An ion-imprinted polymer supported by attapulgite with a chitosan incorporated sol-gel process for selective separation of Ce(Ⅲ)

The surface ion-imprinting concept and chitosan incorporated sol-gel process were applied to the synthesis of a new attapulgitesupported polymer for selective separation of Ce(Ⅲ) from aqueous solution.The imprinting mechanism of prepared ion-imprinted polymer were discussed with the Characteristics of FT-IR and SEM.Results from the experiments of adsorption capacity and selectivity suggested that ion-imprinted polymer offered a fast kinetics for the adsorption of Ce(Ⅲ) under the optimum conditions. Its m...     

An Ion-imprinted Silica Gel Polymer Prepared by Surface Imprinting Technique Combined with Aqueous Solution Polymerization for Selective Adsorption of Ni(Ⅱ) from Aqueous Solution

A novel Ni(Ⅱ) ion-imprinted silica gel polymer was prepared via the surface imprinting technique combined with aqueous solution polymerization by using 2-acrylamido-2-methyl-1-propanesulfonic acid(AMPS) as a functional monomer for the selective separation of Ni(Ⅱ) from aqueous solution. The sorbent showed good chemical and thermal stability. Kinetics studies indicated that the equilibrium adsorption was achieved within 10 min and the adsorption kinetics fitted well with the pseudo-second-order kinetic model. The maximum adsorption capacity of the ion-imprinted polymer towards Ni(Ⅱ) at the optimal p H of 7.0 was 66.22 mg·g~(-1). The relative selectivity coefficients of the sorbent were 9.23, 15.71, 14.72 and 20.15 for Ni(Ⅱ)/Co(Ⅱ), Ni(Ⅱ)/Cu(Ⅱ), Ni(Ⅱ)/Zn(Ⅱ) and Ni(Ⅱ)/Pb(Ⅱ), respectively. The adsorption isotherm fitted well with Langmuir isotherm model. The thermodynamic results indicated that the adsorption of Ni(Ⅱ) was a spontaneous and endothermic process. The sorbent showed good reusability evidenced by six cycles of adsorption/desorption experiments. The precision of this method is satisfactory. Thus, the prepared sorbent can be considered as a promising sorbent for selective separation of Ni(Ⅱ) in real water samples.     

An imprinted polymer for removal of Cd<Superscript>2+</Superscript> from water samples: Optimization of adsorption and recovery steps by experimental design

A new ion-imprinted polymer（ⅡP） was synthesized by copolymerization of 4-vinylpyridine（monomer）, ethyleneglycoldimethacrylate（cross-linker） and 2,2-azobis-isobutyronitrile（initiator） in the presence of Cd²⁺ and quinaldic acid（complexing agent）.It was found that the adsorption capacity of IIP and blank polymer were 45.0 and 6.2 mg g^-1, respectively.The relative selectivity coefficients of the imprinted polymer for different binary mixture were also calculated. Compared to non-imprinted polymer（NIP）,theⅡP had higher selectivity for Cd（Ⅱ）.TheⅡP was used as a sorbent for cadmium extraction from water samples by using a simple batch extraction procedure.The effect of different parameters on Cd²⁺ extraction and its recovery from theⅡP were evaluated and optimized by using experimental design methodology.The optimized adsorption/desorption procedure was applied for cadmium removal from the real water samples.The obtained recoveries proved that thisⅡP could be used for removal of trace cadmium ions from water samples.     

STUDY ON THE ADSORPTION OF OXIDATION OF CROSSLINKED β—CYCLODEXTRIN AND ITS CXOMPOSITE ADSORBENT WITH DIALYTIC MEMBRANE

An urea adsorbent with an aldo structure was obtained by the oxidation of a crosslinked β-cyclodextrin polymer.The highest urea adsorption capacity reached 56.7mg/g in 0.05Maqueous phosphate buffer 37℃ and pH=7.4,and decrease to 4.8mg/g in in aqueous human serum albumin.The composite adsorbent was prepared by the oxidation of a crosslinked β-cyclodextrin and dialytic membrane.It was found that the composite adsorbent has a higher urea adsorption selectivity and capacity compared to that of the oxidation of a crosslinked β-cyclodextrin adsorbent when urea is in aqueous human serum albumin.     

A NOVEL MOLECULARLY IMPRINTED POLYMER： SYNTHESIS AND ADSORPTION BEHAVIOR OF GATIFLOXACIN

A kind of molecularly imprinted polymer （MIPs） with high selectivity was prepared using methacrylic acid （MAA） as functional monomer, ethylene glycol dimethacrylate （EDMA） as crosslinker and Gatifloxacin as template. The effect of various parameters such as volume of solvent, functional monomer dosage, crosslinker dosage and polymerization time were investigated. The selective binding experiment for substrates show that the affinity and selectivity for Gatifloxacin were higher than that for blank polymer. Scatchard analysis show that the MIPs recognized template with two kinds of binding sites. The dissociation constant Kd and maximum adsorption quantity Qmax of these two kinds of binding sites were calculated： Kd1 and Qmax1 of the binding sites with high affinity were 8.67×10^-4 mol/L and 28.19μmol/g, while Kd2 and Qmax2 of the binding sites with low affinity were 1.05×10^-3 mol/L and 33.20μmol/g respectively.     

ADSORPTION BEHAVIOR OF Pb（II） ON POTASSIUM HEXATITANATE WHISKER BY FAAS

Based on the advantage of high surface area and strong adsorption ability of potassium hexatitanate whisker, a method to determine trace Pb（II） content by combining solid phase extraction with Flame atomic absorption spectrometry （FAAS） was established. The adsorptive behavior of potassium hexatitanate whisker to Pb（II）, primary influencing factors of adsorption and elution and effect of coexistence ions were investigated systemically. The optimal analytical conditions were discussed and examined. It was found that the adsorption rate of potassium hexatitanate whisker to Pb（II） was 100% at pH 4.0. Pb（II） could be eluted from potassium tetratitanate whisker with HCl （2mol/L） under boiling water for 30min. The detection limit was 5.75ng/mL, and relative standard deviation was 1.66% （n=9, Cpb=2.0μg/mL）.     

Highly selective determination of palladium(II) after preconcentration using Pd(II)-imprinted functionalized silica gel sorbent prepared by a surface imprinting technique

A novel Pd(II)-imprinted amino-functionalized silica gel sorbent was prepared with the help of a surface-imprinting technique for the preconcentration and separation of Pd(II) prior to its determination by inductively coupled plasma atomic emission spectrometry. Compared to the traditional solid sorbents and non-imprinted polymer particles, the ion-imprinted polymers (IIPs) had a higher adsorption capacity and selectivity for Pd(II). The maximum static adsorption capacity of the imprinted and non-imprinted sorbent for Pd(II) was 26.71 mg g⁻¹ and 10.13 mg g⁻¹, respectively. The relative selectivity factor (α_r) of Pd(II)/Zn(II), Pd(II)/Au(III), Pd(II)/Ru(III), Pd(II)/Rh(III), Pd(II)/Pt(IV), Pd(II)/Ir(III), Pd(II)/Fe(III) and Pd(II)/Zn(II) is 39.0, 60.2, 92.0, 85.0, 50.0, 58.0 and 45.0, respectively. The detection limit (3σ) of the method is 0.36 μg L⁻¹. The relative standard deviation was 3.2% for eight replicate determinations of 10 μg of Pd²⁺ in 200 mL water sample. The method was validated by analyzing a standard reference material, and the results obtained were in good agreement with the standard values. The method was also applied to the determination of trace palladium in geological samples with satisfactory results.     

Hemoglobin-imprinted polymer gel prepared using modified glucosamine as functional monomer

A new functional glycomonomer was obtained from modified glucosamine. Hemoglobin-imprinted polymer gel was prepared with allyl-bromide modified glucosamine as functional monomer, poly（ethylene-glycol）diacrylate （PEGDA） as cross-linker and ammonium persulfate [（NHn）2S2O8]/sodium hydrogen sulfite （NaHSO3） as initiators in a phosphate buffer. The adsorption capacity and selective adsorption of the molecular imprinting polymer （MIP） were also discussed.     

ADSORPTION OF TANNIN ACID ONTO AN AMINATED MACROPOROUS RESIN FROM AQUEOUS SOLUTIONS

A macroporous polymeric adsorbent NG-8 was synthesized with divinylbenzene using conventional suspension polymerization technique.Its aminated product NG-9 was prepared by introducing tertiary amino groups into NG-8 for removal of tannin acid from aqueous solutions.NG-9 could be used directly without a wetting process and had higher adsorption capacity than NG-8,which might be attributed to the enhanced adsorbent-adsorbate interaction due to the tertiary amino groups on the polymeric matrix.The Langmuir equation was successfully employed to describe the adsorption process.The adsorption enthalpy change further validated the uptake of tannin acid on NG-9 to be an enhanced physical adsorption because of the Lewis acid-base interaction.In addition,adsorption kinetic studies testified that the tertiary amino groups on the polymer matrix could decrease the adsorption rate maybe for the hindrance of the tertiary amino groups and water clusters built up.     

Preparation and performance evaluation of resin-derived carbon spheres for desulfurization of fuels

A polystyrene-based ion-exchange resin was employed as the precursor for preparation of resin-derived carbon spheres(RCSs) through KOH activation with various impregnation ratios.Pore structure,yield and hardness,surface functional groups of the samples and their adsorption performance towards dibenzothiophene(DBT) were investigated.The RCSs with large surface areas(up to 2696m2/g) and total pore volumes(up to 1.46 cm3/g) exhibited larger adsorption capacities than a commercial activated carbon,F400.Polanyi-Dubinin-Mane(PDM) model was applied to fit the adsorption data,which proved that micropore filling was involved during the adsorption process.Moreover,a good linear relationship was observed between the extra-micropore volume and adsorption capacity.Intra-particle diffusion(IPD) model was used to describe the kinetic data of DBT onto the adsorbents.The adsorption processes were divided into three stages according to the different diffusion parameter.The selective adsorption towards DBT in the presence of competing compounds was also investigated and the high selectivity of the RSCs towards DBT may be attributed to the large quantity of acidic oxygen-containing groups.     

Acyl Thioacetamide-group Chelated Nanofiber to Adsorb Silver Ions from Aqueous Systems

The acyl thioacetamide-group chelated nanofiber was prepared from polyacrylonitrile（PAN） fiber with thioacetamide as vulcanization agent by an electrospinning process combined with chemical modification.It was found that the chelated nanofiber displays a high adsorption capacity and adsorption selectivity for Ag（Ⅰ） ions from aqueous systems.The adsorption capacity of Ag（Ⅰ） ions on chelated nanofiber increases with the increase of adsorption time.Kinetics of the Ag（Ⅰ） ions adsorption was found to follow pseudo-second-order rate equation.Based on the characterization results,a possible mechanism of Ag（Ⅰ） ions adsorbed on the acyl thioacetamide-group chelated nanofiber was proposed.The chelated nanofiber could not only chelate to Ag（Ⅰ） ions but also reduce them.This study provides a promising nanofiber material for removing heavy metal ions.     

Preparation of a Hybrid Organic-inorganic Monolith for Extraction and Purification of Quercetin and Myricetin from Chamaecyparis obtusa

A new hybrid organic-inorganic monolithic cartridge was synthesized and used as the selective sorbent for the extraction and purification of quercetin and myricetin from Chamaecyparis obtusa via a solid-phase extraction method.The morphology of the monolithic material was examined by field emission-scanning electron microscopy and a Brunauer-Emmett-Teller（BET） test.The adsorption capacity of the obtained material for quercetin and myricetin was investigated by fitting the adsorption data to four different adsorption equations,of which the LangmuirFreundlich isotherm was selected as the most suitable model.Under optimized conditions,good calibration curves were observed at nine concentrations ranged from 0.5 μg/mL to 100.0 μg/mL of quercetin and myricetin.The extraction recovery ranged from 74.5％ to 84.6％ and the inter-and intra-day relative standard deviations were ＜6％.This type of hybrid monolith has potential for the separation and purification of bioactive compounds from natural plant extracts.     

TPD STUDY OF STEAM ADSORPTION ON Ni-RE CATALSTS

Adsorbability to steam of nickel catalysts unpromoted and promot-ed with rare earth for hydrocarbon steam reforming has been comparativelyinvestigated using TPD technique.The results showed that the adsorptive ca-pacity for steam of promoted Ni catalyst was mainly attributed to the rareearth additive and the amounts of adsorbed steam on reduction state catalystswere 1—1.4 times more than those on oxidation state catalysts.The adsorp-tive capacity for steam depended on not only the impregnation mode but alsothe contents of rare earth.At high contents of rare earth,there were threedifferent adsorption sites on the surface of catalysts.But when less than1.3%,the effect on adsorbability to steam became negnigible.The promotedNi-catalyst exhibited good coking-resistance and sulfur-tolerance.This mightbe attributed to its great capacity of adsorption to steam.     

Lead and Cadmium Adsorption onto Iron Oxides and Manganese Oxides in the Natural Surface Coatings Collected on Natural Substances in the Songhua River of China

Natural surface coatings collected from natural substances(NSCsNS)were employed to study the roles of the main chemical components(iron oxides,manganese oxides,and other components)in controlling the adsorption of lead(Pb)and cadmium(Cd)in aquatic environments.The selective chemical extraction followed by the adsorption of Pb and Cd experiments and statistical analysis,were used to investigate the adsorption property of each component.Hydroxylamine hydrochloride was used to remove manganese oxides selectively,and sodium dithionite was used to extract iron oxides and manganese oxides.The result indicated that iron oxides and manganese oxides played an important role in the adsorption of Pb and Cd on NSCsNS,and the relative contribution was about two-thirds.The contribution of manganese oxides was the greatest,with a lesser role indicated for other components.The adsorption ability of manganese oxides for Pb and Cd was greater than that of iron oxides or other components for Pb and Cd.The Pb adsorption observed in each component was greater than Cd adsorption.     

PREPARATION AND ADSORBABILITY OF DEXTRAN MICROSPHERES WITH UNIFORM DIAMETER

The method of preparing uniform dextran microspheres with a narrow diameter distribution was introduced and the adsorbability of these microspheres was evaluated. The microspheres were prepared in W/O microemulsion using 0.5% dextran solution as the aqueous phase and n-hexane as the oil phase. Characteristics of the prepared dextran microspheres were examined with laser light blocking technique, optical microscope and ultraviolet spectrometer. The results show that the prepared dextran microspheres have uniform morphology and narrow diameter distribution, nearly 92% of them having a diameter of 56.6μm. In vitro evaluation of adsorbability, wet dextran microspheres have good adsorption of 98.32mg/g of model drug methylene blue in 20.86mg/L methylene blue solution at 25℃, The adsorption of dried dextran microspheres under the same condition is 132.15mg/g, which is even higher. And the adsorbability of dextran microspheres has significant relationship with the concentration of methylene blue and temperature. The adsorbability is better at lower temperature and higher concentration of methylene blue.     

Fabrication and evaluation of molecularly imprinted regenerated cellulose composite membranes via atom transfer radical polymerization

A simple and effective method for surface molecularly imprinted composite membranes （MICMs） for artemisinin （Ars） based on regenerated cellulose membranes was first prepared through surface- initiated atom transfer radical polymerization （ATRP）, and the as-prepared MICMs were then evaluated as adsorbents for selective recognition and separation of Ars molecules. Batch rebinding studies were conducted to determine the specific adsorption equilibrium, kinetics and selective permeation performance. The adsorption capacity of MICMs toward Ars by the Langmuir isotherm model was 2.008 mgg-1, which was nearly 5.0 times higher than non-molecularly imprinted composite membranes （NICMs）. The kinetic property of MICMs was well-fitted by the pseudo-second-order rate equation. The selective permeation experiments were successfully investigated to prove the excellent selective permeation performance for Ars than the competitive analog （artemether）.     

Structure controlling and adsorption application of polyethersulfone porous microspheres prepared via electrospraying

The focus of this work is to control the structure of electrosprayed polymer microspheres and then study the effect of different structures on the microspheres＇ adsorption properties. Scanning electron microscopy （SEM） coupled with image analysis software was employed to evaluate the size distributions and the structure of microspheres. According to the observation and analysis results, two types of polyethersulfone （PES） porous microspheres （perfect sphere-shaped and collapsed） were prepared via electrospraying technology by adjusting the solvent and polymer molecular weight. The porous PES microspheres can remove bisphenol A （BPA） from its aqueous solution effectively. Compared with collapsed microspheres, the rough microspheres had much higher specific surface area and better mobility in the BPA aqueous solution, so it showed a better adsorption capacity than that of collapsed microspheres. The solvent evaporation rate and the occurrence rate of phase separation significantly affect the structure and morphology of microspheres.     

ADSORPTION OF 2,4-DICHLOROPHENOL IN AQUEOUS SOLUTION ONTO ADSORPTION RESIN MODIFIED BY N-ACETYLANILINE

A hypercrosslinked adsorption resin （ZH-05） modified by N-acetylaniline in the post crosslinking process was prepared. The adsorption properties of ZH-05 toward 2,4-dichlorophenol in comparison with granular activated carbon （GAC） and Amberlite XAD-4 were observed. The present study mainly focuses on the static equilibrium adsorption behaviors, desorption profiles and the proof of chemisorption. The results show that the Langmuir equation can give a perfect fitting to experimental data, and high temperature was favorable for adsorption of 2,4-dichlorophenol on ZH-05. A related equation was used to correlate the amount of chemisorption and the suppositionai chemisorption equilibrium concentration of adsorbate in aqueous solution. The adsorption capacities from different ranges of temperature and the static desorption experiment both reveal the same conclusion, i.e., the adsorption of 2,4-dichlorophenol from water on ZH-05 is a coexistent process of physical adsorption and chemical transition as on GAC.     

Metsulfuron-methyl Molecularly Imprinted Stir Bar Sorptive Extraction Coupled with High Performance Liquid Chromatography for Trace Sulfonylurea Herbicides Analysis in Complex Samples

Metsulfuron-methyl molecularly imprinted polymer(MIP)-coated stir bar was prepared for sorptiveextraction of sulfonylurea herbicides in complex samples. The MIP-coating was about 21.3 祄 thickness with the relative standard deviation(RSD) of 4.4%(n=10). It was homogeneous and porous with good thermal stability and chemical stability. The extraction capability of the MIP-coating was 2.8 times over that of the non-imprinted polymer (NIP)-coating in hexane. The MIP-coating exhibited selective adsorption ability to the template and its analogues. The extraction conditions, including extraction solvent, desorption solvent, extraction time, desorption time and stirring speed, were optimized. A method for the determination of six sulfonylurea herbicides by MIP-coated stir bar sorptive extraction coupled with high performance liquid chromatography(HPLC) was developed. The linear range was 10-200 礸/L and the detection limits were within a range of 2.0-3.3 礸/L. It was also applied to the analysis of sulfonylurea herbicides in spiked river water, soil and rice samples.     

Study of preparation and adsorption properties of imidacloprid mesoporous surface molecularly imprinted polymerEI北大核心CSCD

Imidacloprid mesoporous surface molecularly imprinted polymer (MIP) was rapidly synthesized by one[1]step method, with imidacloprid as template molecule, methacrylic acid (MAA) as functional monomer, azodiisobutyronitrile (AIBN) as initiator and ethylene glycol dimethacrylate (EGDMA) as crosslinker. The characterization of MIP was completed by SEM, TEM, FT-IR, and nitrogen adsorption-desorption isotherms. The adsorption conditions were optimized. At the imidacloprid concentration of 100 µg/mL, MIP reached adsorption saturation and the adsorption time was shorter than that of the corresponding non-imprinted polymer (NIP), with the saturated adsorption value of 3.628 mg/g, and the imprinting factor of 1.27, indicating that the mesoporous structure and surface imprinting improved the mass transfer rate of imidacloprid in the adsorption process, so as to improving the adsorption capacity. In addition, under the same conditions, the adsorption capacity of MIP for imidacloprid was higher than acetamiprid, thiacloprid and thiamethoxam, indicating that MIP had better specific recognition ability. The imidacloprid mesoporous surface MIP can be prepared simply and rapidly, which may be a potential material in the field of sample pretreatment and rapid detection. © 2023, Youke Publishing Co.,Ltd. All rights reserved.