ANSI T 529 OM-2009 Surface pH measurement of paper.pdf
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1、TAPPI/ANSI T 529 om-14 PROVISIONAL METHOD 1974 OFFICIAL METHOD 1982 REVISED 1998 REVISED 1999 REVISED 2004 REVISED 2009 REAFFIRMED 2014 2014 TAPPI The information and data contained in this document were prepared by a technical committee of the Association. The committee and the Association assume n
2、o liability or responsibility in connection 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 Sp
3、ecific Interest Group for this Test Method 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 responsibl
4、e for determining that the safety precautions 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 heal
5、th hazards to humans. Procedures for the handling 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 t
6、his method, the user must determine whether 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. Surf
7、ace pH measurement of paper 1. Scope 1.1 This non-destructive test may be used to measure the hydrogen ion concentration (pH) on the surface of the paper in books and documents that constitute the collections of libraries and government archives. 1.2 This method serves as an alternative to TAPPI T 5
8、09 “Hydrogen Ion Concentration (pH) of Paper Extracts - Cold Extraction Method,” and TAPPI T 435 “Hydrogen Ion Concentration (pH) of Paper Extracts - Hot Extraction Method,” because it avoids the destruction of printed material in the determination of the permanence expected for paper (see also 11.2
9、). 1.3 pH values obtained through the application of this method to sized materials such as writing, printing, and industrial papers reflect only the pH of the surface of these materials and should not be construed as pH values which may be determined by the cold water extraction method of the same
10、material (1). 2. Summary A flat combination electrode is immersed in a drop of water on the surface of the paper sample. The pH of the surface of the paper is determined with high accuracy and repeatability without the requirement of sample destruction (2,3). 3. Significance 3.1 Because the useful l
11、ife of most papers is primarily a function of the acidity of the paper (4,5), it is necessary that the concentration of the hydrogen ion in the paper be known (4) so that appropriate preservation and/or restoration techniques may be employed to extend the useful life of books and documents which are
12、 determined to be acidic. 3.2 Since books and documents (some of which are very valuable or irreplaceable) cannot be destroyed or otherwise defaced for the purpose of pH determination, a need exists for a convenient procedure which is accurate but T 529 om-14 Surface pH measurement of paper / 2 does
13、 not require destruction or extensive water soaking of the paper samples to be tested. This non-destructive method accomplishes this need (6,7,8,9). 4. Apparatus 4.1 Commercial pH meter, with flat combination electrode1, which can be immersed in a single drop of water. The pH meter must measure pH w
14、ith a precision of 0.1 pH unit and should include temperature compensation. 4.2 Backing material, non-absorbent material, such as gum rubber, to allow firm contact of electrode against surface of paper. 4.3 Absorbent cotton, to remove water after completion of test. 4.4 Timer, stopwatch or electric
15、timer. 4.5 Thermometer, 0-100C range. 4.6 Volumetric flasks, 1000 mL, for buffer solutions. 5. Reagents 5.1 Water. Reagent grade water used in this test method shall conform to ASTM Specification D 1193, Type I or II, Standard Specifications for Water (10). NOTE 1: Water meeting this specification i
16、s typically sold by many manufacturers for use in HPLC, residue analysis, and spectrometry, and is packaged under nitrogen. 5.2 Standard buffer solutions: 5.2.1 Potassium hydrogen phthalate buffer, pH 4.01 at 25C; dissolve 10.21 g of KHC8H4O4(A.C.S. primary standard or certified grade) in water and
17、dilute to 1000 mL. NOTE 2: The buffer capacity of this buffer solution is rather low and the solution should be protected from contamination with acids or alkalis. Its pH, however, is not affected by atmospheric carbon dioxide. Replace the buffer solution every six weeks or if mold appears. 5.2.2 Ph
18、osphate buffer, pH 6.86 at 25C: dissolve 3.40 g of monobasic potassium phosphate (KH2PO4, A.C.S. primary standard) and 3.55 g of anhydrous dibasic sodium phosphate, Na2HPO4, in carbon dioxide-free water and dilute to 1000 mL. When protected from undue atmospheric exposure, this buffer solution is qu
19、ite stable. NOTE 3: The Na2HPO4will absorb moisture from the air at relative humidities exceeding 40% at 25C and should be dried at 100 to 130C for 2 h before use. 5.2.3 Borax buffer, pH 9.18 at 25C: dissolve 3.81g of sodium tetraborate Na2B4O7 10 H2O in carbon dioxide-free water and dilute to 1000
20、mL. NOTE 4: The dilution value of this buffer solution is so small that changes in the water content of the borax are usually of no concern. Precautions should be taken to protect solution form prolonged atmospheric exposure and subsequent CO2absorption. The shelf life of this solution is about one
21、month. 5.2.4 Propriety buffer solutions: These are commercially available and may be purchased in a ready-to-use solution form. The pH of these buffer solutions, however, must be accurately known if they are used. 6. Calibration 6.1 Connect the combination surface electrode to the pH meter. 6.2 Soak
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