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4HPDC对胡萝卜汁品质的作用Effect of high pressure carbon dioxide on the quality of carrot juice.

4HPDC对胡萝卜汁品质的作用Effect of high pressure carbon dioxide on the quality of carrot juice.
4HPDC对胡萝卜汁品质的作用Effect of high pressure carbon dioxide on the quality of carrot juice.

Effect of high pressure carbon dioxide on the quality of carrot juice

Linyan Zhou 1,Yuanyuan Wang 1,Xiaosong Hu,Jihong Wu,Xiaojun Liao ?

College of Food Science and Nutritional Engineering,China Agricultural University,China Key Lab of Fruit and Vegetable Processing,Ministry of Agriculture,China

Engineering Research Centre for Fruit and Vegetable Processing,Ministry of Education,Beijing 100083,China

a b s t r a c t

a r t i c l e i n f o Article history:

Received 10July 2008Accepted 11January 2009Keywords:

High pressure carbon dioxide Carrot juice Color Cloud

Particle size distribution

The effect of high pressure carbon dioxide (HPCD)on the quality of carrot juice was investigated.The L -value of HPCD-treated juices increased signi ?cantly (P b 0.05)as compared to untreated juices,and the a -value exhibited an increase tendency with increasing the treatment time.However,the b -value of HPCD-treated juices did not change.The browning degree (BD)and pH of HPCD-treated juices decreased,the cloud and titratable acidity (TA)increased signi ?cantly,the UV –visible spectra of juices were lower,but the total soluble solid (TSS)and the carotenoids of juices were stable.The particle size of juices treated by HPCD for 15,30and 45min increased signi ?cantly (P b 0.05),for 60min showed a noticeable decrease and was almost close to untreated juice.HPCD treatment could not alter the Newtonian ?ow behavior of the carrot juice,but caused a signi ?cant increase in juice viscosity (P b 0.05).

Industrial relevance:Carrot juice is one of the most popular vegetable juices,but it requires severe heat treatment for protection from spoilage due to a higher pH,its heat-sensitive quality is inevitably destructed.In this study,HPCD can avoid the drawbacks of the heat treatment as a novel non-thermal pasteurization,available data are provided for the application and evaluation of HPCD in the juice industry.

?2009Elsevier Ltd.All rights reserved.

1.Introduction

Carrot juice is one of the most popular vegetable juices (Marx,Stuparic,Schieber,&Carle,2003),and it is preferably used as a natural source of provitamin A in the carotenoid drinks (Yoon,Cha,Shin,&Kim,2005).In many countries,a steady increase of carrot juice consumption has been reported.From 1995to 1999,German carrot juice production increased by 69%(Schieber,Stintzing,&Carle,2001).The consumption of carrot juice is increasing very fast in China (Wang et al.,2006).Since carrot juice is a low-acid food of approximately pH 6.0,it has a higher risk of bacterial contamination than other acidic foods (Park,Lee,&Park,2002).Hence,it requires severe heat treatment (105to 121°C)for protection from spoilage (Kim &Gerber,1988;Chen,Peng,&Chen,1995).However,thermal energy inevitably leads to destruction of heat-sensitive nutrients,texture,color,and ?avor (Kim &Gerber,1988).

High pressure carbon dioxide (HPCD)is a novel non-thermal technology for pasteurization or sterilization.Many investigations have shown that this technology can effectively inactivate micro-organisms (Corwin &Shellhammer,2002;Liao,Hu,Chen,Wu,&Liao,2007)and enzymes (Truong,Boff,Min,&Shellhammer,2002;Kincal et al.,2006).However,there have been relatively few studies,which monitor the physical,chemical and sensory quality of liquid foods following HPCD treatment (Garcia-Gonzalez et al.,2007).Damar and

Balaban (2006)described that HPCD retained the fresh-like sensory,nutritional,and physical properties of many liquid foods by avoiding thermal effects of traditional pasteurization.Studies with orange juice showed that HPCD treatment could improve some physical and nutritional quality attributes such as cloud formation and stability,color,and ascorbic acid retention (Arreola et al.,1991;Kincal,2000;Kincal et al.,2006).Dagan and Balaban (2006)observed that aroma and ?avor of HPCD-treated beer was not signi ?cantly different from fresh beer,but beer haze was signi ?cantly reduced by HPCD.Yagiz,Lim,and Balaban (2005)reported that HPCD enhanced cloud up to 38.4%,increased lightness and yellowness,and decreased redness of mandarin juice.Damar and Balaban (2005)concluded that overall likeability of HPCD-treated coconut water was not signi ?cantly different from fresh control,whereas heat-pasteurized samples were rated signi ?cantly lower.Park et al.(2002)studied the carrot juice using a combination of 4.9MPa HPCD and 600MPa ultra-high pressure.However,the effect of HPCD alone at higher pressures on the quality of carrot juice was not evaluated until today.

Recently,the industrial application of HPCD was developed by Praxair Inc.(Burr Bidge,IL,US).Based on the technology licensed from the University of Florida (Balaban,Marshall,&Wicker,1995;Balaban,2004),Praxair developed a continuous system which uses HPCD process as a non-thermal alternative to thermal pasteurization (Connery,Shah,Coleman,&Hunek,2005).This system has been commercialized under the Trade Mark “Better Than Fresh (BTF)”.Praxair has constructed four mobile BTF units for processing about 1.5L per minute of juice for demonstration purposes (Connery et al.,2005).

Innovative Food Science and Emerging Technologies 10(2009)321–327

?Corresponding author.Tel.:+861062737434602;fax:+861062737434604.E-mail address:liaoxjun@https://www.doczj.com/doc/151952710.html, (X.Liao).1

Were equally the ?rst

authors.

1466-8564/$–see front matter ?2009Elsevier Ltd.All rights reserved.doi:

10.1016/j.ifset.2009.01.002

Contents lists available at ScienceDirect

Innovative Food Science and Emerging Technologies

j o u r n a l h o me p a g e :w w w.e l sev i e r.c om /l o c a t e /i fs e t

This work aimed to evaluate the effect of HPCD on the quality of carrot juice,the quality indices included color,pH,TA,TSS,carotenoid, cloud,particle size distribution(PSD)and?ow behavior.

2.Materials and methods

2.1.Preparation of carrot juice

The carrot de?ned as No.1Orange-red variety grew in Beijing Vegetable Experimental Station of the Chinese Academy of Agriculture Science in2006autumn season.After harvesting,the fresh carrot was transported to the laboratory by truck at about20°C,and stored in woven polypropylene bags(75g/m2)in batches of approximately15kg each.Storage temperature was0±1°C and the relative humidity was 85–95%.The storage time was less than1month before processing.

