Effects of water quality on the coagulation performances of humic acids irradiated with UV light

The presence of humic acid in drinking water treatment has received significant attention in recent years because of its adverse effects on the removal of many pollutants in coagulation. In this paper, the effects of water quality including pH, turbidity, alkalinity, and hardness on the removal of humic acid were investigated in a UV light hybridized coagulation process. Our results suggested that UV light radiation could effectively improve the removal rate of humic acid in coagulation under both neutral and basic conditions, and the variations of the selected water quality parameters had little adverse effect on the function of UV light. After UV light radiation, the removal rate of the nitro-humic acid (NHA) increased from 20% to 60% in coagulation, and increased further to 75% and 85% for the raw waters with 10.0 NTU kaolin and 100 mg·L^-1 hardness, respectively. In addition to NHA, the removal rates of the humic acid extracted from peat coal (PHA) and the humic acid provided by Japan metals and chemicals company (JHA) in coagulation were also improved, both in the range of 80%–90% after undergoing UV light radiation. By changing the radiation location from prior to coagulation to the flocculation process, similar experimental results were obtained. The formation of positive charged sites after UV light radiation was considered to be the primary factor that led to an enhanced removal of the humic acid in coagulation.     

Preparation of floating BiOCl0.6I0.4/ZnO photocatalyst and its inactivation of Microcystis aeruginosa under visible light

Frequent occurrence of harmful algal blooms has already threatened aquatic life and human health. In the present study, floating BiOCl_0.6I_0.4/ZnO photocatalyst was synthesized in situ by water bath method, and and applied in inactivation of Microcystis aeruginosa under visible light. The composition, morphology, chemical states, optical properties of the photocatalyst were also characterized. The results showed that BiOCl_0.6I_0.4 exhibited laminated nanosheet structure with regular shape, and the light response range of the composite BZ/EP-3 (BiOCl_0.6I_0.4/ZnO/EP-3) was tuned from 582 to 638 nm. The results of photocatalytic experiments indicated that BZ/EP-3 composite had stronger photocatalytic activity than a single BiOCl_0.6I_0.4 and ZnO, and the removal rate of chlorophyll a was 89.28% after 6 hr of photocatalytic reaction. The photosynthetic system was destroyed and cell membrane of algae ruptured under photocatalysis, resulting in the decrease of phycobiliprotein components and the release of a large number of ions (K⁺, Ca²⁺ and Mg²⁺). Furthermore, active species trapping experiment determined that holes (h⁺) and superoxide radicals (·O₂⁻) were the main active substance for the inactivation of algae, and the p-n mechanism of photocatalyst was proposed. Overall, BZ/EP-3 showed excellent algal removal ability under visible light, providing fundamental theories for practical algae pollution control.     

Spatial,temporal, and environmental limits on xanthotoxin induction in wild parsnip foliage

Summary Although present constitutively in large amounts, furanocoumarins in leaves of wild parsnip,Pastinaca sativa, are inducible to even higher concentrations by mechanical and insect damage. We conducted several experiments in order to characterize the nature and extent of xanthotoxin inducibility inP. sativa foliage. In order to determine the extent to which induction is localized, we mechanically damaged a single leaflet of a compound leaf on seven plants. Xanthotoxin concentrations increased significantly only in the damaged leaflet and in the half of the terminal leaflet closest to the damaged leaflet; thus, xanthotoxin induction is localized to the immediate vicinity of damage. To determine whether xanthotoxin induction results fromin situ biosynthesis or translocation from other plant parts, we detached individual leaflets from ten plants, damaged half of these detached leaflets, and compared xanthotoxin concentrations after 6 h in damaged and intact leaflets. We found that xanthotoxin concentrations increased 41% in damaged leaflets compared to detached leaflets that were not damaged. We also determined the rapidity and duration of the induction response. In leaflets that were damaged and then harvested after 0, 3, 24, 72, 120 and 168 h, xanthotoxin concentrations increased rapidly compared to undamaged leaflets on the opposite side of the leaf, reaching maximum levels within 24 h. This response was of comparatively short duration; concentrations declined to preinduction levels after seven days. To determine whether availability of resources influences the induced response, we performed two experiments, one in which soil nutrients were manipulated and one in which light level was manipulated. The low nutrient treatment was sufficiently extreme to cause cessation of aboveground growth, and the low light treatment caused etiolation. Extremes of resource limitation notwithstanding, leaflets significantly increased xanthotoxin production (2 to 3-fold increase under nutrient limitation and 3-fold increase under light limitation) in response to damage in both experiments.     

