CN114953293A - Preparation process of medical gloves capable of dividing holding force grades - Google Patents
Preparation process of medical gloves capable of dividing holding force grades Download PDFInfo
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- CN114953293A CN114953293A CN202210439649.8A CN202210439649A CN114953293A CN 114953293 A CN114953293 A CN 114953293A CN 202210439649 A CN202210439649 A CN 202210439649A CN 114953293 A CN114953293 A CN 114953293A
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- 238000002360 preparation method Methods 0.000 title claims abstract description 13
- 239000012748 slip agent Substances 0.000 claims abstract description 37
- 239000004816 latex Substances 0.000 claims abstract description 33
- 229920000126 latex Polymers 0.000 claims abstract description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 33
- 238000005406 washing Methods 0.000 claims abstract description 4
- 230000003068 static effect Effects 0.000 claims description 20
- 239000000701 coagulant Substances 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 230000003078 antioxidant effect Effects 0.000 claims description 4
- BYLSIPUARIZAHZ-UHFFFAOYSA-N 2,4,6-tris(1-phenylethyl)phenol Chemical compound C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C(C)C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 BYLSIPUARIZAHZ-UHFFFAOYSA-N 0.000 claims description 3
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 claims description 3
- 239000012190 activator Substances 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 3
- 239000005018 casein Substances 0.000 claims description 3
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 claims description 3
- 235000021240 caseins Nutrition 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims description 3
- 150000003751 zinc Chemical class 0.000 claims description 3
- 239000011667 zinc carbonate Substances 0.000 claims description 3
- 235000004416 zinc carbonate Nutrition 0.000 claims description 3
- 229910000010 zinc carbonate Inorganic materials 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- -1 accelerator Substances 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 claims 1
- 238000004073 vulcanization Methods 0.000 claims 1
- 238000002791 soaking Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 5
- 238000002955 isolation Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 230000003712 anti-aging effect Effects 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- TZZWIGRPBKTNGV-UHFFFAOYSA-N naphthalen-1-ylsulfonyloxymethyl naphthalene-1-sulfonate;sodium Chemical compound [Na].[Na].C1=CC=C2C(S(=O)(OCOS(=O)(=O)C=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 TZZWIGRPBKTNGV-UHFFFAOYSA-N 0.000 description 2
- 235000011118 potassium hydroxide Nutrition 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- KMNUDJAXRXUZQS-UHFFFAOYSA-L zinc;n-ethyl-n-phenylcarbamodithioate Chemical compound [Zn+2].CCN(C([S-])=S)C1=CC=CC=C1.CCN(C([S-])=S)C1=CC=CC=C1 KMNUDJAXRXUZQS-UHFFFAOYSA-L 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002695 general anesthesia Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/02—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor for making articles of definite length, i.e. discrete articles
- B29C41/14—Dipping a core
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/34—Component parts, details or accessories; Auxiliary operations
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C41/00—Shaping by coating a mould, core or other substrate, i.e. by depositing material and stripping-off the shaped article; Apparatus therefor
- B29C41/34—Component parts, details or accessories; Auxiliary operations
- B29C41/46—Heating or cooling
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L21/00—Compositions of unspecified rubbers
- C08L21/02—Latex
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/48—Wearing apparel
- B29L2031/4842—Outerwear
- B29L2031/4864—Gloves
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- C08K2003/265—Calcium, strontium or barium carbonate
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Gloves (AREA)
Abstract
Description
技术领域technical field
本发明涉及医疗器械技术领域,尤其是涉及一种可分握持力等级的医用手套制备工艺。The invention relates to the technical field of medical devices, in particular to a preparation process of medical gloves capable of separating holding force levels.
背景技术Background technique
天然乳胶手套因具有良好的柔软性和弹性,对人的贴合性及穿戴后对物体的触感是其他材料手套不可比拟的,固橡胶医用手套近百年来依然是外科手术的主要防护器械。Due to its good softness and elasticity, natural latex gloves are incomparable to other materials in terms of fit to people and touch of objects after wearing. Solid rubber medical gloves have remained the main protective equipment for surgical operations for nearly a hundred years.
