CN1731168A - Method for measuring general quantity of released gas during cable material combustion - Google Patents

Abstract

The invention discloses a method for measuring the released brine sour gas content during the burning of the cable material, which comprises: first using NaOH solution to absorb the brine sour gas from burning cable material; then using HNO3 solution to adjust PH value 2-9; then adding potassium chloride solution as basic solution, and recording the usage; then using silver electrode as indication electrode, saturated calomel electrode as reference electrode to detect electrode electric potential, at the same time, using AgNO3 solution titration, when it arrives the equivalence point electric potential, recording the AgNO3 solution usage; at last computing brine sour ion total content of the detected solution by the usage of AgNO3 solution, then subtracting the chloride ion content of basic test solution so as to obtain the brine sour gas total content of the cable material.

Description

The assay method of general quantity of released gas during cable material combustion

Technical field

The present invention relates to a kind of material analysis technology, relevant with the assay method of general quantity of released gas during cable material combustion, be specially adapted to detect and disengage the sample of halogen acid gas amount, to remedy the deficiency of GB/T 17650.1-1998 test method less than 5mg/g.

Background technology

Since the seventies in 20th century, because property loss and casualties that fire causes have caused the attention of countries in the world, so the fire-retardant problem of electric wire has risen to important status.The performance of flame retardant cable is far superior to traditional plain edition cable, and when fire took place, flame-proof power cable flame reduced along spreading significantly of cable line, and especially during cable lifting, situation is all the more so; The sour gas of zero-halogen low-smoke flame-retardant electrical cable Halogen, generation is few, so that switchgear, computer network etc. all can not be subjected to the influence of corrosivity smog; The smog and the toxic gas that distribute significantly reduce, thereby help withdrawing of personnel.

Produce in the zero-halogen low-smoke flame-retardant electrical cable in research and development, total amount of halogen acid gas is most important after measuring cable material combustion, it not only can check whether conformance with standard of product, more can pass through this mensuration, help the research staff to select more suitably cable material, thereby produce standard compliant high-quality flame-retardant electric wire and cable.

" GB/T 17650.1-1998 " stipulated the assay method of total amount of halogen acid gas, and its analysis principle is: the halogen acid gas that cable material combustion generates adds HNO after being absorbed by NaOH again ₃Acidifying, then, with a certain amount of and excessive AgNO ₃Reaction generates silver halide precipitation, makes indicator with ammonium ferric sulfate again, with the AgNO of ammonium thiocyanate back titration surplus ₃Thereby, calculate total amount of halogen acid gas.

Its chemical equation following (halogen acid gas is represented with hydrogen chloride):

Surplus

Work as NH ₄The same AgNO of SCN ₃After reacting completely, excessive SCN ^-Same NH ₄Fe (SO ₄) ₂Generate red [Fe (SCN) ₆ ^3-] complex ion, thereby directing terminal.But the indicator discoloration utmost point is not easy to observe in the case, and the terminal point that in other words is exactly this kind analytical approach can't judge accurately that it is inaccurate to have caused this analytical approach to measure.

Therefore, in GB/T 17650.1-1998, spell out to guaranteeing the accuracy of experiment, its assay method is not suitable for and disengages the sample of halogen acid gas amount less than 5mg/g, and promptly the hydracid ion (comprises cl in the NaOH absorption liquid ^-, Br ^-, I ^-) content is less than 10 ^-4The sample of mol/L, and recommend to use GB/T 17650.2-1998 to measure the acidity of gas by measuring pH value and conductivity, yet can only measure material disengages gas when burning acidity with the method for GB/T 17650.2-1998, but can not go out the total amount of halogen acid gas that sample discharges by accurate response.In the analysis to the low smoke, zero halogen cable material under actual conditions, the research staff is necessary again this halogen acid gas amount is analyzed, so, cause many manufacture of materials producers and cable manufacturing enterprise all have to adopt GB/T 17650.1-1998 standard, measured total amount of halogen acid gas data are very inaccurate.