可见光催化剂Ag_3PO_4/海泡石的制备及降解染料废水性能

以沉淀法、离子交换法和原位法制备了Ag_3PO_4/海泡石复合光催化剂,采用XRD、FTIR、UV-Vis-DRS对其结构进行了表征,以可见光驱动催化降解日落黄染料为探针反应,考察了制备方法对催化剂光催化性能的影响。结果表明:Ag_3PO_4与海泡石成功复合并产生了协同作用,催化剂中Ag_3PO_4均为立方晶型,部分Ag_3PO_4进入了海泡石层间,改变了其晶面有序性并拓宽了层间距,海泡石对Ag_3PO_4的复合提高了Ag_3PO_4的稳定性和光催化活性;其中,离子交换法制备的光催化剂中Ag_3PO_4与海泡石的复合程度最高,Ag_3PO_4稳定性最强,光催化活性最好,在可见光驱动下,该催化剂对50 mg/L的日落黄降解率可达97.16%,并且对其他3种50 mg/L的染料废水的降解率也在86%以上,此外,该催化剂再生2次后仍保持良好的活性和稳定性。     

底泥厌氧环境和光照对菹草萌发和幼苗生理的影响

通过向底泥中投加不同量的蔗糖使其发生厌氧反应以模拟不同程度的底泥厌氧环境，研究这种环境和光照强度对菹草石芽萌发和幼苗生理作用的影响。实验结果表明，底泥厌氧环境能显著降低菹草石芽的最终萌发率，且低光照会加剧这种趋势；尽管低光照不一定会提高最终的萌发率，但对提早石芽的萌发是有利的。在01%蔗糖投加处理中，幼苗的叶绿素和可溶性蛋白含量最高(平均为250和1928 mg/g FW)，其后随投加量的升高而降低，而游离氨基酸的含量却一直呈上升趋势，最高时达到024 mg/g FW ，但低光照却使它下降；可溶性糖含量基本不受底泥厌氧水平的影响，但随着光照减少而降低。随着厌氧水平的增加（从对照到05%蔗糖投加量），菹草的超氧物歧化酶(SOD)活性呈现上升趋势，但在10%蔗糖投加处理中活性降至最低；而过氧化物酶(POD)活性一直处于下降趋势。研究结论是：底泥厌氧对菹草石芽萌发影响显著，这种影响可能比低光照的限制作用还要重要。轻度的厌氧环境反而能促进菹草幼苗的生理代谢，但随厌氧水平的升高对碳氮平衡和其它生理活动产生不利影响。此外，底泥厌氧环境对菹草幼苗的抗氧化系统也有明显刺激作用。     

UV/Fenton光解处理含三唑磷废水的研究

采用类UV／Fenton法对模拟三唑磷废水进行处理。在模拟废水中人工投加H2O2和Fe^3＋试剂能产生类Fenton试剂，类Fenton试剂在光照条件过程中可以产生大量活性羟基．OH，能够很好地氧化降解废水中的有机化合物。本方法可以有效的处理低浓度的含三唑磷的废水，提供三唑磷农药水样的UV／Fenton催化氧化过程的一级动力学方程。     

Phototransformation of Clodinafop-Propargyl

Abstract

Photodegradation of the herbicide clodinafop-propargyl was investigated on glass surface under sunlight and UV light. Four photoproducts were identified by NMR, IR, and MS. Major photolysis products were 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoic acid and prop-2-ynyl-2-[(5-chloro-3-hydroxy-2-pyridyloxy) phenoxy] propanoate, while minor were ethyl 2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate and 1-hydroxypropanyl-2-[(5-chloro-3-fluoro-2-pyridyloxy) phenoxy] propanoate. Rate of photodegradation followed first-order kinetics with significant correlation coefficient. The major photoproducts were observed in maximum quantity on the 7th and 10th day and further degraded within 15–20 days.     