在进行检查及手术过程中,橡胶手套能提供最大的灵活性和可操作性,同时可以根据使用者的要求,制成局部麻面、全部麻面或者光面,以增加手套表面的摩擦力,便于抓着器械。但设计成局部麻面或者全麻面时,医生动手术使用时候通常感到手套滑爽度不够,握持手术器械有点涩或者有点粘,操作起来不方便,而全光面的手套,医生使用起来通常觉得有点滑,使用起来手术器械容易滑脱,手握不稳。During inspection and surgery, rubber gloves can provide maximum flexibility and maneuverability. At the same time, according to the user's requirements, it can be made into partial pockmarked surface, full pockmarked surface or smooth surface to increase the friction of the glove surface. Ease of gripping the instrument. However, when it is designed as a local anesthesia or a general anesthesia, doctors usually feel that the gloves are not smooth enough when they are used for surgery, and the surgical instruments are a bit astringent or sticky, which is inconvenient to operate, and full-gloss gloves are used by doctors. It usually feels a little slippery, and the surgical instruments are easy to slip off when using, and the hand is unstable.
以及每个人的体质不同,手掌的皮肤性质不同,同样的医疗手套佩戴后的感觉也不同,而目前的医用手套粘滑程度(或称握持力等级)基本上统一设置,无法满足不同用户的使用需求。And each person's physique is different, the skin properties of the palm are different, and the same medical gloves feel different after wearing, and the current medical gloves' stick-slip degree (or grip level) is basically set uniformly, which cannot meet the needs of different users. Usage requirements.
发明内容SUMMARY OF THE INVENTION
本发明的目的在于提供一种可分握持力等级的医用手套制备工艺,以解决现有技术中存在的至少一个上述技术问题。The purpose of the present invention is to provide a process for preparing medical gloves with different holding force levels, so as to solve at least one of the above-mentioned technical problems existing in the prior art.
为解决上述技术问题,本发明提供的一种可分握持力等级的医用手套制备工艺,包括如下步骤:In order to solve the above-mentioned technical problems, the present invention provides a process for preparing medical gloves that can be divided into grades of holding force, including the following steps:
S10.将干燥脱模后的乳胶手套放入温水中泡洗,后将手套投入到摇箱内进行处理;S10. Put the dried and demolded latex gloves into warm water for washing, and then put the gloves into a shaking box for processing;
S11.待摇箱内手套表面潮湿但没有游离状水分时,加入浓度为2.0-8.0%的滑爽剂继续摇,直至手套表面再次没有游离状水分;后关掉摇箱的蒸汽阀门,打开排气扇,温度降至40℃±2℃(需要时间约为20min)后停止运行;S11. When the surface of the gloves in the shaking box is wet but there is no free moisture, add a slip agent with a concentration of 2.0-8.0% and continue to shake until there is no free moisture on the surface of the gloves again; then turn off the steam valve of the shaking box and open the exhaust Air fan, the temperature drops to 40℃±2℃ (it takes about 20min) to stop running;
S12.通过调节步骤S11中不同浓度的滑爽剂即可得到不同握持力等级的医用手套。S12. Medical gloves with different gripping force levels can be obtained by adjusting the different concentrations of the slip agent in step S11.
本申请中,投入滑爽剂的时间点尤为关键,即手套表面没有游离水分子的时候为投入滑爽剂的最佳时间点,因为手套太干,滑爽剂不易与手套发生反应或者发生物理吸附,手套表面存在游离状水分时,滑爽剂无法吸附在手套表面或者即便吸附也是不牢固或者会发生脱落,当这个工艺状态确定后,则才可以通过调节滑爽剂的浓度来精准控制手套的最终粘滑程度,即握持力等级。In this application, the time point for adding the slip agent is particularly critical, that is, when there are no free water molecules on the surface of the glove, it is the best time point for adding the slip agent, because the gloves are too dry, and the slip agent is not easy to react with the gloves or physically occur. Adsorption, when there is free moisture on the surface of the glove, the slip agent cannot be adsorbed on the surface of the glove, or even if it is adsorbed, it is not firm or will fall off. When the process state is determined, the concentration of the slip agent can be adjusted to accurately control the gloves. The final stick-slip degree of , the grip level.
