Biodegradation of Cyanide Complex Compounds in Aqueous Media by Pseudomonas resinovorans

2013 ◽  
Vol 30 (12) ◽  
pp. 757-764 ◽  
Author(s):  
Abdoul-Raimi Bouari ◽  
Shamim Ara Begum ◽  
Ynoussa Maiga ◽  
Nosa O. Egiebor
Keyword(s):  
Aqueous Media ◽  
Complex Compounds ◽  
Cyanide Complex ◽  
Pseudomonas Resinovorans

scholarly journals Removability Efficiency of Heavy Metals with Modified Humate from Aqueous Media

2014 ◽  
Vol 16 (4) ◽  
Author(s):  
A.S. Taubayeva ◽  
U.Z. Dzhusipbekov ◽  
G.О. Nurgalieva ◽  
A.K. Shakirova ◽  
H. Temel ◽  
...  
Keyword(s):  
Metal Ions ◽  
Sorption Capacity ◽  
Humic Acids ◽  
Aqueous Media ◽  
Toxic Metal ◽  
High Reactivity ◽  
Complex Compounds ◽  
Sorption Ability ◽  
Maximum Sorption ◽  
High Sorption

<p>The main aim of this work was to study the possibility of using amine-modified humate as a sorbent for the purification of water from heavy metal ions (Cu&amp;Co). One of the effective methods of creating new sorbents of humic acids is chemical modification based on the high reactivity of the functional groups in the composition of humic acids. The possibility of modification of humic acid with bis(3-aminopropyl)  amine was illustrated. Modification was carried out with the aim of increasing its sorption capacity. Metal-humate complexes were also obtained by an ion-exchange procedure with modified humate (Mod-Hum) by employing metal salts such as Cu(CH<sub>3</sub>COO)<sub>2</sub>·H<sub>2</sub>O, Co(CH<sub>3</sub>COO)<sub>2</sub>·4H<sub>2</sub>O. Maximum sorption percentages of Mod-Hum achieved were about 99.2% for Cu (II) and 90% for Co (II). The sorption degree depending on pH changes was studied in the range of 2 to 8, the sorption ability of the sorbents was stated to increase with the increase in pH. The degree of sorption of copper (ІІ) on Mod-Hum in the studied range of рН 5 was higher and of cobalt (II) for which the sorption is optimal at higher values (рН 7-8). It is stated that sorption degree increases with the increase in time from 15 min to 2 h. The adsorption of toxic metal ions with Mod-Hum was measured by atomic absorption spectroscopy (AAS). The experimental results on determination of the adsorption isotherm were evaluated with the Langmuir equation. It is shown that the sorbent develops a high sorption capacity in regard to ions of Cu (18.42 mg/g) and Со (16.25 mg/g). All the obtained complex compounds were analyzed and characterized by FT infrared spectroscopy (FTIR), scanning electron microscopy (SEM).</p>

Highly efficient and selective photocatalytic CO2 to CO conversion in aqueous solution

2020 ◽  
Vol 56 (27) ◽  
pp. 3851-3854 ◽  
Author(s):  
Xiaomin Chai ◽  
Hai-Hua Huang ◽  
Huiping Liu ◽  
Zhuofeng Ke ◽  
Wen-Wen Yong ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Performance ◽  
Aqueous Media ◽  
Highly Efficient ◽  
Co Conversion

A Co-based complex displayed the highest photocatalytic performance for CO2 to CO conversion in aqueous media.

Detection of a covalent-ionic carbinolamine intermediate in aqueous media by SDTLC on silica gel plates

2007 ◽  
Vol 20 (3) ◽  
pp. 227-230 ◽  
Author(s):  
Ana Reverdito ◽  
Mariano García ◽  
Alejandra Salerno ◽  
Oscar Locani ◽  
Isabel Perillo
Keyword(s):  
Silica Gel ◽  
Aqueous Media

Temperature Dependence of the Self-Assembled Styrene Based Random Ionomers in Aqueous Solution

2003 ◽  
Vol 775 ◽  
Author(s):  
Sung-Hwa Oh ◽  
Ju-Myung Song ◽  
Joon-Seop Kim ◽  
Hyang-Rim Oh ◽  
Jeong-A Yu
Keyword(s):  
Partition Coefficients ◽  
Room Temperature ◽  
Aqueous Media ◽  
The Self ◽  
Spectroscopic Methods ◽  
Ion Content ◽  
Repeat Units ◽  
Notable Effect ◽  
Order Of Magnitude ◽  
Experimental Errors

