Removing Cd^(2+) by Composite Adsorbent Nano-Fe_3O_4/Bacterial Cellulose

A new composite adsorbent, nano-Fe3O4/bacterial cellulose（BC）, was prepared through blending method. The process of adsorbing Cd2＋ including its isotherm and kinetics measured was studied. The results show that the adsorption efficiency is improved because of huge surface area and surface coordination of nano-Fe3O4 particles. Its adsorption capacity is 27.97 mg/g and the maximum of Cd2＋ removal is 74%. The adsorption kinetics can be described by pseudo-second rate model and the adsorption equilibrium by Langmuir type. The superparamagnetism of nano-Fe3O4 particles can help to solve the difficult separation of single BC adsorbent and lead to the quick separation of composite adsorbent from the liquid if a magnetic field was applied. Cd2＋ can be desorbed effectively by EDTA and HCl from the composite adsorbent, which can make it be reused.

Fabrication and Thermal Conductivity Improvement of Novel Composite Adsorbents adding with Nanoparticles

Thermal conductivity is one of key parameters of adsorbents, which will affect the overall system performance of adsorption chiller. To improve adsorbent＇s thermal conductivity is always one of research focuses in chemisorption field. A new chemical composite adsorbent is fabricated by adding carbon coated metal（Aluminum and Nickel） nanoparticles with three different addition amounts into the mixture of chloride salts and natural expanded graphite aiming to improve the thermal conductivity. The preparation processes and its thermal conductivity of this novel composite adsorbent are reported and summarized. Experimental results indicate that the nanoparticles are homogenously dispersed in the composite adsorbent by applying the reported preparation processes. The thermal conductivity of the composite adsorbent can averagely enlarge by 20% when the weight ratio of the added nanoparticles is 10 wt%. Moreover, carbon coated aluminum nanoparticles exhibit more effective enlargement in thermal conductivity than nickel nanoparticles. As for the composite adsorbent of CaCl2-NEG, there is a big reinforcement from 30% to 50% for Al@C nanoparticles, however only 10% in maximum caused by Ni@C nanoparticles. The proposed research provides a methodology to design and prepare thermal conductive chemical composite adsorbent.

Preparation of Ammonium Tungstophosphate-Calcium Alginate Composite Adsorbent and the Separation of Rubidium and Potassium

As a kind of rare metals,rubidium is often used to prepare special glass,photomultiplier tubes,thermoelectric converter,organic catalysts and antidepressants.Rubidium forms no minerals of its own,hence,it often coexists with

Composite adsorbents of CaCI2 and sawdust prepared by carbonization for ammonia adsorption refrigeration

Composite adsorbents of CaC12 and sawdust prepared by carbonization for adsorption refrigeration with NH3 as refrigerant are tested, and the effects of carboniza tion temperature on the sorption capacity and rate are analyzed. The results show that the amount of pores in the sawdust of the composite adsorbents carbonized, apart from the content of CaCI2, is the most dominant factor influencing the NH3 sorption on composite adsorbents. The optimum carbonization temperature is 700℃, which gives the maximal NH3 sorption capacity as high as 0.774 kg of NH3 per kg of the composite, and the specific cooling power is approximately between 338 and 869 W/kg with the cycle duration varying from 5 to 20 minutes. The present study demonstrates that the composite absorbent of CaC12 and sawdust prepared by carbonization is more promising and competitive for adsorption refrigeration application.

Novel Nanosized Adsorbing Composite Cathode Materials for the Next Generational Lithium Battery

A novel carbon-sulfur nano-composite material was synthesized by heating sublimed sulfur and high surface area activated carbon （HSAAC） under certain conditions. The physical and chemical per- formances of the novel carbon-sulfur nano-composite were characterized by scanning electron microscopy （SEM）, Brunauer-Emmett-Teller （BET） and X-ray diffraction （XRD）. The electrochemical performances of nano-composite were characterized by charge-discharge characteristic, cyclic voltammetry and electrochemical impendence spectroscopy （EIS）. The experimental results indicate that the electrochemical capability of nano- composite material was superior to that of traditional S-containing composite material. The cathode made by carbon-sulfur nano-composite material shows a good cycle ability and a high specific charge-discharge capacity. The HSAAC shows a vital role in adsorbing sublimed sulfur and the polysulfides within the cathode and is an excellent electric conductor for a sulfur cathode and prevents the shuttle behavior of the lithium-sulfur battery.

Constructing porous ZnFC-PA/PSF composite spheres for highly efficient Cs^(+) removal

Radioisotope leaking from nuclear waste has become an intractable problem due to its gamma radiation and strong water solubility.In this work,a novel porous ZnFC-PA/PSF composite sphere was fabricated by immobilization of ferrocyanides modified zinc phytate into polysulfone(PSF)substrate for the treatment of Cs-contaminated water.The maximum adsorption capacity of ZnFC-PA/PSF was 305.38 mg/g,and the removal efficiency of Cs+was reached 94.27%within 2 hr.The ZnFC-PA/PSF presented favorable stability with negligible dissolution loss of Zn^(2+)and Fe^(2+)(<2%).The ZnFC-PA/PSF achieved high-selectivity towards Cs+(K_(d)=2.24×10^(4)mL/g)even in actual geothermal water.The adsorption mechanism was inferred to be the ion-exchange between Cs^(+)and K^(+).What’s more,ZnFC-PA/PSF worked well in the fixed-bed adsorption(E=91.92%),indicating the application potential for the hazardous Cs^(+)removal from wastewater.

Decoupling the adsorption mechanisms of arsenate at molecular level on modified cube-shaped sponge loaded superparamagnetic iron oxide nanoparticles

In this study, a commercial cube-shaped open-celled cellulose sponge adsorbent was modified by in-situ co-precipitation of superparamagnetic iron oxide nanoparticles(SPION) and used to remove As(V) from aqueous solutions. Fe K-edge X-ray absorption spectroscopy(XAS) and TEM identified maghemite as the main iron phase of the SPION nanoparticles with an average size 13 nm. Batch adsorption experiments at 800 mg/L showed a 63% increase of adsorption capacity when loading 2.6 wt.% mass fraction of SPION in the cube-sponge.Experimental determination of the adsorption thermodynamic parameters indicated that the As(V) adsorption on the composite material is a spontaneous and exothermic process.As K-edge XAS results confirmed that the adsorption enhancement on the composite can be attributed to the nanoparticles loaded. In addition, adsorbed As(V) did not get reduced to more toxic As(Ⅲ) and formed a binuclear corner-sharing complex with SPION. The advantageous cube-shape of the sponge-loaded SPION composite together with its high affinity and good adsorption capacity for As(V), good regeneration capability and the enhanceddiffusion attributed to its open-celled structure make this adsorbent a good candidate for industrial applications.

Renewable molybdate complexes encapsulated in anion exchange resin for selective and durable removal of phosphate

The existence of many anions in wastewater reduces the removal efficiency of phosphate by adsorbents under realistic conditions.Facing this challenge,the study reports on an insistent and stable composite adsorbent of molybdate complexes Fe-(MoO_(x))embedded in a macroporous anion exchange resin(D-201).[Fe(MoO_(x))]-D-201 shows 93.7%adsorption capacity(28.3 mg/g)for phosphate even when the molar concentration of coexisting ions is 5 times higher than phosphate.The capacity of adsorbent is maintained more than 84.2%after five regeneration cycles to remove phosphate in the wastewater containing coexisting ions.The ability of highly selective removal of phosphate is maintained during the regeneration cycles explained by the change of the binding of molybdate clusters with phosphate,which is due to the different structures of molybdate clusters depending on various pH.In general,this work puts forward a new idea for the development of phosphorus removal adsorbents for the treatment of wastewater containing coexisting ions.