scholarly journals Hydrogel Functionalized Polyester Fabrics by UV-Induced Photopolymerization

Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1329 ◽  
Author(s):  
Emanuela Lorusso ◽  
Wael Ali ◽  
Marcus Hildebrandt ◽  
Thomas Mayer-Gall ◽  
Jochen S. Gutmann

We address a strategy to graft hydrogels onto polyethylene terephthalate (PET) fabrics using different acrylate-based monomers. The hydrogel-modified fabrics were prepared by a two-step modification. To this end, double functional groups were firstly introduced onto the PET surface via an aminolysis reaction involving allylamine. The final grafted polymer networks were then obtained after UV-induced radical photopolymerization by varying acrylate monomer types in the presence of a cross-linker. After characterization, the resulting hydrogels showed different morphologies and abrasion resistance performances depending on their chemical nature. UV-photopolymerization is a fast and low-cost method to achieve technical fabrics with specific desired properties.


2021 ◽  
pp. 096739112110245
Author(s):  
Amrita Sharma ◽  
PP Pande

It has been observed that acrylate monomers are very difficult to polymerize with the low cost nitroxide catalyst 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO). Therefore, costly acyclic nitroxides such as N-tert-butyl-N-(1-diethylphosphono-2,2-dimethyl)-N-oxyl, (SG1), 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide (TIPNO) and TIPNO derivatives have to be used for the polymerization of the acrylic acid derivatives. There are very few reports on the use of TEMPO-derivatives toward the polymerization of n-butyl acrylate. Generally different reducing agents viz. glucose, ascorbic acid, hydroxyacetone etc. have been used to destroy excess TEMPO during the polymerization reaction. The acrylate polymerizations fail in the presence of TEMPO due to the strong C–O bond formed between the acrylate chain end and nitroxide. To the best of our knowledge, no literature report is available on the use of TEMPO without reducing agent or high temperature initiators, toward the polymerization of n-butyl acrylate. The present study has been carried out with a view to re-examine the application of low cost nitroxide TEMPO, so that it can be utilized towards the polymerization of acrylate monomers (e.g. n-butyl acrylate). We have been able to polymerize n-butyl acrylate using the nitroxide TEMPO as initiator (via a macroinitiator). In this synthesis, a polystyrene macroinitiator was synthesized in the first step from TEMPO, after this TEMPO end-capped styrene macroinitiator (PSt-TEMPO) is used to polymerize n-butyl acrylate monomer. The amount of macroinitiator taken was varied from 0.05% to 50% by weight of n-butyl acrylate monomer. The polymerization was carried out at 120°C by bulk polymerization method. The experimental findings showed a gradual increase in molecular weight of the polymer formed and decrease in the polydispersity index (PDI) with increase in amount of PSt-TEMPO macroinitiator taken. In all experiments conversion was more than 80%. These results indicate that the polymerization takes place through controlled polymerization process. Effect of different solvents on polymerization has also been investigated. In the following experiments TEMPO capped styrene has been used as macroinitiator leading to the successful synthesis of poly n-Butyl acrylate. It has been found that styrene macroinitiator is highly efficient for the nitroxide mediated polymerization, even in very small concentration for the synthesis of poly n-butyl acrylate. High concentration of macroinitiator results in the formation of block copolymers of polystyrene and poly ( n-butyl acrylate) viz. polystyrene-block-poly-( n-butyl acrylate). The use of TEMPO toward controlled polymerization is of much importance, because it is the nitroxide commercially available at the lowest cost.



Sensors ◽  
2021 ◽  
Vol 21 (21) ◽  
pp. 7410
Author(s):  
Ruey-Ching Twu ◽  
Kai-Hsuan Li ◽  
Bo-Lin Lin

A low-cost polyethylene terephthalate fluidic sensor (PET-FS) is demonstrated for the concentration variation measurement on fluidic solutions. The PET-FS consisted of a triangular fluidic container attached with a birefringent PET thin layer. The PET-FS was injected with the test liquid solution that was placed in a common path polarization interferometer by utilizing a heterodyne scheme. The measured phase variation of probe light was used to obtain the information regarding the concentration change in the fluidic liquids. The sensor was experimentally tested using different concentrations of sodium chloride solution showing a sensitivity of 3.52 ×104 deg./refractive index unit (RIU) and a detection resolution of 6.25 × 10−6 RIU. The estimated sensitivity and detection resolutions were 5.62 × 104 (deg./RIU) and 6.94 × 10−6 RIU, respectively, for the hydrochloric acid. The relationship between the measured phase and the concentration is linear with an R-squared value reaching above 0.995.





Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1625 ◽  
Author(s):  
Rijeesh Kizhakidathazhath ◽  
Hiroya Nishikawa ◽  
Yasushi Okumura ◽  
Hiroki Higuchi ◽  
Hirotsugu Kikuchi

The widespread electro–optical applications of polymer dispersed liquid crystals (PDLCs) are hampered by their high-driving voltage. Attempts to fabricate PDLC devices with low driving voltage sacrifice other desirable features of PDLCs. There is thus a clear need to develop a method to reduce the driving voltage without diminishing other revolutionary features of PDLCs. Herein, we report a low-voltage driven PDLC system achieved through an elegantly simple and uniquely designed acrylate monomer (A3DA) featuring a benzene moiety with a dodecyl terminal chain. The PDLC films were fabricated by the photopolymerization of mono- and di-functional acrylate monomers (19.2 wt%) mixed in a nematic liquid crystal E7 (80 wt%). The PDLC film with A3DA exhibited an abrupt decline of driving voltage by 75% (0.55 V/μm) with a high contrast ratio (16.82) while maintaining other electro–optical properties almost the same as the reference cell. The response time was adjusted to satisfactory by tuning the monomer concentration while maintaining the voltage significantly low (3 ms for a voltage of 0.98 V/μm). Confocal laser scanning microscopy confirmed the polyhedral foam texture morphology with an average mesh size of approximately 2.6 μm, which is less in comparison with the mesh size of reference PDLC (3.4 μm), yet the A3DA-PDLC showed low switching voltage. Thus, the promoted electro–optical properties are believed to be originated from the unique polymer networks formed by A3DA and its weak anchoring behavior on LCs. The present system with such a huge reduction in driving voltage and enhanced electro–optical performance opens up an excellent way for abundant perspective applications of PDLCs.



2012 ◽  
Vol 27 (4) ◽  
pp. 639-652 ◽  
Author(s):  
Lihua Zhao ◽  
Zhang-Lin Zhou ◽  
Zengshan Guo ◽  
Gary Gibson ◽  
James A. Brug ◽  
...  

Abstract



2019 ◽  
Vol 2019 ◽  
pp. 1-28 ◽  
Author(s):  
Shem M. Ndirangu ◽  
Yanyan Liu ◽  
Kai Xu ◽  
Shaoxian Song

This paper aims at demonstrating the significance of biochar risk evaluation and reviewing risk evaluation from the aspects of pyrolysis process, feedstock, and sources of hazards in biochar and their potential effects and the methods used in risk evaluation. Feedstock properties and the resultant biochar produced at different pyrolysis process influence their chemical, physical, and structural properties, which are vital in understanding the functionality of biochar. Biochar use has been linked to some risks in soil application such as biochar being toxic, facilitating GHGs emission, suppression of the effectiveness of pesticides, and effects on soil microbes. These potential risks originate from feedstock, contaminated feedstock, and pyrolysis conditions that favor the creation of characteristics and functional groups of this nature. These toxic compounds formed pose a threat to human health through the food chain. Determination of toxicity levels is a first step in the risk management of toxic biochar. Various sorption methods of biochar utilized low-cost adsorbents, engineered surface functional groups, and nZVI modified biochars. The mechanisms of organic compound removal was through sorption, enhanced sorption, modified biochar, postpyrolysis thermal air oxidation and that of PFRs degradation was through activation, photoactive functional groups, magnetization, and hydrothermal synthesis. Emissions of GHGs in soils amended with biochar emanated through physical and biotic mediated mechanisms. BCNs have a significance in reducing the health quotient indices for PTEs risk contamination by suppressing cancer risk arising from consumption of contaminated food. The degree of environmental risk assessment of HM pollution in biomass and biochars has been determined by using potential ecological risk index and RAC while organic contaminant degradation by EPFRs was considered when assessing the environmental roles of biochar in regulating the fate of contaminants removal. The magnitude of technologies’ net benefit must be considered in relation to the associated risks.



2011 ◽  
Author(s):  
Kapil Pandey ◽  
Rahul Bharadwaj ◽  
Swapna Sethi
Keyword(s):  


RSC Advances ◽  
2016 ◽  
Vol 6 (40) ◽  
pp. 33971-33982 ◽  
Author(s):  
F. Karasu ◽  
C. Rocco ◽  
Y. Zhang ◽  
C. Croutxé-Barghorn ◽  
X. Allonas ◽  
...  

LED-cured IPN-based coatings bearing hydrophobic functional groups have been developed in order to obtain hydrophobic self-replenishing surfaces with improved mechanical properties.



2017 ◽  
Vol 23 (12) ◽  
pp. 5653-5668 ◽  
Author(s):  
Jiajing Zhu ◽  
Yanling Tian ◽  
Chengjuan Yang ◽  
Liangyu Cui ◽  
Fujun Wang ◽  
...  


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