ISRN Inorganic Chemistry

Volume 2013 (2013), Article ID 167206, 4 pages

http://dx.doi.org/10.1155/2013/167206

Research Article

Synthesis and Improvement of Activity of Cobalt Organic Salts as Drier

Nader Zabarjad Shiraz,¹ Bahram Letafat,¹ Elaheh Sadat Sharifzadeh,² and Anahita Rabii³

¹Department of Chemistry, Islamic Azad University, Central Tehran Branch, Tehran 1467686831, Iran

²Young Researchers Club, Islamic Azad University, Central Tehran Branch, B.O. Box 13185/768, Tehran, Iran

³Department of Environmental Engineering, Graduate Faculty of Environment, University of Tehran, Tehran 1417853111, Iran

Received 28 November 2012; Accepted 17 December 2012

Academic Editors: M. Cieslak-Golonka and J. Moncol

Copyright © 2013 Nader Zabarjad Shiraz et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Organic salts of cobalt were synthesized in the presence of amine, ethanol, and ethyl methyl ketoxime and were used as drier for alkyd resin. Considering the drying time of alkyd resin containing synthesized compound showed that amines, as electron releasing groups (ERG), increased the oxidizing activity of drier and shortened drying time about an hour, whereas ethyl methyl ketoxime delayed the drying of resin 2 hours. Two methods of synthesis, including solution and precipitation processes of synthesis, were compared in terms of convenience, cost, and environmental aspects.

1. Introduction

Metal alkanoates, metallic soaps, possessing interesting structural, and magnetic and photochemical properties have variety of applications in important areas such as material science, catalysis, and paint industries [1]. Among them, metal 2-ethyl hexanoates and their analogues are also used as fungicide, lubricating agents, plastic stabilizers, waterproof agents, and fuel additives [2]. As a catalyst, they are used in Ziegler nickel catalyst [3], stereoselective Diels-Alder reactions [4], and especially for oxidation and oligomerization of unsaturated chain of alkyd resin in paint industries [5].

Driers are a group of metallic soaps or salts containing either alkaline-earth metals or heavy metals. Common organic acids used are linolenic acid, rosin acids, tall fatty acid, naphthenic acid, and 2-ethyl hexanoic acid (2-EHA) [6]. Driers are added to air-drying coating systems to catalyze the oxidative cross-linking reactions [7]. Most of drier metals are in the oxidation state of +2 and usually dissolved in hydrocarbon solvents such as mineral spirit (clear liquid including a mixture of typically >65% C10 or higher of aliphatic and aromatic hydrocarbons) or aliphatic solvents.

Driers are often divided into two categories: primary and secondary driers. Primary (catalytic, surface, or oxidative) driers promote rapid surface drying [7]. Cobalt, manganese, vanadium, cerium, and iron-based catalysts belong to this group. Several physical and chemical experiments have been done to understand the nature of paint films during drying process [8]. Generally, evaporation of volatile materials, absorption of oxygen from the air, and formation of larger molecules from smaller ones take place to form dried film of paint [9]. Driers promote oxygen uptake, peroxide formation, and decomposition at ambient temperature. Free radicals produced in the process lead to the formation of polymer-polymer cross-links.

Drier accelerators such as 2,2-bipyridine (bpy) and 1,10-phenantroline are also extensively used. They function as chelating agents to form complexes with the primary driers. They apparently increase the activity of the metal towards decomposing peroxides [7]. Other chelating agents such as 2-aminomethylpyridine (amp) and 2-hydroxymethylpyridine (hmp) were recently reported in combination with manganese-based catalysts [10].

Cobalt-based driers are often used in combination with other metals such as zirconium and calcium to obtain uniform drying. Bismuth soaps combined with cobalt driers were found to shorten the drying time of alkyd paints particularly under adverse conditions such as low temperature and high humidity [11]. It has also been reported that combination of aluminium compounds with cobalt driers leads to a significant increase in the hardness of the alkyd paint films [12].