The raw material carrot was randomly separated into3batches,and each batch of carrot was separately pressed into juice and was separate into6×3portions,each portion of juice was used as a replication.Fresh carrot was washed with tap water,and blemished carrots were discarded,then carrots of good quality were sliced into about2mm thick.The pressing of juice was?nished with ZHJ-308A1juice extractor (Fushan Ouke Electric Appliance Co.,China),and the ratio of carrot slices and de-ionized water(2000D de-ionized water machine, Changfeng Instrument Co.,Ltd,China)was1:0.5(w/w).4-fold cheesecloth was used for juice?ltration,and then the juice was centrifuged using Model TDL-5-A Centrifuge(Shanghai Yiheng Scienti?c and Technology Co.,Shanghai,China)at3000rpm for 5min at ambient temperature(approx.25°C).The resulting juice was treated by HPCD immediately or stored at4°C.

2.2.HPCD process system

The diagram of the HPCD system was described by Liao et al.(2007), as shown in Fig.1.The stainless steel pressure vessel with a volume of 850mL was designed to withstand a pressure of50MPa.The vessel temperature was maintained by a THYS-15thermostatic bath(Ningbo Tianheng Instrument Factory,Zhejiang,China).An XMTA-7512tem-perature controller(Yuyao Temperature Meter Factory,Zhejiang,China) was used to monitor the temperature with two thermocouples.One thermocouple was?xed in the vessel lid to monitor the CO2temperature in the upper part of the vessel and the other was placed at the middle wall of the vessel to monitor the temperature of carrot juice in the vessel. A2TD plunger pump(Huaan Supercritical Fluids Extraction Co.Ltd., Jiangsu,China)with a maximum pressure of50MPa and a maximum ?ow rate50l/h was used to pressurize the vessel.A DBY-300pressure transducer(Shanxi Qingming Electronic Group Corporation,Shanxi, China)was?xed in the vessel lid to monitor the vessel pressure.All the data of temperature and pressure were displayed on a control panel.All parts of the system exposed to high pressure were made of stainless steel.The vessel had gas-tight connections to the gas inlet and outlet, and the?uid sample inlet and outlet.The vessel lid could be sealed by screws during HPCD processing.A2XZ-4vacuum pump(Huangyan Qiujing Vacuum Pump Factory,Zhejiang,China)was connected to the vessel for evacuating the air in the vessel and building the vacuum state of the vessel.The carrot juice samples were drawn into the vessel by negative pressure in the vessel.A DL-CJ-1F biohazard containment unit (Donglian Electron Technology Co.,Ltd,Haerbin,China)was used for aseptic https://www.doczj.com/doc/151952710.html,mercially available CO2of99.5%purity was purchased from Beijing Jingcheng Co.(Beijing,China),and was passed through an active carbon?lter before entering the pressure vessel.

2.3.Processing of carrot juice using HPCD system

After being rinsed and sanitized,the pressure vessel was heated to the required temperature,and was evacuated.A200mL sample of carrot juice was drawn to the evacuated pressure vessel by opening the sample inlet valve.The sample inlet valve was then closed and the CO2inlet valve was opened.The vessel was pressurized by the plunger pump to the required pressure level,and the required pressure was held for the required treatment time.Then the depressurization was performed by opening the pressure relief valve at CO2outlet on the pressure vessel.The compression time was in the range of2.5–4min, the depressurization time between3and5min and the minimum temperature of the product immediately after treatment was about ?5°C due to Joule–Thomson cooling effect depending on applied pressures.Equilibration of the temperature was achieved rapidly due to the use of a thermostatic bath.After HPCD treatment,the treated samples were?lled into a sterile bottle through a sample outlet valve. The HPCD system was rinsed and washed three times with de-ionized water after processing of each sample.

To determine the effect of HPCD on the quality of carrot juice,the pressure was10,20,and30MPa,the treatment time was15,30,

45 Fig.1.Diagram of high pressure carbon dioxide processing equipment.1CO2cylinder;2CO2?lter;3Pressure gauge;4Cooling unit;5Plunger pump;6Pressure transducer; 7Biohazard clean safety facility for aseptic operation;8High pressure vessel;9Thermocouples;10Thermostatic bath;11Vacuum pump;12Displaying panel.

322L.Zhou et al./Innovative Food Science and Emerging Technologies10(2009)321–327

and60min,and the temperature was25°C.The parameters of pressure and time were selected based on Liao et al.(2007)study,and were effective in inactivating microbes.

2.4.Heat treatment of carrot juice

Carrot juice was placed in a stainless steel cup(80×100mm,wall thickness1.15mm)and heated to90°C at the centre of juice for1min in a water bath.The heated juice was immediately cooled to about15°C in ice water bath,and then stored at4°C for various measurements.

2.5.Measurements of quality indices

2.5.1.Determination of color

Color assessment was conducted at25°C,using a SC-80Color Difference Meter(Kangguang Co.,China)in the re?ectance mode. Hunter L-,a-,and b-value of juices was measured and the total color difference(ΔE)was calculated as:

ΔE=L?L0

eT2+a?a0

eT2+b?b0

eT2

h i1=2

where L—lightness of treated juice,L0—lightness of untreated juice,a—redness of treated juice,b—yellowness of treated juice,a0—redness of untreated juice,and b0—yellowness of untreated juice(Gui et al., 2006b).

2.5.2.Determination of browning degree(BD)

Juice BD was evaluated using a spectrophotometric method described by Roig,Bello,and Rivera(1999).Carrot juice was centrifuged with a TGL-16G-A refrigerated centrifuge(Anting apparatus Co.,Shanghai,China)at 10,000×g at4°C for20min,and then passed through a0.45μm cellulose nitrate membrane(Beijing Bomex Co.,Beijing,China).The BD value was determined by measuring A420(absorbance at420nm)using an UV-762 spectrophotometer(Lingguang,Shanghai,China)at ambient tempera-ture(25±1°C)with a1cm path length cell.

2.5.

