Crosslinking of cotton cellulose in the presence of serine and glycine. II. Pore structures and agent distribution

2006 ◽  
Vol 102 (2) ◽  
pp. 1578-1584 ◽  
Author(s):  
You-Jen Chen ◽  
Jui-Chin Chen ◽  
Wei-Hua Yao ◽  
Cheng-Chi Chen
Keyword(s):  
Cotton Cellulose ◽  
Pore Structures

Crosslinking of Cotton Cellulose in the Presence of Alpha-aminoacids Part III: Pore Structures

2006 ◽  
Vol 76 (4) ◽  
pp. 336-342 ◽  
Author(s):  
Chang Wang ◽  
Jui-Chin Chen ◽  
Wei-Hua Yao ◽  
Cheng-Chi Chen
Keyword(s):  
Cotton Cellulose ◽  
Pore Structures

Substrate templated synthesis of single-phase and uniform Zr-porphyrin-based metal–organic frameworks

2020 ◽  
Vol 7 (1) ◽  
pp. 221-231
Author(s):  
Seong Won Hong ◽  
Ju Won Paik ◽  
Dongju Seo ◽  
Jae-Min Oh ◽  
Young Kyu Jeong ◽  
...  
Keyword(s):  
Chemical Bath Deposition ◽  
Single Phase ◽  
Metal Organic Frameworks ◽  
Templated Synthesis ◽  
Pore Structures ◽  
Phase Pure ◽  
Metal Organic ◽  
Cbd Method

We successfully demonstrate that the chemical bath deposition (CBD) method is a versatile method for synthesizing phase-pure and uniform MOFs by controlling their nucleation stages and pore structures.

Tuning the pore structures and photocatalytic properties of a 2D covalent organic framework with multi-branched photoactive moieties

Nanoscale ◽  
2020 ◽  
Vol 12 (30) ◽  
pp. 16136-16142
Author(s):  
Xuan Wang ◽  
Ming-Jie Dong ◽  
Chuan-De Wu
Keyword(s):  
Photocatalytic Properties ◽  
Effective Strategy ◽  
Covalent Organic Framework ◽  
Highly Efficient ◽  
Pore Structures ◽  
Local Connection ◽  
Organic Framework

An effective strategy to incorporate accessible metalloporphyrin photoactive sites into 2D COFs by establishing a 3D local connection for highly efficient photocatalysis was developed.

scholarly journals Tailoring of the pore structures of wood pyrolysis chars for potential use in energy storage applications

2021 ◽  
Vol 286 ◽  
pp. 116431
Author(s):  
Przemyslaw Maziarka ◽  
Peter Sommersacher ◽  
Xia Wang ◽  
Norbert Kienzl ◽  
Stefan Retschitzegger ◽  
...  
Keyword(s):  
Energy Storage ◽  
Wood Pyrolysis ◽  
Pore Structures ◽  
Energy Storage Applications ◽  
Potential Use

scholarly journals Modification of cotton fabrics with 2-diethylaminoethyl chloride for salt-free dyeing with anionic dyes

Cellulose ◽  
2021 ◽  
Author(s):  
Peixin Tang ◽  
Leilah-Marie E. Lockett ◽  
Mengxiao Zhang ◽  
Gang Sun
Keyword(s):  
Electrostatic Interactions ◽  
Light Exposure ◽  
Dye Adsorption ◽  
Cost Effective ◽  
Cotton Fabrics ◽  
Cotton Cellulose ◽  
Hydroxyl Groups ◽  
Anionic Dyes ◽  
Free System ◽  
Untreated Cotton

AbstractA chemical modification of cotton fabrics by 2-diethylaminoethyl chloride (DEAE-Cl) was achieved, and the resulted cotton fabrics demonstrated salt-free dyeing properties with anionic dyes. Nucleophilic property of hydroxyl groups in cotton cellulose was enhanced under alkaline conditions and could react with DEAE-Cl, a chemical possessing both nucleophilic and electrophilic sites. The monolayered DEAE-grafted cotton cellulose could further react with DEAE-Cl to form multiple cationic quaternary ammonium salts (denoted as DEAE@Cotton), which are highly interactive with anionic dye molecules. The strong electrostatic interactions between the DEAE@Cotton and the dyes eliminated the use of inorganic salts in cotton dyeing process. The chemical structure and property of DEAE@Cotton were characterized and compared with untreated cotton. The DEAE@Cotton can be dyed in a salt-free system, and the dye exhaustion was faster than the conventional dyeing method due to the robust electrostatic interactions of the fabrics with anionic dyes. The dyed fabrics demonstrated outstanding color fastness under repeated washing, light exposure, and crocking. The dye adsorption process on DEAE@Cotton follows Langmuir isotherm model (R2 = 0.9667). The mechanism of enhanced dyeability was experimentally proved by treating the fabric with other anionic dyes in a salt-free system, proving the process to be environmentally friendly and cost-effective. Graphic abstract

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