Risk analysis studies showed that inhalation exposure to cobalt in humans has been reported to result in cough, dyspnea, decreased pulmonary function, weight loss, diffuse nodular fibrosis, and respiratory hypersensitivity. Contact with cobalt in humans has resulted in dermatitis, with eruptions of the erythematous papular type on the ankles, elbows, and neck [13]. Chronic exposure to cobalt by inhalation in humans results in effects on the respiratory system, such as respiratory irritation, wheezing, asthma, pneumonia, and fibrosis. Other effects include cardiac effects, such as functional effects on the ventricles and enlargement of the heart; congestion of the liver, kidneys, and conjunctiva; and immunological effects that include cobalt sensitization, which can precipitate an asthmatic attack in sensitized individuals [14].

However the increase in environmental regulations makes the knowledge of cobalt drier chemistry of the utmost importance. Replacement of the toxic cobalt salts as driers in alkyd paint still poses a challenge [15]. Although exclusion of cobalt drier is an ultimate favourite method to eliminate its environmental risks in resin and paint industries, reduction of its consumption may be an alternate to diminish resulting hazards. In this paper we try to use some electron donating ligands to improve the drying activity of cobalt octoate, and consequently decrease dosage of cobalt drier in alkyd resins and paints.

2. Experimental

Long oil alkyd (60% in mineral spirit) was used as blank resin. Aniline, ethanolamine, ethyl amine, ethyl methyl ketoxime, cobalt sulfate, and cobalt hydroxide were purchased from fluka and were used without further purification.

2.1. General Procedure for Synthesis of Cobalt Octoate (3)  (Solution Method)

A mixture of Co(OH)₂ (1) (93 g, 1 mol) and 2-EHA (2) (288 g, 2 mol) in mineral spirit (1 L) was stirred magnetically and heated up to 150–160°C to separate the produced H₂O (33.1 mL, 92%) by Dean-Stark apparatus. After departure of the H₂O as by-product, the mixture was heated for an hour and the drier obtained as a deep violet solution. The metal content of drier was adjusted to 10% by adding adequate mineral spirit.

2.2. General Procedure for Synthesis of Cobalt Drier (3)  (Precipitation Method)

To a magnetically stirred solution of CoSO₄ (4) (15.5 g, 0.1 mol) in H₂O (50 mL) was added dropwise a solution of organic acid (2) (0.2 mol) in NaOH solution (10%, 50 mL). After 2 hours refluxing, the precipitate (3) was filtered, washed with water, and dried at room temperature (32.8 g, 95%). The solid was dissolved in mineral spirit to prepare 10% cobalt drier solution.

2.3. Technique to Evaluate Drier Activity

Conventional methods used to determine drying time of oil or paint film often involved a drying time recorder [16]. Other methods for determining the activity of driers are included; for example, the measurement of viscosity change and sample weight increase over time [17] or more modern techniques such as ¹³C NMR [18], GC [9], HPLC [19], FTIR [20], and MS [21] have been used to study the effects of drier on the paint film. However, in this project finger touch method was employed for drying time study [22].

To have a blank sample, 1 kg of alkyd resin (60%) was mixed with calcium drier (5 g, 5% metal) and lead drier (5 g, 32% metal). Synthesized cobalt drier (3 or 6) (0.5 gr) was added to 100 g of prepared blank and stirred thoroughly to get homogeneous liquid. Then a layer of resin (100 micron) was applied on the glass and the touch drying time of resin was measured according to ISO 9117-6 procedure. The results of touch drying time were summarized in Table 1.

Table 1: Comparison of the effect of ligand on the activity of cobalt drier (3), and of 6.

Drier
(nm)
 mol⁻¹cm⁻¹
Drying (hr)
Explanation

Blank
—
—
>24
Cross-linking did not take place.

3
625
300
4
As reference.

6a
690
370
3
Electron donating of nitrogen increased the reactivity of cobalt.

6b
630
320
3
Resonance of electron pair of nitrogen with aromatic ring made aniline ineffective.

6c
626
305
4
Positive charge of nitrogen resulted from the coordination to cobalt made Et₃N unreactive.

