ASM1中废水和污泥组分浓度的测定方法研究

对呼吸计量法应用于校准ASM1作了简明的阐述.在呼吸速率与模型组分关系的基础上,介绍了ASM1中废水与污泥各组分浓度的测定方法,并指出模型组分细化的意义.     

活性污泥数学模型(ASM1)入流组分测定及应用

阐述了活性污泥 1号模型 (ASM1)入流中 7个含碳有机物、4个含氮物质、碱度等四大类 13种组分的分析方法 ,并用这些方法测定了西安市北石桥、电子村两个排放口的城市污水水质。实验结果表明快速可生物降解有机物 (SS)采用间歇实验法、慢速可生物降解有机物 (XS)采用测定BOD5间接计算法既操作简单又准确可靠 ,能为利用活性污泥 1号模型进行污水处理厂的设计、模拟及管理提供入流组分分析依据     

活性污泥数学模型（ASMl）入流组分测定及应用

阐述了活性污泥1号模型(ASM1)入流中7个含碳有机物、4个含氮物质、碱度等四大类13种组分的分析方法，并用这些方法测定了西安市北石桥、电子村两个排放口的城市污水水质。实验结果表明快速可生物降解有机物(Ss)采用间歇实验法、慢速可生物降解有机物(X5)采用测定BOD5间接计算法既操作简单又准确可靠，能为利用活性污泥1号模型进行污水处理厂的设计、模拟及管理提供入流组分分析依据。     

简化活性污泥数学模型在城市污水厂中的应用

以活性污泥 1号模型 (ASM1 )为开发平台 ,建立了简化的活性污泥数学模型 (ASM CN)。该模型主要描述了碳氧化和硝化过程 ,其中模型组分、反应过程和参数的数量都少于ASM1 ,从而提高了该模型在城市污水厂中的实用性。通过测定模型组分、化学计量系数和动力学参数 ,为模型的应用提供了重要的前提和基础。最后利用ASM CN模型对实际城市污水厂的运行进行了动态模拟 ,模拟结果良好 ,验证了ASM CN模型的实用性和有效性 ,并且也验证了模拟程序的准确性。     

简化活性污泥1号模型在间歇式循环上流污泥床中的应用

以活性污泥1号模型(ASM1)为基础,结合间歇式循环上流污泥床工艺结构和实际进水水质特征,建立了简化的活性污泥模型(ASM1-S),该模型与ASM1模型相比,减少了反应过程、进水组分和参数,大大减少了模型参数测定的工作量和模拟过程中的计算量,从而提高了模型的实用性。本文通过测定模型进水组分和对模型模拟结果影响较大的4个参数(YH、μH、μA、bH)值进行测量,并利用Matlab编制模拟程序,就ASM1-S模型对间歇式循环上流污泥床实际运行状况进行了动态模拟,并将出水中COD、氨氮和总氮模型预测值与实测值进行对比,结果表明:该模型对出水中COD、氨氮和总氮的浓度模拟效果较好,最大误差小于10%,从而验证了ASM1-S模型的可靠性和实用性。     

活性污泥法模型的发展

详细阐述了国际水质协会（IAWQ）推出的活性污泥1号模型（ASM1）、2号模型（ASM2）、3号模型（ASM3）的组分、特点和缺陷，论述了活性污泥模型在废水处理中的重要作用，指出活性污泥模型研究、应用中的障碍。     

ASM系列模型在MBR仿真中的应用研究进展

膜生物反应器(MBR)正越来越多地被应用于城市污水以及工业废水的处理中,其运行模型化工作主要集中在描述反应器内生化反应过程以及实现低成本运营的设计等方面。ASM(活性污泥数学模型)系列模型最初主要应用于常规活性污泥法工艺的仿真,但也逐渐应用于膜生物反应器的仿真当中。相较于常规活性污泥工艺,MBR独有的一些特点使应用ASM模型模拟MBR时需要对原有的模型做出修改。有鉴于此,文章旨在整合已经报道的关于ASM系列模型在MBR仿真中的应用,并将重点放在进水组分的划分,动力学参数的确定,可溶性微生物产物(SMP)以及胞外聚合物(EPS)的模拟上。并提供了一些仿真效果较好的案例以及未来膜生物反应器仿真中需要解决的问题的建议。     

厌氧消化1号模型(ADM1)简介

介绍了2002年2月国际水质学会(IWA)推出的厌氧消化1号模型(ADM1).该模型主要描述了厌氧消化中的生化和物化过程,共涉及厌氧体系中的七大类微生物、19个生化动力学过程、3个气液传质动力学过程,共有26个组分和8个隐式代数变量,能够对厌氧生物处理工艺进行较好的预测和模拟.ADM1还提供了开放的建模平台以及与活性污泥模型(ASM)的接口,可广泛应用于对各种厌氧-好氧组合工艺的过程模拟.      

A/O法活性污泥系统计算机模拟研究

介绍了以活性污泥 1号模型 (ASM1 )和固体通量沉淀模型为基础 ,结合反应器原理 ,用VB6 .0计算机语言建立A/O法活性污泥模拟器的方法 ,探讨了A/O法活性污泥系统的模拟工艺流程、各组分的物料平衡关系和欧拉法数值积分的步长选取等问题。模拟器的校准结果表明 ,该模拟器建立的思路和方法完全正确 ,可以用于A/O法活性污泥系统的模拟和预测。     

ASM1耦合曝气模型对污水处理厂的模拟研究

为了更好地模拟污水处理厂实际的曝气方式及溶解氧浓度,采用更加精确的曝气模型对某污水处理厂进行了模拟研究.该模型考虑了污泥浓度、堵塞及温度等因素对氧传质的影响,并将该曝气模型与ASM1相耦合.首先,通过灵敏度分析确定了对该污水处理厂出水指标影响较大的参数,分别为异养菌产率系数YH、异养菌最大比增长速率μH、自养菌最大比增长速率μA及自养菌氧利用半饱和系数KOA.然后,测定部分灵敏度较高的参数并使用测量结果对模型进行校正,校正结果使用希尔系数表征.最后,使用另一批数据对校正参数进行验证.模拟的COD、氨氮、总氮和好氧池末端溶解氧的希尔不等系数分别是0.13、0.23、0.20和0.15,而通过控制溶解氧浓度或理论氧转移效率模型模拟则出现氨氮、溶解氧、总氮及COD的希尔不等系数不同程度上升的结果.校验后的ASM1/曝气耦合模型参数可以很好地应用于污水处理厂的模拟当中,对于优化污水厂曝气控制具有重要意义.     

甲萘酚和甲萘胺在超高交联吸附树脂上的协同吸附行为

研究了水溶液中甲萘酚和甲萘胺在超高交联吸附树脂NDA103、NDA100上的协同吸附行为.实验结果表明,在较高平衡浓度范围内该吸附树脂对双组分水溶液中甲萘酚和甲萘胺双组分(摩尔比分别为3∶1、1∶1、1∶3)的吸附总量大于相同平衡浓度下对单组分水溶液中甲萘酚和甲萘胺的吸附量,呈现协同吸附现象,其主导机制是2种吸附质分子之间的氢键作用.单组分甲萘酚或甲萘胺水溶液和双组分共存水溶液中吸附质分子在吸附树脂上的吸附等温线均符合Langmuir模型.吸附温度由293K升至313K时,甲萘酚和甲萘胺在NDA103上的协同吸附效应的变化明显大于NDA100.NDA103树脂结构上的胺基既加强了对甲萘酚的吸附亲和力又增加了甲萘酚的协同吸附系数.     

北京市大气环境PM2.5和PM1及其碳质组分季节变化特征及来源分析

大气颗粒物是影响我国大多数城市环境空气质量的首要污染物,近年来随着监测技术的进步和采样设备的改进,相关研究对象逐渐从大粒径的PM_10、PM_(2.5)转移到更小粒径的PM_1上.碳质组分是大气颗粒物的重要组成部分.以北京市为研究区域,选取2016年7月、10月及2017年1月、4月作为4个季节的代表月,对大气环境中的PM_(2.5)和PM_1进行采集,分析了二者的质量浓度和季节变化特征.采用两层嵌套气象-空气质量模型系统(WRF-CMAQ)耦合模型对采样时段进行了模拟,分析观测期间PM_(2.5)和PM_1的来源贡献,并使用因子分析法解析了碳质组分的来源.结果表明,PM_(2.5)和PM_1的质量浓度均呈现春、夏、秋、冬这4个季节递增的趋势;PM_1是PM_(2.5)中的主要组成,而且秋冬季节随着灰霾发生频率的增加,PM_1质量浓度占PM_(2.5)的比值明显升高;北京市大气环境中存在明显的二次污染,且SOC更容易在粒径更小的PM_1中积聚.散煤燃烧、机动车尾气排放、居民面源及生物质燃烧排放是北京市大气颗粒物的重要贡献来源;汽油车尾气、柴油车尾气、生物质燃烧和燃煤排放是北京市大气颗粒物中碳质组分的主要来源.     

螺旋藻多糖SPS-1的组成与结构研究

利用IR、UV、C13-NMR光谱分析技术和元素分析、HPAEC-PAD液相色谱法,对冷水提取的螺旋藻多糖SPS-1进行结构和糖基组成研究。结果发现,螺旋藻多糖的糖环是吡喃环,单糖以α-型糖苷键相连。是硫酸粘多糖,糖环上连有甲氧基和乙酰氨基,组成的糖基有六种,已知的糖基分别是D-岩藻糖、D-鼠李糖,D-葡萄糖,相对应的摩尔比为5.0:1:63.5。     

Effects of the surface chemistry of macroreticular adsorbents on the adsorption of 1-naphthol/1-naphthylamine mixtures from water

The adsorption behaviors of 1-naphthol, 1-naphthylamine and l-naphthol/l-naphthylamine mixtures in water over two macroreticular adsorbents were investigated in single or binary batch systems at 293 K, 303 K and 313 K respectively. All the adsorption isotherms in the studied systems can be adequately fitted by Langmuir model. In the case of aminated macroreticular adsorbent NDA103, 1-naphthol is adsorbed to a larger extent than 1-naphthylamine; while, the opposite trend is found for nonpolar macroreticular adsorbent NDA100. It is noteworthy that at higher temperature（303 K and 313 K）, the total uptake amounts of 1-naphthol and 1-naphthylamine in all binary-component systems are obvious larger than the pure uptake amounts in single-component systems, which is presumably due to the cooperative effect primarily arisen from the hydrogen-bonding interaction between the loaded 1-naphthol and 1-naphthylamine molecules. The simultaneous adsorption systems were confirmed to be helpful to the selective adsorption towards 1-naphthol according to the larger selective index.     

1-羟基芘的制备及其质谱光谱解析

报告了由芘制备1-羟基芘的方法,对所得产品进行了元素含量、质谱、核磁共振、紫外光谱、红外光谱和荧光光谱的分析。确定其组成为C_(6)H_(10)O_5,羟基在C_1位上;解析了质谱图中主要裂解产物的结构;给出特征光谱图,克分子消光(λ345nm)为3822.6。产品为较好的色谱纯品。     

First-trimester maternal serum schwangerschafts protein 1 (SP1) in pregnancies associated with chromosomal anomalies