3.Measurement of residual activity of polyphenol oxidase

The activity of polyphenol oxidase(PPO)was assayed by a spectro-photometric method(Sánchez-Ferrer,Bru,Cabanes,&Garcia-Carmona, 1988)with some modi?cations.Catechol was chosen as the substrate, and0.1M catechol substrate solution was prepared with0.1M phosphate buffer(pH6.5).The assay was performed for all samples by adding 100μL juice into2.9mL substrate solution.The increase in absorbance at 420nm was monitored at intervals of0.1s?1immediately after incubation with a Cary50spectrophotometer(Varian Co.Ltd.,California, USA),which was equipped with a peltier thermostatted cell holder,a water pump(Varian Co.Ltd.,California,USA)to keep temperature at 20±0.1°C and an inbuilt electromagnetic stirring to mix up the substrate and juice.Prior to measurement,a pre-equilibrium at20°C of the substrate solution as well as the peach juice by the peltier thermostatted cell holder is obtained.The slope of the very?rst linear part of the reaction curve was taken as the PPO speci?c activity(Abs/min).The PPO residual activity was estimated with the following equation.

Residual activity=

specific activity of PPO after treatment specific activity of PPO before treatment

×100k:

2.5.4.Determination of UV–visible spectroscopy

Carrot juice was centrifuged with a TGL-16G-A refrigeration centrifuge(Anting apparatus Co.,Shanghai,China)at10,000×g at 4°C for20min,and then the supernatant passed through a0.45μm cellulose nitrate membrane(Beijing Bomex Co.,Beijing,China).The supernatant was scanned from200to800nm,using a Cary-50UV–visible spectrophotometer(Varian Co.,Palo Alto,USA)at ambient temperature(25±1°C)with a1cm path length cell.2.5.5.Determination of pH

pH was measured at20°C with a Thermo Orion868pH meter (Thermo Fisher Scienti?c,Inc.,MA,U.S.A),which was calibrated with pH4.0and7.0buffer.

2.5.6.Determination of titratable acidity(TA)

10mL juice was titrated using standardized0.02mol/L NaOH to the phenolphthalein end point(pH=8.2±0.1).The volume of NaOH was converted to mg citric acid per L juice(Rodrigo et al.,2003). 2.5.7.Determination of total soluble solid(TSS)

Juice TSS was determined as Brix using a WAY-2S digital Abbe Refractionmeter(Shanghai Precision and Scienti?c Instrument Co., Shanghai,China)at20°C(Wang et al.,2006).

2.5.8.Determination of carotenoids

The measurement of carotenoids was proposed by Liao et al. (2007)with a little modi?cation,which was determined by measur-ing the A450(absorbance at450nm)at ambient temperature by a spectrophotometer(UV-762,Lingguang,Shanghai,China).2mL of carrot juice was mixed with10mL chloroform/methanol of analytical grade(2:1,V/V)in a separator funnel.After shaking,the organic phase separating from the aqueous phase was dehydrated with anhydrous sodium sulfate,?ltered using Bush funnel and then collected.The aqueous phase was repeatedly extracted with5mL chloroform/ methanol(2:1,V/V)until it was colorless.All the extracts collected were mixed and diluted to a?nal50mL with chloroform/methanol (2:1,V/V).

2.5.9.Determination of cloud

The cloud of carrot juice was determined using a portable WGZ-200turbidimeter(Shanke apparatus Co.,Shanghai,China),and was reported as Nephelometric Turbidity Units(NTU)(Reiter,Stuparic, Neidhart,&Carle,2003).Carrot juice was diluted with distilled water (1:25,V/V)and measured in a5cm cuvette.

2.5.10.Determination of particle size distribution(PSD)

PSD of juice was determined by a LS230particle size analyzer (Beckman coulter,Inc.,Florida,U.S.A).The system used a laser light with a wavelength of750nm to measure particles from0.4to 2000μm by light diffraction.Fourier optics collected the diffracted light and the PSD was calculated by Fraunhofer model.

Firstly,distilled water from a tank was pumped into a sample cell at the speed of approximately8L/min until the cell was full.The juice was added into the cell using a pipette and mixed with distilled water. Particles in juice were dispersed and suspended in distilled water. When the obscuration percentage increased from0to10%,the measurement was performed.Data obtained were analyzed using software LS v3.29.Volume mean diameter D[4,3]and surface mean diameter D[3,2]were determined for all samples.

2.5.11.Determination of viscosity

The dynamic viscosity of carrot juice was determined using an AR550 rheometer(TA Instruments,Waters Co.,Ltd.,Surrey,Great Britain)with a Conical End Concentric Cylinder(stator radius=15.00mm,rotor radius=14.00mm,immersed height=42.00mm,gap=5920μm).

19.6mL juice was applied at each measurement with25±0.1°C controlled by circulating water in a thermostatic system.Viscosities were calculated from the average of seven points of the?ow curves obtained in the shear rate range between4and63s?1.

2.6.Statistical analysis

Analysis of variance(ANOVA)was carried out by using the software Microcal Origin7.5(Microcal Software,Inc.,Northampton,U.S.A). ANOVA test was carried out for all experimental runs to determine

323

L.Zhou et al./Innovative Food Science and Emerging Technologies10(2009)321–327

signi ?cance at α=0.05level.All experiments were performed in triplicates.

3.Results and discussion 3.1.Effect on juice color

The effect of HPCD and heat treatment on juice color was shown in Table 1.As compared with untreated and HPCD-treated juices,the value of L ,a ,and b for heated juice decreased signi ?cantly (P b 0.05).The decrease in L of heated juice re ?ected the darkening of juice surface color,and the decrease in a and b indicated less red and less yellow in juice color,which was possibly due to the susceptibility of juice particles to the coagulation and precipitation after exposure to heat.A noticeable difference can be visualized between two colors when they differ by ΔE N 2–3.5(Krapfenbauer,Kinner,Gossinger,Schonlechner,&Berghofer,2006).The ΔE values of all heated juices were greater than 2,indicating that heating resulted in a visible color difference.

The L -value of HPCD-treated juices increased signi ?cantly (P b 0.05)as compared with that of untreated juices,and the a -value exhibited an increase tendency with increasing the treatment time (Table 1).Park et al.(2002)reported that HPCD alone showed a signi ?cant increase of the L -value of carrot juice.Kincal et al.(2006)also reported a signi ?cant increase of the L -value of HPCD-treated orange juice.In contrast,Park et al.(2002)and Kincal et al.(2006)reported that HPCD resulted in a signi ?cant decrease in the a -value of carrot juice and orange juice.For the b -value,it exhibited no signi ?cant change (P N 0.05)after HPCD treatment in this study,which was in agreement with the observation displayed by Kincal et al.(2006).However,Park et al.(2002)reported that HPCD at 4.9MPa raised signi ?cantly the b -value of carrot juice.The ΔE values of the juices treated at 10MPa for 45and 60min,at 20or 30MPa for 60min were greater than 2,suggesting that longer treatment time of HPCD leads to a visible color difference of juice.

