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CN102505473B - Anti-scald textile and preparation method thereof - Google Patents

Anti-scald textile and preparation method thereof Download PDF

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CN102505473B
CN102505473B CN201110303495.1A CN201110303495A CN102505473B CN 102505473 B CN102505473 B CN 102505473B CN 201110303495 A CN201110303495 A CN 201110303495A CN 102505473 B CN102505473 B CN 102505473B
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scald
textile
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textiles
grafted monomers
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CN102505473A (en
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李景烨
于洋
邓波
李林繁
虞鸣
蒋海青
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Shanghai Institute of Applied Physics of CAS
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Abstract

本发明公开了一种防烫伤纺织品的制备方法,其特征在于:其包括下述步骤:在溶剂中,在无氧条件以及惰性气体保护下,辐照纺织品以及接枝单体,使所述纺织品以及所述接枝单体发生共辐照接枝反应,即得防烫伤纺织品;其中所述的接枝单体为在32℃以上会从亲水性转变成疏水性的具有温敏特性的化合物。本发明还公开了一种由该方法制得的防烫伤纺织品。本发明的制备方法操作简便,大大延长了纺织品在防烫伤效果方面的持久性,同时将防烫伤纺织品的使用厚度降低至较低水平。本发明的防烫伤纺织品能够在保留纺织品本身所具有的亲肤性、透水性的前提下,实现防烫伤效果。并且本发明的防烫伤纺织品能够多次反复使用,都能保持良好的防烫伤效果。The invention discloses a method for preparing anti-scald textiles, which is characterized in that it comprises the following steps: in a solvent, under anaerobic conditions and protection of an inert gas, irradiating textiles and grafted monomers to make the textiles And the grafting monomer undergoes a co-irradiation grafting reaction to obtain an anti-scald textile; wherein the grafting monomer is a compound with temperature-sensitive properties that will change from hydrophilic to hydrophobic above 32°C . The invention also discloses an anti-scald textile made by the method. The preparation method of the invention is easy to operate, greatly prolongs the durability of the anti-scald effect of the textile, and simultaneously reduces the thickness of the anti-scald textile to a relatively low level. The anti-scald textile of the present invention can realize the anti-scald effect on the premise of retaining the skin-friendly property and water permeability of the textile itself. Moreover, the anti-scald textile of the present invention can be used repeatedly, and can maintain a good anti-scald effect.

Description

一种防烫伤纺织品及其制备方法A kind of anti-scald textile and preparation method thereof

技术领域 technical field

本方法涉及一种纺织品的整理方法,尤其涉及一种温敏及防烫伤纺织品及其制备方法。The method relates to a finishing method of textiles, in particular to a temperature-sensitive and anti-scald textile and a preparation method thereof.

背景技术 Background technique

日常生活、工作中,烫伤常常发生。尤其在纺织品被浸湿后,高温水的残留与皮肤接触使得烫伤进一步加重。因此,研制防烫伤的纺织品迫在眉睫。In daily life and work, burns often occur. Especially after the textile is soaked, the residue of high temperature water contacts with the skin and further aggravates the burn. Therefore, it is imminent to develop anti-scald textiles.

目前,纺织品防烫伤的主要方法是加厚纺织品的厚度以及采用特种功能整理,主要采用复合纺织品,即纺织品内衬或外覆绝热层。复合纺织品的绝热层主要有以下几种:纳米孔隔热材料、无机矿物纤维类隔热材料以及有机-金属复合类材料。At present, the main method of textile anti-scalding is to thicken the thickness of textiles and adopt special functional finishing, mainly adopt composite textiles, that is, textile lining or outer covering heat insulation layer. The thermal insulation layer of composite textiles mainly includes the following types: nanoporous thermal insulation materials, inorganic mineral fiber thermal insulation materials, and organic-metal composite materials.

