FIELD APPLICATION OF A REAGENT FOR IN SITU CHEMICAL REDUCTION AND ENHANCED REDUCTIVE DICHLORINATION TREATMENT OF AN AQUIFER CONTAMINATED WITH TETRACHLOROETHYLENE (PCE), TRICHLOROETHYLENE, 1,1-DICHLOROETHYLENE, DICHLOROPROPANE AND 1,1,2,2-TETRACHLOROETHANE (R-130)

2020 ◽  
Vol 19 (10) ◽  
pp. 1791-1796
Author(s):  
Alberto Leombruni ◽  
Michael Mueller ◽  
Alan Seech ◽  
Daniel Leigh
Keyword(s):  
Chemical Reduction ◽  
Field Application

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.

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.

scholarly journals Live-Scale Testing of Granular Materials Stabilized with Alkali-Activated Waste Glass and Carbide Lime

2021 ◽  
Vol 11 (23) ◽  
pp. 11286
Author(s):  
Marina Paula Secco ◽  
Débora Thaís Mesavilla ◽  
Márcio Felipe Floss ◽  
Nilo Cesar Consoli ◽  
Tiago Miranda ◽  
...  
Keyword(s):  
Portland Cement ◽  
Mechanical Performance ◽  
Raw Materials ◽  
Sodium Hydroxide Solution ◽  
Fine Sand ◽  
Field Application ◽  
Natural Soil ◽  
In Situ Tests ◽  
Alkali Activated

The increasingly strong search for alternative materials to Portland cement has resulted in the development of alkali-activated cements (AAC) that are very effective at using industrial by-products as raw materials, which also contributes to the volume reduction in landfilled waste. Several studies targeting the development of AAC—based on wastes containing silicon and calcium—for chemical stabilization of soils have demonstrated their excellent performance in terms of durability and mechanical performance. However, most of these studies are confined to a laboratory characterization, ignoring the influence and viability of the in situ construction process and, also important, of the in situ curing conditions. The present work investigated the field application of an AAC based on carbide lime and glass wastes to stabilize fine sand acting as a superficial foundation. The assessment was supported on the unconfined compressive strength (UCS) and initial shear modulus (G0) of the developed material, and the field results were compared with those prepared in the laboratory, up to 120 days curing. In situ tests were also developed on the field layers (with diameters of 450 and 900 mm and thickness of 300 mm) after different curing times. To establish a reference, the mentioned precursors were either activated with a sodium hydroxide solution or hydrated with water (given the reactivity of the lime). The results showed that the AAC-based mixtures developed greater strength and stiffness at a faster rate than the water-based mixtures. Specimens cured under controlled laboratory conditions showed better results than the samples collected in the field. The inclusion of the stabilized layers clearly increased the load-bearing capacity of the natural soil, while the different diameters produced different failure mechanisms, similar to those found in Portland cement stabilization.

scholarly journals Exploring the Utility of Compound-Specific Isotope Analysis for Assessing Ferrous Iron-Mediated Reduction of RDX in the Subsurface

2020 ◽  
Author(s):  
Yiran Tong ◽  
Matthew J. Berens ◽  
Bridget A. Ulrich ◽  
Jakov Bolotin ◽  
Jennifer H. Strehlau ◽  
...  
Keyword(s):  
Groundwater Contamination ◽  
Ferrous Iron ◽  
Chemical Reduction ◽  
Isotope Analysis ◽  
Enrichment Factors ◽  
Isotope Enrichment ◽  
Compound Specific Isotope Analysis ◽  
A Site ◽  
Mediated Reduction

This work determines isotope enrichment factors for RDX during reduction by iron minerals. The values determined are used to assess the transformation of RDX at a site with groundwater contamination and in laboratory column reactors simulating in situ chemical reduction treatment.

Optimizing Preloading Pressure of Precharged Gas for Isobaric Gas-Tight Hydrothermal Samplers

2018 ◽  
Vol 140 (2) ◽  
Author(s):  
Haocai Huang ◽  
Liang Huang ◽  
Wei Ye ◽  
Shijun Wu ◽  
Canjun Yang ◽  
...  
Keyword(s):  
Volume Change ◽  
Theoretical Models ◽  
Sample Volume ◽  
Field Application ◽  
Laboratory Simulation ◽  
Application Process ◽  
Sampling Depth ◽  
Ambient Temperatures ◽  
Gas Tight

Isobaric gas-tight hydrothermal samplers, with the ability to maintain pressure, can be used to keep in situ chemical and biological sample properties stable. The preloading pressure of the precharged gas is a major concern for isobaric gas-tight hydrothermal samplers, especially when the samplers are used at different sampling depths, where the in situ pressures and ambient temperatures vary greatly. The most commonly adopted solution is to set the preloading pressure for gas-tight samplers as 10% of the hydrostatic pressure at the sampling depth, which might emphasize too much on pressure retention; thereby, the sample volume may be unnecessarily reduced. The pressure transition of the precharged gas was analyzed theoretically and modeled at each sampling stage of the entire field application process. Additionally, theoretical models were built to represent the pressure and volume of hydrothermal fluid samples as a function of the preloading pressure of the precharged gas. Further, laboratory simulation and examination approaches were also adopted and compared, in order to obtain the volume change of the sample and accumulator chambers. By using theoretical models and the volume change of the two chambers, the optimized preloading pressure for the precharged gas was obtained. Under the optimized preloading pressure, the in situ pressure of the fluid samples could be maintained, and their volume was maximized. The optimized preloading pressure obtained in this study should also be applicable to other isobaric gas-tight hydrothermal samplers, by adopting a similar approach to pressure maintenance.

Preparation of Pd@Gr Composite Materials and Research on Catalytic Performance

2019 ◽  
Vol 944 ◽  
pp. 671-677
Author(s):  
Jin Feng Leng ◽  
Kang Wang ◽  
Chang Peng Xia
Keyword(s):  
Reduction Method ◽  
Chemical Reduction ◽  
Great Influence ◽  
Pd Nanoparticles ◽  
Catalytic Performance ◽  
Chemical Oxidation ◽  
Chemical Reduction Method ◽  
Graphene Surface ◽  
Oxidation Reduction

In this work, the preparation of graphene by chemical oxidation reduction method and a series of chemical reactions to get graphene oxide, with the preparation of graphene composites by simply chemical reduction method for the preparation of palladium/graphene composites. Through the chemical reduction method, the small size of Pd nanoparticles is acquired by controlling the content of reducing agent. The Pd nanoparticles on graphene surface is 10nm size and evenly distributed. Pd2+ adsorption on graphene surface and in situ were partially reduced to Pd to Pd2+ nanoparticles by the reducibility of graphene. In the process, the graphene was reduced to graphene and the final compound was thinner and more transparent than the pre-experiment oxide. The oxygen-containing functional groups on the surface of the graphene have influence to the nucleation and growth of metal nanoparticles and KI can control the morphology and size of nanoparticles. The particle size and dispersion uniformity have great influence on the catalytic performance of composites, the smaller particles have better catalytic performance. Keywords:palladium, graphene composites, nanoparticles

Sign in / Sign up

Export Citation Format

Share Document