6d
688
346
3
Electron donating of nitrogen increased the reactivity of cobalt.

6e
635
332
5
Electronegativity of oxygen decreased the nucleophilicity of the ligand.

6f
618
216
9
The stability of redox reaction products postponed the cross linking.

3. Results and Discussions

There are several methods for synthesis of metal alkanoates including metathesis reactions [23–25], ligand exchange reactions [7], and anodic dissolution of metal in alkanoic acid. In this project the reaction of CoSO₄ (1) with 2-EHA (2) in the presence of NaOH solution led to synthesis of cobalt octoate (3) (Scheme 1).

Scheme 1: Synthesis of cobalt octoate in NaOH solution.

In an alternative method, cobalt octoate (3) was synthesized via the reaction of Co(OH)₂ (4) and 2-EHA (2) in mineral spirit as solvent (Scheme 2).

Scheme 2: Synthesis of cobalt octoate in mineral spirit.

Comparison of drier production methods showed that solvent process was time consuming. In solution method, water was removed continuously using Dean-Stark, which could be used as an easy procedure for monitoring of the reaction progress. In solvent process, the product was homogeneous. Because of the lack of interfering by-product, there was no problem in production of insoluble salt.

In spite of difficulties of precipitation method such as filtration and elution, it benefited from some advantages. Solid content of drier was 100%, which not only made the transportation easier and safer, but also provided the ability to produce driers with high metal content.

To investigate effects of organic ligands on the reactivity of cobalt drier, some ligands (L-H, 5) were added to cobalt octoate (3) solution and refluxed at 150–160°C for 2 hrs (Scheme 3).

Scheme 3: Modification of cobalt octoate (3) by ligands (5).

Resulted modified driers (6) were added to alkyd resin, the drying time was measured according to finger touch method and results and some explanations were summarized in Table 1.

Comparison of behaviour and activity of ligands showed that amines, good electron donors, helped Co (II) to increase the rate of oxidation in unsaturated chains of alkyd resin. Aliphatic amine (5a) was more efficient than aromatic ones. Amine 3° was not suitable for this purpose because positive charge on nitrogen appeared as a result of attack of amine to cobalt (Scheme 4(a)).

Scheme 4: Effect of ligands on activity of Co²⁺.

Alcohols and amino alcohol were not efficient for this purpose either, because oxygen is more electronegative than nitrogen, so it does not have much nucleophilicity (Scheme 4(b)).

It seemed that Co (II) formed an unstable complex with oxime [26] and had not adequate tendency to react with polymer and delayed drying time (Scheme 4(c)).

Although various spectroscopic methods such as X-ray, crystallography, ¹H, 13C NMR, EPR, and UV-Vis spectra have been employed for identification and characterization of metal alkanoates, in this study, added ligands (5) changed the color of drier. So, UV-Vis spectrum was used to measure of drier (Table 1) [27]. Cobalt octoate had  nm and appropriate absorption ( mol⁻¹ cm⁻¹) in the visible region due to ⁴T₁  to ⁴T₂  transitions. The deep color of cobalt drier made it unsuitable for white paints. The visible spectrum of driers possessing oxime showed that the had shifted to shorter wave length (618 nm) and molar absorption coefficient had reduced ( mol⁻¹ cm⁻¹) in the visible region. The visible spectra patterns of the driers except aniline were the same as the blank drier and showed that unpaired electrons of nitrogen participated in resonance with the ring instead of coordinating to cobalt. Visible spectrum of the drier including ethyl amine or ethanol amine showed that coordination of amine to Co (II) made shifted to 690 and 688 nm, respectively, and caused an increase in the oxidizing ability of Co (II).

4. Conclusions

Comparison of drier production methods showed that selection of method depends on the raw materials, transportation, desire metal content of drier, and tendency to have a facility for production monitoring. Thanks to good electron releasing power of amines, they were the best choice for increasing the efficiency of driers.

Although modification of cobalt drier reduced the amount of cobalt consumption and consequently could help environmental protection, many efforts are essential to use environmentally friendly driers instead of cobalt drier.

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