CN104459038A - Detecting absorption reagent for benzene series compounds and preparation method of detecting absorption reagent - Google Patents
Detecting absorption reagent for benzene series compounds and preparation method of detecting absorption reagent Download PDFInfo
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- CN104459038A CN104459038A CN201410663035.3A CN201410663035A CN104459038A CN 104459038 A CN104459038 A CN 104459038A CN 201410663035 A CN201410663035 A CN 201410663035A CN 104459038 A CN104459038 A CN 104459038A
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Abstract
The invention relates to a detecting absorption reagent for benzene series compounds and a preparation method of the detecting absorption reagent, and belongs to the field of detecting reagents. The detecting absorption reagent for the benzene series compounds comprises the following raw materials in parts by mass: 35-48 parts of nanometer titania, 5-16 parts of sodium dodecyl alcohol polyvinyl ether sulfate, 2-8 parts of sorbitan fatty acid ester, 5-14 parts of rose essential oil, 9-20 parts of alga oligosaccharides, 6-10 parts of licoflavone, 5-10 parts of N-sodium lauroyl sarcosine, 5-12 parts of ethylene glycol and 35-45 parts of water. The detecting absorption reagent disclosed by the invention has good absorptivity on the benzene series compounds; the absorptivity on methylbenzene can be up to 90%; the absorptivity on xylene can be up to 95%; in addition, the detecting absorption reagent also has good detecting performance on the benzene series compounds; and presence of the benzene series compounds can be rapidly detected.
Description
Technical field
The invention belongs to and detect reagent field, be specifically related to a kind of benzene homologues and detect absorption reagent and preparation method thereof.
Background technology
Benzene and benzene homologues are light yellow liquid, have strong aroma gases, and volatile is steam, and inflammable poisonous.In current interior decoration, multiplex toluene, dimethylbenzene replace purified petroleum benzin to make solvent or the thinning agent of various glue paint and anti-hydrolyzed material.And benzene compounds is defined as strongly carcinogenic material by the World Health Organization (WHO) at present.Owing to using benzene homologues in current indoor hardware fitting, people there will be the phenomenon of central nervous system anesthesia when sucking the benzene homologues of high concentration at short notice, the lighter can dizzy, headache, nauseating, uncomfortable in chest, weak, clouding of consciousness, and severe patient can cause stupor so that breathing, circulatory failure and dead.
Benzene homologues mainly in following several ornament materials content higher: paint, the adjuvant of various paint and thinning agent, various adhesive, waterproof material etc.Therefore in order to keep the living environment of good health, the detection of benzene homologues and absorption are had great importance.
But the effect of existing benzene homologues absorbing agent is still barely satisfactory, lower to the absorptivity of benzene homologues, and cannot detect whether benzene homologues still exists.
Therefore the technical barrier having field urgently to be resolved hurrily that the deficiencies in the prior art have become existing how is overcome.
Summary of the invention
The object of the invention is to solve the deficiencies in the prior art, provide a kind of benzene homologues to detect absorption reagent and preparation method thereof, this detection absorbing agent has good absorption to benzene homologues, sensitiveer to the detection of benzene homologues.
The technical solution used in the present invention is as follows:
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 35-48 part, dodecyl alcohol polyvinylether sodium sulphate 5-16 part, sorbitan fatty acid esters 2-8 part, Rosa Damascana 5-14 part, alga oligosaccharides 9-20 part, licoflavone 6-10 part, N-sodium lauroyl sarcosine 5-10 part, ethylene glycol 5-12 part, water 35-45 part.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 37-46 part, dodecyl alcohol polyvinylether sodium sulphate 7-14 part, sorbitan fatty acid esters 3-7 part, Rosa Damascana 6-13 part, alga oligosaccharides 10-18 part, licoflavone 7-9 part, N-sodium lauroyl sarcosine 6-9 part, ethylene glycol 6-11 part, water 37-43 part.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 39-44 part, dodecyl alcohol polyvinylether sodium sulphate 9-12 part, sorbitan fatty acid esters 4-6 part, Rosa Damascana 7-12 part, alga oligosaccharides 11-17 part, licoflavone 7-8 part, N-sodium lauroyl sarcosine 6-8 part, ethylene glycol 8-10 part, water 39-42 part.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 37 parts, 7 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 3 parts, Rosa Damascana 6 parts, alga oligosaccharides 10 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 6 parts, 37 parts, water.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 46 parts, 14 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 7 parts, Rosa Damascana 13 parts, alga oligosaccharides 18 parts, licoflavone 9 parts, N-sodium lauroyl sarcosine 9 parts, ethylene glycol 11 parts, 43 parts, water.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 39 parts, 9 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 4 parts, Rosa Damascana 7 parts, alga oligosaccharides 11 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 8 parts, 39 parts, water.
