scholarly journals Novel long-chain aliphatic polyamide/surface-modified silicon dioxide nanocomposites: in-situ polymerization and properties

2021 ◽  
Vol 20 ◽  
pp. 100450
Author(s):  
H. Baniasadi ◽  
J. Seppälä
2006 ◽  
Vol 15 (5) ◽  
pp. 096369350601500 ◽  
Author(s):  
Jingyu Wang ◽  
Guoping Chen ◽  
Quan Zhou

A method to synthesize completely delaminated polymer/lamellar aluminophosphate (Mu-4) nanocomposites has been successfully developed, wherein organo-modification of Mu-4 followed by in situ polymerization was applied. It can be found that the long chain n-dodecylamine molecules can favor the intercalation of Mu-4 and thus readily make the Mu-4 layers delaminated in the polymer matrix compared with the short chain N,N-dimethylpropane-1,3-diamine.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
S. C. Nagaraju ◽  
Aashis S. Roy ◽  
J. B. Prasanna Kumar ◽  
Koppalkar R. Anilkumar ◽  
G. Ramagopal

Polyaniline- (PANI) praseodymium Oxide (Pr2O3) composites have been synthesized by in situ polymerization method with different weight percentages. The synthesized composites have been characterized by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy. The temperature dependent conductivity shows that the conductivity is due to the hopping of polarons and bipolarons. These composites show negative thermal coefficient (α) behavior as a function of temperature, which is characteristic behavior of semiconducting materials. Sensor studies have been carried out by two-probe method and found that the sensitivity increases with increase in % RH. It is noticed that stability increase is due to the presence of Pr2O3in polyaniline up to 30 wt%. A fast recovery and response time along with high sensitivity make these composites suitable for humidity sensors.


Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2252 ◽  
Author(s):  
Nicholas S. Emonson ◽  
Daniel J. Eyckens ◽  
Benjamin J. Allardyce ◽  
Andreas Hendlmeier ◽  
Melissa K. Stanfield ◽  
...  

Silk fibroin is an excellent biopolymer for application in a variety of areas, such as textiles, medicine, composites and as a novel material for additive manufacturing. In this work, silk membranes were surface modified by in situ polymerization of aqueous acrylic acid, initiated by the reduction of various aryldiazonium salts with vitamin C. Treatment times of 20 min gave membranes which possessed increased tensile strength, tensile modulus, and showed significant increased resistance to needle puncture (+131%), relative to ‘untreated’ standards. Most interestingly, the treated silk membranes were able to be reversibly formed into various shapes via the hydration and plasticizing of the surface bound poly(acrylic acid), by simply steaming the modified membranes. These membranes and their unique properties have potential applications in advanced textiles, and as medical materials.


2016 ◽  
Vol 29 (7) ◽  
pp. 797-807 ◽  
Author(s):  
Chunyan Wang ◽  
Jianping Xu ◽  
Junxin Yang ◽  
Yong Qian ◽  
Hesheng Liu

In this study, strong multiwalled carbon nanotube (MWNT)–polyimide (PI) matrix interfaces were designed and constructed to obtain high-performance nanocomposites via in-situ polymerization. MWNTs with reactive amino groups were produced by the covalent linking of phenylenediamine to the surface of MWNTs by amide bonds; this material exhibited excellent dispersibility and compatibility with the PI matrix. The incorporation of amine-functionalized MWNT (MWNT-NH2) significantly improved the macroscopic properties of the PI-based nanocomposites. A 50.5% increase in the tensile strength and an 83.1% increase in the Young’s modulus were achieved by 3.0 wt% MWNT-NH2 loading. Furthermore, the storage modulus, thermal stability, and glass transition temperature of the nanocomposite clearly increased by adding MWNT-NH2. The success of this method provides a good rational for developing high-performance polymer-based nanocomposites.


2005 ◽  
Vol 72 ◽  
pp. 177-188 ◽  
Author(s):  
Félix M. Goñi ◽  
F-Xabier Contreras ◽  
L-Ruth Montes ◽  
Jesús Sot ◽  
Alicia Alonso

In the past decade, the long-neglected ceramides (N-acylsphingosines) have become one of the most attractive lipid molecules in molecular cell biology, because of their involvement in essential structures (stratum corneum) and processes (cell signalling). Most natural ceramides have a long (16-24 C atoms) N-acyl chain, but short N-acyl chain ceramides (two to six C atoms) also exist in Nature, apart from being extensively used in experimentation, because they can be dispersed easily in water. Long-chain ceramides are among the most hydrophobic molecules in Nature, they are totally insoluble in water and they hardly mix with phospholipids in membranes, giving rise to ceramide-enriched domains. In situ enzymic generation, or external addition, of long-chain ceramides in membranes has at least three important effects: (i) the lipid monolayer tendency to adopt a negative curvature, e.g. through a transition to an inverted hexagonal structure, is increased, (ii) bilayer permeability to aqueous solutes is notoriously enhanced, and (iii) transbilayer (flip-flop) lipid motion is promoted. Short-chain ceramides mix much better with phospholipids, promote a positive curvature in lipid monolayers, and their capacities to increase bilayer permeability or transbilayer motion are very low or non-existent.


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