ANSI T 282 OM-2013 Hexeneuronic acid content of chemical pulp.pdf

1、 TAPPI/ANSI T 282 om-13 PROVISIONAL METHOD 2007 REVISED AND UPGRADED TO OFFICIAL METHOD 2013 2013 TAPPI The information and data contained in this document were prepared by a technical committee of the Association. The committee and the Association assume no liability or responsibility in connection

2、 with the use of such information or data, including but not limited to any liability under patent, copyright, or trade secret laws. The user is responsible for determining that this document is the most recent edition published. Approved by the Standard Specific Interest Group for this Test Method

3、TAPPI CAUTION: This Test Method may include safety precautions which are believed to be appropriate at the time of publication of the method. The intent of these is to alert the user of the method to safety issues related to such use. The user is responsible for determining that the safety precautio

4、ns are complete and are appropriate to their use of the method, and for ensuring that suitable safety practices have not changed since publication of the method. This method may require the use, disposal, or both, of chemicals which may present serious health hazards to humans. Procedures for the ha

5、ndling of such substances are set forth on Material Safety Data Sheets which must be developed by all manufacturers and importers of potentially hazardous chemicals and maintained by all distributors of potentially hazardous chemicals. Prior to the use of this method, the user must determine whether

6、 any of the chemicals to be used or disposed of are potentially hazardous and, if so, must follow strictly the procedures specified by both the manufacturer, as well as local, state, and federal authorities for safe use and disposal of these chemicals. Hexeneuronic acid content of chemical pulp 1. S

7、cope This method describes a procedure to determine hexeneuronic acid groups (HexA) in chemical pulps. HexA affects the kappa number determination by reaction with permanganate, and can react with certain bleaching chemicals, e.g. chlorine dioxide and ozone, but not with some others such as oxygen a

8、nd peroxide. 2. Summary The method is based on the highly selective hydrolysis of HexA from a pulp sample in a mercuric chloride-sodium acetate solution. Complete hydrolysis of HexA from pulps is achieved within 30 minutes by choosing the appropriate hydrolysis conditions (the concentration of the h

9、ydrolysis agent and the composition of the hydrolysis solution) and temperature. The amount of HexA is directly determined by UV spectrophotometry from the resulting hydrolysis solution (1). A dual-wavelength spectroscopic technique (at 260 and 290 nm) is used to eliminate the spectral interference

10、from the leached lignin in the resulting solution. 3. Significance The presence of the HexA increases chlorine dioxide consumption in chlorine dioxide bleaching. It also causes overestimation of the residual lignin in pulps, which could lead to over dosage of peroxide in peroxide bleaching. Even a s

11、mall amount of HexA can bond with transition metals and reduce pulp brightness stability. These effects are more significant for hardwood chemical pulps. Because pulping temperature and alkaline profiles can affect HexA formation and degradation, the variation of HexA in chemical pulps is significan

12、t. Accurate quantification of HexA content in chemical pulps has practical importance. 4. Definition The main uronic acid group in chemical pulps is 4-deoxy-L-threo-hex-4-enopyranosyluronic acid (hexenuronic acid, HexA). This acid does not exist in native wood but is formed in chemical (alkaline) pu

13、lping through -elimination of methoxyl groups from 4-methylglucuronic acid (MeGlcA). T 282 om-13 Hexeneuronic acid content of chemical pulp / 2 5. Apparatus 5.1 A UV-spectrophotometer with a diode array detector or spectrum scanning capability for measuring absorption at multiple wavelengths. 5.2 Sa

14、mple cell, optical pass of about 10 mm, such as a quartz or fused silica cell. 5.3 Sample vial, 20 mL, can be sealed by a septum 5.4 Water bath. 5.5 Plastic syringe, 3 mL. 5.6 Syringe filter, 0.2 m. 6. Reagents 6.1 Mercuric chloride (HgCl2, analytical grade) 6.2 Sodium acetate trihydrate (CH3COONa 3

15、H2O, analytical grade) 6.3 Distilled water 6.4 Weigh 6 0.006 g of HgCl2and 7 0.007 g of CH3COONa 3H2O and add them into a beaker together with about 500 mL distilled water for dissolution. Transfer the solution to a 1-L volumetric flask and fill distilled water to the 1-L mark. This makes a hydrolys

