滦河水体溶解性有机物的综合分级表征及其混凝去除过程

天然水体溶解性有机物(DOM)是微污染物的潜在载体,是消毒副产物的主要前驱物,自身又可能成为微污染物,因此研究其内在特性和去除机理有着重要的基础性科学意义.本研究综合利用化学、物理分级方法(即树脂和超滤分级法),对中国北方典型饮用水源--滦河水体的DOM进行全面分级表征.此水体DOM基本化学分级特征是憎水酸(HoA)、亲水性物质(HiM)含量较高,且具有季节稳定性;其物理分级特征是分子量＜1 kDa及3 kDa～10 kDa的组分含量较高,也表现出一定的时间稳定性.选用工业聚合铝(PAC)研究此DOM的基本混凝特征和内在混凝机理,结果表明,强憎水部分HoA及3 kDa～10 kDa间的有机物较易被去除,而较大分子量范围10 kDa～30 kDa间的有机物去除率较低,说明混凝过程中此DOM的物理性质不起主要作用,而化学性质更为重要.特别对DOM各组分作进一步(结合)分级研究,发现HoA主要在＞10 kDa范围.＜1 kDa的有机物中主要为HiM,但其中还含有HoA和弱憎水酸(WHoA),这使特定条件下部分＜1 kDa有机物被混凝去除成为可能.另外,HoA中按分子量大小仍可分为易去除和难去除部分,但分布不连续,易去除部分在3 kDa～10 kDa和＞30 kDa区间,而其10 kDa～30 kDa部分较难去除,说明可能存在其他结构性影响因素,值得深入研究.     

Atmospheric bulk deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in the vicinity of an iron and steel making plant

An IRA-743 resin bulk sampler was validated to monitor long-term bulk deposition of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). Six consecutive sampling campaigns (2008-2009) were conducted at four sites around steel complexes in Pohang, South Korea to investigate spatial and seasonal variations of PCDD/F bulk deposition. The bulk deposition within the steel complex showed the highest ∑_4-8PCDD/F (Tetra-Octa) fluxes, ranging from 204 to 608 (mean: 352) pg m⁻² d⁻¹, indicating steel complexes were major sources of PCDD/Fs. The homologue profiles were dominated with lower chlorinated PCDFs. Furthermore, the prevailing winds were confirmed to influence the spatial distribution of PCDD/F deposition. There were apparent seasonal variations of the bulk deposition at each site, and seasonal homologue patterns of PCDD/Fs were clearly observed. According to the passive air sampling, however, no significant seasonal change of ambient air concentrations of PCDD/Fs was observed. Therefore, it was concluded that the seasonal variations of deposition fluxes of PCDD/Fs probably resulted from temperature-dependent gas/particle partitioning.     

Adsorption thermodynamics and kinetic investigation of aromatic amphoteric compounds onto different polymeric adsorbents

The adsorption behavior of p-aminobenzoic acid and o-aminobenzoic acid onto the different polymeric adsorbents was systematically investigated as a function of the solution concentration and temperature.Experimental results indicated that the equilibrium adsorption data of the four polymeric adsorbents fitted well in the Freundlich isotherm.The adsorption capacity of multi-functional polymeric adsorbent NJ-99 was the highest,which might be attributed to the strong hydrogen-bonding interaction between the amino groups on the resin and the carboxyl group of aminobenzoic acid.The adsorption capacity of o-aminobenzoic acid onto any adsorbent was higher than p-aminobenzoic acid.Thermodynamic studies suggested the exothermic,spontaneous physical adsorption process.Adsorption kinetics results showed that the adsorption followed the pseudo-second-order kinetics model and the intraparticle mass transfer process was the rate-controlling step.     

Transformations of particles, metal elements and natural organic matter in different water treatment processes

Characterizing natural organic matter （NOM）, particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Preozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon （GAC） filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant （HPAC） was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.     

太阳光Fenton氧化对含酚废水生物降解影响研究

研究了太阳光Fenton氧化预处理对含酚废水生物降解性的影响及太阳光Fenton氧化-生化法联合工艺对煤气含酚废水的处理效果。结果表明,煤气含酚废水和模拟含酚废水的生物降解性均较差,太阳光Fenton氧化预处理可明显提高含酚废水的生物降解性,随着H2O2投加量的增加,废水的BOD5/COD比值逐渐增大,生物降解性明显增强。煤气含酚废水直接进行生化处理的COD和挥发酚去除率均较低。当太阳光Fenton氧化过程H2O2用量为22.5%理论投加量时,采用太阳光Fenton氧化-生化法联合工艺可使煤气含酚废水的COD由1357mg/L降低至104mg/L,挥发酚由198.2mg/L降低至0.47mg/L,COD和挥发酚均达到国家二级排放标准。     

树脂吸附-Fenton试剂氧化法处理水杨醛生产废水

采用树脂吸附-Fenton试剂氧化法处理水杨醛生产废水。XF-01树脂和XF-02树脂静态吸附水杨醛生产废水时,COD去除率均在85％以上,挥发酚去除率均高于90％。XF-02树脂对水杨醛生产废水的处理效果更佳。动态吸附随废水流量增大,吸附出水的COD和挥发酚质量浓度均增加。适宜的废水流量为15BV,树脂的最佳脱附温度为80℃。在连续4批的吸附-脱附实验中,吸附出水的平均COD约为1200mg／L,平均挥发酚质量浓度小于10mg／L。在Fenton试剂氧化中,铁屑和铁粉的催化效果差别很小,都好于FeSO4·7H2O。以铁屑为催化剂、H2O2溶液加入量为1％时,氧化出水的COD小于150mg／L,挥发酚质量浓度小于0．5mg／L。     

水体中酚类化合物分光光度分析方法的研究

对国内外水体中酚类化合物现有的分光光度分析方法进行了文献综述 ,内容包括可见光分光光度法、紫外光分光光度法、荧光分光光度法和流动注射分光光度法。在总结归纳的基础上 ,提出了水体中酚类化合物分光光度分析方法的发展方向。     

A miniature stainless steel net dumbbell-shaped stir-bar for the extraction of phthalate esters in instant noodle and rice soup samples

Abstract

This work reports the development of a very-simple-to-construct stir-bar extraction device so called “a dumbbell-shaped stainless steel stir-bar.” The extraction device was assembled from a rolled up stainless steel net filled with an XAD-2 sorbent and a metal rod to allow the use of a magnetic stirrer during extraction. The dumbbell-shaped stainless steel stir-bar was used to extract diethyl phthalate (DEP), dibutyl phthalate (DBP), and di(2-ethylhexyl) phthalate (DEHP) before analysis by a gas chromatograph equipped with an electron capture detector (GD-ECD). Under the optimal conditions, the developed method provided a good linearity from 10.0 to 1,000.0?ng mL^?1 for all three compounds. Limits of detection and limits of quantification were 9.37?±?0.29?ng mL^?1 and 31.22?±?0.95?ng mL^?1 for DEP, 5.73?±?0.31?ng mL^?1 and 19.1?±?1.0?ng mL^?1 for DBP and 3.30?±?0.06?ng mL^?1 and 11.0?±?0.19?ng mL^?1 for DEHP, respectively. Good recoveries in the range of 81.89?±?0.17 to 109.5?±?2.0% were achieved when the method was used to extract phthalate esters in five instant noodle and two rice soup samples.     

Nitrogen removal efficiencies and microbial communities in full-scale IFAS and MBBR municipal wastewater treatment plants at high COD:N ratio

• Two IFAS and two MBBR full-scale systems (high COD:N ratio 8:1) were characterized. • High specific surface area carriers grew and retained slow-growing nitrifiers. • High TN removal is related to high SRT and low DO concentration in anoxic tanks. The relative locations of AOB, NOB, and DNB were examined for three different kinds of carriers in two types of hybrid biofilm process configurations: integrated fixed-film activated sludge (IFAS) and moving bed biofilm reactor (MBBR) processes. IFAS water resource recovery facilities (WRRFs) used Anodkalness^TM K1 carriers (KC) at Broomfield, Colorado, USA and polypropylene resin carriers (RC) at Fukuoka, Japan, while MBBR WRRFs used KC carriers at South Adams County, Colorado, USA and sponge carriers (SC) at Saga, Japan. Influent COD to N ratios ranged from 8:1 to 15:1. The COD and BOD removal efficiencies were high (96%–98%); NH₄⁺-N and TN removal efficiencies were more varied at 72%–98% and 64%–77%, respectively. The extent of TN removal was higher at high SRT, high COD:N ratio and low DO concentration in the anoxic tank. In IFAS, RC with high specific surface area (SSA) maintained higher AOB population than KC. Sponge carriers with high SSA maintained higher overall bacteria population than KC in MBBR systems. However, the DNB were not more abundant in high SSA carriers. The diversity of AOB, NOB, and DNB was fairly similar in different carriers. Nitrosomonas sp. dominated over Nitrosospira sp. while denitrifying bacteria included Rhodobacter sp., Sulfuritalea sp., Rubrivivax sp., Paracoccus sp., and Pseudomonas sp. The results from this work suggest that high SRT, high COD:N ratio, low DO concentration in anoxic tanks, and carriers with greater surface area may be recommended for high COD, BOD and TN removal in WRRFs with IFAS and MBBR systems.     

改性三聚氰胺甲醛树脂的合成及性能研究

研究了反应物配比、反应时间、反应温度、ＰＨ值对丙烯酰胺改性三聚氰胺甲醛树脂絮凝效果的影响，实验结果表明絮凝效果最佳的合成反应条件为三聚氰胺／甲醛／丙烯酰胺（质量比）＝１／５（２－３），反应温度为７０℃，反应时间为４ｈ，ＰＨ值为９．０左右。