3.2.Effect on juice BD,PPO residual activity and UV –visible spectra As shown in Table 1,the BD value of HPCD-or heat-treated juices decreased signi ?cantly (P b 0.05)as compared to untreated juices.This difference possibly resulted from the enzymatic browning in juices.As shown in Fig.2,PPO in untreated juice was active and catalyzed the

browning reaction.However,the residual activity of PPO for HPCD-treated juices was 2–3%independent of pressure and could not be detected for heat-treated juices,indicating that PPO in carrot juices was inactivated after heat or HPCD-treatment.Similar observations were previously reported.Kim,Park,Cho,and Park (2001)investi-gated that thermal treatment of carrot juices caused 98.3%loss of PPO.Kincal et al.(2006)suggested that a reduction of PPO activity was 89%using HPCD.Park et al.(2002)reported that a combined treatment of HPCD and 400MPa high hydrostatic pressure showed a residual PPO activity of 19%.Although the BD values of HPCD-or heat-treated juices showed ?uctuation,there was no signi ?cant difference (P N 0.05).

Furthermore,the UV –visible absorbance spectra of all the juices at different conditions were measured.Fig.3shows the spectral curves of HPCD-treated juices at 10MPa as a function of treatment time.Since the spectral curves of HPCD-treated juices at 20or 30MPa were similar,related data are not shown.Obviously,the spectral curve of untreated juice was higher than those of HPCD-or heat-treated juices,and the curves of HPCD-or heat-treated juices almost superposed.These observations also con ?rmed that HPCD and heat treatment effectively inhibited the enzymatic browning in juices.

Table 1

Characteristics of carrot juices treated by different HPCD treatment conditions.Treatment conditions Color BD

pH TA

(mg/L)TSS (Brix)Carotenoids (mg/100mL)Cloud (NTU)Viscosity (mPa s)D [4,3](μm)D [3,2](μm)L a b ΔE Untreated

A

24.01c

11.39b

22.58a

0.000.644a 6.74a 0.38b 4.30a 5.27a 72.5c 1.23c 3.38d 1.44d 10Mpa,15min 24.51c 11.21b 22.78a 1.070.348b 5.95b 1.09a 4.30a 5.27a 80.0bc 1.20c 22.12b 5.56b 10MPa,30min 24.73b c 11.51b 23.39a 1.420.359b 5.95b 1.06a 4.30a 5.34a 83.5bc 1.20c 17.30c 3.07c 10MPa,45min 25.44b 12.20b 23.28a 2.080.357b 5.94b 1.04a 4.30a 5.57a 91.0b 1.24c 16.42c 3.18d 10MPa,60min 26.70a 14.20a 22.72a 4.000.306b 5.93b 1.12a 4.35a 5.62a 115.5a 1.27b 6.50d 1.87d Heat treatment 22.65d 11.13c 20.25b 2.750.328b 6.69a 0.37b 4.30a 5.13a 67.0d 1.51a 57.43a 21.87a Untreated B

24.65c 11.09c 24.14a 0.000.779a 6.55a 0.50b 4.60a 5.18a 65.0c 1.30c 3.63d 1.48d 20MPa,15min 25.49b 12.12ab 24.82a 1.610.272b 6.02b 0.99a 4.50a 5.22a 76.5b 1.24c 15.75b 3.07b 20MPa,30min 25.39b 11.93b 23.96a 1.200.258b 5.99b 1.04a 4.50a 5.19a 79.5b 1.23c 13.60bc 2.69c 20MPa,45min 25.37b 12.25ab 24.38a 1.580.278b 6.00b 0.97a 4.50a 5.22a 82.0ab 1.24c 12.71c 2.84c 20MPa,60min 26.11a 12.91a 24.64a 2.460.247b 6.09b 0.91a 4.55a 5.15a 94.0a 1.33b 3.79d 1.57d Heat treatment 22.30d 10.68d 19.09b 5.590.242b 6.54a 0.48b 4.60a 5.25a 38.5d 1.37a 73.32a 27.12a Untreated C

25.14c 11.63c 23.96a 0.000.461a 6.63a 0.46b 5.10a 5.99a 71.5c 1.22c 2.85d 1.44d 30MPa,15min 25.83b 11.95bc 23.93a 0.790.208b 6.18b 0.84a 5.05a 6.21a 77.0bc 1.26c 17.49b 3.95b 30MPa,30min 25.86b 12.12ab 23.60a 0.950.207b 6.21b 0.83a 5.05a 5.94a 80.5bc 1.38b 10.71c 2.90c 30MPa,45min 26.27b 12.84ab 23.50a 1.720.205b 6.20b 0.82a 5.05a 5.79a 83.5b 1.46b 10.47c 3.10c 30MPa,60min 26.97a 13.01a 23.68a 2.310.228b 6.15b 0.97a 5.00a 5.69a 90.0a 1.39b 3.16d 1.57d Heat treatment

24.32d

11.43d

21.66b

2.48

0.209b

6.57a

0.48b

4.95a

5.52a

54.5d

1.46a

50.54a

18.22a

Values are means,n =3;TA,titratable acidity;TSS,total soluble solid.A,B,C

represent the ?rst,second and third batch of carrot juice,respectively.a,b,c,d

different letters represent a signi ?cant difference within the same column (P b

0.05).

Fig.2.The residual activity of PPO in untreat juice and HPCD-treated carrot juices at different pressures for 15min at 25°C.

324L.Zhou et al./Innovative Food Science and Emerging Technologies 10(2009)321–327

3.3.Effect on juice TSS,carotenoids,pH and TA

The heat treatment caused no signi ?cant alteration in TSS,carot-enoids,pH and TA of juice (P N 0.05).However,HPCD had a different in ?uence on these indices of juices (Table 1).The pH of the juices decreased and its TA increased signi ?cantly (P b 0.05)after HPCD treatment.Park et al.(2002)observed a similar decrease of pH from 6.5to 4.4in juices after HPCD treatment.Gui,(2006a)also reported a pH reduction from 5.6to 5.3in horseradish peroxide solution.The decrease pH and increase in TA was due to CO 2dissolution into juices or solutions,which further dissociated into bicarbonate,carbonate and hydrogen ions.However,Kincal et al.(2006)found an increase in TA and no alteration in pH of HPCD-treated orange juice.This was attributed to a lower pH (3.7–3.8)in original orange juice,at this pH the carbonic acid formed by CO 2dissolution into juice dif ?cultly dissociated into free hydrogen ions,because the dissociation constants of carbonic acid and bicarbonate were pKa=6.57and pKa=10.62(Damar &Balaban,2006),respectively.The TSS and carotenoids of juices showed ?uctuations,but did not change signi ?cantly after HPCD treatment.

3.4.Effect on juice cloud

Cloud stability is an important quality parameter in fresh un-pasteurized juice (Park et al.,2002).As shown in Table 1,the cloud of heated juices decreased.The larger particles of protein coagulation induced by heat rapidly precipitated and caused the loss of juice cloudiness.Blanching of carrots was a practice to inactivate pectin-esterase (PE)or pectin methyl-esterase (PME)to maintain the cloud stability of carrot juice prior to pressing.However,the cloud of HPCD-treated juices increased signi ?cantly (P b 0.05),it was hypothesized that HPCD led to the homogenization effect causing smaller particles of the juice colloid (Kincal et al.,2006).This observation was in agreement with previous investigations.Arreola et al.(1991)reported that HPCD treatment of orange juice stabilized and enhanced cloud,even in the presence of active PE.Kincal et al.(2006)investigated that the cloud for the HPCD-treated juice increased in spite of active PE.It was well known that the cloud of citrus juice is related to the activity of PE,which could lead to precipitation of pectin in juice with subsequent loss of cloud.Therefore,no link was found between PE inactivation and cloud retention in juice with HPCD (Kincal et al.,2006).

The increase in the cloud of HPCD-treated carrot juice was incon-sistent with the observation obtained by Park et al.(2002),who

reported that HPCD caused a loss of carrot juice cloud in a non-enzymatic way.This contradiction was possibly due to a larger difference in parameters of HPCD.In this study,the pressure (≥10MPa)and

the

Fig.3.The UV –visible spectra of carrot juice exposed to HPCD at 10MPa and 25°C for 15,30,45and 60min and heat

treatment.

Fig.4.The cumulative volume (%)against PSD of carrot juice with HPCD a)at 10MPa and 25°C;b)at 20MPa and 25°C;c)at 30MPa and 25°C.○Untreated;■15min;?

30min;△45min;?60

min;he

time (≥15min)were far greater than that (4.9MPa and 10min)in Park et al.(2002)study,the HPCD-induced homogenization effect was more intensive than the acid-induced coagulation and precipita-tion of HPCD.

It was dif ?cult to evaluate the cloud of HPCD-treated juices at 10,20and 30MPa for the same treatment time due to different batches of carrot juice in this study.However,it was comparable for those juices treated by the same pressure level due to the same batch juices.At the same pressure level,the juice cloud increased signi ?cantly (P b 0.05)with increasing the treatment time,indicating that the longer the treatment time was,the more intensive the HPCD-induced homo-genization effect was.3.5.Effect on juice PSD

Fig.4a –c showed the change in PSD against the cumulative volume of juices at different conditions.Obviously,the particle size of heat-treated juice signi ?cantly increased as compared with that of untreated juice at the same cumulative volume (P b 0.05).D [4,3]and D [3,2]for heated juices was maximized and for untreated juices was minimized (Table 1),this was possibly attributed to heat-induced protein coagulation.Reiter et al.(2003)reported that heat-coagulated proteins were supposed to cause cloud particle precipitation following thermal treatment of juices extracted from unblanched carrots.

The particle size of HPCD-treated juices for 15,30and 45min increased signi ?cantly as compared with untreated juices (P b 0.05)(Fig.4a –c).However,for the 60min treatment,it showed a noticeable decrease and was almost close to untreated juice.The HPCD-induced increase of juice particle size was possibly due to acid-induced protein coagulation.Precipitation caused by pH shift was characteristic of proteins (Reiter et al.,2003).As previously suggested in this study,pH decline of HPCD-treated juices was due to the dissociation of carbonic acid formed by CO 2dissolution into the juices.The decrease in particle size of HPCD-treated juices for 60min was probably attributed to HPCD-induced homogenization effect which caused smaller juice particle (Kincal et al.,2006).The longer the treatment time or the higher the pressure was,the more intensive the homogenization effect was.Therefore,the alteration of the particle size for HPCD-treated juices was an interaction between the acid-induced protein coagulation and the HPCD-induced homogenization effect,the acid-induced protein coagulation seemed to dominate for a short treatment time and the HPCD-induced homogenization effect alter-nated for longer treatment time.

3.6.Effect on juice ?ow behavior and viscosity

Fig.5showed the viscosity of HPCD-treated juices at 10MPa as a function of shear rate.The viscosity of all the juices at different conditions showed no signi ?cant alteration in the shear rate range between 4and 63s ?1(P N 0.05,)suggesting that the juices followed the Newtonian ?ow behavior.This result was similar to what Reiter et al.(2003)proposed,indicating that HPCD or heat treatment didn't change the ?ow behavior of the carrot juice.Since the viscosity of HPCD-treated juices at 20or 30MPa exhibited similar trends,related data were not shown.

However,the viscosity of heat-treated juice was signi ?cantly higher than that of untreated juice (P b 0.05),which could be attributed to an increase in solubilization of pectin in cell walls.With HPCD at 10MPa for 30,45and 60min,or at 20MPa for 60min,or at 30MPa for 15,30,45and 60min,the viscosity of juices also increased signi ?cantly (P b 0.05,Table 1),indicating that pressure or time had a signi ?cant in ?uence on juice viscosity.The HPCD-induced homogenization effect under these conditions possibly contributed to an increase in solu-bilization of pectin in cell walls into juices.4.Conclusions

The browning degree and pH of HPCD-treated carrot juices decreased,the cloud and the titratable acidity increased signi ?cantly (P b 0.05),the UV –visible spectra lowed,polyphenol oxidase was inactivated,and the total soluble solid and carotenoids were stable.As compared with untreated juices,the particle size of HPCD-treated juices for 15,30and 45min increased signi ?cantly (P b 0.05)in a similar way and showed a noticeable decrease for the 60min treatment getting close to that of untreated juice.HPCD could not alter the Newtonian ?ow behavior of the carrot juice,but caused a signi ?cant increase in carrot juice viscosity.Acknowledgments

This research work was supported by Project No.20060019016of Doctoral Foundation of Ministry of Education and Project No.2006BAD05A02of the Science and Technology Support in the Eleventh Five Plan of China.References

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胡萝卜橙子汁的功效 很多人都喜欢买个榨汁机,自己在家里榨果汁或者蔬菜汁喝,因为榨出来的果汁和蔬菜汁不仅可以当水喝,而且自身有丰富的营养价值。胡萝卜这种蔬菜具有丰富的维生素,对于预防夜盲症有着很好的效果,橙子也是大家家中常见的一种水果,它里面也含有丰富的维生素,那么使用胡萝卜和橙子一起榨汁的功效是什么呢? 橙子能和胡萝卜一起榨汁吗 当然是可以的呀。不但好喝,两者混着的营养价值非常高的,建议每天喝一杯对身体健康很有帮助。 橙子的功效作用 1、和胃降逆,橙子味酸,性寒凉,入肝、胃经。有和中开胃,降逆止呕之功。善用于饮食停滞而引起的呕吐,胃中浮风恶气,肝胃郁热等疾病。 2、宽胸开结,橙子性寒,有清热降逆之功、善清肺胸之热,由于肺中蕴热,或外感风热,热灼津液为痰,痰热结于胸中,气机痹阻,引起胸部疼痛,咳喘,咯痰黄稠,甚则咳血,或痰腥臭,烦闷发热,苔黄腻,脉象滑数,治宜用橙子,泄热涤痰,宽胸开结,凉血止血,功效显著。 3、消瘿,因外邪所侵,或情志内伤,以及体质虚弱,使气机阻滞,津液积聚为痰。 4、杀鱼蟹之毒,橙子味酸芳香,酸能杀菌,有除醒脾,和胃

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4.职责类:恪尽职守、尽职尽责、爱岗敬业、治学严谨、教学有方、诲人不倦、以校为家、爱厂如家、关心下属、秉公执法、不徇私情、勇于探索、锐意进取、敢于创新、技术精湛、才华横溢、博学善谈、以身殉职、奉公守法、铁面无私、赏罚分明、妙手回春、文武双全、智勇双全、博古通今、见多识广、明察秋毫、严以律己、临危不惧、 (反面:以权谋私、徇私枉法、畏首畏尾、墨守成规、贪生怕死) 5. 品质类:洁身自好、淡泊名利、安贫乐道、仁义守信、乐善好施、虚怀若谷、胸有大志、志存高远、心胸宽广、宽宏大量、豁达大度、坦荡无私、德艺双馨、诚实守信、有责任心、孝顺、清正廉洁、知恩图报、宠辱不惊、有修养、礼贤下士、宠辱不惊、言而有信、表里如一、言行一致、德才兼备、不耻下问、与世无争、不慕权贵、自知之明、知错就改、 (反面:爱慕虚荣、追名逐利、鼠肚鸡肠、投机取巧) 6.大爱类:热爱集体、爱国、没有民族偏见、居安思危、忍辱负重、关注民生、忧国忧民、精忠报国、壮志凌云、民族气节、舍生取义、浩然正气、无私无畏、勇于担当、深明大义、识见高远、顾大体识大局、有领导组织才干、尊重弱者、关爱他人、乐于助人、舍生取义、忠心耿耿、公而忘私、大义灭亲、嫉恶如仇、扶危济困、刚正不阿、远见卓识、 (反面:狭隘的爱国主义、有民族偏见、) 概括景、物特点常用词语:(外形、颜色、 神态、氛围) 素雅、灿烂、柔弱、清丽、俊美、柔婉美丽、美好可爱、乖巧可爱、惹人爱怜、优美、美妙、多彩、清新脱俗、生动活泼、妖娆、葱茏、郁郁葱葱、鲜妍明媚、袅娜多姿、生机勃勃、生命力旺盛、富有活力、辉煌、雄浑、壮美、旷远、恢弘博大、气势非凡、气势磅礴、宏伟壮丽、圣洁、广阔、雄壮、豪迈、强劲、刚

土豆胡萝卜苹果汁

自制土豆胡萝卜苹果汁 土豆胡萝卜苹果汁的疗效很神奇,他的舅舅有肺癌,但天天坚持喝土豆胡萝卜苹果汁,把病根都清除了。但是生土豆一定要精选没发芽的,表皮没发青的。因为发芽发青的土豆都有毒。我半信半疑他说的神奇疗效,但却对这种三合一蔬菜水果汁饶有兴趣。 购买了胡萝卜,生土豆,红苹果,另外还买了两根鲜玉米棒。先全部都洗净了,然后把一根玉米棒一粒一粒的剥下来盛在碗里,再把一根胡萝卜切成薄片,把马铃薯去皮后切成薄片,把苹果去核切成片,满满一大碗倒入豆浆机里,掺入一小杯纯净水把黏糊的“果煳”倒入过滤杯中,用附送的搅拌器搅拌压榨“果煳”,清香的液态果汁透过滤网坠流入杯底,不一会儿一大杯纯液态的果汁浮现在眼前。把榨干的果渣倒掉,把果汁重新倒入豆浆机中,再掺入一杯酸奶,两勺白糖,在启动“果汁/搅拌”功能,立刻一大杯土豆胡萝卜苹果汁新鲜“出炉”了。 色泽呈奶黄,轻摇杯体,一条乳白色的晕圈淡淡浮现,又慢慢消散开来。轻轻品一口,一种酸酸的,微甜又微苦,“胛”舌而耐人回味的复杂味道填满了口中。把吸管插入杯中,斜坐在书房窗台边的摇椅,脚搭在书桌上慢慢的品尝起来。客厅播放着音乐,窗外暖暖的阳光撒在身上,周末的早上难得的悠闲时刻呀。 上网查了一下,原来这生土豆胡萝卜和苹果榨汁是一个日本高僧的偏方,确实有许多的神奇疗效: 胡萝卜苹果汁 原料:4个胡萝卜,2个大的苹果 做法:将胡萝卜擦洗干净,保留其顶部的有机叶子。将苹果洗净。先将胡萝卜榨汁,然后再将苹果榨汁。混合、搅拌,并立即饮用。 功效:这是少数几种能混合的果蔬汁之一。 胡萝卜、苹果汁不但美味,而且是你能找到的最好的排毒剂和身体补充剂之一。这道混合汁还具有美容的作用,非常有益于皮肤。红苹果的味道很甜,因此如果在榨汁时你用的是红苹果,由于胡萝卜也很甜,这会使得榨出来的汁非常甜。所以,你也可以用青苹果来榨汁。β-胡萝卜素、叶酸、维生素C、钙、果胶、镁、钾、磷。维生素B1、维生素B2、维生素B3、维生素B6和维生素E、铜、铁、锌 胡萝卜苹果土豆汁:均衡营养,针对贫血 现代人尽管在饮食上可选择性大,却容易因缺乏必要的养分而导致营养失调。吃,并不等于平息空腹感。最重要的是要让身体获得必要的养分,早餐辟谷法里的胡萝卜苹果土豆汁,就是营养均衡的选择。人体所需的维生素、矿物质,胡萝卜苹果汁里几乎都有。胡萝卜被欧美自然疗法医师认为是可治百病的最佳药方,其中所含的矿物质具有强效净化力,所含胡萝卜素等的植化素可增强抵抗力。而苹果所含有的钙质具有利尿作用,能有效改善水肿。胡萝卜和苹果都是性温平的食物,饮用时最好兑入温水(无论天气冷暖),在温热的温度喝下,就不会有寒凉的感觉。土豆含有丰富的B族维生素和优质纤维素,在人体延缓衰老过程中有重要作用。土豆中含的优质蛋白首屈一指,即使是人体需要的其他营养素如碳水化合物、各种维生素、矿物质等,也都比米面更全面。同时,中医认为土豆能和胃调中、健脾益气,对治疗胃溃疡,习惯性便秘等疾病有裨益,还有解毒、消炎的作用。早上只喝生姜红枣茶就可以了,但肌肤干燥、有贫血现象的人,再搭配胡萝卜苹果土豆汁效果更好。 具体做法 材料:胡萝卜2根,苹果1个,土豆一个,柠檬汁少许。 做法:①挤入柠檬汁,柠檬具有防止氧化的效果。 ②洗净的胡萝卜、土豆和苹果连皮带籽直接切成适当大小放进果汁机榨汁。 ③杯上放滤茶器,将步骤2倒入杯里,搅拌均匀即可。

蜜薯的营养价值

蜜薯的营养价值 与普通的红薯不同,蜜薯是一种甜味更家的地瓜,而且蜜薯的营养价值也与普通的地瓜不同。蜜薯在补气和血方面的具有较大的作用,所以每天吃一些蜜薯可以让脸色看起来更加的红润,让人更显年轻。另外,蜜薯还有很好的提高免疫力的作用,可以起到预防感冒提高身体健康指数的作用。 蜜薯的功效与作用 1、补气和血:常吃蜜薯,皮肤会逐渐变得润泽,气色会变得红润。其补气血的作用可以跟大枣相提并论,且不容易生湿热。 2、提高免疫力:比一般蔬菜含有更多的抗氧化物,可以预防感冒、提高免疫力。 3、双向调节肠道功能:便秘的人可以常吃煮红薯来促进肠胃蠕动、润肠通便;而脾胃不好经常腹泻的人,可以吃烤红薯来缓解不适并加强肠道功能。 4、净化血液:蜜薯中丰富的叶绿素可以帮助排出毒素从而起到净化血液的功效。 5、预防高血压:蜜薯中含有丰富的钾,有助于控制血压。 6、改善更年期症状:通过蜜薯中含有的植固醇起到类似于荷尔蒙的调节身体机能的作用。 7、外用(消炎去毒):将生蜜薯捣碎敷在热毒疮的周围,不仅可以缓解疼痛,还能促进皮肤生长、加快伤口愈合。 蜜薯的营养价值

1、蜜薯中含有丰富的膳食纤维,有利于女性排毒养颜。蜜薯虽然味道甘甜,但热量很低,同等质量的蜜薯和大米,蜜薯的热量只有大米的1/3,低脂肪低热量使其成为健美人士、减肥人士的理想之选。 2、蜜薯所含的膳食纤维和粘液蛋白等成份也可以润滑关节、润肠通便、防癌的功效,是老少皆宜的食品。 3、蜜薯中富含β-胡萝卜素,β-胡萝卜素在人体内可以转化为维生素A,100g蜜薯含有125个单位的维生素A,可以有效预防维生素A缺乏症,并起到保护视力的作用。 4、蜜薯中含有较多的叶黄素。叶黄素有“植物黄体素”之称,能够预防心血管疾病以及衰老引起的多种退化性疾病。 这样看来,蜜薯中富含的各种营养物质对身体健康起着积极促进的作用,也带来了许多神奇的功效。大家可以适当地多吃一些蜜薯,让自己变得更加美丽又健康。

描述个人品质常用英语单词一览

able 有才干的,能干的 active 主动的,活跃的 adaptable 适应性强的 aggressive 有进取心的 alert 机灵的 ambitious 有雄心壮志的 amiable 和蔼可亲的 analytical 善于分析的 apprehensive 有理解力的 aspiring 有志气的,有抱负的 audacious 大胆的,有冒险精神的capable 有能力的,有才能的 careful 办理仔细的 candid 正直的 charitable 宽厚的 competent能胜任的 confident 有信心的 conscientious 认真的,自觉的considerate 体贴的 constructive 建设性的 contemplative 好沉思的 cooperative 有合作精神的 creative 富创造力的 dashing 有一股子冲动劲的,有拼搏精神的dedicated 有奉献精神的 devoted 有献身精神的 dependable 可靠的 diplomatic 老练的,有策略的 disciplined 守纪律的 discreet (在行动、说话等方面)谨慎的dutiful 尽职的 dynamic 精悍的 earnest 认真的 well-educated 受过良好教育的 efficient 有效率的 energetic 精力充沛的

enthusiastic 充满热情的expressivity 善于表达 faithful 守信的,忠诚的 forceful (性格)坚强的 frank直率的,真诚的 friendly 友好的 frugal 俭朴的 generous 宽宏大量 genteel有教养的 gentle 有礼貌的 hard-working 勤劳的 hearty 精神饱满的 honest 诚实的 hospitable 殷勤的humble 恭顺的humorous 有幽默i mpartial 公正的independent 有主见的industrious 勤奋的 ingenious 有独创性的 initiative 首创精神 have an inquiring mind爱动脑筋intellective 有智力的 intelligent 理解力强的 inventive有发明才能,有创造力的just 正直的 kind-hearted 好心的knowledgeable 有见识的 learned 精通某门学问的 liberal 心胸宽大的 logical 条理分明的 loyal 忠心耿耿的 methodical 有方法的 modest 谦虚的 motivated 目的明确的 objective 客观的 open-minded 虚心的 orderly 守纪律的

胡萝卜汁的加工工艺

胡萝卜汁的加工工艺 胡萝卜中含有丰富的胡萝卜素和大量的维生素及矿物质,因此作为营养价值很高的蔬菜被人们广泛的接受。胡萝卜汁是用新鲜的胡萝卜为原料,通过破碎取汁或打浆等工艺制得的产品,在风味和营养上十分接近于新鲜原料,所以它营养丰富,是良好的保健食品。 一、工艺流程 胡萝卜清洗→去皮→切分→热烫→打浆→酶反应→灭酶→榨汁→过滤→杀菌→冷却→灌装→清汁产品 二、操作要点 1、原料选择:用于制汁的胡萝卜一般选择脆嫩,味甜,含纤维素少,色彩艳丽的,剔除病虫害和腐烂者。 2、去皮:有化学去皮和人工去皮法。生产中一般采用碱液去皮法,碱液浓度为2%—4%,温度为70—95℃,煮制时间为1—3min。然后用清水冲洗干净,修整切片。 3、热烫:这一过程主要作用是钝化酶活性,防止酶褐变,软化原料组织,提高出汁率。预煮液中加人少量的柠檬酸、醋酸或维生素C以维持原料的色泽和稳定性。 4、酶处理:在果蔬汁生产中加入酶制剂,可以显著提高果蔬的出汁率及压榨性能。常用的有果胶酶、纤维素酶、半纤维素酶等。常用温度是在90℃作用,作用时5—10min。 5、调配:调配时主要考虑产品的风味和价格因素。常用的甜味剂有蔗糖、葡萄糖、麦芽糖醇、甜蜜素、甘草等,酸度调节剂有柠檬酸、

乳酸、苹果酸、酒石酸等。此外,还可适量加入食用香料、着色剂、防腐剂、抗氧化剂、增稠剂等。 6、均质,脱气:均质的目的是使胡萝卜中的悬浮颗粒进一步破碎细化,使果胶均匀的分布于汁液中,防止出现分层的现象。脱气可以减少或避免胡萝卜汁的氧化,减少其色泽和风味的破坏以及营养成分和维生素C的氧化。据报道,生产上目前多采用真空脱气机,温度控制在40—50℃,压力在0.008—0.01MPa之间,均质压力在20MPa左右,2—3min。 7、杀菌:杀菌的目的在于杀死致病菌和钝化酶的活性。包括冷杀菌和热力杀菌两种,热力杀菌主要采用高温短时杀菌(一般温度为95℃,时间为l5—20s)和超高温瞬时杀菌(杀菌温度为120—130 ℃,时间为3—6s)。

紫茉莉花语

紫茉莉花语 紫茉莉的俗名是胭脂花,也称野茉莉。其实紫茉莉的外型一点也不像茉莉,但有淡淡的茉莉香,而“野”字却当之无愧——因为随便丢几粒种子到土里,紫茉莉便生机勃勃地长出一大丛,并且年复一年扩大自己的领域。紫茉莉的花语是什么呢,它又有什么美丽的花语传说呢?一起来看看吧。 紫茉莉花语贞洁、质朴、玲珑、臆测、猜忌、成熟美、胆小、怯懦 什么是紫茉莉紫茉莉(学名:Mirabilis jalapa L.):草本,高可达1米。根肥粗,倒圆锥形,黑色或黑褐色。茎直立,圆柱形,多分枝,无毛或疏生细柔毛,节稍膨大。叶片卵形或卵状三角形,全缘,两面均无毛,脉隆起。花常数朵簇生枝端,总苞钟形,长约1厘米,5裂,裂片三角状卵形;花被紫红色、黄色、白色或杂色,高脚碟状,筒部长2-6厘米,檐部直径2.5-3厘米,5浅裂;花午后开放,有香气,次日午前凋萎。瘦果球形,直径5-8毫米,革质,黑色,表面具皱纹;种子胚乳白粉质。花期6-10月,果期8-11月。原产热带美洲。中国南北各地常栽培,为观赏花卉,有时逸为野生。根、叶可供药用,有清热解毒、活血调经和滋补的功效。种子白粉可去面部癍痣粉刺。 紫茉莉名字由来紫茉莉,又叫草茉莉、胭脂花、地雷花、粉豆花,是紫茉莉科、紫茉莉属的多年生草本花卉,因其花朵紫红,香如茉莉

而得名,是常见的观赏花卉。 紫茉莉因紫红色的花朵而得名,但它的花色丰富,常见的有红色、黄色、白色、杂色,夏季开花时,一株上密布着许多不同颜色的紫茉莉花朵,非常可爱美观。紫茉莉花朵娇艳,清香宜人,常被种植在花坛、路边做观赏用,也可制作成盆景放在家中观赏。 紫茉莉生长健壮,极易成活。而且有抗二氧化硫的特性,因此无论居民阳台或工矿污染区均可栽植。家庭养殖时,若能不时以洗肉鱼水、淘米水浇之,则花开更旺,花色愈艳。 胭脂花不仅幽香,其种子和叶尚有美容、清热和解毒的功效。种子成熟时,外观黑色如球形,内呈白色。美容时可采取成熟种子若干,研成粉末,去皮后取粉搽脸,可除面斑等,使面部光洁、白皙,收美容之功效。 另外,手面上生有水泡疮时,亦可取粉加水调匀抹于患处,收除湿解毒之功效。当皮肤创伤或行痈疮时,摘取胭脂花鲜叶数片,捣烂敷于创处患处即可。 紫茉莉形态特征紫茉莉是一年生草本植物,高可达1米。根肥粗,倒圆锥形,黑色或黑褐色。茎直立,圆柱形,多分枝,无毛或疏生细柔毛,节稍膨大。叶片卵形或卵状三角形,长3-15厘米,宽2-9厘米,顶端渐尖,基部截形或心形,全缘,两面均无毛,脉隆起;叶柄长1-4厘米,上部叶几无柄。花常数朵簇生枝端;花梗长1-2毫米;总苞钟形,长约1厘米,5裂,裂片三角状卵形,顶端渐尖,无毛,具脉纹,果时宿存;花被紫红色、黄色、白色或杂色,高脚碟状,筒部

实验六 胡萝卜汁饮料制造实验

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4结论与讨论 (10) 参考文献 (10) 致谢 (11)

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