Summary of the invention

The object of the present invention is to provide a kind of assay method of general quantity of released gas during cable material combustion, it can measure general quantity of released gas during cable material combustion exactly, be specially adapted to detect and disengage the sample of halogen acid gas amount, to remedy the deficiency of GB/T17650.1-1998 test method less than 5mg/g.

For reaching above-mentioned purpose, solution of the present invention is:

The halogen acid gas that cable material combustion is generated absorbs with NaOH solution earlier; Use HNO again ₃It is 2～9 that solution is transferred PH; Then, add chloride solution, and write down the basic test solution consumption that is added as basic test solution; Then, make indicator electrode with silver electrode, saturated calomel electrode is made contrast electrode, and the potential electrode current potential simultaneously, is used AgNO ₃The solution titration, Ag in detected solution ⁺After hydracid ion complete reaction, arrive the equivalent point current potential, record AgNO ₃Solution usage; At last, by AgNO ₃Solution usage calculates hydracid ion total content in the detected solution, deducts chloride ion content in the aforementioned basic test solution that adds again, promptly gets total amount of halogen acid gas in the cable material.

Wherein, the above-mentioned HNO that uses ₃Solution is transferred PH to 5～6 the bests.

Concrete steps: the halogen acid gas that the burning of cable material sample is generated absorbs with NaOH solution earlier, and is appended to 1000ml; Get 200ml solution in beaker, stir, drip 2 1% phenolphthalein indicators, drip dense HNO ₃Take off to redness; In test solution, add and contain the basic test solution of Kcl 2mg, and---silver electrode, contrast electrode---saturated calomel electrode of in test solution, placing indicator electrode, AgNO used ₃Standard solution carries out titration, when indicating potential arrives equivalent point current potential 267mV, represents titration end-point; The hydracid total amount is shown as follows with the milligram numerical table of the hydrogen chloride of every gram sample:

$\frac{(V_1-V_0)M\×36.5\×(1000/200)}{m}$

In the formula: V ₀Be titration used AgNO when containing the basic test solution of Kcl 2mg ₃The volume of standard solution, unit/ml;

V ₁Be the used AgNO of whole titration process ₃The volume of standard solution, unit/ml;

M is AgNO ₃The volumetric molar concentration of standard solution, the mol/L of unit;

M is a sample weight, the g of unit.

The principle of the inventive method is:

With the silver ion electrode is indicator electrode, and saturated calomel electrode is made contrast electrode, in tested test solution, following electrode reaction takes place: (I handle herein) its electrode potential nernst equation $E={{{E^0}_{\mathrm{Ag}}}^{+}}_{/\mathrm{Ag}}+\frac{\mathrm{RT}}{\mathrm{nF}}\·\ln \frac{a_{{\mathrm{Ag}}^{+}}}{a_{\mathrm{Ag}}}$ Expression because the ortho states of going back of silver electrode is solid-state, so its activity is considered as 1, changes natural logarithm into common logarithm, (all can generally at room temperature use) in the time of 25 ℃, and nernst equation can be expressed as:

E＝E ⁰ _Ag ⁺ _/Ag+0.0592lg α _Ag ⁺，

∵α _Ag ⁺＝k _sp/α _cl ^-

∴E＝E ⁰ _Ag ⁺ _/Ag+0.0592lg k _sp/a _c1 ^-＝E ⁰ _Ag ⁺ _/Ag+0.0592lg k _sp 0.0592lg α _cl ^-

With E ⁰ _Ag ⁺ _{/ Ag}=0.800V, k _Sp=1.82 * 10 ^-10, the substitution following formula,

Get E=0.800+0.0592lg 1.82 * 10 ^-100.0592lg α _Cl ^-=0.222-0.0592lg α _Cl ^-,

Under certain condition, in very rare solution, usable concentration replaces activity, i.e. E=0.222-0.0592lg[cl ^-].

