In the first part of the present work, relevant findings concerning the laccase (Lacc) activation of alkyl gallates, and its implementation in developing hydrophobic properties on cellulose-based substrates are reported. Surface state energy by water contact angle (CA), absorption tests, and Cobb60 measurements were used to assess the hydrophobic behavior of treated substrates. SEM images of paper samples treated with functionalization solutions (FS) revealed the presence of lauryl gallate (LG, dodecyl 3,4,5,-trihydroxybenzoate) particles attached to fiber surfaces. Secondly, the chemical structure of the enzyme-oxidized LG and several gallates of variable chain length was elucidated by using Fourier transform infrared (FTIR) spectroscopy, ...
The aim of this work was to develop an innovative method for the internal sizing of paper by use of ...
In the present work various laccases (Lac) and different phenolic compounds potentially possessing a...
We investigate the use of laccase enzymes to couple short nonpolar chains containing aromatic groups...
In this work, we studied the influence of the alkyl chain length in enzymatically-oxidized gallates ...
In the present work we investigated the chemical changes undergone by enzyme-oxidized lauryl gallate...
A new biotechnological procedure using laccase in combination with a hydrophobic phenolic compound (...
The covalent grafting of alkyl gallates on wool through a laccase catalysed reaction in 80/20 (v/v, ...
A new approach for the hydrophobization of finished cellulosic substrates based on a previously repo...
An innovative method has been developed for the surface hydrophobisation of cellulose-based material...
To confer hydrophobic properties to Kraft pulp, an environmentally friendly process using laccase an...
The present work describes a new method for the surface functionalization of cellulosic sheets, over...
In the present work we investigate the physicochemical interactions between silica and nanofibrillar...
Nanofibrillated cellulose, NFC, is an interesting wood fibre-based material that could be utilized i...
Laccase-mediated grafting on lignocelluloses has gained considerable attention as an environmentally...
We investigate the use of laccase enzymes to couple short nonpolar chains containing aromatic groups...
The aim of this work was to develop an innovative method for the internal sizing of paper by use of ...
In the present work various laccases (Lac) and different phenolic compounds potentially possessing a...
We investigate the use of laccase enzymes to couple short nonpolar chains containing aromatic groups...
In this work, we studied the influence of the alkyl chain length in enzymatically-oxidized gallates ...
In the present work we investigated the chemical changes undergone by enzyme-oxidized lauryl gallate...
A new biotechnological procedure using laccase in combination with a hydrophobic phenolic compound (...
The covalent grafting of alkyl gallates on wool through a laccase catalysed reaction in 80/20 (v/v, ...
A new approach for the hydrophobization of finished cellulosic substrates based on a previously repo...
An innovative method has been developed for the surface hydrophobisation of cellulose-based material...
To confer hydrophobic properties to Kraft pulp, an environmentally friendly process using laccase an...
The present work describes a new method for the surface functionalization of cellulosic sheets, over...
In the present work we investigate the physicochemical interactions between silica and nanofibrillar...
Nanofibrillated cellulose, NFC, is an interesting wood fibre-based material that could be utilized i...
Laccase-mediated grafting on lignocelluloses has gained considerable attention as an environmentally...
We investigate the use of laccase enzymes to couple short nonpolar chains containing aromatic groups...
The aim of this work was to develop an innovative method for the internal sizing of paper by use of ...
In the present work various laccases (Lac) and different phenolic compounds potentially possessing a...
We investigate the use of laccase enzymes to couple short nonpolar chains containing aromatic groups...