Described benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 44 parts, 12 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 6 parts, Rosa Damascana 12 parts, alga oligosaccharides 17 parts, licoflavone 8 parts, N-sodium lauroyl sarcosine 8 parts, ethylene glycol 10 parts, 42 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
compared with prior art, its beneficial effect is in the present invention:
The present invention detects absorbing agent and has good absorptivity to benzene homologues, wherein, can up to 90% to the absorptivity of toluene, the absorptivity of P-xylene can up to 95%; In addition, the present invention detects absorbing agent and also has good detection perform to benzene homologues, can detect the existence of benzene homologues fast; Preparation method of the present invention is simple, easy and simple to handle, can promote the use of on a large scale.
Embodiment
Below in conjunction with embodiment, the present invention is described in further detail, the raw material used in the present invention unless otherwise noted, all by commercial acquisition.
embodiment 1
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 35 parts, 5 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 2 parts, Rosa Damascana 5 parts, alga oligosaccharides 9 parts, licoflavone 6 parts, N-sodium lauroyl sarcosine 5 parts, ethylene glycol 5 parts, 35 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
embodiment 2
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 48 parts, 16 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 8 parts, Rosa Damascana 14 parts, alga oligosaccharides 20 parts, licoflavone 10 parts, N-sodium lauroyl sarcosine 10 parts, ethylene glycol 12 parts, 45 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
embodiment 3
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 37 parts, 7 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 3 parts, Rosa Damascana 6 parts, alga oligosaccharides 10 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 6 parts, 37 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
embodiment 4
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 46 parts, 14 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 7 parts, Rosa Damascana 13 parts, alga oligosaccharides 18 parts, licoflavone 9 parts, N-sodium lauroyl sarcosine 9 parts, ethylene glycol 11 parts, 43 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
embodiment 5
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 39 parts, 9 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 4 parts, Rosa Damascana 7 parts, alga oligosaccharides 11 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 8 parts, 39 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
embodiment 6
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 44 parts, 12 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 6 parts, Rosa Damascana 12 parts, alga oligosaccharides 17 parts, licoflavone 8 parts, N-sodium lauroyl sarcosine 8 parts, ethylene glycol 10 parts, 42 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
reference examples 1
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 37 parts, 7 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 3 parts, Rosa Damascana 6 parts, alga oligosaccharides 10 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 6 parts, 37 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana and alga oligosaccharides are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
reference examples 2
Benzene homologues detects absorption reagent, comprises the following raw material according to mass fraction meter: nano titanium oxide 37 parts, 7 parts, dodecyl alcohol polyvinylether sodium sulphate, alga oligosaccharides 10 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 6 parts, 37 parts, water.
Described benzene homologues detects the preparation method of absorption reagent, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
performance test
Detect with the embodiment of the present invention 1 to 6 and reference examples 1 to 2 products obtained therefrom and absorb carbon monoxide, test result sees the following form 1.
Table 1 properties of product test data
Visible, the embodiment of the present invention 1 to 6 gained finished product all has excellent performance, and wherein, embodiment 3 can be considered most preferred embodiment.
Claims (8)
1. benzene homologues detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 35-48 part, dodecyl alcohol polyvinylether sodium sulphate 5-16 part, sorbitan fatty acid esters 2-8 part, Rosa Damascana 5-14 part, alga oligosaccharides 9-20 part, licoflavone 6-10 part, N-sodium lauroyl sarcosine 5-10 part, ethylene glycol 5-12 part, water 35-45 part.
2. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 37-46 part, dodecyl alcohol polyvinylether sodium sulphate 7-14 part, sorbitan fatty acid esters 3-7 part, Rosa Damascana 6-13 part, alga oligosaccharides 10-18 part, licoflavone 7-9 part, N-sodium lauroyl sarcosine 6-9 part, ethylene glycol 6-11 part, water 37-43 part.
3. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 39-44 part, dodecyl alcohol polyvinylether sodium sulphate 9-12 part, sorbitan fatty acid esters 4-6 part, Rosa Damascana 7-12 part, alga oligosaccharides 11-17 part, licoflavone 7-8 part, N-sodium lauroyl sarcosine 6-8 part, ethylene glycol 8-10 part, water 39-42 part.
4. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 37 parts, 7 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 3 parts, Rosa Damascana 6 parts, alga oligosaccharides 10 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 6 parts, 37 parts, water.
5. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 46 parts, 14 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 7 parts, Rosa Damascana 13 parts, alga oligosaccharides 18 parts, licoflavone 9 parts, N-sodium lauroyl sarcosine 9 parts, ethylene glycol 11 parts, 43 parts, water.
6. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 39 parts, 9 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 4 parts, Rosa Damascana 7 parts, alga oligosaccharides 11 parts, licoflavone 7 parts, N-sodium lauroyl sarcosine 6 parts, ethylene glycol 8 parts, 39 parts, water.