16、is solution of 0.6% mercuric chloride and 0.7% sodium acetate. 7. Pulp sample Obtain an unbleached pulp sample, equivalent to 5 g air-dried pulp handsheet. Wash the pulp thoroughly using distilled water for slush pulps. Determine the moisture content and the oven-dry weight (w) of the pulp sample us

17、ing TAPPI T 210 (“Weighing, Sampling and Testing Pulp for Moisture”). 8. Procedure 8.1 Weigh 0.05 0.0005 g pulp sample using an analytical balance accurate to 0.0002 g with known moisture content from the sample obtained from Section 7 and add it into a 20-mL vial containing 10 mL of hydrolysis solu

18、tion. Seal the vial by a septum. Handshake the vial to mix the chemicals with the sample. For samples where anticipated level (or the measured level of HexA found in a preliminary analysis) is below 5 mol/g, the analysis should be repeated using a 0.5 0.005 g sample to increase sensitivity. 8.2 Heat

19、 the vial for 30 0.5 minutes in a water bath at 65 1C. 8.3 Remove from water bath and cool with tap water to room temperature. 8.4 Use a 3-mL plastic syringe to retrieve the resulting solution from vial . 8.5 Use a 0.2-m syringe filter on the plastic syringe to filter finers and fines before dispens

20、ing the filtrate into a silica sampling cell for UV absorption measurements. 8.6 Conduct UV absorption measurements of the filtered solution in the 10-mm path length quartz or fused silica sample cell. Record the absorption signals at 260 and 290 nm. Sample dilution may be necessary for UV measureme

21、nts to ensure absorption signal at 260 nm is not saturated. 8.7 Conduct UV absorption measurements of the fresh hydrolysis solution (as the blank) in a 10-mm path length sample cell. 9. Calculation 9.1 Absorption signal determination: Spectrophotometers automatically subtract the measured absorbance

22、 of the blank (fresh hydrolysis) solution from the absorbance of the filtered sample solution. Calculate HexA content according to 9.2.using the absorption signal readings from the instrument directly. 9.2 HexA content determination: )()()2.1(287.0)/(290260gwmLVAAgmolCHexA 3 / Hexeneuronic acid cont

23、ent of chemical pulp T 282 om-13 where 0.287 = calibration constant obtained using a standard pulp (2). This calibration constant can be universally used to calculate HexA content in any pulps. There is no need to conduct calibration. 1.2 = ratio between lignin absorption at 260 nm and 290 nm that i

24、s used to correct lignin absorption on HexA determination (1) V = the volume of the testing hydrolysis solution in mL w = weight of the oven-dry mass of the pulp sample used in hydrolysis in grams. 10. Report Report HexA content as an average of two determinations in mol/g to three significant figur

25、es. 11. Precision 11.1 A round robin study was conducted by 5 laboratories: two from the United States, one from Canada, one from China, and one from Spain. Three kraft eucalyptus pulp samples were produced and sent to these 5 laboratories. The variations in HexA among these samples were not signifi

26、cant but apparent. The reported data were averages of replicate measurements in each laboratory. The repeatability and reproducibility were determined in accordance with the definitions of the terms in TAPPI T 1200 “Interlaboratory Evaluation of Standards to Determine TAPPI Repeatability and Reprodu

27、cibility.” 11.2 Repeatability: (within a laboratory) = 3%. 11.3 Reproducibility: .(between laboratories) = 9% 12. Safety Collect the hydrolysis solution that may contain mercuric compounds for proper disposal. 13. Additional information 13.1 Effective date of issue: April 30, 2013. 13.2 The 2013 rev

28、ision added precision data so that this standard could be upgraded to Official Method status. Several editorial changes were also made. 14. Keywords Hexeneuronic acid, Acid groups, Chemical pulps, Ultraviolet spectroscopy, Hydrolysis Literature cited 1. Chai, X.S., Zhu, J.Y., and Li, J., “A Simple a

29、nd Rapid Method to Determine Hexenuronic Acid Groups in Chemical Pulps,“ J. Pulp Paper Sci., 27(5):165 (2001) 2. Gellerstedt, G. and Li, J., “An HPLC method for the quantitative determination of hexenuronic acid groups in chemical pulp”, Carbohydr. Res., 294:41, 1996. Your comments and suggestions on this procedure are earnestly requested and should be sent to the TAPPI Standards Department.