CN111707514A - Method for evaluating uniformity of glass batch - Google Patents

Method for evaluating uniformity of glass batch Download PDF

Info

Publication number
CN111707514A
CN111707514A CN202010556366.2A CN202010556366A CN111707514A CN 111707514 A CN111707514 A CN 111707514A CN 202010556366 A CN202010556366 A CN 202010556366A CN 111707514 A CN111707514 A CN 111707514A
Authority
CN
China
Prior art keywords
glass batch
uniformity
parts
grinding
filtrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202010556366.2A
Other languages
Chinese (zh)
Inventor
蔡礼貌
孙雪峰
何智钢
韩正伟
李彦涛
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hebei Window Glass Co ltd
CSG Holding Co Ltd
Original Assignee
Hebei Window Glass Co ltd
CSG Holding Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hebei Window Glass Co ltd, CSG Holding Co Ltd filed Critical Hebei Window Glass Co ltd
Priority to CN202010556366.2A priority Critical patent/CN111707514A/en
Publication of CN111707514A publication Critical patent/CN111707514A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/28Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/28Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/38Diluting, dispersing or mixing samples
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/16Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using titration
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00Sampling; Preparing specimens for investigation
    • G01N1/28Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/286Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q involving mechanical work, e.g. chopping, disintegrating, compacting, homogenising
    • G01N2001/2866Grinding or homogeneising

Abstract

The invention provides a method for evaluating the uniformity of a glass batch, which comprises the following steps: (1) taking 10-20 parts of a glass batch sample, and grinding each part of glass batch respectively to obtain 10-20 parts of grinding materials; (2) respectively dissolving the grinding materials obtained in the step (1) by using hydrochloric acid, and filtering the dissolved solution to obtain filtrate; (3) and (3) respectively measuring the MgO content in each filtrate obtained in the step (2), and calculating the uniformity according to the obtained MgO content. The method can realize accurate measurement of the uniformity of the glass batch under the condition of sampling 10-20 parts, and the accuracy of the uniformity test is improved by taking the MgO content as the uniformity test standard because the MgO content in the glass batch, particularly the cover plate glass batch, is low. The method is simple and convenient to operate, and rapid evaluation of the uniformity of the glass batch is realized.

