Determination of Residual Chlorothalonil in Textiles

An effective method was established to determine the content of residual chlorothalonil in textiles by gas chromatography/mass spectrometry-selected ion monitoring coupled with ultrasonic extraction technique. Residual chlorothalonil in textiles was ultrasonically extracted using ethyl acetate as the extraction solvent. The extract was condensed and analyzed by gas chromato-graphy/mass spectrometry in selected ion monitoring mode (GC/MS-SIM). The concentration of chlorothalonil was calibrated by the external standard method. Good linearity existed between the peak area and the mass concentration of chlorothalonil in the mass concentration range from 0.2 μg/mL to 42.8 μg/mL. The equation was A = 95,399ρ − 50,848, with a correlation coefficient of 0.9999. The limit of detection was 0.1 mg/kg for chlorothalonil. The blank samples were spiked at three concentration levels, and the spiked average recoveries changed from 81.9% to 95.4% while the relative standard devi-ation (RSD) changed from 1.8% to 5.2%. The proposed method was simple, rapid, sensitive and the limit of detection could meet the limit requirements of relevant regulations. Commercially available textiles were measured by this method, and chlorothalonil at different concentration levels was detected in some samples.


Introduction
Chlorothalonil is a broad-spectrum and high-efficiency agricultural fungicide. Chlorothalonil interacts with glyceraldehyde triphosphate dehydrogenase in fungal cells and binds to cysteine-containing proteins in the enzyme, thereby destroying the activity of the enzyme. Therefore, the metabolism of fungal cells is destroyed and loses vitality [1]. Chlorothalonil has good bactericidal properties against fungi such as Ascomycetes, Basidiomycetes, and Deuteromycetes. Chlorothalonil is widely used in the United States, France, China, Brazil, and Japan.
Chlorothalonil is widely used as a fruit preservative and insecticide in agriculture, and is used as an antifungal agent for leather, paint, paper and cloth in industry [2] [3]. However, chlorothalonil is a strong allergen that can cause delayed allergic dermatitis [4]. Chlorothalonil is listed in the list of Class  [5]. The content of chlorothalonil in samples such as leather, food, environmental samples, paints and et al. can be determined by liquid chromatography, gas chromatography, gas chromatography-mass spectrometry, etc. [6]- [14], but no literature has been reported on the determination of residual chlorothalonil in textiles. In this paper, residual chlorothalonil in textiles was first ultrasonically extracted using ethyl acetate as the extraction solvents and the extract was then determined by GC/MS-SIM technique.

