茶叶吸附染料作用的初步研究

本文证实了茶叶经化学处理后，可以吸附水中阳离子型染料。三种染料的脱色率均在９０％以上。吸附后的茶叶可以再生处理，循环使用。     

PVA/GA/β-CD纳米纤维的制备及染料吸附性能

利用静电纺丝技术,以六氟异丙醇(HFIP)和水为溶剂,制备了环糊精(β-CD)含量为70%(质量分数)的聚乙烯醇(PVA)/β-CD纳米纤维,并经戊二醛(GA)交联处理得到了可用于染料吸附的PVA/GA/β-CD纳米纤维.通过红外光谱和扫描电子显微镜研究了交联反应前后纳米纤维组成和形貌的变化;考察了PVA/GA/β-CD纳米纤维对7种水溶性染料的吸附性能.结果表明,PVA/GA/β-CD纳米纤维对孔雀石绿、甲基紫和刚果红的吸附效果较好,最大吸附量分别为124.71,121.14和127.39 mg/g,4次吸附-解吸附循环后,染料去除率仍保持80%左右,在染料废水处理中具有良好的应用前景.     

有机-无机杂化聚离子液体材料制备及其对染料吸附性能的评价

以烯丙基三乙氧基硅烷与1-乙烯基-3-辛基咪唑溴盐离子液体为单体通过自由基聚合及溶胶-凝胶制备了有机-无机杂化聚离子液体材料。通过红外光谱和扫描电镜对所制备的杂化聚离子液体材料进行了表征,并考察了其对柠檬黄、日落黄、苋菜红以及诱惑红等常见染料的吸附性能。研究结果表明:所制备的聚离子液体材料对日落黄和诱惑红具有优异的吸附性能,其吸附容量分别为29.20和86.17 mg/g;当吸附时间为5 min时,该材料对诱惑红和日落黄的吸附分别达到平衡时吸附量的87.5%和72.8%,显示了较快的吸附速率。     

卟啉钒在改性高岭土上的吸附行为及机理研究

利用酸改性和负载钼的酸改性高岭土作为吸附剂研究了环己烷中的卟啉钒(钒氧-2,3,7,8,12,13,17,18-八乙基卟啉,VO-OEP)在这两种吸附剂上的吸附行为,从热力学角度探讨了吸附机理。结果表明,两种吸附剂对卟啉钒的吸附符合Langmuir吸附等温线,卟啉钒单层吸附在改性高岭土上;吸附表现为自发热过程,吸附热均大于40 kJ/mol,说明吸附形成了化学键。     

高岭土吸附稀土元素的实验研究

为更好了解粘土矿物对稀土元素(REE)的吸附及其控制因素,进行了不同溶液介质条件(平衡时间、REE含量、pH＝3～6.5) 1 g·L-1高岭土对REE吸附的系列实验.结果表明: 稀土在较短时间内(24 h)吸附/解吸过程达到平衡;Langmuir吸附等温线能模拟REE在高岭土上的吸附,总的趋势是REE含量越高,分馏越不明显;此外,pH对REE吸附和分馏有很大影响,REE分配系数随pH值增加而增加,且在pH近中性时,出现了明显的重稀土比轻稀土更多的被吸附.     

水蒸气对高岭土高温吸附铅的影响

使用沉降炉开展了水蒸气对高岭土高温吸附铅影响的实验研究,其中铅的形态为PbO和PbCl₂两种。首先研究了0-20%水蒸气对高岭土吸附PbO(1100-1300℃)和PbCl₂(800-1300℃)的影响规律,然后基于XRD、SEM和残余羟基率等分析,掌握了水蒸气影响高岭土高温吸附的机理。结果表明,水蒸气可以减少高岭土表面羟基的高温脱落,从而阻碍了PbO吸附、促进了PbCl₂吸附。综合高温下惰性莫来石的出现和高岭土孔隙结构的坍塌等因素,PbO和PbCl₂的最佳吸附温度分别为1200和1000℃。     

碱活化高岭土对亚甲基蓝的吸附研究

本研究通过碱活化的方法对天然高岭土进行改性,制备高岭土基吸附剂,通过静态吸附实验考察了其对亚甲基蓝的吸附行为。实验结果表明:与天然高岭土相比,碱活化高岭土的结构发生了明显改变,进而影响了其吸附亚甲基蓝的性能。该吸附过程可以用伪二级动力学模型和Freundlich等温吸附模型来描述。由吸附热力学可知,该吸附过程可以自发的进行且为吸热过程。     

