CN106635412A - Processing and separation method of oil and application thereof - Google Patents
Processing and separation method of oil and application thereof Download PDFInfo
- Publication number
- CN106635412A CN106635412A CN201710041086.6A CN201710041086A CN106635412A CN 106635412 A CN106635412 A CN 106635412A CN 201710041086 A CN201710041086 A CN 201710041086A CN 106635412 A CN106635412 A CN 106635412A
- Authority
- CN
- China
- Prior art keywords
- oil
- range
- separation method
- tea
- boiling range
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000926 separation method Methods 0.000 title claims abstract description 51
- 238000003672 processing method Methods 0.000 title abstract description 4
- 239000003921 oil Substances 0.000 claims abstract description 108
- 239000010495 camellia oil Substances 0.000 claims abstract description 83
- 238000009835 boiling Methods 0.000 claims abstract description 64
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000010742 number 1 fuel oil Substances 0.000 claims abstract description 26
- 238000001704 evaporation Methods 0.000 claims abstract description 22
- 239000010779 crude oil Substances 0.000 claims abstract description 20
- 238000000199 molecular distillation Methods 0.000 claims abstract description 18
- 239000000047 product Substances 0.000 claims abstract description 13
- 238000009833 condensation Methods 0.000 claims abstract description 12
- 230000005494 condensation Effects 0.000 claims abstract description 12
- 239000002537 cosmetic Substances 0.000 claims abstract description 11
- 239000012535 impurity Substances 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000004615 ingredient Substances 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- 238000004821 distillation Methods 0.000 claims description 7
- 241000196324 Embryophyta Species 0.000 claims description 5
- 235000009754 Vitis X bourquina Nutrition 0.000 claims description 4
- 235000012333 Vitis X labruscana Nutrition 0.000 claims description 4
- 235000014787 Vitis vinifera Nutrition 0.000 claims description 4
- 102000004190 Enzymes Human genes 0.000 claims description 3
- 108090000790 Enzymes Proteins 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 240000007817 Olea europaea Species 0.000 claims description 2
- 239000003463 adsorbent Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000005352 clarification Methods 0.000 claims 3
- 239000012467 final product Substances 0.000 claims 2
- 244000269722 Thea sinensis Species 0.000 claims 1
- 240000006365 Vitis vinifera Species 0.000 claims 1
- 238000010521 absorption reaction Methods 0.000 claims 1
- 239000010269 danmu Substances 0.000 claims 1
- 239000000284 extract Substances 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 238000007670 refining Methods 0.000 abstract description 24
- 230000008020 evaporation Effects 0.000 abstract description 19
- 238000005070 sampling Methods 0.000 abstract description 9
- 235000013305 food Nutrition 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 238000011084 recovery Methods 0.000 abstract description 3
- 238000001179 sorption measurement Methods 0.000 abstract description 3
- 239000006227 byproduct Substances 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 235000019198 oils Nutrition 0.000 description 78
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 46
- 238000003825 pressing Methods 0.000 description 26
- 239000002253 acid Substances 0.000 description 25
- 241001122767 Theaceae Species 0.000 description 24
- 229930003427 Vitamin E Natural products 0.000 description 23
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 23
- 235000013616 tea Nutrition 0.000 description 23
- 235000019165 vitamin E Nutrition 0.000 description 23
- 229940046009 vitamin E Drugs 0.000 description 23
- 239000011709 vitamin E Substances 0.000 description 23
- 150000002978 peroxides Chemical class 0.000 description 21
- 229930182558 Sterol Natural products 0.000 description 20
- 150000003432 sterols Chemical class 0.000 description 20
- 235000003702 sterols Nutrition 0.000 description 20
- 241000526900 Camellia oleifera Species 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000008169 grapeseed oil Substances 0.000 description 15
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 13
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 13
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 13
- 229940031439 squalene Drugs 0.000 description 13
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 13
- 239000004927 clay Substances 0.000 description 10
- 235000020334 white tea Nutrition 0.000 description 10
- 235000015112 vegetable and seed oil Nutrition 0.000 description 9
- 239000005909 Kieselgur Substances 0.000 description 8
- 238000007689 inspection Methods 0.000 description 7
- 150000001336 alkenes Chemical class 0.000 description 4
- 235000018597 common camellia Nutrition 0.000 description 4
- 235000016709 nutrition Nutrition 0.000 description 4
- 241000209507 Camellia Species 0.000 description 3
- 241000219095 Vitis Species 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 239000012230 colorless oil Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000005265 energy consumption Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 238000009874 alkali refining Methods 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000008157 edible vegetable oil Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002481 ethanol extraction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000011031 large-scale manufacturing process Methods 0.000 description 2
- 230000035764 nutrition Effects 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 235000008390 olive oil Nutrition 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 229930195730 Aflatoxin Natural products 0.000 description 1
- XWIYFDMXXLINPU-UHFFFAOYSA-N Aflatoxin G Chemical compound O=C1OCCC2=C1C(=O)OC1=C2C(OC)=CC2=C1C1C=COC1O2 XWIYFDMXXLINPU-UHFFFAOYSA-N 0.000 description 1
- 235000019489 Almond oil Nutrition 0.000 description 1
- 244000144725 Amygdalus communis Species 0.000 description 1
- 235000011437 Amygdalus communis Nutrition 0.000 description 1
- 240000001548 Camellia japonica Species 0.000 description 1
- 244000147058 Derris elliptica Species 0.000 description 1
- 238000012356 Product development Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000005409 aflatoxin Substances 0.000 description 1
- 235000020224 almond Nutrition 0.000 description 1
- 239000008168 almond oil Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001139 anti-pruritic effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 210000003372 endocrine gland Anatomy 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229940087559 grape seed Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000002398 materia medica Substances 0.000 description 1
- 238000000874 microwave-assisted extraction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004770 neurodegeneration Effects 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229940068065 phytosterols Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 235000017709 saponins Nutrition 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000000526 short-path distillation Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000194 supercritical-fluid extraction Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/001—Refining fats or fatty oils by a combination of two or more of the means hereafter
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/02—Other edible oils or fats, e.g. shortenings or cooking oils characterised by the production or working-up
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS OR COOKING OILS
- A23D9/00—Other edible oils or fats, e.g. shortenings or cooking oils
- A23D9/02—Other edible oils or fats, e.g. shortenings or cooking oils characterised by the production or working-up
- A23D9/04—Working-up
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B1/00—Production of fats or fatty oils from raw materials
- C11B1/06—Production of fats or fatty oils from raw materials by pressing
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/003—Refining fats or fatty oils by enzymes or microorganisms, living or dead
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/008—Refining fats or fatty oils by filtration, e.g. including ultra filtration, dialysis
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/10—Refining fats or fatty oils by adsorption
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B3/00—Refining fats or fatty oils
- C11B3/12—Refining fats or fatty oils by distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Biochemistry (AREA)
- Cosmetics (AREA)
- Fats And Perfumes (AREA)
Abstract
本发明公开了一种油的加工分离方法,其特征在于包括以下步骤:步骤一,分离:将毛油以短程分子蒸馏进行分离处理,得到高沸程油和低沸程油;其中,分离处理的条件为:进样速率与蒸发面积的比值在10~100L/(h*m2)范围内,蒸发温度在100~200℃之间,刮板速率在100~300rad/min范围内,冷凝温度在0~35℃之间;步骤二,精制:将步骤一所得低沸程油进行脱酸处理,即得无色澄清透明的高品质化妆品及药用油;将步骤一所得高沸程油进行脱胶处理,即得食用级油。与现有主要利用物理化学吸附等处理方式相比,本发明采用分子蒸馏进行无色茶油的分离,最大程度减少后续颜色恢复的影响因素,并减少精炼步骤,缩短生产周期,降低精炼损失,开发出高品质的深加工油脂产品以及食用级油作为副产品。The invention discloses an oil processing and separation method, which is characterized in that it comprises the following steps: Step 1, separation: the crude oil is subjected to separation treatment by short-range molecular distillation to obtain high boiling range oil and low boiling range oil; wherein, the conditions for separation treatment It is: the ratio of the sampling rate to the evaporation area is in the range of 10-100L/(h*m 2 ), the evaporation temperature is in the range of 100-200°C, the scraper speed is in the range of 100-300rad/min, and the condensation temperature is in the range of 0 ~35°C; step 2, refining: deacidify the low boiling range oil obtained in step 1 to obtain a colorless, clear and transparent high-quality cosmetic and medicinal oil; degumming the high boiling range oil obtained in step 1, namely Get food grade oil. Compared with the existing treatment methods mainly using physical and chemical adsorption, the present invention uses molecular distillation to separate the colorless tea oil, which minimizes the factors affecting subsequent color recovery, reduces refining steps, shortens the production cycle, and reduces refining losses. Developed high-quality deep-processed oil products and edible-grade oil as by-products.
Description
技术领域technical field
本发明属于农产品加工领域,具体涉及一种油的加工分离方法及其应用。The invention belongs to the field of agricultural product processing, and in particular relates to an oil processing and separation method and its application.
背景技术Background technique
油茶(Camellia oleifrea Abel)为山茶科山茶属植物,具有悠久的栽培历史,最初起源于中国,为世界四大木本油料树种其中之一。我国的油茶主要分布在南方,如广西、湖南、浙江、江西等地区,目前在国内具有较大的规模及产量。茶油是从山茶属油茶树的种子中提取的木本植物油,富含不饱和脂肪酸,色清质纯,营养丰富,略带茶油特有的芬芳,是一种高级食用油。茶油中不饱和脂肪酸含量占总脂肪酸含量的90%,其中油酸含量高达80%以上,可与目前世界上公认的保健油—橄榄油相媲美,具有“东方橄榄油”与“油中珍品”之称。《本草纲目》记载:“茶油性偏凉,有凉血、止血、清热、解毒之功效,主治肝血亏损、马卜虫、益肠胃、明目”。据《中外医药大辞典》记载,茶油不仅营养丰富,促进内分泌腺体激素分泌,防治神经功能卜降,提高人体免疫力等功效。因此,茶油是一种值得推荐的对人体健康有益的保健型营养油。因此,茶油是一种值得推荐的对人体健康有益的保健型营养油,适合于长期食用。Camellia oleifrea (Camellia oleifrea Abel) is a plant of the genus Camellia in the family Theaceae. It has a long history of cultivation. It originally originated in China and is one of the four major woody oil tree species in the world. Camellia oleifera in my country is mainly distributed in the south, such as Guangxi, Hunan, Zhejiang, Jiangxi and other regions, and currently has a relatively large scale and output in China. Camellia oil is a woody vegetable oil extracted from the seeds of Camellia oleifera. It is rich in unsaturated fatty acids, pure in color, rich in nutrition, and has a unique fragrance of camellia oil. It is a high-grade edible oil. The unsaturated fatty acid content in camellia oil accounts for 90% of the total fatty acid content, among which the oleic acid content is as high as 80%, which is comparable to the currently recognized health oil in the world—olive oil. "The name. "Compendium of Materia Medica" records: "Tea oil is cool in nature, has the effects of cooling blood, stopping bleeding, clearing away heat, and detoxifying. According to the "Chinese and Foreign Medicine Dictionary", tea oil is not only rich in nutrition, but also promotes the secretion of endocrine gland hormones, prevents neurological decline, and improves human immunity. Therefore, camellia oil is a health-care nutritional oil that is worth recommending and beneficial to human health. Therefore, camellia oil is a recommended health-care nutritional oil beneficial to human health and suitable for long-term consumption.
茶油与橄榄油相似,属于不干性油,精制茶油性质稳定,不易被氧化。茶油渗透性强易吸收,对紫外线有吸收作用,不含一般植物油中存在的黄曲霉毒素,含有少量维生素E、游离氨基酸、茶多酚、茶皂甙等成分而具有杀菌止痒作用,所以茶油非常适合作为化妆品及药用的油脂类原料。据报道在日本每年用于高端化妆品中的茶油高达数百吨。传统的油脂精炼方法能使茶油符合食用标准,但在色泽等品质方面很难满足化妆品用茶油的标准。Camellia oil is similar to olive oil and belongs to non-drying oil. Refined tea oil is stable and not easy to be oxidized. Tea oil has strong permeability and is easy to absorb, absorbs ultraviolet rays, does not contain aflatoxin in general vegetable oils, contains a small amount of vitamin E, free amino acids, tea polyphenols, tea saponins and other ingredients, and has bactericidal and antipruritic effects, so tea The oil is very suitable as a raw material of oils and fats for cosmetics and medicines. It is reported that the camellia oil used in high-end cosmetics in Japan is as high as hundreds of tons every year. Traditional oil refining methods can make camellia oil meet edible standards, but it is difficult to meet the standards of cosmetics in terms of quality such as color and luster.
中国发明专利申请CN200810029411.8公开了一种化妆品用的山茶油制备方法,选用优质油茶籽低温烘烤,常温压榨,加温过滤杂质,碱炼和乙醇萃取两步法脱酸脱胶,再用活性炭与活性白土的混合物作为脱色剂脱色,通过脱嗅去除氧化物和杂味,最后得到基本无色、晶莹透明、无异味的山茶油。中国发明专利公开号CN1017691.A公开了一种利用短程蒸馏精制化妆品级山茶油的方法,该法利用三级蒸馏制备低酸价山茶油与高价值油酸。但上述专利中,所采用的碱炼、乙醇萃取等步骤较繁琐,对油品质有一定影响,能耗较高且容易造成二次污染;而三级蒸馏制备仅作为降低酸值的技术使用,未能很好的解决存在的色泽问题。因此需要开发一种简单易行的绿色生产制备技术进行规模化生产。Chinese invention patent application CN200810029411.8 discloses a method for preparing camellia oil for cosmetics. High-quality camellia seeds are roasted at low temperature, pressed at room temperature, heated to filter impurities, deacidified and degummed by two-step method of alkali refining and ethanol extraction, and then activated carbon The mixture with activated clay is used as a decolorizing agent for decolorization, and oxides and miscellaneous odors are removed by deodorization, and finally camellia oil is basically colorless, crystal clear, and odorless. Chinese Invention Patent Publication No. CN1017691.A discloses a method for refining cosmetic-grade camellia oil by short-path distillation. The method uses three-stage distillation to prepare camellia oil with low acid value and high-value oleic acid. However, in the above-mentioned patents, the steps of alkali refining and ethanol extraction are relatively cumbersome, which have a certain impact on oil quality, high energy consumption and easy to cause secondary pollution; while the three-stage distillation preparation is only used as a technology to reduce the acid value. Failed to solve the existing color problem well. Therefore, it is necessary to develop a simple and feasible green production preparation technology for large-scale production.
