全自动凯氏定氮仪测定化肥中的含氮量

建立全自动凯氏定氮仪检测化肥中氮含量的分析方法。称取总氮量在0.03~0.3 g范围的样品,经消解仪消解及全自动凯氏定氮仪碱化蒸馏,以硼酸为接收液,用0.15~0.20 mol/L的盐酸标准溶液进行自动滴定。该方法加标回收率为99.0%~101.5%,测定结果的相对标准偏差小于1.0%(n=6)。与国标GB/T 8527–2010法测定结果无显著性差异,全自动凯式定氮仪法的准确度、精密度均优于国标方法,而且所用试剂少、分析时间短,满足实验室快速检测大批量化肥中含氮量的需要。     

Flow injection conductometric system with gas diffusion separation for the determination of Kjeldahl nitrogen in milk and chicken meat

A simple flow injection (FI) conductometric system with gas diffusion separation was developed for the determination of Kjeldahl nitrogen (or proteins) in milk and chicken meat. The sample was digested according to the Kjeldahl standard method and the digest was diluted and directly injected into the donor stream consisting of 4 M NaOH. In alkaline medium, ammonium was converted to ammonia, which diffused through the PTFE membrane to dissolve in an acceptor stream (water). Dissociation of ammonia caused a change in conductance of the acceptor solution, which was linearly proportional to the concentration of ammonium originally present in the injected solution. A conductometric flow through cell and an amplifier circuit was fabricated, which helped improve sensitivity of the conductometric detection system. With using a plumbing Teflon tape as a gas diffusion membrane and without thermostating control of the system, a linear calibration graph in range of 10-100 mg L⁻¹ N-NH₄ was obtained, with detection limit of 1 mg L⁻¹ and good precision (relative standard deviation of 0.3% for 11 replicate injections of 50 mg L⁻¹ N-NH₄). The developed method was validated by the standard Kjeldahl distillation/titration method for the analysis of milk and chicken meat samples. The proposed system had sample throughput of 35 h⁻¹ and consumed much smaller amounts of chemical than the standard method (275 mg vs 17.5 g of NaOH per analysis, respectively).     

Rapid coulometric method for the Kjeldahl determination of nitrogen

A rapid coulometric method for the Kjeldahl determination of nitrogen is described. The samples are digested by means of the Tecator AB digestion system which permits forty samples to be digested at the same time. The digestion products are diluted to 75 ml and 1 ml is coulometrically titrated in 1-2 min: 20-30 determinations can be performed per hour. For substances containing nitrogen in the per cent range the relative standard deviations for eight different substances were 0.1-1%.     

Flow-injection determination of ammonia in kjeldahl digests by gas diffusion and conductometry

A flow injection/conductometric method is proposed for determing ammonia in solutions obtained from Kjeldahl digestion. The method is based on diffusion of ammonia through a PTFE membrane from an alkaline (NaOH/EDTA) medium to a deionized water stream. The change in conductance of the deionized water stream is proportional to the ammonia concentration present in the digest. The effects of flow parameters, temperature and potential interferences are reported. Approximately 100 samples can be injected per hour; the precision is about 1%. Results for total nitrogen in vegetable tissues, animal feeds and fertilizers are in good agreement with those obtained by the usual distillation/titration method.     

Fast neutron activation: Sample preparation utilizing graphite as a diluent

A method has been developed for the preparation of irradiation samples which ensures that both standard and unknown samples are of the same size, shape, density and composition. Powdered standard and unknown samples were diluted with graphite to give homogeneous mixtures containing ≥80% graphite; these mixtures were pressed into cylindrical pellets. This method of sample preparation has been applied to the determination of nitrogen in organic and polymeric compounds. The results generally agree with Kjeldahl analyses within 5%. This work was supported by the United States Atomic Energy Commission.     

Determination of ammonium in Kjeldahl digests by gas-diffusion flow-injection analysis with a bulk acoustic wave-impedance sensor

A novel flow-injection analysis (FIA) system has been developed for the rapid and direct determination of ammonium in Kjeldahl digests. The method is based on diffusion of ammonia across a PTFE gas-permeable membrane from an alkaline (NaOH/EDTA) stream into a stream of diluted boric acid. The trapped ammonium in the acceptor is determined on line by a bulk acoustic wave (BAW)-impedance sensor and the signal is proportional to the ammonium concentration present in the digests. The proposed system exhibits a favorable frequency response to 5.0 x 10(-6)-4.0 x 10(-3) mol l(-1) ammonium with a detection limit of 1.0 x 10(-6) mol l(-1), and the precision was better than 1% (RSD) for 0.025-1.0 mM ammonium at a through-put of 45-50 samples h(-1). Results obtained for nitrogen determination in amino acids and for proteins determination in blood products are in good agreement with those obtained by the conventional distillation/titration method, respectively. The effects of composition of acceptor stream, cell constant of conductivity electrode, sample volume, flow rates and potential interferents on the FIA signals were discussed in detail.     