AbstractSolution behaviors of poly(styrene-co-sodium methacrylate) were studied by fluorescence spectroscopic methods using pyrene as a probe. The mol% of methacrylate was in the range 3.6–9.4. Water and N,N-dimethylforamide(DMF) mixture was used as a solvent (DMF/water = 0.2 mol %). The critical micelle (or aggregation) concentrations of ionomers and the partition coefficients of pyrene were obtained the temperature range 10–80°C. At room temperature, the values of CMCs (or CACs) were in the range 4.7 ×10-6 5.3 ×10-6 g/mL and we could not find any notable effect of the content of ionic repeat units within the experimental errors. Unlike CMCs, as the ion content increased, partitioning of pyrene between the hydrophobic aggregates and an aqueous media decreased from 1.5 ×105 to 9.4 ×104. As the temperature increased from 10 to 80 °C, the values of CMCs increased less than one order of magnitude. While, the partition coefficients of pyrene decreased one order of magnitude and the effect of the ion content became negligible.

Host-Guest Interactions on Electrode Surfaces for Immobilization of Molecular Catalysts

2020 ◽  
Author(s):  
Laurent Sévery ◽  
Jacek Szczerbiński ◽  
Mert Taskin ◽  
Isik Tuncay ◽  
Fernanda Brandalise Nunes ◽  
...  
Keyword(s):  
Aqueous Media ◽  
Heterogeneous Systems ◽  
Catalytic Systems ◽  
New Approach ◽  
Molecular Systems ◽  
Electrode Surfaces ◽  
Catalytic Surfaces ◽  
Oxide Electrodes ◽  
The Stability ◽  
Molecular Catalysts

The strategy of anchoring molecular catalysts on electrode surfaces combines the high selectivity and activity of molecular systems with the practicality of heterogeneous systems. The stability of molecular catalysts is, however, far less than that of traditional heterogeneous electrocatalysts, and therefore a method to easily replace anchored molecular catalysts that have degraded could make such electrosynthetic systems more attractive. Here, we apply a non-covalent “click” chemistry approach to reversibly bind molecular electrocatalysts to electrode surfaces via host-guest complexation with surface-anchored cyclodextrins. The host-guest interaction is remarkably strong and allows the flow of electrons between the electrode and the guest catalyst. Electrosynthesis in both organic and aqueous media was demonstrated on metal oxide electrodes, with stability on the order of hours. The catalytic surfaces can be recycled by controlled release of the guest from the host cavities and readsorption of fresh guest. This strategy represents a new approach to practical molecular-based catalytic systems.

Self-Recognizing π-π Stacking Interactions Designed for the Generation of Ultrastable Mesoporous Hydrogen-Bonded Organic Frameworks

2019 ◽  
Author(s):  
KAIKAI MA ◽  
Peng Li ◽  
John Xin ◽  
Yongwei Chen ◽  
Zhijie Chen ◽  
...  
Keyword(s):  
Pore Size ◽  
Fiber Composite ◽  
Aqueous Media ◽  
Stacking Interactions ◽  
Mustard Gas ◽  
X Ray Diffraction ◽  
X Ray ◽  
Expansion Strategy ◽  
Π Stacking ◽  
Hydrogen Bonded

Creating crystalline porous materials with large pores is typically challenging due to undesired interpen-etration, staggered stacking, or weakened framework stability. Here, we report a pore size expansion strategy by self-recognizing π-π stacking interactions in a series of two-dimensional (2D) hydrogen–bonded organic frameworks (HOFs), HOF-10x (x=0,1,2), self-assembled from pyrene-based tectons with systematic elongation of π-conjugated molecular arms. This strategy successfully avoids interpene-tration or staggered stacking and expands the pore size of HOF materials to access mesoporous HOF-102, which features a surface area of ~ 2,500 m2/g and the largest pore volume (1.3 cm3/g) to date among all reported HOFs. More importantly, HOF-102 shows significantly enhanced thermal and chemical stability as evidenced by powder x-ray diffraction and N2 isotherms after treatments in chal-lenging conditions. Such stability enables the adsorption of dyes and cytochrome c from aqueous media by HOF-102 and affords a processible HOF-102/fiber composite for the efficient photochemical detox-ification of a mustard gas simulant.

Sign in / Sign up

Export Citation Format

Share Document