CN1225514C - Phosphate intercalation water talc and its preparation method and use as fire retardant - Google Patents
Phosphate intercalation water talc and its preparation method and use as fire retardant Download PDFInfo
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- CN1225514C CN1225514C CN 03120913 CN03120913A CN1225514C CN 1225514 C CN1225514 C CN 1225514C CN 03120913 CN03120913 CN 03120913 CN 03120913 A CN03120913 A CN 03120913A CN 1225514 C CN1225514 C CN 1225514C
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- ldhs
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Abstract
The present invention provides a phosphate radical intercalation water talc, a preparation method thereof and an application as a fire retardant thereof. The present invention uses a water talc LDH-CO#-[3] having interlayer negative ions CO#+[-]#-[3] as a precursor, phosphate radical negative ions are inserted into the position among the layers of the water talc, the phosphate radical negative ions completely or partly replace CO#-[3]#+[2-], and an LDHs having the interlayer phosphate radical negative ions is obtained, wherein phosphate radicals are from 20 to 100 wt% of the interlayer negative ions, and the phosphate radicals mainly exist among the layers in the mode of dihydrogen phosphate radicals. The phosphate radical intercalation water talc is the good fire retardant, and after the water talc is compounded with PE, PVC, EVA, PP and various rubbery materials, the water talc, PE, PVC, EVA, PP and the rubbery materials all have good smoke suppressing performance and fire retardant performance.
Description
Affiliated field: the present invention relates to a kind of phosphate pillared ht and preparation method thereof and this hydrotalcite is used as fire retardant.
Background technology: document Arira Ookubo, Kenta Ooi and Hiromu Hayashi.Langmuir, 1993,9,1418-1422 and A.Legrouri, M.Badreddine, A.Barroug, A.De Roy, and J.P.Besse.Journal of Materials Science Letters, 1999,18,1077-1079 all adopts ion exchange method, under alkaline condition, respectively with Mg-Al-Cl LDHs, Zn-Al-NO
3LDHs is a precursor, and the preparation interlayer anion is the intercalation LDHs of phosphoric acid one hydrogen root.Preceding a kind of preparation method's weak point is: intercalation precursor Mg-Al-ClLDHs and intercalation product Mg-Al-HPO
4The preparation condition of LDHs is all very harsh, needs regulation and control pH value, the down long-time reaction of low temperature; The weak point of a kind of method in back is: use N
2The protection complicated operation, and the pH value should not regulate and control, and the compound with regular structure of intercalation product is relatively poor.And not mentioned phosphate radical intercalation LDHs is applied to the fire retardant aspect.
The inventor has studied a kind of super-fine high smoke-suppressing type inorganic combustion inhibitor and preparation method thereof in patent application 02100800, the structure of this fire retardant is [Mg
2+ 1-xAl
3+ x(OH)
2] (CO
3)
2- X/2MH
2O, it is a laminate structure, laminate is Mg
2+And Al
3+Oxyhydroxide, this fire retardant is to take off H with thermal decomposition process
2O and release CO
2Fire retardation is brought into play in absorbing and cooling temperature, dilution, the mode of isolation inflammable gas in polymeric substrate, the product after the decomposition is alkaline porous material, specific surface is big, can adsorb particularly sour gas of obnoxious flavour, thus have good flame retardancy, but the smoke suppressing relative mistake some.
Summary of the invention: the present invention utilizes hydrotalcite (Layered Double Hydroxides is abbreviated as LDHs) but has the performance of intercalation assembling, phosphate anion in the assembling of hydrotalcite layers intercalation, and object is the intercalation LDHs material of phosphate radical between prepared layer.This phosphate pillared ht has promptly kept LDHs inherent flame retardant properties preferably, simultaneously its smoke suppressing is increased substantially.
The present invention is CO with the interlayer anion
3 2-Hydrotalcite (be abbreviated as: LDH-CO
3) be precursor, under acidic conditions, phosphate radical anion is inserted into all or part of replacement of this hydrotalcite layers CO
3 2-, obtain the LDHs that interlayer contains phosphate radical anion, wherein phosphate radical accounts for the 20-100wt% of interlayer anion total amount, and phosphate radical mainly exists with the dihydrogen phosphate form.
