ASTM D7723-2017 red 4375 Standard Test Method for Rubber Property&x2014 Macro-Dispersion of Fillers in Compounds《橡胶特性-化合物填料的粗粒分散体的标准试验方法》.pdf

《ASTM D7723-2017 red 4375 Standard Test Method for Rubber Property&x2014 Macro-Dispersion of Fillers in Compounds《橡胶特性-化合物填料的粗粒分散体的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM D7723-2017 red 4375 Standard Test Method for Rubber Property&x2014 Macro-Dispersion of Fillers in Compounds《橡胶特性-化合物填料的粗粒分散体的标准试验方法》.pdf（5页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: D7723 11D7723 17Standard Test Method forRubber PropertyMacro-Dispersion of Fillers inCompounds1This standard is issued under the fixed designation D7723; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of last

2、 revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon () indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers a procedure to measure the macro-dispersion of fillers in a rubber matrix by quantifying the surfa

3、ceroughness of a freshly cut specimen using an optical microscope in reflection mode.1.2 The method provides a procedure to measure the quality of mixing of reinforcing fillers such as silica and carbon black, aswell as inert fillers such as chalk, clay and other solids.1.3 The method includes a sam

4、ple preparation procedure for filled uncured rubber compounds as well as filled cured rubbercompounds.1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.1.5 This standard does not purport to address all of the safety concerns

5、, if any, associated with its use. It is the responsibilityof the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatorylimitations prior to use.1.5 This standard does not purport to address all of the safety concerns, if any, associa

6、ted with its use. It is the responsibilityof the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability ofregulatory limitations prior to use.1.6 This international standard was developed in accordance with internationally recognize

7、d principles on standardizationestablished in the Decision on Principles for the Development of International Standards, Guides and Recommendations issuedby the World Trade Organization Technical Barriers to Trade (TBT) Committee.2. Referenced Documents2.1 ASTM Standards:2D2663 Test Methods for Carb

8、on BlackDispersion in RubberD3053 Terminology Relating to Carbon Black3. Terminology3.1 Definitions of Terms Specific to This Standard:3.1.1 agglomerates, nany number of filler aggregates held together by van der Waals Forces (carbon black) or hydrogenbonding (silica).3.1.2 macro dispersion, ndegree

9、 of distribution of filler into a compound, generally on a scale of less than 100 m but greaterthan 2 m; represents micron range agglomeration.3.1.3 nodges, nbumps in a cut surface caused by filler agglomerates in a rubber matrix.3.1.4 surface roughness, nthe bumps (nodges), or hills and valleys tha

10、t are on the visible side of a sample.3.1.5 white area, nthe portion of the scan area which contains nodges, or other surface defects; it is described here as white,because the reflected light from these surface defects is white.1 This test method is under the jurisdiction of ASTM Committee D11 on R

11、ubber and Rubber-like Materials and is the direct responsibility of Subcommittee D11.12 onProcessability Tests.Current edition approved May 1, 2011Dec. 1, 2017. Published July 2011January 2018. Originally approved in 2011. Last previous edition approved in 2011 as D7723 11.DOI: 10.1520/D7723-11.10.1

12、520/D7723-17.2 For referencedASTM standards, visit theASTM website, www.astm.org, or contactASTM Customer Service at serviceastm.org. For Annual Book of ASTM Standardsvolume information, refer to the standards Document Summary page on the ASTM website.This document is not an ASTM standard and is int

13、ended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Becauseit may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the curr

14、ent versionof the standard as published by ASTM is to be considered the official document.Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States14. Summary of Test Method4.1 This standard uses mathematical algorithms to quantify the surface

15、roughness of freshly cut rubber specimens as measuredby a reflected light optical method in two dimensions.4.2 The reflected light optical method, generally used to determine a comparative dispersion rating, is expanded to givequantitative data as to the size and number of nodges. Nodges do not show

