scholarly journals Evaluation of adsorption and desorption of chafing dish odor on woolen fabric

Author(s):  
Mi Li ◽  
Shaofeng Yuan ◽  
Qili Zhong ◽  
Yahui Guo ◽  
Yuliang Cheng ◽  
...  
2011 ◽  
Vol 37 (1) ◽  
pp. 103-106
Author(s):  
Jian-xin LUO ◽  
Wei GUO ◽  
Hui YAN ◽  
Qiong YANG ◽  
Xin-liang DONG ◽  
...  

1986 ◽  
Vol 176 (1-2) ◽  
pp. 134-156 ◽  
Author(s):  
E.G. Seebauer ◽  
A.C.F. Kong ◽  
L.D. Schmidt

2019 ◽  
Vol 74 ◽  
pp. 199-207 ◽  
Author(s):  
Ji Hye Park ◽  
Ra Hyun Hwang ◽  
Hyung Chul Yoon ◽  
Kwang Bok Yi

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4686
Author(s):  
Jerzy Podobiński ◽  
Mariusz Gackowski ◽  
Grzegorz Mordarski ◽  
Katarzyna Samson ◽  
Michał Śliwa ◽  
...  

The properties of both Cu2+ and Cu+ ions in zeolite CuY were followed with NO and CO as probe molecules. Cu2+ was found to be located in SII, SII*, and SIII sites, whereas Cu+ was found in SII and SII* sites. The fine analysis of the spectra of Cu2+-NO and Cu+-CO adducts suggests that both in SII and in SII* sites two kinds of Cu cations exist. They differ in the positive charge, which may be related to the varying numbers of AlO4− in close proximity. The experiments of NO and CO adsorption and desorption evidenced that both Cu2+ and Cu+ sites of highest positive charge bind probe molecules most strongly but activate them to a lesser extent than the Cu sites of lowest positive charge. The experiments of reduction with hydrogen evidenced that the Cu ions of higher positive charge are first reduced by hydrogen. On the other hand, Cu sites of the lowest positive charge are first oxidized by oxygen. The experiments with CuNaY zeolites of various Cu contents suggest that the first introduced Cu (at low Cu contents) created Cu+, which was the most neutralized by framework oxygens. Such Cu cations are the most stabilized by framework oxygens.


2019 ◽  
Vol 9 (22) ◽  
pp. 4805 ◽  
Author(s):  
Shuang Zhang ◽  
Naoki Kano ◽  
Kenji Mishima ◽  
Hirokazu Okawa

In order to obtain the adsorption mechanism and adsorption structures of Rare Earth Elements (REEs) ions adsorbed onto layered double hydroxides (LDH), the adsorption performance of LDH and ethylenediaminetetraacetic acid (EDTA) intercalated LDH for REEs was investigated by batch experiments and regeneration studies. In addition to adsorption capacity, the partition coefficient (PC) was also evaluated to assess their true performance metrics. The adsorption capacity of LDH increases from 24.9 μg·g−1 to 145 μg·g−1 for Eu, and from 20.8 μg·g−1 to 124 μg·g−1 for La by intercalating EDTA in this work; and PC increases from 45.5 μg·g−1·uM−1 to 834 μg·g−1·uM−1 for Eu, and from 33.6 μg·g−1·μM−1 to 405 μg·g−1·μM−1 for La. Comparison of the data indicates that the adsorption affinity of EDTA-intercalated LDH is better than that of precursor LDH no matter whether the concept of adsorption capacity or that of the PC was used. The prepared adsorbent was characterized by XRD, SEM-EDS and FT-IR techniques. Moreover, quantum chemistry calculations were also performed using the GAUSSIAN09 program package. In this calculation, the molecular locally stable state structures were optimized by density functional theory (DFT). Both the quantum chemistry calculations and the experimental data showed that REEs ions adsorbed by EDTA-intercalated LDH are more stable than those adsorbed by precursor LDH. Furthermore, the calculation results of adsorption and desorption rates show that adsorption rates are larger for Eu(III) than for La(III), which agrees with the experimental result that Eu(III) has a higher adsorption ability under the same conditions. The LDHs synthesized in this work have a high affinity for removing REEs ions.


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