Evidence map›Paper›PMID 41529183›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2026

Stretching and Compressing Capillary Bridges on Hydrophilic, Hydrophobic, and Liquid-Infused Surfaces.

Sarah J Goodband, Ke Sun, Kislon Voïtchovsky, Halim Kusumaatmaja

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Sarah J GoodbandDepartment of Physics, Durham University, Durham DH1 3LE, U.K.
Ke SunDepartment of Physics, Durham University, Durham DH1 3LE, U.K.ORCID 0000-0003-4144-7485
Kislon VoïtchovskyDepartment of Physics, Durham University, Durham DH1 3LE, U.K.ORCID 0000-0001-7760-4732
Halim KusumaatmajaInstitute for Multiscale Thermofluids, School of Engineering, The University of Edinburgh, Edinburgh EH9 3FB, U.K.ORCID 0000-0002-3392-9479

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aqueous capillary liquid bridges are ubiquitous in nature and in technological processes. Here, we comparatively investigate capillary bridges formed between three distinct types of surfaces: (i) hydrophilic glass, (ii) hydrophobic dichlorodimethylsilane (DMS)-functionalized glass, and (iii) liquid-infused (LIS). We combine experimental measurements and computer simulations of the capillary bridges' evolution upon changes in the gap size between the surfaces, deriving in each case the bridge geometry and the resulting capillary force. The results, also compared with predictions from the existing theory, follow expected trends on glass and DMS-functionalized surfaces: contact line pinning dominates the bridge behavior on glass with a characteristic stick-slip motion, whereas a pronounced advancing and receding hysteresis is observed on DMS surfaces. On LIS, the absence of pinning leads to minimal force variation, gravity-driven breaking of the bridge symmetry, and possible liquid exchange between LIS through bridge cloaking. These effects become particularly significant in asymmetric bridge configurations combining LIS and DMS surfaces, where the transfer of lubricant from LIS to DMS modifies the effective surface tension and alters bridge-surface interactions. Our systematic comparison of the capillary bridge behavior across solid and liquid interfaces with varying wettability provides a foundation for designing functional surface applications with controlled bridge-surface interactions.

Identifiers

PMID41529183
PMCPMC12856891

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.