Experimental
Chlorothalonil standard (purity 99.0%) was purchased from Dr. Ehrenstorfer GmbH, Germany. Chromatographic pure methanol was purchased from Fisher Scientific, Pittsburgh, Pennsylvania, USA. Chlorothalonil was first dissolved in chromatographic pure methanol to prepare a standard stock solution with a mass concentration of 428 μg/ml, then diluted with methanol to prepare a series of standard working solutions whose mass concentration was 42. 8 Four positive samples were prepared through impregnation-baking technique.
Chlorothalonil powder purchased from Sichuan Runer Technology Co., Ltd. was dissolved in water to obtain a high concentration aqueous solution of chlorothalonil. Polyerster lining cloth, nylon lining cloth, cotton lining cloth and wool lining cloth were selected to be blank substrates. They were first dipped into the aqueous solution of chlorothalonil for two days. They were then washed completely by water and dried. Therefore, four positive samples (sample 1#: polyester, sample 2#: nylon, 3#: cotton, 4#: wool) with different concentration levels of chlorothalonil were prepared.
The samples were cut into 5 mm × 5 mm pieces by QYB-3 automatic sample preparation machine purchased from Zhongshan Qiyuan Machinery Technology Co. Ltd., China Accurately weigh 1.0 g of the sample and placed in a 35 mL glass reaction flask containing 30 mL of ethyl acetate. The sample was ultrasonically extracted at 45˚C for 35 min. The extract was then filtered to a chicken heart bottle and evaporated to near dryness in a Heidolph 4003 rotary evaporator purchased from Heidolph, Germany. The chicken heart bottle was trans-ferred to an N-Evap 112 nitrogen blowing apparatus purchased from Organomation Associates USA and slowly dried with dry nitrogen. The residue was dissolved in 1mL of methanol, and the resulting solution was filtered used 0.45 μm filtering membrane purchased from CNW Technologist Co. Germany.
Analysis was carried out with an Agilent 6890A-7000B triple quadrupole gas chromatography/mass spectrometry supplied by Agilent USA. Chromatographic separation was performed on a DB-5MS column (30 m × 0.25 mm × 0.25 μm) supplied by Agilent USA with an initial temperature of 90˚C. The temperature raised to 290˚C at the rate of 40˚C/min after maintained for 1 min at the initial temperature and then maintained for 2min at 290˚C. The carrier gas was high purity helium (purity > 99.999%) and the carrier gas flow rate was 1 mL/min. The sample was injected in splitless mode and the injection volume was 1 μl. The inlet temperature, the transmission line temperature and the ion source temperature was 270˚C, 280˚C and 290˚C, respectively. The ionization mode was EI and the ionization energy was 70 eV. The qualitative analysis was carried out in full scan mode and the qualitative ion was m/z 264, m/z 268, and m/z 109. The quantitative analysis was carried out in selected ion monitoring mode and the quantitative ion was m/z 266.

Optimization of Analysis Conditions
The intensity of the mass spectrometry signal in splitless injection mode was affected by the inlet temperature (factor A), ion source temperature (factor B), and carrier gas flow rate (factor C). The effects of these three factors on the intensity of the mass spectrometry signal were first investigated separately. The results showed that the peak area of chlorothalonil reached the maximum when the inlet temperature was 260˚C or the ion source temperature was 280˚C or the carrier gas flow rate was 1.2 ml, respectively. Therefore, the orthogonal experiment was carried out according to the conditions in Table 1. The peak area under the nine experimental conditions was determined, and the k value and the maximum difference of each factor were calculated, thus the optimal scheme was given out, as shown in Table 1. It could be seen from the data in Table 1 that the factor A had the largest maximum difference and the factor B had the smallest maximum difference. Therefore, the factor that had the greatest impact on the peak area was the inlet temperature (factor A), followed by the carrier gas flow rate (factor C) and the ion source temperature (factor B). Through the orthogonal experiment, it was determined that the optimal scheme is A 3 B 3 C 2 , that is to say, the 9 th condition in Table 1

