3 research outputs found

    Distribution of pesticides in different commonly grown vegetables of Cameron Highlands, Pahang, Malaysia

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    Gas chromatography-electron capture detector (GC-ECD) is used to extract and analyse pesticides in vegetable samples collected from Cameron Highlands, Pahang, Malaysia. The limit of detection (LOD) for all pesticides was in the range of 0.03 to 4.5 ng g-1. Recoveries in cabbage, lettuce, and celery ranged from 61.8%-121%, 60-128% and 60%-114%, respectively. The relative standard deviation (RSD) ranged 0.2-15% in cabbage, 0.5-18% in lettuce and 3-19.8% in celery. Organochlorine pesticides (OCPs) concentrations increased down the valley with dichlorodiphenyldichloroethylene (DDE) having the highest concentration at 233 μg kg-1. Organophosphorus pesticides (OPPs) were found to be dispersed throughout the valley, with the highest concentration of parathion ethyl (133 μg kg-1) whereas the pyrethroid pesticides (PYRs) concentrations were comparatively less. The detection frequency in the wet season was highest (5 < - < 100 μg kg-1) for most pesticides. However, in the dry season the pesticides concentrations were higher, at < 5 μg kg-1. PCA analysis indicated that farmers were using a mixture of pesticides

    Development of Flow Injection Spectrophotometric Method for 1-Napthylthiourea Using Sodium Nitrite and Sulphanilic Acid Diazotization Reaction

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    A simple spectrophotometric method in conjunction with flow injection analysis is developed for the quantitative analysis of 1-napthylthiourea (ANTU). The reaction is based on the alkaline hydrolysis of ANTU to 1-naphthylamine at 30°C, coupled with diazotized sulphanilic acid resulting in 4-(sulphophenylazo)-1-naphthylamine which is monitored at 495 nm. The limit of detection (S/N = 3) is 0.01 mg/L with a sampling throughput of 45/h. The method is linear over the range of 0.05–120 mg/L (R2=0.9995,n=7), with calibration equation y = 0.031x−0.018 (y = absorbance; x = mg/L) and relative standard deviation (n=3) 1.8–3.6%. Experimental variables are optimised, and the interfering effects of different pesticides, organic compounds, cations, and anions at environmentally relevant concentrations are investigated. The analysis of ANTU in spiked water samples is extracted with solid phase procedure using disposable Sep-Pak C18 cartridges, and the recovery was 93 ± 1.9–110 ± 3.0%. The results of the proposed method are compared with the HPLC method by applying the F-test and paired Student t-test at 95% confidence level
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