Sentence examples for pore expanded from inspiring English sources

Biodiesel synthesis from acid oil (AO) containing high free fatty acids (FFA) over pore expanded sulfonic acid functionalized mesostructured SBA-15 was studied.

With the aim to overcome these limitations, an effort has been undertaken in the current work to use organically modified pore expanded MCM-41 mesoporous silica (MS) as filler for fabrication of PLA based composites via solution casting method.

A 350 nm nanopore in a 300 nm thick membrane was processed at 1150°C for 50 min. The pore expanded in size to 1.5 μm (Figure 4).

Three-dimensional cubic ordered mesoporous carbons with tunable pore sizes have been synthesized by using cubic Ia3d mesoporous KIT-6 silica as the hard template and boric acid as the pore expanding agent.

In summary, we synthesized 3-D cubic OMCs with tunable pore sizes in the range of 3.9 9.4 nm by using KIT-6 silica as the hard template and boric acid as the pore expanding agent.

Herein, on the basis of this method, we report the synthesis of three-dimensional (3-D) cubic OMCs with tunable pore size distributions using KIT-6 silica as the template and boric acid as the pore expanding agent.

Recently, Lee et al. [12] reported the synthesis of two-dimensional (2-D) hexagonal OMCs with controllable pore sizes in the range of 3 10 nm using MSU-H silica as the hard template and boric acid as the pore expanding agent, which was considered to be a facile method for the pore size control of OMCs.

Therefore pores expanded slightly at low concentrations of KCl, but were unable, because of their cross-linked structure, to expand enough to accommodate the amount of water needed to abolish a large osmotic pressure gradient.

This work will focus on the growth mechanism behind the currentline pores, expanding the work presented in [16].

In addition, fusion pores expand slowly and are a mechanical barrier to content release [16], [17].

The growth of carbon nanotubes (CNTs) in the pores of expanded graphite by chemical vapor deposition with and without a catalyst was investigated and their microstructure was studied by scanning electron microscopy.