CN109580310A - Naphthalene-methanol solution standard substance preparation method - Google Patents
Naphthalene-methanol solution standard substance preparation method Download PDFInfo
- Publication number
- CN109580310A CN109580310A CN201811619132.7A CN201811619132A CN109580310A CN 109580310 A CN109580310 A CN 109580310A CN 201811619132 A CN201811619132 A CN 201811619132A CN 109580310 A CN109580310 A CN 109580310A
- Authority
- CN
- China
- Prior art keywords
- naphthalene
- solution
- methanol
- methanol solution
- concentration
- 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
Links
- 239000000126 substance Substances 0.000 title claims abstract description 29
- MFGWMAAZYZSWMY-UHFFFAOYSA-N (2-naphthyl)methanol Chemical compound C1=CC=CC2=CC(CO)=CC=C21 MFGWMAAZYZSWMY-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 57
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims abstract description 53
- 239000000243 solution Substances 0.000 claims abstract description 53
- 239000012086 standard solution Substances 0.000 claims abstract description 17
- 238000001514 detection method Methods 0.000 claims abstract description 12
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 claims abstract description 7
- 238000001816 cooling Methods 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 4
- 238000005303 weighing Methods 0.000 claims description 4
- 239000003708 ampul Substances 0.000 claims description 3
- 239000012925 reference material Substances 0.000 claims description 3
- PBLNHHSDYFYZNC-UHFFFAOYSA-N (1-naphthyl)methanol Chemical compound C1=CC=C2C(CO)=CC=CC2=C1 PBLNHHSDYFYZNC-UHFFFAOYSA-N 0.000 claims description 2
- 239000012491 analyte Substances 0.000 abstract description 2
- 238000007710 freezing Methods 0.000 abstract description 2
- 230000008014 freezing Effects 0.000 abstract description 2
- 238000005259 measurement Methods 0.000 abstract description 2
- 238000005057 refrigeration Methods 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract 1
- 238000002474 experimental method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012795 verification Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000011022 operating instruction Methods 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
- G01N30/02—Column chromatography
- G01N30/04—Preparation or injection of sample to be analysed
- G01N30/06—Preparation
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N2001/2893—Preparing calibration standards
Landscapes
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
Abstract
The present invention provides naphthalene-methanol solution standard substance preparation methods, raw material is weighed using high Accuracy Electronic Balance, and gas chromatography-mass spectrometry can be qualitative simultaneously and quantitative to sample, and multiple restrictive condition is arranged to the concentration for preparing solution to filter out the standard solution closer to theoretical concentration value;Using relatively narrow standard curve range and repeatedly measurement, keep detectable concentration more accurate;And then using low dose of cooling package standard solution, the volatilization of solvent was both reduced, has ensured the accurate of concentration, and had in turn avoided dispensing the standard solution freezing bottle of large capacity into the risk that possible standard substance is precipitated again after refrigeration.The naphthalene prepared by the method-methanol solution standard substance, which uses, to be more convenient, and uses it more acurrate, reliable as calibrating analyte detection result.
Description
[technical field]
The present invention relates to standard solution fields, and in particular to a kind of preparation method of naphthalene-methanol solution standard substance.
[background technique]
Currently, most analytical reagents are molten according to standard specified in GB/T 15000 " standard sample work directive/guide "
The preparation method of liquid is prepared, but since national standard method is as a kind of regulatory documents, there is no for specific substance
Detailed operating instruction, and it is multifarious due to chemical substance property, and there were significant differences for the concentration of standard solution produced.
Naphthalene-methanol solution standard substance is used as Verification of Liquid Chromatograph solution reference material, the chemistry as known content
Ingredient standard is mainly used for the calibrating of high performance liquid chromatograph, ultraviolet-visible detector, diode array detector.Standard
The concentration of substance will be directly related to verification result.
[summary of the invention]
Based on this, it is necessary to provide a kind of preparation method of naphthalene-methanol solution standard substance, prepared standard solution
Concentration value uses user of service more convenient closer to theoretical value.
The technical problems to be solved by the invention are achieved by the following technical programs:
A kind of preparation method of naphthalene-methanol solution standard substance, comprising the following steps:
By pre-determined naphthalene-methanol concentration of standard solution value M0, calculate required naphthalene, methanol usage;With accurate electricity
Sub- balance weighs the naphthalene of calculation amount, is accurate to 0.00001 gram;
Naphthalene after weighing is dissolved in the methanol of calculation amount;
By the quality and actual methanol usage of practical weighed naphthalene, naphthalene-methanol solution compound concentration M is calculated1, and
M1With M0Between need to meet relationship: ∣ M1-M0∣/M0≤ 0.1%;
Through gas chromatography-mass spectrometry is qualitative and quantitative detection naphthalene-methanol solution concentration value, taken after five tests
Average value, and will be between 0.98 × M0~1.02 × M0Between average value as naphthalene-methanol solution detectable concentration M2;
After detecting, Fu He ∣ M2-M0∣/M0≤ 2.0% naphthalene-methanol solution is that the calibration concentration configured is M2Naphthalene-
Methanol solution standard substance.
