沂沭河底泥中污染物空间分布特征及评价

测定沂沭河底泥的有机质(OM)、总氮(TN)、总磷(TP)及有效磷含量,分析了污染物之间的相关性,评价了沂沭河底泥的污染状况。结果表明:沂沭河流域表层沉积物中TN、TP分布特性相似,沂河中OM含量远低于沭河,OM、TN、TP分布的空间差异较大。有效磷含量约占TP含量的17.7%,表明农田及人类活动对流域水环境造成了一定程度的污染。C/N、N/P及OM与氮、磷含量的回归分析表明,碳、氮具有同源性,底质中OM及氮主要源于生物沉降,而磷主要源于外部输入。经评价,沂沭河底质沉积物环境质量整体较好,污染程度属于清洁水平。     

Synergistic effects of organically modified montmorillonite in combination with metal oxides on the fire safety enhancement of intumescent flame-retarded epoxy resins

Synergistic effects of organically modified montmorillonite (OMMT) in combination with different metal oxides (Bi₂O₃, Sb₂O₃, and MoO₃) on the fire safety enhancement of the intumescent flame-retarded epoxy resins (EPs) were systematically evaluated. The results from X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses show that the OMMT and metal oxides acquire a uniform distribution in the EP matrix, and OMMT platelets exhibit a fully exfoliated state. The flammability and thermogravimetry (TG) tests show that the intumescent flame retardant (IFR)-OMMT-metal oxide ternary system can endow EPs with the higher synergistic efficiencies on the enhancement of flame retardancy, smoke suppression properties, and charring ability compared to those of IFR or IFR-OMMT system, and the synergistic efficiency is the following order: IFR/OMMT/Sb₂O₃ > IFR/OMMT/MoO₃ > IFR/OMMT/Bi₂O₃. In particular, the sample, filled with 1.5 wt% OMMT, 1.5 wt% Sb₂O₃, and 27 wt% IFR, passes the UL94 V-0 rating and acquires the highest limiting oxygen index value of 28.5% among the samples. The IFR-OMMT-metal oxide ternary system exerts a better synergistic effect on the generation of crosslinking and aromatic structures that supply the excellent charring effect and barrier effect for the EPs, and the synergistic efficiency of IFR-OMMT-metal oxide ternary system is varied with the types of metal oxides.     

Nitric Oxide (NO) Scaffolds the Peroxisomal Protein–Protein Interaction Network in Higher Plants

The peroxisome is a single-membrane subcellular compartment present in almost all eukaryotic cells from simple protists and fungi to complex organisms such as higher plants and animals. Historically, the name of the peroxisome came from a subcellular structure that contained high levels of hydrogen peroxide (H₂O₂) and the antioxidant enzyme catalase, which indicated that this organelle had basically an oxidative metabolism. During the last 20 years, it has been shown that plant peroxisomes also contain nitric oxide (NO), a radical molecule than leads to a family of derived molecules designated as reactive nitrogen species (RNS). These reactive species can mediate post-translational modifications (PTMs) of proteins, such as S-nitrosation and tyrosine nitration, thus affecting their function. This review aims to provide a comprehensive overview of how NO could affect peroxisomal metabolism and its internal protein-protein interactions (PPIs). Remarkably, many of the identified NO-target proteins in plant peroxisomes are involved in the metabolism of reactive oxygen species (ROS), either in its generation or its scavenging. Therefore, it is proposed that NO is a molecule with signaling properties with the capacity to modulate the peroxisomal protein-protein network and consequently the peroxisomal functions, especially under adverse environmental conditions.     

氮气氛下直拉硅中氮含量的红外光谱测定

提出了利用直拉硅中与氮有关的特征红外吸收峰９６３、９９６、１０８１－１及１０２７ｃｍ－１确定直拉硅中氮含量的计算公式，并进行了多种样品实测。该法克服了只用９６３ｃｍ－１峰测定直拉硅中氮使结果偏低的弊病，方法相对偏差为５％～２０％     

膜曝气提升菌藻生物膜反应器效能及稳定性

比较曝气头曝气以及膜曝气两种曝气方式支持的菌藻共生系统在不同的运行条件下对污染物的去除效能,探讨去除机理。结果表明,以膜曝气为基础的MABAR对氨氮、总氮、磷、化学需氧量（COD）的去除负荷相对于以曝气头曝气为基础的HABAR,最高分别提升1.44、21.22、3.08、52.09 kg/m²/m³。藻类积累方面,MABAR在5个阶段的积累量都高于HABAR,最高提升15.17 mg/cm²。这不但归因于膜曝气良好的无吹脱和高效的碳化能力为自养藻类提供了充足的无机碳,而且膜曝气为一些十分有利于藻类生长的细菌,例如Acidovorax、Rhodobacter和Acinetobacter,提供了良好的生存环境。MABAR不但能够提升去除效能,还能够促使光生物膜反应器抵抗冲击,维持稳定,这对未来光生物反应器的实际应用提供了一种新的运行方式。     

