一种阳离子型有机高分子水处理剂的研制及其性能

利用胺、甲醛、尿素、环氧氯丙烷这些便宜、易得的工业原料制得了一系列有机高分子水处理剂。研究了胺的种类、聚合单体与环氧氯丙烷的比例对产品性能的影响。利用充气浮选法对所合成的药剂进行了除油效果的评价，结果表明：当胺为二甲胺、二乙胺、甲胺，聚合单体（以胺计）与环氧氯丙烷的摩尔比为1：2时，产品的除油效果最佳。     

制氢弛放气中CO2胺法捕集工艺模拟及优化

为降低PSA制氢装置弛放气中CO2捕集系统蒸汽消耗量,利用Aspen Hysys软件建立了CO2捕集工艺模型并对捕集工艺进行模拟研究。考察了胺液循环量、解吸系统贫胺液CO2负载量、富胺液进解吸塔温度和解吸压力对蒸汽消耗量的影响。模拟结果表明,随着胺液循环量和解吸系统贫胺液CO2负载量的增大,CO2解吸单耗先降低后升高,最低约为2.04t水蒸气/tCO2。提高富胺液进解吸塔温度或提高解吸压力均有利于降低CO2解吸单耗。     

DTC型采出水净化剂研究进展概述

二硫代胺基甲酸盐（DTC）是一种高效、多功能采出水净化剂，它由二硫化碳与伯胺或仲胺反应生成二硫代胺基甲酸，然后再与碱反应而制备。其作用机理是与采出水中的铁或其它溶解金属反应形成絮体，絮体迅速聚结形成网状而包裹油，从而使油去除。DTC具有净化作用快，除油功效高，适用于分离、重力沉降和浮选等水处理过程。目前，国外DTC型冷水剂已发展到第三代。     

有机胺烟气脱硫在燃煤电厂中的应用

在燃煤电厂的"十二五"规划中,SO_2的减排仍是节能减排的主要任务。有机胺脱硫作为一种新兴的资源再生型脱硫工艺,能有效对燃煤电厂烟气中的SO_2进行资源化回收,实现"零污染"。文章重点介绍了有机胺脱硫的国内外研究情况,以及有机胺脱硫工艺的特点及其在燃煤电厂应用的优越性。     

氯消毒新工艺对大肠杆菌灭活作用的研究

研究了短时游离氯后转氯胺的联合消毒方法对大肠杆菌的灭活作用,并对其协同作用以及pH值和温度对协同作用的影响进行了探讨。结果表明：pH值在6．5～8范围内,温度不超过30℃时,短时游离氯后转氯胺的消毒方法对大肠杆菌的灭活具有协同作用,且随pH值的降低而加强,在低温下该方法的协同效果更加明显。     

高效液相色谱串联质谱检测地表水中五种生物胺

采用固相萃取及高效液相色谱串联质谱技术,建立了地表水中5种生物胺（腐胺、尸胺、2-苯乙胺、酪胺、色胺）的测定方法。水样中2-苯乙胺、酪胺和色胺可直接进样测定,腐胺和尸胺经HLB固相萃取柱富集,乙腈洗脱,氮吹浓缩至1.0mL后进样液相色谱串联质谱分析,以选择离子监测（SRM）模式定量分析。在本实验条件下,加标回收率在89.4%～122%之间,相对标准偏差2.15%～11.9%（n=7）,检出限在0.05～5μg/L。     

油气田气体脱硫装置热稳态盐去除应用研究

气体脱硫及胺液再生是油气田和炼厂重要的生产环节。胺液降解会导致产生的热稳态盐积累,严重影响脱硫及胺液再生装置的安全生产,必须及时去除。基于离子交换技术的胺液净化装置去除热稳态盐效果明显,经过70d的运行将热稳态盐浓度从6.3%降至1%以下,泡沫高度降至2.3cm,消泡时间降至1.8s,脱硫效果明显提高,对脱硫及溶剂再生装置的安全高效运行起到了十分重要的作用。     

有机胺分子结构对固态胺材料吸脱附CO_2的动力学常数研究

本文从6组不同种类的固态胺的吸脱附动力学入手,测出3种温度下的6组胺吸、脱附CO_2时的质量变化数据,通过Avrami动力学模型拟合得到不同温度下吸、脱附的动力学常数k。本文发现N,N’-二乙基乙二胺作为一种乙基仲胺,其吸、脱附动力学常数k比其他胺高,是一种吸、脱附性能都比较好的胺,这种类型的胺更适合在密闭空间中作为高效的固态胺吸附剂使用。     

改性钛管基复合吸附剂及其在油田伴生气中CO_2脱除的应用

通过湿式浸渍法制备了胺改性复合吸附剂用于油田伴生气中的CO_2捕集回收。采用物理吸附仪(BET-BJH)、热重分析仪(TG)考察了复合吸附剂的微观结构和热稳定性;通过等温吸附曲线研究了胺改性钛管对CO_2的吸附特性和对CH4/CO_2的吸附选择性。实验结果表明,胺改性复合吸附剂适用于150℃下的操作环境,在75℃时对CO_2的吸附容量可高达110mg/g;其对CO_2的吸附符合准二级动力学模型。40PEI/HTO对CO_2亲和性强,是分离CO_2/CH4的优异吸附剂。     

用改进的吡啶—吡唑啉酮法测定氰化物

前言根据康尼反应原理制定的比色法广泛地应用于氰化物的微量测定。这个特殊反应先是由氧化剂将氰离子氧化成活泼的卤化氰,卤化氰打开吡啶环,生成共轭的戊烯二醛中间体,这个中间体与含有伯胺或活泼亚甲基的偶联剂偶合成有色物质。人们用不同的偶联剂,先后提出了吡啶—吡唑啉酮法、吡啶—联苯胺法和吡啶—巴比妥酸法等。吡啶—联苯胺法的优点是试剂稳定和易于配制,而试剂的强烈毒性和显色液的不稳定性是该法的致命缺点。由于吡啶有恶臭,石井等提出     

Fenton试剂与改性凹凸棒石联合处理微污染水中苯酚的实验研究

研究了Fenton试剂联合聚二甲基二烯丙基氯化铵（PDMDAAC）改性凹凸棒石对模拟微污染水中苯酚的去除效果。考察了pH值、反应时间、投加量、温度等因素对苯酚去除效果的影响。结果表明：先采用Fenton试剂氧化再用改性凹凸棒石吸附对微污染水中苯酚具有较好的去除效果,在pH=9、温度为25℃、改性凹凸棒石投加量为5g／L、吸附时间20min的条件下,苯酚去除率达98．2％。     

Cellulose-based anion exchanger with tertiary amine functionality for the extraction of arsenic(V) from aqueous media

A novel cellulose-based anion exchanger (Cell-AE) with tertiary amine functionality was synthesized by graft polymerization reaction of cellulose and glycidyl methacrylate using N,N′-methylene-bis-acrylamide as a crosslinker and benzoyl peroxide as an initiator, followed by dimethylamine (amination) and acid (HCl) treatment. The chemical modification was confirmed by infrared spectroscopy and CHN analysis. The anion exchanger was used in batch processes to study AS(V) adsorption in solutions. The operating variables studied were pH, contact time, initial As(V) concentration, sorbent mass, and ionic strength. The process was affected by solution pH with an optimum adsorption occurring at pH 6.0. Adsorption equilibrium was achieved within 1 h. Increasing ionic strength of solution negatively affected the arsenic uptake. The adsorption process performed more than 99.0% of As(V) removal from an initial concentration of 25.0 mg/L. The process of adsorption followed pseudo-second-order kinetics. The adsorption equilibrium isotherm data were analyzed using the Langmuir, Freundlich, Redlich–Peterson and Langmuir–Freundlich equations. The Langmuir–Freundlich isotherm described the adsorption data over the concentration range 25–400 mg/L. The adsorption mechanism appears to be a ligand-exchange process. A simulated groundwater sample was treated with Cell-AE to demonstrate its efficiency in removing As(V). The adsorbed As(V) ions were desorbed effectively by a 0.1 M NaOH solution.     