Description

Method for evaluating uniformity of glass batch
Technical Field
The invention belongs to the technical field of glass preparation, relates to a method for evaluating the uniformity of a glass batch, and particularly relates to a method for evaluating the uniformity of the glass batch.
Background
The glass batch is the product of mixing different materials, and the essence of the material mixing process is to reduce or eliminate the difference between two or more kinds of powder. Such differences are manifold and simultaneous, such as chemical composition, density, particle size, substance concentration, and mixing time, among others. The greater the difference between the materials, the less easily the materials can be mixed. The main purpose of mixing in the glass industry is therefore to eliminate the differences in chemical composition between the different materials in order to facilitate the homogeneous progress of the chemical reactions during melting. There are still differences in the glass batch obtained by mechanical mixing through the compounder, and uniformity is a measure of such differences.
The prior art methods for determining the homogeneity of glass batch materials include conductivity, light reflection density and pH titration, as is known in Yanlun entitled glass batch homogeneity (glass and enamel 1999,12(6): 39-49). The method comprises the steps of measuring the content of sodium carbonate in the batch by the consumption of hydrochloric acid, and calculating the content difference of sodium carbonate in each batch to obtain the uniformity of the glass batch, wherein certain glass batches contain sodium carbonate and potassium carbonate and/or calcium oxide with high mass fraction, so that the measurement of the uniformity of the glass batch is directly influenced.
The conductivity rule is that the uniformity is calculated by measuring and calculating the conductivity of each part of glass batch, and sodium carbonate and sodium sulfate in the glass batch provide the main oxides Na of the glass2And O, the two salts can be completely dissolved in water, and the charged particles generated after dissolution move under the influence of an electric field to transfer electrons, thereby finally showing the conductive property. However, the glass batch not only contains sodium carbonate and sodium sulfate, but also potassium salt in the glass batch has influence on the numerical value of the conductivity, and the mass fraction of the soluble sodium salt and the soluble potassium salt in the glass batch is generally more than 20 percentThe uniformity of the glass batch measured by the conductivity method has the defect of large error.
The light reflection density law is that parallel light emitted by a light source is projected on the surface of powder according to the capacity of reflecting light on the surface of glass batch, the reflection capacity of the powder can be obtained according to the relation between the luminous flux of incident light and the luminous flux of reflected light, and then the light reflection density of the powder is obtained through photoelectric signal conversion. Generally, the light reflection capability depends on the light absorption performance and the surface roughness of the solid surface, and the accuracy of the value obtained by the light reflection density method is directly influenced by the thickness of the powder to be measured and the sample preparation condition, so that the measurement error is large during the measurement by the light reflection density method.
CN 103323479a discloses a method for measuring the uniformity of glass batch, comprising the following steps: (1) preparing a sample: preparing a glass batch sample and a glass batch standard sample into a glass batch sample piece and a glass batch standard sample piece which are suitable for measurement of an X-ray fluorescence spectrometer; (2) making a standard curve: preparing a standard curve corresponding to each element or each oxide by adopting a glass batch standard sample; (3) determination of the ingredients in the glass batch samples: measuring the fluorescence X-ray intensity of each element in the glass batch sample by using an X-ray fluorescence spectrometer, and calculating the content of each element or each oxide in the glass batch sample according to a standard curve corresponding to each element or each oxide; (4) and calculating the uniformity of the glass batch according to the calculated content of each element or each oxide of the glass. The measuring method needs to measure the contents of multiple groups of elements and needs to use an X-ray fluorescence spectrometer, and the equipment cost and the time cost of measurement are high.
Along with the requirement on the glass quality is higher and higher, the requirement on the uniformity of the glass batch inevitably exists, so that the method which is simple in batch uniformity test and high in accuracy is provided, the quality of glass preparation is favorably improved, and the efficiency of glass preparation is improved.
Disclosure of Invention
Aiming at the defects in the prior art, the invention aims to provide a method for evaluating the uniformity of a glass batch, in particular to a method for evaluating the uniformity of a cover plate glass batch, which can realize simple and rapid measurement of the glass batch under the condition of less sampling quantity and has smaller measurement error.
In order to achieve the purpose, the invention adopts the following technical scheme:
the invention provides a method for rapidly evaluating the uniformity of a glass batch, which comprises the following steps:
(1) taking 10-20 parts of a glass batch sample, and grinding each part of glass batch respectively to obtain 10-20 parts of grinding materials;
(2) respectively dissolving the grinding materials obtained in the step (1) by using hydrochloric acid, and filtering the dissolved solution to obtain filtrate;
(3) and (3) respectively measuring the MgO content in each filtrate obtained in the step (2), and calculating the uniformity according to the obtained MgO content.
The method provided by the invention utilizes the characteristics that the MgO in the glass batch is low in mass percentage and is easy to dissolve in hydrochloric acid, and can realize the rapid measurement of the uniformity of the glass batch only by taking a small amount of glass batch samples. Because the sampling is less and the cost of hydrochloric acid is lower, the method provided by the invention has the characteristics of simple and convenient operation, economy and high measurement accuracy.
The sampling part of the glass batch sample is 10-20 parts, such as 10 parts, 12 parts, 15 parts, 16 parts, 18 parts or 20 parts, but the sampling part is not limited to the enumerated values, and other non-enumerated values in the numerical range are also applicable; the skilled person can select a proper sampling part within 10-20 parts according to the total amount and sampling amount of the glass batch of the same batch, and the uniformity can be measured within the value range to obtain better effect.