When equivalent point, [Ag ⁺] [cl ^-]=k _Sp=1.82 * 10- ¹⁰,

$\left[{\mathrm{cl}}^{-}\right]=\sqrt{K_{\mathrm{SP}}}=\sqrt{1.82\×{10}^{-10}}=1.35\×{10}^{-5},$

So E=0.222-0.0592lg 1.35 * 10 ^-5=0.222+0.287=0.509V is 509mV, and the saturated calomel electrode current potential is 242mV, therefore, with the silver ion electrode is indicator electrode, and saturated calomel electrode is made contrast electrode, and potential value is E=509mV-242mV=267mV when equivalent point, that is to say, in tested test solution, use standard A gNO ₃When solution carried out titration to the hydracid ion, when showing that current potential is 267mV, reaction was quantitatively finished.

Certainly, in measuring test solution during the hydracid ion, possible cl ^-, Br ^-, I ^-All exist, or only have one of them.If only there is Br in the sample solution ^-, I ^-, and do not have cl ^-, then the equivalent point current potential is not 267mV just.According to solubility product constant K _{SP (Agl)}=8.3 * 10 ^-17, K _{SP (AgBr)}=5.0 * 10 ^-13, K _{SP (Agcl)}=1.82 * 10 ^-10As can be known, having cl ^-, Br ^-, I ^-In the test solution that exists, Ag ⁺At first with I ^-Generation AgI ↓, again with Br ^-Generate AgBr ↓, at last just with cl ^-Generation Agcl ↓.Therefore, no matter whether sample solution exists cl ^-,, reaching [Ag if in sample solution, add known quantitative chloride (as a Kcl) solution earlier ⁺] [cl ^-] during equivalent point current potential 267mV, i.e. I in the test solution ^-, Br ^-, cl ^-All same sequentially Ag ⁺React completely.

After adopting said method, the present invention is by adding basic test solution control equivalent point current potential, and the numerical value by the potential electrode current potential, accurately judge the terminal point of drop reaction, the method is not subjected to the muddiness of detected solution, influence such as coloured grade, without any need for indicator, not only the analytical approach accuracy than present use is significantly increased, and, be applicable to the cable material sample analysis low to hydracid content, promptly be applicable to the test solution that titration concentration is rarer, sensitivity and accuracy height, reliably, operating process is simple, can satisfy fully and analyze requirement, be particularly useful for detecting and disengage the sample of halogen acid gas amount less than 5mg/g, promptly the hydracid ion (comprises cl ^-, Br ^-, I ^-) content is less than 10 ^-4The tested test solution of mol/L has remedied the deficiency of GB/T 17650.1-1998 test method.

Specific embodiment

The measuring process explanation:

Earlier with the halogen acid gas of NaOH solution (also can with KOH solution or have other solution that waits same-action) absorption cable material combustion generation.

Use HNO again ₃It is 2～9 that solution is transferred PH, is best test condition with PH=5～6.

Then, add Klorvess Liquid as basic test solution (also can have with Nacl solution or other waits the solution of same-action to replace), and write down the basic test solution consumption that is added.

Then, make indicator electrode with 216 type silver electrodes, 232 type saturated calomel electrodes are made contrast electrode, and the potential electrode current potential simultaneously, is used AgNO ₃The solution titration, Ag in detected solution ⁺After hydracid ion complete reaction, arrive the equivalent point current potential.

At last, by AgNO ₃Solution usage calculates hydracid ion total content in the detected solution, deducts chloride ion content in the aforementioned basic test solution that adds again, promptly gets total amount of halogen acid gas in the cable material.

The actual analysis process:

Test procedure is with GB/T 17650.1-1998.The halogen acid gas that the burning of cable material sample is generated absorbs with NaOH solution earlier, and is appended to 1000ml.Analytic process is as follows: get 200ml solution in beaker, beaker is placed on the magnetic stirring apparatus stir.Drip 2 1% phenolphthalein indicators, drip dense HNO ₃Take off to redness.In test solution, add the basic test solution that contains Kcl 2mg, and in test solution, place, use AgNO as the silver electrode of indicator electrode, as the saturated calomel electrode of contrast electrode ₃Standard solution carries out titration.When indicating potential arrives equivalent point current potential 267mV, represent titration end-point.Can calculate the milligram number of hydracid total amount by formula with the hydrogen chloride of every gram sample.

