Evidence map›Paper›PMID 34442900›Full record

ArticleMaterials (Basel, Switzerland)2021

Influence of the Surface Chemistry of Graphene Oxide on the Structure-Property Relationship of Waterborne Poly(urethane urea) Adhesive.

Abir Tounici, José Miguel Martín-Martínez

Abstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Effects of Modified AlMaterials (Basel, Switzerland) · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Abir TouniciAdhesion and Adhesives Laboratory, Department of Inorganic Chemistry, University of Alicante, 03080 Alicante, Spain.
José Miguel Martín-MartínezAdhesion and Adhesives Laboratory, Department of Inorganic Chemistry, University of Alicante, 03080 Alicante, Spain.ORCID 0000-0002-7230-6581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small amounts-0.04 wt.%-graphene oxide derivatives with different surface chemistry (graphene oxide-GO-, amine-functionalized GO-A-GO-, reduced GO-r-GO) were added during prepolymer formation in the synthesis of waterborne poly(urethane urea) dispersions (PUDs). Covalent interactions between the surface groups on the graphene oxide derivatives and the end NCO groups of the prepolymer were created, these interactions differently altered the degree of micro-phase separation of the PUDs and their structure-properties relationships. The amine functional groups on the A-GO surface reacted preferentially with the prepolymer, producing new urea hard domains and higher percentage of soft segments than in the PUD without GO derivative. All GO derivatives were well dispersed into the PU matrix. The PUD without GO derivative showed the most noticeable shear thinning and the addition of the GO derivative reduced the extent of shear thinning differently depending on its functional chemistry. The free urethane groups were dominant in all PUs and the addition of the GO derivative increased the percentage of the associated by hydrogen bond urethane groups. As a consequence, the addition of GO derivative caused a lower degree of micro-phase separation. All PUs containing GO derivatives exhibited an additional thermal decomposition at 190-206 °C which was ascribed to the GO derivative-poly(urethane urea) interactions, the lowest temperature corresponded to PU+A-GO. The PUs exhibited two structural relaxations, their temperatures decreased by adding the GO derivative, and the values of the maximum of tan delta in PU+r-GO and PU+A-GO were significantly higher than in the rest. The addition of the GO derivative increased the elongation-at-break, imparted some toughening, and increased the adhesion of the PUD. The highest T-peel strength values corresponded to the joints made with PUD+GO and PUD+r-GO, and a rupture of the substrate was obtained.

Indexed as

adhesiongraphene oxide derivativemicro-phase separationstructure–property relationshipsurface chemistrywaterborne poly(urethane urea)

Identifiers

PMID34442900
PMCPMC8399831

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