When the sampling number of the glass batch sample exceeds 20 parts, the uniformity of the glass batch can be determined and higher accuracy can be obtained, but the increase of the sampling number increases the total sampling amount and the subsequent consumption of hydrochloric acid, and is not beneficial to reducing the measurement cost. When the number of sampled parts is less than 10 parts, a smaller amount of sample is disadvantageous for improving the accuracy of the final result.
The formula for calculating the uniformity is as follows:
H=100%-E
Figure BDA0002544447390000041
Figure BDA0002544447390000042
Figure BDA0002544447390000043
in the above formula: h is the uniformity, E is the relative dispersion, S is the mean square error,
Figure BDA0002544447390000044
is an average value, n is the number of samples, XiThe MgO content of the i-th sample was measured. The relative dispersion E of MgO is calculated by the above formula, and the uniformity of the glass batch is H100% -E.
Preferably, the glass batch is a cover glass batch.
The cover plate glass has higher requirement on the uniformity of the glass batch, and the uniformity of the batch cannot be accurately measured by measuring the sodium carbonate by using a conventional conductivity method, a light reflection density method or a titration method. In contrast, the invention selects the necessary component MgO in the cover plate glass batch as the measuring object, and measures the MgO with relatively less mass fraction, thereby improving the accuracy of uniformity detection and overcoming the K2O and Na2The measurement error caused by high and unstable O content.
Preferably, the cover plate glass batch comprises the following components in percentage by mass: al (Al)2O34.5-21%,CaO 0-6%,MgO 3-10%,K2O1-5% and Na210-15% of O and the balance of SiO2
The cover glass includes low-aluminum cover glass, medium-aluminum cover glass and high-aluminum cover glass, wherein the content of CaO in the medium-aluminum cover glass batch and the high-aluminum cover glass batch is 0%, and the content of CaO in the low-aluminum cover glass batch is 0 to 6%, but not 0%, and for example, 0.5%, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5%, 5%, 5.5% or 6%, but not limited to the recited values, and other values not recited in the numerical range are also applicable.
Al in the cover plate glass batch2O3The percentage by mass of (B) is 4.5 to 21%, and may be, for example, 4.5%, 5%, 8%, 10%, 12%, 15%, 16%, 18% or 21%, but is not limited to the values recited, and other values not recited in the numerical range are also applicable.
The percentage by mass of MgO in the cover glass batch is 3-10%, for example 3%, 4%, 5%, 6%, 7%, 8%, 9% or 10%, but is not limited to the values listed, and other values not listed in the range of values are equally applicable.
K in the cover plate glass batch2The percentage by mass of O is 1 to 5%, and may be, for example, 1%, 1.5%, 2%, 2.5%, 3%, 3.5%, 4%, 4.5% or 5%, but is not limited to the recited values, and other values not recited in the numerical range are also applicable.
Na in the cover plate glass batch2The percentage by mass of O is 10 to 15%, and may be, for example, 10%, 11%, 12%, 13%, 14% or 15%, but is not limited to the values recited, and other values not recited in the numerical range are also applicable.
Preferably, the grinding material in the step (1) is undersize obtained by sieving with a 200-mesh sieve after grinding.
Preferably, the hydrochloric acid in step (2) has a concentration of 1 to 5mol/L, for example, 1mol/L, 2mol/L, 3mol/L, 4mol/L or 5mol/L, but is not limited to the recited values, and other values not recited in the numerical range are also applicable.
Preferably, the dissolving temperature in step (2) is 80-90 ℃, for example, 80 ℃, 81 ℃, 82 ℃, 83 ℃, 84 ℃, 85 ℃, 86 ℃, 87 ℃, 88 ℃, 89 ℃ or 90 ℃, but not limited to the recited values, and other values not recited in the numerical range are also applicable; the time is 5-30min, for example 5min, 10min, 15min, 20min, 25min or 30min, but is not limited to the values listed, and other values not listed in the numerical range are equally applicable.
Preferably, the solid-to-liquid ratio of each part of the grinding material and the hydrochloric acid in the step (2) is 1 (2-10), and can be, for example, 1:2, 1:4, 1:5, 1:6, 1:8 or 1:10, but is not limited to the enumerated values, and other unrecited values in the numerical range are also applicable, and the unit of the solid-to-liquid ratio is g/mL.
Preferably, the determination in step (3) is performed after the MgO content in each filtrate is adjusted to 0.01 to 2 mass% of Mg ions in each filtrate, and may be, for example, 0.01%, 0.05%, 0.1%, 0.3%, 0.5%, 0.8%, 1%, 1.2%, 1.5%, 1.8%, or 2%, but is not limited to the values recited, and other values not recited in the numerical range are also applicable.
Preferably, the determination method comprises atomic absorption spectrometry and/or titrimetry, preferably titrimetry.
The titration analysis method is simple and feasible, and can complete the determination of magnesium ions without large-scale determination equipment, and the titration analysis method disclosed by GB/T9857-1988.
Preferably, the specific operation of taking 10-20 parts of the glass batch sample in the step (1) is as follows: 10-20 parts of glass batch samples of the same batch are taken at a feed opening of the mixer according to time intervals.
Preferably, the time interval is 3 to 8s, and may be, for example, 3s, 3.5s, 4s, 4.5s, 5s, 5.5s, 6s, 6.5s, 7s, 7.5s or 8s, but is not limited to the values recited, and other values not recited within the range of values are equally applicable.
As a preferred technical scheme of the method, the method comprises the following steps:
(1) taking 10-20 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent glass batch samples is 3-8 s; grinding the glass batch respectively, and sieving by a 200-mesh sieve to obtain 10-20 parts of grinding material;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 1-5mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1 (2-10), and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 80-90 ℃ and the time is 5-30 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 0.01-2%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
The recitation of numerical ranges herein includes not only the above-recited numerical values, but also any numerical values between non-recited numerical ranges, and is not intended to be exhaustive or to limit the invention to the precise numerical values encompassed within the range for brevity and clarity.
Compared with the prior art, the invention has the beneficial effects that:
the method provided by the invention can realize accurate measurement of the uniformity of the glass batch under the condition of sampling 10-20 parts, and the accuracy of uniformity test is improved by taking the MgO content as the uniformity test standard because the MgO content in the glass batch, particularly the cover plate glass batch, is low; the method is simple and convenient to operate, and rapid evaluation of the uniformity of the glass batch is realized.
Detailed Description
The technical solution of the present invention is further explained by the following embodiments.
Example 1
The embodiment provides a method for evaluating the uniformity of a cover plate glass batch, which comprises the following components in percentage by mass: al (Al)2O312%,CaO 3%,MgO 5%,K2O3% and Na2O12% and the balance of SiO2(ii) a The method comprises the following steps:
(1) taking 15 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent glass batch samples is 5 s; grinding the glass batch respectively, and sieving with a 200-mesh sieve to obtain 15 parts of grinding materials;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 3mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1:6, and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 85 ℃, and the time is 18 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 0.5%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
In 15 parts of the measured glass batch, the content of MgO is 4.98%, 4.99%, 4.97%, 4.98%, 5.01%, 5.02%, 4.98%, 4.99%, 5.02%, 4.99%, 4.98%, 5.00%, 5.02%, 4.99% and 4.99% in sequence by mass percent, and the uniformity of the obtained cover plate glass batch is calculated to be 99.98%.
Example 2
The embodiment provides a method for evaluating the uniformity of a cover plate glass batch, which comprises the following components in percentage by mass: al (Al)2O38%,CaO 4%,MgO 6%,K2O2% and Na2O11%, the balance being SiO2(ii) a The method comprises the following steps:
(1) taking 12 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent parts of glass batch samples is 6 s; grinding the glass batch respectively, and sieving with a 200-mesh sieve to obtain 12 parts of grinding material;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 4mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1:4, and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 82 ℃ and the time is 12 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 0.1%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
In 12 parts of the measured glass batch, the content of MgO is 6.02%, 6.03%, 6.01%, 5.99%, 5.95%, 6.03%, 5.97%, 6.03%, 5.99% and 6.02% in sequence by mass percent, and the uniformity of the obtained cover plate glass batch is calculated to be 99.99%.
Example 3
The embodiment provides a method for evaluating the uniformity of a cover plate glass batch, which comprises the following components in percentage by mass: al (Al)2O318%,CaO 2%,MgO 8%,K2O4% and Na2O13% and the balance of SiO2(ii) a The method comprises the following steps:
(1) taking 18 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent parts of glass batch samples is 4 s; grinding the glass batch respectively, and sieving with a 200-mesh sieve to obtain 18 parts of grinding material;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 2mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1:8, and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 88 ℃ and the time is 24 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 1%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
In 18 parts of the measured glass batch, the content of MgO is 8.06%, 8.09%, 8.05%, 7.99%, 8.07%, 7.92%, 7.93%, 7.90%, 8.10%, 8.01%, 7.97%, 8.04%, 8.01%, 7.99%, 8.08%, 8.05%, 7.95% and 8.06% in sequence by mass percent, and the uniformity of the obtained cover plate glass batch is calculated to be 99.57%.
Example 4
The embodiment provides a method for evaluating the uniformity of a cover plate glass batch, which comprises the following components in percentage by mass: al (Al)2O321%,MgO 3%,K2O1% and Na2O10%, and the balance SiO2(ii) a The method comprises the following steps:
(1) 20 parts of glass batch samples in the same batch are taken from a feed opening of a mixer, and the sampling time interval of two adjacent glass batch samples is 3 s; grinding the glass batch respectively, and sieving the ground glass batch with a 200-mesh sieve to obtain 20 parts of grinding material;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 5mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1:2, and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 80 ℃, and the time is 30 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 0.01%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
In 20 parts of the measured glass batch, the content of MgO is 3.09%, 2.92%, 2.95%, 3.06%, 3.02%, 2.90%, 3.10%, 3.00%, 3.05%, 3.03%, 3.00%, 2.95%, 2.92%, 3.09%, 3.10%, 3.09%, 2.91%, 3.07% and 3.01% in sequence by mass percent, and the uniformity of the obtained cover plate glass batch is calculated to be 98.48%.
Example 5
The embodiment provides a method for evaluating the uniformity of a cover plate glass batch, which comprises the following components in percentage by mass: al (Al)2O34.5%,CaO 6%,MgO 10%,K2O5% and Na2O15% and the balance of SiO2(ii) a The method comprises the following steps:
(1) taking 10 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent glass batch samples is 8 s; grinding the glass batch respectively, and sieving by a 200-mesh sieve to obtain 10 parts of grinding materials;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 1mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1:10, and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 90 ℃, and the time is 5 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 2%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
In 10 parts of the measured glass batch, the content of MgO is 10.05%, 9.96%, 10.03%, 9.97%, 9.98%, 10.04%, 9.98% and 9.97% in sequence by mass percent, and the uniformity of the obtained cover plate glass batch is calculated to be 99.53%.
In conclusion, the method provided by the invention can realize accurate measurement of the uniformity of the glass batch under the condition of sampling 10-20 parts, and the uniformity test accuracy is improved by taking the MgO content as the uniformity test standard because the MgO content in the glass batch, particularly the cover plate glass batch is lower; the method is simple and convenient to operate, and rapid evaluation of the uniformity of the glass batch is realized.
The above-mentioned embodiments are intended to illustrate the objects, technical solutions and advantages of the present invention in further detail, and it should be understood that the above-mentioned embodiments are only exemplary embodiments of the present invention, and are not intended to limit the present invention, and any modifications, equivalents, improvements and the like made within the spirit and principle of the present invention should be included in the protection scope of the present invention.