It further include that the naphthalene-methanol solution standard substance that will be prepared is dispensed using ampoule bottle is cooling in above-mentioned preparation method
Step.
1. naphthalene provided by the invention-methanol solution standard substance preparation method has the following beneficial effects: using high-precision
Electronic balance, the concentration of standard solution value of preparation is closer to theoretical value;2. can be same to sample using gas chromatography-mass spectrometry
When it is qualitative and quantitative;3. keeping calibration concentration more accurate using relatively narrow standard curve range and repeatedly measurement;4. using small dose
Cooling package standard solution is measured, both reduced the volatilization of solvent, ensured the accurate of concentration, and in turn avoided the standard of large capacity
Solution freezing bottle dispenses the risk that possible standard substance is precipitated again after refrigeration.Naphthalene-the methanol prepared by the method
Solution reference material, which uses, to be more convenient, and uses it more acurrate, reliable as calibrating analyte detection result.
[Detailed description of the invention]
Fig. 1 is the naphthalene-methanol solution standard substance gas chromatogram prepared in the embodiment of the present invention 1.
[specific embodiment]
Naphthalene provided by the invention-methanol solution standard substance preparation method, comprising the following steps:
Concentration value preparing standard solution according to the rules;
It formulates and requires about standard solution referring to GB/T 15000 " standard sample work directive/guide ", calculate dense according to the rules
Spend M0Naphthalene quality, methanol usage needed for being worth preparing standard solution;
The naphthalene that calculation amount is weighed with precision electronic balance is accurate to 0.00001 gram, is dissolved in constant volume methanol;According to reality
The naphthalene quality that border weighs calculates naphthalene-methanol solution compound concentration value, that is, passes through the pure of the quality and naphthalene for weighing obtained naphthalene
Degree, methanol usage, calculate naphthalene-methanol solution compound concentration M1, compound concentration M1With normal concentration M0Between relationship need
It can continue subsequent step in the condition for meeting 0.1%≤(compound concentration value-normal concentration value)/normal concentration value≤0.1%
Suddenly;If M1With M0Between do not meet above-mentioned condition, then need to weigh naphthalene again, prepare solution and calculate M1Until making itself and M0Meet
Condition;
In compound concentration M1After meeting above-mentioned condition, gas chromatography-mass spectrometry is qualitative and quantitative detection naphthalene-methanol
The concentration value of solution, the result that sample is tested through five times is as average value, if the average value is in normal concentration value M0×(1±
2.0%) (that is, 0.98 × M in0≤ average value≤1.02 × M0), then using the average value as naphthalene-methanol solution detectable concentration
M2;If average value deviates from (1 ± 2.0%) × M0, then detectable concentration M must not be used as2;
For naphthalene-methanol detectable concentration M2, then need to further conform to detectable concentration value normal concentration value ±
Condition in 2.0% range, that is, | detectable concentration value-normal concentration value |/normal concentration value≤2.0%;It is only qualified
It could be as qualified naphthalene-methanol solution standard substance, qualified detectable concentration M2The calibration of the as standard substance is dense
Degree;The solution for not meeting the condition must not be used as standard solution.
Standard solution after qualification is distributed into finished product inner wrapping unit using ampoule bottle cooling, for using.
The present invention will now be described in detail with reference to examples.
Embodiment 1
Preparation specification is M0The naphthalene of=1.0mg/mL-methanol solution standard substance
Prepare solution: referring to GB/T 15000 " standard sample work directive/guide " about standard solution constituting criterion.Experiment institute
It is 99.8% with the purity of naphthalene, 0.10020 ± 0.00010g of naphthalene, methanol 100mL should be weighed by being computed;Actually use precise electronic
It 0.10028 gram of balance precise, after being completely dissolved with methanol, is transferred in the container of 100mL capacity, again with methanol constant volume,
It obtains and prepares solution;
Compound concentration value: M1=0.10028g × 0.998 × 103/ 100mL=1.0008mg/mL, in setting
Between 0.999mg/mL~1.001mg/mL;
It is computed, (M1-M0)/M0=(1.0008-1)/1=0.0008=0.08% < 0.1%, it is eligible;
Use gas chromatography-mass spectrometry qualitative and quantitative detection to solution is prepared, detection parameters are as follows:
The chromatogram of detection is as shown in Fig. 1.