7. benzene homologues according to claim 1 detects absorption reagent, it is characterized in that, comprise the following raw material according to mass fraction meter: nano titanium oxide 44 parts, 12 parts, dodecyl alcohol polyvinylether sodium sulphate, sorbitan fatty acid esters 6 parts, Rosa Damascana 12 parts, alga oligosaccharides 17 parts, licoflavone 8 parts, N-sodium lauroyl sarcosine 8 parts, ethylene glycol 10 parts, 42 parts, water.
8. benzene homologues according to claim 1 detects the preparation method of absorption reagent, it is characterized in that, comprise the steps: according to quality proportioning, nano titanium oxide, dodecyl alcohol polyvinylether sodium sulphate, N-sodium lauroyl sarcosine are added to the water successively, stir, again ethylene glycol, sorbitan fatty acid esters, Rosa Damascana, alga oligosaccharides and licoflavone are added wherein successively, stir, obtain described benzene homologues and detect absorption reagent.
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Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4039941A (en) * | 1975-05-09 | 1977-08-02 | Stanford Research Institute | Gas sensor |
JPH04256436A (en) * | 1991-02-05 | 1992-09-11 | Kuraray Chem Corp | Colored activated carbon |
CN1565718A (en) * | 2003-06-30 | 2005-01-19 | 中国石油化工股份有限公司 | Paraxylene sorbent and its preparing method |
CN101259360A (en) * | 2007-12-17 | 2008-09-10 | 昆明理工大学 | Purifying method of waste gases containing benzenes compounds |
CN101301606A (en) * | 2008-07-04 | 2008-11-12 | 内蒙古大学 | Method for preparing doped nanometer titanium oxide photocatalyst |
CN201600356U (en) * | 2009-05-15 | 2010-10-06 | 北京联合大学生物化学工程学院 | Benzene series gas detecting pipe |
CN203203930U (en) * | 2013-04-28 | 2013-09-18 | 北京兰康保科技有限公司 | Air benzene series self-detection box |
CN103537171A (en) * | 2013-10-30 | 2014-01-29 | 许征 | Emulsified liquid for processing organic waste gas, device for processing organic waste gas and method for processing organic waste gas |
CN103551010A (en) * | 2013-09-29 | 2014-02-05 | 安徽华印机电股份有限公司 | Preparation method of nano-grade purifying scavenger |
CN103865337A (en) * | 2012-12-18 | 2014-06-18 | 李辉 | Emulsion paint capable of decomposing formaldehyde |
CN203772749U (en) * | 2013-12-27 | 2014-08-13 | 北京六角体科技发展有限公司 | Formaldehyde/benzene series/ammonia gas rapid self-testing box |
-
2014
- 2014-11-19 CN CN201410663035.3A patent/CN104459038A/en not_active Withdrawn
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4039941A (en) * | 1975-05-09 | 1977-08-02 | Stanford Research Institute | Gas sensor |
JPH04256436A (en) * | 1991-02-05 | 1992-09-11 | Kuraray Chem Corp | Colored activated carbon |
CN1565718A (en) * | 2003-06-30 | 2005-01-19 | 中国石油化工股份有限公司 | Paraxylene sorbent and its preparing method |
CN101259360A (en) * | 2007-12-17 | 2008-09-10 | 昆明理工大学 | Purifying method of waste gases containing benzenes compounds |
CN101301606A (en) * | 2008-07-04 | 2008-11-12 | 内蒙古大学 | Method for preparing doped nanometer titanium oxide photocatalyst |
CN201600356U (en) * | 2009-05-15 | 2010-10-06 | 北京联合大学生物化学工程学院 | Benzene series gas detecting pipe |
CN103865337A (en) * | 2012-12-18 | 2014-06-18 | 李辉 | Emulsion paint capable of decomposing formaldehyde |
CN203203930U (en) * | 2013-04-28 | 2013-09-18 | 北京兰康保科技有限公司 | Air benzene series self-detection box |
CN103551010A (en) * | 2013-09-29 | 2014-02-05 | 安徽华印机电股份有限公司 | Preparation method of nano-grade purifying scavenger |
CN103537171A (en) * | 2013-10-30 | 2014-01-29 | 许征 | Emulsified liquid for processing organic waste gas, device for processing organic waste gas and method for processing organic waste gas |
CN203772749U (en) * | 2013-12-27 | 2014-08-13 | 北京六角体科技发展有限公司 | Formaldehyde/benzene series/ammonia gas rapid self-testing box |
Non-Patent Citations (2)
Title |
---|
王贤亲等: "空气中苯系物TiO2光催化降解研究进展", 《化学研究与应用》 * |
许涛: "苯系物测定方法的研究", 《四川环境》 * |
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