Claims (10)

1. A method of evaluating the uniformity of a glass batch, comprising the steps of:
(1) taking 10-20 parts of a glass batch sample, and grinding each part of glass batch respectively to obtain 10-20 parts of grinding materials;
(2) respectively dissolving the grinding materials obtained in the step (1) by using hydrochloric acid, and filtering the dissolved solution to obtain filtrate;
(3) and (3) respectively measuring the MgO content in each filtrate obtained in the step (2), and calculating the uniformity according to the obtained MgO content.
2. The method of claim 1, wherein the glass batch material is a cover glass batch material.
3. The method according to claim 1 or 2, characterized in that the composition of the cover glass batch is, in mass percent: al (Al)2O34.5-21%,CaO 0-6%,MgO 3-10%,K2O1-5% and Na210-15% of O and the balance of SiO2
4. The method according to any one of claims 1 to 3, wherein the grinding material in the step (1) is undersize obtained by sieving with a 200-mesh sieve after grinding.
5. The method according to any one of claims 1 to 4, wherein the concentration of the hydrochloric acid in the step (2) is 1 to 5 mol/L.
6. The method of claim 5, wherein the dissolving in step (2) is carried out at a temperature of 80-90 ℃ for a period of 5-30 min.
7. The method as claimed in claim 6, wherein the solid-to-liquid ratio of each part of the millbase and the hydrochloric acid in the step (2) is 1 (2-10), and the unit of the solid-to-liquid ratio is g/mL.
8. The method according to any one of claims 1 to 7, wherein the determination in step (3) is performed after the MgO content in each filtrate is adjusted to 0.01 to 2 mass% of Mg ions in each filtrate;
preferably, the determination method comprises atomic absorption spectrometry and/or titrimetry, preferably titrimetry.
9. The method according to any one of claims 1 to 8, wherein the step (1) of taking 10 to 20 parts of the glass batch sample comprises the following specific operations: taking 10-20 parts of glass batch samples of the same batch at a feed opening of a mixer at time intervals;
preferably, the time interval is 3-8 s.
10. A method according to any of claims 1-9, characterized in that the method comprises the steps of:
(1) taking 10-20 parts of glass batch samples of the same batch at a feed opening of a mixer, wherein the sampling time interval of two adjacent glass batch samples is 3-8 s; grinding the glass batch respectively, and sieving by a 200-mesh sieve to obtain 10-20 parts of grinding material;
(2) respectively dissolving the grinding materials obtained in the step (1) by using 1-5mol/L hydrochloric acid, and filtering the dissolved solution to obtain filtrate; the solid-liquid ratio of the grinding materials to the hydrochloric acid is 1 (2-10), and the unit of the solid-liquid ratio is g/mL; the dissolving temperature is 80-90 ℃ and the time is 5-30 min;
(3) adjusting the mass percent of Mg ions in each part of filtrate to be 0.01-2%, measuring the MgO content in each part of filtrate by a titration analysis method, and calculating the uniformity by the obtained MgO content.
CN202010556366.2A 2020-06-17 2020-06-17 Method for evaluating uniformity of glass batch Pending CN111707514A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010556366.2A CN111707514A (en) 2020-06-17 2020-06-17 Method for evaluating uniformity of glass batch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010556366.2A CN111707514A (en) 2020-06-17 2020-06-17 Method for evaluating uniformity of glass batch

