A Novel Technique for Large-Scale Fabrication of 3D Colloidal Crystals: Suspending Self-Assembly in Water Medium (SSAM)

Author(s):  
Zhengting Zhang ◽  
Guiyun Yi ◽  
Xiaodong Wang ◽  
Peng Li ◽  
Zhuoyan Wan ◽  
...  
2013 ◽  
Vol 2013 ◽  
pp. 1-14 ◽  
Author(s):  
Binfu Bao ◽  
Duo Liu ◽  
Youyou Yang ◽  
Zhehong Shen ◽  
Bo You

Self-assembly of colloidal spheres is the most frequently used method for structural colors, but the chroma of the structural colors is usually so low that people cannot observe it under natural conditions. This paper presents a facile method for fabrications of vivid structural colors by doping carbon black into the self-assembly of colloidal polymer spheres and nanosilica particles. This approach can generate very gorgeous structural colors which can be very easily seen under natural conditions. The fabrication conditions for the self-assembly of composite dispersions of polymer/silica/carbon black were optimized to obtain colloidal crystals with vivid colors. Thus, robust mechanical properties, large-scale, and brilliant structural colors can guarantee the obtained crystal films to find practical applications, which are demonstrated by the fact that the successful applications of structural colors beautify the original simple and tedious surface of bamboo strand board (BSB).


2019 ◽  
Vol 4 (1) ◽  
pp. 68-74
Author(s):  
Aleš Dakskobler ◽  
Matjaz Valant

Background: Studies on the formation of colloidal crystals in concentrated suspensions have mainly been based on dispersed suspensions with a repulsive inter-particle potential of hard or nearly hard spheres. The self-assembly in weakly-flocculated suspensions has still been unrealized. Here, we report on the formation of ordered structures in concentrated suspensions of nearly-hard spherical particles with weakly-attractive inter-particle interactions that are an order of magnitude higher than the particles’ thermal energy. Methods: In our case, the self-assembly in such suspensions is not thermodynamically driven, but an external shear force must be applied. The driving force for the particles’ ordering is an increase in the inter-particle interactions. This manifests itself in a decrease in the average angle between the interparticle interaction direction and the applied shear stress direction. Results: For a successful ordering into a large-scale closed packed assembly, the external shear force must not exceed the inter-particle attractive interaction for the minimum possible average angle (as in the closed packed structures) but be high enough to enable the particles to move in the highly loaded suspension. Conclusion: The developed method for the self-assembly of the weakly flocculated systems can be applied very generally e.g. a control over a composition of heterogeneous colloidal crystals, manufacturing of the large-scale photonic crystals or preparation of very densely packed compacts of particles needed for the production of sintered ceramics.


2018 ◽  
Vol 5 (6) ◽  
pp. 171522 ◽  
Author(s):  
Haitong Tang ◽  
Xinru Yu ◽  
Shi Jin ◽  
Fanling Meng ◽  
Yan Yan ◽  
...  

Hierarchical carbon nanofibre (CNF)/SnO 2 /Ni nanostructures of graphitized carbon nanofibres and SnO 2 nanocrystallines and Ni nanocrystallines have been prepared via divalent tin–alginate assembly on polyacrylonitrile (PAN) fibres, controlled pyrolysis and ball milling. Fabrication is implemented in three steps: (1) formation of a tin–alginate layer on PAN fibres by coating sodium alginate on PAN in a water medium followed by polycondensation in SnCl 2 solution; (2) heat treatment at 450°C in a nitrogen atmosphere; (3) ball milling the mixture of CNF/SnO 2 fibres and Ni powder. The CNF/SnO 2 /Ni nanocomposite exhibits good lithium ion storage capacity and cyclability, providing a facile and low-cost approach for the large-scale preparation of anode materials for lithium ion batteries.


2021 ◽  
Vol 11 (15) ◽  
pp. 6688
Author(s):  
Jesús Romero Leguina ◽  
Ángel Cuevas Rumin ◽  
Rubén Cuevas Rumin

The goal of digital marketing is to connect advertisers with users that are interested in their products. This means serving ads to users, and it could lead to a user receiving hundreds of impressions of the same ad. Consequently, advertisers can define a maximum threshold to the number of impressions a user can receive, referred to as Frequency Cap. However, low frequency caps mean many users are not engaging with the advertiser. By contrast, with high frequency caps, users may receive many ads leading to annoyance and wasting budget. We build a robust and reliable methodology to define the number of ads that should be delivered to different users to maximize the ROAS and reduce the possibility that users get annoyed with the ads’ brand. The methodology uses a novel technique to find the optimal frequency capping based on the number of non-clicked impressions rather than the traditional number of received impressions. This methodology is validated using simulations and large-scale datasets obtained from real ad campaigns data. To sum up, our work proves that it is feasible to address the frequency capping optimization as a business problem, and we provide a framework that can be used to configure efficient frequency capping values.


Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1094
Author(s):  
Bastian Klose ◽  
Daniel Kremer ◽  
Merve Aksit ◽  
Kasper P. van der Zwan ◽  
Klaus Kreger ◽  
...  

Polystyrene foams have become more and more important owing to their lightweight potential and their insulation properties. Progress in this field is expected to be realized by foams featuring a microcellular morphology. However, large-scale processing of low-density foams with a closed-cell structure and volume expansion ratio of larger than 10, exhibiting a homogenous morphology with a mean cell size of approximately 10 µm, remains challenging. Here, we report on a series of 4,4′-diphenylmethane substituted bisamides, which we refer to as kinked bisamides, acting as efficient supramolecular foam cell nucleating agents for polystyrene. Self-assembly experiments from solution showed that these bisamides form supramolecular fibrillary or ribbon-like nanoobjects. These kinked bisamides can be dissolved at elevated temperatures in a large concentration range, forming dispersed nano-objects upon cooling. Batch foaming experiments using 1.0 wt.% of a selected kinked bisamide revealed that the mean cell size can be as low as 3.5 µm. To demonstrate the applicability of kinked bisamides in a high-throughput continuous foam process, we performed foam extrusion. Using 0.5 wt.% of a kinked bisamide yielded polymer foams with a foam density of 71 kg/m3 and a homogeneous microcellular morphology with cell sizes of ≈10 µm, which is two orders of magnitude lower compared to the neat polystyrene reference foam with a comparable foam density.


1999 ◽  
Vol 28 (11) ◽  
pp. 1221-1222 ◽  
Author(s):  
Akio Kishida ◽  
Fusako Seto ◽  
Ken-ichiro Hiwatari ◽  
Takeshi Serizawa ◽  
Youichiro Muraoka ◽  
...  

Particuology ◽  
2011 ◽  
Vol 9 (6) ◽  
pp. 559-565 ◽  
Author(s):  
Zhirong Li ◽  
Jingxia Wang ◽  
Yanlin Song

Soft Matter ◽  
2012 ◽  
Vol 8 (25) ◽  
pp. 6684 ◽  
Author(s):  
Matthew M. Shindel ◽  
Szu-Wen Wang ◽  
Ali Mohraz

2005 ◽  
Vol 4 (1) ◽  
pp. 81-91 ◽  
Author(s):  
Martin Nilsson Jacobi ◽  
Steen Rasmussen ◽  
Kolbjørn Tunstrøm

This paper is a discussion on how reaction kinetics and three-dimensional (3D) lattice simulations can be used to elucidate the dynamical properties of micelles as a possible minimal protocell container. We start with a general discussion on the role of molecular self-assembly in prebiotic and contemporary biological systems. A simple reaction kinetic model of a micellation process of amphiphilic molecules in water is then presented and solved analytically. Amphiphilic molecules are polymers with hydrophobic (water-fearing), e.g. hydrocarbon tail groups, and hydrophilic (water-loving) head groups, e.g. fatty acids. By making a few simplifying assumptions an analytical expression for the size distribution of the resulting micelles can be derived. The main part of the paper presents and discusses a lattice gas technique for a more detailed 3D simulation of molecular self-assembly of amphiphilic polymers in aqueous environments. Water molecules, hydrocarbon tail groups and hydrophilic head groups are explicitly represented on a three-dimensional discrete lattice. Molecules move on the lattice proportional to their continuous momentum. Collision rules preserve momentum and kinetic energy. Potential energy from molecular interactions are also included explicitly. The non-trivial thermodynamics of large-scale and long-time dynamics are studied. In this paper we specifically demonstrate how, from a random initial distribution, micelles are formed and grow until they destabilize and can divide. Eventually a steady state of growing and dividing micelles is formed. Towards the end of the paper we discuss the relevance of the presented results to the design of a minimal artificial protocell.


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