进一步地,将相同的医疗手套上平整部位上下叠放在一起,测量手套的静摩擦系数和动摩擦系数,并根据静摩擦系数和动摩擦系数不同将手套的握持力等级(粘滑程度)定义如下:Further, the flat parts on the same medical glove are stacked up and down, the static friction coefficient and the kinetic friction coefficient of the glove are measured, and the gripping force level (stick-slip degree) of the glove is defined as follows according to the difference between the static friction coefficient and the dynamic friction coefficient:
1)静摩擦系数为0.71-0.75;动摩擦系数为0.68-0.74的手套为S级;1) The static friction coefficient is 0.71-0.75; the glove with the dynamic friction coefficient is 0.68-0.74 is grade S;
2)静摩擦系数为0.76-0.82;动摩擦系数为0.74-0.80的手套为L级;2) The static friction coefficient is 0.76-0.82; the glove with the dynamic friction coefficient is 0.74-0.80 is L grade;
3)静摩擦系数为0.83-1.0;动摩擦系数为0.82-1.0的手套为T级;3) The static friction coefficient is 0.83-1.0; the glove with the dynamic friction coefficient is 0.82-1.0 is T grade;
4)静摩擦系数为1.1-1.2;动摩擦系数为1.2-1.3的手套为uL级。4) The static friction coefficient is 1.1-1.2; the glove with the dynamic friction coefficient is 1.2-1.3 is uL grade.
其中,S级手套使用时手感太滑,不建议使用;L级手套使用时手感为中高度滑,可以作为产品握持力等级下限;T级手套使用时手感为中度粘滑,粘滑度适中;uL级手套使用时手感为较粘,可以作为产品握持力等级上限。Among them, the S grade gloves feel too slippery when used, and it is not recommended to use them; the L grade gloves feel medium to high slippery when used, which can be used as the lower limit of the product's grip level; the T grade gloves feel moderately sticky and slippery when used. Moderate; uL-grade gloves feel sticky when used, which can be used as the upper limit of the product's grip level.
以及,静摩擦系数超过1.2,动摩擦系数超过1.3的手套,佩戴者手感较差,本申请中不建议作为主要产品推广使用。In addition, gloves with a static friction coefficient exceeding 1.2 and a dynamic friction coefficient exceeding 1.3 have poor hand feel to the wearer, and are not recommended for promotion and use as a main product in this application.
进一步地,步骤S11中,所述滑爽剂的浓度为4-5.0%,制得的手套为S级;所述滑爽剂的浓度为6-8%,制得的手套为L级;所述滑爽剂的浓度为3-4%,制得的手套为T级;所述滑爽剂的浓度为2-3%,制得的手套为uL级。Further, in step S11, the concentration of the slip agent is 4-5.0%, and the prepared gloves are S grade; the concentration of the slip agent is 6-8%, and the prepared gloves are L grade; The concentration of the slip agent is 3-4%, and the prepared gloves are T grade; the concentration of the slip agent is 2-3%, and the prepared gloves are uL grade.
本申请通过精准调控,从而获得不同粘滑等级的医用手套,使用者通过比较可选择一种适合自己的手套佩戴,从而满足不同用户的使用需求。In the present application, medical gloves with different stick-slip grades can be obtained through precise regulation, and users can choose a suitable glove to wear by comparison, so as to meet the needs of different users.
进一步地,所述步骤S10中,温水的温度为48±2℃。Further, in the step S10, the temperature of the warm water is 48±2°C.
进一步地,所述步骤S11和S12中,所述摇箱的蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分。Further, in the steps S11 and S12, the steam flow rate of the shaking box is 0.45-0.6MPa; the temperature is set to 95±3°C, and the rotation speed is 30 rpm.
进一步地,所述步骤S11和S12中,手套的投入量不超过摇箱容量的75%。Further, in the steps S11 and S12, the input amount of gloves does not exceed 75% of the capacity of the shaking box.
进一步地,所述滑爽剂为丙烯酸混合液或水性聚氨酯乳液。Further, the slip agent is an acrylic mixed solution or an aqueous polyurethane emulsion.
进一步地,所述手套的乳胶组份按照重量计包括:Further, the latex component of the glove comprises by weight:
进一步地,所述稳定剂为氢氧化钾、氢氧化钠、干酪素和氨水中的一种或者若干种。Further, the stabilizer is one or several of potassium hydroxide, sodium hydroxide, casein and ammonia water.
进一步地,所述促进剂为促进剂ZDC(二乙基二硫代氨基甲酸锌)、促进剂PX(乙基苯基二硫代氨基甲酸锌)中的一种或两种。Further, the accelerator is one or both of the accelerator ZDC (zinc diethyl dithiocarbamate) and the accelerator PX (zinc ethyl phenyl dithiocarbamate).