Wherein: the divalent-metal ion in the precursor hydrotalcite can be Mg
2+, Ni
2+, Zn
2+, Fe
2+Or Cu
2-In any, preferred Mg
2+Or Zn
3+Trivalent metal ion can be Co
3+, Fe
3+, Ti
3+, Al
3+Or Ga
3+In any, preferred Al
3+
The phosphate pillared ht preparation process is as follows:
A. adopt known hydrotalcite preparation method to prepare required LDHs-CO
3, its structural formula is: [M
2+ 1-xM
3+ x(OH)
2]
X+(CO
3)
2- X/2MH
2O, (wherein 0.2≤x≤0.33, m is an interlayer crystal water molecule number), its laminate divalence, Tricationic mol ratio M
2+/ M
3+=2-4: 1; M
2+Be Mg
2+, Ni
2+, Zn
2+, Fe
2+Or Cu
2+Any in the divalent-metal ion; M
3+Be Co
3+, Fe
3+, Ti
3+, Al
3+Or Ga
3+Any in the trivalent metal ion.M
2+Preferred Mg
2+, Zn
3+, M
3+Preferred Al
3+
B. be the phosphate solution of 0.1-1.0M with the bigger phosphoric acid salt compound concentration of solubleness.Phosphoric acid salt preferably phosphoric acid sodium or potassiumphosphate;
C. the LDHs that steps A is prepared joins in the container that fills deionized water by the amount of 20-30g/L, and the room temperature lower magnetic force stirs, and obtains hydrotalcite suspension;
D. the volume ratio with hydrotalcite suspension and phosphate solution is 1: the ratio of 0.5-3, press phosphate anion and the interior CO of LDHs in the phosphate solution
3 2-The exchange ratio is determined the phosphate solution add-on, stir on one side, add in the C solution on one side, with the H of 0.1M
3PO
4Solution is regulated pH=4.5-5.0, drips to finish, and condensing reflux 1-2h filters, washs neutrality, and 60-100 ℃ of dry 24h obtains containing the pillared LDHs of dihydrogen phosphate.The concentration or the add-on of control phosphate solution, the degree that adjustable intercalation carries out can obtain the serial intercalated houghite that dihydrogen phosphate accounts for the 20-100wt% of interlayer anion total amount respectively.
The intercalated houghite that obtains is carried out XRD, IR, elemental analysis demonstration, and dihydrogen phosphate has been assembled into stratified material LDHs interlayer.
This hydrotalcite and PE, PVC, EVA, PP and multiple elastomeric material is compound, carry out flame retardant resistance, smoke-suppressing test discovery, its flame retardant properties is compared with the LDHs fire retardant in the patent application 02100800, and its fire-retardant and smoke suppressing all improves a lot than the LDHs of intercalation not.And phosphate radical accounts for the phosphate pillared ht of negatively charged ion total amount 45-100wt%, has better smoke suppressing and flame retardant properties during as fire retardant.So this phosphate pillared ht is a kind of high cigarette halogen-free inorganic flame retardant that presses down.
Table 1 has provided fire-retardant, the smoke suppressing test result of the matrix material of different fire retardants and PE/EVA, and wherein the mass ratio of PE and EVA is 90: 10.
Table 1. different flame retardant is fire-retardant, the smoke suppressing test result
Annotate: limiting oxygen index(LOI)
*Pressing GB/T2406-93 measures; Maximum smoke density
*Pressing ASTME662-95 measures.
| Fire retardant kind addition/100phr | No fire retardant 0 | LDHs 70phr | 50% phosphate radical intercalation LDHs 70phr | 100% phosphate radical intercalation LDHs 70phr |
| The maximum smoke density of limiting oxygen index(LOI) LOI/% ** | 17.1 / | 23.7 252.8 | 29.1 187.4 | 29.8 238.1 |
Data as can be seen from table 1, under identical addition, the limited oxygen index that with dihydrogen phosphate intercalation LDHs is the matrix material of fire retardant is that the matrix material of fire retardant extremely all improves a lot than blank sample and with the LDHs of intercalation not, and maximum smoke density index also obviously reduces.The flame retardant resistance ratio of dihydrogen phosphate intercalation LDHs not intercalation LDHs increases, and its smoke suppressing is improved largely than LDHs.