It prepares solution to detect through five times, test data is as follows:
It is 0.99658mg/mL according to detectable concentration average value, since the average value is in M0± 2.0% range in, meet
Experiment imposes a condition, which is the detectable concentration value M for preparing solution2。
The present embodiment Zhong , ∣ M2-M0∣/M0=∣ 0.99658-1.0 ∣/1.0=0.00342=0.342% < 2%, therefore M2
Standardizing of solution concentration value is as configured, that is, the naphthalene prepared-methanol solution standard substance calibration concentration is 0.99658mg/mL.
After the completion of detection, qualified naphthalene-methanol solution standard substance is encapsulated using brown glass ampoules bottle, and cold
Hiding storage, for using.
Embodiment 2
Preparation specification is M0The naphthalene of=0.2mg/mL-methanol solution standard substance
Prepare solution: referring to GB/T 15000 " standard sample work directive/guide " about standard solution constituting criterion.Experiment institute
It is 99.8% with the purity of naphthalene, 0.20040 ± 0.00020g of naphthalene, methanol 1L should be weighed by being computed;It is practical to use precise electronic day
0.20028 gram of flat precise, after being completely dissolved with methanol, is transferred in the container of 1L capacity, and again with methanol constant volume is matched
Solution processed;
Compound concentration value: M1=0.20028g × 0.998 × 103/ 1000mL=0.19988mg/mL, in setting
Between 0.1998mg/mL~0.2002mg/mL;
It is computed , ∣ M1-M0∣/M0=∣ 0.19988-0.2 ∣/0.2=0.0006=0.06% < 0.1%, it is eligible;
Use gas chromatography-mass spectrometry qualitative and quantitative detection to solution is prepared, detection parameters and embodiment 1 are consistent,
It detects obtained chromatogram and embodiment 1 is close.
It prepares solution to detect through five times, test data is as follows:
It is 0.20048mg/mL according to detectable concentration average value, since the average value is in M0± 2.0% range in, meet
Experiment imposes a condition, which is the detectable concentration value M for preparing solution2。
The present embodiment Zhong , ∣ M2-M0∣/M0=∣ 0.20048-0.2 ∣/0.2=0.0024=0.24% < 2%, therefore M2I.e.
To configure standardizing of solution concentration value, that is, the naphthalene prepared-methanol solution standard substance calibration concentration is 0.10024mg/mL.
After the completion of detection, qualified naphthalene-methanol solution standard substance is encapsulated using brown glass ampoules bottle, and cold
Hiding storage, for using.
The embodiments described above only express several embodiments of the present invention, and the description thereof is more specific and detailed, but simultaneously
Limitations on the scope of the patent of the present invention therefore cannot be interpreted as.It should be pointed out that for those of ordinary skill in the art
For, without departing from the inventive concept of the premise, various modifications and improvements can be made, these belong to guarantor of the invention
Protect range.Therefore, the scope of protection of the patent of the invention shall be subject to the appended claims.
Claims (2)
1. a kind of naphthalene-methanol solution standard substance preparation method, comprising the following steps:
By pre-determined naphthalene-methanol concentration of standard solution value M0, calculate required naphthalene, methanol usage;Use precision electronic balance
The naphthalene for weighing calculation amount is accurate to 0.00001 gram;
Naphthalene after weighing is dissolved in the methanol of calculation amount;
By the quality and actual methanol usage of practical weighed naphthalene, naphthalene-methanol solution compound concentration M is calculated1, and M1With
M0Between need to meet relationship: ∣ M1-M0∣/M0≤ 0.1%;
Through gas chromatography-mass spectrometry is qualitative and quantitative detection naphthalene-methanol solution concentration value, it is averaged after five tests
Value, and will be between 0.98 × M0~1.02 × M0Between average value as naphthalene-methanol solution detectable concentration M2;
After detecting, Fu He ∣ M2-M0∣/M0≤ 2.0% naphthalene-methanol solution is that the calibration concentration configured is M2Naphthalene-methanol
Solution reference material.