对于一般纺织品而言,防烫伤主要是加厚其厚度,降低热传导,从而达到防烫伤的目的。由此带来的问题就是,由于织物过厚而导致穿着、使用不便。对于复合纺织品,纳米孔隔热材料主要采用硅质、硬硅钙石类,这些材料隔热效果优良,这类材料的缺点是耐磨性较差;对于无机矿物纤维类隔热材料,主要有石英纤维棉、硅酸铝纤维棉、碳纤维棉以及石墨纤维棉等,这些材料具有质地轻、耐高温等优点,然而这类材料使用厚度较大;对于有机-金属复合类材料,主要是将耐高温聚合物涂覆在金属表面,再与其他材料复合制成复合材料,这类材料的主要问题是耐高温聚合物容易脱落、防烫伤性能不持久。因此,提供耐久性更好、使用厚度更小的纺织品改性方法,必将提高纺织品的功能应用空间。For general textiles, anti-scald is mainly to thicken its thickness and reduce heat conduction, so as to achieve the purpose of anti-scald. The resulting problem is exactly that it is inconvenient to wear and use because the fabric is too thick. For composite textiles, nanoporous thermal insulation materials mainly use silicon and xonotlite, which have excellent thermal insulation effects. The disadvantage of this type of material is poor wear resistance; for inorganic mineral fiber thermal insulation materials, there are mainly Quartz fiber cotton, aluminum silicate fiber cotton, carbon fiber cotton and graphite fiber cotton, etc. These materials have the advantages of light texture and high temperature resistance, but the thickness of these materials is relatively large; for organic-metal composite materials, it is mainly the resistance The high-temperature polymer is coated on the metal surface, and then compounded with other materials to form a composite material. The main problem of this type of material is that the high-temperature-resistant polymer is easy to fall off, and the anti-scald performance is not durable. Therefore, providing a textile modification method with better durability and smaller thickness will definitely improve the functional application space of textiles.

对于纺织品的整理方式,目前主要有机械整理,如定幅整理、机械手感整理及防缩整理等,形态记忆整理,如湿交联、离子交联等,特种功能整理,如拒水拒油整理、阻燃整理、卫生整理等(Rong Li,KeLu Yan,LatestDevelopment of Textile Finishing Technologies Overseas,China Textile Leader,2009.No.5,75~78)。机械整理即应用机械方式赋予织物各种特殊的手感、外观和形态;形态记忆整理即应用交联剂进行交联,使织物拥有保持平整外观、从折皱中恢复原状的功能;特种功能整理即应用物理、化学或物理化学方法将功能高分子与织物结合,使织物具有特种功能。For the finishing methods of textiles, there are mainly mechanical finishing, such as fixed-width finishing, mechanical feel finishing and anti-shrink finishing, shape memory finishing, such as wet cross-linking, ion cross-linking, etc., special function finishing, such as water-repellent and oil-repellent finishing , flame retardant finishing, hygienic finishing, etc. (Rong Li, KeLu Yan, Latest Development of Textile Finishing Technologies Overseas, China Textile Leader, 2009.No.5, 75~78). Mechanical finishing refers to the application of mechanical methods to give fabrics various special feel, appearance and shape; shape memory finishing refers to the application of crosslinking agents for crosslinking, so that the fabric has the function of maintaining a flat appearance and recovering from wrinkles; special functional finishing refers to the application of Physical, chemical or physicochemical methods combine functional polymers with fabrics to make fabrics have special functions.

发明内容 Contents of the invention

本发明所要解决的技术问题在于克服了现有的防烫伤纺织品厚度较大不利于使用或穿着,或经过物理方法整理的纺织品及复合纺织品耐磨性较差,防烫效果不持久等缺陷,提供了一种新的防烫伤纺织品及其制备方法。本发明的制备方法操作简便,采用辐照接枝法将功能高分子以化学键连接至纺织品表面,大大延长了纺织品在防烫伤效果方面的持久性,同时将防烫伤纺织品的使用厚度降低至较低水平。本发明的防烫伤纺织品能够在保留纺织品本身所具有的亲肤性、透水性的前提下,实现防烫伤效果。并且本发明的防烫伤纺织品能够多次反复使用,都能保持良好的防烫伤效果。The technical problem to be solved by the present invention is to overcome the disadvantages of the existing anti-scald textiles which are too thick to be used or worn, or the textiles and composite textiles that have been physically arranged have poor wear resistance, and the anti-scald effect is not durable, etc., providing A new anti-scald textile and its preparation method. The preparation method of the present invention is easy to operate, and the functional polymer is chemically bonded to the surface of the textile by using the irradiation grafting method, which greatly prolongs the durability of the anti-scald effect of the textile, and at the same time reduces the thickness of the anti-scald textile to a minimum level. The anti-scald textile of the present invention can realize the anti-scald effect on the premise of retaining the skin-friendly property and water permeability of the textile itself. Moreover, the anti-scald textile of the present invention can be used repeatedly, and can maintain a good anti-scald effect.

本发明提供了一种防烫伤纺织品的制备方法,其包括下述步骤:在溶剂中,在无氧条件以及惰性气体保护下,辐照纺织品以及接枝单体,使所述纺织品以及所述接枝单体发生共辐照接枝反应,即得防烫伤纺织品;其中所述的接枝单体为具有温敏特性的单体,本发明中所述的温敏特性指在32℃以上时从亲水性化转变为疏水性的化合物,即具有烯基基团并同时具有亲水和疏水基团的化合物,较佳地为N-异丙基丙烯酰胺和/或N-乙基丙烯酰胺。The invention provides a method for preparing anti-scald textiles, which comprises the following steps: irradiating textiles and grafted monomers in a solvent under anaerobic conditions and inert gas protection to make the textiles and the grafted Grafting monomers undergo a co-irradiation grafting reaction to obtain scald-resistant textiles; wherein the grafting monomers are monomers with temperature-sensitive properties, and the temperature-sensitive properties described in the present invention refer to when the temperature is above 32 ° C. The compound converted from hydrophilic to hydrophobic, that is, the compound having an alkenyl group and both hydrophilic and hydrophobic groups, is preferably N-isopropylacrylamide and/or N-ethylacrylamide.

本发明中,所述的纺织品是指由各种天然纤维和/或人造纤维制备得到的产品,本发明中对于所述纺织品没有特殊要求,可为各种常规的市售纺织品。其中,所述的天然纤维较佳地为棉纤维、麻纤维、丝纤维和毛纤维中的一种或多种,更佳地为棉纤维和/或麻纤维,但不局限于此。所述的人造纤维较佳地为锦纶纤维、涤纶纤维和丙纶纤维中的一种或多种,但并不局限于此。In the present invention, the textiles refer to products prepared from various natural fibers and/or man-made fibers. In the present invention, there is no special requirement for the textiles, and they can be various conventional commercially available textiles. Wherein, the natural fiber is preferably one or more of cotton fiber, hemp fiber, silk fiber and wool fiber, more preferably cotton fiber and/or hemp fiber, but not limited thereto. The man-made fibers are preferably one or more of nylon fibers, polyester fibers and polypropylene fibers, but are not limited thereto.

本发明中,较佳地对所述纺织品进行预处理,该预处理为本领域的常规预处理方法,以清洁所述的纺织品,去除所述纺织品中的杂质。所述的预处理方法较佳地为用丙酮抽提所述纺织品,水洗后干燥即可。In the present invention, the textiles are preferably pretreated, which is a conventional pretreatment method in the art, to clean the textiles and remove impurities in the textiles. The pretreatment method is preferably to extract the textile with acetone, wash it with water and then dry it.

本发明中,所述的溶剂为本领域此类反应常规使用的溶剂,较佳地为水和/或碳原子数1-3的一元醇(如甲醇、乙醇和异丙醇等中的一种或多种)。In the present invention, described solvent is the conventionally used solvent of this type of reaction in this field, is preferably water and/or the monohydric alcohol of carbon atom number 1-3 (such as a kind of in methanol, ethanol and isopropanol etc. or more).

本发明中,所述接枝单体与所述溶剂的质量/体积比较佳地为1~50g/100mL,更佳地为5~30g/100mL,最佳地为10~20g/100mL。在该质量/体积比范围内能够使纺织品保持其原有的透水性,不会使该纺织品的透水性在所述接枝反应后显著下降。In the present invention, the mass/volume ratio of the graft monomer to the solvent is preferably 1-50 g/100 mL, more preferably 5-30 g/100 mL, most preferably 10-20 g/100 mL. Within the mass/volume ratio range, the original water permeability of the textile can be maintained, and the water permeability of the textile will not decrease significantly after the grafting reaction.

本发明中,所述溶剂中还可含有阻聚剂,所述阻聚剂为选用此类反应各种常规的阻聚剂,如硫酸亚铁铵和/或硫酸铜。所述阻聚剂的含量为本领域此类反应的常规用量,较佳地为4mmol/L溶剂以下。In the present invention, the solvent may also contain a polymerization inhibitor, which is selected from various conventional polymerization inhibitors of this type of reaction, such as ferrous ammonium sulfate and/or copper sulfate. The content of the polymerization inhibitor is a conventional amount for this type of reaction in the art, preferably below 4 mmol/L solvent.

本发明中,所述的无氧条件可采用本领域常规的方法获得,一般为脱气后抽真空。其中,所述的脱气可采用本领域常规的方法进行,如超声波震荡脱气,可在超声波清洗机中进行,但并不局限于此。In the present invention, the oxygen-free conditions can be obtained by conventional methods in the art, generally vacuumizing after degassing. Wherein, the degassing can be carried out by conventional methods in the art, such as ultrasonic vibration degassing, which can be carried out in an ultrasonic cleaning machine, but is not limited thereto.

本发明中,所述的共辐照接枝反应可采用本领域常规的辐照接枝反应条件进行。所述共辐照接枝反应的辐照源较佳地为钴源。所述共辐照接枝反应的辐照剂量较佳地为5kGy~50kGy,更佳地为15kGy~30kGy。In the present invention, the co-irradiation grafting reaction can be carried out using conventional irradiation grafting reaction conditions in the art. The radiation source of the co-irradiation grafting reaction is preferably a cobalt source. The irradiation dose of the co-irradiation grafting reaction is preferably 5kGy-50kGy, more preferably 15kGy-30kGy.

本发明的共辐照接枝反应结束后较佳地进行后处理以除去未接枝的接枝单体以及所述接枝单体的均聚物。所述的后处理较佳地按下述步骤进行:以溶剂抽提防烫伤纺织品即可;所述的溶剂为能够溶解所述接枝单体以及接枝单体的均聚物的溶剂,较佳地为甲醇和/或乙醇。所述的抽提较佳地在索氏提取器中进行,如用500mL容量的索氏提取器中抽提72小时。After the co-irradiation grafting reaction of the present invention is completed, post-treatment is preferably performed to remove ungrafted grafted monomers and homopolymers of the grafted monomers. Described aftertreatment preferably carries out by following steps: get final product with solvent extraction anti-scald textile; Described solvent is the solvent that can dissolve the homopolymer of described graft monomer and graft monomer, relatively Preferably methanol and/or ethanol. The extraction is preferably carried out in a Soxhlet extractor, such as extracting for 72 hours in a Soxhlet extractor with a capacity of 500 mL.

在本发明一较佳的实施方式中,所述的制备方法按下述步骤进行:将所述纺织品置入含有所述接枝单体的溶液的辐照管中,经过脱气、抽真空,通入惰性气体后,将该辐照管置入钴源室内进行共辐照接枝反应,将辐照后的纺织品用溶剂进行抽提,即可;其中含有所述接枝单体的溶液中的溶剂同前所述,所述的溶液中较佳地还含有阻聚剂。In a preferred embodiment of the present invention, the preparation method is carried out according to the following steps: the textile is placed in an irradiation tube containing the solution of the grafted monomer, degassed, vacuumized, After passing through the inert gas, put the irradiation tube into the cobalt source chamber to carry out the co-irradiation grafting reaction, and extract the irradiated textiles with a solvent; The solvent is the same as mentioned above, and preferably also contains a polymerization inhibitor in the described solution.

本发明还提供了一种由上述制备方法制得的防烫伤纺织品。其中所述防烫伤纺织品中所述接枝单体的接枝率为1~50%,较佳地为5~30%。The present invention also provides an anti-scald textile prepared by the above preparation method. Wherein the grafting rate of the grafted monomer in the anti-scald textile is 1-50%, preferably 5-30%.

本发明的防烫伤纺织品具有温敏特性,即在32℃以上时该纺织品具有疏水性。在低温时(低于32℃时),该防烫伤纺织品的接枝链上的分子与水的相互作用主要是亲水基团与水分子之间的氢键作用,表现为亲水性;当温度在相变点以上时,接枝链分子内及分子间的疏水相互作用加强,形成疏水层,此时,接枝链分子的形态由疏松的线团结构变为紧密的胶粒状结构,从而表现出温敏性。若温度较高的水泼溅到纺织品表面,当该纺织品的温度达到32℃以上时,由于其疏水性,高温水不会被该纺织品吸收,亦不停留在该纺织品表面,从而达到防烫伤的目的。The anti-scald textile of the present invention has temperature-sensitive properties, that is, the textile has hydrophobicity when the temperature is above 32°C. At low temperature (less than 32°C), the interaction between the molecules on the grafted chain of the anti-scald textile and water is mainly the hydrogen bond between the hydrophilic group and the water molecule, showing hydrophilicity; When the temperature is above the phase transition point, the hydrophobic interaction between the molecules of the graft chain and between molecules is strengthened to form a hydrophobic layer. At this time, the shape of the graft chain molecules changes from a loose coil structure to a compact colloidal structure, thereby Exhibits thermosensitivity. If water with a high temperature is splashed on the surface of the textile, when the temperature of the textile reaches above 32°C, due to its hydrophobicity, the high-temperature water will not be absorbed by the textile, nor will it stay on the surface of the textile, so as to achieve the effect of preventing burns. Purpose.

本发明中,上述优选条件在符合本领域常识的基础上可任意组合,即得本发明各较佳实施例。In the present invention, the above-mentioned preferred conditions can be combined arbitrarily on the basis of conforming to common knowledge in the field, so as to obtain various preferred embodiments of the present invention.

本发明的原料和试剂皆市售可得。The starting materials and reagents of the present invention are all commercially available.

本发明的积极进步效果在于:The positive progress effect of the present invention is:

1、本发明中将辐射接枝法引入纺织品整理中,将功能化合物以化学键连接至纺织品上,成功地解决了具有防烫伤功能的纺织品的耐久使用性问题,能够重复使用和洗涤。1. In the present invention, the radiation grafting method is introduced into the finishing of textiles, and the functional compounds are chemically bonded to the textiles, successfully solving the problem of durability of textiles with anti-scald function, which can be reused and washed.

2、本发明仅仅是对市售的纺织品进行整理,不需要复合或加厚,整理后纺织品的厚度变化量非常小(低于0.5mm),解决了常规的加厚防烫伤纺织品不利于使用和穿着的缺陷。2. The present invention only arranges the commercially available textiles without compounding or thickening, and the thickness variation of the textiles after finishing is very small (less than 0.5 mm), which solves the problem that conventional thickened anti-scald textiles are not conducive to use and Clothing defects.

3、本发明的防烫伤纺织品与市售的纺织品的透水性几乎没有影响。如:棉布在改性前可以在5秒内将水滴完全吸收,改性后的防烫伤棉布在30℃以下可在10秒内将水滴完全吸收;改性后的尼龙布及涤纶布的接触角无明显变化,也说明改性后的纺织品的亲水性近似无变化。3. The water permeability of the anti-scald textiles of the present invention has almost no effect on that of commercially available textiles. For example: cotton cloth can completely absorb water droplets within 5 seconds before modification, and the modified anti-scald cotton cloth can completely absorb water droplets within 10 seconds below 30°C; the contact angle of modified nylon cloth and polyester cloth There is no obvious change, which also shows that the hydrophilicity of the modified textile has almost no change.

4、本发明的防烫伤纺织品不会改变纺织品在常规使用环境下的透水性,仍能够使纺织品具有较好的使用舒适感。4. The anti-scald textiles of the present invention will not change the water permeability of the textiles in the normal use environment, and can still make the textiles have better use comfort.

5、本发明采用是的通用平台,如果需要实现纺织品的其他功能化,只需要对实验过程中的功能化合物进行相应改变即可实现。5. The present invention adopts the general-purpose platform. If it is necessary to realize other functionalization of textiles, it only needs to make corresponding changes to the functional compounds in the experimental process.

附图说明 Description of drawings

图1为接触角的示意图。Figure 1 is a schematic diagram of the contact angle.

图2为实施例1中未改性棉布和改性棉布在不同温度下的接触角测试图,其中图2a为未改性棉布,图2b为改性棉布。Fig. 2 is the contact angle test chart of the unmodified cotton cloth and the modified cotton cloth at different temperatures in Example 1, wherein Fig. 2a is the unmodified cotton cloth, and Fig. 2b is the modified cotton cloth.

图3为实施例2中未改性尼龙布和改性尼龙布在不同温度下的接触角测试图,其中图3a为未改性尼龙布,图3b为改性尼龙布。Fig. 3 is the test diagram of the contact angle of unmodified nylon cloth and modified nylon cloth at different temperatures in Example 2, wherein Fig. 3a is the unmodified nylon cloth, and Fig. 3b is the modified nylon cloth.

具体实施方式 Detailed ways

下面用实施例来进一步说明本发明,但本发明并不受其限制,实施例中的原料均为常规市售产品。The following examples are used to further illustrate the present invention, but the present invention is not limited thereto, and the raw materials in the examples are conventional commercially available products.

说明一:Explanation one:

本发明以及所有实施例中所述的吸收剂量是辐射化学中描述电离辐射给予样品的平均授与能量的概念,其定义为电离辐射向无限小体积内授与的平均能量除以该体积内物质的质量而得到的商。The absorbed dose described in the present invention and all the examples is a concept in radiation chemistry describing the average imparted energy given to a sample by ionizing radiation, which is defined as the average energy imparted by ionizing radiation to an infinitely small volume divided by the mass of the substance in the volume And get the business.

说明二:Explanation 2:

所有实施例中所述的接枝率是高分子化学中描述接枝程度的概念,其定义为样品在接枝反应前、后的质量变化占原始样品质量的百分比,其表达式为:The grafting rate described in all embodiments is the concept of describing the degree of grafting in polymer chemistry, which is defined as the percentage of the mass change of the sample before and after the grafting reaction that accounts for the original sample mass, and its expression is:

DG = w g - w 0 w 0 × 100 % 式1 DG = w g - w 0 w 0 × 100 % Formula 1

其中,Wg为接枝后样品质量,Wo为接枝前样品质量。Among them, W g is the weight of the sample after grafting, and W o is the weight of the sample before grafting.

说明三:Explanation three:

所有实施例中所述的接触角是材料化学中描述材料亲疏水程度的概念,其定义为在固、液、气三相接触达到平衡时,三相接触周边的任一点上,液气界面切线与固体表面间形成的、包含液体的夹角,如图1所示的θ角。The contact angle described in all the examples is a concept describing the degree of hydrophilicity and hydrophobicity of materials in material chemistry, which is defined as the tangent line of the liquid-gas interface at any point on the periphery of the three-phase contact when the three-phase contact of solid, liquid and gas reaches equilibrium. The angle formed with the solid surface, including the liquid, is the angle θ shown in Figure 1.