发明内容Contents of the invention
本发明所要解决的技术问题是针对上述现有技术存在的不足而一种油的加工分离方法及其产品、应用,减少精炼步骤,缩短生产周期,降低精炼损失,最大程度减少后续颜色恢复的影响因素,开发出高品质的深加工油脂产品,以及食用级油作为副产品,实现油的定向优化,充分利用。The technical problem to be solved by the present invention is an oil processing and separation method and its products and applications aimed at the shortcomings of the above-mentioned prior art, reducing refining steps, shortening the production cycle, reducing refining losses, and minimizing the impact of subsequent color recovery Factors, develop high-quality deep-processed oil products, and edible-grade oil as a by-product, to achieve directional optimization of oil and make full use of it.
本发明为解决上述提出的问题所采用的技术方案为:The technical scheme that the present invention adopts for solving the above-mentioned problem is:
一种油的加工分离方法,其特征在于包括以下步骤:A method for processing and separating oil, characterized in that it comprises the following steps:
步骤一,分离:将毛油以短程分子蒸馏进行分离处理,得到高沸程油和低沸程油;其中,分离处理的条件为:进样速率与蒸发面积的比值在10~100L/(h*m2)范围内,蒸发温度在100~200℃之间,刮板速率在100~300rad/min范围内,冷凝温度在0~35℃之间;Step 1, separation: the crude oil is separated by short-range molecular distillation to obtain high-boiling range oil and low-boiling range oil; wherein, the conditions for separation treatment are: the ratio of the sampling rate to the evaporation area is 10-100L/(h*m 2 ) within the range, the evaporation temperature is between 100-200°C, the scraper speed is within the range of 100-300rad/min, and the condensation temperature is between 0-35°C;
步骤二,精制:将步骤一所得低沸程油进行脱酸处理,即得无色澄清透明的高品质化妆品及药用油;将步骤一所得高沸程油进行脱胶处理,即得食用级油。Step 2, refining: deacidifying the low boiling range oil obtained in step 1 to obtain colorless, clear and transparent high-quality cosmetic and medicinal oil; degumming the high boiling range oil obtained in step 1 to obtain edible grade oil.
按上述方案,所述毛油包括油茶、翅果、葡萄籽、橄榄、巴旦木等的油料,即茶油、翅果油、葡萄籽油、橄榄油、巴旦木油等。进一步地,本发明所述毛油优选茶油。According to the above scheme, the crude oil includes oil plants such as camellia oleifera, samara, grape seed, olive, almond, ie tea oil, samara oil, grape seed oil, olive oil, almond oil and the like. Further, the crude oil described in the present invention is preferably camellia oil.
按上述方案,所述毛油可以通过冷榨压榨、超临界萃取、微波辅助萃取或压榨等方式制备得到。According to the above scheme, the crude oil can be prepared by cold pressing, supercritical extraction, microwave-assisted extraction or pressing.
优选地,本发明所述毛油通过冷榨压榨方式制备得到,具体步骤为:选取成熟的油料,其中的含壳率在2~12%(质量百分比)且水分含量在2~8%(质量百分比)的范围,然后进行冷榨压榨,榨膛温度为50~100℃,出油温度为30~80℃;所压榨出的油经过滤去除杂质后,即得到毛油。Preferably, the crude oil of the present invention is prepared by cold pressing, and the specific steps are: select mature oil plants, wherein the shell content is 2-12% (mass percentage) and the moisture content is 2-8% (mass percentage); Percentage), then carry out cold pressing, the temperature of the pressing chamber is 50-100°C, and the temperature of the oil outlet is 30-80°C; the squeezed oil is filtered to remove impurities to obtain crude oil.
进一步地,本发明所述油料的含壳率优选在4~8%,水分含量优选在4~6%的范围。Furthermore, the shell content of the oil in the present invention is preferably in the range of 4-8%, and the moisture content is preferably in the range of 4-6%.
进一步地,所述榨膛温度优选为70~90℃,出油温度优选为30~60℃。Further, the temperature of the press chamber is preferably 70-90°C, and the oil outlet temperature is preferably 30-60°C.
按上述方案,短程分子蒸馏过程中,蒸发冷凝后收集的无色澄清透明的油组分为低沸程油,自蒸发器收集的未蒸发的油组分为高沸程油。According to the above scheme, in the short-range molecular distillation process, the colorless, clear and transparent oil component collected after evaporation and condensation is low boiling range oil, and the unevaporated oil component collected from the evaporator is high boiling range oil.
按上述方案,所述步骤一中,短程分子蒸馏进行分离处理时,分离处理的条件优选为:进样速率与蒸发面积的比值在40~60L/(h*m2)范围内,蒸发温度在120~160℃之间,刮板速率在150~250rad/min范围内,冷凝温度在15~25℃之间。According to the above scheme, in the first step, when short-range molecular distillation is used for separation treatment, the conditions for separation treatment are preferably: the ratio of the sampling rate to the evaporation area is within the range of 40-60L/(h*m 2 ), and the evaporation temperature is within the range of Between 120-160°C, the scraper speed is in the range of 150-250rad/min, and the condensation temperature is between 15-25°C.
按上述方案,步骤二中,低沸程油可以采用短程分子蒸馏进行二次蒸馏工艺实现脱酸,也可以通过添加吸附剂进行物理吸附的方式实现脱酸。优选地,本发明中所述低沸程油中添加白土、硅藻土后,经搅拌、固液分离实现脱酸处理,得到无色澄清透明的化妆品级油。其中,白土、硅藻土和低沸程油以质量比(0.1~0.5):(0.1~0.5):10混合。According to the above scheme, in step 2, the low boiling range oil can be deacidified by short-range molecular distillation for secondary distillation, or by adding an adsorbent for physical adsorption. Preferably, after clay and diatomaceous earth are added to the low boiling range oil in the present invention, the deacidification treatment is realized by stirring and solid-liquid separation to obtain a colorless, clear and transparent cosmetic-grade oil. Among them, clay, diatomite and low boiling range oil are mixed in a mass ratio of (0.1-0.5):(0.1-0.5):10.
按上述方案,步骤二中,高沸程油可以采用酶法工艺进行脱胶处理,也可以采用水化法进行脱胶处理。优选地,本发明采用水化法进行脱胶处理,具体方法为:将高沸程油升温至70~80℃,然后加入温度70~80℃的水进行脱胶,加水量为高沸程油质量的6~7%,脱胶时间为10~20min,经离心、过滤、真空干燥、冷却后,得到食用级油。According to the above scheme, in the second step, the high boiling range oil can be degummed by an enzymatic process, or can be degummed by a hydration method. Preferably, the present invention adopts the hydration method for degumming treatment, the specific method is: heating the high boiling range oil to 70-80°C, and then adding water at a temperature of 70-80°C for degumming, the amount of water added is 6-7% of the mass of the high boiling range oil , the degumming time is 10-20 minutes, after centrifugation, filtration, vacuum drying and cooling, edible grade oil is obtained.
与现有的技术相比,本发明的有益效果是:Compared with prior art, the beneficial effect of the present invention is:
(1)对于无色油尤其是茶油的制备,现有的仍主要延用物理化学吸附等经典的处理方式,步骤较繁杂且能耗及油品损耗较多,而短程分子蒸馏现今是在工业上主要用来进行功效成分的富集分离纯化(如DHA、EPA的富集)或者对油进行脱酸处理等,而其在色素类相关应用又局限于脱除溶剂残留等,故未见有本领域技术人员将其进行无色油品分离方面的拓展尝试及应用。而本发明首次采用短程分子蒸馏进行无色油的分离,首先将有色组分分离出来,最大程度减少后续颜色恢复的影响因素,并减少精炼步骤,缩短生产周期,降低精炼损失,进而开发出高品质的深加工油脂产品(即高品质化妆品及药用油);而有色组分可应用于食品领域。尤其是,在具体实施案例中无色茶油维生素E、角鲨烯、植物甾醇等功效活性成分具有富集效应,含量均出现50%以上的增加,稳定性更佳;(1) For the preparation of colorless oil, especially camellia oil, the existing methods mainly continue to use classic treatment methods such as physical and chemical adsorption, the steps are more complicated and the energy consumption and oil loss are more, while short-range molecular distillation is currently used in In industry, it is mainly used for the enrichment, separation and purification of functional components (such as the enrichment of DHA and EPA) or for deacidification of oil, etc., but its application in pigments is limited to the removal of solvent residues, etc., so it has not been seen. Those skilled in the art have tried to expand and apply it to the separation of colorless oil. However, the present invention adopts short-range molecular distillation for the first time to separate the colorless oil, and firstly separates the colored components, which minimizes the factors affecting subsequent color recovery, reduces refining steps, shortens the production cycle, and reduces refining losses, thereby developing a high-efficiency High-quality deep-processed oil products (that is, high-quality cosmetics and medicinal oils); and colored components can be used in the food field. In particular, in specific implementation cases, functional active ingredients such as colorless tea oil, vitamin E, squalene, and phytosterols have an enrichment effect, and the content increases by more than 50%, and the stability is better;
(2)本发明针对高沸程油有胶质低酸价、低沸程油无胶质酸价较高的特征,分别进行精制处理,实现能耗的定向优化利用,节约能源,油的利用率高,总收率达到96%以上。其中,短程分子蒸馏出的低沸程油收率高,无色澄清透明,维生素E、植物甾醇等功效成分含量较高且易于被皮肤吸收,适用于化妆品、药品等领域,而分离出的高沸程油符合国家食用茶油的相关规定,可应用于食品领域。尤其是,无色茶油收率较高,达到40%以上,而高沸程的茶油仍是优良的食用油原料;(2) The present invention aims at the characteristics that high boiling range oil has colloid and low acid value, and low boiling range oil has no colloid and high acid value, respectively carries out refining treatment, realizes the directional optimized utilization of energy consumption, saves energy, and has high oil utilization rate , the total yield reaches more than 96%. Among them, the low-boiling range oil obtained by short-range molecular distillation has a high yield, is colorless, clear and transparent, has high content of functional ingredients such as vitamin E and phytosterol, and is easily absorbed by the skin. It is suitable for cosmetics, pharmaceuticals and other fields. The oil complies with the relevant national regulations on edible tea oil and can be used in the food field. In particular, the yield of colorless camellia oil is higher, reaching more than 40%, and the tea oil with high boiling range is still an excellent edible oil raw material;
(3)本发明中涉及工艺均在较低温度下进行,蒸馏过程中油样与蒸馏加热面接触时间短,较大程度上保证了油品的高品质;(3) The processes involved in the present invention are all carried out at a lower temperature, and the contact time between the oil sample and the distillation heating surface is short during the distillation process, which ensures the high quality of the oil product to a large extent;
(4)本发明产品定位准确实用性强,涉及步骤均采用物理加工工艺,工艺简单易行损耗低,对环境污染少,容易控制,绿色高效适合规模化生产,符合现代绿色加工及高附加值产品开发要求。(4) The product of the present invention has accurate positioning and strong practicability. The steps involved adopt physical processing technology. The process is simple and easy to operate with low loss, less environmental pollution, easy to control, green and efficient, suitable for large-scale production, in line with modern green processing and high added value Product development requirements.
具体实施方式detailed description
为了更好地理解本发明,下面结合实施例进一步阐明本发明的内容,但本发明不仅仅局限于下面的实施例。In order to better understand the present invention, the content of the present invention is further illustrated below in conjunction with the examples, but the present invention is not limited to the following examples.
实施例1Example 1
一种茶油的加工分离方法,具体包括以下步骤:A method for processing and separating camellia oil, specifically comprising the following steps:
(1)预处理:选取成熟的油茶籽,去除杂质(去除茶籽中可能存在的泥沙枝叶等杂质)并脱壳得到茶籽仁,仁中含壳率为6%,并调整茶籽仁中水分含量在6%;(1) Pretreatment: select mature camellia oleifera seeds, remove impurities (removal of impurities such as silt, branches and leaves that may exist in the tea seeds) and shell them to obtain tea seed kernels, with a shell rate of 6% in the kernels, and adjust the tea seed kernels The moisture content in the medium is 6%;
(2)初榨:将脱壳后的茶籽仁进行冷榨压榨,榨膛温度为90℃,出油温度为40℃,将压榨出的茶油过滤去除杂质(除去压榨过程中产生的残渣等),得到初榨茶油,即毛油;(2) Virgin pressing: the tea seed kernels after shelling are subjected to cold pressing, the temperature of the pressing chamber is 90°C, and the temperature of the oil outlet is 40°C, and the pressed tea oil is filtered to remove impurities (remove the residue generated during the pressing process) etc.), to obtain virgin camellia oil, i.e. crude oil;
(3)分离:过滤后的茶油以短程分子蒸馏(旋转刮板式)进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度140℃,刮板速率200rad/min,冷凝温度15℃,分离得到高沸程茶油和低沸程茶油;( 3 ) Separation: The filtered camellia oil is separated by short-range molecular distillation (rotary scraper type). The plate speed is 200rad/min, the condensation temperature is 15°C, and high boiling range tea oil and low boiling range tea oil are separated;
(4)精制:将分离后的高沸程茶油和水同时升温至70℃,加水量6%,脱胶时间10min,厢式压滤机过滤,得到食用级油茶籽油;而分离所得低沸程茶油,按照白土、硅藻土、低沸程茶油的质量比为0.5:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白茶油。(4) Refining: heat up the separated high-boiling tea oil and water to 70°C at the same time, add 6% water, degumming time 10min, filter with a chamber filter press to obtain edible-grade camellia oleifera seed oil; and separate the obtained low-boiling tea The oil is mixed according to the mass ratio of clay, diatomaceous earth, and low-boiling range tea oil of 0.5:0.5:10, stirred for 30 minutes, and centrifuged to obtain colorless, clear and transparent cosmetic-grade white tea oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨茶油的酸价0.36mgKOH/g、过氧化值0.78mmol/kg、维生素E 0.347mg/g、甾醇0.774mg/g、角鲨烯0.335mg/g;经过分离、精制后的食用级油茶籽油的收率为56%的水平,酸价0.12mgKOH/g、过氧化值0.28mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白茶油的收率为42%的水平,酸价0.07mgKOH/g、过氧化值0.67mmol/kg、维生素E 0.564mg/g、甾醇1.24mg/g、角鲨烯0.612mg/g,可直接应用于高端护肤产品。According to relevant national standards and landmark inspection standards, in this example, the acid value of the obtained virgin tea oil is 0.36mgKOH/g, peroxide value 0.78mmol/kg, vitamin E 0.347mg/g, sterol 0.774mg/g, squal alkenes 0.335mg/g; the yield of food-grade Camellia oleifera oil after separation and refining is 56%, acid value 0.12mgKOH/g, peroxide value 0.28mmol/kg, and vitamin E, sterols, squalene Compared with ordinary refined oil, the ingredients are also at a higher level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white tea oil is 42%, the acid value is 0.07mgKOH/g, and the peroxide value is 0.67mmol/kg , vitamin E 0.564mg/g, sterol 1.24mg/g, squalene 0.612mg/g, which can be directly applied to high-end skin care products.
实施例2Example 2
一种茶油的加工分离方法,具体包括以下步骤:A method for processing and separating camellia oil, specifically comprising the following steps:
(1)预处理:选取成熟的油茶籽,去除杂质并脱壳得到茶籽仁,仁中含壳率为6%,并调整茶籽仁中水分含量在4%;(1) Pretreatment: select mature camellia oleifera seeds, remove impurities and dehull to obtain tea seed kernels, with a shell rate of 6% in the kernels, and adjust the moisture content in the tea seed kernels to 4%;
(2)初榨:将脱壳后的茶籽仁进行冷榨压榨,榨膛温度为80℃,出油温度为35℃,将压榨出的茶油过滤去除杂质,得到初榨茶油,即毛油;(2) Virgin pressing: the tea seed kernels after shelling are subjected to cold pressing, the temperature of the pressing chamber is 80°C, and the oil outlet temperature is 35°C, and the pressed tea oil is filtered to remove impurities to obtain virgin tea oil, namely crude oil;
(3)分离:过滤后的茶油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度135℃,刮板速率180rad/min,冷凝温度15℃,分离得到高沸程茶油和低沸程茶油;(3) Separation: The filtered camellia oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 40L/(h·m 2 ), the evaporation temperature is 135°C, and the scraper speed is 180rad/min. , the condensation temperature is 15°C, and the tea oil with high boiling range and tea oil with low boiling range are obtained through separation;
(4)精制:将分离后的高沸程茶油和水同时升温至80℃,加水量6%,脱胶时间20min,厢式压滤机过滤,得到食用级油茶籽油;而分离所得低沸程茶油,按照白土、硅藻土、低沸程茶油的质量比为0.1:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白茶油。(4) Refining: heat up the separated high-boiling tea oil and water to 80°C at the same time, add 6% water, degumming time 20min, filter with a chamber filter press to obtain edible-grade camellia oleifera seed oil; and separate the obtained low-boiling tea The oil is mixed according to the mass ratio of clay, diatomaceous earth, and low-boiling tea oil of 0.1:0.5:10, stirred for 30 minutes, and centrifugally filtered to obtain colorless, clear and transparent cosmetic-grade white tea oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨茶油的酸价0.40mgKOH/g、过氧化值0.66mmol/kg、维生素E 0.235mg/g、甾醇0.662mg/g、角鲨烯0.301mg/g;经过分离、精制后的食用级油茶籽油的收率为53%的水平,酸价0.14mgKOH/g、过氧化值0.20mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白茶油的收率为44%的水平,酸价0.09mgKOH/g、过氧化值0.50mmol/kg、维生素E 0.442mg/g、甾醇1.04mg/g、角鲨烯0.598mg/g,可直接应用于高端护肤产品。According to relevant national standards and landmark inspection standards, in this example, the acid value of the obtained virgin tea oil is 0.40mgKOH/g, peroxide value 0.66mmol/kg, vitamin E 0.235mg/g, sterol 0.662mg/g, squal alkenes 0.301mg/g; the yield of food grade Camellia oleifera seed oil after separation and refining is 53%, acid value 0.14mgKOH/g, peroxide value 0.20mmol/kg, vitamin E, sterols, squalene Compared with ordinary refined oil, the ingredients are also at a higher level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white tea oil is 44%, the acid value is 0.09mgKOH/g, and the peroxide value is 0.50mmol/kg , vitamin E 0.442mg/g, sterol 1.04mg/g, squalene 0.598mg/g, which can be directly applied to high-end skin care products.
实施例3Example 3
一种茶油的加工分离方法,具体包括以下步骤:A method for processing and separating camellia oil, specifically comprising the following steps:
(1)预处理:选取成熟的油茶籽,去除杂质并脱壳得到茶籽仁,仁中含壳率为10%,并调整茶籽仁中水分含量在6%;(1) Pretreatment: select mature camellia oleifera seeds, remove impurities and dehull to obtain tea seed kernels, with a shell rate of 10% in the kernels, and adjust the moisture content in the tea seed kernels to 6%;
(2)初榨:将脱壳后的茶籽仁进行冷榨压榨,榨膛温度为80℃,出油温度为40℃,将压榨出的茶油过滤去除杂质,得到初榨茶油,即毛油;(2) Virgin pressing: the tea seed kernels after shelling are subjected to cold pressing, the temperature of the pressing chamber is 80°C, and the oil outlet temperature is 40°C, and the pressed tea oil is filtered to remove impurities to obtain virgin tea oil, namely crude oil;
(3)分离:过滤后的茶油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值50L/(h·m2),蒸发温度140℃,刮板速率220rad/min,冷凝温度10℃,分离得到高沸程茶油和低沸程茶油;(3) Separation: The filtered camellia oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 50L/(h·m 2 ), the evaporation temperature is 140°C, and the scraper speed is 220rad/min. , the condensation temperature is 10°C, and the tea oil with high boiling range and tea oil with low boiling range are obtained through separation;
(4)精制:将分离后的高沸程茶油和水同时升温至80℃,加水量4%,脱胶时间20min,厢式压滤机过滤,得到食用级油茶籽油;而分离所得低沸程茶油,按照白土、硅藻土、低沸程茶油的质量比为0.2:0.4:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白茶油。(4) Refining: heat up the separated high-boiling tea oil and water to 80°C at the same time, add 4% water, degumming time 20min, filter with a chamber filter press to obtain edible-grade camellia oleifera seed oil; and separate the obtained low-boiling tea The oil is mixed according to the mass ratio of clay, diatomaceous earth, and low-boiling camellia oil of 0.2:0.4:10, stirred for 30 minutes, and centrifuged to obtain colorless, clear and transparent cosmetic-grade white tea oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨茶油的酸价0.33mgKOH/g、过氧化值0.80mmol/kg、维生素E 0.454mg/g、甾醇0.712mg/g、角鲨烯0.313mg/g;经过分离、精制后的食用级油茶籽油的收率为50%的水平,酸价0.10mgKOH/g、过氧化值0.33mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白茶油的收率为47%的水平,酸价0.07mgKOH/g、过氧化值0.47mmol/kg、维生素E 0.779mg/g、甾醇1.31mg/g、角鲨烯0.589mg/g,可直接应用于高端护肤产品。According to relevant national standards and landmark inspection standards, in this example, the acid value of the obtained virgin tea oil is 0.33mgKOH/g, peroxide value 0.80mmol/kg, vitamin E 0.454mg/g, sterol 0.712mg/g, squal ene 0.313mg/g; after separation and refining, the yield of food-grade Camellia oleifera seed oil is 50%, acid value 0.10mgKOH/g, peroxide value 0.33mmol/kg, and vitamin E, sterols, squalene Compared with ordinary refined oils, the ingredients are also at a higher level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white tea oil is 47%, the acid value is 0.07mgKOH/g, and the peroxide value is 0.47mmol/kg , vitamin E 0.779mg/g, sterol 1.31mg/g, squalene 0.589mg/g, which can be directly applied to high-end skin care products.
实施例4Example 4
一种茶油的加工分离方法,具体包括以下步骤:A method for processing and separating camellia oil, specifically comprising the following steps:
(1)预处理:选取成熟的油茶籽,去除杂质并脱壳得到茶籽仁,仁中含壳率为6%,并调整茶籽仁中水分含量在6%;(1) Pretreatment: select mature camellia oleifera seeds, remove impurities and dehull to obtain tea seed kernels, with a shell rate of 6% in the kernels, and adjust the moisture content in the tea seed kernels to 6%;
(2)初榨:将脱壳后的茶籽仁进行冷榨压榨,榨膛温度为90℃,出油温度为40℃,将压榨出的茶油过滤去除杂质,得到初榨茶油,即毛油;(2) Virgin pressing: the tea seed kernels after shelling are subjected to cold pressing, the temperature of the pressing chamber is 90°C, and the oil outlet temperature is 40°C, and the pressed tea oil is filtered to remove impurities to obtain virgin tea oil, namely crude oil;
(3)分离:过滤后的茶油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度140℃,刮板速率200rad/min,冷凝温度15℃,分离得到高沸程茶油和低沸程茶油;(3) Separation: The filtered camellia oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 40L/(h·m 2 ), the evaporation temperature is 140°C, and the scraper speed is 200rad/min. , the condensation temperature is 15°C, and the tea oil with high boiling range and tea oil with low boiling range are obtained through separation;
(4)精制:将分离后的高沸程茶油和水同时升温至70℃,加水量6%,脱胶时间10min,厢式压滤机过滤,得到食用级油茶籽油;而分离所得低沸程茶油,按照白土、硅藻土、低沸程茶油的质量比为0.5:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白茶油。(4) Refining: heat up the separated high-boiling tea oil and water to 70°C at the same time, add 6% water, degumming time 10min, filter with a chamber filter press to obtain edible-grade camellia oleifera seed oil; and separate the obtained low-boiling tea The oil is mixed according to the mass ratio of clay, diatomaceous earth, and low-boiling range tea oil of 0.5:0.5:10, stirred for 30 minutes, and centrifuged to obtain colorless, clear and transparent cosmetic-grade white tea oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨茶油的酸价0.44mgKOH/g、过氧化值0.87mmol/kg、维生素E 0.300mg/g、甾醇0.677mg/g、角鲨烯0.274mg/g;经过分离、精制后的食用级油茶籽油的收率为57%的水平,酸价0.20mgKOH/g、过氧化值0.32mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白茶油的收率为42%的水平,酸价0.10mgKOH/g、过氧化值0.40mmol/kg、维生素E 0.612mg/g、甾醇1.08mg/g、角鲨烯0.551mg/g,可直接应用于高端护肤产品。According to relevant national standards and landmark inspection standards, in this example, the acid value of the obtained virgin tea oil is 0.44mgKOH/g, peroxide value 0.87mmol/kg, vitamin E 0.300mg/g, sterol 0.677mg/g, squal alkenes 0.274mg/g; the yield of food-grade Camellia oleifera oil after separation and refining is 57%, acid value 0.20mgKOH/g, peroxide value 0.32mmol/kg, and vitamin E, sterols, squalene Compared with ordinary refined oil, the ingredients are also at a higher level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white tea oil is 42%, the acid value is 0.10mgKOH/g, and the peroxide value is 0.40mmol/kg , vitamin E 0.612mg/g, sterol 1.08mg/g, squalene 0.551mg/g, which can be directly applied to high-end skin care products.
实施例5Example 5
一种茶油的加工分离方法,具体包括以下步骤:A method for processing and separating camellia oil, specifically comprising the following steps:
(1)预处理:选取成熟的油茶籽,去除杂质并脱壳得到茶籽仁,仁中含壳率为6%,并调整茶籽仁中水分含量在6%;(1) Pretreatment: select mature camellia oleifera seeds, remove impurities and dehull to obtain tea seed kernels, with a shell rate of 6% in the kernels, and adjust the moisture content in the tea seed kernels to 6%;
(2)初榨:将脱壳后的茶籽仁进行冷榨压榨,榨膛温度为90℃,出油温度为40℃,将压榨出的茶油过滤去除杂质,得到初榨茶油,即毛油;(2) Virgin pressing: the tea seed kernels after shelling are subjected to cold pressing, the temperature of the pressing chamber is 90°C, and the oil outlet temperature is 40°C, and the pressed tea oil is filtered to remove impurities to obtain virgin tea oil, namely crude oil;
(3)分离:过滤后的茶油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度140℃,刮板速率200rad/min,冷凝温度15℃,分离得到高沸程茶油和低沸程茶油;(3) Separation: The filtered camellia oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 40L/(h·m 2 ), the evaporation temperature is 140°C, and the scraper speed is 200rad/min. , the condensation temperature is 15°C, and the tea oil with high boiling range and tea oil with low boiling range are obtained through separation;
(4)精制:将分离后的高沸程茶油加入水和酶,加水量为高沸程茶油质量的6%,加酶量为高沸程茶油质量的1%,于温度40℃搅拌30min进行脱胶,然后采用厢式压滤机过滤,得到食用级油茶籽油;而分离所得低沸程茶油,按照白土、硅藻土、低沸程茶油的质量比为0.5:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白茶油。(4) Refining: adding water and enzyme to the high boiling range camellia oil after separation, the amount of water added is 6% of the quality of high boiling range camellia oil, the amount of enzyme added is 1% of the quality of high boiling range tea oil, degumming is carried out at 40°C of temperature and stirred for 30min, then Adopt chamber type filter press to filter, obtain edible grade Camellia oleifera seed oil; And the low-boiling range camellia oil of separation gained, according to the mass ratio of clay, diatomaceous earth, low-boiling range camellia oil is 0.5:0.5:10 mixes, stirs 30min, After centrifugal filtration, a colorless, clear and transparent cosmetic-grade white tea oil is obtained.
经相关国标及地标检验标准检测,本实施例中,所得初榨茶油的酸价0.27mgKOH/g、过氧化值0.71mmol/kg、维生素E 0.412mg/g、甾醇0.566mg/g、角鲨烯0.289mg/g;经过分离、精制后的食用级油茶籽油的收率为53%的水平,酸价0.13mgKOH/g、过氧化值0.31mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白茶油的收率为45%的水平,酸价0.08mgKOH/g、过氧化值0.40mmol/kg、维生素E 0.656mg/g、甾醇0.899mg/g、角鲨烯0.523mg/g,可直接应用于高端护肤产品。According to relevant national standards and landmark inspection standards, in this example, the acid value of the obtained virgin tea oil is 0.27mgKOH/g, peroxide value 0.71mmol/kg, vitamin E 0.412mg/g, sterol 0.566mg/g, squal alkenes 0.289mg/g; the yield of food-grade Camellia oleifera oil after separation and refining is 53%, acid value 0.13mgKOH/g, peroxide value 0.31mmol/kg, vitamin E, sterols, squalene Compared with ordinary refined oil, the ingredients are also at a higher level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white tea oil is 45%, the acid value is 0.08mgKOH/g, and the peroxide value is 0.40mmol/kg , vitamin E 0.656mg/g, sterol 0.899mg/g, squalene 0.523mg/g, which can be directly applied to high-end skin care products.
实施例6Example 6
一种翅果油的加工分离方法,具体包括以下步骤:A method for processing and separating samara oil, specifically comprising the following steps:
(1)预处理:选取成熟的翅果,去除杂质并脱壳得到翅果仁,仁中含壳率为6%,并调整翅果仁中水分含量在6%;(1) pretreatment: select ripe Samara, remove impurities and shell to obtain Samara Kernel, the shell rate in Kernel is 6%, and adjust the moisture content in Samara Kernel to 6%;
(2)初榨:将脱壳后的翅果仁进行冷榨压榨,榨膛温度为90℃,出油温度为40℃,将压榨出的翅果油过滤去除杂质,得到初榨翅果油,即毛油;(2) Virgin pressing: the shelled samara kernels are cold-pressed, the temperature of the pressing chamber is 90°C, and the oil outlet temperature is 40°C, and the pressed samara oil is filtered to remove impurities to obtain virgin samara oil , namely crude oil;
(3)分离:过滤后的翅果油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度140℃,刮板速率200rad/min,冷凝温度15℃,分离得到高沸程翅果油和低沸程翅果油;(3) Separation: The filtered samara oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 40L/(h·m 2 ), the evaporation temperature is 140°C, and the scraper speed is 200rad/ min, the condensation temperature is 15°C, and the high boiling range samara oil and the low boiling range samara oil are separated;
(4)精制:将分离后的高沸程翅果油和水同时升温至70℃,加水量6%,脱胶时间10min,采用厢式压滤机过滤,得到食用级翅果油;而分离所得低沸程翅果油,按照白土、硅藻土、低沸程翅果油的质量比为0.5:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白翅果油。(4) Refining: heat up the separated high boiling range samara oil and water to 70°C at the same time, add 6% water, degumming time 10min, filter with a chamber filter press to obtain edible grade samara oil; Cheng samara oil is mixed according to the mass ratio of clay, diatomaceous earth, and low boiling range samara oil of 0.5:0.5:10, stirred for 30 minutes, and centrifuged to obtain colorless, clear and transparent cosmetic grade samara oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨翅果油的酸价1.25mgKOH/g、过氧化值1.04mmol/kg、维生素E 0.755mg/g、甾醇0.641mg/g;经过分离、精制后的食用级翅果油的收率为57%的水平,酸价0.54mgKOH/g、过氧化值0.78mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白翅果油的收率为40%的水平,酸价0.16mgKOH/g、过氧化值1.22mmol/kg、维生素E1.87mg/g、甾醇1.11mg/g,为优质的护肤用油。According to relevant national standards and landmark inspection standards, in this embodiment, the acid value of the obtained virgin samara oil is 1.25mgKOH/g, the peroxide value is 1.04mmol/kg, vitamin E is 0.755mg/g, and sterol is 0.641mg/g; The yield of the separated and refined edible grade samara oil is 57%, the acid value is 0.54mgKOH/g, and the peroxide value is 0.78mmol/kg, while vitamin E, sterols, squalene and other components are comparable to ordinary refined oil The ratio is also at a relatively high level, which is a high-quality food-grade oil; while the yield of cosmetic-grade white winged fruit oil is 40%, the acid value is 0.16mgKOH/g, the peroxide value is 1.22mmol/kg, and vitamin E is 1.87mg /g, sterol 1.11mg/g, is a high-quality skin care oil.
实施例7Example 7
一种葡萄籽油的加工分离方法,具体包括以下步骤:A method for processing and separating grapeseed oil, specifically comprising the following steps:
(1)预处理:选取新鲜的葡萄籽,去除杂质并干燥,并调整葡萄籽中水分含量在6%;(1) Pretreatment: select fresh grape seeds, remove impurities and dry, and adjust the moisture content in grape seeds to 6%;
(2)初榨:将上述葡萄籽进行冷榨压榨,榨膛温度为90℃,出油温度为40℃,将压榨出的葡萄籽油过滤去除杂质,得到初榨葡萄籽油,即毛油;(2) Virgin pressing: the above grape seeds are subjected to cold pressing, the temperature of the pressing chamber is 90°C, and the temperature of the oil outlet is 40°C, and the pressed grape seed oil is filtered to remove impurities to obtain virgin grape seed oil, namely crude oil ;
(3)分离:过滤后的葡萄籽油以短程分子蒸馏进行分离处理,分离条件为:进样速率与蒸发面积的比值40L/(h·m2),蒸发温度140℃,刮板速率200rad/min,冷凝温度15℃,分离得到高沸程葡萄籽油和低沸程葡萄籽油;(3) Separation: The filtered grape seed oil is separated by short-range molecular distillation. The separation conditions are: the ratio of the sampling rate to the evaporation area is 40L/(h·m 2 ), the evaporation temperature is 140°C, and the scraper speed is 200rad/ min, condensing temperature 15°C, separated to obtain high boiling range grape seed oil and low boiling range grape seed oil;
(4)精制:将分离后的高沸程葡萄籽油和水同时升温至70℃,加水量6%,脱胶时间10min,厢式压滤机过滤,得到食用级油葡萄籽籽油;而分离所得低沸程葡萄籽油,按照白土、硅藻土、低沸程葡萄籽油的质量比为0.5:0.5:10混合,搅拌30min,离心过滤,得到无色澄清透明的化妆品级白葡萄籽油。(4) Refining: the separated high-boiling range grape seed oil and water are heated up to 70°C simultaneously, the amount of water added is 6%, the degumming time is 10min, and the chamber filter press is filtered to obtain edible-grade oil grape seed oil; The boiling range grape seed oil is mixed according to the mass ratio of clay, diatomaceous earth, and low boiling range grape seed oil of 0.5:0.5:10, stirred for 30 minutes, and centrifuged to obtain colorless, clear and transparent cosmetic grade white grape seed oil.
