{"title":"多分散性和浓度对稀聚合物溶液弹性毛细管减薄的影响","authors":"Vincenzo Calabrese, Amy Q. Shen, Simon J. Haward","doi":"10.1103/physrevx.15.021025","DOIUrl":null,"url":null,"abstract":"The self-thinning of liquid bridges under the action of capillarity occurs in widespread processes like jetting, dripping, and spraying and gives rise to a strong extensional flow capable of stretching dissolved polymers. If the resulting elastic stress exceeds the viscous stress, an exponential “elastocapillary” (EC) thinning regime arises, yielding a timescale τ</a:mi>EC</a:mi></a:mrow></a:msub></a:math> that is commonly considered equivalent to the longest relaxation time of the polymer <c:math xmlns:c=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><c:mi>λ</c:mi></c:math>. A long-standing question is why <e:math xmlns:e=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><e:msub><e:mi>τ</e:mi><e:mrow><e:mi>EC</e:mi></e:mrow></e:msub></e:math> depends strongly on the polymer concentration, even at high dilutions where <g:math xmlns:g=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><g:mi>λ</g:mi></g:math> should be constant in theory. To date, this is understood in terms of intermolecular interactions that arise due to “self-concentration” effects as polymers stretch. However, <i:math xmlns:i=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><i:mi>λ</i:mi></i:math> depends on the polymer molecular weight <k:math xmlns:k=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><k:mi>M</k:mi></k:math>, and we show how the concentration dependence of <m:math xmlns:m=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><m:msub><m:mi>τ</m:mi><m:mrow><m:mi>EC</m:mi></m:mrow></m:msub></m:math> can be explained by considering the molecular weight distribution (MWD) inherent in real polymer samples, without the need to invoke self-concentration. We demonstrate this by blending low-<o:math xmlns:o=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><o:mi>M</o:mi></o:math> and high-<q:math xmlns:q=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><q:mi>M</q:mi></q:math> polymer samples with narrow MWDs at dilute concentrations and in different proportions and by measuring <s:math xmlns:s=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><s:msub><s:mi>τ</s:mi><s:mrow><s:mi>EC</s:mi></s:mrow></s:msub></s:math> for each blend in capillary thinning experiments. Through a simple model that qualitatively reproduces the experimental results, we show how elastic stresses generated by the polymer build up prior to the EC regime due to the sequential stretching of progressively decreasing molecular weight species in the MWD. Since the elastic stress generated by each species depends on its concentration, the fraction of the MWD that is required to stretch in order to induce the EC regime depends on the total polymer concentration <u:math xmlns:u=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><u:mi>c</u:mi></u:math> in the solution. For higher <w:math xmlns:w=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><w:mi>c</w:mi></w:math>, the EC regime is induced by stretching of a higher-<y:math xmlns:y=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><y:mi>M</y:mi></y:math> (longer λ</ab:mi></ab:math>) fraction of the MWD and results in a longer measurement of <cb:math xmlns:cb=\"http://www.w3.org/1998/Math/MathML\" display=\"inline\"><cb:msub><cb:mi>τ</cb:mi><cb:mrow><cb:mi>EC</cb:mi></cb:mrow></cb:msub></cb:math>. Our results have significant implications for the application of capillary thinning measurements to extensional rheometry, for the interpretation of such measurements, and for the understanding of elastocapillary thinning dynamics in general. <jats:supplementary-material> <jats:copyright-statement>Published by the American Physical Society</jats:copyright-statement> <jats:copyright-year>2025</jats:copyright-year> </jats:permissions> </jats:supplementary-material>","PeriodicalId":20161,"journal":{"name":"Physical Review X","volume":"13 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of Polydispersity and Concentration on Elastocapillary Thinning of Dilute Polymer Solutions\",\"authors\":\"Vincenzo Calabrese, Amy Q. Shen, Simon J. Haward\",\"doi\":\"10.1103/physrevx.15.021025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The self-thinning of liquid bridges under the action of capillarity occurs in widespread processes like jetting, dripping, and spraying and gives rise to a strong extensional flow capable of stretching dissolved polymers. If the resulting elastic stress exceeds the viscous stress, an exponential “elastocapillary” (EC) thinning regime arises, yielding a timescale τ</a:mi>EC</a:mi></a:mrow></a:msub></a:math> that is commonly considered equivalent to the longest relaxation time of the polymer <c:math xmlns:c=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><c:mi>λ</c:mi></c:math>. A long-standing question is why <e:math xmlns:e=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><e:msub><e:mi>τ</e:mi><e:mrow><e:mi>EC</e:mi></e:mrow></e:msub></e:math> depends strongly on the polymer concentration, even at high dilutions where <g:math xmlns:g=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><g:mi>λ</g:mi></g:math> should be constant in theory. To date, this is understood in terms of intermolecular interactions that arise due to “self-concentration” effects as polymers stretch. However, <i:math xmlns:i=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><i:mi>λ</i:mi></i:math> depends on the polymer molecular weight <k:math xmlns:k=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><k:mi>M</k:mi></k:math>, and we show how the concentration dependence of <m:math xmlns:m=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><m:msub><m:mi>τ</m:mi><m:mrow><m:mi>EC</m:mi></m:mrow></m:msub></m:math> can be explained by considering the molecular weight distribution (MWD) inherent in real polymer samples, without the need to invoke self-concentration. We demonstrate this by blending low-<o:math xmlns:o=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><o:mi>M</o:mi></o:math> and high-<q:math xmlns:q=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><q:mi>M</q:mi></q:math> polymer samples with narrow MWDs at dilute concentrations and in different proportions and by measuring <s:math xmlns:s=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><s:msub><s:mi>τ</s:mi><s:mrow><s:mi>EC</s:mi></s:mrow></s:msub></s:math> for each blend in capillary thinning experiments. Through a simple model that qualitatively reproduces the experimental results, we show how elastic stresses generated by the polymer build up prior to the EC regime due to the sequential stretching of progressively decreasing molecular weight species in the MWD. Since the elastic stress generated by each species depends on its concentration, the fraction of the MWD that is required to stretch in order to induce the EC regime depends on the total polymer concentration <u:math xmlns:u=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><u:mi>c</u:mi></u:math> in the solution. For higher <w:math xmlns:w=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><w:mi>c</w:mi></w:math>, the EC regime is induced by stretching of a higher-<y:math xmlns:y=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><y:mi>M</y:mi></y:math> (longer λ</ab:mi></ab:math>) fraction of the MWD and results in a longer measurement of <cb:math xmlns:cb=\\\"http://www.w3.org/1998/Math/MathML\\\" display=\\\"inline\\\"><cb:msub><cb:mi>τ</cb:mi><cb:mrow><cb:mi>EC</cb:mi></cb:mrow></cb:msub></cb:math>. Our results have significant implications for the application of capillary thinning measurements to extensional rheometry, for the interpretation of such measurements, and for the understanding of elastocapillary thinning dynamics in general. <jats:supplementary-material> <jats:copyright-statement>Published by the American Physical Society</jats:copyright-statement> <jats:copyright-year>2025</jats:copyright-year> </jats:permissions> </jats:supplementary-material>\",\"PeriodicalId\":20161,\"journal\":{\"name\":\"Physical Review X\",\"volume\":\"13 1\",\"pages\":\"\"},\"PeriodicalIF\":15.7000,\"publicationDate\":\"2025-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Physical Review X\",\"FirstCategoryId\":\"101\",\"ListUrlMain\":\"https://doi.org/10.1103/physrevx.15.021025\",\"RegionNum\":1,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHYSICS, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physical Review X","FirstCategoryId":"101","ListUrlMain":"https://doi.org/10.1103/physrevx.15.021025","RegionNum":1,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHYSICS, MULTIDISCIPLINARY","Score":null,"Total":0}
Effects of Polydispersity and Concentration on Elastocapillary Thinning of Dilute Polymer Solutions
The self-thinning of liquid bridges under the action of capillarity occurs in widespread processes like jetting, dripping, and spraying and gives rise to a strong extensional flow capable of stretching dissolved polymers. If the resulting elastic stress exceeds the viscous stress, an exponential “elastocapillary” (EC) thinning regime arises, yielding a timescale τEC that is commonly considered equivalent to the longest relaxation time of the polymer λ. A long-standing question is why τEC depends strongly on the polymer concentration, even at high dilutions where λ should be constant in theory. To date, this is understood in terms of intermolecular interactions that arise due to “self-concentration” effects as polymers stretch. However, λ depends on the polymer molecular weight M, and we show how the concentration dependence of τEC can be explained by considering the molecular weight distribution (MWD) inherent in real polymer samples, without the need to invoke self-concentration. We demonstrate this by blending low-M and high-M polymer samples with narrow MWDs at dilute concentrations and in different proportions and by measuring τEC for each blend in capillary thinning experiments. Through a simple model that qualitatively reproduces the experimental results, we show how elastic stresses generated by the polymer build up prior to the EC regime due to the sequential stretching of progressively decreasing molecular weight species in the MWD. Since the elastic stress generated by each species depends on its concentration, the fraction of the MWD that is required to stretch in order to induce the EC regime depends on the total polymer concentration c in the solution. For higher c, the EC regime is induced by stretching of a higher-M (longer λ) fraction of the MWD and results in a longer measurement of τEC. Our results have significant implications for the application of capillary thinning measurements to extensional rheometry, for the interpretation of such measurements, and for the understanding of elastocapillary thinning dynamics in general. Published by the American Physical Society2025
期刊介绍:
Physical Review X (PRX) stands as an exclusively online, fully open-access journal, emphasizing innovation, quality, and enduring impact in the scientific content it disseminates. Devoted to showcasing a curated selection of papers from pure, applied, and interdisciplinary physics, PRX aims to feature work with the potential to shape current and future research while leaving a lasting and profound impact in their respective fields. Encompassing the entire spectrum of physics subject areas, PRX places a special focus on groundbreaking interdisciplinary research with broad-reaching influence.