复合絮凝剂PSAM在电厂冲灰水处理中的应用研究

以水玻璃、聚合氯化铝(PAC)、非离子型聚丙烯酰胺(N-PAM)为原料,制备了复合型无机高分子絮凝剂PSAM,初步验证了其对电厂冲灰废水的絮凝净化效果,考察了投药量、铝与硅摩尔比、水样pH等因素对絮凝效果的影响,并与聚硅酸铝(PACS)及传统使用的PAC进行了比较.结果表明,PSAM稳定性良好、有较宽的pH适用范围,絮体颗粒粗大、密实,沉降速度快, 余浊低,优于所对比药剂.     

倒极电解法合成聚合氯化铝絮凝剂

为减少电解制备絮凝剂过程中的极化现象,用特制的自动倒极电源装置合成聚合氯化铝(PAC)絮凝剂。确定了合成的最佳工艺条件：电解槽电压2V;电流密度6A／dm2;倒极周期1s。与不采用倒极装置相比,在最佳条件下合成PAC时,该装置可明显抑制极化现象。处理模拟水样试验表明,该法制备产品的絮凝效果优于一般电解法制备产品及市售产品的絮凝效果。     

酰基化反应废水的综合利用

以含AlCl3的酰基化反应工业废水为原料，采用聚芳醚砜酮中空纤维超滤膜为反应介质制备聚合氯化铝（PAC）。通过正交实验考察了碱浓度、碱化度、碱类型和加碱速率对PAC絮凝性能的影响。经优化后的试制参数用于PAC的放大实验，并将试制产品应用于染料废水的处理，考察了PAC对一定浓度的染料废水（达旦黄、活性红、甲基橙和食品黄）的脱色效果。实验结果表明，在NaOH溶液浓度0．5mol／L、渗透压0．2MPa、碱化度2．0时制备的PAC对4种染料的脱色率均大于96％。     

双氰胺-甲醛聚合物-聚合氯化铝复合絮凝剂的合成及应用

以双氰胺、甲醛、氯化铝为主要原料，加入添加剂合成了双氰胺-甲醛聚合物（DF）-聚合氯化铝（PAC）复合絮凝剂。采用模拟印染废水考察了各种因素对DF—PAC复合絮凝剂混凝脱色性能的影响。实验结果表明，在双氰胺、甲醛、氯化铝、添加剂加入量分别为29．1，57．8，4．8，12．5g，反应温度（70±1）℃、反应时间2．5h的条件下制得的DF—PAC复合絮凝剂的絮凝脱色性能良好，COD去除率不小于90％，色度去除率不小于99％。与PAC和DF絮凝剂相比，DF—PAC复合絮凝剂对实际印染废水的絮凝脱色效果更好。     

含羧甲基淀粉复合絮凝剂的絮凝性能

以酸性铝盐和碱式铝盐为基本原料,引入羧甲基淀粉,制备新型无机-有机复合高分子絮凝剂(PASC).分别对硅藻土悬浮液和染料溶液进行絮凝实验,并与传统絮凝剂聚合氯化铝(PAC)进行对比实验.对于不同初始浊度的硅藻土悬浮液,当剩余浊度达1 NTU时,PASC加入量较PAC分别减少57.56%～75.31%.PASC加入量为12 mg/L时,分散橙染料溶液色度去除率达98.14%;PASC加入量为18 mg/L时,活性红染料溶液色度去除率达81.18%.     

铁-镁-铝无机复合脱色絮凝剂的制备与应用研究

以铁、镁、铝盐为原料制备出一种高效新型复合絮凝剂(PFMA)。研究了该絮凝剂对染料溶液的脱色效果。试验结果表明,PFMA是一种性能优良的无机高分子絮凝剂,对多种染料溶液均具有很强的脱色效果,其脱色性能优于传统的絮凝剂——聚合氯化铝、聚合硫酸铁和硫酸铝。絮凝机理研究结果表明,PFMA的絮凝既有羟基架桥作用,也有压缩双电层和吸附电中和作用。     