A microscale Kjeldahl nitrogen determination for environmental waters

A microscale Kjeldahl system has been designed which has been homemade reduced. The digestor unit of a macroKjeldahl system and a modified glassware microdistillation unit have been used. The optimal conditions for digestion and distillation have been established for ammonium and methylamine as model compound of organic amino nitrogen. The optimised procedure has been applied to the determination of Kjeldahl nitrogen in water samples. Recoveries near 100% and good precision have been achieved. This procedure combines nitrogen miniaturized system and the use of a selective ion electrode for ammonia detection. The analysis time was reduced 4.8 times and the analysis cost 6.6 times compared with classical procedure. The residues generated have been also markedly minimized. A preconcentration factor of 4 instead of 1.5 obtained by the macroscale design has been achieved.     

Rapid estimation of global sugars by UV photodegradation and UV spectrophotometry

The UV/UV method developed for the measurement of specific wastewater pollution parameters (ammonium, Kjeldahl nitrogen, total phosphorus) is adapted to the determination of sugars in fruit juices and soft drinks. The procedure is based on the UV spectrophotometric detection of by-products of UV photodegradation of carbohydrates. Time of analysis is greatly reduced by using specific pH conditions and diluted samples.     

Improved diffusion methods for nitrogen and 15nitrogen analysis of Kjeldahl digests

Simple methods are described that permit the use of either H3BO3 indicator solution or acidified filter disks to collect NH3 liberated by treatment of Kjeldahl digests with NaOH. These methods incorporate modifications to improve reliability, analytical capacity, and convenience. A semimicro digest was diluted to 25 mL with deionized water, and a 10 mL aliquot, containing up to 4 mg N (150 microg N for diffusions into acidified disks), was transferred to a shell vial, which was placed inside a 473 mL (1 pint) Mason jar containing 10 mL 10N NaOH. The NH3 liberated by overturning the vial was collected after 12 to 48 h at ambient temperature, or after 4 h at 45 to 50 degrees C on a hotplate, for quantitative and/or isotope-ratio analyses. With either H3BO3 indicator solution or acidified filter disks, recovery of diffused N was quantitative. Isotope-ratio analyses of diffused N from 15N-labeled chemical, plant, and soil samples were within 3% of analyses using steam distillation.     

Optimisation of focused-microwave assisted digestion procedure for Kjeldahl nitrogen determination in bean samples by factorial design and Doehlert design

In the present paper a focused-microwave Kjeldahl digestion procedure without metal catalyst for nitrogen determination in bean samples was developed. Temperature at which the decomposition plateau occurs, mass of potassium sulphate and either volume of sulphuric acid or hydrogen peroxide were optimised. Results of the two-level full factorial design (2⁴) based on an analysis of variance demonstrated that only the decomposition plateau temperature and the sulphuric acid volume were statistically significant. Optimal conditions for the digestion of bean samples were obtained by using Doehlert design. The modified digestion procedure of 0.25 g of bean samples has been performed in 27 min at optimised conditions. The accuracy of the developed procedure by the analysis of the two certified reference materials, peach leaves (NIST 1547) and apple leaves (NIST 1515). The t-test applied to the results revealed that they are in agreement (p > 0.05) with the certified values. The precision, expressed as relative standard deviation (R.S.D.) was of 0.96% for four successive Kjeldahl nitrogen determinations. In addition, interlaboratory exercises were performed with several bean samples in reference Brazilian food control laboratory.     

全自动凯氏定氮仪在测定干旱区土壤中全氮量的研究

本实验采用了UDK159全自动凯氏定氮仪对干旱区土壤全氮量的方法以及试验部分影响因素进行研究,结果表明：精密度试验中RSD在0.01919%～0.1073%之间(≤1%),用标准物质硫酸铵进行回收率检验,其回收率达99.5% 以上,检测准确度和精密度都符合国家标准的要求;在消化时间的选择上,变异系数为0.0088,表明土壤中有机物在30 min时已完全消化;而关于硫酸用量在10~15mL时为最佳值,干旱区土壤中氮一般含量为(0.260±0.003) %(P =0.95)。     

Repeatability and reproducibility of determination of the nitrogen content of fishmeal by the combustion (Dumas) method and comparison with the Kjeldahl method: interlaboratory study

Ten fishmeal samples (hidden duplicates of 4 meals plus 2 high-protein meals as a Youden pair), tryptophan, and nicotinic acid were analyzed by 18 laboratories using the Dumas method. Thirteen of the laboratories also analyzed the same 12 samples using their current Kjeldahl method. Recoveries (+/-SR) of tryptophan and nicotinic acid were 99.3+/-1.04 and 98.8+/-2.11% by Dumas and 97.1+/-3.03 and 74.6+/-26.76% by Kjeldahl. The Dumas method gave significantly greater values (P < 0.001) than the Kjeldahl method. For fishmeals, Kjeldahl N = 0.989 of Dumas N (P < 0.001). A similar proportionate difference (0.984 of Dumas N) was observed with tryptophan. Most laboratories failed to determine nicotinic acid correctly by Kjeldahl. For fishmeals, the relative standard deviations for repeatability and reproducibility were for Dumas 1.48 and 2.01% and Kjeldahl 1.62 and 2.37%, respectively. A single analysis conducted in 2 laboratories should not differ by more than 5.63% of the mean value when measured by Dumas or by more than 6.64% by Kjeldahl. It is concluded that with fishmeal, Dumas gives a more reliable measure of organic nitrogen than Kjeldahl, and, therefore, Dumas should be the method of choice.     

Measurement of protein in serum and rodent embryos by spectrophotometry at 215 and 225 nm

The Waddell quantitative method for total protein estimation was slightly modified and applied to sera and rodent embryos, and also compared to the Lowry method. It was not necessary to employ the Kjeldahl method to determine an instrument correction factor; reference sera were used to establish a standard curve. The results from this simplified Waddell method were reproducible from day to day with a high degree of accuracy. Comparative data obtained by total protein determination in three commercially available reference sera demonstrated a sensitivity in the modified Waddell method of 4.8 μg/ml with a precision of >96% and an accuracy of >93%. The overall precision in the determination of the total protein by the method in Day 12 rat embryos was >91% as compared to >86% in the Lowry method.     

Standard-addition determination of nitrogen in coal with an ammonia-sensitive electrode

After semimicro Kjeldahl digestion of the coal sample with a K(2)SO(4)-V(2)O(5)-Se catalyst and sulphuric acid, the digest is cooled, diluted with water, neutralized and then made alkaline with NaOH/EDTA solution. The ammonia thus formed is determined by measuring the potential of a properly conditioned ammonia-sensitive electrode containing an appropriate filling solution; a gravimetric standard-addition technique is used. Known additions of 1-2 mug of N per g to blank solutions enables all measurements of potential to be made in the linear region of the electrode-response curve. The electrode measurement procedure gives blank-corrected recoveries of between 99.0 and 101.0% for synthetic sample solutions. Results obtained for nitrogen in reference coal samples by the electrode procedure have been found to agree well with those obtained by other methods.     

Determination of phosphorous in organic compounds and metal complexes by inductively-coupled plasma atomic emission spectrometry

Phosphorus is determined by inductively-coupled plasma atomic emission spectrometry at 213.618 nm. Different types of organic and inorganic phosphorus compounds and metal complexes were examined after direct dissolution in water, aqueous ethanol or acid, or after decomposition by oxygen flask combustion or Kjeldahl digestion; results were within the usual limit of precision and accuracy for such determinations. The effect of small (<20%) ethanol concentrations in the aqueous solution on the signals obtained from a low-power (1200 W) argon plasma is examined and discussed.     

Rapid method for determination of protein content in cereals and oilseeds: validation, measurement uncertainty and comparison with the Kjeldahl method

The objective of this research was to test suitability of the Dumas combustion method to completely substitute the Kjeldahl method in routine laboratory determination of crude protein content in cereals and oilseeds. The validation of the method demonstrated that it is able to determine crude protein content in cereals and oilseeds in an efficient and accurate manner, with a detection limit w(N) = 0.006%, quantification limit w(N) = 0.019%, repeatability precision RSD _r = 0.41%, intra-laboratory reproducibility precision RSD _R = 0.74%, trueness, expressed in terms of bias b = 0.43%, and linear response between (2.36–19.2) mg N. Measurement uncertainty, expressed as relative expanded uncertainty (coverage factor k = 2, confidence level 95%), was calculated from validation data (U _rel = 2.24%). In order to examine the relationship between two methods, 15 cereal grain and oilseed samples were analyzed using Dumas and Kjeldahl procedure. The Kjeldahl procedure gave slightly lower w(N) values than the Dumas procedure: w _K(N) = 0.9905 w _D(N) = 0.0376 (R ²  = 0.9996). Relative standard deviations and results of homogeneity test obtained during analysis of complex cereal products (cereal breakfast and muesli bars) show that the Dumas combustion method may be less suitable for analysis of such samples compared to Kjeldahl method.     

Lead in micro-samples of whole blood by Rhenium-cup in-torch vaporization-inductively coupled plasma-atomic emission spectrometry (ITV-ICP-AES)

A method is described for screening of lead in diluted micro-samples of whole blood by a Re-cup, in-torch vaporization (ITV) sample introduction system for inductively coupled plasma-atomic emission spectrometry (ICP-AES). The method required minimum sample preparation. For example, blood was diluted with water and Triton X-100 in 0.5% HNO3 and, 5 microL were deposited on the Re-cup of the ITV sample introduction system. Samples were dried and charred in-situ prior to vaporization. Levels 1, 2, 3 and 4 (Pb concentration: 4.04, 10.3, 20.59 and 39.36 microg/dL) of NIST Standard Reference Material 955b 'lead in bovine blood' were used to test accuracy and precision. Accuracy was acceptable and precision was below 10% for levels 2-4 and 15% for level 1.     

Uncertainty of nitrogen determination by the Kjeldahl method

 The uncertainty of the Kjeldahl method for determination of nitrogen in insulin was evaluated according the procedure described in the Guide to the Expression of Uncertainty in Measurement. The relative standard uncertainty of the method was found to be 0.19%, compared to the relative intermediate precision experimentally found to be 0.085%. The uncertainty components were organized in Tables, which allowed an easy overview and evaluation. The largest contribution to the uncertainty came from volumetric equipment. Systematic uncertainty budgets such as the design presented here facilitate the uncertainty evaluation process and makes it easier to compare uncertainty evaluations performed by different analysts. Received: 5 April 1999 / Accepted: 31 August 1999     

Chemical stability of midazolam injection by high performance liquid chromatography

The chemical stability of midazolam hydrochloride injection, undiluted or diluted with dextrose sterile solution, was studied at different storage conditions by LC. The study was performed at room temperature (23 +/- 2 degrees C) under light exposure and light protection, +8 +/- 1 degrees C and -20 +/- 0.5 degrees C, in glass and plastic containers over 14 days with midazolam hydrochloride injection, undiluted or diluted with 5% dextrose sterile solution. Chromatographic separation was carried out on a RP-18(e) column, using a mobile phase consisting of ACN-phosphate buffer (pH 3.3; 0.1 M) (30:70 v/v) at a flow rate of 1.0 mL/min and UV detection at 220 nm. The concentrations of all samples remained greater than 90% of the original concentration. The chromatographic assay exhibited an adequate linearity (r(2) >0.999), selectivity, precision (RSD <3.1), and accuracy (recoveries from 100.46 to 101.40%). Injectable midazolam hydrochloride was chemically stable in all conditions that were studied.     

Semimicro spectrophotometric determination of nitroglycerine in propellants by use of 2,4-xylenol

A semimicro spectrophotometric method using 2,4-xylenol is proposed for the determination of nitroglycerine in propellants. The propellant is extracted with methylene chloride, the extract is diluted, and a 10-ml aliquot is evaporated just to dryness. Then 2,4-xylenol reagent and 63% v/v sulphuric acid are added to hydrolyse the nitroglycerine to nitrate and form 6-nitro-2,4-xylenol which is steam-distilled in a Parnas-Wagner Kjeldahl distillation apparatus into a water-ammonia-isopropyl alcohol mixture. The absorbance of the yellow solution of the anion of the 6-nitro-2,4-xylenol is measured. The calibration curve is prepared from potassium nitrate and an empirical factor (5.50) is used to convert from nitrogen content to nitroglycerine (the theoretical factor is 5.40). The 2,4-xylenol should be added before the sulphuric acid in order to prevent interference from diphenylamine and ethyl centralite. The method is designed for the usual nitrocellulose double-base propellants containing 8-50% of nitroglycerine.