Copper precipitation of Cu-monoethanolamine preservative in wood

Holzforschung ◽  
2012 ◽  
Vol 66 (8) ◽  
pp. 1017-1024 ◽  
Author(s):  
Myung Jae Lee ◽  
Paul Cooper

Abstract Copper precipitation is one of the important Cu fixation mechanisms of Cu-amine-treated wood. In the present work, possible pathways of Cu precipitation have been investigated via in vitro and in situ studies focusing on effects of pH and temperature and Cu species formed in Cu-monoethanolamine (Cu-Mea)-treated wood. Higher-concentration Cu-Mea solutions required a lower pH and higher amounts of acid for the precipitation because of the higher amount of free Mea in the preservative-wood system. For this reason, Cu fixation during wet conditioning of wood treated to high Cu retention (2.0% treating solution) resulted in only a slight pH decrease and low Cu fixation. When lower-concentration solutions (0.67% and 0.2%) were applied, the pH decreased enough for Cu precipitation, and the much higher Cu fixation rate was driven by both chemisorption and precipitation. Evaluation of leaching after wet conditioning and drying showed that additional Cu precipitation could occur during drying. Wet conditioning of Cu-Mea-treated wood at 50°C showed outwardly faster and higher Cu fixation, but resulted in higher Cu leaching. According to X-ray diffraction analysis, the in vitro precipitated Cu was a mixture of azurite and malachite, and possibly, Cu2O formed as a result of Cu-Mea decomposition.

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3920
Author(s):  
Martin Weber ◽  
Gábor Balázs ◽  
Alexander V. Virovets ◽  
Eugenia Peresypkina ◽  
Manfred Scheer

By reacting [{Cp‴Fe(CO)2}2(µ,η1:1-P4)] (1) with in situ generated phosphenium ions [Ph2P][A] ([A]− = [OTf]− = [O3SCF3]−, [PF6]−), a mixture of two main products of the composition [{Cp‴Fe(CO)2}2(µ,η1:1-P5(C6H5)2)][PF6] (2a and 3a) could be identified by extensive 31P NMR spectroscopic studies at 193 K. Compound 3a was also characterized by X-ray diffraction analysis, showing the rarely observed bicyclo[2.1.0]pentaphosphapentane unit. At room temperature, the novel compound [{Cp‴Fe}(µ,η4:1-P5Ph2){Cp‴(CO)2Fe}][PF6] (4) is formed by decarbonylation. Reacting 1 with in situ generated diphenyl arsenium ions gives short-lived intermediates at 193 K which disproportionate at room temperature into tetraphenyldiarsine and [{Cp‴Fe(CO)2}4(µ4,η1:1:1:1-P8)][OTf]2 (5) containing a tetracyclo[3.3.0.02,7.03,6]octaphosphaoctane ligand.


2019 ◽  
Vol 92 (7) ◽  
pp. 1013-1019 ◽  
Author(s):  
P. A. Novikov ◽  
A. E. Kim ◽  
K. A. Pushnitsa ◽  
Wang Quingsheng ◽  
M. Yu. Maksimov ◽  
...  

2008 ◽  
Vol 23 (2) ◽  
pp. 175-175 ◽  
Author(s):  
C. Hesse ◽  
F. Goetz-Neunhoeffer ◽  
J. Neubauer ◽  
M. Braeu ◽  
P. Gaeberlein ◽  
...  

2016 ◽  
Vol 120 (27) ◽  
pp. 14984-14990 ◽  
Author(s):  
Qin Pan ◽  
Ching-Chang Chung ◽  
Nanfei He ◽  
Jacob L. Jones ◽  
Wei Gao

CrystEngComm ◽  
2018 ◽  
Vol 20 (22) ◽  
pp. 3105-3116 ◽  
Author(s):  
Roman Svoboda ◽  
Roman Bulánek ◽  
Dušan Galusek ◽  
Roghayeh Hadidimasouleh ◽  
Yadolah Ganjkhanlou

Differential scanning calorimetry and in situ X-ray diffraction analysis were used to study the products and mechanism of crystal formation in VOx–ZrO2 ceramics.


2005 ◽  
Vol 275 (1-2) ◽  
pp. e1793-e1798 ◽  
Author(s):  
L. O’Mahony ◽  
D. Zemlyanov ◽  
M. Mihov ◽  
T. Curtin ◽  
B.K. Hodnett

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