BLOOD FLOW SIMULATION USING SPH METHOD IN LS-DYNA, ANALYSIS OF ADVANTAGES AND DISADVANTAGES

M. Topalovic, A. Nikolic, M. Zivkovic
{"title":"BLOOD FLOW SIMULATION USING SPH METHOD IN LS-DYNA, ANALYSIS OF ADVANTAGES AND DISADVANTAGES","authors":"M. Topalovic, A. Nikolic, M. Zivkovic","doi":"10.46793/iccbi21.255t","DOIUrl":null,"url":null,"abstract":"The purpose of this research was to investigate the possibility of blood flow modelling in LS-DYNA using its SPH solver and SPH-FEM coupling. SPH and FEM methods are both based on the continuum mechanics, and SPH uses Lagrangian material framework, while FEM can use both Lagrangian for solid, and Eulerian formulation for fluid analysis. SPH implementation is mesh-free giving it the capability to model very large deformations without mesh distortions. However, this comes at a high computational price, so the number of SPH particles needs to be significantly lower in comparison to the number of FEM elements in the Eulerian analysis of the same fluid domain. In the case of combined SPH-FEM analysis, the blood vessel wall is modelled with FEM shell elements, while the blood inside is modelled with SPH particles. The contact between the two is done using nodes to surface algorithm, while if we use the SPH only, there is no need for the specific contact definition. The Lagrangian framework of the SPH method means that we need to generate particles at one end, and to destroy them on the other, in order to generate a continuous fluid flow. To do this we used activation and deactivation planes, which is a solution implemented in the commercial LS-Dyna SPH solver. In the results section of the paper, the velocity field of blood obtained by implementation of described modelling methodology is shown. SPH-FEM coupling offers greater possibilities to study the effects of wall deformations, tracking of movement of solid particle inclusion, or mixing two different fluids, but it requires elaborate contact definition, and prolonged analysis time in comparison to the FEM CFD analysis.","PeriodicalId":9171,"journal":{"name":"Book of Proceedings: 1st International Conference on Chemo and BioInformatics,","volume":"40 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Book of Proceedings: 1st International Conference on Chemo and BioInformatics,","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46793/iccbi21.255t","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The purpose of this research was to investigate the possibility of blood flow modelling in LS-DYNA using its SPH solver and SPH-FEM coupling. SPH and FEM methods are both based on the continuum mechanics, and SPH uses Lagrangian material framework, while FEM can use both Lagrangian for solid, and Eulerian formulation for fluid analysis. SPH implementation is mesh-free giving it the capability to model very large deformations without mesh distortions. However, this comes at a high computational price, so the number of SPH particles needs to be significantly lower in comparison to the number of FEM elements in the Eulerian analysis of the same fluid domain. In the case of combined SPH-FEM analysis, the blood vessel wall is modelled with FEM shell elements, while the blood inside is modelled with SPH particles. The contact between the two is done using nodes to surface algorithm, while if we use the SPH only, there is no need for the specific contact definition. The Lagrangian framework of the SPH method means that we need to generate particles at one end, and to destroy them on the other, in order to generate a continuous fluid flow. To do this we used activation and deactivation planes, which is a solution implemented in the commercial LS-Dyna SPH solver. In the results section of the paper, the velocity field of blood obtained by implementation of described modelling methodology is shown. SPH-FEM coupling offers greater possibilities to study the effects of wall deformations, tracking of movement of solid particle inclusion, or mixing two different fluids, but it requires elaborate contact definition, and prolonged analysis time in comparison to the FEM CFD analysis.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用SPH方法模拟ls-dyna中的血流,分析其优缺点
本研究的目的是探讨在LS-DYNA中使用SPH求解器和SPH- fem耦合进行血流建模的可能性。SPH方法和FEM方法均基于连续介质力学,SPH方法采用拉格朗日材料框架,而FEM方法对固体可以采用拉格朗日公式,对流体可以采用欧拉公式。SPH实现是无网格的,这使它能够在没有网格扭曲的情况下模拟非常大的变形。然而,这需要很高的计算代价,因此在相同流体域的欧拉分析中,SPH粒子的数量需要明显低于FEM单元的数量。在SPH-FEM联合分析中,血管壁采用FEM壳单元模拟,血管内部的血液采用SPH粒子模拟。两者之间的接触使用节点表面算法,而如果我们只使用SPH,则不需要特定的接触定义。SPH方法的拉格朗日框架意味着我们需要在一端产生粒子,并在另一端破坏它们,以产生连续的流体流动。为此,我们使用了激活和停用平面,这是在商用LS-Dyna SPH求解器中实现的解决方案。在论文的结果部分,展示了通过实施所描述的建模方法获得的血液速度场。SPH-FEM耦合提供了更大的可能性来研究壁面变形的影响,跟踪固体颗粒包裹体的运动,或混合两种不同的流体,但它需要复杂的接触定义,与FEM CFD分析相比,分析时间更长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
ELECTROPHILIC ORGANOSELENIUM COMPOUNDS AND SARS-COV-2: PRO-OXIDANT ACTIVITY AS A MORE PROMISING WAY TOWARDS THE DRUGGABILITY DIRECT SCAVENGING ACTIVITY OF 4,7-DIHYDROXYCOUMARIN DERIVATIVE TOWARDS SERIES OF CHLOROMETHYLPEROXY RADICALS PLATINUM(IV) COMPLEX AND ITS CORRESPONDING LIGAND SUPPRESS CELL MOTILITY AND PROMOTE EXPRESSION OF FRIZZLED-7 RECEPTOR IN COLORECTAL CANCER CELLS A META-HEURISTIC MULTI-OBJECTIVE APPROACH TO THE MODEL SELECTION OF CONVOLUTION NEURAL NETWORKS FOR URINARY BLADDER CANCER DIAGNOSIS NOVEL LIGANDS OF HUMAN CYP7 ENZYMES – POSSIBLE MODULATORS OF CHOLESTEROL BLOOD LEVEL: COMPUTER SIMULATION STUDIES
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1