聚硅硫酸铝的制备及其絮凝性能

以Na2SiO3·9H2O，Al2（SO4）3·18H2O为原料，加入一定量稳定剂，采用复合法制备出高铝含量且稳定的聚硅硫酸铝（PASS）。研究结果表明：采用磷酸氢二钠与烷基糖苷（质量比为1：1）作为复合稳定剂，在碱化度为1．5～1．8、Ⅳ（A1）：Ⅳ（Si）=1．0～3．0的条件下，合成的PASS絮凝效果最佳；复合稳定剂对废水的COD去除率及浊度去除率影响不大，但能显著改善絮凝产品的稳定性；PASS可用于处理pH范围较宽（pH为6．0—11．0）的工业废水，且处理前后废水pH变化不大；PASS对低温低浊度废水有较好的絮凝效果；在加入量相同的情况下，PASS的絮凝性能明显优于聚合硫酸铝、硫酸铝、聚合硫酸铁，当PASS加入量为40～100恤L／L时，废水浊度去除率达98％以上。     

利用含铝废盐酸制备聚合氯化铝

以某医药企业产生的含铝废盐酸为原料制备了液体聚合氯化铝(PAC)。确定了适宜的有机物去除方法和碱化剂,考察了碱化剂投加量、废盐酸铝离子含量等合成条件对PAC产品指标的影响,并比较了自制PAC和市售PAC对该企业污水站二沉池出水的混凝效果。实验结果表明:采用活性炭吸附法去除废盐酸中有机物,选择固体Ca O作为碱化剂,在活性炭投加量1‰(w)、吸附时间1 h、铝离子含量9.5%(w,以Al_2O_3计)、CaO投加量80 g/L、反应时间24 h的条件下,制备的液体PAC达到行业标准HG/T 2677—2017《工业聚氯化铝》中的Ⅲ类标准;自制PAC对废水COD和SS的去除率均优于市售PAC,不仅可替代其使用,还可外售产生经济效益。     

聚硅酸铝铁-海藻酸钠复合絮凝剂的制备

以硅酸钠、硫酸铝、氯化铁、海藻酸钠（SA）为原料制备了聚硅酸铝铁-海藻酸钠（PSAFe-SA）絮凝剂，并采用SEM、FTIR、XRD、TGA技术进行了表征，分析了影响PSAFe-SA絮凝沉降效果的主要因素，并考察了该絮凝剂对松花江水样的处理效果。实验结果表明：在制备聚硅酸的pH为3.0、n(Al+Fe)∶n(Si)为1.0、n(Al)∶n(Fe)为4.0、m(SA)∶m(Si)为0.04的条件下，所制备的PSAFe-SA絮凝剂性能最好；在水样pH为6.0、PSAFe-SA投加量为28 mg/L、沉降时间为20 min的最佳絮凝条件下，松花江水样的浊度去除率为94.50%。     

聚硫氯化铝絮凝效果及在水处理中的应用

采用聚硫氯化铝（ＰＡＣＳ）为絮凝剂进行废水处理试验,对其絮凝效果及影响因素进行了研究,试验结果表明,ＰＡＣＳ的ＳＯ４＾２－含量,碱化度,投加量和水的ｐＨ对絮凝效果有影响,当Ａｌ＾３＋／ＳＯ４＾２－（摩尔比）为１４￣１６,碱化度为６５％￣７０％,ｐＨ为６￣９、ＰＡＣＳ投加量为２￣４ｍｇ／Ｌ时,絮凝效果最佳,试验结果还表明,ＰＡＣＳ比聚氯化铝（ＰＡＣ）的絮凝效果好。     

聚合氯化铝锌絮凝剂的制备及其性能

用在AlCl，与ZnCl2溶液中加NaOH溶液的方法制备无机高分子絮凝剂聚合氯化铝锌（PAZC），通过正交实验确定的最佳制备条件为：反应时间10min、碱化度2．2、氯化铝浓度0．5mol／L、NaOH溶液浓度0．5mol／L。在n（Zn）：n（Al）=0．6、水样pH=7．8、PAZC加入量为5mg／L的条件下，浊度和COD去除率分别为98．9％和88．2％。PAZC与聚合氯化铝对各种工业废水的处理效果比较结果表明，PAZC对各种工业废水的处理效果较好。从废水处理成本来看，PAZC具有较好的经济效益。     

废弃SCR催化剂中钒和钨的浸出及回收

采用NaOH溶液一次性浸出废弃SCR催化剂中的钒和钨,并用硫酸对浸出液进行除杂,再利用NH4Cl和硫酸分步对浸出液中的钒和钨进行沉淀回收。在NaOH质量分数40%、液固比8、浸出时间4 h、浸出温度90℃的最佳碱浸条件下,钒和钨的浸出率分别达到90.44%和84.49%。除杂过程的铝去除率达到100%,硅去除率达到77.56%。在沉钒pH为8.0、n(NH_4~+)∶n(V)为4的最佳沉钒条件下,钒回收率达到82.79%。在n(SO_4~(2-))∶n(W)为2的最佳沉钨条件下,钨回收率达到76.41%。     