Optimization of Ultrasonic Extraction Conditions
The ultrasonic extraction efficiency depended on four factors such as the type of   extraction solvent, extraction temperature (factor A), extraction time (factor B), and extraction solvent volume (factor C). In order to investigate the effect of Factor A, Factor B and Factor C on the extraction amount, four self-made positive samples were ultrasonically extracted with acetone as the extraction solvent.
In each experiment, only one factor changed while the other two factors remained the same. The results showed that the extraction amount reached the maximum when the extraction time was 30 min for sample 1# and sample 2# while the extraction amount reached the maximum when the extraction time was 35 min for sample 3# and sample 4#. The extraction amount reached the maximum when the extraction temperature was 35˚C for sample 2# and 40˚C for sample 1#, sample 3# and sample 4#. The extraction amount reached the maximum when the volume of the extraction solvent was 20 ml, 30 ml, 20 ml and 25 ml for sample 1#, sample 2#, sample 3# and sample 4#, respectively. In order to investigate the combined effects of these three factors on the extraction amount, an orthogonal experiment was designed according to Table 2. Four self-made positive samples were tested under each condition using acetone as the extraction solvent, and the extraction amounts were listed in Table 2. The k value and the maximum difference of each factor were calculated according to data in Table 2 to give out the optimal scheme as shown in Table 3. The results showed that the optimal schemes of sample 1#, sample 2#, sample 3# and sample 4# were A 3 B 3 C 3 , A 3 B 2 C 3 , A 3 B 3 C 3 , and A 3 B 3 C 1 , respectively. Taking all factors into consideration, the final optimal scheme was A 3 B 3 C 3 , that is to say, the extraction temperature, extraction time and extraction solvent volume were 45˚C, 35 min, and 30 ml, respectively. Under the ultrasonic extraction conditions mentioned above, four self-made positive samples were ultrasonically extracted using common solvents such as ethyl acetate, acetone, n-hexane, methanol, ethanol, acetonitrile, dichloromethane, petroleum ether, t-butyl methyl ether, ethyl acetate/dichloromethane (1:1, V/V) and n-hexane/acetone (1:1, V/V) as the extraction solvents. The extraction results were shown in Table 4. Samples of different materials had different optimal extraction solvents. The optimal extraction solvent was ethyl acetate for sample 1# and sample 3# whose substrate was polyester and   cotton, respectively. The optimal extraction solvent was dichloromethane and ethanol for sample 2# and sample 4#, respectively whose substrate was nylon and wool, respectively. In order to ensure that the final optimal extraction solvent had a good extraction effect on all samples, the solvent with the largest total extraction amount was selected as the final optimal extraction solvent. According to the data in Table 4, the total extraction amount reached the largest when ethyl acetate was used as the extraction solvent. Therefore, the ultrasonic extraction conditions were finally optimized as follows: 30 ml of ethyl acetate was used as the extraction solvent, the extraction temperature was 45˚C, and the extraction time was 35 min.

Linearity and Limit of Detection
The sensitivity was tested by analyzing a series of standard working solution. Linear calibration curve was studied by plotting the pear areas against the mass concentrations of chlorothalonil. Excellent linearity was found over the range of 0.2 μg/ml to 42.8 μg/ml for chlorothalonil and the correlation coefficient was 0.9999. The limit of detection (LOD) was taken when the ratio of signal to noise (S/N) was three and the limit of detection (LOD) was 0.1 mg/kg for chlorothalonil.

Recoveries and Precision Studies
Three levels (1.1 μg, 5.4 μg and 21.4 μg) of chlorothalonil were added to polyester lining cloth, nylon lining cloth, cotton lining cloth and wool lining cloth, which originally contained no chlorothalonil. The spiked average recoveries and the relative standard deviations (RSDs) of nine replicate measurements were determined as shown in Table 5. The spiked average recoveries ranged from 81.9% to 95.4% while the relative standard deviations (RSDs) varied from 1.8% to 5.2%. The inner-day and inter-day RSDs were used to examine the repeatability of the proposed method. Inner-day precision was evaluated using nine injection containing chlorothalonil at 5.4 μg/ml in 1 day while inter-day precision was assessed using nine determinations containing chlorothalonil at 5.4 μg/ml on different days. The inner-day and inter-day precision (n = 9) for chlorothalonil was 2.5% and 3.9%, respectively, which could be considered acceptable. This result demonstrated that no significant influence of the chlorothalonil stability on the experimental results was found during sample preparation and GC/MS-SIM determination.

Analysis of Commercial Textile Samples
To evaluate the applicability of the proposed method, the contents of residual chlorothalonil in 157 commercial textile samples were determined using the previous described procedure. Quantification was based on the external standard

Conclusion
An effective method was established to determine the content of residual chlorothalonil in textiles using gas chromatography/mass spectrometry in selected ion monitoring mode, coupled with ultrasonic extraction technique. A good  C. Y. Wang et al. linearity existed between the peak area and the mass concentration of chlorothalonil in the mass concentration from 0.2 μg/ml to 42.8 μg/ml. The proposed method was simple, rapid and sensitive. The limit of detection was as low as 0.1 mg/kg, far lower than the requirements of relevant regulations. The proposed method was applied in the routine analysis of chlorothalonil in commercially available textiles and chlorothalonil was detected in some of the samples.