CN105233630A - Hydroxyethyl carboxymethyl cellulose applied benzene series discharge exhaust gas treatment liquid and preparation method thereof - Google Patents
Hydroxyethyl carboxymethyl cellulose applied benzene series discharge exhaust gas treatment liquid and preparation method thereof Download PDFInfo
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- CN105233630A CN105233630A CN201510645223.8A CN201510645223A CN105233630A CN 105233630 A CN105233630 A CN 105233630A CN 201510645223 A CN201510645223 A CN 201510645223A CN 105233630 A CN105233630 A CN 105233630A
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Abstract
The invention relates to a hydroxyethyl carboxymethyl cellulose applied benzene series discharge exhaust gas treatment liquid and a preparation method thereof. Raw materials of the treatment liquid have the characteristics of easy degradation and low price, and are mixed according to a special ratio to realize cooperative effects, so the organic exhaust gas absorption rate of the treatment liquid is greatly removed, and benzene series discharge exhaust gases are effectively removed.
Description
Technical field
The present invention relates to a kind of liquid for treating waste gas, particularly a kind of benzene series discharging waste gas treatment fluid applying hydroxyethyl carboxymethyl cellulose.
The invention still further relates to the preparation method of above-mentioned treatment fluid.
Background technology
Toluene, dimethylbenzene, benzene, be industrially commonly called as " triphen ", is widely used in fuel, agricultural chemicals, production of flavor, makes paint, pharmacy, the industries such as Furniture manufacture as industrial chemicals or solvent.In recent years along with the development of electronics industry, machinery, automobile making, printing, shoemaking, coatings industry, application toluene, benzene etc. get more and more as the occasion of solvent, thus cause and volatilize a large amount of gas benzene in air.Therefore waste gas containing benzene is also day by day serious for the pollution of air.They are poisonous organic compound, and leukaemia is the modal malignant tumour relevant with benzene poisoning, and toluene poisoning main manifestations is the impression to nervous centralis, and dimethylbenzene toxicity major effect renal function, embryo or reproductive system.
Processing method for " triphen " generally have combustion method, active carbon adsorption,
Combustion method not easily processes large quantity of exhaust gas, and complicated operation has certain danger.After active carbon adsorption adsorbs certain waste gas, adsorption capacity can decline, and needs the activated carbon that more renews or to its regeneration process, be therefore only applicable to the waste gas that low concentration, tolerance are little, and continuation is not high, easy secondary pollution.
At Chinese patent 200710032770.4, a kind of method of waste gas containing benzene liquid-spraying purified liquid process waste gas is proposed in 201410447382.2 and 201110150485.9, although said method is simple to operate, cost is low, effect stability, but its purifying rate need further raising, and when it using halogen-containing material, if improper use, easily cause the pollution to environment.
Summary of the invention
The present invention completes to solve above-mentioned deficiency of the prior art, the object of this invention is to provide a kind of benzene series discharging waste gas treatment fluid applying hydroxyethyl carboxymethyl cellulose, this treatment fluid is by special hydroxyethyl-carboxymethyl preparation method, and use the particular composition with it with cooperative effect, effectively improve the assimilation effect of " triphen " waste gas, and its configuration simple, with low cost, effectively overcome deficiency of the prior art.
Technical scheme of the present invention is as described below:
1, apply a benzene series discharging waste gas treatment fluid for hydroxyethyl carboxymethyl cellulose, it is characterized in that being made up of following raw material by weight:
80-110 part water, 2-12 part sodium carbonate, 1-5 sodium humate, 2-8 part acetic acid, 2-8 part defoamer 664,1-10 HPMA (HPMA), 1-10 part neopelex, 2-4 part hydroxy silicon oil, 5-15 part hydroxyethyl carboxymethyl cellulose, 2-4 part modified sodium lignosulfonate.
2, the treatment fluid according to 1, it is characterized in that the preparation method of described hydroxyethyl carboxymethyl cellulose is: purified cotton powder 10 powder, expoxy propane 5-20 part, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, react 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose.
Present invention also offers above-mentioned 1, the preparation method of the treatment fluid of 2, is characterized in that:
1) purified cotton powder 10 powder, expoxy propane 5-20 part, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 5-15 part of obtaining, joined in 80-110 part water, then 2-12 part sodium carbonate is added successively, 1-5 sodium humate, 2-8 part acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then 2-8 part defoamer 664 is added, 1-10 HPMA (HPMA), 1-10 part neopelex improves temperature to 40 degrees Celsius of Keep agitation 1 hour, add 2-4 part hydroxy silicon oil again, 2-4 part modified sodium lignosulfonate, stirs 30 minutes, mixes and obtain finished product.
Detailed description of the invention
Below in conjunction with embodiment and comparative example, the present invention is described in detail, and following embodiment is only used for the detailed explanation to description, not as restriction of the present invention.
Embodiment 1
1) purified cotton powder 10 powder, expoxy propane 5 parts, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 5 parts that obtains, joined in 80 parts of water, then added 2 parts of sodium carbonate successively, 1 sodium humate, 2 parts of acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then add 2 parts of defoamers, 664,1 part of HPMA (HPMA), 1 part of neopelex improves temperature to 40 degrees Celsius of Keep agitation 1 hour, add 2 parts of hydroxy silicon oils again, 2 parts of modified sodium lignosulfonates, stir 30 minutes, mix and obtain finished product.
Embodiment 2
1) purified cotton powder 10 powder, expoxy propane 15 parts, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 10 parts that obtains, joined in 95 parts of water, then added 8 parts of sodium carbonate successively, 3 sodium humates, 5 parts of acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then add 5 parts of defoamers 664,6 HPMA (HPMA), 6 parts of neopelexes improve temperature to 40 degrees Celsius of Keep agitation 1 hour, add 3 parts of hydroxy silicon oils again, 3 parts of modified sodium lignosulfonates, stir 30 minutes, mix and obtain finished product.
Embodiment 3
1) purified cotton powder 10 powder, expoxy propane 20 parts, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 15 parts that obtains, joined in 110 parts of water, then added 12 parts of sodium carbonate successively, 5 sodium humates, 8 parts of acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then add 8 parts of defoamers 664,10 HPMA (HPMA), 10 parts of neopelexes improve temperature to 40 degrees Celsius of Keep agitation 1 hour, add 4 parts of hydroxy silicon oils again, 4 parts of modified sodium lignosulfonates, stir 30 minutes, mix and obtain finished product.
Comparative example 1
Common commercially available hydroxyethyl carboxymethyl cellulose 5 parts, joined in 80 parts of water, then added 2 parts of sodium carbonate successively, 1 sodium humate, 2 parts of acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then add 2 parts of defoamers, 664,1 part of HPMA (HPMA), 1 part of neopelex improves temperature to 40 degrees Celsius of Keep agitation 1 hour, add 2 parts of hydroxy silicon oils again, 2 parts of modified sodium lignosulfonates, stir 30 minutes, mix and obtain finished product.
Comparative example 2
1) purified cotton powder 10 powder, expoxy propane 5 parts, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 5 parts that obtains, joined in 80 parts of water, then added 2 parts of sodium carbonate successively, 1 sodium humate, 2 parts of acetic acid, 2 parts of defoamers, 664,1 part of HPMA (HPMA), 1 part of neopelex, 2 parts of hydroxy silicon oils, 2 parts of modified sodium lignosulfonates, stir 1 hour, mix and obtain finished product.
Test case 1
Get the treatment fluid of above-described embodiment 1-3, comparative example 1-2 respectively, mixing organic exhaust gas benzene,toluene,xylene concentration being 100ppm passes in treatment fluid with the speed of 8L/min, and control liquid-gas ratio is 15L/m
2, obtain the extraction efficiency of benzene,toluene,xylene waste gas, concrete numerical value is listed in table 1 below.
Table 1
Benzene clearance | Toluene removal rate | Dimethylbenzene clearance | |
Embodiment 1 | 85.8% | 85.3% | 89.8% |
Embodiment 2 | 87.3% | 87.7% | 89.9% |
Embodiment 3 | 84.9% | 84.1% | 87.8% |
Comparative example 1 | 75.5% | 75.3% | 78.1% |
Comparative example 2 | 81.6% | 81.4% | 82.2% |
Can be found out by above-mentioned numerical value, the benzene,toluene,xylene clearance of embodiment 1-3 is greatly improved than the clearance in Chinese patent 201410447382.2, hydroxyethyl-carboxymethyl is prepared by using specific process, and itself and particular components are configured as treatment fluid, effectively improve the absorption clearance containing benzene organic exhaust gas.The hydroxyethyl carboxymethyl cellulose of specific process modification is not used in comparative example 1, and employ common commercially available hydroxyethyl carboxymethyl cellulose, its clearance decreases than embodiment 1-3, therefore can find out that the carboxymethyl hydroxyethyl cellulose that Special Modifying Method obtains has a significant impact raising organic benzene, organic clearance, and only by each mixing of materials in comparative example 2, its organic benzene, organic clearance also decreases, and therefore can find out that the preparation method for the treatment of fluid, incorporation time, temperature also have certain influence for the clearance of final benzene.
beneficial effect
Can be found out by the data of above-described embodiment and comparative example, the hydroxyethyl carboxymethyl cellulose prepared by the present invention coordinates the absorptivity for the treatment of fluid to waste gas containing benzene of particular components to significantly improve, effectively eliminate the toxic gas at waste gas end, and treatment fluid safety of the present invention, economy are not easy to cause secondary pollution.
Above-mentionedly only several specific embodiments in the present invention to be illustrated; but can not as protection scope of the present invention; every according to the change of the equivalence done by design spirit in the present invention or to modify or equal proportion zooms in or out, all should think and fall into protection scope of the present invention.
Claims (3)
1. apply a benzene series discharging waste gas treatment fluid for hydroxyethyl carboxymethyl cellulose, it is characterized in that being made up of following raw material by weight:
About 80-110 part water, 2-12 part sodium carbonate, 1-5 sodium humate, 2-8 part acetic acid, 2-8 part defoamer 664,1-10 HPMA (HPMA), 1-10 part neopelex, 2-4 part hydroxy silicon oil, 5-15 part hydroxyethyl carboxymethyl cellulose, 2-4 part modified sodium lignosulfonate.
2. treatment fluid according to claim 1, it is characterized in that the preparation method of described hydroxyethyl carboxymethyl cellulose is: purified cotton powder 10 powder, expoxy propane 5-20 part, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, react 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose.
3. the preparation method of the benzene series discharging waste gas treatment fluid of the application hydroxyethyl carboxymethyl cellulose according to claim 1-2, is characterized in that:
1) purified cotton powder 10 powder, expoxy propane 5-20 part, monoxone 4 parts, isopropyl alcohol 50 parts, 100 parts, water, 30 parts, potassium hydroxide, by above-mentioned mixing of materials, reacts 4 hours at 50 c, with acetone precipitation, alcoholic solvent washs, and drying obtains water soluble hydroxyethyl carboxymethyl cellulose;
2) step 1 is got) hydroxyethyl carboxymethyl cellulose 5-15 part of obtaining, joined in 80-110 part water, then 2-12 part sodium carbonate is added successively, 1-5 sodium humate, 2-8 part acetic acid was 30 degrees Celsius of lower stirring and dissolving 30 minutes, then 2-8 part defoamer 664 is added, 1-10 HPMA (HPMA), 1-10 part neopelex improves temperature to 40 degrees Celsius of Keep agitation 1 hour, add 2-4 part hydroxy silicon oil again, 2-4 part modified sodium lignosulfonate, stirs 30 minutes, mixes and obtain finished product.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1459464A (en) * | 2002-05-23 | 2003-12-03 | 武汉理工大学 | Preparation method of water soluble hydroxyethyl carboxymethyl cellulose thickener |
CN103157362A (en) * | 2011-12-09 | 2013-06-19 | 中国科学院广州地球化学研究所 | Preparation method of micro-emulsion absorption liquid used for processing organic exhaust gas |
CN103752157A (en) * | 2014-01-26 | 2014-04-30 | 河北工程大学 | Catching agent of benzene series compounds and preparation method thereof |
CN104275074A (en) * | 2014-05-13 | 2015-01-14 | 浙江大学 | Absorption liquid for treating benzene series organic waste gas and preparation method of absorption liquid for treating benzene series organic waste gas |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1459464A (en) * | 2002-05-23 | 2003-12-03 | 武汉理工大学 | Preparation method of water soluble hydroxyethyl carboxymethyl cellulose thickener |
CN103157362A (en) * | 2011-12-09 | 2013-06-19 | 中国科学院广州地球化学研究所 | Preparation method of micro-emulsion absorption liquid used for processing organic exhaust gas |
CN103752157A (en) * | 2014-01-26 | 2014-04-30 | 河北工程大学 | Catching agent of benzene series compounds and preparation method thereof |
CN104275074A (en) * | 2014-05-13 | 2015-01-14 | 浙江大学 | Absorption liquid for treating benzene series organic waste gas and preparation method of absorption liquid for treating benzene series organic waste gas |
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Application publication date: 20160113 |