Carbon paste electrodes modified with biosolids, soils and biocomposites utilized to study the interaction between organic matter and copper

Carbon paste electrodes (CPEs) modified with a biosolid, two types of soils with different amounts of organic matter (OM), and two biocomposites (soils mixed with a biosolid) were used to assess and compare the Cu(II) ion retention properties of the organic matter contained in the samples. The accumulation of Cu(II) on the surface of the modified carbon paste electrodes (MCPEs) was performed under open-circuit conditions. When comparing the response of the MCPEs while assessing parameters such as pH, preconcentration time, and adsorption/desorption capacity, it was found that the reaction mechanism of the two soils is different between the soils and dissimilar from the biosolid; while the biocomposites show reaction mechanisms that are intermediate between those of the soils and the biosolid. This was proven with the use of infrared spectroscopy, since the FTIR spectra show similarities between the two soils and significant differences between the soils and the biosolid.     

酸改性壳聚糖载体对漆酶的固定化

利用有机酸改性壳聚糖和交联法制备酸化壳聚糖载体,然后用改性壳聚糖载体固定漆酶。结果表明,甲酸、酒石酸改性壳聚糖的最适条件是壳聚糖与酸的量比分别为100/1(g/mol)、100/0.5(g/mol),戊二醛的浓度分别为1%、2%,缓冲溶液的pH分别为4.4、3.6,反应时间分别为3h、4.5h。两种酸改性的壳聚糖用于漆酶的固定,其酶活都有所提高,尤其用酒石酸改性的壳聚糖载体的效果最好,其酶活提高了57%。     

Removal of phosphorus from aqueous solutions using chemically modified sawdust of Aleppo pine (<Emphasis Type="Italic">Pinus halepensis Miller</Emphasis>): kinetics and isotherm studies

In the present study, chemically modified Aleppo pine (Pinus halepensis Miller) sawdust was used for the removal of phosphate from water. Biosorbent preparation process included size fractionation, extraction for surface activation, acid prehydrolysis, and treatment with urea. Sorption of phosphate ions onto biosorbent was studied using the batch technique. The effect of different parameters such as contact time, adsorbate concentration, and temperature was investigated. The adsorption kinetics data were best described by the pseudo-second-order rate equation, and equilibrium was achieved after 40 and 80 min for modified and unmodified sawdust, respectively. The Langmuir and Freundlich equations for describing adsorption equilibrium were applied to data. The constants and correlation coefficients of these isotherm models were calculated and compared. The adsorption isotherms obey the Freundlich equation. The thermodynamic parameters like free energy, enthalpy, and entropy changes for the adsorption of phosphate ions have been evaluated, and it has been found that the reaction was spontaneous and endothermic in nature. The low value of activated energy of adsorption, 3.088–3.540 kJ mol⁻¹, indicates that the phosphate ions are easily adsorbed on the sawdust. Results suggest that the prepared chemically modified Aleppo pine sawdust has potential in remediation of contaminated waters by phosphate.     

Feasibility of CO₂/SO₂ uptake enhancement of calcined limestone modified with rice husk ash during pressurized carbonation

The calcination/carbonation cycle using calcium-based sorbents appears to be a viable method for carbon dioxide (CO?) capture from combustion gases. Recent attempts to improve the CO?/SO? uptake of a calcium-based sorbent modified by using rice husk ash (RHA) in the hydration process have succeeded in enhancing its effectiveness. The optimal mole ratio of RHA to calcined limestone (M(Si/Ca)) was adjusted to 0.2. The cyclic CO? capture characteristics and the SO? uptake activity of the modified sorbent were evaluated in a calcination/pressurized carbonation reactor system. Scanning electron microscope (SEM) images and X-ray diffraction (XRD) spectrum of the sorbent were also taken to supplement the study. The results showed that the carbonation conversion was greatly increased for the sorbent with M(Si/Ca) ratio of 0.2. For this sorbent formulation the optimal operating conditions were 700-750 °C and 0.5-0.7 MPa. CO? absorption was not proportional to CO? concentration in the carbonation atmosphere, but was directly related to reaction time. The CO? uptake decreased in the presence of SO?. SO? uptake increased, and the total calcium utilization was maintained over multiple cycles. Analysis has shown that the silicate component is evenly or well distributed, and this serves as a framework to prevent sintering, thus preserving the available microstructure for reaction. The sorbent also displayed high activity to SO? absorption and could be used to capture CO? and SO? simultaneously.     

二甲基二烯丙基氯化铵－丙烯酰胺的合成及其在含油污水处理中的应用

以二甲胺、氯丙烯等为原料合成二甲基二烯丙基氯化铵（ＤＭＤＡＡＣ），再与丙烯酰胺（ＡＭ）共聚生成共聚物。利用胶体滴定法测定共聚物的阳离子度、一点法测定特性粘数，并利用充气浮选法对阳离子共聚物进行浮选效果评价。结果表明，当产品的阳离子度在３０％～４０％的范围内除油效果最好，其效果明显优于阳离子聚丙烯酰胺（ＣＰＡＭ），与复配的聚合铝加聚丙烯酰胺（ＰＡＣ＋ＰＡＭ）相当。     

Experimental evaluation of the catalytic efficiency of calcium based natural and modified catalyst for biodiesel synthesis

Transesterification of a mixture of vegetable oils with methanol using metal oxide catalysts derived from snail shell (SS) for biodiesel production was investigated. The metal oxides obtained from calcined snail shells in the temperature range of 650°–950 °C and modified by loading different potassium salts were used as a catalyst in the process. The catalysts were characterized by FT-IR, XRD, SEM-EDS, XPS and TGA. Catalytic activities of developed catalysts were also tested by Hammet indicator method and ion exchange method. The best calcination conditions were observed at 850°C for 4 hours based on biodiesel yield. The KF loaded snail shell gave highest biodiesel yield of 98 ± 1% in a batch reactor with highest basicity (15.9 mmoles/g) and basic strength measured by Hammet method. The optimized reaction conditions were: reaction temperature 65°C, reaction time 3 hours, methanol to oil molar ratio 9:1 and catalyst concentration 3wt%. Leaching and reusability tests confirm the stability of the catalyst as it encounters only 3% of leaching and small changes in catalytic activity up to five runs in terms of biodiesel yield.     

Promotional effect of transition metal doping on the properties of KF/CaO catalyst for biodiesel synthesis

A series of heterogeneous KF/CaO catalysts modified with transition metals (lanthanum, cerium, and zirconium) were prepared via wet impregnation method and applied to the trsansesterification process of waste cooking oil (WCO) as feedstock with methanol to biodiesel production. The structure, performance of the solid catalysts was characterized by X-ray diffraction (XRD), temperature programmed desorption of CO₂ (CO₂-TPD), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS). The effect of methanol/oil molar ratio, ¹reaction time, reaction temperature, catalyst amount, and stability was investigated. The results showed that 10 wt% of lanthanum, cerium, and zirconium improved the catalytic activity of KF/CaO catalyst. The maximum catalytic activity using the lanthanum doping of 10wt% on KF/CaO catalyst was reached 98.7% under the optimal reaction condition of methanol/oil molar ratio of 12:1, reaction for 1 h at reaction temperature of 65°C, and 4% (wt/wt oil) catalyst amount. In addition, the FAME yield of KF/CaO/La catalyst remained higher than 95% after 10 cycles. The promotional effect of lanthanum doping could be attributed to the enhancement of the basicity strength of KF/CaO catalyst and block the leach of Ca²⁺ in the transesterification reaction.     

富马酸二甲酯合成的新工艺

以顺酐和甲醇为原料,在浓盐酸的作用下采用一锅法合成富马酸二甲酯.通过正交实验考查了醇解和酯化过程中甲醇用量、时间、温度和异构化过程中浓盐酸用量、时间、温度等因素对反应的影响,得到最优化条件,收率达90.19％.