Production of hydrogen by steam gasification of dehydrochlorinated poly(vinyl chloride) or activated carbon in the presence of various alkali compounds

Steam gasification of dehydrochlorinated poly(vinyl chloride) (PVC) or activated carbon was carried out in the presence of various alkali compounds at 3.0 MPa and 560°C–660°C in a batch reactor or in a semi-batch reactor with a flow of nitrogen and steam. Hydrogen and sodium carbonate were the main products, and methane and carbon dioxide were the minor products. Yields of hydrogen were high in the presence of sodium hydroxide and potassium hydroxide. The acceleration effect of the alkali compounds on the gasification reaction was as follows: KOH > NaOH > Ca(OH)₂ > Na₂CO₃. The rate of gasification increased with increasing partial steam pressure and NaOH/C molar ratio. However, the rate became saturated at a molar ratio of NaOH/C greater than 2.0.     

无机-有机复合絮凝剂PACSAM的制备及其脱色性能

以聚合氯化铝（PAC）和淀粉-丙烯酰胺接枝聚合物（ST-AM）为原料,合成了一种新型的无机-有机复合絮凝剂（PACSAM）。考察了PACSAM对活性染料、直接染料模拟印染废水及实际印染废水的脱色效果,并初步探讨了絮凝机理。实验结果表明：在很宽的pH范围内,PACSAM均表现出了良好的脱色性能;在PACSAM加入量为25m g/L时,PACSAM对实际印染废水的脱色率、COD去除率、浊度去除率分别为96.4%,92.1%,98.5%,废水处理效果明显好于壳聚糖和PAC。PACSAM的絮凝机理包括化学反应、分子间氢键、电中和及架桥作用等。     

Evaluation of chemical stability of heavy metals in industrial waste slag by infrared spectroscopy

Our aim was to clarify the chemical bonding type and stability of heavy metals in industrial waste slag (IWS) by using Fourier transform infrared (FT-IR) spectroscopy. The chemical composition of the IWS sample used in this study was an Al/Si ratio of 0.50 with Fe, Pb, and other minor heavy metals present. The IR peak position of the Si-OSi( M) band (M: Al, Pb, or Fe) was lower for IWS (971 cm⁻¹) than for synthetic Si-Al glass with an Al/Si ratio of 0.5 (1029 cm⁻¹). This implies the formation of covalent Si-O-Pb and Si-O-Fe bonds in the IWS, which caused a shift in the peak position toward a lower wavenumber. FT-IR spectra of synthetic Si-Al-Pb and Si-Al-Fe glasses with various Pb/Si and Fe/Si ratios with a constant Al/Si ratio of 0.5 showed that the peak position of the Si-O-Si(M) band continuously shifted toward lower wavenumbers with increasing Pb/Si and Fe/Si ratios. This suggests that covalent Si-O-Pb and Si-O-Fe bonds are formed in IWS. The comparison of peak positions of the Si-O-Si(M) band between IWS and Si-Al-Fe glass indicated that not only Pb but also other minor heavy metals such as Cu and Cr were included by covalent bonds into the structure of IWS. Therefore, we concluded that most of the heavy metals in IWS formed covalent Si-O-M bodings and were chemically stable.     

液晶屏抛光废液的资源化利用

以液晶屏抛光废液为原料制备冰晶石，首先加入碳酸钠，反应生成氟硅酸钠沉淀，去除废液中的氟硅酸根;再向滤液中加入NaOH和NaAlO2混合溶液，反应生成冰晶石。最佳工艺条件为:碳酸钠加入量为理论加入量的2.2倍，冰晶石制备反应温度为80℃，反应原料中n(HF)∶n(NaAlO2)为5.4、n(Na)∶n(Al)为3.4、NaOH和NaAlO2质量分数为20%。在最佳条件下制得的冰晶石产品中n(Na)∶n(Al)为2.84，达到GB/T4291-2007《冰晶石》中牌号CH-1的质量标准。采用该工艺可实现液晶屏抛光废液的资源化综合利用。     

赤泥制备含钛聚硅酸铝铁及亚甲基蓝溶液的混凝脱色

以拜耳法赤泥为原料、Na Cl为助溶剂,采用酸浸法溶出赤泥中的铁、铝元素,再与硅酸钠、硫酸氧钛反应制备出高效混凝剂含钛聚硅酸铝铁(T-PSAF),并将其用于模拟亚甲基蓝印染废水的脱色。实验结果表明:在硫酸浓度为8 mol/L、液固比(硫酸体积与干赤泥质量之比)为14 m L/g、酸浸温度为80℃、酸浸时间为80 min、Na Cl加入量为0.10 g/g(以干赤泥计)的优化酸浸条件下,铁、铝的浸出率分别为88.25%和73.21%;在n(Fe+Al)∶n(Ti)∶n(Si)=0.3∶0.3∶1、熟化p H为4~5、熟化时间为2 h、混凝剂加入量为25 m L/L的优化混凝条件下,初始亚甲基蓝质量浓度为10 mg/L的废水的脱色率可达87.1%,而当初始亚甲基蓝质量浓度增至150~200 mg/L时废水脱色率可达99%以上。     

混凝—气浮工艺预处理ABS树脂生产废水

采用混凝—气浮工艺对ABS树脂生产过程中的丁二烯聚合工段和乳液接枝工段混合废水进行预处理,优化了工艺条件。实验结果表明：最佳药剂组合为CaCl₂和阳离子型聚丙烯酰胺（FO4440SSH）,最佳CaCl₂投加量为75 mg/L,最佳FO4440SSH投加量为10 mg/L,最佳废水pH范围为5~7;最优操作条件为以288 r/min的转速搅拌混凝1 min,再以72 r/min的转速搅拌絮凝20 min;混凝阶段的最佳G值为159.9 s^-1、GT值为9 594,絮凝阶段的最佳G值为24.5 s^-1、GT值为29 400;优化条件下,废水的浊度与COD去除率均可达98%以上。     

从含铬铝泥中回收铝的新工艺

采用"打浆水洗除Cr(Ⅵ)—电渗析除Cr(Ⅵ)—碱浸提铝—碳酸化分解法精制Al_2O_3"的新工艺处理含铬铝泥(以下简称铝泥),并回收Al_2O_3。实验结果表明:铝泥在70℃下经3次打浆水洗后,w(Na_2CrO_4)(以干铝泥计)降至5.0%;采用电渗析除Cr(Ⅵ)工艺可有效去除铝泥中以结合态和结晶态形式存在的Na_2CrO_4,在55 V直流电压下电渗析6h后铝泥中的w(Na_2CrO_4)降至0.98%;在碱浸温度为100℃、碱浸时间为3 h、NaOH质量浓度为150 g/L的优化碱浸条件下,铝浸出率(以Al_2O_3计)高达90.0%;经3次碳酸化分解处理后,Al_2O_3产品的纯度达98.65%,满足GB/T 24487-2009《氧化铝》中的一级标准,Al_2O_3回收率为96.37%。     

Application of quadratic regression model for Fenton treatment of municipal landfill leachate

The effectiveness of Fenton process in municipal landfill leachate treatment, as a pre- or post-treatment approach, has been demonstrated. However, no general recommendations of universal validity could be made in the term of optimized conditions affecting Fenton process. At the first stage of this study, collected leachate samples from Aradkooh site, Tehran, Iran, were investigated using one-factor-at-a-time method to find out optimum coagulation pH and flocculation time values. Subsequently, the obtained results in addition to data issued previously by the authors were employed to develop a predictive model of the true response surface, namely chemical oxygen demand (COD) removal efficiency. Finally, the main parameters of Fenton procedure, i.e. initial pH, [H(2)O(2)]/[Fe(2+)] molar ratio, Fe(2+) dosage, and coagulation pH were optimized taking advantage of the above-mentioned quadratic model. The derived second-order model included both significant linear and quadratic terms and seemed to be adequate in predicting responses (R(2)=0.9896 and prediction R(2)=0.6954). It was found that the interaction between initial pH and Fe(2+) dosage has a significant effect on COD removal. While, the optimal [H(2)O(2)]/[Fe(2+)] molar ratio was independent of ferrous ion dosage. The optimum conditions for the maximum COD removal of 50.76% for the parameters of initial pH, [H(2)O(2)]/[Fe(2+)] molar ratio, Fe(2+) dosage, and coagulation pH were found to be 5.8, 8.0, 22,500mg/L, and 8.7 respectively.