Meso-Architecture Block Copolymers with High Surface Area Styrene-Bridged Organosilica Particles as Constituent for the Stimuli-Responsive Remediation of Water

Author(s):  
Dennis Kollofrath ◽  
Marcel Geppert ◽  
Sebastian Polarz

The development of drugs for birth-control has changed society, and they are used by billions of woman on an every day basis. As for every mass product, there are problems associated with the waste it causes. One has found that residues of hormones in the urine of woman cannot be removed sufficiently from waste-water and this, in-turn, has already observable and undesired consequences in the biosphere. Apart from the removal of drugs, one is in general seeking new methods for the removal of hydrophobic impurities from waste-water. An ideal system would quantitatively take up the impurity, entrap it followed by preferably simple separation. Finally, one wants to reuse the absorbent, which implies the possibility for regeneration and recycling. Such as complex set of tasks requires a relatively complex materials architecture. Functional organic polymers with high affinity towards the drug, with stable open porosity and high surface area, stimuli-responsive properties and in the form of colloidal dispersions could do the job. Unfortunately, such a system does not exist. We solved this problem by generating mesoporous organosilica nanoparticles, which are monomers at the same time. Initiation of the polymerization reaction by surface-bound pore-walls leads to the formation of a special type of block-copolymer. The pore-walls are covered by the polymer, which cannot leach. An orthogonal modification was achieved by modification of the external surfaces of the particles with a thermoresponsive polymer by click-chemistry. The final core-shell system was able to remove hydrophobic molecules such as the hormone progesterone from water. A change of temperature induces the collapse of the thermoresponsive polymer, which closes the pores and induces aggregation of the particles. After separation of the particles, and thus also the entrapped impurity, from the solvent, one can re-open the pores, which leads to a release of the adsorbed compound(s).

2020 ◽  
Author(s):  
Dennis Kollofrath ◽  
Marcel Geppert ◽  
Sebastian Polarz

The development of drugs for birth-control has changed society, and they are used by billions of woman on an every day basis. As for every mass product, there are problems associated with the waste it causes. One has found that residues of hormones in the urine of woman cannot be removed sufficiently from waste-water and this, in-turn, has already observable and undesired consequences in the biosphere. Apart from the removal of drugs, one is in general seeking new methods for the removal of hydrophobic impurities from waste-water. An ideal system would quantitatively take up the impurity, entrap it followed by preferably simple separation. Finally, one wants to reuse the absorbent, which implies the possibility for regeneration and recycling. Such as complex set of tasks requires a relatively complex materials architecture. Functional organic polymers with high affinity towards the drug, with stable open porosity and high surface area, stimuli-responsive properties and in the form of colloidal dispersions could do the job. Unfortunately, such a system does not exist. We solved this problem by generating mesoporous organosilica nanoparticles, which are monomers at the same time. Initiation of the polymerization reaction by surface-bound pore-walls leads to the formation of a special type of block-copolymer. The pore-walls are covered by the polymer, which cannot leach. An orthogonal modification was achieved by modification of the external surfaces of the particles with a thermoresponsive polymer by click-chemistry. The final core-shell system was able to remove hydrophobic molecules such as the hormone progesterone from water. A change of temperature induces the collapse of the thermoresponsive polymer, which closes the pores and induces aggregation of the particles. After separation of the particles, and thus also the entrapped impurity, from the solvent, one can re-open the pores, which leads to a release of the adsorbed compound(s).


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Garima Rathee ◽  
Amardeep Awasthi ◽  
Damini Sood ◽  
Ravi Tomar ◽  
Vartika Tomar ◽  
...  

Abstract It would be of great significance to introduce a new biocompatible Layered Double Hydroxide (LDH) for the efficient remediation of wastewater. Herein, we designed a facile, biocompatible and environmental friendly layered double hydroxide (LDH) of NiFeTi for the very first time by the hydrothermal route. The materialization of NiFeTi LDH was confirmed by FTIR, XRD and Raman studies. BET results revealed the high surface area (106 m2/g) and the morphological studies (FESEM and TEM) portrayed the sheets-like structure of NiFeTi nanoparticles. The material so obtained was employed as an efficient adsorbent for the removal of organic dyes from synthetic waste water. The dye removal study showed >96% efficiency for the removal of methyl orange, congo red, methyl blue and orange G, which revealed the superiority of material for decontamination of waste water. The maximum removal (90%) of dyes was attained within 2 min of initiation of the adsorption process which supported the ultrafast removal efficiency. This ultrafast removal efficiency was attributed to high surface area and large concentration of -OH and CO32− groups present in NiFeTi LDH. In addition, the reusability was also performed up to three cycles with 96, 90 and 88% efficiency for methyl orange. Furthermore, the biocompatibility test on MHS cell lines were also carried which revealed the non-toxic nature of NiFeTi LDH at lower concentration (100% cell viability at 15.6 μg/ml). Overall, we offer a facile surfactant free method for the synthesis of NiFeTi LDH which is efficient for decontamination of anionic dyes from water and also non-toxic.