16、 the actual size of filler agglomerates. It is assumed thatas the sample is cut, large agglomerates are pushed to one side or the other leaving a contoured surface.The diameter and frequencyof the surface contours are measured using image processing. These contours are referred to as “nodges” to dif

17、ferentiate them fromactual agglomerates. This data is presented in histogram form of count versus nodge diameter, and allows calculating a measureof dispersion.5. Significance and Use5.1 The incorporation of fillers into the rubber matrix is characterized by their macrodispersion as an indicator of

18、the qualityof mixing. This test method provides a measure of the macro-dispersion of reinforcing fillers, like silica and carbon black, as wellas of inert fillers. Based on their polymer nature, different types of rubbers can show a different degree of acceptance for theincorporation of fillers, as

19、indicated by their macro-dispersion.5.2 Macro-dispersion of carbon black and silica in rubber compounds may be measured by different methods. Carbon blackprovides a direct physical reinforcement; silica requires a silane coupling agent in order to initiate reinforcement, and therefore,a different te

20、chnology of mixing. Silica is also a non-conductor, making electrical methods of dispersion measurementimpracticable. This test method is specifically appropriate for the characterization of the microdispersion in silica technology.5.3 This test method also can measure the mixing quality of colored

21、rubbers. It uses variable exposure in order to be able toimage a wide range of colors.5.4 This test method is intended for use in research and development as well as in quality control of filler processability inrubber and may be used for both the evaluation of production processes or referee purpos

22、es.6. Apparatus6.1 Razor Blade (recommended) or Sharp KnifeThe specimen may be prepared using a static cut as shown in Fig. 1 or cutwhile being bi-directionally elongated as shown in Fig. 2.6.2 Reflected Light Microscope, with the following specifications:6.2.1 Imaging power to resolve to 1 m, 3 m,

23、or 10 m depending on the instrument used.6.2.2 Dark field illumination as shown in Fig. 3.6.3 The light microscope is to be equipped with an image sensor. The sensor used to capture the image is a common CCD(Charged Coupled Device) or CMOS (Complementary Metal Oxide Semiconductor) sensor. In the dar

24、k field mode, an apertureis lit at a 30 angle for analysis. The sensor picks up the reflection of bumps on the surface, nodges representing undispersed filler.Flat areas of the sample surface are dark.6.4 A scan is made by taking a digital gray-level image in the dark field mode of the microscope wi

25、th 1 m, 3 m, or 10 mresolution.6.5 The image captured by the sensor shall be digitized and analyzed by the image processing software. The area of nodges isrepresented as “White Area.” The percent White Area, URF%, is the percentage of the white area representing the nodges to thetotal area of the im

26、age. Based on this area ratio, percent dispersion can be calculated.7. Calculation7.1 As the specimen is cut, the underlying agglomerates are pushed to one side or another resulting in hills and valleys on thecut surface. They represent agglomerates under the surface of the cut. The nodge diameter t

27、hat is calculated from these images islarger than the underlying agglomerate. For simplification, nodge size is reported as Agglomerate Size and represented by ahistogram (Fig. 4).FIG. 1 Static CutD7723 1727.2 In order to stay within the 2-100 m range of macro-dispersion defined in Terminology D3053

28、, it is necessary to disregardsmall nodges that are covering the smaller agglomerates by introducing a threshold of 5 m for the nodge size. threshold. Twodifferent values for the threshold may be used: 5 m and 23 m. The threshold value cannot be selected below the resolution ofthe microscope as stat

29、ed in 6.2.1. The frequency of occurrence of nodges decreases with a higher level of dispersion. Dispersion,therefore, is calculated from the white area, which is determined from the radius and frequency of all nodges greater than the nodgethreshold.7.3 Calculate the White Area, URF%,URF, as a ratio

30、to the total scan area.7.4 Calculate the percent dispersion of fillers as follows:Dispersion %51002100 URF%/L (1)Dispersion %5100 2 100 3 URF! /L (1)where:where:URF% = % of total scan from of undispersed filler measured in reflectionURF = fraction of total scan area from undispersed filler measured

