醋酸乙烯生产过程废触媒的资源化回收

采用正交实验研究了微波、超声波条件对废触媒解吸效果的影响,对比实验结果表明,1次微波2次超声波联用技术锌的洗脱率较高,回收的活性炭超过了林业局粉状活性炭二级品指标.用洗脱的醋酸锌溶液制备的磷酸锌符合防锈颜料要求.最终的废液采用电石废渣中和后达到国家废水处理三级排放标准.实现了废触媒的综合回收利用.     

废活性炭微波再生新工艺的研究

提出用微波加热一二氧化碳活化法再生乙酸乙烯合成用触媒载体废活性炭工艺。采用条件实验法研究了活化时间、二氧化碳流量和微波功率对活性炭碘吸附值，亚甲基蓝吸附值和再生得率的影响，得到微波辐射加热二氧化碳活化再生乙酸乙烯用触媒载体废活性炭的最佳工艺条件为活化时间25min，二氧化碳流量0．2L／min，微波功率700w。在此条件下制得的活性炭碘吸附值为1158．02mg／g、亚甲基蓝吸附值为240mv,／g、得率为74．19％。并对活性炭进行了比表面积的测定和孔结构的分析，活性炭的比表面积为1308．13m^2／g，总孔容为0．76mL／g。     

废活性炭微波再生新工艺的研究

提出用微波加热-二氧化碳活化法再生乙酸乙烯合成用触媒载体废活性炭工艺.采用条件实验法研究了活化时间、二氧化碳流量和微波功率对活性炭碘吸附值,亚甲基蓝吸附值和再生得率的影响,得到微波辐射加热二氧化碳活化再生乙酸乙烯用触媒载体废活性炭的最佳工艺条件为活化时间25 min,二氧化碳流量0.2 L/min,微波功率700 W.在此条件下制得的活性炭碘吸附值为1158.02 mg/g、亚甲基蓝吸附值为240 mg/g、得率为74.19%.并对活性炭进行了比表面积的测定和孔结构的分析,活性炭的比表面积为1308.13 m2/g,总孔容为0.76 mL/g.     

超声波—微波联合处理废活性炭制备载铜活性炭

扑热息痛生产过程中产生的废水需要活性炭来处理,因此会产生大量废活性炭。若废活性炭不能有效利用,将对环境造成严重影响,所以其循环利用引起广泛关注。采用超声波—微波联合处理扑热息痛生产中处理废水产生的废活性炭,硝酸铜为活性前驱体制备载铜活性炭,考察焙烧温度和时间对其性能的影响,通过氮气吸附/脱附、扫描电子显微镜、X射线衍射和傅立叶变换红外光谱等表征其性能。结果表明,经超声波预处理,微波焙烧温度800℃、焙烧时间30min时制备的载铜活性炭亚甲基蓝吸附值为150mg/g,比表面积达到985.371m~2/g,实现了在活性炭表面负载Cu及其氧化物。     

废汞触媒中汞的浸出及其再生活性炭的吸附性能

对电石法生产聚氯乙烯产生的废汞触媒进行浸出及再生活性炭的研究,以6 mol·L~(-1)HCl溶液作为浸出剂,在浸出反应温度为65℃、浸出反应时间为90 min和液固比为15∶1的实验条件下得到Hg~(2+)的优化浸出率为61.25%。采用扫描电镜(SEM)、Brunauer-Emmet-Tller(BET)比表面积等方法分析再生活性炭特征。结果表明焙烧废汞触媒浸出渣热再生活性炭是可行的,焙烧最佳工艺条件为:焙烧温度850℃,焙烧时间90 min。得到的焙烧产物亚甲基蓝吸附值为120.5 mg·g~(-1),BET表面积为704.25 m~2·g~(-1),平均孔径为3.28 nm。再生前后的汞含量与从1.067%降至0.351%,再生后能再次作为汞触媒生产的催化剂载体材料,同时减缓固废堆积过程中汞流失造成的一系列环境问题。     

微波加热及真空集成再生活性炭

吸附法油气回收技术中，吸附剂的再生是一个难点和研究重点。微波加热再生作为一种新技术，受到人们的广泛关注。运用正交实验，研究了微波功率、辐照时间、活性炭量和真空度对吸附了汽油油气的富活性炭的再生率和损耗率的影响，发现影响顺序为微波功率〉辐照时间〉活性炭量〉真空度。综合考虑各方面因素，得出实验的最优方案为微波功率300W、辐照时间240s、活性炭量4g、真空度O．06MPa。还研究了活性炭多次吸附一再生后平衡吸附率和表面结构的变化。结果表明，微波和真空法对活性炭的表面结构影响不大，有利于活性炭的多次循环利用。综合比较真空再生法、真空和加热再生法、微波和真空再生法的再生效果，结果表明，微波和真空再生法稳定性较好。     