进一步地,所述防老剂为264(BHT2,6-二叔丁基对甲酚)、SP-P苯乙烯化苯酚种的一种或两种。Further, the antioxidant is one or two of 264 (BHT2,6-di-tert-butyl-p-cresol) and SP-P styrenated phenol.
进一步地,所述活性剂为氧化锌、碳酸锌、等锌盐中的一种或多种。Further, the active agent is one or more of zinc oxide, zinc carbonate, and other zinc salts.
进一步地,所述分散剂为平平加O、NF(亚甲基二萘磺酸二钠)等中的一种或者多种。Further, the dispersing agent is one or more of Peregrine O, NF (disodium methylene dinaphthalene sulfonate) and the like.
进一步地,所述填充剂为白炭黑、碳酸钙中一种或者两种。Further, the filler is one or both of white carbon black and calcium carbonate.
其中,制备手套时,包括如下步骤:Wherein, when preparing gloves, the following steps are included:
S20.将原胶乳压至搅拌罐,在搅拌的状态下,依次加入稳定剂、扩散剂;S20. Press the raw latex into a stirring tank, and in a state of stirring, add a stabilizer and a diffusing agent in turn;
开启热水循环泵升温(全部过程中热水罐水温不能超过70℃)胶乳通过夹套的循环热水进行升温预处理(胶乳配制罐夹套水温全部过程中不得超过55℃),温度30℃~45℃之间,处理时间不少于3小时;Turn on the hot water circulation pump to heat up (the water temperature of the hot water tank cannot exceed 70°C during the whole process). Between ~45°C, the treatment time is not less than 3 hours;
S21.在胶温36℃以上时,依次加入硫化剂、促进剂、防老剂、活化剂;继续升温至40-55℃(具体温度视氯仿值的需求而进行调控);保温时间4小时以上且达到氯仿值需求时间放料停放48小时以上;S21. When the glue temperature is above 36 ℃, add vulcanizing agent, accelerator, anti-aging agent and activator in turn; continue to heat up to 40-55 ℃ (the specific temperature is adjusted according to the demand of chloroform value); the holding time is more than 4 hours and The time required to reach the chloroform value is to discharge and park for more than 48 hours;
S22.清洗并烘干模具;S22. Clean and dry the mold;
S23.将烘干之后的模具浸入凝固剂中,凝固剂的温度为48-60℃,模具在凝固剂中停留的时间为3-5秒;将附着有凝固剂的模具烘干,之后,浸入乳胶中,乳胶的温度为常温(25-28)℃,模具在乳胶中停留的时间为8-12秒,将附着有乳胶的模具取出硫化烘干,之后,将干燥硫化之后带有卷边乳胶膜的模具浸入热水中,热水的温度为75℃,模具在热水中停留的时间为16秒;将进入热水中的模具取出烘干,再将模具浸入隔离剂中(模具在隔离剂中停留的时间为10秒),然后取出干燥、脱模,即可得到乳胶手套。S23. Immerse the dried mold in a coagulant, the temperature of the coagulant is 48-60°C, and the time for the mold to stay in the coagulant is 3-5 seconds; dry the mold with the coagulant attached, and then immerse the mold into the coagulant. In the latex, the temperature of the latex is normal temperature (25-28) ℃, the time of the mold staying in the latex is 8-12 seconds, the mold with the latex is taken out and vulcanized and dried, and then the dried and vulcanized latex with curling The mold of the film is immersed in hot water, the temperature of the hot water is 75 ° C, and the time of the mold staying in the hot water is 16 seconds; the mold entering the hot water is taken out and dried, and then the mold is immersed in the isolation agent (the mold is in isolation. The residence time in the agent is 10 seconds), then take out, dry and demould to obtain latex gloves.
采用上述技术方案,本发明具有如下有益效果:Adopt above-mentioned technical scheme, the present invention has following beneficial effect:
本发明提供的一种可分握持力等级的医用手套制备工艺,避免了传统方法处理的手套全光面手套太滑,部分麻面或者全麻面的又有点粘或者有点涩的技术问题。The invention provides a process for preparing medical gloves with different holding force grades, which avoids the technical problems that the full-gloss gloves treated by the traditional method are too slippery, and the partial or full hemp surface is sticky or astringent.
本申请可有效、精准地控制医用手套的握持力等级,可以制备出多种不同粘度、不同抓握力的医用手套,可满足不同医用工作者的使用要求。The application can effectively and accurately control the gripping force level of the medical gloves, and can prepare a variety of medical gloves with different viscosities and different gripping forces, which can meet the use requirements of different medical workers.
具体实施方式Detailed ways
下面结合具体的实施方式对本发明做进一步的解释说明。显然,所描述的实施例是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。The present invention will be further explained below in conjunction with specific embodiments. Obviously, the described embodiments are some, but not all, embodiments of the present invention. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.
本实施例公开了一种可分握持力等级的医用手套制备工艺,包括如下步骤:The present embodiment discloses a preparation process for medical gloves with separable holding force levels, including the following steps:
S10.将干燥脱模后的乳胶手套放入温水中泡洗,后将手套投入到摇箱内进行处理;S10. Put the dried and demolded latex gloves into warm water for washing, and then put the gloves into a shaking box for processing;
S11.待摇箱内手套表面潮湿但没有游离状水分时,加入浓度为2.0-8.0%的滑爽剂继续摇,直至手套表面再次没有游离状水分;后关掉摇箱的蒸汽阀门,打开排气扇,温度降至40℃±2℃(需要时间约为20min)后停止运行;S11. When the surface of the gloves in the shaking box is wet but there is no free moisture, add a slip agent with a concentration of 2.0-8.0% and continue to shake until there is no free moisture on the surface of the gloves again; then turn off the steam valve of the shaking box and open the exhaust Air fan, the temperature drops to 40℃±2℃ (it takes about 20min) to stop running;
S12.通过调节步骤S11中不同浓度的滑爽剂即可得到不同握持力等级的医用手套。S12. Medical gloves with different gripping force levels can be obtained by adjusting the different concentrations of the slip agent in step S11.
其中,将相同的医疗手套上平整部位上下叠放在一起,测量手套的静摩擦系数和动摩擦系数,并根据静摩擦系数和动摩擦系数不同将手套的握持力等级(粘滑程度)定义如下:Among them, the flat parts on the same medical gloves are stacked up and down, the static friction coefficient and kinetic friction coefficient of the gloves are measured, and the gripping force level (stick-slip degree) of the gloves is defined as follows according to the difference between the static friction coefficient and the dynamic friction coefficient:
1)静摩擦系数为0.71-0.75;动摩擦系数为0.68-0.74的手套为S级;1) The static friction coefficient is 0.71-0.75; the glove with the dynamic friction coefficient is 0.68-0.74 is grade S;
2)静摩擦系数为0.76-0.82;动摩擦系数为0.74-0.80的手套为L级;2) The static friction coefficient is 0.76-0.82; the glove with the dynamic friction coefficient is 0.74-0.80 is L grade;
3)静摩擦系数为0.83-1.0;动摩擦系数为0.82-1.0的手套为T级;3) The static friction coefficient is 0.83-1.0; the glove with the dynamic friction coefficient is 0.82-1.0 is T grade;
4)静摩擦系数为1.1-1.2;动摩擦系数为1.2-1.3的手套为uL级。4) The static friction coefficient is 1.1-1.2; the glove with the dynamic friction coefficient is 1.2-1.3 is uL grade.
其中,S级手套使用时手感太滑,不建议使用;L级手套使用时手感为中高度滑,可以作为产品握持力等级下限;T级手套使用时手感为中度粘滑,粘滑度适中;uL级手套使用时手感为较粘,可以作为产品握持力等级上限。Among them, the S grade gloves feel too slippery when used, and it is not recommended to use them; the L grade gloves feel medium to high slippery when used, which can be used as the lower limit of the product's grip level; the T grade gloves feel moderately sticky and slippery when used. Moderate; uL-grade gloves feel sticky when used, which can be used as the upper limit of the product's grip level.
以及,静摩擦系数超过1.2,动摩擦系数超过1.3的手套,佩戴者手感较差,本申请中不建议作为主要产品推广使用。In addition, gloves with a static friction coefficient exceeding 1.2 and a dynamic friction coefficient exceeding 1.3 have poor hand feel to the wearer, and are not recommended for promotion and use as a main product in this application.
步骤S11中,所述滑爽剂的浓度为4-5.0%时,制得的手套为S级;所述滑爽剂的浓度为6-8%时,制得的手套为L级;所述滑爽剂的浓度为3-4%时,制得的手套为T级;所述滑爽剂的浓度为2-3%时,制得的手套为uL级。所述滑爽剂的浓度低于2%时,制得的手套过于粘涩,不推荐使用。In step S11, when the concentration of the slip agent is 4-5.0%, the prepared gloves are grade S; when the concentration of the slip agent is 6-8%, the prepared gloves are grade L; the When the concentration of the slip agent is 3-4%, the prepared gloves are T grade; when the concentration of the slip agent is 2-3%, the prepared gloves are uL grade. When the concentration of the slip agent is lower than 2%, the prepared gloves are too sticky and not recommended for use.
本申请通过精准调控,从而获得不同粘滑等级的医用手套,使用者通过比较可选择一种适合自己的手套佩戴,从而满足不同用户的使用需求。In the present application, medical gloves with different stick-slip grades can be obtained through precise regulation, and users can choose a suitable glove to wear by comparison, so as to meet the needs of different users.
其中,所述步骤S10中,温水的温度为48±2℃。步骤S11和S12中,所述摇箱的蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分。Wherein, in the step S10, the temperature of the warm water is 48±2°C. In steps S11 and S12, the steam flow rate of the shaking box is 0.45-0.6MPa; the temperature is set to 95±3°C, and the rotation speed is 30 rpm.
以及,手套的投入量可以控制在摇箱容量的70±5%。投入的量太大手套会造成摇不均匀,滑爽剂在手套外表面的分散不均匀,手套量太少会,耗电多、手套表面聚集的滑爽剂过多造成手套过滑、粉量过多。And, the input amount of gloves can be controlled at 70±5% of the capacity of the shaking box. Too large amount of gloves will cause uneven shaking, uneven dispersion of the slip agent on the outer surface of the gloves, too little amount of gloves will cause excessive power consumption, and too much slip agent accumulated on the surface of the gloves will cause the gloves to be too slippery and powdery. excessive.
本实施例中,手套的乳胶组份优选地按照重量计包括:In this embodiment, the latex component of the glove preferably comprises by weight:
其中,稳定剂为氢氧化钾、氢氧化钠、干酪素和氨水中的一种或者若干种。促进剂为促进剂ZDC(二乙基二硫代氨基甲酸锌)、促进剂PX(乙基苯基二硫代氨基甲酸锌)中的一种或两种。防老剂为264(BHT2,6-二叔丁基对甲酚)、SP-P苯乙烯化苯酚种的一种或两种。活性剂为氧化锌、碳酸锌、等锌盐中的一种或多种。分散剂为平平加O、NF(亚甲基二萘磺酸二钠)等中的一种或者多种。填充剂为白炭黑、碳酸钙中一种或者两种。Wherein, the stabilizer is one or several of potassium hydroxide, sodium hydroxide, casein and ammonia water. The accelerator is one or both of the accelerator ZDC (zinc diethyl dithiocarbamate) and the accelerator PX (zinc ethyl phenyl dithiocarbamate). The antioxidant is one or two of 264 (BHT2, 6-di-tert-butyl-p-cresol) and SP-P styrenated phenol. The active agent is one or more of zinc oxide, zinc carbonate, and other zinc salts. The dispersant is one or more of peregalin O, NF (disodium methylene dinaphthalene sulfonate) and the like. The filler is one or two of silica and calcium carbonate.