2. naphthalene according to claim 1-methanol solution standard substance preparation method, which is characterized in that further include that will match
The naphthalene of system-methanol solution standard substance is using ampoule bottle cooling the step of dispensing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811619132.7A CN109580310A (en) | 2018-12-28 | 2018-12-28 | Naphthalene-methanol solution standard substance preparation method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811619132.7A CN109580310A (en) | 2018-12-28 | 2018-12-28 | Naphthalene-methanol solution standard substance preparation method |
Publications (1)
Publication Number | Publication Date |
---|---|
CN109580310A true CN109580310A (en) | 2019-04-05 |
Family
ID=65933254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811619132.7A Pending CN109580310A (en) | 2018-12-28 | 2018-12-28 | Naphthalene-methanol solution standard substance preparation method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109580310A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113030297A (en) * | 2021-02-19 | 2021-06-25 | 广东省计量科学研究院(华南国家计量测试中心) | 2,2',4,4' -tetrabromodiphenyl ether solution standard substance in methanol and preparation method thereof |
CN115684515A (en) * | 2021-07-28 | 2023-02-03 | 上海市质量监督检验技术研究院 | Preparation method of low-concentration total organic carbon standard solution |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107290475A (en) * | 2016-04-13 | 2017-10-24 | 深圳市博林达科技有限公司 | A kind of preparation method of standard liquid |
-
2018
- 2018-12-28 CN CN201811619132.7A patent/CN109580310A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107290475A (en) * | 2016-04-13 | 2017-10-24 | 深圳市博林达科技有限公司 | A kind of preparation method of standard liquid |
Non-Patent Citations (1)
Title |
---|
张凌: "滴定分析概论", 《分析化学(上)》 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113030297A (en) * | 2021-02-19 | 2021-06-25 | 广东省计量科学研究院(华南国家计量测试中心) | 2,2',4,4' -tetrabromodiphenyl ether solution standard substance in methanol and preparation method thereof |
CN115684515A (en) * | 2021-07-28 | 2023-02-03 | 上海市质量监督检验技术研究院 | Preparation method of low-concentration total organic carbon standard solution |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104007218A (en) | Determination method of bisphenol S transfer volume in plastic food packaging materials | |
Pacquette et al. | Determination of total iodine in infant formula and nutritional products by inductively coupled plasma/mass spectrometry: single-laboratory validation | |
CN109580310A (en) | Naphthalene-methanol solution standard substance preparation method | |
CN108760949B (en) | Detection method of plant growth regulator ethephon in biological fluid | |
Uchiyama et al. | Absolute purity determination of a hygroscopic substance, indocyanine green, using quantitative NMR (qNMR) | |
CN104251889B (en) | The measuring method of Phenylephrine Hydrochloride, chlorpheniramine maleate and Ibuprofen BP/EP three kinds of component contents in compound flu tablet | |
CN110261360A (en) | A kind of method and application based on fluorometric determination sulphite | |
CN110068643A (en) | A method of based on vitamin in Liquid Chromatography-Tandem Mass Spectrometry measurement medical food | |
CN110007034A (en) | A method of based on amino acid in Liquid Chromatography-Tandem Mass Spectrometry measurement medical food | |
CN104198611A (en) | Oxiracetam sample impurity detection device | |
CN109061003A (en) | The measuring method of alkyl phenol polyoxyethylene ether content in a kind of liquid tea product | |
CN110320308A (en) | The measuring method of 2- methoxyacetophenone in honey | |
Jing et al. | Determination of free and total carnitine and choline in infant formulas and adult nutritional products by UPLC/MS/MS: Single-laboratory validation, first action 2014.04 | |
CN112844217A (en) | Preparation method of dicofol standard solution | |
CN112697934A (en) | Method for detecting content of pyroglutamic acid in compound amino acid injection | |
Tarkase Kailash et al. | Development and validation of UV-Spectrophotometric methods for estimation of Indapamide in bulk and tablet dosage form | |
CN115308343B (en) | Acid red solution standard substance and preparation method and application thereof | |
CN108896505A (en) | The detection method of content and Ketoprofen injection of Ketoprofen injection | |
Hendrix et al. | Collaborative study of the analysis of tetracycline by liquid chromatography on poly (styrene-divinylbenzene) | |
CN110988173B (en) | A gas chromatography-mass spectrometry method for determination of clotrimazole content in medicine | |
CN114236017B (en) | Method for detecting ascorbyl palmitate and impurities thereof | |
Chhalotiya et al. | Development and validation of an ultra performance liquid chromatography method for venlafaxine hydrochloride in bulk and capsule dosage form | |
CN103728386B (en) | A kind of method utilizing liquid phase method to measure Nu-Iron dissolution rate | |
CN117250276A (en) | Method for measuring residual quantity of bentazone and metabolite thereof in tea | |
CN116794174A (en) | Determination method of RCF based on the integration of qNMR and chromatography technology |
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 | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20190405 |
|
WD01 | Invention patent application deemed withdrawn after publication |