CN1294805C - Water retaining penetration film produced by milling and its preparation method - Google Patents
Water retaining penetration film produced by milling and its preparation method Download PDFInfo
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- CN1294805C CN1294805C CN 200510004881 CN200510004881A CN1294805C CN 1294805 C CN1294805 C CN 1294805C CN 200510004881 CN200510004881 CN 200510004881 CN 200510004881 A CN200510004881 A CN 200510004881A CN 1294805 C CN1294805 C CN 1294805C
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 174
- 230000035515 penetration Effects 0.000 title claims abstract description 51
- 238000003801 milling Methods 0.000 title claims description 46
- 238000002360 preparation method Methods 0.000 title claims description 19
- 239000000835 fiber Substances 0.000 claims abstract description 96
- 239000000843 powder Substances 0.000 claims abstract description 45
- 239000011248 coating agent Substances 0.000 claims abstract description 21
- 238000000576 coating method Methods 0.000 claims abstract description 21
- 239000004927 clay Substances 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 238000005097 cold rolling Methods 0.000 claims abstract description 4
- 239000000243 solution Substances 0.000 claims description 31
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 26
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 22
- 239000003513 alkali Substances 0.000 claims description 20
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- 238000012545 processing Methods 0.000 claims description 14
- 230000003647 oxidation Effects 0.000 claims description 13
- 238000007254 oxidation reaction Methods 0.000 claims description 13
- KSZVHVUMUSIKTC-UHFFFAOYSA-N acetic acid;propan-2-one Chemical compound CC(C)=O.CC(O)=O KSZVHVUMUSIKTC-UHFFFAOYSA-N 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 12
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 238000000465 moulding Methods 0.000 claims description 9
- 238000006386 neutralization reaction Methods 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 8
- 229920000742 Cotton Polymers 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 6
- 239000011118 polyvinyl acetate Substances 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 238000005098 hot rolling Methods 0.000 claims description 5
- -1 polyethylene Polymers 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 4
- 229960000583 acetic acid Drugs 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 239000012362 glacial acetic acid Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 4
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 3
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 3
- 239000002250 absorbent Substances 0.000 claims description 3
- 230000002745 absorbent Effects 0.000 claims description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 3
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 claims description 3
- 239000012990 dithiocarbamate Substances 0.000 claims description 3
- HOIQWTMREPWSJY-GNOQXXQHSA-K iron(3+);(z)-octadec-9-enoate Chemical compound [Fe+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O HOIQWTMREPWSJY-GNOQXXQHSA-K 0.000 claims description 3
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 3
- 235000020778 linoleic acid Nutrition 0.000 claims description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims description 2
- 229940080818 propionamide Drugs 0.000 claims description 2
- 239000002689 soil Substances 0.000 abstract description 22
- 230000004083 survival effect Effects 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 238000005096 rolling process Methods 0.000 abstract 7
- 239000012943 hotmelt Substances 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 description 12
- 230000008595 infiltration Effects 0.000 description 7
- 238000001764 infiltration Methods 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- 238000007306 functionalization reaction Methods 0.000 description 4
- 238000012856 packing Methods 0.000 description 4
- 238000013461 design Methods 0.000 description 3
- 241000223025 Caragana microphylla Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000018650 Pinus massoniana Species 0.000 description 2
- 235000011610 Pinus tabuliformis Nutrition 0.000 description 2
- 241000219000 Populus Species 0.000 description 2
- 241000220317 Rosa Species 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 239000008398 formation water Substances 0.000 description 2
- 238000003973 irrigation Methods 0.000 description 2
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- 235000007630 Elaeagnus umbellata var parvifolia Nutrition 0.000 description 1
- 240000000950 Hippophae rhamnoides Species 0.000 description 1
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- 235000015459 Lycium barbarum Nutrition 0.000 description 1
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- 235000002413 Prunus ansu Nutrition 0.000 description 1
- 244000046101 Sophora japonica Species 0.000 description 1
- 235000010586 Sophora japonica Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 240000003243 Thuja occidentalis Species 0.000 description 1
- 235000008109 Thuja occidentalis Nutrition 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
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- Cultivation Of Plants (AREA)
Abstract
The present invention relates to a rolling water storing penetration film. The raw material mainly adopts water guiding fibre and hot melt powder; firstly, natural fiber is made into the water guiding fibre in the manufacture process, and then the water guiding fibre and the hot melt powder are divided into layers and spread over a workbench of a rolling machine after the water guiding fibre is crushed; the rolling machine manufactures the rolling water storing penetration film after the heat roasting, heat rolling and cold rolling processes; the rolling water storing penetration film is placed at the root part of a plant after filled with water, and then water in the film forms a water potential gradient difference with water in the soil outside the film along the water guiding fibre in the film; the water guiding fibre has a water guiding function under the action of the water potential gradient difference and releases water molecules along the water guiding fibre, and reasonable humidity in the soil is ensured. Both the amount of clay contained in a single root of water guiding fibre after the functionalized coating of the water guiding fibre is completed and the content of the water guiding fibre influence the water guiding speed; because the water potential gradient difference is directly related to the moisture conditions of the outside soil, the water penetration speed of the rolling water storing penetration film can carry out self regulation according to the moisture conditions of the outside soil; the characteristics can ensure the survival of plants in arid and semiarid areas.
Description
Technical field
The present invention relates to a kind of forestry and agriculture field is device of plant water supply and preparation method thereof, relates in particular to a kind of water retaining penetration film produced by milling and preparation method thereof.
Background technology
Along with the development of the society progress with science and technology, the ability that people conquer nature with nature remodeling is progressively improving.People have caused very big destruction to natural environment in the process that conquers nature with nature remodeling.It has been recognized that the problem that this is serious now, afforestation is the best way in the process that transforms barren hills with the desert, but in these regional tree planting processes how for plant provide for a long time sufficient water source be one for a long time can't fine solution problem, this just causes tree planting to do every year, loses the phenomenon of woods exactly.In agricultural production, also there is above-mentioned problem equally.The survival rate average out to 70% of the tree planting of western arid and semiarid zone, the area that has only is 20%~30%, in order to improve the mode that survival rate generally adopts groundwater abstraction, causes subterranean water level to reduce, ecology further worsens.
The way that addresses this problem at present is to drip infiltration irrigation technology, and this technology comes from Israel, though can realize water-saving irrigation, disposable input is huge, is not suitable for applying on ecological recovery.Other has a kind of technology is the container of water storage directly to be put into underground, and the amount that goes out of water droplet realizes long-term water supply in the control container, and the shortcoming of this method is to regulate output according to soil tilth and floristics, causes very big waste; Also to take out after having the container of water storage to use up again, cause waste of manpower resource, otherwise pollute the environment.
Summary of the invention
In view of above-mentioned existing in prior technology problem, the purpose of this invention is to provide and a kind ofly can satisfy above-mentioned requirements, can be long-term be plant water supply according to soil tilth and floristics, but need not to take out the water retaining penetration film produced by milling of natural degradation after using up.
The objective of the invention is to be achieved through the following technical solutions:
A kind of water retaining penetration film produced by milling, it is characterized in that preparing burden water-release fibre and thermal fusing powder are formed; Its percentage by weight is:
Water-release fibre 0.1%~40%;
Thermal fusing powder 60%~99.9%;
Each component percentage by weight summation is 100%.Be directed to different plant varieties and choose different proportionings with soil condition.
The raw material of described water-release fibre is a native fiber, is adopted as cotton fiber usually.
Thermal fusing powder comprises molding powder, low thermal oxidation agent and flexibilizer, and the shared total weight percent of each component is:
Molding powder 60%~99.9%;
Low thermal oxidation agent 0%~3%;
The percentage by weight that each component percentage by weight summation accounts for gross weight is 60%~99.9%.
Described molding powder is polyvinyl acetate, polyethylene, polyvinyl chloride and/or Merlon.
Described low thermal oxidation agent is mixed by arbitrary proportion by in the following material one or more and forms:
Dibutyl tin laurate, acetate acetone close manganese, acetate acetone and close that iron, acetate acetone close cobalt, acetate acetone closes nickel, dithiocarbamate iron, iron oleate, linoleic acid iron, naphthane;
The each component optimum weight percentage of above-mentioned thermal fusing powder is:
Polyvinyl acetate 60%~97.9%;
Low thermal oxidation agent 2%;
The preparation method of described water retaining penetration film produced by milling is characterized in that, comprising:
A, native fiber is made water-release fibre through submissiveization processing;
Concrete steps also comprise:
A1, native fiber is carried out the alkali lye preliminary treatment;
Adopting alkali lye is that concentration is 6%~26% sodium hydrate aqueous solution or ammoniacal liquor, and native fiber was soaked in alkali lye 20 minutes~100 minutes;
A2, the pretreated native fiber of alkali lye is carried out the acid solution neutralisation treatment;
Adopting acid solution is that concentration is 4%~6% glacial acetic acid solution, and the pretreated native fiber of alkali lye was soaked in acid solution 25 minutes~35 minutes;
A3, the native fiber after the sour neutralisation treatment is carried out the face coat processing;
Also can be divided into following two steps:
A31, preparation coating solution;
Described coating solution batching is made up of clay powders, hydrophilizing agent and water, and its percentage by weight is:
Clay powders 5%~45%;
Hydrophilizing agent 0.50%~15%;
Water surplus.
Each component percentage by weight summation is 100%;
Described clay powders granularity is smaller or equal to 0.2 millimeter; Described hydrophilizing agent can be super absorbent resin, can be polyvinyl alcohol, poly-propionamide;
Its compound method be with clay powders and hydrophilizing agent in accordance with regulations percentage by weight add in an amount of water and stir, be heated to 85 ℃~90 ℃ simultaneously.
A32, the native fiber after the acid neutralization of A2 step is soaked oven dry then in coating solution, perhaps coating solution is sprayed on the native fiber back and dries.
Native fiber shredding after A4, the face coat processing is handled and is made water-release fibre.
B, to water-release fibre and thermal fusing powder in accordance with regulations percentage by weight intersperse among on the roll mill workbench;
Usually water-release fibre is blown to by air-flow on the workbench of roll mill, water-release fibre falls naturally to scatter and reticulates; By the vibratory sieve on the workbench thermal fusing powder is evenly distributed on the workbench of roll mill.Water-release fibre that is scattered and thermal fusing powder can be respectively one or more layers and arrange at interval.
To 90 ℃~180 ℃, hot rolling or cold rolling go out water retaining penetration film produced by milling through the heat baking for C, roll mill.
By above technical scheme water retaining penetration film produced by milling of the present invention as can be known, raw material mainly adopts water-release fibre and thermal fusing powder, in manufacturing process, earlier native fiber is made water-release fibre, then water-release fibre is pulverized the back and intersperse among on the workbench of roll mill with the thermal fusing powder layering.Roll mill goes out water retaining penetration film produced by milling through heat baking, hot rolling.
Since water-release fibre be by native fiber through alkali, sour preliminary treatment, realize functional fibre after the functionalization coating with molecule water guide characteristic.Be mixed and made into water retaining penetration film produced by milling with this water-release fibre and thermal fusing powder.Utilize this water retaining penetration film produced by milling dress water to be placed on plant roots, the water formation water potential gradient outside the water-release fibre of the water in the film in film and the film in the soil is poor.Water-release fibre has the water guide function under the effect of water potential gradient difference, discharge hydrone along water-release fibre, and guaranteeing has a rational humidity in the plant soil on every side.For a single water-release fibre, what of institute's argillaceous directly influence the water transmitting ability of water-release fibre after the functionalization coating, and many water guides of content speed of clay is fast, clay contain that many water guides speed is slow less.In addition, can also control the overall rate of oozing out of water by the content that changes water-release fibre in the water retaining penetration film produced by milling, many water retaining penetration film produced by milling of content water guide speed of water-release fibre is fast, and the few water retaining penetration film produced by milling water guide speed of the content of water-release fibre is slow.Have, because water potential gradient difference and extraneous soil moisture content have direct relation, the speed of the more little infiltration of soil moisture is fast more again, and the speed of the big more infiltration of soil moisture is slow more, when soil moisture reaches 40% left and right sides, stops outside infiltration.Therefore the seepage velocity of water retaining penetration film produced by milling can be according to extraneous soil moisture content self-control.Above characteristic can guarantee plant surviving and survive in the arid and semi-arid lands.
Embodiment
The embodiment of its composition of water retaining penetration film produced by milling of the present invention is:
The first step, choose the raw material that cotton fiber is a water-release fibre, it carried out following processing:
1, native fiber is carried out the alkali lye preliminary treatment;
Because the complexity of the cellulosic aggregation bunch structure in the native fiber has high-crystallinity simultaneously again.Make cellulose low to the accessibility of hydrophilic reagent.Thereby the effect of direct coating is relatively poor, so need carry out the alkali lye preliminary treatment to native fiber.Its processing method is:
Adopting alkali lye is that concentration is 6%~26% sodium hydrate aqueous solution or ammoniacal liquor, and native fiber was soaked in alkali lye 20 minutes~100 minutes.
2, the pretreated native fiber of alkali lye is carried out the acid solution neutralisation treatment;
Because of native fiber having been carried out the alkali lye processing, so also need the pretreated native fiber of alkali lye is carried out the acid solution neutralisation treatment.Its processing method is:
Adopting acid solution is that concentration is 4%~6% glacial acetic acid solution, and the pretreated native fiber of alkali lye was soaked in acid solution 25 minutes~35 minutes.
3, the native fiber after the sour neutralisation treatment is carried out the face coat processing;
Through the surperficial amorphous enlarged areas of the native fiber after the processing of above-mentioned 1 and 2 processes, accessibility increases, and is right to carry out the face coat processing.Its process can be divided into following two steps:
(1) preparation coating solution;
Described coating solution batching is made up of clay powders, hydrophilizing agent and water, and its percentage by weight is:
Clay powders 5%~45%;
Hydrophilizing agent 0.50%~15%;
Water surplus.
Each component percentage by weight summation is 100%;
Above-mentioned clay powders granularity is smaller or equal to 0.2 millimeter; Above-mentioned hydrophilizing agent can be polyvinyl alcohol;
Its compound method be with clay powders and hydrophilizing agent in accordance with regulations percentage by weight add in an amount of water and stir, be heated to 85 ℃~90 ℃ simultaneously.
In addition, hydrophilizing agent herein is a super absorbent resin, can also adopt the macromolecule solvent of carboxyl, hydroxyl, amide groups, amido and ether.These groups not only can make macromolecule have transmissibility, also have cohesive, film forming, lubricity, one-tenth colloidality, dispersiveness simultaneously and increase the property received.
(2) face coat processing
Native fiber after step 1 and 2 processing is soaked oven dry then in coating solution, also coating solution can be sprayed on back oven dry on the native fiber.
4, the native fiber shredding after the face coat processing is handled and is made water-release fibre.
Second step, preparation thermal fusing powder
Described thermal fusing powder comprises molding powder, low thermal oxidation agent and flexibilizer, is that the shared total weight percent of example each component is with the polyvinyl acetate molding powder:
Polyvinyl acetate 60%~97.9%;
Low thermal oxidation agent 2%;
The percentage by weight that each component percentage by weight summation accounts for gross weight is 60%~99.9%.
Described molding powder can also use polyethylene, polyvinyl chloride and/or polycarbonate plastic powder.
Described low thermal oxidation agent is mixed by arbitrary proportion by in the following material one or more and forms:
Dibutyl tin laurate, acetate acetone close manganese, acetate acetone and close that iron, acetate acetone close cobalt, acetate acetone closes nickel, dithiocarbamate iron, iron oleate, linoleic acid iron, naphthane;
Above-mentioned each component percentage by weight in accordance with regulations mixed get final product.
The preparation method of the 3rd step, water retaining penetration film produced by milling
1, the water-release fibre with required percentage by weight blows to by air-flow on the workbench of roll mill, and water-release fibre falls naturally to scatter and reticulates;
2, be evenly distributed on the netted water-release fibre that cloth is good on the roll mill workbench by the thermal fusing powder of the vibratory sieve on the workbench required percentage by weight;
3, repeat 1 and 2 steps up to the regulation technological requirement;
4, to 90 ℃~180 ℃, hot rolling or cold rolling go out water retaining penetration film produced by milling to roll mill through the heat baking.
Water retaining penetration film produced by milling of the present invention at first will be determined the raw material proportioning of water retaining penetration film produced by milling according to the soil condition of locality and the kind of the plant of being planted when practical application.Concrete example is as follows:
To be example in arid and semi-arid lands plantation Chinese pine, the raw material weight percentage of its water retaining penetration film produced by milling is:
Cotton fiber 12%;
Polyvinyl acetate 86%;
Low thermal oxidation agent 2%.
Its coating solution ingredients by weight percentage is:
Clay powders (granularity is smaller or equal to 0.2 millimeter) 25%;
Polyvinyl alcohol 8%;
Water 67%.
Three kinds of batch mixes are stirred, be heated to 85 ℃~90 ℃ simultaneously, make coating solution
Is to soak 60 minutes in 16% the sodium hydrate aqueous solution cotton fiber in concentration.The cotton fiber of alkalization being adopted concentration is that 5% glacial acetic acid solution soaked 30 minutes again.Cotton fiber after handling is soaked oven dry then in coating solution.Standby.Water retaining penetration film produced by milling is made in method hot rolling according to the 3rd step.
Through above-mentioned preparation method it is made and to make water retaining penetration film produced by milling, in use water retaining penetration film produced by milling is made water bag, at any water of on-the-spot can locality of planting trees, the water bag that will fill water then is positioned over the sapling root and afforests.Its modes of emplacement can be according to the kind difference of nursery stock, with water bag horizontal positioned or vertical the placement.Certainly the size and the quantity of water bag also are to do corresponding adjustment according to the kind of nursery stock.
Since water-release fibre be by native fiber through alkali, sour preliminary treatment, realize functional fibre after the functionalization coating with molecule water guide characteristic.Be mixed and made into water retaining penetration film produced by milling with this water-release fibre and thermal fusing powder.Utilize this water retaining penetration film produced by milling dress water to be placed on plant roots, the water formation water potential gradient outside the water-release fibre of the water in the film in film and the film in the soil is poor.Water-release fibre has the water guide function under the effect of water potential gradient difference, discharge hydrone along water-release fibre, and guaranteeing has a rational humidity in the plant soil on every side.For a single water-release fibre, what of institute's argillaceous directly influence the water transmitting ability of water-release fibre after the functionalization coating, and many water guides of content speed of clay is fast, clay contain that many water guides speed is slow less.In addition, can also control the overall rate of oozing out of water by the content that changes water-release fibre in the water retaining penetration film produced by milling, many water retaining penetration film produced by milling of content water guide speed of water-release fibre is fast, and the few water retaining penetration film produced by milling water guide speed of the content of water-release fibre is slow.Have, because water potential gradient difference and extraneous soil moisture content have direct relation, the speed of the more little infiltration of soil moisture is fast more again, and the speed of the big more infiltration of soil moisture is slow more, when soil moisture reaches 40% left and right sides, stops outside infiltration.Therefore the seepage velocity of water retaining penetration film produced by milling can be according to extraneous soil moisture content self-control.Above characteristic can guarantee plant surviving and survive in the arid and semi-arid lands.
The seepage velocity of above factor affecting water retaining penetration film produced by milling can adopt a unified parameter to weigh, and is exactly a day water percolating capacity, generally is unit with the gram.The general parameter that also adopts day water percolating capacity is just determined the packing water yield of different nursery stocks aspect afforestation.As table 1 is optimal design table at the seedling packing water yield of different nursery stocks or different seedling ages.
Because what the plastic film of water retaining penetration film produced by milling adopted is degradable polyethylene, contain the low thermal oxidation agent in the material because of degradable polyethylene, plastic film is at short notice with regard to degradable under the effect of low thermal oxidation agent, growth to plant can not impact, and has possessed environment protecting simultaneously yet.
The raw material proportioning of the above water retaining penetration film produced by milling only is preferable embodiment and the representational embodiment of the present invention; And the preparation method of described water retaining penetration film produced by milling only is the preferable preparation method of the present invention; The structure of described water retaining penetration film produced by milling also only is representational structure simultaneously; But protection scope of the present invention is not limited thereto, and anyly is familiar with those skilled in the art in the technical scope that the present invention discloses, and the variation that can expect easily or replacement all should be encompassed within protection scope of the present invention.Therefore, protection scope of the present invention should be as the criterion with the protection domain of claims.
Table 1 is at the optimal design table of the different seedling packing water yields
Seeds | Seedling age (year) | Packing water design (kg) | Day water percolating capacity (g) |
Populus simonii | 1 | 3 | 50 |
In black anti-willow | 1 | 3 | 50 |
Baicheng poplar No. 2 | 2 | 4 | 67 |
The Xinjiang poplar | 3 | 4 | 67 |
Chinese scholar tree | 2 | 3 | 50 |
English walnut | 2 | 3 | 50 |
Elm | 1 | 3 | 50 |
Arrow-leaved oleaster | 1 | 3 | 50 |
Red building | 1 | 2 | 34 |
Apple | 1 | 2 | 34 |
The sand ground elm | 2 | 3 | 50 |
Vertical elm | 3 | 4 | 67 |
The elm paulownia | 2 | 3 | 50 |
Ansu apricot | 1 | 2 | 34 |
Matrimony vine | 1 | 2 | 34 |
Sacsaoul | 1 | 1 | 17 |
Sea-buckthorn | 1 | 1 | 17 |
Water is cured | 4 | 3 | 50 |
Sabina vulgaris | 2 | 2 | 34 |
Chinese pine | 3 | 2 | 34 |
Dragon spruce | 5 | 2 | 34 |
Arbor-vitae | 3 | 2 | 34 |
Larix principis-rupprechtii | 2 | 1 | 17 |
Caragana microphylla | 1 | 1 | 17 |
White caragana microphylla | 1 | 1 | 17 |
Cloves | 1 | 1 | 17 |
The thorn rose | 1 | 1 | 17 |
Yellow thorn plum | 1 | 1 | 17 |
Many seasons rose | 1 | 1 | 17 |
Claims (10)
1, a kind of water retaining penetration film produced by milling, it is characterized in that preparing burden water-release fibre and thermal fusing powder are formed; Its percentage by weight is:
Water-release fibre 0.1%~40%;
Thermal fusing powder 60%~99.9%;
Each component percentage by weight summation is 100%.
2, water retaining penetration film produced by milling according to claim 1, the raw material that it is characterized in that described water-release fibre is a native fiber, described native fiber can be cotton fiber.
3, water retaining penetration film produced by milling according to claim 1 is characterized in that described thermal fusing powder comprises molding powder and low thermal oxidation agent, and the shared total weight percent of each component is:
Molding powder 60%~99.9%;
Low thermal oxidation agent 0%~3%;
The percentage by weight that each component percentage by weight summation accounts for gross weight is 60%~99.9%.
4, water retaining penetration film produced by milling according to claim 3 is characterized in that described molding powder is polyvinyl acetate, polyethylene, polyvinyl chloride and/or Merlon;
Described low thermal oxidation agent is mixed by arbitrary proportion by in the following material one or more and forms:
Dibutyl tin laurate, acetate acetone close manganese, acetate acetone and close that iron, acetate acetone close cobalt, acetate acetone closes nickel, dithiocarbamate iron, iron oleate, linoleic acid iron, naphthane.
5, a kind of preparation method of described water retaining penetration film produced by milling is characterized in that, comprising:
A, native fiber is made water-release fibre;
B, to water-release fibre and thermal fusing powder in accordance with regulations percentage by weight intersperse among on the roll mill workbench;
To 90 ℃~180 ℃, hot rolling or cold rolling go out water retaining penetration film produced by milling through the heat baking for C, roll mill.
6, the preparation method of water retaining penetration film produced by milling according to claim 5 is characterized in that, described steps A comprises:
A1, native fiber is carried out the alkali lye preliminary treatment;
A2, the pretreated native fiber of alkali lye is carried out the acid solution neutralisation treatment;
A3, the native fiber after the sour neutralisation treatment is carried out the face coat processing;
Native fiber after A4, the face coat processing carries out shredding and is processed into water-release fibre.
7, the preparation method of water retaining penetration film produced by milling according to claim 6 is characterized in that:
The alkali lye that described steps A 1 adopts is that concentration is 6%~26% sodium hydrate aqueous solution or ammoniacal liquor, and native fiber was soaked in alkali lye 20 minutes~100 minutes;
The acid solution that described steps A 2 adopts is that concentration is 4%~6% glacial acetic acid solution, and the native fiber that alkali lye is given after the processing soaked in acid solution 25 minutes~35 minutes;
Described steps A 3 also comprises:
A31, preparation coating solution;
A32, the native fiber after the acid neutralization of A2 step is soaked oven dry then in coating solution, perhaps coating solution is sprayed on the native fiber back and dries.
8, the preparation method of water retaining penetration film produced by milling according to claim 7 is characterized in that: steps A 31 described coating solution batchings are made up of clay powders, hydrophilizing agent and water, and its percentage by weight is:
Clay powders 5%~45%;
Hydrophilizing agent 0.50%~15%;
Water surplus.
Each component percentage by weight summation is 100%;
Described clay powders granularity is smaller or equal to 0.2 millimeter; Described hydrophilizing agent can be super absorbent resin, can be polyvinyl alcohol, poly-propionamide;
Its compound method be with clay powders and hydrophilizing agent in accordance with regulations percentage by weight add in an amount of water and stir, be heated to 85 ℃~90 ℃ simultaneously.
9, the preparation method of water retaining penetration film produced by milling according to claim 5 is characterized in that, described step B also comprises: water-release fibre is blown to by air-flow on the workbench of roll mill, and water-release fibre falls naturally to scatter and reticulates; By the vibratory sieve on the workbench thermal fusing powder is evenly distributed on the workbench of roll mill.
10, the preparation method of water retaining penetration film produced by milling according to claim 9 is characterized in that, water-release fibre that is scattered and thermal fusing powder can be respectively one or more layers and arrange at interval.
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CN103535244B (en) * | 2013-10-18 | 2015-05-06 | 中国矿业大学(北京) | Water permeating material and method for manufacturing same |
CN104335881B (en) * | 2014-09-25 | 2016-06-22 | 中国矿业大学(北京) | A kind of infiltrating irrigation core and preparation method |
CN104663363B (en) * | 2015-02-03 | 2017-07-18 | 武汉纺织大学 | A kind of Complex subsurface irrigation pipe of adjustable infiltration |
CN114868625B (en) * | 2022-05-19 | 2023-04-14 | 山东省水利科学研究院 | Water-saving composite infiltrating irrigation pipe and preparation method thereof |
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