微波辐照废木屑活性炭制备工艺优化及其应用

以微波为热源，Na2CO3为活化剂，采用化学活化法制备废木屑活性炭（AC）。采用Taguchi法考察了微波辐照功率、辐照时间、活化剂浓度、固液比对活性炭碘吸附值的影响。结果表明，微波辐照功率对活性炭碘吸附值的影响最显著，辐照时间次之，而固液比的影响不显著。优化的工艺参数为微波辐照功率440W、辐照时间9min、Na2CO3浓度15％、固液比1：2．5，该条件下AC的碘吸附值为1230．40mg／g，实验结果验证了Taguchi法的有效性。该条件下制得的AC用于处理印染废水，结果显示，对COD为239．5mg／L废水投加3g／L活性炭，在pH为11时吸附70min，COD的去除率达77．9％。     

微波紫外耦合辐射降解间硝基苯磺酸钠及活性炭再生

针对活性炭吸附法处理污水所面临的吸附剂物耗大及其所形成的危险废弃物处置难题,采用微波紫外耦合辐射技术对活性炭无害化再生。以活性炭吸附电镀废水中的间硝基苯磺酸钠(3-NBSA)为研究对象,考察了p H对活性炭吸附3-NBSA效果的影响,研究了活性炭的吸附动力学和吸附等温线,最后探讨了微波功率、微波辐照时间、空气流量及再生次数对活性炭再生效果和再生损耗率的影响。实验结果表明,p H在2~8范围内对活性炭吸附效果影响不大,活性炭吸附动力学符合准二级动力学模型,等温吸附特性可用Freundlich等温方程式来描述。活性炭再生实验的最佳工艺条件:微波功率为500W,微波辐照时间为10 min,空气流量为0.024 m3/h。最佳工艺条件下活性炭的再生率达到99.62%,且连续再生5次后仍能达到90.02%。实验表明,在微波紫外耦合辐射作用下比只在微波作用下,活性炭的再生效果和3-NBSA的降解效果更好。     

不同再生工艺对活性炭吸附性能的影响分析

吸附法油气回收技术中,吸附剂的再生是一个难点和研究重点。微波加热作为一种新的再生技术,受到人们日益的重视。实验利用比表面积及孔隙分析仪测定了经多次微波真空,加热真空和加热再生后的活性炭的表面结构变化,通过对比分析,探讨了3种工艺多次再生活性炭对活性炭表面结构的影响。结果表明,3种工艺均对活性炭结构都有所破坏,但微波真空再生对活性炭比表面积和孔容破坏最小,净吸附容量最大,从效率及能耗上都比较好。     

串联式氨解脱离子交换法处理味精等电点废母液

提出了一种味精生产污染物控制新技术，采用四只串联的离子交换柱连续，交替吸附味精生产等电点废母液中残留的谷氨酸，通氨洗脱树脂吸附的谷氨酸，回收谷氨酸生产味精。     

烤胶废料活性炭对含铬废水的处理能力

介绍了微波照射下氯化锌法制取烤胶废料活的方法,用该方法所制烤胶废料活性炭处理含废水的结果表明,烤胶废料活性炭具有吸附容量大,过滤速度快,操作控制方便等优点,活性炭对铬的吸附容量是市售一级粉末活性炭的１．８倍。     

微波解吸柠檬酸盐溶液中SO2实验研究

结合微波具有的热效应、非热效应特性,利用经改装的微波反应装置,研究了微波场下柠檬酸浓度、微波作用时间、微波功率、SO2初始浓度和搅拌速率对解吸柠檬酸盐溶液中SO2的影响,得出了影响SO2解吸率的基本规律和最佳解吸条件,并进行了分析.     

微波解吸柠檬酸盐溶液中SO2实验研究

结合微波具有的热效应、非热效应特性，利用经改装的微波反应装置，研究了微波场下柠檬酸浓度、微波作用时间、微波功率、SO2初始浓度和搅拌速率对解吸柠檬酸盐溶液中SO2的影响，得出了影响SO2解吸率的基本规律和最佳解吸条件，并进行了分析。     

盐液浸提辅助微波再生废油脱水树脂及机制分析

对用于废油脱水的聚丙烯酸钠树脂在盐液浸提辅助微波脱附再生过程中的脱附特性和再生使用性能进行了研究。实验结果表明,盐液浸提辅助微波处理的脱附速率是普通热处理的5～6倍,且能耗更低,脱附率更高,树脂床层温升速率更快,温度峰值却更低,说明盐液浸提对微波处理具有明显辅助效果;树脂再生性能测试结果表明,盐液浸提辅助微波处理的树脂再生使用性能最好,孔结构破坏更少。分析认为,微波选择加热特性以及盐液浸提导致树脂内外渗透压降低和方向改变是盐液浸提辅助微波处理具有良好脱附效果的关键机制。     

Experimental study and modeling of the transfer of zinc in a low reactive sand column in the presence of acetate