水蒸气对高岭土高温吸附铅的影响

使用沉降炉开展了水蒸气对高岭土高温吸附铅影响的实验研究，其中铅的形态为PbO和PbCl₂两种。首先研究了0-20%水蒸气对高岭土吸附PbO（1100-1300 ℃）和PbCl₂（800-1300 ℃）的影响规律，然后基于XRD、SEM和残余羟基率等分析，掌握了水蒸气影响高岭土高温吸附的机理。结果表明，水蒸气可以减少高岭土表面羟基的高温脱落，从而阻碍了PbO吸附、促进了PbCl₂吸附。综合高温下惰性莫来石的出现和高岭土孔隙结构的坍塌等因素，PbO和PbCl₂的最佳吸附温度分别为1200和1000 ℃。     

一步法制备聚脲多孔材料及其对染料的吸附

以甲苯二异氰酸酯为单体, 在水和丙酮混合溶剂中不用致孔剂且无需任何高分子改性一步法合成了聚脲多孔材料(PPU), 通过扫描电镜和BET氮气吸附法对其表面形貌和孔参数进行了表征. 以酸品红(AF)溶液模拟染料废水, 对其在PPU上的吸附进行了研究, 讨论了pH、 吸附时间、 AF初始浓度及吸附剂用量对吸附过程的影响, 优化了吸附条件. 结果表明, PPU对染料AF具有优异的吸附效果. PPU在30℃, pH=3时对AF的最大吸附量为44.60 mg/g. PPU对AF的吸附过程更接近于Langmuir等温吸附的单分子层吸附机理. PPU对水溶性染料刚果红(CR)也有很好的吸附能力. 使用水、 乙醇和水混合溶剂以及NaOH水溶液对染料吸附后的解吸附结果表明, 乙醇和水混合溶剂对吸附染料的解吸效率最高, 对2种染料的解吸附都达90%以上. 解吸后PPU的再吸附能力略有下降, 但第三次吸附量仍达到首次吸附的80%以上.     

新型多胺模板树脂对水溶性染料的吸附及动力学

新型多胺模板树脂对水溶性染料的吸附及动力学;模板树脂;吸附容量;吸附动力学;染料     

Cyclodextrin-Cross-Linked Hydrogels for Adsorption and Photodegradation of Cationic Dyes in Aqueous Solution

Possessing three-dimensional porous structures and tunable mechanical strengths, cyclodextrin-containing polymeric hydrogels are one of the most promising water-based adsorbent materials due to their easy availability, simple chemical modification and environmental friendliness. In this work, two kinds of hydrogels were prepared via the copolymerization with acrylic acid and vinyl-derivatized β-cyclodextrins in water. These two gels have showed good adsorption performance towards cationic dyes through the noncovalent interactions with their anionic backbones and porous network. Meanwhile, pseudo-second-order model was selected to clarify the adsorption kinetics process. Moreover, nano-scaled TiO₂ was doped into these resultant cyclodextrins-based hydrogels to achieve efficient degradation of dyes upon light irradiation. The obtained TiO₂-loaded hydrogels could exhibit improved adsorption performance and make the adsorbed dyes photo-degraded with the decolorization rates above 95%. It can be envisioned that such cyclodextrin-based soft materials may find applications in dye clearance and water treatment.     

Cross-Linked Ionic Liquid Polymer for the Effective Removal of Ionic Dyes from Aqueous Systems: Investigation of Kinetics and Adsorption Isotherms

In the current study, we have synthesized an imidazolium based cross-linked polymer, namely, 1-vinyl-3-ethylimidazolium bis(trifluoromethylsulfonyl)imide (poly[veim][Tf₂N]-TRIM) using trimethylolpropane trimethacrylate as cross linker, and demonstrated its efficiency for the removal of two extensively used ionic dyes—methylene blue and orange-II—from aqueous systems. The detailed characterization of the synthesized poly[veim][Tf₂N]-TRIM was performed with the help of ¹H NMR, TGA, FT-IR and FE-SEM analysis. The concentration of dyes in aqueous samples before and after the adsorption process was measured using an UV-vis spectrophotometer. The process parameters were optimised, and highest adsorption was obtained at a solution pH of 7.0, adsorbent dosage of 0.75 g/L, contact time of 7 h and dye concentrations of 100 mg/L and 5.0 mg/L for methylene blue and orange-II, respectively. The adsorption kinetics for orange-II and methylene blue were well described by pseudo-first-order and pseudo–second-order models, respectively. Meanwhile, the process of adsorption was best depicted by Langmuir isotherms for both the dyes. The highest monolayer adsorption capacities for methylene blue and orange-II were found to be 1212 mg/g and 126 mg/g, respectively. Overall, the synthesized cross-linked poly[veim][Tf₂N]-TRIM effectively removed the selected ionic dyes from aqueous samples and provided >90% of adsorption efficiency after four cycles of adsorption. A possible adsorption mechanism between the synthesised polymeric adsorbent and proposed dyes is presented. It is further suggested that the proposed ionic liquid polymer adsorbent could effectively remove other ionic dyes and pollutants from contaminated aqueous systems.     

3D Porous Structure-Inspired Lignocellulosic Biosorbent of Medulla tetrapanacis for Efficient Adsorption of Cationic Dyes

The focus of this work was on developing a green, low-cost, and efficient biosorbent based on the biological structure and properties of MT and applying it to the remediation of cationic dyes in dye wastewater. The adsorption performance and mechanism of MT on methylene blue (MB) and crystal violet (CV) were investigated by batch adsorption experiments. The results demonstrated that the highest adsorption values of MT for MB (411 mg/g) and CV (553 mg/g) were greatly higher than the reported values of other biosorbents. In addition, the adsorption behaviors of methylene blue (MB) and crystal violet (CV) by MT were spontaneous exothermic reactions and closely followed the pseudo-second-order (PSO) kinetics and Langmuir isotherm. Further, the depleted MT was regenerated using pyrolysis mode to convert depleted MT into MT-biochar (MBC). The maximum adsorption of Cu²⁺ and Pb²⁺ by MBC was up to 320 mg/g and 840 mg/g, respectively. In conclusion, this work presented a new option for the adsorption of cationic dyes in wastewater and a new perspective for the treatment of depleted biosorbents.     

Octa[4‐(9‐carbazolyl)phenyl]silsesquioxane‐Based Porous Material for Dyes Adsorption and Sensing of Nitroaromatic Compounds

A new fluorescent hybrid porous polymer (HPP) is synthesized by an anhydrous FeCl₃‐mediated oxidative coupling reaction of octa[4‐(9‐carbazolyl)phenyl]silsesquioxane (OCPS). The polymer possesses a surface area of 1741 m² g^?1 and hierarchical bimodal micropores (1.41 and 1.69 nm) and mesopores (2.65 nm). The material serves as an excellent adsorbent for CO₂ and dyes with high adsorption capacity for CO₂ (8.53 wt %,1.94 mmol g^?1), congo red (1715 mg g^?1) and rhodamine B (1501 mg g^?1). In addition, the presence of peripheral cabozolyl groups with extended π‐conjugation in the crosslinked framework imparts luminescent character to the polymer and offers the detection of nitroaromatic compounds.     

A Carboxyl-Functionalized Covalent Organic Framework Synthesized in a Deep Eutectic Solvent for Dye Adsorption

Instead of using organic solvents, a deep eutectic solvent (DES) composed of tetrabutylammonium bromide and imidazole (Bu₄NBr/Im) was employed as a solvent for the first time to synthesize covalent organic frameworks (COFs). Due to the low vapor pressure of the Bu₄NBr/Im-based DES, a new carboxyl-functionalized COF (TpPa-COOH) was synthesized under environmental pressure. The as-synthesized TpPa-COOH has open channels, and the DES can be removed completely from the pores. The dye adsorption performance of TpPa-COOH was examined for three organic dyes with similar molecular sizes: one anionic dye (eosin B, EB) and two cationic dyes (methylene blue, MB and safranine T, ST). TpPa-COOH showed an excellent selective adsorption effect on MB and ST. The electronegative keto form in TpPa-COOH might help to form electrostatic and π–π interactions between the π-stacking frameworks of TpPa-COOH and the positive plane MB and ST molecules. The adsorption isotherms of MB and ST on TpPa-COOH were further investigated in detail, and the equilibrium adsorption was well modeled by using a Langmuir isotherm model. Together with hydrogen bonding, TpPa-COOH showed higher adsorption capacity for ST than for MB (1135 vs. 410 mg g⁻¹). These results could provide a guidance for the green synthesis of adsorbents in removing organic dyes from wastewater.     

A Branched Pore Model Analysis for the Adsorption of Acid Dyes on Activated Carbon

A new branched-pore adsorption model has been developed using an external mass transfer coefficient, K _f, an effective diffusivity, D _eff, a lumped micropore diffusion rate parameter, K _b, and the fraction of macropores, f, to describe sorption kinetic data from initial adsorbent-adsorbate contact to the long-term adsorption phase. This model has been applied to an environmental pollution problem—the removal of two dyes, Acid Blue 80 (AB80) and Acid Red 114 (AR114), by sorption on activated carbon. A computer program has been used to generate theoretical concentration-time curves and the four mass transfer kinetic parameters adjusted so that the model achieves a close fit to the experimental data. The best fit values of the parameters have been determined for different initial dye concentrations and carbon masses. Since the model is specifically applicable to fixed constant values of these four parameters, a further and key application of this project is to see if single constant values of these parameters can be used to describe all the experimental concentration-time decay curves for one dye-carbon system.The error analysis and best fit approach to modeling the decay curves for both dye systems show that the correlation between experimental and theoretical data is good for the fixed values of the four fitted parameters. A significantly better fit of the model predictions is obtained when K _f, K _b and f are maintained constant but D _eff is varied. This indicates that the surface diffusivity may vary as a function of surface coverage.     

The Removal of Victoria Blue from Aqueous Solution by Adsorption on a Low-Cost Material

The use of perlite for the removal of victoria blue from aqueous solution at different concentration, ionic strength, pH and temperature has been investigated. Adsorption process is attained to the equilibrium within 1 h. It is found that the adsorption capacity of perlite samples for the removal of victoria blue increased by increasing pH and temperature, and decreased by expansion and ionic strength. The adsorption isotherms are described by means of the Langmuir and Freundlich isotherms. The adsorption isotherm was measured experimentally at different conditions, and the experimental data were correlated reasonably well by the adsorption isotherm of the Langmuir, and the isotherm parameters (Q _m and K) have been calculated for perlite samples as well. It is concluded that victoria blue is physically adsorbed onto the perlite. The removal efficiency (P) and dimensionless seperation factor (R) have shown that perlite can be used for removal of victoria blue from aqueous solutions, but unexpanded perlite is more effective.     

Adsorption of Acid Dyes from Aqueous Solutions by Calcined Alunite and Granular Activated Carbon

Dyestuff production units and dyeing units have always had a pressing need for techniques that allow economical pretreatment for color in the effluent. The effectiveness of adsorption for dye removal from wastewaters had made it an ideal alternative to other expensive treatment options. This paper deals with an investigation on alunite, existing wide reserves in Türkiye and in the world, for dye removal. Calcined alunite was utilized for this study and its performance evaluated against that of granular activated carbon (GAC). The use of calcined alunite for the removal of Acid Blue 40 and Acid Yellow 17 (AB 40 and AY 17) from aqueous solution at different calcination temperature and time, particle size, pH, agitation time and dye concentration has been investigated. The adsorption followed by Langmuir and Freundlich isotherms. The process follows first order adsorption rate expression and the rate constant was found to be 7.65 × 10^–2 and 5.74 × 10^–2 min^–1 for adsorption of AB 40 and AY 17 on calcined alunite, and 8.41 × 10^–2 and 10.04 × 10^–2 min^–1 for adsorption of AB 40 and AY 17 on GAC, respectively. The equilibrium saturation adsorption capacities were 212.8 mg dye/g calcined alunite and 151.5 mg dye/g calcined alunite for AB 40 and AY 17, respectively. The adsorption capacities were found to be 57.47 mg and 133.3 mg dye per g of GAC for AB 40 and AY 17, respectively. The results indicate that, for the removal of acid dye, calcined alunite was most effective adsorbent, although comparable dye removals were exhibited by GAC.     

Statistically Optimum HKUST-1 Synthesized by Room Temperature Coordination Modulation Method for the Adsorption of Crystal Violet Dye

Due to its excellency and versatility, many synthesis methods and conditions were developed to produce HKUST-1 ([Cu₃(BTC)₂(H₂O)₃]_n). However, the diversity of HKUST-1 was actually generated both in terms of characteristics and morphologies. Hence, the consistency of HKUST-1 characteristics and morphologies needs to be maintained. The statistical analysis and optimization provide features to determine the best synthesis condition. Here, a room-temperature coordination modulation method was proposed to maintain the morphology of HKUST-1 while reducing energy consumption. In addition, response surface methodology (RSM) was used to demonstrate the statistical analysis and optimization of the synthesis of HKUST-1. The molar ratio of ligand to metal, reaction time, and acetic acid concentration were studied to determine their effects on HKUST-1. The optimum HKUST-1 was obtained by the synthesis with a molar ratio of ligand to metal of 0.4703 for 27.2 h using 5% v/v acetic acid concentration. The statistical analysis performed a good agreement with the experimental data and showed the significance of three desired parameters on HKUST-1. The optimum HKUST-1 had the adsorption capacity of 1005.22 mg/g with a removal efficiency of 92.31% towards CV dye. It could be reused up to 5 cycles with insignificant decrease in performance.