飞机蒙皮用含氟聚氨酯涂层老化原因分析

选用飞机蒙皮常用的含氟聚氨酯涂层体系为研究对象,结合飞机服役环境的主要特点,开展了实验室模拟加速老化试验研究,并利用电化学阻抗谱对老化试验后的涂层进行了表征.结果表明,紫外线仅对涂层的表面结构产生影响,紫外试验后的涂层电阻下降较慢.在紫外-盐雾循环试验中,紫外线引起涂层表面结构发生变化,涂层的耐水性变差,水更快地进入涂...     

太阳跟踪反射聚光户外加速试验研究

太阳辐射是引起有机材料老化的最主要原因.由于拉萨高原地区的太阳辐射年总量比内地同纬度高出约1倍,在拉萨进行有机涂层样品的户外暴露试验,其老化速度可大大提高.通过在拉萨试验站对4种常用的有机防护涂层开展太阳跟踪反射聚光户外加速试验和自然暴露试验对比研究,优选出了环境适应性好的材料,并验证了其加速性.     

疏水性超高交联吸附树脂对氯代烃蒸气的固定床吸附特性研究

采用固定床吸附法研究了三氯乙烯（TCE）、 1,2-二氯乙烷（DCE）和三氯甲烷（TCM）共3种氯代烃类蒸气在疏水性超高交联吸附树脂LC-1上的动态吸附行为.结果表明, TCE、 DCE和TCM蒸气的初始浓度、 气体流速和吸附温度均会影响动态吸附过程,随着初始浓度、 气体流速和吸附温度的增大,穿透时间变短,传质区长度增大,其中气体流速的影响最大;采用半经验数学模型Yoon-Nelson模型对吸附穿透实验数据进行拟合,拟合相关性系数R²≥0.994.     

雷达吸波涂层海洋大气环境适用性试验研究

目的 分析一种雷达吸波隐身涂层在海洋大气自然环境下性能的变化规律。方法 对12个月不同阶段涂层的常规物理性能和电性能进行检测,其中常规物理性能包括宏观形貌、金相形貌、微观性能、附着力、抗冲击强度和红外光谱。结果 从宏观形貌看,涂层明度和色差值呈上升趋势,12个月明度增加1.22,色差值增加2.91,颜色向绿色和蓝色发展,失光率先增大、后减小,最大失光率为9个月时的34%。涂层附着力和试验时间呈现非线性关系,6个月时,附着力降低了18%,12个月时增大了24%。涂层在2～18GHz的频率范围内,吸波曲线大体呈“U”形,最低反射率随时间向低频方向偏移。涂层金相形貌、微观性能、抗冲击强度和红外光谱特征总体变化不明显。结论 在1a内,自然海洋大气环境对雷达吸波隐身涂层常规物理性能和电性能产生了一定影响,但在试验时间相对较短情况下,海洋大气环境对涂层老化的影响作用尚未充分显示,需要结合更长周期的试验数据进一步分析。     

Role of water chemistry on estrone removal by nanofiltration with the presence of hydrophobic acids

Hydrophobic acid organic matter (HpoA) extracted from treated effluent has been known to improve the rejection of steroid hormone estrone by reverse osmosis (RO) and nanofiltration (NF) membranes. In this study, the effects of solution chemistry (solution pH and ionic strength) on the estrone rejection by NF membrane with the presence of HpoA were systematically investigated. Crossflow nanofiltration experiments show that the presence of HpoA significantly improved estrone rejection at all pH and ionic strength levels investigated. It is consistently shown that the “enhancement effect” of HpoA on estrone rejection at neutral and alkaline pH is attributed to the binding of estrone by HpoA macromolecules via hydrogen bonding between phenolic functional groups in feed solutions, which leads to an increase in molecular weight and appearance of negative charge. The membrane exhibited the best performance in terms of estrone rejection at pH 10.4 (compared to pH 4 and pH 7) as a result of strengthening the electrostatic repulsion between estrone and membrane with the presence of HpoA. At neutral pH level, the ability of HpoA macromolecules to promote estrone rejection became stronger with increasing ionic strength due to their more extended conformation, which created more chances for the association between estrone and HpoA. The important conclusion of this study is that increasing solution pH and salinity can greatly intensify the “enhancement effect” of HpoA. These results can be important for NF application in direct/indirect potable water reuse.     

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.     

有机质官能团及微孔特性对疏水性有机污染物吸附的影响机制

作为重要的地质吸附剂,土壤/沉积物中的有机质是环境中疏水性有机污染物主要的汇.由于有机质的结构异质性,疏水性有机污染物一旦进入其中,会被吸附在不同的位点上,反应活性和生态风险进而会发生变化.对疏水性有机污染物在有机质上的吸附进行研究有助于了解其在环境中的分布,传输及生物有效性.本文就疏水性有机污染物在土壤/沉积物中的有机质上吸附的国内外研究进展进行了综述,讨论了重要有机质组分(腐殖质和碳黑)的结构和吸附作用差异性,重点分析了有机质的微孔特性和官能团对吸附的影响机制.     

包膜材料对土壤酶活性的影响

以自然资源＂水冬瓜果油＂为包膜材料,利用盆栽试验,共设5个处理,研究在有菊花吸收养分的情况下,水冬瓜（Idesia polycarpa maxim.var.vestita dies）油包膜材料在土壤中的降解性能及对土壤酶活性的影响。结果表明：水冬瓜油包膜材料随土壤含水量的增加,降解速率加快。种植菊花的土壤过氧化氢酶、蔗糖酶、脲酶活性也呈现先上升、后下降的趋势。在土壤含水量为30%时,包膜材料半衰期只有62 d;在处理3（果油85%＋调理剂15%）中,土壤过氧化氢酶、土壤蔗糖酶和脲酶数量增加最多。因此,水冬瓜果油85%＋调理剂15%和土壤含水量30%,有利于土壤酶活性的提高,从而加快包膜材料的降解速度。     

广东省家具行业基于涂料类型的VOCs排放特征及其环境影响

为掌握不同涂料类型废气之间的排放差异,基于溶剂型、水性、溶剂型辐射固化（ultra-violet,UV）、水性UV和粉末等不同涂料类型,选取典型家具制造企业进行废气采样,对比研究不同涂料类型废气挥发性有机物（volatile organic compounds,VOCs）排放浓度和组分差异,并对不同涂料类型废气的臭氧生成潜势（ozone formation potential,OFP）和二次有机气溶胶生成潜势（secondary organic aerosol formation potential,SOAFP）进行分析.结果表明,溶剂型涂料废气的总挥发性有机化合物（total volatile organic compound,TVOC）浓度、OFP和SOAFP均高于水性、溶剂型UV、水性UV和粉末涂料废气.不同涂料类型有组织废气VOCs浓度水平和组成差异较大.溶剂型涂料和溶剂型UV涂料废气以芳香烃和含氧挥发性有机物（oxygenated volatile organic compounds,OVOCs）为主,芳香烃的占比分别为41.91%~60.67%和42.51%~43.00%,OVOCs的占比分别为24.75%~41.29%和41.34%~43.21%.水性涂料、水性UV涂料和粉末涂料废气中VOCs占比最高的是OVOCs,占比分别为54.02%~62.10%、55.23%~64.81%和42.98%~46.45%.溶剂型涂料废气的主要组分为苯乙烯（14.68%）,水性涂料废气的主要组分为甲缩醛（14.61%）,溶剂型UV涂料和水性UV涂料废气的主要组分均为乙酸丁酯（15.36%和20.56%）,粉末涂料废气的主要组分是3-乙氧基丙酸乙酯（20.19%）.芳香烃对溶剂型涂料和溶剂型UV涂料废气的OFP贡献最大,分别为79.84%和80.32%.水性涂料和水性UV涂料废气OFP的主要贡献者是芳香烃（51.48%和36.71%）和OVOCs（42.30%和41.03%）.芳香烃（43.46%）、OVOCs（28.06%）和烯烃（25.24%）是粉末涂料OFP的主要贡献者.芳香烃是溶剂型涂料、水性涂料、溶剂型UV涂料、水性UV涂料和粉末涂料废气SOAFP的绝对贡献者,占比均超过99%.     

发酵制药废水二级出水中溶解性有机物特性分析

溶解性有机物（DOM）是发酵制药废水二级生化尾水深度处理工艺的主要去除对象,深入解析废水中DOM的特性是将其有效去除的前提和关键.本研究采集氨基酸类、头孢类、抗生素类、维生素类、阿维菌素类5种发酵制药废水二级出水,通过XAD-8树脂亲疏水性分离、凝胶色谱分子量分级、傅里叶变换红外光谱和三维荧光表征对二级出水中的DOM进行特性分析.结果表明,5种发酵制药废水二级出水的盐度和色度高,废水中有机物浓度高、波动大（48.60~245.40 mg·L^-1）.DOM大多数以疏水性组分为主,分子量分布广泛（210~10000 Da）.二级出水DOM均含有大量的不饱和双键、苯环结构,同时含有—OH、—NH₂和C=O等发色团和助色基团,造成废水色度较高.通过对发酵制药废水二级出水进行EEM-PARAFAC分析确定了4种荧光组分特征峰,包括3种腐殖质类（C1、C3、C4）和1种类蛋白类组分（C2）.发酵制药废水二级出水中DOM主要是以类腐殖质有机物为主（C1、C3）.全方面识别和解析发酵制药废水DOM的组成,可为废水深度处理工艺的优化提供指导.