Nowadays, it is necessary to understand and identify the reactions governing the fate of heavy metals introduced into the environment with low complexing organic compounds, particularly when they are transferred through soils in urban areas. In this work the concomitant influence of pH and acetate on the fate of zinc on siliceous sand was studied in batch and non-saturated column experiments. Total zinc concentrations varied between 2 and 20 mg/l, and total acetate concentrations were fixed at 22, 72, 132, and 223 mM to obtain solution pHs of 4, 5, 6 and 7, respectively. Natural sand (diameter, 0.3-2 mm), mainly constituted of silica, was used. In batch adsorption experiments, zinc adsorption is insignificant at pH 4, low and linear at pH 5, and increasingly nonlinear, of the Langmuir type, at pH 6 and 7 indicating near-saturation conditions of surface sites at these high pH values. In column experiments, Zn retardation increases and the maximum outlet concentration of Zn decreases with rising pH and acetate concentrations. Previous column tracer experiments revealed the occurrence of regionalized water transport in the column. Modeling these data was based on a non-electrostatic approach. Batch and column data modeling was based on the PHREEQC code that allows concomitant resolution of chemical speciation and regionalized water transport. The speciation calculation indicates that the ZnAcetate+ species is the dominant Zn species in the solutions used. Batch experimental curves are correctly modeled assuming the formation of the three surface species triple bond SiOZn+, triple bond SiOH-Zn Acetate+ and triple bond SiO-Zn(Acetate)2-. The column data could be adequately modeled assuming a two-region water transport and the formation of the same three species with the same thermodynamic constants determined in the batch experiments. The hypothesis of the modeling leads to a slight overestimation of the quantities of zinc eluted (10%) at pH 6 and 7, mostly in the desorption phase. These results show that the methodology used facilitates the correct modeling of both batch and transport experiments and formulation of the hypothesis on the interactions between the low reactive sand and a complex solution.     

Studies on the sorption and desorption characteristics of Zn(II) on the surface soils of nuclear power plant sites in India using a radiotracer technique

Zinc adsorption was studied in the soils of three nuclear power plant sites of India. 65Zn was used as a radiotracer to study the sorption characteristics of Zn(II). The sorption of zinc was determined at 25 and 45 degrees C at pH 7.8+/-0.2 in the solution of 0.01 M Ca(NO3)2 as supporting electrolyte. The sorption data was tested both in Freundlich and Langmuir isotherms and could be described satisfactorily. The effect of organic matter and other physico-chemical properties on the uptake of zinc was also studied in all the soil samples. The results showed that the cation exchange capacity, organic matter, pH and clay content were the main contributors to zinc sorption in these soils. The adsorption maximum was found to be higher in the soil on Kakarpara Atomic Power Plant sites soils having high organic matter and clay content. The zinc supply parameters of the soils are also discussed. In the desorption studies, the sequential extraction of the adsorbed zinc from soils showed that the diethylene triamine penta acetic acid extracted maximum amount of adsorbed zinc than CaCl2 and Mg(NO3)2. The zinc sorption on the soil and amount of zinc retention after extractants desorption shows a positively correlation with vermiculite and smectite mineral content present in the clay fraction of the soil. The amount desorbed by strong base (NaOH) and demineralised water was almost negligible from soils of all the sites, whereas the desorption by strong acid (HNO3) was 75-96% of the adsorbed zinc.     

Influence of soil properties on heavy metal sequestration by biochar amendment: 2. Copper desorption isotherms

Contaminant desorption constrains the long-term effectiveness of remediation technologies, and is strongly influenced by dynamic non-equilibrium states of environmental and biological media. Information is currently lacking in the influence of biochar and activated carbon amendments on desorption of heavy metal contaminants from soil components. In this study, copper sorption-desorption isotherms were obtained for clay-rich, alkaline San Joaquin soil with significant heavy metal sorption capacity, and eroded, acidic Norfolk sandy loam soil having low capacity to retain copper. Acidic pecan shell-derived activated carbon and basic broiler litter biochar were employed in desorption experiments designed to address both leaching by rainfall and toxicity characteristics. For desorption in synthetic rain water, broiler litter biochar amendment diminished sorption-desorption hysteresis. In acetate buffer (pH 4.9), significant copper leaching was observed, unless acidic activated carbon (pH_pzc = 3.07) was present. Trends observed in soluble phosphorus and zinc concentrations for sorption and desorption equilibria suggested acid dissolution of particulate phases that can result in a concurrent release of copper and other sorbed elements. In contrast, sulfur and potassium became depleted as a result of supernatant replacements only when amended carbon (broiler litter biochar) or soil (San Joaquin) contained appreciable amounts. A positive correlation was observed between the equilibrium aluminum concentration and initial copper concentration in soils amended with acidic activated carbon but not basic biochar, suggesting the importance of cation exchange mechanism, while dissolution of aluminum oxides cannot be ruled out.     

微波解吸技术及其应用

通过实验数据对活性炭的升温行为进行了定量描述并对微波解吸动力学模式进行了分析。结果表明,活性炭升温行为可分为2个阶段进行描述,微波解吸再生载乙醇活性炭的速度很快,1 min即可达到80％以上的脱附率,一般3～4 min后脱附率达90％以上,整个解吸过程所用的时间不到6 min.