Publications (1)

Publication Number Publication Date
CN111707514A true CN111707514A (en) 2020-09-25

Family

ID=72541073

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010556366.2A Pending CN111707514A (en) 2020-06-17 2020-06-17 Method for evaluating uniformity of glass batch

Country Status (1)

Country Link
CN (1) CN111707514A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113945598A (en) * 2021-09-07 2022-01-18 河北光兴半导体技术有限公司 Evaluation method of glass strengthening ion exchange efficiency
CN117368423A (en) * 2023-12-07 2024-01-09 上海百奥恒新材料有限公司 Quality inspection method for geopolymer and application thereof

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3806396A (en) * 1971-02-24 1974-04-23 Glaverbel Control of flow of glass to a glass ribbon being drawn
US20060230787A1 (en) * 2004-11-12 2006-10-19 Lehman Richard L System for and method of batch analysis and optimization for glass manufacturing
CN103149230A (en) * 2011-12-07 2013-06-12 郑州旭飞光电科技有限公司 Method of directly detecting chemical components of flat glass substrate based on X-ray fluorescence
CN103323479A (en) * 2013-06-18 2013-09-25 芜湖东旭光电科技有限公司 Glass mixed batch uniformity determination method
WO2015118964A1 (en) * 2014-02-04 2015-08-13 オーエムジー株式会社 Near-infrared absorbing/high-contrast glass lens
CN105548280A (en) * 2015-12-30 2016-05-04 东旭科技集团有限公司 Method for determining uniformity of mixed batch for alkali-free glass and method for preparing mixed batch
JP2017078003A (en) * 2015-10-22 2017-04-27 日本電気硝子株式会社 Glass tube for medicine containers, and method for producing the same
CN106770407A (en) * 2016-11-25 2017-05-31 成都中光电科技有限公司 A kind of fuse piece X-fluorescence assay method of the glass batch entirety uniformity
CN107843610A (en) * 2017-10-31 2018-03-27 巨石集团九江有限公司 A kind of method of testing of cell furnace batch uniformity
CN108181244A (en) * 2017-11-30 2018-06-19 彩虹(合肥)液晶玻璃有限公司 A kind of method for measuring TFT-LCD liquid crystal substrate glass batch uniformities