Advantage of the present invention is:
First intercalation to have prepared interlayer anion be univalent dihydrogen phosphate hydrotalcite material;
2. the preparation method's intercalation precursor that is adopted is easy to preparation, and technology is simple, and cost is low, and intercalation is easy to carry out, and does not need N
2Severe condition such as protection;
3. by phosphatic concentration in the control solution, adjustable intercalation enters the amount of the dihydrogen phosphate of hydrotalcite layers.
4. dihydrogen phosphate intercalation LDHs is a kind of fire retardant preferably, and its flame retardant resistance and smoke suppressing are improved than LDHs.
Embodiment:
Embodiment 1:
Steps A: with the solid Mg (NO of 61.5g (0.24mol)
3)
26H
2Solid Al (the NO of O and 45.0g (0.12mol)
3)
39H
2O is dissolved in 225mLH
2Among the O; Other is with the solid Na of 25.3g (0.24mol)
2CO
3And the solid NaOH of 23.0g (0.58mol) is dissolved in 225mLH
2Among the O, under the room temperature rapidly with alkaline solution and salts solution nucleation in full back-mixing rotation liquid film reactor, with the 100 ℃ of crystallization 6h of slurries that obtain, centrifugation, with the sample that obtains wash to the pH value less than 8,70 ℃ of dry 24h, obtain Mg-Al-CO
3LDHs, its Mg
2+/ Al
3+=2: 1.
Step B: take by weighing 17.90g (0.05mol) Na
2HPO
412H
2O is mixed with the phosphate solution of 1.0M.
Step C: the LDHs 4.76g (0.01mol) that steps A is obtained joins in the container of containing the 100mL deionized water, and the room temperature lower magnetic force stirs, and obtains hydrotalcite suspension.
Step D: stir on one side, on one side phosphate solution is added in the LDHs suspension, drip the H of 0.1M then
3PO
4, regulate pH=4.5, drip and finish, condensing reflux 2h filters, washs to pH value and is about 7,70 ℃ of dry 24h, and intercalation is assembled and is obtained dihydrogen phosphate intercalation configuration LDHs material.
By XRD spectra as can be known, the hydrotalcite layers negatively charged ion that obtains is a dihydrogen phosphate all, is the dihydrogen phosphate intercalation configuration LDHs material that a kind of crystal crystalline phase is single, structure is consistent.
This product and PE material is undertaken compound by 70: 100 mass ratio, record the limiting oxygen index(LOI) LOI=29.8% of matrix material, maximum smoke density D
m=238.1.
Embodiment 2:
Steps A: the steps A by embodiment 1 prepares Mg-Al-CO
3The LDHs precursor.
Step B: take by weighing 7.16g (0.02mol) Na
2HPO
412H
2O is mixed with the phosphate solution of 0.5M.
Step C: get the LDHs 4.76g (0.01mol) that steps A obtains and join in the container of containing the 100mL deionized water, the room temperature lower magnetic force stirs, and obtains hydrotalcite suspension.
Step D: stir on one side, on one side phosphate solution is added in the LDHs suspension, drip the H of 0.1M then
3PO
4, regulate pH=4.5, drip and finish, condensing reflux 1.5h filters, washs to the pH value and is about 7.90 ℃ of dry 24h, the intercalation assembling obtains about 50% dihydrogen phosphate intercalation configuration LDHs material.
Learn that by XRD spectra, IR spectrogram and ultimate analysis the hydrogen phosphate negatively charged ion partly replaces CO among the LDHs
3 2-Enter the LDHs interlayer, wherein the amount of dihydrogen phosphate is about 50% of interlayer anion total amount.
This product and PE material is undertaken compound by 70: 100 mass ratio, record the limiting oxygen index(LOI) LOI=29.1% of matrix material, maximum smoke density D
m=187.4.
Embodiment 3:
Steps A: obtain compound with regular structure Zn-Al-CO preferably by embodiment 1 step
3The LDHs precursor.
