Red rice was obtained from the Meili Lake Market in Jinan City, Shandong Province, China. Red rice was milled to coarse particles by a disc-mill, then, screened through different sized sieves to separate granulates (d < 1 mm ), the superfine powders with the size of 156.74, 69.53, 26.35 and 10.68 µm were obtained in an BL-32 type micronizer (Beili Powder Machinery Company, Jinan, Shandong, China). The particle size (D₉₀) was tested using a laser particle size instrument (Weina-16, Jinan , Shandong , China ). The particle size distributions of the powder were: D₉₀ = 156.74, 59.53, 21.35, and 10.68 μm. Three measurements were carried out for each red rice powder.

The bulk density (g/ml) was the density including pores and interparticle voids. Four types of red rice powders were filled in a 10 ml volumetric flask (W₁) up to the mark and were weighed (W₂) separately. The bulk density of the red rice powders was calculated as follows: d₀ = (W₂ − W₁)/10 [11] . Where W₂ was the total weight of the red rice powder and flask, and W₁ was the weight of the flask only. The experiments were repeated five times and the measurement of each sample was repeated three times.

The angle of repose was measured using the sequence of steps stated here [12] . Firstly, a filler was fixed above some graph paper so that the distance of the paper from the outlet of the filler (H) was 3 cm , and the filler was vertical to the paper. Then the red rice powder of different size was separately poured into the filler until the tip of the powder cone touched the outlet of the filler. The diameter (2R) of the cone was measured for each type powder. The angle of repose (θ) was calculated as the following formula: Θ = arctg(2R/H).

The slide angle was determined according to method of Ileleji and Zhou [13] with some slight modification. The 5.000 g of red rice samples were separately weighed. Then red rice powder was poured on glass plane with a length (L) of 130 mm and width of 100 mm . The sliding angle of repose was estimated by gradually lifting the glass plane until the surface of the red rice powder began to be slide. The angle between the inclined glass and horizontal was called the angle of slide. The vertical distance (H) between the top of inclined glass plane and the horizontal was measured. The angle of slide (α) was calculated as the following formula: α = arcsin(H/L).

The water solubility index (WSI) was determined according to the method of Zhao et al. [10] with some modifications. The 1.000 g of sample was measured and dispersed in tubers with 50 ml distilled water. The tubers were placed in a reciprocating water bath shaking instrument and shaken for 30 min at different temperatures of 60˚C, 80˚C, and 100˚C, respectively. Then, the tubers were centrifuged at 3000 r/min for 30 min, excess water of the clear supernatant solution was drained off by evaporation. Finally, the samples were dried at 105˚C and weight of red rice powder (A) dissolved in water with different temperatures could be obtained. The WSI was caculated as WSI(%) = A × 100%.

This parameter was determined according to the method reported by Wu et al. [14] with some modifications. Firstly, the weights of cleaned centrifuge tubes (M) and different sized samples (M₁) were measured. Then the samples (M₁) were dispersed in water (M₂) according to M₁:M₂ = 1:20 at 20˚C and poured into the centrifuge tubes placed in a water bath at 70˚C, 80˚C, and 90˚C, respectively. The tubes were held for 15 min separately and then they were placed in cold water for 30 min, followed by centrifugation for 20 min at 3000 r/min. The supernatant liquid was removed and the centrifuge tubes with the powders (M₃) were weighed again. The formula to calculate water holding capacity (WHC) was as follows: WHC(g/g) = (M₃ − M)/M_1.

Enzymatic digestibility with α-amylase was performed according to the method described by Liu et al. [15] . Approximately 1 g of sample was added to 30 ml of phosphate buffer (0.2 mol/l, pH 6.9) in a test tube and allowed to stand for 30 min in a 95˚C water bath. After cooling at 25˚C, α-amylase (320 unit, A6380, Sigma-Al- drich) was added and incubated with shaking at 30˚C for up to 14 h. After digestion, the undigested sample was removed by centrifugation and analyzed by gravimetric methods.

