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H Zainal

Publications and source records attributed to H Zainal.

3 recordsLinked to original sources

Nitrile glove permeation of benomyl.

The aim of this study was to investigate permeation of the fungicide benomyl at its highest field application concentration (0.70 mg/mL) in Benlate 50 WP aqueous solution (1.4 mg/mL) through two types of unsupported and unlined nitrile gloves--a disposable latex glove (Safeskin) and an industrial chemical-resistant glove (Solvex)--using an American Society for Testing and Materials (ATSM)-type permeation cell with isopropanol collection medium. The permeation cell was contained in a moving-tray water bath at 30.0 degrees C +/- 0.5 degrees C. The collection medium was evaporated and the residue derivatized with an optimized method (2,3,4,5,6-pentafluoro)benzyl bromide to form the disubstituted derivative of carbendazim (CARB), CARB.2PFB. The latter in isooctane was then quantified by gas chromatography- 63Ni-electron capture detection (GC-ECD) by the internal standard method. GC-ECD, GC-mass spectrometry (GC-MS), and reflectance infrared investigations showed that little degradation of benomyl occurred in the challenge solution of aqueous Benlate during an 8-hour exposure period. Benomyl was collected as a mixture of CARB and benomyl as shown by the presence of a diagnostic chromatographic peak identified by GC-MS. The amounts permeated during the same time period were always higher for Safeskin than for Solvex gloves, with the latter being approximately 18 times more protective than the former after 8 hours of continuous exposure. Although the Solvex gloves were safe to wear at least for 4 hours and for almost 8 hours, the ASTM breakthrough threshold was used as reference and thus ignored carcinogenic effects. Reflectance infrared investigations detected benomyl and CARB on the glove challenge surface after drying and confirmed that the cleaned glove surfaces after permeation experiments did not differ in infrared reflectance spectra from the corresponding surfaces just before the permeation experiments.

Benomyl↗

Folpet permeation through nitrile gloves.

The aim of this study was to investigate whether two different brands of unsupported and unlined nitrile gloves protected against aqueous emulsions of a Folpet wettable powder (50% Folpet) using an ASTM type-I-PTC 600 permeation cell at 30.0 +/- 0.1 degrees C held in a shaking water bath. An analytical method to determine Folpet using the internal standard method was first developed based on gas chromatography-mass spectrometry (GC-MS), and gas chromatography-electron capture detection (GC-ECD). A novel pyrolysis GC-ECD technique that quantified the thermal degradation product phthalimide had pg sensitivity suitable to detect the trace amounts of Folpet that permeated. The on-column conversion was (68.0 +/- 9.5) percent at 170 degrees C over the folpet injected mass range of 3 to 148 pg. The challenge solution in the permeation cell was 1.4 mg/mL aqueous emulsion of Folpet wettable powder, and 2-propanol was the collection solvent. After evaporation of the collection solvent, the time weighted average rate of permeation of Folpet through SafeSkin nitrile (an exams type of glove) after 8 hours was (42.1 +/- 2.9) ng/cm(2)/min compared with (2.04 +/- 0.69) ng/cm(2)/min for the Sol-Vex nitrile (industrial chemical resistant), the latter being about 21 times more protective and also near the limits of detection. The respective values after 4 hours of exposure were (28.4 +/- 1.2) and (0.65 +/- 0.36) ng/cm(2)/min. Diagnostic reflectance infrared minima of both challenge and collection sides of the gloves showed small changes in wave number and intensity values after 8 hours of exposure, with Folpet being detected in dried spots on the challenge side. GC-ECD-based permeation and IR reflectance data indicated high chemical resistance of the Sol-Vex gloves to an aqueous emulsion of Folpet.

Chromatography, Gas↗

Selenomethionine content of candidate reference materials.

Selenium has been identified as an antioxidant of importance in the diet. Accurate determination of its chemical forms depends on the availability of suitable reference materials (RMs). Two candidate reference materials for determination of selenomethionine (Semet) in food-related materials, a standard wheat gluten sample (NIST RM 8418 Wheat Gluten) and a commercial selenium enriched yeast, have been examined by use of a gas chromatography-isotope dilution mass spectrometry (IDMS) procedure, after treatment of the matrix with 0.1 mol L(-1) hydrochloric acid containing stannous chloride, addition of CNBr, and extraction with chloroform. This procedure results in cleavage of the CH3Se group to form volatile CH3SeCN. Addition of isotopically enriched 74Semet to an analytical sample enables estimation of the naturally occurring protein-bound 80Semet by IDMS without a protein-digestion process. We found that the Wheat Gluten RM contains a significant amount of Semet as a portion of its assigned value of 2.58 microg Se(total g(-1). Commercial selenium yeast tablets are labeled as containing an elevated level of "organic selenium", usually as Semet. The sample we investigated contained 210 microg Se(total) g(-1) sample as determined separately by IDMS, measuring elemental selenium after digestion. 73% of this total (153 +/- 21 microg Se(semet) g(-1); n = 23) was present as Semet. Thus, these two materials contain significant amounts of their total selenium content as Semet and would be good candidates for further study and characterization as reference materials for determining this important food component. The CNBr reaction used will also enable the determination of Se-(methyl)selenocysteine, the biological role of which is of recent interest. In addition to matrix RMs for Semet, it is important to have standard materials of the pure substance. We have examined a sample of a candidate standard material of selenomethionine being prepared by the USP. It was confirmed that this material is pure selenomethionine.

Cold Temperature↗