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1.
Polymers (Basel) ; 15(5)2023 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-36904473

RESUMO

To prepare a novel cassava starch-based phosphorus releasing super-absorbent polymer (CST-PRP-SAP), the single factor and orthogonal experiment were applied to analyze the effects of different reaction conditions on the absorption and phosphorus release capacities of CST-PRP-SAP samples. The structural and morphological characteristics of the cassava starch (CST), powdered rock phosphate (PRP), cassava starch-based super-absorbent polymer (CST-SAP) and CST-PRP-SAP samples were all compared with various technologies, such as the Fourier transform infrared spectroscopy and X-ray diffraction pattern, etc. The results showed that the CST-PRP-SAP samples had good performances of water retention and phosphorus release which were synthesized, such as the reaction temperature, starch content, P2O5 content, crosslinking agent, initiator, neutralization degree, and acrylamide content, which were 60 °C, 20% w/w, 10% w/w, 0.02% w/w, 0.6% w/w, 70% w/w, and 15% w/w, respectively. The water absorbency of CST-PRP-SAP was almost larger than that of the CST-SAP sample with a P2O5 content of 5.0% and 7.5%, and they all gradually decreased after three consecutive water absorption cycles. The CST-PRP-SAP sample could maintain about 50% of the initial water content after 24 h, even at the temperature of 40 °C. The swelling process of CST-PRP-SAP conformed to the non-Fickian diffusion, which was determined by the diffusion of water molecules and the relaxation process of polymer chain segments. The cumulative phosphorus release amount and release rate of the CST-PRP-SAP samples were increased with the increasing PRP content and the decreasing neutralization degree. After a 216 h immersion, the cumulative phosphorus release amount and release rate of the CST-PRP-SAP samples with different PRP contents were increased by 17.4 and 3.7 times, respectively. The rough surface of the CST-PRP-SAP sample after swelling was beneficial to the performance of water absorption and phosphorus release. The crystallization degree of PRP in the CST-PRP-SAP system was decreased and most of the PRP existed in the form of physical filling, and the available phosphorus content was increased to a certain extent. It was concluded that the CST-PRP-SAP synthesized in this study has excellent properties of continuous water absorption and retention with functions of promotion and the slow-release phosphorus.

2.
Sci Rep ; 6: 21027, 2016 Feb 16.
Artigo em Inglês | MEDLINE | ID: mdl-26878770

RESUMO

A soil remediation method based on magnetic beneficiation is reported. A new magnetic solid chelator powder, FS@IDA (core-shell Fe3O4@SiO2 nanoparticles coated with iminodiacetic acid chelators), was used as a reactive magnetic carrier to selectively capture non-magnetic heavy metals in soil by chelation and removal by magnetic separation. FS@IDA was prepared via inorganic-organic and organic synthesis reactions that generated chelating groups on the surface of magnetic, multi-core, core-shell Fe3O4@SiO2 (FS) nanoparticles. These reactions used a silane coupling agent and sodium chloroacetate. The results show that FS@IDA could chelate the heavy metal component of Cd, Zn, Pb, Cu and Ni carbonates, lead sulfate and lead chloride in water-insoluble salt systems. The resulting FS@IDA-Cd and FS@IDA-Pb chelates could be magnetically separated, resulting in removal rates of approximately 84.9% and 72.2% for Cd and Pb, respectively. FS@IDA could not remove the residual heavy metals and those bound to organic matter in the soil. FS@IDA did not significantly alter the chemical composition of the soil, and it allowed for fast chelating capture, simple magnetic separation and facilitated heavy metal elution. FS@IDA could also be easily prepared and reprocessed.


Assuntos
Quelantes/química , Nanopartículas de Magnetita/química , Metais Pesados/química , Poluentes do Solo/química , Solo/química , Adsorção , Cádmio/química , Cátions , Concentração de Íons de Hidrogênio , Chumbo/química , Solubilidade
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