1998 ◽  
Vol 549 ◽  
Author(s):  
H. Koike ◽  
Y. Oki ◽  
Y. Takeuchi

AbstractContinuous titania fibers were prepared by a polytitanoxane precursor method. Polytitanoxane was synthesized through hydrolysis and polymerization reaction between partially chelated titanium isopropoxide and water without acid catalyst. Polytitanoxane, which was precipitated from an isopropanol solution by adding adequate amount of water to titanium isopropoxide, was then dried and dissolved in tetrahydrofuran. The concentrated viscous solution of polytitanoxane was considerably stable to further self-condensation and had good spinnability. The precursor fiber which was obtained by spinning the solution was calcined to form titania fibers.Two types of titania fibers were obtained under different calcination conditions from the same precursor fiber; Dense fiber with high tensile strength of higher than 1 GPa, and porous fiber with high surface area of more than 10 m2/g.Photocatalytic activity of those fibers was studied using the phenol mineralization reaction in water. The phenol degradation ability of high-surface-area titania fiber was almost the same as that of commercial titania powder for photocatalyst.


2021 ◽  
Author(s):  
Ehsan Valiey ◽  
Mohammad G. Dekamin

In this work, novel pyromellitic diamide-diacid bridged mesoporous organosilica (PMAMOS) nanospheres with controllable morphologies and active catalytic centers were designed and prepared with high surface area and uniform pore size...


2018 ◽  
Vol 6 (44) ◽  
pp. 21901-21905 ◽  
Author(s):  
S. Grätz ◽  
M. Oltermann ◽  
E. Troschke ◽  
S. Paasch ◽  
S. Krause ◽  
...  

An oxidative polymerization reaction was brought into the solvent-free environment of a ball mill, yielding a porous polymer with a defined structure and high surface area.


Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith

<p>This study evaluated the performance of the commonly used strong buffer electrolytes, i.e. phosphate buffers, during CO<sub>2</sub> electroreduction in neutral pH conditions by using in-situ surface enhanced infrared absorption spectroscopy (SEIRAS). Unfortunately, the buffers break down a lot faster than anticipated which has serious implications on many studies in the literature such as selectivity and kinetic analysis of the electrocatalysts. Increasing electrolyte concentration, surprisingly, did not extend the potential window of the phosphate buffers due to dramatic increase in hydrogen evolution reaction. Even high concentration phosphate buffers (1 M) break down within the potentials (-1 V vs RHE) where hydrocarbons are formed on copper electrodes. We have extended the discussion to high surface area electrodes by evaluating electrodes composed of copper nanowires. We would like highlight that it is not possible to cope with high local current densities on these high surface area electrodes by using high buffer capacity solutions and the CO<sub>2</sub> electrocatalysts are needed to be evaluated by casting thin nanoparticle films onto inert substrates as commonly employed in fuel cell reactions and up to now scarcely employed in CO<sub>2</sub> electroreduction. In addition, we underscore that normalization of the electrocatalytic activity to the electrochemical active surface area is not the ultimate solution due to concentration gradient along the catalyst layer.This will “underestimate” the activity of high surface electrocatalyst and the degree of underestimation will depend on the thickness, porosity and morphology of the catalyst layer. </p> <p> </p>


Nanoscale ◽  
2015 ◽  
Vol 7 (25) ◽  
pp. 10974-10981 ◽  
Author(s):  
Xiulin Yang ◽  
Ang-Yu Lu ◽  
Yihan Zhu ◽  
Shixiong Min ◽  
Mohamed Nejib Hedhili ◽  
...  

High surface area FeP nanosheets on a carbon cloth were prepared by gas phase phosphidation of electroplated FeOOH, which exhibit exceptionally high catalytic efficiency and stability for hydrogen generation.


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