Step B: take by weighing 1.74g (0.01mol) K
2HPO
4, be mixed with the phosphate solution of 0.2M.
Step C:6.40g (0.01mol) LDHs joins in the container of containing the 100mL deionized water, and the room temperature lower magnetic force stirs, and obtains hydrotalcite suspension.
Step D: stir on one side, on one side phosphate solution is added in the LDHs suspension, drip the H of 0.1M
3PO
4, regulate pH=5.0, drip and finish, condensing reflux 1h filters, washs to the pH value and is about 7.60 ℃ of dry 24h, the intercalation assembling obtains about 25% dihydrogen phosphate intercalation configuration LDHs material.
Learn that by XRD spectra and IR spectrum analysis the hydrogen phosphate negatively charged ion partly replaces CO among the LDHs
3 2-Enter the LDHs interlayer, wherein the amount of dihydrogen phosphate is about 25% of interlayer anion total amount.
Its flame-retardant smoke inhibition performance of this dihydrogen phosphate intercalation LDHs material undetermined.
Claims (3)
1. the preparation method of a phosphate pillared ht, step is as follows:
A. adopting known hydrotalcite LDHs preparation method to prepare interlayer anion is CO
3 2-Hydrotalcite LDHs-CO
3, its structural formula is: [M
2+ 1-xM
3+ x(OH)
2]
X+(CO
3)
2- X/2MH
2O, 0.2≤x≤0.33 wherein, m is an interlayer crystal water molecule number, its laminate divalence, Tricationic mol ratio M
2+/ M
3+=2-4: 1; M
2+Be Mg
2+, Ni
2+, Zn
2+, Fe
2+Or Cu
2+Any in the divalent-metal ion; M
3+Be Co
3+, Fe
3+, Ti
3+, Al
3+Or Ga
3+Any in the trivalent metal ion;
B. be the phosphate solution of 0.1-1.0M with the bigger phosphoric acid salt compound concentration of solubleness;
C. the LDHs that steps A is prepared joins in the container that fills deionized water by the amount of 20-30g/L, and the room temperature lower magnetic force stirs, and obtains hydrotalcite suspension;
D. the volume ratio with hydrotalcite suspension and phosphate solution is 1: the ratio of 0.5-3, press phosphate anion and the interior CO of LDHs in the phosphate solution
3 2-The exchange ratio is determined the add-on of phosphate solution, stir on one side, on one side phosphate solution is added in the hydrotalcite suspension, with the H of 0.1M
3PO
4Solution is regulated pH=4.5-5.0, drips to finish, and condensing reflux 1-2h filters, washs neutrality, and 60-100 ℃ of dry 24h obtains containing the pillared LDHs of dihydrogen phosphate.
2. the preparation method of borate intercalation hydrotalcite according to claim 1 is characterized in that the laminate divalent-metal ion of hydrotalcite precursor prepared in the steps A is Mg
2+Or Zn
2+Trivalent metal ion is Al
3+The used phosphoric acid salt of step B is sodium phosphate or potassiumphosphate.
3. the preparation method of borate intercalation hydrotalcite according to claim 1, it is characterized in that concentration or add-on by the phosphate solution of controlled step B, the degree that the regulation and control intercalation carries out obtains the serial intercalated houghite that dihydrogen phosphate accounts for interlayer anion total amount 20-100wt%.
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|---|---|---|---|
| CN 03120913 CN1225514C (en) | 2003-03-25 | 2003-03-25 | Phosphate intercalation water talc and its preparation method and use as fire retardant |
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| CN1225514C true CN1225514C (en) | 2005-11-02 |
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- 2003-03-25 CN CN 03120913 patent/CN1225514C/en not_active Expired - Fee Related
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Assignee: Sijiantong Sci. & Tech. Dev. Co., Ltd., Beijing Assignor: Beijing University of Chemical Technology Contract fulfillment period: 2006.10.20 to 2012.10.20 contract change Contract record no.: 2008990001354 Denomination of invention: Phosphate intercalation water talc and its preparation method and use as fire retardant Granted publication date: 20051102 License type: Exclusive license Record date: 2008.12.4 |
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