The relationship between first-trimester maternal serum Schwangerschafts protein 1 (SP1) and the karyotype of the pregnancy was examined in 692 women who underwent chorionic villus biopsy at 6–12 weeks. There were 30 pregnancies with abnormal karyotypes, consisting of 14 Down's syndrome (DS), eight trisomy 18, and eight other anomalies, two of which were mosaics. The normal ranges and medians for gestation were defined from the 662 cases in which the karyotype was normal. The median SP1 (0·5 MOM) of the abnormal group was significantly lower than that of the normal group (10 MOM). This relationship was maintained for the DS pregnancies (0·4 MOM) and for anomalies other than trisomy 18 (0·43 MOM) but not trisomy 18 (1·1 MOM). It is possible that the use of SP1 as a screening test for chromosome anomalies in the first trimester could have a 43 per cent detection rate for a 5 per cent false-positive rate.     

Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36

Deletion of the distal end of the short arm of chromosome 1 (1p36) is thought to be a common terminal chromosomal deletion. However, few cases prospectively diagnosed prenatally have been reported. In this case, prenatal ultrasound at 21 weeks of gestation noted the fetus to have mild ventriculomegaly (Vhanterior = 11 mm and Vhposterior = 12 mm) and increased nuchal edema (6 mm). Maternal serum α-fetoprotein was normal unlike in a majority of previously described cases. The prenatal ultrasound features were further clarified with fetal MRI. Chromosome analysis following amniocentesis demonstrated a 1p36 deletion, which was confirmed by fluorescence in situ hybridization (FISH). The syndrome associated with 1p36 deletion is well described in infants and is characterized by typical facial features (prominent forehead, straight eyebrows. deep-set eyes, flat nasal bridge and a pointed chin). Other associated features are neurodevelopmental delay, seizures, cardiomyopathy and neurosensory hearing impairment. This case supplements our knowledge of the prenatal features of 1p36. Identification of this deletion by direct chromosomal analysis can be technically difficult and vigilance is required to improve diagnosis. FISH analysis is an important diagnostic adjunct where the diagnosis is suspected following classical G-banding techniques. However, in this chromosomal anomaly there remain few characteristic prenatal signs that are readily diagnosed with prenatal imaging. Copyright © 2007 John Wiley & Sons, Ltd.     

GIM（1）灰色模型预测环保投资趋势的可行性探析

环保投资作为环保系统的一个子系统，并不一定具有指数函数规律。本文利用ＧＩＭ（１）灰色模型，探析了它在环保投资趋势预测应用中的可行性。初步应用表明，在序列不完全满足光滑化条件时，ＧＩＭ（１）灰色模型对系统变量的“白化”能力较ＧＭ（１，１）强，而与ＧＳＭ（１）灰色模型相当，信息利用率高，是分析、预测环保投资动态发展趋势一条切实可行的途径。     

LncRNA PU.1 AS regulates arsenic-induced lipid metabolism through EZH2/Sirt6/SREBP-1c pathway

Arsenic (As) is an omnipresent metalloid toxicant, which has elicited serious environmental pollution and health risky problems. Previous studies have uncovered that the As exposure could also cause markedly reduction of serum triglycerides in mice. However, the regulation mechanisms are still largely unknown. The present study is aimed to elucidate the molecular mechanisms of lncRNAs in As-induced lipid metabolic disequilibrium. We demonstrated that lncRNA PU.1 AS was significantly induced in the liver of As-feed mice companied with lower serum triglycerides contents; further in vitro experiment confirmed that PU.1 AS regulated liver cells lipid accumulation by nile red fluorescence staining. Intensive mechanistic investigations illustrated that PU.1 AS could interact with EZH2 protein to regulate its downstream target gene expression, and As-induced PU.1 AS attenuated EZH2-supppressed Sirt6 expression, thereafter leading to a decreased SREBP-1c protein expression, as well as the diminished synthesis of triglycerides in hepatocytes. In conclusion, this study provided a new lncRNA-related regulatory signaling pathway participating in As-induced abnormal lipid metabolism.