Scavenging activity of the extracts against DPPH (2, 2-diphenyl-1-picrylhydrazyl) radical was measured based on Wu et al. [14] . Positive control was prepared by mixing 2 ml of ascorbic acid (0.05 mg/ml) and 3 ml of DPPH (0.04 mg/ml), whereas negative control was prepared by mixing 2 ml of distilled water with 3 ml of DPPH. The 2 ml of the extract (final concentrations were 25, 50, 100, and 150 μg/ml, respectively) prepared from working solution was added to 3 ml of DPPH. The mixture was gently homogenized and left to stand at room temperature for 30 min. Absorbance was read using a spectrophotometer at a wavelength of 517 nm. Activity of scavenging DPPH radicals was calculated using the following equation: Scavenging activity (%) = [(A₍₋₎ − A_s)/(A₍₋₎ − A₍₊₎)] × 100, where, As is the absorbance of the sample, A₍₋₎ and A₍₊₎ are the absorbance values of negative and positive controls, respectively.

The reducing power of the extracts from different sized powder was determined by the method of Fu et al. [16] with minor modification. Different amounts of working solution (final concentrations were 200, 400, and 600 μg/ml, respectively) were mixed with 2.5 ml of phosphate buffer (0.2 mol/l, pH 6.6) and 2.5 ml of potassium ferricyanide [0.03 mol/l, K₃Fe(CN)₆]. Aliquots (2.5 ml) of 0.6 mol/l trichloroacetic acid were added to the mixture, which were then centrifuged for 10 min at 1000 × g (Hitachi SCR20BC, Japan ). The upper layer of solution (2.5 ml) was mixed with 2.5 ml of distilled water and 0.5 ml of 0.006 mol/l FeCl₃, and the absorbance was measured at a wavelength of 700 nm in a spectrophotometer.

Phenolic were extracted by the method of Jeng et al. [5] . The content of total phenolic in extract was estimated using the Folin-Ciocalteu assay [17] . The absorption value was determined at a wavelength of 735 nm with gallic acid used as standard.

The statistical analysis was carried out using SPSS 17.0 (SPSS Inc., Chicago , IL ). Results were expressed as mean values ± standard deviation. Means were compared by univariate variable analysis. A difference was considered statistically significant when P < 0.05.

Bulk densities of the red rice powders varied with their particle sizes (Table 1). The bulk density of the red rice was in the range of 0.624 g /ml - 0.745 g /ml, and the bulk density increased as the particle size decreased. The results confirmed the significant effect of the particle size on the bulk density (P < 0.05). The reason for this might be that, as particle size decreased, pore spaces between particles decreased resulting in the increase in the bulk density [18] .

The angle of repose and slide could reflect the variations in the fluidity of the powder. The angle of repose and slide values of red rice particles were showed in Table 1, which ranged from 74.67˚ (156.74 µm) to 61.41˚ (10.68 µm) and 38.99˚ (156.74 µm) to 26.42˚ (10.68 µm), accordingly. Significant differences (P < 0.05) were existed in angle of repose and slide among the red rice particles. Powder of 10.68 µm had a lower angle of repose and slide than the others followed by 26.35 µm (65.80˚ and 30.31˚) and 69.53 µm (70.84˚ and 35.50˚), the highest were 156.74 µm (74.67˚ and 38.99˚). As the angle of repose and slide increased so did the granular bulk become less flowable [13] .

As described above, superfine powders with 26.35 and 10.68 µm had better flow behavior and the surface attachment of the powder would also be higher, which was in agreement with the investigations of Zhao et al. [10] and Santomaso et al. [19] . The angle of repose and slide of red rice powders usually decreased with powder size reduction, the reason might appear to be the formation of aggregates. The aggregates tended to arrange in a cone the angle of which was much lower than expected for red rice powders. Therefore, the quality of red rice superfine powders would be better, and the mixture in food containing red rice powder would also be uniform and no separable.

As shown in Figure 1(a), the WSI increased with decreasing size at the same temperature. The WSI increased with increasing temperature, and significant difference was found between the different particles (P < 0.05). The values of WSI of red rice with particle sizes of 156.74 µm - 10.68 varied from 5.42% to 9.33%, 5.93% to 10.15%, 6.04% to 11.47%, 6.16% to 12.61%, for 60˚C, 80˚C, 100˚C, respectively.

Meanwhile, as shown in Figure 1(b), the WHC rised with the size decreasing, and significant difference was found (P < 0.05), however, no significant difference was found when the temperature of samples reached 90˚C (P > 0.05). The values of WHC with particle of 156.74 - 10.68 µm varied from 6.52 to 9.62, 8.23 to 11.66, 8.59 to 12.11, 8.70 to 12.34, for 70˚C, 80˚C, 90˚C, respectively. The results indicated that superfine ground enhanced WHC under high temperature of red rice, provided the better hydrophilic and avoided the water lose, which was favor to alleviate the retrogradation of products made by red rice powder.

As demonstrated in Figure 1(a) and Figure 1(b), it was noted that the WHC and WSI values of smaller particle size was higher than others during soaking. It might be due to the fact that after superfine grinding, the surface properties, such as surface area and surface energy had been increased. Moreover, the hydrophilic groups in red rice might had been exposed, which resulted in an easy integration with water, and the dispensability and solubility increased, finally, the value of WCH and WSI increased. The results indicated that the size was smaller for the red rice particle and greater for the solubilization and retaining water capacity of red rice powder.

Each value represents mean ± standard deviation of three replicates; different letters in the same column mean significant difference (P < 0.05).

The digestibility of different sized red rice powder by α-amylase was shown in Figure 1(c). The values of starch digestibility by α-amylase of red rice with particle sizes of 156.74 µm, 69.53 µm, 26.35 µm and 10.68 µm was 37.10%, 46.25%, 53.52% and 60.58%, respectively. Significant differences were found between the four particles (P < 0.05) and the enzymatic hydrolysis increased with the decreased parameters of red rice powder. After superfine ground of red rice, most of the crystalline state converted to a non-crystalline state with reduced mean granule particle size and increased granule specific surface area [20] , and structure of cellulose and hemicelluloses in red pericarp of red rice kernels was broken [21] , which made powder susceptible to enzymatic hydrolysis.

The scavenging activity on DPPH radical was related to the concentration of extracts, the activity increased as a result of increasing concentration for each stage (Table 2). The scavenging effect of extracts from four stages of FLJ flowers on the DPPH radical ranked as 10.68 µm > 36.25 µm > 69.53 µm > 156.74 µm, and was 92.62%, 88.41%, 80.03% and 74.28% at the concentration of 200 μg/ml, respectively. A significant difference of the scavenging effect on DPPH was found between particles of 69.53 µm and stage particles of 36.25 µm (P < 0.05), while no significant difference was found between particles of 36.25 µm and particles of 10.68 µm (P > 0.05). The order of reducing capacity in different sized particles at the amount of 600 μg/ml, comparing with the positive controls, was BHA > 10.68 µm > 36.25 µm > 69.53 µm > 156.74 µm (Table 2). Hu et al. [22] found superfine grinding enhanced antioxidant activity by increased extraction of green tea, although the differences were

The concentration of red rice extract was 200 μg/ml for DPPH radical scavenging activity determination; the concentration of red rice extract was 600 μg/ml for reducing power determination. Each value represents mean ± standard deviation of three replicates; different letters in the same column mean significant difference (P < 0.05).

not statistically significant (P > 0.05). Report in fiber from wine grape pomace showed that superfine grinding strengthened the ABTS radical scavenging activity and ferric reducing antioxidant power [23] . Observation in wheat bran dietary fiber, chelating activity and reducing power increased after superfine grinding, however, DPPH radical scavenging activity decreased [24] . These results above indicated superfine grinding treatment influenced the antioxidant activity depending on the methods employed for antioxidant activity determination and food materials.

Phenolic compounds including phenolic acids and flavonoid were a group of aromatic secondary metabolites ubiquitously distributed in natural plants, crops, fruits, and vegetables. These compounds were of great interest in the food industry due to their beneficial health effects [25] [26] . In the present study, we evaluated total phenolic contents in extracts of four sized red rice powder (Table 2). The most abundant total phenolic content occurred in rice of 10.68 µm, followed by rice with 36.25 µm, 69.53 µm, and 156.74 µm, and their contents were 12.98 GAE/g, 12.64 GAE/g, 10.12 GAE/g, and 6.36 mg GAE/g in extracts, respectively. The soluble phenolic compounds increased with the smaller particle, therefore, superfine ground enhanced the antioxidant activity and related compounds of red rice, which was in agreement with the observation in tea powder [23] and in dietary fiber of wheat bran [24] and wine grape pomace [23] .