1963
DOI: 10.1016/0095-8522(63)90059-x
|View full text |Cite
|
Sign up to set email alerts
|

Nonionic surface-active compounds. VII. Interfacial tensions of solutions of nonionic surface-active agents

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
9
0
1

Year Published

1964
1964
1997
1997

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 37 publications
(10 citation statements)
references
References 10 publications
0
9
0
1
Order By: Relevance
“…In view of Becher's [1] oil/water interracial tension measurements, from which he deduced in effect that the degree of penetration depends on the hydrophobicity of the surfactant, a further temperature effect might be expected with nonionic surfactants at the oil/water interface in addition to that observed here at the melting point of the disperse phase. We would anticipate not only a reduction in adsorbed layer thickness arising from penetration of the oil/ water interface by the stabilising surfactant but also a reduction from the ongoing tendency of the dehydrating surfactant to sink still deeper into the oil phase as temperature increases further.…”
Section: Colloid Stabilitymentioning
confidence: 80%
See 1 more Smart Citation
“…In view of Becher's [1] oil/water interracial tension measurements, from which he deduced in effect that the degree of penetration depends on the hydrophobicity of the surfactant, a further temperature effect might be expected with nonionic surfactants at the oil/water interface in addition to that observed here at the melting point of the disperse phase. We would anticipate not only a reduction in adsorbed layer thickness arising from penetration of the oil/ water interface by the stabilising surfactant but also a reduction from the ongoing tendency of the dehydrating surfactant to sink still deeper into the oil phase as temperature increases further.…”
Section: Colloid Stabilitymentioning
confidence: 80%
“…This assumption however is not expected to have quantitative validity for sterically stabilised dispersions/emulsions. Here the stabilising polymer or surfactant may penetrate the liquid/liquid interface of an emulsion drop which it can not do at the solid/ liquid interface [1,2]. For this reason the adsorption properties and colloid stabilising ability of a given polymer or surfactant may differ depending on whether the substrate is in solid or liquid state.…”
Section: Introductionmentioning
confidence: 98%
“…For the n-octane/oxethylated lauryl alcohol system Becher 33 found that ␥ Despite the deviations stated, and the fact that nonidentical values for the solid surface tension of nonpolar solids and the Lifshitz-van der Waals contribution to surfactant surface tension yield an interfacial tension contribution (see Eqn [13]), Becher 33 assumed that ␥ sl almost exclusively stems from the polar contribution of the EO chains in the water phase.…”
Section: Donor-acceptor (␥ +/ϫ ) and Lifshitz-van Der Waals (␥ Lw ) Pmentioning
confidence: 96%
“…29 But they cannot suppress a certain depth influence of the oxygen atoms. If one considers both (1) the differences in the specific area per molecule [(with similar packing at both interfaces, 33 at the liquid/vapour interface 40 Å 2 (22) 26 and 50 Å 2 (3) 26,27 ] and (2) in (22) the significantly greater distance to the solid surface of the second oxygen atom (Fig. 12, right-hand diagram), an effective reduction of the polarity for 22 can be assumed.…”
Section: Solid/liquid Interfacial Tension (␥ Sl )mentioning
confidence: 99%
“…A existência de um ponto mínimo da tensão superficial está de acordo com os rebotados descritos por Becher (1963) e Hansen e Fagerheim (1998).…”
Section: Determinação Da Tensão Interfacial Entre Tergitol 15-s E Comunclassified