说明四:Explanation four:

实施例1所述的棉布的接触角为0°,因为棉布的亲水性极好,水滴在5秒钟内在棉布表面完全铺展而被吸收,按接触角的定义,该棉布的接触角为0°。The contact angle of the cotton cloth described in Example 1 is 0°, because the hydrophilicity of the cotton cloth is excellent, and the water drop is completely spread and absorbed on the surface of the cotton cloth within 5 seconds. According to the definition of the contact angle, the contact angle of the cotton cloth is 0° °.

实施例1Example 1

将棉布按照尺寸10cm×15cm进行剪裁,清洗干燥后,精确称量其质量为1.7243g,将此棉布装入辐照管中备用。配制质量/体积比15g/100mL的N-异丙基丙烯酰胺的甲醇溶液(即每100mL甲醇中有15g N-异丙基丙烯酰胺)100mL,另外,在此溶液中加入40mg的硫酸铜作为阻聚剂。取此溶液40mL加入前述装有棉布的辐照管中。经超声波震荡脱气、抽真空后,再通入氮气后,将辐照管密封并置入钴源室进行共辐照接枝,其吸收剂量为15kGy。辐照结束后,取出棉布并以甲醇为纯化试剂于索氏提取器进行纯化。纯化结束后,将防烫伤棉布干燥至恒重,精确称量其质量为2.0521g。根据式1计算该样品的接枝率为19.01%。分别在不同温度下检测未改性前的棉布,以及改性后的防烫伤棉布的厚度和左部、右部的接触角,取其平均值,具体见表1、图2。Cut the cotton cloth according to the size of 10cm×15cm, after cleaning and drying, accurately weigh its mass as 1.7243g, and put the cotton cloth into the irradiation tube for later use. Prepare 100mL of a methanol solution of N-isopropylacrylamide with a mass/volume ratio of 15g/100mL (that is, 15g of N-isopropylacrylamide per 100mL of methanol), and add 40mg of copper sulfate to this solution as a barrier. Polymer. Take 40mL of this solution and add it to the aforementioned irradiation tube equipped with cotton cloth. After degassing by ultrasonic vibration, vacuuming, and nitrogen gas, the irradiation tube was sealed and placed in the cobalt source chamber for co-irradiation grafting. The absorbed dose was 15kGy. After the irradiation, the cotton cloth was taken out and purified in a Soxhlet extractor using methanol as the purification reagent. After the purification, the anti-scald cotton cloth was dried to constant weight, and its mass was accurately weighed to be 2.0521g. According to Formula 1, the grafting ratio of the sample was calculated to be 19.01%. The thickness and the contact angles of the left and right parts of the unmodified cotton cloth and the modified anti-scald cotton cloth were measured at different temperatures, and the average values were taken. See Table 1 and Figure 2 for details.

表1Table 1

由表1和图2可见,用本发明的方法得到的防烫伤棉布在常规的室温环境下仍能够保持棉布固有的亲水性,当温度高于30℃以后,改性棉布的接触角显著提高,证明其转变为疏水性,从而能够实现很好的防烫伤效果。并且改性棉布的厚度仅增加了0.2mm。另外棉布在改性前可以在5秒内将水滴完全吸收,改性后的防烫伤棉布在30℃以下可在10秒内将水滴完全吸收,表明改性方法对于棉布本身的透水性没有产生不利影响,仍能够保持棉布优良的透水亲肤效果。It can be seen from Table 1 and Fig. 2 that the anti-scald cotton cloth obtained by the method of the present invention can still maintain the intrinsic hydrophilicity of the cotton cloth under conventional room temperature environment, and when the temperature is higher than 30 ° C, the contact angle of the modified cotton cloth is significantly improved , which proves that it is transformed into hydrophobicity, so that it can achieve a good anti-scald effect. And the thickness of the modified cotton only increased by 0.2mm. In addition, the cotton cloth can completely absorb water droplets within 5 seconds before modification, and the modified anti-scald cotton cloth can completely absorb water droplets within 10 seconds below 30°C, indicating that the modification method has no disadvantages for the water permeability of the cotton cloth itself. It can still maintain the excellent water-permeable and skin-friendly effect of cotton cloth.

实施例2Example 2

将尼龙布按照尺寸10cm×15cm进行剪裁,清洗干燥后,精确称量其质量为0.7040g,将此尼龙布装入辐照管中备用。配制质量/体积浓度为16.7g/100mL的N-乙基丙烯酰胺的乙醇溶液100mL,另外,在此溶液中加入40mg的硫酸铜作为阻聚剂。取此溶液40mL加入前述装有尼龙布的辐照管中。经超声波震荡脱气、抽真空,再通入氮气后,将辐照管密封并置入钴源室进行共辐照接枝,其吸收剂量为30kGy。辐照结束后,取出尼龙布并以乙醇为纯化试剂应用索氏提取器进行纯化。纯化结束后,将防烫伤尼龙布干燥至恒重,精确称量其质量为0.9077g。根据式1计算该样品的接枝率为28.93%。分别在不同温度下检测未改性前的尼龙布,以及改性后的防烫伤尼龙布的厚度和左部、右部的接触角,取其平均值,具体见表2、图3。Cut the nylon cloth according to the size of 10cm×15cm, after cleaning and drying, accurately weigh its mass to 0.7040g, and put the nylon cloth into the irradiation tube for later use. Prepare 100 mL of an ethanol solution of N-ethylacrylamide with a mass/volume concentration of 16.7 g/100 mL, and add 40 mg of copper sulfate to the solution as a polymerization inhibitor. Take 40mL of this solution and add it to the aforementioned irradiation tube equipped with nylon cloth. After degassing by ultrasonic vibration, vacuuming, and nitrogen gas, the irradiation tube was sealed and placed in the cobalt source chamber for co-irradiation grafting. The absorbed dose was 30kGy. After the irradiation, the nylon cloth was taken out and purified with a Soxhlet extractor using ethanol as the purification reagent. After the purification, the anti-scald nylon cloth was dried to a constant weight, and its mass was accurately weighed to be 0.9077g. According to Formula 1, the grafting ratio of the sample was calculated to be 28.93%. The thickness and contact angles of the left and right parts of the unmodified nylon cloth and the modified anti-scald nylon cloth were measured at different temperatures, and the average values were taken. See Table 2 and Figure 3 for details.

表2Table 2

由表2和图3可见,用本发明的方法得到的防烫伤棉尼龙布在常规的室温环境下接触角无明显变化,表明其亲水性和透水性没有显著变化。As can be seen from Table 2 and Figure 3, the contact angle of the anti-scald cotton nylon cloth obtained by the method of the present invention has no significant change under conventional room temperature environment, indicating that its hydrophilicity and water permeability have no significant change.

实施例3Example 3

将棉布按照尺寸10cm×15cm进行剪裁,清洗干燥后,精确称量其质量为1.9724g,将此棉布装入辐照管中备用。配制质量/体积比1g/100mL的N-异丙基丙烯酰胺的水溶液100mL,另外,在此溶液中加入40mg的硫酸铜作为阻聚剂。取此溶液40mL加入前述装有棉布的辐照管中。经超声波震荡脱气、抽真空后,再通入氮气后,将辐照管密封并置入钴源室进行共辐照接枝,其吸收剂量为5kGy。辐照结束后,取出棉布并以甲醇为纯化试剂于索氏提取器进行纯化。纯化结束后,将防烫伤棉布干燥至恒重,精确称量其质量为2.1521g。根据式1计算该样品的接枝率为9.11%。分别在不同温度下检测未改性前的棉布,以及改性后的防烫伤棉布左部以及右部的接触角,取其平均值,具体见表3。Cut the cotton cloth according to the size of 10cm×15cm, after cleaning and drying, accurately weigh its mass as 1.9724g, and put the cotton cloth into the irradiation tube for later use. Prepare 100 mL of an aqueous solution of N-isopropylacrylamide with a mass/volume ratio of 1 g/100 mL, and add 40 mg of copper sulfate to the solution as a polymerization inhibitor. Take 40mL of this solution and add it to the aforementioned irradiation tube equipped with cotton cloth. After degassing by ultrasonic vibration, vacuuming, and nitrogen gas, the irradiation tube was sealed and placed in the cobalt source chamber for co-irradiation grafting. The absorbed dose was 5kGy. After the irradiation, the cotton cloth was taken out and purified in a Soxhlet extractor using methanol as the purification reagent. After the purification, the anti-scald cotton cloth was dried to constant weight, and its mass was accurately weighed to be 2.1521g. According to Formula 1, the grafting ratio of the sample was calculated to be 9.11%. The contact angles of the unmodified cotton cloth and the left and right parts of the modified anti-scald cotton cloth were measured at different temperatures, and the average values were taken, as shown in Table 3.

表3table 3

实施例4Example 4

将涤纶布按照尺寸10cm×15cm进行剪裁,清洗干燥后,精确称量其质量为0.6804g,将此涤纶布装入辐照管中备用。配制质量/体积比为50g/100ml的N-乙基丙烯酰胺的水溶液100mL,另外,在此溶液中加入40mg的硫酸铜作为阻聚剂。取此溶液40mL加入前述装有涤纶布的辐照管中。经超声波震荡脱气、抽真空,再通入氮气后,将辐照管密封并置入钴源室进行共辐照接枝,其吸收剂量为50kGy。辐照结束后,取出涤纶并以乙醇为纯化试剂应用索氏提取器进行纯化。纯化结束后,将防烫伤涤纶布干燥至恒重,精确称量其质量为0.9877g。根据式1计算该样品的接枝率为45.16%。分别在不同温度下检测未改性前的涤纶布,以及改性后的防烫伤涤纶布左部以及右部的接触角,取其平均值,具体见表4。Cut the polyester cloth according to the size of 10cm×15cm, after cleaning and drying, accurately weigh its mass to 0.6804g, and put the polyester cloth into the irradiation tube for later use. 100 mL of an aqueous solution of N-ethylacrylamide with a mass/volume ratio of 50 g/100 ml was prepared, and 40 mg of copper sulfate was added to the solution as a polymerization inhibitor. Take 40 mL of this solution and add it to the aforementioned irradiation tube equipped with polyester cloth. After degassing by ultrasonic vibration, vacuuming, and nitrogen gas, the irradiation tube was sealed and placed in the cobalt source chamber for co-irradiation grafting, and the absorbed dose was 50kGy. After the irradiation, the polyester was taken out and purified with a Soxhlet extractor using ethanol as the purification reagent. After the purification, the anti-scald polyester cloth was dried to constant weight, and its mass was accurately weighed to be 0.9877g. According to Formula 1, the grafting ratio of the sample was calculated to be 45.16%. The contact angles of the unmodified polyester cloth and the left and right parts of the modified anti-scald polyester cloth were measured at different temperatures, and the average values were taken. See Table 4 for details.

表4Table 4

Claims (16)

1. the preparation method of an Anti-scald textile, it is characterized in that: it comprises the steps: in solvent, under oxygen free condition and inert gas shielding, irradiation textiles and grafted monomers, make described textiles and described grafted monomers generation mutual radiation graft reaction, obtain Anti-scald textile; Wherein said grafted monomers is can be transformed into the hydrophobic compound with temperature-sensing property from hydrophily more than 32 DEG C; Described grafted monomers is N-ethyl acrylamide, and described grafted monomers is 1~50g/100mL with the mass/volume ratio of described solvent.
2. preparation method as claimed in claim 1, is characterized in that: described textiles is the product being prepared by natural fabric and/or artificial fibre.
3. preparation method as claimed in claim 2, it is characterized in that: described natural fabric is one or more in cotton fiber, flax fibre, silk fiber and wool fibre, described artificial fibre is one or more in nylon fibre, polyster fibre and polypropylene fiber.
4. preparation method as claimed in claim 1, is characterized in that: described textiles is carrying out carrying out preliminary treatment according to following step before described mutual radiation graft reaction: with textiles described in acetone extracting, dry after washing.
5. preparation method as claimed in claim 1, is characterized in that: described solvent is the monohydric alcohol of water and/or carbon number 1-3.
6. preparation method as claimed in claim 5, is characterized in that: the monohydric alcohol of described carbon number 1-3 is one or more in methyl alcohol, ethanol and isopropyl alcohol.
7. the preparation method as described in any one in claim 1~6, is characterized in that: described grafted monomers is 5~30g/100mL with the mass/volume ratio of described solvent.
8. preparation method as claimed in claim 7, is characterized in that: described grafted monomers is 10~20g/100mL with the mass/volume ratio of described solvent.
9. preparation method as claimed in claim 1, is characterized in that: in described solvent, also contain polymerization inhibitor.
10. preparation method as claimed in claim 9, is characterized in that: described polymerization inhibitor is iron ammonium sulfate and/or copper sulphate; The content of described polymerization inhibitor is below 4mmol/L solvent.
11. preparation methods as claimed in claim 1, is characterized in that: the irradiation dose of described mutual radiation graft reaction is 5kGy~50kGy.
12. preparation methods as claimed in claim 11, is characterized in that: the irradiation dose of described mutual radiation graft reaction is 15kGy~30kGy.
13. preparation methods as claimed in claim 1, is characterized in that: after described mutual radiation graft reaction finishes, carry out in the steps below post processing: can dissolve the solvent extraction Anti-scald textile of homopolymers of described grafted monomers and described grafted monomers.
14. preparation methods as claimed in claim 13, is characterized in that: the solvent of the described homopolymers that can dissolve described grafted monomers and described grafted monomers is methyl alcohol and/or ethanol; Described extracting is carried out in apparatus,Soxhlet's.
15. Anti-scald textiles that made by the preparation method described in any one in claim 1~14; The percent grafting of grafted monomers described in wherein said Anti-scald textile is 1~50%.
16. Anti-scald textiles as claimed in claim 15, is characterized in that, the percent grafting of grafted monomers described in described Anti-scald textile is 5~30%.
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