$\frac{(V_1-V_0)M\×36.5\×(1000/200)}{m}$

Each symbolic representation such as front solution are listed in the formula, do not do at this and give unnecessary details.

The test of method accuracy:

Instrument and reagent: magnetic force heating stirrer

PHS-3C type precision digital PH meter

216 type silver electrodes

232 type saturated calomel electrodes

0.01mol/L AgNO ₃Standard solution, (being 1.7mg/ml)

Kcl, KBr, KI standard solution 1.000g/L, (being 1mg/ml)

The basis test solution is for containing Kcl 2mg

See Table 1---the analytical approach accuracy table of comparisons.Table 1 has been introduced in the testing liquid of being made up of different compositions, uses 0.01mol/L AgNO ₃Standard solution titration, when reaching the equivalent point current potential, the actual AgNO that consumes ₃Quality is with consuming AgNO in theory ₃The contrast of quality, and the error of analytical approach.

The table 1 analytical approach accuracy table of comparisons

Test solution is formed	Equivalent point current potential (mV)	Consume AgNO 3Solution (ml number)	Consumption AgNO 3Quality (mg)	Theory should consume AgNO 3Quality (mg)	Error (%)
						(basic test solution) Kcl 2mg	267	2.75	4.675	4.56	2.5
(basic test solution)+KBr 2mg	267	4.40	7.48	7.42	0.8
						(basic test solution)+KI 2mg	267	3.85	6.55	6.61	-0.9
Each 2mg of (basic test solution)+KBr+KI	267	5.65	9.605	9.47	1.4

Find out that from above data the analysis data that its analytical approach draws and the relative error of gross data are less, illustrate that this potentiometric titration can satisfy the analysis requirement.

Claims (2)

1, the assay method of general quantity of released gas during cable material combustion is characterized in that:

The halogen acid gas that cable material combustion is generated absorbs with NaOH solution earlier; Use HNO again ₃It is 2～9 that solution is transferred PH; Then, add chloride solution, and write down the basic test solution consumption that is added as basic test solution; Then, make indicator electrode with silver electrode, saturated calomel electrode is made contrast electrode, and the potential electrode current potential simultaneously, is used AgNO ₃The solution titration, Ag in detected solution ⁺After hydracid ion complete reaction, arrive the equivalent point current potential, record AgNO ₃Solution usage; At last, by AgNO ₃Solution usage calculates hydracid ion total content in the detected solution, deducts chloride ion content in the aforementioned basic test solution that adds again, promptly gets total amount of halogen acid gas in the cable material.

2, the assay method of general quantity of released gas during cable material combustion according to claim 1 is characterized in that: the halogen acid gas that the burning of cable material sample is generated absorbs with NaOH solution earlier, and is appended to 1000ml; Get 200ml solution in beaker, stir, drip 2 1% phenolphthalein indicators, drip dense HNO ₃Take off to redness; In test solution, add and contain the basic test solution of Kcl 2mg, and---silver electrode, contrast electrode---saturated calomel electrode of in test solution, placing indicator electrode, AgNO used ₃Standard solution carries out titration, when indicating potential arrives equivalent point current potential 267mV, represents titration end-point; The hydracid total amount is shown as follows with the milligram numerical table of the hydrogen chloride of every gram sample:

$\frac{(V_1-V_0)M\×36.5\×(1000/200)}{m}$

In the formula: V ₀Be titration used AgNO when containing the basic test solution of Kcl 2mg ₃The volume of standard solution, unit/ml;

V ₁Be the used AgNO of whole titration process ₃The volume of standard solution, unit/ml;

M is AgNO ₃The volumetric molar concentration of standard solution, the mol/L of unit;

M is a sample weight, the g of unit.