影响,监测了不同海水温度下微絮凝过程中产生絮体的絮凝指数、分形维数等特性,考察了微絮凝对超滤膜污染的减缓作用.实验结果表明,当FeCl_3投加量为1.0 mg·L~(-1)时,对5℃、10℃、15℃、20℃海水的UV254去除率分别为84.4%、81.3%、78.1%、71.9%,DOC去除率分别为81.8%、75.8%、65.0%、57.5%,微絮凝-超滤工艺对低温海水的去除效果优于常温海水,可去除海水中的芳香族蛋白类和腐殖酸类有机物;温度对絮凝指数FI的影响较小,说明其不同温度下微絮凝形成的絮体粒径变化不大;但低温海水形成的絮体分形维数要小于常温海水,说明低温海水的絮体结构更加疏松,疏松的絮体结构更有利于减缓后续超滤膜通量的下降.     

气浮中试工艺中若干运行参数

为找出气浮(DAF)工艺的最佳运行工艺参数,对影响气浮工艺出水效果较大的预处理条件、混凝剂投量、水力负荷、水力条件、回流比、刮渣周期等运行参数做了大量的中试试验研究,发现适当的预臭氧处理可以提高UV254的去除,预加氯可以提高对浊度和藻类的去除,预加高锰酸盐可以提高对浊度、藻类、嗅味和UV254等的去除,预加粉末活性炭可以提高对有机物、色度、嗅味的去除,混凝剂投量从10 mg/L增加到50 mg/L,气浮工艺对有机物的去除率提高了30%~40%,水力负荷越高气浮出水浊度越高,回流比越大气浮出水浊度越低,气浮池过长的刮渣周期也会降低出水水质。总之,合理调整气浮池的工艺参数,可以提高气浮出水水质,降低运行成本。     

渤海海水淡化反渗透法的预处理工艺

采用“消毒-混凝-澄清一砂滤”、“消毒-混凝-澄清-砂滤-超滤”以及“消毒-砂滤-超滤”三套海水淡化预处理工艺进行了试验对比。试验的目的在于获取可行的反渗透预处理工艺。表明,采用“消毒-混凝-澄清-砂滤-超滤”工艺或“消毒-砂滤-超滤”工艺是技术可行的反渗透预处理工艺,其中次氯酸钠为可选消毒剂,三氯化铁为较好的混凝剂,而超滤是不可或缺的单元处理工艺。     

SPME-GC-MS联用快速检测赤潮海水中的有机物

本文用固相微萃取（ＳＰＭＥ）样品预处理技术，分离富集海水中的有机物，结合气相色谱－质谱（ＧＣ－ＭＳ）联用技术进行海水中有机物的快速检测，研究了赤潮发生时海水中有机物的种类及含量的变化规律，初步探讨了其变化原因，为研究赤潮的发生机理和赤潮预报提供了科学依据。     

铁盐和铝盐混凝剂对消毒副产物的控制作用及机制研究

以三氯化铁和硫酸铝为研究对象,探讨了两种混凝剂对三氯甲烷生成量的控制作用及控制机制．结果表明,与硫酸铝相比,三氯化铁可以更好地控制三氯甲烷的生成量,对有机物的去除方面,也具有良好的效果．E4／E6变化表明,三氯化铁和硫酸铝对水中有机物的去除机制不同,硫酸铝主要去除水中大分子的有机物,三氯化铁更倾向于去除水中小分子有机物,而这些小分子有机物通常是消毒副产物的前体物,从而使三氯化铁对消毒副产物的控制作用较硫酸铝明显．     

生物陶粒柱—PAC—膜过滤装置系统处理饮用水实验研究

生物陶粒柱和粉末活性炭作为淹没式中空纤维膜过滤装置的预处理工艺不仅解决了膜过滤装置氨氮去除不利的弱点，避免了亚硝酸盐氮的积累，而且在浊度、细菌、有机物等方面极大地降低了膜过滤装置的负荷。生物陶粒柱－PAC－膜过滤装置系统高锰酸盐指数平均去除率为76．97％，氨氮和亚硝酸盐氮的平均去除率分别达到顾95．50％和99．15％。     

低温下曝气生物滤池预处理污染河水的试验研究

采用两段曝气生物滤床串联工艺预处理入滇新运粮河河水,研究了其在冬天低温条件下对有机物和氨氮的去除效果,并考察了pH值的变化。结果表明,在进水流量为2.4 m3.d-1、水温为13-16℃、原水ρ（CODCr）为66.46-107.82 mg·L-1、ρ（氨氮）为22.15-30.68 mg·L-1的水质特征条件下,系统对CODCr和氨氮的去除率分别为36.08%-50.37%和76.98%-93.56%。其中,碳氧化段以去除有机物为主,硝化段以去除氨氮为主;系统中硝酸氮质量浓度明显升高,无亚硝氮的积累;装置对总氮的平均去除率为19.56%,可以认为总氮的去除是同步硝化反硝化的结果。系统中pH值有所变化但维持在7-8之间,其中碳氧化段pH值升高,硝化段pH值下降。系统对有机物和氨氮良好的去除效果为后续进一步的生物处理提供了条件。     

水中天然含氮有机物的形成、迁移转化及分布

天然含氮有机物是水环境中的重要组成部分,其在天然水体中的形态及分布对环境质量有显著影响.本文围绕水中天然含氮有机物在氮循环中的地位、迁移转化以及其在国内主要水域中的分布情况,对天然含氮有机物的研究现状进行了梳理.我国不同水域中溶解性含氮有机物(DON)浓度相差较大;其中水体中DON浓度一般在1.0 mg?L-1以下;沉...     

糖蜜酒精废水两相UASB处理有机物去除特征

应用气相色谱研究了糖蜜酒精废水两相ＵＡＳＢ处理工艺段中有机物的去除情况，结果表明，酸化反应器内，易降解有机物的去除率上为１００％，产甲烷段反应器内，因易降解化合物在酸化反应器内大部分被去除，剩下的化合物的在该段反应器内去除率偏小，仅为８０％。质谱结果证实，进水中的酚类化合物经两级处理后，被有效去除。     

水中天然有机物的臭氧氧化处理特性

通过小型实验和液相色谱分析，研究了水中天然有机物的臭氧氧化反应的特性和反应前后有机物分子量的变化情况。结果表明，臭氧氧化的主要功效不在于降低以TOC为代表的水中有机物总量，而是改变了有机物的性质和结构。通过臭氧氧化处理，水中大分子有机物分解氧化为小分子有机物分解氧化为小分子有机物，且具有饱和构造的有机物成分明显增加。     

Isolation and Chemical Characterization of Dissolved and Colloidal Organic Matter

An overview of the methods used for the isolation and characterization of organic matter in natural waters is presented. Commonly used techniques for the concentration and isolation of organic matter from water, such as preparative chromatography, ultrafiltration and reverse osmosis, and the methods used to analyze the organic matter obtained by these methods are reviewed. the development of methods to obtain organic matter that is associated with fractions of the dissolved organic carbon other than humic substances, such as organic bases, hydrophilic organic acids and colloidal organic matter are discussed. Methods specifically used to study dissolved organic nitrogen and dissolved organic phosphorous are also discussed.     

Isolation and Chemical Characterization of Dissolved and Colloidal Organic Matter

An overview of the methods used for the isolation and characterization of organic matter in natural waters is presented. Commonly used techniques for the concentration and isolation of organic matter from water, such as preparative chromatography, ultrafiltration and reverse osmosis, and the methods used to analyze the organic matter obtained by these methods are reviewed. the development of methods to obtain organic matter that is associated with fractions of the dissolved organic carbon other than humic substances, such as organic bases, hydrophilic organic acids and colloidal organic matter are discussed. Methods specifically used to study dissolved organic nitrogen and dissolved organic phosphorous are also discussed.     

Removal of organic matter and disinfection by-products precursors in a hybrid process combining ozonation with ceramic membrane ultrafiltration

The performance of an integrated process including coagulation, ozonation, ceramic ultrafiltration (UF) and biologic activated carbon (BAC) filtration was investigated for the removal of organic matter and disinfection by-products (DBPs) precursors from micro-polluted surface water. A pilot scale plant with the capacity of 120 m³ per day was set up and operated for the treatment of drinking water. Ceramic membranes were used with the filtration area of 50 m² and a pore size of 60 nm. Dissolved organic matter was divided into five fractions including hydrophobic acid (HoA), base (HoB) and neutral (HoN), weakly hydrophobic acid (WHoA) and hydrophilic matter (HiM) by DAX-8 and XAD-4 resins. The experiment results showed that the removal of organic matter was significantly improved with ozonation in advance. In sum, the integrated process removed 73% of dissolved organic carbon (DOC), 87% of UV₂₅₄, 77% of trihalomethane (THMs) precursors, 76% of haloacetic acid (HAAs) precursors, 83%of trichloracetic aldehyde (CH) precursor, 77% of dichloroacetonitrile (DCAN) precursor, 51% of trichloroacetonitrile (TCAN) precursor, 96% of 1,1,1-trichloroacetone (TCP) precursor and 63% of trichloronitromethane (TCNM) precursor. Hydrophobic organic matter was converted into hydrophilic organic matter during ozonation/UF, while the organic matter with molecular weight of 1000–3000 Da was remarkably decreased and converted into lower molecular weight organic matter ranged from 200–500 Da. DOC had a close linear relationship with the formation potential of DBPs.     

Exudation of dissolved organic carbon by brown algae

The release via exudation of dissolved organic carbon by Ascophyllum nodosum (L.) Le Jol. was investigated under laboratory conditions. In contrast to results previously reported by Sieburth (1969), continuous release of organic matter was found with only 1 specimen out of 21 tested either in stagnant sea water or in sea water flowing through the system. The holdfast of the plants was found to release relatively large amounts of organic material; however, this release lasted only for short periods, and was most probably due to damage caused by removing the plants from their substrate. The possible reasons for the failure to detect exudation are discussed. With Fucus vesiculosus L., no reliable results could be obtained, most probably due to particulate matter sloughing off the plants during the washings and during the experiments under conditions of photosynthesis.     

Surface water treatment benefits from the presence of algae: Influence of algae on the coagulation behavior of polytitanium chloride

• Emerging titanium coagulation was high-efficient for algae-laden water treatment. • Polytitanium coagulation was capable for both algae and organic matter removal. • Surface water purification was improved by around 30% due to algae inclusion. • Algae functioned as flocculant aid to assist polytitanium coagulation. • Algae could enhance charge neutralization capability of polytitanium coagulant. Titanium-based coagulation has proved to be effective for algae-laden micro-polluted water purification processes. However, the influence of algae inclusion in surface water treatment by titanium coagulation is barely reported. This study reports the influence of both Microcystis aeruginosa and Microcystis wesenbergii in surface water during polytitanium coagulation. Jar tests were performed to evaluate coagulation performance using both algae-free (controlled) and algae-laden water samples, and floc properties were studied using a laser diffraction particle size analyzer for online monitoring. Results show that polytitanium coagulation can be highly effective in algae separation, removing up to 98% from surface water. Additionally, the presence of algae enhanced organic matter removal by up to 30% compared to controlled water containing only organic matter. Polytitanium coagulation achieved significant removal of fluorescent organic materials and organic matter with a wide range of molecular weight distribution (693–4945 Da) even in the presence of algae species in surface water. The presence of algae cells and/or algal organic matter is likely to function as an additional coagulant or flocculation aid, assisting polytitanium coagulation through adsorption and bridging effects. Although the dominant coagulation mechanisms with polytitanium coagulant were influenced by the coagulant dosage and initial solution pH, algae species in surface water could enhance the charge neutralization capability of the polytitanium coagulant. Algae-rich flocs were also more prone to breakage with strength factors approximately 10% lower than those of algae-free flocs. Loose structure of the flocs will require careful handling of the flocs during coagulation-sedimentation-filtration processes.     

High amounts of free aromatic amino acids in the protein-like fluorescence of water-dissolved organic matter

Fluorescence spectroscopy is widely used to study water pollution. The fluorescence of water natural organic matter can be classified into two groups: the protein-like fluorescence originating from aromatic amino acids and the humic fluorescence originating from humic substances. Actually, the precise molecular origin of the protein-like fluorescence is unknown because this fluorescence may be caused by either free amino acids, peptides or proteins. Therefore, we studied the molecular origin of the protein-like fluorescence of Suwannee River natural organic matter and fractions A, B and C + D obtained by size exclusion chromatography/polyacrylamide gel electrophoresis. Fractions were analyzed by reversed-phase high-performance liquid chromatography. The electrophoretic mobilities of fractions varied in the order C + D > B > A and the molecular size in the opposite order. Our results show that the protein-like fluorescence is almost exclusively located in high molecular size fraction A and medium molecular size fraction B. Retention times and fluorescence emission spectra of authentic free aromatic amino acids tyrosine and tryptophan were identical with the retention times and emission spectra of several chromatographic peaks of fractions A and B. More than 50 % of the protein-like fluorescence is due to free aromatic amino acids incorporated in water natural organic matter.     

石灰预处理对树叶堆肥过程中养分转化的影响

以树叶干质量的0%、1.00%、2.50%和4.00%的石灰预处理树叶,24h后分别将预处理后的树叶与鸡粪联合堆肥,研究不同用量石灰预处理树叶对树叶堆肥过程中养分转化的影响。试验在自制的堆肥反应器内进行,采用间歇式强制通风的方式,进行为期59d的堆肥试验。结果表明:石灰预处理树叶24h可以有效的降低树叶中的有机质质量分数,以4.00%的石灰预处理的树叶其有机质降幅达6.00%;石灰预处理24h后,各处理pH相差不大;EC的变化与pH相似;预处理前后,各处理总氮、总磷和总钾的质量分数相差不大。用石灰预处理后的树叶堆肥有利于堆肥有机质的降解,尤以2.50%石灰预处理的效果最好;有利于堆肥w(C)/w(N)的降低,其降低幅度与石灰用量成正比;有利于减少堆肥过程中氮素的损失,且氮素损失与石灰使用量呈反比;有利于堆肥NH4 -N质量分数的降低;提高堆肥终产品NO3--N的质量分数,其质量分数与石灰用量呈正比;有利于堆肥中钾的浓缩;对堆肥的pH、EC、w(NH4 -N)/w(NO3--N)和总磷的影响不大。综合考虑试验结果后认为,以4.00%石灰预处理的效果最为理想。     

Identification of Anthropogenic Organic Contamination Associated with the Sediments of a Hypereutropic Tropical Lake, Venezuela

The concentrations of organic carbon (Corg), inorganic carbon (Cinorg), organic nitrogen (Norg) and total aromatic (Arom_T) were determined in 25 samples of bottom sediments from the Lake Valencia, Venezuela, as a contribution to the knowledge about pollution by organic compounds in tropical lakes. Results demonstrate that the Corg and Norg concentrations do not show the pollution indexes by themselves. This is a consequence of the masking effect of naturally derived organic matter from the decay of algae and organisms in the water column and terrestrial plants, which are transported to the lake. Nevertheless, the Arom_T concentrations and the normalised Arom_T (normalized to organic carbon) make it possible to detect organic matter of anthropogenic origin, in the Arom_T levels are about nine times higher than those natural. The variation in the band intensity of the IRFT spectra for some functional groups present in the saturate and aromatic hydrocarbon fractions gives an indication of anthropogenic contribution for some zones of the lake. With the ¹H NMR spectra it was not possible to differentiate a natural source from an anthropogenic one in the lake. Naturally occurring organic compounds (eicosane, pentacosane, and hexacosane) were detected with GC technique in the saturated hydrocarbon fraction. The presence of an unresolved complex mixture (UCM) in the GC chromatograms indicates pollution by branched and cyclic hydrocarbons. These compounds are probably produced by the incomplete combustion of oil products. Potentially toxic organic compounds such as anthracene, phenanthrene and chrysene were found in the aromatic hydrocarbon fraction, which despite presenting low concentrations (ppb order) accumulate in the lake sediments along with the natural source organic matter. The main access paths of organic pollutants to the lake are the rivers which cross the two urban and industrial areas (Maracay and Valencia cities). The mixture of polluted sediments with bottom natural sediments and the autochthonous contribution of organic matter mitigate the pollution levels progressively towards the center of the lake.     

Molecular weight fractionation of dissolved organic matter in coastal seawater by ultrafiltration

Fractionation of molecular weight of dissolved organic matter (DOM) in coastal seawater of Tokyo Bay (Japan) was performed by ultrafiltration. Ultrafiltration membranes Diaflo UM-05, UM-10 and XM-100 were used for DOM fractionation, and dissolved organic carbon (DOC) was determined for ultrafiltrates of each membrane. In surface water of Station 1, near the center of Tokyo Bay, low-molecular weight DOM (molecular weight less than 500) which passed through a Diaflo UM-05 membrane was 0.3 to 2.6 mgC/l (24 to 42% of the total DOC) during August, 1971 to September, 1972. The macromolecular DOM (molecular weight greater than 100,000) retained on an XM-100 membrane, ranged from 0.1 to 1.0 mgC/l. These fractions accounted for 8 to 23% of the total DOC. The precision of the method was within ± 0.1 mgC/l, and therefore may be employed for coastal seawater of high DOC content.