其中,制备手套时,包括如下步骤:Wherein, when preparing gloves, the following steps are included:
S20.将原胶乳压至搅拌罐,在搅拌的状态下,依次加入稳定剂、扩散剂;S20. Press the raw latex into a stirring tank, and in a state of stirring, add a stabilizer and a diffusing agent in turn;
开启热水循环泵升温(全部过程中热水罐水温不能超过70℃)胶乳通过夹套的循环热水进行升温预处理(胶乳配制罐夹套水温全部过程中不得超过55℃),温度30℃~45℃之间,处理时间不少于3小时;Turn on the hot water circulation pump to heat up (the water temperature of the hot water tank cannot exceed 70°C during the whole process). Between ~45°C, the treatment time is not less than 3 hours;
S21.在胶温36℃以上时,依次加入硫化剂、促进剂、防老剂、活化剂;继续升温至40-55℃(具体温度视氯仿值的需求而进行调控);保温时间4小时以上且达到氯仿值需求时间放料停放48小时以上;S21. When the glue temperature is above 36 ℃, add vulcanizing agent, accelerator, anti-aging agent and activator in turn; continue to heat up to 40-55 ℃ (the specific temperature is adjusted according to the demand of chloroform value); the holding time is more than 4 hours and The time required to reach the chloroform value is to discharge and park for more than 48 hours;
S22.清洗并烘干模具;S22. Clean and dry the mold;
S23.将烘干之后的模具浸入凝固剂中,凝固剂的温度为48-60℃,模具在凝固剂中停留的时间为3-5秒;将附着有凝固剂的模具烘干,之后,浸入乳胶中,乳胶的温度为常温(25-28)℃,模具在乳胶中停留的时间为8-12秒,将附着有乳胶的模具取出硫化烘干,之后,将干燥硫化之后带有卷边乳胶膜的模具浸入热水中,热水的温度为75℃,模具在热水中停留的时间为16秒;将进入热水中的模具取出烘干,再将模具浸入隔离剂中(模具在隔离剂中停留的时间为10秒),然后取出干燥、脱模,即可得到乳胶手套。S23. Immerse the dried mold in a coagulant, the temperature of the coagulant is 48-60°C, and the time for the mold to stay in the coagulant is 3-5 seconds; dry the mold with the coagulant attached, and then immerse the mold into the coagulant. In the latex, the temperature of the latex is normal temperature (25-28) ℃, the time of the mold staying in the latex is 8-12 seconds, the mold with the latex is taken out and vulcanized and dried, and then the dried and vulcanized latex with curling The mold of the film is immersed in hot water, the temperature of the hot water is 75 ° C, and the time of the mold staying in the hot water is 16 seconds; the mold entering the hot water is taken out and dried, and then the mold is immersed in the isolation agent (the mold is in isolation. The residence time in the agent is 10 seconds), then take out, dry and demould to obtain latex gloves.
下面结合具体的实施方式对本发明做进一步的解释说明。The present invention will be further explained below in conjunction with specific embodiments.
实施例1Example 1
取净重为65-68Kg的乳胶手套(尺码为7.5:295-308副),放入48±2℃的温水中泡洗,捞起后放入蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分的摇箱中,摇至手套表面没有游离水分;具体处理时间大概为5-6min;后加入浓度为6-8%的滑爽剂,继续摇直至手套表面没有游离水分(继续运行的时间约为55min),后打开蒸汽阀,打开排风扇,直至摇箱温度降至40±2℃(所需要时间约为18±2min)后停止工作,取出手套即可得到表面太滑不可以接受的医用手套。其中,滑爽剂为丙烯酸混合液。Take latex gloves with a net weight of 65-68Kg (size 7.5: 295-308 pairs), soak them in warm water at 48±2°C, pick them up and put them into steam with a flow rate of 0.45-0.6MPa; set the temperature to 95 ±3°C, in a shaking box with a rotation speed of 30 rpm, shake until there is no free moisture on the surface of the glove; the specific treatment time is about 5-6min; then add a slip agent with a concentration of 6-8%, and continue to shake until the surface of the glove There is no free moisture (the time to continue running is about 55min), then open the steam valve and open the exhaust fan until the temperature of the shaking box drops to 40±2°C (the required time is about 18±2min), then stop working, take out the gloves to get Medical gloves with surfaces too slippery to be accepted. Among them, the slip agent is an acrylic mixed solution.
实施例2Example 2
取净重为68-70Kg的乳胶手套(尺码为7.5:309-318副),放入48±2℃温水中泡洗,捞起放入蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分的摇箱中,摇至手套表面没有游离水分(约5-6min);后加入浓度为4-5.0%的滑爽剂继续摇(继续运行的时间约为58min),直至手套表面没有游离水分,后打开蒸汽阀,打开排风扇,摇至摇箱温度降至40±2℃后停止运行,取出手套即可得到一种制备手套表面滑,但可以接受的医用手套。其中,滑爽剂为丙烯酸混合液。Take latex gloves with a net weight of 68-70Kg (size is 7.5: 309-318 pairs), soak them in 48±2℃ warm water, pick them up and put them in the steam with a flow rate of 0.45-0.6MPa; set the temperature to 95±3 ℃, in a shaking box with a rotation speed of 30 rpm, shake until there is no free moisture on the surface of the glove (about 5-6min); then add a slip agent with a concentration of 4-5.0% and continue to shake (the continuous running time is about 58min) , until there is no free moisture on the surface of the gloves, then open the steam valve, open the exhaust fan, shake until the temperature of the shaking box drops to 40 ± 2 °C, and then stop running, take out the gloves to obtain a medical glove with a smooth but acceptable surface. Among them, the slip agent is an acrylic mixed solution.
实施例3Example 3
取净重为70-72Kg的乳胶手套(尺码为7.5:318-327副),放入48±2℃温水中泡洗,捞起放入蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分的摇箱中,直至手套表面没有游离水分(约5-6min);后加入浓度为3-4%的滑爽剂继续摇(继续运行的时间约为60min),直至手套表面没有游离水分,后打开蒸汽阀,打开排风扇,至摇箱温度降至40±2℃(时间约为20min),取出手套即可得到一种粘滑度适中方便穿戴的医用手套。其中,滑爽剂为丙烯酸混合液。Take latex gloves with a net weight of 70-72Kg (size is 7.5: 318-327 pairs), soak them in 48±2℃ warm water, pick them up and put them in the steam flow rate of 0.45-0.6MPa; set the temperature to 95±3 ℃, in a shaking box with a rotation speed of 30 rpm, until there is no free moisture on the surface of the glove (about 5-6min); then add a slip agent with a concentration of 3-4% and continue to shake (the continuous running time is about 60min), Until there is no free moisture on the surface of the gloves, open the steam valve and open the exhaust fan until the temperature of the shaking box drops to 40±2°C (the time is about 20min). Take out the gloves to obtain a medical glove with moderate stickiness and easy to wear. Among them, the slip agent is an acrylic mixed solution.
实施例4Example 4
取净重为72-75Kg(尺码为7.5:327-341副)的乳胶手套,放入48±2℃温水中泡洗,捞起放入蒸汽流量为0.45-0.6MPa;温度设定为95±3℃,转速为30转/分的摇箱中,直至手套表面没有游离水分子(约5-6min);后加入浓度为2-3%的滑爽剂继续摇(继续运行的时间约为60min),直至手套表面没有游离水分,后打开蒸汽阀,打开排风扇,至摇箱温度降至40±2℃(处理时间约为20min),取出手套即可得到一种粘粘,但可以接受的医用手套。其中,滑爽剂为丙烯酸混合液。Take latex gloves with a net weight of 72-75Kg (size 7.5: 327-341 pairs), soak them in 48±2°C warm water, pick them up and put them in a steam flow rate of 0.45-0.6MPa; set the temperature to 95±3 ℃, the rotation speed is 30 rpm in a shaking box, until there are no free water molecules on the surface of the glove (about 5-6min); then add a slip agent with a concentration of 2-3% and continue to shake (the continuous running time is about 60min) , until there is no free moisture on the surface of the gloves, then open the steam valve, open the exhaust fan, until the temperature of the shaking box drops to 40 ± 2 °C (the processing time is about 20 minutes), take out the gloves to get a sticky, but acceptable medical gloves . Among them, the slip agent is an acrylic mixed solution.
以上实施例试验和检测数据参见下表。See the table below for the test and detection data of the above examples.
本发明提供的一种可分握持力等级的医用手套制备工艺,避免了传统方法处理的手套全光面手套太滑,部分麻面或者全麻面的又有点粘或者有点涩的技术问题。The invention provides a process for preparing medical gloves with different holding force grades, which avoids the technical problems that the full-gloss gloves treated by the traditional method are too slippery, and the partial or full hemp surface is sticky or astringent.
本申请可有效、精准地控制医用手套的握持力等级,可以制备出多种不同粘度、不同抓握力的医用手套,可满足不同医用工作者的使用要求。The application can effectively and accurately control the gripping force level of the medical gloves, and can prepare a variety of medical gloves with different viscosities and different gripping forces, which can meet the use requirements of different medical workers.
最后应说明的是:以上各实施例仅用以说明本发明的技术方案,而非对其限制;尽管参照前述各实施例对本发明进行了详细的说明,本领域的普通技术人员应当理解:其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分或者全部技术特征进行等同替换;而这些修改或者替换,并不使相应技术方案的本质脱离本发明各实施例技术方案的范围。Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention, but not to limit them; although the present invention has been described in detail with reference to the foregoing embodiments, those of ordinary skill in the art should understand that: The technical solutions described in the foregoing embodiments can still be modified, or some or all of the technical features thereof can be equivalently replaced; and these modifications or replacements do not make the essence of the corresponding technical solutions deviate from the technical solutions of the embodiments of the present invention. scope.
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| CN202210439649.8A Pending CN114953293A (en) | 2022-04-25 | 2022-04-25 | Preparation process of medical gloves capable of dividing holding force grades |
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