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3806396A (en) * 1971-02-24 1974-04-23 Glaverbel Control of flow of glass to a glass ribbon being drawn
US20060230787A1 (en) * 2004-11-12 2006-10-19 Lehman Richard L System for and method of batch analysis and optimization for glass manufacturing
CN103149230A (en) * 2011-12-07 2013-06-12 郑州旭飞光电科技有限公司 Method of directly detecting chemical components of flat glass substrate based on X-ray fluorescence
CN103323479A (en) * 2013-06-18 2013-09-25 芜湖东旭光电科技有限公司 Glass mixed batch uniformity determination method
WO2015118964A1 (en) * 2014-02-04 2015-08-13 オーエムジー株式会社 Near-infrared absorbing/high-contrast glass lens
JP2017078003A (en) * 2015-10-22 2017-04-27 日本電気硝子株式会社 Glass tube for medicine containers, and method for producing the same
CN105548280A (en) * 2015-12-30 2016-05-04 东旭科技集团有限公司 Method for determining uniformity of mixed batch for alkali-free glass and method for preparing mixed batch
CN106770407A (en) * 2016-11-25 2017-05-31 成都中光电科技有限公司 A kind of fuse piece X-fluorescence assay method of the glass batch entirety uniformity
CN107843610A (en) * 2017-10-31 2018-03-27 巨石集团九江有限公司 A kind of method of testing of cell furnace batch uniformity
CN108181244A (en) * 2017-11-30 2018-06-19 彩虹(合肥)液晶玻璃有限公司 A kind of method for measuring TFT-LCD liquid crystal substrate glass batch uniformities

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"有色吸热玻璃配合料均匀度的测定" *
何为: "玻璃配合料的均匀度" *
杨伦: "玻璃配合料的均匀度及其测定" *
罗星: "高档玻璃器皿配合料均匀度测定" *
陈静静: "电导率法测定玻璃配合料均匀度" *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113945598A (en) * 2021-09-07 2022-01-18 河北光兴半导体技术有限公司 Evaluation method of glass strengthening ion exchange efficiency
CN117368423A (en) * 2023-12-07 2024-01-09 上海百奥恒新材料有限公司 Quality inspection method for geopolymer and application thereof
CN117368423B (en) * 2023-12-07 2024-02-06 上海百奥恒新材料有限公司 Quality inspection method for geopolymer and application thereof

Similar Documents

Publication Publication Date Title
CN111707514A (en) Method for evaluating uniformity of glass batch
CN109596699B (en) Rare earth single element solution standard substance and preparation thereof
CN103323479A (en) Glass mixed batch uniformity determination method
CN103512911A (en) Metallurgy miscellaneous material fast spectral analysis method
Nakayama et al. Glass beads/x‐ray fluorescence analyses of 42 components in felsic rocks
CN102042982A (en) Method for testing content of boron trioxide in glass containing zinc and lead
CN108593913B (en) Immunoreaction double-pulse detection method based on mass spectrometry technology
CN113092510A (en) X-fluorescence determination method for potassium nitrate as high-alumina glass raw material
CN115598287B (en) Method for detecting copper content in conductive paste
CN108344793B (en) Matrix, preparation method thereof and mass spectrometry detection method of metabolic molecules
CN114964976A (en) Rare earth oxide standard sample and preparation method thereof
CN102062734B (en) Method for analyzing and detecting sodium content and potassium content in covering agent
CN104062285A (en) Determination method for contents of calcium, aluminum and silicon elements in solid surface materials
CN110261418B (en) Method for accurately determining content of beta-tricalcium phosphate in hydroxyapatite
CN111307869A (en) Method for measuring content of elemental boron in boron powder
CN112345620A (en) Method for quantitatively detecting serum elements by inductively coupled plasma mass spectrometry
CN108593906B (en) Metal ion labeled immunoreaction double-pulse detection method
CN112710650A (en) Method for rapidly and accurately measuring main chemical component content of cement
CN111650192A (en) Method for removing lead in lead-bismuth alloy and method for measuring tellurium in lead-bismuth alloy
CN113049718B (en) Preparation of carbon-supported metal oxide composite microspheres and extraction of malachite green and crystal violet from aquatic products by using same
CN105987908A (en) Detection kit for on-site quick detection of nickel ions in water and preparing method
Mao et al. Determination of platinum‐group elements and forty two other elements in two candidate Danish Cretaceous‐Tertiary boundary clay reference materials by INAA, ENAA and RNAA
Trivelpiece et al. Tank 40 Sludge Batch 9 Waste Acceptance Product Specifications (WAPS) Solids and Chemical Analyses
JPS6113140A (en) Quantitative analysis of iron by plasma luminous analysis
CN114527190A (en) Glycosylated hemoglobin detection kit and detection method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination