八种常见吸附剂在蛋白质水解液脱色过程中对氨基酸吸附影响的研究

以八种常见吸附剂作为脱色剂,对蛋白质(猪血为原料)水解液进行了脱色实验并对脱色剂对水解产物——氨基酸的吸附影响进行了研究。结果表明:从脱色和氨基酸吸附两方面考虑,石墨粉是一种优于活性炭的脱色剂。本文还对各种吸附剂在不同pH值下氨基酸的吸附以及石墨粉的反复使用进行了讨论。

超交联多孔材料的合成及吸附氨基酸特性

以苯为反应单体、二甲氧基甲烷(FDA)为交联剂,通过Friedel-Crafts烷基化反应,改变单体与交联剂之间的摩尔比来调控聚合物的孔隙结构,合成了一系列具有高比表面积的多孔芳香交联聚合物HCP-PhH-(1-3)。通过氮气吸附脱附、热失重和红外光谱对其进行表征,聚合物表现出丰富的孔径结构与良好的稳定性。将其对色氨酸(Trp)、苯丙氨酸(Phe)以及苯甘氨酸(Phg)进行了吸附行为研究,结果表明,单体苯与交联剂FDA的摩尔比为1:5时,合成的聚合物HCP-PhH-3具有相对较大的比表面积901.498 m^(2)/g,在25℃时对pH=7、浓度1.5 mmol/L的氨基酸溶液具有较大的吸附能力,吸附量分别为色氨酸(0.199 mmol/g)、苯丙氨酸(0.140mmol/g)、苯甘氨酸(0.034 mmol/g),显示出明显的吸附效果。对HCP-PhH-3吸附氨基酸的过程进行动力学拟合,线性拟合相关度(R2)符合准二级动力学模型。

Synthesis of novel thionocarbamate for copper-sulfur flotation separation and its adsorption mechanism

As a novel collector, O-isopropyl-N,N-diethyl thionocarbamate(IPDTC) was designed and synthesized for copper-sulfur flotation separation. Density functional theory calculations were performed to investigate the electronic structures of IPDTC. The results showed that IPDTC had higher energy of the highest occupied molecular orbital but lower electronegativity than O-isopropyl-N-ethyl thionocarbamate(Z-200). It was predicted that IPDTC had strong collection ability according to the reaction energy criteria. Flotation results demonstrated that the collecting ability of IPDTC to chalcopyrite and pyrite was stronger than that of Z-200. Then, the flotation mechanism was analyzed by measurements of surface tension, adsorption capacity, XPS, FTIR and zeta potential. These results indicated that IPDTC could reduce the solution surface tension. The adsorption capacity of IPDTC on chalcopyrite was higher than that on pyrite, consistent with the results of the flotation tests. FTIR, zeta potential and XPS results also demonstrated that IPDTC was strongly absorbed on the chalcopyrite surface by formation of Cu—S—C bonds, but showed a weak affinity on the pyrite surface.

ADSORPTION OF SAMARIUM(III) ON DIGLYCOLAMIDIC ACID RESIN

The sorption behavior and mechanism of a novel chelate resin, diglycolamidic acid resin (DAAR), for Sm(III) were investigated. The optimal sorption condition of DAAR for Sm(III) is pH=6.0 in HAc-NaAc medium. The statically saturated sorption capacity is 190mg/g resin at 298K. The Sm(III) adsorbed on DAAR can be eluted reaching 100% by 0.5~2.0mol/L HCl used as eluant. The resin can be regenerated and reused without apparent decrease of sorption capacity. The apparent sorption rate constant is k298= 1.96×10-5s-1. The apparent activation energy is 26kJ/mol. The sorption behavior of DAAR for Sm(III) obeys the Freundlich isotherm. The thermodynamic sorption parameters, enthalpy change 腍 of DAAR for Sm(III) is 16.9kJ/mol. The molar coordination ratio of the functional group of DAAR to Sm (III) is 3. The sorption mechanism of DAAR for Sm(III) was examined by using chemical method and IR spectrometry. The coordination bond was formed between oxygen atoms in the functional group of DAAR and Sm(III).

ADSORPTION CHARACTERISTICS OF L-HISTIDINE ON ACTIVE CARBON

Adsorption properties of L-histidine on active carbon were studied in the paper, which are affected by the main parameters, such as the quantity percent of active carbon, pH value of the solution, the thne of adsorption equilibrium and adsorption temperature. The results indicate that adsorption equilibrium time of L-his on active carbon is about 80 minutes. With tire increasing of the quantity percent of active carbon, the adsorbance of L-his decreases sharply, and increases lighter after that. When the quantity percent of active carbon is 10%, the adsorbance reaches the minimum. pH value of solution and extraction temperature have great affection on the adsorption. When the pH value is higher or lower than the pl of L-his, the adsorbance is small, even zero. It is proven that the experimental equilibrium data which are obtained under the conditions of 80 ℃ and pH=1.0, are fitted with the Freundlich equation： q=2.5914c^0.8097. Tire results can provide certain references in L-his adsorption process of industrial operation.

Synthesis of PGMA Microspheres with Amino Groups for High-capacity Adsorption of Cr(VI) by Cerium Initiated Graft Polymerization

Abstract A novel polyglycidylmethacrylate （PGMA） microspheres with high adsorption capacity of Cr（VI） was prepared by cerium（IV） initiated graft polymerization of tentacle-type polymer chains with amino group on polymer microspheres with hydroxyl groups. The micron-sized PGMA microspheres were prepared by a dispersion polym erization method and subsequently modified by ring-opening reaction to introduce functional hydroxyl groups. The polymer microspheres were characterized by scanning electron microscopy （SEM） and Fourier transform infrared spectroscopy （FTIR）. The results indicated that the polymer microspheres had an average diameter of 5 m with uniform size distribution. The free amino group content was determined to be 5.13 mmol·g^-1 for g;PGMA-NH2 microspheres by potentiometric and conductometric titration methods. The Cr（VI） adsorption results indicated that the graft polymerization of tentacle-type polymer chains on the polymer microspheres could produce adsorbents with high adsorption capacity （500 mg-g-l）. The polymer microspheres with grafted tentacle polymer chains have potenial application in large-scale removal of Cr（VI） in aqueous solution.

RECOVERY OF p-AMINOPHENOL (PAP) FROM AQUEOUS SOLUTION BY HYPER-CROSS-LINKED RESIN AND ITS USE FOR WASTEWATER TREATMENT

p-Aminophenol （PAP）, a typical amphoteric compound, has been widely used as raw chemical material and important interrnediate in various fields. To study on the recovery of PAP, an experimental comparison of the adsorption and desorption properties of PAP onto three types of hyper-cross-linked resins in aqueous solutions was performed. This paper focuses on the static equilibrium adsorption and desorption behaviors, the adsorption thermodynamics, the column dynamic adsorption and desorption, and other influencing factors of adsorption, such as temperature and pH values. All the isothermal data fit well to the Freundlich model. The capacity of equilibrium adsorption for PAP on NG-10 is the highest within the temperature range 288K-318K, which may greatly contribute to the advantage in specific surface area, especially the micropore area, of the adsorbent. While in the desorption experiments, NG-9 achieved relative well regeneration efficiency whether by ethanol or by 4% hydrochloric acid. Furthermore, the results of column tests and field applications were also proved that NG-9 was an effective sorbent for the reclamation PAP from wastewater.

SYNTHESIS AND PROPERTIES OF SULFHYDRYL CHITOSAN

A new adsorbent for heavy metal ions, sulfhydryl chitosan (S chitosan), was produced by treatment of chitosan with sulhydryl acetic acid in the presence of sulfuric acid as a catalyst. Its structure was confirmed by elemental analysis and FT IR spectra analysis. The adsorption properties of sulfhydryl chitosan for Cu(Ⅱ), Cd(Ⅱ), Pb(Ⅱ), Cr(Ⅲ) and Ni(Ⅱ) were investigated, and the effect of pH value on adsorption, adsorption kinetics, and selective adsorption was examined. It was shown that S chitosan has good adsorption for Pb(Ⅱ), Cu(Ⅱ) and Cd(Ⅱ) like chitosan, is also insoluble in acid solution; has good adsorption kinetic properties for heavy metal ions; and can be used in acid solution. The adsorption capacities of S chitosan can be affected by media acidity. The adsorbed Cu(Ⅱ) Cd(Ⅱ)and Pb(Ⅱ) could be eluted by diluted chlorhydric acid.

Novel fluorescence sensor based on covalent immobilization of 3-amino-9-ethylcarbazole via electrostatically assembled gold nanoparticle layer

A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors was developed.3-Amino-9-ethylcarbazole(AEC)was attached to the outmost surface of quartz glass slide via aminosilanizing the slide,crosslinking chitosan,adsorbing Au nanoparticle,self-assembling HS(CH2)11OH,and coupling AEC.Thus, an AEC-immobilized optical sensor was obtained.The sensor exhibits a wide linear response range from 7.0×10- 7to 1.0×10 -4 mol/L and a correlation coefficient of 0.995 9 for the detection of 2-nitrophenol.The detection limit and response time of the sensor are 1.0×10- 7mol/L and less than 10 s,respectively.The fluorescence intensity of the used sensor can be restored to the blank value by simply rinsing with blank buffer.A very effective matrix for immobilizing indicator dye is provided by the proposed technique, which is adaptable to other indicator dyes with amino groups besides AEC.

Study of Adsorption Isotherm Curves of Amino Acids on the Kaolinite

This paper studies the adsorption isotherm curves of four amino acids (glycine, aspartic acid, glutamic acid and lysine) and the effects of existences of different concentrations of Cu(II) on them. Both the adsorption isotherm of the amino acids on the kaolinite and that when the copper ion Cu (II) exists belong to the Langmuir type. The slopes of these adsorption isotherm increase with the increasing concentrations of Cu(II) added. It can be explained in terms of formation of the type(I) ternary surface complexes in these systems. The regular pattern of the effects of copper ion Cu(II) on the adsorption isotherm of amino acids on the kaolinite is identical with that of its effects on the exchange and adsorption percentage E (%)-pH on the kaolinite in the same system.

Effects of ammonium application rate on uptake of soil adsorbed amino acids by rice

In recent years, excessive use of chemical nitrogen （N） fertilizers has resulted in the accumulation of excess ammonium （NH4＋） in many agricultural soils. Though rice is known as an NH4＋-tolerant species and can directly absorb soil intact amino acids, we still know considerably less about the role of high exogenous NH4＋ content on rice uptake of soil amino acids. This experiment examined the effects of the exogenous NH4＋ concentration on rice uptake of soil adsorbed glycine in two different soils under sterile culture. Our data showed that the sorption capacity of glycine was closely related to soils＇ physical and chemical properties, such as organic matter and cation exchange capacity. Rice biomass was significantly inhibited by the exogenous NH4＋ content at different glycine adsorption concentrations. A three-way analysis of variance demonstrated that rice glycine uptake and glycine nutritional contribution were not related to its sorption capacity, but significantly related to its glycine：NH4＋ concentration ratio. After 21-d sterile cultivation, the rice uptake of adsorbed glycine accounted for 8.8%-22.6% of rice total N uptake, which indicates that soil adsorbed amino acids theoretically can serve as an important N source for plant growth in spite of a high NH4＋ application rate. However, further studies are needed to investigate the extent to which this bioavailability is realized in the field using the 13C, 15N double labeling technology.

Mesoporous silica SBA-15 functionalized with phosphonate and amino groups for uranium uptake

Mesoporous silicas have a very attractive ability of sorption and enrichment of metal ions due to their huge surface area and facile functionalization by organic ligands. In this work, phosphonate-amino hifunctionalized mesoporous silica SBA-15 （PA-SBA-15） as U（VI） sorbent was fabricated through post-grafting method. The obtained mesoporous silica was character- ized by SEM, XRD, NMR and nitrogen sorption/desorption experiments, which revealed the existence of ordered mesoporous structure with uniform pore diameter and large surface area. The adsorptivity of PA-SBA-15 for U（VI） from aqueous solution was investigated using batch sorption technique under different experimental conditions. The preliminary results show that the U（VI） sorption by PA-SBA-15 is very quick with equilibrium time of less than 1 h, and the U（VI） uptake is as large as 373 mg/g at pH 5.5 under 95℃. The sorption isotherm has been successfully modeled by the Langmuir isotherm, suggesting a monolayer homogeneous sorption of U（VI） in PA-SBA-15. The sorption is pH-dependent due to the pH-dependent charge of sorbent in the aqueous solution. The thermodynamics research shows that the sorption is a feasible and endothermic process. Based on these results, PA-SBA-15 could be a promising solid phase sorbent for highly-efficient removal of U（VI） ions from waste water and enrichment of U（VI） from a solution at a very low level.