31、in reflectionL = the filler volume fraction in the compoundFIG. 2 Bi-Directional CutFIG. 3 Darkfield IlluminationD7723 1737.4.1 For maximum accuracy, the filler volume fraction can be calculated from the following expression, which also appearsin Test Methods D2663:L 5compound density3filler massfil

32、ler density3compound mass (2)L 5 compound density 3filler massfiller density 3compound mass (2)7.5 If the volume percentage of filler in the rubber compound L is either not given or unknown, calculate the weighted percentdispersion or Z Value as follows:Z value51002100 URF%/0.35 (3)Z value5100 2 100

33、 3 URF! /0.35 (3)The Z Value assumes a maximum of 35 % white area.NOTE 1The Z Value assumes a maximum of 35 % white area. Fixing the volume fraction at a maximum value of 0.35 allows the user to skip thetime-consuming step of determining the volume fraction, which is not necessary for quality contro

34、l of a specific compound.8. Test Specimen8.1 The test specimen is prepared from a vulcanized or unvulcanized sample of a filled rubber compound.Arazor blade cut shallbe made, so that two similar surfaces are exposed. The surfaces shall be bigger than 5 by 5 mm.8.1.1 When preparing the test specimen,

35、 it is recommended that a new razor blade be used for each cut. The abrasiveness ofthe rubber as well as contaminates from the rubber left on the blade may affect successive cuts.8.1.2 The thickness of the uncut specimen shall be 5 to 10 mm. Thicker specimens cause excessive drag between the razor b

36、ladeand rubber and may affect the quality of the cut.8.1.3 The specimen shall be cut in one continuous motion.8.2 For unvulcanized samples, porosity which is generated during the slab preparation process should be eliminated. This isaccomplished by pressing a hot sample while cooling. The cut is mad

37、e by placing the unvulcanized sample in a sample preparationsystem, where it is pulled bi-directionally, while a razor cuts. This is not required, but also recommended for cured specimens. Theprocedures specified in 7.1 shall be followed for bi-directionally cut specimens.9. Procedure9.1 A specimen

38、cut according to 8.1 or 8.2 shall be placed in front of the testing window within two minutes after cutting.9.2 Set the threshold to 5 m or 23 m, and adjust the exposure time of the camera if possible (50 ms is recommended).9.3 A minimum of three scans of different locations of the freshly cut surfa

39、ce shall be taken. Five scans of different locationsare recommended. Calculate the average values of the scans. The user does not need to make a fresh cut for each of the five scans.9.4 Apply the calculations expressed in Section 7.10. Report10.1 Percent Dispersion ValuesReport measured dispersion r

40、atings to the nearest 0.1 %.FIG. 4 Example HistogramD7723 17410.2 If the calculation of percent dispersion in 7.4 is used, report the L value used in the calculation. If the calculation of theZ value in 7.5 is used, report the use of the 0.35 Z factor in the calculation.10.3 Agglomerate SizeReport t

41、he agglomerate size as histogram in classes of a width of 3 m.10.4 Report the average agglomerate size. In instances where a bimodal agglomerate distribution exists, two categories may belisted.10.5 Report the setup of the digital acquisition and evaluation: exposure time and threshold value.10.6 Wh

42、ite AreaReport the ratio of area of the undispersed filler to the total area.10.7 Compound IdentificationWhen possible, list pertinent information regarding the following:10.7.1 Filler, type and loading,10.7.2 Other fillers, type and loading,10.7.3 Polymer type, and10.7.4 Extender oil, type and load

43、ing.11. Precision and Bias11.1 A precision and bias study for this test method is currently being planned.12. Keywords12.1 filler; incorporation; macro-dispersion; micro-roughness; reflected light microscopeASTM International takes no position respecting the validity of any patent rights asserted in

44、 connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the re

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46、ul consideration at a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International

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