相对压强对白炭黑氮吸附表面积测试稳定性的影响

研究相对压强对白炭黑氮吸附表面积测试稳定性的影响。结果表明:在相同液氮纯度、脱气温度、脱气时间、氮吸附点数量条件下,与相对压强范围为0.05~0.1时相比,相对压强范围为0.05~0.2时白炭黑的氮吸附表面积测量值偏低,且差值随氮吸附表面积的增大呈增大趋势;相对压强范围较小时,氮吸附表面积测试结果的线性相关因数较大,再现性较好,测试结果较稳定。     

Effect of sulfate on Cu(Ⅱ) sorption to polymer-supported nano-hydrated ferric oxides: Experimental and modeling studies

Incorporating of hydrous ferric oxide(HFO) inside porous supports with large sizes has become an effective way to decontaminate the water from heavy metals. Ubiquitous anions like sulfate are usually present in high concentrations in water, and might greatly affect adsorption behavior of hybrid HFO. Here, a polymer-based HFO-CPS was fabricated by encapsulating nano-HFO inside a chloromethylated polystyrene polymer(CPS) and the reactivity of HFO-CPS with Cu(Ⅱ) was evaluated in the presence of sulfate ions.Surface complexation theory was firstly employed to describe the effect of sulfate on Cu(Ⅱ) adsorption edges of hybrid HFO-CPS, where constant capacitance model(CCM) was adopted. The available weak adsorption site Fe_((2))OH of hybrid HFO-CPS was found to decrease from 20% Fe to 5% Fe, which might be caused by the pore plugging effect after HFO encapsulation. With the assumption that a ternary complex was formed, the effect of sulfate on Cu(Ⅱ) adsorption by HFO-CPS were successfully described by CCM using the optimized Fe_((2))OH site under different sulfate concentrations(1 or 10 mmol·L~(-1)) and Cu/Fe ratios(0.0042 or 0.0252). It is confirmed that the formation of Fe OHCu SO_4 ternary surface complexes played an important role in enhancing Cu(Ⅱ) adsorption on HFO-CPS in the presence of sulfate.     

臭氧脱硝技术在稀贵多金属烟气治理中的应用

主要介绍在面临环境保护要求不断提升,废气排放指标不断降低的情况下,使用臭氧氧化+液碱脱硝技术对稀贵卡尔多炉和旋转顶吹炉生产回收金、银、硒、碲、铅、铋等金属产出的烟气的治理。治理后二氧化硫指标小于50mg/m3、氮氧化合物小于60mg/m3、尘指标小于10mg/m3,满足A类企业环保要求,同时其他重金属指标都满足国家国控指标要求,达到超低排放要求。     

热镀锌TRIP钢还原铁/基板界面表征

 预氧化还原工艺是改善热镀锌先进高强钢(AHSS)可镀性的有效手段之一。当它用于生产热镀锌先进高强钢时,有时也会出现镀层附着性不良的问题。为了明确还原铁/基板界面对热镀锌高强钢镀层附着性的影响,以预氧化还原工艺生产的、镀层附着性不同的热镀锌TRIP钢为研究对象,采用GDOES、SEM、FIB、TEM等手段研究了还原铁/基板界面位置的微观特征。结果表明,镀层附着性不良表现为150~300 nm厚的还原铁层与镀层一起从基板表面脱落,失效发生在还原铁/基板界面,而非镀层/还原铁界面,与常见的镀层/基板界面Fe₂Al₅抑制层缺失引起的镀层附着性不良明显不同。镀层附着性不同的试样在还原铁/基板界面位置均存在硅、锰元素富集,但硅、锰富集程度有差异,镀层附着性不良试样的界面硅、锰富集更高。还原铁/基板界面氧化物形态显著影响了还原铁/基板界面的结合力,当还原铁与基板之间形成连续的氧化膜时,界面结合力较差,易发生界面分离;当还原铁/基板界面形成细小的、不连续的氧化物颗粒时,界面结合力较好。在对热镀锌先进高强钢实施预氧化还原工艺时,为了获得良好的还原铁/基板界面结合力,可以通过提高退火气氛露点促进合金元素内氧化,从而减少和细化还原铁/基板界面氧化物的数量和尺寸,避免形成连续的界面氧化膜。     

取向硅钢氧化膜结构对渗氮层深度的影响

摘要：低温板坯加热技术生产取向硅钢,其关键点之一在于脱碳退火后要进行渗氮处理。通过控制脱碳气氛,获得不同的氧化膜结构;并进一步分析在近似渗氮量条件下,氧化膜结构对渗氮层深度的影响。结果表明：氧化膜分为外层颗粒状氧化膜和内层层片状氧化膜两部分。随着脱碳气氛露点增加,脱碳板O含量增加,氧化膜厚度增厚、层片状氧化膜占氧化膜总厚度的比例下降,渗氮层深度增加。当层片状氧化膜厚度占比较高时,［N］原子积聚在试样的极表层,形成氮沿厚度方向的单峰分布,渗层较浅。当层片状氧化膜厚度占比较低时,［N］原子会越过该层,而在次表层再次发生积聚;从而除了极表层的氮峰外,在次表层形成一个或多个氮峰,渗层较深。