经相关国标及地标检验标准检测,本实施例中,所得初榨葡萄籽油的酸价0.85mgKOH/g、过氧化值1.02mmol/kg、维生素E 0.145mg/g、甾醇1.56mg/g;经过分离、精制后的食用级油葡萄籽油的收率为54%的水平,酸价0.28mgKOH/g、过氧化值0.37mmol/kg,而维生素E、甾醇、角鲨烯等成分与普通精炼油相比也处于较高水平,为优质的食用级油品;而化妆品级白葡萄籽油的收率为44%的水平,酸价0.14mgKOH/g、过氧化值0.50mmol/kg、维生素E 0.250mg/g、甾醇2.55mg/g,为优质的护肤用油。According to relevant national standards and landmark inspection standards, in this embodiment, the acid value of the obtained virgin grape seed oil is 0.85mgKOH/g, peroxide value 1.02mmol/kg, vitamin E 0.145mg/g, sterol 1.56mg/g; The yield of edible-grade grape seed oil after separation and refining is 54%, the acid value is 0.28mgKOH/g, and the peroxide value is 0.37mmol/kg. It is also at a relatively high level, and it is a high-quality food-grade oil; while the yield of cosmetic-grade white grape seed oil is 44%, the acid value is 0.14mgKOH/g, the peroxide value is 0.50mmol/kg, and vitamin E is 0.250 mg/g, sterol 2.55mg/g, it is a high-quality skin care oil.
以上所述仅是本发明的优选实施方式,应当指出,对于本领域的普通技术人员来说,在不脱离本发明创造构思的前提下,还可以做出若干改进和变换,这些都属于本发明的保护范围。The above is only a preferred embodiment of the present invention, it should be pointed out that for those of ordinary skill in the art, without departing from the creative concept of the present invention, some improvements and changes can also be made, and these all belong to the present invention scope of protection.
Claims (10)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710041086.6A CN106635412B (en) | 2017-01-17 | 2017-01-17 | Oil processing and separating method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710041086.6A CN106635412B (en) | 2017-01-17 | 2017-01-17 | Oil processing and separating method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN106635412A true CN106635412A (en) | 2017-05-10 |
| CN106635412B CN106635412B (en) | 2020-11-10 |
Family
ID=58841817
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710041086.6A Active CN106635412B (en) | 2017-01-17 | 2017-01-17 | Oil processing and separating method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106635412B (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108219955A (en) * | 2018-01-24 | 2018-06-29 | 广西壮族自治区农业科学院 | A kind of preparation method and application of hemp essential oil |
| CN115178012A (en) * | 2022-07-12 | 2022-10-14 | 吉水县金海天然香料油科技有限公司 | Tea oil processing equipment for cosmetics and refining process thereof |
| CN116333820A (en) * | 2023-03-15 | 2023-06-27 | 烟台新时代健康产业有限公司 | Method for extracting pollen Pini essential oil from pollen Pini without solvent |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101717691A (en) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | Method for refining cosmetic camellia oil by adopting short-path distillation |
| CN101717690A (en) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | Method for refining camellia oil by adopting short-path distillation |
| CN103113987A (en) * | 2013-03-06 | 2013-05-22 | 曹庸 | Method for removing free fatty acid in tea oil by molecular distillation |
| CN103952237A (en) * | 2014-03-18 | 2014-07-30 | 南宁圣特生物科技有限公司 | Preparation method of camellia seed essential oil |
| CN105462680A (en) * | 2015-12-30 | 2016-04-06 | 德化县祥山大果油茶有限公司 | Camellia oil cold pressing and molecular distillation device and oil preparation method |
-
2017
- 2017-01-17 CN CN201710041086.6A patent/CN106635412B/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101717691A (en) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | Method for refining cosmetic camellia oil by adopting short-path distillation |
| CN101717690A (en) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | Method for refining camellia oil by adopting short-path distillation |
| CN103113987A (en) * | 2013-03-06 | 2013-05-22 | 曹庸 | Method for removing free fatty acid in tea oil by molecular distillation |
| CN103952237A (en) * | 2014-03-18 | 2014-07-30 | 南宁圣特生物科技有限公司 | Preparation method of camellia seed essential oil |
| CN105462680A (en) * | 2015-12-30 | 2016-04-06 | 德化县祥山大果油茶有限公司 | Camellia oil cold pressing and molecular distillation device and oil preparation method |
Non-Patent Citations (2)
| Title |
|---|
| 兰波,等,: ""分子蒸馏分提生产稻米油技术的研究"", 《农产品加工》 * |
| 姜邵通,等: ""稻米油分子蒸馏脱酸工艺优化"", 《食品科学》 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108219955A (en) * | 2018-01-24 | 2018-06-29 | 广西壮族自治区农业科学院 | A kind of preparation method and application of hemp essential oil |
| CN108219955B (en) * | 2018-01-24 | 2021-08-20 | 广西壮族自治区农业科学院 | A kind of preparation method and application of hemp essential oil |
| CN115178012A (en) * | 2022-07-12 | 2022-10-14 | 吉水县金海天然香料油科技有限公司 | Tea oil processing equipment for cosmetics and refining process thereof |
| CN115178012B (en) * | 2022-07-12 | 2024-05-03 | 吉水县金海天然香料油科技有限公司 | Tea oil processing equipment for cosmetics and refining technology thereof |
| CN116333820A (en) * | 2023-03-15 | 2023-06-27 | 烟台新时代健康产业有限公司 | Method for extracting pollen Pini essential oil from pollen Pini without solvent |
Also Published As
| Publication number | Publication date |
|---|---|
| CN106635412B (en) | 2020-11-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101194713B (en) | Method for processing edible camellia oil | |
| CN101880596A (en) | A method for low temperature preparation of oil | |
| CN102766524B (en) | Method for squeezing edible tea seed oil at normal temperature | |
| CN105175266B (en) | One kind chlorogenic acid extracting and caffeinic method from coffee bean | |
| CN111000760B (en) | Method for preparing cosmetic base oil by using peony essential oil and seed oil | |
| CN103739741B (en) | A kind of method extracting pectin from fermentation haw thorn wine pomace | |
| WO2002012159A1 (en) | Process for producing oleanolic acid and/or maslinic acid | |
| CN107858202A (en) | Selenium-rich tea oil and its processing technology | |
| CN102675398B (en) | A kind of method extracting momordica grosvenori glycoside V and farnesol from Grosvenor Momordica | |
| CN106635412B (en) | Oil processing and separating method and application thereof | |
| UA128432C2 (en) | METHOD OF OBTAINING OILS AND DECREASED MEAL BY SOLID/LIQUID EXTRACTION | |
| US20100040758A1 (en) | Integrated production of phytochemical rich plant products or isolates from green vegetation | |
| CN102613639B (en) | Apple processing method based on separation before squeezing | |
| CN110484351A (en) | A kind of physical refining process of original flavor camellia oil | |
| CN111393400B (en) | Method for preparing squalene, vitamin E and sterol from fructus momordicae seed kernels | |
| CN105132138A (en) | Processing technology for camellia seeds | |
| CN103082027A (en) | Advanced woody blend oil and production process thereof | |
| CN101628857B (en) | Production technique for extracting resveratrol from giant knotweed | |
| CN108659954A (en) | A kind of production method of tea seeds refined oil | |
| CN105832579B (en) | The floral wax that is extracted from sunset abelmoschus flower pharmacy procedure by-product, honey, flavones position and its preparation method and application | |
| CN104086467A (en) | Method for preparing sulforaphene by adopting solvent extraction method and molecular distillation method | |
| CN102199487A (en) | Method for producing virgin cold pressed Trichosanthes kirilowii Maxim seed oil | |
| CN105802723B (en) | A kind of preparation method of strong fragrance camellia seed oil | |
| CN113913029A (en) | Method for preparing effective components of gardenia jasminoides | |
| WO2018117158A1 (en) | Palm oil having reduced saturated hydrocarbon content |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |