Functional Poly(p-Xylylene)s via Chemical Reduction of Poly(p-Phenylene Vinylene)s

2019 ◽  
Author(s):  
Ain Uddin ◽  
Weifan Sang ◽  
Yong Gao ◽  
Kyle Plunkett
Keyword(s):  
Film Formation ◽  
Chemical Reduction ◽  
Water Soluble ◽  
Phenylene Vinylene ◽  
Polymer Modification ◽  
Polymer Backbone ◽  
Crosslinking Process ◽  
Conducting Membranes ◽  
In Situ Crosslinking

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.

Functional Poly(p-Xylylene)s via Chemical Reduction of Poly(p-Phenylene Vinylene)s

2019 ◽  
Author(s):  
Ain Uddin ◽  
Weifan Sang ◽  
Yong Gao ◽  
Kyle Plunkett
Keyword(s):  
Film Formation ◽  
Chemical Reduction ◽  
Water Soluble ◽  
Phenylene Vinylene ◽  
Polymer Modification ◽  
Polymer Backbone ◽  
Crosslinking Process ◽  
Conducting Membranes ◽  
In Situ Crosslinking

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.

scholarly journals The convenient preparation of stable aryl-coated zerovalent iron nanoparticles

2015 ◽  
Vol 6 ◽  
pp. 1192-1198 ◽  
Author(s):  
Olga A Guselnikova ◽  
Andrey I Galanov ◽  
Anton K Gutakovskii ◽  
Pavel S Postnikov
Keyword(s):  
Iron Nanoparticles ◽  
Diazonium Salt ◽  
Chemical Reduction ◽  
Water Soluble ◽  
Zerovalent Iron ◽  
Iron Core ◽  
Organic Layer ◽  
Aryl Group ◽  
Surface Modified

A novel approach for the in situ synthesis of zerovalent aryl-coated iron nanoparticles (NPs) based on diazonium salt chemistry is proposed. Surface-modified zerovalent iron NPs (ZVI NPs) were prepared by simple chemical reduction of iron(III) chloride aqueous solution followed by in situ modification using water soluble arenediazonium tosylate. The resulting NPs, with average iron core diameter of 21 nm, were coated with a 10 nm thick organic layer to provide long-term protection in air for the highly reactive zerovalent iron core up to 180 °C. The surface-modified iron NPs possess a high grafting density of the aryl group on the NPs surface of 1.23 mmol/g. FTIR spectroscopy, XRD, HRTEM, TGA/DTA, and elemental analysis were performed in order to characterize the resulting material.

Induced Synthesis of Hydroxyapatite by Chitosan for Enamel Remineralization

2012 ◽  
Vol 530 ◽  
pp. 40-45 ◽  
Author(s):  
Kun Tian ◽  
Min Peng ◽  
Wei Fei ◽  
Chu Hang Liao ◽  
Xiao Hua Ren
Keyword(s):  
Calcium Fluoride ◽  
Dentinal Tubule ◽  
Dental Tissue ◽  
Crosslinking Process ◽  
Parallel Direction ◽  
Biomimetic Method ◽  
Dental Tissue Engineering ◽  
In Situ Crosslinking

The formation of organized nanocrystals that resemble tooth-like hydroxyapatite is crucial for successful enamel remineralization. Based on the principles of biomineralization , spindle - shaped hydroxyapatites (HA) were synthesized through biomimetic method with chitosan as template under a controllable way in vitro. We observed that hydroxyapatite nanorods can be controlled followed by in situ crosslinking process and triggered by conditions of pH and ionic strength. The dentinal tubule were blocked by neonatal hydroxyapatite layer and this composite a continuous structure of columns crystal with size of 10-40nm. At the same time, XRD showed that the precipitation was calcium fluoride phosphate and Ca:P was 1.6. Furthermore, there were column crystal with parallel direction inside, as same as the crystal array in the top of enamel rod. The results suggest that chitosan monolayer may be useful in the modulation of mineral behavior during in situ dental tissue engineering.

scholarly journals A thin, deformable, high-performance supercapacitor implant that can be biodegraded and bioabsorbed within an animal body

2021 ◽  
Vol 7 (2) ◽  
pp. eabe3097
Author(s):  
Hongwei Sheng ◽  
Jingjing Zhou ◽  
Bo Li ◽  
Yuhang He ◽  
Xuetao Zhang ◽  
...  
Keyword(s):  
High Performance ◽  
Electronic Devices ◽  
Form Factors ◽  
Time Frame ◽  
Water Soluble ◽  
Two Dimensional ◽  
Medical Electronics ◽  
Thin Structure ◽  
Shed Light

It has been an outstanding challenge to achieve implantable energy modules that are mechanically soft (compatible with soft organs and tissues), have compact form factors, and are biodegradable (present for a desired time frame to power biodegradable, implantable medical electronics). Here, we present a fully biodegradable and bioabsorbable high-performance supercapacitor implant, which is lightweight and has a thin structure, mechanical flexibility, tunable degradation duration, and biocompatibility. The supercapacitor with a high areal capacitance (112.5 mF cm−2 at 1 mA cm−2) and energy density (15.64 μWh cm−2) uses two-dimensional, amorphous molybdenum oxide (MoOx) flakes as electrodes, which are grown in situ on water-soluble Mo foil using a green electrochemical strategy. Biodegradation behaviors and biocompatibility of the associated materials and the supercapacitor implant are systematically studied. Demonstrations of a supercapacitor implant that powers several electronic devices and that is completely degraded after implantation and absorbed in rat body shed light on its potential uses.

Synthesis and short DNA in situ loading and delivery of 4 nm-aperture flexible organic frameworks

2021 ◽  
Author(s):  
Ze-Kun Wang ◽  
Jia-Le Lin ◽  
Yun-Chang Zhang ◽  
Chen-Wu Yang ◽  
Ya-Kun Zhao ◽  
...  
Keyword(s):  
Cancer Cells ◽  
Water Soluble

Water-soluble hydrazone-connected 3D flexible organic frameworks have been revealed to in situ load and deliver short DNA into normal and cancer cells.

Chemically reduced graphene oxide-coated knitted fabric imparted conductivity and outstanding hydrophobicity

2021 ◽  
pp. 004051752199547
Author(s):  
Min Hou ◽  
Xinghua Hong ◽  
Yanjun Tang ◽  
Zimin Jin ◽  
Chengyan Zhu ◽  
...  
Keyword(s):  
Electrical Conductivity ◽  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Chemical Reduction ◽  
Knitted Fabric ◽  
Mesh Structure ◽  
Reduced Graphene ◽  
Chemically Reduced Graphene Oxide ◽  
Modified Hummers Method

Functionalized knitted fabric, as a kind of flexible, wearable, and waterproof material capable of conductivity, sensitivity and outstanding hydrophobicity, is valuable for multi-field applications. Herein, the reduced graphene oxide (RGO)-coated knitted fabric (polyester/spandex blended) is prepared, which involves the use of graphite oxide (GO) by modified Hummers method and in-situ chemical reduction with hydrazine hydrate. The treated fabric exhibits a high electrical conductivity (202.09 S/cm) and an outstanding hydrophobicity (140°). The outstanding hydrophobicity is associated with the morphology of the fabric and fiber with reference to pseudo-infiltration. These properties can withstand repeated bending and washing without serious deterioration, maintaining good electrical conductivity (35.70 S/cm) and contact angle (119.39°) after eight standard washing cycles. The material, which has RGO architecture and continuous loop mesh structure, can find wide use in smart garment applications.

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