Synthesis of Amino Propionic Acid Modified Polypropylene-Graft-Styrene Fiber

2014 ◽  
Vol 1033-1034 ◽  
pp. 420-423
Author(s):  
Yao Ran Sun ◽  
Shu De Duan ◽  
Rui Xia Guo ◽  
Rui Sheng Hu ◽  
Hai Li Yun

The amino propanoic acid chelating fiber (APACF) was prepared by immobilizing tetraethylenepentamine (TEPA) and propionic acid on polypropylene-graft-styrene (PP-g-ST). The synthetic conditions of amino PP-g-ST fiber and APACF were optimized by the way of L16(45) orthogonal experiment, and the optimizing reaction conditions were obtained. APACF was characterized by FTIR, and the changes of IR spectrum verified the introduction of carboxyl groups to the raw material. The experimental results revealed that the APACF can be used to remove and enrich copper from aqueous solution.

2014 ◽  
Vol 997 ◽  
pp. 169-172 ◽  
Author(s):  
Wei Qing Chen ◽  
Dong Ping Lou

Bamboo shaving is a by-product of bamboo industry, often be discarded or incinerated. In this work, sodium carboxymethyl cellulose (CMC) was prepared from pretreated bamboo shaving as raw material, while the main reaction conditions affecting product properties such as pretreated method, alkalization temperature and time, etherified temperature and time were studied. The results showed that the optimized pretreated conditions for bamboo cellulose were soaked in 15% NaOH at 1:8 (w/v) ratio of cellulose to solvent for 1 h at 95°C, The content of α-cellulose reach to 94.25%. The optimized reaction conditions for CMC synthesis were alkalified at 30°C for 70 min and etherified at 55°C for 90min; afterwards, temperature was kept at 70°C for 10min. Under these conditions, viscosity of 1% CMC aqueous solution was above 260 mPa·s, degree of substitution (DS)≥0.8, and content of chloride and moisture were less than 1.2 % and 10 % respectively.


2011 ◽  
Vol 287-290 ◽  
pp. 2084-2087 ◽  
Author(s):  
Li Wang ◽  
Chun Yan Zhuang ◽  
De Qin Meng

Taking leaching tailings of the nickel ore as raw material, calcium sulfate whiskers were prepared. The effects of Mg/Ca mole ratio, concentration of sulfuric acid, reaction temperature and precipitating time on the recovery of calcium were studied in this paper. The preparation method and reaction conditions of fibrous calcium sulfate whisker have been optimized by an orthogonal experiment, in order to obtain a high grade whisker product which could meet industrial requirements on whiteness and size.


2012 ◽  
Vol 178-181 ◽  
pp. 454-457
Author(s):  
Xiao Qing Niu

In poly ferric sulfate production process with pyrite cinder as the main raw material, the sodium nitrite as catalyst is too toxic to be used largely. By orthogonal experiment and single factor experiments, the best reaction conditions were studied for the sodium nitrite as the catalyst, the amount of catalyst is 0.8%, the reaction temperature is 50°C and the reaction time is 60 minutes. According these conditions, the catalyst (CH-2) was used to promote the oxidation-polymerization reaction. Results showed that the use of this non-sodium nitrite catalyst could not eliminate the product toxicity that would be caused by using sodium nitrite catalyst but also make the toxicity of PFS was eliminated and the performance was better.


2017 ◽  
Author(s):  
Curt Wentrup ◽  
Horst Briehl

Flash vacuum pyrolysis (FVP) of 5-azido-1-aryltetrazoles results in triple N<sub>2</sub> elimination and formation of aryl isocyanides RNC, which rearrange in part to aroylnitriles RCN under the reaction conditions. Similar FVP of 5-azido-1-arenesulfonyltetrazoles generates a compound absorbing in the IR spectrum (77 K) at 2090 cm<sup>-1 </sup>and assigned the structure of arenesulfonyl isocyanide, ArSO<sub>2</sub>NC <b>11</b>. FVP at temperatures above 600 <sup>o</sup>C results in progressively more nitrile ArSO<sub>2</sub>CN <b>12</b>. Compound <b>11</b> also disappears on warming above -80 <sup>o</sup>C


2017 ◽  
Author(s):  
Curt Wentrup ◽  
Horst Briehl

Flash vacuum pyrolysis (FVP) of 5-azido-1-aryltetrazoles results in triple N<sub>2</sub> elimination and formation of aryl isocyanides RNC, which rearrange in part to aroylnitriles RCN under the reaction conditions. Similar FVP of 5-azido-1-arenesulfonyltetrazoles generates a compound absorbing in the IR spectrum (77 K) at 2090 cm<sup>-1 </sup>and assigned the structure of arenesulfonyl isocyanide, ArSO<sub>2</sub>NC <b>11</b>. FVP at temperatures above 600 <sup>o</sup>C results in progressively more nitrile ArSO<sub>2</sub>CN <b>12</b>. Compound <b>11</b> also disappears on warming above -80 <sup>o</sup>C


2020 ◽  
Vol 16 ◽  
Author(s):  
Reda M. El-Shishtawy ◽  
Abdullah M. Asiri ◽  
Nahed S. E. Ahmed

Background: Color effluents generated from the production industry of dyes and pigments and their use in different applications such as textile, paper, leather tanning, and food industries, are high in color and contaminants that damage the aquatic life. It is estimated that about 105 of various commercial dyes and pigments amounted to 7×105 tons are produced annually worldwide. Ultimately, about 10–15% is wasted into the effluents of the textile industry. Chitin is abundant in nature, and it is a linear biopolymer containing acetamido and hydroxyl groups amenable to render it atmospheric by introducing amino and carboxyl groups, hence able to remove different classes of toxic organic dyes from colored effluents. Methods: Chitin was chemically modified to render it amphoteric via the introduction of carboxyl and amino groups. The amphoteric chitin has been fully characterized by FTIR, TGA-DTG, elemental analysis, SEM, and point of zero charge. Adsorption optimization for both anionic and cationic dyes was made by batch adsorption method, and the conditions obtained were used for studying the kinetics and thermodynamics of adsorption. Results: The results of dye removal proved that the adsorbent was proven effective in removing both anionic and cationic dyes (Acid Red 1 and methylene blue (MB)), at their respective optimum pHs (2 for acid and 8 for cationic dye). The equilibrium isotherm at room temperature fitted the Freundlich model for MB, and the maximum adsorption capacity was 98.2 mg/g using 50 mg/l of MB, whereas the equilibrium isotherm fitted the Freundlich and Langmuir model for AR1 and the maximum adsorption capacity was 128.2 mg/g. Kinetic results indicate that the adsorption is a two-step diffusion process for both dyes as indicated by the values of the initial adsorption factor (Ri) and follows the pseudo-second-order kinetics. Also, thermodynamic calculations suggest that the adsorption of AR1 on the amphoteric chitin is an endothermic process from 294 to 303 K. The result indicated that the mechanism of adsorption is chemisorption via an ion-exchange process. Also, recycling of the adsorbent was easy, and its reuse for dye removal was effective. Conclusion: New amphoteric chitin has been successfully synthesized and characterized. This resin material, which contains amino and carboxyl groups, is novel as such chemical modification of chitin hasn’t been reported. The amphoteric chitin has proven effective in decolorizing aqueous solution from anionic and cationic dyes. The adsorption behavior of amphoteric chitin is believed to follow chemical adsorption with an ion-exchange process. The recycling process for few cycles indicated that the loaded adsorbent could be regenerated by simple treatment and retested for removing anionic and cationic dyes without any loss in the adsorbability. Therefore, the study introduces a new and easy approach for the development of amphoteric adsorbent for application in the removal of different dyes from aqueous solutions.


Metals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 259
Author(s):  
Sandra Pavón ◽  
Doreen Kaiser ◽  
Robert Mende ◽  
Martin Bertau

The global market of lithium-ion batteries (LIB) has been growing in recent years, mainly owed to electromobility. The global LIB market is forecasted to amount to $129.3 billion in 2027. Considering the global reserves needed to produce these batteries and their limited lifetime, efficient recycling processes for secondary sources are mandatory. A selective process for Li recycling from LIB black mass is described. Depending on the process parameters Li was recovered almost quantitatively by the COOL-Process making use of the selective leaching properties of supercritical CO2/water. Optimization of this direct carbonization process was carried out by a design of experiments (DOE) using a 33 Box-Behnken design. Optimal reaction conditions were 230 °C, 4 h, and a water:black mass ratio of 90 mL/g, yielding 98.6 ± 0.19 wt.% Li. Almost quantitative yield (99.05 ± 0.64 wt.%), yet at the expense of higher energy consumption, was obtained with 230 °C, 4 h, and a water:black mass ratio of 120 mL/g. Mainly Li and Al were mobilized, which allows for selectively precipitating Li2CO3 in battery grade-quality (>99.8 wt.%) without the need for further refining. Valuable metals, such as Co, Cu, Fe, Ni, and Mn, remained in the solid residue (97.7 wt.%), from where they are recovered by established processes. Housing materials were separated mechanically, thus recycling LIB without residues. This holistic zero waste-approach allows for recovering the critical raw material Li from both primary and secondary sources.


Author(s):  
Laura Wienands ◽  
Franziska Theiß ◽  
James Eills ◽  
Lorenz Rösler ◽  
Stephan Knecht ◽  
...  

AbstractParahydrogen-induced polarization is a hyperpolarization method for enhancing nuclear magnetic resonance signals by chemical reactions/interactions involving the para spin isomer of hydrogen gas. This method has allowed for biomolecules to be hyperpolarized to such a level that they can be used for real time in vivo metabolic imaging. One particularly promising example is fumarate, which can be rapidly and efficiently hyperpolarized at low cost by hydrogenating an acetylene dicarboxylate precursor molecule using parahydrogen. The reaction is relatively slow compared to the timescale on which the hyperpolarization relaxes back to thermal equilibrium, and an undesirable 2nd hydrogenation step can convert the fumarate into succinate. To date, the hydrogenation chemistry has not been thoroughly investigated, so previous work has been inconsistent in the chosen reaction conditions in the search for ever-higher reaction rate and yield. In this work we investigate the solution preparation protocols and the reaction conditions on the rate and yield of fumarate formation. We report conditions to reproducibly yield over 100 mM fumarate on a short timescale, and discuss aspects of the protocol that hinder the formation of fumarate or lead to irreproducible results. We also provide experimental procedures and recommendations for performing reproducible kinetics experiments in which hydrogen gas is repeatedly bubbled into an aqueous solution, overcoming challenges related to the viscosity and surface tension of the water.


2015 ◽  
Vol 1130 ◽  
pp. 685-688
Author(s):  
Rui Yi Fan ◽  
Qing Ping Yi ◽  
Qing Lin Zhang ◽  
Zheng Rong Luo

A biosorbent was prepared by treating the persimmon (Diospyros kaki Thunb.) fallen leaves with sodium hydroxide (NaOH). The NaOH concentration and stirring period for the preparation of the biosorbent were adjusted to optimise the Cd(I) adsorption capacity of the biosorbents. Removal of highly toxic Cadmium metal ions from water system using the optimal biosorbent named ‘NPFL’ was investigated using a mimic industrial column. The result showed that NPFL could remove Cd(II) in large quantities from aqueous solution with coexisting metal ions. The raw material, NPFL and Cd(II) loaded NPFL were characterized by SEM-EDS. The reusability of NPFL was also studied by batch adsorption-desorption test.


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