NivaarExam PrepOfficial exam papers ↗

22-Mec-B2 Environmental Control in Buildings · May 2015

Question 8 of 8: Ideal R-134a vapour-compression chiller, and refrigerant environmental concerns

Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)

Notes on this paper

Paper format. Professional Engineers of Ontario / EGBC annual examination, 07-Mec-B2 (now 22-Mec-B2) Environmental Control in Buildings, May 2015 sitting. Three hours, open book. Eight problems of 20 points each; the candidate is instructed to solve five and to nominate on the cover of the first workbook which five are to be graded. Psychrometric charts and a pressure–enthalpy diagram for the refrigerant are appended to the paper, and candidates are expected to bring an environmental-control text and steam tables. Instruction 1 invites the candidate to submit a clear statement of any interpretation assumptions with the answer — that latitude is used explicitly below wherever the printed data are redundant or incomplete.

All eight problems are worked here. Every psychrometric state has been recomputed from the ASHRAE formulation for saturation vapour pressure rather than scaled off a chart, so the numbers below are tighter than a graphical solution would be; chart-quality agreement (about $\pm 0.2$ K in temperature and $\pm 0.0002$ kg/kg in humidity ratio) is all that an examiner expects, and a candidate reading the appended charts should reproduce every answer to within that band.

Reference texts for this subject.

Psychrometric relations used throughout. At barometric pressure $p$ with saturation vapour pressure $p_{ws}(t)$ from the ASHRAE correlation, the humidity ratio, specific enthalpy and humid volume of moist air are

$$W = 0.621945\,\frac{\phi\,p_{ws}(t)}{p - \phi\,p_{ws}(t)}, \qquad h = 1.006\,t + W\,(2501 + 1.86\,t), \qquad v = \frac{0.287042\,(t + 273.15)\,(1 + 1.6078\,W)}{p}$$

with $h$ in kJ per kg of dry air, $t$ in $\,{}^{\circ}$C and $p$ in kPa. In inch-pound units the enthalpy becomes $h = 0.240\,t + W\,(1061 + 0.444\,t)$ Btu per lb of dry air with $t$ in $\,{}^{\circ}$F. Wet-bulb temperatures are obtained by solving the adiabatic-saturation equation, not by eye. Mixing two air streams is exact in moisture and in enthalpy, so $W$ and $h$ of the mixture are the mass-weighted averages and the mixed dry bulb follows from them; weighting the dry bulb directly is the usual shortcut and differs here by about $0.01$ K.

Question 8: Ideal R-134a vapour-compression chiller, and refrigerant environmental concerns (20 marks: 15 + 5)

Question text not reproduced: the examination questions are © Engineers and Geoscientists BC. Open the official past paper (linked at the top of this page) to read the question, then follow the worked solution below.

(a) The ideal cycle

Given. An ideal (standard) vapour-compression cycle: saturated vapour leaves the evaporator, compression is isentropic, saturated liquid leaves the condenser, and expansion through the valve is isenthalpic. Pressure drops in the heat exchangers and lines are neglected.

Given data
QuantitySymbolValue
Refrigerant—R-134a
Evaporating temperature$t_{evap}$35 °F (1.67 °C)
Condensing temperature$t_{cond}$125 °F (51.67 °C)
Refrigerating capacity$\dot{Q}_e$20 tons (240000 Btu/h, 70.34 kW)

Find. The evaporator and condenser pressures, the refrigerant mass flow rate, the COP, and a comparison with the Carnot COP between the same two temperatures.

200250300350400450200300500700100015002000saturatedliquidsaturatedvapour1234condenser 1374 kPa (199.3 psia) at 125 °Fevaporator 311 kPa (45.1 psia) at 35 °Fisentropiccompressionthrottleq(evap) = 125.35 kJ/kgspecific enthalpy h (kJ/kg)pressure p (kPa, log scale)COP = 4.058
The ideal cycle on the R-134a pressure–enthalpy diagram. 1–2 is isentropic compression from saturated vapour to the condensing pressure, 2–3 condensation to saturated liquid, 3–4 isenthalpic expansion through the valve, and 4–1 evaporation back to saturated vapour.

Approach. Read the saturation pressures and the state enthalpies from the R-134a tables (or the appended p–h diagram), follow the four ideal processes round the cycle to get the specific refrigerating effect and the specific compressor work, and scale by the required capacity to obtain the mass flow.

  1. Saturation pressures. From the R-134a saturation table,$$p_{evap} = p_{sat}(35\,{}^{\circ}\text{F}) = 310.9 \text{ kPa} = \boxed{45.1 \text{ psia}}$$$$p_{cond} = p_{sat}(125\,{}^{\circ}\text{F}) = 1374 \text{ kPa} = \boxed{199.3 \text{ psia}}$$ a pressure ratio of $4.42$, comfortably within single-stage territory.
  2. State 1 — saturated vapour leaving the evaporator.$$h_1 = h_g(35\,{}^{\circ}\text{F}) = 399.57 \text{ kJ/kg}, \qquad s_1 = 1.7262 \text{ kJ/kg}\cdot\text{K}$$
  3. State 2 — isentropic compression to the condenser pressure. Following $s_2 = s_1$ into the superheat region at $1374$ kPa gives$$h_2 = 430.46 \text{ kJ/kg} \quad\text{at}\quad t_2 = 134.4\,{}^{\circ}\text{F}$$ so the discharge is superheated about $5.2$ K above the condensing temperature — a modest and realistic discharge temperature for R-134a.
  4. States 3 and 4 — condensation and expansion. Saturated liquid leaves the condenser and the expansion valve is isenthalpic:$$h_3 = h_f(125\,{}^{\circ}\text{F}) = 274.22 \text{ kJ/kg}, \qquad h_4 = h_3 = 274.22 \text{ kJ/kg}$$
  5. Specific effects and COP. Round the cycle,$$q_e = h_1 - h_4 = 399.57 - 274.22 = 125.35 \text{ kJ/kg}$$$$w_c = h_2 - h_1 = 430.46 - 399.57 = 30.89 \text{ kJ/kg}$$$$\text{COP} = \frac{q_e}{w_c} = \frac{125.35}{30.89} = \boxed{4.058}$$ As a check the condenser must reject $q_c = h_2 - h_3 = 156.24$ kJ/kg, and indeed $q_e + w_c = 125.35 + 30.89 = 156.24$ kJ/kg.
  6. Refrigerant mass flow rate. One ton of refrigeration is 3.5169 kW, so 20 tons is $70.34$ kW and$$\dot{m} = \frac{\dot{Q}_e}{q_e} = \frac{70.337}{125.35} = \boxed{0.5611 \text{ kg/s}}$$ which is $74.2$ lb/min, or $4453$ lb/h. The compressor then absorbs $\dot{m}\,w_c = 17.33$ kW ($23.2$ hp) and the condenser rejects $\dot{m}\,q_c = 87.67$ kW.
  7. Comparison with the Carnot cycle. Between the same two temperatures, expressed absolutely ($T_e = 274.82$ K, $T_c = 324.82$ K),$$\text{COP}_{Carnot} = \frac{T_e}{T_c - T_e} = \frac{274.82}{324.82 - 274.82} = 5.496$$ so the ideal vapour-compression cycle achieves$$\frac{\text{COP}}{\text{COP}_{Carnot}} = \frac{4.058}{5.496} = \boxed{0.738 \;=\; 73.8\ \%}$$ of the Carnot value. The shortfall is not inefficiency in any avoidable sense: it is the price of the two irreversibilities that are built into the standard cycle, namely the throttling valve (which replaces a reversible expander and destroys the work it could have recovered) and the superheat horn on the compression line (which pushes the discharge above the condensing temperature). A real machine, with isentropic compressor efficiency around 70% and finite temperature differences in both heat exchangers, would deliver perhaps 2.5–3.0 rather than $4.06$.

(b) Primary environmental concerns with refrigerants

Four concerns dominate, and they are best kept distinct because they call for different responses. Stratospheric ozone depletion was the original driver: chlorine and bromine released from CFCs and HCFCs catalyse ozone destruction, and the Montreal Protocol, implemented in Canada through the Ozone-depleting Substances and Halocarbon Alternatives Regulations under CEPA, has phased out CFCs entirely and is completing the phase-out of HCFCs such as R-22. R-134a, the refrigerant in this problem, contains no chlorine and has zero ozone depletion potential, which is precisely why it replaced R-12.

Direct global warming is now the binding constraint. R-134a has a 100-year global warming potential of about 1430, so every kilogram leaked is equivalent to roughly 1.4 tonnes of CO₂. The Kigali Amendment to the Montreal Protocol, which Canada has ratified, imposes a stepwise phase-down of HFC consumption, and Canadian regulations already restrict high-GWP refrigerants in new equipment. The industry response is the move to low-GWP alternatives — HFO blends such as R-1234yf and R-513A, and the natural refrigerants ammonia (R-717), CO₂ (R-744) and hydrocarbons — each of which trades the GWP problem for toxicity, pressure or flammability issues that must then be managed by design and by code.

Indirect emissions are usually the larger term and are easy to overlook: the electricity the compressor consumes over the machine's life typically dominates the direct leakage contribution. The total equivalent warming impact (TEWI) framework adds the two together, and it is why a modest gain in COP can outweigh a large reduction in refrigerant GWP. In this cycle the compressor draws 17.3 kW continuously; over 4000 operating hours a year that is roughly 69333 kWh, and on a fossil-fired grid the associated emissions would exceed the direct effect of leaking the entire charge.

Containment, safety and end-of-life complete the picture. Leakage is the mechanism by which every direct impact is realised, so Canadian regulation requires leak testing, record-keeping, certified technicians and the recovery rather than venting of refrigerant at servicing and decommissioning. Safety classification under ASHRAE Standard 34 and the machinery-room requirements of ASHRAE Standard 15 govern toxicity and flammability — the reason ammonia, for all its thermodynamic and environmental merit, is confined to industrial plant rooms. Some newer HFOs also break down in the atmosphere to trifluoroacetic acid, a persistent compound now under active study. Good engineering practice therefore means specifying the lowest-GWP refrigerant compatible with the safety class the occupancy allows, minimising the charge, designing for tightness, and treating efficiency as an environmental measure in its own right.

Final results
QuantitySymbolResult
Evaporator pressure$p_{evap}$45.1 psia (310.9 kPa)
Condenser pressure$p_{cond}$199.3 psia (1374 kPa)
Refrigerating effect$q_e$125.35 kJ/kg
Compressor work$w_c$30.89 kJ/kg
Refrigerant mass flow rate$\dot{m}$0.5611 kg/s (74.2 lb/min, 4453 lb/h)
Compressor power$\dot{W}_c$17.33 kW (23.2 hp)
Condenser heat rejection$\dot{Q}_c$87.67 kW
Cycle COPCOP4.058
Carnot COP between the same temperatures$\text{COP}_{Carnot}$5.496
Fraction of Carnot achieved—73.8%
Back to the paper →