太湖水体光学特征及其对水中初级生产力的影响

对太湖梅梁湾水体实测结果表明 :在水体表面 ,UV -C的强度较小 ,只有 10 -5μE·m-2 ·s-1数量级 ;UV -B的强度随着波长的增加而呈现递增的趋势 ;UV -A的强度较强 ,达 10 -2 μE·m-2 ·s-1数量级 ,并且在水体中衰减较快 ,衰减系数 (Kd)可以达到 12 .5m-1。可见光在水体中Kd 可达 8.2m-1。在水下 0 .5m处 ,紫外线不足表面光强的 1% ,可见光是表面光强的 2 0 %左右。初级生产力在表面相对较小 ,在水下 0 .2m处最大 ,且随水深的增加而减少 ;在水体中直接测定发现 ,0 .2m处溶解氧值较高。初级生产力的这种分布是水体中紫外光与可见光共同作用的结果。     

Tertiary treatment of municipal wastewater using isolated algal strains: treatment efficiency and value-added products recovery

ABSTRACT

Two microalgal strains (Chlorella sorokiniana, A&B,) grown optimally at pH 9 (A) and 7 (B) were isolated from a municipal wastewater treatment plant. These strains were used to check their efficacy for nutrients and organic carbon removal capacities from the tertiary wastewater. The strains were characterised using 18S rDNA sequencing method and both the strains closely related to Chlorella sorokiniana. Different inoculum doses (IDs) of both the strains were tried to check their efficacy on wastewater treatment. Due to the increase in the IDs, hydraulic retention time decreased from 6 d to 1?d. On an average, 12–100% of total kjeldahl nitrogen, 53–96% NO₃–N, and 59–92% PO₄–P, were removed. Despite the same growth environment, strain A with the highest ID (700?mg/L) showed the best performance in terms of overall organic carbon removal, nutrient removal, and value-added products recovery. Strain A showed an increase in carbohydrate and protein content by 42% and 13%, respectively. Both the strains showed luxury phosphorus uptake and found suitable for advanced wastewater treatment.     

Effects of UV-A LED light irradiation on growth of cultured RAW 264.7 cells

The aim of this study was to examine the effects of ultraviolet A (UV-A) irradiation-induced damage on cultured macrophage RAW 264.7 cells and determine which components produced these manifestations. RAW 264.7 cells were irradiated with 365 nm UV-A using a light-emitting diode (LED). Cell viability and damage were determined using a calcein-AM and propidium iodide dual-staining assay and lactate dehydrogenase leakage, respectively. Intracellular reactive oxygen species (ROS) were measured by H₂DCF-DA. The components of ROS in each medium were measured using an electron paramagnetic resonance (EPR) spectrometer in the presence of 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) and 2,2,5,5-tetramethyl-3-pyrroline-3-carboxamide (TPC). While UV-A irradiation for 2 min significantly suppressed cell growth, LDH leakage did not occur. Addition of N-acetyl cysteine restored inhibition of cell proliferation, and reduced intracellular ROS levels. The EPR signal in the presence of TPC increased with time but was decreased by sodium azide. In addition, a typical EPR spectrum was obtained in the presence of DMPO, indicating the presence of a hydroxyradical. The spectrum was diminished by L-histidine. Data suggest that ROS generated in cells or culture medium by UV-A irradiation is predominantly singlet oxygen, and this singlet oxygen suppressed cell proliferation.